| Tag | Content |
|---|
EnhancerAtlas ID | HS086-03052 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr12:121686540-121687580 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr12:121687490-121687501 | GGAGGGTGTGG | - | 6.32 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I121248 | chr12 | 121686081 | 121687090 |
|
Enhancer Sequence | CAACGAACGA CAGGAGGGGT GAGGGGCAGG TGTGGCTGGC TACCGGGGGG CCCTGCCAGC 60
GAGCGGAGCC ACAAGGGCAT GCAGGACGGA GAGGCAAGGG CCTGTGGTCA GGCATGCAAA 120
ACAGCTGGCG AGCAGAGGGC AGGGGTGAGC AAAGGGGCGG AAACATGAAG ACGGAGAGAC 180
AGGACGGGAG GAGCTACAAG GCTGAAATGG AAGTGGGGCG ATTCTCCATC CGGCCCCGGG 240
TCTTGGCCGA AGTGATGGGA ATTTGGCATC TGCCTTGCCT GGCTGCCCAA GGAGCATCCA 300
TCACTCCTCA GCCACAATCC CTGACACCTG GGAGGCTCAG TGCACAGCAG GCAGCATTCT 360
CCCCATCTCA CAGCAGGAGA GGCTTGGAGG CATGGTGGGA CCAGCTGGCA GGACAGGATC 420
AGGAGAGGAC CCAGGCAGGG GTCTGCCCCC TTGGGTCCAA GCCCCAATCC ATGATTTTTT 480
GGGCTGCCTT CTGTTAAGAC CTTCAAATGC CAGTTAGCTA GCTGCCTAGG AAGTCCCAGG 540
GCAAATCTCT AGATTTCCTA GAGGGCCAGA TATATGTGTG TGGCATTAGT GGAGATGTGT 600
AGGGGAATAC ACTTTCCTAA AAGTGCTTTC TGCAAGAGGG TGGGATTCAG CAGGCTGGGG 660
AGGTCGAATT GCTCATTAAT TTCCTCCCAT CCTCACTGCA GTTTCTCAAA GGGACGGGCC 720
TTTGGAAAGG ACCTGAGCTC TGGGAATAGG GTGTGGAGCA CGGAGGCCCC ATGCCGGTCT 780
GCAGAGGGTG GATCCCATCA GCCCACGCCA ATCAGAGCAA GTGCAGGCTG GCGGGTCATA 840
GATCCCACTC CCACAGTCAC AGTGCACACA ATGCCCAAAT CTTCCTACCC AGCCCTCAAC 900
AGCCCCCAGC AGCTCAGAGG CCCTGGGGCA TAGGAGAACA GCGGTGCCAA GGAGGGTGTG 960
GTGCTGTGGA CACAAGGGTG TGGGGTCTGG CTGAGGCATG GCTGAGCCAA ACAATTCCGA 1020
GCACGGGGCA CAGGCTGAGC 1040
|
