Variant report

Variant	nsv565650
Chromosome Location	chr14:97089607-97126153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:100)
CpG islands
(count:550)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:100 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:97113854-97114026	K562	blood:	n/a	n/a
2	ATF1	chr14:97102247-97102558	K562	blood:	n/a	n/a
3	BACH1	chr14:97093553-97093561	K562	blood:	n/a	n/a
4	BHLHE40	chr14:97092811-97093615	K562	blood:	n/a	n/a
5	CEBPB	chr14:97123038-97123338	IMR90	lung:	n/a	chr14:97123165-97123176
6	CEBPB	chr14:97099041-97099257	HepG2	liver:	n/a	n/a
7	CEBPB	chr14:97123014-97123254	K562	blood:	n/a	chr14:97123165-97123176
8	CEBPB	chr14:97123007-97123330	HepG2	liver:	n/a	chr14:97123165-97123176
9	CEBPB	chr14:97123015-97123332	A549	lung:	n/a	chr14:97123165-97123176
10	CTCF	chr14:97109374-97109423	Kidney_OC	kidney:	n/a	n/a
11	E2F4	chr14:97101062-97101293	MCF10A-Er-Src	breast:	n/a	chr14:97101160-97101169
12	E2F4	chr14:97108022-97108207	MCF10A-Er-Src	breast:	n/a	n/a
13	EBF1	chr14:97116241-97116544	GM12878	blood:	n/a	n/a
14	FOS	chr14:97098453-97098517	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr14:97098452-97098557	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr14:97098453-97098628	MCF10A-Er-Src	breast:	n/a	n/a
17	GABPA	chr14:97102189-97102461	K562	blood:	n/a	n/a
18	GABPA	chr14:97093845-97094041	Hela-S3	cervix:	n/a	n/a
19	GABPA	chr14:97093844-97094016	Hela-S3	cervix:	n/a	n/a
20	GATA1	chr14:97126117-97127106	PBDE	blood:	n/a	chr14:97126652-97126661
21	GATA1	chr14:97125943-97127088	K562	blood:	n/a	chr14:97126652-97126661
22	GATA2	chr14:97098757-97099067	SH-SY5Y	brain:	n/a	chr14:97098853-97098863 chr14:97098854-97098861 chr14:97098854-97098863
23	JUND	chr14:97102260-97102364	HepG2	liver:	n/a	chr14:97102348-97102359
24	JUND	chr14:97098324-97098676	K562	blood:	n/a	n/a
25	JUND	chr14:97102256-97102416	K562	blood:	n/a	chr14:97102348-97102359
26	MAFF	chr14:97126044-97126244	HepG2	liver:	n/a	chr14:97126112-97126130
27	MAFF	chr14:97093484-97093715	K562	blood:	n/a	n/a
28	MAFF	chr14:97090507-97090729	HepG2	liver:	n/a	n/a
29	MAFF	chr14:97126105-97126150	K562	blood:	n/a	chr14:97126112-97126130
30	MAFK	chr14:97090463-97090756	HepG2	liver:	n/a	n/a
31	MAFK	chr14:97118784-97118787	HepG2	liver:	n/a	n/a
32	MAFK	chr14:97126006-97126208	HepG2	liver:	n/a	chr14:97126115-97126126 chr14:97126091-97126105 chr14:97126115-97126126 chr14:97126088-97126104 chr14:97126113-97126127
33	MAFK	chr14:97101150-97101275	HepG2	liver:	n/a	n/a
34	MAFK	chr14:97090616-97090736	IMR90	lung:	n/a	n/a
35	MAFK	chr14:97090484-97090789	HepG2	liver:	n/a	n/a
36	MAFK	chr14:97093474-97093679	K562	blood:	n/a	n/a
37	MAFK	chr14:97101134-97101354	HepG2	liver:	n/a	n/a
38	MAX	chr14:97115130-97115314	NB4	blood:	n/a	chr14:97115264-97115274
39	MAZ	chr14:97102391-97102425	K562	blood:	n/a	n/a
40	MAZ	chr14:97093017-97093351	K562	blood:	n/a	n/a
41	MYC	chr14:97114986-97115110	H1-hESC	embryonic stem cell:	n/a	n/a
42	MYC	chr14:97107945-97107965	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr14:97115487-97115564	MCF-7	breast:	n/a	n/a
44	POLR2A	chr14:97098287-97098306	MCF-7	breast:	n/a	n/a
45	POLR2A	chr14:97107904-97108021	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr14:97115869-97115968	MCF-7	breast:	n/a	n/a
47	POLR2A	chr14:97099086-97099256	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr14:97105601-97105786	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr14:97115785-97115794	A549	lung:	n/a	n/a
50	POLR2A	chr14:97095728-97095787	Gliobla	brain:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:97092205-97092255	Caco-2	colon:	n/a
2	chr14:97092205-97092255	Caco-2	colon:	n/a
3	chr14:97092096-97092146	GM12878	blood:	n/a
4	chr14:97091520-97091570	LNCaP	prostate:	n/a
5	chr14:97090367-97090417	LNCaP	prostate:	n/a
6	chr14:97091489-97091539	HNPCEpiC	eye:	n/a
7	chr14:97092205-97092255	PrEC	prostate:	n/a
8	chr14:97092096-97092146	IMR90	lung:	fetal
9	chr14:97090212-97090262	AG10803	skin:	n/a
10	chr14:97092150-97092200	NT2-D1	testis:	n/a
