Variant report

Variant	rs73017572
Chromosome Location	chr1:159945494-159945495
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	chr1:159932000-159949800	Weak transcription	Esophagus	oesophagus
2	chr1:159933200-159947200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:159933400-159950600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:159937400-159947200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:159940200-159947400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr1:159941600-159957800	Weak transcription	Right Atrium	heart
7	chr1:159942000-159951200	Weak transcription	Gastric	stomach
8	chr1:159942000-159951600	Weak transcription	Pancreas	Pancrea
9	chr1:159942200-159947200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr1:159942200-159950000	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr1:159942200-159959400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:159943200-159947400	Weak transcription	Fetal Intestine Small	intestine
13	chr1:159943200-159951200	Weak transcription	Colonic Mucosa	Colon
14	chr1:159943400-159947000	Weak transcription	Stomach Mucosa	stomach
15	chr1:159944600-159947000	Weak transcription	NHEK	skin
16	chr1:159944600-159947200	Weak transcription	Fetal Stomach	stomach
17	chr1:159945000-159946800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:159945200-159946800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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

what's new

Quick links