Variant report

Variant	rs1865746
Chromosome Location	chr10:52067350-52067351
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:52064687..52067489-chr10:52072620..52075726,3	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10825665	0.89[CEU][hapmap];0.82[JPT][hapmap]
rs10825729	0.94[CEU][hapmap];0.94[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10825740	0.90[CEU][hapmap];0.83[JPT][hapmap]
rs11005193	0.95[CEU][hapmap];0.80[CHB][hapmap];0.94[JPT][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2217899	0.95[CEU][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs2304443	0.82[YRI][hapmap]
rs2842096	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs7070330	0.94[CEU][hapmap];0.94[JPT][hapmap]
rs7078238	0.94[CEU][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs7092981	0.95[CEU][hapmap];0.80[CHB][hapmap];0.94[JPT][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7094121	0.94[CEU][hapmap];0.94[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7894586	0.95[CEU][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs7895250	0.95[CEU][hapmap];0.80[CHB][hapmap];0.88[JPT][hapmap];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv518071	chr10:51595893-52157935	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1054775	chr10:51595893-52392361	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv1053903	chr10:51886486-52163991	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv1040661	chr10:51886486-52164585	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1051028	chr10:51886486-52164585	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv1037118	chr10:51886486-52167442	Enhancers ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv1051087	chr10:51886486-52447295	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
8	nsv916214	chr10:51886486-52458983	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv918212	chr10:51886486-52465482	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
10	nsv817412	chr10:51911034-52432990	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
11	esv2830205	chr10:51978430-52135215	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
12	nsv1053293	chr10:51981959-52102649	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
13	nsv1046850	chr10:52009869-52135542	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
14	nsv540625	chr10:52009869-52135542	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
15	esv2762864	chr10:52030945-52107415	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
16	nsv521273	chr10:52051645-52197847	Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52055000-52069200	Weak transcription	Fetal Intestine Small	intestine
2	chr10:52055000-52069200	Weak transcription	HSMMtube	muscle
3	chr10:52059000-52068200	Weak transcription	Primary B cells from cord blood	blood
4	chr10:52061400-52080400	Weak transcription	Psoas Muscle	Psoas
5	chr10:52062200-52075000	Weak transcription	HUVEC	blood vessel
6	chr10:52062400-52070600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr10:52062600-52070200	Weak transcription	Small Intestine	intestine
8	chr10:52063000-52069200	Weak transcription	Fetal Stomach	stomach
9	chr10:52063200-52076600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr10:52064000-52073400	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr10:52064200-52070000	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr10:52064400-52069600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr10:52064600-52071400	Strong transcription	Liver	Liver
14	chr10:52064600-52073000	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr10:52064800-52067800	Weak transcription	Hela-S3	cervix
16	chr10:52064800-52068600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr10:52064800-52070600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:52065000-52069000	Weak transcription	Brain Angular Gyrus	brain
19	chr10:52065000-52069400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr10:52065000-52070600	Weak transcription	Colon Smooth Muscle	Colon
21	chr10:52065000-52072800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr10:52065000-52072800	Weak transcription	HepG2	liver
23	chr10:52065000-52081600	Weak transcription	Stomach Mucosa	stomach
24	chr10:52065200-52067400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr10:52065200-52067600	Weak transcription	Spleen	Spleen
26	chr10:52065200-52068200	Weak transcription	A549	lung
27	chr10:52065200-52069200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr10:52065200-52069600	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr10:52065200-52069600	Weak transcription	NHLF	lung
30	chr10:52065200-52070200	Weak transcription	Fetal Kidney	kidney
31	chr10:52065200-52070200	Weak transcription	NH-A	brain
32	chr10:52065200-52070600	Weak transcription	Esophagus	oesophagus
33	chr10:52065200-52070600	Weak transcription	Fetal Brain Male	brain
34	chr10:52065200-52072400	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr10:52065200-52073000	Weak transcription	Fetal Thymus	thymus
36	chr10:52065200-52076800	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr10:52065400-52067600	Weak transcription	Thymus	Thymus
38	chr10:52065400-52068200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr10:52065400-52069400	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr10:52065400-52071200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr10:52065400-52073000	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr10:52065400-52073000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr10:52065400-52077000	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr10:52065600-52068200	Strong transcription	K562	blood
45	chr10:52065600-52071200	Strong transcription	Fetal Lung	lung
46	chr10:52065600-52071400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr10:52065600-52075000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr10:52065800-52071200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr10:52066000-52069200	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr10:52066200-52070600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links