| Tag | Content |
|---|
EnhancerAtlas ID | HS091-17863 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:70505260-70506440 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr16:70505389-70505410 | GGAGGAGAGAATGAGGGAGGA | + | 6.62 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I070472 | chr16 | 70505601 | 70505750 |
|
Enhancer Sequence | CAGTCACCCT GCATTCCCTC ACCCCCATCT TCAGGCTTTG GGGAGCCCAA GGAGTCCTGG 60
CCCCCACCCC ACTGCGGGGT TCTCTGAGCA CTGGCCCGTG GGACAGGCTG TGAGGAGGGT 120
CGGATGTAGG GAGGAGAGAA TGAGGGAGGA GATAGGGTGA AGATAGGCTG TGAGACCAGC 180
AGAGTCTCCA CAGGCCTTTA CCTCCCTCCT TGCATCTGCT CTGCCAGGTG GGCTGGGTGG 240
GGATTTTGTT TTTTTTCTGG AGATAGAGTC TTGCTCTATC ACCAAGGCTG GAGTGCAGTG 300
GCCCAATCTC AGCTCACTGC AATCTCTGCC TCCCAGGTTC AAGCGATTCT CCTGCCTCAG 360
CCTCACGAAT AGCTGGGACT ACCAGCGTGC ACCACCACGC CCAGCTTAGT AGAGATGGGG 420
TTTCGCCATG CTAGTCTGGT TGGGTGGGGT TGTTGTTTTT TTTTTTTTTT TTGAGACTCA 480
CTCTGTCTCC CAGGCCGGAG TGCAGTGGCG CAATCTTGGC TCACTGCAAG CTCTGCCTCC 540
CGGGTTCACG CCATTTTCCT GCCTCAGCCT CCTGAGTAGC TGGGAGTACA GGCGCCCACC 600
ACCACGCCTG GCAAATTTTT TTGTATTTTT TAGTAGAGAT GAGGTTTCAC CGCGTTAGCC 660
AGGATGGTCT CAATCTCCCG ACCTCAACTG ATCTGCCTGC CTCGGCCTCC CAAAGTGCTG 720
GGATTATAGG TGTGAGCCAC CGCGCACGGC TGGGTGGGGG TTTTTATCCT TATTTGACAG 780
GCTAGAGACT GGGATTCAGA GAGGGAGGTA ACCCGCCTTG GGCTGCAGCC TGTTGTGGTG 840
GGCTGGGCCT GGAACCCAGG GTTCTGCTCC AGATTTCAGG CACCTTGGCG GGAGTGTTGG 900
GGCTGCAGGG CTGAAAACAA TTTCAGAAAT TGCTCCATGG CTGGGTGTAG TGGCTCATGC 960
CTGTAATCTC AACACTCTGG GAGGCCGAGG TGGGAGGCCA GGAGTTCATA CCTGCAGTGA 1020
GCTGACCACA CCACTGCACT CCAGCCTGGG TGGGTCAAGT ATGTTCTTTG TCTGTCTTCC 1080
TGCCCTCATG TGAGCACTTG AGCAGCTCCT GGCCCCCTGG CCGAGTGTCT CTAACCCTTT 1140
CCTGTGGCCC CTGCAGCCCT GACTGCTTCT TCCTCTCCCC 1180
|
