Variant report

Variant	nsv565651
Chromosome Location	chr14:97097653-97137681
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:248)
CpG islands
(count:244)
Chromatin interactive
region (count:36)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:248 , 50 per page) page: 1 2 3 4 5

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	ARID3A	chr14:97126507-97126797	K562	blood:	n/a	n/a
3	ATF1	chr14:97102247-97102558	K562	blood:	n/a	n/a
4	ATF1	chr14:97126481-97126798	K562	blood:	n/a	n/a
5	ATF3	chr14:97129932-97130110	K562	blood:	n/a	n/a
6	BHLHE40	chr14:97127039-97127064	K562	blood:	n/a	n/a
7	BHLHE40	chr14:97129978-97130201	K562	blood:	n/a	n/a
8	CBX3	chr14:97129917-97130313	K562	blood:	n/a	n/a
9	CBX3	chr14:97129812-97130286	K562	blood:	n/a	n/a
10	CCNT2	chr14:97126335-97126729	K562	blood:	n/a	chr14:97126450-97126459
11	CEBPB	chr14:97123015-97123332	A549	lung:	n/a	chr14:97123165-97123176
12	CEBPB	chr14:97123038-97123338	IMR90	lung:	n/a	chr14:97123165-97123176
13	CEBPB	chr14:97099041-97099257	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:97123014-97123254	K562	blood:	n/a	chr14:97123165-97123176
15	CEBPB	chr14:97123007-97123330	HepG2	liver:	n/a	chr14:97123165-97123176
16	CEBPD	chr14:97126470-97126782	K562	blood:	n/a	n/a
17	CEBPD	chr14:97132151-97132601	K562	blood:	n/a	n/a
18	CHD2	chr14:97129970-97130133	K562	blood:	n/a	n/a
19	CTCF	chr14:97132560-97132710	GM12872	blood:	n/a	n/a
20	CTCF	chr14:97137660-97137825	MCF-7	breast:	n/a	chr14:97137729-97137747 chr14:97137730-97137746 chr14:97137724-97137745
21	CTCF	chr14:97132708-97132747	GM13976	blood:	n/a	n/a
22	CTCF	chr14:97132540-97132690	HepG2	liver:	n/a	n/a
23	CTCF	chr14:97132613-97132759	LNCaP	prostate:	n/a	n/a
24	CTCF	chr14:97109374-97109423	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr14:97132629-97132716	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr14:97137681-97137799	MCF-7	breast:	n/a	chr14:97137729-97137747 chr14:97137730-97137746 chr14:97137724-97137745
27	CTCF	chr14:97132516-97132711	HepG2	liver:	n/a	n/a
28	CTCF	chr14:97132569-97132712	NHEK	skin:	n/a	n/a
29	CTCF	chr14:97132560-97132710	MCF-7	breast:	n/a	n/a
30	CTCF	chr14:97132600-97132750	GM12878	blood:	n/a	n/a
31	CTCF	chr14:97137524-97137962	MCF-7	breast:	n/a	chr14:97137729-97137747 chr14:97137730-97137746 chr14:97137724-97137745
32	CTCF	chr14:97132520-97132670	GM12864	blood:	n/a	n/a
33	CTCF	chr14:97132540-97132690	GM12873	blood:	n/a	n/a
34	CTCF	chr14:97132453-97132841	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr14:97137678-97137803	MCF-7	breast:	n/a	chr14:97137729-97137747 chr14:97137730-97137746 chr14:97137724-97137745
36	CTCF	chr14:97137640-97137790	MCF-7	breast:	n/a	chr14:97137729-97137747 chr14:97137730-97137746 chr14:97137724-97137745
37	CTCF	chr14:97132547-97132743	GM12878	blood:	n/a	n/a
38	CTCF	chr14:97137660-97137810	MCF-7	breast:	n/a	chr14:97137729-97137747 chr14:97137730-97137746 chr14:97137724-97137745
39	CTCF	chr14:97132580-97132730	Caco-2	colon:	n/a	n/a
40	CTCF	chr14:97132566-97132726	K562	blood:	n/a	n/a
