Variant report

Variant	rs2339329
Chromosome Location	chr18:24721718-24721719
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10502486	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11083195	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12456507	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12458849	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12956646	0.82[EUR][1000 genomes]
rs12957452	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12958230	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12958264	0.82[EUR][1000 genomes]
rs12958868	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12963367	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12969203	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12969884	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12970303	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1426873	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17632975	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17705635	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34481937	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4800790	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62082885	0.82[EUR][1000 genomes]
rs67364402	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8096346	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs919140	0.82[EUR][1000 genomes]
rs9646527	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9646563	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9748372	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067103	chr18:24524011-24760469	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv543668	chr18:24524011-24760469	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv909473	chr18:24655235-24792075	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv909474	chr18:24683823-24832023	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv909475	chr18:24687324-24776226	Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv530515	chr18:24704459-24883897	Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24716400-24727400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr18:24716600-24722600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr18:24716600-24722600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr18:24716600-24723600	Weak transcription	Gastric	stomach
5	chr18:24716600-24724000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr18:24716600-24730200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr18:24718200-24723600	Weak transcription	Pancreas	Pancrea
8	chr18:24718400-24723600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr18:24718400-24723600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr18:24718400-24727400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr18:24718600-24722800	Weak transcription	Liver	Liver
12	chr18:24718600-24723600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr18:24718800-24722000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr18:24718800-24722000	Weak transcription	HepG2	liver
15	chr18:24718800-24723200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr18:24719000-24722600	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr18:24719000-24723400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr18:24719800-24723400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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