Variant report

Variant	rs72616382
Chromosome Location	chr4:130945103-130945104
allele	C/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:10)

rs_ID	r²[population]
rs61471044	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72616304	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72616305	0.86[ASN][1000 genomes]
rs72616306	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72616307	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72616359	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72616370	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72616371	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72616381	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72616384	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019516	chr4:130754819-130976202	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1017270	chr4:130853337-130982586	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv879936	chr4:130941492-130981535	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:130943000-130947200	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr4:130943200-130952600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr4:130943400-130945600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr4:130943400-130947000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr4:130943400-130947400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr4:130943600-130952600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr4:130943800-130945200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr4:130944000-130945600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr4:130944800-130945200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:130945000-130945400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:130945000-130945600	Enhancers	H1 Cell Line	embryonic stem cell
12	chr4:130945000-130945600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:130945000-130945600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr4:130945000-130946400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr4:130945000-130950400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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