Tag | Content |
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EnhancerAtlas ID | HS086-03859 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr15:73088780-73090140 |
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) |
KLF16 | MA0741.1 | chr15:73089637-73089648 | GGGGGCGTGGC | - | 6.62 | RREB1 | MA0073.1 | chr15:73089983-73090003 | TGGGGTGGGGGGGGTGGGGG | - | 6.38 | RREB1 | MA0073.1 | chr15:73089978-73089998 | GGGGGTGGGGTGGGGGGGGT | - | 6.74 | SP3 | MA0746.2 | chr15:73089636-73089649 | TGGGGGCGTGGCT | - | 6.34 | SP8 | MA0747.1 | chr15:73089636-73089648 | TGGGGGCGTGGC | - | 6.11 | ZNF740 | MA0753.2 | chr15:73089987-73090000 | GTGGGGGGGGTGG | - | 7.52 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_19773 | chr15:73088760-73089969 | CD4p_CD25-_Il17p_PMAstim_Th17 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I072796 | chr15 | 73088742 | 73090061 |
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Enhancer Sequence | CAAGTGAAAC TATCAGATCC CAGGGCGCTC CCGTGCGGTT GTCAGATTTC CCTCCTGTAA 60 AGTGGATGAG TAACCCCACC CCACATGCAC TCCCGTCCAC ACAGCTCTTG AAAGGCCAAA 120 CCAGGCGACG CTGTGGCCCA GAGAGAACCA GAAGAGAGGG TGCGTGGGGT GCACGGCAAG 180 CCATTGAGTC TGTGGCCACA CCTAGGCGGA GAGAGACGAG CTCGGGTGAG GGTGGGCCGC 240 GGGATCCACA GACTCCTCTT CGTGCGGTGG ATGCATCAGG CTCCGTCTCT GAACCTCGGT 300 TTCCCCATCT GCAGAATGGG GATGGGATCT CCTGGTGATG GGGATCTGTG GACGCGGCGC 360 CCTCGGGGGT GCACAGAACT AAGGCCGGCC TGCAGCAGCG ACCTCGGGGG CTGGTGGGGA 420 CGGAAGACCG GACCTCCTGG CCCGAAGGCT GGGCGCAGCC CCCGCCCGCC CGCCTCTTCC 480 CGCCGGCGCC TCCCCGGGGT GGCAGTGTGG GGAGAGTGGC TTGGCGCCCG CAGGGGGCGC 540 CGCGAGCCCA CCGCGAGAGC GGCCGCGGCG CGGGGTGGGT GCCGAACGGG CTGCGCGCCG 600 CGCTGCTCCC GACCCGCGGG TCAAGTCTGG CGCCTGGGAG GTCCTTGAAT TCCGCGGGAT 660 TTGTTTTTCC GCAAAACCAA AAACGCCATC CACTTAACAG ATCCGTGCTA GGAGGCCCTG 720 GCTCAGTCCT TCCACCAAAC ACCTCGGCCC AGCCGCGGCT GTACGGCTCC CAGGCTCCCA 780 GTGTTTCCTC CACGCTTTCA AACCTCAGCG CTGAGGTGAC CGCCTCCGGG CAGCCTTCCC 840 GGACTACCCC AGGACTTGGG GGCGTGGCTC CACAGCGGGC CTAGTTCCGC CCGTGTGCTG 900 GCCTCTTCCA CGACCGGCAG TCTTTGAGGA TGGGGCTTGG CCTCCATCCC CTTGAACCCC 960 TCAGCGTCGC ACCCCAGAGC CACTCTGACC CCTGGCCAAT GATTATAAGT GAGGGAGCCA 1020 CCTCTTCTCC CTGCGTGGCA CAGGCCAGGG TCCGCAGGAA GGGGCCTTGC TCATCCCCAA 1080 TCTTAAGCTC CGCTGAGATG AAGGAACCAA GAGCAGGCTT GGCACTGGGA GGGCGGCTGT 1140 CCCAGTGGCG GGGAGGGGAG CTCTGGATCT GTGGGGGAGT TTGTGCAGCG TGTCAGCGGG 1200 GGGTGGGGTG GGGGGGGTGG GGGCCTGTGG ATGCCCGCAG GTGTTTGTGT TTGTGCATGT 1260 GTAAGTCTCT GTGTGTATAT ATTTGTGGGA AAGCATCTTC TAAATTAAGA ATATATTTGT 1320 GTAGGGTAAA TGGTCAAGTC AAATAGAAAG TGACTTCAAT 1360
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