Tag | Content |
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EnhancerAtlas ID | HS042-03501 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:203605160-203609390 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr1:203606392-203606404 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr1:203606392-203606404 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr1:203606390-203606405 | CTACTAAAAATAGAA | + | 6.57 | ZNF263 | MA0528.1 | chr1:203607244-203607265 | GGAGGAGGGGAGGGGAGATGG | + | 7.34 | ZNF263 | MA0528.1 | chr1:203607241-203607262 | GATGGAGGAGGGGAGGGGAGA | + | 7.5 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_00067 | chr1:203604360-203616001 | Adipose_Nuclei | SE_01479 | chr1:203604870-203605953 | Adrenal_Gland | SE_14468 | chr1:203606593-203608222 | CD4_Memory_Primary_7pool | SE_18521 | chr1:203606441-203608772 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19166 | chr1:203604811-203606059 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19166 | chr1:203606504-203608677 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_25804 | chr1:203604538-203608945 | Duodenum_Smooth_Muscle | SE_26726 | chr1:203604787-203606378 | Esophagus | SE_26726 | chr1:203606391-203609094 | Esophagus | SE_36167 | chr1:203604627-203606500 | HMEC | SE_40816 | chr1:203604708-203609103 | Left_Ventricle | SE_42264 | chr1:203604934-203606364 | Lung | SE_42264 | chr1:203606457-203609147 | Lung | SE_44861 | chr1:203604954-203605705 | NHLF | SE_44861 | chr1:203606743-203607292 | NHLF | SE_45901 | chr1:203604878-203606427 | Osteoblasts | SE_48668 | chr1:203604926-203606222 | Right_Atrium | SE_48668 | chr1:203606480-203609006 | Right_Atrium | SE_54514 | chr1:203604351-203615993 | Stomach_Smooth_Muscle | SE_64830 | chr1:203604851-203606333 | NHEK | SE_65767 | chr1:203604597-203606061 | Pancreatic_islets | SE_65767 | chr1:203606936-203608546 | Pancreatic_islets | SE_65767 | chr1:203608551-203609049 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 5 | ID | Chromosome | Start | End |
GH01I203635 | chr1 | 203604807 | 203606314 | GH01I203637 | chr1 | 203606744 | 203607292 | GH01I203638 | chr1 | 203607729 | 203608129 | GH01I203639 | chr1 | 203608141 | 203608310 | GH01I203641 | chr1 | 203608552 | 203609049 |
