Variant report

Variant	rs73166344
Chromosome Location	chr22:32733032-32733033
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11545749	1.00[ASN][1000 genomes]
rs11703546	1.00[ASN][1000 genomes]
rs12167726	1.00[ASN][1000 genomes]
rs16990408	1.00[ASN][1000 genomes]
rs28783498	1.00[ASN][1000 genomes]
rs35856742	1.00[ASN][1000 genomes]
rs55807703	1.00[ASN][1000 genomes]
rs56028423	1.00[ASN][1000 genomes]
rs56034165	1.00[ASN][1000 genomes]
rs5998418	1.00[ASN][1000 genomes]
rs5998424	1.00[ASN][1000 genomes]
rs5998473	1.00[ASN][1000 genomes]
rs61095402	1.00[ASN][1000 genomes]
rs67737467	1.00[ASN][1000 genomes]
rs68016118	1.00[ASN][1000 genomes]
rs68023238	1.00[ASN][1000 genomes]
rs68125825	1.00[ASN][1000 genomes]
rs73166353	1.00[ASN][1000 genomes]
rs73168708	1.00[ASN][1000 genomes]
rs73168732	1.00[ASN][1000 genomes]
rs73170304	1.00[ASN][1000 genomes]
rs73170321	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948789	chr22:32462505-32764760	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
2	nsv1065175	chr22:32467617-32761093	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
3	nsv544680	chr22:32467617-32761093	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	esv2830423	chr22:32477718-32767825	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	esv2422247	chr22:32486448-32788258	Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
6	nsv459874	chr22:32574274-32866934	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
7	nsv588895	chr22:32574274-32866934	Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
8	nsv1064737	chr22:32603912-32829725	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 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	chr22:32730200-32733200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
2	chr22:32730800-32734600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr22:32731000-32733200	Enhancers	H1 Cell Line	embryonic stem cell
4	chr22:32731000-32737200	Weak transcription	Right Atrium	heart
5	chr22:32731000-32737400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr22:32731200-32734600	Weak transcription	Left Ventricle	heart
7	chr22:32731400-32733400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr22:32731600-32733200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr22:32731800-32733200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr22:32731800-32733600	Enhancers	Fetal Muscle Leg	muscle
11	chr22:32731800-32734000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr22:32731800-32734400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr22:32732000-32733200	Enhancers	Fetal Brain Female	brain
14	chr22:32732000-32733800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr22:32732000-32733800	Enhancers	Brain Anterior Caudate	brain
16	chr22:32732200-32733200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr22:32732200-32733200	Enhancers	Colon Smooth Muscle	Colon
18	chr22:32732200-32735800	Weak transcription	Brain Hippocampus Middle	brain
19	chr22:32732200-32737600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr22:32732400-32733600	Enhancers	Fetal Brain Male	brain
21	chr22:32732600-32735400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr22:32732800-32733200	Weak transcription	Brain Germinal Matrix	brain
23	chr22:32732800-32733200	Weak transcription	HUVEC	blood vessel
24	chr22:32733000-32733200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
25	chr22:32733000-32733600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr22:32733000-32733800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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