Variant report

Variant	rs6022803
Chromosome Location	chr20:52474850-52474851
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr20:52471901..52491673-chr20:55835708..55845674,34	MCF-7	breast:
2	chr17:57932184..57934585-chr20:52473101..52475297,2	MCF-7	breast:
3	chr20:52368202..52371256-chr20:52472915..52475847,3	K562	blood:

Variant related genes	Relation type
ENSG00000101144	Chromatin interaction
ENSG00000226308	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs34340293	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 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
7	nsv586222	chr20:52473679-52506380	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	74 gene(s)	inside rSNPs	diseases
8	esv3378662	chr20:52474345-52485443	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	60 gene(s)	inside rSNPs	diseases
9	esv3341653	chr20:52474345-52485543	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	60 gene(s)	inside rSNPs	diseases
10	esv3381391	chr20:52474445-52485443	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	60 gene(s)	inside rSNPs	diseases
11	nsv820856	chr20:52474672-52484379	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	56 gene(s)	inside rSNPs	diseases
12	nsv828744	chr20:52474672-52484379	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	56 gene(s)	inside rSNPs	diseases
13	nsv828745	chr20:52474735-52484379	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	56 gene(s)	inside rSNPs	diseases
14	nsv962637	chr20:52474736-52483715	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	54 gene(s)	inside rSNPs	diseases
15	nsv828746	chr20:52474785-52484076	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	56 gene(s)	inside rSNPs	diseases
16	esv16592	chr20:52474800-52484346	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	56 gene(s)	inside rSNPs	diseases
17	nsv586223	chr20:52474850-52475882	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
18	nsv586224	chr20:52474850-53279490	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	338 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52453600-52480200	Weak transcription	Small Intestine	intestine
2	chr20:52456600-52476200	Weak transcription	Gastric	stomach
3	chr20:52468800-52476200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr20:52468800-52481400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr20:52471600-52475000	Enhancers	Primary T cells from cord blood	blood
6	chr20:52472200-52476600	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr20:52472400-52480800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr20:52473200-52480200	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr20:52473400-52476200	Weak transcription	Placenta	Placenta
10	chr20:52473400-52476200	Weak transcription	Spleen	Spleen
11	chr20:52473600-52475000	Enhancers	Fetal Lung	lung
12	chr20:52473600-52476400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr20:52474000-52475400	Enhancers	Fetal Intestine Large	intestine
14	chr20:52474000-52476600	Enhancers	Stomach Mucosa	stomach
15	chr20:52474200-52475000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr20:52474200-52475000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr20:52474200-52475000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr20:52474200-52475000	Enhancers	Fetal Heart	heart
19	chr20:52474200-52475000	Enhancers	Fetal Kidney	kidney
20	chr20:52474200-52475000	Flanking Active TSS	HepG2	liver
21	chr20:52474200-52475200	Enhancers	Fetal Intestine Small	intestine
22	chr20:52474200-52475400	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr20:52474200-52476600	Enhancers	Duodenum Mucosa	Duodenum
24	chr20:52474400-52475000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr20:52474400-52475000	Enhancers	Colonic Mucosa	Colon
26	chr20:52474400-52475000	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr20:52474400-52475000	Enhancers	Right Ventricle	heart
28	chr20:52474400-52475000	Weak transcription	Dnd41	blood
29	chr20:52474400-52476200	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr20:52474600-52475000	Enhancers	H1 Cell Line	embryonic stem cell
31	chr20:52474600-52475000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
32	chr20:52474600-52476200	Weak transcription	Aorta	Aorta
33	chr20:52474600-52480200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr20:52474600-52480200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr20:52474600-52481600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr20:52474800-52476200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr20:52474800-52476200	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr20:52474800-52476200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr20:52474800-52476200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr20:52474800-52476200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr20:52474800-52476200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr20:52474800-52476200	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr20:52474800-52476200	Weak transcription	Fetal Muscle Leg	muscle
44	chr20:52474800-52476200	Weak transcription	Fetal Stomach	stomach
45	chr20:52474800-52476200	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr20:52474800-52476200	Weak transcription	K562	blood
47	chr20:52474800-52476400	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr20:52474800-52479600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr20:52474800-52480000	Weak transcription	Ovary	ovary
50	chr20:52474800-52480000	Weak transcription	A549	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links