Variant report

Variant	rs7096690
Chromosome Location	chr10:93989756-93989757
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs35412677	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57762009	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58708663	0.89[AMR][1000 genomes]
rs59509997	0.89[AMR][1000 genomes]
rs59582715	0.89[AMR][1000 genomes]
rs60968131	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6583800	0.89[AMR][1000 genomes]
rs6583808	0.87[AMR][1000 genomes]
rs7074872	1.00[AMR][1000 genomes]
rs7075257	0.89[AMR][1000 genomes]
rs7083185	0.87[AMR][1000 genomes]
rs7084837	0.89[AMR][1000 genomes]
rs73314344	0.89[AMR][1000 genomes]
rs73316068	0.89[AMR][1000 genomes]
rs73316069	0.89[AMR][1000 genomes]
rs73316082	0.89[AMR][1000 genomes]
rs73318015	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73318028	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7907888	0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv975763	chr10:93822289-94105956	Enhancers Bivalent Enhancer Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv1046258	chr10:93866969-94466106	Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93927400-93997800	Weak transcription	Fetal Intestine Large	intestine
2	chr10:93961000-93990800	Weak transcription	Spleen	Spleen
3	chr10:93964200-93993000	Weak transcription	Fetal Brain Female	brain
4	chr10:93964200-93996000	Weak transcription	Brain Germinal Matrix	brain
5	chr10:93964200-93997600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr10:93967600-93990800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr10:93968400-93997000	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr10:93969200-93997800	Weak transcription	Pancreas	Pancrea
9	chr10:93969200-93998600	Weak transcription	Lung	lung
10	chr10:93969600-93997800	Weak transcription	Esophagus	oesophagus
11	chr10:93971000-93990800	Weak transcription	Duodenum Mucosa	Duodenum
12	chr10:93971200-93990400	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr10:93971400-93993200	Weak transcription	Fetal Muscle Leg	muscle
14	chr10:93971400-93997800	Weak transcription	Stomach Mucosa	stomach
15	chr10:93971600-93997000	Weak transcription	Adipose Nuclei	Adipose
16	chr10:93973000-93997000	Weak transcription	Liver	Liver
17	chr10:93974800-93991600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr10:93975400-93998000	Weak transcription	Colonic Mucosa	Colon
19	chr10:93975600-93997000	Weak transcription	HepG2	liver
20	chr10:93976600-93999000	Weak transcription	Aorta	Aorta
21	chr10:93976800-93990600	Weak transcription	Right Ventricle	heart
22	chr10:93976800-93997200	Weak transcription	Stomach Smooth Muscle	stomach
23	chr10:93976800-93998800	Weak transcription	Gastric	stomach
24	chr10:93977000-93998400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr10:93977600-93998000	Weak transcription	Primary B cells from cord blood	blood
26	chr10:93978200-93990600	Weak transcription	Fetal Stomach	stomach
27	chr10:93979000-93991000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr10:93979200-93994600	Weak transcription	Fetal Brain Male	brain
29	chr10:93979400-93998600	Weak transcription	Primary T cells from cord blood	blood
30	chr10:93979800-93996800	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr10:93980400-93990800	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr10:93981600-93990400	Weak transcription	Psoas Muscle	Psoas
33	chr10:93982600-93997800	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr10:93982800-93997600	Weak transcription	Fetal Thymus	thymus
35	chr10:93983200-93998400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr10:93983200-93998400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr10:93983400-93997800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr10:93983400-93998000	Weak transcription	HSMMtube	muscle
39	chr10:93983400-93998200	Weak transcription	HSMM	muscle
40	chr10:93983600-93998400	Weak transcription	Primary hematopoietic stem cells	blood
41	chr10:93984000-93990400	Weak transcription	Rectal Smooth Muscle	rectum
42	chr10:93984400-93992600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr10:93984400-93997000	Weak transcription	Hela-S3	cervix
44	chr10:93984400-93997400	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr10:93984600-93992400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr10:93984600-93992600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr10:93984800-93990400	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr10:93985000-93998800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr10:93986800-93990400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr10:93986800-93993000	Weak transcription	Left Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links