Variant report

Variant	rs7167759
Chromosome Location	chr15:52016771-52016772
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:52010154..52013648-chr15:52016687..52020314,4	MCF-7	breast:
2	chr15:52015204..52021746-chr15:52024939..52031385,17	MCF-7	breast:
3	chr15:52016515..52018648-chr15:52040542..52043046,2	MCF-7	breast:
4	chr15:52015670..52018450-chr15:52021031..52024231,3	K562	blood:
5	chr10:123395216..123396212-chr15:52016350..52016937,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000140280	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1350173	0.83[EUR][1000 genomes]
rs16953082	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes]
rs16964486	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16964488	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs16964505	1.00[CEU][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16964506	1.00[CEU][hapmap];0.82[JPT][hapmap];0.95[EUR][1000 genomes]
rs16964507	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs16964508	1.00[CEU][hapmap];0.82[JPT][hapmap];0.95[EUR][1000 genomes]
rs16964510	0.95[EUR][1000 genomes]
rs16964518	0.95[EUR][1000 genomes]
rs16964528	0.83[EUR][1000 genomes]
rs16964532	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes]
rs16964555	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs16964561	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs16964579	0.85[EUR][1000 genomes]
rs16964585	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs16964596	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs17705373	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs17705685	1.00[YRI][hapmap]
rs1991267	1.00[JPT][hapmap]
rs2414115	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2570232	1.00[CEU][hapmap]
rs2593181	1.00[JPT][hapmap]
rs2899478	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3751595	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3794529	0.88[EUR][1000 genomes]
rs3794533	1.00[YRI][hapmap]
rs4499184	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4775971	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs56221158	0.93[EUR][1000 genomes]
rs60398357	0.83[EUR][1000 genomes]
rs7165594	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7166954	0.91[EUR][1000 genomes]
rs7168775	1.00[YRI][hapmap]
rs7174616	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs7175121	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs7179971	0.91[EUR][1000 genomes]
rs7180093	0.91[EUR][1000 genomes]
rs7180099	1.00[AMR][1000 genomes]
rs73405349	0.83[EUR][1000 genomes]
rs73405355	0.83[EUR][1000 genomes]
rs73405356	0.83[EUR][1000 genomes]
rs73405364	0.85[EUR][1000 genomes]
rs73405388	0.83[EUR][1000 genomes]
rs7342575	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs74015721	0.83[EUR][1000 genomes]
rs74015757	0.86[EUR][1000 genomes]
rs74015761	0.86[EUR][1000 genomes]
rs8034090	1.00[YRI][hapmap]
rs8036648	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8038895	1.00[YRI][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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

No data

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51974200-52018800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:51975600-52017200	Weak transcription	Fetal Brain Male	brain
3	chr15:51984800-52018600	Weak transcription	Brain Hippocampus Middle	brain
4	chr15:51990000-52016800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr15:51991400-52018800	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr15:51992200-52018800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr15:51993600-52016800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr15:51999800-52018200	Weak transcription	Fetal Stomach	stomach
9	chr15:52000800-52024000	Weak transcription	Gastric	stomach
10	chr15:52001000-52018600	Weak transcription	Pancreas	Pancrea
11	chr15:52004800-52018600	Weak transcription	Spleen	Spleen
12	chr15:52006400-52018400	Weak transcription	Fetal Muscle Leg	muscle
13	chr15:52007000-52023400	Weak transcription	Brain Anterior Caudate	brain
14	chr15:52007600-52016800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr15:52007800-52016800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr15:52007800-52018200	Weak transcription	NHDF-Ad	bronchial
17	chr15:52008200-52023200	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr15:52008400-52018400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr15:52008400-52023400	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr15:52010800-52018400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr15:52010800-52018400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr15:52011000-52017000	Weak transcription	Adipose Nuclei	Adipose
23	chr15:52011200-52018400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr15:52011200-52018600	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr15:52011400-52018800	Weak transcription	Brain Cingulate Gyrus	brain
26	chr15:52011400-52023400	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr15:52011600-52018400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr15:52011600-52023400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr15:52011800-52018200	Weak transcription	Hela-S3	cervix
30	chr15:52011800-52018200	Weak transcription	HMEC	breast
31	chr15:52012000-52016800	Strong transcription	Primary B cells from cord blood	blood
32	chr15:52012400-52017000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr15:52012400-52017200	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr15:52012400-52024200	Weak transcription	Fetal Lung	lung
35	chr15:52012800-52017000	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr15:52012800-52017200	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr15:52012800-52017200	Strong transcription	Primary B cells from peripheral blood	blood
38	chr15:52012800-52018400	Weak transcription	Ovary	ovary
39	chr15:52013000-52017200	Strong transcription	Dnd41	blood
40	chr15:52013200-52017000	Strong transcription	GM12878-XiMat	blood
41	chr15:52013400-52018600	Weak transcription	Lung	lung
42	chr15:52013400-52018800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr15:52013400-52023600	Weak transcription	Colonic Mucosa	Colon
44	chr15:52013600-52018400	Weak transcription	Esophagus	oesophagus
45	chr15:52013600-52018400	Weak transcription	Left Ventricle	heart
46	chr15:52013600-52018800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr15:52013600-52019400	Weak transcription	Thymus	Thymus
48	chr15:52013600-52028200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr15:52013600-52028400	Weak transcription	Fetal Brain Female	brain
50	chr15:52013600-52028800	Weak transcription	Fetal Muscle Trunk	muscle

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