Variant report

Variant	rs1208236
Chromosome Location	chr6:134138444-134138445
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	chr6:134136062..134139390-chr6:134141516..134143681,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000223586	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1208234	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1208235	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1208237	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1208239	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1208240	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1208241	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1208242	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1208243	0.89[EUR][1000 genomes]
rs1208244	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1208246	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1208247	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1208249	0.89[EUR][1000 genomes]
rs1208251	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1208252	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1208253	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1208254	0.89[EUR][1000 genomes]
rs1208260	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1208265	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1208267	0.84[EUR][1000 genomes]
rs1575446	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1616030	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1746011	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1746012	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1763941	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1763944	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1763945	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2104261	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs716050	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs942130	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs942131	0.89[EUR][1000 genomes]
rs942132	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv830812	chr6:133993897-134165407	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv34122	chr6:134089019-134378252	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134136000-134141600	Weak transcription	Fetal Kidney	kidney
2	chr6:134136800-134138800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:134136800-134147800	Weak transcription	A549	lung
4	chr6:134137000-134142600	Weak transcription	Aorta	Aorta
5	chr6:134137600-134139200	Enhancers	Ovary	ovary
6	chr6:134137600-134140200	Enhancers	Fetal Stomach	stomach
7	chr6:134138000-134139000	Enhancers	Fetal Muscle Leg	muscle
8	chr6:134138200-134151200	Weak transcription	Fetal Lung	lung

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