Variant report

Variant	rs11181681
Chromosome Location	chr12:43153047-43153048
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11181672	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs11181673	0.99[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs11181674	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs11181675	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs11181676	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs11181677	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs11181678	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11181679	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11181680	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11181682	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12302566	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12313884	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs1356421	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1356422	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs1356423	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs1914486	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs1914487	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs2203734	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs2897590	0.84[CEU][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs57284063	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs60367750	0.99[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs61924560	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs61926694	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs7962745	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7963132	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7963276	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs868765	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs870972	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs955918	0.98[AFR][1000 genomes];0.88[AMR][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	nsv1044790	chr12:42672255-43344184	Enhancers Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
2	nsv541483	chr12:42672255-43344184	Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
3	nsv832389	chr12:43003361-43173896	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	esv16183	chr12:43152222-43153279	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv11145	chr12:43152653-43153149	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:43149600-43153800	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr12:43149600-43154800	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr12:43149600-43156400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:43149800-43153200	Enhancers	H1 Cell Line	embryonic stem cell
5	chr12:43149800-43153600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:43149800-43154000	Enhancers	H9 Cell Line	embryonic stem cell
7	chr12:43149800-43155200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:43149800-43156600	Enhancers	HMEC	breast
9	chr12:43150000-43153800	Enhancers	NHEK	skin
10	chr12:43150200-43154000	Enhancers	Placenta Amnion	Placenta Amnion
11	chr12:43150200-43154400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr12:43150200-43154400	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr12:43150200-43155200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr12:43150400-43154800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr12:43150800-43154800	Enhancers	Fetal Lung	lung
16	chr12:43151000-43153400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr12:43151000-43153400	Enhancers	Brain Germinal Matrix	brain
18	chr12:43151200-43155400	Weak transcription	GM12878-XiMat	blood
19	chr12:43151600-43153600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr12:43151600-43153600	Weak transcription	Hela-S3	cervix
21	chr12:43151800-43153200	Weak transcription	A549	lung
22	chr12:43151800-43153400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr12:43151800-43153400	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr12:43151800-43153400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr12:43151800-43153600	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr12:43151800-43153800	Enhancers	NH-A	brain
27	chr12:43152000-43153400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr12:43152000-43154600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr12:43152200-43153200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:43152200-43153200	Weak transcription	Fetal Muscle Leg	muscle
31	chr12:43152200-43153200	Weak transcription	Osteobl	bone
32	chr12:43152200-43154200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr12:43152200-43154600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr12:43152200-43155600	Weak transcription	HSMM	muscle
35	chr12:43152600-43153400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr12:43152600-43153600	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr12:43152600-43154400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr12:43152600-43154800	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr12:43152800-43153200	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr12:43152800-43153400	Enhancers	Spleen	Spleen
41	chr12:43152800-43153800	Enhancers	Left Ventricle	heart
42	chr12:43152800-43154000	Enhancers	Psoas Muscle	Psoas
43	chr12:43152800-43155000	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr12:43152800-43155400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr12:43153000-43153200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr12:43153000-43153400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr12:43153000-43156800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links