Tag | Content |
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EnhancerAtlas ID | HS187-25125 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr9:102524460-102525560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr9:102524923-102524944 | TTCTCCTTTCAGTTTCCCTTC | + | 7.3 | Nr2f6(var.2) | MA0728.1 | chr9:102524610-102524625 | TGAACTCCTGACCTC | - | 6.22 |
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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 |
GH09I099762 | chr9 | 102524483 | 102525282 |
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Enhancer Sequence | TGGCTCACAG CAACCTCTGC CTCCTGGATT AAGCGATTCT CTTGCCTCAG CCTCCTGAGT 60 AGCCGGGACT ACAGGCGCGC ACCACCACGC CTGGCTAAGT TTTGTATTTT TAGTGGAGAT 120 GGGGTTTCGC CATGTTGGCC AGGCTGGTCT TGAACTCCTG ACCTCAGGTG ATCTACCTGC 180 CTCAGACTCC CAAAGTGCTG GGATTACAGG CATGAACCAC ACCATGCCTG GAATTTTCTT 240 TTTTAAGAGA CATAGTCTTG CCATGTTGCC CAGGCTAGTC TTGGACTCTT GTACTCAAGT 300 GATCCTCCTG CCTCAGCCTC CCCAGTAGCT GGAACTACAG GCATGCACCA CCACACCCAG 360 GTAAGAAAAT GTTTTAAAGC ACACTCATTG TTCAATTGAT AACTGTCAGA AAACAAGAAA 420 GCTCTAAAAC TCAACCACTC TCTCTTTCTA TCCGTGTTGC TGCTTCTCCT TTCAGTTTCC 480 CTTCTATTAC TCTGCTTCCT CTGTTTATGC AGTTTCCATT CTCTGATAGT TTCGGCTAAC 540 ACAGCACAAT GTGGTCACTC CCAATACCTT TTAAACCTTG ATAACTCTCA ACACTTCCTT 600 GTAGTTTCTG CCCCCACTAA TTGGTTCAGT CTCTTAATTT ACCAATTCCA AATGGCCCGT 660 CTTTTCATGC TAGACCATAG AAATGTCACA GAACAGCCTA TGGATGATGG GTACTTGGAT 720 CAGAAGCCCG CTCTATTCCA ATCAGCTGTG ATCCAATCAC ATGGGGAATG GGCAGGATAA 780 CAGGTTTAGA GAATAGACTC ATTGGAAGCA GGGCCCTGAG CAGAAGAGAT TCTTTGAGAA 840 GGAGGTGGGG AAGAGCAAGC AATGTTCAAC ACCTCCAGGG CATTACATTT TCCTGCCTAC 900 CTATTCTCCT ACAAGCACAC CACACTCCTT TCAAAGTGGA ATTGCTATCT CCCAAACCCA 960 TTCCACAATT CATTATCCCA TGCCTTTGCT CACACTGTTC TCTCTGCTTT GAATAATCTC 1020 TAACCCTGTC TTATCATCTC AAAATGTACT AGCCAAAGGA TGTGAGTGGA TATAGAAGTA 1080 ATTCAGAGAA CAGTCAATGT 1100
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