Tag | Content |
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EnhancerAtlas ID | HS190-11657 | Organism | Homo sapiens | Tissue/cell | Treg_cell | Coordinate | chr7:2076760-2078340 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr7:2077695-2077716 | GATAAGAAAGTGAAACTGTCT | - | 6.45 |
| | 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 |
GH07I002037 | chr7 | 2076900 | 2078235 |
| Enhancer Sequence | TACACATCAG ATCTCACCGG TTCCAGTGCC TTCTGCCACG TGGAAATTTC GGCTCCTTCT 60 TTGTCTTCTT AATAGACTCT TCTTTTTTTT TTTTTTTTTT AGAACGGGTT TAGATTTAGA 120 AGAATGGAGA AGATGGTAGA GACTTTTCAC ATATTCCACA CCCAGGTGCC CCACTGTTAA 180 CATCTTACAC GAGCACAGTG TGCTGGCCAC AATAAGGAGC CAGCATGGAC CCAGGCACGC 240 CTTGCTCTCC TGGACTACAC AGATACTGTG CTTCTTACAA ATGGAAGGCT TGTGGCCGTC 300 CTGCCTTCGG CGAGGCACCA TGTTCCCAAC AGCATGTGCT CCCTACACGG CTCTGTCACA 360 TCTGGTAATC CTCATGGCGT TTCAGACATT GTATCACTAT TATATCTGTT GTGGTCTGTA 420 ATGGGTGGTC TCTGATCTTA CTACTGTCAT TGATTCTGGG GCGCCACGTC CTGACTGTAC 480 TTCCGACATT GCATCACTGT TATGTCTGTT GTGGTCTGTG ATCGGCGGTC TCCGATCTTA 540 CTGCTGTCAT TGATTCTGGG ACGCCACACA CTATGCTCCT CAGACGGCAA AAGCTTCACC 600 GACCAACGCT GCTTGTGTCT GGCTGCTTCA CTGACCAGCC ATCTCCCTCC CTCCCTCTCC 660 TTGGGCCTCT CTATTCCCTG GGCGACACAA CAGTATTAAA ATCAGGCCAA TTAATAACCC 720 TACAACAGCC TCTAAGCATT CAAGAGAAAG GAAGAGTCGC ATGTCTCTCC TTTAAACCAA 780 AAGCTAGAAA GGATTAAGCT TAGTGAGGAA GGCGTGCCAA AAGCAAAGAT AAGCCGAAAG 840 CCAGGCCTCT CGTGCCAAAC AGCTCGCCAA GTTGTGAATG CAAAGGGAAA GTTCTTGGAG 900 GAAATTAAAA GTGCTGCTCC ACTGAACACA CCAACGATAA GAAAGTGAAA CTGTCTTATT 960 GCTGATACGG AGAAGTCTGA GTGGTCTGGA TAGATCAAAC CAGCCCCAAC ATTCCCTTAA 1020 GTCAGAGCAA GTTCCACGAG GCTGAGAGAG GTGGGAAAGC TGCAGAATTC AAGTCTGAAG 1080 CTAGCAGAGG TGGGTTCATG AGGTTTACAT TAAGAGGCAG TCCCCATCAC ATAAAAGTAC 1140 AAGGTGAAGC CGCAAGTGCT GACGGAGAAG CTGCAGCAAG TTCTCCAGAA GATCCAGCTA 1200 AGAGCACCAA TGAAGGTGGC CACACTAAAC ACCAGATTTG CAGTGCACAT AAAACAGCCT 1260 TCTGCTGGAA GATGCCGTCT AGGGCTTTTA CAGTTACAGA GGAGAAGTCG ATCCCTGCCT 1320 TCAAAGTTTC AGAGGACAAG CTGATGCTGT TAGGAGATAA TGAAGCTGAT GACTTTTTTT 1380 TTTTTTTTTT TTTTTTTTTT TGAGACACAG TCTCACTCAT TCTGTCACCC AGGCTGGAGC 1440 ACGGTGGCAC AATCTTGGCT CACTGCAACC TCCGCCTTCT GGGTTCAAGC AATTCTCCTG 1500 CCTCAGCCTC CCAAGTAGCC GGGATTACAA GTGTGTGCCA CCACGCCTCA CTAATTTTTT 1560 GTATTTTTAG TAGAGACAGG 1580
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