Variant report

Variant	rs8027276
Chromosome Location	chr15:52340596-52340597
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:52309859..52315433-chr15:52338782..52357079,28	MCF-7	breast:
2	chr15:52331526..52333859-chr15:52340163..52342919,2	K562	blood:
3	chr15:52339219..52341051-chr15:52343518..52345839,3	MCF-7	breast:
4	chr15:52339448..52341029-chr15:52351279..52354022,2	MCF-7	breast:
5	chr15:52339947..52342319-chr15:52368984..52372783,3	MCF-7	breast:
6	chr15:52311160..52314129-chr15:52338657..52341063,3	MCF-7	breast:
7	chr15:52294207..52297195-chr15:52339559..52341402,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000069956	Chromatin interaction
ENSG00000259438	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10152141	0.83[EUR][1000 genomes]
rs10518675	0.83[EUR][1000 genomes]
rs12324384	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12324807	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13379854	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16964720	0.83[EUR][1000 genomes]
rs2001741	0.83[EUR][1000 genomes]
rs2306793	0.83[EUR][1000 genomes]
rs2899484	0.83[EUR][1000 genomes]
rs4774606	0.83[EUR][1000 genomes]
rs4775995	0.83[EUR][1000 genomes]
rs4775996	0.83[EUR][1000 genomes]
rs55705935	0.83[EUR][1000 genomes]
rs55873482	0.83[EUR][1000 genomes]
rs56307802	0.83[EUR][1000 genomes]
rs7177328	0.83[EUR][1000 genomes]
rs73400734	1.00[ASN][1000 genomes]
rs7359204	0.83[EUR][1000 genomes]
rs74013636	0.83[EUR][1000 genomes]
rs74013638	0.83[EUR][1000 genomes]
rs74013640	0.83[EUR][1000 genomes]
rs74013641	0.83[EUR][1000 genomes]
rs74013642	0.83[EUR][1000 genomes]
rs74013644	0.83[EUR][1000 genomes]
rs74013645	0.83[EUR][1000 genomes]
rs74013646	0.83[EUR][1000 genomes]
rs74013647	0.83[EUR][1000 genomes]
rs74013648	0.83[EUR][1000 genomes]
rs74013654	0.83[EUR][1000 genomes]
rs74013656	0.83[EUR][1000 genomes]
rs74013661	0.83[EUR][1000 genomes]
rs7497554	0.83[EUR][1000 genomes]
rs8033365	0.83[EUR][1000 genomes]
rs8036048	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050664	chr15:52265723-52342101	Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52312800-52345400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr15:52314400-52359800	Weak transcription	Fetal Brain Male	brain
3	chr15:52325800-52342200	Weak transcription	HUVEC	blood vessel
4	chr15:52326800-52342800	Weak transcription	Fetal Brain Female	brain
5	chr15:52327000-52340600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr15:52332400-52348200	Weak transcription	Colonic Mucosa	Colon
7	chr15:52332600-52342400	Weak transcription	NHDF-Ad	bronchial
8	chr15:52332600-52349000	Weak transcription	Esophagus	oesophagus
9	chr15:52332600-52349400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr15:52332600-52350800	Weak transcription	Aorta	Aorta
11	chr15:52332600-52361800	Weak transcription	Gastric	stomach
12	chr15:52332800-52344400	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr15:52333000-52341000	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr15:52333000-52341000	Weak transcription	HSMM	muscle
15	chr15:52333000-52344200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr15:52333000-52344400	Weak transcription	Left Ventricle	heart
17	chr15:52333000-52345400	Weak transcription	Lung	lung
18	chr15:52333000-52348200	Weak transcription	HSMMtube	muscle
19	chr15:52333000-52350800	Weak transcription	Right Ventricle	heart
20	chr15:52333000-52351000	Weak transcription	Spleen	Spleen
21	chr15:52333200-52340800	Weak transcription	Adipose Nuclei	Adipose
22	chr15:52333200-52342800	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr15:52333200-52348600	Weak transcription	Colon Smooth Muscle	Colon
24	chr15:52334000-52361400	Weak transcription	Small Intestine	intestine
25	chr15:52334200-52343800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:52334400-52343000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr15:52334600-52344200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr15:52334600-52344200	Weak transcription	Fetal Kidney	kidney
29	chr15:52334600-52357200	Weak transcription	Fetal Heart	heart
30	chr15:52334800-52350200	Weak transcription	Psoas Muscle	Psoas
31	chr15:52335000-52344200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr15:52335000-52344200	Weak transcription	Hela-S3	cervix
33	chr15:52335000-52348000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr15:52335400-52341800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr15:52335400-52344200	Weak transcription	Ovary	ovary
36	chr15:52335400-52350800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr15:52335400-52350800	Weak transcription	Pancreas	Pancrea
38	chr15:52336400-52340800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr15:52337400-52341600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr15:52337600-52344000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr15:52337600-52360600	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr15:52337800-52341400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr15:52337800-52357000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr15:52338000-52344200	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr15:52338200-52341200	Strong transcription	Fetal Thymus	thymus
46	chr15:52338200-52342000	Strong transcription	NHEK	skin
47	chr15:52338200-52342400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr15:52338200-52343200	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr15:52338200-52344200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr15:52338200-52346200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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