Variant report

Variant	rs74071394
Chromosome Location	chr14:85107658-85107659
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs74071312	1.00[AMR][1000 genomes]
rs74071322	1.00[AMR][1000 genomes]
rs74071323	1.00[AMR][1000 genomes]
rs74071365	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74071387	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74071396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751288	chr14:84815330-85704047	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1046875	chr14:84993510-85193250	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv456354	chr14:85046837-85110699	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv565377	chr14:85046837-85110699	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv902162	chr14:85048957-85131164	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv565378	chr14:85070611-85140984	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv1829021	chr14:85106009-85196163	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85106200-85108000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr14:85106400-85108000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr14:85107000-85110600	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr14:85107400-85107800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr14:85107400-85108400	Enhancers	Fetal Lung	lung
6	chr14:85107600-85107800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr14:85107600-85108000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr14:85107600-85108000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr14:85107600-85108600	Enhancers	HUES48 Cell Line	embryonic stem cell

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

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