Variant report

Variant	rs11713171
Chromosome Location	chr3:53066280-53066281
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:53066267..53068975-chr3:53075224..53077291,2	K562	blood:
2	chr3:53065348..53067602-chr3:53078678..53080712,2	MCF-7	breast:
3	chr3:53064347..53066735-chr3:53078484..53080283,2	K562	blood:

Variant related genes	Relation type
ENSG00000163935	Chromatin interaction

Extended variants
information (count: 102 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10510761	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11706035	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11707575	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11707780	1.00[EUR][1000 genomes]
rs11710292	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11710394	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11710707	0.89[EUR][1000 genomes]
rs11711773	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11712653	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11713206	0.89[EUR][1000 genomes]
rs11713290	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11713859	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11714037	0.89[EUR][1000 genomes]
rs11714876	0.94[EUR][1000 genomes]
rs11714902	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11715231	0.84[EUR][1000 genomes]
rs11717132	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11717619	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11717715	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11718388	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11718538	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11718752	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11718834	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11720191	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13058817	0.93[EUR][1000 genomes]
rs13069006	0.89[EUR][1000 genomes]
rs13072395	0.89[EUR][1000 genomes]
rs13072457	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13072818	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13074524	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13078834	0.89[EUR][1000 genomes]
rs13078971	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13084937	0.94[EUR][1000 genomes]
rs13085514	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13085544	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13091844	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13092352	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13320044	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1346719	1.00[EUR][1000 genomes]
rs17052727	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2336540	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2336541	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2564926	0.93[EUR][1000 genomes]
rs2564941	0.80[EUR][1000 genomes]
rs2581807	0.93[EUR][1000 genomes]
rs3097417	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34121720	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34238610	0.95[EUR][1000 genomes]
rs34244302	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34313969	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34340609	1.00[EUR][1000 genomes]
rs34493168	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34754279	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34872575	0.89[EUR][1000 genomes]
rs34933390	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34943350	0.89[EUR][1000 genomes]
rs34979715	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35076015	0.95[EUR][1000 genomes]
rs35163227	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35174175	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35230793	0.84[EUR][1000 genomes]
rs35378159	0.89[EUR][1000 genomes]
rs35384050	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35385050	0.89[EUR][1000 genomes]
rs35507120	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35720014	0.89[EUR][1000 genomes]
rs35737577	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35849389	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs36090694	0.89[EUR][1000 genomes]
rs3796352	0.84[EUR][1000 genomes]
rs3806692	1.00[EUR][1000 genomes]
rs3821872	0.96[EUR][1000 genomes]
rs4478072	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58515094	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs58660500	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59583591	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60887045	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs60942590	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61172708	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6445555	0.91[EUR][1000 genomes]
rs6445556	0.98[EUR][1000 genomes]
rs6445557	0.98[EUR][1000 genomes]
rs71299622	0.84[EUR][1000 genomes]
rs71299700	0.81[EUR][1000 genomes]
rs71301804	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71301808	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs71301809	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs71301811	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs71301814	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs71617204	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs750474	0.98[EUR][1000 genomes]
rs7622420	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7625448	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7640293	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7645611	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9756317	0.93[EUR][1000 genomes]
rs9875573	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1818974	chr3:52966316-53096394	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv876800	chr3:53038786-53113762	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv1823728	chr3:53046712-53080351	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv1820544	chr3:53046712-53096394	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv822094	chr3:53059674-53096460	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11713171	TMEM110	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:53033000-53078400	Weak transcription	Aorta	Aorta
2	chr3:53048800-53077800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr3:53054000-53070600	Weak transcription	Right Ventricle	heart
4	chr3:53056600-53077800	Weak transcription	Fetal Stomach	stomach
5	chr3:53061800-53070000	Weak transcription	Psoas Muscle	Psoas
6	chr3:53061800-53070800	Weak transcription	Left Ventricle	heart
7	chr3:53061800-53074400	Weak transcription	Osteobl	bone
8	chr3:53062200-53074400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr3:53062200-53076800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:53062200-53077000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr3:53062400-53071000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:53062600-53066400	Weak transcription	HepG2	liver
13	chr3:53063200-53067000	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr3:53063400-53067000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr3:53063600-53066800	Enhancers	Primary T cells from cord blood	blood
16	chr3:53063600-53066800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr3:53063600-53067800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr3:53063800-53066800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr3:53064000-53078400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr3:53064800-53066400	Enhancers	Primary T cells fromperipheralblood	blood
21	chr3:53065200-53066600	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr3:53065200-53069000	Weak transcription	Stomach Mucosa	stomach
23	chr3:53065400-53066600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chr3:53065400-53066600	Weak transcription	A549	lung
25	chr3:53065400-53066800	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr3:53065400-53066800	Weak transcription	Liver	Liver
27	chr3:53065400-53068600	Weak transcription	Fetal Intestine Large	intestine
28	chr3:53065400-53068600	Weak transcription	Fetal Intestine Small	intestine
29	chr3:53065400-53068800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr3:53065400-53068800	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr3:53065400-53070200	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr3:53065400-53070200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr3:53065400-53070600	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr3:53065400-53073000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr3:53065400-53073000	Weak transcription	Esophagus	oesophagus
36	chr3:53065400-53074400	Weak transcription	Duodenum Mucosa	Duodenum
37	chr3:53065400-53077600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr3:53065400-53078600	Weak transcription	Gastric	stomach
39	chr3:53065600-53067000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr3:53065600-53072600	Weak transcription	NHEK	skin
41	chr3:53065600-53077000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr3:53065800-53068800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr3:53065800-53070000	Weak transcription	Dnd41	blood
44	chr3:53065800-53070400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr3:53065800-53073000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr3:53065800-53076200	Weak transcription	Primary B cells from cord blood	blood
47	chr3:53066200-53068800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr3:53066200-53069000	Weak transcription	Pancreas	Pancrea
49	chr3:53066200-53070600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr3:53066200-53070800	Weak transcription	Right Atrium	heart

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