Variant report

Variant	rs3846714
Chromosome Location	chr5:150935419-150935420
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	chr5:150901800-150935600	Weak transcription	Fetal Intestine Small	intestine
2	chr5:150908200-150948000	Strong transcription	HMEC	breast
3	chr5:150908400-150944000	Strong transcription	NHEK	skin
4	chr5:150909200-150942400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr5:150911600-150942800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:150914200-150935600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:150914200-150938600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:150918200-150945400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr5:150924600-150935600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:150931000-150942800	Weak transcription	Brain Angular Gyrus	brain
11	chr5:150933400-150936000	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr5:150934200-150949600	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr5:150934600-150936200	Weak transcription	Adipose Nuclei	Adipose
14	chr5:150934600-150937000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr5:150935200-150936600	Strong transcription	Esophagus	oesophagus
16	chr5:150935400-150936600	Strong transcription	Skeletal Muscle Female	skeletal muscle
17	chr5:150935400-150937400	Enhancers	Primary B cells from peripheral blood	blood
18	chr5:150935400-150938800	Enhancers	Primary monocytes fromperipheralblood	blood

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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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