Tag | Content |
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EnhancerAtlas ID | HS187-01565 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:154411800-154416340 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:154415029-154415048 | TGCTGCCCCCTTGAGGCTG | - | 6.18 | EWSR1-FLI1 | MA0149.1 | chr1:154412339-154412357 | CCTGCCTGCCTTCCTTTG | - | 6.35 | EWSR1-FLI1 | MA0149.1 | chr1:154412335-154412353 | CCTGCCTGCCTGCCTTCC | - | 7.45 | HSF1 | MA0486.2 | chr1:154415937-154415950 | TTCTGGAACATTC | + | 6.67 | KLF14 | MA0740.1 | chr1:154415956-154415970 | GGCCCCGCCCACTT | + | 6 | MEF2C | MA0497.1 | chr1:154412922-154412937 | TTCTATTTTTAAATT | - | 6.5 | Nr2f6(var.2) | MA0728.1 | chr1:154413347-154413362 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr1:154414584-154414605 | GGAGGAGGAAGTAGAGTGGGT | + | 6.05 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_00437 | chr1:154410501-154413087 | Adipose_Nuclei | SE_00437 | chr1:154413491-154415294 | Adipose_Nuclei | SE_09189 | chr1:154410306-154416288 | CD14 | SE_14719 | chr1:154413221-154415159 | CD4_Memory_Primary_7pool | SE_16173 | chr1:154413285-154414084 | CD4_Naive_Primary_7pool | SE_16173 | chr1:154414342-154415773 | CD4_Naive_Primary_7pool | SE_17632 | chr1:154411908-154416448 | CD4p_CD25-_CD45RAp_Naive | SE_18405 | chr1:154410428-154416120 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19165 | chr1:154411944-154415379 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_26877 | chr1:154414476-154415277 | Esophagus | SE_26877 | chr1:154415829-154416690 | Esophagus | SE_41647 | chr1:154415442-154416643 | LNCaP | SE_42431 | chr1:154413450-154415385 | Lung | SE_50453 | chr1:154413392-154415195 | Sigmoid_Colon | SE_62668 | chr1:154357227-154415486 | Tonsil | SE_65390 | chr1:154413695-154415264 | Pancreatic_islets | SE_65390 | chr1:154415799-154416809 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr1 | 154411979 | 154412800 | chr1 | 154412800 | 154413166 | chr1 | 154414244 | 154414343 | chr1 | 154412049 | 154412363 | chr1 | 154414475 | 154414753 |
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| Number: 4 | ID | Chromosome | Start | End |
GH01I154439 | chr1 | 154411601 | 154412810 | GH01I154440 | chr1 | 154413232 | 154413861 | GH01I154441 | chr1 | 154414277 | 154415076 | GH01I154442 | chr1 | 154415443 | 154416809 |
