Variant report

Variant	rs1704916
Chromosome Location	chr12:104924173-104924174
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:104919275..104922640-chr12:104923988..104926677,3	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11613208	0.92[CEU][hapmap]
rs1553836	0.96[CEU][hapmap];0.88[CHD][hapmap];0.97[GIH][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1553839	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1625417	0.94[EUR][1000 genomes]
rs1626422	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1628116	0.96[CEU][hapmap];0.88[CHD][hapmap];0.97[GIH][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1704903	1.00[CEU][hapmap];0.98[TSI][hapmap];0.96[EUR][1000 genomes]
rs1704905	0.95[EUR][1000 genomes]
rs1704915	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1704917	0.96[CEU][hapmap];0.88[CHD][hapmap];0.97[GIH][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1704918	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.89[GIH][hapmap];0.87[LWK][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1704921	1.00[CEU][hapmap];0.81[GIH][hapmap];0.87[LWK][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs1704922	1.00[CEU][hapmap];0.81[GIH][hapmap];0.89[LWK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.85[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs1704923	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs1704924	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.89[GIH][hapmap];0.82[MEX][hapmap];0.98[TSI][hapmap];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1704925	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.89[GIH][hapmap];0.82[MEX][hapmap];0.98[TSI][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1704926	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.89[LWK][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1704927	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1704929	0.98[EUR][1000 genomes]
rs17812021	0.86[ASN][1000 genomes]
rs1795851	1.00[CEU][hapmap];0.81[GIH][hapmap];0.98[TSI][hapmap];0.98[EUR][1000 genomes]
rs1795852	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.89[GIH][hapmap];0.82[MEX][hapmap];0.98[TSI][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1795853	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.89[GIH][hapmap];0.82[MEX][hapmap];0.98[TSI][hapmap];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1795854	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.89[GIH][hapmap];0.87[LWK][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1795855	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.87[MEX][hapmap];0.98[TSI][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1795856	0.96[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];0.98[TSI][hapmap];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1795857	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.80[YRI][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1795859	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.87[MEX][hapmap];0.98[TSI][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1795861	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1795862	0.96[CEU][hapmap];0.86[GIH][hapmap];0.95[TSI][hapmap];0.97[EUR][1000 genomes]
rs1795864	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1795867	0.96[CEU][hapmap];0.88[CHD][hapmap];0.97[GIH][hapmap];0.83[MEX][hapmap];0.93[TSI][hapmap];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1795868	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1795870	0.96[CEU][hapmap];0.88[CHD][hapmap];0.97[GIH][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1795872	0.96[CEU][hapmap];0.88[CHD][hapmap];0.97[GIH][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1973589	0.96[CEU][hapmap];0.88[CHD][hapmap];0.97[GIH][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2055861	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.89[GIH][hapmap];0.89[LWK][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2665739	0.88[CHD][hapmap]
rs2665748	1.00[CEU][hapmap];0.98[TSI][hapmap];0.96[EUR][1000 genomes]
rs2706273	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs313325	0.88[CHD][hapmap]
rs6539159	0.92[CEU][hapmap]
rs7968613	0.92[CEU][hapmap]
rs907097	1.00[CHB][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[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	nsv832504	chr12:104853331-105028245	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs1704916	GOLGA2B	cis	parietal	SCAN
rs1704916	UTP20	cis	cerebellum	SCAN
rs1704916	KIAA1033	cis	cerebellum	SCAN

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104915600-104936600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:104917200-104925800	Weak transcription	Lung	lung
3	chr12:104917600-104924600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr12:104917800-104928200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr12:104918000-104934200	Weak transcription	A549	lung
6	chr12:104918200-104928200	Weak transcription	Osteobl	bone
7	chr12:104918200-104928400	Weak transcription	Ovary	ovary
8	chr12:104918400-104927400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr12:104918400-104928200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr12:104918600-104925400	Weak transcription	Spleen	Spleen
11	chr12:104918600-104926600	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr12:104918600-104926800	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr12:104918600-104927600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr12:104919200-104925600	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr12:104919200-104935000	Weak transcription	Primary T cells from cord blood	blood
16	chr12:104919400-104926000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr12:104919400-104928000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr12:104920000-104926400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr12:104920400-104927400	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr12:104920600-104926200	Weak transcription	Fetal Thymus	thymus
21	chr12:104920600-104929400	Weak transcription	Colon Smooth Muscle	Colon
22	chr12:104920800-104924200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
23	chr12:104920800-104926200	Strong transcription	Dnd41	blood
24	chr12:104921000-104929200	Weak transcription	Right Ventricle	heart
25	chr12:104921200-104927000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr12:104921200-104928000	Weak transcription	K562	blood
27	chr12:104921200-104928400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr12:104921400-104925400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr12:104921400-104926600	Weak transcription	Pancreas	Pancrea
30	chr12:104921400-104926800	Weak transcription	Fetal Heart	heart
31	chr12:104921400-104928000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr12:104921400-104928000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr12:104921400-104931600	Weak transcription	Gastric	stomach
34	chr12:104921400-104939000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr12:104921800-104925600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr12:104922200-104928400	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr12:104922400-104924200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr12:104922400-104925600	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr12:104923000-104927800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr12:104923000-104927800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr12:104923200-104926800	Weak transcription	HMEC	breast
42	chr12:104923200-104930200	Weak transcription	NHEK	skin
43	chr12:104923400-104926800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:104923400-104926800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr12:104923400-104928200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr12:104923400-104929800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr12:104923400-104930000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr12:104923600-104925400	Weak transcription	Primary hematopoietic stem cells	blood
49	chr12:104923600-104928000	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr12:104923800-104924400	Enhancers	Primary B cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links