Tag | Content |
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EnhancerAtlas ID | HS053-15514 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr16:67951050-67952460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr16:67951975-67951989 | AGAAGGTGAGTCAT | + | 6.51 | NFIL3 | MA0025.1 | chr16:67951119-67951130 | AGGTTACATAA | - | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_03621 | chr16:67950723-67952149 | Brain_Angular_Gyrus | SE_41735 | chr16:67951057-67951762 | LNCaP | SE_65564 | chr16:67950024-67954491 | Pancreatic_islets |
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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 |
GH16I067915 | chr16 | 67949241 | 67953328 |
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Enhancer Sequence | CAATCTATGA CAACCCTGCC AGGTGGTACG TAATCCCCCA CCTTACAGAT GAGGAAACTG 60 AGGATGGTGA GGTTACATAA CTTGGCCATG GTCTCCCGAC TGGAGGGTGG CACATCTGGG 120 ATTTGATTCC AGGCTGTCTT GGCTTCAGAG TTCTTGGCCT GTCTAGTGCT GCAGTCTGCT 180 CTCCCTGGTA TGTGTGCCTC AGCACGTTGC TGGTTTCTTG TTTCAGTGCT TTCTGGCTGC 240 TGATCAGTGG ACACATCTCT CCTGTCTAGC CTGTAGGGTC CTTGAGGACA GCATGTACAT 300 CAATACATAT GCTGTCCACT GTCGTGTCCA GGCTTAGTGC ACAGTGGTAC CTGTATGCTG 360 GGTTGAACTG CAGTATTTAT AAGTGATAAC TGGTGGGGGA ATTTTCTCTT GGCTTCTCCT 420 GAGGGAAGCA CCAGTGGCTA TTGGTGATGC CCTGGGAAGC GTCCCAAATG TGACTGCTGG 480 CAGGCAGACA GGCTGTGCAG CCAGTGGAGT GCTCCCCTCA AGGGGCCAGA CTCCAGGAGG 540 AAGCAGAGAG CCTGCTGGCA ATGCGCTTAG GGGGCTGCTG GCCACAGCTG CCTGTGGGCA 600 CAGGCAGGGG GAGGATTTAA AGGCCCAGGG CTGGTGTGTG CTTGTCAACT TTTAGGGCAA 660 ATACAAGACT CTTGGAAGAG GGGTAAATGC TGAGGAGGAG ATGACTGGAA AGGAAAAATC 720 TGAATGTTTA CCCAGCACCC AGAGGCACTG GAGTGGAGAG GGCACGCTGG AGTGGAGAGG 780 GCATGCTGGA AGTGGTGGGG AGACACAGGT TGGGAGAGGT AGCGAAGGCC TGTGTGAATG 840 TGAGAGCAGT TTGAGGACAC AGTCACCTTG AGAGGCGGCT TCCTATCACA GGAGGCCTGG 900 AGGAGCTGTT TCTAAAGGAT GACACAGAAG GTGAGTCATC AGCTACAGAC TCATGCTAGA 960 GAACTGTCAG GGTCCTCCAA TGCAGAGAGT CTGTGATTCA CTTGACATGA AATGTGACAT 1020 CCTTGATGTC AGTGCTTTTG TCAAGAGTTC TATTCCTAGA GGCAGGACGG ATGAAGGGGC 1080 TCTTGTAGGA TTGATATTAG AGTGATGCCA TTAGGAGCTT TGCTGTCTGC TGCATTCAGC 1140 ATCCTGAATT ATCACCCTCC TCTGCTTGGC CAGTCTCTGA GCTGTGGGTG AGCCCAGGTG 1200 ACTGTACTAG GAACAGGTGG GCTTGGGTAG AATTTCTCAC AGAGCCTTGT GAGTGCTGCT 1260 GGGCAGGGGA CAGAGTACTG TTGGGAGAGG AAGCCCACCT TCATAGCCAC TCTGCTGCTA 1320 CCTGGGTGAC AAGGGCTGGT GGGAGGTGGC CTCCCAGGGT TGGGTGTCTG GTCTGCAGGT 1380 TGACCATACA TTGATCTGGG GCTAAGTATA 1410
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