Variant report

Variant	nsv912590
Chromosome Location	chr20:1278770-1298397
allele	n/a
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	ARID3A	chr20:1284914-1285109	K562	blood:	n/a	n/a
2	ATF1	chr20:1281704-1281915	K562	blood:	n/a	n/a
3	ATF3	chr20:1289968-1290275	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr20:1294067-1294472	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr20:1289999-1290199	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr20:1280316-1280385	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr20:1294180-1294466	GM12878	blood:	n/a	n/a
8	BHLHE40	chr20:1285433-1285717	K562	blood:	n/a	n/a
9	BHLHE40	chr20:1294195-1294496	K562	blood:	n/a	n/a
10	BHLHE40	chr20:1280237-1280483	K562	blood:	n/a	n/a
11	BRCA1	chr20:1294333-1294360	GM12878	blood:	n/a	n/a
12	BRCA1	chr20:1294316-1294516	HepG2	liver:	n/a	n/a
13	CEBPB	chr20:1294202-1294446	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr20:1294284-1294436	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr20:1294308-1294363	GM12878	blood:	n/a	n/a
16	CHD2	chr20:1294106-1294254	HepG2	liver:	n/a	n/a
17	CHD2	chr20:1294008-1294452	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr20:1290127-1290213	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr20:1280276-1280452	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr20:1294131-1294336	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr20:1291122-1291228	HepG2	liver:	n/a	n/a
22	CTCF	chr20:1290180-1290330	HRE	kidney:	n/a	n/a
23	CTCF	chr20:1280280-1280430	AG04449	skin:	n/a	n/a
24	CTCF	chr20:1285500-1285650	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr20:1280260-1280410	HMF	breast:	n/a	n/a
26	CTCF	chr20:1280320-1280470	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr20:1294220-1294370	NHLF	lung:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
28	CTCF	chr20:1280198-1280512	K562	blood:	n/a	n/a
29	CTCF	chr20:1294010-1294525	MCF-7	breast:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331
30	CTCF	chr20:1294240-1294390	AG04449	skin:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
31	CTCF	chr20:1280300-1280450	SAEC	small airway:	n/a	n/a
32	CTCF	chr20:1294260-1294410	RPTEC	kidney:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
33	CTCF	chr20:1280280-1280430	HepG2	liver:	n/a	n/a
34	CTCF	chr20:1280263-1280467	MCF-7	breast:	n/a	n/a
35	CTCF	chr20:1280252-1280490	GM12878	blood:	n/a	n/a
36	CTCF	chr20:1280257-1280461	GM12891	blood:	n/a	n/a
37	CTCF	chr20:1280280-1280430	GM12874	blood:	n/a	n/a
38	CTCF	chr20:1294075-1294549	A549	lung:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331
39	CTCF	chr20:1280260-1280410	GM12869	blood:	n/a	n/a
40	CTCF	chr20:1294123-1294466	ECC-1	luminal epithelium:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331
41	CTCF	chr20:1294073-1294527	Spleen_OC	spleen:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331
42	CTCF	chr20:1293760-1294857	A549	lung:	n/a	chr20:1294318-1294328 chr20:1294149-1294162 chr20:1294315-1294336 chr20:1294151-1294161 chr20:1294314-1294330 chr20:1294146-1294164 chr20:1294316-1294325 chr20:1294313-1294331
43	CTCF	chr20:1280220-1280370	K562	blood:	n/a	n/a
44	CTCF	chr20:1290057-1290302	H1-hESC	embryonic stem cell:	n/a	chr20:1290141-1290162 chr20:1290146-1290164
45	CTCF	chr20:1280280-1280430	BJ	skin:	n/a	n/a
46	CTCF	chr20:1294220-1294370	HVMF	connective:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
47	CTCF	chr20:1294220-1294370	BE2_C	brain:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
48	CTCF	chr20:1290110-1290237	GM12892	blood:	n/a	chr20:1290141-1290162 chr20:1290146-1290164
49	CTCF	chr20:1294260-1294410	HCPEpiC	choroid plexus:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
50	CTCF	chr20:1280260-1280410	GM12873	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1297651-1297701	ovcar-3	ovarian:	n/a
2	chr20:1293682-1293732	HepG2	liver:	n/a
3	chr20:1294376-1294426	AG04450	lung:	fetal
4	chr20:1293682-1293732	PANC-1	pancreas:	n/a
5	chr20:1294361-1294411	IMR90	lung:	fetal
6	chr20:1283388-1283438	AG09319	gingival:	n/a
7	chr20:1290724-1290774	Hepatocyte	liver:	n/a
8	chr20:1283388-1283438	BE2_C	brain:	n/a
9	chr20:1294858-1294908	PFSK-1	brain:	n/a
10	chr20:1294301-1294351	NH-A	brain:	n/a
11	chr20:1286630-1286680	ECC-1	luminal epithelium:	n/a
12	chr20:1294858-1294908	K562	blood:	n/a
13	chr20:1294814-1294864	RPTEC	kidney:	n/a
14	chr20:1280341-1280391	HCT-116	colon:	n/a
15	chr20:1294313-1294363	BE2_C	brain:	n/a
16	chr20:1285816-1285866	HCF	heart:	n/a
17	chr20:1297651-1297701	ECC-1	luminal epithelium:	n/a
18	chr20:1285816-1285866	ovcar-3	ovarian:	n/a
19	chr20:1297651-1297701	MCF-7	breast:	n/a
20	chr20:1287050-1287100	HUVEC	blood vessel:	n/a
21	chr20:1286558-1286608	HUVEC	blood vessel:	n/a
22	chr20:1294361-1294411	AG09309	skin:	n/a
23	chr20:1294311-1294361	AG09309	skin:	n/a
24	chr20:1289571-1289621	HEK293	kidney:	embryo
25	chr20:1294311-1294361	MCF-7	breast:	n/a
26	chr20:1294858-1294908	AG04450	lung:	fetal
27	chr20:1294858-1294908	BE2_C	brain:	n/a
28	chr20:1287050-1287100	CMK	blood:	n/a
29	chr20:1286630-1286680	HCF	heart:	n/a
30	chr20:1294313-1294363	ovcar-3	ovarian:	n/a
31	chr20:1294021-1294071	HRPEpiC	eye:	n/a
32	chr20:1287050-1287100	HAEpiC	amniotic membrane:	n/a
33	chr20:1286558-1286608	HMEC	breast:	n/a
34	chr20:1280341-1280391	GM12891	blood:	n/a
35	chr20:1287050-1287100	HCT-116	colon:	n/a
