Variant report

Variant	rs13049498
Chromosome Location	chr21:16144749-16144750
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TBL1XR1	chr21:16144746-16144778	K562	blood:	n/a	n/a
2	RCOR1	chr21:16144699-16144833	K562	blood:	n/a	n/a
3	ZNF274	chr21:16144063-16144840	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:16131213..16134500-chr21:16143323..16145254,3	MCF-7	breast:
2	chr21:16142635..16145022-chr21:16234825..16237651,2	MCF-7	breast:
3	chr21:16143951..16146224-chr21:16159304..16162772,3	K562	blood:
4	chr21:16142841..16145561-chr21:16145912..16150073,3	K562	blood:
5	chr21:16144518..16147487-chr21:16436685..16438487,2	MCF-7	breast:

No data

No data

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16143400-16146200	Enhancers	K562	blood
2	chr21:16143600-16144800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr21:16144000-16145200	Enhancers	Primary T cells from cord blood	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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