Tag | Content |
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EnhancerAtlas ID | HS061-08584 | Organism | Homo sapiens | Tissue/cell | GM12892 | Coordinate | chr16:2145290-2147140 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr16:2147049-2147069 | CCCCACCCCACCCTACCCCA | + | 6.26 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTAATCTTA GCTACTTGGG AGGCTGAGGC AGATAACTGC TTGAACGTGG GAGGCAGACT 60 TTGCAGTGAG CCGAGATCAT GCGACTGCAC TCCAGTCTGG GCAACAGAGA CTCCATCTCA 120 AAAAAATAAA TAAAAATAAA AAATAACCCA GCCTCAACTA TTCCTTTATA GCAACACAAA 180 TGACTCAGGG TCTGACTCAG GGAGCAGGCT CTCGCTGGCA GAGACGGAGA ATGGCCAATA 240 GGGAGGCATG GAGTGGCAGG GAATGCCAGG GCAGAGGCGC CGCCAGGACG GAGGGTGCAG 300 GCTCAGGCGC AGGGAAGGCC GTGCTCTGCG TTGGGAAAGG AGCCACGGGA CGCGCTGGAG 360 GCTGCAGTGA GGAAGGACGC AGAGGGGTCC AGGACAAACC CAAGCCTCCG ACCTGGTCAG 420 CCCGAAGCAC TGTCCGAGCA AGGGACGGCC AAGGGTTGAG GAAGCCGGGA GGGTGAGGGC 480 CACGCGCTCT GTGTGGATGC GGAGTCTGAG CTGCCGTCAG AAATCCCCGC GGAAGCACTG 540 AATCTGGATT TCACAGAGCT TTGGGCCGGA GATACCTGGG GCTGGTCAGC ATGTAGTGAC 600 TACCCCTGGA TTTCCCCATA CTCTGTATTT TTAAAACCAA CCAGCAATTT ATTCATAAAG 660 ATGCCCTCAT GTGATGGTTA TCTGCCTTTT GTAAATCAGG AAGTTTTCCT TTTTGTTTGA 720 GTCCAGGGGC AGTTCATACC TCTTTAGTTC TTGGTTGCTT AACAATGAGA AGCACTCAAA 780 GGAATAACAC ACAAATCAAA CTAGATGTGG ATGCAAAAGC AGCAGTCACG CACCACTTAG 840 TGCCAGGGAT GTGTTCTGAG AAATGCGTCA TTAGGTAATT CTGTTGCTGT GCAAATGTCA 900 CAGGGCGTAG TTACCCAAAC CCAGACACCG CAGCCCCTGT GCATGCAGGC CCTGTGGTGT 960 GGCCTGTGGC TCCGGGGCAC CGCACCTGCA CTGCATGCCA CTGCACTGAA TCCTGCAGGC 1020 AGCTGCAGTG CAACGGCAGG GCCGTGTGGA CCTCAGCACA CCTGAGCATA GGAGGGCATG 1080 GCAGAGCCCG GGGTCACACG CGTGGGAACA CGCCGTGGGT GCGCTCCGCC GCCGGCTGCC 1140 ATGTGCGTGA CTATGTGCGT GACTACATAC AAGGTAACCT CTATATGACC ATTTGTTGAT 1200 AAGTTACAAA ACAACCAAGA AATTGAGGAA TTTTTTTGTT TTTGAGACGG AGTTTCGCTC 1260 TTGTTGCCCA GGCTGGAGTG CAGTGGCGCG ATCTCGGCTC ACTACAACCT TCACCTACCA 1320 GGTTCAATCG ATTCTCCTAC CTCAGTCTCC CGAGTAACTG GGACTACAGG CGCCTGCCAG 1380 CATGCCCGGC TAATTTTTTG TATTTTTAGT AGAGACGGGG TTTCGCCATG TTGGCCAGGC 1440 TGGTCTCGAA CTGCTGACCT CAGGTCATCT GCCCACCTCG GCCTCCCAAA GTGCTGGGAT 1500 TACACGTGTG AGCCACCGCG CCCGGCCAAA AATGGGGTAT TTAAAAACCC GCCCATAATT 1560 TCTCACTGCT CTGAGACCAA GATAAAAACG TGGCCCCGGC CAGCCTCACA CAGGAGCCTT 1620 TCTGCTCCTA CAAAGCCCCA TGAGCCTGCT CCCTCCCTAG AGGGAAGGTT CTGGGGCCCT 1680 GGGGATCCCA TGAGGCTCTT TCCACAGACA ACAGAGGTTC AGAGAAGTGA AGTGGTGCAG 1740 CCACAGCCCT GCCCTGGCAC CCCACCCCAC CCTACCCCAG GCGGGAACCA CGGCTGCCTG 1800 GCCTGAGTCC CGGCCCCTCC TCTGGCAATC CCCCCTCCCC CGAGAGCCGG 1850
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