Variant report

Variant	rs11666112
Chromosome Location	chr19:20041801-20041802
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1008112	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs1019280	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10420011	0.86[CEU][hapmap]
rs10420124	0.87[CEU][hapmap]
rs11085283	0.85[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11668581	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11670634	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12151060	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12460570	0.82[EUR][1000 genomes]
rs12608906	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12610295	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1860939	0.81[CEU][hapmap]
rs2110587	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2110589	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs2160157	0.82[EUR][1000 genomes]
rs2335888	0.81[CEU][hapmap]
rs2335889	0.81[CEU][hapmap]
rs2335892	0.81[CEU][hapmap]
rs258575	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs258579	0.88[CEU][hapmap];0.82[EUR][1000 genomes]
rs4563152	0.81[CEU][hapmap]
rs4808223	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4809005	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4809007	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4809014	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58151139	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs60549783	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61699225	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6511066	0.87[CEU][hapmap]
rs6511073	0.87[CEU][hapmap]
rs6511074	0.81[CEU][hapmap]
rs7255064	0.82[EUR][1000 genomes]
rs7256046	0.81[CEU][hapmap]
rs73008647	0.95[EUR][1000 genomes]
rs73008648	0.95[EUR][1000 genomes]
rs73008668	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73008670	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8101213	0.81[CEU][hapmap]
rs8105482	0.87[CEU][hapmap]
rs8106847	0.86[CEU][hapmap]
rs8109457	0.84[CEU][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8111124	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8112738	0.81[CEU][hapmap]
rs9304965	0.93[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063273	chr19:19591146-20061367	ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv519535	chr19:19871250-20595412	Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
3	nsv961192	chr19:19906394-20083740	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	esv3319016	chr19:19917475-20819154	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
5	esv3319017	chr19:19917475-20819154	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
6	esv3413756	chr19:19936066-20072059	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	esv3380276	chr19:19936583-20073601	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	esv3429980	chr19:19943721-20102072	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv1061846	chr19:19946927-20595412	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
10	esv3390957	chr19:19965887-20819154	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
11	nsv869122	chr19:19969851-20595412	ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
12	nsv1057569	chr19:19973268-20193556	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
13	nsv1059158	chr19:19973489-20576161	Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
14	esv3407363	chr19:20000919-20059307	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
15	nsv1056595	chr19:20020626-20061367	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
16	nsv458376	chr19:20021046-20151257	Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
17	nsv578800	chr19:20021046-20151257	Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
18	nsv911319	chr19:20025940-20170214	ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs11666112	ZNF253	cis	Heart Left Ventricle	GTEx
rs11666112	ZNF253	Cis_1M	lymphoblastoid	RTeQTL
rs11666112	ZNF253	cis	multi-tissue	Pritchard
rs11666112	ZNF253	cis	Nerve Tibial	GTEx
rs11666112	ZNF682	cis	Muscle Skeletal	GTEx
rs11666112	ZNF506	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:20012800-20043400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr19:20013200-20043600	Weak transcription	Fetal Brain Male	brain
3	chr19:20027600-20043200	Weak transcription	HSMMtube	muscle
4	chr19:20032000-20046800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
5	chr19:20032600-20042800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr19:20032600-20046400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr19:20032600-20046800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr19:20032600-20047000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr19:20032600-20047000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
10	chr19:20032800-20046600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
11	chr19:20033400-20044200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr19:20033400-20046400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr19:20033400-20046600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
14	chr19:20033400-20047000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr19:20033400-20047800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr19:20033600-20045600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr19:20033800-20044600	Weak transcription	Brain Anterior Caudate	brain
18	chr19:20034000-20044400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
19	chr19:20034000-20046000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
20	chr19:20034000-20046400	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr19:20034000-20046600	ZNF genes & repeats	Brain Germinal Matrix	brain
22	chr19:20034000-20047000	ZNF genes & repeats	Dnd41	blood
23	chr19:20034200-20046000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr19:20034200-20046400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
25	chr19:20034800-20045600	Weak transcription	Pancreas	Pancrea
26	chr19:20035000-20044000	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr19:20035000-20044400	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr19:20036000-20044600	Weak transcription	Rectal Smooth Muscle	rectum
29	chr19:20036200-20044400	Weak transcription	Left Ventricle	heart
30	chr19:20036200-20044400	Weak transcription	Ovary	ovary
31	chr19:20037000-20046400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
32	chr19:20037200-20042200	Weak transcription	Psoas Muscle	Psoas
33	chr19:20037800-20042800	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr19:20038000-20043400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr19:20038200-20044400	Weak transcription	Stomach Mucosa	stomach
36	chr19:20038400-20042000	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr19:20038600-20044000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr19:20038800-20042200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr19:20038800-20042800	Weak transcription	Placenta	Placenta
40	chr19:20039600-20043000	Weak transcription	Osteobl	bone
41	chr19:20039800-20043200	Weak transcription	NHDF-Ad	bronchial
42	chr19:20040000-20042200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr19:20040000-20043000	Weak transcription	Fetal Heart	heart
44	chr19:20040200-20042800	Weak transcription	HSMM	muscle
45	chr19:20040200-20043000	Weak transcription	Fetal Kidney	kidney
46	chr19:20040200-20043200	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr19:20040200-20043200	Weak transcription	HUVEC	blood vessel
48	chr19:20040400-20042200	Weak transcription	Fetal Lung	lung
49	chr19:20040400-20042200	Weak transcription	NH-A	brain
50	chr19:20040400-20043200	ZNF genes & repeats	Fetal Stomach	stomach

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