41	CTCF	chr14:97137660-97137810	GM12864	blood:	n/a	chr14:97137729-97137747 chr14:97137730-97137746 chr14:97137724-97137745
42	CTCF	chr14:97132498-97132829	K562	blood:	n/a	n/a
43	CTCF	chr14:97132500-97132650	GM06990	blood:	n/a	n/a
44	CTCF	chr14:97132486-97132775	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr14:97132557-97132747	GM12892	blood:	n/a	n/a
46	CTCF	chr14:97132506-97132840	GM12878	blood:	n/a	n/a
47	CTCF	chr14:97132427-97132874	HCT-116	colon:	n/a	n/a
48	CTCF	chr14:97132640-97132790	GM12875	blood:	n/a	n/a
49	CTCF	chr14:97132580-97132730	HEK293	kidney:	n/a	n/a
50	CTCF	chr14:97132560-97132710	A549	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:97129577-97129627	ProgFib	skin:	n/a
2	chr14:97135129-97135179	SAEC	small airway:	n/a
3	chr14:97127338-97127388	HIPEpiC	eye:	n/a
4	chr14:97135129-97135179	HCM	heart:	n/a
5	chr14:97129452-97129502	H1-hESC	embryonic stem cell:	embryo
6	chr14:97129577-97129627	SK-N-SH_RA	brain:	n/a
7	chr14:97127338-97127388	K562	blood:	n/a
8	chr14:97135129-97135179	SK-N-MC	brain:	n/a
9	chr14:97135129-97135179	NB4	blood:	n/a
10	chr14:97127338-97127388	A549	lung:	n/a
11	chr14:97129452-97129502	CMK	blood:	n/a
12	chr14:97135129-97135179	GM12891	blood:	n/a
13	chr14:97129577-97129627	HepG2	liver:	n/a
14	chr14:97129452-97129502	HRCEpiC	kidney:	n/a
15	chr14:97127338-97127388	GM12892	blood:	n/a
16	chr14:97129577-97129627	HMEC	breast:	n/a
17	chr14:97129452-97129502	GM12891	blood:	n/a
18	chr14:97129577-97129627	HRPEpiC	eye:	n/a
19	chr14:97127338-97127388	HRE	kidney:	n/a
20	chr14:97129452-97129502	AG09319	gingival:	n/a
21	chr14:97127338-97127388	HUVEC	blood vessel:	n/a
22	chr14:97135129-97135179	RPTEC	kidney:	n/a
23	chr14:97129452-97129502	PANC-1	pancreas:	n/a
24	chr14:97135129-97135179	HEK293	kidney:	embryo
25	chr14:97129452-97129502	GM12878	blood:	n/a
26	chr14:97127338-97127388	NHBE	bronchial:	n/a
27	chr14:97135129-97135179	AG09319	gingival:	n/a
28	chr14:97129452-97129502	SKMC	muscle:	n/a
29	chr14:97127338-97127388	AG04449	skin:	fetal
30	chr14:97127338-97127388	U87	brain:	n/a
31	chr14:97129452-97129502	NT2-D1	testis:	n/a
32	chr14:97129452-97129502	T-47D	breast:	n/a
33	chr14:97135129-97135179	HUVEC	blood vessel:	n/a
34	chr14:97127338-97127388	MCF-7	breast:	n/a
35	chr14:97135129-97135179	K562	blood:	n/a
36	chr14:97127338-97127388	RPTEC	kidney:	n/a
37	chr14:97129452-97129502	HPAEpiC	pulmonary alveolar:	n/a
38	chr14:97127338-97127388	MCF10A-Er-Src	breast:	n/a
39	chr14:97129577-97129627	BE2_C	brain:	n/a
40	chr14:97135129-97135179	SK-N-SH	brain:	n/a
41	chr14:97127338-97127388	BJ	skin:	n/a
42	chr14:97135129-97135179	GM12892	blood:	n/a
43	chr14:97135129-97135179	AG10803	skin:	n/a
44	chr14:97127338-97127388	PFSK-1	brain:	n/a
45	chr14:97129577-97129627	PFSK-1	brain:	n/a
46	chr14:97129452-97129502	ECC-1	luminal epithelium:	n/a
47	chr14:97135129-97135179	Caco-2	colon:	n/a
48	chr14:97127338-97127388	HRPEpiC	eye:	n/a
49	chr14:97135129-97135179	BJ	skin:	n/a
50	chr14:97129452-97129502	HEEpiC	esophagus:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:97050109..97051246-chr14:97131819..97133058,6	MCF-7	breast:
