Variant report

Variant	esv3310838
Chromosome Location	chr14:37636091-37639750
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	chr14:37636859-37637271	K562	blood:	n/a	n/a
2	ARID3A	chr14:37636253-37636339	K562	blood:	n/a	n/a
3	ARID3A	chr14:37637980-37638323	K562	blood:	n/a	n/a
4	ARID3A	chr14:37638798-37638998	K562	blood:	n/a	chr14:37638878-37638894 chr14:37638877-37638893
5	ATF1	chr14:37636855-37637252	K562	blood:	n/a	n/a
6	ATF1	chr14:37637957-37638275	K562	blood:	n/a	n/a
7	ATF2	chr14:37636807-37637410	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr14:37636749-37637333	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr14:37639465-37639767	K562	blood:	n/a	n/a
10	BACH1	chr14:37636808-37637367	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr14:37636967-37637160	K562	blood:	n/a	n/a
12	BHLHE40	chr14:37637932-37638567	K562	blood:	n/a	n/a
13	CBX3	chr14:37637860-37638321	K562	blood:	n/a	n/a
14	CCNT2	chr14:37636844-37637082	K562	blood:	n/a	n/a
15	CCNT2	chr14:37637920-37638412	K562	blood:	n/a	n/a
16	CEBPB	chr14:37637883-37638325	K562	blood:	n/a	n/a
17	CEBPB	chr14:37637050-37637331	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr14:37636269-37636581	A549	lung:	n/a	chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636432-37636445
19	CEBPB	chr14:37637944-37638270	K562	blood:	n/a	n/a
20	CEBPB	chr14:37636272-37636611	HepG2	liver:	n/a	chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636432-37636445
21	CEBPB	chr14:37636301-37636565	K562	blood:	n/a	chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636432-37636445
22	CEBPB	chr14:37636334-37636621	IMR90	lung:	n/a	chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636432-37636445
23	CEBPB	chr14:37636247-37636625	H1-hESC	embryonic stem cell:	n/a	chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636432-37636445
24	CEBPB	chr14:37636249-37636621	K562	blood:	n/a	chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636432-37636445
25	CEBPB	chr14:37636278-37636578	MCF-7	breast:	n/a	chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636432-37636445
26	CEBPB	chr14:37636246-37636660	K562	blood:	n/a	chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636434-37636443 chr14:37636432-37636445
27	CEBPD	chr14:37637817-37638422	K562	blood:	n/a	n/a
28	CEBPD	chr14:37637861-37638375	K562	blood:	n/a	n/a
29	CREB1	chr14:37636830-37637229	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr14:37637938-37638390	K562	blood:	n/a	n/a
31	CUX1	chr14:37637759-37638233	K562	blood:	n/a	n/a
32	CUX1	chr14:37639527-37639894	K562	blood:	n/a	chr14:37639645-37639661
33	CUX1	chr14:37636376-37636407	K562	blood:	n/a	n/a
34	CUX1	chr14:37637412-37637523	K562	blood:	n/a	n/a
35	CUX1	chr14:37636904-37637086	K562	blood:	n/a	n/a
36	CUX1	chr14:37638777-37638930	K562	blood:	n/a	n/a
37	E2F4	chr14:37636086-37636181	MCF10A-Er-Src	breast:	n/a	n/a
38	ELF1	chr14:37636870-37637144	K562	blood:	n/a	n/a
39	EP300	chr14:37637983-37638203	GM12878	blood:	n/a	n/a
40	EP300	chr14:37636810-37637359	H1-hESC	embryonic stem cell:	n/a	n/a
41	EP300	chr14:37637864-37638499	K562	blood:	n/a	n/a
42	EP300	chr14:37636752-37637313	K562	blood:	n/a	n/a
43	EP300	chr14:37636454-37636464	K562	blood:	n/a	n/a
44	EP300	chr14:37637990-37638261	K562	blood:	n/a	n/a
45	ETS1	chr14:37637925-37638267	K562	blood:	n/a	n/a
46	FOS	chr14:37639592-37639776	MCF10A-Er-Src	breast:	n/a	chr14:37639621-37639631 chr14:37639620-37639632 chr14:37639622-37639630 chr14:37639623-37639630 chr14:37639621-37639630 chr14:37639622-37639631
47	FOS	chr14:37639673-37639706	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr14:37639606-37639792	MCF10A-Er-Src	breast:	n/a	chr14:37639621-37639631 chr14:37639620-37639632 chr14:37639622-37639630 chr14:37639623-37639630 chr14:37639621-37639630 chr14:37639622-37639631
49	GABPA	chr14:37637921-37638201	K562	blood:	n/a	n/a
50	GATA1	chr14:37637969-37638288	PBDEFetal	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:37638478-37638528	AG09309	skin:	n/a
2	chr14:37638478-37638528	PFSK-1	brain:	n/a
3	chr14:37638478-37638528	H1-hESC	embryonic stem cell:	embryo
4	chr14:37638478-37638528	HEK293	kidney:	embryo
5	chr14:37638478-37638528	SK-N-MC	brain:	n/a
6	chr14:37638478-37638528	HepG2	liver:	n/a
7	chr14:37638478-37638528	HL-60	blood:	n/a
8	chr14:37638478-37638528	Hela-S3	cervix:	n/a
9	chr14:37638478-37638528	SK-N-SH	brain:	n/a
10	chr14:37638478-37638528	RPTEC	kidney:	n/a
11	chr14:37638478-37638528	HCF	heart:	n/a
12	chr14:37638478-37638528	MCF10A-Er-Src	breast:	n/a
13	chr14:37638478-37638528	HRCEpiC	kidney:	n/a
14	chr14:37638478-37638528	SAEC	small airway:	n/a
15	chr14:37638478-37638528	PANC-1	pancreas:	n/a
16	chr14:37638478-37638528	HAEpiC	amniotic membrane:	n/a
17	chr14:37638478-37638528	HRPEpiC	eye:	n/a
18	chr14:37638478-37638528	HUVEC	blood vessel:	n/a
19	chr14:37638478-37638528	Caco-2	colon:	n/a
20	chr14:37638478-37638528	AoSMC	blood vessel:	n/a
21	chr14:37638478-37638528	NH-A	brain:	n/a
22	chr14:37638478-37638528	PrEC	prostate:	n/a
23	chr14:37638478-37638528	MCF-7	breast:	n/a
24	chr14:37638478-37638528	AG09319	gingival:	n/a
25	chr14:37638478-37638528	NB4	blood:	n/a
