Variant report

Variant	esv15775
Chromosome Location	chr20:23955662-23977093
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	chr20:23976814-23977193	HepG2	liver:	n/a	n/a
2	BATF	chr20:23965266-23965679	GM12878	blood:	n/a	n/a
3	BCL11A	chr20:23959204-23959390	GM12878	blood:	n/a	chr20:23959323-23959332
4	BCL11A	chr20:23959584-23959850	GM12878	blood:	n/a	n/a
5	BCL11A	chr20:23965025-23965194	GM12878	blood:	n/a	n/a
6	BCL11A	chr20:23965421-23965603	GM12878	blood:	n/a	n/a
7	BCL11A	chr20:23970694-23970943	GM12878	blood:	n/a	n/a
8	BCL11A	chr20:23957003-23957211	GM12878	blood:	n/a	n/a
9	BCL3	chr20:23960521-23961246	GM12878	blood:	n/a	chr20:23960654-23960662
10	BCL3	chr20:23960441-23961293	GM12878	blood:	n/a	chr20:23960654-23960662
11	BHLHE40	chr20:23976881-23977143	GM12878	blood:	n/a	n/a
12	CEBPB	chr20:23961806-23961982	HepG2	liver:	n/a	n/a
13	CEBPB	chr20:23961774-23962025	HepG2	liver:	n/a	n/a
14	CTCF	chr20:23976854-23977003	K562	blood:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
15	CTCF	chr20:23968647-23968745	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr20:23959280-23959430	GM12873	blood:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
17	CTCF	chr20:23965300-23965539	MCF-7	breast:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
18	CTCF	chr20:23965285-23965542	Pancreas_OC	pancreas:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
19	CTCF	chr20:23976900-23977050	Hela-S3	cervix:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
20	CTCF	chr20:23976860-23977010	HAc	cerebellar:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
21	CTCF	chr20:23976877-23977171	MCF-7	breast:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
22	CTCF	chr20:23965314-23965525	ProgFib	skin:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
23	CTCF	chr20:23965300-23965537	MCF-7	breast:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
24	CTCF	chr20:23965200-23965350	HMEC	breast:	n/a	chr20:23965234-23965243
25	CTCF	chr20:23965296-23965543	H1-hESC	embryonic stem cell:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
26	CTCF	chr20:23976840-23976990	RPTEC	kidney:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
27	CTCF	chr20:23976900-23977050	HCT-116	colon:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
28	CTCF	chr20:23965260-23965410	GM12864	blood:	n/a	n/a
29	CTCF	chr20:23976900-23977050	GM12869	blood:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
30	CTCF	chr20:23976920-23977070	HPF	lung:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
31	CTCF	chr20:23965420-23965570	HMEC	breast:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965421-23965431
32	CTCF	chr20:23976875-23977132	Lung_OC	lung:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
33	CTCF	chr20:23965220-23965370	Caco-2	colon:	n/a	chr20:23965234-23965243
34	CTCF	chr20:23959285-23959486	HUVEC	blood vessel:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
35	CTCF	chr20:23959320-23959470	A549	lung:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
36	CTCF	chr20:23965260-23965410	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr20:23959320-23959470	MCF-7	breast:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
38	CTCF	chr20:23976866-23977157	GM12878	blood:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
39	CTCF	chr20:23976940-23977090	NHEK	skin:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
40	CTCF	chr20:23965149-23965628	K562	blood:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965234-23965243 chr20:23965413-23965434
41	CTCF	chr20:23965336-23965513	LNCaP	prostate:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
42	CTCF	chr20:23976900-23977050	AoAF	blood vessel:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
43	CTCF	chr20:23959304-23959502	GM19238	blood:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959490-23959498 chr20:23959384-23959402 chr20:23959386-23959407
44	CTCF	chr20:23976891-23977054	ECC-1	luminal epithelium:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
45	CTCF	chr20:23959240-23959390	HBMEC	blood vessel:	n/a	chr20:23959276-23959289
46	CTCF	chr20:23959300-23959450	HepG2	liver:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
47	CTCF	chr20:23976940-23977090	HCM	heart:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
48	CTCF	chr20:23976880-23977030	GM12872	blood:	n/a	chr20:23976966-23976984 chr20:23976961-23976982 chr20:23976968-23976981 chr20:23976972-23976981
49	CTCF	chr20:23961901-23961919	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr20:23965220-23965370	GM06990	blood:	n/a	chr20:23965234-23965243

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23965921-23965971	SK-N-SH	brain:	n/a
2	chr20:23972451-23972501	BE2_C	brain:	n/a
3	chr20:23969237-23969287	U87	brain:	n/a
4	chr20:23970065-23970115	LNCaP	prostate:	n/a
5	chr20:23972451-23972501	AG04449	skin:	fetal
6	chr20:23969832-23969882	AG04450	lung:	fetal
7	chr20:23969397-23969447	BE2_C	brain:	n/a
8	chr20:23969237-23969287	HRPEpiC	eye:	n/a
9	chr20:23969432-23969482	A549	lung:	n/a
