Variant report

Variant	rs73501867
Chromosome Location	chr11:77696773-77696774
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:77696526..77698662-chr11:77704818..77706643,2	K562	blood:
2	chr11:77694947..77697759-chr11:77703796..77706385,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000149262	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11237399	1.00[AMR][1000 genomes]
rs59293034	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60704733	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73492001	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73493811	1.00[AFR][1000 genomes]
rs73493813	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73493836	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73493884	1.00[AMR][1000 genomes]
rs73495954	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73499843	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73501887	1.00[AMR][1000 genomes]
rs73501892	1.00[AMR][1000 genomes]
rs73503564	1.00[AMR][1000 genomes]
rs73503567	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050891	chr11:77416645-77788002	Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv1037292	chr11:77431583-77745934	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv541092	chr11:77431583-77745934	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv949316	chr11:77454076-77769885	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv520740	chr11:77553638-77997936	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
6	nsv1035753	chr11:77577384-77866386	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
7	nsv541093	chr11:77577384-77866386	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv526268	chr11:77688774-77698524	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:77614800-77700200	Weak transcription	Psoas Muscle	Psoas
2	chr11:77625800-77697400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr11:77649200-77701200	Weak transcription	NH-A	brain
4	chr11:77661400-77704400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:77664200-77704000	Weak transcription	NHEK	skin
6	chr11:77665800-77704200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr11:77666000-77704400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr11:77667600-77704200	Weak transcription	NHLF	lung
9	chr11:77668400-77701200	Weak transcription	Aorta	Aorta
10	chr11:77671200-77704200	Weak transcription	NHDF-Ad	bronchial
11	chr11:77672000-77701200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr11:77672000-77703800	Weak transcription	Fetal Brain Male	brain
13	chr11:77679000-77704200	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr11:77680800-77700200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr11:77681000-77704200	Weak transcription	HSMMtube	muscle
16	chr11:77682000-77700200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr11:77682800-77700800	Weak transcription	Right Ventricle	heart
18	chr11:77684200-77702400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr11:77688200-77704800	Weak transcription	Stomach Mucosa	stomach
20	chr11:77688400-77702200	Strong transcription	Dnd41	blood
21	chr11:77688600-77702800	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr11:77688800-77702400	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr11:77688800-77702400	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr11:77688800-77703400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:77688800-77703400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr11:77688800-77703800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr11:77689000-77702600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr11:77689000-77704800	Weak transcription	Fetal Heart	heart
29	chr11:77689200-77700000	Strong transcription	Primary B cells from cord blood	blood
30	chr11:77689200-77703000	Strong transcription	Primary T cells from cord blood	blood
31	chr11:77689200-77704800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr11:77689400-77697400	Strong transcription	Fetal Intestine Large	intestine
33	chr11:77689400-77701400	Strong transcription	Primary B cells from peripheral blood	blood
34	chr11:77689600-77703000	Strong transcription	Fetal Thymus	thymus
35	chr11:77690400-77704200	Weak transcription	HMEC	breast
36	chr11:77690600-77698600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr11:77690600-77700600	Weak transcription	Pancreas	Pancrea
38	chr11:77690600-77700800	Weak transcription	Esophagus	oesophagus
39	chr11:77690600-77700800	Weak transcription	Spleen	Spleen
40	chr11:77690600-77703800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr11:77690600-77704000	Weak transcription	Brain Anterior Caudate	brain
42	chr11:77690600-77704000	Weak transcription	Brain Substantia Nigra	brain
43	chr11:77690600-77704200	Weak transcription	Gastric	stomach
44	chr11:77690600-77704200	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr11:77690600-77704400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr11:77690800-77701000	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr11:77690800-77704200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr11:77690800-77704200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr11:77690800-77704200	Weak transcription	Small Intestine	intestine
50	chr11:77691000-77700000	Weak transcription	Fetal Brain Female	brain

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