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Enhancer Sequence | TGGGGCCAGC TGAGGGAACC TGGGGACTGA GGGCTTCCAG AGTCACCCAC CTAACTTTTG 60 AGGAGACAGG TCCCAGGCTG TAAGAGAAGA AATTCACCAA ACAGCCCAGA GATTGTTGCT 120 GACCAAACCT TTAGTGTCCC TTAGAATTCT CTAATTAGGT GATTCTGAAA GAAACCAGCA 180 AGCAGTGCCT GCCTGGAGCC TTCATGCCTG AGCTAAGCAA GGCCTTCTAG GCACTCCCTT 240 GGCAAGGGCA GCACACCTGG CTGTCCTGTC ATTGACCCAA ATCATTGTGC TACCCACCCC 300 CGCCTCCCCA TCCTGATCGT CGCTCTGGAG AGAGATTGAG TTTCCAGGAT GGCTTCTCTC 360 TCTCTTTTTC TCCCTCTCTT CTCCTGGAAA CCCTGGGGCT AGGCCCTACA TGACTCAGGG 420 CTCTTTTTAC GTAGGCTCAT GTAGGTGACG GCTATTAATC CTTTAGTCAA TTCCCCTTCT 480 GTGTTGGTGA GGGAGCCTGA AAGAGCGGGA GCCAGGAAGT TGGAAGGGGG CAGACAGGGA 540 GGAGTTTGTT CTAGTGGGCT GCCAGGCTTG CCAGAAGAGC ACGGGACTGG GAGTCAGAAA 600 ACTGGTAATC TGGACTCTTG TCTGCTGTGT AACCTTGATT GAAGCAGGGG ATATCTCTGG 660 GCCTTCATCA ACTGCACTGT TACATGAAAC CAAGTTTGGA CATACAGACA TTCCTGATTC 720 AAGACCCTCC TCTTCTATAG AAGACAAAGG AGTAAAACTC TCAATGCCCA AACCAAACTC 780 TTTTATCACA GATAGAGTCT AGCACAATGT AACAATTTGC AGCCAAGTCC CATCCTTCTG 840 CCCAGGATGA CCAGGGGAAA AGAGGCCAAA AAGCATATGG CTTTGAACTG CCACCATTGA 900 TGTTTGGGAG TAGAACAGGT TCTAAGATTT CCCACCTCCA CCTGCCGGGA ACTTCAATTA 960 GGAAGTACCT TCCAAGGCCG TAATTCTGCT ATGTCCTAGG CCAGAAACTA AGGAATATTA 1020 GCTAGAGGTA GAGAAATTCA AACTTTCACA AAGTTTCCTA GGGCACATAA TCCCCCCAAA 1080 AGTTATTATA TTGAACCATA TGAAAATGCC AATATACGGC TGGGTGCGGT GGCTCACGCC 1140 TGTAATCCCA GCACTTTGGA AGGCCGAGGC AGGCGGATCA CGAGGTCAGG AGATTGAAAC 1200 CATCCTGGCT AACACGGTGA AGCCCCGTCT CTACTAAAAA TAGAAAAAAT TAGCCGGGCG 1260 AGGTGGCAGG CGCCTGTAGT CCCAGCTACT GGGGAGGCTG AGGCAGGAGA ATGGCGTGAA 1320 CCCCCGGGGG GGGGCGGAGC CTGCAGTGAG CCGAGATCGC ACCACTGCAC TCCAGCCTGG 1380 GTGACAGAGC AAGACTCTGT CTCAAAAAAA AAAAAAAAAA AAGCCAATAT ACAACCACTT 1440 TTGACCTACA AAGGCAATTT CATGTAGCTC ACCTAACAAT ATTATTCGAC ACTGGAATAA 1500 TGTCAGTGGC ATTACAGTCA GTGTTGTGAG CTGCAGAGAT TAGGTTTTCA TCTGAGCTGT 1560 GGGTTGGATT AGAAATTCAG GCAAAGTTGC CAGCTGCTAG GCCAGCTTAC CCTCCTTGCC 1620 AATCCAGACT TTCAGCCCTA GAGGTAGACA TGTTGGCAGA GCCCTTGTTT GGACTCTGGT 1680 TGAGATTCTA GCATTAGCCT TCCTGGCAAC TGGCCAGGGA AGCTGCCCAA GGTAGAGAGG 1740 AATGTATCAT CCATCTATAG TCTGCTTTTC TTGTGTCCCA AATGCCCTGC TTCCTATCTT 1800 GGGAGCTGAA GACGGAGGAA AATTTAAGAA AGGAGGAAAT GGAAATACTG GCCCTATTCA 1860 TCCTCTGTCT AGTGGGATAC AAGAGCGGGA ACACACACTT GAAATCTCAT CTGGTGCAGG 1920 GACACATGAC CTAGTGATGG CTGGTAACTG CTAATAGGAT GGCTGGGGGC TGAAGGGGTC 1980 TTAGTGGGAA TGGGGAGACT AGAATTTGGC AGGGCTCAAC TGGAAATTAT TCATGGAGGA 2040 GGTGATTGCC AAACAGGATT TTAAAGAGAA AGGACAGATT TGATGGAGGA GGGGAGGGGA 2100 GATGGGGAGG AAGGGGTGTG CTGCTACCAC CCGACTGAGG ACACTCAGAG CATCCTGGAG 2160 AATCGGATAC TCTGGCAGGT GAGGGAGGCT GTCTGATCCC