Variant report

Variant	rs10793267
Chromosome Location	chr11:77693272-77693273
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:77692487..77694366-chr11:77703526..77705740,2	K562	blood:
2	chr11:77683720..77686593-chr11:77691250..77693756,3	K562	blood:

Variant related genes	Relation type
ENSG00000149262	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10899420	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11237331	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11237343	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11826938	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1630344	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1668326	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1668327	0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1790249	0.88[EUR][1000 genomes]
rs2510965	0.95[EUR][1000 genomes]
rs3018165	0.92[EUR][1000 genomes]
rs586363	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs597289	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs607876	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs619142	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs629035	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs632040	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs632412	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6592754	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6592755	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs669327	0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7101610	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7105941	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7124008	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7929510	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs949171	0.88[EUR][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	chr11:77680800-77693400	Weak transcription	Primary hematopoietic stem cells	blood
15	chr11:77680800-77700200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr11:77681000-77704200	Weak transcription	HSMMtube	muscle
17	chr11:77682000-77700200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr11:77682800-77700800	Weak transcription	Right Ventricle	heart
19	chr11:77684200-77702400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr11:77688200-77694200	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr11:77688200-77694600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr11:77688200-77704800	Weak transcription	Stomach Mucosa	stomach
23	chr11:77688400-77694800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr11:77688400-77702200	Strong transcription	Dnd41	blood
25	chr11:77688600-77702800	Strong transcription	Primary T helper cells fromperipheralblood	blood
26	chr11:77688800-77694200	Strong transcription	GM12878-XiMat	blood
27	chr11:77688800-77694800	Strong transcription	Fetal Muscle Trunk	muscle
28	chr11:77688800-77695000	Strong transcription	Liver	Liver
29	chr11:77688800-77695200	Strong transcription	Primary T cells fromperipheralblood	blood
30	chr11:77688800-77702400	Strong transcription	Primary monocytes fromperipheralblood	blood
31	chr11:77688800-77702400	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr11:77688800-77703400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr11:77688800-77703400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr11:77688800-77703800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr11:77689000-77693600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr11:77689000-77693600	Strong transcription	Fetal Intestine Small	intestine
37	chr11:77689000-77694200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr11:77689000-77694400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr11:77689000-77702600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr11:77689000-77704800	Weak transcription	Fetal Heart	heart
41	chr11:77689200-77700000	Strong transcription	Primary B cells from cord blood	blood
42	chr11:77689200-77703000	Strong transcription	Primary T cells from cord blood	blood
43	chr11:77689200-77704800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr11:77689400-77693600	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr11:77689400-77694000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr11:77689400-77694200	Strong transcription	Adipose Nuclei	Adipose
47	chr11:77689400-77694200	Strong transcription	Duodenum Smooth Muscle	Duodenum
48	chr11:77689400-77694200	Strong transcription	HSMM	muscle
49	chr11:77689400-77694400	Strong transcription	Duodenum Mucosa	Duodenum
50	chr11:77689400-77697400	Strong transcription	Fetal Intestine Large	intestine

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