Tag | Content |
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EnhancerAtlas ID | HS150-00798 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr1:118250390-118251590 |
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) |
GSC | MA0648.1 | chr1:118251056-118251066 | GCTAATCCCC | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I117708 | chr1 | 118250679 | 118251611 |
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Enhancer Sequence | GAGGTCTGAG ATGCTGCTGG AGGAGTTTGT ATTCTAGTTC CTGGCAGGAG ATCTGAAGCA 60 TATTTAAGAA TTAAGTGAAT GGGGGGTGGG AGGTGGAAGA GGAAACTGGA GAGAGTAGGA 120 GGCTCCAGGC AGAAGGATCA GCTTCGTCAA AGACTAAGAA GTGAGACTGC ATGGTCCTCA 180 AATCCCTTCT CTTACTCTTC TGCCTTCTTT CCAATTCCCG TTTGTCCCAG GCTAAGGCCT 240 TGCTTAAGTG ATCTCTGTCA GAAGGATGGA GTGAAAGCAG GAAGAGAGTC CCTTCTGGCT 300 CACAAGCAGG GTGGCCAACC ATCACAGTTT GCCTGGGACT GTCCTGGCTT TAGCACTGAA 360 GGGTTCATGT CCTGGAAAAC CTTTGGTCCC TGGATAAACA GGAAAAGTTG GTCACCCTGC 420 TCAGAGGGTT TGTTCTGGTC ACCCAAGTCA CCTGGAAGGA GAAACAGGGC ATCTGAGTGT 480 CTTGGAATGA TCCCTGGGCT GGGGCCAGGA CACCCGGGTT TAAGTCCCAG CTCTGTCCCA 540 CACCAGCCTT GTAATTCTGA GGAAGTTGTG TCTCTAGCCT CCCTATATTG ACAACATTTG 600 CTTAGTTTCT ATATTCTGTA TGCTCTGGAA ATTGGGGCTT CGATCCTAGA GAGATTTCTA 660 GGGCTAGCTA ATCCCCAGAG TAAGCAAATG GCTCCCCGTG GAGCATGCTT TTGATATGCA 720 AACCAGCCAA TCCAGAGCCT GCACCCCCAA CCCTCTCCTT TATCAAACGC TCACACACCA 780 ATGCAATATC TCCCCTGCCC TAAACCACCC CAGGGCCAAG TCCTGGACAA CTAGGGATCA 840 CGCCTATAGC CCAGAACCTA CTGAAATTAT CCAAACTACC CAAAGCTGAA CTTACTCAGC 900 ATAGTTGCAG TACCTTGCCC ATTCCTTCCC ACAGGAACCC CAGTAAAGGC CCTGAGCCAT 960 GCATACTCTC CTCTCCCCTC CCCACTTCTG CCTCCTGACC GACCCAGCGC TTCCTGGGGT 1020 GGCCTGCGTG GCACGCCGTA CCTCCTGTTC TAGAGGCCTG TGAGTATAAA CTTTTTCCTC 1080 CCTGACAATC ATTTCCATTT CTTACCATGC CTGATTAAAA CAAACTCCAG GTCCATTTTA 1140 TCACACTCCT CCCTGCCGTT ATTGGCCCTC CTGCCTCACG GGGTTGTTGC GAGGGCCTAA 1200
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