Variant report

Variant	rs13197492
Chromosome Location	chr6:53677720-53677721
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:53657579..53660733-chr6:53674241..53678049,6	MCF-7	breast:
2	chr6:53588027..53590620-chr6:53675669..53678421,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000228614	Chromatin interaction
ENSG00000137269	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs3000998	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3001002	0.85[ASN][1000 genomes]
rs3001003	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3003489	0.85[ASN][1000 genomes]
rs3003491	0.85[ASN][1000 genomes]
rs3003493	0.85[ASN][1000 genomes]
rs3003496	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3003497	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35709775	0.82[EUR][1000 genomes]
rs4236113	0.85[ASN][1000 genomes]
rs4265033	0.85[ASN][1000 genomes]
rs4269375	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4276503	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4342426	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4351263	0.85[ASN][1000 genomes]
rs4382260	0.85[ASN][1000 genomes]
rs4398733	0.85[ASN][1000 genomes]
rs4421195	0.80[EUR][1000 genomes]
rs4475321	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4484515	0.85[ASN][1000 genomes]
rs4518484	0.80[EUR][1000 genomes]
rs4587161	0.86[EUR][1000 genomes]
rs4591854	0.85[ASN][1000 genomes]
rs4712048	0.85[ASN][1000 genomes]
rs4712049	0.85[ASN][1000 genomes]
rs4715425	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4715426	0.85[ASN][1000 genomes]
rs5001609	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6458958	0.85[ASN][1000 genomes]
rs6458959	0.85[ASN][1000 genomes]
rs6458960	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6458961	0.85[ASN][1000 genomes]
rs6458962	0.85[ASN][1000 genomes]
rs6458966	0.85[ASN][1000 genomes]
rs6458970	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6650996	0.85[ASN][1000 genomes]
rs6900929	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6920743	0.85[ASN][1000 genomes]
rs6934444	0.85[EUR][1000 genomes]
rs7762883	0.85[ASN][1000 genomes]
rs7763147	0.85[ASN][1000 genomes]
rs7767443	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9349686	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9357774	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9357775	0.82[EUR][1000 genomes]
rs9367542	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9370236	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9382239	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034955	chr6:53447607-53931055	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1021506	chr6:53600338-53770482	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:53661400-53688200	Weak transcription	Right Ventricle	heart
2	chr6:53667600-53678400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:53668200-53680200	Weak transcription	Fetal Stomach	stomach
4	chr6:53668800-53680000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr6:53668800-53683800	Weak transcription	Ovary	ovary
6	chr6:53670200-53678000	Weak transcription	Aorta	Aorta
7	chr6:53670200-53686400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr6:53670800-53680000	Weak transcription	Stomach Smooth Muscle	stomach
9	chr6:53670800-53693200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr6:53671000-53680200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr6:53671000-53683600	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr6:53671200-53680400	Weak transcription	Fetal Brain Female	brain
13	chr6:53671400-53679000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr6:53673000-53678400	Weak transcription	Primary B cells from peripheral blood	blood
15	chr6:53673400-53687200	Weak transcription	Fetal Muscle Leg	muscle
16	chr6:53673600-53677800	Weak transcription	Brain Substantia Nigra	brain
17	chr6:53673600-53682800	Weak transcription	Dnd41	blood
18	chr6:53673800-53678600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr6:53674200-53678200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr6:53674800-53678400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:53674800-53679600	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr6:53674800-53680400	Enhancers	Fetal Intestine Small	intestine
23	chr6:53675000-53681200	Weak transcription	Fetal Brain Male	brain
24	chr6:53675400-53679000	Enhancers	Duodenum Mucosa	Duodenum
25	chr6:53675400-53680200	Enhancers	Stomach Mucosa	stomach
26	chr6:53675400-53680400	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr6:53675600-53678200	Enhancers	Rectal Mucosa Donor 29	rectum
28	chr6:53675600-53678800	Enhancers	Hela-S3	cervix
29	chr6:53676200-53677800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:53676200-53677800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr6:53676200-53677800	Weak transcription	Lung	lung
32	chr6:53676200-53678000	Weak transcription	Brain Cingulate Gyrus	brain
33	chr6:53676200-53678400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr6:53676200-53678600	Enhancers	Esophagus	oesophagus
35	chr6:53676200-53678800	Enhancers	Gastric	stomach
36	chr6:53676200-53679200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:53676200-53683600	Weak transcription	Left Ventricle	heart
38	chr6:53676200-53697800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:53676400-53677800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr6:53676400-53678400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr6:53676400-53678400	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr6:53676400-53679200	Weak transcription	Brain Angular Gyrus	brain
43	chr6:53676400-53679800	Weak transcription	Fetal Heart	heart
44	chr6:53676600-53677800	Weak transcription	Brain Hippocampus Middle	brain
45	chr6:53676600-53677800	Weak transcription	HUVEC	blood vessel
46	chr6:53676600-53679400	Weak transcription	Colon Smooth Muscle	Colon
47	chr6:53676800-53678000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr6:53676800-53678000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr6:53676800-53678000	Weak transcription	Fetal Thymus	thymus
50	chr6:53676800-53678600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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