Variant report

Variant	rs61027777
Chromosome Location	chr6:132109844-132109845
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:0)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr6:132109800-132109950	HVMF	connective:	n/a	n/a
2	SMC3	chr6:132109538-132109906	HepG2	liver:	n/a	n/a
3	RAD21	chr6:132109578-132109902	HepG2	liver:	n/a	n/a
4	CTCF	chr6:132109740-132109890	AoAF	blood vessel:	n/a	n/a
5	RAD21	chr6:132109465-132109846	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr6:132109700-132109850	BJ	skin:	n/a	n/a
7	CTCF	chr6:132109566-132109932	IMR90	lung:	n/a	n/a
8	CTCF	chr6:132109760-132109910	HCM	heart:	n/a	n/a
9	CTCF	chr6:132109700-132109850	NHDF-neo	bronchial:	n/a	n/a
10	CTCF	chr6:132109713-132109913	K562	blood:	n/a	n/a
11	RAD21	chr6:132109486-132109981	HepG2	liver:	n/a	n/a
12	CTCF	chr6:132109720-132109870	HFF-Myc	foreskin:	n/a	n/a
13	CTCF	chr6:132109700-132109850	MCF-7	breast:	n/a	n/a
14	CTCF	chr6:132109700-132109850	HCFaa	heart:	n/a	n/a
15	CTCF	chr6:132109700-132109850	NHLF	lung:	n/a	n/a
16	RAD21	chr6:132109601-132109846	HepG2	liver:	n/a	n/a
17	RAD21	chr6:132109294-132109904	IMR90	lung:	n/a	n/a
18	CTCF	chr6:132109820-132109970	HAc	cerebellar:	n/a	n/a
19	CTCF	chr6:132109584-132109904	HepG2	liver:	n/a	n/a
20	RAD21	chr6:132109567-132109887	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr6:132109700-132109850	WI-38	lung:	n/a	n/a

No data

Variant related genes	Relation type
MIR548H5	TF binding region

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12660595	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12661063	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12662953	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12663389	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12664747	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12664750	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12665617	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3908474	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4371863	1.00[AMR][1000 genomes]
rs73537697	1.00[AMR][1000 genomes]
rs73539605	1.00[AMR][1000 genomes]
rs73539606	1.00[AMR][1000 genomes]
rs73539675	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv515476	chr6:131615425-132228577	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv7968	chr6:131917172-132321099	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv830809	chr6:131953928-132126417	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
4	nsv830810	chr6:131960923-132138396	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
5	nsv886670	chr6:132071193-132193395	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
6	nsv886671	chr6:132071193-132203432	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
7	nsv5479	chr6:132101897-132136593	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
8	esv2630901	chr6:132105802-132109925	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv3494780	chr6:132105884-132109857	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv21004	chr6:132106620-132118530	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
11	nsv604667	chr6:132106988-132115081	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132106400-132113000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr6:132107600-132110800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr6:132107800-132110800	Enhancers	NHDF-Ad	bronchial
4	chr6:132108000-132110600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:132108000-132111000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr6:132108600-132110600	Enhancers	NHLF	lung
7	chr6:132108600-132111000	Enhancers	Osteobl	bone
8	chr6:132108800-132110000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr6:132108800-132110800	Enhancers	HSMM	muscle
10	chr6:132109200-132110800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr6:132109800-132110200	Weak transcription	Adipose Nuclei	Adipose
12	chr6:132109800-132112800	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr6:132109800-132112800	Weak transcription	Fetal Stomach	stomach
14	chr6:132109800-132113000	Weak transcription	Fetal Muscle Leg	muscle
15	chr6:132109800-132113200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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