Variant report

Variant	rs73425192
Chromosome Location	chr9:27165340-27165341
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12002056	1.00[AMR][1000 genomes]
rs57788976	1.00[AMR][1000 genomes]
rs59063277	1.00[AMR][1000 genomes]
rs73425189	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73425194	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73425196	1.00[AMR][1000 genomes]
rs73425202	1.00[AMR][1000 genomes]
rs73427104	1.00[AMR][1000 genomes]
rs73427105	1.00[AMR][1000 genomes]
rs73436054	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892862	chr9:26956663-27190655	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1016733	chr9:27073650-27264576	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1022313	chr9:27083369-27250505	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1017802	chr9:27088160-27262682	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1019104	chr9:27088160-27358206	Enhancers Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv892863	chr9:27138898-27170934	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv6512	chr9:27155677-27200455	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:27151000-27172800	Weak transcription	Left Ventricle	heart
2	chr9:27151000-27229200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr9:27152000-27174600	Weak transcription	Fetal Muscle Leg	muscle
4	chr9:27152200-27165400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr9:27152400-27181600	Weak transcription	Adipose Nuclei	Adipose
6	chr9:27157400-27165400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr9:27158200-27165600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr9:27158200-27183600	Weak transcription	Lung	lung
9	chr9:27158400-27165800	Weak transcription	Spleen	Spleen
10	chr9:27162400-27168600	Weak transcription	HSMMtube	muscle
11	chr9:27162600-27172600	Weak transcription	HUVEC	blood vessel
12	chr9:27162800-27177800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:27163000-27178000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr9:27164400-27175400	Weak transcription	Fetal Intestine Small	intestine
15	chr9:27164600-27165800	Enhancers	Fetal Lung	lung
16	chr9:27164600-27166000	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr9:27164600-27166200	Enhancers	Fetal Stomach	stomach
18	chr9:27164800-27165400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr9:27164800-27165600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr9:27164800-27165800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr9:27164800-27165800	Enhancers	Rectal Smooth Muscle	rectum
22	chr9:27164800-27166000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:27164800-27166000	Enhancers	Colon Smooth Muscle	Colon
24	chr9:27164800-27166200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr9:27165000-27165800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr9:27165000-27166000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr9:27165000-27166000	Enhancers	Stomach Smooth Muscle	stomach
28	chr9:27165000-27166200	Enhancers	Placenta	Placenta
29	chr9:27165200-27165400	Enhancers	Ovary	ovary
30	chr9:27165200-27165600	Enhancers	Brain Germinal Matrix	brain
31	chr9:27165200-27165800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:27165200-27165800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr9:27165200-27166200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr9:27165200-27166200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr9:27165200-27166200	Enhancers	HUES6 Cell Line	embryonic stem cell

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