Variant report

Variant	rs10991894
Chromosome Location	chr9:94105104-94105105
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:94103649..94105719-chr9:94123863..94125427,2	MCF-7	breast:
2	chr9:94103409..94105645-chr9:94120684..94122259,2	K562	blood:
3	chr9:94097644..94101149-chr9:94101391..94105187,4	K562	blood:
4	chr9:94087425..94089272-chr9:94102729..94105618,2	K562	blood:
5	chr9:94104145..94106983-chr9:94120665..94122259,2	K562	blood:
6	chr9:94094684..94097540-chr9:94102093..94106003,3	K562	blood:

Variant related genes	Relation type
ENSG00000148090	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1022141	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10512209	1.00[AFR][1000 genomes]
rs10991842	0.83[ASN][1000 genomes]
rs10991844	0.87[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs10991845	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs10991846	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs10991847	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs10991852	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs10991854	0.87[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs10991856	0.83[ASN][1000 genomes]
rs10991857	0.83[ASN][1000 genomes]
rs10991863	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs10991867	1.00[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs10991868	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs10991871	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs10991874	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10991876	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10991879	0.90[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10991883	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10991884	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10991885	0.87[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10991886	0.85[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10991887	1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10991892	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10991893	1.00[CEU][hapmap];0.93[CHB][hapmap];0.95[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10991895	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10991896	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10991897	1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10991901	0.87[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10991903	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10991904	0.87[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10991906	0.87[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12238387	0.83[ASN][1000 genomes]
rs16907250	1.00[AFR][1000 genomes]
rs16907269	0.82[ASN][1000 genomes]
rs16907273	0.82[ASN][1000 genomes]
rs16907280	1.00[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs16907293	1.00[AFR][1000 genomes]
rs16907311	0.87[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs16907384	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2281922	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2292365	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs3811122	0.83[ASN][1000 genomes]
rs3811124	0.83[ASN][1000 genomes]
rs3851540	1.00[AFR][1000 genomes]
rs4430195	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4537426	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs7868771	0.87[CEU][hapmap];0.82[JPT][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	nsv893570	chr9:93973938-94148084	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv482877	chr9:93979351-94157734	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv893571	chr9:94072113-94202927	Genic enhancers Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94052000-94119200	Weak transcription	Small Intestine	intestine
2	chr9:94090200-94106200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr9:94090600-94108400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:94090600-94109400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr9:94093200-94122600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr9:94097800-94121600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr9:94099200-94105400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:94099200-94105600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr9:94099200-94105800	Strong transcription	Primary B cells from peripheral blood	blood
10	chr9:94099800-94108600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr9:94100000-94106800	Strong transcription	Primary B cells from cord blood	blood
12	chr9:94100400-94105200	Strong transcription	Fetal Intestine Large	intestine
13	chr9:94100400-94105400	Strong transcription	HepG2	liver
14	chr9:94100600-94105400	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr9:94101000-94105400	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr9:94101000-94122400	Weak transcription	HUVEC	blood vessel
17	chr9:94101400-94105200	Strong transcription	Primary T cells from cord blood	blood
18	chr9:94101400-94105200	Strong transcription	Brain Germinal Matrix	brain
19	chr9:94101400-94105200	Strong transcription	K562	blood
20	chr9:94101400-94105400	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr9:94101400-94105400	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr9:94101800-94105600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr9:94102000-94106000	Strong transcription	Fetal Stomach	stomach
24	chr9:94102000-94122400	Weak transcription	HMEC	breast
25	chr9:94102400-94119400	Weak transcription	Psoas Muscle	Psoas
26	chr9:94103000-94105200	Genic enhancers	Thymus	Thymus
27	chr9:94103000-94105400	Strong transcription	Fetal Muscle Leg	muscle
28	chr9:94103200-94105200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr9:94103400-94105200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr9:94103400-94105200	Strong transcription	Sigmoid Colon	Sigmoid Colon
31	chr9:94103400-94105400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr9:94103400-94105600	Strong transcription	Placenta	Placenta
33	chr9:94103600-94105200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr9:94103600-94105200	Strong transcription	Fetal Brain Male	brain
35	chr9:94103800-94105200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
36	chr9:94103800-94105400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr9:94103800-94105600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr9:94104000-94105200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
39	chr9:94104200-94105200	Strong transcription	H1 Cell Line	embryonic stem cell
40	chr9:94104200-94105200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr9:94104200-94105200	Strong transcription	Osteobl	bone
42	chr9:94104200-94105400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr9:94104200-94105400	Strong transcription	NHDF-Ad	bronchial
44	chr9:94104200-94105600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr9:94104200-94105800	Strong transcription	Primary T helper cells PMA-I stimulated	--
46	chr9:94104400-94105200	Strong transcription	Primary T cells fromperipheralblood	blood
47	chr9:94104400-94105400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr9:94104400-94105400	Strong transcription	Skeletal Muscle Female	skeletal muscle
49	chr9:94104400-94105600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr9:94104400-94113600	Weak transcription	Hela-S3	cervix

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