Variant report

Variant	rs722796
Chromosome Location	chr6:128733693-128733694
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:128733005..128734621-chr6:128736673..128739211,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10428737	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12110431	0.98[AFR][1000 genomes]
rs1339193	1.00[CEU][hapmap]
rs1612415	0.85[CEU][hapmap]
rs17055854	1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17361665	0.87[EUR][1000 genomes]
rs17459362	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs1891146	1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1891147	1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1891148	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4466261	0.92[CEU][hapmap]
rs58395468	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59893653	0.89[EUR][1000 genomes]
rs66843622	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6939023	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs72974018	0.84[EUR][1000 genomes]
rs72974042	0.81[EUR][1000 genomes]
rs72974046	1.00[EUR][1000 genomes]
rs72974053	1.00[EUR][1000 genomes]
rs72974060	1.00[EUR][1000 genomes]
rs72974074	1.00[EUR][1000 genomes]
rs72974081	0.81[EUR][1000 genomes]
rs7748155	0.83[YRI][hapmap]
rs7764930	1.00[CEU][hapmap];0.80[YRI][hapmap]
rs7774606	0.94[AFR][1000 genomes]
rs9375564	0.94[AFR][1000 genomes]
rs9402035	0.93[YRI][hapmap]
rs946424	1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs953549	0.92[CEU][hapmap]
rs961292	1.00[CEU][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033443	chr6:128306654-128899203	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv538440	chr6:128306654-128899203	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv886649	chr6:128399657-128808054	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv1020071	chr6:128579774-129048919	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh 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
5	nsv538441	chr6:128579774-129048919	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv830800	chr6:128710631-128878435	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128688800-128738800	Weak transcription	Psoas Muscle	Psoas
2	chr6:128698800-128743200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr6:128703200-128743000	Weak transcription	Pancreas	Pancrea
4	chr6:128710200-128739800	Weak transcription	Fetal Intestine Large	intestine
5	chr6:128712000-128733800	Weak transcription	Brain Hippocampus Middle	brain
6	chr6:128715600-128743000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr6:128715800-128736200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:128716600-128736000	Weak transcription	Brain Substantia Nigra	brain
9	chr6:128716600-128739400	Weak transcription	Aorta	Aorta
10	chr6:128716800-128738400	Weak transcription	Fetal Heart	heart
11	chr6:128717200-128739600	Weak transcription	NH-A	brain
12	chr6:128722000-128738600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr6:128722400-128740000	Weak transcription	Right Ventricle	heart
14	chr6:128726200-128733800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:128728000-128736000	Weak transcription	Fetal Kidney	kidney
16	chr6:128728200-128739000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr6:128728400-128738800	Weak transcription	Stomach Smooth Muscle	stomach
18	chr6:128728600-128739400	Weak transcription	Fetal Intestine Small	intestine
19	chr6:128728600-128742800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:128728800-128736200	Weak transcription	HepG2	liver
21	chr6:128728800-128748000	Weak transcription	Ovary	ovary
22	chr6:128731000-128753400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:128731400-128735400	Weak transcription	Small Intestine	intestine
24	chr6:128731800-128734400	Weak transcription	Primary T cells from cord blood	blood
25	chr6:128732200-128738800	Weak transcription	Osteobl	bone
26	chr6:128732200-128739000	Weak transcription	Fetal Thymus	thymus
27	chr6:128732400-128739400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr6:128732400-128739400	Weak transcription	Left Ventricle	heart
29	chr6:128732400-128752400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr6:128732800-128742800	Weak transcription	Brain Angular Gyrus	brain
31	chr6:128733400-128733800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:128733400-128733800	Enhancers	HSMMtube	muscle
33	chr6:128733400-128734600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr6:128733400-128734600	Enhancers	HSMM	muscle
35	chr6:128733600-128733800	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
36	chr6:128733600-128734000	Enhancers	H1 Cell Line	embryonic stem cell
37	chr6:128733600-128734000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr6:128733600-128734000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr6:128733600-128734200	Enhancers	Gastric	stomach
40	chr6:128733600-128734400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr6:128733600-128734400	Enhancers	Brain Anterior Caudate	brain
42	chr6:128733600-128734600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
43	chr6:128733600-128735000	Enhancers	Muscle Satellite Cultured Cells	--
44	chr6:128733600-128735000	Enhancers	NHEK	skin

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