| Tag | Content |
|---|
EnhancerAtlas ID | HS091-23224 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:10687120-10687870 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:10687293-10687308 | TGAACTTCTGACCTC | - | 6.38 | | RARA | MA0729.1 | chr19:10687290-10687308 | TCTTGAACTTCTGACCTC | - | 6.88 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I010576 | chr19 | 10687356 | 10688690 |
|
Enhancer Sequence | GTAGAGATGG GGTTTCACCA TGTTAGCCAG GATGGTCTCG ATCTCCTGAC CTCGTGATCC 60
GCCCACCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGTG CCCTGCCCTA 120
ATTTTTGTAT TTTTAGTAGA GACGGGTTTT CACCATGTTG GCCAGGCTGG TCTTGAACTT 180
CTGACCTCAG GTGATCTGCC CGCTTCAGCC TCCCAAAGTG CTGGGATTAC AGGTATGAGC 240
CACCATGTCT GGCCTTTTAA TCTTTTTTTT TTTTTTTTGA GACGGAGTCT CGTTCTGTTG 300
CCCAGGCTGG AGTGTGCAGT GGCACAATCT CAGCTCACTG CAACCTCTGC CTCCCGGGTT 360
CAAGCAATTC TCCTGCCTCA GTGTCCCGAG TGGCTGGGAT TACAGGCATG CGCCACCACA 420
CCCAGCTAAT TTTTGTACTT TTACTAGAGA CGGATGTTAG CCGTCTCTAT GTTAGCCAGG 480
CTGGGATTTC AGGCGTGAGC CACTGCGCCC AGCTCCTCTT AATATTTTTA TAGAGGCAGG 540
GTCTCACTGT GTTCCCCAGG CTGGTCTCCA GCTCCTGGGT TCAAGCGATC TGCCCGTGTC 600
AGCCTCTCAA AGTACTGGCA TTCCAGTCAT GAGCCATCAC ACCTGACTGG GTCTCTGATT 660
TGTTCTCTGC CTTGTTCTCA TGGCTCCTGG GCAGCCCCCA CACTACTCCA GTCCCCTCCA 720
CCCCCAGATC CCCCGCCAGT CCCTGGTACT 750
|
