Variant report

Variant	rs61549238
Chromosome Location	chr3:100309181-100309182
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:100181471..100182427-chr3:100308979..100310073,6	K562	blood:
2	chr3:100181564..100184311-chr3:100308277..100310597,3	MCF-7	breast:
3	chr3:100034880..100036007-chr3:100308930..100309869,3	MCF-7	breast:
4	chr3:100035487..100036085-chr3:100309070..100309718,3	MCF-7	breast:
5	chr3:100181513..100182449-chr3:100308116..100310031,6	MCF-7	breast:
6	chr3:100181402..100182493-chr3:100308907..100310066,13	MCF-7	breast:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10428254	0.91[ASN][1000 genomes]
rs10511187	0.92[ASN][1000 genomes]
rs10511188	0.92[ASN][1000 genomes]
rs10936264	0.84[ASN][1000 genomes]
rs1165521	0.86[ASN][1000 genomes]
rs12634935	0.92[ASN][1000 genomes]
rs12635503	0.92[ASN][1000 genomes]
rs12636790	0.92[ASN][1000 genomes]
rs12637319	0.92[ASN][1000 genomes]
rs1305373	0.92[ASN][1000 genomes]
rs1305375	0.92[ASN][1000 genomes]
rs13069547	0.86[ASN][1000 genomes]
rs13321761	0.92[ASN][1000 genomes]
rs1842732	0.90[ASN][1000 genomes]
rs2169554	0.87[ASN][1000 genomes]
rs3924054	0.81[AMR][1000 genomes]
rs58618663	0.82[ASN][1000 genomes]
rs60151360	0.91[ASN][1000 genomes]
rs619149	0.86[ASN][1000 genomes]
rs653530	0.92[ASN][1000 genomes]
rs661266	0.92[ASN][1000 genomes]
rs6768258	0.92[ASN][1000 genomes]
rs6770693	0.92[ASN][1000 genomes]
rs6771421	0.92[ASN][1000 genomes]
rs6773148	0.84[ASN][1000 genomes]
rs6783630	0.92[ASN][1000 genomes]
rs6785969	0.92[ASN][1000 genomes]
rs6786853	0.87[ASN][1000 genomes]
rs73141183	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7426414	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9290097	0.91[ASN][1000 genomes]
rs9290098	0.92[ASN][1000 genomes]
rs9290099	0.92[ASN][1000 genomes]
rs9290100	0.92[ASN][1000 genomes]
rs9790050	0.92[ASN][1000 genomes]
rs9790137	0.92[ASN][1000 genomes]
rs9790219	0.92[ASN][1000 genomes]
rs9818800	0.87[ASN][1000 genomes]
rs9829641	0.91[ASN][1000 genomes]
rs9829972	0.90[ASN][1000 genomes]
rs9834474	0.91[ASN][1000 genomes]
rs9834776	0.87[ASN][1000 genomes]
rs9838918	0.90[ASN][1000 genomes]
rs9853434	0.87[ASN][1000 genomes]
rs9856061	0.90[ASN][1000 genomes]
rs9856338	0.84[ASN][1000 genomes]
rs9860005	0.92[ASN][1000 genomes]
rs9874401	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751965	chr3:100299310-100462527	Enhancers Genic enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	esv2751966	chr3:100299310-100468500	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	esv2756284	chr3:100299329-100427937	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2752830	chr3:100299329-100442478	Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv432464	chr3:100299329-100442478	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	esv2751967	chr3:100299329-100455139	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	esv2751968	chr3:100299329-100476713	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	nsv432466	chr3:100299329-100476713	Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
9	nsv536667	chr3:100308355-100445857	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100276800-100309200	Weak transcription	NH-A	brain
2	chr3:100300600-100309200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr3:100304200-100309200	Weak transcription	Fetal Stomach	stomach
4	chr3:100305000-100309200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:100308800-100309200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:100308800-100312000	Enhancers	Fetal Intestine Large	intestine
7	chr3:100309000-100309200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr3:100309000-100309200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:100309000-100309200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:100309000-100309200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr3:100309000-100309200	Enhancers	Muscle Satellite Cultured Cells	--
12	chr3:100309000-100309200	Enhancers	Psoas Muscle	Psoas
13	chr3:100309000-100309200	Enhancers	A549	lung
14	chr3:100309000-100309200	Enhancers	Hela-S3	cervix
15	chr3:100309000-100309200	Enhancers	HSMM	muscle
16	chr3:100309000-100309200	Enhancers	HUVEC	blood vessel
17	chr3:100309000-100309200	Enhancers	NHEK	skin
18	chr3:100309000-100309200	Enhancers	Osteobl	bone
19	chr3:100309000-100309400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr3:100309000-100309400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr3:100309000-100309400	Enhancers	Pancreas	Pancrea
22	chr3:100309000-100309600	Enhancers	Primary B cells from peripheral blood	blood
23	chr3:100309000-100309600	Enhancers	NHDF-Ad	bronchial
24	chr3:100309000-100310200	Enhancers	Liver	Liver

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