Tag | Content |
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EnhancerAtlas ID | HS076-23831 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr17:9142180-9142950 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr17:9142652-9142663 | GGGGGCGTGGT | - | 6.14 | KLF5 | MA0599.1 | chr17:9142200-9142210 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr17:9142651-9142666 | TGGGGGCGTGGTCAG | - | 6.52 | SP3 | MA0746.2 | chr17:9142651-9142664 | TGGGGGCGTGGTC | - | 6.16 | SP4 | MA0685.1 | chr17:9142649-9142666 | GCTGGGGGCGTGGTCAG | - | 6.16 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_01955 | chr17:9142034-9143325 | Aorta | SE_26708 | chr17:9140746-9149651 | Esophagus | SE_44564 | chr17:9142078-9143295 | NHDF-Ad |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I009238 | chr17 | 9141895 | 9149189 |
|
Enhancer Sequence | TCTGTTCAAT CTGAAGCTCT GGGGCGGGGC CCAGCAGTGT ATTTTCACAA GCCGGCCAGG 60 GGATTCTGAT GCATGCTCCA TTTGGGGAAG TCCTTCTACT AGGGAAAATA CTGGCAGAGA 120 ATTTGGAGTA AGAGGAATGG TCTGGGGACC TTGGGCGGCA TGGAGGAAGG GAGGCCACCT 180 GGTAGGGATG GCTTAGGCGT GGGAAGCGGC AGTCCAAGGT TCCCGGGGCT CTGGAAAAGG 240 CACTACGGCC ACCCCAAAGG GTGGGTTCTC ATCTTCTGTC CCTGAGCATT GAGGACCCAT 300 TATGGTTTTC TGAGGCTGGT TGGAGGGCCA GGCTGTGTGT GGAGTGTCAT GAGGGCTGGT 360 GTAAAGTGAC TTGGGCCTTT GGAGAAGCGC ACCCCTGAGG AACCTCCCTC TCCCCGCCAG 420 CACTGCTCTC ACCCGAGCGC CTGCCCTGGG CAGACAGCTT GCCCAGAGTG CTGGGGGCGT 480 GGTCAGCACC TGTAGGCTTC CTGGACAAAG TGGGCCTTGA CAAGGCCAGG AGATGGCTTG 540 TCCCGACGGC AGTGCTGGGT GGCACCCTCA CAGCGTGGGA GGCAAGGCTT CTTGGCCCTG 600 TTGTTAGCAG GTGGGGGTCT ACGATCAGCT TGCCACCACC CACGCGCTCC TGTATGGGCC 660 ACTCTGTGCA GTCACTTCCT GGGGCTGGGT CTCCTTTCCC TTCTCCCCAG GCTCAGGCAG 720 GGCGGACCTA GCCACAGCAG CTGGGAGCCC ACCCGTCTGC CTGTGCTTCC 770
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