Variant report

Variant	nsv909518
Chromosome Location	chr18:29009409-29049018
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	chr18:29016896-29016955	HepG2	liver:	n/a	n/a
2	ATF1	chr18:29043383-29043412	K562	blood:	n/a	n/a
3	ATF2	chr18:29018383-29018706	GM12878	blood:	n/a	n/a
4	ATF2	chr18:29018291-29018807	GM12878	blood:	n/a	n/a
5	BATF	chr18:29018346-29018766	GM12878	blood:	n/a	n/a
6	BATF	chr18:29018420-29018737	GM12878	blood:	n/a	n/a
7	BCL11A	chr18:29018405-29018782	GM12878	blood:	n/a	n/a
8	BCL3	chr18:29018340-29018768	GM12878	blood:	n/a	n/a
9	CBX3	chr18:29033979-29034622	HCT-116	colon:	n/a	n/a
10	CBX3	chr18:29034067-29034484	HCT-116	colon:	n/a	n/a
11	CEBPB	chr18:29026954-29028137	K562	blood:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027139-29027150 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027139-29027150 chr18:29027957-29027970
12	CEBPB	chr18:29025928-29026244	K562	blood:	n/a	n/a
13	CEBPB	chr18:29019860-29020209	IMR90	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
14	CEBPB	chr18:29027850-29028050	Hela-S3	cervix:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027957-29027970
15	CEBPB	chr18:29027614-29028137	HepG2	liver:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027957-29027970
16	CEBPB	chr18:29019854-29020182	A549	lung:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
17	CEBPB	chr18:29034088-29034345	A549	lung:	n/a	n/a
18	CEBPB	chr18:29019855-29020147	K562	blood:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
19	CEBPB	chr18:29019853-29020186	HepG2	liver:	n/a	chr18:29020036-29020049 chr18:29020038-29020047 chr18:29020036-29020047 chr18:29020037-29020048
20	CEBPB	chr18:29027491-29028085	H1-hESC	embryonic stem cell:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027957-29027970
21	CEBPB	chr18:29027824-29028093	A549	lung:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027957-29027970
22	CEBPB	chr18:29034023-29034597	HCT-116	colon:	n/a	chr18:29034579-29034590
23	CEBPB	chr18:29027821-29028120	IMR90	lung:	n/a	chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027970 chr18:29027959-29027970 chr18:29027959-29027968 chr18:29027959-29027968 chr18:29027957-29027968 chr18:29027957-29027970
24	CHD2	chr18:29018582-29018611	GM12878	blood:	n/a	n/a
25	CTCF	chr18:29016920-29017070	Caco-2	colon:	n/a	n/a
26	CTCF	chr18:29016980-29017130	HMEC	breast:	n/a	n/a
27	CTCF	chr18:29016900-29017050	Caco-2	colon:	n/a	n/a
28	CTCF	chr18:29016901-29017147	MCF-7	breast:	n/a	n/a
29	CTCF	chr18:29016926-29017083	HepG2	liver:	n/a	n/a
30	CTCF	chr18:29031660-29031810	BJ	skin:	n/a	n/a
31	CTCF	chr18:29026665-29026744	GM10248	blood:	n/a	n/a
32	CTCF	chr18:29016954-29017116	K562	blood:	n/a	n/a
33	CTCF	chr18:29016966-29017112	MCF-7	breast:	n/a	n/a
34	CTCF	chr18:29016991-29017055	MCF-7	breast:	n/a	n/a
35	CTCF	chr18:29023512-29023552	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr18:29016969-29017100	HepG2	liver:	n/a	n/a
37	CTCF	chr18:29016940-29017090	NHEK	skin:	n/a	n/a
38	CTCF	chr18:29016900-29017050	HMEC	breast:	n/a	n/a
39	CTCF	chr18:29016880-29017030	SAEC	small airway:	n/a	n/a
40	CTCF	chr18:29017020-29017170	HepG2	liver:	n/a	n/a
41	CTCF	chr18:29016957-29017069	GM12878	blood:	n/a	n/a
42	CTCF	chr18:29016980-29017130	MCF-7	breast:	n/a	n/a
43	CTCF	chr18:29016880-29017030	MCF-7	breast:	n/a	n/a
44	CTCF	chr18:29016900-29017050	SAEC	small airway:	n/a	n/a
45	CTCF	chr18:29027680-29027830	HMEC	breast:	n/a	n/a
46	E2F4	chr18:29009647-29009811	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr18:29027652-29027969	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr18:29034103-29034392	MCF10A-Er-Src	breast:	n/a	n/a
49	ELF1	chr18:29009479-29010084	HCT-116	colon:	n/a	chr18:29009818-29009831 chr18:29009819-29009830
50	ELF1	chr18:29009590-29010002	K562	blood:	n/a	chr18:29009818-29009831 chr18:29009819-29009830

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29026303-29026353	AG04450	lung:	fetal
2	chr18:29027701-29027751	GM06990	blood:	n/a
3	chr18:29027658-29027708	AG04449	skin:	fetal
4	chr18:29027701-29027751	BE2_C	brain:	n/a
5	chr18:29027885-29027935	T-47D	breast:	n/a
6	chr18:29027885-29027935	Hepatocyte	liver:	n/a
7	chr18:29027658-29027708	AG04450	lung:	fetal
8	chr18:29027885-29027935	HNPCEpiC	eye:	n/a
9	chr18:29026301-29026351	GM19239	blood:	n/a
10	chr18:29027885-29027935	GM12891	blood:	n/a
11	chr18:29026301-29026351	HCPEpiC	choroid plexus:	n/a
12	chr18:29027885-29027935	H1-hESC	embryonic stem cell:	embryo
13	chr18:29026301-29026351	AG04450	lung:	fetal
14	chr18:29027658-29027708	HEEpiC	esophagus:	n/a
15	chr18:29027701-29027751	PrEC	prostate:	n/a
16	chr18:29027745-29027795	HL-60	blood:	n/a
17	chr18:29027885-29027935	MCF-7	breast:	n/a
18	chr18:29026303-29026353	HepG2	liver:	n/a
19	chr18:29027701-29027751	GM12891	blood:	n/a
20	chr18:29027701-29027751	HUVEC	blood vessel:	n/a
21	chr18:29027658-29027708	GM12892	blood:	n/a
22	chr18:29026303-29026353	T-47D	breast:	n/a
23	chr18:29027885-29027935	PrEC	prostate:	n/a
24	chr18:29027701-29027751	SKMC	muscle:	n/a
25	chr18:29027701-29027751	PFSK-1	brain:	n/a
