Variant report

Variant	rs2726908
Chromosome Location	chr11:108732609-108732610
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:108728605..108731193-chr11:108732068..108735115,3	K562	blood:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10502103	0.80[ASN][1000 genomes]
rs12574721	0.81[ASN][1000 genomes]
rs12574758	0.82[ASN][1000 genomes]
rs12577382	0.81[ASN][1000 genomes]
rs12785398	0.80[ASN][1000 genomes]
rs12794597	0.80[ASN][1000 genomes]
rs12802313	0.81[ASN][1000 genomes]
rs12808674	0.82[ASN][1000 genomes]
rs1365046	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1365047	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1365048	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1462787	0.80[AFR][1000 genomes]
rs17108703	0.80[ASN][1000 genomes]
rs2042677	0.94[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2042678	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2553751	0.80[ASN][1000 genomes]
rs2553754	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2553757	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2553758	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2553760	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2553761	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2615756	0.83[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs2726907	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2726910	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2726911	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2726913	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2726914	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2726915	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2726916	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2726919	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2726920	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34350110	0.81[ASN][1000 genomes]
rs34354308	0.81[ASN][1000 genomes]
rs35244070	0.81[ASN][1000 genomes]
rs35430545	0.82[ASN][1000 genomes]
rs57014838	0.80[ASN][1000 genomes]
rs71489925	0.81[ASN][1000 genomes]
rs898972	0.81[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	nsv1052254	chr11:108122683-108845008	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv541164	chr11:108122683-108845008	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv898386	chr11:108409442-108831875	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv898389	chr11:108724639-108891986	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108707600-108740800	Weak transcription	HMEC	breast
2	chr11:108710200-108735800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr11:108710200-108738200	Weak transcription	Gastric	stomach
4	chr11:108715400-108738200	Weak transcription	K562	blood
5	chr11:108721600-108742200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:108723600-108733200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr11:108725000-108736600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr11:108725000-108737000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:108725000-108739600	Weak transcription	A549	lung
10	chr11:108725000-108740000	Weak transcription	NHDF-Ad	bronchial
11	chr11:108725000-108741000	Weak transcription	HSMMtube	muscle
12	chr11:108725000-108741400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr11:108725400-108734200	Weak transcription	Fetal Intestine Small	intestine
14	chr11:108725400-108737200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr11:108725400-108738400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr11:108725400-108740600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:108725400-108740800	Weak transcription	NHEK	skin
18	chr11:108725400-108741000	Weak transcription	Brain Angular Gyrus	brain
19	chr11:108725600-108733600	Weak transcription	Primary hematopoietic stem cells	blood
20	chr11:108725600-108733800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr11:108725800-108740000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr11:108726000-108732800	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr11:108726000-108733600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr11:108726200-108733600	Weak transcription	GM12878-XiMat	blood
25	chr11:108726200-108740400	Weak transcription	Primary B cells from cord blood	blood
26	chr11:108726200-108768400	Weak transcription	Primary B cells from peripheral blood	blood
27	chr11:108728400-108735600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:108728400-108810600	Weak transcription	Left Ventricle	heart
29	chr11:108728600-108741000	Weak transcription	Primary T cells from cord blood	blood
30	chr11:108729400-108735600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:108729800-108737200	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr11:108730000-108733600	Weak transcription	Dnd41	blood
33	chr11:108730000-108737000	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr11:108730000-108740400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr11:108730600-108733600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:108730600-108735800	Weak transcription	NH-A	brain
37	chr11:108730800-108735600	Weak transcription	Osteobl	bone
38	chr11:108731400-108734200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links