Variant report

Variant	rs58167367
Chromosome Location	chr6:126677275-126677276
allele	A/G
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	chr6:126663600-126678800	Weak transcription	Thymus	Thymus
2	chr6:126663600-126682800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr6:126663800-126678400	Weak transcription	Fetal Lung	lung
4	chr6:126663800-126686400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:126665400-126702200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr6:126665400-126702200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:126668200-126677800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:126671000-126677400	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr6:126671600-126679400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr6:126671600-126679800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:126671600-126680600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr6:126671800-126681000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr6:126673600-126678000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr6:126675400-126681000	Weak transcription	A549	lung
15	chr6:126677000-126678600	ZNF genes & repeats	Dnd41	blood

Quick Search:

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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