Variant report

Variant	rs73853957
Chromosome Location	chr3:112395365-112395366
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:112393886..112395917-chr3:112708547..112711075,2	K562	blood:
2	chr3:112382809..112385022-chr3:112393249..112395898,2	MCF-7	breast:
3	chr3:112358207..112360933-chr3:112392611..112397881,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000272844	Chromatin interaction
ENSG00000091986	Chromatin interaction
ENSG00000163607	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs58079096	0.98[AFR][1000 genomes]
rs58671322	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60413428	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61467102	0.89[AFR][1000 genomes]
rs73853947	0.98[AFR][1000 genomes]
rs73853955	1.00[AFR][1000 genomes]
rs73853956	0.98[AFR][1000 genomes]
rs73853958	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73853962	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3329419	chr3:112236688-112620544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv432477	chr3:112390310-112603310	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112388000-112395800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:112389200-112396800	Enhancers	Osteobl	bone
3	chr3:112389600-112395800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr3:112389600-112396200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr3:112390400-112395800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr3:112391000-112395400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr3:112391200-112395800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr3:112391400-112407800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr3:112391600-112395400	Enhancers	A549	lung
10	chr3:112391600-112395600	Weak transcription	Fetal Lung	lung
11	chr3:112391800-112395400	Weak transcription	Thymus	Thymus
12	chr3:112391800-112395800	Weak transcription	Spleen	Spleen
13	chr3:112392000-112395400	Weak transcription	Primary hematopoietic stem cells	blood
14	chr3:112392000-112397200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr3:112392200-112395600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr3:112392200-112395600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:112392200-112397400	Enhancers	Placenta Amnion	Placenta Amnion
18	chr3:112392400-112395800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr3:112393000-112395400	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr3:112394200-112395400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr3:112394200-112395400	Enhancers	K562	blood
22	chr3:112394200-112396400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr3:112394200-112396400	Enhancers	NH-A	brain
24	chr3:112394200-112396600	Enhancers	NHEK	skin
25	chr3:112394400-112395400	Enhancers	HUVEC	blood vessel
26	chr3:112394400-112396200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr3:112394600-112396200	Enhancers	Primary T cells fromperipheralblood	blood
28	chr3:112394800-112396800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr3:112395000-112395400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr3:112395000-112395400	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr3:112395000-112395400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr3:112395000-112395600	Enhancers	Hela-S3	cervix
33	chr3:112395000-112395600	Enhancers	HMEC	breast
34	chr3:112395000-112396000	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr3:112395000-112396200	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr3:112395000-112396200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr3:112395000-112396200	Enhancers	Duodenum Mucosa	Duodenum
38	chr3:112395000-112396400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr3:112395000-112396400	Enhancers	Primary B cells from peripheral blood	blood
40	chr3:112395000-112396400	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr3:112395000-112397800	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr3:112395200-112395400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr3:112395200-112395400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr3:112395200-112395400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr3:112395200-112395400	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr3:112395200-112395400	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr3:112395200-112395400	Enhancers	HSMMtube	muscle
48	chr3:112395200-112395600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr3:112395200-112395600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr3:112395200-112395600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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