Variant report

Variant	rs73895205
Chromosome Location	chr21:16259534-16259535
allele	C/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	chr21:16249200-16264600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr21:16250600-16261000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr21:16250800-16260000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr21:16252800-16259800	Weak transcription	Small Intestine	intestine
5	chr21:16253000-16260400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr21:16253800-16261200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr21:16255000-16261400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr21:16256800-16259600	Weak transcription	Fetal Muscle Leg	muscle
9	chr21:16258400-16260800	Weak transcription	Psoas Muscle	Psoas
10	chr21:16258600-16260400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr21:16259200-16261600	Enhancers	HepG2	liver
12	chr21:16259200-16262000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr21:16259400-16260600	Enhancers	A549	lung
14	chr21:16259400-16262000	Enhancers	Placenta	Placenta
15	chr21:16259400-16262200	Enhancers	Liver	Liver
16	chr21:16259400-16262600	Enhancers	Fetal Intestine Small	intestine

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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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