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Enhancer Sequence | TATTTTTTGA GACGGAGTCT CGCTCTGTCG CCCAGGCTAG AGTGCAGTGG CGTGATCTCA 60 GCTCAATGCA ACCTCTGCCT CCCGGGTTCA AGCAATTCTC CTATCTCAGC CTCCCGAGTA 120 GCTGGGACTA CAGGCACCTG CCACCATGAC TGGCTAATTT TTATATTTTT AGTGGAGATG 180 GGGTTTCACC ATATTGGTCA GGCTGGTCTT GAACCCCTGA CCTCAGGTGA TTCACCCACC 240 TCAGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACC GCGCCCTGCC CATTTATATT 300 ATTTTTAAGT GCACAGCTCT GTGGCATTAA GTATTGTTGT GCAACCATCA CCACTTTACT 360 TCTCCAGGAC TTTTTTCATC TTGTAAAACT GAAACTCAGA ATCTGTTAAA CAGTAACTTT 420 CCTTTCACCC ACTCCTTCCC CCAGCTCGTG GCAACCACCA GTCTACTTGC TTTTTCTGTG 480 AGTTTGACTA CTCTAGTACT TCATTTGCTT GCTTGCTTGC TTGCATGCCT GCCTACCTGC 540 CTGCCTGCCT TCCTTTGTCT CTTTCTGTCT CTCTCTTTTT CTCTTTTTTT TTGAGACGGA 600 GTCTCACTCT GTCACCCACC CAGGCTGGAG TGCACTGTCG TGACCTTGGC TCACTGCAAC 660 CTCTGCCTCC CGGGTTCAAG CAATTCTCCA GCCTTAGCCT CCTGAGTAGC TGAGATTACA 720 GGCGCCTGCC ACCATGCCTG GCTAATTTTT GTATTTTTTG TAGAGACAAG GTTTCACCAT 780 GTTGCCCAGG CTGCACTCTA GGTACTTCAA ATAAGTGGAA TCAGAGAGTA TTTGTCCTTT 840 GGTGACTGAC TTATTTCACT TAGCATAATG TCCTCAAGGT TTATTCATGT GGTATAACAT 900 GTGTCAGACT TTCCTCCCTT TTTAAGGCTG AATAATATTC CATTGTGTAG AGATACCACA 960 TTGTGTTGAT TCATTCATTT GTCAGGGGAC ACTGGGTTTG CTTCCCCATT TTGGTTGTGC 1020 ATAATGCTGC TATGAACACG GGTGTAAAAT ATCTGTTTAG ATTCCTGCTT TCAGTTCTTT 1080 TGTGTATATA CTCAGAATTA TAATTGTGGC ATTATATGGT AATTCTATTT TTAAATTTTC 1140 ATGGAAATGC CATGCCGTTT TCCACAGTGG CTGCACCATT TTACACTTAC ACCAGAGTGT 1200 ATAAGGGTTC CAGTTTCTCC ACATCCTTGC CAACATTTGT TATTTTTCAT TTTGCTGCAA 1260 TAGTCCTCCT TATGGATGTG AAGTGTTATC TCACTGTGGT TTTGATTTGC ATTTCCCTAA 1320 TGATTAATGT CTTTTTTTTT TTTTTTTTGA GACAGAGTCT CACCCTGTCA CCCAGTCTGG 1380 AGTGCAGTGG GGCGATCTTG GCTCACTGTA ACCTCCACCT CCTGGGGTTC AAGTGATTCT 1440 CGTGCCTCAG CCTCCCGAGT AGTTGAGATT GGCATGCACC ACCACACCCA GCTAATTTTT 1500 GTATTTTTAG CAGAGACGGG GCTTTGCCAT GTTGGCGAGG CTGCTCTTGA ACTCCTGACC 1560 TCAAGTGATC TGCCCATCTA TGCCTCCCAA AGTACTGGGA TTACAGGCGT GAGCCACCAC 1620 ACCCAGGCTG AGGATCTTTT CATGTGCTTC TTGGCCATTC ATATATCTTT GGAGAAATAT 1680 CTATTCAAAT AGAAAGTTCT TTCTTATGTG AACCTAACTC TGGCCTCACT GGCCCTTGCT 1740 CTGTTCTCAG GGATAACCAA TGACAAATTT CCTAGTCTGC TCTCTCTGAA TTCTTTTGGA 1800 GTTCCCAGAC CTGCATCTGC TTGGGCTCCT CTTCCCAGGC TGTTACATGA GATGGTCTGT 1860 GAATTCTTCA CCTTTCTGGC CCCCTTCCCC TGAATCTGGT CTCATTTGTG GATGTCCCTC 1920 TTTAAGTTGC TGACACTCTC CTTCTATTGG AAGATGGTGT GGTGGGGGCT GTCTGGCCAG 1980 CACTGGGTAC GGTCTCCACT TTCCAGCCTC AGGTGGATGT GCTTCTTTGG CATAGACACA 2040 GCTTCTGTGG GAGCTCAGAT AGAACAGTCG GTTTCTTCTC ATGTAAGGAG CGGAAGACTT 2100 TGAGCCCTCC ACCCTATGCA TGTGTGGTTT GAGGCAGGGG AAGTCTTCAA AACCCAGTTG 2160 TGAATATATC CAAGAAAGAA ACCTGCTGCT CCCCTCTCTG CTGAGGGAAG AGCAAGAGGA 2220 ACTTGGATGA TTTTGACGCA AGAGGGGGAT TCAGGTTGGA AATTGGCGGG CAGTTCTGAA 2280 AAATAAGGGG AAGGTTAGAG CACTAGGTGA GGTGTGTGTT ATGGACCACG GTTATTTGGC 2340 TGTTAGGGAC GCATCAGTGT ACTAAACACT GTATCACCGT