Variant report

Variant	rs12491426
Chromosome Location	chr3:194951800-194951801
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:194945629..194947428-chr3:194950514..194952678,2	K562	blood:

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs11918143	0.95[EUR][1000 genomes]
rs11919965	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11921174	1.00[ASN][1000 genomes]
rs11928199	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12485302	0.83[ASN][1000 genomes]
rs12485800	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12486636	0.95[EUR][1000 genomes]
rs12488616	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12491902	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12492289	0.81[EUR][1000 genomes]
rs12492644	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12493888	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12494306	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12495659	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12496459	0.86[AMR][1000 genomes]
rs12496628	0.85[EUR][1000 genomes]
rs12497444	0.95[EUR][1000 genomes]
rs12497906	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12498063	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1808074	0.83[ASN][1000 genomes]
rs35899174	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3773419	0.83[ASN][1000 genomes]
rs3773420	0.83[ASN][1000 genomes]
rs56281422	0.95[EUR][1000 genomes]
rs56835677	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs58113840	1.00[EUR][1000 genomes]
rs60677730	0.95[EUR][1000 genomes]
rs61022222	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66510151	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67413252	0.90[EUR][1000 genomes]
rs67484513	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6777904	1.00[EUR][1000 genomes]
rs6785108	0.85[EUR][1000 genomes]
rs6790425	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6804467	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72499624	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72499625	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72607893	0.87[ASN][1000 genomes]
rs72607894	0.85[ASN][1000 genomes]
rs72607896	0.83[ASN][1000 genomes]
rs72607897	0.83[ASN][1000 genomes]
rs72607898	0.83[ASN][1000 genomes]
rs72607899	0.83[ASN][1000 genomes]
rs72607900	0.83[ASN][1000 genomes]
rs72607901	0.83[ASN][1000 genomes]
rs72607902	0.83[ASN][1000 genomes]
rs72611103	0.81[ASN][1000 genomes]
rs755202	0.87[ASN][1000 genomes]
rs7642127	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007697	chr3:194554814-195009930	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats 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	28 gene(s)	inside rSNPs	diseases
2	nsv536873	chr3:194554814-195009930	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
3	nsv1009796	chr3:194737333-195124248	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
4	nsv461126	chr3:194817484-194961888	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
5	nsv592981	chr3:194817484-194961888	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
6	nsv1014826	chr3:194834615-195631793	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats 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	73 gene(s)	inside rSNPs	diseases
7	nsv536876	chr3:194834615-195631793	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
8	nsv533904	chr3:194868329-195438728	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
9	nsv1009120	chr3:194874494-194974672	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv1010168	chr3:194874494-195135790	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
11	nsv536877	chr3:194874494-195135790	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
12	nsv997956	chr3:194879534-195087539	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking 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	20 gene(s)	inside rSNPs	diseases
13	nsv536878	chr3:194879534-195087539	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
14	esv1832781	chr3:194902818-195528226	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
15	nsv432508	chr3:194916131-195478861	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	59 gene(s)	inside rSNPs	diseases
16	nsv432510	chr3:194935314-195478861	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	59 gene(s)	inside rSNPs	diseases
17	nsv984539	chr3:194945800-194984579	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:194931600-194958800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:194931800-194956600	Weak transcription	K562	blood
3	chr3:194940600-194959000	Weak transcription	Right Ventricle	heart
4	chr3:194942200-194952400	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr3:194944600-194959000	Weak transcription	Ovary	ovary
6	chr3:194945200-194957200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr3:194945200-194958800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr3:194945200-194959200	Weak transcription	NHLF	lung
9	chr3:194945400-194954000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr3:194945400-194958800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr3:194945400-194959200	Weak transcription	Osteobl	bone
12	chr3:194945400-194971600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr3:194945600-194957800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr3:194945600-194959000	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr3:194946000-194957600	Weak transcription	Duodenum Mucosa	Duodenum
16	chr3:194946000-194958800	Weak transcription	Aorta	Aorta
17	chr3:194946000-194958800	Weak transcription	Colon Smooth Muscle	Colon
18	chr3:194946000-194959000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr3:194946000-194971400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr3:194946200-194956600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr3:194946400-194957800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr3:194947000-194959000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr3:194947200-194956600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr3:194947600-194955800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr3:194947600-194956800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr3:194947600-194957000	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr3:194947600-194957400	Weak transcription	Dnd41	blood
28	chr3:194947600-194957600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr3:194947600-194957600	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr3:194947600-194957800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr3:194947600-194962200	Weak transcription	Hela-S3	cervix
32	chr3:194947800-194955200	Weak transcription	Adipose Nuclei	Adipose
33	chr3:194947800-194956400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:194947800-194957000	Weak transcription	Fetal Muscle Trunk	muscle
35	chr3:194947800-194957000	Weak transcription	Fetal Stomach	stomach
36	chr3:194947800-194957400	Weak transcription	Fetal Muscle Leg	muscle
37	chr3:194947800-194958800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr3:194947800-194959000	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr3:194947800-194959400	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr3:194947800-194961200	Weak transcription	Gastric	stomach
41	chr3:194948000-194956200	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr3:194948000-194957400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr3:194948000-194958800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr3:194948000-194959000	Weak transcription	Lung	lung
45	chr3:194948200-194956800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr3:194948200-194959000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr3:194948200-194959200	Weak transcription	HUVEC	blood vessel
48	chr3:194948400-194957600	Weak transcription	Primary T cells from cord blood	blood
49	chr3:194948400-194959400	Weak transcription	Fetal Brain Female	brain
50	chr3:194948600-194958800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links