Variant report

Variant	rs8133782
Chromosome Location	chr21:47241091-47241092
allele	C/T
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:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:47239959..47242449-chr21:47264107..47266678,2	K562	blood:
2	chr21:46961760..46964733-chr21:47240674..47242196,2	MCF-7	breast:
3	chr21:47240324..47241096-chr21:47342788..47343697,3	MCF-7	breast:
4	chr21:46973106..46978237-chr21:47237804..47242212,8	MCF-7	breast:
5	chr21:46901426..46903468-chr21:47240521..47242930,2	K562	blood:
6	chr21:47062419..47066562-chr21:47239039..47241901,3	MCF-7	breast:
7	chr21:46975702..46976554-chr21:47240286..47241105,4	MCF-7	breast:
8	chr21:46962342..46962898-chr21:47240607..47241133,2	MCF-7	breast:
9	chr21:46973481..46977035-chr21:47238682..47244036,11	MCF-7	breast:
10	chr21:47114783..47115552-chr21:47240377..47241099,2	K562	blood:
11	chr21:47240289..47241171-chr21:47342639..47343656,4	MCF-7	breast:
12	chr21:47059881..47063838-chr21:47238507..47241456,3	MCF-7	breast:
13	chr21:46897608..46898629-chr21:47240205..47241125,3	K562	blood:
14	chr21:46974481..46976891-chr21:47239576..47241145,21	MCF-7	breast:
15	chr21:46975863..46976683-chr21:47240184..47241118,3	K562	blood:
16	chr21:46974938..46975481-chr21:47240107..47241154,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000183570	Chromatin interaction
ENSG00000173638	Chromatin interaction

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs11908989	1.00[EUR][1000 genomes]
rs11910200	1.00[EUR][1000 genomes]
rs11910741	1.00[EUR][1000 genomes]
rs11910904	1.00[EUR][1000 genomes]
rs11911016	1.00[EUR][1000 genomes]
rs16978611	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2877093	1.00[EUR][1000 genomes]
rs56789580	1.00[EUR][1000 genomes]
rs58160661	1.00[EUR][1000 genomes]
rs58393620	1.00[EUR][1000 genomes]
rs58476668	1.00[EUR][1000 genomes]
rs58614340	1.00[EUR][1000 genomes]
rs59852288	1.00[EUR][1000 genomes]
rs60300060	1.00[EUR][1000 genomes]
rs60541263	1.00[EUR][1000 genomes]
rs60918845	1.00[EUR][1000 genomes]
rs61151390	1.00[EUR][1000 genomes]
rs61265907	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61398316	1.00[EUR][1000 genomes]
rs73376613	1.00[EUR][1000 genomes]
rs73376621	1.00[EUR][1000 genomes]
rs73376631	1.00[EUR][1000 genomes]
rs73376653	1.00[EUR][1000 genomes]
rs73376677	1.00[EUR][1000 genomes]
rs73376685	1.00[EUR][1000 genomes]
rs73376697	1.00[EUR][1000 genomes]
rs73378536	1.00[EUR][1000 genomes]
rs73378554	1.00[EUR][1000 genomes]
rs73378560	1.00[EUR][1000 genomes]
rs73378572	1.00[EUR][1000 genomes]
rs73378580	1.00[EUR][1000 genomes]
rs73378582	1.00[EUR][1000 genomes]
rs73378589	1.00[EUR][1000 genomes]
rs73378591	1.00[EUR][1000 genomes]
rs73378594	1.00[EUR][1000 genomes]
rs73378597	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73378599	1.00[EUR][1000 genomes]
rs73380609	1.00[EUR][1000 genomes]
rs73380618	1.00[EUR][1000 genomes]
rs73380620	1.00[EUR][1000 genomes]
rs73380624	1.00[EUR][1000 genomes]
rs73380625	1.00[EUR][1000 genomes]
rs73380629	1.00[EUR][1000 genomes]
rs73380634	1.00[EUR][1000 genomes]
rs73380636	1.00[EUR][1000 genomes]
rs73380639	1.00[EUR][1000 genomes]
rs73380641	1.00[EUR][1000 genomes]
rs73380652	1.00[EUR][1000 genomes]
rs73380656	1.00[EUR][1000 genomes]
rs73380658	1.00[EUR][1000 genomes]
rs73380665	1.00[EUR][1000 genomes]
rs73380668	1.00[EUR][1000 genomes]
rs73380670	1.00[EUR][1000 genomes]
rs73380672	1.00[EUR][1000 genomes]
rs73380673	1.00[EUR][1000 genomes]
rs73380675	1.00[EUR][1000 genomes]
rs73380682	1.00[EUR][1000 genomes]
rs73380688	1.00[EUR][1000 genomes]
rs73382504	1.00[EUR][1000 genomes]
rs73382531	1.00[EUR][1000 genomes]
rs73382578	1.00[EUR][1000 genomes]
rs8127953	1.00[EUR][1000 genomes]
rs8129037	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs8133670	1.00[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	nsv531546	chr21:46504151-47411772	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
2	nsv1058665	chr21:46719445-47634282	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	91 gene(s)	inside rSNPs	diseases
3	nsv544486	chr21:46719445-47634282	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	91 gene(s)	inside rSNPs	diseases
4	nsv1059230	chr21:46956877-47907990	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	n/a
5	nsv544491	chr21:46956877-47907990	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	94 gene(s)	inside rSNPs	n/a
6	nsv1058472	chr21:47027823-47797326	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	n/a
7	nsv544492	chr21:47027823-47797326	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	n/a
8	nsv428043	chr21:47179244-47471971	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	n/a
9	nsv1065959	chr21:47188878-48091343	Bivalent Enhancer Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	n/a
10	nsv914078	chr21:47218744-47311686	Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
11	nsv531580	chr21:47221774-48090317	Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:47217800-47260400	Weak transcription	Right Atrium	heart
2	chr21:47236400-47243800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr21:47237200-47241200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr21:47237200-47241400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr21:47238400-47241600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr21:47238800-47241800	Enhancers	Fetal Thymus	thymus
7	chr21:47239000-47241200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr21:47239400-47247200	Weak transcription	Primary T cells from cord blood	blood
9	chr21:47240200-47241200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
10	chr21:47240200-47241800	Enhancers	H1 Cell Line	embryonic stem cell
11	chr21:47240200-47243600	Enhancers	Liver	Liver
12	chr21:47240400-47241200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr21:47240400-47241200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr21:47240400-47241600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr21:47240400-47242400	Enhancers	Fetal Heart	heart
16	chr21:47240600-47256600	Weak transcription	Dnd41	blood
17	chr21:47240800-47241200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr21:47240800-47241600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr21:47240800-47241600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr21:47240800-47241800	Enhancers	NHEK	skin
21	chr21:47240800-47242200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr21:47240800-47242600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr21:47240800-47242600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr21:47240800-47244800	Weak transcription	Thymus	Thymus
25	chr21:47241000-47241200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr21:47241000-47241200	Bivalent Enhancer	Fetal Muscle Leg	muscle
27	chr21:47241000-47241200	Bivalent Enhancer	Fetal Stomach	stomach
28	chr21:47241000-47242000	Weak transcription	Spleen	Spleen
29	chr21:47241000-47242600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr21:47241000-47243200	Weak transcription	HSMM	muscle
31	chr21:47241000-47251800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr21:47241000-47255400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links