Variant report

Variant	nsv912589
Chromosome Location	chr20:1272686-1298397
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	chr20:1289999-1290199	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr20:1294067-1294472	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	chr20:1294195-1294496	K562	blood:	n/a	n/a
8	BHLHE40	chr20:1294180-1294466	GM12878	blood:	n/a	n/a
9	BHLHE40	chr20:1285433-1285717	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	chr20:1294308-1294363	GM12878	blood:	n/a	n/a
15	CHD1	chr20:1294284-1294436	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr20:1294131-1294336	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr20:1290127-1290213	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr20:1280276-1280452	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr20:1291122-1291228	HepG2	liver:	n/a	n/a
20	CHD2	chr20:1294008-1294452	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr20:1294106-1294254	HepG2	liver:	n/a	n/a
22	CTCF	chr20:1280169-1280467	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr20:1294240-1294390	HCPEpiC	choroid plexus:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
24	CTCF	chr20:1280220-1280370	A549	lung:	n/a	n/a
25	CTCF	chr20:1293876-1294671	HCT-116	colon:	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
26	CTCF	chr20:1294220-1294370	GM12869	blood:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
27	CTCF	chr20:1294177-1294178	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr20:1280260-1280410	HCT-116	colon:	n/a	n/a
29	CTCF	chr20:1280260-1280410	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr20:1280260-1280410	GM12866	blood:	n/a	n/a
31	CTCF	chr20:1294220-1294370	GM12867	blood:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
32	CTCF	chr20:1294240-1294390	SK-N-SH_RA	brain:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
33	CTCF	chr20:1294260-1294410	GM12878	blood:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
34	CTCF	chr20:1293910-1294559	HepG2	liver:	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
35	CTCF	chr20:1293929-1294445	K562	blood:	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
36	CTCF	chr20:1294220-1294370	BE2_C	brain:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
37	CTCF	chr20:1280291-1280473	K562	blood:	n/a	n/a
38	CTCF	chr20:1294135-1294467	Kidney_OC	kidney:	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	chr20:1294240-1294390	AG09309	skin:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
40	CTCF	chr20:1290000-1290150	GM12869	blood:	n/a	n/a
41	CTCF	chr20:1294199-1294451	A549	lung:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
42	CTCF	chr20:1290080-1290230	Caco-2	colon:	n/a	chr20:1290141-1290162 chr20:1290146-1290164
43	CTCF	chr20:1280380-1280530	HFF	foreskin:	n/a	n/a
44	CTCF	chr20:1285500-1285650	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr20:1290073-1290167	Medullo	brain:	n/a	chr20:1290141-1290162 chr20:1290146-1290164
46	CTCF	chr20:1293975-1294482	HepG2	liver:	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
47	CTCF	chr20:1290057-1290302	H1-hESC	embryonic stem cell:	n/a	chr20:1290141-1290162 chr20:1290146-1290164
48	CTCF	chr20:1294260-1294410	HCM	heart:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
49	CTCF	chr20:1294240-1294390	HRE	kidney:	n/a	chr20:1294318-1294328 chr20:1294315-1294336 chr20:1294314-1294330 chr20:1294316-1294325 chr20:1294313-1294331
50	CTCF	chr20:1280420-1280570	HFF-Myc	foreskin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1294021-1294071	GM12878	blood:	n/a
2	chr20:1294311-1294361	HRE	kidney:	n/a
3	chr20:1283388-1283438	HMEC	breast:	n/a
4	chr20:1286558-1286608	HL-60	blood:	n/a
5	chr20:1294021-1294071	GM12878	blood:	n/a
6	chr20:1294311-1294361	HRE	kidney:	n/a
7	chr20:1283388-1283438	HMEC	breast:	n/a
8	chr20:1286558-1286608	HL-60	blood:	n/a
