Tag | Content |
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EnhancerAtlas ID | HS147-04326 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:205262440-205265710 |
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) |
FOSL2 | MA0478.1 | chr1:205263880-205263891 | GGATGACTCAT | + | 6.62 | IRF2 | MA0051.1 | chr1:205263976-205263994 | GGAAAGAGAAAGGAAAAG | + | 6.03 | JUN(var.2) | MA0489.1 | chr1:205263882-205263896 | ATGACTCATCCCCC | - | 6.22 | JUNB | MA0490.1 | chr1:205263880-205263891 | GGATGACTCAT | + | 6.62 | PRDM1 | MA0508.2 | chr1:205262631-205262641 | GTGAAAGTGA | - | 6.02 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_02431 | chr1:205262567-205264599 | Astrocytes | SE_05801 | chr1:205262462-205264469 | Brain_Hippocampus_Middle | SE_11085 | chr1:205262547-205264187 | CD20 | SE_26974 | chr1:205262635-205264492 | Esophagus | SE_26974 | chr1:205265274-205265884 | Esophagus | SE_29391 | chr1:205262567-205264765 | Fetal_Intestine_Large | SE_32765 | chr1:205262511-205264574 | H1 | SE_38936 | chr1:205262243-205265794 | IMR90 | SE_46173 | chr1:205262329-205265260 | Osteoblasts | SE_50327 | chr1:205262518-205264578 | Sigmoid_Colon | SE_52983 | chr1:205262582-205264598 | Small_Intestine | SE_54130 | chr1:205262477-205264677 | Spleen | SE_55645 | chr1:205263252-205263684 | Thymus | SE_56704 | chr1:205262588-205264656 | u87 | SE_56704 | chr1:205264714-205265918 | u87 | SE_58462 | chr1:205242169-205295027 | Ly1 | SE_58967 | chr1:205242236-205295022 | Ly3 | SE_60263 | chr1:205242326-205284722 | Ly4 | SE_60576 | chr1:205242267-205294889 | DHL6 | SE_61365 | chr1:205242037-205294994 | HBL1 | SE_61423 | chr1:205183427-205322469 | Toledo | SE_62465 | chr1:205242393-205294944 | Tonsil | SE_65493 | chr1:205262566-205265065 | Pancreatic_islets | SE_68815 | chr1:205262515-205265189 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 205262860 | 205263030 | chr1 | 205265393 | 205265497 | chr1 | 205262798 | 205264485 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I205293 | chr1 | 205262232 | 205274585 |
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Enhancer Sequence | CTTGATTTAA CTATCAAGTT CCCCTTTATA AGGGGCTGGG GCCAGGAAAG CGGGTGGAGG 60 CCCTTTATTA AACATTTATT GAGTACCTGT TCTCACTCCT TAGGTTTTCT CCAGTGATGT 120 ATTGCTTAAA AAGCATGTTC ATGTGTTGTC TCATTTAATC CTTGCAGTAA TGTGATGGGT 180 GTGAGCTGAC TGTGAAAGTG ACTCTCTAAG TCATTGCAAT GCACTCTGTG GGAAGAATGT 240 GCTAGCCCAG CAAGGCTGTC TTTGTGATGT CCGATGTGTA CGTGCGTGGG GAGGCGCTCC 300 CAAAAGCTGC GCTGGGGCAG GGTGTCCTGA ACGGCGTTAC CAGATGTATC TTGACAAAGA 360 GGTTGGCACC ACCATGAAGA CCAATTCAAC CAGCTCTCCT AGCCCAGCTT CCATGCTCTT 420 CAAGGAGACT TCCCACTGAA CTTCCGAATA CCCTTGTGTG AAACTGCCAC AGGCAGTGAA 480 TGTGCTCATC AGCAAACCCA AGTATCTGGT TGGTTTGACA GGGGTTTTGT TATTCATTAG 540 AAATGAATGA ATTGGCATGT TGGCTGAATC CATTCCTCTC CTAGAGCTCA GTGAGTCTGC 600 TCCTGAGCCT CCTAGCCTGT TGATAAGCAA GGTTTCTGAG CAGCAAAGTG AGGCTGCTCA 660 CTTTGGCAAA CAGGTCTTCA GGTGAGCCCG GCCACCATGT GAGGCCCTGT TGGCAGGCCA 720 GGCTCTCCCC AGGCCCCACC TGGCCTCACC AATGGCTCTT GGATTCACAG