Variant report

Variant	rs61926194
Chromosome Location	chr12:32759076-32759077
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs61926163	0.81[EUR][1000 genomes]
rs61926164	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61926168	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61926169	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61926170	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61926171	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61926172	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61926173	0.81[EUR][1000 genomes]
rs61926174	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61926176	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61926186	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61926187	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61926188	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61926189	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61926190	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61926191	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61926192	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61926193	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61926195	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62642552	1.00[EUR][1000 genomes]
rs74072673	0.81[EUR][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	nsv531960	chr12:32257285-32775277	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32713000-32780400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr12:32713400-32796200	Weak transcription	Fetal Lung	lung
3	chr12:32715200-32760200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr12:32720000-32764800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:32720200-32778400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr12:32722600-32764800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr12:32722600-32764800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr12:32722600-32764800	Weak transcription	Psoas Muscle	Psoas
9	chr12:32722600-32779400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr12:32725200-32778600	Weak transcription	Fetal Brain Male	brain
11	chr12:32733200-32764800	Weak transcription	Esophagus	oesophagus
12	chr12:32735400-32765000	Weak transcription	Small Intestine	intestine
13	chr12:32736200-32764000	Weak transcription	Brain Germinal Matrix	brain
14	chr12:32736400-32760200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr12:32739600-32760200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr12:32739800-32764600	Weak transcription	NHLF	lung
17	chr12:32741200-32762000	Weak transcription	Right Ventricle	heart
18	chr12:32741600-32761200	Weak transcription	Brain Anterior Caudate	brain
19	chr12:32741800-32769600	Weak transcription	Stomach Mucosa	stomach
20	chr12:32742000-32764800	Weak transcription	Spleen	Spleen
21	chr12:32742400-32765600	Weak transcription	Primary B cells from peripheral blood	blood
22	chr12:32743800-32764600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr12:32744200-32797600	Weak transcription	Fetal Heart	heart
24	chr12:32744800-32762000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:32744800-32765000	Weak transcription	Brain Substantia Nigra	brain
26	chr12:32745000-32764400	Weak transcription	Lung	lung
27	chr12:32747200-32760600	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr12:32749000-32764200	Weak transcription	Stomach Smooth Muscle	stomach
29	chr12:32749000-32764800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr12:32750000-32762200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr12:32750000-32765000	Strong transcription	Adipose Nuclei	Adipose
32	chr12:32750000-32770400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr12:32752000-32762000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr12:32753000-32774200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr12:32754200-32795200	Weak transcription	Primary B cells from cord blood	blood
36	chr12:32754600-32766800	Weak transcription	NH-A	brain
37	chr12:32754800-32764600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr12:32755000-32760000	Weak transcription	Aorta	Aorta
39	chr12:32755000-32760200	Weak transcription	Fetal Muscle Leg	muscle
40	chr12:32755000-32762000	Weak transcription	Left Ventricle	heart
41	chr12:32755000-32764800	Weak transcription	Colonic Mucosa	Colon
42	chr12:32755000-32775800	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr12:32755200-32762200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr12:32755400-32760400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr12:32755400-32760800	Weak transcription	Fetal Brain Female	brain
46	chr12:32755400-32800600	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr12:32755600-32759400	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr12:32755600-32764400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr12:32755600-32764600	Weak transcription	Brain Hippocampus Middle	brain
50	chr12:32755600-32765200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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