Variant report

Variant	rs78139328
Chromosome Location	chr2:21205796-21205797
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3442930	chr2:21205632-21205966	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 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	chr2:21201400-21205800	Weak transcription	Fetal Muscle Leg	muscle
5	chr2:21203800-21206800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:21204800-21207000	Enhancers	Fetal Muscle Trunk	muscle
7	chr2:21205200-21206800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr2:21205400-21206000	Enhancers	Fetal Kidney	kidney
9	chr2:21205600-21208600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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