Variant report

Variant	rs17095858
Chromosome Location	chr12:45798732-45798733
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10736025	1.00[CEU][hapmap]
rs12578337	1.00[TSI][hapmap]
rs12578638	1.00[TSI][hapmap]
rs17095779	1.00[CEU][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17095781	1.00[CEU][hapmap];0.92[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17095830	0.92[MKK][hapmap];1.00[TSI][hapmap]
rs17095835	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17095855	0.85[AMR][1000 genomes]
rs17095860	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17095861	1.00[CEU][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17095862	1.00[CEU][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17095868	0.91[LWK][hapmap];0.80[MKK][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes]
rs17095871	0.91[YRI][hapmap];0.91[AFR][1000 genomes]
rs17095884	1.00[CEU][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17095890	1.00[CEU][hapmap];0.83[JPT][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17095914	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17121366	0.91[ASN][1000 genomes]
rs3803177	1.00[CEU][hapmap];0.83[JPT][hapmap];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs41338444	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4512918	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57056104	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57160874	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57455310	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58028140	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58152224	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58213849	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58940403	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60794282	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61276164	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61351713	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61484865	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7138332	0.92[MKK][hapmap];1.00[TSI][hapmap]
rs7296058	1.00[CEU][hapmap]
rs74081808	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74081818	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs74081821	1.00[EUR][1000 genomes];0.94[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	nsv1050923	chr12:45581310-45808289	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:45744800-45809200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:45752200-45803800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr12:45752200-45809200	Weak transcription	Small Intestine	intestine
4	chr12:45759000-45805200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr12:45759200-45822600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr12:45764400-45802800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr12:45764400-45821000	Weak transcription	Brain Cingulate Gyrus	brain
8	chr12:45764600-45815400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr12:45772600-45815400	Weak transcription	K562	blood
10	chr12:45773400-45803800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr12:45774800-45811400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr12:45778800-45803400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr12:45780400-45829800	Weak transcription	Brain Anterior Caudate	brain
14	chr12:45780800-45802000	Weak transcription	Right Ventricle	heart
15	chr12:45783200-45818800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr12:45783400-45826400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr12:45783600-45799800	Weak transcription	HepG2	liver
18	chr12:45786000-45799800	Weak transcription	Primary hematopoietic stem cells	blood
19	chr12:45786000-45800800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr12:45786200-45801000	Weak transcription	Psoas Muscle	Psoas
21	chr12:45786200-45801200	Weak transcription	Spleen	Spleen
22	chr12:45786200-45805400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr12:45786200-45806200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr12:45786200-45809200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:45786400-45806200	Weak transcription	Esophagus	oesophagus
26	chr12:45786600-45803600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr12:45786600-45803800	Weak transcription	Gastric	stomach
28	chr12:45786600-45806000	Weak transcription	Ovary	ovary
29	chr12:45786600-45827000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr12:45792000-45799800	Strong transcription	Skeletal Muscle Female	skeletal muscle
31	chr12:45792000-45828600	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr12:45792200-45802000	Strong transcription	Adipose Nuclei	Adipose
33	chr12:45792600-45800200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr12:45792600-45822600	Weak transcription	Colonic Mucosa	Colon
35	chr12:45792600-45827000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr12:45792800-45811800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr12:45793000-45803200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr12:45793000-45827600	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr12:45794000-45801000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr12:45794200-45807400	Strong transcription	A549	lung
41	chr12:45794200-45823200	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr12:45794400-45800000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:45794400-45807400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:45794600-45798800	Strong transcription	Primary T cells from cord blood	blood
45	chr12:45794600-45803000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr12:45794600-45804400	Strong transcription	HMEC	breast
47	chr12:45794600-45806800	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr12:45794600-45809200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr12:45794600-45812200	Weak transcription	Fetal Brain Male	brain
50	chr12:45794800-45807600	Strong transcription	HUES64 Cell Line	embryonic stem cell

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