Variant report

Variant	rs12629742
Chromosome Location	chr3:121614895-121614896
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10934565	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11923248	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11928871	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12488334	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12488851	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12491991	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12493408	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12493952	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12496318	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12497349	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12498028	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12630486	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12632345	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12634032	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12637351	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12637968	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12638492	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs13067270	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13083557	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13089878	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1344279	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1920290	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1920291	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1920297	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1920298	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1920299	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1920309	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1986368	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1986712	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2091664	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2141487	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2332033	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2689285	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2689290	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2877560	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34158925	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34181646	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34478505	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34543553	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34566912	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34696871	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34837785	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35101693	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35415993	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35737776	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35902163	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3942629	0.84[EUR][1000 genomes]
rs4118376	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4285028	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4305455	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4676758	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6790281	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs71329246	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs71329247	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73855465	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73855476	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73855480	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73855481	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7615571	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7623901	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7637495	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7640872	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7651226	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9823335	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432480	chr3:121355723-121629928	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS 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	39 gene(s)	inside rSNPs	diseases
2	nsv432482	chr3:121364236-121629634	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv432481	chr3:121364236-121637178	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv516233	chr3:121419301-121670405	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv877383	chr3:121465220-121650736	Strong transcription Enhancers Weak transcription ZNF genes & repeats 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 miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv432483	chr3:121488995-121629634	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats 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	8 gene(s)	inside rSNPs	diseases
7	esv33139	chr3:121500400-122091831	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv877384	chr3:121601577-121659774	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs12629742	IQCB1	Cis_1M	lymphoblastoid	RTeQTL
rs12629742	IQCB1	cis	Esophagus Muscularis	GTEx
rs12629742	SLC15A2	Cis_1M	lymphoblastoid	RTeQTL
rs12629742	EAF2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121555800-121615600	Weak transcription	Primary T cells from cord blood	blood
2	chr3:121592800-121646800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr3:121593000-121615400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr3:121593000-121632400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr3:121610600-121621800	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr3:121612400-121616000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr3:121612800-121615000	Active TSS	Fetal Muscle Trunk	muscle
8	chr3:121613000-121615000	Enhancers	H9 Cell Line	embryonic stem cell
9	chr3:121613000-121615200	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr3:121613000-121615600	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr3:121613000-121616600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr3:121613000-121616800	Strong transcription	GM12878-XiMat	blood
13	chr3:121613000-121620600	Strong transcription	Primary B cells from cord blood	blood
14	chr3:121613000-121621800	Strong transcription	Primary B cells from peripheral blood	blood
15	chr3:121613000-121622000	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr3:121613200-121619400	Strong transcription	Primary hematopoietic stem cells	blood
17	chr3:121613400-121615400	Weak transcription	Pancreas	Pancrea
18	chr3:121613400-121622000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr3:121613400-121626400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr3:121613600-121615200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr3:121613600-121617400	Weak transcription	Aorta	Aorta
22	chr3:121613800-121615000	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr3:121613800-121615000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr3:121613800-121615200	Active TSS	Fetal Muscle Leg	muscle
25	chr3:121613800-121615600	Enhancers	H1 Cell Line	embryonic stem cell
26	chr3:121613800-121647200	Weak transcription	Left Ventricle	heart
27	chr3:121614000-121617200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr3:121614000-121632800	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr3:121614000-121633200	Weak transcription	Fetal Kidney	kidney
30	chr3:121614000-121637800	Weak transcription	Spleen	Spleen
31	chr3:121614200-121615000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr3:121614200-121615000	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr3:121614200-121615200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr3:121614200-121615400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr3:121614200-121615400	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr3:121614200-121615600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr3:121614200-121617400	Weak transcription	Brain Substantia Nigra	brain
38	chr3:121614200-121631600	Weak transcription	Brain Anterior Caudate	brain
39	chr3:121614200-121634400	Weak transcription	Brain Cingulate Gyrus	brain
40	chr3:121614400-121615400	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr3:121614600-121615000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr3:121614600-121615400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr3:121614800-121615000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:121614800-121615000	Enhancers	Brain Hippocampus Middle	brain
45	chr3:121614800-121615000	Enhancers	Right Atrium	heart
46	chr3:121614800-121615400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr3:121614800-121616400	Enhancers	Placenta	Placenta
48	chr3:121614800-121617600	Enhancers	Placenta Amnion	Placenta Amnion

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links