9	chr20:1289571-1289621	SK-N-SH_RA	brain:	n/a
10	chr20:1294376-1294426	ECC-1	luminal epithelium:	n/a
11	chr20:1294311-1294361	BE2_C	brain:	n/a
12	chr20:1294361-1294411	SKMC	muscle:	n/a
13	chr20:1294361-1294411	HCT-116	colon:	n/a
14	chr20:1294311-1294361	Caco-2	colon:	n/a
15	chr20:1294858-1294908	RPTEC	kidney:	n/a
16	chr20:1297651-1297701	Hepatocyte	liver:	n/a
17	chr20:1286558-1286608	GM12892	blood:	n/a
18	chr20:1294814-1294864	T-47D	breast:	n/a
19	chr20:1285816-1285866	SK-N-SH_RA	brain:	n/a
20	chr20:1294313-1294363	ECC-1	luminal epithelium:	n/a
21	chr20:1286630-1286680	NHDF-neo	bronchial:	n/a
22	chr20:1294361-1294411	ECC-1	luminal epithelium:	n/a
23	chr20:1290724-1290774	U87	brain:	n/a
24	chr20:1294301-1294351	NT2-D1	testis:	n/a
25	chr20:1294021-1294071	SAEC	small airway:	n/a
26	chr20:1294021-1294071	SK-N-MC	brain:	n/a
27	chr20:1287050-1287100	Hela-S3	cervix:	n/a
28	chr20:1275312-1275362	ovcar-3	ovarian:	n/a
29	chr20:1285816-1285866	NHDF-neo	bronchial:	n/a
30	chr20:1289571-1289621	GM12891	blood:	n/a
31	chr20:1294814-1294864	RPTEC	kidney:	n/a
32	chr20:1294313-1294363	NH-A	brain:	n/a
33	chr20:1276904-1276954	AG09309	skin:	n/a
34	chr20:1275425-1275475	HUVEC	blood vessel:	n/a
35	chr20:1277001-1277051	BJ	skin:	n/a
36	chr20:1286630-1286680	BJ	skin:	n/a
37	chr20:1294313-1294363	HCT-116	colon:	n/a
38	chr20:1289571-1289621	HCPEpiC	choroid plexus:	n/a
39	chr20:1294311-1294361	HCT-116	colon:	n/a
40	chr20:1280341-1280391	PFSK-1	brain:	n/a
41	chr20:1285816-1285866	RPTEC	kidney:	n/a
42	chr20:1294313-1294363	HIPEpiC	eye:	n/a
43	chr20:1294814-1294864	HCPEpiC	choroid plexus:	n/a
44	chr20:1294814-1294864	HAEpiC	amniotic membrane:	n/a
45	chr20:1280341-1280391	SK-N-MC	brain:	n/a
46	chr20:1277001-1277051	RPTEC	kidney:	n/a
47	chr20:1272984-1273034	GM12892	blood:	n/a
48	chr20:1294311-1294361	HCF	heart:	n/a
49	chr20:1277043-1277093	HCF	heart:	n/a
50	chr20:1294858-1294908	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr20:1261527..1264873-chr20:1277243..1279340,3	K562	blood:
2	chr20:1282248..1284954-chr20:1288783..1291101,2	MCF-7	breast:
3	chr20:1296607..1299079-chr20:1367748..1369670,2	K562	blood:
4	chr20:1274563..1276619-chr20:1279112..1281898,2	K562	blood:
5	chr20:1271210..1274105-chr20:1276784..1280464,4	K562	blood:
6	chr1:33005017..33005864-chr20:1276425..1276945,3	HCT-116	colon:
7	chr20:1280644..1283563-chr20:1283914..1285559,2	MCF-7	breast:
8	chr20:1283698..1286846-chr20:1286878..1289632,3	K562	blood:
9	chr20:1275541..1277248-chr20:1306085..1307627,2	K562	blood:
10	chr20:1293745..1297831-chr20:1304825..1308186,3	MCF-7	breast:
11	chr20:1279418..1283217-chr20:1283449..1287758,5	K562	blood:
12	chr20:1271210..1274105-chr20:1276784..1280464,4	K562	blood:
13	chr20:1274563..1276619-chr20:1279112..1281898,2	K562	blood:
14	chr20:1205252..1207423-chr20:1288622..1291157,2	K562	blood:
15	chr20:1205295..1208138-chr20:1282456..1285112,2	K562	blood:
16	chr20:1280644..1283563-chr20:1283914..1285559,2	MCF-7	breast:
17	chr20:1272392..1273936-chr20:1275888..1278512,2	K562	blood:
18	chr20:1272718..1276817-chr20:1277279..1280817,5	MCF-7	breast:
19	chr20:1292210..1295153-chr20:1372716..1374404,2	MCF-7	breast:
20	chr20:1272718..1276817-chr20:1277279..1280817,5	MCF-7	breast:
21	chr20:1282248..1284954-chr20:1288783..1291101,2	MCF-7	breast:
22	chr20:1281423..1283535-chr20:1306063..1308157,2	K562	blood:
23	chr20:1283698..1286846-chr20:1286878..1289632,3	K562	blood:
24	chr20:1279418..1283217-chr20:1283449..1287758,5	K562	blood:
25	chr20:1286013..1291003-chr20:1304965..1309000,4	K562	blood:
26	chr20:1296232..1299079-chr20:1367748..1370124,3	K562	blood:
27	chr20:1279250..1281881-chr20:1447982..1450441,2	K562	blood:
28	chr20:1196637..1198683-chr20:1279227..1282045,2	K562	blood:
29	chr20:1285641..1287786-chr20:1289716..1291902,2	K562	blood:
30	chr20:1272392..1273936-chr20:1275888..1278512,2	K562	blood:

