Variant report

Variant	rs11923612
Chromosome Location	chr3:142290490-142290491
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1129391	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11708470	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11715514	0.81[EUR][1000 genomes]
rs11718899	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11916455	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12629001	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12629713	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12634255	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12638158	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12639363	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13063075	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13065800	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13066441	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13068397	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13070239	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];0.90[MKK][hapmap];0.98[TSI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13071750	0.85[CEU][hapmap]
rs13072346	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13072355	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13082648	0.91[CHB][hapmap];0.95[CHD][hapmap];0.85[GIH][hapmap]
rs13085247	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13085261	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13089219	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13092234	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13092593	0.80[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs13093304	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13099184	0.93[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.98[TSI][hapmap]
rs2227929	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2227931	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2306699	0.91[CHB][hapmap]
rs34392719	0.85[CEU][hapmap];0.92[GIH][hapmap];0.89[TSI][hapmap]
rs3923464	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4256152	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4558780	0.82[EUR][1000 genomes]
rs4582075	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4683427	0.81[TSI][hapmap]
rs57299906	0.84[ASN][1000 genomes]
rs6440085	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6776402	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6786320	0.89[CHB][hapmap]
rs6809448	0.87[GIH][hapmap];0.83[MKK][hapmap]
rs7432464	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7623785	0.91[CHB][hapmap];0.95[CHD][hapmap];0.85[GIH][hapmap]
rs7636909	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7641914	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7643377	0.91[CHB][hapmap];0.95[CHD][hapmap];0.83[GIH][hapmap]
rs953135	0.91[CHB][hapmap];0.95[CHD][hapmap];0.85[GIH][hapmap]
rs9814159	0.91[CHB][hapmap];0.95[CHD][hapmap];0.85[GIH][hapmap]
rs9829125	0.91[CHB][hapmap];0.95[CHD][hapmap];0.85[GIH][hapmap]
rs9859834	0.91[CHB][hapmap];0.95[CHD][hapmap];0.85[GIH][hapmap]
rs9867210	0.91[CHB][hapmap];0.95[CHD][hapmap];0.83[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877556	chr3:141898980-142331360	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv877558	chr3:142123841-142331360	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv877559	chr3:142132749-142331360	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv877560	chr3:142132749-142362179	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv877561	chr3:142152925-142331360	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
6	nsv932989	chr3:142204208-142423305	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats 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	33 gene(s)	inside rSNPs	diseases
7	nsv591919	chr3:142219542-142308070	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11923612	TRPC1	cis	parietal	SCAN
rs11923612	XRN1	cis	cerebellum	SCAN

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142231600-142295800	Weak transcription	Small Intestine	intestine
2	chr3:142244400-142295600	Weak transcription	Fetal Heart	heart
3	chr3:142253800-142296400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr3:142269200-142292600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr3:142272600-142296200	Weak transcription	Brain Angular Gyrus	brain
6	chr3:142272600-142296200	Weak transcription	Psoas Muscle	Psoas
7	chr3:142272800-142293400	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr3:142274800-142296200	Weak transcription	NHLF	lung
9	chr3:142274800-142296400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr3:142275000-142293600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr3:142275600-142296400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr3:142276000-142291200	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr3:142276800-142296600	Weak transcription	Ovary	ovary
14	chr3:142277400-142296600	Weak transcription	Esophagus	oesophagus
15	chr3:142278400-142295800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:142278400-142296200	Weak transcription	Colon Smooth Muscle	Colon
17	chr3:142279200-142296400	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr3:142279800-142295600	Weak transcription	Thymus	Thymus
19	chr3:142280200-142296200	Weak transcription	Fetal Lung	lung
20	chr3:142282000-142293600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr3:142282200-142296200	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr3:142282400-142292000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr3:142282600-142296200	Weak transcription	Rectal Smooth Muscle	rectum
24	chr3:142282800-142296400	Weak transcription	Fetal Kidney	kidney
25	chr3:142283800-142291400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr3:142283800-142296400	Weak transcription	Colonic Mucosa	Colon
27	chr3:142284000-142294400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr3:142284000-142295800	Weak transcription	HUVEC	blood vessel
29	chr3:142284000-142296000	Weak transcription	Adipose Nuclei	Adipose
30	chr3:142284200-142293600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr3:142284200-142296400	Weak transcription	Left Ventricle	heart
32	chr3:142284600-142293600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr3:142285000-142291800	Weak transcription	Stomach Smooth Muscle	stomach
34	chr3:142285000-142292400	Weak transcription	GM12878-XiMat	blood
35	chr3:142285000-142294400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr3:142285000-142294400	Weak transcription	Osteobl	bone
37	chr3:142285200-142291800	Weak transcription	A549	lung
38	chr3:142285200-142293600	Weak transcription	Duodenum Mucosa	Duodenum
39	chr3:142285200-142294000	Weak transcription	Brain Anterior Caudate	brain
40	chr3:142285200-142294200	Weak transcription	Fetal Thymus	thymus
41	chr3:142285200-142294400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr3:142285200-142294400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr3:142285200-142294400	Weak transcription	NH-A	brain
44	chr3:142285200-142294800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr3:142285200-142295600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr3:142285200-142295600	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr3:142285200-142295600	Weak transcription	HSMM	muscle
48	chr3:142285200-142295800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr3:142285200-142296200	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr3:142285200-142296200	Weak transcription	Skeletal Muscle Female	skeletal muscle

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