Variant report

Variant	rs566558663
Chromosome Location	chr6:38132851-38132852
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:38129827..38133473-chr6:38138909..38141756,3	K562	blood:

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028825	chr6:37495154-38278320	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1020625	chr6:37833591-38155622	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv1021991	chr6:37893949-38738720	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	esv2754649	chr6:37985025-38147910	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv534620	chr6:38049585-38602064	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv524213	chr6:38106844-38160627	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
8	nsv517973	chr6:38131442-38152460	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA miRNA target site	n/a	inside rSNPs	diseases
9	nsv522522	chr6:38131442-38207636	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
10	esv3447385	chr6:38132274-38136172	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3407137	chr6:38132799-38135547	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv3437086	chr6:38132849-38135472	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38091400-38141800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr6:38111800-38138200	Weak transcription	Fetal Brain Female	brain
3	chr6:38112400-38138200	Weak transcription	Fetal Brain Male	brain
4	chr6:38113200-38134400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:38113200-38138000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr6:38114400-38138200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr6:38117600-38137200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr6:38119800-38134800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:38121000-38159600	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr6:38121200-38136400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:38121400-38136600	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr6:38121400-38141000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr6:38121600-38137800	Weak transcription	Colonic Mucosa	Colon
14	chr6:38121800-38138000	Weak transcription	Dnd41	blood
15	chr6:38121800-38153600	Weak transcription	Primary B cells from peripheral blood	blood
16	chr6:38122000-38137600	Weak transcription	Esophagus	oesophagus
17	chr6:38122200-38134200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:38122800-38135800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr6:38123200-38136800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr6:38123200-38153200	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr6:38123400-38155400	Weak transcription	Aorta	Aorta
22	chr6:38123400-38157000	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr6:38123400-38176800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr6:38123600-38138400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr6:38123600-38140800	Weak transcription	Placenta	Placenta
26	chr6:38123600-38144200	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr6:38123600-38153000	Weak transcription	Primary B cells from cord blood	blood
28	chr6:38123800-38141400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:38123800-38151200	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr6:38124000-38152200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:38124200-38137000	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr6:38124200-38151800	Weak transcription	Brain Anterior Caudate	brain
33	chr6:38124400-38136200	Weak transcription	Fetal Lung	lung
34	chr6:38124400-38144200	Weak transcription	Primary hematopoietic stem cells	blood
35	chr6:38127400-38137800	Weak transcription	Gastric	stomach
36	chr6:38127400-38141000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr6:38127600-38140600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr6:38128800-38133600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr6:38129200-38145600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr6:38129400-38136400	Weak transcription	Brain Germinal Matrix	brain
41	chr6:38129400-38137000	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr6:38129400-38141200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:38129400-38141200	Weak transcription	Lung	lung
44	chr6:38129400-38144600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr6:38129600-38137800	Weak transcription	Stomach Smooth Muscle	stomach
46	chr6:38129600-38138200	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr6:38129600-38141200	Weak transcription	Primary T cells from cord blood	blood
48	chr6:38130000-38135400	Weak transcription	Fetal Intestine Small	intestine
49	chr6:38130000-38144400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr6:38130200-38140800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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