Variant report

Variant	rs55705559
Chromosome Location	chr20:53226782-53226783
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:53221224..53225981-chr20:53225997..53231429,8	MCF-7	breast:
2	chr20:53226045..53227848-chr20:53245304..53248217,2	MCF-7	breast:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10154005	0.93[AMR][1000 genomes]
rs10485784	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13433172	0.93[AMR][1000 genomes]
rs17327539	0.88[EUR][1000 genomes]
rs28663252	0.82[EUR][1000 genomes]
rs55960128	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56138015	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56187828	0.84[AMR][1000 genomes]
rs56294816	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56371656	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57120787	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs58298733	0.81[EUR][1000 genomes]
rs6014078	0.83[EUR][1000 genomes]
rs6014080	0.83[EUR][1000 genomes]
rs6014087	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6014089	0.97[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6023382	0.86[EUR][1000 genomes]
rs6023383	0.86[EUR][1000 genomes]
rs6023394	0.83[EUR][1000 genomes]
rs6023396	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6023397	0.83[EUR][1000 genomes]
rs6023398	0.83[EUR][1000 genomes]
rs6023401	0.83[EUR][1000 genomes]
rs6023403	0.83[EUR][1000 genomes]
rs6023422	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6091933	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6091939	0.88[AMR][1000 genomes]
rs6098093	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6098099	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6098103	0.83[EUR][1000 genomes]
rs6098104	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6098105	0.83[EUR][1000 genomes]
rs6098111	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6098116	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6098118	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6098123	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6098129	0.88[AMR][1000 genomes]
rs6098130	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62214427	0.82[EUR][1000 genomes]
rs62214433	0.87[AMR][1000 genomes]
rs67907005	0.88[EUR][1000 genomes]
rs7269966	0.83[EUR][1000 genomes]
rs73140147	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73144055	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs73144063	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73144072	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73144079	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73144086	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73146053	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73146055	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv586224	chr20:52474850-53279490	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	338 gene(s)	inside rSNPs	diseases
2	nsv1067497	chr20:53146241-53751820	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
3	nsv1064144	chr20:53175264-53750137	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
4	nsv544302	chr20:53175264-53750137	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
5	nsv586282	chr20:53218978-53254815	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:53202200-53230800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr20:53204600-53240600	Weak transcription	Left Ventricle	heart
3	chr20:53215200-53236400	Weak transcription	Aorta	Aorta
4	chr20:53216400-53227000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr20:53216800-53226800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr20:53217000-53235800	Weak transcription	Brain Germinal Matrix	brain
7	chr20:53217400-53240600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr20:53217800-53227000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr20:53217800-53227400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr20:53221600-53239000	Weak transcription	Osteobl	bone
11	chr20:53223400-53227600	Weak transcription	Fetal Muscle Leg	muscle
12	chr20:53225400-53227600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr20:53225600-53227200	Weak transcription	Ovary	ovary
14	chr20:53225800-53226800	Enhancers	Fetal Brain Female	brain
15	chr20:53226000-53228400	Weak transcription	Adipose Nuclei	Adipose
16	chr20:53226200-53227600	Enhancers	Fetal Brain Male	brain
17	chr20:53226400-53228600	Weak transcription	Fetal Muscle Trunk	muscle
18	chr20:53226600-53227400	Strong transcription	Cortex derived primary cultured neurospheres	brain

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