Variant report

Variant	rs12406444
Chromosome Location	chr1:95608534-95608535
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:95602168..95604701-chr1:95606457..95608618,2	K562	blood:
2	chr1:95549452..95551789-chr1:95607274..95610071,2	K562	blood:
3	chr1:95607723..95611080-chr1:95611882..95614538,3	K562	blood:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10782998	1.00[AMR][1000 genomes]
rs11165320	1.00[AMR][1000 genomes]
rs12035503	1.00[AMR][1000 genomes]
rs2391630	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6695720	1.00[AMR][1000 genomes]
rs7517250	1.00[AMR][1000 genomes]
rs7520889	1.00[AMR][1000 genomes]
rs7526279	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7532269	1.00[AMR][1000 genomes]
rs915502	1.00[AMR][1000 genomes]
rs915503	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830636	chr1:95495849-95703126	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv870669	chr1:95586773-95690269	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95584000-95629400	Weak transcription	Aorta	Aorta
2	chr1:95585400-95636800	Weak transcription	Colon Smooth Muscle	Colon
3	chr1:95590000-95611000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:95592800-95634200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr1:95592800-95661800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr1:95594600-95610600	Weak transcription	A549	lung
7	chr1:95598600-95612400	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr1:95598800-95633800	Weak transcription	Fetal Heart	heart
9	chr1:95600000-95650200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr1:95601200-95618400	Weak transcription	Pancreas	Pancrea
11	chr1:95601800-95633600	Weak transcription	HepG2	liver
12	chr1:95602200-95615400	Weak transcription	Ovary	ovary
13	chr1:95602200-95628000	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr1:95602800-95628800	Weak transcription	Adipose Nuclei	Adipose
15	chr1:95602800-95634200	Weak transcription	Left Ventricle	heart
16	chr1:95603000-95640800	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr1:95604200-95609800	Weak transcription	Liver	Liver
18	chr1:95604200-95630000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr1:95605600-95618000	Weak transcription	Fetal Lung	lung
20	chr1:95606000-95610600	Weak transcription	K562	blood
21	chr1:95607600-95609200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr1:95607800-95609000	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr1:95607800-95609000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
24	chr1:95608000-95609000	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr1:95608000-95609000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr1:95608000-95609000	Active TSS	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links