Variant report

Variant	rs16870345
Chromosome Location	chr8:104348947-104348948
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:104309275..104311438-chr8:104347221..104349478,2	MCF-7	breast:
2	chr8:104345079..104346663-chr8:104348274..104351227,2	MCF-7	breast:
3	chr8:104311034..104312841-chr8:104347572..104350173,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164930	Chromatin interaction
ENSG00000247081	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1403295	1.00[AMR][1000 genomes]
rs16870264	1.00[AMR][1000 genomes]
rs16870288	1.00[AMR][1000 genomes]
rs16870308	1.00[AMR][1000 genomes]
rs16870347	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1982891	1.00[AMR][1000 genomes]
rs59556900	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60542330	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs703808	0.87[AFR][1000 genomes]
rs827532	0.87[AFR][1000 genomes]
rs827542	0.87[AFR][1000 genomes]
rs827544	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429931	chr8:104097396-104878014	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	esv1848810	chr8:104128496-104369288	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	esv1844303	chr8:104128696-104369090	Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv1015965	chr8:104192086-104361108	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv1023181	chr8:104298542-104366365	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv1020476	chr8:104312212-104924482	Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	nsv539704	chr8:104312212-104924482	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS 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	42 gene(s)	inside rSNPs	diseases
8	nsv1016395	chr8:104327541-104473005	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104312000-104350200	Weak transcription	Esophagus	oesophagus
2	chr8:104312400-104350000	Weak transcription	Lung	lung
3	chr8:104312600-104350000	Weak transcription	Colon Smooth Muscle	Colon
4	chr8:104317400-104354000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr8:104321400-104358800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr8:104321600-104350200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:104322800-104350200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr8:104328200-104355800	Weak transcription	Gastric	stomach
9	chr8:104328200-104361200	Weak transcription	Pancreas	Pancrea
10	chr8:104330400-104350200	Weak transcription	Psoas Muscle	Psoas
11	chr8:104331800-104352000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr8:104337800-104350200	Weak transcription	Brain Angular Gyrus	brain
13	chr8:104337800-104351800	Weak transcription	Aorta	Aorta
14	chr8:104338000-104350000	Weak transcription	Brain Anterior Caudate	brain
15	chr8:104340600-104349000	Weak transcription	Fetal Kidney	kidney
16	chr8:104340800-104350000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr8:104342400-104349200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr8:104342400-104357600	Weak transcription	Placenta	Placenta
19	chr8:104342400-104360000	Weak transcription	Duodenum Mucosa	Duodenum
20	chr8:104342600-104352000	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr8:104343000-104350000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr8:104343000-104350000	Weak transcription	Stomach Smooth Muscle	stomach
23	chr8:104343000-104350000	Weak transcription	NHLF	lung
24	chr8:104343200-104349000	Weak transcription	NHDF-Ad	bronchial
25	chr8:104343200-104355800	Weak transcription	HUVEC	blood vessel
26	chr8:104343800-104350000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr8:104343800-104350000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr8:104343800-104352200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr8:104343800-104352200	Weak transcription	NHEK	skin
30	chr8:104343800-104357600	Weak transcription	Adipose Nuclei	Adipose
31	chr8:104343800-104357600	Weak transcription	Ovary	ovary
32	chr8:104344000-104349200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr8:104344000-104352200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:104345800-104350200	Weak transcription	Left Ventricle	heart
35	chr8:104346000-104351200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr8:104346400-104349000	Weak transcription	Fetal Heart	heart
37	chr8:104346800-104349000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr8:104347600-104350600	Enhancers	Fetal Thymus	thymus
39	chr8:104347800-104349200	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr8:104347800-104350400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr8:104347800-104350800	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr8:104348200-104349200	Enhancers	Primary T cells fromperipheralblood	blood
43	chr8:104348200-104349400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr8:104348200-104349400	Flanking Active TSS	Dnd41	blood
45	chr8:104348200-104350200	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr8:104348200-104350400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr8:104348200-104350600	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr8:104348200-104350600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr8:104348400-104349200	Flanking Active TSS	Primary T cells from cord blood	blood
50	chr8:104348400-104349200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood

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