Variant report

Variant	rs1255896
Chromosome Location	chr14:64444876-64444877
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10149728	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10498512	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10873172	0.87[CEU][hapmap];0.80[CHB][hapmap]
rs11623650	0.89[EUR][1000 genomes]
rs12147217	0.82[CHB][hapmap]
rs1255856	0.88[EUR][1000 genomes]
rs1255857	0.80[EUR][1000 genomes]
rs1255867	0.97[EUR][1000 genomes]
rs1255869	0.97[EUR][1000 genomes]
rs1255872	0.97[EUR][1000 genomes]
rs1255873	0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1255874	0.97[EUR][1000 genomes]
rs1255875	0.97[EUR][1000 genomes]
rs1255876	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1255877	0.96[EUR][1000 genomes]
rs1255878	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1255879	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1255880	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1255881	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1255882	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1255883	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1255885	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1255887	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1255890	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1255891	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1255892	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1255900	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1255901	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1255902	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1255903	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1255905	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1255908	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1262235	0.93[EUR][1000 genomes]
rs1262237	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1266870	0.97[EUR][1000 genomes]
rs1270526	0.97[EUR][1000 genomes]
rs1271567	0.96[CEU][hapmap];1.00[CHB][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1272156	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1272714	0.92[EUR][1000 genomes]
rs1273192	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12878653	0.83[EUR][1000 genomes]
rs2184292	0.89[EUR][1000 genomes]
rs2357175	0.89[EUR][1000 genomes]
rs2357176	0.81[EUR][1000 genomes]
rs2792201	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28483877	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2884111	0.89[EUR][1000 genomes]
rs2994421	0.97[EUR][1000 genomes]
rs2994422	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35224808	0.86[EUR][1000 genomes]
rs61984073	0.88[EUR][1000 genomes]
rs7156570	0.89[EUR][1000 genomes]
rs8009321	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9323442	0.91[EUR][1000 genomes]
rs9323443	0.89[EUR][1000 genomes]
rs945027	0.97[EUR][1000 genomes]
rs945028	0.97[EUR][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	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	nsv1038825	chr14:64109441-64491720	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	esv1793389	chr14:64346190-64457224	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	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

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64395000-64491000	Weak transcription	Psoas Muscle	Psoas
2	chr14:64416800-64458600	Weak transcription	Gastric	stomach
3	chr14:64417000-64459200	Weak transcription	NHEK	skin
4	chr14:64417000-64466000	Weak transcription	Colon Smooth Muscle	Colon
5	chr14:64417200-64458600	Weak transcription	Esophagus	oesophagus
6	chr14:64417400-64466200	Weak transcription	Right Ventricle	heart
7	chr14:64417600-64459200	Weak transcription	Pancreas	Pancrea
8	chr14:64418000-64463000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr14:64418200-64450800	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr14:64418400-64458600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr14:64419000-64463000	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr14:64419200-64489000	Weak transcription	Small Intestine	intestine
13	chr14:64419400-64448200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr14:64419400-64459000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr14:64419400-64459200	Weak transcription	HMEC	breast
16	chr14:64420000-64458000	Weak transcription	Colonic Mucosa	Colon
17	chr14:64420200-64459000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr14:64420600-64462600	Weak transcription	HUVEC	blood vessel
19	chr14:64421600-64466000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr14:64423800-64463000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr14:64428400-64459400	Weak transcription	Aorta	Aorta
22	chr14:64429600-64458000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr14:64431000-64458200	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr14:64431200-64463800	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr14:64431200-64464800	Weak transcription	Stomach Mucosa	stomach
26	chr14:64432400-64452600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr14:64432600-64453200	Weak transcription	Duodenum Mucosa	Duodenum
28	chr14:64432800-64457200	Weak transcription	Fetal Thymus	thymus
29	chr14:64433400-64448600	Weak transcription	Fetal Muscle Leg	muscle
30	chr14:64433400-64465800	Weak transcription	Fetal Heart	heart
31	chr14:64434800-64458600	Weak transcription	Lung	lung
32	chr14:64435200-64448600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr14:64435200-64457600	Weak transcription	Adipose Nuclei	Adipose
34	chr14:64435200-64458200	Weak transcription	Fetal Muscle Trunk	muscle
35	chr14:64435200-64471800	Weak transcription	Hela-S3	cervix
36	chr14:64435400-64453200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr14:64435400-64463600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr14:64435600-64452800	Weak transcription	Brain Germinal Matrix	brain
39	chr14:64437600-64449800	Strong transcription	Dnd41	blood
40	chr14:64438200-64446200	Weak transcription	Fetal Intestine Small	intestine
41	chr14:64438400-64452800	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr14:64439200-64465600	Weak transcription	Rectal Smooth Muscle	rectum
43	chr14:64439600-64462800	Weak transcription	Fetal Brain Male	brain
44	chr14:64439800-64445600	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr14:64439800-64467800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr14:64440000-64457200	Weak transcription	Fetal Brain Female	brain
47	chr14:64440400-64450000	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr14:64440800-64466000	Weak transcription	Primary B cells from peripheral blood	blood
49	chr14:64440800-64480400	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr14:64441000-64451600	Strong transcription	Placenta	Placenta

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