Variant report

Variant	rs6705192
Chromosome Location	chr2:64137828-64137829
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	chr2:64137390..64139134-chr2:64141328..64143487,2	MCF-7	breast:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10171008	0.87[ASN][1000 genomes]
rs10201844	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10207847	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11125985	0.80[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs11125986	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12611543	0.83[ASN][1000 genomes]
rs12612549	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12612596	0.82[EUR][1000 genomes]
rs12613707	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12615049	0.83[ASN][1000 genomes]
rs13384707	0.81[EUR][1000 genomes]
rs1362797	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1440004	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2054119	0.81[EUR][1000 genomes]
rs2080649	0.91[EUR][1000 genomes]
rs2165210	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2302809	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2901636	0.89[EUR][1000 genomes]
rs329477	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs329486	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3980405	0.91[EUR][1000 genomes]
rs4072113	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4359637	0.81[EUR][1000 genomes]
rs4399712	0.80[EUR][1000 genomes]
rs6546027	0.81[EUR][1000 genomes]
rs6546038	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6546039	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6546040	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6546042	0.83[ASN][1000 genomes]
rs6546043	0.81[ASN][1000 genomes]
rs6546046	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6716322	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6716558	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6724024	0.86[ASN][1000 genomes]
rs6727120	0.87[EUR][1000 genomes]
rs6736556	0.83[ASN][1000 genomes]
rs6737855	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6746875	0.92[EUR][1000 genomes]
rs6757168	0.88[ASN][1000 genomes]
rs7420396	0.87[ASN][1000 genomes]
rs7560265	0.83[ASN][1000 genomes]
rs7589241	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7596262	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7602952	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7608885	0.88[EUR][1000 genomes]
rs9309356	0.81[EUR][1000 genomes]

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:120 , 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	chr2:64119600-64139600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr2:64126000-64138000	Weak transcription	Brain Angular Gyrus	brain
7	chr2:64126200-64138800	Weak transcription	Brain Cingulate Gyrus	brain
8	chr2:64127200-64138000	Weak transcription	HSMMtube	muscle
9	chr2:64127400-64138600	Weak transcription	Psoas Muscle	Psoas
10	chr2:64129200-64138000	Weak transcription	Left Ventricle	heart
11	chr2:64129600-64138200	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr2:64129600-64138200	Weak transcription	NH-A	brain
13	chr2:64129600-64139000	Weak transcription	Spleen	Spleen
14	chr2:64129600-64153200	Weak transcription	Thymus	Thymus
15	chr2:64129600-64153600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr2:64129600-64153600	Weak transcription	Aorta	Aorta
17	chr2:64129600-64153600	Weak transcription	Pancreas	Pancrea
18	chr2:64129600-64154000	Weak transcription	Colonic Mucosa	Colon
19	chr2:64129600-64164000	Weak transcription	NHLF	lung
20	chr2:64129600-64201000	Weak transcription	Hela-S3	cervix
21	chr2:64129800-64154200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:64130000-64138000	Weak transcription	Lung	lung
23	chr2:64130000-64153200	Weak transcription	Gastric	stomach
24	chr2:64130000-64153600	Weak transcription	Rectal Smooth Muscle	rectum
25	chr2:64130000-64153800	Weak transcription	Esophagus	oesophagus
26	chr2:64130200-64138200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr2:64130200-64149200	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr2:64130200-64153200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr2:64130200-64153600	Weak transcription	Fetal Intestine Small	intestine
30	chr2:64130200-64153600	Weak transcription	Ovary	ovary
31	chr2:64130200-64153800	Weak transcription	Fetal Stomach	stomach
32	chr2:64130400-64138400	Weak transcription	NHDF-Ad	bronchial
33	chr2:64130400-64138800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr2:64130400-64144400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr2:64130400-64155000	Strong transcription	HepG2	liver
36	chr2:64130400-64167600	Weak transcription	Fetal Heart	heart
37	chr2:64130400-64168400	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr2:64130400-64211200	Weak transcription	Fetal Brain Male	brain
39	chr2:64130600-64138000	Weak transcription	HUVEC	blood vessel
40	chr2:64130600-64140800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr2:64130600-64144400	Weak transcription	HMEC	breast
42	chr2:64130600-64153600	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr2:64130600-64168000	Weak transcription	Colon Smooth Muscle	Colon
44	chr2:64130800-64138000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr2:64130800-64174800	Weak transcription	Stomach Mucosa	stomach
46	chr2:64131000-64138200	Weak transcription	NHEK	skin
47	chr2:64131000-64154200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr2:64131200-64138000	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr2:64131400-64155000	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr2:64131600-64141400	Strong transcription	Duodenum Mucosa	Duodenum

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