Variant report

Variant	rs28881835
Chromosome Location	chr1:213086628-213086629
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10140072	0.82[EUR][1000 genomes]
rs12323509	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12589535	0.81[AFR][1000 genomes]
rs12893016	0.82[AFR][1000 genomes]
rs12893778	0.81[AFR][1000 genomes]
rs28532336	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28562831	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4898562	0.87[EUR][1000 genomes]
rs5002354	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs66794842	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008383	chr1:213025546-213114894	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv3437401	chr1:213082329-213088502	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	esv3337955	chr1:213083029-213088127	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv3428295	chr1:213083029-213088127	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1000808	chr1:213083340-213087446	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
6	nsv511730	chr1:213083776-213086646	Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213073800-213089000	Weak transcription	Pancreas	Pancrea
2	chr1:213079600-213090000	Weak transcription	Right Atrium	heart
3	chr1:213081600-213088000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:213083200-213088000	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr1:213083200-213089000	Active TSS	H9 Cell Line	embryonic stem cell
6	chr1:213083400-213088000	Active TSS	iPS-18 Cell Line	embryonic stem cell
7	chr1:213084200-213088600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:213086200-213086800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
9	chr1:213086200-213088000	Active TSS	H1 Cell Line	embryonic stem cell
10	chr1:213086400-213087200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr1:213086400-213087400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
12	chr1:213086400-213087800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr1:213086400-213088000	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr1:213086400-213088000	Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr1:213086400-213088000	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr1:213086400-213088000	Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr1:213086400-213088000	Active TSS	iPS-15b Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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