| Tag | Content |
|---|
EnhancerAtlas ID | HS026-32599 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr8:38507590-38508680 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr8:38508421-38508435 | GGGGCCTTCGGGGG | + | 6.82 |
|
| | 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 |
| GH08I038650 | chr8 | 38507537 | 38509759 |
|
Enhancer Sequence | GGCTTATACT TAATTAGGGA AACACACAGA AGGAAAGATC AGTGGAAGCT TGAGAGGTCA 60
GGAAGGGCTT CATAGATGAA AATAAACTTG AGGTAGACCT CAGAACGGGG AACAGATTTG 120
GATTGACCTG AAGAGAACAG GGGATTCCAC GCAGGAGGAA AAGCTGGGGT CAGAATAAGC 180
CTGACTTCTG TTAGTTAGCC TTGCTGAGCA GTCGTATTTG CTTTGGGAAA GGAACAGGAG 240
ATAAGTTGAG TAGGTAGGGT AGGGCTAGAG CATTGAATGC CAGGAGAAGG TAGAGGGTAT 300
GAATGGAAAT GGGATGAGAG CCTAAGCAAG GTTTAATTTA AAACTTCCAG CAAACTGAGA 360
TCAAAAGAAC GTGGCCTTCT AGCCAGTCTT TCCATGGAGA CAACTGAGGA GCCTGGAGTG 420
GGCAAAGGAC CCTCGGGCTT GCGGTGGCCA CGGGCACCCC AGAGGGACGG AGGGCGCCAT 480
ACCGCGGTTG CCATGTTCCT GCATGTGTTT GAAATCTGGG CTGACAAGAA GAGCTGGACA 540
ATTTTGCTCC GTTACGTATT GAATTCTCTT CTCTGTGGTA CAGGATCCCC TTGAAGCGTG 600
ACAGCTGCAA TGACTTCCAG ATGTCCGCCT CCTGTCTCCT AGCCGACTGG GGTGGATGTG 660
GTAAACTCCG CGATGGAAAC CAAAACCCCC ACCAGATGTG CCATGTCAAC GTCAGCCTCG 720
CGCACATCTG GCTTCAATGC CGGCCGCCAG CCCCAGAACA AATGGCGGCT TTCCCGCTGT 780
ATTCAGCTAG TCAGCGTTCC CCGGTTAAAA GGCGCTGGGG CAGGAACGGC CGGGGCCTTC 840
GGGGGCGCGA CGCGGCGACG CCCAGCCTGG GAAGGGGCGC GGGGCCCGTG TTGGCCGCGG 900
TGGGTCCCGG CTCCCTGGAG GCTGAGCCCC GGGCGCTCTT TCCTCGCGGC GCTGCCGTGG 960
GGTGGCCGGG AGGGCAGAAC GAGGGGCTGC GGGACGGTGT TCGGAAGAAA ATCGTGCGAG 1020
TTTAAAAACA TCCAAAGTGA GCCGAGCTGG GCCCCAAGCC TCGGCCTCGC GCACTCGCCA 1080
GGCCCAGGAG 1090
|
