Variant report

Variant	rs2237944
Chromosome Location	chr11:17838116-17838117
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:17825311..17828756-chr11:17836792..17840310,3	MCF-7	breast:
2	chr11:17837704..17839963-chr11:17840786..17842611,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1005008	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10160556	0.88[EUR][1000 genomes]
rs10466421	0.84[AMR][1000 genomes]
rs10766440	0.88[EUR][1000 genomes]
rs10832860	0.85[EUR][1000 genomes]
rs11024415	0.82[CHB][hapmap];0.92[AMR][1000 genomes]
rs11821847	0.82[CHB][hapmap]
rs1548528	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2079227	0.92[CEU][hapmap];0.91[EUR][1000 genomes]
rs2107427	0.90[CHB][hapmap]
rs2158395	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs2158396	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2237943	0.89[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.87[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2237946	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2237948	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2237949	0.93[YRI][hapmap]
rs2237950	0.92[CEU][hapmap];0.89[EUR][1000 genomes]
rs2237952	0.89[EUR][1000 genomes]
rs2283249	0.90[CHB][hapmap]
rs2299632	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs2299633	0.91[CHB][hapmap]
rs3802969	0.89[CEU][hapmap];0.87[EUR][1000 genomes]
rs4757589	0.88[CEU][hapmap]
rs4757591	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs4757593	0.80[CHB][hapmap];0.90[JPT][hapmap]
rs6486398	0.96[CEU][hapmap];0.81[CHB][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6486399	0.81[CHB][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7106840	0.89[JPT][hapmap]
rs7109837	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7115183	0.90[CHB][hapmap]
rs7124199	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs718439	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs765989	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7929668	0.90[CHB][hapmap];0.83[AMR][1000 genomes]
rs7932686	0.91[CHB][hapmap]
rs7935967	0.82[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832078	chr11:17780503-17953521	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
2	nsv1043973	chr11:17781560-17869896	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
3	nsv949248	chr11:17791822-18692687	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
4	nsv897026	chr11:17823296-18084878	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 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	chr11:17806800-17867400	Weak transcription	Primary B cells from cord blood	blood
2	chr11:17808200-17861400	Weak transcription	Thymus	Thymus
3	chr11:17815600-17841400	Weak transcription	HepG2	liver
4	chr11:17818600-17843200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:17825400-17843400	Weak transcription	Lung	lung
6	chr11:17831200-17849400	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr11:17832000-17849600	Weak transcription	Primary T cells from cord blood	blood
8	chr11:17832400-17838600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr11:17833000-17843800	Weak transcription	HSMMtube	muscle
10	chr11:17833800-17843000	Weak transcription	Fetal Heart	heart
11	chr11:17833800-17867400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr11:17834800-17838800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr11:17834800-17843400	Weak transcription	Stomach Mucosa	stomach
14	chr11:17835000-17838400	Weak transcription	Fetal Intestine Large	intestine
15	chr11:17835000-17843000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr11:17835000-17843400	Weak transcription	Brain Angular Gyrus	brain
17	chr11:17835000-17849600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr11:17835000-17869400	Weak transcription	Fetal Intestine Small	intestine
19	chr11:17835200-17842600	Weak transcription	Aorta	Aorta
20	chr11:17835200-17884200	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr11:17835600-17843200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr11:17835800-17838200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr11:17835800-17838200	Weak transcription	NHEK	skin
24	chr11:17836400-17843200	Weak transcription	Colon Smooth Muscle	Colon
25	chr11:17836600-17842400	Weak transcription	Psoas Muscle	Psoas
26	chr11:17837400-17838400	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr11:17837400-17838600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr11:17837400-17838600	Enhancers	Fetal Kidney	kidney
29	chr11:17837600-17838400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr11:17837600-17838400	Enhancers	Adipose Nuclei	Adipose
31	chr11:17837600-17838400	Enhancers	Placenta	Placenta
32	chr11:17837600-17838400	Enhancers	Left Ventricle	heart
33	chr11:17837600-17838400	Enhancers	Stomach Smooth Muscle	stomach
34	chr11:17837600-17838600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr11:17837600-17838600	Enhancers	Fetal Lung	lung
36	chr11:17837600-17838600	Enhancers	Fetal Muscle Leg	muscle
37	chr11:17837600-17838600	Enhancers	Fetal Stomach	stomach
38	chr11:17837800-17838200	Enhancers	Rectal Smooth Muscle	rectum
39	chr11:17837800-17838600	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr11:17837800-17838600	Enhancers	HMEC	breast
41	chr11:17838000-17838400	Enhancers	Esophagus	oesophagus
42	chr11:17838000-17838400	Active TSS	Fetal Brain Male	brain
43	chr11:17838000-17838400	Enhancers	Fetal Muscle Trunk	muscle
44	chr11:17838000-17838400	Enhancers	Gastric	stomach
45	chr11:17838000-17838600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr11:17838000-17838600	Enhancers	Ovary	ovary
47	chr11:17838000-17838600	Enhancers	Pancreas	Pancrea
48	chr11:17838000-17838600	Enhancers	Right Atrium	heart
49	chr11:17838000-17838600	Enhancers	Right Ventricle	heart
50	chr11:17838000-17838600	Enhancers	Sigmoid Colon	Sigmoid Colon

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