Tag | Content |
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EnhancerAtlas ID | HS190-01850 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr10:90843350-90844390 |
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) |
IRF1 | MA0050.2 | chr10:90844213-90844234 | AAACCAAAAATGAAAACAAAA | - | 6.14 | IRF1 | MA0050.2 | chr10:90844331-90844352 | AAATAGAAAGTGAAAGAACTA | - | 7.54 | Nr2f6(var.2) | MA0728.1 | chr10:90843971-90843986 | AAGGTTAAGAGATCA | + | 6.15 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH10I089084 | chr10 | 90843758 | 90845130 |
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Enhancer Sequence | TAATCTAGGT ACATTTGCTG GCATCTCCTG ATGTTCTGTC TTTCCATAGT TAAAATTTGG 60 GCTGAGCTTT AAGGAAATTA AGGAAAGACT ACTTTCACCT TTTGAGGCTC CCACTGTTCT 120 GATAGGCAAG CTTGAATAGC TAGGCTACAG GACAGCGCAT TTTTCATTTT CCCATTTGGG 180 ACCAGAATTG CAGCCTATAT GCAATTACCA AGACTAGTCT CTGAGGCAGT AGTCTCTGAC 240 CATCCACTTC AACTGCACTC CTGCATGATG CCCTTACATT TCTGTTGTCT GTGTTGAGGA 300 AAATCTGGGA CATGAACGCA TGTGGTAAAC TACAGAACAA TAGTAATAAA ATAGTTTTCA 360 TTTGTGAAAC CCTTCTTTGT TCTAGAAGCT GTACTCTATA GTTTACAGGC CATCTCCTTC 420 AGTACTGTCA TCACCAAGAG GTGGATATTA TTGTCCCTTC CATTTTACAA GTGAGAAAAT 480 TGAGGCCAAG TTAGGTGGGT AGTTTAATAT AAGACTCTGC CTCAGGAGAG GTATGCAGGA 540 TTAAAAATAA ATTTAGAGGC CCAGCGTGGT GGCTCACACC TGTAATCCCA GCTCTTTGAG 600 AGGCCGAGGC AGGCGGATCA CAAGGTTAAG AGATCAAGAC CATCCTGTCC AACATGGTGA 660 AACTCCATCT CTACTAAAAA TAAAAAAAAT TAGCTGGGCA AGGTGGCACA TACCTGTAGT 720 CCCAGCTACT CAGGAGGCTG AGGCAGGAGG ATCACTTGAA TTCGGGAGGC AGAGGTTGCA 780 GTGAGCCGAT ATCATGCCAC TGCACTCCAC CCTGGTGGCA GAGCGAGACT CCGTCTAAAA 840 AAAAGAAAAA AGAAAAAAGA AAAAAACCAA AAATGAAAAC AAAAAATAAA AATAAAAAAA 900 TAAATTTAGA AACTCACAGC TCACAGCCCA CACAGATACC ATGGACTTTC ACTTTCCATG 960 GTTGCATCAG AATAACATAT GAAATAGAAA GTGAAAGAAC TAAAGACAGA ACTTTGAGCA 1020 ACATCAATAT TTAAGTGGCA 1040
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