Variant report

Variant	rs7895551
Chromosome Location	chr10:116625481-116625482
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:116620510..116622671-chr10:116624179..116626213,2	K562	blood:

Variant related genes	Relation type
ENSG00000151553	Chromatin interaction

Extended variants
information (count: 126 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:121)

rs_ID	r²[population]
rs10444099	1.00[JPT][hapmap]
rs1045657	1.00[JPT][hapmap]
rs1046492	1.00[CEU][hapmap];0.91[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10490908	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10510007	0.95[CEU][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10885613	0.88[AFR][1000 genomes]
rs10885614	0.92[YRI][hapmap];0.90[AFR][1000 genomes]
rs10885633	1.00[JPT][hapmap]
rs10885634	1.00[JPT][hapmap]
rs10885636	1.00[JPT][hapmap]
rs10885638	1.00[JPT][hapmap]
rs10885639	1.00[JPT][hapmap]
rs11196929	0.82[AFR][1000 genomes]
rs11196930	0.88[AFR][1000 genomes]
rs11196932	0.88[AFR][1000 genomes]
rs11196935	0.83[AFR][1000 genomes]
rs11196936	0.88[AFR][1000 genomes]
rs11196937	0.88[AFR][1000 genomes]
rs11196939	0.91[YRI][hapmap];0.88[AFR][1000 genomes]
rs11196941	0.86[AFR][1000 genomes]
rs11196943	0.85[AFR][1000 genomes]
rs11196944	0.87[AFR][1000 genomes]
rs11196945	0.92[YRI][hapmap];0.83[AFR][1000 genomes]
rs11196948	0.84[AFR][1000 genomes]
rs11196950	0.84[AFR][1000 genomes]
rs11196951	0.84[AFR][1000 genomes]
rs11196952	0.86[AFR][1000 genomes]
rs11196953	0.86[AFR][1000 genomes]
rs11196963	1.00[CHB][hapmap]
rs11196984	1.00[JPT][hapmap]
rs11196996	1.00[JPT][hapmap]
rs11196999	1.00[JPT][hapmap]
rs11197000	1.00[JPT][hapmap]
rs11197007	1.00[JPT][hapmap]
rs11197010	1.00[JPT][hapmap]
rs11197011	1.00[JPT][hapmap]
rs11197012	1.00[JPT][hapmap]
rs11818115	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12098332	1.00[JPT][hapmap]
rs12218498	0.87[AFR][1000 genomes]
rs12265048	1.00[JPT][hapmap]
rs12269261	1.00[JPT][hapmap]
rs12415173	0.90[AFR][1000 genomes]
rs12761122	1.00[JPT][hapmap]
rs12764662	1.00[JPT][hapmap]
rs12765350	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12771956	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12772800	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12773943	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12775180	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1359079	0.91[YRI][hapmap];0.86[AFR][1000 genomes]
rs17092497	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17092542	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17586888	0.82[AFR][1000 genomes]
rs17663670	0.91[YRI][hapmap];0.85[AFR][1000 genomes]
rs17721283	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17721905	1.00[JPT][hapmap]
rs17794346	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17795212	1.00[JPT][hapmap]
rs1966384	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2105001	1.00[JPT][hapmap]
rs2146805	0.85[AFR][1000 genomes]
rs2146806	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2420065	0.88[AFR][1000 genomes]
rs2420066	0.88[AFR][1000 genomes]
rs2420067	0.91[YRI][hapmap];0.86[AFR][1000 genomes]
rs2420069	0.91[YRI][hapmap];0.86[AFR][1000 genomes]
rs3180654	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34064819	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34187191	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34683721	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35010779	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35622181	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35628210	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36036948	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36089581	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3758603	0.86[AFR][1000 genomes]
rs41284358	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55711292	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58587374	0.85[AFR][1000 genomes]
rs60820172	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61596353	0.84[AFR][1000 genomes]
rs61867965	0.87[AFR][1000 genomes]
rs61867966	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61867967	1.00[ASN][1000 genomes]
rs61868018	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6585309	1.00[JPT][hapmap]
rs6585310	1.00[JPT][hapmap]
rs6585311	1.00[JPT][hapmap]
rs68085797	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7071789	1.00[JPT][hapmap]
rs7071812	1.00[JPT][hapmap]
rs7072356	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7072364	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7074729	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7075888	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7079877	0.86[AFR][1000 genomes]
rs7089973	0.86[CEU][hapmap];1.00[JPT][hapmap]
rs7093674	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7094072	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7099565	1.00[JPT][hapmap]
rs7099590	1.00[JPT][hapmap]
rs7100026	1.00[JPT][hapmap]
rs749649	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7897937	0.92[YRI][hapmap];0.88[AFR][1000 genomes]
rs7898249	1.00[JPT][hapmap]
rs7903663	0.86[AFR][1000 genomes]
rs7904188	0.90[AFR][1000 genomes]
rs7904605	1.00[JPT][hapmap]
rs7908069	1.00[JPT][hapmap]
rs7908464	1.00[JPT][hapmap]
rs7909566	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7909657	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7914792	0.88[AFR][1000 genomes]
rs7918253	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7918388	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7919649	0.90[AFR][1000 genomes]
rs7920216	0.92[YRI][hapmap];0.90[AFR][1000 genomes]
rs7923295	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8181444	0.88[AFR][1000 genomes]
rs881192	1.00[JPT][hapmap]

