Variant report

Variant	rs414174
Chromosome Location	chr21:46557261-46557262
allele	C/G
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:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:46395302..46396927-chr21:46557197..46559182,2	MCF-7	breast:
2	chr21:46492190..46501097-chr21:46553481..46562048,38	K562	blood:
3	chr21:46370881..46371402-chr21:46556771..46557622,2	MCF-7	breast:
4	chr21:46220183..46220714-chr21:46556779..46557402,2	MCF-7	breast:
5	chr21:46557040..46559507-chr21:46738434..46740061,2	MCF-7	breast:
6	chr21:46369431..46370294-chr21:46556979..46557669,4	MCF-7	breast:
7	chr21:46556762..46557633-chr21:46898156..46898795,2	K562	blood:
8	chr21:46552512..46554278-chr21:46555488..46557400,3	MCF-7	breast:
9	chr21:46372367..46372964-chr21:46556977..46557491,2	MCF-7	breast:
10	chr21:46376597..46379233-chr21:46555743..46557641,2	K562	blood:
11	chr21:46312837..46313337-chr21:46556640..46557461,2	MCF-7	breast:
12	chr21:46363498..46366270-chr21:46557131..46558741,2	MCF-7	breast:
13	chr21:46372382..46374637-chr21:46555803..46558629,2	K562	blood:
14	chr21:46546584..46551511-chr21:46553581..46558677,4	K562	blood:
15	chr21:46350869..46353170-chr21:46557195..46559661,2	MCF-7	breast:
16	chr21:46495902..46496885-chr21:46556392..46557286,2	K562	blood:
17	chr21:46369431..46369974-chr21:46556933..46557673,2	MCF-7	breast:
18	chr21:46367892..46370514-chr21:46556035..46557918,2	K562	blood:
19	chr21:46556578..46559478-chr21:46562183..46565396,3	MCF-7	breast:
20	chr21:46492248..46501057-chr21:46545477..46562980,48	K562	blood:
21	chr21:46518590..46519096-chr21:46556955..46557660,2	MCF-7	breast:
22	chr21:46548264..46550888-chr21:46555243..46558018,2	MCF-7	breast:
23	chr21:46345835..46349084-chr21:46555674..46558816,3	MCF-7	breast:
24	chr21:46369385..46370766-chr21:46556658..46557681,11	K562	blood:
25	chr21:46493470..46497016-chr21:46556393..46558721,5	MCF-7	breast:
26	chr21:46555863..46558704-chr21:46711445..46713394,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000197381	Chromatin interaction
ENSG00000160256	Chromatin interaction
ENSG00000268856	Chromatin interaction
ENSG00000223768	Chromatin interaction
ENSG00000235374	Chromatin interaction
ENSG00000160255	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs420499	0.83[EUR][1000 genomes]
rs430446	0.91[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	nsv916258	chr21:45995986-46624705	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
2	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

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46532600-46570600	Weak transcription	Dnd41	blood
2	chr21:46544200-46558200	Weak transcription	HepG2	liver
3	chr21:46544200-46560400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr21:46548600-46571600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr21:46548800-46558400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr21:46549800-46559400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr21:46549800-46567600	Weak transcription	Gastric	stomach
8	chr21:46550000-46567800	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr21:46550400-46571200	Weak transcription	Brain Germinal Matrix	brain
10	chr21:46550800-46563600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr21:46551000-46562400	Weak transcription	HMEC	breast
12	chr21:46551200-46557400	Weak transcription	Fetal Intestine Large	intestine
13	chr21:46551400-46567400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr21:46551600-46557400	Weak transcription	Colonic Mucosa	Colon
15	chr21:46551600-46562400	Weak transcription	Brain Angular Gyrus	brain
16	chr21:46551600-46562600	Genic enhancers	HSMM	muscle
17	chr21:46551800-46565400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr21:46553400-46558600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr21:46553400-46561600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr21:46553400-46568600	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr21:46553400-46570600	Weak transcription	Esophagus	oesophagus
22	chr21:46553400-46574600	Weak transcription	Fetal Heart	heart
23	chr21:46553600-46558800	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr21:46553600-46562600	Weak transcription	Placenta	Placenta
25	chr21:46553600-46563000	Weak transcription	Lung	lung
26	chr21:46553800-46561800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr21:46554200-46557400	Genic enhancers	Fetal Muscle Trunk	muscle
28	chr21:46554400-46557600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr21:46554600-46557800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr21:46554800-46558600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr21:46554800-46559200	Strong transcription	Primary B cells from cord blood	blood
32	chr21:46554800-46564600	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr21:46555200-46558000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr21:46555200-46558200	Weak transcription	Adipose Nuclei	Adipose
35	chr21:46555200-46558600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr21:46555200-46574600	Weak transcription	Right Atrium	heart
37	chr21:46555400-46557400	Weak transcription	Fetal Intestine Small	intestine
38	chr21:46555400-46558000	Weak transcription	NHEK	skin
39	chr21:46555400-46562400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr21:46555400-46562400	Weak transcription	Left Ventricle	heart
41	chr21:46555400-46562400	Weak transcription	Right Ventricle	heart
42	chr21:46555600-46557600	Enhancers	NH-A	brain
43	chr21:46555600-46558400	Enhancers	Muscle Satellite Cultured Cells	--
44	chr21:46555600-46571600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr21:46555800-46557400	Enhancers	HSMMtube	muscle
46	chr21:46555800-46557600	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr21:46555800-46558600	Strong transcription	Aorta	Aorta
48	chr21:46555800-46562600	Weak transcription	Primary T cells from cord blood	blood
49	chr21:46555800-46570800	Weak transcription	Fetal Lung	lung
50	chr21:46555800-46571600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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