Variant report

Variant	rs4896849
Chromosome Location	chr6:146120858-146120859
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	chr6:146120708..146122690-chr6:146126076..146128209,2	MCF-7	breast:
2	chr6:146047378..146061811-chr6:146118130..146137627,77	K562	blood:

Variant related genes	Relation type
ENSG00000270828	Chromatin interaction
ENSG00000270638	Chromatin interaction
ENSG00000112425	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs17223456	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17821586	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17821684	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17821702	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17822170	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1856245	1.00[ASN][1000 genomes]
rs1935614	1.00[ASN][1000 genomes]
rs1988640	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2068029	1.00[ASN][1000 genomes]
rs28568954	1.00[ASN][1000 genomes]
rs3891273	1.00[ASN][1000 genomes]
rs4343934	1.00[ASN][1000 genomes]
rs4895680	1.00[ASN][1000 genomes]
rs4895681	1.00[ASN][1000 genomes]
rs4895685	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4895686	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4896823	1.00[ASN][1000 genomes]
rs4896825	1.00[ASN][1000 genomes]
rs4896830	1.00[ASN][1000 genomes]
rs4896834	1.00[ASN][1000 genomes]
rs4896845	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4896846	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4896847	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56241331	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56954340	0.97[AFR][1000 genomes]
rs57057101	0.97[AFR][1000 genomes]
rs58588227	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60043524	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61041405	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6570721	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6570722	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6900565	0.94[AFR][1000 genomes]
rs6914746	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6920248	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6921551	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6938028	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6938895	0.96[AFR][1000 genomes]
rs6940256	0.86[AFR][1000 genomes]
rs7341315	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs734166	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73568138	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73570006	0.96[AFR][1000 genomes]
rs73570010	0.97[AFR][1000 genomes]
rs73570014	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73570033	0.95[AFR][1000 genomes]
rs73570037	0.95[AFR][1000 genomes]
rs73572161	0.90[AFR][1000 genomes]
rs73579478	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9497352	1.00[ASN][1000 genomes]
rs9497355	1.00[ASN][1000 genomes]
rs9497366	1.00[ASN][1000 genomes]
rs9497368	1.00[ASN][1000 genomes]
rs9767028	1.00[ASN][1000 genomes]
rs999860	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034226	chr6:146071068-146306942	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:146100600-146123200	Weak transcription	HUVEC	blood vessel
2	chr6:146104600-146127000	Weak transcription	Brain Hippocampus Middle	brain
3	chr6:146105000-146123200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr6:146105200-146134400	Weak transcription	Thymus	Thymus
5	chr6:146105400-146125800	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr6:146105800-146125600	Weak transcription	Fetal Kidney	kidney
7	chr6:146106000-146133600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr6:146106600-146122200	Weak transcription	NHLF	lung
9	chr6:146106800-146121200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr6:146106800-146122800	Weak transcription	HSMMtube	muscle
11	chr6:146107000-146122200	Weak transcription	Left Ventricle	heart
12	chr6:146107000-146125600	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr6:146110200-146135000	Weak transcription	Pancreas	Pancrea
14	chr6:146112400-146122200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:146112400-146122400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr6:146112400-146122400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:146112400-146122400	Weak transcription	Adipose Nuclei	Adipose
18	chr6:146112400-146123000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr6:146112400-146125400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr6:146112400-146125400	Weak transcription	Fetal Stomach	stomach
21	chr6:146112400-146125600	Weak transcription	Aorta	Aorta
22	chr6:146112400-146125600	Weak transcription	Brain Substantia Nigra	brain
23	chr6:146112400-146135000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr6:146112600-146121200	Weak transcription	Osteobl	bone
25	chr6:146112600-146122200	Weak transcription	Primary B cells from cord blood	blood
26	chr6:146112600-146124600	Weak transcription	Liver	Liver
27	chr6:146112600-146125800	Weak transcription	Fetal Brain Female	brain
28	chr6:146112800-146122000	Weak transcription	NHEK	skin
29	chr6:146113000-146123200	Weak transcription	HMEC	breast
30	chr6:146113200-146122200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr6:146113200-146122800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr6:146113400-146122800	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr6:146113400-146133600	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr6:146113600-146122200	Weak transcription	Psoas Muscle	Psoas
35	chr6:146113600-146122800	Weak transcription	Primary B cells from peripheral blood	blood
36	chr6:146113800-146124000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:146113800-146126000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr6:146114200-146122200	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr6:146114200-146122200	Weak transcription	A549	lung
40	chr6:146114200-146123000	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr6:146114400-146121200	Weak transcription	K562	blood
42	chr6:146114400-146123200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr6:146114400-146125400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr6:146114600-146121600	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr6:146114600-146122400	Weak transcription	Primary hematopoietic stem cells	blood
46	chr6:146114600-146122800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr6:146115600-146121200	Weak transcription	Hela-S3	cervix
48	chr6:146116400-146126600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr6:146116600-146123200	Weak transcription	Fetal Lung	lung
50	chr6:146116600-146124600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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