Variant report

Variant	rs73172384
Chromosome Location	chr21:16374565-16374566
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs7282564	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs73170302	1.00[AMR][1000 genomes]
rs73172303	1.00[AMR][1000 genomes]
rs73172306	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73172383	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73172388	1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs8132326	1.00[AMR][1000 genomes];0.89[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	nsv1060151	chr21:16295713-16435497	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv544378	chr21:16295713-16435497	Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv834048	chr21:16324481-16489570	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16340600-16375800	Weak transcription	Right Ventricle	heart
2	chr21:16340800-16375800	Weak transcription	Gastric	stomach
3	chr21:16340800-16375800	Weak transcription	Lung	lung
4	chr21:16340800-16377600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr21:16341200-16388600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr21:16341600-16377000	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr21:16358800-16377600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr21:16360400-16380200	Weak transcription	Fetal Muscle Trunk	muscle
9	chr21:16360400-16402600	Weak transcription	Placenta	Placenta
10	chr21:16361600-16374600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr21:16361800-16375800	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr21:16362200-16377600	Weak transcription	Fetal Stomach	stomach
13	chr21:16362200-16385800	Weak transcription	K562	blood
14	chr21:16363400-16383000	Weak transcription	Primary B cells from peripheral blood	blood
15	chr21:16363600-16375800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr21:16363600-16377600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr21:16363600-16377600	Weak transcription	Thymus	Thymus
18	chr21:16363800-16376800	Weak transcription	Dnd41	blood
19	chr21:16364800-16423000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr21:16366000-16379000	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr21:16366200-16375800	Weak transcription	Fetal Thymus	thymus
22	chr21:16368600-16374800	Enhancers	HepG2	liver
23	chr21:16368600-16414600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr21:16368800-16374600	Weak transcription	Esophagus	oesophagus
25	chr21:16369000-16374800	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr21:16369000-16375800	Weak transcription	HUVEC	blood vessel
27	chr21:16369000-16377600	Weak transcription	NHEK	skin
28	chr21:16369200-16377800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr21:16370200-16374800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr21:16370200-16375000	Enhancers	Fetal Intestine Large	intestine
31	chr21:16370200-16383600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr21:16370800-16377400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr21:16371000-16375800	Weak transcription	Right Atrium	heart
34	chr21:16371600-16374600	Weak transcription	Colonic Mucosa	Colon
35	chr21:16371600-16375000	Enhancers	Fetal Intestine Small	intestine
36	chr21:16371600-16375800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr21:16371600-16375800	Weak transcription	Left Ventricle	heart
38	chr21:16371600-16375800	Weak transcription	Spleen	Spleen
39	chr21:16371800-16375000	Enhancers	Osteobl	bone
40	chr21:16372000-16377200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr21:16372200-16374800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr21:16372200-16375000	Enhancers	NHLF	lung
43	chr21:16372200-16379200	Weak transcription	Primary B cells from cord blood	blood
44	chr21:16372400-16374600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr21:16372400-16375200	Enhancers	Liver	Liver
46	chr21:16372600-16376800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr21:16373000-16375200	Enhancers	NH-A	brain
48	chr21:16373200-16374800	Enhancers	Stomach Mucosa	stomach
49	chr21:16373200-16374800	Enhancers	HSMMtube	muscle
50	chr21:16373200-16375000	Enhancers	Skeletal Muscle Male	skeletal muscle

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