Variant report

Variant	rs912710
Chromosome Location	chr6:5001604-5001605
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:4991690..4994969-chr6:5000168..5002505,4	K562	blood:
2	chr6:4995264..4998093-chr6:5000328..5002613,2	K562	blood:
3	chr6:4980886..4983187-chr6:5000128..5002637,2	K562	blood:
4	chr6:4948514..4950542-chr6:5000037..5002807,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs11758411	0.81[EUR][1000 genomes]
rs11759046	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1417656	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1749154	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1749161	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1749165	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1771865	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1771866	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1771867	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1771871	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1886567	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2326574	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764102	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764103	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764104	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764105	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764106	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764107	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764108	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2764109	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764112	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764114	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764115	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764116	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764120	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764121	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764123	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764124	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764125	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764126	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764127	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2764129	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764130	1.00[ASN][1000 genomes]
rs2764132	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2764134	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764135	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764137	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764138	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764139	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764141	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764142	1.00[ASN][1000 genomes]
rs2764143	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764145	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764148	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2764149	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764151	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764152	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764166	1.00[ASN][1000 genomes]
rs2764169	1.00[ASN][1000 genomes]
rs2764185	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2764186	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2764191	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764192	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2793240	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2793241	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2793242	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2793245	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2793247	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2793249	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2793250	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2793251	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2985675	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2994694	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34471690	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4960056	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5018030	0.90[AMR][1000 genomes]
rs62385141	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6905084	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6912320	1.00[ASN][1000 genomes]
rs795809	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs795810	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs795811	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs912709	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs912711	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs947153	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9502260	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	esv2422499	chr6:4745428-5073222	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv830577	chr6:4834567-5050544	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv462622	chr6:4904380-5172009	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv600871	chr6:4904380-5172009	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats 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 miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv1033905	chr6:4955826-5080904	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv600872	chr6:4975313-5342190	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
8	nsv1031837	chr6:4996667-5418726	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4985600-5003000	Weak transcription	HUVEC	blood vessel
2	chr6:4985600-5003200	Weak transcription	Hela-S3	cervix
3	chr6:4985800-5003600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr6:4987600-5003000	Weak transcription	GM12878-XiMat	blood
5	chr6:4987600-5003600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:4988200-5003600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:4988800-5003600	Weak transcription	HMEC	breast
8	chr6:4989200-5003600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr6:4990000-5003600	Weak transcription	Fetal Lung	lung
10	chr6:4990400-5003600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr6:4990400-5003600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:4990800-5003000	Weak transcription	Fetal Heart	heart
13	chr6:4990800-5003600	Weak transcription	Right Ventricle	heart
14	chr6:4991000-5002600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:4991200-5002400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:4992200-5003400	Weak transcription	NH-A	brain
17	chr6:4992400-5003600	Weak transcription	Small Intestine	intestine
18	chr6:4992800-5003600	Weak transcription	Brain Germinal Matrix	brain
19	chr6:4993000-5003600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:4993400-5002400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr6:4993400-5003400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:4993600-5003600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:4993600-5003600	Weak transcription	Colon Smooth Muscle	Colon
24	chr6:4994400-5003600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr6:4994600-5002200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr6:4994600-5002400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr6:4994600-5002400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr6:4994600-5003600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr6:4994800-5002400	Strong transcription	Adipose Nuclei	Adipose
30	chr6:4994800-5002400	Strong transcription	Liver	Liver
31	chr6:4995000-5002200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:4995200-5003000	Weak transcription	Fetal Brain Female	brain
33	chr6:4995200-5003600	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr6:4996400-5002400	Strong transcription	Fetal Muscle Trunk	muscle
35	chr6:4996400-5002400	Strong transcription	Fetal Stomach	stomach
36	chr6:4996400-5003600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr6:4997000-5003600	Weak transcription	Fetal Kidney	kidney
38	chr6:4997200-5003200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr6:4997200-5003600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr6:4997600-5003400	Weak transcription	Colonic Mucosa	Colon
41	chr6:4997600-5003600	Weak transcription	Brain Cingulate Gyrus	brain
42	chr6:4997800-5001800	Weak transcription	Aorta	Aorta
43	chr6:4997800-5002400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:4997800-5003600	Weak transcription	Ovary	ovary
45	chr6:4998000-5002200	Strong transcription	HUES64 Cell Line	embryonic stem cell
46	chr6:4998000-5002400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr6:4998000-5003600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr6:4998000-5003600	Weak transcription	Thymus	Thymus
49	chr6:4998200-5003200	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr6:4998200-5003600	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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