Variant report

Variant	rs543942876
Chromosome Location	chr18:13131209-13131210
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:13124233..13126010-chr18:13129729..13132355,2	K562	blood:
2	chr18:13130413..13132086-chr18:13135033..13137817,2	MCF-7	breast:
3	chr18:13128234..13129969-chr18:13130472..13133331,2	K562	blood:

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	nsv1062014	chr18:12687210-13183383	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv543655	chr18:12687210-13183383	Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
3	nsv1057083	chr18:12916779-13207538	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	nsv576524	chr18:12918318-13183609	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv1056593	chr18:12926314-13183383	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
6	nsv1064364	chr18:12926314-13207686	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv833591	chr18:13093777-13253748	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv515878	chr18:13122618-13142415	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv909408	chr18:13122618-13308950	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv817785	chr18:13130681-13133577	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:13106800-13135400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr18:13118200-13132600	Weak transcription	HepG2	liver
3	chr18:13118400-13135600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr18:13118400-13136200	Weak transcription	Psoas Muscle	Psoas
5	chr18:13118800-13136800	Weak transcription	HSMMtube	muscle
6	chr18:13119000-13133400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr18:13119000-13134200	Weak transcription	Fetal Lung	lung
8	chr18:13119000-13136400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr18:13119200-13135800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr18:13119200-13136400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr18:13119400-13133600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr18:13119600-13135400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr18:13121200-13136400	Weak transcription	NHDF-Ad	bronchial
14	chr18:13121400-13134000	Weak transcription	HMEC	breast
15	chr18:13121400-13136600	Weak transcription	Brain Angular Gyrus	brain
16	chr18:13121600-13131600	Weak transcription	Fetal Kidney	kidney
17	chr18:13121600-13135800	Weak transcription	Fetal Brain Male	brain
18	chr18:13121600-13136000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr18:13121800-13134200	Weak transcription	HUVEC	blood vessel
20	chr18:13121800-13136400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr18:13122000-13136400	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr18:13123800-13136400	Weak transcription	HSMM	muscle
23	chr18:13124800-13131400	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr18:13125600-13135800	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr18:13126600-13135000	Weak transcription	Ovary	ovary
26	chr18:13126800-13133400	Weak transcription	K562	blood
27	chr18:13127000-13133400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr18:13127000-13135200	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr18:13127000-13136200	Weak transcription	Primary B cells from peripheral blood	blood
30	chr18:13127000-13136200	Weak transcription	Placenta	Placenta
31	chr18:13127200-13135800	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr18:13127200-13136200	Weak transcription	Brain Anterior Caudate	brain
33	chr18:13127400-13132000	Weak transcription	Fetal Intestine Large	intestine
34	chr18:13127400-13132000	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr18:13127400-13134200	Weak transcription	NHEK	skin
36	chr18:13127400-13135600	Weak transcription	Primary hematopoietic stem cells	blood
37	chr18:13127400-13135800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr18:13127400-13135800	Weak transcription	GM12878-XiMat	blood
39	chr18:13127400-13136400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr18:13127600-13132400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr18:13127600-13132400	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr18:13127600-13133200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr18:13127600-13134800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr18:13127600-13135200	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr18:13127600-13135400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr18:13127600-13135600	Weak transcription	Fetal Brain Female	brain
47	chr18:13127600-13135800	Weak transcription	Duodenum Mucosa	Duodenum
48	chr18:13127600-13135800	Weak transcription	Left Ventricle	heart
49	chr18:13127600-13135800	Weak transcription	Thymus	Thymus
50	chr18:13127600-13136000	Weak transcription	Adipose Nuclei	Adipose

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