Variant report

Variant	rs7683115
Chromosome Location	chr4:75964721-75964722
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10007853	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10012438	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10015360	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10015456	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10018358	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1043633	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1043634	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10518133	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11943279	0.89[ASN][1000 genomes]
rs1346138	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs16997586	0.92[ASN][1000 genomes]
rs17000108	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs17000109	0.92[ASN][1000 genomes]
rs17000112	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs17000114	0.94[ASN][1000 genomes]
rs17000141	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17000149	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17000150	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17198085	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17250403	0.96[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs17250773	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28461358	0.89[ASN][1000 genomes]
rs3733466	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3733467	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3775530	0.94[ASN][1000 genomes]
rs3796683	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6824037	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6829853	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6836425	0.96[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6851144	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72660383	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs72660386	0.96[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs72660401	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7654416	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7680016	0.93[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs890289	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9090	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005324	chr4:75689880-76233555	Bivalent/Poised TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv537142	chr4:75689880-76233555	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7683115	DKFZP564O0823	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:75940000-75976200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr4:75944200-75971000	Weak transcription	Fetal Muscle Trunk	muscle
3	chr4:75951800-75965200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr4:75954400-75971000	Weak transcription	Fetal Heart	heart
5	chr4:75956400-75976000	Weak transcription	Spleen	Spleen
6	chr4:75956600-75964800	Weak transcription	Stomach Mucosa	stomach
7	chr4:75956800-75967600	Weak transcription	Colon Smooth Muscle	Colon
8	chr4:75956800-75982800	Weak transcription	Pancreas	Pancrea
9	chr4:75957200-75976400	Weak transcription	Colonic Mucosa	Colon
10	chr4:75957600-75971200	Weak transcription	Fetal Intestine Small	intestine
11	chr4:75962000-75966000	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr4:75962600-75966000	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr4:75962600-75971000	Weak transcription	Right Atrium	heart
14	chr4:75962800-75971200	Weak transcription	Fetal Muscle Leg	muscle
15	chr4:75962800-75975800	Weak transcription	Fetal Intestine Large	intestine
16	chr4:75963000-75964800	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr4:75963000-75966200	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr4:75963000-75967600	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr4:75963000-75970400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:75963000-75971000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:75963000-75971000	Weak transcription	Aorta	Aorta
22	chr4:75963000-75971000	Weak transcription	GM12878-XiMat	blood
23	chr4:75963200-75976000	Weak transcription	Adipose Nuclei	Adipose
24	chr4:75963400-75971200	Weak transcription	Left Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links