26	chr18:29027745-29027795	GM06990	blood:	n/a
27	chr18:29026303-29026353	HEEpiC	esophagus:	n/a
28	chr18:29027885-29027935	ECC-1	luminal epithelium:	n/a
29	chr18:29027745-29027795	GM12878	blood:	n/a
30	chr18:29027745-29027795	HIPEpiC	eye:	n/a
31	chr18:29027658-29027708	Jurkat	blood:	n/a
32	chr18:29027885-29027935	GM12878	blood:	n/a
33	chr18:29027701-29027751	ProgFib	skin:	n/a
34	chr18:29027701-29027751	NHBE	bronchial:	n/a
35	chr18:29027885-29027935	A549	lung:	n/a
36	chr18:29027745-29027795	HPAEpiC	pulmonary alveolar:	n/a
37	chr18:29027885-29027935	SK-N-SH	brain:	n/a
38	chr18:29026303-29026353	NH-A	brain:	n/a
39	chr18:29027658-29027708	LNCaP	prostate:	n/a
40	chr18:29026303-29026353	GM12878	blood:	n/a
41	chr18:29026301-29026351	A549	lung:	n/a
42	chr18:29027701-29027751	K562	blood:	n/a
43	chr18:29027701-29027751	AoSMC	blood vessel:	n/a
44	chr18:29027658-29027708	ProgFib	skin:	n/a
45	chr18:29027701-29027751	Hepatocyte	liver:	n/a
46	chr18:29027745-29027795	NH-A	brain:	n/a
47	chr18:29026303-29026353	NHDF-neo	bronchial:	n/a
48	chr18:29027658-29027708	GM19239	blood:	n/a
49	chr18:29027885-29027935	HMEC	breast:	n/a
50	chr18:29027701-29027751	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
2	chr18:29046909..29049478-chr18:29076853..29079838,2	K562	blood:
3	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:
4	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:
5	chr18:29033071..29035215-chr18:29036604..29039421,3	K562	blood:
6	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
7	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:
8	chr18:29042545..29045965-chr18:29077171..29079744,3	K562	blood:
9	chr18:28786778..28788708-chr18:29017378..29018896,2	MCF-7	breast:
10	chr18:29038496..29040369-chr18:29042094..29044336,2	K562	blood:
11	chr18:29044429..29046768-chr18:29048309..29050870,3	K562	blood:
12	chr18:29038234..29040822-chr18:29041279..29043976,2	MCF-7	breast:
13	chr18:29007636..29009624-chr18:29016577..29018951,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000266729	TF binding region
DSG3	TF binding region
ENSG00000266729	CpG island
DSG3	CpG island
ENSG00000266521	chromatin interactions
ENSG00000046604	chromatin interactions

Extended variants
information (count: 1649 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12961029	chr18:29009409-29009410	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146359281	chr18:29009459-29009460	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs557827981	chr18:29009497-29009498	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs570519735	chr18:29009517-29009518	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs539156266	chr18:29009563-29009564	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs531279149	chr18:29009608-29009609	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs570150471	chr18:29009628-29009629	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs182537022	chr18:29009652-29009653	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs72929966	chr18:29009675-29009676	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs186259788	chr18:29009694-29009695	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs139417809	chr18:29009705-29009706	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs555808715	chr18:29009719-29009720	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs190636070	chr18:29009741-29009742	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs560252565	chr18:29009764-29009765	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs573933301	chr18:29009833-29009834	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs184172026	chr18:29009845-29009846	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs543937815	chr18:29009882-29009883	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs541219471	chr18:29009923-29009924	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs188828117	chr18:29009947-29009948	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs143682629	chr18:29009953-29009954	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs574143524	chr18:29009979-29009980	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs150054129	chr18:29009995-29009996	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561681124	chr18:29010007-29010008	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs559852523	chr18:29010090-29010091	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs527597461	chr18:29010092-29010093	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs80055261	chr18:29010166-29010167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs8094890	chr18:29010191-29010192	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149022310	chr18:29010194-29010195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551133698	chr18:29010195-29010196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569368856	chr18:29010198-29010199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536300599	chr18:29010210-29010211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548582351	