Variant report

Variant	rs200292451
Chromosome Location	chr5:9154784-9154785
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv881438	chr5:8728874-9695667	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
2	nsv461944	chr5:8758041-9209831	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv597069	chr5:8758041-9209831	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1016937	chr5:8824417-9402871	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
5	nsv537638	chr5:8824417-9402871	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
6	nsv918004	chr5:8824417-9402871	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
7	nsv1015378	chr5:9053542-9617963	Genic enhancers Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
8	nsv537640	chr5:9053542-9617963	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
9	nsv830200	chr5:9081023-9269495	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv880683	chr5:9091164-9170323	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv880323	chr5:9100211-9157454	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv597070	chr5:9100211-9280338	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv1020815	chr5:9135207-9425649	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv498044	chr5:9143754-9402870	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	nsv530183	chr5:9146506-9413373	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
16	esv3363022	chr5:9154560-9154979	Weak transcription Strong transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:9134400-9156600	Weak transcription	Brain Cingulate Gyrus	brain
2	chr5:9136800-9176400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr5:9136800-9189000	Weak transcription	Pancreas	Pancrea
4	chr5:9143600-9161000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:9145000-9158000	Weak transcription	Esophagus	oesophagus
6	chr5:9145200-9157200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:9145200-9160800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr5:9145400-9163200	Weak transcription	Fetal Kidney	kidney
9	chr5:9145600-9235400	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr5:9148600-9155600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr5:9150400-9156000	Weak transcription	Dnd41	blood
12	chr5:9151000-9169000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr5:9151200-9156400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr5:9151200-9168800	Weak transcription	NH-A	brain
15	chr5:9151600-9157800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr5:9151800-9154800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr5:9152000-9155200	Strong transcription	Fetal Muscle Trunk	muscle
18	chr5:9152000-9155200	Strong transcription	Fetal Muscle Leg	muscle
19	chr5:9152000-9155400	Strong transcription	Cortex derived primary cultured neurospheres	brain
20	chr5:9152200-9154800	Strong transcription	Placenta Amnion	Placenta Amnion
21	chr5:9152400-9155400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr5:9152400-9155600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr5:9152400-9156400	Weak transcription	Spleen	Spleen
24	chr5:9152400-9156600	Weak transcription	Left Ventricle	heart
25	chr5:9152400-9171800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr5:9152600-9155200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr5:9152600-9156200	Weak transcription	NHDF-Ad	bronchial
28	chr5:9152600-9156200	Weak transcription	NHLF	lung
29	chr5:9152600-9157600	Weak transcription	Right Ventricle	heart
30	chr5:9153000-9155000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:9153400-9155000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr5:9153600-9154800	Strong transcription	Fetal Intestine Small	intestine
33	chr5:9153600-9155200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr5:9153600-9157800	Weak transcription	Fetal Heart	heart
35	chr5:9153800-9155400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:9153800-9183400	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr5:9154000-9226200	Weak transcription	Fetal Intestine Large	intestine
38	chr5:9154200-9155400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr5:9154400-9154800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr5:9154400-9154800	Strong transcription	Aorta	Aorta
41	chr5:9154400-9154800	Strong transcription	Fetal Stomach	stomach
42	chr5:9154400-9155000	Strong transcription	Liver	Liver
43	chr5:9154400-9155000	Strong transcription	Brain Hippocampus Middle	brain

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