Tag | Content |
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EnhancerAtlas ID | HS177-13749 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr20:34652310-34653220 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr20:34652732-34652742 | GCCCCGCCCC | + | 6.02 | RFX1 | MA0509.2 | chr20:34652638-34652654 | GGCTGCCATGGCAACG | + | 6.01 | RFX2 | MA0600.2 | chr20:34652638-34652654 | GGCTGCCATGGCAACG | + | 6.28 | RFX2 | MA0600.2 | chr20:34652638-34652654 | GGCTGCCATGGCAACG | - | 6.3 | RFX5 | MA0510.2 | chr20:34652638-34652654 | GGCTGCCATGGCAACG | + | 6.77 | RFX5 | MA0510.2 | chr20:34652638-34652654 | GGCTGCCATGGCAACG | - | 6.81 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_24902 | chr20:34652078-34654000 | Colon_Crypt_3 | SE_27150 | chr20:34651941-34653968 | Esophagus | SE_57668 | chr20:34652759-34653492 | VACO_503 |
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Enhancer Sequence | TCTTCCTGGG GGGCGGTGCA GGGTCAGGTG AGCAGCTGGG GCTCCGGAGG GTCTGGGTCT 60 CTGTCACTTC TTGCTGCGTC GCCTTCTGTG AGTCCTTCCC AGCCCCCTAA TCATGCCCGC 120 CTGAGCAAGA GGATGAGAAA ATGCCGACCC CGTAGCGGGG ACTCTGCTGC TGTGCGGGGC 180 GCGGTTCGCC GAACCCACTG GCCGCTTCTA GAGAGTCGGC CCCAGGGCCA GGACCTCCAC 240 TTGGCAGGCG CTGGGGCGCC CAGGGGCAGG GCCAGCGCGG GAAAGGCCGC GAGTCCTTCG 300 ACCCCCTGGC AGTCTGGGAG CCGGCCGCGG CTGCCATGGC AACGCCCGGA AGCTGCCGGG 360 AGGGGAGGCA GGCCCAGCCG GGACGAGGCC CTGCCTCCAG CCAACGCTCC GCCCAGAACG 420 AAGCCCCGCC CCGGAACGAA GCCCCGCCTC CAGCAACTCT CTGCCCGGAG AGAGGCCCGA 480 CAGCTGCGAC CCGACTGGTT CTGTCCGAGC CCGACGGGCC GCGCTGACCC AGCGACTGTG 540 CCTGACTGAC CACAGGTGCC GCCACCGCCT GATAATACGA GTGTGTCAGC TTCCGTCTGA 600 CTGAACGCAG GTTTCATGGG TGCCTGACAG ACCAAGACTG CTGGATCTGT CAGCCTGGCC 660 GCAGCTGGCT GACTGGCTGA CTGGCTGGCT GGTTGACTGG CTGGCTGACT GGCTGCCTGG 720 CTGGCTGGCT GGCTGGCTGC TCTTGCCCGG CCGCCATCTG GGCCTGACGG GCTGCGTCTG 780 ACCGGGCGGC CTATCTGCCT CTGCCTGACC AGCCTCCATC TGTGCTTGGC GAGCTGTGTG 840 ACCGGCCGCG ACGGTCTGTG TCTGACTGAG CACAAGGTTC CTAGCGGCCG ATCAGCTGCT 900 TGACCCCATC 910
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