Tag | Content |
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EnhancerAtlas ID | HS128-01795 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr1:204591180-204593610 |
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) |
Nr2f6(var.2) | MA0728.1 | chr1:204592333-204592348 | TGACCTTTAGACCCT | - | 6.32 | RARA | MA0729.1 | chr1:204592330-204592348 | CCCTGACCTTTAGACCCT | - | 6.22 | ZEB1 | MA0103.3 | chr1:204593286-204593297 | CGCACCTGCCC | + | 6.02 | ZIC4 | MA0751.1 | chr1:204593292-204593307 | TGCCCCCTGCTGGGC | + | 6.04 |
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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: 2 | ID | Chromosome | Start | End |
GH01I204623 | chr1 | 204592131 | 204593213 | GH01I204624 | chr1 | 204593221 | 204593263 |
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Enhancer Sequence | AGCAAGATAC AAGAATCAAC CCAAGTCCAG GGGGCTGTGT GCCGTTTACA CTTCACATCT 60 GTGCTGCCAG GTCTGTCTGA TCTGACCCTG CCCTGGGCCT CTGGAGGGTC TGGGATGCAC 120 TGAATGCTGC AGCTGCAGGC CCTGTGCCTG TTCTCGTCCC CTGGGGTGAT GACTCCTTAC 180 CAGGCAGCTG CAGAAAGCTT GGAGCTATGT CTCCTGCCAC CATCCAGGCA GGTGCCTCTC 240 AGCGGGCCAG AGGGGCTCTT CACCTCCCTC ATCCTGCTTC CAGGATGCTA GGGCTTGGGA 300 GGGGAGCAGC TGGAGGCAGG GTCCCGTTCC CTGAGCAGGA ACACAGCAAG CCTATTTACA 360 TTTGGCTACT TCCCACTTTC CTCTGCAGCT ATTTCTGAAG GTGGGAAAAA CAACCGCGAC 420 TTCAAAGGCA CAGAGGTTTT GATAGGGGTG TGTGTGCACC GACACGTAAA ACTCAGTGTG 480 AACAAACACA TGTGTACACA TGCATGCATG CCTGCATACC TGTGCAAGGG GAACCCAGCT 540 ACCCAAGCCA GTGTATGGGG GTCAGGAAGC AGGGAGGGAA TTTTGTGGTG GTCTAGGTGG 600 GTGGAAAGGA AGGAGGGAAC AAGCTGAGTC TCCGAGAGGT CCCTGTTGTG GAACTGGATC 660 TATGGCCAGT AATCCTGCCA CACTTACATA CCAGAGACCC CTGACTGCCA CCTAGACCTG 720 CTGTGAGAGA GCAGACCTAC CGGCAAATAG ATCAGGACCC AAATCGCGGC CCTACCACTC 780 ACTACCCAAG TACCTGAGGC AAAGCTACTT GACTGCTCTG AGCAACCATT TCCTTCTGTA 840 TTACATGAGA TTGTCATTGG AGTTAAATGA GTGTGTTGCA CACAGAAAGA ACTGGACAAA 900 TGTTAGCTCT CTTCCAGCTC CAGTCATCCC TCAGGGTCAG GAGGTTCTCC AGCTATAGGA 960 CTTCTTAGGG GACAATAGAA GTTGGCTCCT AGGACTCCTA GGGCTCGATA AGTTAGCAAG 1020 TGCCATGCTA GTTGGGGAGG CAGGTTCAAA AACACGAAAC AACTAGGAGA GCCCAAGACA 1080 TTTCCCAAGT GGAGAGAAGG GTGAGGGCTG GAGGAGGTGG AGAGGGGTCT TCAGCTGGGC 1140 CCCAGCATCT CCCTGACCTT TAGACCCTAC CCGAGTCCAG TTTCCCTTCT TCATCAACAC 1200 TTGGTTCTAA GCGCTGAGTC CGTGCTCAAC TGCACTGAGG GGATCAAGGA ACCATTTAAA 1260 ACTTCATTGA AACCCTCCAG GCACTTGCCT TTCCCCTTCA CCCCAGACTG CTGCCCCTTC 1320 CTTCCCTCCC CTGGTTGGGC TGGGTGGATG AGGCAGAGGT CGTGGCTCCT GGGCCGGGAG 1380 CCTGGGGCTG GGCCTCGGGA TCCAGAGGCA GTGACTTGAT GACTCATGTT CACACTGCAC 1440 CTCTGACCCC AAGGCTTGGC AAAGGCCCAG ACAAGTCCAC CCCCTCACTG CTGAGCATGC 1500 AGCTCTTTCC AGGATGCAGC TCAGAGCTGC CCTCTCACCT GCCATCACCA CCTAAGGCTG 1560 CCTTGCACAT GGCCCGCTCA TGCAGGCTGA TTAGCAGTTT CTACCGGGGA GCTGCAGAGA 1620 AAGCTAATTG TCTTTCATCT GTAATCTCCA GGGGTGATCA GGAGTTCAGA CTGTCACGTG 1680 TATACTTTCC CCAATTGGAT TCCGAGCTTC TTGAGGCAGG GGCCATATCT TACATGCTTT 1740 TTGTGTCCCC AGAGCACCAA GTGTAGGATT GAGCATGTAG CAGGTGCTTG AGAGTTGCTA 1800 TAGTGAAATG TGTAGAGAAC ACGCATTGCA TTTAATCCCC CCAACAACCC TGTGTGTAGG 1860 CAAGAAGGGA TTATTTAGCT CCATTTTGCC AGGGAGGCAA CTGAGAGTCA GAAACGTTAG 1920 GTGATTCATC AGAGGTTGCA CAGCTTCTAT GCAGTGGGGT CAGGATTCAA ACCCAGGGTC 1980 TTTGACTCTA CATCCTGCCT CACCAGCCCA GCCAATGTGG ATCAGCACCT GTTTTACAGG 2040 AGCAGAGGGC AAGGCTGCCT CAGTTGCAAA TCCCTTCAGA GAAAACCTGA GTCCTCAGCT 2100 CCTCCACGCA CCTGCCCCCT GCTGGGCCCC TCAGCTCCTG TTCCTTGACT CCTGCCTAGA 2160 ACAACCCCCC TGGGGGACAG TGTGGGGAAG GACACTGTTC CTGTGTGTGT GTGTGGCTGG 2220 GCCTGGAACC ACAGGGACAA ACAGAGCCAG CTGCTGCACA CAGACCTCAG CCTGCCTTCT 2280 GAATGGGGGC TGGGGGCTGC TTTTTGCGCA GCCAGTGACT GCTGGCCAGC TGTGGGCTTC 2340 AGGGACAGGA GACAAAAGCC CTAGAGCCGT ATTCCAAGAA GCAGGGTTGG TTGCCCACTC 2400 CAAGGGCAAG TTTCTCTCTT GGAAAGGCTG 2430
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