Variant report

Variant	rs7719113
Chromosome Location	chr5:127737033-127737034
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10040416	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10041869	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10044959	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10046007	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10055617	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10057231	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10057405	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10057855	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10059301	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10062686	1.00[ASN][1000 genomes]
rs10063393	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10067405	0.92[AFR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10070076	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10071920	0.92[AFR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10074194	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10074198	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10076728	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10477683	1.00[ASN][1000 genomes]
rs10477684	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10478811	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10519994	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11950890	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11951790	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11951921	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11952130	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11955447	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13360784	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1396477	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1561006	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17164115	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17608692	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17676426	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs17677244	0.85[YRI][hapmap]
rs1848501	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1858080	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1978439	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2063248	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28579194	1.00[ASN][1000 genomes]
rs28800517	1.00[ASN][1000 genomes]
rs3792871	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs3792873	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3816905	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs3909897	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4492151	1.00[CEU][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55733883	1.00[ASN][1000 genomes]
rs56228613	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59535791	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59820839	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6867183	1.00[ASN][1000 genomes]
rs6873360	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6881856	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6883276	0.88[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7356632	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7700287	0.83[ASN][1000 genomes]
rs7731176	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9327476	1.00[ASN][1000 genomes]
rs989548	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs989549	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[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	nsv531991	chr5:127624564-127966085	Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs7719113	FBN2	cis	Thyroid	GTEx
rs7719113	FBN2	cis	Nerve Tibial	GTEx
rs7719113	FBN2	cis	Whole Blood	GTEx
rs7719113	FBN2	cis	Artery Aorta	GTEx
rs7719113	FBN2	cis	Artery Tibial	GTEx
rs7719113	FBN2	cis	lung	GTEx

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:127672000-127746000	Weak transcription	NHDF-Ad	bronchial
2	chr5:127675600-127742200	Weak transcription	Fetal Intestine Small	intestine
3	chr5:127686000-127738400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:127686000-127742000	Weak transcription	A549	lung
5	chr5:127695200-127737800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr5:127696800-127738200	Weak transcription	Fetal Lung	lung
7	chr5:127704800-127741800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr5:127714600-127743000	Weak transcription	HMEC	breast
9	chr5:127716600-127744800	Weak transcription	Fetal Kidney	kidney
10	chr5:127720000-127739000	Weak transcription	NHEK	skin
11	chr5:127724200-127738600	Weak transcription	Fetal Brain Female	brain
12	chr5:127725400-127738400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:127725400-127743000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr5:127725600-127743800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:127725800-127738600	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr5:127725800-127739000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:127725800-127743400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr5:127725800-127765600	Weak transcription	Fetal Muscle Trunk	muscle
19	chr5:127726000-127745000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr5:127726200-127739200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr5:127727800-127740600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:127728400-127741800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr5:127728400-127744200	Weak transcription	NH-A	brain
24	chr5:127729000-127742200	Weak transcription	Ovary	ovary
25	chr5:127729200-127740600	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr5:127731400-127747000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr5:127731800-127738400	Weak transcription	Fetal Muscle Leg	muscle
28	chr5:127731800-127740000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr5:127731800-127740200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr5:127731800-127740600	Weak transcription	Fetal Stomach	stomach
31	chr5:127732200-127740000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:127732200-127740000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr5:127732200-127740000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr5:127732800-127739400	Weak transcription	Placenta	Placenta
35	chr5:127733200-127744400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr5:127733800-127737600	Weak transcription	HUVEC	blood vessel
37	chr5:127733800-127744200	Weak transcription	Right Ventricle	heart
38	chr5:127734400-127742600	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr5:127734600-127740000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr5:127734800-127737400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr5:127735200-127739000	Weak transcription	Fetal Heart	heart
42	chr5:127736200-127737200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:127736400-127737800	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr5:127736400-127745000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr5:127737000-127738200	Weak transcription	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links