Tag | Content |
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EnhancerAtlas ID | HS118-16612 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr6:137469260-137470670 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr6:137469361-137469373 | GTTTGTTTGTTT | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH06I137147 | chr6 | 137468960 | 137470834 |
| Enhancer Sequence | TTATAAATGT AGGGAGTGTT AGATTCTTAG CAGAATAAAG ATGGAAACAT ACAAATTACT 60 TTCCTCTGTT TATTGGAAGG GCTTTTCTTA ATCTGACTTT TGTTTGTTTG TTTGGTTGGT 120 TGGTTTTGGG TTTTTTTTTG AGACAGGATC TCATTATGTT GCCCAGGCTG GGCTCAAACT 180 CCTGTACTCA AGTGATTCTC CTTCAGCTTC CTGAGTAGCT GAGATTACAG GTGCATGCCA 240 CCACATCCAG GCTAGTCTGA CTTTTTATTG ACAGTGTAGC CCTTGGAGGT TCTAAGACTT 300 TTGTAGGGGT ATTAGTTCTA ACTCCCTGCC TTGTGCTGGC CTAAAACCTT GTCTTTTGTC 360 CTGGGAGTGG CTGTTACCAC TTAGGGTCTA GTTACCACAT CCAGCAAATG CCTTCAGGGC 420 AGCTGGGGCA GTCACTGTGT TGGTCTTCTG GTTCCCCTTT GATTTCCGTT TACTTTGTTT 480 TGGCCCCCAA GGATTCCCTT TATTTTTATT TTTGCCCCTC TGTGGAGTTT GGAGAATGTG 540 TTTTATCCAG AATTTCTAAG TGTTTTAGAA GAAGAGAGTT TCCTACTCCC AGGCTATTTA 600 ATTTGGAACC ATAAGTTTTT AAAGCACTTT CCAACTATAT TGGAATAATG GGATAGTTAA 660 CTTTAAATAA ACATGTCCCT TTTGTAGTGA GGCACATATT TCAGGCATTG TCCTATCAGT 720 GAGTCAGCTG CGGACATCAC AGGGCTCCTG GCTTATGATC TGTGATGCTA GATTTTGCAA 780 TTGATTGCAA AATCAGTTTT GCAATCAGTT GCAAGTTTCT TGACCCATTC ACTGGATTGT 840 GATTGTGTTA CAAGACCAAG TCAAGATTAT TTGACCTCAT AGCACTTTAC TCTTTAACAG 900 CTCTCTCCTT GAAATATTAC CTTCCCGCAC TATTCATGAA CATATCAGCC CACAGATTTC 960 CTCCTACCTC TTTGGCTATT CCTTCTCAGT CTCCTTTTAA GATTTTTCTT ACTCAGGCAT 1020 CTTTGGGTGA AAGTCCCTCA ATATCTGGTC TTACTCAAAA CTGCCTCTCA CTCACTACTC 1080 TCTCCCTAGG CAATCCTATC AATGTCCACT GTACTGTATG CATGAAATGA CTCACAAATT 1140 TTTGTCTCTA ATAAAGACTT TACTTTGAGT CTTGGATCTG AAGAGATATG TCCCCTGGAT 1200 CTCTTAAAAG CATATTAAGC TTAACATATT CAAAACCAAA CTCATAATCT CTATTACCTT 1260 GCATCCCACC AAACTGGTCT TTTTCATCAA ACCCCATCAA AAAGATCTCA GCAATTCATC 1320 TAATTATGCA TGCAAGAAAC TTAGAGGTCA TCTTTGACAT GTCCTCTTCA CCATTATATC 1380 CGATCTATCA CCTGGTCCTG CCAATGTTGC 1410
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