Tag | Content |
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EnhancerAtlas ID | HS162-00656 |
Organism | Homo sapiens |
Tissue/cell | Plasma_cell_myeloma |
Coordinate | chr1:156197310-156198830 |
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 | chr1:156197944-156197959 | TGAACTCCTGACCTT | - | 6.04 | PRDM1 | MA0508.2 | chr1:156198308-156198318 | TCACTTTCAC | + | 6.02 | Zfx | MA0146.2 | chr1:156197990-156198004 | CCCGCCTCGGCCTC | + | 6.01 |
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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 | AGAGTCTTGC TCTGTCGCCC AGGCTAGAGT ATAGTGGTGC GATTTCAGCT CACCGCAATC 60 TCCGCCTCCC GGGTTCAAGC GATTCTCATG CCTCAGCCTC CTGAGTAGCT GGGATTACAG 120 GTGCCTACTA CCATGCCTGG CTCATTTTTT ATATTTTTAG TAGAGATGGG TTTTCTCCAT 180 TTTGGTCAGG CTGGTCTCGA ACTCCCGACT TCAAGTGATC CCCCTGCCTT AGCCTCCCAA 240 AGTGCTGGGA TAACAGGTGT GAGCCACTGC GCCTGGCCTT AAATTTTTTT TTATTGAGAC 300 AGGTTCTTGC TGTGTTGCAC AGGCTGGTCT CCAACTCCTG GGCTCAAGTG ATCCTCCTGC 360 CTCAGCCTCA CAAAATGCTG GGATTACAGG CGTGAGCCAC TGCACCTGAC TATGATTTTT 420 TTTTTTTTTT TTGAGACGGA GTTTCATTCT TGTTGCCCAC ACTGGGGTGC AATGGCATGA 480 TCTCAGCTCA CTGCAACCTC CGCCTCCCGG GTTCAAGTGA TTCTCCTGCC TCAGCCTCCG 540 AAGTAGCTGG GATTACAGAC ATGCGCTACC ACACCCAGCT AATTTTTGTA TTTTTAGTAA 600 AGATAGGGTT TCATCATGTT AGTCAGGCTG GTCTTGAACT CCTGACCTTA GGTGATCTGC 660 TCCTGACCTC AGGTGATCTG CCCGCCTCGG CCTCCCAAAG TGCTGGGATT ACAGGCGTGA 720 GCCACCGCAC CTGGCGATTT TTTTTTTTTT TTTTTTTTTT TTTTTTTTTA GTGTATCACT 780 TTCCTGCTTC TCCCTGAGTA TATTTTTCAG AAAATCCACA AGGGCATTCA AAACATTCCC 840 AATTCTGCAT TGGCTCTCAA GAAAGACATC ACCTTCTTCC TGTACTCACT GACACTGGCA 900 CCAGTCTGGC TGCCTTTCTC CTTGGTTAAG CCACATTGTC CTGTTAGCAT ATATTTCATC 960 TTGTGTCTGT GTATGAGTGT GTGTGTTTCT GTGGTCCTTC ACTTTCACTG AATTATCATA 1020 CCATAAAGGA GACCTCAGAA CAGGTCACAG CCAGCGCTGG TGGTCAGAAT TTGCTTCACC 1080 CCTGCCCTGG GCCCTATCCG CTGTCAGCTG CCTGAGCTGA AGAGAGATGC GTCCAGCTCA 1140 GACCCTCCGC CTGCTGAGTA GGCTGGGTGG AGGAACAGGA TCTCCCATGT CTAAGCCAAA 1200 CCTGTTTTAA GCCACAATTA CCCAGTTTCA ATTCCAGCCC TGCTTGGTCA GCATCATGTG 1260 TTCCTCCACG TTCCTCCTGG TAGCCACAGA CTGCGTGGCT AGTCAGGCCA GCAGCAAAAC 1320 AAGATATCTG GGAGTCTGCT GAGGGTTGAA GGAATGCCCA TCGTCTATTC TGTGTACAGT 1380 ATTGTTTTTA TTTTTGTTTT GTTTTTTGAG ACGGAGTCTT GCTGTGTCGC CCAGGCTGGA 1440 GTGCAGTGGC GTGATCTCAG CTCACTGCAA CCTCCGCCTC CCAGGTTCAA GTGATTCTCC 1500 TGCCTCAGCC TCCTGAGTAG 1520
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