Variant report

Variant	rs5762418
Chromosome Location	chr22:28341443-28341444
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs118839	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs138631	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs138638	0.88[CEU][hapmap];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs138650	0.89[CEU][hapmap];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs138675	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs138685	0.81[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs1548235	0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs2038158	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2267121	0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs2267124	0.88[ASN][1000 genomes]
rs4140571	0.89[CEU][hapmap];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs470100	0.86[CHB][hapmap];0.91[JPT][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs470105	0.81[CHB][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs5752667	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs5762393	0.87[ASN][1000 genomes]
rs5762416	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5997319	0.95[CHB][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap]
rs6005671	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs720621	0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs73425788	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs738451	0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs7625	0.84[ASN][1000 genomes]
rs957601	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062877	chr22:28163507-28866350	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:28316400-28342600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr22:28316400-28358600	Weak transcription	Placenta	Placenta
3	chr22:28316400-28370200	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr22:28316400-28376800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr22:28316400-28378000	Weak transcription	Esophagus	oesophagus
6	chr22:28316600-28348400	Weak transcription	Brain Substantia Nigra	brain
7	chr22:28317000-28348200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr22:28317800-28342600	Weak transcription	Small Intestine	intestine
9	chr22:28317800-28345200	Weak transcription	HepG2	liver
10	chr22:28318800-28382000	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr22:28319600-28358000	Weak transcription	Brain Germinal Matrix	brain
12	chr22:28319600-28383000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr22:28320800-28347800	Weak transcription	HUVEC	blood vessel
14	chr22:28321000-28354800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr22:28321200-28358400	Weak transcription	Fetal Muscle Trunk	muscle
16	chr22:28321400-28379000	Weak transcription	Primary B cells from cord blood	blood
17	chr22:28321600-28345000	Weak transcription	Fetal Lung	lung
18	chr22:28321800-28342800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr22:28322000-28365200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr22:28322000-28366200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr22:28323800-28346000	Weak transcription	Dnd41	blood
22	chr22:28326800-28368600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr22:28327000-28348000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr22:28327000-28348400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr22:28327400-28347800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr22:28329400-28347800	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr22:28329400-28348200	Weak transcription	Adipose Nuclei	Adipose
28	chr22:28329400-28377800	Weak transcription	Primary T cells from cord blood	blood
29	chr22:28329800-28344000	Weak transcription	Liver	Liver
30	chr22:28332200-28345400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr22:28332600-28343000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr22:28333600-28343400	Weak transcription	Fetal Heart	heart
33	chr22:28339400-28352400	Weak transcription	Fetal Stomach	stomach
34	chr22:28339400-28367800	Weak transcription	Fetal Intestine Small	intestine

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