| Tag | Content |
|---|
EnhancerAtlas ID | HS098-51497 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr7:27129740-27130710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr7:27130153-27130168 | TGAACTTTGACCTCT | - | 7.99 | | Hnf4a | MA0114.3 | chr7:27130151-27130167 | CATGAACTTTGACCTC | - | 7.01 | | NR2C2 | MA0504.1 | chr7:27130153-27130168 | TGAACTTTGACCTCT | - | 6.99 | | Nr2f6 | MA0677.1 | chr7:27130153-27130167 | TGAACTTTGACCTC | - | 6.83 | | Rxra | MA0512.2 | chr7:27130153-27130167 | TGAACTTTGACCTC | - | 7.38 | | ZNF263 | MA0528.1 | chr7:27130602-27130623 | AGAGGAGGGGGCAGGAGAAGG | + | 6.37 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCACAAGGA GTCCTAAGGC AGAATTTTTG TGTGTTCTCA CAAATGCAGG CACAAAGGGG 60
ACTTATCTAA GGCAGAGGGT CACCAAAGTT GACCAGTGAC TAGCTTATCC CAATAGTGGC 120
ATGCTAACTA AAGGGTGTTC TTGTATGTAC TGAAAAAGCC ATAGCGTTTC TTTTACAGCC 180
CCATCCAATA TAAAGAAAGA TGTTGTTCAT GCACTAATTT CAGTATTTTT AAGCACAGGA 240
GTTGCCTGTC TCTCAAAATA AATTAAAGCC TGAAATGCCT AGAGCTTCTG CTTTAAGAAT 300
GATTATTCTT AAGGAGGAAA CACAAACAGC AGTGACCATT TTTCACAGAC GTGCTCAGCC 360
ATCAGGAAAG CTTAATAAAT CCCTATTTAG TATGCATTTA TGCAGTGATT ACATGAACTT 420
TGACCTCTGA AGAGCTGTAG CAATTAGCTT CAGTGTCTAG CATCTTCTAC TCACCATTCC 480
CCACTGGCTT CCTTGTGTCT TCCTTTTTCA TCTCTCAATA CTTCATGCAT TAAGAAGGCG 540
TAAAATTTAA AAGTTGACTT TCCACCTGAG GTATTTGCTT CTGCGCAAGC CAATTCTCCC 600
TCCCCCCTTT CCCACTCAAC AGCCATCTCA GATGGATATT GGGGCTCTGA TTGTCAATAT 660
TACTCAAACA CAAATGGATT TCAATTCAAT CTTGCCCTGT ACTTTCACAA AGATAAACTC 720
TAATGGCCCA AAGAGCTTCA TTTCATAGCT TGTGGCATCT GAAATAAATC AGATATCTTC 780
TGTCAGACTA ATTTAACATT TTAACAATAT TTGATGTGAT TTATTTAAAG TCAAATGAAA 840
CTGAATGGAT TGGCAGAAAA CTAGAGGAGG GGGCAGGAGA AGGGCAGCTG GAAGCTTCCA 900
AAAAACAAAA AACAAAAAAG AAAAAAAGGA AGAAAAGAAA AGAACCAAGA GGGGAGAGGA 960
AAGTGTTTTA 970
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