Tag | Content |
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EnhancerAtlas ID | HS148-04047 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr12:31901900-31902710 |
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 | TATCACTAAG AATATAGGAA GCCTTAAGAA TTGAATATGG TGGTTCAAAA TTAGTATTTT 60 TCCTCTTTGT AGGGGAAATC ACCCAAAAGT AACAATCAGA ACTGTTACCA CCTGACTGGT 120 TCTTGCCCAC TGCACAGATA AAACCAAAAC ACTGAGCCAG CAGGAGTTGC AGCAGAGAAA 180 GAGTTTGATT ATTGCAAGGC AATAGAGTGA GGAGGACGGG ATACATTTCC CAGATCCACC 240 TCACCAAGAA TTCAGAGGCT AAGGTTTTTA AGGATGATTT GGCAGGTAGG GCATTAGGAA 300 ACAGATGTTG TGGATTGGTT GGGGGATGAA ATCATAGGAG TGTTGAAACT GTCTTCATGT 360 GCTGAGTCAT TTCCTGCAGG GGAGTGGTCA GAGGACCGGT TGAGTCAGTT CCTTTGTTGC 420 AGTCACGGTC ACTGTTCAAG CTGGTGTCAG TTGATTCACC TGAAGGCAAA GTCTGAAAAA 480 TATCTCAGAG ATCAGTCTCA GGTTTCACAA TAGCGCTTGT GACTGCCTGT TACATAACTC 540 CTGAGCAATA AGCAATTATA GAAAAGCAAA CAAGAGAACA ATGATGGGCT ATCATTCAAC 600 TACGCCTACA GCTTAAGAGG TGAGCTCCCT GGTGATTGAA ACTGCTTGCA CTCCTCAGTT 660 GATCCAACTT CTGGAAAATA CAAAGGCAGT CTGCATGACT TAAAGATCAT TGTTTCTTTT 720 TCTTTTTTTT TTTTTTTTTG AGACAGAGTC TTGGTCTGTC GCCGAGGCTG GAGTGCAGTG 780 GCACAACCTG GGCTCACTGC AACCTCCGCC 810
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