Tag | Content |
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EnhancerAtlas ID | HS129-01140 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:53039720-53041310 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:53040198-53040219 | TTATGGAAAGTGAAAGAACAT | - | 6.08 | SOX10 | MA0442.2 | chr1:53041121-53041132 | TTCTTTGTTTT | - | 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 |
GH01I052574 | chr1 | 53039998 | 53041010 |
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Enhancer Sequence | GCACTTTGGA AGGCCAAGGA GGAAGGATTG CTTGAGGCCA GGAGTTCAAC ACAAGCCTAG 60 GCAGCAAAAC AAGATTCTGT CTCTACAAAA AAATATTAAA AATTAGCTGG GCATGGTGAT 120 GCATGCCTAT AGTCGTAGCT ACTCGGGAGG ATGAGATAGG AGGCTCGCTT GAGCCCAGGA 180 GTTTGAGGCT GCAGTGAGCT ATGACTGCGC CACTGCACTC CAGCCTGGGA AATAGCGTAA 240 GACCCTCACT CTAAAAAATA AAGGAATAAA TAAAAGTATT GTACTTTTAG CTACACTAAA 300 AACTTCACAA GGTCATTGTC AGGCCCCATC CTTTCCTCAA AGAACACAGA CCTTAGAGTC 360 ACATAGATTT GGATTCAAAT TTAGACCCAC TGCTTTCCAC GATCTTGAGC AAGTCTCTCA 420 ATCTTTCAGA TCACCTTCTC ATAAAAAATG TAGACCATAA TTCTCACCTC TTAAGTTCTT 480 ATGGAAAGTG AAAGAACATA TAAAAAGTGC CTAGCACAGA CCCTGGCACA TAACAGGTGC 540 TCAAGACCCC CTTGCCATTT CCTAAACATG CCTTAGACTT GCATCCTACT AAACCTTTGC 600 AACATGGTGC TTCCTTGGCC TGATAAACCA TACTGCTTTT GTCTGCTGCC AAACTCTGTT 660 CATTCTGCGT CACCCAACTT AAATACATTC TTCTCTCTGA AGCTTCCCTT GGCTTCTTTG 720 GAGAGAATGA GTCACTCTGT CTTGTTCAGT TCTGCAGGAT TTACCACTAT CGCCTCACTT 780 GATCACATTG TGTTGTAATT GCTTATTTAT GAATCTTCTC CCTCACCAGA TTTTATGGTC 840 CTCCTCCATG GCTGAAGCCA CATATTTTCA CAGCACCTAG CATGGTACTT GGCCCTCAAT 900 AAATGTTTCA ATGAATGGAG GAATAATAAT AGCAAACAGT CAGTGCTTAA TTCTAGGCAT 960 TATTCCAAGT GCTTTACAAA TATTATTAAC TTGTTTAATC TTCATGACAA TTCTATGAAT 1020 TATTATCATT TCTCTCTTAC AGATGAGGAA AATGGCACAT AGAAAAGTTA TGTAATTTGT 1080 CTAAGGTCAC TCAGCTATTA ACTGTCAAAG CCAGGATTCA AACCCAAGCA GTTGGTGTGA 1140 GTCCAGACTT TTAGCCAACA CACTACAATG CCTCCCAGTG AACAAAGGAA TGAACAATCA 1200 CAAACAAATT TGCTTTTCCC AAATGTCTTT CTTTCTCAGG TTTTGGAATG GCTCATCCAT 1260 TCATTTAACA AACACTTTAC ATAGAGTTTT CTATGTGTAT AATTATCACA CTAAACACCA 1320 ATCTCTGTTT TCCTCACCCC GGCCACACCC CACTTCACAC AATCTTCACT GCTTGCCCCT 1380 AACCTCGACT GCTCTGTGAA TTTCTTTGTT TTGTTTTGCT GGAGACAGGG TCTCACCCTG 1440 TCACTCAGGT TGGAGAGTAG TGGCATGATC ATAGTTCACT GTAGCCTGGA ACTCCTGGGC 1500 TCAAATGAGC CTCCTGCCTC AGCCTCCAGC CTCCAGCCTG AGTACGTAGG ACTTCAGGTG 1560 CCCATCATCA CACCTGGCTA ATTTTTAATA 1590
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