Variant report

Variant	rs558480922
Chromosome Location	chr16:30428761-30428762
allele	C/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:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:30428172..30431085-chr17:59475920..59478019,2	MCF-7	breast:
2	chr16:30426230..30430771-chr16:30440207..30443266,5	K562	blood:
3	chr16:30367168..30369191-chr16:30427259..30429781,3	MCF-7	breast:
4	chr16:30427757..30432109-chr16:30437396..30442167,10	MCF-7	breast:
5	chr16:30133035..30135349-chr16:30425863..30428832,2	MCF-7	breast:
6	chr16:30428282..30430706-chr16:30650260..30652815,2	MCF-7	breast:
7	chr16:30100427..30103235-chr16:30427361..30429315,2	MCF-7	breast:
8	chr16:30427326..30429415-chr16:30670296..30671867,2	MCF-7	breast:
9	chr16:30427103..30429593-chr16:30455374..30458526,5	MCF-7	breast:
10	chr16:30427599..30430058-chr16:30620615..30623502,2	MCF-7	breast:
11	chr16:30387643..30390000-chr16:30427735..30430082,2	MCF-7	breast:
12	chr16:30428232..30430752-chr16:30661502..30664068,2	MCF-7	breast:
13	chr16:30427799..30431834-chr16:30534294..30540593,7	MCF-7	breast:
14	chr16:30428527..30430623-chr16:30582267..30583993,2	MCF-7	breast:
15	chr16:30378643..30380815-chr16:30427484..30429569,2	MCF-7	breast:
16	chr16:30427113..30429104-chr16:30669120..30671415,2	MCF-7	breast:
17	chr16:30428344..30430995-chr16:30535727..30539808,4	MCF-7	breast:
18	chr16:30428007..30431562-chr16:30708422..30711318,5	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000180035	Chromatin interaction
ENSG00000156858	Chromatin interaction
ENSG00000239791	Chromatin interaction
ENSG00000156860	Chromatin interaction
ENSG00000156853	Chromatin interaction
ENSG00000149922	Chromatin interaction
ENSG00000169957	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000080603	Chromatin interaction
ENSG00000179958	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000180209	Chromatin interaction
ENSG00000169221	Chromatin interaction
ENSG00000179918	Chromatin interaction
ENSG00000102882	Chromatin interaction
ENSG00000261840	Chromatin interaction
ENSG00000229809	Chromatin interaction
ENSG00000267131	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065915	chr16:29967090-30486120	Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	229 gene(s)	inside rSNPs	diseases
2	nsv542897	chr16:29967090-30486120	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	229 gene(s)	inside rSNPs	diseases
3	nsv1056897	chr16:30363683-30457504	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
4	nsv905724	chr16:30368591-30438930	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
5	nsv532531	chr16:30370550-30581820	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	113 gene(s)	inside rSNPs	diseases
6	nsv827612	chr16:30371538-30429862	Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
7	esv3394301	chr16:30426951-30431549	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	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	chr16:30419200-30428800	Weak transcription	Small Intestine	intestine
2	chr16:30419800-30428800	Weak transcription	Gastric	stomach
3	chr16:30420000-30428800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr16:30421200-30437600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr16:30421200-30437600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr16:30421400-30428800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr16:30426800-30428800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr16:30427200-30430200	Strong transcription	HepG2	liver
9	chr16:30427400-30428800	Enhancers	Fetal Heart	heart
10	chr16:30427600-30430600	Weak transcription	K562	blood
11	chr16:30428200-30428800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
12	chr16:30428200-30429800	Flanking Active TSS	Stomach Smooth Muscle	stomach
13	chr16:30428200-30430000	Enhancers	Fetal Brain Male	brain
14	chr16:30428400-30428800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr16:30428400-30428800	Flanking Active TSS	Primary T cells from cord blood	blood
16	chr16:30428400-30428800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
17	chr16:30428400-30428800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
18	chr16:30428400-30428800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
19	chr16:30428400-30428800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
20	chr16:30428400-30428800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
21	chr16:30428400-30428800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
22	chr16:30428400-30428800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
23	chr16:30428400-30428800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr16:30428400-30428800	Flanking Active TSS	Brain Hippocampus Middle	brain
25	chr16:30428400-30428800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr16:30428400-30428800	Flanking Active TSS	Duodenum Mucosa	Duodenum
27	chr16:30428400-30428800	Flanking Active TSS	Fetal Brain Female	brain
28	chr16:30428400-30428800	Flanking Active TSS	Fetal Intestine Small	intestine
29	chr16:30428400-30428800	Enhancers	Fetal Lung	lung
30	chr16:30428400-30428800	Flanking Active TSS	Thymus	Thymus
31	chr16:30428400-30428800	Flanking Active TSS	GM12878-XiMat	blood
32	chr16:30428400-30429000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
33	chr16:30428400-30429000	Flanking Active TSS	Primary B cells from cord blood	blood
34	chr16:30428400-30429000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
35	chr16:30428400-30429000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
36	chr16:30428400-30429000	Flanking Active TSS	NHEK	skin
37	chr16:30428400-30429200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr16:30428400-30429600	Flanking Active TSS	Primary hematopoietic stem cells	blood
39	chr16:30428400-30429600	Active TSS	Brain Angular Gyrus	brain
40	chr16:30428400-30429600	Active TSS	Brain Germinal Matrix	brain
41	chr16:30428400-30429800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr16:30428400-30429800	Active TSS	Rectal Smooth Muscle	rectum
43	chr16:30428400-30429800	Active TSS	A549	lung
44	chr16:30428400-30429800	Active TSS	Osteobl	bone
45	chr16:30428400-30430000	Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr16:30428400-30430000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr16:30428400-30430000	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr16:30428400-30430200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr16:30428400-30430200	Active TSS	Brain Anterior Caudate	brain
50	chr16:30428400-30430200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle

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