36	chr20:1294313-1294363	MCF-7	breast:	n/a
37	chr20:1280341-1280391	MCF-7	breast:	n/a
38	chr20:1287050-1287100	MCF10A-Er-Src	breast:	n/a
39	chr20:1286630-1286680	AG09319	gingival:	n/a
40	chr20:1283388-1283438	PFSK-1	brain:	n/a
41	chr20:1293560-1293610	AG10803	skin:	n/a
42	chr20:1289571-1289621	AG09309	skin:	n/a
43	chr20:1294301-1294351	ECC-1	luminal epithelium:	n/a
44	chr20:1290724-1290774	HepG2	liver:	n/a
45	chr20:1293682-1293732	PFSK-1	brain:	n/a
46	chr20:1280341-1280391	CMK	blood:	n/a
47	chr20:1294301-1294351	HL-60	blood:	n/a
48	chr20:1293560-1293610	GM19239	blood:	n/a
49	chr20:1286558-1286608	GM12892	blood:	n/a
50	chr20:1283388-1283438	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:1285641..1287786-chr20:1289716..1291902,2	K562	blood:
2	chr20:1292210..1295153-chr20:1372716..1374404,2	MCF-7	breast:
3	chr20:1274563..1276619-chr20:1279112..1281898,2	K562	blood:
4	chr20:1282248..1284954-chr20:1288783..1291101,2	MCF-7	breast:
5	chr20:1296607..1299079-chr20:1367748..1369670,2	K562	blood:
6	chr20:1281423..1283535-chr20:1306063..1308157,2	K562	blood:
7	chr20:1205295..1208138-chr20:1282456..1285112,2	K562	blood:
8	chr20:1283698..1286846-chr20:1286878..1289632,3	K562	blood:
9	chr20:1261527..1264873-chr20:1277243..1279340,3	K562	blood:
10	chr20:1296232..1299079-chr20:1367748..1370124,3	K562	blood:
11	chr20:1286013..1291003-chr20:1304965..1309000,4	K562	blood:
12	chr20:1283698..1286846-chr20:1286878..1289632,3	K562	blood:
13	chr20:1280644..1283563-chr20:1283914..1285559,2	MCF-7	breast:
14	chr20:1272718..1276817-chr20:1277279..1280817,5	MCF-7	breast:
15	chr20:1282248..1284954-chr20:1288783..1291101,2	MCF-7	breast:
16	chr20:1279418..1283217-chr20:1283449..1287758,5	K562	blood:
17	chr20:1279250..1281881-chr20:1447982..1450441,2	K562	blood:
18	chr20:1280644..1283563-chr20:1283914..1285559,2	MCF-7	breast:
19	chr20:1271210..1274105-chr20:1276784..1280464,4	K562	blood:
20	chr20:1279418..1283217-chr20:1283449..1287758,5	K562	blood:
21	chr20:1293745..1297831-chr20:1304825..1308186,3	MCF-7	breast:
22	chr20:1205252..1207423-chr20:1288622..1291157,2	K562	blood:
23	chr20:1196637..1198683-chr20:1279227..1282045,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNPH-3	chr20:1291041-1291229	NONHSAT078097
2	lnc-SNPH-3	chr20:1290266-1290556	NONHSAT078097

Variant related genes	Relation type
SDCBP2	TF binding region
SDCBP2	CpG island
ENSG00000234684	chromatin interactions
ENSG00000088832	chromatin interactions
ENSG00000244588	chromatin interactions
ENSG00000125775	chromatin interactions
ENSG00000088833	chromatin interactions

Extended variants
information (count: 937 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:937 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4814078	chr20:1278770-1278771	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73073684	chr20:1278780-1278781	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186594477	chr20:1278842-1278843	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537450431	chr20:1278864-1278865	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569618971	chr20:1278887-1278888	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150752436	chr20:1278925-1278926	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7354581	chr20:1278958-1278959	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534403338	chr20:1278969-1278970	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529176008	chr20:1278974-1278975	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542947390	chr20:1279035-1279036	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559922481	chr20:1279036-1279037	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112179953	chr20:1279054-1279055	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573339215	chr20:1279108-1279109	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545546825	chr20:1279115-1279116	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190578398	chr20:1279158-1279159	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs117870485	chr20:1279189-1279190	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535150420	chr20:1279251-1279252	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549249674	chr20:1279252-1279253	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs561260702	chr20:1279283-1279284	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs34554664	chr20:1279306-1279307	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373960328	chr20:1279328-1279329	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs386811599	chr20:1279336-1279337	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs6041234	chr20:1279337-1279338	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534919114	chr20:1279340-1279341	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200421186	chr20:1279434-1279435	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552301569	chr20:1279441-1279442	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs146310808	chr20:1279449-1279450	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs58322191	chr20:1279478-1279479	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs60327946	chr20:1279482-1279483	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs3038999	chr20:1279489-1279490	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs34011198	chr20:1279496-1279497	