Variant report

Variant	rs4344406
Chromosome Location	chr10:50318109-50318110
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:50314500..50318570-chr10:50326499..50328270,3	K562	blood:
2	chr10:50298074..50299624-chr10:50316267..50318551,2	K562	blood:

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10218995	0.83[JPT][hapmap]
rs11100988	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11100989	0.92[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11100990	0.88[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12240534	1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12246766	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12255055	0.87[CEU][hapmap];1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12267388	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12765281	0.94[CHB][hapmap]
rs12776553	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13088	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17773851	0.94[CHB][hapmap]
rs17782733	0.94[CHB][hapmap];0.84[ASN][1000 genomes]
rs1986725	0.89[CEU][hapmap];1.00[CHB][hapmap];0.90[EUR][1000 genomes]
rs2003044	0.88[CHB][hapmap]
rs2466756	0.83[JPT][hapmap]
rs2725179	0.88[CHB][hapmap]
rs2725180	0.83[JPT][hapmap]
rs2725181	0.94[CHB][hapmap]
rs2725192	0.83[JPT][hapmap]
rs2725200	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2804930	0.82[CHB][hapmap]
rs2804931	0.88[CHB][hapmap]
rs2804932	0.88[CHB][hapmap]
rs2804933	0.83[JPT][hapmap]
rs2804934	0.94[CHB][hapmap]
rs2804937	0.94[CHB][hapmap]
rs2804939	0.88[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes]
rs2804940	0.88[EUR][1000 genomes]
rs35007047	0.80[ASN][1000 genomes]
rs35285557	0.83[ASN][1000 genomes]
rs35666409	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs36015645	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4073711	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4073712	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4240499	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4240500	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4319434	0.83[JPT][hapmap]
rs4350286	0.92[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4364979	0.83[ASN][1000 genomes]
rs4412679	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4417190	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4497320	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4509682	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4532948	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4558091	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4559606	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4620641	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4644582	0.83[ASN][1000 genomes]
rs4838365	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4838367	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4838446	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4838447	0.91[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6537497	0.96[CEU][hapmap]
rs6537499	0.83[JPT][hapmap]
rs7072243	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7094217	0.83[JPT][hapmap]
rs7100655	1.00[CHB][hapmap]

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	nsv831866	chr10:50165180-50335276	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
2	esv2761593	chr10:50276812-50336129	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	esv1824894	chr10:50309905-50340304	Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50312200-50320400	Enhancers	Colon Smooth Muscle	Colon
2	chr10:50312600-50322800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:50314400-50321400	Genic enhancers	Fetal Stomach	stomach
4	chr10:50314600-50319800	Enhancers	Lung	lung
5	chr10:50314600-50320200	Enhancers	Right Atrium	heart
6	chr10:50314600-50321000	Genic enhancers	Fetal Muscle Leg	muscle
7	chr10:50315000-50318800	Weak transcription	Psoas Muscle	Psoas
8	chr10:50315000-50322600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr10:50315400-50319400	Weak transcription	Aorta	Aorta
10	chr10:50315400-50319600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr10:50315400-50323000	Weak transcription	Pancreas	Pancrea
12	chr10:50315600-50323000	Weak transcription	Spleen	Spleen
13	chr10:50315800-50320600	Enhancers	Fetal Lung	lung
14	chr10:50315800-50322200	Enhancers	Left Ventricle	heart
15	chr10:50315800-50322600	Weak transcription	Liver	Liver
16	chr10:50316000-50321200	Enhancers	Right Ventricle	heart
17	chr10:50316000-50321600	Enhancers	Ovary	ovary
18	chr10:50316600-50318200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr10:50316600-50320200	Weak transcription	Fetal Thymus	thymus
20	chr10:50317000-50320400	Enhancers	NHDF-Ad	bronchial
21	chr10:50317200-50318800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr10:50317200-50319200	Enhancers	Brain Substantia Nigra	brain
23	chr10:50317200-50319400	Enhancers	Brain Angular Gyrus	brain
24	chr10:50317200-50320600	Enhancers	NHLF	lung
25	chr10:50317200-50321000	Enhancers	Adipose Nuclei	Adipose
26	chr10:50317200-50321600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr10:50317200-50321600	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr10:50317400-50318200	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr10:50317400-50319000	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr10:50317400-50322000	Weak transcription	K562	blood
31	chr10:50317600-50318200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr10:50317600-50318600	Enhancers	Fetal Heart	heart
33	chr10:50317600-50318600	Flanking Active TSS	Stomach Smooth Muscle	stomach
34	chr10:50317800-50318200	Active TSS	Rectal Smooth Muscle	rectum
35	chr10:50317800-50318400	Enhancers	H1 Cell Line	embryonic stem cell
36	chr10:50317800-50318600	Enhancers	Muscle Satellite Cultured Cells	--
37	chr10:50317800-50318600	Enhancers	Brain Cingulate Gyrus	brain
38	chr10:50317800-50318600	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr10:50317800-50319000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr10:50317800-50319200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr10:50318000-50318200	Enhancers	Brain Hippocampus Middle	brain
42	chr10:50318000-50318200	Enhancers	Esophagus	oesophagus
43	chr10:50318000-50318200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
44	chr10:50318000-50318200	Enhancers	HSMM	muscle
45	chr10:50318000-50318400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr10:50318000-50318600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr10:50318000-50318600	Enhancers	Fetal Muscle Trunk	muscle
48	chr10:50318000-50318800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr10:50318000-50319000	Weak transcription	Placenta	Placenta
50	chr10:50318000-50320600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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