Tag | Content |
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EnhancerAtlas ID | HS128-14513 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr22:19748820-19750760 |
Target genes | Number: 12 | Name | Ensembl ID |
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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) |
PLAG1 | MA0163.1 | chr22:19748928-19748942 | CCCCTCTGGGCCCC | - | 6.36 | RUNX1 | MA0002.2 | chr22:19749648-19749659 | CTCTGTGGTTT | + | 6.14 | Zfx | MA0146.2 | chr22:19748902-19748916 | GGGGGCGCGGCCTG | + | 6.44 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I019760 | chr22 | 19747720 | 19755972 |
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Enhancer Sequence | CACGCCGCGA CCCTCCCCAC GTGCTGCCGC CAGGGCTGCG GGCCTCCGCC TGATCCGCGC 60 GAGCGGGGCC GAAAGCCGGG TCGGGGGCGC GGCCTGGCCA CCTGCGGGCC CCTCTGGGCC 120 CCGCTGCCTC CTTCGCTGTT CGCCGTCCCG GCTCCGGCGA CAGCCGCCCG GCGCTCCCCT 180 CCTAACACCT ATCCTCCGCC GGGGCGGGAG GAGACGGCGC GGGCCGCACG GGAACGGCGA 240 GGAGCCCCGC GGGACTCGCC CGCCCGCCCC GCAGCCCCAG GACGCCGCGC GGCCCAGAAA 300 CCGGCCCGGC TTGGGGCGCA CCCGGCTGGG GGCAGGCAGC GGCGTCCAGG GGGCCTCACC 360 GCCCGGCCGA CTCCTAGTAA ATCCCACCTC AAGAAAACTC TGGTTCAGTT CTGGAGTTCA 420 GTCTATGCGG GCAAGATAAA GAGCGGCAGC CGGGCAACTC TCTGGACACT TTCAGGAGAG 480 GATTACCCTT AAAAACAGCG TGCACTGTTG CGTGGAAGTT GCTACCCAGT TTCCTTCAAC 540 CTAGATCCCT ATAGTTGTGG GGCCTGGCTC TGTATCCAGC GGCCCGTCAC CTCCCAACCG 600 GCCTGTATTT GTTTTAAAGA CCAAGAGACA AGGGGAACAA GTTTTGCAGA TGCACCCGAT 660 TTGACCGGTA GACAAAGGCG GGTGCCGCGC TGTGTCTAAT GTACACACCA GCTCGGAGTC 720 CGAACAGCCA AGGGGAGCTC AGGGCCTGTT TGCAAAGCCT TCTCGTGGTT TCTGTTTCCC 780 TGCTGCCGGC GTCCTTTCTG AGGAACCTGG GCCTGTGCTC TGCTCCAGCT CTGTGGTTTT 840 TTTCCAGGCC CTCCTTGCTG TCCCCAGGCA CACAGGCCCT CCTGAGGACA GCGGCAGCCC 900 AGCCGCTGGC TCAGGCCAGC CCGGCAAGGG CCTTGTCGGC GCTGGGCTTC ACCCGGGAGC 960 CCACGTCCCG CAGCACCCTC CAGCCTGCAG AGGCTTCGGG TGGGGGAGGG AGCGGGCCTG 1020 TCCTAGAGGC TGGCTCCTGG CATCTGTCTT CTGCCCACCG CCTGCAGGGA GTTGCTTGTG 1080 AGGGGAGGCA GAGGGGACGG CAAGTGAGGG CCAATCCTTG TGTTGTCCTG AAGGGCCCCA 1140 CGGCCACTAC TGCTGTGCCA TCATGTGGGG GTAGCCCATG GCCTACACCC GTCCAGGCAC 1200 TGCAGAATGT CCTTTCAAGA GCCCTGACTG GTCACTGAGC CAGGGTCCAA AGCGGGGGAG 1260 ATTTGAGGAA CAGGAAAGAC ACAAACTGAG TACACTCTGG GTAGCTGCGT CTTGGGGTTA 1320 TGTGTCTTAA GGGGAGTGGA AGCTTGCCCT GTGCCCTGAG GAAGGTGGGG AGACTCTTAT 1380 CATGGGGCCA TGATAGAGAG GGGCCCTGAG AGTCAGGGGA GGGAGGGCTC TGAGCCTTGG 1440 CCTCACTGAG GGGATTGGGT AACAGCCGAA GACCCAGCTA AAAGGGCAGC GGGGACGCCT 1500 TGAACTCACA CAGGACTACC CGGTTTCACT TTGTTGGAGC CGGGAGCTGC TTCGATCAAG 1560 CTGGGGAGGC TCTGCTAAGG GCGCACGTTA GGCACCCTGC TGCCGGCCGA AGCTGGGACC 1620 AAGAGGCCAA AAAGTCAGCA AGGGCGAGGC CGAGTTTATG TAGGCCAAGG TTGCCGAAGG 1680 TGGGGGCTCC AGCGCTGGGC TGGCCATTTC TGTGTCCAGG AACGGCCCAG GAGGCTCCCC 1740 TGCTGCGCCA AGCTCCCAGT TGAGTAGGGG CCTGCCCAGA TTAGAGCAGC TAAGCCAGGA 1800 AAGATGGAGC CCAAGGGCTG GGACGACACA GCAGCCCCCA GAGGCTGGAG GGAGGGGCCG 1860 AGCAGAGGGG CCGCCAGCCC CAGGCAGGTC AAGGGGGGCT GCCTTCCACC AGCTAGGGTG 1920 ACCCAAGGCC TCATCACCCC 1940
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