| Tag | Content |
|---|
EnhancerAtlas ID | HS060-24249 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr3:47388520-47389600 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr3:47389564-47389575 | TTCTTTGTTTT | - | 6.62 |
|
| | 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 |
| GH03I047346 | chr3 | 47388488 | 47389524 |
|
Enhancer Sequence | GGACTGCATA TTGGTGCCTG TCCTGATCGC CCCTACTCTC GGATTTCCCC TTTTCTCCAT 60
TCACTGCCCT AAAACTCCAG AGTTTCCCAG TGGAATGTGG CTGCCTGTTG ACTGCCTGGA 120
ATCAGCATCT CCAGCTCCTT TTTTATGCTC TAGGCGAGAG GTGCTTTAAC TTTGGTGCAC 180
ATAAAAGTCA CTGGAAAATG TTTAAACCAC AGATCCGTTC CTAAGTCCCT CTCTAGAGAC 240
AGGTTCCCTA GGGCTGGGGT GCAGCTCAGC ATTCTGGCGT GAGCAAGTTT CCTTGGTGAT 300
TTGCATGCTC TTCAGTGTGA GAACTATACT CCCATCTTCA GTTTCACTTC CCCAAATACA 360
GCCGCATTCC AGATCTGCTC TTCCAAGATT ACACTGTGGT TAGTGTGGTT TTGCCTGTTG 420
GGAAACTCTT CAGTCACACT TTTCCAAAAG TCAGCTTGTG ATCAATCTTG TCCATTGGAC 480
TCCTGGATGG CAACTTAATT TTTTTAAGTT TTTGGAAGGC ATATCACTCC CACACACACC 540
CCACCAGGAC ATGTCTTACA TATAAACACT CTTATCAGTT GAATCTCACA TGGTCCTCAG 600
TAATCCCCAC GGAGCAGGTA ACATTTTAGC ATAAGGAAAC TGCCTCAGAA TGGCCAAGTA 660
ATTGACCTGA CTCCAGCTAA CCAGTGGCAT TGTGAGAAAT TGAGACCAGA TCTCCACACT 720
CACAGTCCAG TCTGCCTAAG GACAGCAGTG TCTTCCACCT GTGAAGGGAG CAGCATTCCT 780
CCCAACAGTC ATAGACCTTG GAAAAGCAGA CTGGGCAGCA AGGGGAAGAG TGAAGAAGCA 840
GGTGCCTTCA TGCTGAAAGA GATAGCCAGA CTATCTGGGA ACTCTGCCCT CTGGGAGAAA 900
GGCCTGTTGC TTGTAAAGTA GTAGCAGCCC TTTCCATGTA ATCTATGCCC CCTTGACCAG 960
AGCCAAAGAG CCCCATAGGT GAAGAGTGGA CTGCTAAGTC AAACTGGATT CATCTGCTTG 1020
ACTTTCCATT TCTTTTTTCT TTCTTTCTTT GTTTTTGTTA TTTGGACTCC TTTCCCCCTC 1080
|
