Variant report

Variant	rs9288803
Chromosome Location	chr3:105132008-105132009
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:105131124..105132764-chr3:105135409..105137743,2	MCF-7	breast:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1036581	0.94[AFR][1000 genomes]
rs13100997	0.81[AFR][1000 genomes]
rs2033802	1.00[ASW][hapmap];1.00[LWK][hapmap];0.82[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs2053307	0.91[AFR][1000 genomes]
rs4894924	0.88[ASW][hapmap];0.80[LWK][hapmap];0.86[YRI][hapmap]
rs6790159	0.92[AFR][1000 genomes]
rs7428824	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs7641185	0.94[ASW][hapmap];0.94[LWK][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs9827147	1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs9827196	0.93[AFR][1000 genomes]

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	nsv525071	chr3:105004853-105409321	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv829650	chr3:105070893-105255036	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv877304	chr3:105122214-105198374	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:105119000-105133600	Weak transcription	Brain Angular Gyrus	brain
2	chr3:105121000-105134800	Weak transcription	NHLF	lung
3	chr3:105121600-105136600	Weak transcription	HSMM	muscle
4	chr3:105121800-105133600	Weak transcription	NH-A	brain
5	chr3:105121800-105133800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr3:105122400-105133000	Weak transcription	Gastric	stomach
7	chr3:105122400-105136600	Weak transcription	Osteobl	bone
8	chr3:105122600-105133200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr3:105122600-105135800	Weak transcription	NHEK	skin
10	chr3:105123000-105134800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr3:105123800-105135800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr3:105126600-105133400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr3:105128800-105136600	Weak transcription	HMEC	breast
14	chr3:105130400-105134000	Weak transcription	A549	lung
15	chr3:105130600-105132200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr3:105130600-105132400	Weak transcription	Brain Hippocampus Middle	brain
17	chr3:105130600-105133400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:105130600-105133800	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr3:105130800-105133000	Weak transcription	Brain Anterior Caudate	brain
20	chr3:105131200-105133800	Weak transcription	Brain Substantia Nigra	brain
21	chr3:105131600-105133600	Weak transcription	Fetal Heart	heart
22	chr3:105132000-105134400	Enhancers	Brain Cingulate Gyrus	brain

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