Variant report

Variant	rs11828946
Chromosome Location	chr11:59728374-59728375
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59726800-59728400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr11:59727400-59729600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr11:59727600-59728600	Enhancers	Fetal Intestine Large	intestine
4	chr11:59727800-59728400	Enhancers	Primary hematopoietic stem cells	blood
5	chr11:59727800-59728400	Enhancers	Stomach Mucosa	stomach
6	chr11:59727800-59736600	Enhancers	Fetal Heart	heart
7	chr11:59728000-59728400	Enhancers	Ovary	ovary
8	chr11:59728000-59728400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
9	chr11:59728000-59728400	Enhancers	Sigmoid Colon	Sigmoid Colon
10	chr11:59728000-59728600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr11:59728000-59729200	Enhancers	Pancreas	Pancrea
12	chr11:59728000-59729800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:59728000-59730600	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr11:59728200-59728400	Enhancers	K562	blood
15	chr11:59728200-59729000	Enhancers	Gastric	stomach
16	chr11:59728200-59730200	Enhancers	HepG2	liver

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