Variant report

Variant	rs2049754
Chromosome Location	chr6:147319672-147319673
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147311400-147321200	Weak transcription	HSMM	muscle
2	chr6:147312600-147321000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr6:147313400-147320800	Weak transcription	K562	blood
4	chr6:147318600-147320800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:147318600-147320800	Weak transcription	NHDF-Ad	bronchial
6	chr6:147318600-147321000	Weak transcription	A549	lung
7	chr6:147318600-147321200	Weak transcription	HSMMtube	muscle
8	chr6:147318600-147321200	Weak transcription	NHLF	lung
9	chr6:147318600-147321200	Weak transcription	Osteobl	bone
10	chr6:147318600-147321400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr6:147318600-147321400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:147318800-147320800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:147318800-147321000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr6:147318800-147321000	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr6:147318800-147321000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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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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