Variant report

Variant	rs10773981
Chromosome Location	chr12:1816712-1816713
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:1815296..1817227-chr12:1871744..1873347,2	MCF-7	breast:
2	chr12:1815063..1817215-chr12:1824872..1827970,3	K562	blood:
3	chr12:1799438..1802227-chr12:1816513..1818304,2	MCF-7	breast:
4	chr12:1814191..1816713-chr12:1818333..1820469,2	K562	blood:

Variant related genes	Relation type
ENSG00000006831	Chromatin interaction

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

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

rs_ID	r²[population]
rs1058322	0.83[ASN][1000 genomes]
rs10735000	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10744548	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10744549	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10744550	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10773979	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10773987	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10848554	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10848568	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11832522	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12296831	0.81[EUR][1000 genomes]
rs2058112	0.81[EUR][1000 genomes]
rs4766414	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57216374	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs60523400	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61518726	0.81[ASN][1000 genomes]
rs703176	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73040720	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7488369	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs767870	0.96[ASN][1000 genomes]
rs7963224	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7975375	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9805042	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9805109	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9888418	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[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	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

No data

Chromatin state (count:90 , 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	chr12:1807400-1819200	Weak transcription	Primary T cells from cord blood	blood
16	chr12:1807400-1822000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr12:1807400-1823400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr12:1807600-1821600	Weak transcription	Ovary	ovary
19	chr12:1807800-1817400	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr12:1808200-1820400	Weak transcription	Fetal Lung	lung
21	chr12:1808200-1820400	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr12:1808400-1830800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr12:1810600-1819800	Weak transcription	Fetal Intestine Small	intestine
24	chr12:1811200-1816800	Enhancers	HepG2	liver
25	chr12:1812400-1817000	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr12:1812600-1817000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr12:1812600-1819400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:1813200-1819400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr12:1813200-1823400	Weak transcription	Left Ventricle	heart
30	chr12:1813400-1819200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr12:1813800-1816800	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr12:1813800-1816800	Enhancers	A549	lung
33	chr12:1813800-1817800	Enhancers	Brain Substantia Nigra	brain
34	chr12:1814000-1816800	Enhancers	Adipose Nuclei	Adipose
35	chr12:1814400-1825400	Weak transcription	Colon Smooth Muscle	Colon
36	chr12:1814800-1818400	Enhancers	Brain Hippocampus Middle	brain
37	chr12:1815200-1817000	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr12:1815200-1817000	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr12:1815200-1817000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr12:1815200-1823800	Weak transcription	HSMM	muscle
41	chr12:1815200-1827800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr12:1815400-1816800	Enhancers	NHLF	lung
43	chr12:1815400-1817000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:1815400-1817000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:1815600-1817600	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr12:1815800-1816800	Enhancers	Primary B cells from cord blood	blood
47	chr12:1815800-1816800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr12:1815800-1817000	Enhancers	Primary T cells fromperipheralblood	blood
49	chr12:1816000-1816800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr12:1816000-1817000	Enhancers	Duodenum Smooth Muscle	Duodenum

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