Variant report

Variant	rs59347138
Chromosome Location	chr5:176926987-176926988
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr5:176926840-176926990	AG04450	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:176730450..176733119-chr5:176926735..176928384,3	MCF-7	breast:
2	chr5:176926429..176929073-chr5:177031602..177034332,2	K562	blood:
3	chr5:176814610..176818995-chr5:176923007..176929143,6	MCF-7	breast:

Variant related genes	Relation type
PDLIM7	TF binding region
ENSG00000027847	Chromatin interaction
ENSG00000169228	Chromatin interaction
ENSG00000169230	Chromatin interaction
ENSG00000131183	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs73349165	1.00[AMR][1000 genomes]
rs73349168	1.00[AMR][1000 genomes]
rs73349170	1.00[AMR][1000 genomes]
rs73349177	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73349179	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916108	chr5:176688459-177078723	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
2	nsv883158	chr5:176726635-176931706	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	120 gene(s)	inside rSNPs	diseases
3	nsv883160	chr5:176740996-176952919	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
4	nsv1024444	chr5:176751921-177427715	Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	142 gene(s)	inside rSNPs	diseases
5	nsv883161	chr5:176754722-176958397	Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
6	nsv1020334	chr5:176779108-176954933	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
7	nsv883164	chr5:176780545-177003616	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
8	esv1816147	chr5:176787037-176966509	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
9	nsv883166	chr5:176817636-176940384	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
10	nsv883170	chr5:176824137-176952919	Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
11	nsv883173	chr5:176842474-176931706	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
12	nsv883174	chr5:176842474-176940384	Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
13	nsv883175	chr5:176842474-176952919	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
14	nsv1030965	chr5:176851182-176937654	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
15	nsv1026103	chr5:176851182-176942552	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
16	nsv1022832	chr5:176861503-176937654	Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
17	nsv1018088	chr5:176861503-176942552	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
18	nsv1028123	chr5:176861503-176949149	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
19	nsv537965	chr5:176861503-176949149	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
20	nsv883177	chr5:176868358-177003616	Genic enhancers Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
21	esv2752795	chr5:176898619-177488281	Active TSS Strong transcription Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
22	nsv883180	chr5:176912073-176937177	Genic enhancers Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
23	nsv984570	chr5:176923414-176956300	Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:176925400-176927600	Weak transcription	NHDF-Ad	bronchial
2	chr5:176925400-176927800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr5:176925400-176928000	Weak transcription	Brain Angular Gyrus	brain
4	chr5:176925400-176930000	Weak transcription	Gastric	stomach
5	chr5:176925400-176930600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr5:176925400-176937200	Weak transcription	Aorta	Aorta
7	chr5:176925400-176937200	Weak transcription	Dnd41	blood
8	chr5:176925600-176927000	Enhancers	Fetal Kidney	kidney
9	chr5:176925600-176927000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr5:176925600-176927600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr5:176925600-176927600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr5:176925600-176927600	Weak transcription	Brain Cingulate Gyrus	brain
13	chr5:176925600-176927600	Weak transcription	Colon Smooth Muscle	Colon
14	chr5:176925600-176927600	Weak transcription	Hela-S3	cervix
15	chr5:176925600-176927800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:176925600-176927800	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr5:176925600-176927800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr5:176925600-176927800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr5:176925600-176927800	Weak transcription	Liver	Liver
20	chr5:176925600-176927800	Weak transcription	HMEC	breast
21	chr5:176925600-176928000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr5:176925600-176928400	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr5:176925600-176928600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr5:176925600-176928600	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr5:176925600-176928800	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr5:176925600-176929400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr5:176925600-176929600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr5:176925600-176929600	Weak transcription	Esophagus	oesophagus
29	chr5:176925600-176930800	Weak transcription	Lung	lung
30	chr5:176925600-176930800	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr5:176925600-176934400	Weak transcription	Pancreas	Pancrea
32	chr5:176925600-176942400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr5:176925800-176927000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr5:176925800-176927000	Weak transcription	NHLF	lung
35	chr5:176925800-176927400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr5:176925800-176927600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:176925800-176927600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr5:176925800-176927600	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr5:176925800-176927600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr5:176925800-176927600	Weak transcription	Brain Anterior Caudate	brain
41	chr5:176925800-176927600	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr5:176925800-176927600	Weak transcription	Fetal Lung	lung
43	chr5:176925800-176927600	Weak transcription	Left Ventricle	heart
44	chr5:176925800-176927600	Weak transcription	A549	lung
45	chr5:176925800-176927600	Weak transcription	Osteobl	bone
46	chr5:176925800-176927800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr5:176925800-176927800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr5:176925800-176927800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr5:176925800-176927800	Weak transcription	Adipose Nuclei	Adipose
50	chr5:176925800-176927800	Weak transcription	HUVEC	blood vessel

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