Variant report

Variant	rs72991942
Chromosome Location	chr6:133632866-133632867
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:22)

rs_ID	r²[population]
rs10485232	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11753937	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11759873	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12523816	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1336521	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17062339	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17301622	0.88[AFR][1000 genomes]
rs211434	0.82[ASN][1000 genomes]
rs2210891	0.91[AFR][1000 genomes]
rs296416	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs296418	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs369425	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs385859	0.86[ASN][1000 genomes]
rs407038	0.83[ASN][1000 genomes]
rs439123	0.91[EUR][1000 genomes]
rs4493757	0.85[ASN][1000 genomes]
rs62430320	0.95[AFR][1000 genomes]
rs62430323	0.85[AFR][1000 genomes]
rs6569876	0.85[ASN][1000 genomes]
rs72991933	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs949767	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs954917	0.89[ASN][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	nsv886679	chr6:133578733-133635272	Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv886680	chr6:133613759-133663021	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 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	chr6:133613000-133655000	Weak transcription	Hela-S3	cervix
2	chr6:133623200-133636200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr6:133627000-133633200	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr6:133627400-133633200	Weak transcription	Psoas Muscle	Psoas
5	chr6:133627600-133637000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr6:133629400-133639600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr6:133629800-133633000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:133631000-133635800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr6:133631200-133639000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr6:133631600-133635400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr6:133632800-133633000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr6:133632800-133633000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr6:133632800-133633000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:133632800-133633000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr6:133632800-133633800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr6:133632800-133634800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr6:133632800-133634800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr6:133632800-133635000	Enhancers	HUES64 Cell Line	embryonic stem cell

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