Variant report

Variant	rs71628384
Chromosome Location	chr1:165364477-165364478
allele	A/G
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	chr1:165362600-165371800	Weak transcription	Lung	lung
2	chr1:165362600-165378200	Weak transcription	Psoas Muscle	Psoas
3	chr1:165362800-165365400	Weak transcription	Esophagus	oesophagus
4	chr1:165362800-165365400	Weak transcription	Fetal Muscle Trunk	muscle
5	chr1:165362800-165366800	Weak transcription	HUVEC	blood vessel
6	chr1:165362800-165367000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr1:165362800-165371800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:165362800-165371800	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr1:165362800-165392200	Weak transcription	Brain Anterior Caudate	brain
10	chr1:165363000-165364600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr1:165363000-165367400	Weak transcription	Fetal Lung	lung
12	chr1:165363000-165368000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr1:165363200-165366800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:165363600-165378400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:165364200-165365600	Enhancers	GM12878-XiMat	blood
16	chr1:165364200-165365800	Enhancers	Fetal Muscle Leg	muscle
17	chr1:165364400-165364600	Bivalent Enhancer	Fetal Thymus	thymus
18	chr1:165364400-165364800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr1:165364400-165365600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin

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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