Tag | Content |
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EnhancerAtlas ID | HS128-17260 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr5:6765550-6768190 |
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) |
GFI1 | MA0038.2 | chr5:6767732-6767744 | TGCTGTGATTTC | - | 6.22 | Gfi1b | MA0483.1 | chr5:6767732-6767743 | TGCTGTGATTT | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I006764 | chr5 | 6764957 | 6768251 |
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Enhancer Sequence | AGGGTAGTCT CGAACTCTTG GGCTCAAGCG ATCCTCCCTC CTCAGCCTCC CAAAGTGCCG 60 TGTGCCACCA TACCCAGCCC CTCTTTGGTT TTTTAAAAGT GCCTGCTAGC TCATCAGCAC 120 AGGAGCAAGG CGACTTGGAG CCACAATGAG ACAGATGATT GCCAGTGTTG TTTCATTTCA 180 GTTCTTAAGT TCCTGCATGG GGTGCTTACT GATGAGTCTG TCTCTCCTCT CAGGTAAGCC 240 AGGCCTCCAT CCACTCCTGC ACAGCAGGGA ACGCTGCACG GTGGCCCAGG GTTCGTGGTG 300 GGCACGCCGT ACCCCTCACC CCCTCCACGT GGAGTCTGGC TGAGGGCTCC CTCCCGCATG 360 CCAGGCCTGG CATGTCGGTG CAGGCCCTTG CATTTCTGGC TGTGCTGCGC AGTCTCACCC 420 TTGAGAAGAA GGGGGCGCTG TTGCCTCAGC CTTGCAGAGT TTCTCTGTGG TCAAACCACC 480 CTGCCAGCCT CCCTGCTGCA GCCGGCAGCA CGTCACTCCA TGCGGGAGGG GAGCCCCACC 540 TAAGGTAGGC TGTGAATTAA TATTTTTTAA AGCCCCAGGT ATTCAGGTTT AAAAAAGGCC 600 CAGGGACATG AGGCTGCAAT TTTTTGCTCT ATTGAAGAAA AGAAAAATCT GTAGAATTTT 660 AACAGTGACA ATGAGGTTGA AGCTACTACA GATGCTGCAC CTTGGGGGTC TTGGGGTCCC 720 TCCTGCTCCC CAGGGGAGTC CATCAGTTCC CACAGAGGGT CTGCTAGAAT TGCTGAAATC 780 AGACTCGCAG CCACCCAGCA AACCTGCACC AAGTTCTGGG GCCAATTCTG GTGTGGGCAG 840 GGGATTGGTG GCCGCTTTGT CGTTAGGGTC CCCGATGTCG GACATGAGCT TGATGAGTGG 900 AGGAGCCGGG CCCCATGAGG ATGCTGGTCT GTTCTTCCCC AGAATCTGCC TATGGCTCAG 960 CCTCAGAACC TCAGGAATGG AAACAGGAGC AGAGAGCTGT CTATGCGGGG AGGTCCTGGG 1020 TCCAGTTTCC ATCTCACTCC CCGATGGGCT TGTGAACTGA GGCGGTGGCA TTCTCTGCCT 1080 GGCCCTTTTG TCTGGTTGGA GAATGAGACC TACTGCCTGG AGCGGTGGGG CCTGGATGCA 1140 GGCCTTGGCG CAGGGCGCTT TGCAAACTGC CTGGTGCTTT GCAGATGCCT CTCACCGCAA 1200 CCTTCCCCTC CAAGCCTGCA GCCTTTAGGA CTTCCTGCTC CTCTGCTGCT CCCTCCCTCC 1260 CTCTCCCCTC GCTGGCACTC TCTGTCTGGC TGCCCAGGGC ACTGACTCAC TGGAGTGCCC 1320 CTGGCTCACC GCCAGCAGAC ATTTCCCTGT CACCGCCAAG GGCTGAGGAG GTGGCTGAGG 1380 CTCTGGCCCC GGAGCCTGGA GGCCAGGGCA GCTGCAGAGG AGCAGCTGGG TGCCATGCGG 1440 GCCTCTGGGA AATGTCCCAG ACACCTGCCT TGGAAGCCCC AGGGGCAAAA CAGCCACTGA 1500 ACTCTACAGG AGCCCCACCC TGAGGCCACT TCTCCCTCAG GGAACCAGTG CGCTGTGTGG 1560 GGTGGAGCGA GTGAGGTCGG GAAGCTGGGG CCATGTCCGG TGACAAGGAG GATCCCTCCC 1620 GGACATGGGC GAGGCTGGGA GTGGGCAGCC AACTAGCCAG CCATGGGTCC TGGGAGCTGG 1680 CTTATTTTGG TTGTTAGGTT TATGGCCATA TTAAGAGAAC AGCAGTTTTG GCAAATGCCC 1740 TACAAGTAGA CACTCAAAAC CTACATTGGT AGAGAATAAA TATTTCTTAT TTTATCAGTG 1800 CAAAAGAACA CAAAACTGTC TTTTCTCTCT CTCCACTCTT TTTTTTTTTT TTTTTTTTTT 1860 GAGACGAAGT CTTGCCCTGT CGCCCAGGCT GGATTGCAGT TTGCAATGGC ACGATCTCGG 1920 CTCACTGCAT CCTCTGCCTC CCGGGTTCAA TCGATTCTCC TGCCTCAGCC TCCCGAGTAG 1980 CTGGGATTAC AGACGTGCAC CACCACTTCT GGTTAATTTT TTGTATCTTT AGACAAAGTT 2040 TCACCATGTC AGCCAGACTG ATCTCGAACT CCTGACCTCA TGATCTGCCC ACCTTGGCCT 2100 CCCAAAGTGC TGGGATTACA GGCGTGATCC ACCACTCCGG GCCCTCTCTC TCCACTCTTT 2160 AAAATAATCC TTGTCTCCTT TTTGCTGTGA TTTCACGTCC TGCAGGTGGG AGGTACCAGC 2220 AGGTCTGGAC AGGCGGGACT TGCCTTGTGT CTTCCAGTCT GGACTGGCTC CATGGCTACC 2280 CTTCCCACAA GGCCTCCGCA TTGGTGCTGG GGAACGAGGC AGCAACTTGA TCCTCAAGTT 2340 GCTCTGATTT GTCCTTACAC AGTAGCCCTC TTCTCTAGCA GGCATGTCAG GGTGGTCAGG 2400 AGACAGGAGG CGGGGGCTGG GGAGGGGTTA GGCCTCAGCC CGCATGGGGG GTGTCCTCTG 2460 CAGGGAGGTG AGCAGCTTAG CATCTGCCAG CACCAATCAT TCTGTGGGCT TCAGGCTGTA 2520 GCGGGGCTCT AGTTGCCTGC TTCCTGGCCC TGGAATGACT TGGGTACGGG GAGTGTTGGC 2580 TGGATGTGCA AGAGTCAGAT AATGGAGGTG GGTGGGAGAT AGGGCTGAGA TGTTTTGTCC 2640
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