Variant report

Variant	rs12269110
Chromosome Location	chr10:91118823-91118824
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10159717	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11203082	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11203083	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11203087	0.83[EUR][1000 genomes]
rs11203088	0.85[AFR][1000 genomes]
rs11203091	0.93[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11203093	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11203095	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12242873	1.00[AMR][1000 genomes]
rs12243051	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12243721	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12243856	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12245646	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12249661	0.81[AFR][1000 genomes]
rs12249707	0.81[AFR][1000 genomes]
rs12250550	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12250610	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12251678	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12252455	1.00[AMR][1000 genomes]
rs12256540	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12259825	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12259887	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12263019	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12263584	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12263989	0.81[AFR][1000 genomes]
rs12264051	0.81[AFR][1000 genomes]
rs12267215	0.83[EUR][1000 genomes]
rs12267943	0.81[AFR][1000 genomes]
rs12268333	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs2151008	0.81[AFR][1000 genomes]
rs4378299	0.81[AFR][1000 genomes]
rs59633641	1.00[EUR][1000 genomes]
rs7074809	1.00[EUR][1000 genomes]
rs7079179	1.00[EUR][1000 genomes]
rs7090951	1.00[EUR][1000 genomes]
rs7910157	1.00[EUR][1000 genomes]
rs7912070	1.00[AMR][1000 genomes]
rs7919999	1.00[EUR][1000 genomes]
rs7922439	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91108600-91122200	Weak transcription	Spleen	Spleen
2	chr10:91112400-91120000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr10:91112400-91122400	Weak transcription	Esophagus	oesophagus
4	chr10:91112400-91127400	Weak transcription	Left Ventricle	heart
5	chr10:91113000-91119200	Weak transcription	Lung	lung
6	chr10:91113200-91122200	Weak transcription	Placenta	Placenta
7	chr10:91116200-91122000	Weak transcription	K562	blood
8	chr10:91116400-91119000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr10:91116600-91120000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr10:91117000-91122000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr10:91117000-91127800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr10:91117200-91119200	Weak transcription	Fetal Intestine Large	intestine
13	chr10:91117200-91119400	Weak transcription	Fetal Intestine Small	intestine
14	chr10:91117200-91119800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr10:91117200-91119800	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr10:91117200-91120000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr10:91117200-91122000	Weak transcription	Fetal Heart	heart
18	chr10:91117200-91127400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr10:91117200-91127400	Weak transcription	Fetal Muscle Leg	muscle
20	chr10:91117400-91120000	Weak transcription	Fetal Kidney	kidney
21	chr10:91117400-91124000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr10:91117600-91120200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr10:91118000-91122200	Weak transcription	Primary hematopoietic stem cells	blood

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