Variant report

Variant	rs72712805
Chromosome Location	chr9:16152566-16152567
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11999673	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12004737	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs55694526	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56077305	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs56268371	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs60287822	0.86[EUR][1000 genomes]
rs7044861	0.80[ASN][1000 genomes]
rs72712803	0.82[EUR][1000 genomes]
rs72712804	0.86[EUR][1000 genomes]
rs72712806	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72712808	0.88[EUR][1000 genomes]
rs72712809	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72712819	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72712821	0.81[ASN][1000 genomes]
rs72712836	0.81[AMR][1000 genomes]
rs729119	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949463	chr9:15970668-16377360	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv429999	chr9:16102066-16389100	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv892638	chr9:16106659-16172580	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16145600-16152600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:16148200-16154600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:16150000-16153000	Enhancers	Colon Smooth Muscle	Colon
4	chr9:16150400-16152800	Enhancers	NHEK	skin
5	chr9:16150600-16153400	Enhancers	Rectal Smooth Muscle	rectum
6	chr9:16150800-16154400	Weak transcription	Adipose Nuclei	Adipose
7	chr9:16151000-16154000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr9:16151000-16154400	Weak transcription	Ovary	ovary
9	chr9:16151000-16155200	Enhancers	Fetal Thymus	thymus
10	chr9:16151000-16155400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr9:16151200-16154000	Enhancers	Fetal Muscle Trunk	muscle
12	chr9:16151400-16154600	Weak transcription	Pancreas	Pancrea
13	chr9:16151400-16154600	Enhancers	Stomach Smooth Muscle	stomach
14	chr9:16151800-16154600	Enhancers	Fetal Muscle Leg	muscle
15	chr9:16151800-16154600	Weak transcription	Dnd41	blood
16	chr9:16152000-16153200	Enhancers	HSMMtube	muscle
17	chr9:16152000-16154200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr9:16152000-16154200	Weak transcription	Primary T cells from cord blood	blood
19	chr9:16152000-16154400	Enhancers	Fetal Brain Female	brain
20	chr9:16152200-16154600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr9:16152200-16154600	Enhancers	Brain Germinal Matrix	brain
22	chr9:16152400-16152800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:16152400-16153000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
24	chr9:16152400-16154200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr9:16152400-16154200	Enhancers	Fetal Brain Male	brain
26	chr9:16152400-16155400	Enhancers	Fetal Stomach	stomach

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