Variant report

Variant	rs11039030
Chromosome Location	chr11:46953118-46953119
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46944800-46958200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:46952000-46957800	Weak transcription	NHLF	lung
3	chr11:46952200-46953200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr11:46952200-46953600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr11:46952200-46957200	Weak transcription	A549	lung
6	chr11:46952200-46957600	Weak transcription	Hela-S3	cervix
7	chr11:46952200-46957800	Weak transcription	NHEK	skin
8	chr11:46952400-46953600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr11:46952400-46953800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr11:46952400-46957000	Weak transcription	Fetal Intestine Small	intestine
11	chr11:46952400-46957600	Weak transcription	Duodenum Mucosa	Duodenum
12	chr11:46952400-46957600	Weak transcription	Fetal Intestine Large	intestine
13	chr11:46952400-46957800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr11:46952400-46957800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr11:46952400-46957800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr11:46952400-46957800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:46952400-46957800	Weak transcription	Stomach Mucosa	stomach
18	chr11:46952400-46957800	Weak transcription	HepG2	liver
19	chr11:46952600-46957800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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