Tag | Content |
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EnhancerAtlas ID | HS080-17446 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr19:41414020-41414680 |
Target genes | Number: 14 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr19:41414293-41414303 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr19:41414290-41414305 | TTAGCCCCGCCCCTC | + | 6.34 | SP2 | MA0516.2 | chr19:41414289-41414306 | CTTAGCCCCGCCCCTCC | + | 6.79 | SP4 | MA0685.1 | chr19:41414290-41414307 | TTAGCCCCGCCCCTCCC | + | 6.39 | ZNF263 | MA0528.1 | chr19:41414562-41414583 | GGAGGAGAGGCGGGAGGGGTG | + | 6.16 | ZNF263 | MA0528.1 | chr19:41414559-41414580 | TGAGGAGGAGAGGCGGGAGGG | + | 7.3 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I040908 | chr19 | 41414106 | 41414905 |
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Enhancer Sequence | TAAAATGGGC ATGAATGCTG TTCCCCTTTG CAGAGGTTTG TGGGCATTAA GTGAGGTGAG 60 CATGCAACGG TTTTTGAACA GAGCTGACAC GGAGGTACTT GTTCAAGAAA TGAGATGCTA 120 TTATTACTAC TCTTTGTAGC ATAGTTTAAG GTTTCCCTTC CTCTCATCCC AGCTCTGAAG 180 GACATCGTCA AGGTGAACTG AGCCCCTTCT GTTTCTTCTC TTCCCCCTAA CCACCTCGCC 240 CCTTCCTTTC CCCCTGTCCT GCCCCCATTC TTAGCCCCGC CCCTCCCGCA GGCCCGCTCC 300 TGGCCCCGCC CTTCCTCTGA TCCCGCCCAC CACGCCGGCA CCAGCACAGC CCTCCCTCAG 360 CAAGGCAAGT AGCACTTGGT GTAGTTTCGT GGGATTGTGA CAAAGCCCAC GTGTTTGGGG 420 GACACAACAA TGTCCTTAGG CGACTGCCGC GATTTGAAGC GGAAGTTCTG CATGATGGTG 480 GTGAGGTAGA GAAAGAGCTC CATTCTGGCC AGGCCTTCTC TGAAACAGTT CCGCCTTCCT 540 GAGGAGGAGA GGCGGGAGGG GTGGAGGTGA AGCCCACTCT TAGTGCAGCC TTGCCCCGCT 600 ACAGACCTCC AGCTGCGGCT CTCCCAGGGA GGAGGGGTGG AATATTATGG CCTGAGAGAC 660
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