Tag | Content |
---|
EnhancerAtlas ID | HS091-45756 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr8:27362660-27364050 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr8:27363447-27363464 | TGCTTTCTATGACTTCC | + | 6.85 | Lhx3 | MA0135.1 | chr8:27363499-27363512 | AACTAATTAATTT | - | 6.29 | mix-a | MA0621.1 | chr8:27363500-27363511 | ACTAATTAATT | - | 6.62 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGGTACGGA GACACTTCCT TATGGCAGAG AAGGATGTTC AGAGATATTG CAACCAGGGA 60 AAAACTGAGG AGTGAGCAGG TGGGATGCAT CTTGGGCCTG GCAGGACAGC TCTGAGTCCA 120 CTTCTCCCAG ACCACGTCTT CTCCTAGAAG ACTGTTACCC ATTCTTTGAT CTAGAAAGTT 180 CTCCCAGAGG TGGGCATTTG GCTCCATTGT ATAGCTCTTA CAGAACTTTG GTCAAAACAG 240 GCATCAGCAA AAGCTGTTTT AGCCCAGCTG CCTCAGTTTA CTTACAAAGA AATGGAGATC 300 CTGGGAGACT TGCAAGGCCA CAAGACTAGT AGTCAGGTTC ATCCCCACAA AGGGTGAGTG 360 AGGACAGGCT CCGGTATTGC CATGCTCTCC CACCAGACAC CCTGTGCCCT GAGCCTGTCT 420 CCAGAGATCA CCTGTCCTAA AGCTCTTTTC TCTTTGTGTG TCTCTACTTT AATCTACAAA 480 AGGTGATTGA ATGGAGATTA AATTCCTTTC CCTCACATTT CCAACCCCCC ACCTCCCCAC 540 AAGCTGACCA GAGCAAACCC TGAACTCTAG CCTTGGAGTC CTCACCATGC TGCATCCTGG 600 GACCTCCCCT TTCACCTCCT GGACTTTGCT TCTTCTCTTC TCAGTGCCTG GAGTCAGCCT 660 CAGAGCAGGG CTCCCAATCT AAGCCTGCAC AGGAATATAT CAGTCTTCCT ATCGATGGCT 720 TCCAGGTTGG ATGAGCTGCT TAGAATTCTA GACTTCCCTT GTCCAAGATG GTAAATGCAT 780 GCACCCATGC TTTCTATGAC TTCCAGGATT TTTCTTCTCT TTTTATTTAT TTATTGTTTA 840 ACTAATTAAT TTATTTTTTC TTAGAGACAG AGCCTCACTC TGTCACCTAG GCTAGAGTGC 900 AGTGAAGCGA TCATAGCTCA CTGCAGCCTC AAACTCCTGA GCTCAAGTGA TCGTCCTGCC 960 TCAGCCTCCC AAGTAGCTAT GACCACAGGT TCATACCACC ATGCATGGCT AATTTTTTAC 1020 ATTCTGTTGT AACGGGGGTC TCACTATATT GTTCATGCTA ATCTTGAACT CCTGGTTTCA 1080 ACCAATCCTT CCAGTCTCCC AAAGTGCTGG GATTACAGGT GTGAGCCATC AAGCCTAGCA 1140 CTTTCTTTAT TACTACATAT AAATTTTTGA TTCATTAAGA ATCTATTTGG GGGTAAGATA 1200 TAAAGTAAGG ATCCATTTTA TTCCCCCAAA CAGTTAACCA GTCATACCAA GGCCATTAAA 1260 CAATCTTCCT TACCAATTGG ACATGACACT TTTCTTAGAA ACTAAATTCT TATTTGTATT 1320 TGGTTCTATT TCATAGACAT GTCTGTTTCT TTTCTAGTGC CAAATTTCTA CCTTTTGTAG 1380 CTTCATCAAT 1390
|