Variant report

Variant	rs11886358
Chromosome Location	chr2:55370692-55370693
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55361800-55373000	Weak transcription	HSMMtube	muscle
2	chr2:55361800-55378600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr2:55365200-55381000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:55365600-55378600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr2:55366200-55378600	Weak transcription	Colon Smooth Muscle	Colon
6	chr2:55366800-55373400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr2:55367200-55378800	Weak transcription	Placenta	Placenta
8	chr2:55367800-55375000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr2:55369600-55374600	Weak transcription	Hela-S3	cervix
10	chr2:55369800-55374800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr2:55369800-55378200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr2:55369800-55378600	Weak transcription	Fetal Stomach	stomach
13	chr2:55370000-55372600	Weak transcription	Stomach Mucosa	stomach
14	chr2:55370000-55375600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr2:55370000-55379600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr2:55370600-55371800	Weak transcription	K562	blood

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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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