Variant report

Variant	rs28711618
Chromosome Location	chr4:74749883-74749884
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:74748840..74751609-chr4:74903470..74906256,2	K562	blood:

Variant related genes	Relation type
ENSG00000163734	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10000849	1.00[ASN][1000 genomes]
rs10003573	1.00[ASN][1000 genomes]
rs10007450	1.00[ASN][1000 genomes]
rs10014539	1.00[ASN][1000 genomes]
rs10017601	1.00[ASN][1000 genomes]
rs10024248	1.00[ASN][1000 genomes]
rs10028241	1.00[ASN][1000 genomes]
rs10034225	1.00[ASN][1000 genomes]
rs10470727	1.00[ASN][1000 genomes]
rs13435411	1.00[ASN][1000 genomes]
rs184761	1.00[ASN][1000 genomes]
rs2564595	1.00[ASN][1000 genomes]
rs28378124	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28433328	1.00[AMR][1000 genomes]
rs28439247	1.00[AMR][1000 genomes]
rs28481533	1.00[ASN][1000 genomes]
rs28522863	1.00[ASN][1000 genomes]
rs28538897	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28563821	1.00[ASN][1000 genomes]
rs28589827	1.00[ASN][1000 genomes]
rs28602974	1.00[ASN][1000 genomes]
rs28634348	1.00[ASN][1000 genomes]
rs28652714	1.00[ASN][1000 genomes]
rs28673400	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28681485	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28719470	1.00[EUR][1000 genomes]
rs28872183	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34943257	1.00[ASN][1000 genomes]
rs352017	1.00[ASN][1000 genomes]
rs352022	1.00[ASN][1000 genomes]
rs447672	1.00[ASN][1000 genomes]
rs485912	1.00[ASN][1000 genomes]
rs525317	1.00[ASN][1000 genomes]
rs61734750	1.00[EUR][1000 genomes]
rs648318	1.00[ASN][1000 genomes]
rs6817745	1.00[AMR][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	nsv1001725	chr4:74354050-74860924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv530126	chr4:74376622-74843892	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv432612	chr4:74723372-74774372	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv525980	chr4:74731526-75382209	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74747600-74752200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr4:74748200-74752000	Enhancers	Muscle Satellite Cultured Cells	--
3	chr4:74748600-74750000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:74748800-74750200	Enhancers	NHEK	skin
5	chr4:74749000-74750000	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr4:74749400-74751000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:74749400-74751200	Weak transcription	NH-A	brain
8	chr4:74749400-74751400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:74749400-74751400	Weak transcription	NHLF	lung
10	chr4:74749600-74750600	Weak transcription	NHDF-Ad	bronchial
11	chr4:74749600-74751200	Weak transcription	Osteobl	bone
12	chr4:74749600-74751600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr4:74749600-74756800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:74749600-74756800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr4:74749800-74751000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:74749800-74751400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr4:74749800-74751400	Weak transcription	HMEC	breast
18	chr4:74749800-74751600	Weak transcription	HSMM	muscle

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