Variant report

Variant	rs210931
Chromosome Location	chr6:11744180-11744181
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:11743683..11746205-chr6:11753336..11755527,2	K562	blood:
2	chr6:11743986..11745912-chr6:11747510..11751154,3	MCF-7	breast:
3	chr6:11742447..11744431-chr6:11745938..11748190,2	K562	blood:

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs191921	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs210890	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs210899	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs210905	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs210910	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs210911	0.80[CEU][hapmap];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs210913	0.90[AMR][1000 genomes]
rs210914	0.90[AMR][1000 genomes]
rs210915	0.90[AMR][1000 genomes]
rs210917	0.88[AMR][1000 genomes]
rs210918	0.88[AMR][1000 genomes]
rs210926	1.00[CEU][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs210933	1.00[CEU][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2235397	0.81[CEU][hapmap]
rs2743953	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2781127	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4713852	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs6457810	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9394295	0.85[CEU][hapmap]

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	esv2758036	chr6:11679753-11822351	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2759407	chr6:11679753-11822351	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv428470	chr6:11686198-11747850	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11719400-11762200	Weak transcription	Colonic Mucosa	Colon
2	chr6:11723600-11744200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr6:11725200-11748600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:11726400-11744600	Weak transcription	Right Atrium	heart
5	chr6:11732400-11744800	Weak transcription	Fetal Intestine Small	intestine
6	chr6:11732400-11750400	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr6:11732800-11750400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr6:11734600-11745000	Weak transcription	HSMMtube	muscle
9	chr6:11735200-11744600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:11735600-11754800	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr6:11736200-11744600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:11736200-11752400	Weak transcription	NHEK	skin
13	chr6:11736200-11754800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr6:11736600-11750600	Weak transcription	Stomach Mucosa	stomach
15	chr6:11737600-11744800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:11738600-11762000	Weak transcription	Gastric	stomach
17	chr6:11739000-11755000	Weak transcription	HMEC	breast
18	chr6:11739200-11744600	Weak transcription	Adipose Nuclei	Adipose
19	chr6:11739600-11751800	Weak transcription	HUVEC	blood vessel
20	chr6:11741600-11745400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr6:11742000-11755000	Weak transcription	HSMM	muscle
22	chr6:11743400-11744400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:11743400-11744800	Weak transcription	Ovary	ovary
24	chr6:11743400-11745000	Weak transcription	Aorta	Aorta
25	chr6:11743600-11745400	Enhancers	Pancreas	Pancrea
26	chr6:11743800-11744200	Enhancers	K562	blood
27	chr6:11743800-11744600	Weak transcription	Duodenum Mucosa	Duodenum
28	chr6:11743800-11744600	Weak transcription	Placenta	Placenta
29	chr6:11743800-11745000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr6:11743800-11745200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr6:11743800-11750200	Weak transcription	Small Intestine	intestine
32	chr6:11744000-11744800	Weak transcription	Lung	lung

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