Variant report

Variant	rs624829
Chromosome Location	chr6:119473094-119473095
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:119471765..119474178-chr6:119478318..119480105,2	K562	blood:
2	chr6:119465818..119467517-chr6:119472124..119474189,2	K562	blood:
3	chr6:119470210..119471903-chr6:119471905..119473640,2	K562	blood:
4	chr6:119470751..119473289-chr6:119476279..119478742,2	MCF-7	breast:
5	chr6:119471416..119474795-chr6:119668550..119671355,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000111885	Chromatin interaction
ENSG00000111879	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12190611	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1891540	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2558	0.81[JPT][hapmap]
rs601575	0.81[CHB][hapmap];0.84[CHD][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs608541	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs611211	0.81[CEU][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs638368	0.84[CEU][hapmap];0.83[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.97[TSI][hapmap];0.80[YRI][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs656012	0.84[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs660682	0.85[JPT][hapmap]
rs666655	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs678974	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs682949	0.88[CEU][hapmap];0.83[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.97[TSI][hapmap];0.83[YRI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs683488	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6910397	0.89[ASW][hapmap];0.87[CEU][hapmap];0.91[GIH][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.94[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6928078	0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6934752	0.87[CEU][hapmap];0.86[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6935092	0.95[EUR][1000 genomes]
rs733259	0.87[CEU][hapmap];0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs733260	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7775389	0.88[CEU][hapmap];0.91[GIH][hapmap];0.86[JPT][hapmap];0.91[MEX][hapmap];0.92[TSI][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9387637	0.88[CEU][hapmap];0.91[GIH][hapmap];0.86[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9398502	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9398503	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9401130	0.88[CEU][hapmap];0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.95[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	nsv1025995	chr6:119407742-119709548	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv886570	chr6:119450888-119600556	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1017507	chr6:119465981-119664949	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs624829	FAM184A	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119457000-119474800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:119469800-119476800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:119470200-119482400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:119470600-119473800	Weak transcription	HepG2	liver
5	chr6:119471200-119478200	Weak transcription	NHDF-Ad	bronchial
6	chr6:119472200-119473600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr6:119472800-119477800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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