Variant report

Variant	rs7595938
Chromosome Location	chr2:148840271-148840272
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:148839523..148841211-chr2:148842127..148844445,2	K562	blood:

Extended variants
information (count: 90 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10180655	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs10205246	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10209751	0.93[ASN][1000 genomes]
rs10439198	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10439199	0.94[ASN][1000 genomes]
rs10928374	0.86[ASN][1000 genomes]
rs10928375	0.96[ASN][1000 genomes]
rs10928377	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10928378	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11676430	0.85[ASN][1000 genomes]
rs11685710	0.94[ASN][1000 genomes]
rs12105745	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs1234396	0.93[ASN][1000 genomes]
rs1234397	0.93[ASN][1000 genomes]
rs1234402	1.00[ASN][1000 genomes]
rs1234405	1.00[ASN][1000 genomes]
rs1234410	1.00[ASN][1000 genomes]
rs1234413	0.99[ASN][1000 genomes]
rs1234416	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1234418	0.94[ASN][1000 genomes]
rs1234429	0.99[ASN][1000 genomes]
rs1234430	1.00[ASN][1000 genomes]
rs1234433	1.00[ASN][1000 genomes]
rs1238800	0.99[ASN][1000 genomes]
rs12472291	0.86[ASN][1000 genomes]
rs12479178	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12615059	0.97[ASN][1000 genomes]
rs12622150	0.89[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap]
rs13016893	0.84[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1312025	1.00[ASN][1000 genomes]
rs13398026	0.93[ASN][1000 genomes]
rs13411680	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13430086	1.00[CEU][hapmap]
rs1375859	0.93[ASN][1000 genomes]
rs1449958	0.96[ASN][1000 genomes]
rs1597406	0.96[ASN][1000 genomes]
rs1872198	0.93[ASN][1000 genomes]
rs1901013	0.89[ASN][1000 genomes]
rs2100469	0.93[ASN][1000 genomes]
rs2113792	0.86[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap]
rs2382202	0.93[ASN][1000 genomes]
rs2603597	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2603599	0.91[ASN][1000 genomes]
rs2603600	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs28475125	0.90[ASN][1000 genomes]
rs28870981	0.93[ASN][1000 genomes]
rs2890922	0.94[ASN][1000 genomes]
rs3768684	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs3768686	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs3768688	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs3820716	1.00[JPT][hapmap]
rs6430287	0.97[ASN][1000 genomes]
rs6430288	0.97[ASN][1000 genomes]
rs6430291	0.93[ASN][1000 genomes]
rs6430298	0.89[ASN][1000 genomes]
rs6727415	0.94[ASN][1000 genomes]
rs6731371	0.82[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs6753116	0.84[ASN][1000 genomes]
rs73005159	0.82[ASN][1000 genomes]
rs7422771	0.90[ASN][1000 genomes]
rs7423983	0.82[ASN][1000 genomes]
rs7558404	0.93[ASN][1000 genomes]
rs7568722	0.91[ASN][1000 genomes]
rs7569629	0.96[ASN][1000 genomes]
rs7577025	0.93[ASN][1000 genomes]
rs7580420	0.96[ASN][1000 genomes]
rs7580610	0.96[ASN][1000 genomes]
rs7587464	0.86[ASN][1000 genomes]
rs979636	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916286	chr2:148438001-148977722	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv529388	chr2:148471340-148934846	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	esv3392562	chr2:148476961-148843061	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv1009602	chr2:148668195-148844240	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv535967	chr2:148668195-148844240	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv1002358	chr2:148703807-148942372	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv1007683	chr2:148717347-148942372	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv535971	chr2:148717347-148942372	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv869326	chr2:148727068-148859804	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv817366	chr2:148727068-148879681	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv1000852	chr2:148730825-148934986	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	nsv535972	chr2:148730825-148934986	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
13	nsv916766	chr2:148743880-148955720	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
14	nsv1005805	chr2:148755022-148842566	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	nsv535976	chr2:148755022-148842566	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	nsv1001339	chr2:148755022-149020866	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
17	nsv535977	chr2:148755022-149020866	Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
18	nsv1014570	chr2:148780080-148869729	Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
19	nsv535978	chr2:148780080-148869729	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
20	nsv869146	chr2:148787051-149060763	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
21	nsv535979	chr2:148822091-148859805	Weak transcription Strong transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7595938	ORC4L	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:148779600-148844600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:148795600-148843800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr2:148799400-148844000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:148800000-148844600	Weak transcription	Fetal Lung	lung
5	chr2:148805600-148846200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr2:148807000-148844600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr2:148812600-148845000	Weak transcription	HSMM	muscle
8	chr2:148821200-148857600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr2:148826000-148861000	Weak transcription	Left Ventricle	heart
10	chr2:148826200-148840600	Weak transcription	Psoas Muscle	Psoas
11	chr2:148826200-148842400	Weak transcription	Primary T cells from cord blood	blood
12	chr2:148826600-148844800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:148832600-148842400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr2:148834200-148844800	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr2:148834600-148856400	Weak transcription	HSMMtube	muscle
16	chr2:148834800-148844600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:148836400-148844800	Weak transcription	Fetal Kidney	kidney
18	chr2:148836800-148853400	Weak transcription	NHDF-Ad	bronchial
19	chr2:148837000-148849200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr2:148837400-148853000	Weak transcription	HUVEC	blood vessel
21	chr2:148837600-148866800	Weak transcription	Ovary	ovary
22	chr2:148838000-148844400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:148838000-148844800	Weak transcription	Adipose Nuclei	Adipose
24	chr2:148838200-148844400	Weak transcription	Fetal Thymus	thymus
25	chr2:148838800-148844600	Weak transcription	Liver	Liver
26	chr2:148839000-148840800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:148839000-148842400	Weak transcription	Primary B cells from cord blood	blood
28	chr2:148839200-148840400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr2:148839200-148840400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr2:148839400-148840400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr2:148839400-148842600	Weak transcription	Aorta	Aorta
32	chr2:148839400-148844800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr2:148839400-148844800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr2:148839600-148844000	Weak transcription	Primary hematopoietic stem cells	blood
35	chr2:148839600-148844600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr2:148839800-148844200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr2:148839800-148844800	Weak transcription	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