Variant report

Variant	rs12197051
Chromosome Location	chr6:2362123-2362124
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WRNIP1-35	chr6:2356966-2362624	NONHSAT106650

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

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

rs_ID	r²[population]
rs12193414	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12193650	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12211058	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17134937	0.96[ASN][1000 genomes]
rs1887419	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2104592	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4144237	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4502983	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58112041	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59711442	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs60259303	0.94[ASN][1000 genomes]
rs6899468	0.86[AMR][1000 genomes]
rs6903122	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6915462	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6916208	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6917662	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6936023	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7755421	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7767356	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9501822	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9503136	0.81[AMR][1000 genomes]
rs9503146	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9503147	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9503150	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[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	nsv531295	chr6:1773436-2724986	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
2	nsv883388	chr6:2093432-2514911	Strong transcription Enhancers ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
3	nsv883389	chr6:2093432-2776303	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
4	nsv1021573	chr6:2246721-2832408	Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
5	nsv538102	chr6:2246721-2832408	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
6	nsv883390	chr6:2265344-2584919	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv883391	chr6:2282747-2507448	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:2339200-2370000	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr6:2344400-2377400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr6:2345400-2365800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:2347000-2362800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr6:2352000-2362400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr6:2352400-2376400	Weak transcription	HSMMtube	muscle
7	chr6:2353800-2376400	Weak transcription	Pancreas	Pancrea
8	chr6:2354200-2362200	Weak transcription	Ovary	ovary
9	chr6:2354200-2363200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:2354200-2363200	Weak transcription	Adipose Nuclei	Adipose
11	chr6:2354200-2366800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr6:2354200-2367200	Weak transcription	Stomach Smooth Muscle	stomach
13	chr6:2354200-2371600	Weak transcription	Right Ventricle	heart
14	chr6:2354200-2376400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr6:2356000-2363400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:2356200-2362800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr6:2356200-2369800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr6:2356200-2382200	Weak transcription	Aorta	Aorta
19	chr6:2356600-2382800	Weak transcription	Psoas Muscle	Psoas
20	chr6:2356800-2363400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:2357000-2363800	Weak transcription	Brain Anterior Caudate	brain
22	chr6:2357400-2363400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:2358000-2370000	Weak transcription	Esophagus	oesophagus
24	chr6:2358600-2363800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr6:2358800-2364000	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr6:2359000-2365000	Weak transcription	Gastric	stomach
27	chr6:2359200-2362800	Weak transcription	Fetal Lung	lung
28	chr6:2359800-2362400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:2360000-2362400	Strong transcription	Primary B cells from cord blood	blood
30	chr6:2360000-2362600	Weak transcription	Brain Hippocampus Middle	brain
31	chr6:2360200-2362200	Strong transcription	Fetal Stomach	stomach
32	chr6:2360400-2362800	Strong transcription	Left Ventricle	heart
33	chr6:2360400-2379600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr6:2361000-2362600	Strong transcription	Fetal Intestine Large	intestine
35	chr6:2361000-2363200	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr6:2361200-2362400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr6:2361400-2362400	Strong transcription	Fetal Intestine Small	intestine
38	chr6:2361400-2370000	Weak transcription	Duodenum Mucosa	Duodenum
39	chr6:2361800-2362400	Strong transcription	Liver	Liver

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