Variant report

Variant	rs564292647
Chromosome Location	chr21:17795564-17795565
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TCF7L2	chr21:17795180-17795790	HEK293	kidney:	n/a	chr21:17795362-17795372 chr21:17795620-17795636
2	ZNF217	chr21:17795419-17795943	MCF-7	breast:	n/a	n/a
3	GATA3	chr21:17795531-17796171	MCF-7	breast:	n/a	n/a
4	NFIC	chr21:17794868-17795608	ECC-1	luminal epithelium:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:17793428..17795619-chr21:17796309..17799030,2	MCF-7	breast:
2	chr21:17795082..17798298-chr21:17801061..17804757,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000270139	TF binding region

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064857	chr21:17628760-18533131	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	345 gene(s)	inside rSNPs	diseases
2	nsv544382	chr21:17628760-18533131	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	345 gene(s)	inside rSNPs	diseases
3	nsv913416	chr21:17728224-17863882	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv913419	chr21:17775056-17826260	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv470880	chr21:17777827-17820111	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv459100	chr21:17777966-17826260	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv587077	chr21:17777966-17826260	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv913420	chr21:17777966-17826260	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv913421	chr21:17786219-17826260	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv913422	chr21:17791751-17826260	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv459101	chr21:17794432-17819036	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv587078	chr21:17794432-17819036	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17790400-17797000	Active TSS	Skeletal Muscle Female	skeletal muscle
2	chr21:17791200-17797000	Active TSS	Fetal Brain Female	brain
3	chr21:17791400-17795600	Active TSS	Brain Germinal Matrix	brain
4	chr21:17791400-17796800	Active TSS	Skeletal Muscle Male	skeletal muscle
5	chr21:17791400-17797000	Active TSS	Stomach Smooth Muscle	stomach
6	chr21:17791400-17797200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr21:17791400-17797200	Active TSS	Breast Myoepithelial Primary Cells	Breast
8	chr21:17791600-17796200	Active TSS	Liver	Liver
9	chr21:17791600-17796400	Active TSS	Cortex derived primary cultured neurospheres	brain
10	chr21:17791600-17796600	Active TSS	Fetal Brain Male	brain
11	chr21:17791600-17796800	Active TSS	Fetal Stomach	stomach
12	chr21:17791600-17797200	Active TSS	HSMMtube	muscle
13	chr21:17791800-17796400	Active TSS	Adipose Nuclei	Adipose
14	chr21:17791800-17797400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr21:17793000-17796000	Weak transcription	Psoas Muscle	Psoas
16	chr21:17793000-17796200	Weak transcription	Fetal Lung	lung
17	chr21:17793000-17796400	Weak transcription	Brain Substantia Nigra	brain
18	chr21:17793000-17796400	Weak transcription	Ovary	ovary
19	chr21:17793000-17796400	Weak transcription	Rectal Smooth Muscle	rectum
20	chr21:17793000-17796400	Weak transcription	Right Ventricle	heart
21	chr21:17793000-17796400	Weak transcription	NHLF	lung
22	chr21:17793200-17796000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr21:17793200-17796000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr21:17793200-17796400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr21:17793200-17796400	Weak transcription	NHEK	skin
26	chr21:17793400-17796200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr21:17793600-17796200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr21:17793800-17796400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr21:17794000-17796400	Weak transcription	Colon Smooth Muscle	Colon
30	chr21:17794000-17796600	Weak transcription	Fetal Heart	heart
31	chr21:17794400-17796200	Enhancers	Osteobl	bone
32	chr21:17794400-17796800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr21:17794400-17797200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
34	chr21:17794400-17797800	Active TSS	Right Atrium	heart
35	chr21:17794600-17796200	Weak transcription	Brain Anterior Caudate	brain
36	chr21:17794800-17795800	Enhancers	HSMM	muscle
37	chr21:17794800-17796000	Enhancers	Hela-S3	cervix
38	chr21:17795000-17798200	Flanking Active TSS	HUVEC	blood vessel
39	chr21:17795200-17796000	Weak transcription	HMEC	breast
40	chr21:17795200-17796200	Weak transcription	A549	lung
41	chr21:17795200-17796800	Active TSS	Brain Inferior Temporal Lobe	brain
42	chr21:17795400-17795800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr21:17795400-17796200	Enhancers	Muscle Satellite Cultured Cells	--
44	chr21:17795400-17796200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr21:17795400-17796200	Enhancers	NH-A	brain
46	chr21:17795400-17796400	Weak transcription	Brain Angular Gyrus	brain
47	chr21:17795400-17796400	Weak transcription	Brain Hippocampus Middle	brain
48	chr21:17795400-17796400	Weak transcription	Fetal Kidney	kidney
49	chr21:17795400-17796400	Weak transcription	Fetal Muscle Leg	muscle
50	chr21:17795400-17797200	Active TSS	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links