Variant report

Variant	rs73844420
Chromosome Location	chr3:87013224-87013225
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10514743	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17028628	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1898266	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1898267	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1898268	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1946747	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55854261	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56077607	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56338126	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56346369	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56781488	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57070008	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs57383190	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57543641	0.90[ASN][1000 genomes]
rs57604593	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59090592	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59701679	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61594756	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6551256	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6762893	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6763484	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6784668	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6788077	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6802660	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72916057	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72916059	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72916062	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72916064	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72916069	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72916081	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72916083	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72916086	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72916091	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72916092	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72916098	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72916100	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72916102	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72918103	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72918106	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72918107	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72918108	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72918113	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72918116	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72918121	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72918124	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72918169	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73844421	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73844432	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73844434	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73844442	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73844457	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7617401	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7627441	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7645797	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7649313	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs959081	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534036	chr3:86967129-87283600	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:86986800-87014400	Weak transcription	Aorta	Aorta
2	chr3:86988200-87013400	Weak transcription	Ovary	ovary
3	chr3:86993800-87014200	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr3:86998000-87019800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr3:86998800-87036000	Weak transcription	Psoas Muscle	Psoas
6	chr3:87003800-87014200	Weak transcription	Fetal Muscle Leg	muscle
7	chr3:87004200-87014400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr3:87004400-87014200	Weak transcription	Adipose Nuclei	Adipose
9	chr3:87007000-87013400	Genic enhancers	Osteobl	bone
10	chr3:87007200-87026600	Weak transcription	Esophagus	oesophagus
11	chr3:87007200-87038400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr3:87008000-87016200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr3:87008000-87016600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr3:87008000-87022600	Weak transcription	HMEC	breast
15	chr3:87008000-87028800	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr3:87008000-87032000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr3:87008000-87034200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr3:87008200-87014600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr3:87008200-87016200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr3:87008200-87022600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr3:87008600-87014200	Weak transcription	Colon Smooth Muscle	Colon
22	chr3:87009800-87016400	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr3:87010800-87016800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr3:87010800-87020000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr3:87011000-87014600	Weak transcription	Fetal Intestine Small	intestine
26	chr3:87011000-87016200	Weak transcription	A549	lung
27	chr3:87011400-87015600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr3:87011400-87015800	Strong transcription	Muscle Satellite Cultured Cells	--
29	chr3:87011600-87014000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr3:87011600-87014400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr3:87011600-87014600	Weak transcription	Fetal Intestine Large	intestine
32	chr3:87011600-87016600	Strong transcription	HSMM	muscle
33	chr3:87011600-87017800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr3:87011600-87022600	Weak transcription	HUVEC	blood vessel
35	chr3:87011600-87026600	Weak transcription	Rectal Smooth Muscle	rectum
36	chr3:87012400-87017600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr3:87012400-87018000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr3:87012600-87014400	Weak transcription	Hela-S3	cervix
39	chr3:87012600-87016200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr3:87012600-87016200	Strong transcription	HSMMtube	muscle
41	chr3:87012600-87032600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr3:87012800-87016000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr3:87012800-87022200	Strong transcription	NH-A	brain
44	chr3:87013000-87013400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:87013000-87014800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr3:87013000-87020800	Strong transcription	NHLF	lung
47	chr3:87013200-87013400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr3:87013200-87014000	Strong transcription	Placenta	Placenta
49	chr3:87013200-87014600	Strong transcription	NHDF-Ad	bronchial
50	chr3:87013200-87016600	Strong transcription	Fetal Lung	lung

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