Tag | Content |
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EnhancerAtlas ID | HS098-24358 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:47856440-47858090 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:47857235-47857254 | TAGTGACATCTGCTGGCAA | - | 6.64 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 47857344 | 47857551 | chr17 | 47857737 | 47857832 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I049779 | chr17 | 47856547 | 47857969 |
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Enhancer Sequence | TGCACACTCC TAAGGAATTG CAGGAAGGCC AGTGAAGCTG CGGCACTGAG AAGGAAGCAG 60 GTTTGTGTGA GATGGGCCTG AAGAGTTAGC CAGAAGACAG ACCAGGCAGG ACACTGAAGG 120 CCAGGGAAGG ATTTCTGTCT TTACCCCTCC ATGGATAGGC ACATGGAATG AAGGTCTTTA 180 AAGAAGAGCT GCCAATGGTT CTTTCTCCCA GATTACTAAT GCTACTTACA GTTGTCTGGA 240 AGGAGAACAG TCATGACGGT CTAAGCTGCT AGGAACTTCC CAGCATCCTG ACATGGTGTG 300 GCTATGCCTG GCTGTCACTG GGGAGCCCCC AGAACCCATG GATCAGCCCT AGCCTACAGC 360 CCTCAGGCAA GGGATAGCCC CCACCCATGT GGACAAAGGG GCAGGGTGGA GGGTGGGTGG 420 AGTGCTTTGC CTGAGATCTC AGCTCTGCAT GACATTTGGA ACAGCCCCAA GACTATGGCT 480 CTTTTTCCTA GATAACTCTA TCATGTGTAC CCCCCATTTA AATGGCCTGC CGCCCTTCCT 540 ACAGCAGCTG TGCTCCCCAC CCAATCTGGA GAAGGTCCCT GGATAAGAAC TCTGACTCTG 600 CCCAGAGACT TGGGTCTTGA CCTGCTAAGT TTAGGCCTCA GGACTGTTGG GAACCATGGA 660 TATATACATA TCCTTGATAG TTTTCCAGGG GTATTAATGG AAGCCATTGG AGAAGAGGGT 720 CACAATTGTT GGACTCAGCC TTTCTAAAGC CAGTCCTTTC CTTCCAGTCA TATCTTTGGA 780 AAATGTGGTT TGGTGTAGTG ACATCTGCTG GCAAGGCTAG GCACATAATA CAATGACTGG 840 ATGTCCACTC ATCCTCATGT AATTTCCAGA CTAGCAAGAA AATCGTTCTT AACTTCTGAG 900 ATTGGATTGG GCTCAGTAAC CTCAGTTGGC AAGAGCAAGA CTAAGATGTC CAAGGATGTG 960 GGTCTGAACT ATGTATGGGC TAGTTTGCCT TAAATAGAGA AAATGTGTTT CCTAGTTGTG 1020 GCTTATACCC CTCCCATTGG TCAGTTGATT CATATTTGGG TACAGTTAAT CACAAGGGAG 1080 ATTGGGCAAA CATGTATAAA TGACTCAGAG GAACCCGTTC CTAGCCCCTA TGCCTGGGAA 1140 AGCATCTCCC AACAAATAAA AAGACCCACA TTTTACAAAT GGCAAAATGC AGTGTCATTT 1200 TTTTATCCTC CTGAGGTTGA CTAGTTTGGG AAACTTTTTA GTTTCTCCCA GGTCACCAGG 1260 AAAGTAGTGT CTACAGAATC ATCTTCATGG TTCTTATAGT GGGCAAGACT GACTAGGGCT 1320 TTTATAATGG CCCCTCCACA CATGCTGGGG TAAGGGCAGT GGCGTGATCT TGGCTAACTG 1380 AAACCGCCGC CTCCTGGGCT CAAGCAATCC TCCCACCTTA GCCTCCCAAG TAACTGGGAC 1440 TACAGGTCCA CCAGTAATTT TTTGTATTTT TAGTACAGAT GGGGTTTTCC CATGTTGGGC 1500 AGGCTGGTCT TGAACTCCTG GCCTCAAGTG ATCTGCCTGT CTCAGCCTCC GAAAAGTGCT 1560 GGGACTACAG GCGTGAGCTA CCGCGCCCAG CCTCTCCTCA CCACTTTCAT CCATGCCATG 1620 TACACATTCT GTTTACAATC TCACCCTTTT 1650
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