Variant report

Variant	rs35286649
Chromosome Location	chr19:51416451-51416452
allele	-/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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	nsv1060760	chr19:50883425-51463712	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
2	nsv1058177	chr19:50984774-51463712	Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
3	esv3438577	chr19:51414940-51419738	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
4	esv3512692	chr19:51415440-51418251	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
5	esv3512693	chr19:51415440-51418251	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
6	esv3345084	chr19:51416258-51418089	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51410800-51418400	Weak transcription	Right Atrium	heart
2	chr19:51415600-51416600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
3	chr19:51415600-51416600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr19:51415800-51416600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
5	chr19:51415800-51416600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
6	chr19:51416000-51416600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
7	chr19:51416000-51416600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr19:51416000-51416600	Bivalent Enhancer	HMEC	breast
9	chr19:51416000-51416800	Bivalent Enhancer	Esophagus	oesophagus
10	chr19:51416200-51416800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
11	chr19:51416400-51416600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
12	chr19:51416400-51416600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
13	chr19:51416400-51416600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
14	chr19:51416400-51416600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr19:51416400-51416600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
16	chr19:51416400-51416800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr19:51416400-51416800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
18	chr19:51416400-51416800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast

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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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