Variant report

Variant	rs16929850
Chromosome Location	chr12:26144849-26144850
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs16929805	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs16929965	0.88[CHB][hapmap];0.91[CHD][hapmap];0.90[GIH][hapmap];1.00[YRI][hapmap]
rs2048608	1.00[CEU][hapmap];0.83[TSI][hapmap];0.94[EUR][1000 genomes]
rs2172912	0.90[CHB][hapmap];1.00[YRI][hapmap]
rs58597112	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs59714345	0.94[EUR][1000 genomes]
rs61914180	0.92[EUR][1000 genomes]
rs61914181	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61914182	0.92[EUR][1000 genomes]
rs61914183	0.92[EUR][1000 genomes]
rs61914184	0.92[EUR][1000 genomes]
rs61914186	0.94[EUR][1000 genomes]
rs61914187	0.94[EUR][1000 genomes]
rs61914211	0.94[EUR][1000 genomes]
rs61914212	0.94[EUR][1000 genomes]
rs61914216	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61914242	0.81[ASN][1000 genomes]
rs61914243	0.83[ASN][1000 genomes]
rs61914244	0.81[ASN][1000 genomes]
rs61914245	0.83[ASN][1000 genomes]
rs7962900	0.85[ASN][1000 genomes]
rs7963582	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7965337	0.92[EUR][1000 genomes]
rs7965449	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758300	chr12:25992331-26161116	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
2	esv2759886	chr12:25992331-26161116	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
3	nsv898931	chr12:26123345-26192936	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv522351	chr12:26127230-26149703	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv983482	chr12:26142257-26146356	Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26117600-26150000	Weak transcription	Hela-S3	cervix
2	chr12:26131000-26145400	Weak transcription	Lung	lung
3	chr12:26131000-26146000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr12:26131000-26146200	Weak transcription	HSMM	muscle
5	chr12:26132400-26146800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr12:26133000-26145200	Weak transcription	NH-A	brain
7	chr12:26133000-26145200	Weak transcription	Osteobl	bone
8	chr12:26134200-26148000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr12:26134400-26145400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr12:26134400-26145400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr12:26134400-26147800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr12:26138400-26146800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr12:26138800-26145400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr12:26139200-26145200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr12:26139200-26147400	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr12:26139400-26146000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr12:26139400-26150600	Weak transcription	Brain Angular Gyrus	brain
18	chr12:26139600-26145800	Weak transcription	Brain Substantia Nigra	brain
19	chr12:26139600-26160000	Weak transcription	Pancreas	Pancrea
20	chr12:26139800-26145000	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr12:26139800-26146800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr12:26140200-26145400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr12:26140200-26145600	Weak transcription	Aorta	Aorta
24	chr12:26140200-26147600	Weak transcription	Ovary	ovary
25	chr12:26141800-26146800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr12:26142000-26145200	Weak transcription	Fetal Lung	lung
27	chr12:26142000-26149000	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr12:26142200-26145000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr12:26142200-26145000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr12:26142200-26145200	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr12:26142200-26145400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr12:26142200-26145600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr12:26142200-26145600	Weak transcription	Stomach Smooth Muscle	stomach
34	chr12:26142200-26146400	Weak transcription	Brain Cingulate Gyrus	brain
35	chr12:26142200-26146400	Weak transcription	Brain Hippocampus Middle	brain
36	chr12:26142200-26146400	Weak transcription	Fetal Stomach	stomach
37	chr12:26142200-26155600	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr12:26142400-26145400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr12:26142800-26145400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr12:26142800-26145400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr12:26143200-26145000	Weak transcription	Rectal Smooth Muscle	rectum
42	chr12:26143800-26147400	Enhancers	Brain Anterior Caudate	brain
43	chr12:26143800-26151200	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr12:26143800-26151200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr12:26144000-26151200	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr12:26144000-26151600	Enhancers	Colon Smooth Muscle	Colon
47	chr12:26144400-26145400	Enhancers	HUVEC	blood vessel
48	chr12:26144400-26145800	Enhancers	Right Atrium	heart
49	chr12:26144400-26146000	Enhancers	Right Ventricle	heart
50	chr12:26144400-26146200	Enhancers	Left Ventricle	heart

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