26	chr14:37638478-37638528	GM12878	blood:	n/a
27	chr14:37638478-37638528	CMK	blood:	n/a
28	chr14:37638478-37638528	K562	blood:	n/a
29	chr14:37638478-37638528	GM19239	blood:	n/a
30	chr14:37638478-37638528	SK-N-SH_RA	brain:	n/a
31	chr14:37638478-37638528	HRE	kidney:	n/a
32	chr14:37638478-37638528	NHDF-neo	bronchial:	n/a
33	chr14:37638478-37638528	HIPEpiC	eye:	n/a
34	chr14:37638478-37638528	ECC-1	luminal epithelium:	n/a
35	chr14:37638478-37638528	AG04449	skin:	fetal
36	chr14:37638478-37638528	AG04450	lung:	fetal
37	chr14:37638478-37638528	ovcar-3	ovarian:	n/a
38	chr14:37638478-37638528	GM06990	blood:	n/a
39	chr14:37638478-37638528	HCT-116	colon:	n/a
40	chr14:37638478-37638528	BJ	skin:	n/a
41	chr14:37638478-37638528	LNCaP	prostate:	n/a
42	chr14:37638478-37638528	HNPCEpiC	eye:	n/a
43	chr14:37638478-37638528	HEEpiC	esophagus:	n/a
44	chr14:37638478-37638528	A549	lung:	n/a
45	chr14:37638478-37638528	IMR90	lung:	fetal
46	chr14:37638478-37638528	BE2_C	brain:	n/a
47	chr14:37638478-37638528	Hepatocyte	liver:	n/a
48	chr14:37638478-37638528	HCM	heart:	n/a
49	chr14:37638478-37638528	Jurkat	blood:	n/a
50	chr14:37638478-37638528	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:37639061..37645694-chr14:37661777..37669317,18	MCF-7	breast:
2	chr14:37619150..37623313-chr14:37636849..37639143,3	K562	blood:
3	chr14:37638241..37643981-chr14:37665773..37670423,8	MCF-7	breast:
4	chr14:37439762..37441841-chr14:37637700..37639770,2	K562	blood:
5	chr14:37635891..37637422-chr14:37666864..37668416,2	MCF-7	breast:
6	chr14:37131202..37132825-chr14:37638068..37640984,2	K562	blood:
7	chr14:37639697..37645467-chr14:37664720..37672395,14	K562	blood:
8	chr14:37636501..37638947-chr14:37664211..37667966,4	K562	blood:
9	chr14:37639617..37644848-chr14:37662875..37669924,15	K562	blood:
10	chr14:37638513..37640081-chr14:37646893..37648669,2	MCF-7	breast:

Variant related genes	Relation type
SLC25A21-AS1	TF binding region
SLC25A21-AS1	CpG island
ENSG00000198807	chromatin interactions
ENSG00000151338	chromatin interactions

Extended variants
information (count: 121 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:121 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183421235	chr14:37636107-37636108	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs17106483	chr14:37636115-37636116	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs546125517	chr14:37636122-37636123	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs559648154	chr14:37636125-37636126	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs143796791	chr14:37636153-37636154	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs371329476	chr14:37636172-37636173	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs548360385	chr14:37636174-37636175	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs188766906	chr14:37636211-37636212	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs148144758	chr14:37636277-37636278	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374299239	chr14:37636291-37636292	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs192468618	chr14:37636424-37636425	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs537635625	chr14:37636427-37636428	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs570134147	chr14:37636439-37636440	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs144020943	chr14:37636450-37636451	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs8003685	chr14:37636477-37636478	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs566813346	chr14:37636512-37636513	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs535698820	chr14:37636551-37636552	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs184967091	chr14:37636561-37636562	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs575715083	chr14:37636566-37636567	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs147294735	chr14:37636596-37636597	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs372286139	chr14:37636600-37636601	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs578078717	chr14:37636652-37636653	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs200205653	chr14:37636693-37636694	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs56933807	chr14:37636715-37636716	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs559730297	chr14:37636753-37636754	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs138053138	chr14:37636810-37636811	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs143521638	chr14:37636880-37636881	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs10140952	chr14:37636921-37636922	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs530592039	chr14:37636923-37636924	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs550264200	chr14:37636934-37636935	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs553737610	chr14:37636942-37636943	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs2180633	chr14:37636948-37636949	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs571899204	chr14:37637051-37637052	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs115989779	