Tag | Content |
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EnhancerAtlas ID | HS118-13384 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr3:148755270-148756830 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr3:148755394-148755406 | CCTGAGTAAACA | - | 6.37 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAAAAAAGAA AATACAACAG ACCATACCAT ATCCATGATA TTCACCCATG AAGGCCTAAG 60 TATGATGACC CTAGTTATAA TCTTACTGAG AAGGATACCG TCAGTTGAGG GAGGAAAAAG 120 GAAGCCTGAG TAAACATATA TGCATCAACA AGGTAGCCTC ACCCAAGTAA CTAAAATTTA 180 TATCTCAGTA GTATTCCTAC ATGTATCTCA GTAGAATTCC TACATGTTAA AAATCTTCTG 240 AGTTTCAGGT AACAAGTTAC AACCACAAAT CTTAAGTCTG AATGCACAGA AACAGCAGAG 300 GGTTGCCTTT AGCCCACATA GTACCCAGTG CAAATTAGAA ACTGAATTAG TCCAAGGTCC 360 TCTCAGGCCA AACAGCCCCT TTGTACACGT AGAAAAACAC GCTCCTATGT GAATGCACGT 420 CCAGGTCACA CAGCTTGGTG AGTAAAGTTC AAAGTGAATT TTAGCCTCTG TTCTACCTTC 480 ATGCCTGTAC TACACAACCA CAACTGACTG CACTATATTA GGCATTAAAA CGTACTCAGA 540 ACATTCCATT AATGATAATT TGTTTCTCAA ATTGTGATCC TAGACCACCT GTACCTCAAT 600 CACCTATGAT ATATGCTAAA AATGCAGCTT CCTGGGTCTA ATCCTAGAAC TCCTAAGTCT 660 CTACGTTGAA TGCAAAGGAA ATTGCATTTT ACCTAATTCT TATGCACATT AAAGCTTAAG 720 ACTACTAGAA CCGTGATGGT AATCATTTTG TCTATCTTGT TTATAGTTAG ATTCCCAGTG 780 CCTATAAAAA CTGACGCAAA GCAGGATCTC ATTATTTGCT GGCTGAATGA ACCACTACCC 840 TAAAAAGCAT TACAGTTAAT ATTTATTATA GAAGAAAAGT AGAATAGCAT AGCATAATAG 900 TACTTAAATA TTTACATGGA CTATGATTCT GGTTTTGCCT ATTACTAACT GTATGATACT 960 GGGCACATTA TTTACTTTTC TGTGCTTCAG TTGCCTCTTC AGTAAAACAG AGCATTTTTT 1020 TTCTTTTTTT TCTTTCAGAG ACGGGTTCTT GCTCTGTCAC CCAGGCTGGA GTGCAGTGAC 1080 AGGAGCATGG CTCACTGAAA CTTCAACCTC CTGGGCCCAA GCAATCAATC TTTCCGACTT 1140 AGCCCTGCAA GTAGCTGGGA CTACAAGCAC AAACCACTAC ACCAGAGTAA CTTTTCTGGT 1200 ACTTTTTTTT GTAGAGATGG GGTTTTGCCA TGTTGCCTAG GCTGCTCTCA AACTCCTGAG 1260 CTCAGGCAAT CCATTCACCT TGGCCTCCCA AAGTGCTGGG ATTACAGGCA TGTGCCACAG 1320 CACCTGGCCA AAACAGAGCA TTTAATAATG GTATCTACCT CATAAGGATG TTGTGAGGAT 1380 TTCAGTAAAG TGCTTAAGAG AAAGCTCTTA ATCCACATTT ACTAAGTTTT TGTTATTTAT 1440 TTCTAAAGTT TGCCTAAGAA TTTTCACAGT TAATTATAAC TATGAAGGTA TTTACCAAAT 1500 AGTTTTTTGT CTTATTTTTT TGAAAGAAGT ACTAAGATTC TGAAAAAATT TACAGAACTA 1560
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