Variant report

Variant	rs369689274
Chromosome Location	chr11:17556580-17556581
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv469895	chr11:17368270-17584220	Weak transcription Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv1040065	chr11:17556031-17753467	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17538400-17562200	Weak transcription	Small Intestine	intestine
2	chr11:17547200-17563200	Genic enhancers	Fetal Intestine Small	intestine
3	chr11:17553600-17557000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr11:17553600-17557200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr11:17553600-17561800	Weak transcription	Gastric	stomach
6	chr11:17553600-17562200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr11:17553800-17556600	Weak transcription	Brain Anterior Caudate	brain
8	chr11:17553800-17556800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr11:17553800-17558200	Weak transcription	Stomach Mucosa	stomach
10	chr11:17553800-17558600	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr11:17553800-17563200	Weak transcription	Colonic Mucosa	Colon
12	chr11:17555400-17560400	Weak transcription	Duodenum Mucosa	Duodenum
13	chr11:17555800-17562400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr11:17556000-17558000	Enhancers	Hela-S3	cervix
15	chr11:17556200-17556800	Weak transcription	Fetal Intestine Large	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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