Variant report

Variant	rs6583804
Chromosome Location	chr10:93935403-93935404
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10786029	0.95[ASN][1000 genomes]
rs10786031	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10786033	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10882028	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10882042	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1099379	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11186915	0.82[AMR][1000 genomes]
rs1229578	0.86[ASN][1000 genomes]
rs1229579	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1622656	0.81[ASN][1000 genomes]
rs1711849	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1971471	0.92[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2254667	0.85[AMR][1000 genomes]
rs2767654	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2771248	0.85[AMR][1000 genomes]
rs3781229	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3824734	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4642988	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4933227	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4933228	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4933229	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs701844	0.85[ASN][1000 genomes]
rs701846	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7071943	0.84[ASN][1000 genomes]
rs7078559	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7087501	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7090737	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7091853	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7897555	0.85[ASN][1000 genomes]
rs7908721	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7914436	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7919840	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7920520	0.88[ASN][1000 genomes]
rs833385	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs855698	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs855699	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs855702	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs855703	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs855704	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs855707	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs855708	0.88[ASN][1000 genomes]
rs855710	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][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:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93911800-93953200	Weak transcription	Pancreas	Pancrea
2	chr10:93926400-93976000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr10:93926600-93976000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr10:93926800-93941200	Weak transcription	Brain Anterior Caudate	brain
5	chr10:93926800-93941200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr10:93926800-93942000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr10:93926800-93982400	Weak transcription	HSMMtube	muscle
8	chr10:93927000-93938600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr10:93927000-93940200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr10:93927000-93940600	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr10:93927000-93947600	Weak transcription	Primary B cells from cord blood	blood
12	chr10:93927000-93963800	Weak transcription	Brain Angular Gyrus	brain
13	chr10:93927000-93966200	Weak transcription	Ovary	ovary
14	chr10:93927000-93970800	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr10:93927200-93967600	Weak transcription	Adipose Nuclei	Adipose
16	chr10:93927200-93980400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr10:93927400-93960000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr10:93927400-93966600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr10:93927400-93970800	Weak transcription	Duodenum Mucosa	Duodenum
20	chr10:93927400-93997800	Weak transcription	Fetal Intestine Large	intestine
21	chr10:93928400-93936200	Weak transcription	Primary B cells from peripheral blood	blood
22	chr10:93928600-93942600	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr10:93928800-93949000	Weak transcription	Liver	Liver
24	chr10:93929200-93984800	Weak transcription	Fetal Intestine Small	intestine
25	chr10:93929400-93967800	Weak transcription	Colon Smooth Muscle	Colon
26	chr10:93929600-93938800	Weak transcription	Fetal Stomach	stomach
27	chr10:93930000-93958200	Weak transcription	Hela-S3	cervix
28	chr10:93932400-93940800	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr10:93933000-93940400	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr10:93933200-93941400	Weak transcription	Fetal Heart	heart
31	chr10:93934000-93940400	Weak transcription	Brain Substantia Nigra	brain
32	chr10:93934000-93940600	Strong transcription	Primary monocytes fromperipheralblood	blood
33	chr10:93934200-93936200	Weak transcription	Brain Hippocampus Middle	brain
34	chr10:93934200-93936400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr10:93934200-93940200	Weak transcription	Psoas Muscle	Psoas
36	chr10:93934200-93949400	Weak transcription	Lung	lung
37	chr10:93934200-93976200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr10:93935000-93935600	ZNF genes & repeats	Brain Cingulate Gyrus	brain
39	chr10:93935000-93936400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr10:93935200-93935800	Strong transcription	Left Ventricle	heart
41	chr10:93935400-93936400	Strong transcription	Duodenum Smooth Muscle	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links