Variant report

Variant	rs1783552
Chromosome Location	chr11:75233263-75233264
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:75232287..75234755-chr11:75237989..75239575,2	MCF-7	breast:
2	chr11:75220615..75223491-chr11:75231021..75233361,2	MCF-7	breast:
3	chr11:75230382..75233335-chr11:75236668..75238207,2	MCF-7	breast:
4	chr11:75223800..75226938-chr11:75231769..75233776,3	MCF-7	breast:
5	chr11:75218684..75220369-chr11:75232244..75234821,2	K562	blood:
6	chr11:75224068..75229006-chr11:75230364..75234823,7	K562	blood:
7	chr11:75217621..75220369-chr11:75231791..75234821,5	K562	blood:

Variant related genes	Relation type
ENSG00000254460	Chromatin interaction
ENSG00000158555	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1557472	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1557473	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1630251	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1631039	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs590260	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs600867	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs604252	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs607775	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs614227	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs615983	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs616422	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs630776	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs633602	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs634530	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs634890	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs686084	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7924708	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7934513	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7949062	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7949091	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3381903	chr11:75123498-75587233	Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	81 gene(s)	inside rSNPs	diseases
2	nsv897923	chr11:75129007-75302855	Active TSS Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75216200-75233600	Genic enhancers	Fetal Intestine Small	intestine
2	chr11:75217800-75234800	Weak transcription	Ovary	ovary
3	chr11:75220400-75235200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr11:75227800-75234200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:75227800-75234400	Enhancers	Fetal Intestine Large	intestine
6	chr11:75228600-75234400	Weak transcription	Lung	lung
7	chr11:75228800-75234800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr11:75229000-75233600	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr11:75229000-75234400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr11:75229400-75233800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr11:75229400-75234200	Enhancers	HSMMtube	muscle
12	chr11:75229600-75235200	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr11:75230200-75233400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr11:75230200-75233400	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr11:75230200-75233400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr11:75230400-75233400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr11:75230400-75233800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:75230400-75233800	Weak transcription	Primary B cells from peripheral blood	blood
19	chr11:75230400-75234000	Weak transcription	GM12878-XiMat	blood
20	chr11:75230600-75233600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr11:75230800-75235400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr11:75231000-75234200	Enhancers	Adipose Nuclei	Adipose
23	chr11:75231400-75234400	Enhancers	Pancreas	Pancrea
24	chr11:75231600-75234600	Enhancers	Placenta	Placenta
25	chr11:75232000-75233400	Genic enhancers	Spleen	Spleen
26	chr11:75232000-75235400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr11:75232200-75233400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr11:75232200-75233600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr11:75232200-75235000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr11:75232200-75235600	Weak transcription	Right Atrium	heart
31	chr11:75232200-75236200	Weak transcription	Aorta	Aorta
32	chr11:75232400-75234600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr11:75232400-75234600	Weak transcription	Hela-S3	cervix
34	chr11:75232400-75234800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr11:75232400-75234800	Weak transcription	Psoas Muscle	Psoas
36	chr11:75232400-75235200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr11:75232600-75233800	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr11:75232600-75234800	Weak transcription	Liver	Liver
39	chr11:75232800-75234600	Transcr. at gene 5' and 3'	HepG2	liver
40	chr11:75233000-75234200	Weak transcription	HSMM	muscle
41	chr11:75233000-75234400	Enhancers	Primary T cells fromperipheralblood	blood
42	chr11:75233000-75234600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
43	chr11:75233200-75233400	Enhancers	Fetal Brain Female	brain
44	chr11:75233200-75233800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr11:75233200-75233800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:75233200-75234000	Enhancers	Fetal Brain Male	brain

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