Variant report

Variant	esv2751914
Chromosome Location	chr20:41744586-41890453
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:977)
CpG islands
(count:976)
Chromatin interactive
region (count:30)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:41816377-41816695	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:41816403-41816671	K562	blood:	n/a	n/a
3	ARID3A	chr20:41767058-41767218	HepG2	liver:	n/a	n/a
4	ATF3	chr20:41867500-41867825	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr20:41867573-41867779	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr20:41867526-41867815	GM12878	blood:	n/a	n/a
7	ATF3	chr20:41867540-41867771	K562	blood:	n/a	n/a
8	BACH1	chr20:41817618-41817818	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr20:41827269-41827705	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr20:41820686-41820961	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr20:41818772-41819165	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr20:41834788-41835095	GM12878	blood:	n/a	chr20:41834913-41834922
13	BATF	chr20:41834770-41835045	GM12878	blood:	n/a	chr20:41834913-41834922
14	BCL3	chr20:41830817-41831026	GM12878	blood:	n/a	n/a
15	BCL3	chr20:41832137-41832351	GM12878	blood:	n/a	n/a
16	BHLHE40	chr20:41816417-41816700	GM12878	blood:	n/a	n/a
17	BRCA1	chr20:41816564-41816702	HepG2	liver:	n/a	n/a
18	BRCA1	chr20:41816481-41816725	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr20:41752864-41753060	HepG2	liver:	n/a	chr20:41752931-41752942
20	CEBPB	chr20:41839547-41839860	A549	lung:	n/a	chr20:41839683-41839694
21	CEBPB	chr20:41790474-41790761	HepG2	liver:	n/a	chr20:41790641-41790652
22	CEBPB	chr20:41794198-41794422	A549	lung:	n/a	n/a
23	CEBPB	chr20:41839565-41839828	HepG2	liver:	n/a	chr20:41839683-41839694
24	CEBPB	chr20:41818934-41819178	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr20:41813986-41814119	HepG2	liver:	n/a	chr20:41814088-41814101
26	CEBPB	chr20:41816312-41816697	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr20:41773257-41773543	HepG2	liver:	n/a	chr20:41773388-41773399
28	CHD2	chr20:41816411-41816727	HepG2	liver:	n/a	n/a
29	CHD2	chr20:41816422-41816725	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTBP2	chr20:41817711-41818431	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr20:41820632-41820956	MCF-7	breast:	n/a	n/a
32	CTCF	chr20:41820522-41820994	MCF-7	breast:	n/a	n/a
33	CTCF	chr20:41816140-41816290	Caco-2	colon:	n/a	n/a
34	CTCF	chr20:41834480-41834630	RPTEC	kidney:	n/a	n/a
35	CTCF	chr20:41816460-41816610	HEEpiC	esophagus:	n/a	chr20:41816561-41816574 chr20:41816560-41816576 chr20:41816559-41816577 chr20:41816561-41816574
36	CTCF	chr20:41820720-41820870	HCT-116	colon:	n/a	n/a
37	CTCF	chr20:41820600-41820750	HFF-Myc	foreskin:	n/a	n/a
38	CTCF	chr20:41816424-41816699	ECC-1	luminal epithelium:	n/a	chr20:41816561-41816574 chr20:41816560-41816576 chr20:41816559-41816577 chr20:41816561-41816574
39	CTCF	chr20:41872380-41872530	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr20:41878360-41878510	GM12868	blood:	n/a	n/a
41	CTCF	chr20:41872440-41872590	MCF-7	breast:	n/a	n/a
42	CTCF	chr20:41872440-41872590	RPTEC	kidney:	n/a	n/a
43	CTCF	chr20:41872444-41872574	GM19240	blood:	n/a	n/a
44	CTCF	chr20:41816469-41816717	H1-hESC	embryonic stem cell:	n/a	chr20:41816561-41816574 chr20:41816560-41816576 chr20:41816559-41816577 chr20:41816561-41816574
45	CTCF	chr20:41872455-41872562	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr20:41820700-41820850	AG04449	skin:	n/a	n/a
47	CTCF	chr20:41872360-41872510	BE2_C	brain:	n/a	n/a
48	CTCF	chr20:41872380-41872653	LNCaP	prostate:	n/a	n/a
49	CTCF	chr20:41816870-41816885	ProgFib	skin:	n/a	n/a
50	CTCF	chr20:41820720-41820870	SK-N-SH_RA	brain:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:41817476-41817526	HEEpiC	esophagus:	n/a
2	chr20:41820798-41820848	GM06990	blood:	n/a
3	chr20:41818905-41818955	GM19239	blood:	n/a
4	chr20:41823021-41823071	SK-N-SH	brain:	n/a
5	chr20:41814797-41814847	SKMC	muscle:	n/a
6	chr20:41817476-41817526	AG10803	skin:	n/a
7	chr20:41817903-41817953	BE2_C	brain:	n/a
8	chr20:41820798-41820848	PrEC	prostate:	n/a
9	chr20:41818356-41818406	AoSMC	blood vessel:	n/a
10	chr20:41819125-41819175	MCF10A-Er-Src	breast:	n/a
11	chr20:41818574-41818624	AoSMC	blood vessel:	n/a
12	chr20:41823021-41823071	GM19239	blood:	n/a
13	chr20:41818574-41818624	BE2_C	brain:	n/a
14	chr20:41817476-41817526	LNCaP	prostate:	n/a
15	chr20:41818788-41818838	LNCaP	prostate:	n/a
16	chr20:41818905-41818955	HNPCEpiC	eye:	n/a
17	chr20:41818788-41818838	GM19239	blood:	n/a
18	chr20:41817903-41817953	NB4	blood:	n/a
19	chr20:41817903-41817953	Caco-2	colon:	n/a
