Variant report

Variant	rs73402869
Chromosome Location	chr15:52424491-52424492
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:52419157..52422953-chr15:52424329..52426526,3	MCF-7	breast:
2	chr15:52309643..52312109-chr15:52424380..52429568,4	MCF-7	breast:
3	chr15:52417291..52418865-chr15:52424187..52426510,2	MCF-7	breast:
4	chr15:52415685..52419897-chr15:52423776..52427123,4	K562	blood:
5	chr15:52389425..52391021-chr15:52422602..52424878,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000259438	Chromatin interaction
ENSG00000069956	Chromatin interaction
ENSG00000069966	Chromatin interaction
ENSG00000259709	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10400852	1.00[EUR][1000 genomes]
rs16953085	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16964735	1.00[EUR][1000 genomes]
rs16964737	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16964750	1.00[EUR][1000 genomes]
rs16964770	1.00[EUR][1000 genomes]
rs2231296	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28656256	1.00[EUR][1000 genomes]
rs28663157	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41494446	1.00[EUR][1000 genomes]
rs59195841	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59289747	1.00[EUR][1000 genomes]
rs60397096	1.00[EUR][1000 genomes]
rs7162885	0.82[AFR][1000 genomes]
rs7163133	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7164357	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7165157	1.00[EUR][1000 genomes]
rs7165527	1.00[EUR][1000 genomes]
rs7165708	1.00[EUR][1000 genomes]
rs7167133	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7171700	1.00[EUR][1000 genomes]
rs7172939	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7178038	1.00[EUR][1000 genomes]
rs730945	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73402803	1.00[EUR][1000 genomes]
rs73402824	1.00[EUR][1000 genomes]
rs73402826	1.00[EUR][1000 genomes]
rs73402833	1.00[EUR][1000 genomes]
rs73402839	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73402853	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73402857	0.96[AFR][1000 genomes]
rs73402859	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73402879	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73404813	1.00[EUR][1000 genomes]
rs8023921	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8024311	1.00[EUR][1000 genomes]
rs8024767	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8035146	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8040458	1.00[EUR][1000 genomes]
rs8041042	1.00[EUR][1000 genomes]
rs8041128	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8041233	1.00[EUR][1000 genomes]
rs8041355	1.00[EUR][1000 genomes]
rs8041504	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv471244	chr15:52305463-52511465	Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv984198	chr15:52319726-52481137	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv1054372	chr15:52369078-52579464	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv542387	chr15:52369078-52579464	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv833005	chr15:52389869-52541330	Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52404800-52428000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr15:52405000-52427400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr15:52405000-52427800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr15:52405000-52428800	Weak transcription	Fetal Heart	heart
5	chr15:52405400-52426000	Weak transcription	Spleen	Spleen
6	chr15:52406400-52427800	Weak transcription	Fetal Brain Male	brain
7	chr15:52407400-52427600	Weak transcription	HSMMtube	muscle
8	chr15:52407600-52441600	Weak transcription	Fetal Lung	lung
9	chr15:52407800-52428800	Weak transcription	Brain Hippocampus Middle	brain
10	chr15:52407800-52440400	Weak transcription	Brain Substantia Nigra	brain
11	chr15:52408200-52425800	Weak transcription	Small Intestine	intestine
12	chr15:52408600-52425600	Weak transcription	Primary hematopoietic stem cells	blood
13	chr15:52408800-52428000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr15:52409000-52426800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr15:52409800-52425400	Weak transcription	Fetal Intestine Small	intestine
16	chr15:52410000-52428600	Weak transcription	Hela-S3	cervix
17	chr15:52410200-52424800	Weak transcription	Fetal Muscle Leg	muscle
18	chr15:52410200-52441600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr15:52410600-52427800	Weak transcription	Adipose Nuclei	Adipose
20	chr15:52410600-52441400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr15:52411000-52425800	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr15:52411200-52428600	Weak transcription	Left Ventricle	heart
23	chr15:52412000-52427200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr15:52412000-52427800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr15:52412000-52441200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr15:52412200-52436000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr15:52413600-52431800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr15:52413800-52428400	Weak transcription	Rectal Smooth Muscle	rectum
29	chr15:52414200-52427800	Strong transcription	Primary B cells from peripheral blood	blood
30	chr15:52414400-52428400	Weak transcription	Colon Smooth Muscle	Colon
31	chr15:52416000-52427800	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr15:52416000-52432800	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr15:52416200-52431600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr15:52416800-52426800	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr15:52417000-52425800	Weak transcription	A549	lung
36	chr15:52417000-52427600	Weak transcription	HSMM	muscle
37	chr15:52417000-52436000	Weak transcription	Lung	lung
38	chr15:52417200-52428600	Weak transcription	NHLF	lung
39	chr15:52417200-52428800	Weak transcription	Gastric	stomach
40	chr15:52417200-52431200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr15:52417200-52431800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr15:52417200-52436200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr15:52417400-52425800	Weak transcription	Duodenum Mucosa	Duodenum
44	chr15:52417400-52426200	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr15:52417400-52429000	Weak transcription	K562	blood
46	chr15:52417400-52431800	Weak transcription	HMEC	breast
47	chr15:52417400-52432000	Weak transcription	NHDF-Ad	bronchial
48	chr15:52417600-52424600	Weak transcription	HepG2	liver
49	chr15:52417600-52425000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr15:52417600-52435400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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