Variant report

Variant	nsv514871
Chromosome Location	chr18:44546006-44562254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:362)
CpG islands
(count:1404)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr18:44549353-44549656	GM12878	blood:	n/a	n/a
2	BCL11A	chr18:44555313-44555571	GM12878	blood:	n/a	n/a
3	BHLHE40	chr18:44547816-44548107	HepG2	liver:	n/a	n/a
4	BHLHE40	chr18:44553731-44554022	HepG2	liver:	n/a	n/a
5	BHLHE40	chr18:44552793-44553372	HepG2	liver:	n/a	n/a
6	BHLHE40	chr18:44546870-44547457	HepG2	liver:	n/a	n/a
7	CTCF	chr18:44552060-44552210	HepG2	liver:	n/a	n/a
8	CTCF	chr18:44554040-44554190	AG04450	lung:	n/a	n/a
9	CTCF	chr18:44550236-44550581	K562	blood:	n/a	n/a
10	CTCF	chr18:44562140-44562290	SAEC	small airway:	n/a	n/a
11	CTCF	chr18:44552256-44552456	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr18:44546352-44546572	K562	blood:	n/a	n/a
13	CTCF	chr18:44554040-44554190	HA-sp	spinal cord:	n/a	n/a
14	CTCF	chr18:44556144-44556568	K562	blood:	n/a	n/a
15	CTCF	chr18:44557309-44557626	K562	blood:	n/a	n/a
16	CTCF	chr18:44556180-44556382	K562	blood:	n/a	n/a
17	CTCF	chr18:44553366-44553476	GM19239	blood:	n/a	n/a
18	CTCF	chr18:44557429-44557536	LNCaP	prostate:	n/a	n/a
19	CTCF	chr18:44551498-44551626	LNCaP	prostate:	n/a	n/a
20	CTCF	chr18:44550232-44550622	K562	blood:	n/a	n/a
21	CTCF	chr18:44557382-44557538	LNCaP	prostate:	n/a	n/a
22	CTCF	chr18:44553344-44553385	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr18:44557477-44557530	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr18:44557427-44557512	GM20000	blood:	n/a	n/a
25	CTCF	chr18:44547459-44547559	GM19239	blood:	n/a	n/a
26	CTCF	chr18:44561451-44561458	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr18:44547080-44547230	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr18:44551550-44551578	LNCaP	prostate:	n/a	n/a
29	CTCF	chr18:44552060-44552210	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr18:44552308-44552416	Gliobla	brain:	n/a	n/a
31	CTCF	chr18:44551620-44551770	AG10803	skin:	n/a	n/a
32	CTCF	chr18:44561700-44561850	HEK293	kidney:	n/a	n/a
33	CTCF	chr18:44547080-44547230	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr18:44546361-44546519	HepG2	liver:	n/a	n/a
35	CTCF	chr18:44552363-44552374	A549	lung:	n/a	n/a
36	CTCF	chr18:44552060-44552210	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr18:44557269-44557573	K562	blood:	n/a	n/a
38	CTCF	chr18:44547060-44547210	GM12868	blood:	n/a	n/a
39	CTCF	chr18:44552040-44552190	AG04449	skin:	n/a	n/a
40	CTCF	chr18:44546374-44546519	Gliobla	brain:	n/a	n/a
41	CTCF	chr18:44551296-44551735	K562	blood:	n/a	n/a
42	CTCF	chr18:44561420-44561449	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr18:44551208-44551848	K562	blood:	n/a	n/a
