Variant report

Variant	rs882099
Chromosome Location	chr1:151977172-151977173
allele	A/G
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:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:151940219..151941099-chr1:151976121..151977198,6	MCF-7	breast:
2	chr1:151861047..151861926-chr1:151976278..151977205,2	MCF-7	breast:
3	chr1:151880825..151882446-chr1:151974960..151977633,2	K562	blood:
4	chr1:151906232..151907079-chr1:151976438..151977221,2	MCF-7	breast:
5	chr1:151906723..151908280-chr1:151976802..151979658,2	MCF-7	breast:
6	chr1:151860828..151863330-chr1:151976166..151978262,2	MCF-7	breast:
7	chr1:151879997..151882325-chr1:151975828..151977633,2	K562	blood:
8	chr1:151958520..151979218-chr1:151992734..152014750,97	MCF-7	breast:
9	chr1:151520240..151522190-chr1:151976261..151978118,2	MCF-7	breast:
10	chr1:151879750..151883668-chr1:151974501..151979582,5	MCF-7	breast:
11	chr1:151976242..151977190-chr1:151986239..151986739,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000159445	Chromatin interaction
ENSG00000163191	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11204923	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1490188	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1602252	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1602254	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1967084	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1967085	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1979638	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2932567	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2932572	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2932573	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2999535	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2999536	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2999537	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2999538	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3007713	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3007714	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6587641	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6704157	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs882100	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs959945	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs994974	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007097	chr1:151832796-152227977	Strong transcription Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
2	nsv1012327	chr1:151835544-152200890	Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
3	nsv535159	chr1:151835544-152200890	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
4	nsv872441	chr1:151850072-152034430	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	191 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151967800-151977200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr1:151974200-151977200	Enhancers	NHEK	skin
3	chr1:151975600-151977200	Enhancers	Esophagus	oesophagus
4	chr1:151975600-151977200	Enhancers	Left Ventricle	heart
5	chr1:151975800-151977200	Enhancers	Fetal Heart	heart
6	chr1:151975800-151977200	Enhancers	Right Atrium	heart
7	chr1:151976000-151978400	Enhancers	Right Ventricle	heart
8	chr1:151976400-151977200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr1:151976400-151977400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:151976600-151977600	Weak transcription	Hela-S3	cervix
11	chr1:151976600-151979400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr1:151976600-151979400	Weak transcription	HMEC	breast
13	chr1:151976800-151977200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr1:151976800-151993600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr1:151977000-151978000	Weak transcription	Stomach Mucosa	stomach
16	chr1:151977000-151979200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:151977000-151986000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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