Variant report

Variant	rs10207372
Chromosome Location	chr2:37389133-37389134
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr2:37389107-37389270	HepG2	liver:	n/a	n/a
2	RAD21	chr2:37389111-37389315	H1-hESC	embryonic stem cell:	n/a	n/a
3	MAFK	chr2:37389015-37389151	HepG2	liver:	n/a	n/a
4	RAD21	chr2:37389084-37389345	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr2:37389128-37389220	HepG2	liver:	n/a	n/a
6	RAD21	chr2:37388993-37389294	H1-hESC	embryonic stem cell:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:37382848..37386165-chr2:37386168..37391618,9	MCF-7	breast:
2	chr2:37387188..37389991-chr2:37393391..37396132,3	MCF-7	breast:
3	chr2:37383824..37387146-chr2:37387589..37390750,4	K562	blood:
4	chr2:37383207..37386416-chr2:37387973..37392066,4	MCF-7	breast:

No data

No data

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37388600-37389400	Enhancers	HepG2	liver
2	chr2:37389000-37390400	Enhancers	Primary neutrophils fromperipheralblood	blood

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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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