Variant report

Variant	rs74065328
Chromosome Location	chr14:70843360-70843361
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:70831727..70833563-chr14:70842326..70845155,2	MCF-7	breast:
2	chr14:70839508..70842169-chr14:70842644..70844318,2	MCF-7	breast:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs17108067	0.83[EUR][1000 genomes]
rs35051921	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55754533	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56258216	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56979041	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57900246	1.00[AMR][1000 genomes]
rs58148118	0.83[EUR][1000 genomes]
rs60037800	0.83[EUR][1000 genomes]
rs61008071	1.00[AMR][1000 genomes]
rs61977511	0.82[AFR][1000 genomes]
rs7141890	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74062883	0.83[EUR][1000 genomes]
rs74062886	0.83[EUR][1000 genomes]
rs74062887	0.83[EUR][1000 genomes]
rs74062891	0.83[EUR][1000 genomes]
rs74062892	0.83[EUR][1000 genomes]
rs74062893	0.83[EUR][1000 genomes]
rs74062894	0.83[EUR][1000 genomes]
rs74062895	0.83[EUR][1000 genomes]
rs74062897	0.83[EUR][1000 genomes]
rs74065305	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74065319	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74065320	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74065324	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74065325	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74065327	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74065329	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74065332	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74065333	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74065334	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74065335	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv902075	chr14:70612618-70919016	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70826800-70857600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:70827000-70855200	Weak transcription	Esophagus	oesophagus
3	chr14:70827000-70857600	Weak transcription	Small Intestine	intestine
4	chr14:70827000-70864200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr14:70827200-70864200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr14:70827200-70864400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr14:70827200-70882600	Weak transcription	A549	lung
8	chr14:70827200-70882600	Weak transcription	NH-A	brain
9	chr14:70827400-70845800	Weak transcription	HSMM	muscle
10	chr14:70827400-70846200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr14:70832000-70872400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr14:70832200-70864200	Weak transcription	GM12878-XiMat	blood
13	chr14:70832600-70858000	Weak transcription	Stomach Mucosa	stomach
14	chr14:70832800-70856600	Weak transcription	HUVEC	blood vessel
15	chr14:70833800-70882400	Weak transcription	NHDF-Ad	bronchial
16	chr14:70834000-70858400	Weak transcription	HepG2	liver
17	chr14:70834200-70864600	Weak transcription	Fetal Thymus	thymus
18	chr14:70834400-70843400	Weak transcription	Fetal Heart	heart
19	chr14:70834400-70847800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr14:70834600-70844000	Weak transcription	Thymus	Thymus
21	chr14:70835400-70856000	Strong transcription	Primary T cells from cord blood	blood
22	chr14:70835600-70853800	Strong transcription	Liver	Liver
23	chr14:70836000-70864200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr14:70836600-70864600	Weak transcription	Brain Germinal Matrix	brain
25	chr14:70836800-70850400	Strong transcription	Primary T cells fromperipheralblood	blood
26	chr14:70837000-70843600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr14:70837000-70844000	Strong transcription	Duodenum Smooth Muscle	Duodenum
28	chr14:70837000-70850000	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr14:70837000-70850600	Strong transcription	Primary T helper cells PMA-I stimulated	--
30	chr14:70838400-70844200	Strong transcription	Rectal Mucosa Donor 31	rectum
31	chr14:70838600-70870000	Weak transcription	NHEK	skin
32	chr14:70838600-70882400	Weak transcription	Hela-S3	cervix
33	chr14:70839000-70843600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr14:70839000-70844000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr14:70839000-70845000	Weak transcription	Fetal Intestine Small	intestine
36	chr14:70839000-70850400	Strong transcription	Primary B cells from cord blood	blood
37	chr14:70839200-70843600	Strong transcription	HUES48 Cell Line	embryonic stem cell
38	chr14:70839400-70843600	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr14:70839600-70858600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
40	chr14:70840000-70847800	Weak transcription	Ovary	ovary
41	chr14:70840200-70847800	Weak transcription	Brain Substantia Nigra	brain
42	chr14:70840200-70850000	Weak transcription	Osteobl	bone
43	chr14:70840200-70852200	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr14:70840200-70864200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr14:70840200-70864400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr14:70840200-70864400	Weak transcription	Spleen	Spleen
47	chr14:70840200-70882400	Weak transcription	Colon Smooth Muscle	Colon
48	chr14:70840200-70882600	Weak transcription	Colonic Mucosa	Colon
49	chr14:70840400-70849400	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr14:70840400-70854800	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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