Tag | Content |
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EnhancerAtlas ID | HS187-03589 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr10:89824240-89825450 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx3-2 | MA0122.3 | chr10:89824999-89825012 | TTTAAGTGGTTCA | - | 6.33 | SOX10 | MA0442.2 | chr10:89825423-89825434 | AAAACAAAGGA | + | 6.32 | Sox3 | MA0514.1 | chr10:89825423-89825433 | AAAACAAAGG | - | 6.02 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_09860 | chr10:89821159-89829084 | CD14 | SE_25726 | chr10:89818943-89828511 | DND41 | SE_32551 | chr10:89821298-89831261 | GM12878 | SE_39532 | chr10:89821269-89824947 | Jurkat | SE_54094 | chr10:89822016-89828486 | Spleen | SE_59698 | chr10:89821239-89881250 | Ly4 | SE_66780 | chr10:89821269-89824947 | Jurkat |
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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 |
GH10I088061 | chr10 | 89821559 | 89828156 |
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Enhancer Sequence | ATCCTCGTAA GATGTTAACA ACTTTAAGTC CTGTGGTGGT ATGGGGGACC TGAACACCTG 60 GGTGCATTTT CTTTTATTTA CTCTAACAGG GACACAGACC TCTGGCTTCT TTCATAGAAA 120 CCCCCCTTTT TGAAATGTCT CTGTTTTGTT CATTCAGGAG AACAGATCAG CATCTCTCAT 180 GCAAGGCCTG GCTCTGTGCC CATCTCACTT TTGCAATGAA TTTAGCAACA TCTGCTTTGC 240 CCATTAAAGT GATTTTTCTC TTCCTGGCCC TGAGCCTGTA TGCTTGCTGC AATTGATTAC 300 TAGCAATTTC CTTCCCAAAC CAGAGAGTTC AGTGAACTCT AAATTGAATT GTTGCTCACT 360 GGTCTCCTTT GGACCAATTG CATATGGCTT ACGTGCAAAA TGGTCAAGCC ACTCAGTTCC 420 CGAATCTATA GGCTGATGAT TCTGGTTAAA CGTGGGAGAG GACCTGATGA GTGACATTTC 480 CCATTTTTGC ACACAGTGGC CTAGGACTGT GGTCACTTCT GTGTTTCTCA ATTTCAGGTG 540 GGGGGAGGGG ATGAAGCCAC CTTGCTTACA GCAAGGCTGT TGAAGTACAC ACCCTCTTTC 600 CTTTCAGTCA TATTGCAGCA CCAATGGCCT CAGATGTAGT TGCCTGGAAA CCTTGTTTCA 660 GAGACATCTG AGAAACATAT ATCTAGCTCC AGAAGTGGCT TAGAAAGACC TCAGGAAGAT 720 GCATATCACT GTACTCTTTT GAAGGCAGCA GTGGGTCCCT TTAAGTGGTT CAGGCAGCTT 780 TTTAAGATAA AGCAACGCCC AAAGTGATGC TGAGCCTGTA TACCTGGCCT GCTGCTCCAT 840 CTTGATTGGC GGATATCTAG TTATCCTTTG AGATGTAGTC TGAGTGTTAC CTCTCAGGGA 900 GTCTGCCCAT GTCTCACTCA GCCCTGTATT CCCAATATCT AGCACAGTGA GTACATGTAG 960 TGCACCCTCA GTGAAAGGAC AAATGAGTGA AGGATGCTGC TCTTCTCGTG AGAAGATTTT 1020 AAACTGGTAC TTTGCTCTGA GCTGTCCTTG AAGTGTCTCT CCTTCCCCAC AGCCATGATA 1080 GCTTTACACA GGGACAGTGA GGAGTTGTTG GTTATTTAGA GAAGTGAAAG TCAGGAGTCT 1140 CCTCTGCCAC ATAGTCCTAA AAAAAAAAAA CAACAAAAAA CCCAAAACAA AGGAACTTAT 1200 TACTGACCAA 1210
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