Variant report

Variant	rs17107998
Chromosome Location	chr14:79109618-79109619
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10483908	1.00[CEU][hapmap];0.82[TSI][hapmap]
rs10483909	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs10483910	1.00[EUR][1000 genomes]
rs10483911	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1558954	0.93[EUR][1000 genomes]
rs17094080	1.00[EUR][1000 genomes]
rs17107940	0.90[EUR][1000 genomes]
rs17107945	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs17107950	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs17107955	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs17107963	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs17107972	0.97[EUR][1000 genomes]
rs17107982	1.00[EUR][1000 genomes]
rs17108027	0.85[TSI][hapmap]
rs17757034	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs17835469	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17835493	0.87[EUR][1000 genomes]
rs17835635	0.85[GIH][hapmap];0.82[MEX][hapmap]
rs55853427	0.83[EUR][1000 genomes]
rs57609667	0.90[EUR][1000 genomes]
rs59429125	0.90[EUR][1000 genomes]
rs60339939	1.00[EUR][1000 genomes]
rs60501605	0.93[EUR][1000 genomes]
rs61314717	0.93[EUR][1000 genomes]
rs61976090	0.93[EUR][1000 genomes]
rs61976091	0.93[EUR][1000 genomes]
rs61976094	0.92[EUR][1000 genomes]
rs61976095	0.93[EUR][1000 genomes]
rs61976097	0.90[EUR][1000 genomes]
rs61976098	0.90[EUR][1000 genomes]
rs61976099	0.90[EUR][1000 genomes]
rs61976100	0.93[EUR][1000 genomes]
rs61976101	0.90[EUR][1000 genomes]
rs61976102	0.90[EUR][1000 genomes]
rs61976103	0.90[EUR][1000 genomes]
rs61976104	0.90[EUR][1000 genomes]
rs61976105	0.90[EUR][1000 genomes]
rs61976106	0.93[EUR][1000 genomes]
rs61976107	0.93[EUR][1000 genomes]
rs61976109	0.93[EUR][1000 genomes]
rs61976112	0.97[EUR][1000 genomes]
rs61976113	0.97[EUR][1000 genomes]
rs61976114	0.97[EUR][1000 genomes]
rs61976115	0.97[EUR][1000 genomes]
rs61976117	1.00[EUR][1000 genomes]
rs61976118	1.00[EUR][1000 genomes]
rs61976119	1.00[EUR][1000 genomes]
rs61976120	0.86[EUR][1000 genomes]
rs61976134	1.00[EUR][1000 genomes]
rs61976135	1.00[EUR][1000 genomes]
rs61976136	1.00[EUR][1000 genomes]
rs61976137	1.00[EUR][1000 genomes]
rs61976139	1.00[EUR][1000 genomes]
rs61976140	0.95[EUR][1000 genomes]
rs61976142	1.00[EUR][1000 genomes]
rs61976143	0.87[EUR][1000 genomes]
rs61976144	0.87[EUR][1000 genomes]
rs61976145	0.86[EUR][1000 genomes]
rs6574456	1.00[CEU][hapmap]
rs72683546	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72683554	0.93[EUR][1000 genomes]
rs72683556	0.93[EUR][1000 genomes]
rs72683559	0.93[EUR][1000 genomes]
rs72683565	0.95[EUR][1000 genomes]
rs72683567	1.00[EUR][1000 genomes]
rs72683573	0.87[EUR][1000 genomes]
rs8017659	1.00[CEU][hapmap]
rs8019422	1.00[CEU][hapmap];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760000	chr14:78875607-79173528	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2758363	chr14:78903610-79173528	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv34435	chr14:79055398-79111151	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
4	esv2757578	chr14:79055398-79140536	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79106000-79111000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr14:79106200-79111000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr14:79106200-79111000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr14:79106200-79111000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr14:79106200-79111200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr14:79106200-79111200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr14:79108200-79123600	Weak transcription	Brain Germinal Matrix	brain

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