Variant report

Variant	rs2589583
Chromosome Location	chr1:220740156-220740157
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220724400-220743400	Weak transcription	Fetal Brain Male	brain
2	chr1:220724600-220741600	Weak transcription	Aorta	Aorta
3	chr1:220728000-220745200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr1:220730400-220747400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:220737800-220746400	Weak transcription	Fetal Brain Female	brain
6	chr1:220738800-220743000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr1:220739000-220740400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:220739200-220741200	Weak transcription	Left Ventricle	heart
9	chr1:220739200-220741600	Weak transcription	Fetal Heart	heart
10	chr1:220739200-220747200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:220739200-220748200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:220739400-220746200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr1:220739800-220741000	Weak transcription	Cortex derived primary cultured neurospheres	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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