Variant report

Variant	rs12581815
Chromosome Location	chr12:1853316-1853317
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:1838787..1840977-chr12:1852855..1855148,3	K562	blood:
2	chr12:1846841..1849389-chr12:1852680..1854549,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10848566	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11061918	0.92[ASN][1000 genomes]
rs11061935	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11061946	0.90[ASN][1000 genomes]
rs11061952	0.90[ASN][1000 genomes]
rs11061956	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11061962	0.83[ASN][1000 genomes]
rs11061967	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11061973	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11833054	0.85[ASN][1000 genomes]
rs12230440	0.81[AFR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12231894	0.83[ASN][1000 genomes]
rs12579507	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12582624	0.81[ASN][1000 genomes]
rs12810020	0.81[ASN][1000 genomes]
rs12821401	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16928704	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2058033	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34375871	0.83[ASN][1000 genomes]
rs4766413	0.81[ASN][1000 genomes]
rs66590925	0.83[ASN][1000 genomes]
rs71454839	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7297509	0.81[ASN][1000 genomes]
rs73040715	0.88[ASN][1000 genomes]
rs73040736	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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	nsv832304	chr12:1710249-1868642	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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

No data

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1816200-1857800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr12:1816200-1866400	Weak transcription	Esophagus	oesophagus
3	chr12:1816200-1897400	Weak transcription	Aorta	Aorta
4	chr12:1817000-1856600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:1823000-1866600	Weak transcription	Gastric	stomach
6	chr12:1824000-1866600	Weak transcription	HSMM	muscle
7	chr12:1825200-1855400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr12:1826000-1885400	Weak transcription	NH-A	brain
9	chr12:1828600-1855800	Weak transcription	Fetal Intestine Large	intestine
10	chr12:1831400-1857800	Weak transcription	Lung	lung
11	chr12:1836800-1855400	Weak transcription	Primary hematopoietic stem cells	blood
12	chr12:1837000-1861600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr12:1837200-1855400	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr12:1840800-1854000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr12:1840800-1855600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr12:1842400-1854200	Weak transcription	Dnd41	blood
17	chr12:1845600-1885200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:1847600-1854200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr12:1847600-1857800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr12:1847600-1863800	Weak transcription	Ovary	ovary
21	chr12:1847600-1885200	Weak transcription	Right Atrium	heart
22	chr12:1849800-1855400	Weak transcription	Left Ventricle	heart
23	chr12:1849800-1868400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr12:1849800-1868800	Weak transcription	Pancreas	Pancrea
25	chr12:1849800-1905600	Weak transcription	Small Intestine	intestine
26	chr12:1850000-1856800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr12:1850000-1866600	Weak transcription	Fetal Lung	lung
28	chr12:1850200-1854000	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr12:1850200-1855600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr12:1850200-1856000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr12:1850200-1856000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr12:1850200-1856600	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr12:1850200-1865800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr12:1850200-1885200	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr12:1850400-1855800	Weak transcription	Fetal Intestine Small	intestine
36	chr12:1850400-1856200	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr12:1850400-1863400	Weak transcription	Fetal Stomach	stomach
38	chr12:1850400-1870400	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr12:1850400-1904800	Weak transcription	Fetal Kidney	kidney
40	chr12:1850600-1854200	Weak transcription	Primary T cells from cord blood	blood
41	chr12:1850600-1854400	Weak transcription	NHDF-Ad	bronchial
42	chr12:1850600-1856000	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr12:1850800-1854200	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr12:1850800-1855600	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr12:1850800-1863400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr12:1850800-1863400	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr12:1850800-1885200	Weak transcription	Right Ventricle	heart
48	chr12:1851000-1854200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr12:1851000-1854200	Weak transcription	A549	lung
50	chr12:1851000-1854400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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