Variant report

Variant	rs35826725
Chromosome Location	chr15:41713219-41713220
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:41693298..41696074-chr15:41713088..41714637,2	MCF-7	breast:
2	chr15:41711628..41713417-chr15:41713793..41716319,2	MCF-7	breast:
3	chr15:41708317..41710602-chr15:41711098..41714425,3	MCF-7	breast:
4	chr15:41706897..41710806-chr15:41711426..41714664,8	MCF-7	breast:

Variant related genes	Relation type
ENSG00000137806	Chromatin interaction
ENSG00000137815	Chromatin interaction

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10152497	0.93[ASN][1000 genomes]
rs10152702	0.83[EUR][1000 genomes]
rs10153010	0.93[ASN][1000 genomes]
rs10467974	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10518718	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11630191	0.93[ASN][1000 genomes]
rs11631770	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11633799	0.93[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs12324291	0.90[ASN][1000 genomes]
rs13379756	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap]
rs16971767	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs16971798	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs16971806	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs16971832	0.85[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs16971834	0.85[CEU][hapmap];0.93[CHB][hapmap];0.92[CHD][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs1757455	0.87[ASN][1000 genomes]
rs1757463	0.81[CHB][hapmap]
rs2015781	0.93[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2777491	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs28393472	0.93[ASN][1000 genomes]
rs28526381	0.93[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs28578057	0.83[ASN][1000 genomes]
rs28583065	0.83[ASN][1000 genomes]
rs28600680	0.89[ASN][1000 genomes]
rs28643296	0.87[ASN][1000 genomes]
rs28655070	0.96[ASN][1000 genomes]
rs28716108	0.85[ASN][1000 genomes]
rs28792672	0.87[ASN][1000 genomes]
rs28847691	0.96[ASN][1000 genomes]
rs316605	0.93[CHB][hapmap];0.86[CHD][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs316609	0.93[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs316610	0.86[CHB][hapmap];0.86[CHD][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs316613	0.92[ASN][1000 genomes]
rs316614	0.93[CHB][hapmap];0.86[CHD][hapmap];0.91[JPT][hapmap];0.92[ASN][1000 genomes]
rs316615	0.87[ASN][1000 genomes]
rs316617	0.81[CHB][hapmap]
rs3743038	0.86[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs55782852	0.83[ASN][1000 genomes]
rs58335029	0.82[ASN][1000 genomes]
rs58910172	0.87[ASN][1000 genomes]
rs59590312	0.87[ASN][1000 genomes]
rs61037359	0.82[ASN][1000 genomes]
rs61127691	0.87[ASN][1000 genomes]
rs6650519	0.80[ASN][1000 genomes]
rs66538814	0.89[ASN][1000 genomes]
rs7161772	0.83[ASN][1000 genomes]
rs7163649	0.82[ASN][1000 genomes]
rs7163788	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7165675	0.83[ASN][1000 genomes]
rs7166469	0.91[MKK][hapmap]
rs7167498	0.85[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7167729	0.95[ASN][1000 genomes]
rs7168177	0.96[ASN][1000 genomes]
rs7172148	1.00[ASN][1000 genomes]
rs7175690	0.87[ASN][1000 genomes]
rs7175800	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7176314	0.87[ASN][1000 genomes]
rs7176588	0.86[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7177641	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7178634	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap]
rs7178777	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap]
rs7180418	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap]
rs7180492	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7181911	0.89[ASN][1000 genomes]
rs7182667	0.88[ASN][1000 genomes]
rs7183337	0.82[ASN][1000 genomes]
rs73404980	0.82[ASN][1000 genomes]
rs73404987	0.88[ASN][1000 genomes]
rs73404994	0.93[ASN][1000 genomes]
rs73404995	0.93[ASN][1000 genomes]
rs73404996	0.93[ASN][1000 genomes]
rs73405000	0.91[ASN][1000 genomes]
rs73405001	0.91[ASN][1000 genomes]
rs73407109	0.93[ASN][1000 genomes]
rs8023619	0.83[ASN][1000 genomes]
rs8026197	0.93[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs8027626	0.95[ASN][1000 genomes]
rs8031932	0.87[GIH][hapmap]
rs8032838	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs8034626	0.81[ASN][1000 genomes]
rs8034819	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8036498	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs8036527	0.87[ASN][1000 genomes]
rs8037824	0.93[ASN][1000 genomes]
rs8041325	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap]
rs823716	0.92[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs919961	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs9302109	0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs9672866	0.89[ASN][1000 genomes]
rs9972288	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044438	chr15:41560160-41745480	Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
2	nsv1038923	chr15:41585028-41754890	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv1045142	chr15:41585044-41738314	Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
4	nsv1039283	chr15:41620499-41745480	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	63 gene(s)	inside rSNPs	diseases
5	nsv933757	chr15:41641236-41773058	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	27 gene(s)	inside rSNPs	diseases
6	nsv524476	chr15:41689232-41820200	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	nsv569232	chr15:41694377-41730246	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41710400-41713400	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr15:41710400-41715600	Weak transcription	Lung	lung
3	chr15:41710400-41724600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr15:41710400-41745200	Weak transcription	Esophagus	oesophagus
5	chr15:41710400-41750000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:41710600-41714600	Weak transcription	Stomach Mucosa	stomach
7	chr15:41710600-41715000	Weak transcription	Ovary	ovary
8	chr15:41710600-41716200	Weak transcription	Stomach Smooth Muscle	stomach
9	chr15:41710600-41717000	Weak transcription	Fetal Stomach	stomach
10	chr15:41710600-41721200	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr15:41710600-41721200	Weak transcription	Right Atrium	heart
12	chr15:41710600-41723800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr15:41710600-41723800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr15:41710600-41729800	Weak transcription	Brain Substantia Nigra	brain
15	chr15:41710600-41731600	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr15:41710600-41731600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr15:41710600-41731800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr15:41710600-41733600	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr15:41710600-41745200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr15:41710800-41716200	Weak transcription	Fetal Brain Female	brain
21	chr15:41710800-41716400	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr15:41710800-41718800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr15:41710800-41718800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr15:41710800-41718800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr15:41710800-41718800	Weak transcription	HMEC	breast
26	chr15:41710800-41718800	Weak transcription	NH-A	brain
27	chr15:41710800-41718800	Weak transcription	NHLF	lung
28	chr15:41710800-41720800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr15:41710800-41720800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr15:41710800-41721200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr15:41710800-41724200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr15:41710800-41724800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr15:41710800-41724800	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr15:41710800-41726600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr15:41710800-41727800	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr15:41710800-41729800	Weak transcription	Brain Cingulate Gyrus	brain
37	chr15:41710800-41729800	Weak transcription	Psoas Muscle	Psoas
38	chr15:41710800-41730200	Weak transcription	Fetal Intestine Large	intestine
39	chr15:41710800-41730600	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr15:41710800-41731600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr15:41710800-41731800	Weak transcription	Left Ventricle	heart
42	chr15:41710800-41733400	Weak transcription	Brain Hippocampus Middle	brain
43	chr15:41710800-41733400	Weak transcription	HSMMtube	muscle
44	chr15:41711000-41714200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr15:41711000-41718800	Weak transcription	HSMM	muscle
46	chr15:41711000-41729800	Weak transcription	Placenta	Placenta
47	chr15:41711000-41730200	Weak transcription	Adipose Nuclei	Adipose
48	chr15:41711000-41730600	Weak transcription	Osteobl	bone
49	chr15:41711200-41715400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr15:41711200-41718800	Weak transcription	Fetal Muscle Trunk	muscle

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