Variant report

Variant	rs1196152
Chromosome Location	chr2:182944448-182944449
allele	C/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:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:182606478..182612379-chr2:182941539..182945973,8	MCF-7	breast:
2	chr2:182817984..182820031-chr2:182941799..182945080,3	MCF-7	breast:
3	chr2:182753389..182769521-chr2:182932013..182949608,79	MCF-7	breast:
4	chr2:182787158..182788882-chr2:182942568..182944661,2	MCF-7	breast:
5	chr2:182944117..182946257-chr2:182954795..182956782,2	MCF-7	breast:
6	chr2:182807209..182809576-chr2:182943543..182945117,2	MCF-7	breast:
7	chr2:182941653..182947128-chr2:182990854..182994247,10	MCF-7	breast:
8	chr2:182601592..182603449-chr2:182943212..182945378,2	MCF-7	breast:
9	chr2:182940136..182945901-chr2:182990915..182998605,17	MCF-7	breast:
10	chr2:182799515..182801884-chr2:182939610..182944921,5	MCF-7	breast:
11	chr2:182753988..182769660-chr2:182938612..182954194,58	MCF-7	breast:
12	chr2:182943137..182945042-chr2:182998880..183001308,2	MCF-7	breast:
13	chr2:182880362..182889935-chr2:182937119..182944893,30	MCF-7	breast:
14	chr2:182932067..182937899-chr2:182939888..182947237,17	MCF-7	breast:
15	chr2:182814166..182817095-chr2:182942432..182944854,2	MCF-7	breast:
16	chr2:182943683..182945595-chr2:183046138..183048424,2	MCF-7	breast:
17	chr2:182590275..182592284-chr2:182942786..182945570,2	MCF-7	breast:
18	chr2:182942463..182945440-chr2:182995161..182998579,4	MCF-7	breast:
19	chr2:182880158..182888359-chr2:182937576..182947086,29	MCF-7	breast:

No data

No data

No data

Variant related genes	Relation type
ENSG00000221023	Chromatin interaction
ENSG00000150722	Chromatin interaction
ENSG00000260742	Chromatin interaction
ENSG00000138434	Chromatin interaction

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs17648206	0.85[CEU][hapmap];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875477	chr2:182938377-183086478	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182934000-182944800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:182942200-182944600	Enhancers	Fetal Intestine Large	intestine
3	chr2:182942200-182944800	Enhancers	Fetal Intestine Small	intestine
4	chr2:182942400-182945200	Enhancers	Hela-S3	cervix
5	chr2:182942600-182945800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr2:182944200-182944600	Enhancers	Small Intestine	intestine
7	chr2:182944400-182944600	Enhancers	Duodenum Mucosa	Duodenum
8	chr2:182944400-182946000	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr2:182944400-182946000	Weak transcription	Fetal Lung	lung

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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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