Variant report

Variant	rs11761827
Chromosome Location	chr7:112051706-112051707
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:11)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr7:112051135-112051753	HCT-116	colon:	n/a	chr7:112051633-112051642
2	RAD21	chr7:112051134-112051733	A549	lung:	n/a	n/a
3	CTCF	chr7:112050499-112051895	A549	lung:	n/a	chr7:112051633-112051642
4	CTCF	chr7:112050711-112051887	SK-N-SH	brain:	n/a	chr7:112051633-112051642
5	CTCF	chr7:112051236-112051719	MCF-7	breast:	n/a	chr7:112051633-112051642
6	JUND	chr7:112049554-112051862	SK-N-SH	brain:	n/a	n/a
7	SMC3	chr7:112050105-112051862	SK-N-SH	brain:	n/a	chr7:112050653-112050661
8	RAD21	chr7:112050034-112052306	SK-N-SH	brain:	n/a	n/a
9	RAD21	chr7:112051126-112051766	MCF-7	breast:	n/a	n/a
10	RAD21	chr7:112051184-112051734	HCT-116	colon:	n/a	n/a
11	RAD21	chr7:112051200-112051720	MCF-7	breast:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:112049730..112052171-chr7:112053926..112056276,3	K562	blood:
2	chr7:112045125..112048422-chr7:112049738..112053855,5	K562	blood:
3	chr12:74795006..74795737-chr7:112051152..112051706,2	MCF-7	breast:
4	chr7:112050573..112053136-chr7:112089164..112091552,2	MCF-7	breast:
5	chr7:112048671..112054554-chr7:112088966..112092653,8	K562	blood:
6	chr7:111403379..111404358-chr7:112051159..112051887,3	MCF-7	breast:
7	chr7:112050774..112053695-chr7:112073947..112076333,2	K562	blood:
8	chr7:112049693..112052446-chr7:112089375..112092902,3	K562	blood:
9	chr7:112051238..112053639-chr7:112090198..112091815,2	MCF-7	breast:
10	chr7:111592856..111595719-chr7:112049563..112051825,3	MCF-7	breast:
11	chr7:112045125..112047686-chr7:112049738..112051786,2	K562	blood:

No data

No data

No data

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11771128	0.84[EUR][1000 genomes]
rs12216563	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13223482	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34020242	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35734252	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4730544	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58295122	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62474016	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6944057	0.87[EUR][1000 genomes]
rs6969907	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6976652	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs720639	0.89[EUR][1000 genomes]
rs7780160	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7798715	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7810707	0.87[EUR][1000 genomes]
rs9649350	0.88[EUR][1000 genomes];0.94[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	nsv532335	chr7:111411990-112054905	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv531436	chr7:111856171-112585407	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
3	nsv831097	chr7:112000837-112113173	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 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	chr7:112046000-112060400	Weak transcription	Brain Angular Gyrus	brain
2	chr7:112050200-112051800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr7:112050600-112052800	Enhancers	HepG2	liver
4	chr7:112051000-112051800	Enhancers	Brain Hippocampus Middle	brain
5	chr7:112051000-112053000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:112051200-112051800	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr7:112051200-112054800	Weak transcription	Fetal Lung	lung
8	chr7:112051400-112052000	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr7:112051400-112053400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:112051400-112055400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr7:112051600-112052000	Enhancers	HUVEC	blood vessel
12	chr7:112051600-112053400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr7:112051600-112055200	Weak transcription	Primary hematopoietic stem cells	blood
14	chr7:112051600-112055200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:112051600-112062000	Weak transcription	Right Atrium	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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