10	chr20:23969397-23969447	HL-60	blood:	n/a
11	chr20:23970065-23970115	T-47D	breast:	n/a
12	chr20:23970162-23970212	HL-60	blood:	n/a
13	chr20:23969832-23969882	Jurkat	blood:	n/a
14	chr20:23970162-23970212	H1-hESC	embryonic stem cell:	embryo
15	chr20:23969429-23969479	NH-A	brain:	n/a
16	chr20:23969832-23969882	NHDF-neo	bronchial:	n/a
17	chr20:23970162-23970212	HMEC	breast:	n/a
18	chr20:23970162-23970212	BJ	skin:	n/a
19	chr20:23969429-23969479	PFSK-1	brain:	n/a
20	chr20:23969432-23969482	BJ	skin:	n/a
21	chr20:23969832-23969882	HPAEpiC	pulmonary alveolar:	n/a
22	chr20:23965841-23965891	NB4	blood:	n/a
23	chr20:23969429-23969479	ProgFib	skin:	n/a
24	chr20:23965841-23965891	Hela-S3	cervix:	n/a
25	chr20:23969237-23969287	NHBE	bronchial:	n/a
26	chr20:23969429-23969479	HRE	kidney:	n/a
27	chr20:23969397-23969447	ProgFib	skin:	n/a
28	chr20:23965921-23965971	HMEC	breast:	n/a
29	chr20:23965921-23965971	Hela-S3	cervix:	n/a
30	chr20:23970065-23970115	GM12892	blood:	n/a
31	chr20:23970162-23970212	SAEC	small airway:	n/a
32	chr20:23968830-23968880	NB4	blood:	n/a
33	chr20:23972451-23972501	AG10803	skin:	n/a
34	chr20:23969432-23969482	T-47D	breast:	n/a
35	chr20:23969397-23969447	NB4	blood:	n/a
36	chr20:23969832-23969882	RPTEC	kidney:	n/a
37	chr20:23969237-23969287	MCF-7	breast:	n/a
38	chr20:23965841-23965891	HNPCEpiC	eye:	n/a
39	chr20:23965921-23965971	AG04449	skin:	fetal
40	chr20:23970065-23970115	GM19239	blood:	n/a
41	chr20:23965841-23965891	GM12878	blood:	n/a
42	chr20:23969429-23969479	BE2_C	brain:	n/a
43	chr20:23965921-23965971	GM06990	blood:	n/a
44	chr20:23968830-23968880	BE2_C	brain:	n/a
45	chr20:23970162-23970212	NHBE	bronchial:	n/a
46	chr20:23969429-23969479	PrEC	prostate:	n/a
47	chr20:23965841-23965891	HRCEpiC	kidney:	n/a
48	chr20:23969429-23969479	H1-hESC	embryonic stem cell:	embryo
49	chr20:23972451-23972501	NT2-D1	testis:	n/a
50	chr20:23969832-23969882	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23976507..23978682-chr20:23981230..23983499,2	K562	blood:
2	chr20:23917806..23918382-chr20:23976746..23977457,2	MCF-7	breast:
3	chr20:23870254..23870831-chr20:23976722..23977413,2	MCF-7	breast:
4	chr20:23917673..23918874-chr20:23976593..23977514,3	K562	blood:
5	chr20:23870329..23871235-chr20:23976503..23977926,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000236168	TF binding region
GGTLC1	TF binding region
POM121L3P	TF binding region
ENSG00000236168	CpG island
GGTLC1	CpG island
POM121L3P	CpG island

Extended variants
information (count: 886 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:886 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534205205	chr20:23955674-23955675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373209767	chr20:23955694-23955695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567809483	chr20:23955711-23955712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs755031	chr20:23955742-23955743	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs755032	chr20:23955778-23955779	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs541369993	chr20:23955796-23955797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116688839	chr20:23955806-23955807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577653352	chr20:23955817-23955818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543493271	chr20:23955831-23955832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539303296	chr20:23955839-23955840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529416977	chr20:23955848-23955849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs755033	chr20:23955858-23955859	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs566693972	chr20:23955866-23955867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138409756	chr20:23955898-23955899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528788235	chr20:23955918-23955919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73326801	chr20:23955928-23955929	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs571254142	chr20:23955930-23955931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545574160	chr20:23955943-23955944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs118011290	chr20:23955961-23955962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550675092	chr20:23955987-23955988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368280711	chr20:23956021-23956022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs76597862	chr20:23956022-23956023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536404924	chr20:23956044-23956045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552894591	chr20:23956047-23956048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566706882	chr20:23956057-23956058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538546624	chr20:23956064-23956065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374556964	chr20:23956074-23956075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73106893	chr20:23956102-23956103	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs368966944	