Tag | Content |
---|
EnhancerAtlas ID | HS091-20264 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:48497020-48498510 |
Target genes | Number: 21 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr17:48497858-48497873 | CCTGACCTTGGCCTC | - | 6.4 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I050420 | chr17 | 48497802 | 48499910 |
|
Enhancer Sequence | TGCCGGTACA GGCACACTGT GGGTGATCAG GCCACGCTTC CACTCAAATG GAGTGGGCAA 60 GTTCCAAAGA CTAGTCTTAC CAAGTTTCAG ATGTCTGGAC TCCAAGTGCC AGTTCCTTCC 120 TGGTGTTCAG CCACTGCGTT GATCCTCCAT GGGGGCCTGC CACATGCTGC TCTGGCAAGG 180 CGTTCCACCG GGGCAATTGC TTACCTGGGA TCGCTCTCAG GATCCGCATC GCTCAAGCTG 240 GCTGGAGTCC CCCGCAGGGA TGCTCCACAG GGCAGGCCTA AGCCACCTAA GGGGCTGCCT 300 CAACCATCCA TTCATCACCA TGCTTCCCGG TCAGGGAACC AAGAAATGAA GCGTGACAAG 360 CTGCAGACAA AACCCCTCAG ACACTGAGTT AAAGAAGGAA GGGCTTTATT CGGCTGGGAG 420 CTTCGGCAAG ACTCACGTCT CCAACAACCG AGCTCTCCAA GTGAGCAATT CCTGTCCCTT 480 TTAAGGGCTC ACAACTCTAA GGAGGTCCAC GTGAGAGGGT CATGATCGAT TGAGCAAGCA 540 GGGGGTACGT GACTGGGGGC TGCATGTACC AGTAATTAGA ACGGAACAGA ACAGGACAGG 600 GATTTTCACA GTGCTTTTCT ATACAATGTC TGTAATCTAT AGATAATATG ACCAATTAGG 660 TCAGGGGTCG ATCTTTAACT ACCAGGCCCA GGTGTGGCGC TGGGCTGTCT GCTTGTGGAT 720 TTCATTTTTG CCTTTTAGTT TTTATTTCTT CTTTCTTTGG AGGCAGAAAT TGGGCATAAG 780 ACAATATGAG GGGTGGTCTC CTCCCTTATC GCCATGTTGA CCAAGCTGGT CTCAAACTCC 840 TGACCTTGGC CTCCCAAATT GCTGGGATTA CAGGCATGAG CCACCGCGCC CAGCCCAACA 900 CTTTAATTTT AATTGCGTAA GACTCTCTTC AGACTTCTGG CCTCCAGAAC TGTAAGACAA 960 TAAATTTCTG GGGTTTTAAG CCACTACATG TGTGCAATTT GTTCCAGCAG CAATAGGAAA 1020 CTGACGCACT GCTTCTTTCT CAGGACTAGA TGCAAACCTC CAGGAGGCCT TCTGCAACAC 1080 ACCTTGGGTA GGTGCCTCTC CCCTAGCCTT GCTCACACAG CACTGGCCGC ACTGCAGGCC 1140 ATTGTCAGTC TCAGGGTTGG TGTTTTCTCC TAGACAGTGA GCTCATTGAG AGCAGACACC 1200 ATGTCTCATT CATATCATGC TTGTCAGCAA GTAGTTACTC AATGAATGAA TGCTGAACCA 1260 ATGAATAAAA AAAGAAAGTT AAATTAGATT TGGTTTAACA CTGGGTCTTT ATCCAAGACT 1320 TCACAGTTGA CTTTAGTTCT TGACTTTGAC CCAAGAAAAG TAAAATATTA CACCATCCAA 1380 ATAAAGATTT TTGTCCTATC CTCTTACAAA AGCAAGGCTT TCACAGTTTT TTTGGCAGTT 1440 GCTGGGATTA TGGCTTAGTT TTCAATTTGG GGATGTAAGC AAGAAAATAC 1490
|