Variant report

Variant	rs2371002
Chromosome Location	chr2:211471071-211471072
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10165443	0.85[CEU][hapmap];0.92[MEX][hapmap];0.89[TSI][hapmap];0.81[EUR][1000 genomes]
rs10184633	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10191702	0.81[EUR][1000 genomes]
rs1047883	0.96[CEU][hapmap]
rs11685955	0.81[EUR][1000 genomes]
rs12694201	0.85[EUR][1000 genomes]
rs12694202	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12694203	0.96[CEU][hapmap];0.89[TSI][hapmap];0.87[EUR][1000 genomes]
rs12694204	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2229589	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2287599	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2302910	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2370997	0.92[CEU][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes]
rs2370998	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs2371000	0.96[CEU][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4312427	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs4396646	0.85[CEU][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4399666	0.85[CEU][hapmap];0.83[MEX][hapmap];0.89[TSI][hapmap];0.81[EUR][1000 genomes]
rs6435577	0.80[CEU][hapmap]
rs6435578	0.90[EUR][1000 genomes]
rs6721477	0.92[CEU][hapmap];0.89[TSI][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6734696	0.96[CEU][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7573258	0.96[CEU][hapmap];0.83[MEX][hapmap];0.89[TSI][hapmap];0.87[EUR][1000 genomes]
rs7582951	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7583822	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7593211	0.81[EUR][1000 genomes]
rs7598448	0.84[CEU][hapmap];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3398091	chr2:211315261-211634200	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1013658	chr2:211447246-211809945	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv536135	chr2:211447246-211809945	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2371002	CPS1	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211442400-211484200	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr2:211442800-211477800	Strong transcription	Liver	Liver
3	chr2:211448600-211480800	Weak transcription	Aorta	Aorta
4	chr2:211448800-211475400	Weak transcription	Ovary	ovary
5	chr2:211450200-211481400	Strong transcription	Duodenum Mucosa	Duodenum
6	chr2:211458600-211485000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr2:211459000-211475600	Strong transcription	Hela-S3	cervix
8	chr2:211463800-211474800	Weak transcription	Left Ventricle	heart
9	chr2:211464400-211480600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr2:211467200-211482000	Weak transcription	HepG2	liver
11	chr2:211467400-211475200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr2:211469400-211474400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:211469800-211471400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:211469800-211474800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr2:211470000-211475600	Strong transcription	Fetal Intestine Large	intestine
16	chr2:211470200-211471400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr2:211471000-211471800	Strong transcription	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links