Tag | Content |
---|
EnhancerAtlas ID | HS091-49420 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chrX:46971220-46972800 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
YY1 | MA0095.2 | chrX:46971646-46971658 | CAAGATGGCTGA | + | 6.04 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTAAAACCC CGTCTCTACT AAAAATACAA AAATTAGCTG AGTGTGGTGA CGGGCACCTG 60 TAATCCCAGC TACTCGGGAG GCTGAGGCAA GAGAATTGCT TCAGCCCGGG AGGCGGAGGT 120 TGCAGTGAGC TGAGATCGCA CCACTGCACT CCAGCCTGGG CGATAGGGCA AGACTCCATC 180 TTGGGGGGGA AAAAAAAGCT TACTAATCAT GCAACAAGGC AGGAAAATAT GAAGACAACA 240 GTCAATCAAG GAAAACCAAC CCAGATTTGA TGCATAAATT AATTAGCAGA TAAGGACATT 300 AAGAGTTATT AAAGCTATGT TCCACAAGTT CATAAGAGTT CAACAAGAGA CATAGAAGAT 360 ATAAAAATGA CCCAATGGTG CAACATTTTT AAAAGAATGA ATTTTAAAAA CTGTCAACCT 420 AGGGAGCAAG ATGGCTGAAT AAAAGCCTCC TGATCATCCT CTTCACAGGA ATGCTGAATT 480 GAACACCTAT CCACACAATA AAGCACCTTC ATAAGAACCA AAAATCAGGT GAGCAATCAC 540 AGTACCTGGT TTTAACTTCC TATCACTGAA AGAGGCACTA AAGTGGGTAG GGAAGACAGC 600 TTTGAATCAC CTACACCACC CCGCCCCCAT CCCCTGGTAG TAGGTGTGTG GCAGAGAGAG 660 AGAATCTGTG CACTTGGGGG CAGGAGAGCA CAGCAATCGT GAGACTTTGC GCTGGAACTC 720 GGTGCTTCCC TGTCACAACA GAAAGCAAAA ACCGGAGAGA ACTAAGCCGG CACCCATAAG 780 GGGAGCACTT GGACCAGCCC TAGCCAGAGG CAAACTGTCC ATCCCAGCAG TCAGAACCTG 840 AGTTTTGGCA AGCCTCACCA CCGTGGGCTA AAGTGCTCTG CAGTCCTAAA TAAACTTGAA 900 AGTCAGTCTG GGCTACAAGG ACTGCCGTTC CTGGGCAAGT CCTGTTGCTG TGCTGGGCTT 960 GGAGCCAGTG GATTTGGACA CACAACCCAG TGAAACATCA GCTGGGGTGG CCAAGGGAGT 1020 GCTTGAGCCA CCCCTCTCCC AACCCCAAGC AGTGCAGCTC AAACCACTGA AAGAGATTCC 1080 TTTCCTCTAC TTGAGGAGAG GAGCGGGGAG AGTAAAGAGG ACTTTGTCTT GCAACTTGGA 1140 AGCCAGCTCA GCCACAGTAG GATATGGCAC CAGGCAGAGT CCTGAAGTCC CCATTCCAGG 1200 CCCTAGCTCC CAGATGACAT TTTTCACACT TTTTTTAGAA GGAGTCTCAT TCTGTCACCC 1260 AGGCTGGAGT GCAGTGGTGC GATCTCGGCT CACTGCAAAC TCCGCCTCCC AGGTTCAAGC 1320 AATTCTCCCT GCCTCAGCCT CCCAAGTAGC TGGGATTACA GTCACGTGCC ATCACGCCTG 1380 GCTAATTTTT GTATTTTTAG TAGAGACGGG GTTTCACCAT GTTGGCCAGG CTGGTCTCAA 1440 ACTCCTGGCC TCAAGTGATC CGCCCACCTC GGCCTCCTAA AGTGCTGGGA TTACAGGCGT 1500 GAGCCACTGT GCCTGGCCCC AAATGACATT TCTAGACACA CTTTGGGCCA TAAGAGAACC 1560 TGCTGCCTTG AAGGGAAGGC 1580
|
| |
|
|
|