Variant report

Variant	rs62009342
Chromosome Location	chr15:78464513-78464514
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:78455141..78458694-chr15:78463989..78467554,5	MCF-7	breast:
2	chr15:78425346..78429501-chr15:78464309..78466788,4	MCF-7	breast:
3	chr15:78445643..78447208-chr15:78463043..78465753,2	MCF-7	breast:
4	chr15:78447133..78448969-chr15:78464297..78466316,2	K562	blood:

Variant related genes	Relation type
ENSG00000166411	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11854120	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11856106	0.94[ASN][1000 genomes]
rs17479031	1.00[ASN][1000 genomes]
rs17479135	1.00[ASN][1000 genomes]
rs17850483	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17850484	1.00[ASN][1000 genomes]
rs3825847	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4570804	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57867560	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62009331	0.92[EUR][1000 genomes]
rs62009333	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62009334	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62009335	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62009336	1.00[EUR][1000 genomes]
rs62009337	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62009339	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62009340	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62009341	1.00[EUR][1000 genomes]
rs62009343	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62009347	0.89[EUR][1000 genomes]
rs62009348	0.89[EUR][1000 genomes]
rs7165154	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529491	chr15:77932659-78751516	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv948437	chr15:78435527-78504662	Strong transcription Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS 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	15 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	chr15:78442800-78465600	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr15:78446600-78465200	Strong transcription	Fetal Intestine Large	intestine
3	chr15:78446800-78466000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr15:78447000-78475200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr15:78448000-78465200	Strong transcription	Primary T cells fromperipheralblood	blood
6	chr15:78448000-78465800	Strong transcription	Fetal Muscle Trunk	muscle
7	chr15:78448600-78465400	Strong transcription	Placenta	Placenta
8	chr15:78448800-78466600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr15:78449000-78467800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr15:78449400-78465200	Strong transcription	Rectal Mucosa Donor 31	rectum
11	chr15:78449800-78465400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr15:78450000-78464600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr15:78450000-78465200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr15:78450000-78465200	Strong transcription	Osteobl	bone
15	chr15:78450000-78466200	Strong transcription	Left Ventricle	heart
16	chr15:78450200-78465200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr15:78450200-78465400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr15:78450200-78465400	Strong transcription	Sigmoid Colon	Sigmoid Colon
19	chr15:78450600-78465200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr15:78451000-78466200	Strong transcription	Duodenum Smooth Muscle	Duodenum
21	chr15:78451200-78467000	Strong transcription	Stomach Smooth Muscle	stomach
22	chr15:78451200-78467600	Strong transcription	Brain Cingulate Gyrus	brain
23	chr15:78451400-78467200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr15:78452200-78467400	Strong transcription	Brain Angular Gyrus	brain
25	chr15:78452200-78467400	Strong transcription	Brain Inferior Temporal Lobe	brain
26	chr15:78453400-78465200	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr15:78453600-78464600	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr15:78453600-78464600	Strong transcription	Colon Smooth Muscle	Colon
29	chr15:78453600-78467400	Strong transcription	Fetal Brain Female	brain
30	chr15:78454600-78467400	Strong transcription	Brain Substantia Nigra	brain
31	chr15:78454800-78465600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr15:78455600-78465000	Strong transcription	HSMM	muscle
33	chr15:78455800-78464800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr15:78455800-78465200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr15:78456000-78464800	Strong transcription	HUES64 Cell Line	embryonic stem cell
36	chr15:78456000-78465200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr15:78456600-78466200	Weak transcription	HUVEC	blood vessel
38	chr15:78457000-78466800	Strong transcription	Rectal Smooth Muscle	rectum
39	chr15:78457000-78468400	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr15:78458000-78465000	Strong transcription	Hela-S3	cervix
41	chr15:78458000-78465200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr15:78458200-78466000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr15:78458200-78466600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr15:78458400-78465800	Genic enhancers	Fetal Thymus	thymus
45	chr15:78458800-78468800	Weak transcription	Stomach Mucosa	stomach
46	chr15:78459000-78470000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr15:78459400-78464600	Enhancers	Primary B cells from cord blood	blood
48	chr15:78459600-78464600	Strong transcription	Small Intestine	intestine
49	chr15:78460000-78464600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr15:78460200-78466400	Weak transcription	Fetal Brain Male	brain

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