Variant report

Variant	rs4748836
Chromosome Location	chr10:23337395-23337396
allele	A/G
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	chr10:23335200-23340200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr10:23335200-23341400	Weak transcription	Fetal Muscle Leg	muscle
3	chr10:23335200-23341800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr10:23335800-23337600	Enhancers	Placenta Amnion	Placenta Amnion
5	chr10:23336200-23337400	Enhancers	Hela-S3	cervix
6	chr10:23336600-23340800	Weak transcription	Fetal Kidney	kidney
7	chr10:23336600-23341800	Weak transcription	Brain Hippocampus Middle	brain
8	chr10:23336600-23348800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr10:23336800-23340600	Weak transcription	HSMMtube	muscle
10	chr10:23336800-23342000	Weak transcription	Fetal Stomach	stomach
11	chr10:23337000-23337400	Enhancers	K562	blood
12	chr10:23337000-23340400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr10:23337000-23340800	Weak transcription	NHEK	skin
14	chr10:23337000-23341200	Weak transcription	Stomach Mucosa	stomach
15	chr10:23337000-23341800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr10:23337200-23337400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr10:23337200-23337400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr10:23337200-23337400	Enhancers	Left Ventricle	heart

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

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