Variant report

Variant	rs74013659
Chromosome Location	chr15:52352792-52352793
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:52309859..52315433-chr15:52338782..52357079,28	MCF-7	breast:
2	chr15:52311321..52313850-chr15:52352707..52354984,2	K562	blood:
3	chr15:52310181..52316125-chr15:52344513..52354209,17	MCF-7	breast:
4	chr15:52351509..52353613-chr15:52377181..52378749,2	MCF-7	breast:
5	chr15:52351076..52352912-chr15:52353054..52355889,3	K562	blood:
6	chr15:52351123..52352912-chr15:52353054..52354974,2	K562	blood:
7	chr15:52339448..52341029-chr15:52351279..52354022,2	MCF-7	breast:
8	chr15:52351305..52354173-chr15:52357852..52359999,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000069956	Chromatin interaction
ENSG00000259438	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10152141	0.81[ASN][1000 genomes]
rs10518675	0.85[ASN][1000 genomes]
rs16964694	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16964700	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16964705	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16964720	0.97[ASN][1000 genomes]
rs17540338	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17612255	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17612326	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2001741	0.81[ASN][1000 genomes]
rs2017967	0.85[ASN][1000 genomes]
rs2246726	1.00[EUR][1000 genomes]
rs2306793	0.81[AMR][1000 genomes]
rs2414120	1.00[EUR][1000 genomes]
rs2414123	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2441779	1.00[EUR][1000 genomes]
rs2470593	1.00[EUR][1000 genomes]
rs2470594	1.00[EUR][1000 genomes]
rs2470595	1.00[EUR][1000 genomes]
rs2899484	1.00[ASN][1000 genomes]
rs4375608	1.00[EUR][1000 genomes]
rs4456445	1.00[EUR][1000 genomes]
rs4491448	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4774606	0.97[ASN][1000 genomes]
rs4775995	0.85[ASN][1000 genomes]
rs4775996	0.97[ASN][1000 genomes]
rs55705935	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs55714716	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs55873482	0.81[ASN][1000 genomes]
rs56307802	0.85[ASN][1000 genomes]
rs56677715	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs58936667	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs61546369	0.81[ASN][1000 genomes]
rs7177328	0.81[ASN][1000 genomes]
rs74013638	0.81[ASN][1000 genomes]
rs74013640	0.81[ASN][1000 genomes]
rs74013641	0.81[ASN][1000 genomes]
rs74013642	0.81[ASN][1000 genomes]
rs74013644	0.85[ASN][1000 genomes]
rs74013645	0.85[ASN][1000 genomes]
rs74013646	0.85[ASN][1000 genomes]
rs74013647	0.85[ASN][1000 genomes]
rs74013648	0.85[ASN][1000 genomes]
rs74013653	0.96[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs74013654	0.85[ASN][1000 genomes]
rs74013656	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs74013657	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs74013661	0.97[ASN][1000 genomes]
rs7497554	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs751560	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8033365	0.88[ASN][1000 genomes]
rs8033840	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8036048	0.90[ASN][1000 genomes]
rs8041281	1.00[EUR][1000 genomes]
rs9796534	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530681	chr15:52297253-52390470	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	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
3	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

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52314400-52359800	Weak transcription	Fetal Brain Male	brain
2	chr15:52332600-52361800	Weak transcription	Gastric	stomach
3	chr15:52334000-52361400	Weak transcription	Small Intestine	intestine
4	chr15:52334600-52357200	Weak transcription	Fetal Heart	heart
5	chr15:52337600-52360600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr15:52337800-52357000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
7	chr15:52339400-52359200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr15:52339600-52357000	Strong transcription	Fetal Intestine Large	intestine
9	chr15:52340200-52362200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr15:52341600-52357600	Strong transcription	Cortex derived primary cultured neurospheres	brain
11	chr15:52341800-52358000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
12	chr15:52343000-52359400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr15:52344200-52356600	Strong transcription	Primary T cells from cord blood	blood
14	chr15:52344400-52357200	Strong transcription	Left Ventricle	heart
15	chr15:52344600-52362000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr15:52345000-52357200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr15:52345000-52357800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr15:52345000-52358600	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr15:52345200-52358000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr15:52345600-52358000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr15:52345600-52358800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr15:52345600-52358800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr15:52345800-52359200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr15:52346200-52359000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr15:52346400-52357200	Strong transcription	NHEK	skin
26	chr15:52347000-52357600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr15:52347200-52353200	Strong transcription	Rectal Mucosa Donor 31	rectum
28	chr15:52347200-52356200	Strong transcription	Fetal Lung	lung
29	chr15:52347200-52356600	Strong transcription	Placenta	Placenta
30	chr15:52347200-52357000	Strong transcription	Fetal Thymus	thymus
31	chr15:52347200-52357200	Strong transcription	Fetal Muscle Trunk	muscle
32	chr15:52347200-52358800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr15:52347400-52357400	Strong transcription	HUES6 Cell Line	embryonic stem cell
34	chr15:52347600-52354400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr15:52347600-52356000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr15:52347600-52356400	Strong transcription	Sigmoid Colon	Sigmoid Colon
37	chr15:52347600-52356400	Strong transcription	HepG2	liver
38	chr15:52347600-52358800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr15:52347800-52353400	Strong transcription	Primary hematopoietic stem cells	blood
40	chr15:52347800-52354800	Strong transcription	HMEC	breast
41	chr15:52347800-52356400	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr15:52347800-52356400	Strong transcription	Muscle Satellite Cultured Cells	--
43	chr15:52347800-52357600	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr15:52347800-52358800	Strong transcription	HSMM	muscle
45	chr15:52348000-52356200	Strong transcription	A549	lung
46	chr15:52348000-52357200	Strong transcription	GM12878-XiMat	blood
47	chr15:52348000-52357600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr15:52348000-52361200	Weak transcription	Stomach Mucosa	stomach
49	chr15:52348200-52356200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr15:52348200-52356200	Strong transcription	Hela-S3	cervix

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