Variant report

Variant	rs7282521
Chromosome Location	chr21:15741370-15741371
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:15738236..15741507-chr21:15753904..15757362,3	K562	blood:
2	chr21:15738717..15742131-chr21:15743462..15746963,4	K562	blood:
3	chr21:15741032..15742950-chr21:15746679..15748662,2	MCF-7	breast:
4	chr21:15740980..15743787-chr21:15748039..15750871,3	K562	blood:
5	chr21:15733062..15735967-chr21:15740026..15741975,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000155304	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1040330	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12479	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13048179	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13048477	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2037941	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2142240	0.81[AMR][1000 genomes]
rs2822624	0.87[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2822629	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2822631	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2822632	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2822636	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2822638	0.90[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2822642	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2822644	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2822652	0.91[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs2822655	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2822661	0.83[JPT][hapmap]
rs2822662	1.00[JPT][hapmap]
rs7276170	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9305301	0.86[ASN][1000 genomes]
rs9978374	0.80[ASN][1000 genomes]
rs9982492	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064554	chr21:15676222-15809321	Strong transcription Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1061686	chr21:15724570-15765777	Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv962647	chr21:15739771-15741418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15731600-15744800	Weak transcription	Hela-S3	cervix
2	chr21:15734400-15745600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr21:15734600-15744800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr21:15734600-15744800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr21:15734600-15745400	Weak transcription	HUVEC	blood vessel
6	chr21:15734800-15745400	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr21:15735200-15744600	Weak transcription	NHEK	skin
8	chr21:15735200-15744800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr21:15735200-15744800	Weak transcription	HMEC	breast
10	chr21:15735200-15745200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr21:15737400-15745400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr21:15738600-15746000	Weak transcription	Ovary	ovary
13	chr21:15739000-15744600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr21:15739200-15745000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr21:15739200-15747800	Weak transcription	Esophagus	oesophagus
16	chr21:15739600-15745000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr21:15739800-15742400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr21:15739800-15743800	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr21:15739800-15744600	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr21:15739800-15745600	Weak transcription	GM12878-XiMat	blood
21	chr21:15739800-15746000	Weak transcription	K562	blood
22	chr21:15740400-15744800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr21:15740400-15745200	Weak transcription	Brain Germinal Matrix	brain
24	chr21:15740400-15746000	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr21:15740600-15744800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr21:15740600-15745000	Weak transcription	Primary B cells from cord blood	blood
27	chr21:15740600-15745000	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr21:15740600-15745400	Weak transcription	Stomach Smooth Muscle	stomach
29	chr21:15740600-15746000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr21:15740600-15746000	Weak transcription	NHLF	lung
31	chr21:15740800-15746000	Weak transcription	Left Ventricle	heart
32	chr21:15741000-15744400	Weak transcription	Placenta	Placenta
33	chr21:15741000-15744600	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr21:15741000-15745000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr21:15741000-15745000	Weak transcription	Fetal Brain Female	brain
36	chr21:15741000-15745200	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr21:15741000-15745400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr21:15741000-15746000	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr21:15741000-15746000	Weak transcription	Fetal Muscle Leg	muscle
40	chr21:15741200-15744600	Weak transcription	Fetal Intestine Large	intestine
41	chr21:15741200-15744800	Weak transcription	Primary B cells from peripheral blood	blood
42	chr21:15741200-15745000	Weak transcription	Brain Cingulate Gyrus	brain
43	chr21:15741200-15745800	Weak transcription	Brain Hippocampus Middle	brain
44	chr21:15741200-15745800	Weak transcription	Fetal Muscle Trunk	muscle
45	chr21:15741200-15745800	Weak transcription	Thymus	Thymus
46	chr21:15741200-15746000	Weak transcription	Aorta	Aorta
47	chr21:15741200-15746000	Weak transcription	Right Ventricle	heart
48	chr21:15741200-15748000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links