Tag | Content |
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EnhancerAtlas ID | HS092-05395 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:246957510-246959050 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr1:246958047-246958059 | CAGTAAACAGAA | + | 6.02 | PAX6 | MA0069.1 | chr1:246958948-246958962 | CACTTATGCGTGAA | - | 6.09 |
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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: 1 | ID | Chromosome | Start | End |
GH01I246794 | chr1 | 246957671 | 246958925 |
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Enhancer Sequence | CGGCTGAGTA CCAGCTTGAA TGAAGTACTT GAGCACCCTG GTGAGCTGAG GGTCCTCGCT 60 GAGGTTAAGA AGGTGAGGGA AGGTCATCAT CTGCCGCTCC TGCAGGAGAA GTGGAGAGGG 120 TTGGGTGTCA CCAGTCCGCA CCAGCCCACT GGGGAGAGCA ACACTTCTTT CCCGTCTCTG 180 TGCACCTTGT CAACCCTCCT GGGGAGGGAG GAAAGCTGAG AGGGGCTGGG GCATTGCTGA 240 TGGTGGGGTG GAGTCTCAGG CAGGCCAGCC GTCAGGAGTC TGAGTACATC TGGACTGGAC 300 AGTTCCAAGG AGCTGTCTCC CGGCTGCCCT CCCCAGCTGT CTGCATGCCC CGCTCTGGTC 360 CCCTGCCTGG GCAGCCCCTC CCCATGTCTC CATGCAGCCT CTCATTCTCC CGAAGTGCTG 420 CTGGCTGGCT GAGAATCAGA TGTTGATGGC AAAAAGTGGG GTATGGCACG AACCCTCGCC 480 TGGCAACCTG AACATGTCAT TCGTCCACAC AAGGATTGTT GTGGCGTAGG GATTTGACAG 540 TAAACAGAAC GGGGATGATT ATGCAGCCAC GAGGAAGACT TTTACAGCTT GAAATCCTCT 600 CTGACAAAGA GTAAAGAGGG CAAAAACCCT TCCAATTTTT ACTGTATATG CAGAACCCAA 660 AATCCCGTAT TCCTCCATGT GACCTTACTT GACCCTTGAA GCTGAGAGTC CCAGCCACCA 720 CTTACACAGA ACGTGACTCA GTACAGCCCT AACTGTCTGG TTTCCTGATG CCACAGACCC 780 CACCCTGCTC CACCCCCCAG GCCCTGAGGC CGTAGTTAGG CAGTATGAGG TTCCGGAATC 840 CCCAGCTCCA GTCCCCTAGT ACTCCAGGTC TGATCCTCAA CTTTGGGATT TTCCCAGGGC 900 CTCGTGGCCA CGGGGAGTGG GGTGGGGTGG AAGCCGGGGT GGCCAGGGGA GGCCGAAATT 960 CAATCACAGC CCATTTAGGG TGTGATATCA TCAGCGAATG CCAGGATAGA CACCCGGCCT 1020 TACGCCCTGC CAGGCCCCGA GTCCTCCCCG TTTCCCTCGC TGGCATGCCC TGATGTTCTC 1080 TCCCTAGCTC TGCCAGTAGC ATCATTACCA GTCACACATT ACACATTCAC CAAAAAAGCC 1140 TCGCCACAGT CGGGCCTGGC CAGCCAGACT GCAGCCTGTG CCTGGCCCCC TGCCCTGGGC 1200 TCAGCCTCCG CAGGTGGCGG AGGTGAAGCT CACCTGGGCC CTCTCCAGCA GGTGTGCCCA 1260 GGTCACCTGA TCAGGAGTCC CCAGCTGCTG CTCTGCCTGG AGACAGGCCG ACGGCTCTGG 1320 AAGGAGGGAG GCATTTTAAG CGGCGGGTCT GCGGTGCCAG GGGGAGTCAC GGGATAGCTA 1380 GTGTGTCTCT GGCTCTGTTC TCAAAGCCCA GGATCCCGGC AGCAGCAGGA ATGCAGCACA 1440 CTTATGCGTG AAGACGAGAT CTTTCGGTAA GTCCTACAAA GAGGACTTTT AATTCCCCTC 1500 CTAATTCGTA AGACGTTAGT GCAAGAAGGT CCTTTAAGGG 1540
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