Variant report

Variant	rs11061940
Chromosome Location	chr12:1822392-1822393
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:1805073..1809008-chr12:1822212..1826429,4	K562	blood:
2	chr12:1817051..1819015-chr12:1820770..1822956,2	K562	blood:
3	chr12:1817233..1819242-chr12:1821456..1823051,3	K562	blood:

Variant related genes	Relation type
ENSG00000271500	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1029629	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10773982	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10773986	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10773989	0.84[ASN][1000 genomes]
rs10848553	0.82[AMR][1000 genomes]
rs10848558	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10848569	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11061919	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11061920	0.82[AMR][1000 genomes]
rs11061921	0.82[AMR][1000 genomes]
rs11061923	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11061924	0.82[AMR][1000 genomes]
rs11061925	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11061927	0.82[AMR][1000 genomes]
rs11061937	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11061957	0.85[AMR][1000 genomes]
rs11061962	0.87[AMR][1000 genomes]
rs11061968	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11061974	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1136213	0.82[AMR][1000 genomes]
rs11614639	0.86[ASN][1000 genomes]
rs11832817	0.85[AMR][1000 genomes]
rs12230579	0.85[AMR][1000 genomes]
rs12231894	0.87[AMR][1000 genomes]
rs12342	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12582624	0.87[AMR][1000 genomes]
rs12810020	0.87[AMR][1000 genomes]
rs12812707	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12813694	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12828908	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12831353	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2058034	0.82[AMR][1000 genomes]
rs2058035	0.82[AMR][1000 genomes]
rs2068485	0.86[ASN][1000 genomes]
rs2240613	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2286385	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2370055	0.83[AMR][1000 genomes]
rs34375871	0.87[AMR][1000 genomes]
rs3809266	0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4766413	0.80[AMR][1000 genomes]
rs6489323	0.83[AMR][1000 genomes]
rs6489324	0.87[AMR][1000 genomes]
rs66590925	0.87[AMR][1000 genomes]
rs7132033	0.82[AMR][1000 genomes]
rs7297509	0.87[AMR][1000 genomes]
rs7313760	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7975826	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7978818	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs929434	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	nsv1045312	chr12:1805856-1843202	Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv3446685	chr12:1819204-1825021	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1801600-1823400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr12:1801600-1827800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr12:1801800-1823800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr12:1801800-1828200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr12:1801800-1830800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr12:1802200-1822800	Weak transcription	Thymus	Thymus
7	chr12:1802400-1822800	Weak transcription	Fetal Thymus	thymus
8	chr12:1802400-1823000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr12:1802400-1824600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr12:1802400-1841200	Weak transcription	HMEC	breast
11	chr12:1806000-1840000	Weak transcription	Spleen	Spleen
12	chr12:1806200-1823400	Weak transcription	Dnd41	blood
13	chr12:1806200-1844400	Weak transcription	NHEK	skin
14	chr12:1807200-1847400	Weak transcription	Fetal Stomach	stomach
15	chr12:1807400-1823400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr12:1808400-1830800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr12:1813200-1823400	Weak transcription	Left Ventricle	heart
18	chr12:1814400-1825400	Weak transcription	Colon Smooth Muscle	Colon
19	chr12:1815200-1823800	Weak transcription	HSMM	muscle
20	chr12:1815200-1827800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr12:1816200-1825200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr12:1816200-1825400	Weak transcription	Osteobl	bone
23	chr12:1816200-1836400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr12:1816200-1849400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr12:1816200-1857800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr12:1816200-1866400	Weak transcription	Esophagus	oesophagus
27	chr12:1816200-1897400	Weak transcription	Aorta	Aorta
28	chr12:1816400-1823000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr12:1816400-1824600	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr12:1816400-1825200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr12:1816400-1840200	Weak transcription	Colonic Mucosa	Colon
32	chr12:1816400-1841400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr12:1816400-1841400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr12:1816600-1827600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr12:1816600-1846200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr12:1816800-1822800	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr12:1816800-1823800	Weak transcription	Primary B cells from cord blood	blood
38	chr12:1816800-1825400	Weak transcription	A549	lung
39	chr12:1817000-1823400	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr12:1817000-1823600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr12:1817000-1824600	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr12:1817000-1825200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr12:1817000-1835200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr12:1817000-1856600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:1818400-1822600	Enhancers	HepG2	liver
46	chr12:1819200-1822400	Enhancers	Psoas Muscle	Psoas
47	chr12:1819200-1826600	Enhancers	Stomach Mucosa	stomach
48	chr12:1819200-1833800	Enhancers	Liver	Liver
49	chr12:1819800-1822400	Enhancers	Right Atrium	heart
50	chr12:1819800-1827200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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