Variant report

Variant	rs35830608
Chromosome Location	chr10:91117083-91117084
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:91115941..91117620-chr10:91122098..91123707,2	MCF-7	breast:

Extended variants
information (count: 59 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10509571	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10509572	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10788642	0.83[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs10887950	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10887953	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10887957	0.87[ASN][1000 genomes]
rs10887959	0.83[ASN][1000 genomes]
rs11203063	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11203066	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs11203070	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11203072	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11203090	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11203099	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11203105	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs11203106	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs11203109	0.83[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs11203112	0.80[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs11203115	0.88[ASN][1000 genomes]
rs11203119	0.81[ASN][1000 genomes]
rs11819073	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12248331	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12255504	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12356008	0.80[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs12772449	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs12781453	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12781505	0.84[ASN][1000 genomes]
rs1332330	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1591051	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17096301	0.81[AMR][1000 genomes]
rs17120001	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17120004	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17121248	0.82[ASN][1000 genomes]
rs2070845	0.87[AMR][1000 genomes]
rs2274878	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34032344	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs34234196	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34712773	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35833529	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3740027	0.84[AMR][1000 genomes]
rs3780878	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4339948	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6586182	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6586183	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7073534	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7085361	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7088579	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7097569	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs71479013	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7897619	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7897873	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7910389	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7916812	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs884407	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9733018	0.85[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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs35830608	IFIT5	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:36 , 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	chr10:91114600-91117200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr10:91114600-91117400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr10:91114800-91117200	Enhancers	NHLF	lung
10	chr10:91114800-91117400	Enhancers	NHDF-Ad	bronchial
11	chr10:91115000-91117200	Enhancers	Osteobl	bone
12	chr10:91115400-91117200	Enhancers	Brain Germinal Matrix	brain
13	chr10:91115400-91117400	Enhancers	Fetal Lung	lung
14	chr10:91116000-91117200	Enhancers	Fetal Muscle Leg	muscle
15	chr10:91116200-91122000	Weak transcription	K562	blood
16	chr10:91116400-91117200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr10:91116400-91119000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr10:91116600-91117200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr10:91116600-91117200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr10:91116600-91117200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr10:91116600-91117200	Enhancers	Fetal Intestine Small	intestine
22	chr10:91116600-91117800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr10:91116600-91118000	Enhancers	Primary hematopoietic stem cells	blood
24	chr10:91116600-91120000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr10:91116800-91117200	Enhancers	H1 Cell Line	embryonic stem cell
26	chr10:91116800-91117200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr10:91116800-91117200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr10:91116800-91117200	Enhancers	Fetal Heart	heart
29	chr10:91116800-91117200	Enhancers	Fetal Stomach	stomach
30	chr10:91116800-91117400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr10:91116800-91117400	Enhancers	Fetal Kidney	kidney
32	chr10:91117000-91117200	Enhancers	Fetal Intestine Large	intestine
33	chr10:91117000-91117400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr10:91117000-91118200	Weak transcription	GM12878-XiMat	blood
35	chr10:91117000-91122000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr10:91117000-91127800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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