Variant report

Variant	rs73419728
Chromosome Location	chr9:14936613-14936614
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs55690915	1.00[AMR][1000 genomes]
rs57954003	1.00[AMR][1000 genomes]
rs59461104	1.00[AMR][1000 genomes]
rs60047223	1.00[AMR][1000 genomes]
rs73419726	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73419730	0.91[AFR][1000 genomes]
rs73419735	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73642484	1.00[AMR][1000 genomes]
rs73642486	1.00[AMR][1000 genomes]
rs73642488	1.00[AMR][1000 genomes]
rs73642489	1.00[AMR][1000 genomes]
rs73642494	1.00[AMR][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	nsv1029491	chr9:14033607-14942373	Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv613637	chr9:14524438-15011915	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv831518	chr9:14760638-14953501	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv613647	chr9:14852141-15016475	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv892620	chr9:14922877-15086021	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv892621	chr9:14928013-15043692	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14925200-14945400	Weak transcription	Aorta	Aorta
2	chr9:14927600-14937000	Weak transcription	Fetal Lung	lung
3	chr9:14933000-14941800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:14933200-14957200	Weak transcription	Fetal Muscle Leg	muscle
5	chr9:14934600-14937400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr9:14934600-14938200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:14935000-14937600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr9:14935200-14937000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr9:14935200-14937200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr9:14935200-14937200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr9:14935200-14937200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr9:14935200-14937400	Enhancers	Colon Smooth Muscle	Colon
13	chr9:14935200-14937600	Enhancers	Fetal Stomach	stomach
14	chr9:14935200-14939200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr9:14935400-14937400	Enhancers	Fetal Brain Female	brain
16	chr9:14935800-14937000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr9:14935800-14938800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:14936000-14936800	Enhancers	Fetal Heart	heart
19	chr9:14936000-14937200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:14936200-14937200	Enhancers	Fetal Brain Male	brain
21	chr9:14936600-14936800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr9:14936600-14937200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr9:14936600-14942000	Weak transcription	Fetal Kidney	kidney

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