Variant report

Variant	rs3791855
Chromosome Location	chr2:171690731-171690732
allele	A/G
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	chr2:171681200-171693800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:171682200-171691600	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr2:171683600-171694200	Genic enhancers	Cortex derived primary cultured neurospheres	brain
4	chr2:171685600-171692600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:171685800-171699000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:171686400-171699200	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr2:171687400-171691400	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr2:171687800-171712600	Weak transcription	Brain Anterior Caudate	brain
9	chr2:171688800-171690800	Enhancers	K562	blood
10	chr2:171688800-171719000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr2:171689000-171693400	Weak transcription	Brain Germinal Matrix	brain
12	chr2:171689400-171694400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:171689800-171696200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:171689800-171705400	Weak transcription	Aorta	Aorta
15	chr2:171690000-171715000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr2:171690200-171698800	Weak transcription	NHEK	skin
17	chr2:171690600-171700400	Weak transcription	Hela-S3	cervix

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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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