Variant report

Variant	rs10151127
Chromosome Location	chr14:64494278-64494279
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10140978	0.91[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10146667	0.82[ASN][1000 genomes]
rs11844088	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11844628	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1255954	0.84[CEU][hapmap];0.81[TSI][hapmap]
rs1255959	0.84[CEU][hapmap]
rs1255960	0.87[CHD][hapmap]
rs1255961	0.87[CHD][hapmap]
rs1255965	0.91[CEU][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1255966	0.84[CEU][hapmap]
rs1255967	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs1255968	0.91[CHD][hapmap]
rs12586503	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1262240	0.84[CEU][hapmap]
rs1262241	0.83[ASN][1000 genomes]
rs1890907	0.81[ASN][1000 genomes]
rs1890908	0.91[CHD][hapmap]
rs2153477	0.81[ASN][1000 genomes]
rs2153478	0.81[ASN][1000 genomes]
rs2153481	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28572628	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28609254	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3829767	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs3866737	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4027402	0.91[CEU][hapmap];0.81[JPT][hapmap];0.85[TSI][hapmap]
rs4027404	0.91[CEU][hapmap];0.81[JPT][hapmap];0.85[TSI][hapmap];0.83[YRI][hapmap]
rs4027405	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4275767	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4462521	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4899131	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4902264	0.91[CEU][hapmap];0.86[GIH][hapmap];0.92[TSI][hapmap]
rs6573542	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6573544	0.83[ASN][1000 genomes]
rs7144722	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7147157	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7153376	0.83[ASN][1000 genomes]
rs7157594	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7158401	0.84[CEU][hapmap]
rs8010699	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs8010911	0.84[CEU][hapmap]
rs963289	0.84[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915909	chr14:63620440-64560369	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv902019	chr14:64395569-64882380	Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv456326	chr14:64420413-64754361	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv564905	chr14:64420413-64754361	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv902020	chr14:64434288-64506541	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv1821411	chr14:64488037-64506541	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64457000-64502000	Strong transcription	Placenta	Placenta
2	chr14:64457000-64519200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr14:64460000-64513400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr14:64460600-64495000	Weak transcription	NHDF-Ad	bronchial
5	chr14:64466600-64513200	Weak transcription	NHEK	skin
6	chr14:64466600-64593200	Weak transcription	Colon Smooth Muscle	Colon
7	chr14:64468800-64527200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr14:64469600-64518400	Weak transcription	HMEC	breast
9	chr14:64471800-64505200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr14:64473000-64515000	Weak transcription	Hela-S3	cervix
11	chr14:64474400-64505000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr14:64475200-64527200	Weak transcription	Fetal Heart	heart
13	chr14:64475600-64505600	Weak transcription	Esophagus	oesophagus
14	chr14:64475600-64518400	Weak transcription	Gastric	stomach
15	chr14:64479200-64526200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr14:64481400-64503000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:64481400-64574000	Weak transcription	Stomach Mucosa	stomach
18	chr14:64481600-64502400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr14:64482200-64500200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:64482400-64503800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr14:64482600-64496000	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr14:64482800-64503800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr14:64483800-64503800	Strong transcription	Primary T cells fromperipheralblood	blood
24	chr14:64484000-64503800	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr14:64484200-64500400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr14:64484400-64499200	Strong transcription	Primary T cells from cord blood	blood
27	chr14:64485800-64499000	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr14:64486000-64497800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr14:64486000-64503200	Strong transcription	Dnd41	blood
30	chr14:64486200-64501800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr14:64486800-64498600	Strong transcription	Duodenum Mucosa	Duodenum
32	chr14:64487000-64499200	Strong transcription	Rectal Mucosa Donor 29	rectum
33	chr14:64487200-64500400	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr14:64487400-64494600	Strong transcription	Rectal Mucosa Donor 31	rectum
35	chr14:64487400-64495600	Strong transcription	Fetal Intestine Large	intestine
36	chr14:64487400-64499000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr14:64487600-64498800	Strong transcription	HUES48 Cell Line	embryonic stem cell
38	chr14:64487800-64499200	Strong transcription	Liver	Liver
39	chr14:64487800-64501600	Weak transcription	NHLF	lung
40	chr14:64488000-64494800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
41	chr14:64488000-64495400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr14:64488000-64500200	Strong transcription	Left Ventricle	heart
43	chr14:64488400-64499000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
44	chr14:64488400-64500400	Strong transcription	Fetal Muscle Leg	muscle
45	chr14:64489000-64518400	Weak transcription	HUVEC	blood vessel
46	chr14:64489200-64500200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr14:64489200-64526600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr14:64489400-64568600	Weak transcription	Small Intestine	intestine
49	chr14:64490000-64515800	Weak transcription	Right Ventricle	heart
50	chr14:64490200-64499200	Strong transcription	Adipose Nuclei	Adipose

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