Variant report

Variant	rs10912966
Chromosome Location	chr1:175323386-175323387
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11800933	1.00[ASN][1000 genomes]
rs16848218	1.00[ASN][1000 genomes]
rs16848281	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16848304	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17304735	1.00[ASN][1000 genomes]
rs17375910	1.00[ASN][1000 genomes]
rs17376706	1.00[ASN][1000 genomes]
rs17376819	1.00[ASN][1000 genomes]
rs35604600	1.00[ASN][1000 genomes]
rs61805066	1.00[ASN][1000 genomes]
rs61805071	1.00[ASN][1000 genomes]
rs61806379	1.00[ASN][1000 genomes]
rs61806380	1.00[ASN][1000 genomes]
rs61808381	1.00[ASN][1000 genomes]
rs6425350	1.00[ASN][1000 genomes]
rs6662518	1.00[ASN][1000 genomes]
rs983058	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949473	chr1:175151666-175391741	Enhancers ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv831948	chr1:175229631-175407303	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175284200-175343000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr1:175288800-175343200	Weak transcription	Brain Angular Gyrus	brain
3	chr1:175288800-175343200	Weak transcription	Brain Substantia Nigra	brain
4	chr1:175312200-175324600	Weak transcription	Pancreas	Pancrea
5	chr1:175319400-175340000	Weak transcription	Fetal Brain Female	brain
6	chr1:175321400-175323400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr1:175321800-175336600	Weak transcription	Brain Germinal Matrix	brain
8	chr1:175322000-175323400	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr1:175322000-175323800	Enhancers	Placenta	Placenta
10	chr1:175322000-175325200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:175322600-175323600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr1:175322600-175323800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr1:175323200-175323800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:175323200-175324200	Strong transcription	Brain Inferior Temporal Lobe	brain

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