Variant report

Variant	rs6716558
Chromosome Location	chr2:64136847-64136848
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10171008	0.80[ASN][1000 genomes]
rs10187013	0.88[YRI][hapmap]
rs10201844	0.89[CHB][hapmap];1.00[YRI][hapmap]
rs10207847	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11125986	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12612549	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs13006124	0.85[CHB][hapmap]
rs13384707	0.90[CHB][hapmap]
rs1362797	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1440004	0.84[EUR][1000 genomes]
rs17619717	0.85[CHB][hapmap]
rs2080649	0.84[EUR][1000 genomes]
rs2165210	0.81[EUR][1000 genomes]
rs2302809	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2901636	0.82[EUR][1000 genomes]
rs329477	0.82[EUR][1000 genomes]
rs329486	0.90[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs3980405	0.84[EUR][1000 genomes]
rs4072113	0.84[CHB][hapmap];1.00[YRI][hapmap]
rs6546038	0.95[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6546039	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6546040	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6546043	0.95[CHB][hapmap];0.92[JPT][hapmap]
rs6546046	0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs6705192	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6716322	0.85[EUR][1000 genomes]
rs6726257	0.84[CHB][hapmap]
rs6727120	0.81[EUR][1000 genomes]
rs6737855	0.90[CHB][hapmap];1.00[YRI][hapmap]
rs6746875	0.85[EUR][1000 genomes]
rs6757168	0.81[ASN][1000 genomes]
rs7420396	0.80[ASN][1000 genomes]
rs7589241	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs7596262	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7597935	0.84[CHB][hapmap]
rs7602952	0.82[EUR][1000 genomes]
rs7608885	0.81[EUR][1000 genomes]
rs9309356	0.90[CHB][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013375	chr2:63969820-64231550	ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv531376	chr2:64094322-64521876	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv521717	chr2:64104132-64186582	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:64114000-64212000	Weak transcription	Small Intestine	intestine
2	chr2:64114200-64174800	Weak transcription	Right Ventricle	heart
3	chr2:64116800-64138600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr2:64118200-64153600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:64118400-64137800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr2:64119600-64139600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr2:64126000-64138000	Weak transcription	Brain Angular Gyrus	brain
8	chr2:64126200-64138800	Weak transcription	Brain Cingulate Gyrus	brain
9	chr2:64127200-64138000	Weak transcription	HSMMtube	muscle
10	chr2:64127400-64138600	Weak transcription	Psoas Muscle	Psoas
11	chr2:64129200-64138000	Weak transcription	Left Ventricle	heart
12	chr2:64129600-64138200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr2:64129600-64138200	Weak transcription	NH-A	brain
14	chr2:64129600-64139000	Weak transcription	Spleen	Spleen
15	chr2:64129600-64153200	Weak transcription	Thymus	Thymus
16	chr2:64129600-64153600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr2:64129600-64153600	Weak transcription	Aorta	Aorta
18	chr2:64129600-64153600	Weak transcription	Pancreas	Pancrea
19	chr2:64129600-64154000	Weak transcription	Colonic Mucosa	Colon
20	chr2:64129600-64164000	Weak transcription	NHLF	lung
21	chr2:64129600-64201000	Weak transcription	Hela-S3	cervix
22	chr2:64129800-64154200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:64130000-64138000	Weak transcription	Lung	lung
24	chr2:64130000-64153200	Weak transcription	Gastric	stomach
25	chr2:64130000-64153600	Weak transcription	Rectal Smooth Muscle	rectum
26	chr2:64130000-64153800	Weak transcription	Esophagus	oesophagus
27	chr2:64130200-64137800	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr2:64130200-64138200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr2:64130200-64149200	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr2:64130200-64153200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr2:64130200-64153600	Weak transcription	Fetal Intestine Small	intestine
32	chr2:64130200-64153600	Weak transcription	Ovary	ovary
33	chr2:64130200-64153800	Weak transcription	Fetal Stomach	stomach
34	chr2:64130400-64137000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:64130400-64138400	Weak transcription	NHDF-Ad	bronchial
36	chr2:64130400-64138800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr2:64130400-64144400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr2:64130400-64155000	Strong transcription	HepG2	liver
39	chr2:64130400-64167600	Weak transcription	Fetal Heart	heart
40	chr2:64130400-64168400	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr2:64130400-64211200	Weak transcription	Fetal Brain Male	brain
42	chr2:64130600-64137800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr2:64130600-64138000	Weak transcription	HUVEC	blood vessel
44	chr2:64130600-64140800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr2:64130600-64144400	Weak transcription	HMEC	breast
46	chr2:64130600-64153600	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr2:64130600-64168000	Weak transcription	Colon Smooth Muscle	Colon
48	chr2:64130800-64137200	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr2:64130800-64138000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr2:64130800-64174800	Weak transcription	Stomach Mucosa	stomach

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