Variant report

Variant	rs6929743
Chromosome Location	chr6:151007388-151007389
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:151002149..151004353-chr6:151006799..151008917,2	MCF-7	breast:
2	chr6:150739625..150740200-chr6:151007043..151007665,2	MCF-7	breast:
3	chr6:151006847..151007653-chr6:151136348..151136865,2	MCF-7	breast:
4	chr6:150738919..150740367-chr6:151006693..151007780,5	MCF-7	breast:
5	chr6:151005271..151008219-chr6:151020756..151022583,2	K562	blood:
6	chr6:151007139..151009866-chr6:151010268..151011885,2	MCF-7	breast:
7	chr6:151006793..151007729-chr6:151062617..151063276,4	MCF-7	breast:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10872666	0.84[AMR][1000 genomes]
rs12664686	0.93[CEU][hapmap]
rs17080073	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17080108	0.93[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2345745	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4036092	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4869926	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4869927	0.93[CEU][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4869928	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4869929	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4869930	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4869931	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55646755	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58824807	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59155780	0.91[AFR][1000 genomes]
rs59466561	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6899782	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6908127	0.93[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73010188	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7738394	0.96[YRI][hapmap];0.94[AFR][1000 genomes]
rs7749222	0.96[YRI][hapmap];0.94[AFR][1000 genomes]
rs9478775	0.93[CEU][hapmap];0.83[AMR][1000 genomes]
rs9478780	0.93[CEU][hapmap];0.86[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9478783	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9480514	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9480526	0.93[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9480528	0.93[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9480529	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9480530	0.92[CEU][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9480531	0.93[CEU][hapmap];0.86[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9480533	0.93[CEU][hapmap];1.00[CHB][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9885650	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9885699	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9885836	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886772	chr6:150743364-151024280	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1030326	chr6:150967665-151641372	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150980600-151008800	Weak transcription	Gastric	stomach
2	chr6:150980800-151014800	Weak transcription	Pancreas	Pancrea
3	chr6:150989400-151007800	Weak transcription	Ovary	ovary
4	chr6:150990600-151008800	Weak transcription	Rectal Smooth Muscle	rectum
5	chr6:150990600-151016600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr6:150990800-151011800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:150995000-151008800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr6:150995400-151008800	Weak transcription	Small Intestine	intestine
9	chr6:150996600-151008000	Weak transcription	Fetal Intestine Large	intestine
10	chr6:151000800-151010000	Enhancers	Primary B cells from peripheral blood	blood
11	chr6:151001600-151008200	Genic enhancers	Fetal Thymus	thymus
12	chr6:151002400-151007800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:151003400-151007400	Genic enhancers	Thymus	Thymus
14	chr6:151003600-151007600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:151003600-151011400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:151003800-151007400	Weak transcription	NHEK	skin
17	chr6:151003800-151015000	Weak transcription	Brain Substantia Nigra	brain
18	chr6:151004800-151012000	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr6:151005000-151017400	Weak transcription	Aorta	Aorta
20	chr6:151005200-151007400	Enhancers	HUVEC	blood vessel
21	chr6:151005800-151008000	Enhancers	Placenta	Placenta
22	chr6:151005800-151018400	Weak transcription	Psoas Muscle	Psoas
23	chr6:151006000-151007400	Enhancers	Right Ventricle	heart
24	chr6:151006000-151008000	Enhancers	Left Ventricle	heart
25	chr6:151006000-151018400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr6:151006200-151007600	Weak transcription	Fetal Muscle Leg	muscle
27	chr6:151006400-151007600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr6:151006600-151007600	Weak transcription	Fetal Lung	lung
29	chr6:151006600-151007800	Weak transcription	Lung	lung
30	chr6:151006600-151007800	Weak transcription	Spleen	Spleen
31	chr6:151006600-151008000	Weak transcription	Stomach Mucosa	stomach
32	chr6:151006600-151008400	Weak transcription	Liver	Liver
33	chr6:151006600-151011400	Enhancers	Primary B cells from cord blood	blood
34	chr6:151006600-151011800	Weak transcription	Primary hematopoietic stem cells	blood
35	chr6:151006600-151011800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr6:151006600-151014600	Weak transcription	Right Atrium	heart
37	chr6:151006800-151007800	Weak transcription	Esophagus	oesophagus
38	chr6:151006800-151008400	Weak transcription	Duodenum Mucosa	Duodenum
39	chr6:151006800-151008800	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr6:151006800-151008800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr6:151006800-151017200	Weak transcription	Fetal Stomach	stomach
42	chr6:151007000-151007400	Weak transcription	Adipose Nuclei	Adipose
43	chr6:151007000-151007600	Enhancers	Fetal Kidney	kidney
44	chr6:151007000-151007800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr6:151007000-151008000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:151007000-151008400	Enhancers	HMEC	breast
47	chr6:151007000-151009400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:151007200-151007400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr6:151007200-151008000	Enhancers	Placenta Amnion	Placenta Amnion
50	chr6:151007200-151008200	Weak transcription	Rectal Mucosa Donor 31	rectum

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