44	CTCF	chr18:44554020-44554170	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr18:44556001-44556074	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr18:44547060-44547210	WI-38	lung:	n/a	n/a
47	CTCF	chr18:44547080-44547230	HEK293	kidney:	n/a	n/a
48	CTCF	chr18:44556177-44556405	K562	blood:	n/a	n/a
49	CTCF	chr18:44546337-44546544	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr18:44557210-44557657	K562	blood:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44561718-44561768	GM12878	blood:	n/a
2	chr18:44561718-44561768	GM12878	blood:	n/a
3	chr18:44562063-44562113	ProgFib	skin:	n/a
4	chr18:44551732-44551782	PANC-1	pancreas:	n/a
5	chr18:44561725-44561775	SK-N-MC	brain:	n/a
6	chr18:44560277-44560327	K562	blood:	n/a
7	chr18:44561188-44561238	NT2-D1	testis:	n/a
8	chr18:44555308-44555358	SK-N-SH_RA	brain:	n/a
9	chr18:44553084-44553134	Hepatocyte	liver:	n/a
10	chr18:44562136-44562186	ECC-1	luminal epithelium:	n/a
11	chr18:44560277-44560327	HUVEC	blood vessel:	n/a
12	chr18:44557732-44557782	HPAEpiC	pulmonary alveolar:	n/a
13	chr18:44561130-44561180	HPAEpiC	pulmonary alveolar:	n/a
14	chr18:44562030-44562080	IMR90	lung:	fetal
15	chr18:44561130-44561180	HRPEpiC	eye:	n/a
16	chr18:44562136-44562186	H1-hESC	embryonic stem cell:	embryo
17	chr18:44562056-44562106	GM12878	blood:	n/a
18	chr18:44555308-44555358	BJ	skin:	n/a
19	chr18:44561725-44561775	SKMC	muscle:	n/a
20	chr18:44561188-44561238	BJ	skin:	n/a
21	chr18:44558967-44559017	PrEC	prostate:	n/a
22	chr18:44561385-44561435	NB4	blood:	n/a
23	chr18:44551732-44551782	NHBE	bronchial:	n/a
24	chr18:44558967-44559017	HCM	heart:	n/a
25	chr18:44561188-44561238	HRPEpiC	eye:	n/a
26	chr18:44562113-44562163	Caco-2	colon:	n/a
27	chr18:44551732-44551782	ovcar-3	ovarian:	n/a
28	chr18:44557635-44557685	AG04449	skin:	fetal
29	chr18:44558967-44559017	SK-N-SH	brain:	n/a
30	chr18:44551732-44551782	AG09319	gingival:	n/a
31	chr18:44557647-44557697	AG04449	skin:	fetal
32	chr18:44562063-44562113	HRE	kidney:	n/a
33	chr18:44561130-44561180	HCM	heart:	n/a
34	chr18:44562030-44562080	CMK	blood:	n/a
35	chr18:44557673-44557723	SKMC	muscle:	n/a
36	chr18:44562019-44562069	GM19239	blood:	n/a
37	chr18:44551719-44551769	NH-A	brain:	n/a
38	chr18:44557635-44557685	GM12878	blood:	n/a
39	chr18:44551719-44551769	PANC-1	pancreas:	n/a
40	chr18:44562063-44562113	GM12878	blood:	n/a
41	chr18:44557673-44557723	HCT-116	colon:	n/a
42	chr18:44561385-44561435	Hepatocyte	liver:	n/a
43	chr18:44557635-44557685	AG09309	skin:	n/a
44	chr18:44555308-44555358	GM12892	blood:	n/a
45	chr18:44562030-44562080	H1-hESC	embryonic stem cell:	embryo
46	chr18:44557673-44557723	K562	blood:	n/a
47	chr18:44557635-44557685	CMK	blood:	n/a
48	chr18:44557673-44557723	HRE	kidney:	n/a
49	chr18:44562030-44562080	RPTEC	kidney:	n/a
50	chr18:44562019-44562069	AG04449	skin:	fetal

