Variant report

Variant	rs7145918
Chromosome Location	chr14:77865227-77865228
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:77790168..77792372-chr14:77864392..77868587,4	MCF-7	breast:
2	chr14:77858452..77860278-chr14:77863182..77865442,2	MCF-7	breast:
3	chr14:77777582..77780078-chr14:77863177..77865968,2	MCF-7	breast:
4	chr14:77837819..77844743-chr14:77858917..77867107,14	MCF-7	breast:
5	chr14:77865069..77868017-chr14:77924592..77926353,2	MCF-7	breast:
6	chr14:77781806..77790093-chr14:77860676..77869624,28	MCF-7	breast:
7	chr14:77767421..77771659-chr14:77864356..77866894,5	MCF-7	breast:
8	chr14:77854656..77856694-chr14:77864255..77865846,2	MCF-7	breast:
9	chr14:77864538..77867025-chr14:78015900..78017650,2	MCF-7	breast:

No data

No data

No data

Variant related genes	Relation type
ENSG00000100577	Chromatin interaction
ENSG00000009830	Chromatin interaction
ENSG00000100580	Chromatin interaction
ENSG00000100583	Chromatin interaction
ENSG00000100591	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs2178874	0.80[YRI][hapmap]
rs35913082	1.00[AMR][1000 genomes]
rs4903587	0.85[AMR][1000 genomes]
rs56686781	0.81[AFR][1000 genomes]
rs60966860	0.83[AFR][1000 genomes]
rs7141816	0.89[YRI][hapmap];0.81[AFR][1000 genomes]
rs7141931	0.80[YRI][hapmap];1.00[AMR][1000 genomes]
rs7142535	0.87[YRI][hapmap]
rs7144628	1.00[AMR][1000 genomes]
rs7144883	0.81[AFR][1000 genomes]
rs7148278	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7149349	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7150614	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs760253	1.00[AMR][1000 genomes]
rs760254	1.00[AMR][1000 genomes]
rs8015874	0.80[YRI][hapmap];1.00[AMR][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	nsv902107	chr14:77790416-77871777	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1362	chr14:77853202-77898605	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77859600-77886200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr14:77860000-77872400	Weak transcription	Brain Anterior Caudate	brain
3	chr14:77862600-77872600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr14:77863800-77870800	Weak transcription	Primary hematopoietic stem cells	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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