| Tag | Content |
|---|
EnhancerAtlas ID | HS091-23012 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:5893300-5894680 |
Target genes | | Number: 17 | Name | Ensembl ID |
|
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr19:5894602-5894613 | TCTTATCTCCC | + | 6.62 | | Mecom | MA0029.1 | chr19:5894597-5894611 | CCTTATCTTATCTC | - | 6.42 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I005894 | chr19 | 5894041 | 5895941 |
|
Enhancer Sequence | TCTACAAAAA ATAAAAATAA AAACAATTAG CTGGCTGTAG TGGTGCACAC CTGCAGTCCC 60
AGCTACCAGG GAGGCTGAGA TGAGAGAGTC GCATAAGCCA GGAAGGTCAA GGTTCCAGTG 120
AGCCATGATC CTGCCACTGC CCTCCAGCTT GAGAGACAGA GCAAGACTAT GTCTCAAAAA 180
GACGAATTTT TGGTAGAGAC AGGGTCTCAC TGCGTTGCCC AGGCTGGTTC CAAGCTCCTG 240
GCCTCAAGCA ATCCTCCCAC CTCAACCTCC AAAAGTGCTG AGATTACAGG CTCAAACCAC 300
CAGGCCCAGC CTACAACATT TTTTAAAAAA ATTAACCAGG CATAGTGGCG GTGGCCATAG 360
TCCTGGCTAC TCGGGAGGCT GAGGTGGGAG GATTGCTTGG GCCCGGGAGT TCCAGGCTGA 420
GTTACTACTC GGGGGTGGAC AGAGAAGGAT ATGAGGCTGA AAGTGAAGTT TGGCTTTTCA 480
CATCTAGGCC CCGCGGATGG GCTTGAGAAA AGGGAAGAGA TGGGGCCGGA TACGGGTCAG 540
GAGGGCCATA GCCAGCCCTG CCGGTTCCTG CTGTCCCCGG CCCACCAGCA GGGCCCAGAT 600
CCATCCCAGC CAGGGCTGTG CACAGCTCCG CTCCCCTGGG TGGAGCCTGG AGCGCCCTAA 660
TTTGCAGCCC ACCGCAGCAT GTGGGAGCTT GCAGGCTTCC TCTCCAGCTG CCAGGGAGCA 720
TGAGCCAGTT CTGGAGAAGG GGCCCGGGGT GGTGCCAGCA TTCCAGGGCC ACCTAAATCA 780
CTGGCCTGAC AGGTGGCAGG AAGGGATCGC AATTCTTTCC CTTGTCGCTG CCACCAGCCA 840
GGTGCTGAGG GGGGTCCTGT CCCGCTCTGC CCTAGCCCCA GGGGCTGCGA GTGACCTGCC 900
GGATGGGGAC GGCTGCTGGA CCAGCCTGTC CGGGGCTCTC CGCTCCAGTG CCCAGGAATT 960
TGGAGACAGG GCCTGGGCGT GTTTTCCACA TGTTGTTGGC TTTGGGGACA GGCCCAGAGA 1020
AAGGATGGCT CAAGATCTGC AGGGGGGTTG TGACCAGAGC CCACAGCGCT GAGGGAAGGG 1080
CTGTGGGCGG CAGGGCCCAT TTTCCACTTG CTGGCAGGTC ACTGGCACGC TCCTGCCCTG 1140
CCCTGGGAAC TGGGGGAAGC AGAGGCTGGG GCGCATCCCA GCCGTCTCCC CTCCTGGGCT 1200
CCCGATGGCC CCAGCCTGAT GCACTACCAG TTCTGTGGGG CCAGGCTGGT ACCCTTGGCA 1260
GGGACGGCAG GCGGCAGGCA GGCGCGTGTG CAGGGGGCCT TATCTTATCT CCCTTCCTCA 1320
CTCCCTCCCA GATCCGCCCT CACCGGCTGC TGTGTCGCCG TCATCAAGCC CTCCGGACAC 1380
|
