| Tag | Content |
|---|
EnhancerAtlas ID | HS076-24488 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr17:33923290-33924220 |
Target genes | |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr17:33923528-33923549 | TATTTCTTTCTTTTTTTTTTT | + | 6.2 | | NHLH1 | MA0048.2 | chr17:33923786-33923796 | CGCAGCTGCG | + | 6.02 | | NHLH1 | MA0048.2 | chr17:33923786-33923796 | CGCAGCTGCG | - | 6.02 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH17I035596 | chr17 | 33923661 | 33923790 | | GH17I035597 | chr17 | 33923985 | 33925257 |
|
Enhancer Sequence | GCTGGATTTG GCAGGATGGG ACATGGTGAA GAGTCCTATG AAGAATGACT CTTTAAAGGG 60
CCCAGCTTTT CTTGCTATGC TACTTTTGTA GCTGTTGATT AAATAGAAAT TTTGGAACAA 120
TTTTTTTGCC TTATTGGCCA TGGATATTGA AACGAAAAAG TGCTCTACTT CTGTGTCTTA 180
CTAATTTCAT CCTTTCCACA TAATGGTTTC AGGCAAATCA CGTAGTGTTT GTCCCCACTA 240
TTTCTTTCTT TTTTTTTTTT TTGGAGGAGG GGAGGTCAGG TTTTAATGTC CCAGTCCTCG 300
GGCGCCGTCA TCCCGCGCCT GCCAGGCCCG GCGGCCATGT CGCTCACTCG GGTGGCGGCC 360
AGCCTGCCTC ATCAGGGCCT TCCGCGGAGG CCGCCCCGTC GCCCTCGAGC ACCAGCTTCA 420
CGTCCAGCTC CAGCTGCCCG GTGTAGAAGC CCACGGCGGC GCACACCCAG AGCGGGCTGG 480
TGGCGAGTAC AGCGCCCGCA GCTGCGCCCC CTAGCGTCAG CTGCATGGGC CCCCGCAGCG 540
CTGCCAGGCC CCGCAGGCGC TGCCCCACAC CGCACACAGG CCGCCCAGCA GGAAGAAGCC 600
ATATGCTGCT TCGTGATCCA TGTCACTCTG CATGAAGGAG ATAACCCCGA TGCCCTATGC 660
CAGGAGGCCA TTGTGGAACC AGGAGAAGAA AGCTGTCTCG TGCGCCTTTC GGAGAGGAGC 720
CTGGCGCCTG CACGGTCCAG CTCGGACACA GGTGGCGGCG AAGCCCCGTT GTGGGGGCCG 780
TGGCCGGGGG CGAAGGACCC CTGGGCGCCC CCGCTCCGGG GCCACTGAGG CAGCAGTAGC 840
GACCTCCGGA AGCGGAGACT GTCCCCACTG TTTCTATGCT GGTAAATGAG ATCTGGTTGA 900
AAGGAACGAC AGGAACAGTC TTGAAGGTGG 930
|
