Variant report

Variant	rs6097634
Chromosome Location	chr20:52467455-52467456
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr20:52466894..52469692-chr20:52471207..52473335,2	K562	blood:
2	chr17:57969168..57971185-chr20:52467018..52469521,2	MCF-7	breast:
3	chr20:50292654..50294989-chr20:52467138..52468915,2	MCF-7	breast:
4	chr20:52324403..52325048-chr20:52466907..52467868,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000108443	Chromatin interaction
ENSG00000108423	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs6091757	0.82[AFR][1000 genomes]
rs6091760	1.00[AFR][1000 genomes]
rs6097620	0.82[AFR][1000 genomes]
rs6097621	0.82[AFR][1000 genomes]
rs6097622	0.85[AFR][1000 genomes]
rs6097623	0.85[AFR][1000 genomes]
rs6097624	0.85[AFR][1000 genomes]
rs6097626	0.85[AFR][1000 genomes]
rs6097627	0.85[AFR][1000 genomes]
rs6097633	1.00[AFR][1000 genomes]
rs7261242	0.82[AFR][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	esv34060	chr20:52251863-52702186	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	296 gene(s)	inside rSNPs	diseases
2	nsv834008	chr20:52368660-52533410	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	185 gene(s)	inside rSNPs	diseases
3	nsv834009	chr20:52386050-52590795	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	182 gene(s)	inside rSNPs	diseases
4	nsv1060372	chr20:52409008-52502100	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	122 gene(s)	inside rSNPs	diseases
5	esv1831516	chr20:52437245-52514913	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	98 gene(s)	inside rSNPs	diseases
6	esv18025	chr20:52464720-52486135	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	67 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52453600-52480200	Weak transcription	Small Intestine	intestine
2	chr20:52456600-52468400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr20:52456600-52476200	Weak transcription	Gastric	stomach
4	chr20:52459600-52468400	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr20:52459600-52472600	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr20:52462800-52468200	Weak transcription	Osteobl	bone
7	chr20:52463000-52468400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr20:52463000-52474000	Weak transcription	A549	lung
9	chr20:52464200-52468600	Weak transcription	NHEK	skin
10	chr20:52464400-52467600	Enhancers	Primary B cells from peripheral blood	blood
11	chr20:52464400-52468000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr20:52464400-52472400	Weak transcription	Fetal Stomach	stomach
13	chr20:52464600-52472800	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr20:52464600-52474200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr20:52465000-52468400	Weak transcription	HepG2	liver
16	chr20:52465200-52468200	Weak transcription	Primary T cells from cord blood	blood
17	chr20:52465200-52468200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr20:52465200-52468400	Weak transcription	K562	blood
19	chr20:52465200-52472000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr20:52465200-52472000	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr20:52465200-52472200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr20:52465200-52472200	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr20:52465200-52472400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr20:52465400-52468400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr20:52465400-52468400	Weak transcription	Dnd41	blood
26	chr20:52466200-52468400	Weak transcription	Fetal Thymus	thymus
27	chr20:52466200-52472200	Weak transcription	Thymus	Thymus
28	chr20:52467200-52471600	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr20:52467200-52472600	Weak transcription	Adipose Nuclei	Adipose
30	chr20:52467400-52469400	Weak transcription	GM12878-XiMat	blood
31	chr20:52467400-52471600	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr20:52467400-52471600	Weak transcription	Monocytes-CD14+_RO01746	blood

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