Variant report

Variant	rs7262310
Chromosome Location	chr20:41772739-41772740
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs56164211	1.00[EUR][1000 genomes]
rs6065584	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs6103166	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6103173	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6103177	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7270191	1.00[YRI][hapmap]
rs73106044	1.00[EUR][1000 genomes]
rs73106069	1.00[EUR][1000 genomes]
rs947198	0.87[ASW][hapmap];0.87[YRI][hapmap];0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063450	chr20:41409901-41880620	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1060690	chr20:41413369-41851935	Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1066088	chr20:41417205-42060036	Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	esv2751914	chr20:41744586-41890453	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41767200-41775000	Weak transcription	Brain Cingulate Gyrus	brain
2	chr20:41769200-41774400	Weak transcription	Brain Substantia Nigra	brain
3	chr20:41769400-41774000	Weak transcription	Brain Hippocampus Middle	brain
4	chr20:41770000-41774800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr20:41770200-41774800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr20:41771400-41772800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr20:41772400-41772800	Enhancers	Breast Myoepithelial Primary Cells	Breast

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links