Variant report

Variant	rs72679720
Chromosome Location	chr1:62658647-62658648
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12122973	1.00[ASN][1000 genomes]
rs12131839	1.00[ASN][1000 genomes]
rs12136917	1.00[ASN][1000 genomes]
rs12141623	1.00[ASN][1000 genomes]
rs2457828	1.00[ASN][1000 genomes]
rs2481696	1.00[ASN][1000 genomes]
rs72679729	1.00[ASN][1000 genomes]
rs72679734	1.00[ASN][1000 genomes]
rs7412990	1.00[ASN][1000 genomes]
rs870906	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004446	chr1:62394631-62813533	Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
2	nsv534984	chr1:62394631-62813533	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
3	nsv870842	chr1:62644118-62679202	Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1009398	chr1:62656660-62780644	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62646600-62660400	Weak transcription	Right Atrium	heart
2	chr1:62649800-62660000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:62650400-62658800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr1:62652000-62660200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:62657400-62659000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr1:62657600-62660000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr1:62657600-62660000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr1:62658400-62658800	Enhancers	H9 Cell Line	embryonic stem cell
9	chr1:62658400-62659000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr1:62658400-62659000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr1:62658400-62659200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr1:62658600-62658800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr1:62658600-62658800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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