Variant report

Variant	rs10229016
Chromosome Location	chr7:128062660-128062661
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr7:128045147..128050080-chr7:128061541..128066850,10	MCF-7	breast:
2	chr7:128035982..128041518-chr7:128062564..128068284,7	MCF-7	breast:
3	chr7:128048177..128050685-chr7:128059766..128063238,3	MCF-7	breast:
4	chr7:128055955..128059453-chr7:128060667..128062980,3	K562	blood:
5	chr7:128044912..128048334-chr7:128062375..128066541,5	K562	blood:
6	chr7:128042298..128048334-chr7:128059762..128065417,7	K562	blood:
7	chr7:128056824..128058697-chr7:128060667..128062977,2	K562	blood:
8	chr7:128060108..128063097-chr7:128063704..128066560,3	K562	blood:
9	chr7:128048374..128053724-chr7:128060919..128066147,7	K562	blood:
10	chr7:128044762..128048052-chr7:128061346..128064155,3	MCF-7	breast:
11	chr7:127982008..127984015-chr7:128061546..128064363,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000106344	Chromatin interaction
ENSG00000106348	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10229394	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10230632	0.83[AMR][1000 genomes]
rs10245559	0.83[AMR][1000 genomes]
rs11770116	0.82[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11980741	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1560214	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2288548	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2288549	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2402895	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2562730	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2562732	0.82[AMR][1000 genomes]
rs2562734	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2562737	0.85[AMR][1000 genomes]
rs2732394	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2732397	0.87[AMR][1000 genomes]
rs2732432	0.83[AMR][1000 genomes]
rs3097361	0.85[AMR][1000 genomes]
rs4728108	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4731446	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4731448	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4731450	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4731453	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4731454	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4731455	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6467178	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6947697	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6948333	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs930106	0.89[AMR][1000 genomes];0.86[EUR][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	nsv831124	chr7:127970345-128147910	Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	nsv889191	chr7:127973133-128073326	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128051400-128086200	Weak transcription	Right Atrium	heart
2	chr7:128055800-128063800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:128056000-128062800	Weak transcription	Brain Hippocampus Middle	brain
4	chr7:128059000-128063200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:128060400-128065000	Enhancers	Fetal Muscle Leg	muscle
6	chr7:128060600-128063600	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr7:128060600-128064800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr7:128061000-128063800	Weak transcription	Stomach Smooth Muscle	stomach
9	chr7:128061000-128064000	Enhancers	Primary T cells fromperipheralblood	blood
10	chr7:128061000-128065200	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr7:128061800-128063000	Weak transcription	Placenta	Placenta
12	chr7:128061800-128063800	Enhancers	Fetal Brain Male	brain
13	chr7:128062200-128064000	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr7:128062200-128064000	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr7:128062400-128063800	Enhancers	Fetal Brain Female	brain
16	chr7:128062600-128064200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr7:128062600-128064800	Enhancers	HepG2	liver

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