chr18:29010244-29010245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373413397	chr18:29010307-29010308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs193223033	chr18:29010339-29010340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376690480	chr18:29010358-29010359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182577844	chr18:29010363-29010364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577064564	chr18:29010421-29010422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142055976	chr18:29010442-29010443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556293509	chr18:29010462-29010463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529409382	chr18:29010536-29010537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577871038	chr18:29010546-29010547	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs574202910	chr18:29010574-29010575	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs187710295	chr18:29010683-29010684	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs75855470	chr18:29010715-29010716	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs147810378	chr18:29010905-29010906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72929968	chr18:29010933-29010934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs564361937	chr18:29010957-29010958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531581090	chr18:29010959-29010960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550002199	chr18:29010960-29010961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4102545	chr18:29010981-29010982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29006600-29010600	Enhancers	Placenta Amnion	Placenta Amnion
2	chr18:29007200-29010800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr18:29007400-29010800	Enhancers	NHEK	skin
4	chr18:29008200-29010600	Enhancers	Stomach Mucosa	stomach
5	chr18:29008200-29010800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr18:29008400-29009800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr18:29008400-29010600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr18:29008800-29009600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr18:29008800-29010600	Enhancers	HMEC	breast
10	chr18:29009000-29010400	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr18:29009200-29010200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr18:29009200-29010200	Enhancers	Fetal Intestine Large	intestine
13	chr18:29009200-29010400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr18:29009200-29010600	Enhancers	Hela-S3	cervix
15	chr18:29009400-29009800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr18:29009400-29010400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr18:29009600-29010200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr18:29009800-29010200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr18:29009800-29010400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr18:29010000-29010200	Enhancers	Small Intestine	intestine
21	chr18:29010200-29010400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr18:29010600-29012200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr18:29010800-29019800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr18:29012200-29012600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr18:29012600-29016800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr18:29016800-29017400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr18:29017200-29017400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr18:29019600-29020400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr18:29019800-29020200	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr18:29019800-29020600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr18:29019800-29020800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr18:29019800-29020800	Enhancers	NHEK	skin
33	chr18:29020400-29022400	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr18:29020600-29021000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr18:29020800-29021800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr18:29020800-29021800	Flanking Active TSS	NHEK	skin
37	chr18:29021000-29021400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr18:29021400-29021800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr18:29021800-29022200	Enhancers	NHEK	skin
40	chr18:29021800-29026800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr18:29022200-29022600	Weak transcription	NHEK	skin
42	chr18:29022400-29023000	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr18:29022600-29022800	Enhancers	NHEK	skin
44	chr18:29022800-29026600	Weak transcription	NHEK	skin
45	chr18:29024400-29024800	Enhancers	Esophagus	oesophagus
46	chr18:29024800-29027600	Weak transcription	Esophagus	oesophagus
47	chr18:29026600-29027000	Active TSS	K562	blood
48	chr18:29026600-29027200	Enhancers	NHEK	skin
49	chr18:29026800-29027000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr18:29026800-29027200	Enhancers	HMEC	breast

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