Variant report

Variant	rs1773353
Chromosome Location	chr1:211898313-211898314
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	chr1:211879200-211913600	Weak transcription	Right Atrium	heart
2	chr1:211896400-211909000	Weak transcription	Fetal Intestine Small	intestine
3	chr1:211896600-211898800	Enhancers	Pancreas	Pancrea
4	chr1:211896600-211898800	Enhancers	Spleen	Spleen
5	chr1:211897000-211898400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:211897200-211899200	Enhancers	HepG2	liver
7	chr1:211897600-211898800	Enhancers	Fetal Muscle Leg	muscle
8	chr1:211897600-211898800	Enhancers	Ovary	ovary
9	chr1:211897800-211898600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr1:211898000-211898600	Enhancers	Brain Substantia Nigra	brain
11	chr1:211898000-211898600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr1:211898000-211898600	Enhancers	Fetal Muscle Trunk	muscle
13	chr1:211898000-211898600	Enhancers	Right Ventricle	heart
14	chr1:211898000-211898800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:211898000-211898800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:211898200-211898600	Enhancers	Psoas Muscle	Psoas
17	chr1:211898200-211898800	Enhancers	Brain Hippocampus Middle	brain
18	chr1:211898200-211900200	Enhancers	Brain Inferior Temporal Lobe	brain

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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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