Variant report

Variant	rs57724305
Chromosome Location	chr22:30352323-30352324
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:30346859..30350735-chr22:30351458..30355335,4	K562	blood:
2	chr22:30349519..30352332-chr22:30354507..30356583,2	MCF-7	breast:

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs16988115	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16988122	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16988151	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28647168	1.00[AMR][1000 genomes]
rs56733052	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57258477	1.00[AMR][1000 genomes]
rs5763560	1.00[ASN][1000 genomes]
rs58255360	1.00[AMR][1000 genomes]
rs58952888	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs59580785	1.00[AMR][1000 genomes]
rs5997540	1.00[AMR][1000 genomes]
rs5997565	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6006297	1.00[AMR][1000 genomes]
rs6006299	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6006301	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6006309	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6006317	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6006318	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6006331	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60245742	1.00[AMR][1000 genomes]
rs60964812	1.00[AMR][1000 genomes]
rs61043203	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61191536	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61540772	1.00[AMR][1000 genomes]
rs73162767	1.00[ASN][1000 genomes]
rs73394851	1.00[AMR][1000 genomes]
rs73394860	1.00[AMR][1000 genomes]
rs73394861	1.00[AMR][1000 genomes]
rs73394863	1.00[AMR][1000 genomes]
rs73394876	1.00[AMR][1000 genomes]
rs73396842	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73396845	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73398604	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73398634	0.87[AFR][1000 genomes]
rs73398637	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73398640	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73398663	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73400621	0.83[AMR][1000 genomes]
rs73400633	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73400648	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73400675	1.00[AMR][1000 genomes]
rs73400689	1.00[AMR][1000 genomes]
rs73402619	1.00[AMR][1000 genomes]
rs73402627	1.00[AMR][1000 genomes]
rs73402640	1.00[AMR][1000 genomes]
rs73402644	1.00[AMR][1000 genomes]
rs73402647	1.00[AMR][1000 genomes]
rs73402653	1.00[AMR][1000 genomes]
rs73402667	1.00[AMR][1000 genomes]
rs9620939	0.83[AMR][1000 genomes]
rs9625903	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064081	chr22:29826745-30623965	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv544677	chr22:29826745-30623965	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv1064489	chr22:30316627-30361881	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv869764	chr22:30323649-30367813	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv523696	chr22:30326102-30381789	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1058511	chr22:30330447-30361881	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	esv2763694	chr22:30330459-30361881	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv588883	chr22:30333405-30365842	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv3591	chr22:30344208-30388897	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30313600-30354200	Weak transcription	Small Intestine	intestine
2	chr22:30334200-30374800	Weak transcription	Thymus	Thymus
3	chr22:30340200-30355400	Weak transcription	Fetal Intestine Small	intestine
4	chr22:30340200-30374800	Weak transcription	Fetal Thymus	thymus
5	chr22:30340600-30360400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr22:30340600-30370000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr22:30340600-30375000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr22:30340800-30376000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr22:30341200-30353600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr22:30341400-30354400	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr22:30341400-30355200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr22:30342600-30375200	Weak transcription	Spleen	Spleen
13	chr22:30344200-30375000	Weak transcription	HMEC	breast
14	chr22:30344400-30376000	Weak transcription	HSMMtube	muscle
15	chr22:30344600-30357600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr22:30344600-30357800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr22:30344600-30358400	Weak transcription	Fetal Stomach	stomach
18	chr22:30344600-30367200	Weak transcription	Brain Anterior Caudate	brain
19	chr22:30344600-30370000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr22:30344600-30374600	Weak transcription	Adipose Nuclei	Adipose
21	chr22:30344600-30375600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr22:30345000-30352800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr22:30345000-30358600	Weak transcription	Fetal Lung	lung
24	chr22:30345000-30367200	Weak transcription	Brain Cingulate Gyrus	brain
25	chr22:30345000-30367600	Weak transcription	Brain Germinal Matrix	brain
26	chr22:30345000-30375400	Weak transcription	Fetal Brain Female	brain
27	chr22:30345400-30356400	Weak transcription	Fetal Brain Male	brain
28	chr22:30345400-30370000	Weak transcription	HSMM	muscle
29	chr22:30345400-30371600	Weak transcription	Lung	lung
30	chr22:30345400-30379000	Weak transcription	Esophagus	oesophagus
31	chr22:30345800-30363200	Weak transcription	Liver	Liver
32	chr22:30346200-30355200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr22:30347000-30373800	Weak transcription	Left Ventricle	heart
34	chr22:30347200-30357800	Weak transcription	Fetal Muscle Trunk	muscle
35	chr22:30347200-30369600	Weak transcription	Pancreas	Pancrea
36	chr22:30347600-30359600	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr22:30347600-30360000	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr22:30347800-30353800	Weak transcription	Primary B cells from cord blood	blood
39	chr22:30348000-30374800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr22:30348200-30354200	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr22:30348200-30357600	Weak transcription	Primary T cells from cord blood	blood
42	chr22:30348200-30363200	Weak transcription	Duodenum Mucosa	Duodenum
43	chr22:30348400-30352400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr22:30348400-30352400	Weak transcription	NHEK	skin
45	chr22:30348400-30366200	Weak transcription	Colon Smooth Muscle	Colon
46	chr22:30348400-30373800	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr22:30348400-30387200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr22:30348600-30358400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr22:30348600-30366600	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr22:30348800-30354400	Weak transcription	Primary neutrophils fromperipheralblood	blood

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