Variant report

Variant	rs16922981
Chromosome Location	chr10:23369213-23369214
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23359000-23369600	Weak transcription	Stomach Smooth Muscle	stomach
2	chr10:23366400-23370000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr10:23366400-23370200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr10:23366400-23383600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr10:23368600-23369400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr10:23368600-23369600	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr10:23368600-23370000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr10:23368600-23371200	Enhancers	Fetal Muscle Leg	muscle
9	chr10:23368800-23370000	Enhancers	Hela-S3	cervix
10	chr10:23368800-23370200	Weak transcription	Brain Germinal Matrix	brain
11	chr10:23369000-23369400	Enhancers	Ovary	ovary
12	chr10:23369000-23370000	Weak transcription	Psoas Muscle	Psoas
13	chr10:23369200-23370200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr10:23369200-23370400	Enhancers	Fetal Kidney	kidney
15	chr10:23369200-23370600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr10:23369200-23371200	Enhancers	Fetal Stomach	stomach
17	chr10:23369200-23383800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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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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