Variant report

Variant	rs7867069
Chromosome Location	chr9:97380597-97380598
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:97379626..97381399-chr9:97382615..97384650,2	K562	blood:
2	chr9:97377917..97381579-chr9:97382484..97386312,5	MCF-7	breast:
3	chr9:97369469..97371530-chr9:97378423..97380826,2	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10993270	1.00[YRI][hapmap]
rs12683407	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12684849	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16910850	0.89[CEU][hapmap];0.80[CHB][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs16910853	0.89[CEU][hapmap];0.80[CHB][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs16910860	0.89[CEU][hapmap];0.80[CHB][hapmap];0.89[GIH][hapmap];0.88[JPT][hapmap];0.94[TSI][hapmap];0.86[EUR][1000 genomes]
rs2296707	0.80[CEU][hapmap];0.86[JPT][hapmap];0.81[EUR][1000 genomes]
rs28369691	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28369738	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28369782	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28369786	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28402377	0.88[EUR][1000 genomes]
rs28402378	0.88[EUR][1000 genomes]
rs28402384	0.88[EUR][1000 genomes]
rs28402386	0.88[EUR][1000 genomes]
rs28402389	0.88[EUR][1000 genomes]
rs28402390	0.88[EUR][1000 genomes]
rs28402396	0.88[EUR][1000 genomes]
rs28402397	0.88[EUR][1000 genomes]
rs28402401	0.85[EUR][1000 genomes]
rs28402404	0.88[EUR][1000 genomes]
rs4111369	0.80[CEU][hapmap];0.80[CHB][hapmap];1.00[GIH][hapmap];0.94[TSI][hapmap]
rs4574908	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs573212	0.88[CHD][hapmap];0.88[JPT][hapmap];0.81[MEX][hapmap];0.89[MKK][hapmap]
rs59327242	0.88[EUR][1000 genomes]
rs59727084	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7019207	0.82[CEU][hapmap];0.88[EUR][1000 genomes]
rs7028990	0.80[CEU][hapmap];0.80[CHB][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];0.94[TSI][hapmap]
rs7849320	0.80[CEU][hapmap];0.86[JPT][hapmap];0.81[EUR][1000 genomes]
rs7850385	0.81[EUR][1000 genomes]
rs7859022	0.81[EUR][1000 genomes]
rs7859489	0.80[CEU][hapmap];0.84[JPT][hapmap];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041195	chr9:97054795-97402378	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv893596	chr9:97321172-97598966	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
3	nsv614918	chr9:97380597-97412037	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv893597	chr9:97380597-97463435	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97364400-97382800	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr9:97364800-97382800	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr9:97366600-97384400	Weak transcription	Small Intestine	intestine
4	chr9:97370000-97382400	Weak transcription	Lung	lung
5	chr9:97371400-97401000	Weak transcription	Spleen	Spleen
6	chr9:97371600-97384200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:97372400-97384400	Weak transcription	Gastric	stomach
8	chr9:97373000-97381200	Weak transcription	Fetal Stomach	stomach
9	chr9:97374600-97380600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr9:97374600-97384400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr9:97374600-97392600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr9:97374600-97393400	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr9:97374800-97381000	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr9:97374800-97384200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr9:97375200-97385600	Weak transcription	Stomach Mucosa	stomach
16	chr9:97375400-97382800	Strong transcription	Duodenum Mucosa	Duodenum
17	chr9:97375400-97382800	Strong transcription	Fetal Intestine Large	intestine
18	chr9:97375400-97383000	Strong transcription	Fetal Intestine Small	intestine
19	chr9:97375800-97380600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr9:97375800-97381000	Weak transcription	Pancreas	Pancrea
21	chr9:97376200-97385800	Strong transcription	Liver	Liver

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