Variant report

Variant	rs564078689
Chromosome Location	chr19:36209458-36209459
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:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:36034283..36038136-chr19:36206970..36210335,6	K562	blood:
2	chr19:36027447..36030155-chr19:36207019..36209668,2	K562	blood:
3	chr19:36136475..36140054-chr19:36207952..36210367,3	MCF-7	breast:
4	chr19:36133592..36136218-chr19:36207471..36210079,2	MCF-7	breast:
5	chr19:35757743..35760122-chr19:36207492..36209553,2	MCF-7	breast:
6	chr19:36034638..36039287-chr19:36205354..36210335,7	K562	blood:
7	chr19:36208185..36209878-chr19:36358146..36361161,3	K562	blood:
8	chr19:36018973..36020669-chr19:36208062..36210070,2	K562	blood:
9	chr19:36207787..36211113-chr19:36265053..36268029,3	K562	blood:
10	chr19:36208378..36210285-chr19:36358548..36361708,3	K562	blood:
11	chr19:36208921..36210608-chr19:36499552..36501350,2	MCF-7	breast:
12	chr19:36208210..36211144-chr19:36264877..36267691,4	MCF-7	breast:
13	chr19:36047300..36050125-chr19:36207207..36209834,3	K562	blood:
14	chr19:36207151..36210695-chr19:36264649..36268718,5	K562	blood:
15	chr19:36035974..36038022-chr19:36207371..36209822,3	MCF-7	breast:
16	chr19:36133481..36135868-chr19:36206189..36210381,3	K562	blood:
17	chr19:35758844..35760411-chr19:36208018..36210634,2	MCF-7	breast:
18	chr19:36047138..36050303-chr19:36204932..36209680,5	K562	blood:
19	chr19:36208544..36210188-chr19:36360524..36362280,2	MCF-7	breast:
20	chr19:36207946..36209485-chr19:36241921..36244354,2	MCF-7	breast:
21	chr19:36203511..36205032-chr19:36208383..36210782,2	MCF-7	breast:
22	chr19:36208682..36209521-chr20:37100779..37101545,2	HCT-116	colon:
23	chr19:36208456..36210034-chr19:36345854..36347720,2	K562	blood:
24	chr19:36206099..36210841-chr19:36246614..36251827,8	MCF-7	breast:
25	chr19:36035457..36038261-chr19:36205897..36210098,5	MCF-7	breast:
26	chr19:36207379..36214815-chr19:36234227..36241330,25	MCF-7	breast:
27	chr19:36205476..36213390-chr19:36226310..36233646,27	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000267796	Chromatin interaction
ENSG00000105663	Chromatin interaction
ENSG00000126267	Chromatin interaction
ENSG00000126259	Chromatin interaction
ENSG00000011590	Chromatin interaction
ENSG00000105698	Chromatin interaction
ENSG00000161265	Chromatin interaction
ENSG00000105290	Chromatin interaction
ENSG00000004777	Chromatin interaction
ENSG00000126246	Chromatin interaction
ENSG00000267120	Chromatin interaction
ENSG00000267439	Chromatin interaction
ENSG00000105675	Chromatin interaction
ENSG00000161270	Chromatin interaction
ENSG00000205155	Chromatin interaction
ENSG00000189001	Chromatin interaction
ENSG00000188223	Chromatin interaction
ENSG00000170471	Chromatin interaction
ENSG00000236144	Chromatin interaction
ENSG00000167595	Chromatin interaction
ENSG00000105672	Chromatin interaction
ENSG00000004776	Chromatin interaction
ENSG00000181392	Chromatin interaction
ENSG00000105679	Chromatin interaction
ENSG00000105677	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv911630	chr19:36149761-36290977	Enhancers Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	69 gene(s)	inside rSNPs	diseases
3	nsv458566	chr19:36156588-36265508	Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
4	nsv579422	chr19:36156588-36265508	Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
5	nsv911631	chr19:36169285-36290977	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
6	nsv911632	chr19:36174176-36288297	Strong transcription Active TSS Flanking Active TSS Enhancers Weak 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	66 gene(s)	inside rSNPs	diseases
7	nsv911633	chr19:36206050-36283847	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
8	nsv911634	chr19:36206050-36290977	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
9	nsv828544	chr19:36207191-36210758	Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	36 gene(s)	inside rSNPs	diseases
10	esv3365662	chr19:36208037-36210160	Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	35 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	chr19:36206600-36209800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
2	chr19:36206600-36210000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr19:36206600-36210200	Active TSS	H9 Cell Line	embryonic stem cell
4	chr19:36206800-36210200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr19:36206800-36210200	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr19:36206800-36210400	Active TSS	iPS-18 Cell Line	embryonic stem cell
7	chr19:36207000-36210000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr19:36207000-36210000	Active TSS	NHDF-Ad	bronchial
9	chr19:36207000-36210200	Active TSS	HUES64 Cell Line	embryonic stem cell
10	chr19:36207000-36210400	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr19:36207000-36210400	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr19:36207200-36209600	Active TSS	Gastric	stomach
13	chr19:36207200-36209800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr19:36207200-36209800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr19:36207200-36209800	Active TSS	Fetal Intestine Large	intestine
16	chr19:36207200-36209800	Active TSS	Sigmoid Colon	Sigmoid Colon
17	chr19:36207200-36210000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr19:36207200-36210000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr19:36207200-36210000	Active TSS	Aorta	Aorta
20	chr19:36207200-36210000	Active TSS	Left Ventricle	heart
21	chr19:36207200-36210000	Active TSS	Psoas Muscle	Psoas
22	chr19:36207200-36210000	Active TSS	Small Intestine	intestine
23	chr19:36207200-36210600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr19:36207400-36209600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
25	chr19:36207400-36209600	Active TSS	Brain Substantia Nigra	brain
26	chr19:36207400-36209600	Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr19:36207400-36209600	Active TSS	Placenta Amnion	Placenta Amnion
28	chr19:36207400-36209600	Active TSS	Rectal Smooth Muscle	rectum
29	chr19:36207400-36209600	Active TSS	Right Ventricle	heart
30	chr19:36207400-36209800	Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr19:36207400-36209800	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr19:36207400-36209800	Active TSS	Brain Angular Gyrus	brain
33	chr19:36207400-36209800	Active TSS	Brain Anterior Caudate	brain
34	chr19:36207400-36209800	Active TSS	Brain Cingulate Gyrus	brain
35	chr19:36207400-36209800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
36	chr19:36207400-36209800	Active TSS	Colon Smooth Muscle	Colon
37	chr19:36207400-36209800	Active TSS	Esophagus	oesophagus
38	chr19:36207400-36209800	Active TSS	Fetal Intestine Small	intestine
39	chr19:36207400-36209800	Active TSS	Fetal Lung	lung
40	chr19:36207400-36209800	Active TSS	Fetal Stomach	stomach
41	chr19:36207400-36209800	Active TSS	Stomach Mucosa	stomach
42	chr19:36207400-36210000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr19:36207400-36210000	Active TSS	Ovary	ovary
44	chr19:36207400-36210200	Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr19:36207600-36209600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
46	chr19:36207600-36209600	Active TSS	Primary T helper naive cells from peripheral blood	blood
47	chr19:36207600-36209600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
48	chr19:36207600-36209600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr19:36207600-36209600	Active TSS	Brain Hippocampus Middle	brain
50	chr19:36207600-36209600	Active TSS	Fetal Brain Female	brain

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