Variant report

Variant	rs72996087
Chromosome Location	chr1:151433054-151433055
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HCFC1	chr1:151430201-151433371	Hela-S3	cervix:	n/a	n/a
2	MAX	chr1:151432940-151433055	NB4	blood:	n/a	chr1:151432973-151432983 chr1:151433033-151433043

No data

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

No.	Distal block	Cell Line	Cell type
1	chr1:151431720..151433397-chr1:151480112..151483047,2	K562	blood:
2	chr1:151421812..151434588-chr1:151506621..151515599,30	MCF-7	breast:
3	chr1:151413939..151417832-chr1:151429782..151433498,5	K562	blood:
4	chr1:151431438..151433634-chr1:151734265..151736700,2	K562	blood:
5	chr1:151371183..151372890-chr1:151431011..151433472,2	MCF-7	breast:
6	chr1:151427202..151436068-chr1:151477865..151490153,60	MCF-7	breast:
7	chr1:151270824..151272634-chr1:151430532..151433338,2	MCF-7	breast:
8	chr1:151411812..151418574-chr1:151428106..151433466,11	MCF-7	breast:
9	chr1:151431826..151434593-chr1:151511133..151514053,3	K562	blood:
10	chr1:151429965..151433300-chr1:151491808..151494354,4	MCF-7	breast:
11	chr1:151225884..151227392-chr1:151432640..151434874,2	K562	blood:
12	chr1:151423878..151427557-chr1:151430240..151433379,4	K562	blood:
13	chr1:151430095..151434593-chr1:151511133..151513913,5	K562	blood:
14	chr1:151387420..151389134-chr1:151433019..151434724,2	K562	blood:

No data

Variant related genes	Relation type
POGZ	TF binding region
ENSG00000143442	Chromatin interaction
ENSG00000159352	Chromatin interaction
ENSG00000143436	Chromatin interaction
ENSG00000143367	Chromatin interaction
ENSG00000143393	Chromatin interaction
ENSG00000143375	Chromatin interaction
ENSG00000143450	Chromatin interaction
ENSG00000232536	Chromatin interaction
ENSG00000159377	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs35198305	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57098736	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59506235	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59863461	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61147726	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6702368	1.00[AMR][1000 genomes]
rs72996003	1.00[AMR][1000 genomes]
rs72996015	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72996022	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72996027	1.00[AMR][1000 genomes]
rs72996035	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72996038	1.00[AMR][1000 genomes]
rs72996040	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72996059	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72996068	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72996077	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72996084	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72996090	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72996094	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7530212	0.88[AFR][1000 genomes];1.00[AMR][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	nsv916272	chr1:150961809-151557253	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
2	nsv831581	chr1:151289151-151478605	Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
3	esv1811070	chr1:151403570-151433317	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	esv3393715	chr1:151430153-151433301	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	n/a
5	esv3392140	chr1:151430178-151433126	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151431000-151445000	Weak transcription	Spleen	Spleen
2	chr1:151432200-151433200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
3	chr1:151432400-151433200	Enhancers	Liver	Liver
4	chr1:151432400-151434000	Weak transcription	Left Ventricle	heart
5	chr1:151432400-151434200	Weak transcription	Right Ventricle	heart
6	chr1:151432400-151434600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:151432400-151437800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:151432600-151434400	Weak transcription	HSMMtube	muscle
9	chr1:151432600-151434800	Weak transcription	Duodenum Mucosa	Duodenum
10	chr1:151432600-151436400	Weak transcription	Stomach Smooth Muscle	stomach
11	chr1:151432600-151436800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr1:151432600-151445000	Weak transcription	Fetal Intestine Small	intestine
13	chr1:151432600-151445000	Weak transcription	Pancreas	Pancrea
14	chr1:151432800-151433200	Enhancers	Dnd41	blood
15	chr1:151433000-151434200	Weak transcription	K562	blood

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