| Tag | Content |
|---|
EnhancerAtlas ID | HS091-14742 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr15:51120550-51121650 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr15:51120632-51120647 | TGAACTCCTGACCTC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr15 | 51120677 | 51120745 | | chr15 | 51120901 | 51121466 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH15I050828 | chr15 | 51120647 | 51121751 |
| Enhancer Sequence | TTATAGGCAC CTGCCACCAT GCCTGGCTAA TTTTTGTATT TTTAGTAGAG ATGGGGTTTC 60
ACCATGCTGG CCAGGCTGGT CTTGAACTCC TGACCTCAGG CGATCCACCC ACCTTGGCCT 120
CCCAAGTGCT GGGATTACAG ACGTGAGCCA CCGCGCCTGG CCACTGTCTC ATTTTTTAAA 180
TGGGCACATG GTATTCTTTT GTAAGCACTG CAAAAATACA TTATTGTACA TATACCTGTC 240
TTCCTTCATC TCTTTTTCTA CGAGGGCACA TACTTTCCCT TGAGAATGAA GGGGAAACTG 300
CAGGTGCATA GGGGACTACC TAGAGAAAAT AAGGAGAAGA ATGATTCTGC TCTATCCTGG 360
AGGCTCTTAA GTCCATAGTC ATATTGTTAT CTTGACATGG CAATTTATGG CTTATGATTG 420
CTTTCATATT TCATTTGATC TTTATTCAAA CCTATGAAGT GGCTAGACCC GACAGTAAAA 480
TCATTGCTAT TTTACAGTCT CAGAGGTATT GAGTGACCAG CCTCATGCCT CACAGCTAGT 540
TAGGGACAGT ATGCAGTTAG AATCCATGTC TTCTATCTTT CAGTCCACTG CTATTGCACA 600
ATGGACAGCT GCTCCCTGCA ACCACATGTG GGAGGAGAAT TGGGAGGACT GAAAAAAAAC 660
TGTGTAGTGA TTCACAGGGA ACTTGGGATA ATGGTCGTCA AGAATGTGCT ATGTCAGCCA 720
GTTGGTGTCG TGCTGAGCAG TGTTGGTTTG GGTTTTTTTT TTATATGGTG AGAAAGAGAA 780
TGAATGTCTC TCCATGTGTT TCTAGGTATA TCAGTGATTT CTGCTTTCAC AGTAGAGACA 840
GTCATAATAA GCATATGCAC TTGTATCCTT AAAAGTAAGG CAGAGCATTA TTCTAAGCGA 900
AGTAACTCAG GAATGGAAAA CCAAGTGTCT TATGTTCTCA CTTATAAATG GGAGCTAAGC 960
TATGAGGATG CAAAAACATA CAGAGTGATA TAATGGACTT TGGGGACTCG GGGGGAGGCT 1020
GGGAAGGGGA CAAGGGATAA AAGACAACAT ATTGGGTACA GTGGACACTG CTCAAGTGCC 1080
AGGTGCACAC AAATCTCAGA 1100
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