Variant report

Variant	rs7779933
Chromosome Location	chr7:117838552-117838553
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:117834706..117839817-chr7:117854613..117858941,5	K562	blood:
2	chr7:117838537..117840659-chr7:117840686..117843099,2	MCF-7	breast:
3	chr7:117792505..117794134-chr7:117837460..117839603,2	K562	blood:

Variant related genes	Relation type
ENSG00000106013	Chromatin interaction

Extended variants
information (count: 125 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:123)

rs_ID	r²[population]
rs10085904	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1015782	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10226152	0.93[EUR][1000 genomes]
rs10227326	0.93[EUR][1000 genomes]
rs10229589	0.93[EUR][1000 genomes]
rs10241875	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10252627	0.81[EUR][1000 genomes]
rs10267938	0.87[EUR][1000 genomes]
rs10487390	0.93[EUR][1000 genomes]
rs1054032	0.93[EUR][1000 genomes]
rs1061731	0.93[EUR][1000 genomes]
rs10953864	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1117254	0.89[EUR][1000 genomes]
rs11486992	0.93[EUR][1000 genomes]
rs11487110	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs11543742	0.92[EUR][1000 genomes]
rs11761947	0.80[EUR][1000 genomes]
rs11768889	0.81[EUR][1000 genomes]
rs11770353	0.90[EUR][1000 genomes]
rs11979012	0.90[EUR][1000 genomes]
rs12537795	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12666439	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12667103	0.84[EUR][1000 genomes]
rs13224397	0.81[EUR][1000 genomes]
rs13224733	0.91[EUR][1000 genomes]
rs17584359	0.81[EUR][1000 genomes]
rs194577	0.81[EUR][1000 genomes]
rs194578	0.81[EUR][1000 genomes]
rs194579	0.81[EUR][1000 genomes]
rs2058416	0.90[EUR][1000 genomes]
rs2058417	0.91[EUR][1000 genomes]
rs2058418	0.82[AFR][1000 genomes]
rs20598	0.81[EUR][1000 genomes]
rs2191920	0.90[EUR][1000 genomes]
rs2402322	0.93[EUR][1000 genomes]
rs2896242	0.93[EUR][1000 genomes]
rs34029977	0.81[EUR][1000 genomes]
rs34847140	0.80[EUR][1000 genomes]
rs35382009	0.80[EUR][1000 genomes]
rs3802012	0.91[EUR][1000 genomes]
rs4141028	0.91[EUR][1000 genomes]
rs41900	0.87[EUR][1000 genomes]
rs41901	0.87[EUR][1000 genomes]
rs41902	0.87[EUR][1000 genomes]
rs41905	0.87[EUR][1000 genomes]
rs41906	0.86[EUR][1000 genomes]
rs41909	0.87[EUR][1000 genomes]
rs41910	0.85[EUR][1000 genomes]
rs41911	0.85[EUR][1000 genomes]
rs41915	0.83[EUR][1000 genomes]
rs41916	0.83[EUR][1000 genomes]
rs41926	0.83[EUR][1000 genomes]
rs41933	0.82[EUR][1000 genomes]
rs41934	0.83[EUR][1000 genomes]
rs41935	0.83[EUR][1000 genomes]
rs41938	0.83[EUR][1000 genomes]
rs41939	0.83[EUR][1000 genomes]
rs41945	0.83[EUR][1000 genomes]
rs41946	0.81[EUR][1000 genomes]
rs41947	0.81[EUR][1000 genomes]
rs41948	0.81[EUR][1000 genomes]
rs41949	0.81[EUR][1000 genomes]
rs41950	0.81[EUR][1000 genomes]
rs41951	0.81[EUR][1000 genomes]
rs41952	0.81[EUR][1000 genomes]
rs41953	0.81[EUR][1000 genomes]
rs41954	0.81[EUR][1000 genomes]
rs41955	0.81[EUR][1000 genomes]
rs41956	0.81[EUR][1000 genomes]
rs41957	0.81[EUR][1000 genomes]
rs41958	0.81[EUR][1000 genomes]
rs41961	0.81[EUR][1000 genomes]
rs41963	0.81[EUR][1000 genomes]
rs41964	0.81[EUR][1000 genomes]
rs41967	0.81[EUR][1000 genomes]
rs41968	0.80[EUR][1000 genomes]
rs41969	0.81[EUR][1000 genomes]
rs41970	0.81[EUR][1000 genomes]
rs41977	0.81[EUR][1000 genomes]
rs41979	0.81[EUR][1000 genomes]
rs41980	0.81[EUR][1000 genomes]
rs41982	0.81[EUR][1000 genomes]
rs41983	0.80[EUR][1000 genomes]
rs41984	0.81[EUR][1000 genomes]
rs41985	0.80[EUR][1000 genomes]
rs41986	0.81[EUR][1000 genomes]
rs41987	0.81[EUR][1000 genomes]
rs41988	0.81[EUR][1000 genomes]
rs41990	0.81[EUR][1000 genomes]
rs41991	0.81[EUR][1000 genomes]
rs41993	0.81[EUR][1000 genomes]
rs41994	0.80[EUR][1000 genomes]
rs41995	0.80[EUR][1000 genomes]
rs41996	0.80[EUR][1000 genomes]
rs41997	0.80[EUR][1000 genomes]
rs42234	0.81[EUR][1000 genomes]
rs42376	0.81[EUR][1000 genomes]
rs4535672	0.81[EUR][1000 genomes]
rs4727865	0.81[EUR][1000 genomes]
rs5002233	0.93[EUR][1000 genomes]
rs61328879	0.81[AFR][1000 genomes]
rs6466648	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs68189275	0.81[EUR][1000 genomes]
rs6942513	0.81[AFR][1000 genomes]
rs6944524	0.93[EUR][1000 genomes]
rs6946855	0.91[EUR][1000 genomes]
rs6948096	0.93[EUR][1000 genomes]
rs6956486	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6964911	0.91[EUR][1000 genomes]
rs6965144	0.93[EUR][1000 genomes]
rs769435	0.81[AFR][1000 genomes]
rs7796145	0.93[EUR][1000 genomes]
rs7796148	0.93[EUR][1000 genomes]
rs7797855	0.93[EUR][1000 genomes]
rs7799229	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7806490	0.81[EUR][1000 genomes]
rs917761	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9655829	0.93[EUR][1000 genomes]
rs9656259	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs9656260	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs979652	0.93[EUR][1000 genomes]
rs989899	0.90[EUR][1000 genomes]
rs992035	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869971	chr7:117420583-118274149	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	nsv889088	chr7:117744660-117913648	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7779933	LSM8	cis	multi-tissue	Pritchard

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117825000-117842200	Weak transcription	Aorta	Aorta
2	chr7:117825800-117842600	Weak transcription	Brain Hippocampus Middle	brain
3	chr7:117828800-117838800	Weak transcription	Primary B cells from cord blood	blood
4	chr7:117829800-117840800	Weak transcription	Primary T cells from cord blood	blood
5	chr7:117830400-117842400	Weak transcription	Fetal Lung	lung
6	chr7:117831200-117842400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr7:117831400-117839800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr7:117832800-117842200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:117833000-117854000	Weak transcription	HSMM	muscle
10	chr7:117833400-117842200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:117833600-117854000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:117834000-117839400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr7:117834000-117842000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr7:117834400-117843400	Weak transcription	Fetal Thymus	thymus

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