Variant report

Variant	rs2861309
Chromosome Location	chr10:98038542-98038543
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98032400-98047200	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr10:98034200-98042200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr10:98036200-98038800	Weak transcription	Stomach Mucosa	stomach
4	chr10:98036400-98041600	Weak transcription	Liver	Liver
5	chr10:98036400-98044800	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr10:98036400-98045200	Weak transcription	Gastric	stomach
7	chr10:98036600-98039200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr10:98037000-98040800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr10:98037200-98040400	Weak transcription	NHEK	skin
10	chr10:98037400-98039400	Weak transcription	Primary B cells from cord blood	blood
11	chr10:98037400-98040000	Weak transcription	HMEC	breast
12	chr10:98037400-98041000	Weak transcription	Esophagus	oesophagus
13	chr10:98037600-98040800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr10:98037800-98038800	Weak transcription	Primary B cells from peripheral blood	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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