Variant report

Variant	rs11124924
Chromosome Location	chr2:21206275-21206276
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21200000-21206400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr2:21200200-21207000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr2:21201200-21206400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:21203800-21206800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:21204800-21207000	Enhancers	Fetal Muscle Trunk	muscle
6	chr2:21205200-21206800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr2:21205600-21208600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr2:21205800-21207400	Enhancers	Fetal Muscle Leg	muscle
9	chr2:21206000-21206400	Weak transcription	Fetal Kidney	kidney
10	chr2:21206200-21207000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr2:21206200-21208200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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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