Variant report

Variant	rs74067145
Chromosome Location	chr14:79316893-79316894
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs60924894	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832838	chr14:79306627-79445382	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79314000-79317000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr14:79314200-79317800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr14:79314200-79317800	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr14:79314400-79317800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr14:79314600-79317800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr14:79314600-79318200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr14:79314800-79317800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr14:79314800-79318000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr14:79315600-79318000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr14:79316600-79317600	Weak transcription	Fetal Brain Male	brain
11	chr14:79316600-79324400	Weak transcription	H1 Cell Line	embryonic stem cell

Quick Search:

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

what's new

Quick links