Variant report

Variant	rs74146256
Chromosome Location	chr10:89806555-89806556
allele	A/T
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	chr10:89801600-89808400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr10:89802200-89806600	Enhancers	Primary hematopoietic stem cells	blood
3	chr10:89802600-89822200	Weak transcription	Aorta	Aorta
4	chr10:89803400-89822000	Weak transcription	Psoas Muscle	Psoas
5	chr10:89803600-89806600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr10:89803600-89807800	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr10:89804600-89807200	Enhancers	Fetal Thymus	thymus
8	chr10:89804800-89806800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr10:89805000-89807200	Enhancers	Fetal Muscle Leg	muscle
10	chr10:89805000-89808400	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr10:89805200-89806600	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr10:89805600-89806600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr10:89805600-89806600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr10:89806200-89806600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr10:89806200-89806800	Enhancers	Lung	lung
16	chr10:89806400-89806800	Enhancers	Adipose Nuclei	Adipose
17	chr10:89806400-89807200	Weak transcription	Brain Hippocampus Middle	brain
18	chr10:89806400-89810800	Enhancers	Dnd41	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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