Tag | Content |
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EnhancerAtlas ID | HS091-13769 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:77799620-77801150 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr14:77800234-77800245 | TCAAGGTCAAT | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr14:77799867-77799882 | TGATCTCTTGACCTT | - | 6.93 |
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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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Enhancer Sequence | TCCTCCTAAC TTTTAGTGTT TTGTTTTTGT TTTTTTTTTT TTTTTTGGAG ACAGAGTCTC 60 ACTCTCTCGC CAGGCTGGAG TGCAGTGGAG CGATCTCGGT TCACTGCAAC CTCCGCCTCC 120 CAGGTTCAAG GGATTCTCCT GCCTCAGCCT CCCAAGTAGC TGGGACTGCA GGCCCACGCC 180 ACCACACCCA GCTAATTTTT GTATTTTTAG TAGAGACAGG GTTTCACCAT GTTGGCCAGA 240 ATGGTCTTGA TCTCTTGACC TTGTGATCCA CCTGCCTCGG TCTCCCAAAG TGCTGGGATT 300 ACAGGTGTGA GCCACCACGC CCGGCCTAGA TATTTTATTT AAAAAAAATT TTTTTAGAGA 360 TGGAGTCTCA CTGTGTTGCC CAGGCTGATC TTGATCCTCC CGCCTCAGCC TCCCAAGTAG 420 CTGGGCCAGC TCTTACTTCT AAACATAACT TATTTAGCTC TTGCTTCCAA GGTCACAGCA 480 ATTCTACTTT CAGAGAATAC TTTGAACTAA GGATAGCTGC TGAGTTTAAG CCAGAAGTGC 540 ACAGGTTAAA GAACATCAAG GCTGAATGTC AAGAGCTGTA ATGTGTGAGC TGCCTTTTGT 600 AATCCTGAGC TATGTCAAGG TCAATGATAT GACACATATG AATGCTTTTA AAAGTTAAAA 660 AATAATCTTA AGGCCAGGTG CGGTGGCTCA CACCTGTAAT CCTAGCACTT TGGGAGGCTG 720 AGGCGGGTGG ATTGCCTGAG CTCAGGAGTT CAAGACCAGC CTGGGTAACA TGGTGAAACC 780 CTGTCTCTAC TAAAATACAA AAAATTAGCT GGGCGTGGTG GCATGTGCCT GTAATTCCAG 840 CTACTCAGGA GGCTGAGACA GGAGAATTGC TTGAACCAGG GAGGCGGAGG TTGCAGTAAG 900 CCGAGATCAT GCCACTGCAC TCCAGCCTGG CGACAAAGTG AGACTCCATC TCAAAAAATA 960 ATAATAATCT TAAATATATT ATGTGTTCAC AGTGACATAT TACATCCAGC ATACCCAAAC 1020 ATGAATCATT AATGATCTCC AGCTACATGG AATCTGCCTG GGCTTTTTGT TACTTGTAGG 1080 GTAGTTTGGT GATTACATTC AACTGAATTG TTTCAGATCC CTTCTCTTTC ATGCTTCAAC 1140 CTCTAAAATA TGTTGCAACA GAAAGCAGAG AATGATCTAA CAGGTTCATT TTAGCATCAC 1200 AGATATCACT GAAGGAAATA TTTAAATGCC ACCCTTCCCT GCTCAGATGT GAGTCCTTAT 1260 TCTGCAACAG ACACTAGGGA TGTGGAGAGG CAGTGTTTTA AAAGACAGCA AAGATATATT 1320 ATGGTGTCAC TTTTTGTAAA TGAAAATAGG CTGAATTCAT ATCACCCAGA TTACGTTAAT 1380 GATTGGCCTG GTATCCGAAG TCGAGGTTCC AAATTTGAAC AGAATATCTT CATGGGGAAA 1440 CAGGCCTCAC TGGGACCAAA TGCTGACATA AAACTCAGAA CTTATTAATC ATCACTATAA 1500 ACCCAGTTTT TCCATTCCCA GTTCCCAGGT 1530
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