Variant report

Variant	rs2728704
Chromosome Location	chr12:32442805-32442806
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1151038	0.82[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1151039	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1151045	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs155201	0.84[ASN][1000 genomes]
rs161979	0.84[ASN][1000 genomes]
rs161980	0.84[ASN][1000 genomes]
rs161981	0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs185487	0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs2129590	0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs2594000	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs261868	0.84[ASN][1000 genomes]
rs261869	0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs261870	0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs261874	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs261875	0.95[CEU][hapmap];0.85[CHB][hapmap];0.86[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs261876	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs261877	1.00[CEU][hapmap];0.86[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2632344	0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs2632359	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs2650137	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2728705	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2728800	0.85[ASN][1000 genomes]
rs708225	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs708226	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs708227	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs751720	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs753296	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs792473	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs792474	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs792861	0.90[ASN][1000 genomes]
rs792863	0.82[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs792866	0.88[ASN][1000 genomes]
rs806784	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs813784	0.87[CEU][hapmap];0.80[AMR][1000 genomes]
rs814243	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs901598	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531960	chr12:32257285-32775277	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	esv2751096	chr12:32280340-32702784	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv558171	chr12:32287259-32559693	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription 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	13 gene(s)	inside rSNPs	diseases
4	nsv832366	chr12:32328559-32511360	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32426600-32443400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr12:32426800-32443200	Weak transcription	NH-A	brain
3	chr12:32426800-32446800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr12:32427000-32443400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr12:32427000-32458600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr12:32427000-32459400	Weak transcription	Aorta	Aorta
7	chr12:32427000-32463000	Weak transcription	NHLF	lung
8	chr12:32427200-32463000	Weak transcription	Fetal Intestine Small	intestine
9	chr12:32427400-32445200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr12:32427600-32454400	Weak transcription	Primary B cells from cord blood	blood
11	chr12:32434800-32443000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:32435200-32448200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr12:32438200-32443200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr12:32438200-32443200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr12:32438200-32443200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr12:32438200-32449600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr12:32438800-32443200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr12:32438800-32443400	Weak transcription	Ovary	ovary
19	chr12:32438800-32449600	Weak transcription	Fetal Brain Female	brain
20	chr12:32439600-32443000	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr12:32439800-32443200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr12:32439800-32447000	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr12:32440000-32443400	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr12:32440200-32443200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:32440200-32458600	Weak transcription	Thymus	Thymus
26	chr12:32441000-32448800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr12:32442400-32451800	Weak transcription	Primary B cells from peripheral blood	blood
28	chr12:32442800-32443000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr12:32442800-32443200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr12:32442800-32443600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr12:32442800-32443800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr12:32442800-32443800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr12:32442800-32443800	Enhancers	HSMMtube	muscle
34	chr12:32442800-32443800	Enhancers	Osteobl	bone
35	chr12:32442800-32444000	Enhancers	A549	lung
36	chr12:32442800-32444000	Enhancers	K562	blood
37	chr12:32442800-32444200	Enhancers	Hela-S3	cervix

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