Tag | Content |
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EnhancerAtlas ID | HS010-01823 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr17:2717430-2718730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr17:2718026-2718046 | ACCCCCCCCAACCCCAACAC | + | 6.09 | ZNF740 | MA0753.2 | chr17:2718024-2718037 | CCACCCCCCCCAA | + | 6.37 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65245 | chr17:2717416-2718706 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 2717801 | 2718168 | chr17 | 2718511 | 2718548 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I002813 | chr17 | 2717254 | 2719453 |
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Enhancer Sequence | GTGGGGACCC CAGCTTACTG ATTGATTTGT GGGCTTGGCA GTCAGGCAGC CTCTGTTTAA 60 ATCCTGACTC TACCAGCTGG GTGACCTTGG ACAAGTTACT TAACCTCTCT GTGCCTCTGT 120 CAGTTCTGGT TTTGTTTTCT CACAATCGTG CCTCCTCTTG ATCTTCAGCT GCAGCCCGAG 180 GGTGGAACTT GCTGTGTGTG GCTGGGCACT TTCGCCTGTG GCTGTGCTGC TCTGCCCACA 240 GGGAACATGC CTTTGCTGCC CCTTCCCTGT CAGCATCAGG GTCACAACCT GCCCGTCCTT 300 CCAGGGCCAG CTTCCATGCA GCTTCCTCCA CGCACAGCCC CTTCCCCATC GGCATGGAAG 360 GCTCTCTTCC TTGTGCCCCT GGGGCAGCCG GAACCTCAGG TCACATGCAG CTCCTCCCGC 420 GCCGTGGGGA TCTGGTGGTT TCTGTCTGAG TTCCTCCCCA CTTGGGGTCT GAGACCGTGG 480 GAGCCTCTAG CGTGCCCAGC TCGGGCTGTC TCACTGTTTG TTACCCAGGT GAGGTGGCTG 540 TCCCCTCCCT ACCTTGGGTT GAGCTGTGAA CCAGTAGGTT ACCGCAGTGT GGTACCACCC 600 CCCCCAACCC CAACACCCAG CTCATTCTGA GAGGGTGGAG TGGGCGGAAA TCCGTGCCTG 660 GCAGACCACA AAGCCACATA ACTGACTTTT GTAGCCCTGC CCTGGGGTGT TGGGGGGGAG 720 GGTTGACGGC AGCCATTGCC CCTTTCTTCG GTGCTTTGCC ACCAGCAGAC GCCCCGTGGA 780 ATTGAGGAGC TTTGTTCTAC GAGCTCGGGA ACGGGACTTG GGAGGGACAG CCCCTGTCCC 840 ACCCTGCCAT GCCCTGTTCA ACCCTGTCAG GCAGCTGAAC GTAGGCTGGA CCCATGGCTG 900 CCCACCCTGG CTGCAGTACA GAATCACCTA GGGGACCTCG TTAAAATGCA GCTTCCGGAC 960 CCCACCCTGG GGCTTGGGGA TTCTGCCTCA TCAGCCTGGG TGGGGCCCAG GAAACCTGTG 1020 TGTTACCAGC GCTGAGGTGC TGCTGATGAG GCAGCTGGCT TCACAGCTGC ACGGGAACCA 1080 GTGCCGTTTA AAGCACTTTC CCCCACAGTG CGGCTCCAGC AGTCAGGTTC ACGTACTCTG 1140 GGTGACCTGG GGCAGGCTGC GCAACCTCTC TGTGCCCCAG TTTCTTTGTC TGAGGATAAT 1200 AACAGTACCT GCACGTGGGT GCGCTTGTTG TGAGGCTTAA ATGAGATTAT CCAGGTGAAA 1260 TGGGAACAGA GTGCCTGGTA CCTAGTGCTC AACACATGTA 1300
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