Variant report

Variant	rs422205
Chromosome Location	chr21:46525101-46525102
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:46221400..46223268-chr21:46524948..46526484,2	MCF-7	breast:
2	chr21:46524740..46528756-chr21:46537470..46542914,5	K562	blood:
3	chr21:46523822..46526157-chr21:46543907..46545528,2	MCF-7	breast:
4	chr21:46493396..46496965-chr21:46524044..46525744,3	MCF-7	breast:
5	chr21:46492354..46499042-chr21:46517406..46531809,25	K562	blood:

Variant related genes	Relation type
ENSG00000197381	Chromatin interaction
ENSG00000235374	Chromatin interaction
ENSG00000268856	Chromatin interaction
ENSG00000184787	Chromatin interaction
ENSG00000236519	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17004737	0.93[ASN][1000 genomes]
rs2032253	0.93[ASN][1000 genomes]
rs2838772	0.92[EUR][1000 genomes]
rs2838775	0.93[ASN][1000 genomes]
rs2838777	0.93[ASN][1000 genomes]
rs2838779	0.93[ASN][1000 genomes]
rs2838780	0.93[ASN][1000 genomes]
rs2838784	0.93[ASN][1000 genomes]
rs2838785	0.93[ASN][1000 genomes]
rs3171490	0.93[ASN][1000 genomes]
rs373249	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs375621	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs387536	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs406923	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs407157	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs412431	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs420499	0.81[EUR][1000 genomes]
rs423892	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs425176	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs437833	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs444789	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs451550	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73230667	0.93[ASN][1000 genomes]
rs73230670	0.93[ASN][1000 genomes]
rs73230679	0.93[ASN][1000 genomes]
rs73230680	0.93[ASN][1000 genomes]
rs73230681	0.93[ASN][1000 genomes]
rs73232640	0.93[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	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	nsv3541	chr21:46496415-46536629	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	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:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46512200-46525600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr21:46513200-46529200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr21:46516400-46525600	Weak transcription	K562	blood
4	chr21:46516400-46549400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr21:46519400-46526800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr21:46520400-46525400	Weak transcription	Fetal Brain Female	brain
7	chr21:46520600-46525200	Enhancers	Left Ventricle	heart
8	chr21:46521200-46527000	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr21:46521200-46528800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr21:46521400-46525200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr21:46521400-46526400	Enhancers	Adipose Nuclei	Adipose
12	chr21:46521600-46525200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr21:46521600-46525200	Enhancers	HMEC	breast
14	chr21:46521600-46526400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr21:46521600-46526800	Genic enhancers	HSMM	muscle
16	chr21:46521800-46526600	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr21:46521800-46526800	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr21:46522000-46525200	Enhancers	Primary T cells fromperipheralblood	blood
19	chr21:46522000-46525200	Enhancers	Right Atrium	heart
20	chr21:46522000-46526400	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr21:46522000-46527000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr21:46522200-46527200	Enhancers	Colon Smooth Muscle	Colon
23	chr21:46522400-46525600	Weak transcription	Osteobl	bone
24	chr21:46522600-46538600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr21:46522800-46529600	Weak transcription	NH-A	brain
26	chr21:46523000-46525200	Weak transcription	Fetal Brain Male	brain
27	chr21:46523000-46525600	Weak transcription	Brain Angular Gyrus	brain
28	chr21:46523000-46525600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr21:46523000-46526200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr21:46523000-46529200	Weak transcription	Colonic Mucosa	Colon
31	chr21:46523000-46529400	Weak transcription	NHLF	lung
32	chr21:46523000-46532600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr21:46523000-46548200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr21:46523200-46525600	Weak transcription	Brain Cingulate Gyrus	brain
35	chr21:46523200-46529000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr21:46523400-46525800	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr21:46523400-46526800	Enhancers	Fetal Heart	heart
38	chr21:46523400-46527000	Enhancers	Primary T cells from cord blood	blood
39	chr21:46523600-46526200	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr21:46523600-46526800	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr21:46523800-46525200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr21:46523800-46526000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr21:46523800-46527000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr21:46524000-46525200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr21:46524000-46525200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr21:46524000-46525400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
47	chr21:46524000-46526400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr21:46524000-46527200	Enhancers	HSMMtube	muscle
49	chr21:46524200-46527000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr21:46524400-46525800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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