11	chr14:97090212-97090262	HL-60	blood:	n/a
12	chr14:97090212-97090262	LNCaP	prostate:	n/a
13	chr14:97091489-97091539	HMEC	breast:	n/a
14	chr14:97092205-97092255	HEEpiC	esophagus:	n/a
15	chr14:97090367-97090417	NH-A	brain:	n/a
16	chr14:97092096-97092146	Hela-S3	cervix:	n/a
17	chr14:97092096-97092146	AG04449	skin:	fetal
18	chr14:97091520-97091570	PFSK-1	brain:	n/a
19	chr14:97092150-97092200	H1-hESC	embryonic stem cell:	embryo
20	chr14:97091067-97091117	Hepatocyte	liver:	n/a
21	chr14:97092205-97092255	HRCEpiC	kidney:	n/a
22	chr14:97091520-97091570	H1-hESC	embryonic stem cell:	embryo
23	chr14:97092096-97092146	NT2-D1	testis:	n/a
24	chr14:97091902-97091952	HAEpiC	amniotic membrane:	n/a
25	chr14:97090367-97090417	HIPEpiC	eye:	n/a
26	chr14:97092096-97092146	ovcar-3	ovarian:	n/a
27	chr14:97091520-97091570	MCF-7	breast:	n/a
28	chr14:97091902-97091952	HRE	kidney:	n/a
29	chr14:97091067-97091117	NT2-D1	testis:	n/a
30	chr14:97091067-97091117	MCF10A-Er-Src	breast:	n/a
31	chr14:97092096-97092146	GM06990	blood:	n/a
32	chr14:97091067-97091117	NHBE	bronchial:	n/a
33	chr14:97092150-97092200	SKMC	muscle:	n/a
34	chr14:97092205-97092255	SK-N-SH_RA	brain:	n/a
35	chr14:97092150-97092200	Caco-2	colon:	n/a
36	chr14:97092150-97092200	HRE	kidney:	n/a
37	chr14:97091520-97091570	A549	lung:	n/a
38	chr14:97091520-97091570	Caco-2	colon:	n/a
39	chr14:97091489-97091539	AG04449	skin:	fetal
40	chr14:97090212-97090262	HCM	heart:	n/a
41	chr14:97092205-97092255	HRE	kidney:	n/a
42	chr14:97091902-97091952	IMR90	lung:	fetal
43	chr14:97090367-97090417	Hela-S3	cervix:	n/a
44	chr14:97091902-97091952	AoSMC	blood vessel:	n/a
45	chr14:97090367-97090417	AG04449	skin:	fetal
46	chr14:97090367-97090417	HRE	kidney:	n/a
47	chr14:97091520-97091570	HCPEpiC	choroid plexus:	n/a
48	chr14:97091520-97091570	AoSMC	blood vessel:	n/a
49	chr14:97091902-97091952	HNPCEpiC	eye:	n/a
50	chr14:97091520-97091570	Hepatocyte	liver:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:97040936..97041835-chr14:97100556..97101428,4	MCF-7	breast:
2	chr14:97098302..97100960-chr14:97102875..97104630,2	K562	blood:
3	chr14:97084192..97086627-chr14:97090861..97093279,2	MCF-7	breast:
4	chr14:97091981..97093780-chr14:97101556..97103907,3	MCF-7	breast:
5	chr14:97040398..97040962-chr14:97100553..97101449,2	MCF-7	breast:
6	chr14:97085374..97088173-chr14:97091908..97094865,2	K562	blood:
7	chr14:97041013..97042090-chr14:97100546..97101489,8	MCF-7	breast:
8	chr14:97047039..97047841-chr14:97100546..97101485,3	MCF-7	breast:
9	chr14:97105478..97107756-chr14:97114890..97116903,2	MCF-7	breast:
10	chr14:97093078..97095980-chr14:97096287..97099015,3	MCF-7	breast:
11	chr14:97093078..97095980-chr14:97096287..97099015,3	MCF-7	breast:
12	chr14:97121918..97124905-chr14:97127753..97129733,2	K562	blood:
13	chr14:97040333..97042090-chr14:97100526..97101489,19	MCF-7	breast:
14	chr14:97047308..97047841-chr14:97100928..97101485,2	MCF-7	breast:
15	chr14:97096962..97100936-chr14:97101885..97104048,3	K562	blood:
16	chr14:97125727..97128111-chr14:97129743..97131813,3	K562	blood:
17	chr14:97105478..97107756-chr14:97114890..97116903,2	MCF-7	breast:
18	chr14:97125727..97127557-chr14:97130189..97131813,2	K562	blood:
19	chr14:93483695..93484309-chr14:97100592..97101400,2	MCF-7	breast:
20	chr14:97100866..97101454-chr14:97138053..97138598,2	MCF-7	breast:
21	chr14:97098302..97100960-chr14:97102875..97104630,2	K562	blood:
22	chr14:97091981..97093780-chr14:97101556..97103907,3	MCF-7	breast:
23	chr14:97100553..97101432-chr14:97126836..97127804,5	MCF-7	breast:
24	chr14:97096962..97100936-chr14:97101885..97104048,3	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG2B-8	chr14:97104524-97104851	NONHSAT039549

No data

Variant related genes	Relation type
RN7SKP108	TF binding region
RN7SKP108	CpG island

Extended variants
