Variant report

Variant	rs16940314
Chromosome Location	chr15:58739540-58739541
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:58739121..58741793-chr15:58746543..58749268,3	K562	blood:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs16940315	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41292484	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57774188	1.00[EUR][1000 genomes]
rs73420582	1.00[EUR][1000 genomes]
rs74016103	1.00[EUR][1000 genomes]
rs74016175	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051058	chr15:58519922-59092530	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS 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 lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv542401	chr15:58519922-59092530	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529717	chr15:58519923-58756814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1042201	chr15:58520746-58780710	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv569598	chr15:58552606-58852463	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv904267	chr15:58699010-58769583	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1047048	chr15:58701400-58784800	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	esv3362898	chr15:58705732-58850860	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1043362	chr15:58726337-58756571	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv457173	chr15:58731567-58779039	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv569600	chr15:58731567-58779039	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58730400-58746200	Weak transcription	GM12878-XiMat	blood
2	chr15:58733200-58739600	Weak transcription	Fetal Kidney	kidney
3	chr15:58734200-58739800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr15:58734400-58739600	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr15:58734400-58739800	Weak transcription	Brain Anterior Caudate	brain
6	chr15:58734400-58740400	Weak transcription	Pancreas	Pancrea
7	chr15:58734600-58739800	Weak transcription	Brain Cingulate Gyrus	brain
8	chr15:58735000-58740200	Weak transcription	Small Intestine	intestine
9	chr15:58735400-58740400	Weak transcription	Colonic Mucosa	Colon
10	chr15:58736600-58746200	Weak transcription	Spleen	Spleen
11	chr15:58736800-58740200	Weak transcription	Fetal Intestine Large	intestine
12	chr15:58737000-58739600	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr15:58737200-58740200	Weak transcription	Fetal Intestine Small	intestine
14	chr15:58737400-58749800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr15:58737400-58761800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr15:58737600-58739600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr15:58737800-58739600	Weak transcription	Adipose Nuclei	Adipose
18	chr15:58737800-58740000	Weak transcription	HepG2	liver
19	chr15:58737800-58740600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr15:58737800-58746600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr15:58737800-58748200	Weak transcription	Left Ventricle	heart
22	chr15:58738600-58739600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:58738600-58740800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr15:58738600-58740800	Enhancers	Liver	Liver
25	chr15:58738600-58741400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr15:58738600-58741400	Enhancers	Dnd41	blood
27	chr15:58738800-58739600	Enhancers	Gastric	stomach
28	chr15:58738800-58740600	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr15:58738800-58740800	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr15:58738800-58740800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr15:58738800-58741000	Enhancers	Fetal Thymus	thymus
32	chr15:58739000-58739600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr15:58739000-58740600	Weak transcription	Lung	lung
34	chr15:58739200-58740600	Enhancers	NHDF-Ad	bronchial
35	chr15:58739200-58741200	Enhancers	Thymus	Thymus
36	chr15:58739400-58739600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr15:58739400-58739600	Enhancers	Fetal Muscle Trunk	muscle
38	chr15:58739400-58739800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr15:58739400-58739800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr15:58739400-58739800	Enhancers	Esophagus	oesophagus
41	chr15:58739400-58740000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr15:58739400-58740000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr15:58739400-58740000	Enhancers	Duodenum Mucosa	Duodenum
44	chr15:58739400-58740000	Enhancers	HSMMtube	muscle
45	chr15:58739400-58740200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr15:58739400-58740200	Enhancers	HSMM	muscle
47	chr15:58739400-58740200	Enhancers	NH-A	brain
48	chr15:58739400-58740400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr15:58739400-58740400	Enhancers	Aorta	Aorta
50	chr15:58739400-58740400	Enhancers	Brain Substantia Nigra	brain

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