Variant report

Variant	rs71317727
Chromosome Location	chrX:122868456-122868457
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:122867200-122870200	Weak transcription	NHLF	lung
2	chrX:122867200-122870400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chrX:122867400-122869600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chrX:122867400-122869600	Weak transcription	Fetal Intestine Small	intestine
5	chrX:122867400-122869600	Weak transcription	A549	lung
6	chrX:122867400-122869600	Weak transcription	HSMMtube	muscle
7	chrX:122867400-122869800	Weak transcription	Fetal Intestine Large	intestine
8	chrX:122867400-122869800	Weak transcription	HepG2	liver
9	chrX:122867400-122869800	Weak transcription	HSMM	muscle
10	chrX:122867400-122869800	Weak transcription	Osteobl	bone
11	chrX:122867400-122870200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chrX:122867400-122870200	Weak transcription	NH-A	brain
13	chrX:122867400-122870200	Weak transcription	NHDF-Ad	bronchial
14	chrX:122867400-122870400	Weak transcription	Fetal Heart	heart
15	chrX:122867400-122872200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chrX:122867400-122874400	Weak transcription	K562	blood
17	chrX:122867600-122870400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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