Tag | Content |
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EnhancerAtlas ID | HS118-13409 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr3:149995820-149997310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr3:149996877-149996890 | AAATAATTAATTA | - | 6.71 | TFAP2C | MA0524.2 | chr3:149996935-149996947 | TGCCCTGAGGCA | - | 6.18 |
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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 |
GH03I150277 | chr3 | 149995138 | 149997706 |
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Enhancer Sequence | TTGACTTGAA GCTGAATCTG TTTTCTCAAT TTTTTGAGTG ACTATTCTCT AAAGAAAGTA 60 TTATTAAAAG CAGACTTCCC CCAAATTGAC TTTAACAGCA ATTATTTTCT TTGAATATGA 120 GAAGGATATT TTGATTTCCC AAATGCACGT TAACTGAATT TTTGAACTGG ATCTTTTATG 180 GCTGAGTTTT CTCTATTTTT TTCTGTAACA GAAACATTAC ATTACATTGT CTCCCTGAGA 240 ACCCTAAAGC TGGAGGTTCC ATGGTATGTG TCTTGCATAA AATAAAACAG CAGATGACAG 300 CAAATTCATT TTCCTACTCT GCCATAGCTC CTATGGCTCA CTAACTTTTG AACTGTGGCT 360 GTGCTGAGTG AATTTTCTTG TCAGGCCCTG TAAAACTGCT TTACAGAGAG AGCAAAAGCA 420 ACTTGAGTTT TCTCAAAGGG ACCTGTGATA ATGGACAAGT CACACTGCTT TTCTGGGCAT 480 CAGTAACTTC TACTGTATAA ATAAGAACTT TCAGATAGAA TAATCTCCAG GGTTTGTTTT 540 TTTGTCTTTC TAGCAATAAA AAAGTATTGA CTCTGTTAAC CAATATTTAA TCATTTTAAG 600 TCAAACAAAA CAAATTTTTA CATCATTGTA GTGTTACAAA TGTATTTGGT TTCTTTTATA 660 CTGCTTAGAG ATAACTTCTT AAATATATAT TGGATTTCAG TATTCTATAT ATAAATTTGA 720 GCATTTCTTA ATGGGGGAAA AAGATTAAAA CTCATATTGG CTCAATTATA CTGGAGCAGG 780 GTGAGAACAT CTCACCAGGC AAGAGCAAAG ACAGCCCCGA ATGTCTCCTC CCCTTTGTTG 840 AAATATTACC AGCAAAACCC AAGTGATCAA AAAAGACTCA CAAATTATAT GGCAGTCCAT 900 GCCCATAAAA CATGATACAA TTCGGTCAAG GTACACTAGG TCAGTTGCTA AGAACCTCGT 960 GTTTCTTCTA GTAGTTACGT AAACAGTTAG ATGTGTTTGC TTTTTTTTTT TTTTTTCAAA 1020 GACTAAGGAA AAGGGAAAAT TGCCAACACA ATTACCAAAA TAATTAATTA AAAGCCAGCC 1080 CAGTCCGCAA CAGCTGCTTT CAGTTGTCCG GAGTGTGCCC TGAGGCAACA GCACCTTACA 1140 GCTCCTTTCT CAGGCAAGGA ATGCTGCCAT TATCTCGTTC TCAATGGAAA ACCACCTCCC 1200 CTGCCACATC CCTGTAAATT GTTGAACCTA AAGGGCTTTT TTCTCCACCC AGAAAAGAAG 1260 GTAATGGAAA CTAAAGTAGG CTGTTCAACC ATAAGCCTTG GGAAGCTTCC AAAAGCTTTC 1320 ATTCCTGTCC AGAAGCTTCT AAAGAGGAGG CCTACGATTA GGGAGATAAG CAATACTATC 1380 AAATTTTTGG AGCCTGGAAA TGCTTTCCCC AACCCCATTT TTCTTTTAAG TAAGGGACCC 1440 AGAATGAGAA ATAAATATTT GGGAAAGACA CAGGAACTAC ATTTCCATCT 1490
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