chr14:37637060-37637061	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs10589340	chr14:37637085-37637086	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs188168141	chr14:37637092-37637093	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs567087623	chr14:37637099-37637100	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs375052792	chr14:37637224-37637225	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs549384089	chr14:37637225-37637226	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191428932	chr14:37637281-37637282	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs183996397	chr14:37637285-37637286	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs8007988	chr14:37637291-37637292	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs559016250	chr14:37637306-37637307	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs371971662	chr14:37637371-37637372	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs578144349	chr14:37637391-37637392	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs112871824	chr14:37637406-37637407	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs534211506	chr14:37637453-37637454	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs554191133	chr14:37637535-37637536	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs139440297	chr14:37637542-37637543	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs544795743	chr14:37637654-37637655	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37630000-37638000	Weak transcription	Pancreas	Pancrea
2	chr14:37631600-37636200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr14:37635000-37636800	Enhancers	K562	blood
4	chr14:37635200-37636200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr14:37635200-37636800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr14:37635400-37636400	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr14:37636000-37636800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr14:37636000-37638600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr14:37636200-37637200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr14:37636200-37637200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr14:37636400-37638600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr14:37636400-37638600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr14:37636400-37638800	Enhancers	H1 Cell Line	embryonic stem cell
14	chr14:37636400-37638800	Enhancers	H9 Cell Line	embryonic stem cell
15	chr14:37636600-37637200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr14:37636800-37637000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr14:37636800-37637000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr14:37636800-37637000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr14:37636800-37639000	Flanking Active TSS	K562	blood
20	chr14:37637000-37637200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr14:37637000-37637200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr14:37637200-37637400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr14:37637200-37637600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr14:37637200-37637600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr14:37637200-37637600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr14:37637200-37637600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr14:37637200-37638000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr14:37637200-37638200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr14:37637400-37638200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr14:37637600-37638400	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr14:37637600-37638600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr14:37637600-37638600	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr14:37637600-37639000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr14:37637800-37638000	Enhancers	Fetal Heart	heart
35	chr14:37637800-37638400	Enhancers	Duodenum Mucosa	Duodenum
36	chr14:37638000-37638600	Enhancers	Pancreas	Pancrea
37	chr14:37638000-37638800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr14:37638000-37639000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr14:37638200-37638400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr14:37638200-37638400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr14:37638200-37638600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr14:37638400-37638600	Flanking Active TSS	Duodenum Mucosa	Duodenum
43	chr14:37638400-37640800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr14:37638400-37641000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr14:37638600-37638800	Enhancers	Small Intestine	intestine
46	chr14:37638600-37639000	Enhancers	Duodenum Mucosa	Duodenum
47	chr14:37638600-37639600	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr14:37638600-37639600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr14:37638600-37640400	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr14:37638600-37640400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links