Variant report

Variant	rs73545122
Chromosome Location	chr13:96693886-96693887
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 106 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10450823	1.00[AMR][1000 genomes]
rs12872370	1.00[AMR][1000 genomes]
rs1411556	1.00[AMR][1000 genomes]
rs2389392	1.00[AMR][1000 genomes]
rs2389393	1.00[AMR][1000 genomes]
rs35123499	1.00[AMR][1000 genomes]
rs57094206	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57235111	1.00[AMR][1000 genomes]
rs57754676	1.00[AMR][1000 genomes]
rs57982590	1.00[AMR][1000 genomes]
rs58004448	1.00[AMR][1000 genomes]
rs58055473	1.00[AMR][1000 genomes]
rs5805947	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58267899	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58887467	1.00[AMR][1000 genomes]
rs59489368	1.00[AMR][1000 genomes]
rs59577050	1.00[AMR][1000 genomes]
rs59735887	1.00[AMR][1000 genomes]
rs59810714	1.00[AMR][1000 genomes]
rs59906993	1.00[AMR][1000 genomes]
rs60431735	1.00[AMR][1000 genomes]
rs61262042	1.00[AMR][1000 genomes]
rs61380463	1.00[AMR][1000 genomes]
rs7335644	1.00[AMR][1000 genomes]
rs73545107	1.00[AMR][1000 genomes]
rs73545110	1.00[AMR][1000 genomes]
rs73545120	1.00[AMR][1000 genomes]
rs73545141	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73545164	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73556728	1.00[AMR][1000 genomes]
rs73556737	1.00[AMR][1000 genomes]
rs73556739	1.00[AMR][1000 genomes]
rs73556741	1.00[AMR][1000 genomes]
rs73556742	1.00[AMR][1000 genomes]
rs73556744	1.00[AMR][1000 genomes]
rs73556746	1.00[AMR][1000 genomes]
rs73556758	1.00[AMR][1000 genomes]
rs73556766	1.00[AMR][1000 genomes]
rs73556769	1.00[AMR][1000 genomes]
rs73556770	1.00[AMR][1000 genomes]
rs73556777	1.00[AMR][1000 genomes]
rs73556778	1.00[AMR][1000 genomes]
rs73556780	1.00[AMR][1000 genomes]
rs73556783	1.00[AMR][1000 genomes]
rs73556788	1.00[AMR][1000 genomes]
rs73556793	1.00[AMR][1000 genomes]
rs73556795	1.00[AMR][1000 genomes]
rs73556796	1.00[AMR][1000 genomes]
rs73556802	1.00[AMR][1000 genomes]
rs73558608	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73558612	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73558615	1.00[AMR][1000 genomes]
rs73558627	1.00[AMR][1000 genomes]
rs73558628	1.00[AMR][1000 genomes]
rs73558630	1.00[AMR][1000 genomes]
rs73558636	1.00[AMR][1000 genomes]
rs73558639	1.00[AMR][1000 genomes]
rs73558645	1.00[AMR][1000 genomes]
rs73558650	1.00[AMR][1000 genomes]
rs73558660	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73558663	1.00[AMR][1000 genomes]
rs73558671	1.00[AMR][1000 genomes]
rs73558676	1.00[AMR][1000 genomes]
rs73558684	1.00[AMR][1000 genomes]
rs73558693	1.00[AMR][1000 genomes]
rs73558699	1.00[AMR][1000 genomes]
rs73560803	1.00[AMR][1000 genomes]
rs73560812	1.00[AMR][1000 genomes]
rs73560818	1.00[AMR][1000 genomes]
rs73560819	1.00[AMR][1000 genomes]
rs73560823	1.00[AMR][1000 genomes]
rs73560841	1.00[AMR][1000 genomes]
rs73560842	1.00[AMR][1000 genomes]
rs73560849	1.00[AMR][1000 genomes]
rs73560858	1.00[AMR][1000 genomes]
rs73560863	1.00[AMR][1000 genomes]
rs73560864	1.00[AMR][1000 genomes]
rs73560867	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73560873	1.00[AMR][1000 genomes]
rs73560875	1.00[AMR][1000 genomes]
rs73560887	1.00[AMR][1000 genomes]
rs73560888	1.00[AMR][1000 genomes]
rs73560891	1.00[AMR][1000 genomes]
rs73560896	1.00[AMR][1000 genomes]
rs73560901	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73562903	1.00[AMR][1000 genomes]
rs73562904	1.00[AMR][1000 genomes]
rs73562906	1.00[AMR][1000 genomes]
rs73562910	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73562913	1.00[AMR][1000 genomes]
rs73562923	1.00[AMR][1000 genomes]
rs73562929	1.00[AMR][1000 genomes]
rs73562932	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73562935	1.00[AMR][1000 genomes]
rs73562939	1.00[AMR][1000 genomes]
rs73562959	1.00[AMR][1000 genomes]
rs7984382	1.00[AMR][1000 genomes]
rs7989952	1.00[AMR][1000 genomes]
rs9669909	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050430	chr13:96508530-97020734	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv541883	chr13:96508530-97020734	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1041165	chr13:96522021-96966520	Enhancers Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1051574	chr13:96550653-96779248	Strong transcription Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1040320	chr13:96573646-96790859	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv869471	chr13:96622327-97223956	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
7	nsv530390	chr13:96681439-97193029	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96613200-96694200	Weak transcription	A549	lung
2	chr13:96668600-96704400	Weak transcription	Stomach Smooth Muscle	stomach
3	chr13:96669200-96694000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr13:96669400-96694000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr13:96669400-96704600	Weak transcription	Brain Anterior Caudate	brain
6	chr13:96673000-96698400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:96677600-96704200	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr13:96678400-96704400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr13:96678600-96698800	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr13:96683400-96704200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr13:96686800-96698400	Weak transcription	Fetal Lung	lung
12	chr13:96687000-96694200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr13:96687000-96698800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr13:96687200-96694000	Weak transcription	Gastric	stomach
15	chr13:96687200-96698800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr13:96687200-96698800	Weak transcription	Ovary	ovary
17	chr13:96687200-96699000	Weak transcription	Left Ventricle	heart
18	chr13:96687200-96704600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr13:96687200-96705000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr13:96687400-96694200	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr13:96687400-96694400	Weak transcription	Fetal Muscle Trunk	muscle
22	chr13:96687400-96698800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr13:96687400-96699200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr13:96688800-96694000	Weak transcription	Fetal Muscle Leg	muscle
25	chr13:96688800-96694800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr13:96689200-96694000	Weak transcription	Pancreas	Pancrea
27	chr13:96691600-96699000	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr13:96692800-96694600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr13:96693000-96694400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr13:96693200-96694000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr13:96693200-96694600	Enhancers	H9 Cell Line	embryonic stem cell
32	chr13:96693400-96694600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr13:96693400-96694600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr13:96693400-96697800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr13:96693600-96694000	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr13:96693600-96694400	ZNF genes & repeats	Fetal Intestine Small	intestine
37	chr13:96693600-96694400	ZNF genes & repeats	Fetal Stomach	stomach
38	chr13:96693800-96694000	ZNF genes & repeats	Aorta	Aorta
39	chr13:96693800-96694200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr13:96693800-96694200	Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr13:96693800-96694400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr13:96693800-96694600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr13:96693800-96694600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr13:96693800-96694600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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