Variant report

Variant	rs533467779
Chromosome Location	chr3:112134901-112134902
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002567	chr3:112088498-112144063	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2830128	chr3:112090292-112144026	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv591294	chr3:112091220-112208750	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1010208	chr3:112098542-112227212	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv997659	chr3:112099148-112135687	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1003936	chr3:112125931-112274613	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv998309	chr3:112130290-112278804	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
8	esv3331778	chr3:112134311-112164058	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112126200-112135200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:112126600-112135200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr3:112126600-112135400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr3:112126800-112135200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr3:112126800-112136400	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr3:112130800-112136400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr3:112130800-112136400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr3:112130800-112137200	Weak transcription	Right Atrium	heart
9	chr3:112130800-112137600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr3:112132600-112135400	Weak transcription	Primary B cells from cord blood	blood
11	chr3:112132800-112135400	Weak transcription	Placenta	Placenta
12	chr3:112132800-112137600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:112132800-112144200	Weak transcription	Primary B cells from peripheral blood	blood
14	chr3:112134000-112136400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr3:112134200-112136600	Strong transcription	H1 Cell Line	embryonic stem cell
16	chr3:112134400-112135800	Enhancers	iPS-15b 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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