Variant report

Variant	rs73054336
Chromosome Location	chr2:190679440-190679441
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1046196	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1233267	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1233270	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1233273	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1233274	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1233286	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13404927	0.82[EUR][1000 genomes]
rs2544054	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs5742924	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5742949	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5742955	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5742962	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5742965	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs5742976	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5742991	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5742993	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5742994	0.81[EUR][1000 genomes]
rs5742997	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5743003	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5743024	0.91[AFR][1000 genomes]
rs5743028	0.91[AFR][1000 genomes]
rs5743048	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs5743067	0.95[AFR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs5743090	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs5743102	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs5743130	0.82[EUR][1000 genomes]
rs58147864	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60386871	0.82[EUR][1000 genomes]
rs6750293	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73042330	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73054335	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73054339	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73054342	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs735558	0.82[EUR][1000 genomes]
rs7579156	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv3080	chr2:190661654-190706515	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:190649800-190713400	Weak transcription	Gastric	stomach
2	chr2:190650000-190688200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr2:190650400-190686800	Weak transcription	Thymus	Thymus
4	chr2:190650400-190688400	Weak transcription	Colonic Mucosa	Colon
5	chr2:190650400-190689800	Weak transcription	Rectal Smooth Muscle	rectum
6	chr2:190650400-190711400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr2:190650600-190683200	Weak transcription	Fetal Brain Male	brain
8	chr2:190650600-190688800	Weak transcription	Fetal Heart	heart
9	chr2:190650600-190693200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr2:190650600-190700400	Weak transcription	Hela-S3	cervix
11	chr2:190656800-190685000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr2:190656800-190721000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr2:190658200-190743800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr2:190659000-190685000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:190659200-190681200	Weak transcription	Spleen	Spleen
16	chr2:190659800-190686800	Weak transcription	Fetal Stomach	stomach
17	chr2:190659800-190743600	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr2:190661400-190717800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr2:190662600-190683000	Weak transcription	Adipose Nuclei	Adipose
20	chr2:190662600-190686800	Weak transcription	Left Ventricle	heart
21	chr2:190662800-190719000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr2:190663000-190682600	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr2:190663000-190682800	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr2:190663000-190683000	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr2:190663000-190685600	Weak transcription	Brain Anterior Caudate	brain
26	chr2:190663000-190701600	Weak transcription	Psoas Muscle	Psoas
27	chr2:190663000-190712800	Weak transcription	Aorta	Aorta
28	chr2:190663200-190683000	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr2:190663200-190700600	Weak transcription	Colon Smooth Muscle	Colon
30	chr2:190663200-190712400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr2:190663400-190683400	Weak transcription	Brain Hippocampus Middle	brain
32	chr2:190664600-190680000	Weak transcription	Stomach Smooth Muscle	stomach
33	chr2:190664600-190683600	Weak transcription	Brain Cingulate Gyrus	brain
34	chr2:190664800-190686800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr2:190664800-190741800	Weak transcription	Brain Angular Gyrus	brain
36	chr2:190665000-190683000	Weak transcription	HUVEC	blood vessel
37	chr2:190665000-190684400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr2:190665000-190696600	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr2:190666600-190683600	Strong transcription	HSMM	muscle
40	chr2:190667400-190683200	Weak transcription	NHLF	lung
41	chr2:190667600-190683600	Weak transcription	HMEC	breast
42	chr2:190667800-190686800	Weak transcription	Pancreas	Pancrea
43	chr2:190668400-190684400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr2:190669400-190683800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr2:190669400-190686800	Weak transcription	Lung	lung
46	chr2:190669400-190743800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr2:190669600-190709600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr2:190669600-190713200	Weak transcription	Ovary	ovary
49	chr2:190669800-190679800	Weak transcription	Fetal Muscle Trunk	muscle
50	chr2:190669800-190709000	Weak transcription	Placenta	Placenta

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