| Tag | Content |
|---|
EnhancerAtlas ID | HS091-45400 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr8:6698170-6699180 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr8:6698327-6698346 | CACCCAGTAGGTGGCGCTG | + | 6.53 | | IRF1 | MA0050.2 | chr8:6698812-6698833 | GTTTCCTTTCTCTTTCTCCTC | + | 6.29 | | ZNF263 | MA0528.1 | chr8:6698813-6698834 | TTTCCTTTCTCTTTCTCCTCC | - | 7.12 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I006840 | chr8 | 6697781 | 6699182 |
|
Enhancer Sequence | GCATAGATAG CAGATCATGA GAGTGTGCAC AGCGTATAAT GCCTTCTCAG TGCATGTTGG 60
GTGTATGAAT GAATAAGTGA ATAAACAAGT AAGTGAATGA ATGAAAGCAA GCAGCCAGGA 120
AGCGCTGCAG CTCAGTCTAG TCTTTTCCCA GGGCAAACAC CCAGTAGGTG GCGCTGTTGC 180
ACCGGCGGTT GCAAACCCTC AGAGCACGTT TAAACAGAGC TCTCTGACTC TGGGACAGAG 240
GATGTGGAAA ACCTGTGTCT TCAAATCACG TCATTAGGTT TGAAGATGAC TTAATGTGAA 300
AATAAATGTA TTTTAACGTC ATTAAAATAA TCCTTAGTAC TTTAAAATCT CAGCTAGCTT 360
CTGAATGCTT TGGGAATACT TTCTCCATAG TTAACTGCAC ACAAGCCCGT GGGGTGGGCA 420
GGGCAGGTAT TTGCTCTCTG AGATCCAAAG AGGGCAGTTT CTCGGCTGGT AGAGGCAGAG 480
CTGGATGCAG AGCCAGGCAC AGAGCCAAGG CGCGTCTGAC CCCAGTCCAG CGGGATCTCC 540
TGCAAGCCGC AGTGTTTCCA GAGGCGCACT TCAGTGTGTG GAGTGAAGGG AGAGTCTCCG 600
GACATGAGAA GAGCTGCTCT GAGCAGTGTG GCGGCCGTTT TTGTTTCCTT TCTCTTTCTC 660
CTCCTGGGGC TAGGCAGACA CCGGGCACAA AGAAGGAAAC AGGCCTTCTG TGAGTGCAGC 720
AGCAATCAAT AAAGAAGCAG CCCAGAGCGG CCATCCCTCT TCTGTCTGCT GTGACGCTCC 780
GGCCCAGGTG TCCCTGGGGC TGCCCTCCCC AGGGCCTGTG TGTTGCATAT ATGGGGTGGG 840
GTGAGGGCAG CTGGAATTGA GGTGGGGACC CTGCAATTGT GAGGGGCTGC GTGGCAGAGG 900
TGGGCGGCTC TCGCAGGCCT CTTCCTGGAC ACTTGCACCC CCTCATCCTG CTCTCTTTTT 960
CTTCCTGCAC TTACATCATC TCATTTGTTT ATTTTCTCAT TGTCCGTCTC 1010
|
