Tag | Content |
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EnhancerAtlas ID | HS187-10597 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:46914240-46915590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr17:46914790-46914805 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr17:46914341-46914356 | TGAACTCCTGACCTC | - | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 46914946 | 46915429 | chr17 | 46914603 | 46914733 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I048837 | chr17 | 46914503 | 46915949 |
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Enhancer Sequence | CCTTCTGAGT AGCTGGAATT ACAGATGCAT GCCACCACAC CCAGCTAATT TTTTGTATTT 60 TTAGTAGAAA TGGGGTTTCA CCATGTTAGC CAGCCTGCTC TTGAACTCCT GACCTCAGGT 120 GATCTGCCTG CCTTGGCCTC CCAGTGCTGG GATTACAGGC ATGAGCTACC ACACGCAGCA 180 CTCAGAAGAA CACTCAGAAC ACTCTTATCT GAGTGTTCTT CATGATCCGC AAAGGACAAG 240 TTAAGTAATT TTACACGCAC AGATAAATTG GTGCTCCAGG CTTAGGACAG AGGGATATGC 300 TGGCCTCCAT ATGACGGTAG ACCACTTGGA AATAAAGGGT CTGCAAGCTG AGAAACCTCC 360 CTGCCCACTC TCTCATAGCA TCCAAGAGAA ACCCTCATTG TACACAGGTA ACAGTTTATT 420 ATAGGGAAAA ATCTTGACCT AGACTGGAAT GTGAACATTC CCCCACCGTT GAAAAACTCT 480 TTTGAGCCGG GCATGGTGGC TCATGCCTGT AATCCCAGCA CTTTGGGAGG CTGAGGTGGG 540 TGGATCACCT GAGGTCAGGA GTTCAAGACC AGCCTGGCCA ACATGGTGAA ACCCCCTCTG 600 TACTAAAAAT ACAAAAAATT AGCTGGGCAT GGTGGCGTGC ACCTGTAGTC CCAGTTACTC 660 AGGAGGCTGA AGCAGGAGAA TTGCTTGAAC CCCAGAGGCG GAGGTTGCAG TGAGCTGAGA 720 TACCGCCACT GCACTCCAGC CTGGGGAACA GAGCGAAACT CTGTCTAAAA AAAAAAAATG 780 GAAAGAAAAA CTTTTGAGGT TTGAGGTTGA GGATGTGGCT AAACTGTGTC ACAAACCAGA 840 AAGTCAATGC ATTTTTTAGT TCCTTAACTC AATTTCAAGA ATAGACAGTT TAGTGCTCCA 900 AAGTCCTGTT GCCTTCTTTA TGAAAAAACT GACTTCTGGG GAGTTGGAAG AGCAGGCCTG 960 GTTGCTTAGA CTTCAAAGTA AAACCAGTAA ATAGATAGGA TGGGGCTAGA ATAAGTATTA 1020 TGGTTGTTTG GGAGGTCTTG TTTTTTTGGT TATTGTACTT ATTTATTTTT AAAAATTATA 1080 TGTGTGCCAG CCGGGCGCGG TGGCTTACAT TGAAGCAGGA AGAGCCACAG ACAAAACTCC 1140 TCAGACACCG AGTTAACGAA GGATGGGGTT TATTAGGCCG GGGGCATCAG CAAGACTCCT 1200 GTCTCAAGAG CTGAGCTCCC CGAGTGAGCA ATTCCTGTCC CTTTTAAGGG CTAACAACTC 1260 TAAGGGGGTA TGCGTGAGAG GGTCGTGATC AATTGAGCAA GCAGGGGGTA CATGACTGGG 1320 GGCTGCATGT GTCGGTAATT AGATCGTCAC 1350
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