Tag | Content |
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EnhancerAtlas ID | HS193-14279 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr17:44356820-44357750 |
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) |
IRF1 | MA0050.2 | chr17:44356856-44356877 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 44357048 | 44357501 | chr17 | 44356903 | 44357020 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I046279 | chr17 | 44356971 | 44357567 |
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Enhancer Sequence | ATTACAGGCA TGAGCCACCG CACCTGGCCT TTTTTTTCTT TCTTTCTTTT TTTTTTTTTT 60 TTTTTGAGAT AGGGTCTTGT TGTGTCGTCC AGGCTGGAGT GTAGTTGCAT GAACATGGCT 120 CACTGCAGTA TCTGTCTCCT GGGCTTAATC CTCCCACCTC AGCCTCTGGA GTAGCTGGGA 180 TCATGGGTGC ACATCACCAT GCCTGGCTAA TTTTTGTATT TTGTAAAGAT GGGGTTTCCT 240 CATGTTGCCC GGGCTGGTCT AGAATTCCTG GGCTCAAGCA TCCTCCTGCC TCAGCCTCTC 300 AATGTGTTGG GATTACAGGC ATGAACCACC ATTCCCAGCC AACAGGCCCT CCTACACAAC 360 TTTTTGTTTT TAGTGGCGTT TCTAATTGCC TTTCATTTTT ATCCCTGACA TTCTTTGGCT 420 TAATCATAGC CTTATGTTTT TCTGTCTTAA ACAAATTATC TAATGCATGA GTCATTGTCT 480 TGCCCTACTG ACCCTCTGGG GAGTGCTCCA TTCTCCTGCT AGGATTTGGA TTGCTTACCG 540 CACAGCCTGC TGTACAAATG TCACCTTGAG TCAGAGTAAT TCTCATTGCT TTCCCTGAAC 600 CTCTTGTTTT CTGAACCCAA ATAAATAAAA ATGTCTGGCC AGGCGCGGTG GCTCACATCT 660 GTAATCCCAG CACTTTGGGA GGCCAGGGCA GGTGGATCAC TTGCCTTGAG ACCAGCTTGG 720 CCAACATGGC AAAACCCCAT CCCTACTAAA AACACAAAAA TTAGCCAGGT GTGGTGGCAG 780 GCGCCTGTAA TCCCAGCTAC TTGGGAGGCT GAGGCAGGAG AATCGCTTGA ACGCGGGAAG 840 CGGAGGTTGC AGTGAGGTGA GATTGCACCA CTGCACTCCA GCCTGGGCAA CAGAGTGAGA 900 CTCTGTCTCA AAAACACAAA ACAACAGAAA 930
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