Variant report

Variant	rs73483973
Chromosome Location	chr13:51092843-51092844
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	chr13:51085819..51089100-chr13:51090794..51093089,4	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1149854	1.00[EUR][1000 genomes]
rs1149855	1.00[EUR][1000 genomes]
rs1149856	1.00[EUR][1000 genomes]
rs2762044	1.00[EUR][1000 genomes]
rs2762062	1.00[EUR][1000 genomes]
rs55987657	1.00[EUR][1000 genomes]
rs56222340	1.00[EUR][1000 genomes]
rs57723811	1.00[EUR][1000 genomes]
rs57938299	1.00[EUR][1000 genomes]
rs58214088	1.00[EUR][1000 genomes]
rs58521176	1.00[EUR][1000 genomes]
rs58911842	1.00[EUR][1000 genomes]
rs59137919	1.00[EUR][1000 genomes]
rs59729773	1.00[EUR][1000 genomes]
rs59951137	1.00[EUR][1000 genomes]
rs60147627	1.00[EUR][1000 genomes]
rs61382687	1.00[EUR][1000 genomes]
rs7324132	1.00[EUR][1000 genomes]
rs7337343	1.00[EUR][1000 genomes]
rs73483957	1.00[EUR][1000 genomes]
rs73498022	1.00[EUR][1000 genomes]
rs73498030	1.00[EUR][1000 genomes]
rs73498061	1.00[EUR][1000 genomes]
rs73498091	1.00[EUR][1000 genomes]
rs73498093	1.00[EUR][1000 genomes]
rs73498096	1.00[EUR][1000 genomes]
rs73500213	1.00[EUR][1000 genomes]
rs73500225	1.00[EUR][1000 genomes]
rs73500236	1.00[EUR][1000 genomes]
rs73500241	1.00[EUR][1000 genomes]
rs73500242	1.00[EUR][1000 genomes]
rs73500246	1.00[EUR][1000 genomes]
rs73500250	1.00[EUR][1000 genomes]
rs73500259	1.00[EUR][1000 genomes]
rs73500262	1.00[EUR][1000 genomes]
rs73500270	1.00[EUR][1000 genomes]
rs73500278	1.00[EUR][1000 genomes]
rs73500279	1.00[EUR][1000 genomes]
rs73500287	1.00[EUR][1000 genomes]
rs73500290	1.00[EUR][1000 genomes]
rs73500300	1.00[EUR][1000 genomes]
rs73500302	1.00[EUR][1000 genomes]
rs73502108	1.00[EUR][1000 genomes]
rs73502118	1.00[EUR][1000 genomes]
rs73502137	1.00[EUR][1000 genomes]
rs74079205	1.00[EUR][1000 genomes]
rs74079217	1.00[EUR][1000 genomes]
rs74079242	1.00[EUR][1000 genomes]
rs7990648	1.00[EUR][1000 genomes]
rs9591331	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035151	chr13:50513535-51167850	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1254 gene(s)	inside rSNPs	diseases
2	esv2753964	chr13:50545399-51421199	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
3	esv2753492	chr13:50550081-51461720	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
4	nsv1045237	chr13:50976560-51102386	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	esv1815534	chr13:51061044-51092946	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv1816672	chr13:51061044-51092946	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv1830736	chr13:51061044-51092946	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	esv1834352	chr13:51061044-51092946	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	esv1841390	chr13:51061044-51092946	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	esv1843375	chr13:51061044-51092946	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51084200-51093200	Weak transcription	Spleen	Spleen
2	chr13:51084400-51093000	Weak transcription	Lung	lung
3	chr13:51086200-51093000	Weak transcription	Placenta	Placenta
4	chr13:51087200-51095400	Weak transcription	Right Ventricle	heart
5	chr13:51087600-51093000	Weak transcription	Psoas Muscle	Psoas
6	chr13:51087600-51094800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr13:51087600-51095200	Weak transcription	Small Intestine	intestine
8	chr13:51087600-51095600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr13:51087800-51093000	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr13:51087800-51093200	Weak transcription	Fetal Muscle Trunk	muscle
11	chr13:51087800-51102000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr13:51088000-51095200	Weak transcription	Stomach Mucosa	stomach
13	chr13:51088000-51095400	Weak transcription	Stomach Smooth Muscle	stomach
14	chr13:51088200-51093000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr13:51088200-51100800	Weak transcription	Primary B cells from cord blood	blood
16	chr13:51089200-51093200	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr13:51089200-51094600	Weak transcription	Colon Smooth Muscle	Colon
18	chr13:51089200-51095400	Weak transcription	Fetal Intestine Large	intestine
19	chr13:51089200-51095600	Weak transcription	Fetal Intestine Small	intestine
20	chr13:51090200-51099200	Enhancers	Liver	Liver
21	chr13:51090800-51093200	Weak transcription	Gastric	stomach
22	chr13:51090800-51093400	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr13:51090800-51093600	Enhancers	Fetal Muscle Leg	muscle
24	chr13:51090800-51095600	Enhancers	Fetal Lung	lung
25	chr13:51091000-51093400	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr13:51091000-51094800	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr13:51091000-51096600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr13:51091200-51093000	Weak transcription	Fetal Thymus	thymus
29	chr13:51091200-51093000	Weak transcription	Thymus	Thymus
30	chr13:51091600-51093600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr13:51091800-51094400	Weak transcription	Fetal Kidney	kidney
32	chr13:51092200-51093000	Enhancers	Brain Substantia Nigra	brain
33	chr13:51092200-51093400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr13:51092200-51093800	Enhancers	Brain Angular Gyrus	brain
35	chr13:51092400-51093200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr13:51092400-51093400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr13:51092400-51093400	Enhancers	Left Ventricle	heart
38	chr13:51092400-51093400	Enhancers	HSMMtube	muscle
39	chr13:51092400-51093400	Enhancers	Osteobl	bone
40	chr13:51092400-51093600	Enhancers	HSMM	muscle
41	chr13:51092400-51093600	Enhancers	NHLF	lung
42	chr13:51092400-51094800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr13:51092400-51095600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr13:51092400-51098400	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr13:51092600-51093000	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr13:51092600-51093200	Weak transcription	Pancreas	Pancrea
47	chr13:51092600-51093400	Enhancers	Muscle Satellite Cultured Cells	--
48	chr13:51092600-51093400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr13:51092600-51093400	Enhancers	Fetal Stomach	stomach
50	chr13:51092600-51093600	Enhancers	HepG2	liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links