| Tag | Content |
|---|
EnhancerAtlas ID | HS051-19177 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr3:23077150-23077960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REL | MA0101.1 | chr3:23077851-23077861 | GGAAATCCCC | - | 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 |
| GH03I023035 | chr3 | 23077257 | 23079183 |
|
Enhancer Sequence | CCCTCAGCTG CAGGTCTGTT GGAGTTTGCT GGAGGTCCAC TCCAGACCCT GTTTGCCTGG 60
ATATCACCAG CAGAAGCTGC AGAACAGCCA ATATTGCAGA AGGGCAAATA TTGCTGCCTG 120
ATCCTTCCTC TGGAAGCTTC ATCCCAGAAG GGCTCCTGCC TATATGAGTT GTCTGTCGGC 180
CCCTACTGGG AGCTGTCTCC CAGTTAGGCT ACACGGGGGT CAGGGACCCA CTTGAGGAGG 240
CAGTCTGTCC ATTCTCATTC TCAGAGCTCA ACCACTGCTC TGGGAGAACA ACTGCTCTCT 300
TCAAGCTGTC AGACAGGGAC GTTTAAGTCT GCAGAAGCTG TCTGCTGCCT TTTGTTCAAA 360
TATGACCTGC CCACAGAGGT GGAGTCTATA GAGGCAGTAA GCTGTGCTGA GCTGTGGTGG 420
GCTCCACCCA GTTCAAGCTT CCTGGCCTCT TTGTTTACCT ATTCAAGCCT CAGCAATGGT 480
GGACGCCCCT CCCCCATCCA GGCTGCCACC TCGAAGTTTG ATCTCAGACT GCTGCAATAG 540
CAGTGAGCAA GGCTCCATGG GCGTGGGACC TGCCAAGCCA GGCATAAGGG AGAATCTCCT 600
TGTCTGCCAG TTGCTAAGAC CTTGGGAAAA GTGCATTATT CAGGCAGGAG TGTCCCGTTT 660
TTCCAGGTAC AGCCTGTCCT GGCTTCCCTT GGCTAGGAAA GGGAAATCCC CCAACCCCTT 720
GCACTTCCTG GGTGAGACGA CACCCCACCC TGCTTCGGCT CATGCTCCAT GGGCTGTACA 780
CACTGTCCAA ACTGGTTGGA CCCATCTTCT 810
|
