Variant report

Variant	rs17817377
Chromosome Location	chr6:55916978-55916979
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 127 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:112)

rs_ID	r²[population]
rs1028390	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10484704	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10484724	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10807507	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10807508	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10807510	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10948974	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs10948975	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs12189567	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs12189571	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs12190695	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12190930	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs12191931	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12192012	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12194051	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs12194192	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12194397	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12194916	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12194997	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12195340	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs12196213	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12196526	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs12196649	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12196670	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12196709	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12196860	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs12197951	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12201286	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12201413	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12201531	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12203179	0.81[CHD][hapmap];0.89[JPT][hapmap]
rs12203653	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12203768	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12205230	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs12205653	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12206920	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12207120	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs12207662	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12207665	1.00[CHB][hapmap];0.93[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs12207715	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12207719	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12208500	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12208615	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12208823	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12208954	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12209003	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12209420	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12209529	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12210228	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12210402	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12211223	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12212135	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12212143	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12212211	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs12212998	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12213291	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12213571	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12214594	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12214662	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12215027	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs12215913	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12216538	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1555095	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs1555096	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs16887615	1.00[CEU][hapmap];0.85[CHB][hapmap]
rs17218267	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17218309	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17218770	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17219028	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs17219063	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs17219126	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17219382	0.85[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];0.89[JPT][hapmap]
rs17221026	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[YRI][hapmap];0.82[AMR][1000 genomes]
rs17223058	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHB][hapmap];0.92[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.86[TSI][hapmap];1.00[YRI][hapmap]
rs17683841	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17683846	1.00[CHB][hapmap];0.93[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap]
rs17683955	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17751067	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17751085	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17751114	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17751143	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17817407	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17817455	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17817730	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17818151	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17818561	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17818687	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17819585	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];1.00[LWK][hapmap];0.90[MEX][hapmap];1.00[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap];0.85[AMR][1000 genomes]
rs17819753	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.81[AMR][1000 genomes]
rs17819824	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.81[AMR][1000 genomes]
rs1925178	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];0.80[MEX][hapmap];0.91[TSI][hapmap]
rs2076474	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2076475	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes]
rs2143359	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.90[MEX][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes]
rs2894833	0.98[ASN][1000 genomes]
rs35471617	0.81[AMR][1000 genomes]
rs3950155	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs41464152	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs4295483	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4295484	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4336432	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4388288	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4452633	1.00[JPT][hapmap]
rs4469280	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4482975	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4544908	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs57122743	0.85[AMR][1000 genomes]
rs59186267	0.81[AMR][1000 genomes]
rs60913237	0.85[AMR][1000 genomes]
rs7450492	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs763966	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[YRI][hapmap];0.82[AMR][1000 genomes]
rs9382577	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034037	chr6:55222409-56069600	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv830665	chr6:55755560-55920219	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv885911	chr6:55789704-56143231	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	nsv526703	chr6:55810482-56023811	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
5	nsv1023687	chr6:55868611-55940255	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
6	nsv1020208	chr6:55870429-55932120	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
7	nsv538227	chr6:55870429-55932120	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
8	esv3474014	chr6:55907505-55918211	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3474013	chr6:55907507-55918172	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3486610	chr6:55907534-55918254	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3474015	chr6:55907553-55918186	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3474016	chr6:55907647-55918110	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv3486611	chr6:55907647-55918110	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv1029182	chr6:55910866-55991956	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
15	esv3432353	chr6:55912873-55918277	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55899200-55920400	Weak transcription	Fetal Muscle Leg	muscle
2	chr6:55911800-55940800	Weak transcription	Left Ventricle	heart
3	chr6:55915200-55917000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr6:55916000-55919000	Weak transcription	Osteobl	bone
5	chr6:55916000-55920200	Weak transcription	Fetal Lung	lung
6	chr6:55916000-55927000	Weak transcription	Fetal Stomach	stomach
7	chr6:55916200-55922200	Weak transcription	Fetal Muscle Trunk	muscle
8	chr6:55916200-55923400	Weak transcription	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links