Variant report

Variant	rs11203091
Chromosome Location	chr10:91120653-91120654
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11185740	1.00[CEU][hapmap]
rs11203093	0.83[EUR][1000 genomes]
rs11203095	0.83[EUR][1000 genomes]
rs11203100	0.90[CHB][hapmap];0.85[YRI][hapmap];0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12243051	0.83[EUR][1000 genomes]
rs12243721	0.83[EUR][1000 genomes]
rs12243856	0.83[EUR][1000 genomes]
rs12245646	1.00[ASW][hapmap];0.82[LWK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs12250550	0.83[EUR][1000 genomes]
rs12250610	0.83[EUR][1000 genomes]
rs12251678	1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs12255221	1.00[AMR][1000 genomes]
rs12256540	1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs12259825	0.83[EUR][1000 genomes]
rs12259887	0.83[EUR][1000 genomes]
rs12263019	1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs12263584	0.83[EUR][1000 genomes]
rs12268333	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12269110	0.93[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs1332334	1.00[TSI][hapmap]
rs59633641	0.83[EUR][1000 genomes]
rs7067930	0.81[CHB][hapmap]
rs7074809	0.83[EUR][1000 genomes]
rs7076750	1.00[CEU][hapmap]
rs7079179	0.83[EUR][1000 genomes]
rs7090951	0.83[EUR][1000 genomes]
rs7099173	1.00[CEU][hapmap]
rs7907230	1.00[TSI][hapmap]
rs7910157	1.00[TSI][hapmap];0.83[EUR][1000 genomes]
rs7910817	1.00[ASW][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs7912070	1.00[YRI][hapmap]
rs7913002	1.00[CHB][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs7917528	1.00[CEU][hapmap]
rs7919999	0.83[EUR][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	nsv1042848	chr10:90466032-91318474	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv540741	chr10:90466032-91318474	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv1041964	chr10:90861380-91378356	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv1040375	chr10:91022218-91153074	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	esv34085	chr10:91065949-91174175	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
6	nsv528603	chr10:91119644-91124029	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91108600-91122200	Weak transcription	Spleen	Spleen
2	chr10:91112400-91122400	Weak transcription	Esophagus	oesophagus
3	chr10:91112400-91127400	Weak transcription	Left Ventricle	heart
4	chr10:91113200-91122200	Weak transcription	Placenta	Placenta
5	chr10:91116200-91122000	Weak transcription	K562	blood
6	chr10:91117000-91122000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr10:91117000-91127800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr10:91117200-91122000	Weak transcription	Fetal Heart	heart
9	chr10:91117200-91127400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr10:91117200-91127400	Weak transcription	Fetal Muscle Leg	muscle
11	chr10:91117400-91124000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr10:91118000-91122200	Weak transcription	Primary hematopoietic stem cells	blood
13	chr10:91119000-91122200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr10:91119200-91121000	Enhancers	Fetal Intestine Large	intestine
15	chr10:91119400-91122200	Weak transcription	Right Atrium	heart
16	chr10:91119600-91133800	Weak transcription	Pancreas	Pancrea
17	chr10:91120000-91121200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:91120000-91127200	Weak transcription	Duodenum Mucosa	Duodenum
19	chr10:91120200-91122200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr10:91120400-91127000	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr10:91120600-91122200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr10:91120600-91122400	Weak transcription	Fetal Intestine Small	intestine

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