Variant report

Variant	rs712065
Chromosome Location	chr1:224696628-224696629
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10753474	0.84[CEU][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10916628	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10916629	0.87[EUR][1000 genomes]
rs10916630	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10916631	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10916632	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12093242	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12140117	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12140906	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12141016	0.85[ASN][1000 genomes]
rs12141708	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12142949	0.89[EUR][1000 genomes]
rs12566578	1.00[CEU][hapmap];0.94[CHB][hapmap];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16847945	0.90[JPT][hapmap]
rs1891243	0.83[CHB][hapmap]
rs1891244	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2648743	0.92[EUR][1000 genomes]
rs3738367	0.91[EUR][1000 genomes]
rs4294381	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs4653589	1.00[CEU][hapmap];0.94[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];0.81[MEX][hapmap];0.95[TSI][hapmap];0.95[EUR][1000 genomes]
rs59319739	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61825792	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6426133	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6665956	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6688146	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6695773	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6699035	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs712066	0.94[CEU][hapmap];0.94[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];0.81[MEX][hapmap];0.95[TSI][hapmap];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7541723	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7541917	0.88[EUR][1000 genomes]
rs7545252	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7550648	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs791504	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8868	chr1:224383023-224752531	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv1014717	chr1:224551939-224885543	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv535311	chr1:224551939-224885543	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs712065	BPNT1	cis	parietal	SCAN
rs712065	CNIH3	cis	cerebellum	SCAN

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224690000-224699400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:224690000-224702000	Enhancers	Liver	Liver
3	chr1:224690200-224697200	Weak transcription	Gastric	stomach
4	chr1:224691800-224698400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr1:224692000-224697000	Weak transcription	GM12878-XiMat	blood
6	chr1:224692000-224697400	Weak transcription	Fetal Stomach	stomach
7	chr1:224692000-224697400	Enhancers	HepG2	liver
8	chr1:224692000-224698400	Weak transcription	HSMM	muscle
9	chr1:224692000-224698400	Weak transcription	HSMMtube	muscle
10	chr1:224692000-224701600	Weak transcription	Fetal Lung	lung
11	chr1:224692400-224697800	Weak transcription	Placenta	Placenta
12	chr1:224692400-224701600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr1:224692600-224697000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr1:224692600-224697200	Weak transcription	Fetal Thymus	thymus
15	chr1:224692600-224697200	Weak transcription	Stomach Mucosa	stomach
16	chr1:224692600-224697400	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr1:224692600-224698800	Weak transcription	Stomach Smooth Muscle	stomach
18	chr1:224692600-224700600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr1:224693000-224697200	Weak transcription	Lung	lung
20	chr1:224693000-224697200	Weak transcription	Dnd41	blood
21	chr1:224693000-224698400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr1:224693200-224697000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr1:224693200-224697200	Weak transcription	K562	blood
24	chr1:224693600-224699200	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr1:224694200-224697200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:224694200-224704000	Weak transcription	Right Atrium	heart
27	chr1:224694200-224717600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:224694200-224727600	Weak transcription	Brain Anterior Caudate	brain
29	chr1:224694400-224697000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:224694400-224697200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr1:224694400-224697200	Weak transcription	NHLF	lung
32	chr1:224694400-224697400	Weak transcription	Fetal Muscle Trunk	muscle
33	chr1:224694400-224697800	Weak transcription	Esophagus	oesophagus
34	chr1:224694400-224697800	Weak transcription	Osteobl	bone
35	chr1:224694400-224698400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr1:224694400-224698400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:224694600-224697000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr1:224694600-224697200	Weak transcription	NHEK	skin
39	chr1:224694600-224697400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:224694600-224697800	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr1:224694800-224697000	Weak transcription	Adipose Nuclei	Adipose
42	chr1:224695000-224697000	Weak transcription	Colonic Mucosa	Colon
43	chr1:224695000-224697200	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr1:224695200-224698600	Enhancers	Fetal Intestine Large	intestine
45	chr1:224695200-224699000	Enhancers	NHDF-Ad	bronchial
46	chr1:224695800-224697000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr1:224695800-224697400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:224695800-224697400	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr1:224695800-224697800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr1:224695800-224698400	Weak transcription	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links