| Tag | Content |
|---|
EnhancerAtlas ID | HS062-08565 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr19:49111660-49112800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr19:49112512-49112533 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | Nr2f6(var.2) | MA0728.1 | chr19:49112703-49112718 | TGAACTCCTGACCTC | - | 6.22 | | SOX10 | MA0442.2 | chr19:49112252-49112263 | AAAACAAAGAC | + | 6.14 | | ZNF143 | MA0088.2 | chr19:49112226-49112242 | CTCCCACAATGCACCC | + | 6.47 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 49112246 | 49112556 | | chr19 | 49112029 | 49112498 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I048608 | chr19 | 49111888 | 49112613 |
|
Enhancer Sequence | CGCCTGGCCT TTTTCCGTTT TCTTTTTCTT TTCCTTTTTT TTTTTTTTTT TTATTTTTTG 60
AGACAGAGTC TCGCTCGGTC ACCCAGGCTT TAGTGCAGTG GCGCGATCTT GGCTCACTGC 120
AACCTCCACC TCCCAGGTTC TAGCGATTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGACT 180
AGAGATGCAT TCCACCAGGC CCGGCTGATT TTTTGTATTT TTAGTAGAGA CAGGGTTTCC 240
CCATGTTAAT CAGGCTGGTC TGAAACTCCT GACCTCGGGT GATCCACCTG CCTCGGCCTC 300
CCAAAGTGCT GGGATTACAG GTGTGAGCCA CCACGCCCAG CCCAAAAGCT GTGTTTTAAC 360
AAGCGCTCCC AGGGATTCTG GTGCATGCAC AGGGTTGAAA GCCACTGTTC CTGAGCAGTG 420
TTCTCAGCTG GGCACCTGTG CTCCCCAGTG GGCATCTGCG CTGTCTGGAG AGGTTTTCGG 480
TTCTCTAATT GGCAGGGAAA GTCGGGGGTA TGGGGCGTGT GATGCTACTG ACCTCTGCTG 540
GGTGGAGGCT GAAGATGCCG AGGAGCCTCC CACAATGCAC CCAACAGCTC CTAAAACAAA 600
GACTTACCCA GCCCGAGCGT GGGTGCCACC CCTGTTGAGG GACCTGGTTC TAGAGGCTCT 660
AACCCTATCA GCCCATGACA TAGAGGGGGA AACTGAGGCA CAGAGAGGTG AAGTAAGTTG 720
CCTGAAGTCA CACAACGAGG AACTGAGAGA GCTAGAATTT GAATCCAGGC CGTCTGGTCC 780
CAGAGGCCAC ACCCCTCTCC TCCCTAGCTG TGCTGTGACC CTGTGAGGTA GGTGCTGTTA 840
TTATTTGCAG TTTCTTTCTT TCTTTTTTTT TTTTTTTTTT TTTTGCTTTT TTGAGATGGA 900
GTCTTGCTCT GTCTCCCAGG CTGGAGTGCG ACAGCGCGAT CTCGGCTCAC TGCAACCTCT 960
CTCCTGGGTT CAAGCAATTC TCCTGCCTCA ACCTCCCAAG TAGCTGGGAA GACAGGGTTT 1020
CACCATGTTG GCCAGACTGG TCTTGAACTC CTGACCTCAG CCAATCTGCC CGCCTCAGCC 1080
TCTCAAAGTG CTGGGATTAC AGGCGTGAGC CACCATGTCC GGGCATTTTC TTAGATGCTC 1140
|
