Variant report

Variant	rs561052266
Chromosome Location	chr5:16738458-16738459
allele	-/GCTG
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	nsv869660	chr5:16651289-16766428	Genic enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv880373	chr5:16710572-16785604	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1025225	chr5:16714512-17234866	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv520128	chr5:16737513-16746784	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv2363439	chr5:16738458-16738462	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16730800-16741400	Strong transcription	A549	lung
2	chr5:16730800-16744400	Weak transcription	HSMM	muscle
3	chr5:16734600-16744400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:16734800-16739200	Enhancers	Pancreas	Pancrea
5	chr5:16735000-16738600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr5:16735000-16738600	Enhancers	Fetal Lung	lung
7	chr5:16735000-16739400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:16735000-16739400	Enhancers	Stomach Mucosa	stomach
9	chr5:16735200-16746600	Weak transcription	HSMMtube	muscle
10	chr5:16736000-16738800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr5:16736200-16738600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:16736400-16738800	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr5:16736400-16739200	Enhancers	HMEC	breast
14	chr5:16736400-16740200	Weak transcription	Right Ventricle	heart
15	chr5:16736400-16781400	Weak transcription	Esophagus	oesophagus
16	chr5:16736600-16738600	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr5:16736600-16738600	Active TSS	Rectal Mucosa Donor 29	rectum
18	chr5:16736600-16738800	Active TSS	H1 Cell Line	embryonic stem cell
19	chr5:16736600-16740400	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr5:16736800-16738600	Active TSS	H9 Cell Line	embryonic stem cell
21	chr5:16736800-16738600	Active TSS	Brain Germinal Matrix	brain
22	chr5:16736800-16738600	Active TSS	Brain Inferior Temporal Lobe	brain
23	chr5:16736800-16738800	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr5:16736800-16739200	Enhancers	HUVEC	blood vessel
25	chr5:16736800-16740200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr5:16736800-16740600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:16736800-16741800	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr5:16736800-16756600	Weak transcription	Ovary	ovary
29	chr5:16736800-16758200	Weak transcription	Spleen	Spleen
30	chr5:16736800-16761200	Weak transcription	Hela-S3	cervix
31	chr5:16736800-16761800	Weak transcription	Colonic Mucosa	Colon
32	chr5:16736800-16762400	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr5:16737000-16738600	Active TSS	Fetal Intestine Large	intestine
34	chr5:16737000-16738800	Active TSS	Duodenum Mucosa	Duodenum
35	chr5:16737000-16741600	Weak transcription	NHDF-Ad	bronchial
36	chr5:16737000-16742000	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr5:16737000-16742000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr5:16737000-16780400	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr5:16737200-16738600	Enhancers	Gastric	stomach
40	chr5:16737600-16738600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:16737600-16739000	Weak transcription	NHEK	skin
42	chr5:16737600-16739400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr5:16737800-16738600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr5:16737800-16738800	Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr5:16737800-16739400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr5:16737800-16739400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
47	chr5:16737800-16740800	Weak transcription	Fetal Kidney	kidney
48	chr5:16738000-16738600	Enhancers	Fetal Stomach	stomach
49	chr5:16738000-16738800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr5:16738000-16739200	Enhancers	Rectal Mucosa Donor 31	rectum

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