Variant report

Variant	rs61884706
Chromosome Location	chr11:63856611-63856612
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:63849400..63851715-chr11:63854816..63857359,2	K562	blood:
2	chr11:63854385..63857237-chr11:63950908..63953026,2	MCF-7	breast:
3	chr11:63854089..63858016-chr11:63890229..63892946,3	MCF-7	breast:
4	chr11:63831163..63834275-chr11:63854365..63857011,4	K562	blood:
5	chr11:63854748..63858551-chr11:63863184..63865147,4	K562	blood:
6	chr11:63855872..63856739-chr11:63913242..63914073,2	MCF-7	breast:
7	chr11:63856107..63859792-chr11:63865203..63866942,3	K562	blood:
8	chr11:63839378..63841759-chr11:63854044..63857012,2	MCF-7	breast:
9	chr11:63831163..63834046-chr11:63854365..63856884,2	K562	blood:
10	chr11:63852661..63854183-chr11:63856127..63858636,2	K562	blood:
11	chr11:63856543..63858986-chr11:63931216..63932761,2	K562	blood:
12	chr11:63837418..63841150-chr11:63854327..63856960,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000168439	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs56286917	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61884707	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61884708	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7926637	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7944693	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897629	chr11:63664882-63866959	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv897630	chr11:63664882-63924446	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
4	esv1849906	chr11:63719273-63880383	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	esv29993	chr11:63738642-63864211	Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv897642	chr11:63744152-63866959	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
7	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
8	nsv897645	chr11:63754986-63859751	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
9	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
10	nsv897651	chr11:63761169-63863405	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
11	nsv897652	chr11:63761169-63866959	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
12	nsv897653	chr11:63761169-63875456	Strong transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
13	nsv897654	chr11:63772000-63875456	Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	nsv832184	chr11:63787702-63925084	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
16	nsv897657	chr11:63810944-63866959	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
17	nsv897658	chr11:63810944-63897759	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
18	nsv897659	chr11:63813470-63907079	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
19	nsv832185	chr11:63819946-63963532	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	89 gene(s)	inside rSNPs	diseases
20	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63786600-63858000	Weak transcription	Hela-S3	cervix
2	chr11:63846600-63859200	Weak transcription	Fetal Brain Female	brain
3	chr11:63848200-63865600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr11:63848600-63858400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr11:63850800-63860200	Bivalent Enhancer	Fetal Stomach	stomach
6	chr11:63851200-63858800	Enhancers	Fetal Thymus	thymus
7	chr11:63851800-63857000	Weak transcription	Fetal Brain Male	brain
8	chr11:63851800-63868400	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr11:63852000-63858400	Weak transcription	Fetal Heart	heart
10	chr11:63852200-63857200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:63852200-63863400	Weak transcription	Right Atrium	heart
12	chr11:63852400-63857000	Weak transcription	Left Ventricle	heart
13	chr11:63853000-63858600	Enhancers	Brain Germinal Matrix	brain
14	chr11:63853000-63860800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr11:63853000-63869000	Enhancers	Brain Hippocampus Middle	brain
16	chr11:63853000-63871200	Enhancers	Brain Cingulate Gyrus	brain
17	chr11:63853000-63871600	Enhancers	Brain Substantia Nigra	brain
18	chr11:63853400-63856800	Weak transcription	Fetal Lung	lung
19	chr11:63853400-63871200	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr11:63853600-63858000	Enhancers	Colon Smooth Muscle	Colon
21	chr11:63853600-63864400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr11:63853600-63870800	Enhancers	Brain Angular Gyrus	brain
23	chr11:63853800-63857400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:63854000-63858400	Weak transcription	HepG2	liver
25	chr11:63854400-63857200	Weak transcription	Dnd41	blood
26	chr11:63854600-63856800	Weak transcription	Thymus	Thymus
27	chr11:63854600-63858200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:63854600-63861000	Weak transcription	Ovary	ovary
29	chr11:63854600-63864400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr11:63854600-63868400	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr11:63854800-63857200	Weak transcription	HSMMtube	muscle
32	chr11:63854800-63857600	Weak transcription	Liver	Liver
33	chr11:63854800-63862400	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr11:63855000-63857200	Weak transcription	HSMM	muscle
35	chr11:63855200-63857200	Weak transcription	Psoas Muscle	Psoas
36	chr11:63855200-63860800	Weak transcription	Pancreas	Pancrea
37	chr11:63855400-63864800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr11:63855800-63858400	Enhancers	A549	lung
39	chr11:63856000-63856800	Enhancers	Stomach Mucosa	stomach
40	chr11:63856000-63857000	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr11:63856000-63857200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:63856000-63857200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:63856000-63857400	Enhancers	Esophagus	oesophagus
44	chr11:63856000-63857400	Bivalent Enhancer	Fetal Muscle Leg	muscle
45	chr11:63856200-63857400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:63856400-63856800	Active TSS	Spleen	Spleen
47	chr11:63856400-63856800	Bivalent Enhancer	NHEK	skin
48	chr11:63856400-63857400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr11:63856400-63857400	Enhancers	Colonic Mucosa	Colon
50	chr11:63856400-63857600	Enhancers	Rectal Smooth Muscle	rectum

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