No data

Variant related genes	Relation type
TCEB3B	TF binding region
TCEB3CL2	TF binding region
TCEB3CL	TF binding region
TCEB3C	TF binding region
TCEB3B	CpG island
TCEB3CL2	CpG island
TCEB3CL	CpG island
TCEB3C	CpG island

Extended variants
information (count: 600 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560979721	chr18:44546031-44546032	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs529749005	chr18:44546090-44546091	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs112278899	chr18:44546092-44546093	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs549877127	chr18:44546189-44546190	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs369886283	chr18:44546202-44546203	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs563322467	chr18:44546210-44546211	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs532301467	chr18:44546211-44546212	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs150347153	chr18:44546214-44546215	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs565594498	chr18:44546370-44546371	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs138006330	chr18:44546526-44546527	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs149478243	chr18:44546645-44546646	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs534615248	chr18:44546812-44546813	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs548171974	chr18:44547127-44547128	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs147149326	chr18:44547159-44547160	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs568490690	chr18:44547198-44547199	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs141662366	chr18:44547360-44547361	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs138619856	chr18:44547377-44547378	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs78197099	chr18:44547402-44547403	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs71906626	chr18:44547442-44547443	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs150511064	chr18:44547444-44547445	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs139462600	chr18:44547449-44547450	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs71922510	chr18:44547453-44547454	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs368079834	chr18:44547465-44547466	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs199609595	chr18:44547476-44547477	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs189556067	chr18:44547505-44547506	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs67844926	chr18:44547506-44547507	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs72393053	chr18:44547515-44547516	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs537131472	chr18:44547588-44547589	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs557389201	chr18:44547821-44547822	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs555520417	chr18:44547983-44547984	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs147524555	chr18:44548026-44548027	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs149165550	chr18:44548094-44548095	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs142340842	chr18:44548628-44548629	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs201366170	chr18:44549012-44549013	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs577286550	chr18:44549143-44549144	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs539989656	chr18:44549147-44549148	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs553612378	chr18:44549149-44549150	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs573566859	chr18:44549156-44549157	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs199619018	chr18:44549170-44549171	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs542591879	chr18:44549178-44549179	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs75431623	chr18:44549194-44549195	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs554245013	chr18:44549203-44549204	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs574409348	chr18:44549206-44549207	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs148562892	chr18:44549214-44549215	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs201850765	chr18:44549216-44549217	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs200094578	chr18:44549232-44549233	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs543067546	chr18:44549238-44549239	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs112351123	chr18:44549336-44549337	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs200712716	chr18:44549397-44549398	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs56006467	chr18:44549455-44549456	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
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
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
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
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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
small cell lung cancer	17426248	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44538200-44551600	Weak transcription	Gastric	stomach
2	chr18:44545200-44547200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr18:44545200-44552000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr18:44546400-44547000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr18:44547000-44547400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr18:44547000-44547400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr18:44547000-44547400	ZNF genes & repeats	Fetal Stomach	stomach
8	chr18:44547200-44547400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr18:44547200-44547400	ZNF genes & repeats	Fetal Brain Female	brain
10	chr18:44547200-44547400	Bivalent Enhancer	HepG2	liver
11	chr18:44547400-44552000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr18:44547400-44552000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr18:44550200-44556600	Weak transcription	Fetal Lung	lung
14	chr18:44551600-44551800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr18:44551600-44551800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr18:44551800-44553000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr18:44551800-44553000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr18:44552000-44552200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr18:44552000-44552200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr18:44552000-44552400	Enhancers	H1 Cell Line	embryonic stem cell
21	chr18:44552000-44552400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr18:44552000-44552400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr18:44552200-44552400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr18:44552400-44555000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr18:44553000-44553200	Enhancers	Right Ventricle	heart
26	chr18:44553000-44553600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr18:44553000-44553600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr18:44553200-44562600	Weak transcription	Right Ventricle	heart
29	chr18:44553600-44554000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr18:44553600-44555000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr18:44554000-44555400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr18:44554000-44555400	ZNF genes & repeats	Stomach Smooth Muscle	stomach
33	chr18:44554600-44555400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
34	chr18:44555000-44555400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
35	chr18:44555000-44555400	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr18:44555000-44555400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
37	chr18:44555200-44555400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr18:44555400-44560000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr18:44555400-44560000	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr18:44555400-44561400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr18:44555400-44563200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr18:44560000-44560400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr18:44560000-44560600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
44	chr18:44561400-44561600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr18:44561600-44562000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr18:44561800-44562000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

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