Variant report

Variant	rs61286863
Chromosome Location	chr2:173197867-173197868
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10182136	0.88[EUR][1000 genomes]
rs55639081	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55998604	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56004424	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56011402	0.92[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs57200533	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57540835	0.87[ASN][1000 genomes]
rs58198619	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59279316	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59465816	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61071477	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs66486916	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6742648	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73018804	0.92[EUR][1000 genomes]
rs73018829	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7588553	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7591203	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7602327	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];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	nsv3034	chr2:173160295-173200113	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173195200-173199000	Weak transcription	Colonic Mucosa	Colon
2	chr2:173195400-173198000	Weak transcription	Spleen	Spleen
3	chr2:173195400-173199800	Weak transcription	Lung	lung
4	chr2:173195400-173199800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr2:173195400-173204000	Weak transcription	Left Ventricle	heart
6	chr2:173195400-173204000	Weak transcription	Right Ventricle	heart
7	chr2:173195800-173199600	Weak transcription	Stomach Mucosa	stomach
8	chr2:173196000-173198000	Weak transcription	Fetal Intestine Large	intestine
9	chr2:173196000-173199600	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr2:173196200-173198000	Weak transcription	Small Intestine	intestine
11	chr2:173196400-173198400	Enhancers	Pancreas	Pancrea
12	chr2:173196800-173198000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr2:173196800-173198800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:173197200-173198600	Enhancers	Fetal Thymus	thymus
15	chr2:173197200-173198800	Enhancers	Fetal Muscle Leg	muscle
16	chr2:173197400-173198600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:173197400-173198600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr2:173197400-173198800	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr2:173197400-173198800	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr2:173197600-173198200	Enhancers	Brain Cingulate Gyrus	brain
21	chr2:173197600-173198400	Enhancers	Brain Substantia Nigra	brain
22	chr2:173197600-173204000	Weak transcription	Fetal Muscle Trunk	muscle
23	chr2:173197600-173204400	Weak transcription	Thymus	Thymus
24	chr2:173197800-173198000	Enhancers	Gastric	stomach
25	chr2:173197800-173198000	Enhancers	HSMMtube	muscle
26	chr2:173197800-173198200	Enhancers	Psoas Muscle	Psoas
27	chr2:173197800-173198400	Enhancers	Brain Anterior Caudate	brain
28	chr2:173197800-173198600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr2:173197800-173198600	Enhancers	Brain Hippocampus Middle	brain
30	chr2:173197800-173198600	Enhancers	Fetal Intestine Small	intestine
31	chr2:173197800-173198600	Enhancers	Fetal Lung	lung
32	chr2:173197800-173198600	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr2:173197800-173204000	Enhancers	Duodenum Mucosa	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links