Variant report

Variant	rs10177345
Chromosome Location	chr2:37387207-37387208
allele	C/G
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	chr2:37370415..37372075-chr2:37384482..37387450,2	K562	blood:
2	chr2:37385156..37387851-chr2:37415682..37418467,2	K562	blood:
3	chr2:37382848..37386165-chr2:37386168..37391618,9	MCF-7	breast:
4	chr2:37381640..37387428-chr2:37421417..37425727,6	MCF-7	breast:
5	chr2:37387188..37389991-chr2:37393391..37396132,3	MCF-7	breast:
6	chr2:37375493..37378915-chr2:37383921..37387868,3	K562	blood:
7	chr2:37385569..37388130-chr2:37422191..37423882,2	K562	blood:
8	chr2:37382658..37387385-chr2:37421093..37425812,6	MCF-7	breast:

No data

No data

No data

Variant related genes	Relation type
ENSG00000138068	Chromatin interaction
ENSG00000055332	Chromatin interaction
ENSG00000233159	Chromatin interaction
ENSG00000224891	Chromatin interaction
ENSG00000218739	Chromatin interaction

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37385000-37388400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:37385800-37389000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr2:37387200-37387600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr2:37387200-37387600	Enhancers	Esophagus	oesophagus

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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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