Variant report

Variant	rs10186182
Chromosome Location	chr2:20070196-20070197
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:3)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:20066730..20071387-chr2:20098933..20103374,5	MCF-7	breast:
2	chr2:20066412..20068865-chr2:20069307..20071942,2	MCF-7	breast:
3	chr2:20068233..20072834-chr2:20097586..20102817,5	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RHOB-4	chr2:20070186-20070307	ENSG00000228784
2	lnc-RHOB-4	chr2:20070186-20070307	ENSG00000228784
3	lnc-RHOB-4	chr2:20070163-20070307	ENSG00000228784
4	lnc-RHOB-4	chr2:20070163-20070307	XLOC_001379
5	lnc-RHOB-4	chr2:20070163-20070307	NONHSAT069409

No data

Variant related genes	Relation type
ENSG00000183891	Chromatin interaction
ENSG00000228784	Chromatin interaction
ENSG00000271991	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10169726	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11096625	0.90[CEU][hapmap];0.89[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11096626	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11096627	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11096628	1.00[CEU][hapmap];0.90[YRI][hapmap];0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11676372	0.88[CEU][hapmap];0.95[CHB][hapmap];0.82[JPT][hapmap];0.92[ASN][1000 genomes]
rs12615948	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12617511	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1437865	0.89[YRI][hapmap];0.82[AFR][1000 genomes]
rs2276605	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34354920	0.92[ASN][1000 genomes]
rs3731670	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6729518	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6740941	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6747879	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7566500	0.83[JPT][hapmap]
rs7570541	0.88[CEU][hapmap];0.90[CHB][hapmap];0.83[JPT][hapmap];0.92[ASN][1000 genomes]
rs7577847	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7586775	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7595902	0.88[CEU][hapmap];0.95[CHB][hapmap];0.82[JPT][hapmap];0.92[ASN][1000 genomes]
rs7595915	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7608279	0.88[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.92[ASN][1000 genomes]
rs7608518	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9306887	0.81[CHB][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873711	chr2:19950864-20073860	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv873712	chr2:19955245-20131079	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
3	nsv873713	chr2:19955245-20144372	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
4	nsv455819	chr2:19987440-20095690	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv581155	chr2:19987440-20095690	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
6	nsv873714	chr2:20019616-20113088	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
7	nsv873715	chr2:20059323-20144372	ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:20063600-20070600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:20068800-20075600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr2:20068800-20086200	Weak transcription	Spleen	Spleen
4	chr2:20068800-20097200	Weak transcription	Aorta	Aorta
5	chr2:20069000-20098200	Weak transcription	Right Atrium	heart
6	chr2:20069200-20070200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr2:20069200-20072800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr2:20069200-20077600	Weak transcription	Fetal Lung	lung
9	chr2:20069400-20070400	Enhancers	Primary T cells fromperipheralblood	blood
10	chr2:20069400-20070800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr2:20069400-20070800	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr2:20069400-20071200	Weak transcription	Fetal Stomach	stomach
13	chr2:20069400-20072800	Weak transcription	Primary B cells from cord blood	blood
14	chr2:20069400-20075600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr2:20069400-20075800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:20069400-20076000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr2:20069400-20076200	Weak transcription	Primary hematopoietic stem cells	blood
18	chr2:20069400-20078600	Weak transcription	Placenta	Placenta
19	chr2:20069600-20070200	Enhancers	Fetal Thymus	thymus
20	chr2:20069600-20070400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr2:20069600-20071400	Weak transcription	Fetal Muscle Leg	muscle
22	chr2:20069600-20071600	Weak transcription	Thymus	Thymus
23	chr2:20069600-20072200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr2:20069600-20076000	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr2:20069600-20079000	Weak transcription	NHDF-Ad	bronchial
26	chr2:20069600-20079800	Weak transcription	Lung	lung
27	chr2:20069600-20087800	Weak transcription	Gastric	stomach
28	chr2:20069800-20070600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr2:20069800-20071400	Weak transcription	Primary T cells from cord blood	blood
30	chr2:20069800-20072000	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr2:20069800-20072800	Weak transcription	GM12878-XiMat	blood
32	chr2:20069800-20075000	Weak transcription	Primary B cells from peripheral blood	blood
33	chr2:20069800-20079200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr2:20069800-20097200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr2:20070000-20070200	Strong transcription	Fetal Intestine Small	intestine
36	chr2:20070000-20072800	Weak transcription	Fetal Muscle Trunk	muscle
37	chr2:20070000-20073600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr2:20070000-20074000	Weak transcription	Fetal Intestine Large	intestine
39	chr2:20070000-20075400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr2:20070000-20078000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr2:20070000-20081400	Weak transcription	Esophagus	oesophagus

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