chr20:23956141-23956142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188850002	chr20:23956153-23956154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573808024	chr20:23956167-23956168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35994874	chr20:23956173-23956174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200569890	chr20:23956208-23956209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543162567	chr20:23956228-23956229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs137893428	chr20:23956259-23956260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544732594	chr20:23956269-23956270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142323582	chr20:23956428-23956429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556567612	chr20:23956445-23956446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs6114392	chr20:23956447-23956448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192863509	chr20:23956450-23956451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs6114393	chr20:23956465-23956466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6049277	chr20:23956475-23956476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372306772	chr20:23956497-23956498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs5841016	chr20:23956510-23956511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs3071374	chr20:23956532-23956533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6114394	chr20:23956534-23956535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143954987	chr20:23956609-23956610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs6114395	chr20:23956612-23956613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs578070917	chr20:23956639-23956640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545334269	chr20:23956717-23956718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23948800-23959000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:23955400-23956000	Enhancers	Fetal Muscle Trunk	muscle
3	chr20:23955800-23956800	Enhancers	Dnd41	blood
4	chr20:23956200-23959000	Weak transcription	Fetal Muscle Trunk	muscle
5	chr20:23956800-23958600	Weak transcription	Dnd41	blood
6	chr20:23958600-23959000	Enhancers	Dnd41	blood
7	chr20:23959000-23959200	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr20:23959000-23959200	Enhancers	Fetal Thymus	thymus
9	chr20:23959000-23959200	Enhancers	Lung	lung
10	chr20:23959000-23959200	Flanking Active TSS	Dnd41	blood
11	chr20:23959000-23959400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr20:23959000-23959400	Enhancers	Primary T cells fromperipheralblood	blood
13	chr20:23959000-23959600	Enhancers	Fetal Stomach	stomach
14	chr20:23959000-23963400	Enhancers	Fetal Muscle Trunk	muscle
15	chr20:23959200-23959400	Enhancers	Dnd41	blood
16	chr20:23959200-23959600	Enhancers	A549	lung
17	chr20:23959200-23960400	Enhancers	Primary B cells from cord blood	blood
18	chr20:23959200-23960800	Enhancers	Primary B cells from peripheral blood	blood
19	chr20:23959400-23959600	Flanking Active TSS	Dnd41	blood
20	chr20:23959400-23960000	Weak transcription	Lung	lung
21	chr20:23959400-23960600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr20:23959400-23962200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr20:23959600-23960000	Weak transcription	Fetal Stomach	stomach
24	chr20:23959600-23960000	Weak transcription	A549	lung
25	chr20:23959600-23961000	Enhancers	Dnd41	blood
26	chr20:23960000-23960200	Enhancers	A549	lung
27	chr20:23960000-23960400	ZNF genes & repeats	Fetal Stomach	stomach
28	chr20:23960000-23960800	Enhancers	Pancreas	Pancrea
29	chr20:23960000-23961400	Active TSS	Lung	lung
30	chr20:23960200-23963200	Weak transcription	A549	lung
31	chr20:23960200-23963400	Enhancers	Fetal Muscle Leg	muscle
32	chr20:23960400-23960600	Enhancers	Fetal Kidney	kidney
33	chr20:23960400-23960600	Enhancers	Fetal Lung	lung
34	chr20:23960400-23960800	Enhancers	Esophagus	oesophagus
35	chr20:23960400-23960800	Weak transcription	Fetal Thymus	thymus
36	chr20:23960400-23963400	Enhancers	Fetal Stomach	stomach
37	chr20:23960600-23960800	Flanking Active TSS	Duodenum Mucosa	Duodenum
38	chr20:23960600-23961200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr20:23960600-23961200	Flanking Active TSS	Fetal Kidney	kidney
40	chr20:23960600-23961200	Flanking Active TSS	Fetal Lung	lung
41	chr20:23960600-23961400	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr20:23960600-23961800	Enhancers	Fetal Heart	heart
43	chr20:23960600-23962400	Enhancers	HepG2	liver
44	chr20:23960800-23961200	ZNF genes & repeats	Esophagus	oesophagus
45	chr20:23960800-23961400	Genic enhancers	Pancreas	Pancrea
46	chr20:23960800-23962000	Enhancers	Right Ventricle	heart
47	chr20:23961000-23961200	Flanking Active TSS	Fetal Brain Male	brain
48	chr20:23961000-23961400	Enhancers	Right Atrium	heart
49	chr20:23961000-23961800	Enhancers	Fetal Thymus	thymus
50	chr20:23961000-23962800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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