Variant report

Variant	rs601845
Chromosome Location	chr11:64132498-64132499
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:64132487-64132816	K562	blood:	n/a	n/a

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:64130858..64133466-chr11:64138873..64141793,3	K562	blood:
2	chr11:64131252..64134081-chr11:64135368..64138200,2	MCF-7	breast:
3	chr11:64131375..64132916-chr11:64135481..64137117,2	K562	blood:
4	chr11:64036137..64038943-chr11:64132125..64134188,2	K562	blood:
5	chr11:64071859..64073528-chr11:64131116..64134089,2	K562	blood:

No data

Variant related genes	Relation type
MIR1237	TF binding region
ENSG00000221273	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000173153	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1199175	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1318165	0.83[AMR][1000 genomes]
rs477909	1.00[AMR][1000 genomes]
rs483515	1.00[AMR][1000 genomes]
rs484384	1.00[AMR][1000 genomes]
rs488760	0.83[AMR][1000 genomes]
rs494403	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs512372	0.83[AMR][1000 genomes]
rs513264	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs523525	1.00[AMR][1000 genomes]
rs545916	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs550819	0.83[AMR][1000 genomes]
rs558105	0.83[AMR][1000 genomes]
rs558864	0.83[AMR][1000 genomes]
rs564687	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs565221	0.83[AMR][1000 genomes]
rs566049	0.83[AMR][1000 genomes]
rs571379	0.83[AMR][1000 genomes]
rs590103	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs614047	0.83[AMR][1000 genomes]
rs632654	0.83[AMR][1000 genomes]
rs648220	1.00[AMR][1000 genomes]
rs649463	1.00[AMR][1000 genomes]
rs652611	0.83[AMR][1000 genomes]
rs676931	0.83[AMR][1000 genomes]
rs681797	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7941847	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
4	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh 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	237 gene(s)	inside rSNPs	diseases
5	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
6	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' 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	180 gene(s)	inside rSNPs	diseases
7	esv1802320	chr11:63987425-64154633	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
8	nsv897679	chr11:63994692-64150370	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
9	nsv897682	chr11:63999529-64170500	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
10	nsv897685	chr11:64048912-64150370	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
11	nsv897688	chr11:64107735-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
12	nsv897689	chr11:64109118-64148420	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
13	nsv897690	chr11:64118422-64135298	Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
14	nsv897691	chr11:64118422-64137875	Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
15	nsv832187	chr11:64121969-64312300	Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' 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	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64127400-64136000	Weak transcription	Fetal Kidney	kidney
2	chr11:64127400-64140000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:64127400-64144400	Weak transcription	Psoas Muscle	Psoas
4	chr11:64127600-64132800	Weak transcription	Small Intestine	intestine
5	chr11:64127600-64139600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr11:64127800-64132800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr11:64127800-64137600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:64127800-64139800	Strong transcription	Fetal Intestine Small	intestine
9	chr11:64127800-64146800	Weak transcription	Fetal Heart	heart
10	chr11:64128000-64133800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr11:64128000-64135400	Strong transcription	Fetal Stomach	stomach
12	chr11:64128000-64135800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr11:64128000-64136200	Strong transcription	Fetal Muscle Trunk	muscle
14	chr11:64128000-64138000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:64128000-64138200	Strong transcription	HUES6 Cell Line	embryonic stem cell
16	chr11:64128000-64138200	Strong transcription	Left Ventricle	heart
17	chr11:64128000-64138800	Strong transcription	Ovary	ovary
18	chr11:64128000-64139000	Strong transcription	Primary T cells from cord blood	blood
19	chr11:64128000-64139000	Strong transcription	Sigmoid Colon	Sigmoid Colon
20	chr11:64128000-64140000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr11:64128200-64133400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr11:64128200-64134600	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr11:64128200-64135600	Strong transcription	NH-A	brain
24	chr11:64128200-64135800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr11:64128200-64137000	Strong transcription	Colon Smooth Muscle	Colon
26	chr11:64128200-64138200	Strong transcription	Stomach Smooth Muscle	stomach
27	chr11:64128200-64138400	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr11:64128200-64138800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr11:64128200-64138800	Strong transcription	Duodenum Mucosa	Duodenum
30	chr11:64128200-64139400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr11:64128200-64139600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr11:64128200-64139600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr11:64128200-64139800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr11:64128200-64140000	Strong transcription	Lung	lung
35	chr11:64128400-64133800	Strong transcription	NHEK	skin
36	chr11:64128400-64134000	Weak transcription	Fetal Brain Male	brain
37	chr11:64128400-64135600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr11:64128400-64135600	Strong transcription	Fetal Intestine Large	intestine
39	chr11:64128400-64135800	Strong transcription	Brain Substantia Nigra	brain
40	chr11:64128400-64136000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr11:64128400-64136200	Strong transcription	Brain Cingulate Gyrus	brain
42	chr11:64128400-64137000	Strong transcription	Thymus	Thymus
43	chr11:64128400-64138200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr11:64128400-64138200	Strong transcription	Brain Anterior Caudate	brain
45	chr11:64128400-64139000	Strong transcription	Adipose Nuclei	Adipose
46	chr11:64128400-64139400	Strong transcription	Primary T helper cells fromperipheralblood	blood
47	chr11:64128400-64139600	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr11:64128400-64140400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:64128600-64133600	Strong transcription	Muscle Satellite Cultured Cells	--
50	chr11:64128600-64134000	Strong transcription	HMEC	breast

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