information (count: 1555 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1555 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs234587	chr14:97089607-97089608	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189445980	chr14:97089646-97089647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138645298	chr14:97089649-97089650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529391394	chr14:97089651-97089652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541579652	chr14:97089668-97089669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559987333	chr14:97089686-97089687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181486519	chr14:97089696-97089697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186839039	chr14:97089703-97089704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs234586	chr14:97089705-97089706	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs117008888	chr14:97089728-97089729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs142848959	chr14:97089750-97089751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562857883	chr14:97089753-97089754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527989118	chr14:97089772-97089773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147408976	chr14:97089773-97089774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543538862	chr14:97089832-97089833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565157128	chr14:97089958-97089959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138084849	chr14:97089963-97089964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542259542	chr14:97089995-97089996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538423551	chr14:97090046-97090047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562049710	chr14:97090059-97090060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557143988	chr14:97090099-97090100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113510838	chr14:97090107-97090108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529873035	chr14:97090127-97090128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546458684	chr14:97090148-97090149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575429852	chr14:97090160-97090161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143137115	chr14:97090167-97090168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555789516	chr14:97090186-97090187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10129847	chr14:97090197-97090198	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs377433994	chr14:97090211-97090212	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541440780	chr14:97090240-97090241	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191682832	chr14:97090241-97090242	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533482192	chr14:97090258-97090259	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35291807	chr14:97090293-97090294	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs563934835	chr14:97090308-97090309	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181106279	chr14:97090311-97090312	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531093834	chr14:97090316-97090317	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549304031	chr14:97090318-97090319	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560541078	chr14:97090328-97090329	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528029834	chr14:97090340-97090341	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546207155	chr14:97090393-97090394	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs148518222	chr14:97090397-97090398	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538757071	chr14:97090448-97090449	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550489800	chr14:97090456-97090457	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs568468947	chr14:97090457-97090458	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373401953	chr14:97090474-97090475	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374033010	chr14:97090483-97090484	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186377120	chr14:97090487-97090488	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536153417	chr14:97090502-97090503	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554858297	chr14:97090514-97090515	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142795127	chr14:97090540-97090541	Genic enhancers Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Glioblastoma	21080181	CNVD
