Variant report

Variant	rs10863915
Chromosome Location	chr1:211695085-211695086
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:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:211686791..211692090-chr1:211692436..211697358,7	K562	blood:
2	chr1:211694815..211696668-chr1:211701298..211704318,3	K562	blood:
3	chr1:211692734..211695713-chr1:211744143..211747035,2	MCF-7	breast:
4	chr1:211694132..211696485-chr1:211743577..211746464,2	MCF-7	breast:
5	chr1:211687723..211692261-chr1:211692405..211697712,7	MCF-7	breast:
6	chr1:211688371..211691980-chr1:211692436..211695699,4	K562	blood:
7	chr1:211694601..211695455-chr1:211715138..211715915,2	MCF-7	breast:
8	chr1:211690573..211693033-chr1:211694499..211696048,2	MCF-7	breast:
9	chr1:211675520..211676320-chr1:211694611..211695515,3	MCF-7	breast:
10	chr1:211692018..211701005-chr1:211746984..211755135,17	MCF-7	breast:
11	chr1:211692714..211696685-chr1:211696869..211699786,3	K562	blood:
12	chr1:211675520..211676320-chr1:211694790..211695515,2	MCF-7	breast:

No data

No data

No data

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1020335	0.93[CEU][hapmap]
rs11119758	0.89[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1962917	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1962918	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2010504	1.00[JPT][hapmap];0.91[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2032005	1.00[JPT][hapmap];0.92[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2184855	0.93[CEU][hapmap]
rs4951528	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4951758	0.88[YRI][hapmap];0.82[AFR][1000 genomes]
rs4951761	0.87[CEU][hapmap]
rs4951762	0.89[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6664769	0.83[AMR][1000 genomes]
rs6680424	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6693000	0.80[CEU][hapmap]
rs7519203	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][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	nsv832514	chr1:211630247-211794963	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211688200-211701200	Weak transcription	Gastric	stomach
2	chr1:211689400-211701200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:211689400-211715000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr1:211690200-211698400	Enhancers	Liver	Liver
5	chr1:211690400-211695800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr1:211691000-211700400	Weak transcription	Fetal Thymus	thymus
7	chr1:211693400-211697800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:211694400-211695200	Enhancers	Right Atrium	heart
9	chr1:211694600-211695200	Enhancers	A549	lung
10	chr1:211694600-211695800	Weak transcription	Hela-S3	cervix
11	chr1:211694800-211696200	Enhancers	GM12878-XiMat	blood
12	chr1:211694800-211698000	Weak transcription	Fetal Muscle Leg	muscle
13	chr1:211695000-211697400	Weak transcription	K562	blood
14	chr1:211695000-211697800	Weak transcription	Fetal Muscle Trunk	muscle
15	chr1:211695000-211698400	Enhancers	HepG2	liver

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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