Variant report

Variant	rs74119728
Chromosome Location	chr1:166352882-166352883
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs16827930	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16827931	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16827935	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16857036	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16857044	0.83[AMR][1000 genomes]
rs4422983	0.83[AMR][1000 genomes]
rs56945226	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs74119732	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs74119733	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[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	nsv916491	chr1:166000783-166948513	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 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	chr1:166343800-166354200	Weak transcription	Right Atrium	heart
2	chr1:166348200-166354200	Weak transcription	Left Ventricle	heart
3	chr1:166348800-166353000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:166349400-166354200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr1:166352000-166353400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr1:166352000-166360200	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr1:166352200-166353000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr1:166352200-166353000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr1:166352200-166356000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
10	chr1:166352400-166353200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr1:166352600-166353200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:166352600-166353600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:166352600-166354600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:166352800-166353000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr1:166352800-166353000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
16	chr1:166352800-166353000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
17	chr1:166352800-166353200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
18	chr1:166352800-166356200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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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