| Tag | Content |
|---|
EnhancerAtlas ID | HS091-23179 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:10041200-10042180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:10041714-10041733 | CGACCACTAGATGTCGCTC | + | 6.42 | | TBX20 | MA0689.1 | chr19:10042031-10042042 | CTTCACACCTC | - | 6.02 |
|
| | 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 |
| GH19I009930 | chr19 | 10041641 | 10041810 |
|
Enhancer Sequence | CAGCATGGGT GACAGAACAA GACCCCGTCT TAGAAATAGG CCCGGCACCG TGGCTCACGC 60
CTGTAATCCC AGCACTTTGG GAGGCCAAGG CGGGCAGATC ATCTGAGGTC TGGAGTTCGA 120
GACCAGAGTG GGCAACGTGG TGAAACCCTG TCTCTATTAA AAATACAAAA AAAAAAAAAT 180
TTAGCCGGCT GTGGTGCTGT GCGCCTATAA TCCCAGCTAC TCGAGAGGCT GAGCAGGAGA 240
ATCGCTTGAA CCCGGGAGGC AGAGATTGCA GTGAGCCGAA ATCGCACCAC TGCACTCCAG 300
TGTGGACGAC ACAGCAAGAC TCTGTTTCAA ATATCATCAT CATCATCATC ATCAACTTTT 360
TAAAATGTTT GCACCCGCGG CGAGTATCTC ACCTGTTTTA CCCTGACCTG GGCACCCCCA 420
TCCCACATAC GCACGCGCCC ACGCACAGGT GCACAACCAC ACACATTCAC CCACCAGTCA 480
CACAGACGCA CACAGTCCCT GCACAAACCT CACTCGACCA CTAGATGTCG CTCAAGCTCC 540
ATAATCTTAA ATCCAGCCCC AAGGGGCTCT TTCCTACACT AACTCGGAGT CTTTAAATTT 600
CCTTTTACTT CCCTCCACTG GGACATTTAC ATGCTCTAAA GGAGCCCCAG GAGAACATCG 660
TCTTACCCCT AAACAACAGT GCCCTATCGG TGGAATGTCA GGCACAGGTA AAGAAGATGG 720
GTTTTCTTTC TTTCTTTTTT GTGGAGACAG GGTCTCAGTC TGTCGCCCAA GCTGGAGTGC 780
AGTAGTGCAA TGATAGCTCA CTGCAGCCTC AAACTCCTGG GCTCAAGTGA TCTTCACACC 840
TCAGCCTCCT GAGTAGAACT ACAAGCCTGG CCAATTTTTT TTAAAGTTAC TGCAGAGGCC 900
GGGCACGGTG GCTCACGCCT GTAATCCCAG CAGTTTAGGA GGCCGAGGCA GACAAATCAA 960
GATGTCAGGA GTTCGAGACC 980
|
