Variant report

Variant	rs7861470
Chromosome Location	chr9:110870079-110870080
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110858000-110870600	Weak transcription	A549	lung
2	chr9:110863200-110881600	Weak transcription	Gastric	stomach
3	chr9:110866000-110870600	Weak transcription	NHDF-Ad	bronchial
4	chr9:110866200-110870800	Weak transcription	Osteobl	bone
5	chr9:110866400-110870600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr9:110866400-110871200	Weak transcription	Fetal Stomach	stomach
7	chr9:110867400-110880200	Weak transcription	Esophagus	oesophagus
8	chr9:110867600-110881600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr9:110868200-110870400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr9:110868400-110870400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr9:110868600-110870600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:110868600-110870600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:110868600-110870600	Weak transcription	Stomach Mucosa	stomach
14	chr9:110868600-110870800	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr9:110868600-110899800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr9:110868800-110871000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr9:110869800-110870400	Enhancers	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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