Variant report

Variant	rs28796021
Chromosome Location	chr14:64088869-64088870
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:64086921..64089569-chr14:64107307..64109779,2	K562	blood:
2	chr14:64008866..64010910-chr14:64088046..64091397,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000140006	Chromatin interaction
ENSG00000261242	Chromatin interaction
ENSG00000154001	Chromatin interaction

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10083359	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10083535	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10131964	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10132382	0.83[EUR][1000 genomes]
rs10133598	1.00[CHB][hapmap];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10133932	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10137182	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10137805	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10137908	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[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];1.00[ASN][1000 genomes]
rs10137933	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10144435	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10144827	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10148637	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10148797	1.00[CHB][hapmap];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10149710	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10149737	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10149828	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10150009	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10162453	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10498509	1.00[CHB][hapmap];0.96[EUR][1000 genomes]
rs11158505	0.81[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11847188	1.00[CEU][hapmap]
rs11847332	1.00[CEU][hapmap]
rs12323694	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1255792	0.83[ASN][1000 genomes]
rs1262228	0.83[ASN][1000 genomes]
rs17101315	1.00[CEU][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];0.88[TSI][hapmap];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17101326	1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs17101328	1.00[CHB][hapmap];0.96[EUR][1000 genomes]
rs2236339	1.00[CEU][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];0.81[TSI][hapmap];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28373566	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28575623	0.95[ASN][1000 genomes]
rs28590010	0.96[EUR][1000 genomes]
rs28633552	0.83[EUR][1000 genomes]
rs28707240	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28733391	0.96[EUR][1000 genomes]
rs28778590	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28821865	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4420451	0.96[EUR][1000 genomes]
rs55659518	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58485817	0.95[ASN][1000 genomes]
rs60269901	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60327717	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61984037	0.91[ASN][1000 genomes]
rs61984047	0.95[ASN][1000 genomes]
rs61985684	0.91[ASN][1000 genomes]
rs6573525	0.83[EUR][1000 genomes]
rs6573526	1.00[CEU][hapmap];1.00[MEX][hapmap]
rs7142943	0.87[ASN][1000 genomes]
rs7145740	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs7146546	1.00[MEX][hapmap]
rs7148726	0.83[ASN][1000 genomes]
rs7148824	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7152052	1.00[CEU][hapmap];1.00[MEX][hapmap]
rs7154057	1.00[CEU][hapmap];1.00[MEX][hapmap]
rs7154795	1.00[CEU][hapmap];1.00[MEX][hapmap]
rs7155345	1.00[CEU][hapmap]
rs7155351	1.00[CEU][hapmap]
rs7156289	0.87[ASN][1000 genomes]
rs7156393	0.87[ASN][1000 genomes]
rs73263604	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73263616	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73263627	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73280637	0.87[ASN][1000 genomes]
rs73280645	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73280662	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73280667	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73280672	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7359072	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7359073	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs74056152	0.87[ASN][1000 genomes]
rs74056153	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs74056154	0.83[EUR][1000 genomes]
rs8006499	1.00[CEU][hapmap]
rs8007512	0.87[ASN][1000 genomes]
rs8009516	0.95[ASN][1000 genomes]
rs8012130	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8012691	0.83[EUR][1000 genomes]
rs8012866	1.00[CEU][hapmap]
rs8018580	1.00[CEU][hapmap];1.00[MEX][hapmap]
rs8020691	1.00[CEU][hapmap]
rs8020821	0.90[CHD][hapmap];1.00[JPT][hapmap]
rs8022456	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520528	chr14:63400786-64157117	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS 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	49 gene(s)	inside rSNPs	diseases
2	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
3	nsv1048645	chr14:64057327-64283872	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv528691	chr14:64068806-64098555	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64062000-64108000	Weak transcription	Spleen	Spleen
2	chr14:64062200-64107600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr14:64062600-64107000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr14:64062800-64105400	Weak transcription	Hela-S3	cervix
5	chr14:64063200-64092800	Weak transcription	Aorta	Aorta
6	chr14:64063400-64098600	Weak transcription	Small Intestine	intestine
7	chr14:64066200-64097400	Weak transcription	Gastric	stomach
8	chr14:64066200-64099400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr14:64066200-64107600	Weak transcription	Pancreas	Pancrea
10	chr14:64066400-64099400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr14:64066600-64092800	Weak transcription	Duodenum Mucosa	Duodenum
12	chr14:64066600-64093600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr14:64066600-64096200	Weak transcription	K562	blood
14	chr14:64066600-64099400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr14:64066600-64107400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr14:64066600-64107600	Weak transcription	Stomach Smooth Muscle	stomach
17	chr14:64066600-64107800	Weak transcription	Fetal Kidney	kidney
18	chr14:64067000-64107400	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr14:64067200-64096000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr14:64067200-64107800	Weak transcription	HSMMtube	muscle
21	chr14:64067800-64100400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr14:64068200-64100800	Weak transcription	Fetal Intestine Large	intestine
23	chr14:64068200-64105600	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr14:64068200-64107800	Weak transcription	Ovary	ovary
25	chr14:64069000-64098400	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr14:64069000-64107600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr14:64069200-64107600	Weak transcription	Left Ventricle	heart
28	chr14:64070800-64107600	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr14:64071000-64089200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr14:64072000-64100800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr14:64075800-64107400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:64080000-64090600	Weak transcription	Primary hematopoietic stem cells	blood
33	chr14:64082000-64093600	Weak transcription	Brain Anterior Caudate	brain
34	chr14:64082000-64098400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr14:64082000-64102400	Weak transcription	HMEC	breast
36	chr14:64082000-64107200	Weak transcription	HSMM	muscle
37	chr14:64082000-64107800	Weak transcription	Brain Substantia Nigra	brain
38	chr14:64082200-64090600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr14:64082200-64092400	Weak transcription	Brain Hippocampus Middle	brain
40	chr14:64082200-64096000	Weak transcription	Brain Angular Gyrus	brain
41	chr14:64082200-64100600	Weak transcription	NH-A	brain
42	chr14:64082200-64102200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr14:64082400-64095800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr14:64082400-64107600	Weak transcription	NHEK	skin
45	chr14:64082400-64107600	Weak transcription	Osteobl	bone
46	chr14:64082400-64107800	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr14:64082600-64089400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr14:64082600-64100600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr14:64082800-64089000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr14:64082800-64089600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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