Variant report

Variant	rs35660009
Chromosome Location	chr6:15213759-15213760
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:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr6:15211292..15214275-chr6:15361319..15363079,2	K562	blood:
2	chr6:15211327..15214253-chr6:15443742..15445346,2	K562	blood:
3	chr6:15207140..15215305-chr6:15243300..15250227,33	K562	blood:
4	chr6:15212901..15214487-chr6:15252379..15253919,2	K562	blood:
5	chr6:15211290..15214684-chr6:15251009..15254684,5	K562	blood:
6	chr6:15210286..15214983-chr6:15243593..15250047,26	K562	blood:
7	chr6:15210646..15214635-chr6:15377351..15380909,4	K562	blood:
8	chr6:15156210..15158890-chr6:15211476..15214661,3	K562	blood:
9	chr6:15210423..15214380-chr6:15237542..15240375,3	K562	blood:
10	chr6:15210476..15213974-chr6:15388595..15391826,3	K562	blood:
11	chr6:15086750..15092578-chr6:15208564..15214623,13	K562	blood:
12	chr6:14685709..14687762-chr6:15211791..15214339,2	K562	blood:
13	chr6:15211412..15213944-chr6:16209890..16212085,2	K562	blood:
14	chr6:15211921..15214474-chr6:15385655..15388402,2	K562	blood:
15	chr6:15197961..15202582-chr6:15208962..15214320,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000234261	Chromatin interaction
ENSG00000271888	Chromatin interaction
ENSG00000235488	Chromatin interaction
ENSG00000008083	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs13191127	0.93[EUR][1000 genomes]
rs13197919	0.82[EUR][1000 genomes]
rs13198600	0.85[EUR][1000 genomes]
rs13206138	0.93[EUR][1000 genomes]
rs13206695	0.86[EUR][1000 genomes]
rs13209122	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13209721	0.93[EUR][1000 genomes]
rs13210652	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13213534	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13215638	0.86[EUR][1000 genomes]
rs13216551	0.93[EUR][1000 genomes]
rs13216625	0.86[EUR][1000 genomes]
rs13219748	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34048058	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34144528	0.82[EUR][1000 genomes]
rs34156913	0.85[EUR][1000 genomes]
rs34229995	0.85[EUR][1000 genomes]
rs34340185	0.82[EUR][1000 genomes]
rs34390534	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34470245	0.93[EUR][1000 genomes]
rs34488826	0.85[EUR][1000 genomes]
rs34677259	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34790337	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34816087	0.93[EUR][1000 genomes]
rs34816488	0.93[EUR][1000 genomes]
rs34934295	0.93[EUR][1000 genomes]
rs35147300	0.85[EUR][1000 genomes]
rs35378362	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35659244	0.86[EUR][1000 genomes]
rs35981238	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs36058592	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs67845400	0.86[EUR][1000 genomes]
rs71533639	0.93[EUR][1000 genomes]
rs71533640	0.93[EUR][1000 genomes]
rs71533642	0.93[EUR][1000 genomes]
rs71551025	0.93[EUR][1000 genomes]
rs71551028	0.93[EUR][1000 genomes]
rs71551030	0.93[EUR][1000 genomes]
rs71551032	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs71551033	0.93[EUR][1000 genomes]
rs71551034	0.93[EUR][1000 genomes]
rs71551035	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs71551040	0.85[EUR][1000 genomes]
rs71551041	0.85[EUR][1000 genomes]
rs71551042	0.82[EUR][1000 genomes]
rs71551043	0.82[EUR][1000 genomes]
rs71551045	0.82[EUR][1000 genomes]
rs71551046	0.82[EUR][1000 genomes]
rs7740407	0.93[EUR][1000 genomes]
rs9383028	0.86[EUR][1000 genomes]
rs9476760	0.86[EUR][1000 genomes]
rs9476761	0.86[EUR][1000 genomes]
rs9476782	0.93[EUR][1000 genomes]
rs9476783	0.93[EUR][1000 genomes]
rs9476784	0.93[EUR][1000 genomes]
rs9476793	0.93[EUR][1000 genomes]
rs9476794	0.93[EUR][1000 genomes]
rs9476797	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9476798	1.00[AMR][1000 genomes];0.93[EUR][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	nsv830593	chr6:15049636-15244190	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv830594	chr6:15171158-15261296	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv1027010	chr6:15201803-15425629	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15208400-15222000	Weak transcription	Right Atrium	heart
2	chr6:15211400-15218200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:15211600-15222200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr6:15212000-15227600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr6:15213000-15214800	Enhancers	HepG2	liver

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