Tag | Content |
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EnhancerAtlas ID | HS129-36668 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr8:145092420-145094800 |
Target genes | Number: 55 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr8:145093117-145093132 | GAGGTCAAGAGATCA | + | 7.23 |
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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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Enhancer Sequence | CTCTCTGAAA CATGCGCTGT GTCCACTCAG GGTTGAATGG ATTAAGGGGG GTGCAAGATG 60 TGCTTTGTTA AACAGATGCT TGAAGGCAGC ATGCTCGTTA AGAGTCATCA CCACTCCCTA 120 ATCTCAAGTA CCCAGGGACA CAAACACTGT GGAAGGCCGC AGGGTCCTCT GCCTAGGAAA 180 ACCAGAGACC TTTGTTCACT TGTTTATCTG CTGACCTTCC CTCCACTATT GTCCTATGAC 240 CCTGCCCAAT CCCCCTCTGC GAGAAACACC CAAGAATGAT CAATAAAAAT AAATAGATTA 300 ATTAAAAAAA AAAAAAAAGA ATGAATTTTG GCCGGGCTCG GTGGCCACGC CTGTAATCCC 360 AGCACTTTGG GAGGCCAAGG CGGGCAGATC ATGAGGTCAG GAGATCAAGA CCATCCTGGC 420 TAACACGGTG AAACCCTGTC TCTCCTAAAA ATACAAAAAA TTAGCCGGGC GAGGTGGCGG 480 GCGCCTGTAA TCCCAGCTAC GCGAGGCTGA GGCAGGAGAA TGGCGTGAAC CCCGGGGGGC 540 GGAGCCTTCA GTGAGCCGAG ATCGCACCAC TGCACTCCAG CCTGGGCGAC AGTGAGACTC 600 TGTCTCAAAA AAAAAAAAAA AATTGATTTT TACAGCCAGG TGCAGTGGCT CATGCCTGTA 660 ATCCCAGTAC TTTGGGAAGC CCAGGCAGGC AGATCATGAG GTCAAGAGAT CAAAACCATC 720 CTGGTCAACA TGGTGAAACC CCGTCTCTAC TAAAAATACA AAAATTAGCT GGGCCTGGTG 780 GCACACACCT GTAGTCCCAG CTACTCAGGA GGCTGGAGCA GGAGAATCGC TTGAACCCGG 840 GAGGCAGAGG TTGCAGTGAG CCGAGATTGT GCCACTGCAC TCCAGCCTGG GCAACAGAGC 900 GAGACTCTGT CTCAAAAAAA AAAAAAACCG CATGAATTTT ACTTCTTTAA AATTATTATT 960 TTGAGATGGG GTCTCACTCT GTCACCCAGG CTGGAGTGCA GTGGCACGAT CACAGTGCAA 1020 TCATAGCTCA CTGCAGCCTC AACCTCCCGG GCTCAAATGA TCCTCCCACC TCAGCCTCCC 1080 GAGTAGCTGG GACTACAGGT GTGTGCCACC AGGCCCAGCT AATTTTTGTG TTTTTTGTAG 1140 AGACATGGTC TCTCCATATT GAGCAGGCCG GTCTGGAACT CCTGGGCTCA GGCGGTTGAA 1200 TTTTACATTT TTAAATGGTT AAAAGAAGAC TACTATTACA TGACCCATGA AATCCAAAAT 1260 GTCGTATTCA TCCATAAAGG TTTGTTGCCA TACACCCTCC CTCATTCACC TCCGGGTTGC 1320 CCGTGGCTGC CTTCTGAAGG CAACGGCAGG CTTGAGCGGT TGCAACAGAG ACCATATAGC 1380 TGGCAAAGGT GGAAGTATTT ACCTCCAGAC CTTCACAGAA AATGCTTGCC AACTCCTGAG 1440 CTATATACGC ACGGTAGAGA AGGTCTCCAA GGCAACACGC AGCTCCTCAA TAGAGACTAA 1500 CTGTGGGATG ATGGAACTAT CTGTGGCTTT TCATCTTTTT TTTCTGTATT TCCATTCTTT 1560 CTCTATAATA AGCATGTACT GCATTTATAA CAACAAAAGT GGAAGTTCTC AATGAAATTG 1620 CATACTCACA AAAACCTTCT CTGCACTCCC ACCACTACTG CCAGCAGCTG CATCCCCGGG 1680 GATCAGGGGG CTTCTCCCCG AAACAGTGGC CAGAAAAAGG AGCACTCCTC CAGGACCAAG 1740 GAAAGCAGGC TCTCAGGGGC AGGGAGAGAG CATAAAGCAG TGTCTGGGAC CAGGGTGTGT 1800 GACCAGCTCT GACCTGCATC CCTGTTTAGG CCACAGCAAG CCCCACAGGG CAGGGACCAT 1860 GCAAGGGTGC CGGGCCACGT GAGGCTCTGC CCATTGCAGC ACGGACCCCC TGAGGAGCCC 1920 CCACCACAAA GACAGTGGTC AGGAGGCCTG GGCCCTCTTC TCTCCACCGA AGAACAGAGG 1980 GGCCAACTTG GTGACCTGAG AATCCAGCTG CTTGGAGACC CTCTGCTGGG CAAGGGGTGG 2040 GCACGGTTGA GGAAAGGGCA GCGGGACGTC CCCATGGCTG GGGGCAGTGG GCAAGTGGTC 2100 AGAGAAGTGA GCCTGGGAGA ACTGACCCAA AAATCAGGGC TGGAGATGAG GCCTTGGGGA 2160 GCCACTCCCA GGCTCCTCTG AGCAGACACA GACTCCCCAC AGAGGCAGAG ACGCCACCAC 2220 CCTGGCCTGC CTAAGAAGTG AGGCTCAGAG ACCAGGTCGG ACCAGTCAGC TCATCGGGGA 2280 CAGATGGGCA CTATGGCCAG GCCCTACCAC AGTGACAGAG CCTGTGACCA CCCTCGCCGT 2340 GGTCTGGAGG GGCTCCCCTG GGGTCTCAGT GCTTTCTCTG 2380
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