Variant report

Variant	rs59661530
Chromosome Location	chr8:125055906-125055907
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125052600-125083600	Weak transcription	Gastric	stomach
2	chr8:125053000-125060400	Weak transcription	Left Ventricle	heart
3	chr8:125053600-125058600	Enhancers	Fetal Heart	heart
4	chr8:125053800-125056200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr8:125053800-125059800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:125053800-125062400	Weak transcription	Stomach Mucosa	stomach
7	chr8:125054200-125056400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr8:125054200-125056400	Weak transcription	A549	lung
9	chr8:125054200-125061000	Weak transcription	Fetal Stomach	stomach
10	chr8:125054400-125056600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:125054400-125056800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr8:125054600-125066800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr8:125054800-125056000	Weak transcription	Fetal Intestine Large	intestine
14	chr8:125055200-125057800	Enhancers	Fetal Intestine Small	intestine
15	chr8:125055400-125059400	Strong transcription	Adipose Derived Mesenchymal Stem Cell 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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