Variant report

Variant	rs9805042
Chromosome Location	chr12:1893170-1893171
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:1769289..1772102-chr12:1891359..1893235,3	K562	blood:
2	chr12:1888574..1891262-chr12:1892199..1893915,2	MCF-7	breast:
3	chr12:1769289..1772614-chr12:1889825..1893235,5	K562	blood:
4	chr12:1890411..1894703-chr12:1895509..1898196,4	K562	blood:
5	chr12:1892244..1894703-chr12:1895509..1898196,2	K562	blood:

Variant related genes	Relation type
ENSG00000006831	Chromatin interaction
ENSG00000266043	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1058322	0.83[ASN][1000 genomes]
rs10734999	1.00[CHB][hapmap];0.94[CHD][hapmap]
rs10735000	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10744548	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10744549	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10744550	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10773979	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs10773981	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10773987	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10848554	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10848568	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11832522	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11836547	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs12296831	0.89[EUR][1000 genomes]
rs12370189	0.85[CHB][hapmap]
rs1468491	0.91[CEU][hapmap];0.93[EUR][1000 genomes]
rs16928751	0.91[CEU][hapmap];0.93[EUR][1000 genomes]
rs1860054	0.93[EUR][1000 genomes]
rs1860055	0.93[EUR][1000 genomes]
rs2058112	0.91[CEU][hapmap];0.93[TSI][hapmap];0.89[EUR][1000 genomes]
rs2286380	0.90[CEU][hapmap];0.93[EUR][1000 genomes]
rs35854772	0.93[EUR][1000 genomes]
rs4140993	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs4766414	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57216374	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57414925	0.91[EUR][1000 genomes]
rs60523400	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs66673051	0.93[EUR][1000 genomes]
rs67365540	0.93[EUR][1000 genomes]
rs67405160	0.93[EUR][1000 genomes]
rs67567175	0.93[EUR][1000 genomes]
rs703176	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7132184	0.91[CEU][hapmap];0.93[EUR][1000 genomes]
rs7134070	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs7138701	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs7302234	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs73040178	0.93[EUR][1000 genomes]
rs73040720	0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73041873	0.88[EUR][1000 genomes]
rs7311218	1.00[CHB][hapmap]
rs7316374	0.91[CEU][hapmap];0.93[EUR][1000 genomes]
rs7488369	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.94[ASN][1000 genomes]
rs767870	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7963224	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7967137	0.91[CEU][hapmap];0.93[EUR][1000 genomes]
rs7975375	0.91[CEU][hapmap];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9805109	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9888418	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042863	chr12:1163817-1902302	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
2	nsv541345	chr12:1163817-1902302	Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv832305	chr12:1769852-1936054	Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv948480	chr12:1776217-2284333	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv832306	chr12:1847726-2001308	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv1038425	chr12:1857052-1902302	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv430442	chr12:1889823-1982151	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
8	nsv556996	chr12:1891372-1934920	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9805042	ANO2	cis	cerebellum	SCAN

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1816200-1897400	Weak transcription	Aorta	Aorta
2	chr12:1849800-1905600	Weak transcription	Small Intestine	intestine
3	chr12:1850400-1904800	Weak transcription	Fetal Kidney	kidney
4	chr12:1857200-1893400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr12:1862000-1894800	Weak transcription	Colonic Mucosa	Colon
6	chr12:1868200-1901800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr12:1878600-1897800	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr12:1879000-1904800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr12:1880600-1894600	Weak transcription	Esophagus	oesophagus
10	chr12:1881600-1897400	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr12:1881600-1897600	Strong transcription	Dnd41	blood
12	chr12:1881600-1897800	Strong transcription	Fetal Thymus	thymus
13	chr12:1882000-1898200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:1882400-1896000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr12:1882600-1904800	Weak transcription	Stomach Mucosa	stomach
16	chr12:1885200-1904600	Weak transcription	Fetal Brain Male	brain
17	chr12:1885400-1897800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr12:1885400-1898000	Strong transcription	Primary T cells from cord blood	blood
19	chr12:1885600-1895200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr12:1885600-1897600	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr12:1885600-1902600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr12:1885800-1896600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr12:1885800-1904000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr12:1886000-1894600	Weak transcription	Pancreas	Pancrea
25	chr12:1886000-1904200	Weak transcription	Rectal Smooth Muscle	rectum
26	chr12:1886000-1905000	Weak transcription	Fetal Brain Female	brain
27	chr12:1886200-1897800	Strong transcription	Primary T cells fromperipheralblood	blood
28	chr12:1886200-1905400	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr12:1886800-1897200	Strong transcription	Primary B cells from peripheral blood	blood
30	chr12:1886800-1897600	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr12:1886800-1897800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr12:1887000-1896800	Strong transcription	Primary T helper cells fromperipheralblood	blood
33	chr12:1887000-1897400	Strong transcription	Primary B cells from cord blood	blood
34	chr12:1887000-1897600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr12:1887000-1897800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr12:1887200-1905000	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr12:1887600-1896400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr12:1887800-1899000	Strong transcription	Duodenum Mucosa	Duodenum
39	chr12:1888000-1897800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:1888600-1893200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr12:1888800-1894600	Weak transcription	HSMM	muscle
42	chr12:1889200-1894600	Weak transcription	HMEC	breast
43	chr12:1889200-1904800	Weak transcription	Right Atrium	heart
44	chr12:1889400-1893200	Weak transcription	Stomach Smooth Muscle	stomach
45	chr12:1889400-1897400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr12:1889400-1904200	Weak transcription	Brain Germinal Matrix	brain
47	chr12:1889600-1893400	Strong transcription	Fetal Intestine Large	intestine
48	chr12:1889600-1898000	Strong transcription	GM12878-XiMat	blood
49	chr12:1889600-1904000	Weak transcription	Colon Smooth Muscle	Colon
50	chr12:1889600-1905000	Weak transcription	Muscle Satellite Cultured Cells	--

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