Variant report

Variant	rs7866188
Chromosome Location	chr9:94681588-94681589
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:94676298..94678105-chr9:94680028..94681662,2	MCF-7	breast:
2	chr9:94664745..94669992-chr9:94681267..94685780,5	K562	blood:
3	chr9:94673282..94676556-chr9:94680783..94682805,3	K562	blood:
4	chr9:94680096..94683212-chr9:94691490..94694919,3	K562	blood:
5	chr9:94679676..94683212-chr9:94692527..94694919,4	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11795340	0.88[JPT][hapmap]
rs1573979	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16908147	1.00[CHB][hapmap]
rs1954599	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs2049704	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2049705	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2186091	1.00[CHB][hapmap];0.82[EUR][1000 genomes]
rs2297569	1.00[CHB][hapmap]
rs3858082	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59394638	0.83[ASN][1000 genomes]
rs60066947	0.83[ASN][1000 genomes]
rs6479381	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6479382	1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7032998	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7033261	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7038822	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs7046846	1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7048052	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73519162	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73519164	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73519170	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73519172	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73519174	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73519181	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7851545	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7854552	0.83[ASN][1000 genomes]
rs7854566	0.83[ASN][1000 genomes]
rs7854742	0.83[ASN][1000 genomes]
rs7857164	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7857924	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7872177	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7873326	0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7875069	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7875147	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7876056	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7866188	AHSP	trans	lymphoblastoid	seeQTL

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94668800-94682800	Weak transcription	Colonic Mucosa	Colon
2	chr9:94670200-94682800	Weak transcription	Fetal Kidney	kidney
3	chr9:94670400-94682800	Weak transcription	Right Atrium	heart
4	chr9:94670600-94686200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr9:94671600-94682600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:94677400-94683000	Weak transcription	K562	blood
7	chr9:94677600-94682800	Weak transcription	Fetal Intestine Large	intestine
8	chr9:94678000-94685000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr9:94678200-94683600	Enhancers	Colon Smooth Muscle	Colon
10	chr9:94678200-94686600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:94678800-94686200	Weak transcription	Ovary	ovary
12	chr9:94679600-94682800	Weak transcription	Fetal Heart	heart
13	chr9:94679600-94684200	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:94680000-94682000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr9:94680000-94682000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:94680200-94682600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr9:94680200-94682800	Weak transcription	Fetal Stomach	stomach
18	chr9:94680800-94681800	Enhancers	Fetal Lung	lung
19	chr9:94681000-94681800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr9:94681200-94681600	Enhancers	Stomach Mucosa	stomach
21	chr9:94681200-94681800	Enhancers	Gastric	stomach
22	chr9:94681200-94681800	Enhancers	Rectal Smooth Muscle	rectum
23	chr9:94681400-94681600	Enhancers	Stomach Smooth Muscle	stomach
24	chr9:94681400-94682000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr9:94681400-94683200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr9:94681400-94683800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr9:94681400-94691400	Weak transcription	Pancreas	Pancrea

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