Variant report

Variant	rs1172953
Chromosome Location	chr10:97877582-97877583
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:97862903..97865419-chr10:97876280..97877825,2	K562	blood:
2	chr10:97875753..97878264-chr10:97885533..97887892,2	MCF-7	breast:
3	chr10:97848457..97851252-chr10:97877480..97882183,4	MCF-7	breast:
4	chr10:97871710..97874019-chr10:97877046..97879264,2	MCF-7	breast:
5	chr10:97871595..97874047-chr10:97875206..97878090,4	K562	blood:
6	chr10:97863872..97865419-chr10:97876280..97878249,2	K562	blood:
7	chr10:97871721..97873820-chr10:97875416..97878062,2	K562	blood:
8	chr10:97875384..97878140-chr10:97888337..97891215,2	MCF-7	breast:

No data

No data

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97876600-97878200	Weak transcription	HepG2	liver

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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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