Cancer	20164920	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Breast cancer	21509527	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	17426248	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97081600-97090200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:97084000-97090000	Weak transcription	Fetal Brain Male	brain
3	chr14:97084000-97096200	Weak transcription	Right Atrium	heart
4	chr14:97088800-97090600	Weak transcription	Brain Germinal Matrix	brain
5	chr14:97090000-97094600	Enhancers	Fetal Brain Male	brain
6	chr14:97090200-97091600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:97090200-97091600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
8	chr14:97090200-97093200	Weak transcription	Spleen	Spleen
9	chr14:97090400-97093000	Enhancers	Fetal Brain Female	brain
10	chr14:97090600-97091000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr14:97090600-97091600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr14:97090600-97092000	Enhancers	Brain Germinal Matrix	brain
13	chr14:97090800-97091400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr14:97091000-97091200	Bivalent Enhancer	Fetal Stomach	stomach
15	chr14:97091000-97091400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr14:97091000-97091600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr14:97091000-97091600	Bivalent Enhancer	Fetal Muscle Leg	muscle
18	chr14:97091000-97092200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr14:97091200-97091400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr14:97091200-97091400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr14:97091400-97091600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr14:97091400-97092600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr14:97091400-97093000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr14:97091600-97092000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr14:97092000-97092200	Bivalent Enhancer	Brain Hippocampus Middle	brain
26	chr14:97092000-97092400	Flanking Active TSS	Brain Germinal Matrix	brain
27	chr14:97092000-97095800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr14:97092400-97092600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr14:97092400-97094400	Enhancers	Brain Germinal Matrix	brain
30	chr14:97092800-97093000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr14:97093000-97093200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
32	chr14:97093000-97093200	Enhancers	GM12878-XiMat	blood
33	chr14:97093000-97093200	Bivalent/Poised TSS	K562	blood
34	chr14:97093000-97093600	Flanking Bivalent TSS/Enh	NHEK	skin
35	chr14:97093000-97094000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr14:97093000-97094400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr14:97093200-97093400	Enhancers	Spleen	Spleen
38	chr14:97093200-97093600	Flanking Active TSS	GM12878-XiMat	blood
39	chr14:97093200-97093600	Flanking Bivalent TSS/Enh	K562	blood
40	chr14:97093200-97093800	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr14:97093400-97094200	Weak transcription	Spleen	Spleen
42	chr14:97093600-97093800	Bivalent/Poised TSS	K562	blood
43	chr14:97093600-97094000	Active TSS	GM12878-XiMat	blood
44	chr14:97094000-97094600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr14:97094200-97095000	Enhancers	Spleen	Spleen
46	chr14:97095800-97097000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:97096200-97096600	ZNF genes & repeats	Right Atrium	heart
48	chr14:97097000-97098000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr14:97098000-97098400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr14:97098400-97100600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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