Variant report

Variant	rs73103108
Chromosome Location	chr5:59041176-59041177
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:59022602..59025084-chr5:59040662..59042603,2	MCF-7	breast:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs16890086	1.00[AMR][1000 genomes]
rs16890141	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73101121	1.00[AMR][1000 genomes]
rs73101139	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73101141	1.00[AMR][1000 genomes]
rs7713809	0.82[AFR][1000 genomes];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	nsv881708	chr5:58869051-59093198	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1018015	chr5:58889470-59532667	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv537766	chr5:58889470-59532667	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv427720	chr5:58913581-59086987	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
5	nsv534614	chr5:58962510-59388525	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59028000-59043200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr5:59036800-59041600	Enhancers	Hela-S3	cervix
3	chr5:59039400-59041200	Enhancers	Brain Germinal Matrix	brain
4	chr5:59039400-59042600	Enhancers	HMEC	breast
5	chr5:59039400-59059800	Weak transcription	Primary B cells from cord blood	blood
6	chr5:59039600-59043000	Enhancers	HUVEC	blood vessel
7	chr5:59039800-59042600	Enhancers	Rectal Smooth Muscle	rectum
8	chr5:59039800-59042600	Enhancers	NH-A	brain
9	chr5:59040000-59042800	Enhancers	HSMM	muscle
10	chr5:59040200-59041200	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr5:59040200-59041600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr5:59040200-59042600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr5:59040400-59041200	Enhancers	Fetal Lung	lung
14	chr5:59040400-59041200	Flanking Active TSS	A549	lung
15	chr5:59040400-59041600	Enhancers	Brain Substantia Nigra	brain
16	chr5:59040400-59043400	Enhancers	Colon Smooth Muscle	Colon
17	chr5:59040600-59041200	Enhancers	Fetal Brain Female	brain
18	chr5:59040600-59041200	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr5:59040600-59041400	Enhancers	Brain Anterior Caudate	brain
20	chr5:59040600-59041400	Enhancers	Brain Cingulate Gyrus	brain
21	chr5:59040800-59041200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr5:59040800-59041200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr5:59040800-59041200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
24	chr5:59040800-59041200	Flanking Active TSS	HSMMtube	muscle
25	chr5:59040800-59041200	Flanking Active TSS	Osteobl	bone
26	chr5:59040800-59041400	Enhancers	Fetal Heart	heart
27	chr5:59040800-59041400	Enhancers	NHDF-Ad	bronchial
28	chr5:59040800-59041600	Flanking Active TSS	NHEK	skin
29	chr5:59040800-59042200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr5:59040800-59042200	Enhancers	Fetal Stomach	stomach
31	chr5:59041000-59041200	Enhancers	Adipose Nuclei	Adipose
32	chr5:59041000-59041200	Enhancers	Stomach Smooth Muscle	stomach
33	chr5:59041000-59041400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:59041000-59041400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr5:59041000-59041600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr5:59041000-59041600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr5:59041000-59041600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
38	chr5:59041000-59042800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr5:59041000-59043400	Enhancers	Fetal Brain Male	brain
40	chr5:59041000-59047000	Weak transcription	Fetal Intestine Small	intestine

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