Variant report

Variant	rs57976923
Chromosome Location	chr1:220749326-220749327
allele	C/T
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	chr1:220742200-220749600	Weak transcription	Aorta	Aorta
2	chr1:220748000-220755600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr1:220748000-220762200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:220748200-220752400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr1:220748200-220762200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:220748200-220769200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr1:220748400-220762400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr1:220748400-220767200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr1:220748400-220773200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr1:220748600-220749400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:220748600-220750200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr1:220748600-220751000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:220748600-220769800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr1:220748800-220770400	Weak transcription	Fetal Muscle Leg	muscle
15	chr1:220749000-220752600	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:220749000-220767000	Weak transcription	Fetal Muscle Trunk	muscle

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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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