Variant report

Variant	rs73694521
Chromosome Location	chr8:91678818-91678819
allele	G/T
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	chr8:91677600-91679000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:91677800-91679000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:91678400-91679000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:91678400-91679000	ZNF genes & repeats	Aorta	Aorta
5	chr8:91678600-91679000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:91678600-91679000	Weak transcription	A549	lung
7	chr8:91678600-91680600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr8:91678800-91679000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
9	chr8:91678800-91679400	Weak transcription	Fetal Muscle Leg	muscle
10	chr8:91678800-91679600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr8:91678800-91682600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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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