Tag | Content |
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EnhancerAtlas ID | HS113-33769 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr7:29415160-29416640 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr7:29415974-29415989 | GAGGGGCAAAGGCCA | + | 6.22 | LHX2 | MA0700.1 | chr7:29416590-29416600 | ACTAATTAAC | + | 6.02 | RORA | MA0071.1 | chr7:29415708-29415718 | TGACCTTGAT | - | 6.02 |
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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 |
GH07I029375 | chr7 | 29414986 | 29417104 |
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Enhancer Sequence | GTAGAGTTGG AATACTATGT GGTATTGTTC ATTGTTTTAG AAAAAAAGAA CTGATAGCAT 60 CGTGTGTTAC AACATGTGTT CTGCCATCCT CCTCTAGCCT ATGACAGCTG GAACCCAAGA 120 TCCCATTACT CATTGATCTC AGGTGGTGGT GGTAGTGAGA GTGTGGATCC AAACTGAGAC 180 ACAATTGTTA TGCGGAGGTA CTGGCTTTTG TAACACCAAC CTTACTCATC CAAACACAGA 240 GCAAATGTCA CACCTCCATA GGAGTTGCTA CCTACAGCAG CCCCATATTA AGTCTGCTCT 300 GTGACTCAGA GGTCAGGCCC CACAAGTTTT GGGGTGTAAC CAGGGTTATC CAGGAAAAGG 360 AGCAGGTGCA TAATGCTGGA GCTATAGTGA GGATTTAAAG ACATGCTTCA CATTTTGCTC 420 ACCTGGTTAA ACTGTAACTG AGAAATAATG CTGATAAAGG CAGGTTATAC TTTGCTCCAG 480 ATAAGCCATG TCTCCTACTG GCGTGTGGCC TGTCCAACCA AGCACTGAGA GGCTTGGACG 540 TAGATTTCTG ACCTTGATTC TGCTTTCCAT TGGAAAAAAT GTGGATGATG CAATCTCAGA 600 CAGCCTCAAT TTTAATATGA CTATGCTGAA TGATATTACC TAATTATTTA CTTGTTGTCA 660 GTCTTTTAAT AGAAATGACA GCTATCACAT ATGGAGTACT TCCTGTGCCC TGAGCACCGG 720 CTTCAGAGTT TTATGGATGC TACGCCCACC ACAATCCCAT GGGGCTTGTT ATCCCTCTCA 780 CTTTACACAG GAGGAAATGA GACAGGAAGC ACAAGAGGGG CAAAGGCCAG ATTCCAACCC 840 AGATAGTTCA TATCAATGGC TGGGCTTCTA ATCCAGTGAG TCACGGAGTG TGATCCCAGC 900 ATCAGCTGGG AACAGGTGAG AAATGCAGGT TCTGTGGCCC ATCCCACACC TGAATTACAA 960 ACCCTGGAGA TGGGGCCCAG CAATCTGTGT TTTAGCGAGC TCTTCAGGGG ATTCTGATGC 1020 CGCCTTGGGT GTGAGAACTA CTGTTCTAAG GACTGTTCTT GCTTCTCTCT GCTTTCTATT 1080 TCATCCTTCC TCCCTAATCC CTTAGGATAG AAGACTCAAG ATGCTTTTGC CTCCTGGTAA 1140 TGCTTGCTAT TTGCTCAGCA CTTGTGCTAG ACTATTCACG GATTTCAGTG TAGGCACCCA 1200 TAGCCTTCCT TATTTTTCCC AGATGTACTT CCTCCCAGAT GTTATTTTCC ACCCTTTAAA 1260 AATATTTTGT CTTTCTTCTT TGCTATTTCT AACTTTCCTG TACTCTTTTA TGTTGCAGAG 1320 ACCAAATGTG AATCCTGCTT GTAAGGGTGG GGTCAGTACT TGATTAAGCC TGATCTCCTC 1380 CCTCTACCCT CCATTTTCTG GTATTATACT TCTAATGTTA TGTTTGTGTT ACTAATTAAC 1440 AAAGCTATTT CAAATTCAGG TTTTTTTGTT TGCTTGTTTG 1480
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