20	chr20:41819125-41819175	Hepatocyte	liver:	n/a
21	chr20:41817476-41817526	NH-A	brain:	n/a
22	chr20:41818788-41818838	SKMC	muscle:	n/a
23	chr20:41818788-41818838	HCT-116	colon:	n/a
24	chr20:41818756-41818806	CMK	blood:	n/a
25	chr20:41873421-41873471	T-47D	breast:	n/a
26	chr20:41818574-41818624	HAEpiC	amniotic membrane:	n/a
27	chr20:41817011-41817061	HNPCEpiC	eye:	n/a
28	chr20:41818574-41818624	Hepatocyte	liver:	n/a
29	chr20:41819125-41819175	HEK293	kidney:	embryo
30	chr20:41818905-41818955	ovcar-3	ovarian:	n/a
31	chr20:41817476-41817526	BE2_C	brain:	n/a
32	chr20:41820798-41820848	K562	blood:	n/a
33	chr20:41817903-41817953	SAEC	small airway:	n/a
34	chr20:41818788-41818838	PFSK-1	brain:	n/a
35	chr20:41817801-41817851	HNPCEpiC	eye:	n/a
36	chr20:41873421-41873471	MCF-7	breast:	n/a
37	chr20:41823021-41823071	A549	lung:	n/a
38	chr20:41819125-41819175	PFSK-1	brain:	n/a
39	chr20:41819125-41819175	NT2-D1	testis:	n/a
40	chr20:41873421-41873471	AoSMC	blood vessel:	n/a
41	chr20:41818756-41818806	Jurkat	blood:	n/a
42	chr20:41818356-41818406	HRE	kidney:	n/a
43	chr20:41818756-41818806	LNCaP	prostate:	n/a
44	chr20:41823021-41823071	HL-60	blood:	n/a
45	chr20:41818356-41818406	Hela-S3	cervix:	n/a
46	chr20:41817476-41817526	AG09309	skin:	n/a
47	chr20:41814797-41814847	ovcar-3	ovarian:	n/a
48	chr20:41817011-41817061	BE2_C	brain:	n/a
49	chr20:41820798-41820848	RPTEC	kidney:	n/a
50	chr20:41818358-41818408	GM19239	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:41818061..41819755-chr20:41823894..41826162,2	K562	blood:
2	chr20:41825220..41828068-chr20:41830459..41832964,3	K562	blood:
3	chr20:41866721..41868759-chr20:41869246..41871076,2	MCF-7	breast:
4	chr11:5415584..5416428-chr20:41864268..41865032,2	MCF-7	breast:
5	chr20:41810992..41813382-chr20:41815861..41818440,2	K562	blood:
6	chr20:41866721..41868759-chr20:41869246..41871076,2	MCF-7	breast:
7	chr20:40832079..40832639-chr20:41816078..41817042,2	K562	blood:
8	chr20:41403662..41404501-chr20:41816400..41817064,2	MCF-7	breast:
9	chr20:41820316..41821010-chr20:42037578..42038228,2	MCF-7	breast:
10	chr20:41840392..41842138-chr20:41842650..41845553,2	K562	blood:
11	chr1:202926944..202927808-chr20:41777619..41778619,3	Hela-S3	cervix:
12	chr20:41834519..41836308-chr20:41836344..41837935,2	MCF-7	breast:
13	chr20:40584685..40585561-chr20:41816130..41816774,5	MCF-7	breast:
14	chr20:41834519..41836308-chr20:41836344..41837935,2	MCF-7	breast:
15	chr20:41820295..41821061-chr20:42038025..42038531,2	MCF-7	breast:
16	chr20:40832583..40833565-chr20:41816153..41816980,6	MCF-7	breast:
17	chr20:41826202..41828926-chr20:41833025..41835825,2	K562	blood:
18	chr20:40584767..40585608-chr20:41820301..41820945,3	MCF-7	breast:
19	chr20:41820391..41820963-chr20:41872072..41872972,2	MCF-7	breast:
20	chr20:41859597..41861872-chr20:41912468..41914721,2	K562	blood:
21	chr20:41878436..41880626-chr20:41888938..41891800,2	K562	blood:
22	chr20:41816163..41817038-chr20:42037697..42038566,2	K562	blood:
23	chr20:41878436..41880626-chr20:41888938..41891800,2	K562	blood:
24	chr20:41840392..41842138-chr20:41842650..41845553,2	K562	blood:
25	chr20:41826202..41828926-chr20:41833025..41835825,2	K562	blood:
26	chr20:41873999..41876332-chr20:41880534..41882596,2	K562	blood:
27	chr20:41825220..41828068-chr20:41830459..41832964,3	K562	blood:
28	chr20:41816096..41818389-chr20:41830511..41832144,2	K562	blood:
29	chr20:41820391..41820963-chr20:41872072..41872972,2	MCF-7	breast:
30	chr20:41873999..41876332-chr20:41880534..41882596,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRSF6-7	chr20:41882862-41882991	NONHSAT079813
2	lnc-SRSF6-1	chr20:41818756-41818890	NONHSAT079811
3	lnc-SRSF6-8	chr20:41850846-41851147	NONHSAT079812
4	lnc-SRSF6-7	chr20:41851998-41852097	NONHSAT079813
5	lnc-SRSF6-1	chr20:41829236-41830011	ENSG00000233508.1
6	lnc-SRSF6-1	chr20:41829236-41831231	NONHSAT079811
7	lnc-SRSF6-1	chr20:41818862-41818890	ENSG00000233508.1
8	lnc-SRSF6-7	chr20:41875519-41875633	NONHSAT079813
9	lnc-SRSF6-7	chr20:41874209-41874322	NONHSAT079813
10	lnc-SRSF6-7	chr20:41887606-41888416	NONHSAT079813
11	lnc-SRSF6-7	chr20:41883759-41883831	NONHSAT079813
12	lnc-GTSF1L-7	chr20:41764691-41764922	predAs_ge08_MYBL2_2
13	lnc-SRSF6-7	chr20:41886388-41887469	NONHSAT079813

No data

Variant related genes	Relation type
ENSG00000233508	TF binding region
PPIAP21	TF binding region
PTPRT	TF binding region
RN7SL666P	TF binding region
ENSG00000233508	CpG island
PPIAP21	CpG island
PTPRT	CpG island
RN7SL666P	CpG island
ENSG00000159346	chromatin interactions
ENSG00000196090	chromatin interactions
ENSG00000233508	chromatin interactions

Extended variants
