Variant report

Variant	rs17005145
Chromosome Location	chr4:82404511-82404512
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10010140	1.00[ASN][1000 genomes]
rs10010394	1.00[ASN][1000 genomes]
rs10012642	0.95[ASN][1000 genomes]
rs10015146	1.00[ASN][1000 genomes]
rs10023826	0.90[ASN][1000 genomes]
rs12500201	1.00[ASN][1000 genomes]
rs12502814	1.00[ASN][1000 genomes]
rs13102560	0.95[ASN][1000 genomes]
rs13111699	1.00[ASN][1000 genomes]
rs13128387	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13131664	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16998600	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17005142	1.00[ASN][1000 genomes]
rs17005144	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28479652	1.00[ASN][1000 genomes]
rs28767523	1.00[ASN][1000 genomes]
rs28827174	1.00[ASN][1000 genomes]
rs34128580	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34749111	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35010226	0.90[ASN][1000 genomes]
rs35149381	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35991185	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36026752	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41523946	0.90[ASN][1000 genomes]
rs4693274	1.00[ASN][1000 genomes]
rs4693275	0.92[ASN][1000 genomes]
rs4693276	0.92[ASN][1000 genomes]
rs4693277	0.92[ASN][1000 genomes]
rs62303604	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6535252	0.86[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6819741	1.00[ASN][1000 genomes]
rs6819989	1.00[ASN][1000 genomes]
rs6825177	1.00[ASN][1000 genomes]
rs6834665	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7660392	0.95[ASN][1000 genomes]
rs7678464	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7683852	0.90[ASN][1000 genomes]
rs7684580	1.00[ASN][1000 genomes]
rs7688827	0.90[ASN][1000 genomes]
rs7690069	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7691170	0.95[ASN][1000 genomes]
rs9307784	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999729	chr4:81802554-82627820	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv537156	chr4:81802554-82627820	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv829986	chr4:82345163-82509860	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:82395800-82406400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr4:82402600-82404600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr4:82403000-82404600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr4:82403000-82404600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:82403400-82405000	Enhancers	Primary hematopoietic stem cells	blood
6	chr4:82404000-82404800	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr4:82404400-82406200	Weak transcription	Primary B cells from cord blood	blood

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