Variant report

Variant	rs10864925
Chromosome Location	chr2:114597617-114597618
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114574200-114603600	Weak transcription	Primary B cells from cord blood	blood
2	chr2:114586400-114601000	Weak transcription	Primary T cells from cord blood	blood
3	chr2:114589200-114600200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr2:114589200-114600200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:114589200-114600200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:114591600-114597800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:114592800-114599400	Weak transcription	Placenta	Placenta
8	chr2:114595600-114598600	Enhancers	HepG2	liver
9	chr2:114596400-114621000	Weak transcription	Aorta	Aorta
10	chr2:114596600-114603400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr2:114596600-114611600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr2:114596800-114632800	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr2:114597400-114599200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:114597400-114600200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr2:114597600-114598600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr2:114597600-114631400	Weak transcription	Primary T helper cells PMA-I stimulated	--

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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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