Variant report

Variant	rs62282204
Chromosome Location	chr3:138584405-138584406
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:138579482..138585214-chr3:138633331..138636801,5	K562	blood:
2	chr3:138581454..138585634-chr3:138592021..138596158,7	K562	blood:
3	chr3:138580257..138585634-chr3:138593415..138596528,8	K562	blood:
4	chr3:137891312..137893819-chr3:138582385..138585243,2	K562	blood:

Variant related genes	Relation type
ENSG00000138231	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10804659	0.88[EUR][1000 genomes]
rs10935288	0.82[EUR][1000 genomes]
rs11706016	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11706291	0.86[ASN][1000 genomes]
rs11708762	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11711360	0.83[EUR][1000 genomes]
rs11924479	0.81[EUR][1000 genomes]
rs12497815	0.87[EUR][1000 genomes]
rs12631035	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12633714	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13061496	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13072146	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13077455	0.83[EUR][1000 genomes]
rs13100110	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17484361	0.83[EUR][1000 genomes]
rs28826701	0.86[ASN][1000 genomes]
rs35514824	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4894359	0.84[EUR][1000 genomes]
rs62282207	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6773514	0.83[EUR][1000 genomes]
rs6776833	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6791627	0.82[EUR][1000 genomes]
rs71312597	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7613579	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7628172	0.88[EUR][1000 genomes]
rs7634571	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7646689	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7650967	0.88[EUR][1000 genomes]
rs9289566	0.80[EUR][1000 genomes]
rs9812318	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9813576	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9817727	0.88[EUR][1000 genomes]
rs9822500	0.86[EUR][1000 genomes]
rs9851887	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9855727	0.80[EUR][1000 genomes]
rs9870355	0.80[ASN][1000 genomes]
rs9871842	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9881861	0.86[ASN][1000 genomes]
rs9882957	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530057	chr3:138014877-138734390	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv1013074	chr3:138213166-138737688	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1002612	chr3:138213274-138831792	Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv536726	chr3:138213274-138831792	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv1009726	chr3:138219923-138737688	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv869205	chr3:138248190-138775288	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv868955	chr3:138248190-138848947	Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv591854	chr3:138348081-138764229	Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv1010514	chr3:138365640-138737688	Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
10	nsv1000927	chr3:138423543-138632596	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
11	nsv917964	chr3:138440701-138699084	Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs62282204	FAIM	Cis_1M	lymphoblastoid	RTeQTL
rs62282204	CEP70	Cis_1M	lymphoblastoid	RTeQTL
rs62282204	PIK3CB	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138580400-138585000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr3:138582400-138584800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:138582600-138584600	Weak transcription	Left Ventricle	heart
4	chr3:138582600-138585200	Weak transcription	Brain Angular Gyrus	brain
5	chr3:138582600-138586200	Weak transcription	Adipose Nuclei	Adipose
6	chr3:138582600-138586200	Weak transcription	Fetal Muscle Leg	muscle
7	chr3:138582600-138592400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:138582800-138586800	Weak transcription	Hela-S3	cervix
9	chr3:138583000-138592600	Weak transcription	K562	blood
10	chr3:138584200-138591600	Weak transcription	HepG2	liver
11	chr3:138584400-138584600	Weak transcription	Primary monocytes fromperipheralblood	blood

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