Tag | Content |
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EnhancerAtlas ID | HS128-01761 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr1:204101380-204103640 |
Target genes | Number: 13 | 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) |
LMX1B | MA0703.2 | chr1:204102617-204102628 | TTAATTAAATT | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr1:204102879-204102894 | TGATCTTCTGACCTC | - | 6.15 | POU2F2 | MA0507.1 | chr1:204102969-204102982 | TTCATTTGCATTT | + | 6.59 | RARA | MA0729.1 | chr1:204102876-204102894 | TCTTGATCTTCTGACCTC | - | 6.01 | ZNF263 | MA0528.1 | chr1:204103033-204103054 | GAAGGTGGGTGAGGAGGAGAA | + | 6.69 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_65332 | chr1:204095460-204101903 | Pancreatic_islets | SE_65332 | chr1:204102868-204104668 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I204133 | chr1 | 204102869 | 204104668 |
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Enhancer Sequence | GTACCTGTGG GGAAGACAGA AGGAAGCTGG GTGTGAGGAA GAAAGCCAGG TGGGCCCTGC 60 TGGGGGTGCT GACATCATGA GAAAAGTTTT TCAGTGGCTC TAGGCCTATC TAAGTCTGAG 120 CAGATCAACC CCAACCCAGA CTGATTAGTA TTATTATTTC TTTTGCTTCT TTTTAAAATT 180 TTTAATATTT ATTTATTTTG AGACAGGGTC TGGATCTGTC ACCCAGGCTG GAGTGCAATG 240 GCATGATCTT GGCTCACTGC AACCTCTGCC TCCCGGGCTC TGATGATCCT CCCACTCAGC 300 CTCCAGAATA GCTGGGATTA TAGGTGCACG CCACCACACC TGGCTAATAT TTGTATTTTT 360 TGTAGAGACA GGGTTTCACC ATGTTGCCCA GGCTAATCTT GAACTCCTGA GCTCAAGCAA 420 TCCGCCTGCC ATGGCCTCCC AAAGTACTGG GATTACAGGC ATGAGCCACC GTGCCCAGCC 480 TATTTTTTTT TTAACTTCAA CTACATTTTT TTTCTTCTTA GATCAGACTA GAGAAACCCT 540 TCCACAAACA TGCTTGTTTG GAGTTTTGTT TTTACCGTTC TATATTGTTA AGTATATTCA 600 CATTGCTGTG CAAATGAATA TCTACAACTT TTTCCTTTTG GACAACCGAA ACTAGACCTA 660 TTAAGCAATA CTCCCCATTG CTCCCTCTCC CCACCCCCTG GCAACAATTC TACTTGGTTT 720 CTATGGATTT GACTACTTTA GTTATCTCTT AAAGAACCAT ATTTGTCTTT TTGTGACTGG 780 CTTATTTAGC GTAATGTCCT CAAGATTCAT CCACGTTGTA GCAAGTGACA TTTCCTTCGT 840 TTTTAAGGCC AATATTCTAT TGCATGTATA GACTATATTT TATTCATTCA TTCATCTGTT 900 GACAGACAGC TGGGTTGCTT CCATCTCTTG GCTACTATGC CAAGAATAAT GTTGCCATGA 960 ACATAGGTAT ATAAATATTT CTTTGAGAGT TTGCTTTCAA TTATTTTGGC TACCCACCGA 1020 GAAATGAGAT TGTTGGATCA TACGGTAGTT ACATTTTTAT TTTTTGAGGA ACCACCCTAC 1080 TGTTTTCCAT AGTAGCTCAC CATTTTACAT TCCTACCAAT GGTGCAGAAA GGTTCCAATT 1140 CCTGCATATC CTTACCAACA ATTATTATTT TCTGTTTTTT AACAGCAGCC ATCCTAATGG 1200 GTGTGAAGCG ACATCTCACC ATGCTTTGCT TTTTTTTTTA ATTAAATTTT ATTTTTTTAT 1260 CATTTCATTT TATTTTATTT TATTTTTTTT TTTTTTTGAG ACGGAGTCTC GCTCTGTCGC 1320 CCAGGCTGGA GTGCAGTGGC GGGATCTCGG CTCACTGCAA GCTCCGCCTC CCGGGTTCAC 1380 GCCATTCTCC TGCCTCAGCC TCCTGAGTAG CTGGGACTAC AGGCGCCCGC CACCACGCCC 1440 GGCTAATTTT TTGTATTTTT AGTAGAGACG GGGTTTCACC GTGTTAGCCA GGATGGTCTT 1500 GATCTTCTGA CCTCGTGATC CACCCGCCTC AGCCTCCCAA AGTGCTGGGA TTACAGGCGT 1560 GAGCCACCGC GCCCGGCCTC ACCGTGCTCT TCATTTGCAT TTCTCTAATA GTTGTGAACA 1620 CTTTGAAACC AGGGTAGTGA TTCCCTTTCA GCTGAAGGTG GGTGAGGAGG AGAAGGGCAA 1680 GGCCCTGGAC CAGAATGGAA GGAGAAATGA TTCCTGGCCT TAGGTACATA GGAGCCTCAC 1740 AGGACAGGGA CTCCCTGAAT CATCGATACA CAAGCAGCGG CTAGCTACTG AAGGAGTAGC 1800 TGGGGCTGTC GCCCAACCAG AAGGCAGCAT GGTAAACCCT TAACCACTGC ATGGCTTCAG 1860 CAAGTCACTT CTGCTCTCTG GACCTCTGTC CTCTCTGCTG TAAAATGAGG GTAAGACCTA 1920 CAGTCGTTCA GACTGATTTT CAACGATCCC ATCCACCACC AGGCTCTGTG GATAGGTGCG 1980 CTGGAAGCAG GGTGGGGAGT GGAGTAGGCG GTAGGATTTC GTGGGGACTA GCACACCTCC 2040 TACGAGGAAC AGGGAGGATA TGACACTTCT CTTTTCAGAG TGGTACTTTC CTGGCATCCC 2100 CTGGGGATAG TGGCCCCGCT GGAGATGAGC TGGAACGGGG GCGAGTCAGC AGAGCAGGGG 2160 AGCGGACTCT GGGCATTCTG CCTGGGCTGT CCTTTGCCCA CACCCTGGGC TCAACCAAGG 2220 CTCTCCCTTT TCTCCACGTC CCACCATCAC CCCCACACTC 2260
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