Variant report

Variant	rs57696811
Chromosome Location	chr13:111270192-111270193
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:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:111270127..111273388-chr13:111363315..111367711,4	MCF-7	breast:
2	chr13:111268040..111269954-chr13:111270156..111273298,3	K562	blood:
3	chr13:111270148..111271814-chr13:111272109..111273731,2	K562	blood:
4	chr13:111268021..111270238-chr13:111291368..111294151,2	MCF-7	breast:
5	chr13:111266965..111271727-chr13:111364973..111369025,9	MCF-7	breast:
6	chr13:111265756..111270693-chr13:111363417..111370660,10	K562	blood:
7	chr13:111267851..111270253-chr13:111566067..111568371,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000153487	Chromatin interaction
ENSG00000134905	Chromatin interaction
ENSG00000255831	Chromatin interaction
ENSG00000088448	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10467308	1.00[ASN][1000 genomes]
rs11838544	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11838563	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11838902	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11840542	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11841651	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12427561	1.00[ASN][1000 genomes]
rs12428009	1.00[ASN][1000 genomes]
rs55949519	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57658160	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57813755	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59590698	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59764598	1.00[EUR][1000 genomes]
rs60690859	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs718886	1.00[ASN][1000 genomes]
rs73629903	1.00[ASN][1000 genomes]
rs73629967	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046423	chr13:110936104-111286607	Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv832720	chr13:111100235-111295993	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv1044234	chr13:111143053-111370580	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	216 gene(s)	inside rSNPs	diseases
4	nsv949634	chr13:111151460-111582996	Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
5	nsv901010	chr13:111165390-111286592	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	nsv1053922	chr13:111167764-111330876	Flanking Active TSS Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
7	nsv1043849	chr13:111167764-111340418	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
8	nsv541924	chr13:111167764-111340418	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv1036160	chr13:111167764-111347308	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
10	nsv541925	chr13:111167764-111347308	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
11	nsv901011	chr13:111168951-111280002	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
12	nsv901012	chr13:111220842-111340342	Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
13	nsv1038089	chr13:111229517-111274823	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
14	nsv1044340	chr13:111234073-111692994	Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	240 gene(s)	inside rSNPs	diseases
15	nsv563123	chr13:111237260-111292044	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
16	nsv525124	chr13:111261267-111280002	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
17	nsv563124	chr13:111261267-111300943	Enhancers Genic enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
18	nsv1048700	chr13:111265350-111658617	Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	240 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111268400-111270400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
2	chr13:111268600-111270200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
3	chr13:111268600-111270400	Flanking Active TSS	Duodenum Mucosa	Duodenum
4	chr13:111268800-111270200	Flanking Active TSS	Dnd41	blood
5	chr13:111268800-111270200	Flanking Active TSS	NH-A	brain
6	chr13:111268800-111270400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr13:111268800-111270400	Flanking Active TSS	HMEC	breast
8	chr13:111269000-111270200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr13:111269000-111270200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
10	chr13:111269000-111270200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr13:111269000-111270200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
12	chr13:111269000-111270200	Flanking Active TSS	Brain Hippocampus Middle	brain
13	chr13:111269000-111270200	Weak transcription	Lung	lung
14	chr13:111269000-111270400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr13:111269000-111270400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr13:111269000-111270400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr13:111269000-111270400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr13:111269000-111270400	Flanking Active TSS	Liver	Liver
19	chr13:111269000-111270400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
20	chr13:111269000-111270400	Enhancers	Placenta	Placenta
21	chr13:111269000-111270400	Enhancers	Placenta Amnion	Placenta Amnion
22	chr13:111269000-111272200	Enhancers	Pancreas	Pancrea
23	chr13:111269000-111277000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr13:111269000-111277600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr13:111269000-111287000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr13:111269200-111270400	Enhancers	Brain Substantia Nigra	brain
27	chr13:111269200-111270400	Enhancers	Fetal Heart	heart
28	chr13:111269200-111270400	Enhancers	Fetal Muscle Leg	muscle
29	chr13:111269200-111270400	Enhancers	Fetal Thymus	thymus
30	chr13:111269200-111270400	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr13:111269200-111270400	Flanking Active TSS	GM12878-XiMat	blood
32	chr13:111269200-111270600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr13:111269200-111271000	Enhancers	Primary T cells fromperipheralblood	blood
34	chr13:111269200-111271000	Enhancers	Fetal Stomach	stomach
35	chr13:111269200-111271400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr13:111269200-111271400	Enhancers	Stomach Mucosa	stomach
37	chr13:111269200-111274600	Weak transcription	Fetal Muscle Trunk	muscle
38	chr13:111269400-111270200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr13:111269400-111270200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr13:111269400-111270200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr13:111269400-111270200	Weak transcription	Right Atrium	heart
42	chr13:111269400-111270200	Enhancers	HSMMtube	muscle
43	chr13:111269400-111270400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr13:111269400-111270400	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr13:111269400-111270400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr13:111269400-111270400	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr13:111269400-111270400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr13:111269400-111270400	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr13:111269400-111270400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr13:111269400-111270400	Enhancers	Cortex derived primary cultured neurospheres	brain

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