GTGGGGTGAG CTTACCCACC 2400 CCAAGGACCT TCAGCTCTCA AGGCCCAGAC AGACAGGATG CACCTGCCTC CCAGACTAGG 2460 TGTGGGAGTG GTGGCCTTTG GGAGACACAG AGGTCCTGGG AAGCACCTGG GAGTCAGGTT 2520 GTATGACACT GGTAAAGTTA GTTCAGCTCT CAGAGCCTCA GTCTTGTCAT CGGTAAAGTA 2580 GAGATGATAG CACCAATCTT GTTCCTTTCA GAGAGTTTTT GTGAGTCTGA TGAAAAAATA 2640 TTCTTTAGAA ATGCTAAAGC ATACTGCATT TGTAAGGGGA TCAGCAATTA CAGGACAGTG 2700 CTGGTTCTTG GGAGGAGAGT GGGACCAGGG GCATCCCAGA ATCACTATCC TGGATGCCAT 2760 CGTGAACTCA CTGCATTGGA ATCTGGAGGA GGAAGTAGAG TGGGTGGTTT GAGAAAGCTT 2820 TCCTGGTGGT TTTAGTATGT GCTTGAGGGG GCTGGAGGAG GGTGCGTGCC CCACTGTAGT 2880 ATGTCTAATA CGTAATAGAT GGTGTTCACA GCACGATAAG GCCGTAAGCA GACTGTTCTG 2940 TTGGGGCAGT TTAGAGATAG CAGGAAAAGC TTCATGGAGG AGGTGACAAT TGAATTATGT 3000 CTTGAAGGAT GTGTAGGAGG GTCCCAGACA GAAAATGGGG ATTGTAGGCA GAGTACAAAG 3060 GCACGGAGCT GTGAGCAAGG GGAGGGTGGC AGAGAGCTGC TTGGTGAGGC CGACACGTGT 3120 GTGGGTGGGT GGTCTGAGTG GGACAGGTGG AGGCCGGCCT TGGTGGGCCC CTGTAGGAGT 3180 GGAAGTGGAA TGCCATAGAG TGGGGCTCTG GAGCCTGGAC TTCAGCAGGT GCTGCCCCCT 3240 TGAGGCTGGG GCCTGGCCCC CCGCACAGAC TGTAGCCCAG GATAGCCTTT TGTATGAAGT 3300 TGGGGGTCCC AGGGTCACTC TGTCTTAGCC CTGCTTTGGC CAGCAAGGCC AGCACGGTCG 3360 GCAGCTTTCT CTCAAGCGGG AGTTCTGAAT TTATCCTCTC CTGATGGGAG TTCTCCCTGT 3420 CACATCAACA TTGAGTCTGG GGGAATCACA AAATCATTTT CTTCTTTTTT TTTTTTTTCA 3480 GAGATGGTAT CTCATTCTGT TGCCCAAGCC GGAGTGCAGT GGCATAATCA TAGCTCACTC 3540 CAGCCTTGAA CTCCTGCCTC AGCCTCTGAG TAGCTAGGAC TATAGGCATG CATCACGATG 3600 CCCAGCTAAT TTTTTAAAAA ATATTTTACA GAGATGAGGT CACCCTATGT TGCACAGGCC 3660 TTGAGTGATC CTCCTGCCTC AGCCTCCCAA AGCTCTGGGA TTTATAGCCA TGAGCCACTG 3720 TGCCAGGCTG GAGCCCCTTT TCAAAGAGGG CGTGGGGCAA AATGCCTGGG AAAAGCCCAT 3780 TAGGTATAAG GGGGTTATTC CTTGCTTCTC ACAAATAATC CCTTTAACTC CCTCTCCTAT 3840 TCCCCAAGAA TGGGAATCAC ACCTGTTGGA GGAGGTGATA CCAAAGGTTT GCATTTGCAC 3900 ATGAGGGGGT GCCCTGAAGC CAGGACTGGG CGGTCAGTGC CTCCAGCTAC ACGTTATCTT 3960 CTCAAACTCT TTGGCCATCC ATTCTGGAGG AGTTTGTTTT GTTCCTCTCT GCAGCACTCC 4020 CAAGTGGGAC ATTCTGGGGT TAAAGAGCCT TGGTTACACA TTTCCGGAGA GATTTTGCCC 4080 TGTTCACTTA TCCATATGGC ATCCCTGAAT TCCCTCTCTG CCCTGTTTTC TGCAGCTTTC 4140 TGGAACATTC CACTGGGGCC CCGCCCACTT CCACTGCATC ACCTGCCACT TTGTGCAGAG 4200 CACTGGCTCT GGAGTCAGGC AGCATTGGGT CTAGTTGCTG CCCTTGCCCT TGACTAGCAC 4260 GACCCTGGGG AAGTACCTCA CTGAGACTCA GTTTGCTTAT TTGTCAAATG GGAATAATAA 4320 TGCCTGCCTC AAAAAACCCA AACCCCAGCC TTGCTGGGTT GTGAGGCTTC AGTGAGGTGA 4380 GAAGCAATTA GCACAGAGCC TGGCACATGA CAAGGGTGCA ATAAATGCCA GCATGACTGC 4440 CTTTCACCCG TATCTCCTGC CAAGCCTGTC TCTCGAGCTT TGGATTCATG TCTTCAACTT 4500 GGCCCAGACT TCTGGCCAGA TCCTCCCTCC TGTGCCAGGT 4540
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