| Tag | Content |
|---|
EnhancerAtlas ID | HS062-07175 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr17:47856760-47857750 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:47857235-47857254 | TAGTGACATCTGCTGGCAA | - | 6.64 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I049779 | chr17 | 47856547 | 47857969 |
|
Enhancer Sequence | GGGAGCCCCC AGAACCCATG GATCAGCCCT AGCCTACAGC CCTCAGGCAA GGGATAGCCC 60
CCACCCATGT GGACAAAGGG GCAGGGTGGA GGGTGGGTGG AGTGCTTTGC CTGAGATCTC 120
AGCTCTGCAT GACATTTGGA ACAGCCCCAA GACTATGGCT CTTTTTCCTA GATAACTCTA 180
TCATGTGTAC CCCCCATTTA AATGGCCTGC CGCCCTTCCT ACAGCAGCTG TGCTCCCCAC 240
CCAATCTGGA GAAGGTCCCT GGATAAGAAC TCTGACTCTG CCCAGAGACT TGGGTCTTGA 300
CCTGCTAAGT TTAGGCCTCA GGACTGTTGG GAACCATGGA TATATACATA TCCTTGATAG 360
TTTTCCAGGG GTATTAATGG AAGCCATTGG AGAAGAGGGT CACAATTGTT GGACTCAGCC 420
TTTCTAAAGC CAGTCCTTTC CTTCCAGTCA TATCTTTGGA AAATGTGGTT TGGTGTAGTG 480
ACATCTGCTG GCAAGGCTAG GCACATAATA CAATGACTGG ATGTCCACTC ATCCTCATGT 540
AATTTCCAGA CTAGCAAGAA AATCGTTCTT AACTTCTGAG ATTGGATTGG GCTCAGTAAC 600
CTCAGTTGGC AAGAGCAAGA CTAAGATGTC CAAGGATGTG GGTCTGAACT ATGTATGGGC 660
TAGTTTGCCT TAAATAGAGA AAATGTGTTT CCTAGTTGTG GCTTATACCC CTCCCATTGG 720
TCAGTTGATT CATATTTGGG TACAGTTAAT CACAAGGGAG ATTGGGCAAA CATGTATAAA 780
TGACTCAGAG GAACCCGTTC CTAGCCCCTA TGCCTGGGAA AGCATCTCCC AACAAATAAA 840
AAGACCCACA TTTTACAAAT GGCAAAATGC AGTGTCATTT TTTTATCCTC CTGAGGTTGA 900
CTAGTTTGGG AAACTTTTTA GTTTCTCCCA GGTCACCAGG AAAGTAGTGT CTACAGAATC 960
ATCTTCATGG TTCTTATAGT GGGCAAGACT 990
|
