Variant report

Variant	nsv909474
Chromosome Location	chr18:24683823-24832023
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	chr18:24818776-24818854	K562	blood:	n/a	n/a
2	ARID3A	chr18:24722857-24723286	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:24777810-24778518	HepG2	liver:	n/a	n/a
4	ATF1	chr18:24807384-24807646	K562	blood:	n/a	n/a
5	ATF1	chr18:24827298-24827505	K562	blood:	n/a	n/a
6	ATF1	chr18:24815630-24815792	K562	blood:	n/a	n/a
7	ATF1	chr18:24692205-24692289	K562	blood:	n/a	n/a
8	ATF1	chr18:24763423-24763503	K562	blood:	n/a	n/a
9	ATF1	chr18:24707007-24707009	K562	blood:	n/a	n/a
10	ATF1	chr18:24822246-24822493	K562	blood:	n/a	n/a
11	ATF1	chr18:24779782-24779947	K562	blood:	n/a	n/a
12	ATF1	chr18:24761429-24761582	K562	blood:	n/a	n/a
13	ATF1	chr18:24784086-24784430	K562	blood:	n/a	n/a
14	ATF1	chr18:24830641-24830642	K562	blood:	n/a	n/a
15	ATF1	chr18:24761884-24761917	K562	blood:	n/a	n/a
16	ATF1	chr18:24818736-24818908	K562	blood:	n/a	n/a
17	ATF1	chr18:24820083-24820284	K562	blood:	n/a	n/a
18	ATF3	chr18:24716186-24716326	HepG2	liver:	n/a	n/a
19	BACH1	chr18:24764352-24764632	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr18:24709050-24709054	K562	blood:	n/a	n/a
21	BACH1	chr18:24765163-24765182	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr18:24779499-24779643	K562	blood:	n/a	n/a
23	BACH1	chr18:24702204-24702331	K562	blood:	n/a	n/a
24	BCL11A	chr18:24820443-24820728	GM12878	blood:	n/a	n/a
25	BHLHE40	chr18:24715587-24715933	GM12878	blood:	n/a	n/a
26	BHLHE40	chr18:24820205-24820821	GM12878	blood:	n/a	n/a
27	BHLHE40	chr18:24716111-24716471	HepG2	liver:	n/a	n/a
28	BHLHE40	chr18:24819169-24819170	K562	blood:	n/a	n/a
29	BHLHE40	chr18:24819115-24819311	GM12878	blood:	n/a	n/a
30	CBX3	chr18:24729202-24729532	K562	blood:	n/a	n/a
31	CEBPB	chr18:24716075-24716429	Hela-S3	cervix:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
32	CEBPB	chr18:24716131-24716369	HepG2	liver:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
33	CEBPB	chr18:24775015-24775170	A549	lung:	n/a	chr18:24775040-24775051
34	CEBPB	chr18:24716125-24716411	IMR90	lung:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
35	CEBPB	chr18:24716052-24716403	A549	lung:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
36	CEBPB	chr18:24716065-24716475	H1-hESC	embryonic stem cell:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
37	CEBPB	chr18:24819695-24819939	HepG2	liver:	n/a	n/a
38	CEBPB	chr18:24716064-24716457	HepG2	liver:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
39	CEBPB	chr18:24716143-24716486	HepG2	liver:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
40	CEBPB	chr18:24716115-24716315	K562	blood:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
41	CEBPB	chr18:24767247-24767461	HepG2	liver:	n/a	chr18:24767358-24767369 chr18:24767399-24767412
42	CEBPB	chr18:24774994-24775125	H1-hESC	embryonic stem cell:	n/a	chr18:24775040-24775051
43	CEBPB	chr18:24716019-24716509	ECC-1	luminal epithelium:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
44	CEBPB	chr18:24778351-24778577	K562	blood:	n/a	chr18:24778467-24778484 chr18:24778470-24778483
45	CEBPB	chr18:24774989-24775189	HepG2	liver:	n/a	chr18:24775040-24775051
46	CEBPB	chr18:24716078-24716533	HepG2	liver:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
47	CEBPB	chr18:24716155-24716411	MCF-7	breast:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
48	CEBPB	chr18:24777826-24778604	HepG2	liver:	n/a	chr18:24778467-24778484 chr18:24778470-24778483
49	CEBPB	chr18:24716122-24716427	A549	lung:	n/a	chr18:24716255-24716266 chr18:24716257-24716266 chr18:24716255-24716268
50	CEBPB	chr18:24774998-24775161	K562	blood:	n/a	chr18:24775040-24775051

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:24765485-24765535	NH-A	brain:	n/a
2	chr18:24765485-24765535	NH-A	brain:	n/a
3	chr18:24765154-24765204	BJ	skin:	n/a
4	chr18:24765485-24765535	Hela-S3	cervix:	n/a
5	chr18:24765490-24765540	ECC-1	luminal epithelium:	n/a
6	chr18:24762316-24762366	CMK	blood:	n/a
7	chr18:24764966-24765016	HRE	kidney:	n/a
8	chr18:24764966-24765016	AG04449	skin:	fetal
9	chr18:24765781-24765831	GM12892	blood:	n/a
10	chr18:24765154-24765204	SAEC	small airway:	n/a
11	chr18:24765119-24765169	Jurkat	blood:	n/a
12	chr18:24765643-24765693	AG10803	skin:	n/a
13	chr18:24764966-24765016	NB4	blood:	n/a
14	chr18:24765490-24765540	SKMC	muscle:	n/a
15	chr18:24765490-24765540	LNCaP	prostate:	n/a
16	chr18:24764966-24765016	HEEpiC	esophagus:	n/a
17	chr18:24762316-24762366	HIPEpiC	eye:	n/a
18	chr18:24762316-24762366	AG09309	skin:	n/a
19	chr18:24765485-24765535	GM06990	blood:	n/a
20	chr18:24765490-24765540	HUVEC	blood vessel:	n/a
21	chr18:24765781-24765831	HCT-116	colon:	n/a
22	chr18:24764966-24765016	HCM	heart:	n/a
23	chr18:24765119-24765169	NH-A	brain:	n/a
24	chr18:24765485-24765535	HMEC	breast:	n/a
25	chr18:24764599-24764649	AoSMC	blood vessel:	n/a
26	chr18:24765643-24765693	SK-N-MC	brain:	n/a
27	chr18:24764599-24764649	A549	lung:	n/a
28	chr18:24762316-24762366	T-47D	breast:	n/a
29	chr18:24765485-24765535	HAEpiC	amniotic membrane:	n/a
30	chr18:24765643-24765693	HCM	heart:	n/a
31	chr18:24765781-24765831	AG09319	gingival:	n/a
32	chr18:24765473-24765523	SAEC	small airway:	n/a
33	chr18:24765154-24765204	HMEC	breast:	n/a
34	chr18:24765473-24765523	GM19239	blood:	n/a
35	chr18:24765154-24765204	SK-N-SH	brain:	n/a
