Variant report

Variant	rs9944097
Chromosome Location	chr14:78069472-78069473
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:78065290..78070188-chr14:78072894..78075904,4	K562	blood:
2	chr14:78069297..78071425-chr14:78081435..78083020,2	K562	blood:
3	chr14:78064498..78067393-chr14:78068632..78070407,3	K562	blood:
4	chr14:78068423..78071899-chr14:78079739..78082860,4	K562	blood:
5	chr14:78069363..78073512-chr14:78081398..78084592,5	MCF-7	breast:
6	chr14:78063987..78068208-chr14:78069326..78072935,4	MCF-7	breast:
7	chr14:78059041..78061902-chr14:78067196..78069981,2	K562	blood:

Variant related genes	Relation type
ENSG00000100596	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10129280	0.81[CHB][hapmap]
rs10139059	0.81[CHB][hapmap]
rs10139852	0.83[ASN][1000 genomes]
rs10140195	1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10148189	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10873309	0.81[CHB][hapmap];0.88[CHD][hapmap]
rs11626349	0.83[CHD][hapmap]
rs12432164	0.92[ASN][1000 genomes]
rs12587835	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13379058	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs176897	0.92[ASN][1000 genomes]
rs176898	0.92[ASN][1000 genomes]
rs176901	1.00[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs176903	1.00[CHB][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs176907	0.90[ASN][1000 genomes]
rs1990806	0.90[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2267746	0.81[CHB][hapmap]
rs2267747	0.81[CHB][hapmap]
rs2267748	0.81[CHB][hapmap]
rs2267749	0.81[CHB][hapmap]
rs2267750	0.81[CHB][hapmap];0.88[CHD][hapmap]
rs2299921	0.81[CHB][hapmap];0.88[CHD][hapmap]
rs2299922	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2299924	0.81[CHB][hapmap];0.85[CHD][hapmap]
rs2299927	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2299928	0.81[CHB][hapmap];0.88[CHD][hapmap]
rs2299929	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28460392	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28472502	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs58598324	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7144314	0.91[CEU][hapmap];0.84[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];0.82[TSI][hapmap]
rs7157536	0.93[ASN][1000 genomes]
rs7158771	0.95[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	nsv832835	chr14:77906706-78095207	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1053810	chr14:77987871-78148320	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv1051554	chr14:78004196-78122980	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9944097	POMT2	cis	cerebellum	SCAN

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78021800-78071600	Weak transcription	Colon Smooth Muscle	Colon
2	chr14:78047400-78070000	Weak transcription	Fetal Brain Male	brain
3	chr14:78051400-78070200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr14:78051600-78072600	Weak transcription	Psoas Muscle	Psoas
5	chr14:78055000-78081600	Weak transcription	Right Ventricle	heart
6	chr14:78056600-78072800	Weak transcription	Placenta	Placenta
7	chr14:78056800-78070000	Weak transcription	Gastric	stomach
8	chr14:78057400-78070000	Weak transcription	Spleen	Spleen
9	chr14:78057600-78081400	Weak transcription	Rectal Smooth Muscle	rectum
10	chr14:78061600-78070000	Weak transcription	Esophagus	oesophagus
11	chr14:78061800-78069800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr14:78062200-78070200	Weak transcription	Ovary	ovary
13	chr14:78062800-78075000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr14:78063200-78070000	Weak transcription	Brain Germinal Matrix	brain
15	chr14:78063200-78077800	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr14:78063400-78069800	Weak transcription	Liver	Liver
17	chr14:78063400-78070000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr14:78063400-78070200	Weak transcription	Fetal Muscle Trunk	muscle
19	chr14:78063400-78070200	Weak transcription	Fetal Thymus	thymus
20	chr14:78063400-78081600	Weak transcription	Fetal Stomach	stomach
21	chr14:78063600-78069600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr14:78063600-78070200	Weak transcription	Stomach Smooth Muscle	stomach
23	chr14:78063800-78071800	Weak transcription	Fetal Lung	lung
24	chr14:78063800-78072000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr14:78063800-78074000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr14:78063800-78074200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:78064600-78070600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr14:78065200-78070200	Weak transcription	Fetal Intestine Large	intestine
29	chr14:78065400-78069600	Weak transcription	NHDF-Ad	bronchial
30	chr14:78065400-78070000	Weak transcription	Lung	lung
31	chr14:78065400-78071800	Weak transcription	Thymus	Thymus
32	chr14:78065600-78081400	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr14:78065800-78070200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr14:78065800-78070200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr14:78065800-78071800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr14:78066000-78071600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr14:78066000-78079600	Weak transcription	Dnd41	blood
38	chr14:78066200-78069600	Weak transcription	Brain Angular Gyrus	brain
39	chr14:78066200-78070200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr14:78066400-78069800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr14:78066600-78069600	Weak transcription	Primary B cells from cord blood	blood
42	chr14:78066600-78069800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr14:78066600-78070200	Weak transcription	GM12878-XiMat	blood
44	chr14:78066600-78071600	Weak transcription	Fetal Heart	heart
45	chr14:78066600-78074200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr14:78066800-78069600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr14:78066800-78069600	Weak transcription	HMEC	breast
48	chr14:78066800-78069600	Weak transcription	K562	blood
49	chr14:78066800-78069600	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr14:78066800-78070000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links