Variant report

Variant	rs4358650
Chromosome Location	chr6:149309243-149309244
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12194615	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12197795	0.81[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs12202149	0.94[JPT][hapmap]
rs12204964	0.96[CEU][hapmap];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12207855	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12207913	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1384310	0.94[JPT][hapmap];0.80[ASN][1000 genomes]
rs1564601	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1564602	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2340749	0.81[CEU][hapmap];0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs3734376	0.94[JPT][hapmap]
rs3734377	0.94[JPT][hapmap]
rs6932862	0.95[JPT][hapmap]
rs6933251	0.94[JPT][hapmap]
rs6936508	0.81[CEU][hapmap];0.82[EUR][1000 genomes]
rs9322162	0.81[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs9377181	0.95[JPT][hapmap]
rs9377183	0.81[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9377186	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9386241	0.95[ASN][1000 genomes]
rs9404010	0.89[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs9404011	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032690	chr6:149206106-149398712	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1032319	chr6:149271433-149550525	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv538470	chr6:149271433-149550525	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv830842	chr6:149272321-149427340	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149278000-149310600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr6:149286800-149320600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr6:149289200-149314600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:149290800-149311800	Weak transcription	Stomach Smooth Muscle	stomach
5	chr6:149292800-149321200	Weak transcription	Aorta	Aorta
6	chr6:149293800-149309400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:149294000-149320400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:149294200-149319400	Weak transcription	HSMMtube	muscle
9	chr6:149296000-149311400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:149300000-149319800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr6:149300800-149317600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:149301200-149309800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr6:149301600-149309800	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr6:149302000-149310200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr6:149302000-149311600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr6:149302800-149316200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:149304400-149310000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr6:149304400-149314000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr6:149304600-149310000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr6:149304800-149309800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr6:149304800-149311600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr6:149305200-149310000	Weak transcription	Colon Smooth Muscle	Colon
23	chr6:149305200-149311800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:149305400-149381400	Weak transcription	Gastric	stomach
25	chr6:149306000-149311600	Weak transcription	Fetal Muscle Leg	muscle
26	chr6:149306200-149319400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr6:149306400-149310000	Weak transcription	Ovary	ovary
28	chr6:149306400-149316800	Weak transcription	Fetal Heart	heart
29	chr6:149307200-149311400	Enhancers	Primary B cells from peripheral blood	blood
30	chr6:149307400-149310000	Weak transcription	Dnd41	blood
31	chr6:149308000-149319600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr6:149308200-149311200	Enhancers	Primary B cells from cord blood	blood
33	chr6:149308200-149320600	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr6:149308400-149309600	Strong transcription	Lung	lung
35	chr6:149308400-149312000	Weak transcription	Brain Cingulate Gyrus	brain
36	chr6:149308400-149320400	Weak transcription	Right Ventricle	heart
37	chr6:149308600-149309400	Strong transcription	Fetal Stomach	stomach
38	chr6:149308800-149309400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:149309000-149309600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr6:149309000-149310000	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr6:149309000-149310200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr6:149309200-149309400	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr6:149309200-149309400	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:149309200-149309600	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr6:149309200-149309800	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr6:149309200-149311000	Enhancers	H9 Cell Line	embryonic stem cell
47	chr6:149309200-149311200	Enhancers	H1 Cell Line	embryonic stem cell
48	chr6:149309200-149312200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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