Variant report

Variant	rs74128727
Chromosome Location	chr1:172882717-172882718
allele	G/T
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	chr1:172879400-172884200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:172880000-172883800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr1:172881400-172883000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:172881400-172883000	ZNF genes & repeats	Dnd41	blood
5	chr1:172881400-172883000	ZNF genes & repeats	NHEK	skin
6	chr1:172881800-172882800	ZNF genes & repeats	HSMMtube	muscle
7	chr1:172881800-172882800	ZNF genes & repeats	HUVEC	blood vessel
8	chr1:172881800-172883000	ZNF genes & repeats	A549	lung
9	chr1:172882000-172883000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
10	chr1:172882200-172883000	Weak transcription	NHLF	lung
11	chr1:172882200-172885800	Weak transcription	Aorta	Aorta
12	chr1:172882400-172882800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:172882600-172882800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:172882600-172883000	ZNF genes & repeats	HSMM	muscle
15	chr1:172882600-172885200	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