Tag | Content |
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EnhancerAtlas ID | HS118-16127 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr6:43117620-43119000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr6:43118240-43118252 | TTCTGTTTACCT | - | 6.14 | Nr2f6(var.2) | MA0728.1 | chr6:43118779-43118794 | TGAACTCCTGACCTT | - | 6.04 |
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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: 2 | ID | Chromosome | Start | End |
GH06I043151 | chr6 | 43117769 | 43118043 | GH06I043150 | chr6 | 43118161 | 43118310 |
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Enhancer Sequence | GGGAGGTGGA GTGGTAGGCA GGGTGTTCCC TGGCCAGCTA GAGTTGGCAC CAAAGTGCCA 60 TATTGGGTGT GAGTGGGCTG AGGGGAGCCT CAGGAGGATT TTAAGAGAGC AGTGAGTTAG 120 TGACAGAAAT CAAAGACATG GGTCCTGGGT GTTGGCATAA TGGTAGGTAA TGCCTTTTAG 180 AGTAGCTGAT AAGATGATAT CAGAGAGCTG TAATCTGTGA TTGCTTCATG GATCACTTGT 240 GAACTAATGA TGTGATGAGA AGCAGGATCA GCTTAGCACA CCTGGTGGAC CATGCTTTAT 300 GCAGTCAGAT GCCGTGGCAG GAAACAGAAG GCCTCTTGTG AGATCTCATA GCATCACAGT 360 GGGTTAGCCA GAACATGGGC AAACCCCTGG GGTGTTAAAA TTGGAAAGGA AGGAGTGGGT 420 CTGATCTTTA CCAAAGAACG GGTCTTTTAT AACAGTATTT GAGAATTACT CCAGTGGCTA 480 TCTGATGGCA TCTTGCCCAG CATAAAGGAA ACACCGAATT GGCTTGAGTC TAACAGAATT 540 CCCTTTTACT GCCCTTGCTT TCCGGAAGCA CCACCTCTCT GGAAAGATAG CAAGTCAGTT 600 ACCATGCCAA GTCCACCTTC TTCTGTTTAC CTTGACTAGC AGCAGATTGT TTAACTTGTG 660 AGCCAGATCA GAGAGAGCAG GCCAAGGGGA CTCACAAGTC TGATGAGGGC ACGTTACCAA 720 AACCTTTGCC TGCCGCTTAC AGAGAATCAA GCAAGGTTGG ACAATGCCCT GGGATTTTGA 780 AGCCTGAAGT GGAGTTGGCT CTGTTTATGA TGGCCACTGA AGCAGCCTGG CCCCTTTACC 840 ACCAGTGCAC CTGAGGCATT CTGAGGACGG TGCTGCAGGG GTTATTTTAG GGATGTAGAC 900 TCAGCTTTTT TTTTTTTTTT TTTTTTTTTT TTTTCCCGAG ACAGAGTCTC GCTCTGTCTC 960 TGTCACTCAG GCTGGGTTGC AGTGGCACCA TCTCGGCTCA CTGCAGCCTC CGCCTCCCAA 1020 GTAGCTGGGA TCGCTCTTCA AGCGATTCTC CTGCCTTAGC CTCCCGAGTA GCTGGGATTA 1080 CAGGAGCCCG CCACCACACC CAACTAATTT TTGTATTTTT AGCAGGGATG AGGTTTCACC 1140 ATATTGGCCA GGCTGGTCTT GAACTCCTGA CCTTGTGATC CACCCACCTT GGTCTCCCAG 1200 AGTGCTGGGA ATATAGGTGT GAGCCACTGT GCCCAGCCAG ACTCTGCTTT TTCATGGAAA 1260 CCCCAGTGTA CTTCCCTGTA CCCAGAGAAG AGAGGCCCAG TAATCCTGAC ATGCCATCCA 1320 CCTGCCTTCT TTTTTTTTTT TTTCTTGAGA CCGAGTCTCG CTCTGTCGCC CAAGCTGGAG 1380
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