Variant report

No.	Distal block	Cell Line	Cell type
1	chr6:14109682..14112094-chr6:14128047..14131236,3	K562	blood:
2	chr6:13614733..13616816-chr6:14110995..14112952,2	K562	blood:
3	chr6:14100020..14102595-chr6:14109297..14111891,3	K562	blood:
4	chr6:14107830..14114797-chr6:14115908..14119067,6	K562	blood:
5	chr6:14110518..14112309-chr6:14112614..14114768,2	K562	blood:
6	chr6:14106946..14109197-chr6:14110134..14112699,2	K562	blood:

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10080702	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10484346	1.00[EUR][1000 genomes]
rs11965901	1.00[EUR][1000 genomes]
rs16874553	1.00[EUR][1000 genomes]
rs16874594	1.00[EUR][1000 genomes]
rs2068206	1.00[EUR][1000 genomes]
rs55875628	1.00[EUR][1000 genomes]
rs56297167	1.00[EUR][1000 genomes]
rs57376077	1.00[EUR][1000 genomes]
rs60371731	1.00[EUR][1000 genomes]
rs61291802	1.00[EUR][1000 genomes]
rs61466290	1.00[EUR][1000 genomes]
rs6911430	1.00[EUR][1000 genomes]
rs73364380	1.00[EUR][1000 genomes]
rs73366305	1.00[EUR][1000 genomes]
rs73366310	1.00[EUR][1000 genomes]
rs73366314	1.00[EUR][1000 genomes]
rs73366326	1.00[EUR][1000 genomes]
rs73366337	1.00[EUR][1000 genomes]
rs73369927	1.00[EUR][1000 genomes]
rs73369944	1.00[EUR][1000 genomes]
rs73369946	1.00[EUR][1000 genomes]
rs73369951	1.00[EUR][1000 genomes]
rs73373532	1.00[EUR][1000 genomes]
rs73373534	1.00[EUR][1000 genomes]
rs73724053	1.00[EUR][1000 genomes]
rs7757894	1.00[EUR][1000 genomes]
rs9464655	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9464656	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9464658	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9476487	1.00[EUR][1000 genomes]
rs9476502	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9476503	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9476505	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9476506	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	nsv1027179	chr6:14058703-14223055	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:14109400-14111200	Enhancers	Primary B cells from peripheral blood	blood
2	chr6:14110000-14117200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr6:14110200-14117000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:14110200-14117200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr6:14110400-14117200	Weak transcription	Primary B cells from cord blood	blood
6	chr6:14110400-14117400	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr6:14110400-14117400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr6:14110600-14113800	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr6:14110800-14111200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr6:14111000-14111200	Enhancers	K562	blood
11	chr6:14111000-14111400	Enhancers	GM12878-XiMat	blood
12	chr6:14111000-14112000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr6:14111000-14117400	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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