Variant report

Variant	rs206236
Chromosome Location	chr1:165510264-165510265
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165505600-165513000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:165507200-165510400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:165507600-165512800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr1:165508400-165510800	Enhancers	Fetal Muscle Leg	muscle
5	chr1:165508400-165510800	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr1:165508600-165510400	Enhancers	Placenta	Placenta
7	chr1:165508600-165510600	Enhancers	Left Ventricle	heart
8	chr1:165509000-165510400	Enhancers	Adipose Nuclei	Adipose
9	chr1:165509000-165510400	Enhancers	Right Atrium	heart
10	chr1:165509000-165510600	Enhancers	Psoas Muscle	Psoas
11	chr1:165509400-165510400	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr1:165509400-165510400	Enhancers	Right Ventricle	heart
13	chr1:165509600-165510600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr1:165509600-165510600	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr1:165509800-165511400	Weak transcription	Fetal Lung	lung
16	chr1:165509800-165511800	Weak transcription	Fetal Stomach	stomach
17	chr1:165510000-165510800	Enhancers	Fetal Heart	heart
18	chr1:165510200-165511000	Enhancers	Fetal Muscle Trunk	muscle
19	chr1:165510200-165513000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

Quick Search:

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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