Variant report

Variant	rs6658755
Chromosome Location	chr1:221811427-221811428
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:221809737..221812639-chr1:221914030..221916413,2	MCF-7	breast:
2	chr1:221716805..221717802-chr1:221811163..221812344,4	MCF-7	breast:
3	chr1:221651383..221651959-chr1:221811085..221811756,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000143507	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1018334	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10442685	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10495172	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10863640	0.84[AMR][1000 genomes]
rs11118751	0.80[ASN][1000 genomes]
rs11118768	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11118777	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11118778	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11118779	0.94[AFR][1000 genomes]
rs11118780	0.92[AFR][1000 genomes]
rs12023780	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12026281	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12029530	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12029601	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12122580	0.88[AFR][1000 genomes]
rs12748524	0.84[AMR][1000 genomes]
rs12753128	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1338074	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1342092	0.80[ASN][1000 genomes]
rs1538248	0.80[ASN][1000 genomes]
rs1858565	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1879068	0.82[AMR][1000 genomes]
rs1933268	0.84[AMR][1000 genomes]
rs1967553	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3860323	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3860324	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4436399	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4450027	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4484930	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4498809	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6658414	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6658746	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6663135	0.84[AMR][1000 genomes]
rs6663415	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6663637	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6663644	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6666514	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6697462	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6700617	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9660488	0.81[ASN][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	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv873200	chr1:221644180-221843191	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221806200-221813600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr1:221810200-221811600	Enhancers	Brain Anterior Caudate	brain
3	chr1:221810200-221811600	Enhancers	Brain Substantia Nigra	brain
4	chr1:221810200-221811600	Enhancers	NHDF-Ad	bronchial
5	chr1:221810400-221811600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr1:221810400-221811600	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr1:221810400-221811600	Enhancers	Fetal Muscle Leg	muscle
8	chr1:221810400-221811600	Enhancers	HSMMtube	muscle
9	chr1:221810600-221811600	Enhancers	Brain Hippocampus Middle	brain
10	chr1:221810600-221811600	Enhancers	HSMM	muscle
11	chr1:221810600-221811600	Enhancers	Osteobl	bone
12	chr1:221810800-221811600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:221810800-221811600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:221810800-221811600	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr1:221811200-221811600	Enhancers	Fetal Heart	heart
16	chr1:221811400-221817000	Weak transcription	Brain Germinal Matrix	brain

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