| Tag | Content |
|---|
EnhancerAtlas ID | HS081-05285 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr12:110258510-110259440 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr12:110258724-110258735 | ATTGCACAACA | + | 6.14 | | ZNF263 | MA0528.1 | chr12:110259255-110259276 | CCCTCCTGTTTCCCCTGCTCT | - | 6.17 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I109820 | chr12 | 110258477 | 110259394 |
|
Enhancer Sequence | GTACAGACGG GGTTTCATGG TGTTAGCCAG GATGGTCTCG ATCTCCTGAC CTCGTGATCC 60
GCCTGCCTCA GCCTCCCAAA GTGCTGGGAT TATAGGCGTG AGCCACTACG CCCGGCCCTC 120
AGCTGCCCTA TTAAGGGATC GTAATAGGGT CGTTGTGAGA GGTATATACC TTGAGTCAAG 180
TGCCTGGCAT AAAGAAAGCC TCAATAAACA GCAGATTGCA CAACAGATGG CTTCTCTCTG 240
AGAATCCCGG ATTCAAAGGC GGTGGAGGTC TCTGGCTCCG TCCCCATGCC CCAACTTGCG 300
GAGGGTGGAA AAAGGGGCCC ATCCTCGGGG TTACCCGCGG CTTTGCCTGA TCTCATGGAA 360
ACCCTGGCAA ACATTTGTCA AATCCCATCC TCCTGATTAC GTGACCAAGG AAAGCTGCTT 420
AAATCTGGGG GCAAGTTTGG GCATGCAAAC CTGCTCCGCC CCAGCGGGGA GGAATCCAGG 480
GAGCTGGTTT CTCCCGGTTC CCTCCCTTCT GGAATCAATT CATTCCACCA GGCATCAATG 540
CAGTGGCACC TGTTTGCAGG GCACAGGGGA GACATAAAAG TGTGGAACCT CAGAGAACTC 600
GCAGTCCAGG AGGGAAGGCT GATGGCTCTC TCTGCCTCCA GGCCTTTGCC TAGGCTGTTC 660
CCTCCGCCTG GAATGCCCTT CCCTTCGCTG GCTGGCTCCC ACTTACTCCT CAGGCCTCAT 720
GTTAAAGGGC ACTTCCTCTG AAAAGCCCTC CTGTTTCCCC TGCTCTTTAC TCTTAGAGTA 780
ACATGTGCCT TCCTTTACAG CACTTCCCAC GATTAAACTT TTCTATATAT GTATTTTTTT 840
TTTCAAGAGA GTCTCGCTCT GTCCCCCAGG TTGGAGTGCA GTGGCATGAT CTCAGCTCAC 900
TGCAACCTCC GCCTCCTGGG TTCAAGCAAT 930
|
