Variant report

Variant	rs55792263
Chromosome Location	chr8:61820315-61820316
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr8:61820220-61820370	GM12871	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:61812523..61815203-chr8:61818659..61820454,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000254777	TF binding region

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10504321	0.92[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12680914	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12680923	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12682244	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16926576	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16926582	0.87[AFR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4123861	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4609230	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55832112	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57065489	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58187777	0.80[AFR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58610284	0.88[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs59503990	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61356857	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61525594	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72652548	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72652549	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72652550	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7819622	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917756	chr8:60942299-61862796	Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv526196	chr8:61593569-61877623	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	esv1795586	chr8:61733174-61863906	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv429919	chr8:61771472-61979873	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv890947	chr8:61815886-61882751	Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv948922	chr8:61818964-62475097	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:61812200-61821200	Weak transcription	Right Atrium	heart
2	chr8:61816800-61820600	Weak transcription	Small Intestine	intestine
3	chr8:61816800-61821200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:61816800-61821200	Weak transcription	Colonic Mucosa	Colon
5	chr8:61816800-61821200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr8:61816800-61821200	Weak transcription	NH-A	brain
7	chr8:61816800-61821400	Weak transcription	Osteobl	bone
8	chr8:61817000-61820400	Weak transcription	Primary B cells from cord blood	blood
9	chr8:61817000-61821000	Weak transcription	Adipose Nuclei	Adipose
10	chr8:61817000-61821200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr8:61817000-61821200	Weak transcription	HSMM	muscle
12	chr8:61817000-61821400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr8:61817200-61820400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr8:61817200-61820600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr8:61817200-61820800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr8:61817200-61820800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr8:61817200-61820800	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr8:61817200-61820800	Weak transcription	Duodenum Mucosa	Duodenum
19	chr8:61817200-61820800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr8:61817200-61821000	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr8:61817200-61821000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr8:61817200-61821000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr8:61817200-61821000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr8:61817200-61821200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr8:61817200-61821200	Weak transcription	Fetal Lung	lung
26	chr8:61817400-61820400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr8:61817400-61820800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr8:61817400-61820800	Weak transcription	HUVEC	blood vessel
29	chr8:61817400-61821000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:61817800-61821600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr8:61818200-61820600	Weak transcription	Primary T cells from cord blood	blood
32	chr8:61818200-61820800	Weak transcription	Fetal Intestine Large	intestine
33	chr8:61818800-61820400	Weak transcription	Fetal Thymus	thymus
34	chr8:61818800-61821200	Weak transcription	Pancreas	Pancrea
35	chr8:61819000-61822000	Weak transcription	Lung	lung
36	chr8:61819000-61822200	Weak transcription	Gastric	stomach
37	chr8:61819400-61821200	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr8:61819800-61820800	Enhancers	GM12878-XiMat	blood
39	chr8:61820000-61820800	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr8:61820000-61821400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr8:61820200-61820400	Enhancers	Primary T cells fromperipheralblood	blood
42	chr8:61820200-61820400	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr8:61820200-61820600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
44	chr8:61820200-61821000	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr8:61820200-61821200	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr8:61820200-61821400	Enhancers	Primary B cells from peripheral blood	blood
47	chr8:61820200-61821800	Enhancers	Stomach Mucosa	stomach

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