Tag | Content |
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EnhancerAtlas ID | HS010-02547 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr2:137010880-137011660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr2:137011026-137011038 | CCTGTGTAAACA | - | 6.14 | Myog | MA0500.1 | chr2:137011440-137011451 | AACAGCTGCAG | + | 6.02 | Tcf12 | MA0521.1 | chr2:137011440-137011451 | AACAGCTGCAG | + | 6.62 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_09631 | chr2:137010582-137014917 | CD14 | SE_10274 | chr2:137010741-137014409 | CD19_Primary | SE_11065 | chr2:137010304-137014964 | CD20 | SE_61425 | chr2:136945577-137039880 | Toledo | SE_62403 | chr2:136962507-137014815 | Tonsil |
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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 |
GH02I136253 | chr2 | 137010941 | 137014177 |
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Enhancer Sequence | AGTAAGAAAA TGATTTCTTA CTCCTATTTC TGTCTTGGGG AATTGATGCT AACTTGAAGA 60 TTCATAGACA TGTACTTTCT GGTGGGGACA GGATCTTTGA GAACAACTGG TCAAACTTCA 120 TCTGGTTTCA GAATCTCTTC TATGGCCCTG TGTAAACACC TGCCCTGATG TGGATCTCTA 180 ACTACTGAGA CTGCCCCCAG ATGGGACTCT TGGGAAGTTA TTGTTTACTT GAGTTGAAAT 240 CAGCCTCCTG CTGGCTTCAG GCCATTGGTC CCAGTTCTGT TCTGCCATAC TTCAGATTCT 300 CACCATCTTG GAGCTGCTGG GAACCAGGGG CCCTGGGGTC ATCCTTGCAA GGGAACTAGG 360 GAAGAAAGAG GAAGCTGAGG GGCTGGAGCC AACCGTAAGG CGTTCCTCTT TGGGAAGGCT 420 GGCTTGTGAT GGGACTTGCC AGGACCAGCA TGCTGAGAGG AGGAAGCCAG CTCTCAGGTC 480 AAGATTCCGT TGATGTGGAA CAAACTATAA CCCTGCGCCG TTGCTTTCCC AGGCCTCACT 540 TCCCCAAACA GGGGCACGTG AACAGCTGCA GTGGCCTGGT GGCAGCATGC TGGGATCCTT 600 CAGGCCAGGC CAGCAAAAGG GTAAAATCTG GGCCAGTGGG TACCCTCATA GGGACTCTCC 660 AGGCTGCCTT CCTCTTCCAG GTCTTCTGTG AAATTAGCTG GAAAAGGAGA TCACATGCCT 720 GATTCCCCTT TATCCCAGCA AGCCTGGAAA ACAAAGTCCA GCCCCAGTCA AAAGCTTCCT 780
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