| Tag | Content |
|---|
EnhancerAtlas ID | HS091-30537 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr20:31601760-31603240 |
Target genes | | Number: 17 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr20:31602103-31602121 | GAAAGGAAGCCAGGGAGG | + | 6.29 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGGTGGGTGC CTGGTGAGGG CAGGGTCACA GGAATCCCAG ATGCCAAAGC TGTGCTGCTG 60
TTTCCTGAGC TGCCCACTCA GGACTTTAAC CAATGGCCAC AAGGGCCTCA GGGGCCCCCA 120
TTATTGTGCT TGTTTTATGT CGGAGGACAC TGAGGCTCAG AGAGGGGGAG AGGCATGCCT 180
GAGGTCACAC AGCAAGTGAG CGGCCAGAGC CTGGGACCTT TCCATCCCCT GCACCACTTG 240
ACAATACACA CTAGCTATTA GCACACTCTT TGGGGAGGGA TTTTGGGTGG ATCAGACTGG 300
CTGTGAGGAC CTCGGAGACC CACCCCTCCT AGCAGAGATG AGGGAAAGGA AGCCAGGGAG 360
GGCCTGGGAC CCACCAATAG CCAGCTCTCG CAGGCCAGGC CGCTCCCTTC TGCATAAAGG 420
CTGATGGCAG CTCCCGCCTC CAGAGCACTT ATGTGTGCTG AGCATTGTTC AGGCCCTTTC 480
CATAGATCAT TTCGTTTGAT CCTCACAGTA TCCTACCAGG TAGGTGTTAA GTATTTCCTG 540
CATTTTACAG GAGCGCAAAT GGAGGCCCAG AGCAGTTAAG TGACTTGCCT AAGGCCACCG 600
GCTGACAAAT GGTGTAACCA CATTCAGGCC CAGGCAGCCC GACTAATCCC ATGGCTTGCA 660
AATCCCCCTA GACGATGTCT GCACCTTCCC AATGTGAGCG GGGCTTGCTG AGGTGTTGAG 720
CATCTTGGAG GCTTAGAAGA ATGCAACGTA TGCATCAAGA CTGAGCTTTC TCCCCAGAGA 780
GGGATGTGGC TGCGTAAACC CATTCACACT TGTGTCGCAT GATCACCACG TGTGACTCAC 840
GACCCCTCAC TGTCCTTACA GGCAGGGGAT GCTCACAGCT TATTGAAGGG GAAATGGAAG 900
CCCAGAGGCT TTGGGAACAC AGAGGCCACC CTCCCACCTC CCCCCCAGGG AGCTGGTTCA 960
GCAAGGTTGG GCTGTGGCTT GGATCGACAT TTTTGCAAAT CAAGGAACTA TAGGTGCCTA 1020
TGGAGCACTG TTGAGTTGTT TAGAGGGGAA ACGGAGGCCC AGAGTCAGGA AGGGATTTTA 1080
TTAGGTGTGT CACAGAAAAT TGGACCCAAA GCATGAAGCA GACCCAGGAT CCCAGCTCTA 1140
CCCCCTAACC CAACCTTTAC TGGGCTTAGA GTGGCCACGA AGCCAGCTGG CCAAGGTCAT 1200
GGCCAAGTCT GGCTTTTGCA ACGCCCTCTC TGTCTCACGC GCCACATTCT TGGCCATTTC 1260
CAAACCTTGA GATAAATGAC CCTCTCTTTT GAGACTCAAT TTCCTCATCT ATGGGGCCAG 1320
TTATGCCAGC ACTGTGTCTG GCAGATGGCA GGGCATCGAA TGGAATTGAT TGGCCTCCTG 1380
GCTGAGGATA GAGACTTCTC TTCCCAGACG TGCGACTGTG CTGAGTGACG GGACTTAATA 1440
TGTTTGGGAG CCCAGGAACT CTTTCTGTGT TTCTCCCTCA 1480
|
