Tag | Content |
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EnhancerAtlas ID | HS195-01489 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr12:31901820-31902760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:31902606-31902627 | TCATTGTTTCTTTTTCTTTTT | + | 6.02 | JUN(var.2) | MA0489.1 | chr12:31902261-31902275 | CTGAGTCATTTCCT | - | 6.73 | NFE2L1 | MA0089.2 | chr12:31902257-31902272 | TGTGCTGAGTCATTT | - | 6.91 | Nfe2l2 | MA0150.2 | chr12:31902259-31902274 | TGCTGAGTCATTTCC | - | 6.41 | RREB1 | MA0073.1 | chr12:31902205-31902225 | TGTTGTGGATTGGTTGGGGG | - | 6.33 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_09906 | chr12:31898377-31905721 | CD14 | SE_15277 | chr12:31901388-31902876 | CD4_Memory_Primary_7pool | SE_35168 | chr12:31898555-31904362 | HeLa | SE_38691 | chr12:31898993-31904489 | HUVEC | SE_40045 | chr12:31900620-31902995 | K562 | SE_54023 | chr12:31901634-31902971 | Spleen | SE_61892 | chr12:31867411-31932528 | Toledo | SE_62563 | chr12:31867177-31913478 | Tonsil | SE_63403 | chr12:31879241-31906059 | NCI-H69 |
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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 |
GH12I031745 | chr12 | 31898797 | 31905733 |
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Enhancer Sequence | TTCAAGTACA TGTATCTTCA AAATACAAAT ATACTTCAAA GCTACTGTAC TTTGAAATAT 60 GTTATCTTCA AAAATGACAT TATCACTAAG AATATAGGAA GCCTTAAGAA TTGAATATGG 120 TGGTTCAAAA TTAGTATTTT TCCTCTTTGT AGGGGAAATC ACCCAAAAGT AACAATCAGA 180 ACTGTTACCA CCTGACTGGT TCTTGCCCAC TGCACAGATA AAACCAAAAC ACTGAGCCAG 240 CAGGAGTTGC AGCAGAGAAA GAGTTTGATT ATTGCAAGGC AATAGAGTGA GGAGGACGGG 300 ATACATTTCC CAGATCCACC TCACCAAGAA TTCAGAGGCT AAGGTTTTTA AGGATGATTT 360 GGCAGGTAGG GCATTAGGAA ACAGATGTTG TGGATTGGTT GGGGGATGAA ATCATAGGAG 420 TGTTGAAACT GTCTTCATGT GCTGAGTCAT TTCCTGCAGG GGAGTGGTCA GAGGACCGGT 480 TGAGTCAGTT CCTTTGTTGC AGTCACGGTC ACTGTTCAAG CTGGTGTCAG TTGATTCACC 540 TGAAGGCAAA GTCTGAAAAA TATCTCAGAG ATCAGTCTCA GGTTTCACAA TAGCGCTTGT 600 GACTGCCTGT TACATAACTC CTGAGCAATA AGCAATTATA GAAAAGCAAA CAAGAGAACA 660 ATGATGGGCT ATCATTCAAC TACGCCTACA GCTTAAGAGG TGAGCTCCCT GGTGATTGAA 720 ACTGCTTGCA CTCCTCAGTT GATCCAACTT CTGGAAAATA CAAAGGCAGT CTGCATGACT 780 TAAAGATCAT TGTTTCTTTT TCTTTTTTTT TTTTTTTTTG AGACAGAGTC TTGGTCTGTC 840 GCCGAGGCTG GAGTGCAGTG GCACAACCTG GGCTCACTGC AACCTCCGCC TCCTGGGTTC 900 AAGCGATTCT CCTGCTTCAG CCTCCCGAGT AGCTGGGATC 940
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