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs397821289	chr20:1279507-1279508	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs568619630	chr20:1279510-1279511	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537538357	chr20:1279536-1279537	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs6033366	chr20:1279640-1279641	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574452811	chr20:1279645-1279646	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs567694722	chr20:1279662-1279663	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536984711	chr20:1279677-1279678	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs182978339	chr20:1279686-1279687	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573452922	chr20:1279750-1279751	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs74486267	chr20:1279758-1279759	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs6041238	chr20:1279788-1279789	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs137978281	chr20:1279791-1279792	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs116826910	chr20:1279796-1279797	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs561295602	chr20:1279806-1279807	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs114688538	chr20:1279808-1279809	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs540588285	chr20:1279816-1279817	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs149473762	chr20:1279833-1279834	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs532394109	chr20:1279887-1279888	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs552126317	chr20:1279943-1279944	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	17363583	CNVD
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:737 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1248200-1281200	Weak transcription	NHEK	skin
2	chr20:1249000-1281400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr20:1253800-1285400	Weak transcription	Aorta	Aorta
4	chr20:1256800-1281400	Weak transcription	Esophagus	oesophagus
5	chr20:1261400-1278800	Weak transcription	NHLF	lung
6	chr20:1265600-1280400	Weak transcription	K562	blood
7	chr20:1266400-1284800	Weak transcription	Brain Germinal Matrix	brain
8	chr20:1267200-1281400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr20:1267400-1281000	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr20:1267600-1281200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr20:1267800-1281000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr20:1268200-1280600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr20:1268200-1280800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr20:1269200-1283600	Weak transcription	Right Ventricle	heart
15	chr20:1269400-1283200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr20:1271800-1280000	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr20:1271800-1280200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr20:1271800-1280400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr20:1272200-1280000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr20:1272200-1280200	Weak transcription	Fetal Thymus	thymus
21	chr20:1272200-1285400	Weak transcription	Adipose Nuclei	Adipose
22	chr20:1272200-1285400	Weak transcription	Left Ventricle	heart
23	chr20:1272200-1286000	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr20:1272400-1281200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr20:1272400-1281200	Weak transcription	Osteobl	bone
26	chr20:1272400-1285800	Weak transcription	Fetal Muscle Leg	muscle
27	chr20:1272600-1279600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr20:1272600-1294000	Weak transcription	Rectal Smooth Muscle	rectum
29	chr20:1272800-1281200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr20:1272800-1283400	Weak transcription	HSMMtube	muscle
31	chr20:1273000-1281200	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr20:1273000-1294000	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr20:1273800-1280200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr20:1274400-1280000	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr20:1274600-1282200	Strong transcription	Stomach Smooth Muscle	stomach
36	chr20:1274800-1280400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr20:1274800-1280600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr20:1274800-1288200	Weak transcription	Fetal Intestine Small	intestine
39	chr20:1275000-1280200	Weak transcription	Gastric	stomach
40	chr20:1275000-1289400	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr20:1275200-1279600	Weak transcription	Fetal Muscle Trunk	muscle
42	chr20:1275400-1280400	Weak transcription	Brain Hippocampus Middle	brain
43	chr20:1275400-1284000	Weak transcription	Pancreas	Pancrea
44	chr20:1275800-1285400	Weak transcription	Duodenum Mucosa	Duodenum
45	chr20:1275800-1293800	Weak transcription	Brain Substantia Nigra	brain
46	chr20:1276000-1280000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr20:1276000-1280800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr20:1276200-1281000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr20:1276600-1289800	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr20:1276800-1279000	Strong transcription	Brain Cingulate Gyrus	brain

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