Variant report

Variant	rs16971631
Chromosome Location	chr17:34233312-34233313
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:34228200-34233600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr17:34229200-34236800	Weak transcription	K562	blood
3	chr17:34229800-34240000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr17:34230000-34245400	Weak transcription	Primary T cells from cord blood	blood
5	chr17:34230400-34233800	Weak transcription	Fetal Thymus	thymus
6	chr17:34231000-34233800	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr17:34231200-34233400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr17:34231200-34233400	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr17:34231400-34234000	Weak transcription	Thymus	Thymus
10	chr17:34231800-34234200	Enhancers	Fetal Intestine Large	intestine
11	chr17:34233000-34234000	Enhancers	Fetal Intestine Small	intestine
12	chr17:34233000-34234600	Enhancers	Placenta	Placenta
13	chr17:34233200-34235200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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