ACTCGCTGGA AGGCCTCCAG 2220 CCTTTGTCTG AGCCAGTACC GGTACTGTGG GCAGGATGGC ATCTGGCCTC AGCAGCGGCC 2280 TGCCACCTGT CTGCTTTCCT GGCACTTATG GACCATTAGG ATGATTTTTT GATGTTTTCT 2340 CCCTGCTGTC CATATTACAG CCTTCTTTGT GGGGAGCACT CGTACGACAT CTGTTAGGAT 2400 GCAAGGACAG GCACAGCAAG CAGCAAGCAT CCATTCCAGG AGCTTTCTGA CCTTGTACAG 2460 GGGAGGACGG TCACCAGGCT TTGGGCTTGT CACCAGGCTC ATTTTACTGA GACAGAGCAT 2520 TTGAGATGGA CAGAGAACTG GCACCTCGAG ACTTGCCCAA AGACACTGGG TTAGTTTGAG 2580 GCAGAGGTGG GGGTACAGCC TAGTTCTCCC CACTCCAAGA CTGGGACCTC GACCCCATCA 2640 CTGCAACACT GTGTGACCAG ATCAACACCA AACTTCCCTG GTTCCCAATG TCTCTACCCA 2700 CATGGCAGAG AGAACTATCC CCGTCCCTCC AAGGTTGATG TGAGGTCATG TGCTAGGAGC 2760 AGTTTGGAAG ACAGATTCTA GAAACCATAA AGGTGCTGGT GGCATGATTG TTACTGTTGC 2820 TGTTATTATT AACAATTAAG GTCATTAGCA CACAGAAAAT GCAAAGAAGT ATTTGGCACT 2880 GCCCGTATCA CCGTGCAGCT CCTAACAGTC CCCTCCATGG CTCCTCCTCG CACACTGGGC 2940 CTTGAGCTGA GAGAGGCAGA GTAATTGAGA GGGGAAGCAG AAGTCCTGGG AAGAGGTGTG 3000 CAGAGATCTC CTCCTGCCGG GGTATTCTTG GCCCTACGCT TTCCTCAGGG TGTGCCTCCT 3060 CCAAAAGGTC AGAGGAAGTG CAGAGGGGAA GGAGGGGAAG CACTATTAAC TCCATCCTTC 3120 CTTAGCAGCT GACTAAGTCA GGTTGGCTGC TGAGCTCTGA TTTGGGATCT AAGAGTCAAG 3180 AGGGCGGGGC CACCATAATG TGACAGCACA GGCTGATTTG ATTGCCAGAG CCAATCTGTC 3240 ATTCATTTGC TTGTTCACTT ATCCATTTAT TTATCCAACA AACATGAAGC GAGCACAGAC 3300 CATATGCCAA GCACTATGTT AAGGGTTTGG GAAGAAGTGG TATCCGGGAG GCAAAGGAAG 3360 GGCTCAGCAT CACTGATGTT AAGCTCAGGG ATGATTGTCC CAAGCCTGGG GACTCACAGC 3420 AAGCCCCGCT TGTTGGTAGT GCTCTAGGGA GTTTGCATCT GTTTCCCTGG AGAGCACATT 3480 TAACCCTTGA CTTCAGGGAG GTAAGATCTA GACCCGACGC ACAACTGAGC TGGTAGGGGC 3540 CTTAGATATC ATTGCAGGGC AGCCCCTGGT GTTAGCAGTG AGACCATGGC CTGAATGGTA 3600 AAGGGCTTGC GCTTGTCCTT TGCTGAAGAA AGCCTTCTCC TGGACCAGGG CATGGTGCCG 3660 AAGCTGGGTG TGGGTCCAGC CTGGTTTATT CAGCCGCTCG GTTGGCCTCC CAGTGTTACC 3720 TGACTTTACC ATCCCCTGCT TATATCCGGA GCCTCTGCCT CTGATGGGGT GGAGATGTTC 3780 TGTTGCTGGG ATGCCCAGAG GAATCCAAAT GGTACTGAGA AATAGAACAA TACCTCTCCA 3840 GAGAAGCCCT CCAGTTCCTC CTCCAGTCTT TACCTCTCAT TTCAGCCTCT TAATCCCTAT 3900 TTTCAGAGGC AATGTGGTAT AAAGGATAAA GGAGTGGATT TAGCTTCAGT TGGTACATGC 3960 TGTACACATC TGCACCTAGC CTGAGTTTTG CCCTCTTTAA AGTTTGTATA ATATCGCCTT 4020 TCATTACTTA CCCCATAGAG TGTTATGACA GACAAATAAG GTATTGTAGG TAAAAGCATC 4080 CCATAAACAT TAAAGTGCTA GATATACGTA AAGCTTATTA TTCCGGTGAC CCCCTCTTCC 4140 TATTCCCCAC TCTTCATCTC AGTTCCTTCT CTTGACTGCC CAACCCCTTG ACCCCACTCC 4200 CAAGAACATC CTCCTGTTCT CTGTGTGTTC 4230
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