| Tag | Content |
|---|
EnhancerAtlas ID | HS042-22060 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr19:2223940-2225380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr19:2223960-2223981 | CACTCACTCCCCTTCTCCTCC | - | 6.11 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 2224920 | 2225207 | | chr19 | 2224282 | 2224455 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I002223 | chr19 | 2223631 | 2224437 |
|
Enhancer Sequence | ATCTCATCAT CCCCTTGAAA CACTCACTCC CCTTCTCCTC CCAAGAGCCC CTGGCACCCC 60
CCGCCCCCAT CCTACTTTCT GTCTCTGAAT CTGAGGGCTC TAGGGACCTC CTAGGAGCGG 120
AGTCACACAG GATGTGGCCT TTTGTGTCTG GCATCTCTCA CTGAGCGTGA CGTCCTCAAG 180
GTGCATCCTC GGTCCCTGTC GTGGCTGGGT GGTGCTCCAC CATCCATCCG CCCTCCGTGC 240
TAGGCTTGCT TACCCTGGGC GGTTGTGAGC AGCACTGCTG TGGCCATGGG TGTGCGTGTT 300
TGTGTTTGGG AGCAAGTTTC CCGTTTCCTG GTGCCTGGGC GGAGGTGCTG GGTGGCCCGG 360
CCCCCTGGGC TCTCCAGCAG CCACACCATT CCACCCTGCC ACCATGGGTG CACGAGGGTC 420
TGAGGTCCTC AGTCCCCACA TCCTCAACAC ACTGAATTTC TTGTTTTGAT TCTAGCCATC 480
CGAGTCGTCG TGAAGTGATA TAACATGGTA GGGTTTTTTG CTTTTTTTTT TTTTTTTTTC 540
CTGAGACACA GAGTTTTGGT CTGTGGCCCA GGCTGGAGTG CGGTGGCGCG ATCTCGGCTC 600
ACTGACCCTC CGCCTCCTGG GTTCAAGTGA TTCTCCTGCC TCAGCCTCCT GAGTAGTTGT 660
GTCTACAGGC ACACGCTACC ACCGTGCCTC GTTCGTTTTT TTGTTTTATA GAGATCGGGT 720
TTTGCCATGT TGCCCAGGCT GGTCTCAAAC TCCTGGCCTC AAGCCTTCTG CCTCCCAGTG 780
CCTCCCAGCG TGCGCCATCA CAGCCGGCCC TAAGTGTGCT TTTGGTGGTG TTCTGTGTTA 840
GTTCGTTCTG CTCCTTGCCC ACGTGTGCGT GCACGTGTTA CACGAGAAAC ATTGTAGCAC 900
CTGGATGCTC TGTTTTGCAT TGGGATTGCT CAGCTTAGTG GTTTCCAGGA TCTTTAGGAA 960
TTTGTGTGTC CCTGGTGTGT TCTTGGGACA TTGGATCAAA GCGACCCCAT GCAGTGTGTG 1020
GTTGGGCATG TCTTCACGTG CTGGCCTGCA ATGCTGTGGC ATTGTTTGCC ACCTGAGGCA 1080
CCGAGGTCTG AGAGGGGCCG GGAGAGGGAG GTAGGAAGAG AGCTCTGTCT GGGATTCTCA 1140
CACTTCTGTG TGCTGGGAAA TTGCTTCTCC CATTCAGCTG CTGTGCCTGA TCTCTTGGCT 1200
GCTTGTCCCA GCAGAGGCCC TGGAGTCCCT GCCAGGACAG TACCCTTGTG GCACAACAGG 1260
GGTGGATCCC AGGGCCCAGC CACCCAGTCC AGGCCTGGCC CAGGGTGGCT GCACGGGTCC 1320
CCTGTCTGGG CCGAGTGCTT CTCGTTCACC ACCTCCGGAG CTCCCTGGGC TGTTGGCTGT 1380
CAGCATTTGT GTCATTCTTA GTATGCAGCT GGGTTTCAAG CATTAATGAC CTTTTTTTCT 1440
|
