Tag | Content |
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EnhancerAtlas ID | HS184-00891 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:61803530-61805120 |
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) |
Mafb | MA0117.2 | chr1:61803603-61803615 | AAATTGCTGACT | + | 6.92 | NFYA | MA0060.3 | chr1:61805052-61805063 | TCTGATTGGCC | - | 6.02 | NFYB | MA0502.1 | chr1:61805053-61805068 | CTGATTGGCCCCTAT | - | 6.16 | RUNX3 | MA0684.1 | chr1:61803677-61803687 | AAACCGCAAA | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_64290 | chr1:61802112-61805213 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I061336 | chr1 | 61802364 | 61805416 |
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Enhancer Sequence | TGTCAAATAT CACTCCTGGT AGGAACCCAG AAAGTTCTCC TGAAAAATCC ACTACTTCTG 60 CCCATTTCCT TCCAAATTGC TGACTCTATT TTACTTGAAG TTGGTGGAGT GACTTCGAAA 120 CCCTAACTAC TTCACTGGGA AAGAGGAAAA CCGCAAATAC ACACAGGCCA TTGTGACTCT 180 GGCCTGGTGG GCTCTAATTT TCTAGCGGCG GTTTGTACAC CCAAGCCGGC TGCAAGGGTT 240 AAGTAAACTT CGTGGCTAAG GATGACTTCA TGGCCCTGGA ATTTTGAAAA GCCAGGATTC 300 TCAGTACACT GTGGCCAGCC TTAGAGTCTT TGGGTGTGAA AACCACTCTC AGTTACCCGG 360 ACTGATTTTT GGTTCCTGTT GCAGTGCTGC AGAATCTATT AAAATCCGGC AGCTGAATTG 420 TCCTGGCTCT GCCACAAAGC TCAGCTGCCG GGTCCACTAC AGGATTCCTG AGTTGTTTGT 480 CAATGGAGAG TGGGAGTGAA TGGAACCAGG CATATGCCTC AGCCTGGCAT GAGGTGGCAC 540 CCTAGTGGCT GTTTTCTGCC TTAGAAATGT GCGCTCTTTC TATATTTTCA CACAGGAATT 600 GTCATTAACA TCCAAATTGC AGTTCATTTC TAAAGTTCTT TTTGAAGTCT CTGGGTCCTT 660 GTTACGTTTT CAAGTACCCA TATTCAGATG CTTAGATTTT CAGGCTAGTA ATTTAGTAAG 720 AACTATTGGC AATATTCTAA CCTGACATGG TGGAACTTCT AAGACAGAAT GAACTCGGCT 780 ACAAGGCACA ACAAGAAAAC GAAACTCTTG GGTAGGAACA AGCCCAAACT TGAAAATACA 840 AAATGTTCTT GCACAGAAGG ACTAATGAGG AAATGGGTGT AGGATAAGAA ATTCCAGACA 900 TCCAGTCATT TGGGGTGCCA TTTAAACATT CGCAGTACTT TAGATCTTAA TTAAAGTGGG 960 ATAGATTTAA AACTTTCTTT CTAAACTAGT GGCCTGTTGG TTTTCCTGTG TTAAGTAACA 1020 CGATAGCTGT GATCATTGCA TGGAAATTAA TTTTTAAAAT AGCTTATATT CTTAAGCAAG 1080 ATCTTCTTTC AAAAGAAACC ATTTGGGCTC GAGCATTAAA GGAAGAAACA AAAAGAATAT 1140 AATAAAAAAT AGATTGCAGC CCTAGCATGA ACAGTTGCCG TGACCTTGCC TTTTGTTTGC 1200 CATTACACAA TTCAATGGCA GTCTACTCAA ACTATGTGCT CGATCAATAT CCTATTAAAG 1260 CAGCACAAAA AGTCTCCATA AACTTAGTGG TTAGCTATGT TTATAAATGG AACTCGGCAT 1320 AATTGGATGG TCAATAGCAG GCTCTACTAG TAATTTTAAA ATGAACGTCA CACATTTTAT 1380 ATCTGTAGAA GTCAATGGCA CCTCTTCTAG AGTGAAGGTA GAGTGTGGAG CAGACAAAAG 1440 AGTGGGTGGC CCTTTAAAAA AATCATAATG TCTATTTCCA AATGTAGTTT TTAAAGAAAA 1500 TCTAAGTTAT GGAAGAGAAA ATTCTGATTG GCCCCTATAT ATTTTTATTT TGCCTATCTG 1560 AACCACCTTC TTCTGAATAT ATTATGACTT 1590
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