information (count: 5136 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:5136 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16987782	chr20:41744589-41744590	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138497235	chr20:41744590-41744591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559415913	chr20:41744651-41744652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552232231	chr20:41744695-41744696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190044885	chr20:41744735-41744736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528340359	chr20:41744742-41744743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375980008	chr20:41744791-41744792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533101516	chr20:41744803-41744804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568158322	chr20:41744825-41744826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536885174	chr20:41744877-41744878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112582447	chr20:41744907-41744908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183370809	chr20:41744923-41744924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74765087	chr20:41744954-41744955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538766738	chr20:41744985-41744986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558642137	chr20:41745033-41745034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370911155	chr20:41745034-41745035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572411941	chr20:41745044-41745045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188356624	chr20:41745047-41745048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552883503	chr20:41745119-41745120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555293207	chr20:41745133-41745134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs8123075	chr20:41745159-41745160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544066837	chr20:41745163-41745164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs16987784	chr20:41745198-41745199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369764050	chr20:41745221-41745222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576984950	chr20:41745244-41745245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566335646	chr20:41745299-41745300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192038471	chr20:41745318-41745319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147330002	chr20:41745333-41745334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183666829	chr20:41745387-41745388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs139447542	chr20:41745399-41745400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562048361	chr20:41745403-41745404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187914181	chr20:41745428-41745429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550333457	chr20:41745458-41745459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570325615	chr20:41745474-41745475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546706934	chr20:41745476-41745477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6030659	chr20:41745491-41745492	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552642273	chr20:41745499-41745500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373244494	chr20:41745509-41745510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568415110	chr20:41745519-41745520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565929134	chr20:41745528-41745529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149667164	chr20:41745565-41745566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191323382	chr20:41745667-41745668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575241949	chr20:41745707-41745708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144472814	chr20:41745758-41745759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs557556420	chr20:41745767-41745768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78601689	chr20:41745770-41745771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545534978	chr20:41745781-41745782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557359964	chr20:41745791-41745792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569446342	chr20:41745856-41745857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572732967	chr20:41745857-41745858	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	21645411	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	21693616	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Ovarian cancer	19193619	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelodysplastic syndrome	17634407	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ductal carcinoma	22052326	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Malignant melanoma	17260012	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Colorectal cancer	16774939	CNVD
