| Tag | Content |
|---|
EnhancerAtlas ID | HS062-08424 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr19:42076370-42077530 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:42077155-42077174 | GGGCGCCATCTAGTGGGCG | - | 6.65 | | HSF1 | MA0486.2 | chr19:42076624-42076637 | GAAAGTTCTGGAA | - | 6.29 | | Nr5a2 | MA0505.1 | chr19:42077217-42077232 | GCTGGCCTTGGACTA | - | 6.19 | | ZEB1 | MA0103.3 | chr19:42076719-42076730 | CCCACCTGCCC | + | 6.14 | | ZNF263 | MA0528.1 | chr19:42077304-42077325 | GGAGGAGCAGGTGAGGGGAAG | + | 6.52 |
|
| | 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 |
| GH19I041570 | chr19 | 42077081 | 42077230 |
|
Enhancer Sequence | AGCCTAGAGC GGGCCCCACA GCTGTCAGGA AGCCAGGACT CAGCCTCCAG GCGGCAGTCA 60
CCCTGGTGCC ACAGCGACAG CGCTGATGGC CATTCTGAAG ACTGGGGGTG TCAGGAGAGC 120
TGGGCGTCCC ACAGAACTGC ACAGAATAAT GGGGAACGAG GGTGACACAG GACTCAGGAT 180
TTCAGATGGG TAGGTAGGCT CAGCTGGGAG CTCAGGGACA GACCTGAGGA GCCTCAGTGG 240
GAAGTGCTGA AGTGGAAAGT TCTGGAATGT TTCAGGAAAA AGGCTGGAGG CTTAGAGGAA 300
AGGCTGTCGC TCCTAATATG GCTGGCAACC CTGGATGGGC TGTGTTCCTC CCACCTGCCC 360
ATCCTCTCAC TGCTGCCACC TCTAGGGACA CAACCTCTCT TCATGTCCAC CTTCCCAAAC 420
TCACCTGCAC TCCTCCATTA TCTGACTTTA TGTGAAAGCA GTGCTAAGAT CCCTCTCCTG 480
CAATGCAAGA AGGAGATGAG AGGCCCGGGT CCCCACAGAC AACTCAGCAG TGGGGTCCTG 540
CTGAAGTGGG ACCGGGCAGA ATCATGCACT CCCAACATCC TGGATCCTGA CTGGGGGTAA 600
CAGTGAAGTT CAAAGACCAT GCCATCAAAA TCTCCAGAGT GAGGCTCCTC CCTGGGGTCC 660
CTGAGGTCTG TCCAGGAGCT GCTCCCTGAG CAAATCTAGA GTGTGGAGGG CTGGGGTTGT 720
GGCAGTAAAA GCAGCCACAT TTGTCTCAGG GTGGAAAGGG AGACGGTGAG CTCCAGTAAG 780
GGCAAGGGCG CCATCTAGTG GGCGCCTCCT GCTAAGGAGC AAGGAGACCA GGAGAGCGGA 840
GATCAGGGCT GGCCTTGGAC TAAGGGGTGA GTTCAGGTGG AGGGGACTGA GGTGTAAGGA 900
GGCGGGTGAA GTGGGGAAGT GGTGGGGAGA CATGGGAGGA GCAGGTGAGG GGAAGCTTCA 960
GGGAAGCTGC GGGAGGGCAC AGCAGGGCTC TCCACTCCTC AGCATTGACA TTTGGGTGGT 1020
CAAACTGGTG GGGCTCTGTG AACTGCAGGG TGTTCAGCAC CATCCACCCA CTCAATGCCA 1080
GCAGGACTCC CTCCCCCAGC TCTGACAACC AACAATGTTT CCAGACTTTG CCAAATGTCC 1140
CCTAGAGGGC AAAATTTCCC 1160
|
