| Tag | Content |
|---|
EnhancerAtlas ID | HS051-16190 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr2:162094580-162095550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox6 | MA0515.1 | chr2:162095267-162095277 | AAAACAATGG | - | 6.02 | | ZNF263 | MA0528.1 | chr2:162095359-162095380 | CTCCTCCGCGCTCCCTCCTCC | - | 6 | | ZNF263 | MA0528.1 | chr2:162095345-162095366 | TCCTCCCGGCCTCCCTCCTCC | - | 7.26 |
|
| | 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 |
| GH02I161237 | chr2 | 162093712 | 162096390 |
|
Enhancer Sequence | CCGGCCGGGC GCGCCCAGCC TGTGGCGCCT CCTCTCCCGG GCTGCTGCCT CGACAGCTGC 60
TTGTAGCTAC AGTAATTAGA CTGTCAGTGC TTGTTAGAGG AGAGAGGGGA AAACACGCTT 120
CTGACAGCAG ATTCCAAGAC TCCCCAGTTT GTTAATTTCT AAGAGATCTT TAAAGCATTA 180
ATTGAGGTCT CCCCAACTCT CCCCTCCCGT CCCTCTCTGC AACTCCTCCC TTCCCAAAAA 240
TATCTTTAGG AGAAGCGAGT TCTCTCGGCG TGGAAGCAGT GTTTCCCGCA AAACTGCCAG 300
CCCGCCCCCC GCTCACGCAC AGACACCCAA TTTCCCATAT ACAGATAAAT GCACACATGT 360
ATACGCGAAA GGTTAACTCG GCGGAGGACT CGCCCAAATA AGCACCGGGA TTGCATTTAA 420
AATAATAATA ATAAATAAAT AAATAAACTA GGAAGGAAAG CGGGGGGAGG GAAGCAGAAG 480
TCGGGAAGAA AAGAGAAAAG CAGCAGGCTG ATTACGAGGT GTCAAAACTG CCAGGAGCAA 540
GAAGGTGATA GCAATCAGGG GTGAGAAGAG TGCGGCATTC GTGCGGGGCA ACTAATTATC 600
CGTCTCATTT GAGAAGAGCA GCATTTGAGG CAGCAGCGTT CGCCTGCTGA ACGGTGACAG 660
ATTGGCGCGG AGGAGAGGGG AGGTGTTAAA ACAATGGAGC CGGGCGCGCG AGCGCTGCTG 720
CATGCTAATC AGCCCTCCCT CCGCCTGCCT GCCGCGCTCC CTCCTTCCTC CCGGCCTCCC 780
TCCTCCGCGC TCCCTCCTCC CGCCTGCGGC GCTCCCTCCT TTCCAGCGGG CCCCGCGCCG 840
CCGCCGCCAC CCGCTTCCTG CTCCCTCGCT TTCCCGCGCG TCCTTCCCGC CGCTGGCGAG 900
TGGAACCCAG CCACCGCCAC CGAGTCCCTA GCGGGCCAGG AGCCCCCGCG CGGCCCCCAG 960
CGCCGGCCCG 970
|
