Variant report

Variant	rs7023885
Chromosome Location	chr9:12851252-12851253
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1332054	1.00[AMR][1000 genomes]
rs16929880	1.00[AMR][1000 genomes]
rs16929883	1.00[AMR][1000 genomes]
rs4297127	1.00[AMR][1000 genomes]
rs4599899	1.00[AMR][1000 genomes]
rs4741258	1.00[AMR][1000 genomes]
rs7018559	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7034819	1.00[AFR][1000 genomes];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	nsv498136	chr9:12387840-12984158	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	esv2422212	chr9:12448789-13127738	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv892573	chr9:12730636-12874703	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv892574	chr9:12754969-12918226	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv892575	chr9:12804243-12852462	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv613615	chr9:12830070-12947238	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12849400-12852000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr9:12849800-12851800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr9:12850000-12851600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr9:12850400-12853600	Weak transcription	Fetal Intestine Large	intestine
5	chr9:12850400-12859200	Weak transcription	Small Intestine	intestine
6	chr9:12850600-12851400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr9:12850600-12853600	Weak transcription	Fetal Intestine Small	intestine
8	chr9:12850600-12859000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr9:12850800-12853000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr9:12850800-12854200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr9:12851000-12852200	Weak transcription	Fetal Stomach	stomach
12	chr9:12851000-12854200	Weak transcription	HMEC	breast
13	chr9:12851000-12858400	Weak transcription	Stomach Mucosa	stomach
14	chr9:12851200-12851400	Weak transcription	NHDF-Ad	bronchial
15	chr9:12851200-12851800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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