36	chr18:24765781-24765831	HL-60	blood:	n/a
37	chr18:24765119-24765169	K562	blood:	n/a
38	chr18:24764966-24765016	HepG2	liver:	n/a
39	chr18:24765643-24765693	NH-A	brain:	n/a
40	chr18:24765643-24765693	AG09319	gingival:	n/a
41	chr18:24762316-24762366	HRCEpiC	kidney:	n/a
42	chr18:24765781-24765831	RPTEC	kidney:	n/a
43	chr18:24765485-24765535	SAEC	small airway:	n/a
44	chr18:24765643-24765693	HepG2	liver:	n/a
45	chr18:24765119-24765169	SAEC	small airway:	n/a
46	chr18:24765643-24765693	HAEpiC	amniotic membrane:	n/a
47	chr18:24762316-24762366	BE2_C	brain:	n/a
48	chr18:24765119-24765169	A549	lung:	n/a
49	chr18:24765485-24765535	HUVEC	blood vessel:	n/a
50	chr18:24765154-24765204	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:24712355..24714811-chr18:24718073..24719662,2	MCF-7	breast:
2	chr18:24754408..24756988-chr18:24763307..24765193,2	K562	blood:
3	chr18:24712355..24714811-chr18:24718073..24719662,2	MCF-7	breast:
4	chr18:24770863..24773354-chr18:24775315..24777406,2	K562	blood:
5	chr18:24744878..24747343-chr18:24750374..24752456,2	K562	blood:
6	chr18:24754408..24756988-chr18:24763307..24765193,2	K562	blood:
7	chr18:24744878..24747343-chr18:24750374..24752456,2	K562	blood:
8	chr18:24816860..24819247-chr18:24819852..24822725,2	K562	blood:
9	chr14:56390153..56391038-chr18:24814712..24815423,2	MCF-7	breast:
10	chr18:24770863..24773354-chr18:24775315..24777406,2	K562	blood:
11	chr18:24734168..24736128-chr18:24762446..24765149,2	K562	blood:
12	chr18:24734168..24736128-chr18:24762446..24765149,2	K562	blood:
13	chr18:24587162..24589841-chr18:24735427..24737669,2	K562	blood:
14	chr18:24816860..24819247-chr18:24819852..24822725,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAF4B-5	chr18:24827005-24827152	ENSG00000265374.1
2	lnc-TAF4B-5	chr18:24823577-24823630	ENSG00000265374.1
3	lnc-TAF4B-5	chr18:24805706-24805925	ENSG00000265374.1
4	lnc-TAF4B-5	chr18:24815572-24815623	ENSG00000265374.1
5	lnc-TAF4B-5	chr18:24814886-24814966	ENSG00000265374.1
6	lnc-TAF4B-4	chr18:24768707-24770662	ENSG00000260372.2
7	lnc-TAF4B-4	chr18:24727662-24727742	ENSG00000260372.2

Variant related genes	Relation type
ENSG00000265374	TF binding region
CHST9	TF binding region
ENSG00000265374	CpG island
CHST9	CpG island

Extended variants
information (count: 5100 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:5100 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8094101	chr18:24683823-24683824	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75070301	chr18:24683835-24683836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs28713375	chr18:24683860-24683861	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs73404900	chr18:24683892-24683893	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs557952524	chr18:24683988-24683989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527959494	chr18:24683994-24683995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564513069	chr18:24684001-24684002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs8097772	chr18:24684020-24684021	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs183942734	chr18:24684030-24684031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555653290	chr18:24684168-24684169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574129716	chr18:24684275-24684276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189971546	chr18:24684284-24684285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571018243	chr18:24684292-24684293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181627400	chr18:24684366-24684367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553536797	chr18:24684395-24684396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550450493	chr18:24684397-24684398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs578160730	chr18:24684408-24684409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs28607703	chr18:24684423-24684424	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs187047500	chr18:24684516-24684517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs142615172	chr18:24684524-24684525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191839716	chr18:24684579-24684580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538481207	chr18:24684586-24684587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561239891	chr18:24684598-24684599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74343848	chr18:24684628-24684629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369920321	chr18:24684648-24684649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558893488	chr18:24684674-24684675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533061712	chr18:24684779-24684780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371802982	chr18:24684780-24684781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201836383	chr18:24684808-24684809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551145363	chr18:24684866-24684867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569833088	chr18:24684871-24684872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146015150	chr18:24684877-24684878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs372942103	chr18:24684879-24684880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34338004	chr18:24684885-24684886	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs77960463	chr18:24684924-24684925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370712127	