Variant report

Variant	rs74139803
Chromosome Location	chr1:226996098-226996099
allele	A/C
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	chr1:226987200-227001400	Weak transcription	Right Atrium	heart
2	chr1:226987400-226997400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:226989400-227002800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr1:226992800-227003200	Weak transcription	Lung	lung
5	chr1:226993600-227001400	Weak transcription	Thymus	Thymus
6	chr1:226994800-227007000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:226995000-226997400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr1:226995000-226998200	Weak transcription	Fetal Thymus	thymus
9	chr1:226995000-227003400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:226995200-226998200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr1:226995600-226996600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:226995600-226997200	Weak transcription	Brain Anterior Caudate	brain
13	chr1:226995800-227009800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:226996000-226996200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:226996000-226998400	Enhancers	Brain Dorsolateral Prefrontal Cortex	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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