AGGACTGCAC 780 ATTGGACTGG GAGACAGGGC AAGCCAGGGG TCCCTTAGCA GAGAAGGGAT CCCTGCCAGT 840 AACTAGCCTG CTGTGAGTAT GAAGTTGCCA CTTACCAAGG ACCCTCCTGA TGGACACAAC 900 AAAGGCGATG GGTGATTGCT GCCAGGGCTC ATAAAGAGGT GATTCAGAAT CTAGCTGGGG 960 GAACTTTGAA AGGTCATTGC ACCTTGACCC TAGCTTCCAG GCGGGACATG TGGTGAGTTC 1020 TGCTGCAATG GCTGGGTGCC CTCACAGGCC AGAGCTCAGG TTAATGCAGC TCAGAGCTCG 1080 AATTCTGATC ACAGGAAGAG AATGGTGAGG AGGATGGAGG CAGGGGTGCT GGCTGGGCCC 1140 AGAACACCAA AGGCAGAGCT GAACACTTCC ACTGGGAAGT GGGGGTTTTG GCCTCTTGGG 1200 CTGGGAAATT CCTGGCCGGC ACTGTCTGTT TATCAGGGAA GCTGAGTCAG ACTGAAACGT 1260 ATCTCCTAAA AAGCTCTGCT ATTTCTAGGA TTCCATCCGG TCAAAGCCAG CCTCCTCTTC 1320 CCTGGGGAAT TCCTTTGAGG GTGGAGAGAT AGAGGGGACA GACTGGCCTT TTCCTAGACA 1380 TGGAAACCTG AAATCTGAGT TTTTGCCCAT TTATGGACCT GAAATCCCCT CCCCCACCTA 1440 GGATGACTCA TCCCCCAGCT TGACCCAACT GCCCCTAGAG AGGGGAAAGG GTGAAACTGA 1500 GATGGTGGGA TTAGCTCAGG GAGGGGGTTG GAGGCTGGAA AGAGAAAGGA AAAGACAACT 1560 GAAAAGGATG GGGAATTCCT TTGCAAAGAG ATGGTGAGGA GAGGATTTCA GAGCCAAAAA 1620 GAGGCAGAAT GAGAAAGAGA GAAAGATTTT CATCCCAGAG GGAAGCTGCA TGCCTGGCAG 1680 AGTAAAAATC TTCCAGGTTA AGGTAGGTTC AGGCCCTCAC CTTGAGTAAA TTCTGGAACT 1740 TTAGTGTGAT CAGAGCCACT TGCCGTGCTT GTGAAAATGC AGAGATTCCC GTGCCCTCCC 1800 TGGGCTGTGA TCCGCTTCCA GGCTCCTTCA GGGATCTGAA GTAGGAAGTT CTGAAACACA 1860 GAAAGAGGAT TGACTGGGAA TCCTTCTCCC AACCTGGGGC CTCTGCTGTA TAAAGCGACT 1920 CACAACCCCT CTGCAGGTGC CAATGTCAGA GGCAGAGCCC TGGTCCAAGG GTGACGTTTC 1980 TAACATTCTT ATAAAAATCT GTGAAAGACT TTGGCCAGGC CCAGTGGCTC AAGCCTGTGA 2040 TCCCAGCACT TTAGGAGGCT GAGGCAGGTG GATCTCTTGA GGTGAGGAGT TCGAGACCAG 2100 CCTGGCCAAC ATGGCAAAAC CCGTCTCTAC TAAAAATACA AAAAAATTAG CTGGGTGTGG 2160 TGGCATGCAC CTGTAGTCCC AGCTACTGGA GGAGCAGGGG GGCGCTGAGG TGGAGGATCG 2220 CTTGTGCTCA GGAGGTCGAG GCTGCAGTAA GCTGAGATTG CACCATTGTA CTCCAGCCTG 2280 GGCCACAGAG TGAGATCCTG TGTCAAAAAA AAAAAAGACT TTTTATCGGA TGGAGAAAGC 2340 CAGTCCCCAC CAGGCCAAAT ATGCCTCCTC ATTGCAGCAC TGCCCACCTC CCCACATAAT 2400 CATATCAGAG AAGCTTTGGA AAGAACTGCT TTCCTAGTCA ATACAATCCT AGGATCTTTA 2460 CAGCCAGAAG GGACTTCTTC AGGTATCATC TGGCGGGATT TTTCACCTGA AGCAGAAATT 2520 CCTTCTAGCA ACAACCCCCA CATCTCTATC TCCAACCCAA ATCTCTCAAA CTCCAGGCTC 2580 CTCATACCAC TTATCTTTGC CTGGAGGCCT AAGTGCCTCT GACTTCACCT CACACCTCCT 2640 CCATCTGCAA GTCTTCCCCG ACCCAGCTAA TGGACACTCT ACCCTCCAAG TTTCTCAGGC 2700 CAGAGACCAT GGAGTGATTC TTGGTTTCTC TCTTTCTTTC ATACCCTACA TCTAATCCAT 2760 CAGGAAAGCC TGTTGGCTCT AGCTTCAGAA TATGTCAGAA ATCTGACAAC TTGTCATTTC 2820 TTTACTACTG ACTCCAGTCC AAGCCCCATT ACCTCTTTCC AGAATTGGAC AATGTCGACC 2880 CTCCCATGGC TAGTCTCAAC AAGCAGAAGA ATTTTTTTTA ATTCTATCTC AAAAAAAAAA 2940 AATGTCATTC CTTTGCTCAG AACTTCCTGG TGGTTGGCAA TTTCATTCTG AATAAAAGCC 3000 ACAGCCCATG TAATGGTTCA CAAGGCCCTG TGTAATCTAC CTTCCCCACC CTTGTTACCT 3060 CTCCTGACAC GTCTTCTGCT ACTCTCTCAT GCACTCTGCT CCAGCATCAA TGGCTGTTCT 3120 AGAACTTGCA ACCTGCTCTT GCCTTGAGGC CTTTGCAATG GTTGTTCCCT CCACCCTGAA 3180 CACTGTTCCC CCAGATAGCC ACATAGCTAG CTCCACCCCC AACCCCTGCC ACCAGGTTTT 3240 TATTCAAATG CCACCTTCTC AGGAAGGCCT 3270
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