Tag | Content |
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EnhancerAtlas ID | HS147-00642 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:21415840-21416730 |
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) |
GFI1 | MA0038.2 | chr1:21416614-21416626 | TGCTGTGATTTA | - | 6.27 | Gfi1b | MA0483.1 | chr1:21416614-21416625 | TGCTGTGATTT | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 21416392 | 21416539 | chr1 | 21416136 | 21416203 |
|
| Number: 2 | ID | Chromosome | Start | End |
GH01I021089 | chr1 | 21415894 | 21416493 | GH01I021090 | chr1 | 21416695 | 21418292 |
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Enhancer Sequence | CTAAAAACCA AATGTTTCAA ATGTCCTAAA ATGACTAAAT CAATCTCTTC AAAAGCCTTC 60 CCATGATAAA CATTCCATGG AATCTCAAAA CAAACACAAC TATACAATAA GTGTCCAAAC 120 TTTAGACCCA TGATGAGACT CTGCCACCTT TACTTTGTAC TAAAAATAAC TGGCTGGGCA 180 CAGTGGCTCA AGCCTATAAT CCCAACACTT TTGGAGGTCA AACTGAGAGA ATCACTTAAA 240 CCCCAAGAGT TCAAGACAAG CCTGGGCAAC ACAGCAAGAC CTCATCTCTA CTAAATTAGC 300 CGAGTGTGGT TGCCAGCACC TGTAGTCTCC GGGAGGCTGA GGTGGTAGGA TCACTTGAGC 360 ACAGGAGTTT AACAAGTTGC AATTAGCAAA CCTCTCTACC AAAAAAAAAA AAAAGCCTAA 420 ATAAATCAGC ATGAGACAGG AACTGCCAGA AATTTTCTAC AGAATTTGAA TTCAAAGAAA 480 TGACCCATGT AAAACTCTGT ACACTACAAC ATACTTCCTT CCTAATTCTG CCTGCCATTG 540 TGCTTATTAC CAGTTCTCAC CAAACTCTGT ATCTCCAAGC ATAAATCATT GGATGTTTCT 600 TTCCCTCTGA GCTCAAGATA CAGGCAAAAC AGCTTTTCAT AGTGCTACTT AAAATTCTAA 660 TTCAATAAAT GAGCAGTGTA ACATGCACAT ACAATAATCC AGAACATGCT GATTTTTCAT 720 AACCCATGAT TGAAATACAG TAGTACATCC ACTTGATATT TCTGTATTTC AAATTGCTGT 780 GATTTATATC ATTAGGAAGT ACAAGCAAAA CTATTAGTAA GATTACATAG ATGGTATGCA 840 ATACTGAATT AAGACTCTAA GTAGAAATAT AAATGTAAAA AATTTCGAAT 890
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