Variant report

Variant	rs7945405
Chromosome Location	chr11:108414662-108414663
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:108408866..108411436-chr11:108411845..108416177,4	K562	blood:
2	chr11:108414480..108416284-chr4:87927673..87929225,2	K562	blood:
3	chr11:108407718..108412252-chr11:108413139..108417754,5	K562	blood:

Variant related genes	Relation type
ENSG00000110723	Chromatin interaction
ENSG00000172493	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs17108182	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1893996	1.00[ASW][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1893997	1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3092837	1.00[EUR][1000 genomes]
rs4988109	1.00[EUR][1000 genomes]
rs4988134	1.00[EUR][1000 genomes]
rs7103368	1.00[EUR][1000 genomes]
rs7110533	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7116971	1.00[EUR][1000 genomes]
rs7938338	1.00[EUR][1000 genomes]
rs9666757	1.00[EUR][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	nsv1052254	chr11:108122683-108845008	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active 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	28 gene(s)	inside rSNPs	diseases
2	nsv541164	chr11:108122683-108845008	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv898386	chr11:108409442-108831875	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108385000-108422800	Weak transcription	Fetal Intestine Small	intestine
2	chr11:108401600-108420800	Weak transcription	Lung	lung
3	chr11:108407400-108420000	Weak transcription	Esophagus	oesophagus
4	chr11:108409000-108417200	Weak transcription	Pancreas	Pancrea
5	chr11:108409200-108419400	Weak transcription	K562	blood
6	chr11:108409200-108423000	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr11:108409600-108422600	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr11:108409800-108416600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:108409800-108419600	Weak transcription	Liver	Liver
10	chr11:108409800-108422200	Weak transcription	Fetal Kidney	kidney
11	chr11:108409800-108422200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr11:108410000-108422800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr11:108410200-108422000	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr11:108410200-108422400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr11:108412400-108414800	Enhancers	HSMMtube	muscle
16	chr11:108414000-108414800	Enhancers	HSMM	muscle
17	chr11:108414200-108414800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:108414200-108415200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:108414200-108415200	Enhancers	Placenta	Placenta
20	chr11:108414200-108415400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr11:108414200-108415400	Flanking Active TSS	NHEK	skin
22	chr11:108414400-108414800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr11:108414400-108422400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr11:108414600-108414800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:108414600-108415000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr11:108414600-108416800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:108414600-108417000	Weak transcription	H1 Cell Line	embryonic stem cell

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