| Tag | Content |
|---|
EnhancerAtlas ID | HS091-36874 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr4:76806420-76807900 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr4:76807699-76807720 | AAAGAAAAAGTGAAAAAAATA | - | 6.34 | | RFX2 | MA0600.2 | chr4:76807221-76807237 | TGTTGCCATGGTAATC | - | 6.27 | | RFX2 | MA0600.2 | chr4:76807221-76807237 | TGTTGCCATGGTAATC | + | 6.29 | | RFX5 | MA0510.2 | chr4:76807221-76807237 | TGTTGCCATGGTAATC | - | 6.53 | | RFX5 | MA0510.2 | chr4:76807221-76807237 | TGTTGCCATGGTAATC | + | 6.63 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I075885 | chr4 | 76807141 | 76807830 |
|
Enhancer Sequence | AGTTTTCTTT ATGTGAAAGA AAGAAAATCA ATTGCTAAAT ATTTATTTAT TTATTTATGT 60
TTTAAGAGAC AGGGCCTCAC TATGTTGCCC AGGCTGACCT CAAACTCCTG GCCTCAACGA 120
TCCTCCCACT TTAGCCTCCC AAATGCTGGG ATTACAGGCA TGAGCCACTG CACCTGGCCC 180
CTTCTAGTTA TTAACCAAAC ATTTTAAGTT TGTTAAATAG TTTGCAAAAA TGTACTAGAA 240
TATAATGCAA TGCTGACTTT TCTATTATTT ATTTGCTGCA ACAGAGTAGC AAATATTATT 300
AAAAATAATA TCTTAGGCTG GGCACAGTGG CTCACGCCTG TAATACCAAC ACTTTGGGAG 360
CTGAGGTGAG TGGATCACTT GAGCTCAGGG GTTCAAGACC AGCCTGGCCA ACATGGCCAA 420
ACCCCGTCTC TATAAAAAAT ATAAAAAATT AGTCCATCGT AGGCCAGGCG CGGTGGCTCA 480
CACCGGTAAT CCCAGCACTT TGGGAGGCTG AGGCAGGTGG ATCATGAGGT CAGGAGTTCG 540
AGACCAGCCC GGCCAAGATG GTGAAACCCT GTCTCTACTA AAAATACAAA AATTAGCCGG 600
GCGTGGTGGT GCACGCCTGT AGTCCCAGCT ACTTGGGAGG CCGAGGCAGG AGAATCACTT 660
GAACCTGGGA CGCGGAGGTT GCAGTGAGCC GAGATCGTGC CATTGCATTC CAGCCTCGGC 720
GAGAAGAGCG AAACTCTGTC TTAAAAAAAA AAAAATTAGG CCATTATGAG ACAGGTTAGT 780
TTTACCCTAC TGATGATCTG TTGTTGCCAT GGTAATCCTG CTCAGTACCA ACCCGCAGGT 840
TCAGACATTC GGTGTATGTG CTTGGCTAAG GAGCCAATGG GACAAAGCTA CCCTCTGTGG 900
GATTTTGACT GAATGCCTCT AAGTCAGAAT CCCGCCCAGG CTGAACCACA GGGCAGCGCT 960
GCAGGGCCTC AGTTGGCCTC GGATAGCCAG TCTCCCAATG GCCTGGGATA GCCAGTCTCC 1020
TGCCATCCCC GCCGGCCCGC AGTTCGGCTC AGCAAGCGCG CAGGTACCCG AGGCCGGTGC 1080
GGAGAGTCCC TCCTCCTGGG AAACCGGGTG CGGCCGGAAA GGCGGCCGCC CCTCACCCGT 1140
CATGCAACGG CACGTTCGTG GGGAACCTGA CATTAAACTG TTCGTAGATG ACCTGCTTCT 1200
GGGTCAGGAT TTCGCACTGA GCAGAGCAGC TCCCTCGCTG TGATCTACTG AAAGTCAGCC 1260
CTCGACACAA GGGTTTGAAA AAGAAAAAGT GAAAAAAATA AAGAAATTAG GGCATGTTGG 1320
CATGCACTAG TGGTCCCAGC TACTCGGGAG GCTGAGGTGG GAGGATTGCT TGAACCTGGG 1380
AGGCAGAGGT TGCAGTGAGC CTAGATCGCA CCACTGCACT CCAGCCTAGG TGGCAGATTG 1440
AGACCCCCAT CTCAAAAAAA TAAAAATAAA TAATAATATT 1480
|
