Variant report

Variant	rs11181678
Chromosome Location	chr12:43152271-43152272
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:43144917..43147362-chr12:43148881..43152996,3	MCF-7	breast:
2	chr12:42983007..42984827-chr12:43150919..43152450,2	MCF-7	breast:
3	chr12:43149824..43152359-chr12:43167562..43169768,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000139174	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 1 )

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]
rs11181679	0.91[CEU][hapmap];0.86[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[ASW][hapmap];1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][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]
rs11181681	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	1.00[ASW][hapmap];0.85[CEU][hapmap];0.93[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];0.95[TSI][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	nsv558748	chr12:43151728-43152847	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv16183	chr12:43152222-43153279	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11181678	NELL2	cis	cerebellum	SCAN

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:43140800-43152800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:43149600-43153800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr12:43149600-43154800	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr12:43149600-43156400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:43149800-43153200	Enhancers	H1 Cell Line	embryonic stem cell
6	chr12:43149800-43153600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:43149800-43154000	Enhancers	H9 Cell Line	embryonic stem cell
8	chr12:43149800-43155200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:43149800-43156600	Enhancers	HMEC	breast
10	chr12:43150000-43153800	Enhancers	NHEK	skin
11	chr12:43150200-43154000	Enhancers	Placenta Amnion	Placenta Amnion
12	chr12:43150200-43154400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr12:43150200-43154400	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr12:43150200-43155200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr12:43150400-43154800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr12:43150600-43152800	Enhancers	HSMMtube	muscle
17	chr12:43150800-43152400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr12:43150800-43154800	Enhancers	Fetal Lung	lung
19	chr12:43151000-43153400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr12:43151000-43153400	Enhancers	Brain Germinal Matrix	brain
21	chr12:43151200-43155400	Weak transcription	GM12878-XiMat	blood
22	chr12:43151400-43153000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr12:43151600-43152600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr12:43151600-43152600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr12:43151600-43152800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr12:43151600-43153000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr12:43151600-43153600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr12:43151600-43153600	Weak transcription	Hela-S3	cervix
29	chr12:43151800-43152800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr12:43151800-43153200	Weak transcription	A549	lung
31	chr12:43151800-43153400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr12:43151800-43153400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr12:43151800-43153400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr12:43151800-43153600	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr12:43151800-43153800	Enhancers	NH-A	brain
36	chr12:43152000-43153400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr12:43152000-43154600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:43152200-43152600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr12:43152200-43153200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:43152200-43153200	Weak transcription	Fetal Muscle Leg	muscle
41	chr12:43152200-43153200	Weak transcription	Osteobl	bone
42	chr12:43152200-43154200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr12:43152200-43154600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr12:43152200-43155600	Weak transcription	HSMM	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links