Tag | Content |
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EnhancerAtlas ID | HS176-42891 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr9:132796690-132797840 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arid3b | MA0601.1 | chr9:132796850-132796861 | CTAATTAATAT | - | 6.02 | Nr5a2 | MA0505.1 | chr9:132797217-132797232 | GAGTTCAAGGCCAGC | + | 8.25 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_09183 | chr9:132794830-132800143 | CD14 | SE_10876 | chr9:132764194-132806774 | CD20 | SE_17850 | chr9:132796300-132808716 | CD4p_CD25-_CD45ROp_Memory | SE_18285 | chr9:132775338-132806783 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19171 | chr9:132781442-132806573 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22698 | chr9:132796606-132806668 | CD8_primiary | SE_32459 | chr9:132780348-132805546 | GM12878 | SE_58840 | chr9:132746322-132806403 | Ly3 | SE_60636 | chr9:132750718-132808637 | DHL6 | SE_62275 | chr9:132746084-132814849 | 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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Enhancer Sequence | GATTGAGGCT GCAGCGAGCC ATGTTTGTGC CACTGCACTC CAGCCTGGTC AACAGAGTGA 60 GACTCTGTAT TCCTCCTTGT TCTTTCTCAA TTTCCTTAAA AATAGTTTTC GCCAAGACAT 120 ACTTCTGTTG GGCAAATTCA GAAACTTGAT ACTACTCCTA CTAATTAATA TCCACACAAA 180 TTTATTTAAA TTAGAAAAGA GAAACAATAA CTGGCTTTGA AAGGATTAGG AGATTACTAG 240 ACATCTATGA AGCATCTGCT TGAGTACGAG CTTCATTCAT GACTGTTTCT GCTGGCTCTG 300 CAGCATTTAG TGGTGTGAGT CATTGATTCT CAGTGATTCT CAATATGAAT AACATCAACT 360 GTTTTATAAA GCAAAATCTA CTGCAGTGAT GGGGAAATAT GAGTGAGTGG TGGGGATAAA 420 GGGAACTGTG CACTACTAAC ACAGAAGATC CAGTTTTTGG CCAAGTGGCT AATGCCTGTA 480 ATCCCAGCTC TTTGGGAGGC CAAGGTGGAA GGATCACTTG AGCCCAGGAG TTCAAGGCCA 540 GCCTGGGCAG CATAGAAAGA CCCCGTCTCT ACAAAAAAAA TACAAAAATT AGCAGAGTGT 600 GGTGACATGT GCCTGTAATC CCAGCTACTT GGGAGGCTGA GGCAGGAGAA TCACTTGAAC 660 CTAAGAGGCA GAGGTTGCAG TGAGTCGAGA TCGTGCCACT GCACCCCAGC CTGGGCAACA 720 TGGAGAAGTG GCAAAAAATG ACTCGCTGCC CAGCTGCAAG GACTGTGGCT AGCATGCAGC 780 CTCCTTTAGG GTCCACCTCA TCTTTTGAGT CGAGGGCATC TCTTCTTGTA GCACCCCCAG 840 CCAATGACTA AGCAAGCTGG CAGCCAAGGC CATCCTCTTC TTGGGACGAC CTCTGGCCAA 900 TGATAAAGGA AGGCAGAGAT ACAGAGGCCG AGCCATTTCT GCCAGAGGAT TCTTGTGTCT 960 GCTCTGGAGC TCCCCATTGG CCTGGTGGGG ACTCTGTCAG GTCTGCATCG TGATCTGATG 1020 GCTTCCACTC TTTCCCCTTC ACAGGTGTTA CTCCCCAGTA AAACTGTACT AATGACTCCA 1080 TCTAAGCCTC TTCTTCCAGG ATATTGGCAC AAATGGTAGT TACCTTGCTG GATTCTTGTA 1140 ACAAATAAAC 1150
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