Variant report

Variant	rs78727540
Chromosome Location	chr6:110068090-110068091
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949475	chr6:109907936-110160501	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv817322	chr6:109933272-110070574	Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv830769	chr6:109944334-110078120	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv5436	chr6:110052812-110097662	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv886533	chr6:110067773-110126393	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:110013000-110114400	Weak transcription	Right Ventricle	heart
2	chr6:110028000-110071200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:110028200-110080800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr6:110035000-110071400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:110035000-110084000	Weak transcription	GM12878-XiMat	blood
6	chr6:110035200-110094200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr6:110035400-110083000	Weak transcription	Brain Germinal Matrix	brain
8	chr6:110035600-110089000	Weak transcription	Spleen	Spleen
9	chr6:110036800-110115600	Weak transcription	Colonic Mucosa	Colon
10	chr6:110039000-110081000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr6:110041400-110081000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr6:110042200-110088800	Weak transcription	Fetal Intestine Small	intestine
13	chr6:110042400-110089000	Weak transcription	Brain Cingulate Gyrus	brain
14	chr6:110044200-110115400	Weak transcription	Brain Angular Gyrus	brain
15	chr6:110047200-110084000	Weak transcription	Small Intestine	intestine
16	chr6:110047600-110068800	Weak transcription	Dnd41	blood
17	chr6:110048600-110089800	Weak transcription	Fetal Kidney	kidney
18	chr6:110050400-110078400	Weak transcription	Fetal Brain Male	brain
19	chr6:110057200-110089000	Weak transcription	Fetal Brain Female	brain
20	chr6:110057400-110089000	Weak transcription	Esophagus	oesophagus
21	chr6:110057600-110086200	Weak transcription	Brain Anterior Caudate	brain
22	chr6:110058200-110087200	Weak transcription	Rectal Smooth Muscle	rectum
23	chr6:110058200-110089000	Weak transcription	Lung	lung
24	chr6:110058400-110085000	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr6:110058400-110089600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr6:110058800-110112400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr6:110059200-110069400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr6:110059200-110124000	Weak transcription	Colon Smooth Muscle	Colon
29	chr6:110060000-110087800	Weak transcription	Fetal Thymus	thymus
30	chr6:110061200-110089200	Weak transcription	Pancreas	Pancrea
31	chr6:110062600-110089200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr6:110062800-110087400	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr6:110062800-110088000	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr6:110063000-110078000	Weak transcription	Primary hematopoietic stem cells	blood
35	chr6:110065200-110084000	Weak transcription	Left Ventricle	heart
36	chr6:110065200-110089000	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr6:110065200-110111200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr6:110065400-110094200	Weak transcription	Brain Substantia Nigra	brain
39	chr6:110065600-110068200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr6:110065600-110069000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr6:110065600-110069200	Weak transcription	Aorta	Aorta
42	chr6:110065600-110069600	Weak transcription	Liver	Liver
43	chr6:110065600-110070000	Weak transcription	Fetal Muscle Trunk	muscle
44	chr6:110065600-110070400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr6:110065600-110073000	Weak transcription	Stomach Smooth Muscle	stomach
46	chr6:110065600-110074200	Weak transcription	Fetal Intestine Large	intestine
47	chr6:110065600-110074400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr6:110065600-110077800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr6:110065600-110080800	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr6:110065600-110084000	Weak transcription	Placenta	Placenta

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