Tag | Content |
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EnhancerAtlas ID | HS129-03596 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:225638170-225639510 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr1:225638391-225638408 | AAGGTCACAGTGGCCCG | + | 6.23 | ESR2 | MA0258.2 | chr1:225638392-225638407 | AGGTCACAGTGGCCC | + | 6.67 | ZNF263 | MA0528.1 | chr1:225638736-225638757 | TCCCCTTCACTGGCCTCCTCC | - | 6.12 | Zfx | MA0146.2 | chr1:225638225-225638239 | CCGGCCTCGGCCTC | + | 6.28 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_26936 | chr1:225632317-225640379 | Esophagus | SE_54244 | chr1:225637447-225639301 | Spleen | SE_54544 | chr1:225627713-225643546 | Stomach_Smooth_Muscle | SE_61599 | chr1:225612246-225670298 | Toledo |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I225450 | chr1 | 225637903 | 225639303 |
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Enhancer Sequence | GGGGTTTCAC CATGTTGGCC AGGCTGGTCT TGAACTCCTG ACTTCAAGTG ATCTGCCGGC 60 CTCGGCCTCC CAAAGGGTTG GGATTACAGG CGTGAGCCAC CACACCCGGC TGCAACTGTT 120 TCTTCTGATG AATGCAGCTG TGCCAGTTTC CAGGCAGCCT GTGCGAAGCT CTGCCAGCTC 180 ATCGTCCTGC TGTCGCAGCC CTGGGGCTTC CTGTCAAGGG GAAGGTCACA GTGGCCCGTG 240 TAAACCCTCA CTCTGCTTAC ACAGTTGTGA GCAGGGGCAC TCTCTGAACT GCAATGTATA 300 TAACAATAAG TAAACTGCAA AGAGAAAAGG GAAAAAAGGA AATTGTTTTC CTGGCACATA 360 ACCAAAAAGT CTAGGGACAG ATCTGGTGCT TCCGGCTCAA CTTGACCAAG GGACTCATAT 420 GATATCACTG GAGCCACAGT CTCCTAGCCC TTGCCTCCAC TTCTGCTGGA AGCTTGGTTT 480 CATTGTCAGG CCGCAGCAGC TCGAGGACAC AGCCAAACCA TATCACCATC TTTTACCAAG 540 GTGCACACAG CCCTTCAGAA TCCTCCTCCC CTTCACTGGC CTCCTCCTCT GACCCTCTTC 600 CTTCTGCTCA CTCAGCTCTA GCCACAGTGG CCTCCGTGCT GTTGGATTCC ACCTCAGGGC 660 CTTTGCACAT GCTGCCCTCA TGACTGGAAC ACTTCCCCAA CACTCCTGAG GCTCTCTCCC 720 TCTCTTCTTC AGGTCTTGCC TTTGCAGTGA GGCCTTTCCT CACCACTCTG CTGAAAACTG 780 CAACCCATTA CCTGACCCAG TCCCTTTCCT TCCCTGCAGA GCACTTTCCA CCACACACAT 840 ATGTCACTCC TTGTACACCC ATCAGTCTGT CTGGGCTAGA AGAATAGCTC CTGCGGGACA 900 GGGGTTTGTG TCTGTTTTGT TCGCAGCTGC ATTCCCAGTC CTAGAGCAAT GCTTGTGGGG 960 CCTAGCAGGT GCTCGCTAAG TGCTCATGGA TTGGCTGAGA GCTGAGTTGA CTCCATAGGC 1020 TATGCCACAG AGTGGCCCTG GGCAGCTTGC TGTCCTTCCT TCACACGGAC AGAGGCAGTT 1080 GTGGTTTGGT AAGATACCCT CTGAACAGCT AATGTGGGTA AAGAAGCATC TCCCTGTGGG 1140 CAATGGTAGC CATCTGCAGG CCCCTGTGGT TCAGCTCCCT GCTATGGAGG GCTGAGTCAT 1200 TGACGTGGTG GCCTTTTAGA GACACACCTT GCGAGACTCC TTTGTTAGGA CAGAACAGTA 1260 TCTCCTGGAA TCTTTATTTA AATTAAAAAA ATAAAAGTTT CTAAGAACCA GGCCTTCAGA 1320 AAACTTCAGA CTGCCCTTCA 1340
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