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	nsv949138	chr10:116311531-116874477	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1038050	chr10:116315109-116895719	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv533027	chr10:116344641-116856352	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	esv3435429	chr10:116394152-117006347	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv831996	chr10:116601552-116772968	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs7895551	DCP1A	cis	Brain Pons	GTEx
rs7895551	TRUB1	Cis_1M	lymphoblastoid	RTeQTL
rs7895551	FAM160B1	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116589600-116626600	Weak transcription	Stomach Mucosa	stomach
2	chr10:116589600-116640600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:116590800-116625600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr10:116590800-116626400	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr10:116591000-116626600	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr10:116604800-116627200	Weak transcription	Small Intestine	intestine
7	chr10:116609600-116634800	Weak transcription	Spleen	Spleen
8	chr10:116609600-116639400	Weak transcription	Pancreas	Pancrea
9	chr10:116610200-116625600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr10:116610200-116634600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr10:116610400-116628000	Weak transcription	Esophagus	oesophagus
12	chr10:116610600-116628000	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr10:116611600-116641000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr10:116612400-116625800	Weak transcription	Brain Cingulate Gyrus	brain
15	chr10:116612800-116625600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr10:116612800-116626600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr10:116614000-116626200	Strong transcription	Primary hematopoietic stem cells	blood
18	chr10:116614400-116626200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr10:116614800-116628400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr10:116616800-116626400	Weak transcription	Brain Substantia Nigra	brain
21	chr10:116617000-116627400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr10:116617000-116630200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr10:116617400-116640600	Weak transcription	Fetal Intestine Small	intestine
24	chr10:116617600-116625600	Strong transcription	Adipose Nuclei	Adipose
25	chr10:116617800-116626000	Strong transcription	HSMM	muscle
26	chr10:116617800-116626400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr10:116618000-116626400	Strong transcription	Muscle Satellite Cultured Cells	--
28	chr10:116618200-116626000	Strong transcription	Osteobl	bone
29	chr10:116619200-116625600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr10:116619400-116626200	Weak transcription	Psoas Muscle	Psoas
31	chr10:116619400-116627200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr10:116619400-116627400	Weak transcription	Lung	lung
33	chr10:116619400-116634400	Weak transcription	Fetal Brain Male	brain
34	chr10:116619400-116636000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr10:116619400-116636400	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr10:116619400-116641600	Weak transcription	Aorta	Aorta
37	chr10:116619600-116627000	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr10:116619800-116629400	Weak transcription	Colon Smooth Muscle	Colon
39	chr10:116619800-116634800	Weak transcription	Fetal Brain Female	brain
40	chr10:116620600-116635000	Weak transcription	Fetal Stomach	stomach
41	chr10:116621200-116629800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr10:116621400-116626400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr10:116621400-116634800	Weak transcription	HepG2	liver
44	chr10:116621400-116636000	Weak transcription	Right Ventricle	heart
45	chr10:116621600-116628000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr10:116621600-116629400	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr10:116621800-116639600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr10:116621800-116639600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr10:116622000-116639200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr10:116622200-116627200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links