Tag | Content |
---|
EnhancerAtlas ID | HS091-19429 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:31324890-31326380 |
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 | chr17:31325517-31325536 | TGGTGCCCTCTCGTGGCGG | - | 6.73 | RREB1 | MA0073.1 | chr17:31325044-31325064 | TGTGGGCAGGTGTTTGGGGG | - | 6.61 | ZNF263 | MA0528.1 | chr17:31325931-31325952 | CGCCCCCCACCATCCTCCTCC | - | 6.5 | ZNF263 | MA0528.1 | chr17:31325934-31325955 | CCCCCACCATCCTCCTCCACC | - | 6.69 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I032998 | chr17 | 31325299 | 31326418 |
|
Enhancer Sequence | GTGAATATGG CTCTCAGCTC TCAGTGTGTC TGCAGGTGCC ATGTCAGAGC CAGAGCACCT 60 CCGTTTTCCC TCACCTCACC TGTCCGCTTG GGCTGGGTTT CCAGTGGACT CCAGAAAGCC 120 CAGCACCAGA GGCTTACCTC CATTTCTGGT GGCCTGTGGG CAGGTGTTTG GGGGGGGCAC 180 CAGTGCATTT TTTGTCTACC ACACCTGGCA AAATTTGGGT CTAGGGTGGC CAGATTTAAC 240 AAAACAAATA CATAAGAAAC AACAAAAACA GGATGCCCCA GTTTAATTTG AACTTTGGAT 300 ATACAACAGA TAATTTTAAG CATGTCCAAA ATATTGCATA GGAACATATT TATATTAAAA 360 CTATTTGACG TTTATCTAAA ATTTAAACTT AACTGGGTGT CCTATGTTTT ACCTGGCAAC 420 CCTAGCTGGA TCTAGGGCTG TGCACCTCTG GCTTGATTGG GAAGGTTCTT GGGACACTTT 480 TTTTCTGCAG CTTTGGTTGC AGATGGTGGT CACTGTGCTT TGGCCCTCCA GCTGTGACTA 540 CTAACACACA CCCCTGCCAA GCCGGGGGTG CTGCTTGGTC GCGGGAGAAG AATGACCACC 600 CGGAGCTTCT GCTTTCACCT TGCTCTCTGG TGCCCTCTCG TGGCGGAAGA TTCAAGTGCC 660 GCTGATAGAG ACGGTGCGCT CACTTTGCCC ACTACTGCTA GGAGTTTGGA GGATGGGACG 720 GGAGTGACCG TGGCTTTCAA TCCGCACAGC CAGTGCAGCC TTCTGCCTTA GTCAGCACAC 780 GAGAAGCCCA GAAAAAGATA GCGCGGTCCC CTGCTAATCT GGGACGACTG CCTCTAAAGG 840 AGGAAGGTGG GTGGGTCTCA GGATCGCAGT GGATGTGGTG GCAGCAGCAG CAGTTGCAGA 900 GATAGGATGA TGTGTGAGAA GCCTGAGCCC TGAGTTCAGA CTGTAGATTC TTCTGAAAAG 960 GTTCCAAAGA AACCTGTAAG CACTGAACTG TTGGTTGAGG CATGGCTGGT GACTCTTAGG 1020 GAGAGGAGGG GACGACACTG TCGCCCCCCA CCATCCTCCT CCACCTAATT CAGCCACCCT 1080 GAATGCCTCC GGGTCAGCAT ACACCAGAGG GGCGTGGAAT GTCCACAATT AGCGAGTCAG 1140 GCCAGTTTCC TTCCCCTGCT GGTCTGGTCA AGATGATGAT GAAACTTGAG AGCGACTCAT 1200 GCAAGGGGAC AGAGTGGTGA AGAACCCTGC TGGCAGTAGG GGCATCAATG ACTAATGGAG 1260 CTATTAAATC ATAAGTAGGG AGAAGCTGCT GTCTTTTTAA CATCAAGGCA AACACGGTGT 1320 GCCTACCATG TGCCATGCAT TATCTAATCT AGACCCTAGA ACAATAGCTA TGATGCAGCT 1380 ACCATTATGA CCACCATTCC ACAGACAAGG GGAAACAGAG GCTCAGATGA GATAAATTTG 1440 CACCCAGCTC AGTGTGACTC CACATGTACG CTTACTCACT GTACTTTGCC 1490
|