Variant report

Variant	rs12774725
Chromosome Location	chr10:22897321-22897322
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	chr10:22878706..22881547-chr10:22895040..22897400,2	MCF-7	breast:
2	chr10:22894884..22897373-chr10:22931733..22933332,2	K562	blood:

Variant related genes	Relation type
ENSG00000150867	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10764339	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10764344	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs10828323	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10828324	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10828325	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10828328	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs11013052	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11013059	0.89[ASN][1000 genomes]
rs11013066	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11013067	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11013068	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11013077	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11013082	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs11013091	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs1171490	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1171492	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1171497	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1171503	0.88[CEU][hapmap];1.00[CHB][hapmap]
rs1171504	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs1171506	0.88[CEU][hapmap];1.00[CHB][hapmap]
rs1171509	0.87[CEU][hapmap];1.00[CHB][hapmap]
rs12246676	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12253847	1.00[CHB][hapmap]
rs12354766	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12356117	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12357289	0.83[CEU][hapmap];1.00[CHB][hapmap]
rs12357384	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs12357444	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12358560	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12360229	0.96[ASN][1000 genomes]
rs12360495	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12765474	0.96[ASN][1000 genomes]
rs12770214	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12772257	0.96[ASN][1000 genomes]
rs1326340	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1343504	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1409393	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1409395	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1614387	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1750747	0.80[CEU][hapmap]
rs1750748	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1750775	0.80[CEU][hapmap]
rs1750777	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1778334	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1778335	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1778338	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1778339	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1778340	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1778342	0.88[CEU][hapmap]
rs1778345	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1778346	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1778347	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2031620	0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2154053	0.80[CEU][hapmap]
rs2559534	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2798981	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs34786070	0.85[ASN][1000 genomes]
rs35885150	0.89[ASN][1000 genomes]
rs7071306	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs73598577	0.81[AFR][1000 genomes]
rs7912132	0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7917130	0.92[ASN][1000 genomes]
rs7917460	1.00[ASN][1000 genomes]
rs7921549	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs943196	0.88[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs943197	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs943198	0.85[ASN][1000 genomes]
rs9645524	1.00[JPT][hapmap];0.92[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1830947	chr10:22881196-23004381	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:22844200-22904800	Weak transcription	Rectal Smooth Muscle	rectum
2	chr10:22856600-22899200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr10:22858200-22904000	Weak transcription	Colonic Mucosa	Colon
4	chr10:22862400-22902000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr10:22880000-22906800	Weak transcription	Colon Smooth Muscle	Colon
6	chr10:22883200-22899200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr10:22887200-22902400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr10:22888800-22898000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr10:22888800-22905000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr10:22889400-22904400	Weak transcription	Hela-S3	cervix
11	chr10:22891000-22901400	Weak transcription	Gastric	stomach
12	chr10:22891000-22904800	Weak transcription	Right Ventricle	heart
13	chr10:22891200-22904800	Weak transcription	NHLF	lung
14	chr10:22891600-22897600	Weak transcription	Left Ventricle	heart
15	chr10:22893600-22897800	Weak transcription	Fetal Lung	lung
16	chr10:22893600-22902000	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr10:22894000-22898800	Weak transcription	Spleen	Spleen
18	chr10:22894000-22902600	Weak transcription	Right Atrium	heart
19	chr10:22894000-22906600	Weak transcription	Ovary	ovary
20	chr10:22894200-22898400	Weak transcription	Small Intestine	intestine
21	chr10:22894200-22904600	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr10:22894600-22897600	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr10:22894600-22899000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr10:22894600-22903000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr10:22894600-22904400	Weak transcription	NHDF-Ad	bronchial
26	chr10:22894600-22904600	Weak transcription	NHEK	skin
27	chr10:22894600-22905000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr10:22894800-22899400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr10:22894800-22904600	Weak transcription	Adipose Nuclei	Adipose
30	chr10:22894800-22913000	Weak transcription	Fetal Kidney	kidney
31	chr10:22895200-22897400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr10:22895200-22898400	Genic enhancers	Brain Anterior Caudate	brain
33	chr10:22895200-22899200	Genic enhancers	Primary T cells fromperipheralblood	blood
34	chr10:22895400-22898200	Genic enhancers	Brain Inferior Temporal Lobe	brain
35	chr10:22895400-22899400	Genic enhancers	Brain Hippocampus Middle	brain
36	chr10:22895400-22904600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr10:22895600-22897400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr10:22895600-22898000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr10:22895600-22898600	Strong transcription	Thymus	Thymus
40	chr10:22895600-22899400	Weak transcription	HepG2	liver
41	chr10:22895600-22901000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr10:22895600-22902000	Weak transcription	Pancreas	Pancrea
43	chr10:22895600-22902200	Weak transcription	Placenta	Placenta
44	chr10:22895600-22906000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr10:22895800-22899000	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr10:22895800-22900200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr10:22895800-22904600	Weak transcription	HUVEC	blood vessel
48	chr10:22895800-22904800	Weak transcription	NH-A	brain
49	chr10:22896000-22897800	Strong transcription	Aorta	Aorta
50	chr10:22896000-22898000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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