Variant report

Variant	rs7732363
Chromosome Location	chr5:89764225-89764226
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:89763652..89766204-chr5:89766216..89768442,2	K562	blood:
2	chr5:89742379..89744327-chr5:89761998..89764685,2	K562	blood:
3	chr5:89760831..89763273-chr5:89763943..89766948,3	K562	blood:

Variant related genes	Relation type
ENSG00000113356	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10041220	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10043702	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10214167	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10473934	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10942593	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10942594	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11953207	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11956418	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12516555	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13436287	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2303801	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28728101	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28815472	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34397682	0.92[EUR][1000 genomes]
rs3763070	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3763072	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3805478	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59742368	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61610742	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6864062	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6867534	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6872360	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6889253	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6889947	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6890115	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7729481	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7730433	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021142	chr5:89102893-89897826	Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS 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	55 gene(s)	inside rSNPs	diseases
2	nsv537804	chr5:89102893-89897826	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv917025	chr5:89208994-89855436	Enhancers Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	nsv432750	chr5:89410113-90137144	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
5	nsv432751	chr5:89457044-90090444	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
7	nsv518131	chr5:89748142-89781594	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	19 gene(s)	inside rSNPs	diseases
8	nsv882364	chr5:89748142-89808531	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89734600-89769000	Weak transcription	Pancreas	Pancrea
2	chr5:89736400-89767600	Weak transcription	Hela-S3	cervix
3	chr5:89736400-89768400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr5:89743800-89767800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr5:89744400-89768600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr5:89745400-89765800	Weak transcription	A549	lung
7	chr5:89746400-89765200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr5:89747400-89768600	Weak transcription	NHDF-Ad	bronchial
9	chr5:89748000-89768400	Weak transcription	Duodenum Mucosa	Duodenum
10	chr5:89748400-89768600	Weak transcription	Adipose Nuclei	Adipose
11	chr5:89748600-89768200	Weak transcription	Osteobl	bone
12	chr5:89749200-89768400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr5:89749200-89768800	Weak transcription	Brain Germinal Matrix	brain
14	chr5:89749200-89768800	Weak transcription	Ovary	ovary
15	chr5:89749200-89769000	Weak transcription	Left Ventricle	heart
16	chr5:89749400-89767600	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr5:89749400-89768600	Weak transcription	Fetal Intestine Large	intestine
18	chr5:89749800-89768600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr5:89750200-89768800	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr5:89750800-89768800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr5:89751200-89766600	Weak transcription	Fetal Muscle Trunk	muscle
22	chr5:89751200-89769000	Weak transcription	Spleen	Spleen
23	chr5:89751600-89767600	Weak transcription	Brain Anterior Caudate	brain
24	chr5:89751800-89767600	Weak transcription	Fetal Intestine Small	intestine
25	chr5:89752000-89769200	Weak transcription	Small Intestine	intestine
26	chr5:89752200-89768400	Weak transcription	Stomach Smooth Muscle	stomach
27	chr5:89752200-89768800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr5:89752800-89767800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr5:89752800-89768600	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr5:89753200-89767000	Weak transcription	K562	blood
31	chr5:89753200-89768400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr5:89753800-89768400	Weak transcription	Brain Cingulate Gyrus	brain
33	chr5:89753800-89768600	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr5:89755400-89769000	Weak transcription	HSMM	muscle
35	chr5:89755600-89768400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr5:89755600-89768600	Weak transcription	Primary B cells from cord blood	blood
37	chr5:89756000-89767800	Weak transcription	Primary B cells from peripheral blood	blood
38	chr5:89757400-89766000	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr5:89757400-89766800	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr5:89757400-89768800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr5:89757600-89767000	Weak transcription	Brain Angular Gyrus	brain
42	chr5:89758000-89769200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr5:89758600-89768400	Weak transcription	Brain Hippocampus Middle	brain
44	chr5:89759200-89767200	Weak transcription	HepG2	liver
45	chr5:89759200-89768800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr5:89759200-89768800	Weak transcription	Lung	lung
47	chr5:89760400-89768800	Weak transcription	Fetal Stomach	stomach
48	chr5:89761800-89768400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr5:89762000-89768800	Weak transcription	Fetal Kidney	kidney
50	chr5:89763000-89767000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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