Variant report

Variant	rs6963347
Chromosome Location	chr7:50335778-50335779
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:50324971..50327941-chr7:50334805..50336815,2	K562	blood:
2	chr7:50334783..50338754-chr7:50340442..50344598,8	K562	blood:

Variant related genes	Relation type
ENSG00000185811	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs12718255	1.00[AMR][1000 genomes]
rs12718258	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12718259	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12718262	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12718263	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13223507	1.00[CEU][hapmap]
rs13223971	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13225200	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13238273	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34049075	1.00[AMR][1000 genomes]
rs34175022	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34181857	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34243680	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34258132	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34311116	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34484271	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34856226	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34861102	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34919759	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34920847	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34936043	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34967960	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34971464	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35019961	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35042793	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35048559	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35064086	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35295940	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35420653	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35456567	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35487792	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35661691	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35680007	1.00[AMR][1000 genomes]
rs35803603	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35928979	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35946624	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35985210	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs36039109	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6955602	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6962406	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6963656	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6965399	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6979359	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs71538375	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs71538376	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs71538377	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs71538378	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs71538384	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs71538385	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7456833	0.85[JPT][hapmap]
rs7781824	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7811173	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv464444	chr7:49671882-50454736	Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv606897	chr7:49671883-50454736	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv498090	chr7:49708644-50427714	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1020869	chr7:49712860-50457544	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1024102	chr7:50195864-50418159	Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr7:50325000-50340000	Weak transcription	Thymus	Thymus
2	chr7:50325800-50343000	Weak transcription	K562	blood
3	chr7:50331800-50335800	Weak transcription	Primary T cells from cord blood	blood
4	chr7:50332800-50336000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr7:50333000-50336600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr7:50333200-50335800	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr7:50333200-50339600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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