Variant report

Variant	rs7047326
Chromosome Location	chr9:94707277-94707278
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:94706737..94709425-chr9:94709648..94712474,2	MCF-7	breast:
2	chr9:94700947..94708226-chr9:94708551..94712716,11	K562	blood:
3	chr9:94706769..94709242-chr9:94710784..94712955,2	MCF-7	breast:
4	chr9:94696439..94698046-chr9:94704884..94707640,2	K562	blood:
5	chr9:94661900..94664292-chr9:94705248..94709269,4	K562	blood:

Variant related genes	Relation type
ENSG00000169071	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10116249	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10118072	0.85[EUR][1000 genomes]
rs10124760	0.95[EUR][1000 genomes]
rs10125384	0.86[EUR][1000 genomes]
rs10125466	0.86[EUR][1000 genomes]
rs10512220	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10733743	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10761138	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10820931	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12340044	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1316268	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1881391	0.95[EUR][1000 genomes]
rs1892268	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1919100	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2297568	0.85[EUR][1000 genomes]
rs2312739	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2895201	0.84[EUR][1000 genomes]
rs3847308	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6479385	0.82[EUR][1000 genomes]
rs6479386	0.82[EUR][1000 genomes]
rs6479387	0.95[EUR][1000 genomes]
rs6479388	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6479389	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6479400	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6479402	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7020136	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7034357	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7034363	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7037255	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7038017	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7041193	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7042102	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7048699	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7848874	0.83[EUR][1000 genomes]
rs7848987	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7850309	0.82[EUR][1000 genomes]
rs7852032	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7859689	0.85[EUR][1000 genomes]
rs7862779	0.86[EUR][1000 genomes]
rs7863167	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7867072	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7869504	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7871444	0.84[EUR][1000 genomes]
rs9774945	0.82[EUR][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	nsv1047426	chr9:94363211-94758114	Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv949008	chr9:94500776-95182133	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv530946	chr9:94633154-94715023	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1050845	chr9:94687959-95312406	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
5	nsv1046733	chr9:94690622-95138564	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv831653	chr9:94692454-94867542	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv530947	chr9:94697309-95093377	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
8	nsv982625	chr9:94702344-94712887	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	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	chr9:94698000-94708200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:94698400-94707600	Weak transcription	Fetal Intestine Small	intestine
3	chr9:94698600-94708200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:94701400-94707800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:94702400-94707600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr9:94702800-94707800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr9:94702800-94708200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:94703000-94707600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr9:94703000-94707600	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr9:94704600-94707400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:94704600-94708000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr9:94704800-94707600	Enhancers	Fetal Lung	lung
13	chr9:94704800-94707800	Enhancers	Rectal Smooth Muscle	rectum
14	chr9:94706000-94707400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr9:94706200-94708000	Enhancers	Fetal Heart	heart
16	chr9:94706200-94708400	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr9:94706200-94710400	Enhancers	Placenta Amnion	Placenta Amnion
18	chr9:94706400-94707600	Enhancers	Hela-S3	cervix
19	chr9:94706400-94707800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr9:94706400-94708800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr9:94706600-94708200	Enhancers	Fetal Stomach	stomach
22	chr9:94706800-94707400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr9:94706800-94709600	Flanking Active TSS	K562	blood
24	chr9:94707000-94707400	Enhancers	Gastric	stomach
25	chr9:94707000-94708400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr9:94707000-94708400	Bivalent Enhancer	Fetal Brain Male	brain
27	chr9:94707000-94708800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr9:94707000-94708800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr9:94707000-94709800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr9:94707200-94707400	Enhancers	Colon Smooth Muscle	Colon
31	chr9:94707200-94707600	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr9:94707200-94707600	Enhancers	Fetal Kidney	kidney
33	chr9:94707200-94707800	Enhancers	H1 Cell Line	embryonic stem cell
34	chr9:94707200-94708000	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr9:94707200-94708800	Enhancers	Placenta	Placenta

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