Variant report

Variant	rs1711400
Chromosome Location	chr11:102460598-102460599
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:102459731..102462268-chr11:102463599..102465321,2	K562	blood:
2	chr11:102460154..102463687-chr11:102465390..102468477,5	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10895321	0.95[ASN][1000 genomes]
rs10895323	0.88[ASN][1000 genomes]
rs1612069	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1615443	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1632456	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1711399	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1711401	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1711403	0.83[AFR][1000 genomes]
rs1711430	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1711432	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1711434	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1711438	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1711441	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1711442	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1711443	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1784400	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1784405	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1784407	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1784409	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1784410	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1784428	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1784431	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1784432	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1784433	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1784434	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1784435	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1784436	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1784437	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1784438	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1784439	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1784440	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1784441	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1784444	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1784445	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1784446	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1784447	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1784449	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1784451	0.83[AFR][1000 genomes]
rs2292733	0.95[ASN][1000 genomes]
rs2459479	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2459480	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2509015	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2509016	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2509017	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2509018	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2701961	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2846369	0.83[AFR][1000 genomes]
rs7950388	0.95[ASN][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	esv1815657	chr11:102413582-102490794	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv832252	chr11:102445479-102627879	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102451400-102462600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:102451600-102463600	Weak transcription	NHDF-Ad	bronchial
3	chr11:102454600-102461000	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr11:102459200-102461800	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr11:102459400-102462600	Enhancers	Primary B cells from peripheral blood	blood
6	chr11:102460000-102461000	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr11:102460200-102463800	Enhancers	GM12878-XiMat	blood

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