Variant report

Variant	rs3748227
Chromosome Location	chr10:97949901-97949902
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97945600-97956200	Weak transcription	Brain Substantia Nigra	brain
2	chr10:97947000-97950000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr10:97947400-97961800	Weak transcription	Pancreas	Pancrea
4	chr10:97948000-97963800	Weak transcription	Placenta	Placenta
5	chr10:97948200-97963600	Weak transcription	Gastric	stomach
6	chr10:97948200-97979000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr10:97948400-97957000	Weak transcription	Fetal Intestine Small	intestine
8	chr10:97948400-97974200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr10:97948600-97962800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr10:97948600-97969400	Weak transcription	Fetal Stomach	stomach
11	chr10:97948800-97959200	Weak transcription	Spleen	Spleen
12	chr10:97949400-97952000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
13	chr10:97949600-97952200	ZNF genes & repeats	Primary B cells from cord blood	blood
14	chr10:97949600-97956600	Strong transcription	Rectal Mucosa Donor 29	rectum
15	chr10:97949600-97989200	Strong transcription	Liver	Liver
16	chr10:97949800-97952000	ZNF genes & repeats	Fetal Intestine Large	intestine
17	chr10:97949800-97953600	Strong transcription	Duodenum Mucosa	Duodenum
18	chr10:97949800-97953600	ZNF genes & repeats	GM12878-XiMat	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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