Variant report

Variant	rs556442427
Chromosome Location	chr4:106578844-106578845
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv879699	chr4:106212562-106698892	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3467298	chr4:106577722-106583287	Weak transcription Strong transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3467299	chr4:106577722-106583287	Weak transcription Enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv14749	chr4:106577867-106583120	Enhancers Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:106559400-106580000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr4:106559400-106580200	Weak transcription	Fetal Intestine Small	intestine
3	chr4:106559400-106602800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr4:106569800-106600400	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr4:106574400-106585400	Weak transcription	Rectal Smooth Muscle	rectum
6	chr4:106576600-106581400	Strong transcription	Fetal Intestine Large	intestine
7	chr4:106577800-106579200	Enhancers	NHEK	skin
8	chr4:106578000-106579000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr4:106578200-106579200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:106578200-106588200	Weak transcription	Pancreas	Pancrea
11	chr4:106578600-106580200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr4:106578600-106607000	Weak transcription	Small Intestine	intestine
13	chr4:106578800-106579400	Enhancers	HMEC	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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