Tag | Content |
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EnhancerAtlas ID | HS184-04910 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:133775120-133776460 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr10:133775941-133775962 | TTCCGTTTTCATTTTCCTTTT | + | 6.3 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_47883 | chr10:133776060-133776372 | Pancreas |
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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 |
GH10I131961 | chr10 | 133774987 | 133776470 |
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Enhancer Sequence | ACCCAGGGCT CCTTGATCTT TTAGGAACTG CGGCACCCCC GAAGCTGTGA CAGGTGCAGA 60 GGCGCTGCCG TCCTGGGCCG GGCCTCACCT TCCGCCTTGT GTGCTCTGGC GCCAGCACCC 120 AGTCCCAAGG GCACAGCGGC TGCGACTTGC CTCTGGCCAG GGCAGGTGGT GGTGTCATAC 180 CCAGGACGGG AACCCACACT TGATGTCCTC CAGGGTTTTT TTTTTTTACA TTATCTTAAG 240 GACTGACAGT CTCCCACCCC ATCTGCTCCC ATCTGTCCCT AATTTCATGC GCCTCCGCCT 300 GAGTTCCTGC ACGCATTTCC TGAATAAACA CACCCCTGTG CCAGTCAGAA CCCGCGGGGG 360 TTTTGGAAGT GAGAGCCCAG CAAGGCAGCT GGCCAGGGGG CGGCACTGCC CTCCGGGGAG 420 CACCGGTGCC CGGGACTCTG CTTCTGAGGC TGGCCTGTAC GATGATTTTG TATAAATATC 480 TCCAATCAGA ACCTTTTTAG TGTATTTCTT AATATAACAG AAACTGGTGT CTTAAAATAC 540 AAGACTAGCT GCCCGGTGAT GACACCAAAT CGAGCAGCGG GGCTCGCAGT GGCCAGGATC 600 CCCGACAGTG GAATGCTGAG GTTAGAACTG AAACCGCGTT TCGTGAAGTC ATCATCACGC 660 ACGGGAAACA GGTTTGGGGT GAGGGGCGGT CCAGTCCTAA GAAAGCTCTC CAGCTCCACG 720 CGGTCACCTT CACTCACTCA CCAGATGCAG ATTGCAAAGA GGCGAAACCT GTGATTTCTT 780 TAATAATCAC AGTCTCCATC TGGTGAGTGG TTAAAGTCAC GTTCCGTTTT CATTTTCCTT 840 TTGGTGGCTG GGAAATGCTT CTGATAGTAA TAGTTTTCGA TTCTGCAACT CCCATTGTCT 900 TAGGCTCTGT AGCTCTCCAT TTTCTTCTTA TCCTTGGGAC GTGTCTTGGA CGTTTCTAAC 960 AGGCTGTGTT CCTGGACCTG AAACTCAGCT GGAGACTGGG TCCCTTGCAG ATTTGCAGGG 1020 ACCGTCCATC GCTGGTGTGT AGATGCAAAA ACAAAACACT GGCACCACCC AGTCAGAACT 1080 GGCAGGGGCT GCCTGCACTG GGCACCAACC CCGCAGATGG CCAGGCCCAG ACCACGTGAC 1140 TGCCTGCTGG GCTCCACCCC CAACCGCAGC CCAGCCAAGG CAGAGAGGTG GCTGCACTTC 1200 CGCCGATCAG AGGTCCAGAT AGAGCTCCGT CTGCTTGCCT TGGAGTTGTT AGAAAATTAT 1260 CTTTGGGGCT AGGCATGGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA AGCTGAGGTG 1320 GGCGGATCAC GAGGTCAGGA 1340
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