Variant report

Variant	rs73348707
Chromosome Location	chr5:126751672-126751673
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11956397	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11957319	0.87[AMR][1000 genomes]
rs12109001	0.88[AFR][1000 genomes]
rs17164905	0.87[AMR][1000 genomes]
rs17164925	0.87[AMR][1000 genomes]
rs17164941	1.00[AMR][1000 genomes]
rs17164956	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17164963	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55851028	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56853109	1.00[AMR][1000 genomes]
rs57502023	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58718502	1.00[AMR][1000 genomes]
rs59739975	0.87[AMR][1000 genomes]
rs60678437	0.87[AMR][1000 genomes]
rs60694077	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60931267	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61021426	1.00[AMR][1000 genomes]
rs61031224	1.00[AMR][1000 genomes]
rs73331252	0.87[AMR][1000 genomes]
rs73346997	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73348729	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73348755	1.00[AMR][1000 genomes]
rs73348768	0.87[AMR][1000 genomes]
rs73348777	0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033607	chr5:126385181-127304459	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1019821	chr5:126658200-126934917	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv537894	chr5:126658200-126934917	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1032587	chr5:126691103-126826978	Genic enhancers Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv830478	chr5:126721368-126937408	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:126734800-126753400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr5:126742800-126754000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:126742800-126760200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:126742800-126762600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr5:126742800-126782000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:126742800-126792400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr5:126743000-126755600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:126743000-126784800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr5:126743400-126760000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr5:126746200-126752200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr5:126746200-126754800	Weak transcription	Psoas Muscle	Psoas
12	chr5:126746200-126758000	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr5:126746400-126752200	Weak transcription	Brain Hippocampus Middle	brain
14	chr5:126746400-126752200	Weak transcription	Brain Substantia Nigra	brain
15	chr5:126746400-126752400	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr5:126746400-126752400	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr5:126746400-126752800	Weak transcription	Brain Angular Gyrus	brain
18	chr5:126746400-126760800	Weak transcription	HSMM	muscle
19	chr5:126746600-126752600	Weak transcription	Fetal Muscle Trunk	muscle
20	chr5:126747000-126755000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr5:126747000-126759200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr5:126747200-126755000	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr5:126747400-126752800	Weak transcription	Fetal Brain Male	brain
24	chr5:126748000-126752400	Weak transcription	Brain Anterior Caudate	brain
25	chr5:126748400-126755000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr5:126748400-126758600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:126748800-126752400	Weak transcription	HSMMtube	muscle
28	chr5:126749400-126755000	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr5:126749600-126753200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:126749600-126753400	Weak transcription	Fetal Brain Female	brain
31	chr5:126749800-126752600	Genic enhancers	Fetal Muscle Leg	muscle
32	chr5:126750200-126754200	Weak transcription	Brain Germinal Matrix	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links