| Tag | Content |
|---|
EnhancerAtlas ID | HS098-28181 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:46302120-46303120 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox6 | MA0515.1 | chr19:46302127-46302137 | AAAACAATGG | - | 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 |
| GH19I045798 | chr19 | 46302156 | 46303016 |
|
Enhancer Sequence | AAAAACAAAA ACAATGGAAC AATGGGTGGA CACAGATTGG GTGGGGGACA GAAGAGCGTT 60
GGGTGGGTGG GGGCAGAGGA TGGATGGACA AGTGGAGCCT CAAGTTTGTA TCATTTGCTT 120
TCAGAGGAAT GTTGGCATAT CAGGGTATAG CCTGAAGAAG GGAGTTGGCA AAAGCAAACG 180
TGCCTCTTCC CAGCTTCCAG AGAAGGAAAA AATAAATGCC AGGAATGTGT TAAAGTATCC 240
AGATTACATG CAATCCCACC ACGGCTGTGA TTCATACAGG AGCGAATACA GTCCCAGTTC 300
ACATTGAGAT TAAAAACGAA ATTCTAGGAA AAATCATCAT GCCATCTGGT GGACAAAGCT 360
GGTAGGTGCG CCCACCTCCA GCGGCAAACC CCCTGTCACG CAGCAGGGCA GAGGGCTGCC 420
AGGTGCCTGC GGGGGAAGGC TGAAGGACTG TGGGGAGTGT GTAGCTGGGT GGGAGGATGT 480
AGGAGTGACT TTGGCTTGCC ATTCTTGTTT GTTTTTTGAG ACAAGGTCTT GCTCTGTTGC 540
CCAGACTGGA GTGCAGTGGT GCAATCACAG CTCACTGCAA CCTCGATCTC CTGGGCTCAA 600
GCAATCCTTC TGCCTCAGCC CCCTAAGTAG CTGGGACTCT GTAGTCCGTG CCATCATGCC 660
GGGCTGATTT TAAAAATTTT TTTAATTTTT TTTTTTGTAC AGATAGTGTC TTACTGTGTT 720
CCTCTCGCTG GTCTCAAGCT CCTGGGCTCA AGCAATCCTC CCACCTTGGC AACCCAGAGT 780
GCTGGGATTA CAGGCATGAG CCAGTGCACC TGGCCCAAGC TTGCCATTCT TTTTGGAACA 840
ACTGGTGGTG GGAGGGAAGG TTTCTGCCCC ATAGAGAGAA AAGCCTTCCA ACTGGAAGAA 900
CAGGCCGGGT GCGGTGGCTC ATGCCTGTAA TCCTAGCACT TTGGGAGGCC AAGGCGGGCA 960
GATCACTCGA GGTCAGGAGT CTGAGACCAG CCTGGCCAAC 1000
|
