| Tag | Content |
|---|
EnhancerAtlas ID | HS091-11526 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr13:28596300-28597480 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr13:28596839-28596857 | GGAAGGAAGGTAGCCAGA | + | 6.32 | | ZBTB18 | MA0698.1 | chr13:28596328-28596341 | GAACATCTGGCTG | - | 6.32 | | ZNF263 | MA0528.1 | chr13:28596733-28596754 | GAAGGAAGTGGAGGAGAAGAG | + | 6.16 | | ZNF263 | MA0528.1 | chr13:28596742-28596763 | GGAGGAGAAGAGGAGGAGGAG | + | 6.44 | | ZNF263 | MA0528.1 | chr13:28596730-28596751 | GGGGAAGGAAGTGGAGGAGAA | + | 6.65 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I028022 | chr13 | 28596550 | 28597947 |
|
Enhancer Sequence | AGTAGCTGGA ACTGCAGACA CACACCATGA ACATCTGGCT GAGGCAGTAA TTTTTTAAAG 60
AAAAAAGGCC GAGTGTGGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCTGAGGCA 120
GGTGGATTGC TTGAGCTCAG GATTTCAAGA CCAGCCTGGG CAACATGGTG AATTCCCATC 180
TCTATTAAAA TACAAAAAAT TAGCCAGGCA TGCTGGTATG CACCCGTGGT CCCAGCTACA 240
CGGAAGGCCG AGGCATGAGA ATTGCTTGAA CCCAGGAAGC AGAGGTTGTA GTGAGCCAAG 300
ATCACGCCAC TGCACTCCAG CCTGGGCAAC AGAGCGAGAC TGTCTCCAAA AACAAAACAA 360
AACAAAACAA AAAAATACAA TTGAAAGTAG TCTTTCCAAA TTCAGAGAGA AAACAGGAGA 420
GAAGAGGCAA GGGGAAGGAA GTGGAGGAGA AGAGGAGGAG GAGATTAGAA GACTGCAAGA 480
AAAATGAGGG GGAAGAATTT TGGGAAATAA AGAGAAGGTA ATGAAAGGCA AGCAAACGAG 540
GAAGGAAGGT AGCCAGAGAG TGGGCTATGA TCTGCTTATA GGCAGGAGAC ATTTGAAATC 600
ACAGAGAACA GCGGGTGGAA AGGCAGTTCA AAAAGAGTGC AAAATTGGGG TAGAGACATG 660
GTTCACGGCA GGCTCCAGGG CCTTACCAAC GAATGGATCT GGGGTTAGCA ACAGAGGAGG 720
CAGTGAGCCT GCAGGACTGC TGCCAGCCCA CAGCACGCAG GGTGAGAATT AGACAAAGAC 780
ACTCAGGGTG GCTGGCTCGG TTTCAGCCTC CTCTCATCCC CTGGGTTGAA TGCCCACATG 840
CAGGGCACAA CCTGAACAGC CGTTCTGAAA GGGACTGACA ATGCTACGCT TTGTTTTGAG 900
GAAGGATTTC TGAGGACTTC CTATCTCGAC CTTCAGCCTT GGAAGTTTCA GGGGACTTTG 960
TGCAGCCTGG GAGGGCTGTG CTAGCCGTGA CCTCACAAGG GATCCCAGGC CTTTATGCTA 1020
CTACAATTAG CCAAGAGCCA AGGTAACACG CTAGGTGACT CCAACAGTGA ACAGGGGAGA 1080
AAAGGCAGAC TTTAAGGGAT ACAAGTTAAA ATAAACAAGA AAACATATAT AAGCACATCT 1140
TTTCAAATCT TTTTTTTGGT TTGTTTTTTC TTTAAAAGGA 1180
|
