| Tag | Content |
|---|
EnhancerAtlas ID | HS187-14144 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:162094860-162095610 |
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 | GTTTCCCGCA AAACTGCCAG CCCGCCCCCC GCTCACGCAC AGACACCCAA TTTCCCATAT 60
ACAGATAAAT GCACACATGT ATACGCGAAA GGTTAACTCG GCGGAGGACT CGCCCAAATA 120
AGCACCGGGA TTGCATTTAA AATAATAATA ATAAATAAAT AAATAAACTA GGAAGGAAAG 180
CGGGGGGAGG GAAGCAGAAG TCGGGAAGAA AAGAGAAAAG CAGCAGGCTG ATTACGAGGT 240
GTCAAAACTG CCAGGAGCAA GAAGGTGATA GCAATCAGGG GTGAGAAGAG TGCGGCATTC 300
GTGCGGGGCA ACTAATTATC CGTCTCATTT GAGAAGAGCA GCATTTGAGG CAGCAGCGTT 360
CGCCTGCTGA ACGGTGACAG ATTGGCGCGG AGGAGAGGGG AGGTGTTAAA ACAATGGAGC 420
CGGGCGCGCG AGCGCTGCTG CATGCTAATC AGCCCTCCCT CCGCCTGCCT GCCGCGCTCC 480
CTCCTTCCTC CCGGCCTCCC TCCTCCGCGC TCCCTCCTCC CGCCTGCGGC GCTCCCTCCT 540
TTCCAGCGGG CCCCGCGCCG CCGCCGCCAC CCGCTTCCTG CTCCCTCGCT TTCCCGCGCG 600
TCCTTCCCGC CGCTGGCGAG TGGAACCCAG CCACCGCCAC CGAGTCCCTA GCGGGCCAGG 660
AGCCCCCGCG CGGCCCCCAG CGCCGGCCCG GTGGAGTGCA GCCCCGCGCG GGCTCGCCCG 720
AGGGCTCGGC CTGCGCCGCG CGCCCACTCC 750
|
