Tag | Content |
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EnhancerAtlas ID | HS095-20625 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr3:54076010-54077360 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr3:54077189-54077200 | TCAAGGTCATT | + | 6.32 | Esrra | MA0592.2 | chr3:54077188-54077199 | CTCAAGGTCAT | + | 6.02 | Esrrg | MA0643.1 | chr3:54077189-54077199 | TCAAGGTCAT | + | 6.02 | Nfe2l2 | MA0150.2 | chr3:54076423-54076438 | TGCTGGGTCATTGTG | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCCCCTGCTA TGCCTGGAAT AGGCAACGTG AGACCTAGGA GGCCTCGTGC ACTTCCCCCA 60 CCTCCCTGCC CTCTAGGACA CATGGTGCAG GGCAAGGCCA GCTCTCCTGG GGAGGCTGAG 120 TGAGGAATGG AAGGAGGTGT GGGGCTTTGC TGCAAGTCTC CTCCTGGAGA GGAGAGAATT 180 CTCCCTGACC CTTATCCTAC AGAGAGTTTT GCACCTTACT TCTGTCACTA GACCAAATAT 240 ATTTGGACAT CTTTCTATGT CAGAGCATAG GGATCCAATC CATTCTGTTT AGTAGCCGCT 300 TATGACTCCA CTGCTTGGGT GGCCTGATGG ATCCTGATCT CTAAGCACTC TGAGGCCTAC 360 CCACTGCTTT TGCAGTGCAT CAGTTCTGGT GGACCCTCAG AATTGCCCCA TTGTGCTGGG 420 TCATTGTGGA AGTGTGTGCT CTAAACATAA ACCTCCTAAA AATAGTCTTT CTGAGTTTGG 480 TGCTTGTGTA TCTCTCAGTG AATGTCTGCC AACTGGGGCC GCAAGGCTTC CATTAACAAG 540 AATCTCTGAG CAGGTCCTGG GGCCTCCAAA GGAAGGAAGT GGAGTCAAGC CTCTGCCACT 600 CCTTCCAGGG CTGAGGAGTG CTCTGCATTT GAAAAGGCGG GTGTGTGATA CCCTGGATGA 660 TATCCCTGTA TGAGCTCATC TTCCAGGAAT GAAAAGGAGG TGTTCTTTGC CTTCAGGCAG 720 GTGAGACTTT TGCCCTGTAC ATTTGCTTCT ATTGCACACT CAGTTGGCTC TTTCACTGTG 780 CACACTACAA TTAGTGAAGT CTGTTTCGTG CCTGCCACTC CAGGAACAGG CTTTAGACGG 840 TCTTTCATGC CCCCTTTGCT TTATTCAGGG TTTTCATAAA TAATCTTTCT TCTCGCTTAC 900 CTTTTCTTTT CACCTACAAT ATCTGAAACC ACGTAGAATG TTGCCTGCAT ACAGCTCAGC 960 ATCCTTGCAC GGCTCCCCTG TTTAGTTAAA GTGGTTATAG TTTTAGCCTA TTTATTAGTA 1020 AGTAGTTGTA ATTTACTGAG GTGTTGGTGT GCAGCAGGCC TTATGCTAAG CGCTTTGTTG 1080 GAAAAAGCTC CTGGAAGCTT CACCACAGAC TGCTCTTTGA GATATTTTTG TCAGCCCCGT 1140 TTTACAGAGG AGGAAACCAA GGCTGAGGAA GTGACACACT CAAGGTCATT GAGCTAGAAA 1200 GTGGTTGTAT CTGAATCTAT GCCAGCTTAG AAAACCTCCA TTTTTAAGCC CTCTGCCATG 1260 CAGAATTTTT GCCTCACCCC CTCTGTAGGT TCACTGTGGG TCCCCGTAAG AACAAGGTTA 1320 TTCAGCTTCT CAGGAGGACA AGGAGAAATT 1350
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