Variant report

Variant	rs557749035
Chromosome Location	chr4:175376930-175376931
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	esv3361753	chr4:175375852-175377950	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv3371560	chr4:175376377-175377425	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:175371000-175378400	Weak transcription	Esophagus	oesophagus
2	chr4:175371800-175382600	Weak transcription	Small Intestine	intestine
3	chr4:175372000-175377200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr4:175374000-175377800	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr4:175374200-175378800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr4:175374400-175377800	Weak transcription	Stomach Mucosa	stomach
7	chr4:175374600-175382800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr4:175374800-175377000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr4:175375200-175377000	Weak transcription	Fetal Stomach	stomach
10	chr4:175376000-175379400	Enhancers	Colon Smooth Muscle	Colon
11	chr4:175376200-175378800	Weak transcription	Pancreas	Pancrea
12	chr4:175376400-175381600	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr4:175376600-175381600	Weak transcription	Fetal Intestine Small	intestine

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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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