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

Variant related genes	Relation type
SDCBP2	TF binding region
SDCBP2	CpG island
ENSG00000088832	chromatin interactions
ENSG00000125775	chromatin interactions
ENSG00000244588	chromatin interactions
ENSG00000234684	chromatin interactions
ENSG00000088833	chromatin interactions
ENSG00000160062	chromatin interactions

Extended variants
information (count: 1185 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1185 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs912107	chr20:1272686-1272687	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs912106	chr20:1272718-1272719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4813077	chr20:1272734-1272735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570402312	chr20:1272764-1272765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542950181	chr20:1272797-1272798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs3038996	chr20:1272815-1272816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs33968962	chr20:1272816-1272817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs397688836	chr20:1272819-1272820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374524145	chr20:1272820-1272821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368644998	chr20:1272821-1272822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34065876	chr20:1272884-1272885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559638294	chr20:1272907-1272908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528729696	chr20:1272936-1272937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182408713	chr20:1272962-1272963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187144135	chr20:1272985-1272986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143696132	chr20:1273046-1273047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549505457	chr20:1273060-1273061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550795646	chr20:1273088-1273089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148091822	chr20:1273089-1273090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6109303	chr20:1273096-1273097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530103437	chr20:1273111-1273112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6109304	chr20:1273155-1273156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141833572	chr20:1273198-1273199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs6109306	chr20:1273224-1273225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116274571	chr20:1273233-1273234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs744840	chr20:1273265-1273266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552389388	chr20:1273268-1273269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2077304	chr20:1273270-1273271	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs537972654	chr20:1273339-1273340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554226978	chr20:1273350-1273351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34210731	chr20:1273354-1273355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375147445	chr20:1273356-1273357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74831328	chr20:1273477-1273478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377154692	chr20:1273485-1273486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533849258	chr20:1273511-1273512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553482999	chr20:1273518-1273519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138085020	chr20:1273529-1273530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553302945	chr20:1273532-1273533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142601423	chr20:1273570-1273571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201769459	chr20:1273584-1273585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192480430	chr20:1273605-1273606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs79087076	chr20:1273616-1273617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539094807	chr20:1273642-1273643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140098230	chr20:1273660-1273661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575729375	chr20:1273669-1273670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574925984	chr20:1273706-1273707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4814066	chr20:1273711-1273712	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs34713476	chr20:1273740-1273741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530189790	chr20:1273803-1273804	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79058087	chr20:1273859-1273860	Weak transcription Strong transcription Enhancers	n/a	n/a	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:821 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1248000-1278600	Weak transcription	Spleen	Spleen
2	chr20:1248200-1277400	Weak transcription	Fetal Stomach	stomach
3	chr20:1248200-1281200	Weak transcription	NHEK	skin
4	chr20:1249000-1281400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr20:1253000-1274800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr20:1253800-1285400	Weak transcription	Aorta	Aorta
7	chr20:1256000-1277800	Weak transcription	Fetal Brain Female	brain
8	chr20:1256400-1277400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr20:1256800-1281400	Weak transcription	Esophagus	oesophagus
10	chr20:1261400-1278800	Weak transcription	NHLF	lung
11	chr20:1262400-1272800	Weak transcription	Right Atrium	heart
12	chr20:1263200-1276200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr20:1264200-1273400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr20:1264800-1274800	Weak transcription	Gastric	stomach
15	chr20:1265400-1277800	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr20:1265600-1280400	Weak transcription	K562	blood
17	chr20:1266400-1284800	Weak transcription	Brain Germinal Matrix	brain
18	chr20:1267200-1281400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr20:1267400-1281000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr20:1267600-1281200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr20:1267800-1281000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr20:1268200-1280600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr20:1268200-1280800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr20:1268400-1274600	Weak transcription	Stomach Smooth Muscle	stomach
25	chr20:1268600-1278000	Weak transcription	Primary T cells from cord blood	blood
26	chr20:1269000-1274400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr20:1269200-1274200	Weak transcription	Brain Cingulate Gyrus	brain
28	chr20:1269200-1277600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr20:1269200-1283600	Weak transcription	Right Ventricle	heart
30	chr20:1269400-1283200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr20:1271000-1272800	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr20:1271000-1273600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr20:1271400-1273000	Enhancers	Brain Anterior Caudate	brain
34	chr20:1271400-1274600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr20:1271600-1272800	Enhancers	HSMM	muscle
36	chr20:1271600-1272800	Enhancers	HSMMtube	muscle
37	chr20:1271600-1273000	Enhancers	Muscle Satellite Cultured Cells	--
38	chr20:1271600-1273000	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr20:1271600-1273400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr20:1271600-1273400	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr20:1271600-1275200	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr20:1271600-1275800	Enhancers	Brain Angular Gyrus	brain
43	chr20:1271800-1280000	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr20:1271800-1280200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr20:1271800-1280400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr20:1272000-1272800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr20:1272000-1273600	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr20:1272200-1274200	Weak transcription	Pancreas	Pancrea
49	chr20:1272200-1280000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr20:1272200-1280200	Weak transcription	Fetal Thymus	thymus

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