Tag | Content |
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EnhancerAtlas ID | HS118-15997 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr6:33342070-33343600 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr6:33342639-33342654 | TGAACTCCTGACCTC | - | 6.22 |
| | 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 |
GH06I033373 | chr6 | 33341692 | 33344810 |
| Enhancer Sequence | CTTTATCTGC TTCAAGTCCA GACATACCAC AAAGAATAAT TGTTTTCTCT TCCCCTCCCT 60 GTAAGATCAG GAATGGAATC ACACCTGAGC AGGTCCTTTC CCAAAAGAGT CTGTCTCTCA 120 GCTCATTCAC ATTCCACAGG GAACTATTCA AAACTCAATC TCTATCTCTG GGCCCATTCA 180 TTCTCCCTAA TAATCGCCTA TGGCCCCTCA AGAGAATTCC TGTTCCCTAT CCCATAACCT 240 GTTTTGCCAG GATGGTAAAT AAGCTCCTGA ACCCTGTTGT GGATTGGTTA ATCACTCTGT 300 GGTTCTCTCT GTGTACACAT TAATCCATTT ATATGCCTCT TCTCCAATGC ACCTTTTTTT 360 TTTTTGTTTT GTTTTGTTTT GTTTTTTGGA CAGACTCTTG CTCTGTCGAC AGGGCTGGAA 420 TGCAATGGCA CAATCTCAGC TCACTGCAAC CTCCACCTCC TGGGCTCAAG TGATTCTCCT 480 GTCTCAGCTT CCCGAGTAGC TGGGATTACA AGCACACGCC ACTGTGCCCA GCTAATTTTT 540 ATATTTTCAC CATGTTTCCA GGCTGGTTTT GAACTCCTGA CCTCAGGTGA TCCACCCGAC 600 TCAGCCCCCC AAAGTGCTGG GATTACAGAT GTGAACCACC GTGCCCAGCC TGCATCTATC 660 TTTCGTGAGT TAATTTTCCA GCCAACCTTC AGAGGGCGAA AGGGAAGTTT TCCTTTGGCC 720 CATACAGGTT CATTATAGCT ATTCTATGTA GTTTTCTACT TAAGTATGTC ATAATTTCAA 780 AAGAGAAAAA GAGAAGGGAG AAAATTGTTC TAAGCTTTCA ATGTGAAGGC CTGGCACTTT 840 TAAAGAATAA CAGCTTCTGT GGCCAGACTT TTAGTATCAG TATGGACTTT CCCTGGAGAA 900 GTCCAGCCAG ATGGGCAGAC TGGGCAGATG CTTATACTGA TTAGCTAGAT TTAGCTAATG 960 GGCAGAGCCG TCACAATGCA CTGGTTGAAA TGGTGCAAAA AAATAATGTA AGGCTTTTTT 1020 TTTTTTGGTA CAGGATCTGG CTCTGTTGCC TATGCTGGAG TACAGTTGCT CAATCTTGGC 1080 TCACTGTAAC CTCCGTTTCC TGGACTCATG CCATCCTCTC GCTTCAGCCT TCTGAGAAGC 1140 TGGGACTACA GGAATGCACC ATCACACCCG GCTAATTTTT GTATTTTTTG TAGAGATGGG 1200 GTTTCACCGT GTTAACTAGG CTGGTCTCAT AACCGCCCAA TGTGTTTACC TTGCCCGCTG 1260 CCTAGACAGA GCCGATTTCT CAAGACAGAG GAATTGCAAT ATAGAAAGAG TAATTCACGC 1320 AGAGCCTGCT GTGTGGGAGA CAGGAGTTTT ATTATTACTC AAATCAGTCT GCCCAAGAAT 1380 TCGAGGAGCA GAGTTTGTTT TTGTTGTTGT TGTTTTGTTC TGTTTTTTGA GATGGAGTCT 1440 CTCTCTGTCA CCCAGGCTGG AGTGCAATGG CAAAATCTTG GCTCACTGCA ACCTCCACCT 1500 CCCAGGTTCA AGTGATTCTC CTGCCTCAGC 1530
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