Tag | Content |
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EnhancerAtlas ID | HS176-16507 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr17:44356780-44357690 |
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 | CTCAGGTGAT CCATCCACCT TGGCCCTCCA AAGTGCTGGG ATTACAGGCA TGAGCCACCG 60 CACCTGGCCT TTTTTTTCTT TCTTTCTTTT TTTTTTTTTT TTTTTGAGAT AGGGTCTTGT 120 TGTGTCGTCC AGGCTGGAGT GTAGTTGCAT GAACATGGCT CACTGCAGTA TCTGTCTCCT 180 GGGCTTAATC CTCCCACCTC AGCCTCTGGA GTAGCTGGGA TCATGGGTGC ACATCACCAT 240 GCCTGGCTAA TTTTTGTATT TTGTAAAGAT GGGGTTTCCT CATGTTGCCC GGGCTGGTCT 300 AGAATTCCTG GGCTCAAGCA TCCTCCTGCC TCAGCCTCTC AATGTGTTGG GATTACAGGC 360 ATGAACCACC ATTCCCAGCC AACAGGCCCT CCTACACAAC TTTTTGTTTT TAGTGGCGTT 420 TCTAATTGCC TTTCATTTTT ATCCCTGACA TTCTTTGGCT TAATCATAGC CTTATGTTTT 480 TCTGTCTTAA ACAAATTATC TAATGCATGA GTCATTGTCT TGCCCTACTG ACCCTCTGGG 540 GAGTGCTCCA TTCTCCTGCT AGGATTTGGA TTGCTTACCG CACAGCCTGC TGTACAAATG 600 TCACCTTGAG TCAGAGTAAT TCTCATTGCT TTCCCTGAAC CTCTTGTTTT CTGAACCCAA 660 ATAAATAAAA ATGTCTGGCC AGGCGCGGTG GCTCACATCT GTAATCCCAG CACTTTGGGA 720 GGCCAGGGCA GGTGGATCAC TTGCCTTGAG ACCAGCTTGG CCAACATGGC AAAACCCCAT 780 CCCTACTAAA AACACAAAAA TTAGCCAGGT GTGGTGGCAG GCGCCTGTAA TCCCAGCTAC 840 TTGGGAGGCT GAGGCAGGAG AATCGCTTGA ACGCGGGAAG CGGAGGTTGC AGTGAGGTGA 900 GATTGCACCA 910
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