| Tag | Content |
|---|
EnhancerAtlas ID | HS091-00116 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:2427010-2428040 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr1:2427795-2427809 | AGGCCACGTCATCC | + | 6.07 | | HSF1 | MA0486.2 | chr1:2427758-2427771 | GAACCTTCCAGAA | - | 6.19 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I002495 | chr1 | 2427256 | 2428289 |
|
Enhancer Sequence | TAGGTGCCCT GCCCCACGGG GAGGCCCCGC ACACTCCTGG GAGCCTGGCC CAACCGGGCC 60
CTTCTCTGCG GTGACCCCAC CAGGACCATC CCTGAGCAGG GCAGGACCTA CCCCCTTCTT 120
GGCCCCTGGA AGCAGTGAAG TGGTAGGGAG TGTGGTGTGC AGGGCAGGCT GGTGGCTGTG 180
GGCAGTGGGG GCAGGGGCGG CTGAGCAGGT GGCTGGAGGG CCCAGGTCCC CACAGCCCTG 240
GATGCTGCCG GGCTGTCGGC TCTCGGTCCT CACCGCCTCC TCTTATGAGG CCCCCAGCCT 300
CATGCCCTCC CCAGGGGGCA ACAAATGCCT GCCATGAAGT GGCTCCCCCT CTTCCCGTCC 360
AGTCAGGCTG AATTCAAGGC CCAGGCCCCC GTGTCGGAGG CCTTCCTCAG CACTGTCTGG 420
GGTCTCTTTG AGGTCTCAAA CCTACAGGCC CAGAAGGAAC TCCCACCCCT CCCGGACCCT 480
GGGCTCCCCC CGTGCCGCCC ACTCCCTCCT ATTGCCGTCT CCCCTCACTT CCATCCCCCA 540
ATGGTTCCTC CGTGCCCCTC GCCTGGGCAC AGCCCCCTCC TGTCTCATCC CGTCCCACGT 600
GCCAGCCGGG CTCTGCCCTT AGCACACATC TGATCCACGT GTGCCGCTGC CACCCGGCCG 660
ACACGGAGGC CCCCTTGGAC CCTGGCCTCC TCTCCACATA GCGATTCTAG GCCAGACCCA 720
GGCCCCGAGC CCAGCTCTCC CCTGCTCAGA ACCTTCCAGA AGCCCCCACA CCTGCCACGC 780
TTGGCAGGCC ACGTCATCCT CCACTGCACA CAGTGCCTAG GGACTTTGCA CCTGCTGGTA 840
GCTCCCAGCC AGCCCACATC CTGCCCAGCA CTCAGGTTTC CGCAGCCCGC GGCCCAGTCT 900
GGCGTCCGTC TCTGATGGTT CGGGGCCTGC TGCGTGAATT AATGAGGCTG CCCGAGCCCT 960
GGAGCCCGTC TCACGGAGCT GGGTGCCAGG CTGGCCCTGG ACGGGAGGGG TTCTGACCCC 1020
CTGCACCTGC 1030
|
