Variant report

Variant	rs2580769
Chromosome Location	chr2:55214618-55214619
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:55198988..55201900-chr2:55213351..55214997,2	MCF-7	breast:
2	chr2:55205322..55208790-chr2:55211251..55214642,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000115310	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10189094	0.86[YRI][hapmap]
rs10460507	0.82[TSI][hapmap]
rs13031431	1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs17046579	0.91[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs17046586	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs17046589	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1822617	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2255026	0.81[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.93[ASN][1000 genomes]
rs2255393	0.85[CHB][hapmap]
rs2580768	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2580770	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2580771	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2588513	0.81[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap]
rs2588515	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2588516	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2588522	1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs2919126	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2920859	0.81[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs2920892	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2968788	0.81[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs2972063	0.89[ASN][1000 genomes]
rs2972092	0.81[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs34352825	0.92[ASN][1000 genomes]
rs34378852	0.93[ASN][1000 genomes]
rs34928331	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35981204	0.89[ASN][1000 genomes]
rs4672003	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6545464	0.81[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs6545465	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6715980	0.81[ASW][hapmap];0.83[LWK][hapmap];0.81[MKK][hapmap];0.89[YRI][hapmap]
rs6734314	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6739210	0.81[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.96[ASN][1000 genomes]
rs72795434	0.93[ASN][1000 genomes]
rs7355716	0.84[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834069	chr2:55096597-55251680	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv874155	chr2:55205262-55307646	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2580769	PPP1R1C	trans	parietal	SCAN

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55184800-55214800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:55191800-55234200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr2:55193400-55214800	Strong transcription	HepG2	liver
4	chr2:55195000-55215200	Strong transcription	Dnd41	blood
5	chr2:55195800-55216200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:55196200-55226400	Weak transcription	Thymus	Thymus
7	chr2:55196600-55217200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:55196600-55217200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:55198200-55237200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:55198600-55215200	Weak transcription	Lung	lung
11	chr2:55198800-55215200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:55200800-55216600	Weak transcription	Colonic Mucosa	Colon
13	chr2:55203800-55222600	Weak transcription	Spleen	Spleen
14	chr2:55203800-55223800	Weak transcription	Pancreas	Pancrea
15	chr2:55203800-55258400	Weak transcription	Esophagus	oesophagus
16	chr2:55204200-55214800	Strong transcription	Fetal Thymus	thymus
17	chr2:55205200-55220600	Weak transcription	Small Intestine	intestine
18	chr2:55205200-55223800	Weak transcription	Left Ventricle	heart
19	chr2:55205600-55214800	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr2:55205800-55216000	Weak transcription	Fetal Intestine Small	intestine
21	chr2:55206400-55214800	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr2:55206600-55214800	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:55206600-55215200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
24	chr2:55206800-55214800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:55207600-55214800	Strong transcription	K562	blood
26	chr2:55207600-55215200	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr2:55207800-55214800	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr2:55207800-55214800	Strong transcription	Fetal Intestine Large	intestine
29	chr2:55207800-55215200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr2:55208000-55214800	Strong transcription	Primary B cells from peripheral blood	blood
31	chr2:55208200-55216600	Weak transcription	Stomach Mucosa	stomach
32	chr2:55208400-55215000	Strong transcription	Primary B cells from cord blood	blood
33	chr2:55210000-55214800	Genic enhancers	NHDF-Ad	bronchial
34	chr2:55210000-55228200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr2:55210600-55214800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr2:55210600-55214800	Genic enhancers	A549	lung
37	chr2:55210800-55216000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr2:55211000-55214800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr2:55211000-55218600	Weak transcription	Aorta	Aorta
40	chr2:55211200-55214800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr2:55211200-55232000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr2:55211400-55214800	Genic enhancers	NHLF	lung
43	chr2:55211600-55214800	Strong transcription	Duodenum Mucosa	Duodenum
44	chr2:55211600-55215400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr2:55211800-55214800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:55211800-55215000	Strong transcription	Liver	Liver
47	chr2:55212000-55214800	Strong transcription	GM12878-XiMat	blood
48	chr2:55212000-55216000	Weak transcription	Fetal Heart	heart
49	chr2:55212200-55214800	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chr2:55212200-55214800	Strong transcription	HSMMtube	muscle

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