Tag | Content |
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EnhancerAtlas ID | HS129-22436 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr20:34652190-34653720 |
Target genes | Number: 28 | 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 | GGCTGGGCAC AAGGTGAGTG CTCGCCTTGA CATTGTTGCG CCAGATTTCC CTAAGCACAT 60 CACTGCATGG CTGTTCTCTC TTCTGGATAC GGCCGCCCTT TCTGCCTAGA GACGTTTGAT 120 TCTTCCTGGG GGGCGGTGCA GGGTCAGGTG AGCAGCTGGG GCTCCGGAGG GTCTGGGTCT 180 CTGTCACTTC TTGCTGCGTC GCCTTCTGTG AGTCCTTCCC AGCCCCCTAA TCATGCCCGC 240 CTGAGCAAGA GGATGAGAAA ATGCCGACCC CGTAGCGGGG ACTCTGCTGC TGTGCGGGGC 300 GCGGTTCGCC GAACCCACTG GCCGCTTCTA GAGAGTCGGC CCCAGGGCCA GGACCTCCAC 360 TTGGCAGGCG CTGGGGCGCC CAGGGGCAGG GCCAGCGCGG GAAAGGCCGC GAGTCCTTCG 420 ACCCCCTGGC AGTCTGGGAG CCGGCCGCGG CTGCCATGGC AACGCCCGGA AGCTGCCGGG 480 AGGGGAGGCA GGCCCAGCCG GGACGAGGCC CTGCCTCCAG CCAACGCTCC GCCCAGAACG 540 AAGCCCCGCC CCGGAACGAA GCCCCGCCTC CAGCAACTCT CTGCCCGGAG AGAGGCCCGA 600 CAGCTGCGAC CCGACTGGTT CTGTCCGAGC CCGACGGGCC GCGCTGACCC AGCGACTGTG 660 CCTGACTGAC CACAGGTGCC GCCACCGCCT GATAATACGA GTGTGTCAGC TTCCGTCTGA 720 CTGAACGCAG GTTTCATGGG TGCCTGACAG ACCAAGACTG CTGGATCTGT CAGCCTGGCC 780 GCAGCTGGCT GACTGGCTGA CTGGCTGGCT GGTTGACTGG CTGGCTGACT GGCTGCCTGG 840 CTGGCTGGCT GGCTGGCTGC TCTTGCCCGG CCGCCATCTG GGCCTGACGG GCTGCGTCTG 900 ACCGGGCGGC CTATCTGCCT CTGCCTGACC AGCCTCCATC TGTGCTTGGC GAGCTGTGTG 960 ACCGGCCGCG ACGGTCTGTG TCTGACTGAG CACAAGGTTC CTAGCGGCCG ATCAGCTGCT 1020 TGACCCCATC TCTGCTGAGC CGGCCGACAC CGACGGATTG ACTCTGGCAA CGCCTGGCCC 1080 GAGTGGCGCT ACCGGCTTCC AGAGACTTCC TGACCCCTGC CGAGGTTGCA CCGCTCAGCG 1140 CTGCCCTGTG AGGCGCTGAC TGTGGCCGCA GCTGAGTGCG GCTGCCCCTT CACAGACAGG 1200 GCGTGCAGAA TGACGGTCGC CTGGCTGTCC CTCCCTAGGC GCCCCTGGCT AGCTCGGCTT 1260 GCCTGGCAGC GTCTGTGTCT GAGGGACGTG TTGGTGGCCG CCGCTGGCCG CATCTGTCCC 1320 CCTGCAGGTG GGCATCAGGT TGCCCCCGTG AAGTGCAGCT GGGGCCGAGC CTGGCTGAAG 1380 GACGGCCACC TTCTCTCCAG CTGTCCAGCG AGGGCTTCTG AGGTGGTGCC CTCCGGGGCT 1440 CTGTGGCCTG GACCTCTCCA GCCACACACA GTCAGAGCCT TAGGGGATCC CAAGCAAGGG 1500 CACCCACAGG GAAGAGAGCC TAAGACAGAG 1530
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