Variant report

Variant	rs10079614
Chromosome Location	chr5:58604311-58604312
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10036406	0.84[EUR][1000 genomes]
rs10060200	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10070436	0.84[EUR][1000 genomes]
rs10079396	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10079932	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13354210	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17724250	0.84[EUR][1000 genomes]
rs17780213	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17780584	0.85[EUR][1000 genomes]
rs17780740	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1824159	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2044419	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2194210	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56183128	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57516309	0.97[EUR][1000 genomes]
rs60453299	0.84[EUR][1000 genomes]
rs72765993	0.97[EUR][1000 genomes]
rs72767710	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72767722	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9716677	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv598252	chr5:58487764-58618889	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1023628	chr5:58557950-58757438	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv917274	chr5:58565291-58814374	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv1030117	chr5:58587672-58637179	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58593000-58611200	Weak transcription	Right Ventricle	heart
2	chr5:58593200-58612600	Weak transcription	Fetal Lung	lung
3	chr5:58593200-58613400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr5:58593800-58604800	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr5:58594000-58612800	Weak transcription	Stomach Mucosa	stomach
6	chr5:58594400-58606000	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr5:58595400-58604600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:58595600-58609000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr5:58597000-58607600	Weak transcription	Psoas Muscle	Psoas
10	chr5:58597800-58604600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr5:58598000-58604400	Weak transcription	Fetal Intestine Small	intestine
12	chr5:58598000-58604600	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr5:58598000-58607800	Weak transcription	Fetal Heart	heart
14	chr5:58598000-58608600	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr5:58598000-58612600	Weak transcription	Fetal Intestine Large	intestine
16	chr5:58598000-58612800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:58598000-58612800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr5:58598200-58604600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:58599800-58604400	Weak transcription	A549	lung
20	chr5:58600400-58604800	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr5:58602400-58606600	Weak transcription	Hela-S3	cervix

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links