Variant report

Variant	rs2351632
Chromosome Location	chr2:190084184-190084185
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:190054234..190055943-chr2:190083010..190085899,2	MCF-7	breast:
2	chr2:190081415..190084414-chr2:190089702..190092239,3	MCF-7	breast:
3	chr2:190071758..190073666-chr2:190084082..190085954,2	K562	blood:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10165257	0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs10166385	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10167242	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10172607	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10173224	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10184895	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10188246	0.85[EUR][1000 genomes]
rs10755002	0.93[ASN][1000 genomes]
rs10804029	0.87[EUR][1000 genomes]
rs10931401	1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap];0.95[ASN][1000 genomes]
rs10931403	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10931405	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10931411	0.86[ASN][1000 genomes]
rs11676905	0.89[EUR][1000 genomes]
rs11901914	0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12474942	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12621657	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12994482	0.89[EUR][1000 genomes]
rs12999125	0.95[ASN][1000 genomes]
rs13006065	0.98[ASN][1000 genomes]
rs13015183	0.92[ASN][1000 genomes]
rs13018252	1.00[CEU][hapmap];0.94[JPT][hapmap]
rs13028226	0.95[ASN][1000 genomes]
rs13031211	0.80[JPT][hapmap]
rs13031609	0.82[ASN][1000 genomes]
rs13408928	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13411992	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13413518	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1356161	0.96[ASN][1000 genomes]
rs1356166	0.94[ASN][1000 genomes]
rs1464135	1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs1474000	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1515866	0.93[ASN][1000 genomes]
rs1520858	0.95[JPT][hapmap]
rs1533618	0.99[ASN][1000 genomes]
rs1546617	0.94[ASN][1000 genomes]
rs1913892	0.96[ASN][1000 genomes]
rs1973666	0.86[ASN][1000 genomes]
rs1983318	0.94[ASN][1000 genomes]
rs2351631	0.93[ASN][1000 genomes]
rs2351633	0.95[ASN][1000 genomes]
rs2351635	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2351932	0.85[EUR][1000 genomes]
rs2683012	0.87[EUR][1000 genomes]
rs4580411	0.82[EUR][1000 genomes]
rs4667268	0.94[CHB][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes]
rs4667270	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4667271	0.99[ASN][1000 genomes]
rs4667275	0.89[ASN][1000 genomes]
rs4667280	0.82[EUR][1000 genomes]
rs6434334	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6434337	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6434340	0.82[EUR][1000 genomes]
rs6704568	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6728877	0.93[ASN][1000 genomes]
rs6732534	0.95[ASN][1000 genomes]
rs6761868	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7422875	0.89[EUR][1000 genomes]
rs7425383	0.89[EUR][1000 genomes]
rs7574281	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7599222	0.85[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7603704	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9288163	0.89[YRI][hapmap]
rs939158	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs939160	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533029	chr2:189812229-190554339	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv875613	chr2:189999011-190324685	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:190076000-190087200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr2:190076000-190096800	Weak transcription	Aorta	Aorta
3	chr2:190077000-190086000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr2:190077000-190086400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr2:190077000-190086600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr2:190077000-190086600	Weak transcription	Fetal Stomach	stomach
7	chr2:190078400-190087800	Weak transcription	Colon Smooth Muscle	Colon
8	chr2:190078600-190086000	Weak transcription	NHDF-Ad	bronchial
9	chr2:190078600-190086800	Weak transcription	NHLF	lung
10	chr2:190082600-190085800	Weak transcription	HUVEC	blood vessel
11	chr2:190082600-190086000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr2:190082600-190086800	Weak transcription	HSMMtube	muscle
13	chr2:190082800-190084800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:190082800-190086200	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr2:190082800-190087200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:190082800-190087200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr2:190082800-190087200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:190082800-190087200	Weak transcription	Fetal Muscle Leg	muscle
19	chr2:190083000-190085600	Enhancers	A549	lung
20	chr2:190083200-190086800	Weak transcription	NH-A	brain
21	chr2:190083400-190085800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr2:190083400-190086200	Weak transcription	HSMM	muscle
23	chr2:190083600-190087200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr2:190083600-190087400	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr2:190084000-190087200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr2:190084000-190087200	Weak transcription	HUES6 Cell Line	embryonic stem cell

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