Variant report

Variant	rs28497795
Chromosome Location	chr15:100229938-100229939
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12101528	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs13329194	0.89[AFR][1000 genomes]
rs28520235	0.84[AFR][1000 genomes]
rs28834979	0.80[AFR][1000 genomes]
rs28838709	0.87[AFR][1000 genomes]
rs8039892	0.81[AFR][1000 genomes]
rs8042600	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036346	chr15:99752391-100365458	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv542520	chr15:99752391-100365458	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv817201	chr15:99839238-100537341	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv1038005	chr15:100170414-100633714	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv542522	chr15:100170414-100633714	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv904559	chr15:100174907-100255046	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv904560	chr15:100196657-100339331	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv904561	chr15:100204918-100486828	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
9	nsv904562	chr15:100214935-100237682	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:100159000-100253000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:100171200-100232800	Weak transcription	Esophagus	oesophagus
3	chr15:100171200-100248800	Weak transcription	Gastric	stomach
4	chr15:100172000-100230800	Weak transcription	Stomach Mucosa	stomach
5	chr15:100179200-100232600	Weak transcription	Colonic Mucosa	Colon
6	chr15:100181800-100232800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr15:100192000-100230400	Weak transcription	NHLF	lung
8	chr15:100199800-100232600	Weak transcription	Right Ventricle	heart
9	chr15:100209800-100232800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr15:100211800-100232200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr15:100212800-100240000	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr15:100213000-100232600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr15:100213200-100250800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr15:100213400-100232600	Weak transcription	Pancreas	Pancrea
15	chr15:100213600-100243400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr15:100215800-100230800	Weak transcription	Stomach Smooth Muscle	stomach
17	chr15:100216200-100230200	Weak transcription	HMEC	breast
18	chr15:100216200-100232600	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr15:100216200-100233000	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr15:100216800-100230200	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr15:100216800-100230400	Weak transcription	Placenta	Placenta
22	chr15:100216800-100232200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr15:100217000-100232800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr15:100217400-100232600	Weak transcription	Fetal Intestine Small	intestine
25	chr15:100218000-100230400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr15:100218200-100232600	Weak transcription	Hela-S3	cervix
27	chr15:100218200-100232800	Weak transcription	Rectal Smooth Muscle	rectum
28	chr15:100219400-100230200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr15:100219400-100248200	Weak transcription	Small Intestine	intestine
30	chr15:100219600-100248400	Weak transcription	Spleen	Spleen
31	chr15:100219800-100230400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr15:100219800-100230600	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr15:100219800-100243600	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr15:100220400-100232600	Weak transcription	Thymus	Thymus
35	chr15:100220400-100233000	Weak transcription	Right Atrium	heart
36	chr15:100221800-100232000	Weak transcription	Psoas Muscle	Psoas
37	chr15:100222000-100232600	Weak transcription	Aorta	Aorta
38	chr15:100222800-100243600	Weak transcription	Brain Angular Gyrus	brain
39	chr15:100223000-100230400	Weak transcription	Osteobl	bone
40	chr15:100223600-100230000	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr15:100223600-100232600	Weak transcription	NHEK	skin
42	chr15:100223600-100232800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr15:100223600-100236600	Strong transcription	Fetal Lung	lung
44	chr15:100223600-100247400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr15:100223800-100230000	Weak transcription	NH-A	brain
46	chr15:100223800-100230400	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr15:100223800-100232800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr15:100223800-100241000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr15:100223800-100243600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr15:100223800-100246800	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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