Variant report

Variant	rs35975557
Chromosome Location	chr15:51425427-51425428
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:51417258..51420710-chr15:51423538..51426372,3	MCF-7	breast:
2	chr15:51425185..51425710-chr15:51490781..51491753,3	MCF-7	breast:
3	chr15:51424409..51425763-chr15:51694743..51695941,3	MCF-7	breast:
4	chr15:51425211..51425789-chr15:51573674..51574562,2	MCF-7	breast:
5	chr15:51407595..51409362-chr15:51423649..51426297,2	MCF-7	breast:
6	chr15:51424799..51425687-chr15:51484566..51485090,2	K562	blood:
7	chr15:51424780..51426009-chr15:51484368..51485483,10	MCF-7	breast:
8	chr15:51419195..51421876-chr15:51424233..51426848,2	K562	blood:
9	chr15:51425247..51427565-chr15:51436062..51438888,2	K562	blood:
10	chr15:51425013..51425714-chr15:51674755..51675460,2	MCF-7	breast:
11	chr15:51425244..51425785-chr15:51673112..51674004,3	MCF-7	breast:
12	chr15:51425036..51425713-chr15:51484663..51485513,3	MCF-7	breast:
13	chr15:51231463..51232073-chr15:51424824..51425630,2	MCF-7	breast:
14	chr15:51418702..51420720-chr15:51424387..51427020,3	MCF-7	breast:
15	chr15:51424835..51425877-chr15:51454808..51456221,4	MCF-7	breast:

No data

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10851496	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11070836	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11070837	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12440795	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13329067	0.92[ASN][1000 genomes]
rs2141278	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28362014	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35079663	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59415822	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs71471593	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer 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
2	nsv569399	chr15:50874964-51562198	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
3	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
4	nsv904214	chr15:51204364-51535192	Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	nsv1049644	chr15:51265447-51560445	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	esv34532	chr15:51276128-51752856	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	esv2758382	chr15:51282257-51830339	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	esv2760031	chr15:51282257-51830339	Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
9	nsv428634	chr15:51299632-51446666	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv471243	chr15:51345485-52018096	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS 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	39 gene(s)	inside rSNPs	diseases
11	esv2757600	chr15:51352249-51783981	Weak transcription Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51420400-51426400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr15:51423200-51426800	Enhancers	HUVEC	blood vessel
3	chr15:51423800-51425600	Enhancers	NH-A	brain
4	chr15:51423800-51425800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:51423800-51425800	Enhancers	Osteobl	bone
6	chr15:51423800-51426000	Enhancers	NHDF-Ad	bronchial
7	chr15:51423800-51426400	Enhancers	Muscle Satellite Cultured Cells	--
8	chr15:51423800-51426400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr15:51424000-51425800	Enhancers	NHLF	lung
10	chr15:51424000-51426000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr15:51424000-51426000	Enhancers	HMEC	breast
12	chr15:51424000-51426000	Enhancers	HSMM	muscle
13	chr15:51424200-51425800	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr15:51424200-51427200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr15:51424200-51427600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr15:51424400-51425600	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr15:51424400-51425800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr15:51424400-51425800	Enhancers	Brain Germinal Matrix	brain
19	chr15:51424400-51425800	Enhancers	HSMMtube	muscle
20	chr15:51424400-51427000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr15:51424600-51425600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr15:51424800-51425600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr15:51424800-51425600	Flanking Active TSS	Brain Substantia Nigra	brain
24	chr15:51424800-51425800	Enhancers	Brain Angular Gyrus	brain
25	chr15:51424800-51425800	Enhancers	Brain Anterior Caudate	brain
26	chr15:51424800-51425800	Enhancers	Brain Hippocampus Middle	brain
27	chr15:51424800-51425800	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr15:51425000-51425800	Enhancers	Brain Cingulate Gyrus	brain
29	chr15:51425000-51425800	Enhancers	Fetal Muscle Leg	muscle
30	chr15:51425000-51426200	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr15:51425200-51425600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr15:51425200-51425600	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr15:51425200-51425800	Enhancers	Ovary	ovary
34	chr15:51425200-51425800	Active TSS	Hela-S3	cervix
35	chr15:51425200-51426400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr15:51425400-51425600	Flanking Active TSS	HepG2	liver
37	chr15:51425400-51427800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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