Variant report

Variant	rs7121907
Chromosome Location	chr11:34497652-34497653
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11032656	0.92[EUR][1000 genomes]
rs11032672	0.94[EUR][1000 genomes]
rs11032702	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1107573	0.97[EUR][1000 genomes]
rs12269988	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12272630	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12273124	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12275712	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12285026	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12285064	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12288793	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12293745	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12295136	0.97[EUR][1000 genomes]
rs16925514	0.97[EUR][1000 genomes]
rs17883208	0.89[EUR][1000 genomes]
rs17884086	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2057513	0.95[AFR][1000 genomes]
rs57360584	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58817388	0.97[EUR][1000 genomes]
rs59468184	0.97[EUR][1000 genomes]
rs7114869	0.97[EUR][1000 genomes]
rs7125892	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73436768	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7926613	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9282626	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897205	chr11:34248229-34507213	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv897207	chr11:34253683-34621004	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv897208	chr11:34257064-34562247	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv897209	chr11:34309519-34548906	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv832114	chr11:34424428-34607851	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34483400-34501600	Weak transcription	HMEC	breast
2	chr11:34491000-34501800	Weak transcription	Psoas Muscle	Psoas
3	chr11:34492000-34498400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:34493000-34497800	Weak transcription	Small Intestine	intestine
5	chr11:34493000-34498200	Weak transcription	Esophagus	oesophagus
6	chr11:34493200-34497800	Weak transcription	Dnd41	blood
7	chr11:34493200-34497800	Weak transcription	NHLF	lung
8	chr11:34493200-34498000	Weak transcription	Right Ventricle	heart
9	chr11:34494000-34498000	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr11:34494000-34498000	Weak transcription	NHDF-Ad	bronchial
11	chr11:34494000-34498400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr11:34494000-34498400	Weak transcription	Osteobl	bone
13	chr11:34494000-34499400	Weak transcription	HepG2	liver
14	chr11:34494000-34501800	Weak transcription	HSMM	muscle
15	chr11:34494200-34497800	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr11:34494200-34499400	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr11:34494400-34497800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr11:34494400-34498000	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr11:34494400-34498200	Weak transcription	Brain Anterior Caudate	brain
20	chr11:34494400-34498200	Weak transcription	Gastric	stomach
21	chr11:34494400-34498200	Weak transcription	Pancreas	Pancrea
22	chr11:34494400-34498400	Weak transcription	Fetal Muscle Trunk	muscle
23	chr11:34494400-34498600	Weak transcription	Fetal Intestine Large	intestine
24	chr11:34494400-34501400	Weak transcription	Fetal Kidney	kidney
25	chr11:34494600-34498200	Weak transcription	Placenta	Placenta
26	chr11:34494600-34498400	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr11:34494800-34498000	Weak transcription	Fetal Intestine Small	intestine
28	chr11:34495000-34498000	Weak transcription	Brain Angular Gyrus	brain
29	chr11:34495200-34498000	Weak transcription	Ovary	ovary
30	chr11:34495200-34498200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr11:34495200-34499000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:34495200-34499200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr11:34495200-34501800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr11:34495600-34498400	Weak transcription	Stomach Smooth Muscle	stomach
35	chr11:34495600-34498800	Weak transcription	Primary B cells from cord blood	blood
36	chr11:34495600-34500400	Weak transcription	Liver	Liver
37	chr11:34496000-34498400	Weak transcription	Fetal Stomach	stomach
38	chr11:34496400-34498000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr11:34496400-34498000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr11:34496400-34498000	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr11:34496400-34498200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr11:34496600-34498200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:34496600-34498400	Weak transcription	Hela-S3	cervix
44	chr11:34496800-34498400	Weak transcription	Duodenum Mucosa	Duodenum
45	chr11:34496800-34498600	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr11:34496800-34498800	Weak transcription	Adipose Nuclei	Adipose
47	chr11:34496800-34501400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr11:34496800-34501800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr11:34497000-34498600	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr11:34497000-34498600	Weak transcription	Primary T cells from cord blood	blood

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