Variant report

Variant	rs2458634
Chromosome Location	chr19:41670581-41670582
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11671185	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.89[TSI][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1645685	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1645686	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1709116	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1709124	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1709125	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2432221	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs305954	0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs305955	0.82[ASN][1000 genomes]
rs305956	0.82[ASN][1000 genomes]
rs305960	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs305961	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs305962	0.85[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	esv3391909	chr19:41632754-41688263	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv911767	chr19:41649516-41716271	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41662600-41678200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr19:41664200-41675600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:41665200-41671200	Weak transcription	Gastric	stomach
4	chr19:41665400-41672800	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr19:41665400-41673000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr19:41665400-41678200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr19:41665400-41678400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr19:41665400-41678400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr19:41665400-41678600	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr19:41665800-41679000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr19:41666000-41671400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr19:41666000-41681800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr19:41666400-41671000	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr19:41666400-41671200	Weak transcription	Duodenum Mucosa	Duodenum
15	chr19:41666400-41673400	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr19:41666400-41678400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr19:41666600-41671200	Weak transcription	Stomach Mucosa	stomach
18	chr19:41668000-41671000	Weak transcription	Fetal Intestine Large	intestine
19	chr19:41668200-41671000	Weak transcription	Fetal Intestine Small	intestine
20	chr19:41669800-41670600	Enhancers	HepG2	liver
21	chr19:41670400-41670800	Enhancers	Hela-S3	cervix
22	chr19:41670400-41672000	Enhancers	A549	lung

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