| Tag | Content |
|---|
EnhancerAtlas ID | HS062-00067 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr1:8977920-8978760 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:8978669-8978684 | GAGGTCAGGAGTTCA | + | 6.22 | | SOX10 | MA0442.2 | chr1:8978453-8978464 | TGCTTTGTTTT | - | 6.02 |
|
| | 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 |
| GH01I008918 | chr1 | 8978060 | 8978659 |
|
Enhancer Sequence | CTCAGGAATT CAAGACCAGC CTGACCAACA TGGTGAAACC CCATCTCTAC TAAAAATACA 60
AACATTAGCC AGGCACGATG GCTCATGCCT GTAATTCCAG CACTTTGAGA GGCCAAGGTG 120
GGTGGATCAA ACTCCTGAGG TCAGGAGTTT GAGACCAGCC TGACCAACAT GGTGAAACCC 180
TGTCTCTACT AAAAATACAA AAATTAGCCG GGCATGGTGG TGTGCACCTG TAATCCCAGC 240
TACTCGGGAG GCTGAGGCTG GAAGATGGCT TGAACCTGGG AGGCAGAGGT TGCAGTCAGC 300
CAAGATTGTG CCACTGCACT CCAGCCTGGG TGACAGAGCG AGACTCTGCC TCAAATACAA 360
AAACAAAAAC ATAACAAAAA TTCTGCACAG TATTTTTCTG ACCACTGGGT GTCATGAGCG 420
TACAATAAAT GCTTCAGCTG GAAAAACTGC ATATTTACAG GACTGCCTTC AATATGGTGG 480
TGGTTCTCCT GACTGCAGGG GATGCGGCAG CAAGTAATAA ACCCTTCAAA AGTTGCTTTG 540
TTTTTGCAAG CAAGACATTG AGAAGCAGAG AAAATGTAGA CAGTTGAAGA TAAACAAAAA 600
CACAGCACTG GCTGCTTCTT TGCGTTTTCC AGAATATTTC AGTGGAGCAG CTGTTACGGG 660
AGGAATATAA AAATCTAAAG TAAGGCTGGG AGCAGTGGCT CACTACTGTA ATCTCAACAC 720
TTTGGTAGGC TGAGGCAGGA GGATTGCTTG AGGTCAGGAG TTCAAGACTA GCCTGGGCAA 780
TATAGCAAGA CTCTGTCTCT ACCAAAGCCA GAAAAAAAAA ATCTAAAATA AAGTATTCTT 840
|