chr18:24684951-24684952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73944527	chr18:24685000-24685001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs112774108	chr18:24685013-24685014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574844224	chr18:24685038-24685039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577919295	chr18:24685125-24685126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539126474	chr18:24685255-24685256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148662403	chr18:24685302-24685303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189834638	chr18:24685355-24685356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12956646	chr18:24685369-24685370	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs558460132	chr18:24685416-24685417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539153181	chr18:24685428-24685429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182420226	chr18:24685436-24685437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11665636	chr18:24685559-24685560	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs540489214	chr18:24685754-24685755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544029116	chr18:24685762-24685763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
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
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
Sudden cardiac death	19188705	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
Acute myeloid leukemia	19651600	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:836 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:24679000-24691400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr18:24679600-24688000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr18:24684200-24685000	Enhancers	Fetal Brain Male	brain
4	chr18:24685000-24689000	Weak transcription	Fetal Brain Male	brain
5	chr18:24685200-24685600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr18:24685200-24685600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr18:24685400-24685800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr18:24688000-24689400	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr18:24689000-24689200	Enhancers	H9 Cell Line	embryonic stem cell
10	chr18:24689000-24690000	Enhancers	Fetal Brain Male	brain
11	chr18:24689000-24691200	Enhancers	Fetal Stomach	stomach
12	chr18:24689200-24693200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr18:24689200-24703600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr18:24689400-24691400	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr18:24689600-24690000	Enhancers	Fetal Brain Female	brain
16	chr18:24690000-24691800	Weak transcription	Fetal Brain Male	brain
17	chr18:24690400-24690600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr18:24690600-24691600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr18:24691400-24691600	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr18:24691400-24692000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr18:24691400-24692000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
22	chr18:24691600-24691800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr18:24691800-24693200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr18:24692000-24693200	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr18:24692000-24693400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr18:24693200-24694800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr18:24693200-24695200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
28	chr18:24693400-24693600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr18:24693400-24694200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
30	chr18:24693600-24707200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr18:24694200-24699400	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr18:24695200-24699200	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr18:24697600-24697800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr18:24697800-24699000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr18:24698600-24698800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr18:24698600-24698800	ZNF genes & repeats	Pancreas	Pancrea
37	chr18:24698800-24700200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr18:24698800-24715600	Weak transcription	Pancreas	Pancrea
39	chr18:24699000-24699200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr18:24699200-24699600	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr18:24699200-24699800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr18:24699200-24700000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr18:24699400-24700200	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr18:24699600-24700000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr18:24699600-24701800	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr18:24699800-24700800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr18:24700000-24701200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr18:24700000-24701600	Enhancers	Muscle Satellite Cultured Cells	--
49	chr18:24700000-24703400	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr18:24700000-24703800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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