Tag | Content |
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EnhancerAtlas ID | HS141-07069 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr16:23874720-23875870 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF8 | MA0652.1 | chr16:23874937-23874951 | AGTTTCATTTTCGT | - | 6.01 | IRF9 | MA0653.1 | chr16:23874937-23874952 | AGTTTCATTTTCGTA | - | 6.02 | SPI1 | MA0080.4 | chr16:23875259-23875273 | TAAAAGAGGAAGTT | + | 6.83 | SPIC | MA0687.1 | chr16:23875259-23875273 | TAAAAGAGGAAGTT | + | 6.34 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_10067 | chr16:23863461-23878484 | CD14 | SE_10888 | chr16:23856132-23883188 | CD20 | SE_32644 | chr16:23868998-23876906 | GM12878 | SE_60111 | chr16:23838010-23894131 | Ly4 | SE_63093 | chr16:23837102-23894105 | Tonsil | SE_67999 | chr16:23846983-23921777 | TC32 |
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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 |
GH16I023855 | chr16 | 23866922 | 23876752 |
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Enhancer Sequence | TTTGCACTGT GGACTCACCC TGAATTCTTT CTTGTGCAAG ATCCAAGAAC CCTTTCTTGG 60 GGTCTGGATC AGGACTCCTT TCCTGTAATA CAATGTCACA GAGCTCTTAA GTGGCAGAGC 120 TTGGGGCCAA ACTTAGGCTG CTGCACCCGA TGTCCCAGCT CCTCTGCCCT ATCTAGCTGT 180 GGATTTGTGC CTCGAAATAG AATTGCATTT TGAATGCAGT TTCATTTTCG TATGGAAAGT 240 GTCTATCCTG TAAATGTAAC TGTAGCAGCC CCAAAGCTGA GCTGGGCAGT TTTATGGCAG 300 CCTGGAGTCA GTCTTGTCCG CTTCCAATCA GGGTTCCTGG ACTGGCTCCT ATATTAAAAT 360 TGGTATTAGT AGACAATGTT CCAGGCAGAG TTTTGGATAG AAACTATCCA TCAGCACCAA 420 GAATGTGCCT GATTTGGTAA TCTTTTTACC AAAGTAAAAG TCAGTAGTAA GTTGTGGTTA 480 AAAGAGAGGA AGTTCAGAGT TCAGTACGTT ATTTCTCTCT CTCTCTCTCT TTGTTTAAAT 540 AAAAGAGGAA GTTACTGCTC TTATTTTTGT ACCAGCCCGT CAGTAATGGG TACAGAGTAA 600 AATCTTAGCT AAGCTGAGGT CAAACTTCAA AACTTAGTAA TAAGGATCTC CCTTGTTCCT 660 TTGTAGGGCG ACTAACATGA AGGTTCTGAC TCTTAACCCA TAGAGCCACA AAAAATAGTC 720 CTAGGAAAAT CATATGATTT TATTTATTTT AGGAACAGAA ATGGTCCCTT CCGAAGTAGA 780 GGCATTTCTA CTTCTTTCCT AAACACCATC TCTGCTCAGT GAGCTCTCCC ACCCTCAGGT 840 ACTGTGTTTC AGGCTTATTG CTGTATTGCT AGAAGTATCC TCACCTTCGA GATTAAGAAA 900 AGATATTTAT TGCCGGGCAC AGTGGCTCAC GCCTGCAATC CCAGTCTTTT GGGAAGCTGA 960 GACGGGAGGA TCACTTGAGC CCAGGATCTT GAGACCAGCC AGGGCAGTAT AGTGAGAACT 1020 CATCTTGAAA AGAAAAATTT ATTGAGCTCC TACTGTATAC TGGGGATACA GCAATAGGCA 1080 AGATAGCCCT TGCTCCTCAT GTAACCTACA GATAATAAAC AAGATTACAA ACAAACAAAA 1140 TAAGAGGTCG 1150
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