Tag | Content |
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EnhancerAtlas ID | HS150-09239 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr6:41612300-41613700 |
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) |
EWSR1-FLI1 | MA0149.1 | chr6:41612983-41613001 | CCTTTCTTCCTCCCTCCC | - | 6.85 | ZNF263 | MA0528.1 | chr6:41612982-41613003 | CCCTTTCTTCCTCCCTCCCTC | - | 6.3 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_68476 | chr6:41594173-41625301 | TC71 |
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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 | TGTGCTCTGG GCCCAGGGAG GCAGCTGGGC CACAGGATCT TCTCCTCAGC ATGCTTCCAA 60 CTCCCATCCC CCAGGCCTGC ATGCCCAAGC CTCCACTGAT CCCTCTAATT ACCTCCCTCC 120 TCTCTTCTTT GATCTCTCAT CTCCCTCTCT TTGCCTCTCT CCCCCACCCC CACTCTCTCC 180 CTCTCTGTGT CAACCCCTCA CTATTCTCTG TGATTGATTC CATTTCAATT CCCAAGACTA 240 CCCTGTGTCT CTCTGTGTCT CTGTCTCTGC ATGTGCCTCT TTCTGGTCTC TCTGTGGGGT 300 GTGTACTCTT TGGGCTTCCC TGCTGTTTCT CATCATCTCC CTGTCTGCCC GTGTCCCCCT 360 CTGTGTCACT CTGCCTCTCC CCGTGTCCCC CTCTGTGTCA CCCTGCCTCT CCTTGTGTCC 420 CCCTCTGTGT CACCCTGCCT CTCCCTGCGC TCTTTTGGCC TCTGCATCTC TGAGTCTCTT 480 GTTTCTGTGT CTCCTTGCTC CTTCTCCCAA CATGATATTT GGGGAGGGGG CAGGTGGAAG 540 GCCACCCTCT TTAGACCCCT GTCCTTCCAA CTAACTGCAT AGGCTGAGGT CTGATGAGAG 600 GCCCAGGCTG CACCCTACAC CCTTTCATTG CCACAGCCTG GGCCCGCCCC TGACCCCTGG 660 CTGAGTGTGT GGACGCTCGG ACCCCTTTCT TCCTCCCTCC CTCACCTCCC ATCCCCCATC 720 CCTTTTCCCC CTGAGCCTAG GGGCCCTAGT CCTGCAGGCT GGGGAGCTGT GGGTTTGAAG 780 GTGGCTCCAT TTCTGCCTCC TGCCGCCCCT GCACAGAGCC ACTGTAATTA CATGTGGCTG 840 CGGTTCACCT CTTCCCCAGT GCTCCGGCCG GCTCCTTGTC CTCCTCCTGA CTGTAGCCCC 900 TCCCTGCTCC TCACCCCCAG GTTCCTCTGA CTCCTCTATC ATCATCCTCT CTGACCCAGT 960 TTCTCCCGTC TCCCTCCGCG CTCTGTATCA CACAGTGCTA CCTTCTCTGT CGCCTCTGCC 1020 CCTGCCCCAT CTCTATCTTT CTCTCCATTA CTGACTTCCG TGCTATTGCT GCGTCTCACT 1080 CCCGTCTCAG GCTGTCTGTC ACTGGGTCAC TGTGGATCCC TTTTCCGTGC CCAATCTCTC 1140 GCAGTCCGAT GCTCTATCTC CCTTTACCTC TACCTCTCAC TGTCCCTTTG ATTCTCCCTG 1200 TCACTCTCGA TGCCTGTCCC TATCTCTCCG TTGCTGACCG TCCGTCTGTT CTCCCGTGTT 1260 GTGTTTCTGC CTCCTCTCCC TACTTCTCTT TATATTCTGC CATCTCTGCC CCTCCCGACA 1320 CCACATGCAC ACGTGCACAC ACTCAAATGC ATGCACACCC TTGCTCACTC CCAGATTGTG 1380 GTTTGGGAGC TTTCTATTTT 1400
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