Variant report

Variant	rs10743374
Chromosome Location	chr12:20570985-20570986
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs10505865	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10732533	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10732534	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10734701	0.81[EUR][1000 genomes]
rs10743370	0.92[ASN][1000 genomes]
rs10743372	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10743373	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10770649	0.82[ASN][1000 genomes]
rs10770650	0.87[ASN][1000 genomes]
rs10770651	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10770652	0.89[ASN][1000 genomes]
rs10770653	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10770654	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10770655	0.83[EUR][1000 genomes]
rs10770656	0.86[ASN][1000 genomes]
rs10841501	0.92[ASN][1000 genomes]
rs10841509	0.83[ASN][1000 genomes]
rs10841510	0.86[ASN][1000 genomes]
rs10841512	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10841513	0.89[ASN][1000 genomes]
rs10841515	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10841516	0.89[ASN][1000 genomes]
rs11045203	0.82[ASN][1000 genomes]
rs11045206	0.86[ASN][1000 genomes]
rs11045207	0.86[ASN][1000 genomes]
rs11045211	0.84[ASN][1000 genomes]
rs11045218	0.86[ASN][1000 genomes]
rs11045220	0.86[ASN][1000 genomes]
rs11045221	0.86[ASN][1000 genomes]
rs11045222	0.84[ASN][1000 genomes]
rs11045223	0.87[ASN][1000 genomes]
rs11045224	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11045225	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11045226	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11045227	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11045228	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11045230	0.89[ASN][1000 genomes]
rs12297116	0.87[ASN][1000 genomes]
rs12370745	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12370763	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12372457	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1348583	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1444628	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1444629	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1444630	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1444634	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1444635	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1444641	0.97[ASN][1000 genomes]
rs1444643	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1444644	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1444645	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1444646	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16922851	0.81[ASN][1000 genomes]
rs1838447	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1838448	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4762955	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5014033	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5014034	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5014035	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5014036	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5014037	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5014038	0.84[EUR][1000 genomes]
rs5014039	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5014040	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60977432	0.86[ASN][1000 genomes]
rs6487083	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6487084	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6487085	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6487086	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7136586	0.87[ASN][1000 genomes]
rs71450706	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7310385	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7314448	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7954501	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7957567	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7967538	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs935258	0.89[ASN][1000 genomes]
rs978349	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9805045	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048067	chr12:20363755-20874845	Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv541408	chr12:20363755-20874845	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1046870	chr12:20509914-20711535	Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
4	nsv541409	chr12:20509914-20711535	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
5	nsv1042315	chr12:20531641-20629866	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20553200-20571200	Weak transcription	Psoas Muscle	Psoas
2	chr12:20556400-20573200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr12:20556600-20582400	Weak transcription	Osteobl	bone
4	chr12:20558600-20588000	Weak transcription	HUVEC	blood vessel
5	chr12:20559800-20577800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr12:20562800-20573400	Weak transcription	Fetal Kidney	kidney
7	chr12:20563400-20573000	Weak transcription	Fetal Intestine Small	intestine
8	chr12:20564800-20573800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr12:20566600-20572800	Weak transcription	Left Ventricle	heart
10	chr12:20566800-20572200	Weak transcription	Right Ventricle	heart
11	chr12:20566800-20576200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr12:20567200-20573200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr12:20567200-20574400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr12:20568200-20588600	Weak transcription	Small Intestine	intestine
15	chr12:20568600-20588800	Weak transcription	Fetal Muscle Leg	muscle
16	chr12:20568600-20595400	Weak transcription	Pancreas	Pancrea
17	chr12:20568800-20571000	Weak transcription	Right Atrium	heart
18	chr12:20568800-20579400	Weak transcription	Adipose Nuclei	Adipose
19	chr12:20569000-20577800	Weak transcription	NHDF-Ad	bronchial
20	chr12:20569200-20571200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr12:20569200-20573400	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr12:20569200-20574200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:20569800-20571200	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr12:20570000-20572800	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr12:20570400-20571400	Enhancers	Aorta	Aorta
26	chr12:20570600-20571000	Weak transcription	Colon Smooth Muscle	Colon
27	chr12:20570600-20571200	Enhancers	Fetal Intestine Large	intestine
28	chr12:20570800-20573000	Weak transcription	Hela-S3	cervix

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