Variant report

Variant	rs567966475
Chromosome Location	chr6:36952625-36952626
allele	A/G
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:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:36930754..36936310-chr6:36950773..36956274,7	MCF-7	breast:
2	chr6:36952074..36956895-chr6:36967839..36978010,11	MCF-7	breast:
3	chr6:36952261..36954341-chr6:37137585..37140214,3	K562	blood:
4	chr6:36911927..36913902-chr6:36952339..36954357,2	MCF-7	breast:
5	chr6:36561584..36563964-chr6:36951421..36953213,2	MCF-7	breast:
6	chr6:36950922..36953739-chr6:37176914..37178749,2	MCF-7	breast:
7	chr6:36951113..36952947-chr6:36995288..36997269,2	K562	blood:
8	chr6:36852278..36855515-chr6:36952430..36957026,4	MCF-7	breast:
9	chr6:36934908..36939247-chr6:36952489..36955593,6	MCF-7	breast:
10	chr6:36952431..36954730-chr6:36980411..36983158,3	MCF-7	breast:
11	chr6:36646638..36649501-chr6:36950264..36953112,2	MCF-7	breast:
12	chr6:36838369..36843263-chr6:36951921..36955568,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000137168	Chromatin interaction
ENSG00000137193	Chromatin interaction
ENSG00000232598	Chromatin interaction
ENSG00000112081	Chromatin interaction
ENSG00000146192	Chromatin interaction
ENSG00000198663	Chromatin interaction
ENSG00000137409	Chromatin interaction
ENSG00000164530	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030015	chr6:36818510-37104446	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv916833	chr6:36826524-37029833	Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv885815	chr6:36915906-36979583	Active TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv5263	chr6:36941625-36972109	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	22 gene(s)	inside rSNPs	diseases
5	nsv518386	chr6:36942746-37037670	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv602952	chr6:36951210-36978745	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	esv19906	chr6:36951876-36955062	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	22 gene(s)	inside rSNPs	diseases
8	esv3404117	chr6:36952499-36955347	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36951000-36952800	Flanking Active TSS	HUVEC	blood vessel
2	chr6:36951200-36952800	Flanking Active TSS	Right Ventricle	heart
3	chr6:36951400-36953400	Flanking Active TSS	Stomach Smooth Muscle	stomach
4	chr6:36951600-36952800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
5	chr6:36951600-36953000	Flanking Active TSS	Hela-S3	cervix
6	chr6:36951600-36953400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:36951800-36952800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:36951800-36952800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:36951800-36952800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr6:36951800-36952800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr6:36951800-36952800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
12	chr6:36951800-36952800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:36951800-36952800	Flanking Active TSS	Brain Cingulate Gyrus	brain
14	chr6:36951800-36952800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
15	chr6:36951800-36952800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
16	chr6:36951800-36952800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
17	chr6:36951800-36952800	Flanking Active TSS	Fetal Heart	heart
18	chr6:36951800-36952800	Flanking Active TSS	NH-A	brain
19	chr6:36951800-36952800	Flanking Active TSS	Osteobl	bone
20	chr6:36951800-36953000	Flanking Active TSS	Brain Angular Gyrus	brain
21	chr6:36951800-36953000	Flanking Active TSS	Brain Hippocampus Middle	brain
22	chr6:36951800-36953200	Flanking Active TSS	Brain Anterior Caudate	brain
23	chr6:36951800-36953200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr6:36951800-36953400	Flanking Active TSS	Primary T cells from cord blood	blood
25	chr6:36951800-36953400	Flanking Active TSS	Primary hematopoietic stem cells	blood
26	chr6:36951800-36953400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
27	chr6:36952000-36952800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr6:36952000-36952800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
29	chr6:36952000-36952800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:36952000-36952800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
31	chr6:36952000-36952800	Flanking Active TSS	HMEC	breast
32	chr6:36952000-36952800	Transcr. at gene 5' and 3'	K562	blood
33	chr6:36952000-36953000	Flanking Active TSS	Brain Substantia Nigra	brain
34	chr6:36952000-36953000	Flanking Active TSS	Colon Smooth Muscle	Colon
35	chr6:36952000-36953000	Flanking Active TSS	Duodenum Mucosa	Duodenum
36	chr6:36952000-36953000	Flanking Active TSS	NHEK	skin
37	chr6:36952000-36953200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
38	chr6:36952000-36953400	Flanking Active TSS	Adipose Nuclei	Adipose
39	chr6:36952200-36952800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
40	chr6:36952200-36952800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
41	chr6:36952200-36952800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr6:36952200-36952800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr6:36952200-36952800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr6:36952200-36952800	Flanking Active TSS	Fetal Intestine Small	intestine
45	chr6:36952200-36952800	Flanking Active TSS	Fetal Lung	lung
46	chr6:36952200-36952800	Flanking Active TSS	HSMM	muscle
47	chr6:36952200-36953000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr6:36952200-36953000	Flanking Active TSS	Right Atrium	heart
49	chr6:36952200-36953000	Flanking Active TSS	HepG2	liver
50	chr6:36952200-36953200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood

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