Tag | Content |
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EnhancerAtlas ID | HS190-00855 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr1:155606610-155607720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:155607389-155607410 | GAAAGTAAAGTGAAAGCGAAA | - | 6.45 | IRF1 | MA0050.2 | chr1:155607378-155607399 | AAAGCAAAAGTGAAAGTAAAG | - | 9.36 | IRF1 | MA0050.2 | chr1:155607395-155607416 | AAAGTGAAAGCGAAAGTAAAG | - | 9.95 | IRF2 | MA0051.1 | chr1:155607393-155607411 | GTAAAGTGAAAGCGAAAG | + | 6.1 | IRF2 | MA0051.1 | chr1:155607399-155607417 | TGAAAGCGAAAGTAAAGC | + | 6.71 |
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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 |
GH01I155635 | chr1 | 155605592 | 155607989 |
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Enhancer Sequence | GACAGTTTTC CGCCTCTAGC CAGCCCTCAG CTTTTCCCAG GAAAGGTAGA GAAAGGTGGA 60 CCTGGTTCCA GGCAAACCAA CACTCCCAGC CCAGAGGGCC GGGGGTTGTT AGAGAGCCCT 120 TTCCCAGAGA GCCTCACACC TGTGTCTTAA GCCTGGCGGC TGCGCTTGTC ACTTTTTTTT 180 TTTTTTTTGA GATGGAGTCT TGCTCTGTTG CCCAGGCTGG AGTGCAGTGG TGCAATCTCA 240 GCTCACTGCA AGCTCTGCCT CCTGGGTTCC CGCCAATCTC CTGCCTCAGC TTCCCGAGTA 300 CCTGGGACTA CAGGTGCCCA CCACCATGCC TGGCTAATAT TTTTTGTATT TTTAGTAGAG 360 GTGGGGTTTC ACTGTGTTAG CCAGGATGAT CTCAATCTCC TGACCTCGTG ATCCACCCGC 420 CTTGGCCTCC CAAAGTGCTG CAGTTACAGG TGTGAGCCAC TGCACCCGGC CGCTTGTCAC 480 ATTTAAATGG CTGACAGGTG CCTGGTGTTT TCTTCCAATT TCTAATGAGA AGATAGAACA 540 GAATAGCAAG CAAGAGGGGT TCAATGTTAC TCACTGCTTT GGAGAAATCC TGAATGTGTC 600 CCCAGAAATG AGACGAGAAG TCTTCTCCTG ATCAAAGGTC TTTTCTTGAT TGAAGGGTTC 660 GTGGTTTCAC AGGCTTCAAG GAAAGAAGCC ATGGACCTCA GTGGTGAGTG TTACAGCTCC 720 ATTAGAGAAA CATGCAGACC CAAAGAGTGT GCGGTGGCAA GATTTATTAA AGCAAAAGTG 780 AAAGTAAAGT GAAAGCGAAA GTAAAGCTTC CATATGGTGG AAGGGAACCC AGAAGGGTTG 840 CCCAATCCTT TTTTTTTTTG AGATGGAGTC TCGCTGTGTC GCCCAGGCTG GAGTGCAGTG 900 GCGCAATCTC GGCTCACTGC AAGCTGCGCC TCCTGGGTTC ACGCCATTCT CCAGCCTCAG 960 CCTCCCGAGT AGCTGGGATT ACAGGCGCCT GCCACCACGC CCGGCTAATT TTTTGTATTT 1020 TTAGTAGAGA TGGGGTCTCA CTGTGTTAAC CAGGATGGTC TCGATCTCCT GACCTCGTGA 1080 TCCACCCGCC TTGGCCTTCC AAAGTGCTGG 1110
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