Cervical cancer	21062161	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	20585902	CNVD
Ductal carcinoma	18381933	CNVD
Cancer	21129771	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	20864512	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	22860045	CNVD
Cervical cancer	16585170	CNVD
Developmental delay	21373258	CNVD
Breast cancer	21806811	CNVD
Mental retardation	17901693	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Barrett''s esophagus	18559552	CNVD
Renal cell carcinoma	18765545	CNVD
Lung cancer	16740712	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Anaplastic thyroid cancer	18753363	CNVD

Chromatin state (count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41744200-41746600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr20:41746600-41748200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr20:41747400-41752800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr20:41748200-41750000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr20:41750000-41751800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr20:41751800-41752400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr20:41752000-41752400	Enhancers	Fetal Stomach	stomach
8	chr20:41752400-41754200	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr20:41752600-41753600	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr20:41752800-41753400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr20:41753000-41753400	Enhancers	Fetal Brain Male	brain
12	chr20:41753600-41763800	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr20:41754200-41759400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr20:41759400-41760000	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr20:41760000-41766200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr20:41762600-41762800	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr20:41762600-41763200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr20:41762800-41763000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr20:41762800-41763600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr20:41763600-41763800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr20:41763600-41764400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr20:41763800-41767000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr20:41764200-41765400	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr20:41764200-41767400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr20:41764400-41764800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr20:41764400-41765000	Enhancers	Fetal Stomach	stomach
27	chr20:41764800-41771400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr20:41766200-41767200	Enhancers	Brain Anterior Caudate	brain
29	chr20:41766200-41767600	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr20:41766200-41769200	Enhancers	Brain Substantia Nigra	brain
31	chr20:41766400-41766600	Enhancers	Fetal Brain Male	brain
32	chr20:41766400-41767200	Enhancers	Brain Cingulate Gyrus	brain
33	chr20:41766400-41767400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
34	chr20:41766400-41767600	Enhancers	Brain Hippocampus Middle	brain
35	chr20:41766600-41767000	Enhancers	Placenta	Placenta
36	chr20:41766600-41768200	Weak transcription	Fetal Brain Male	brain
37	chr20:41766800-41767000	Bivalent Enhancer	Fetal Stomach	stomach
38	chr20:41766800-41767400	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr20:41766800-41767400	Flanking Bivalent TSS/Enh	HepG2	liver
40	chr20:41767000-41767600	Enhancers	Fetal Intestine Large	intestine
41	chr20:41767000-41768400	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr20:41767200-41768400	Weak transcription	Fetal Stomach	stomach
43	chr20:41767200-41775000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr20:41767400-41767800	Bivalent Enhancer	HepG2	liver
45	chr20:41767400-41768000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr20:41767400-41768200	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr20:41767600-41768800	Weak transcription	Brain Hippocampus Middle	brain
48	chr20:41767600-41772400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr20:41768000-41770000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr20:41768200-41768400	Enhancers	Brain Inferior Temporal Lobe	brain

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