Variant report

Variant	rs12369985
Chromosome Location	chr12:62918780-62918781
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:62914778..62916591-chr12:62918347..62920592,2	K562	blood:
2	chr12:62918451..62921309-chr12:62921578..62923186,2	MCF-7	breast:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10877855	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10877856	1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10877857	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10877859	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10877862	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10877864	1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10877870	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11174487	1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11174494	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11174495	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11174496	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11174498	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11174504	1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11174514	1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11174517	1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11174518	1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11174527	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11174537	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11174557	1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11174568	0.82[EUR][1000 genomes]
rs11174569	0.82[EUR][1000 genomes]
rs11174571	1.00[CHB][hapmap];0.82[EUR][1000 genomes]
rs11174575	1.00[CHB][hapmap]
rs11520127	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11613132	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11614022	1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11614822	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12367878	1.00[CHB][hapmap]
rs12369751	1.00[CHB][hapmap]
rs12369961	1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12370404	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17716977	1.00[CHB][hapmap]
rs17731893	1.00[CHB][hapmap]
rs17732089	1.00[CHB][hapmap];0.80[EUR][1000 genomes]
rs17732182	1.00[CHB][hapmap]
rs2270732	1.00[CHB][hapmap]
rs7301016	1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7302094	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7302456	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7303825	1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73124315	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73141014	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73141045	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7962519	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7975109	1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530690	chr12:62678463-62999462	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv899158	chr12:62783967-62937259	Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv899159	chr12:62783967-62945245	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv821671	chr12:62794304-63007964	Strong transcription ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
5	nsv469418	chr12:62893199-62959137	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
6	nsv559156	chr12:62893199-62959137	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
7	esv3390559	chr12:62902734-62920842	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62863200-62937400	Weak transcription	Pancreas	Pancrea
2	chr12:62863600-62926400	Weak transcription	Colon Smooth Muscle	Colon
3	chr12:62866600-62953200	Weak transcription	Psoas Muscle	Psoas
4	chr12:62871800-62926200	Weak transcription	Fetal Brain Male	brain
5	chr12:62876000-62937400	Weak transcription	Gastric	stomach
6	chr12:62889200-62949600	Weak transcription	Small Intestine	intestine
7	chr12:62894400-62926200	Weak transcription	NH-A	brain
8	chr12:62897600-62931000	Weak transcription	K562	blood
9	chr12:62897600-62944000	Weak transcription	Esophagus	oesophagus
10	chr12:62898000-62923400	Weak transcription	NHDF-Ad	bronchial
11	chr12:62902400-62929200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr12:62902600-62926600	Weak transcription	Stomach Smooth Muscle	stomach
13	chr12:62902600-62927000	Weak transcription	Colonic Mucosa	Colon
14	chr12:62903600-62918800	Weak transcription	Osteobl	bone
15	chr12:62903600-62926200	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr12:62903600-62926200	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr12:62903600-62926200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr12:62903600-62949800	Weak transcription	NHEK	skin
19	chr12:62903800-62924400	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr12:62903800-62926200	Weak transcription	Hela-S3	cervix
21	chr12:62904400-62926200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr12:62904600-62926200	Weak transcription	HMEC	breast
23	chr12:62904600-62927000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr12:62904600-62929200	Weak transcription	HUVEC	blood vessel
25	chr12:62905400-62926600	Weak transcription	HSMMtube	muscle
26	chr12:62906400-62943800	Weak transcription	Aorta	Aorta
27	chr12:62906600-62931600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr12:62906800-62926200	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr12:62906800-62927400	Weak transcription	Brain Germinal Matrix	brain
30	chr12:62907000-62926800	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr12:62907000-62927800	Weak transcription	Lung	lung
32	chr12:62907000-62931000	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr12:62907000-62987200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr12:62907400-62940200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr12:62908200-62926200	Weak transcription	Primary hematopoietic stem cells	blood
36	chr12:62908200-62927600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr12:62908400-62931000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr12:62908800-62926200	Weak transcription	Fetal Lung	lung
39	chr12:62908800-62927400	Weak transcription	Left Ventricle	heart
40	chr12:62909000-62927200	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr12:62909000-62927200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr12:62909200-62926000	Weak transcription	Dnd41	blood
43	chr12:62909200-62926200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr12:62909400-62923400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr12:62909400-62927400	Weak transcription	Fetal Kidney	kidney
46	chr12:62910600-62927000	Weak transcription	Fetal Brain Female	brain
47	chr12:62911400-62944000	Weak transcription	Spleen	Spleen
48	chr12:62911600-62925000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr12:62911800-62930400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr12:62912400-62918800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links