Variant report

Variant	rs73640569
Chromosome Location	chr9:7965454-7965455
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs59429921	1.00[AMR][1000 genomes]
rs60687579	1.00[AMR][1000 genomes]
rs7018764	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73640565	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73640570	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73640571	1.00[AMR][1000 genomes]
rs73640572	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7854969	0.94[AFR][1000 genomes];1.00[AMR][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	nsv1033077	chr9:7358832-7990735	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv539977	chr9:7358832-7990735	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv995116	chr9:7682729-8065192	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv8414	chr9:7827373-8511613	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1024456	chr9:7887727-8157591	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv539979	chr9:7887727-8157591	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv892216	chr9:7910934-7985651	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv892217	chr9:7919153-7978514	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7959800-7967200	Weak transcription	Dnd41	blood
2	chr9:7961000-7967200	Weak transcription	Primary T cells from cord blood	blood
3	chr9:7961400-7967200	Weak transcription	Thymus	Thymus
4	chr9:7961800-7966800	Weak transcription	Stomach Mucosa	stomach
5	chr9:7962600-7967600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:7962800-7969800	Weak transcription	Fetal Brain Male	brain
7	chr9:7963600-7965800	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr9:7963600-7967200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr9:7963600-7967400	Weak transcription	Fetal Intestine Small	intestine
10	chr9:7963600-7967600	Weak transcription	Fetal Intestine Large	intestine
11	chr9:7963800-7966200	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr9:7964000-7966800	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr9:7964000-7967200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr9:7964400-7968000	Weak transcription	Fetal Stomach	stomach
15	chr9:7964600-7977200	Weak transcription	Fetal Heart	heart
16	chr9:7965000-7965600	Enhancers	Fetal Lung	lung
17	chr9:7965200-7967200	Enhancers	Primary monocytes fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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