2	chr14:97125727..97127557-chr14:97130189..97131813,2	K562	blood:
3	chr14:97093078..97095980-chr14:97096287..97099015,3	MCF-7	breast:
4	chr14:97049843..97051026-chr14:97131982..97133064,8	MCF-7	breast:
5	chr14:97040333..97042090-chr14:97100526..97101489,19	MCF-7	breast:
6	chr14:97121918..97124905-chr14:97127753..97129733,2	K562	blood:
7	chr14:97133535..97135440-chr14:97140308..97142145,2	MCF-7	breast:
8	chr14:97137196..97139523-chr14:97142703..97145275,2	MCF-7	breast:
9	chr14:97100553..97101432-chr14:97126836..97127804,5	MCF-7	breast:
10	chr14:97127931..97131812-chr14:97133536..97135209,3	K562	blood:
11	chr14:97098302..97100960-chr14:97102875..97104630,2	K562	blood:
12	chr14:97105478..97107756-chr14:97114890..97116903,2	MCF-7	breast:
13	chr14:97040936..97041835-chr14:97100556..97101428,4	MCF-7	breast:
14	chr14:97127690..97129431-chr14:97133268..97135036,2	K562	blood:
15	chr14:97105478..97107756-chr14:97114890..97116903,2	MCF-7	breast:
16	chr14:97047308..97047841-chr14:97100928..97101485,2	MCF-7	breast:
17	chr14:97127931..97131812-chr14:97133536..97135209,3	K562	blood:
18	chr14:97047039..97047841-chr14:97100546..97101485,3	MCF-7	breast:
19	chr14:97100553..97101432-chr14:97126836..97127804,5	MCF-7	breast:
20	chr14:97096962..97100936-chr14:97101885..97104048,3	K562	blood:
21	chr14:97041013..97042090-chr14:97100546..97101489,8	MCF-7	breast:
22	chr14:97136763..97139575-chr14:97158044..97160413,2	MCF-7	breast:
23	chr14:97100866..97101454-chr14:97138053..97138598,2	MCF-7	breast:
24	chr14:97125727..97128111-chr14:97129743..97131813,3	K562	blood:
25	chr14:97098302..97100960-chr14:97102875..97104630,2	K562	blood:
26	chr14:97130230..97132435-chr14:97152874..97154643,2	MCF-7	breast:
27	chr14:97096962..97100936-chr14:97101885..97104048,3	K562	blood:
28	chr14:97135759..97137328-chr14:97140118..97143356,3	MCF-7	breast:
29	chr14:97091981..97093780-chr14:97101556..97103907,3	MCF-7	breast:
30	chr14:97050265..97051308-chr14:97136874..97138151,3	MCF-7	breast:
31	chr14:97125727..97127557-chr14:97130189..97131813,2	K562	blood:
32	chr14:97121918..97124905-chr14:97127753..97129733,2	K562	blood:
33	chr14:97040398..97040962-chr14:97100553..97101449,2	MCF-7	breast:
34	chr14:97125727..97128111-chr14:97129743..97131813,3	K562	blood:
35	chr14:97127690..97129431-chr14:97133268..97135036,2	K562	blood:
36	chr14:93483695..93484309-chr14:97100592..97101400,2	MCF-7	breast:

(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: 1493 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1493 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs735408	chr14:97097653-97097654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs367908554	chr14:97097660-97097661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527845131	chr14:97097661-97097662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78816228	chr14:97097682-97097683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552757436	chr14:97097688-97097689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571134162	chr14:97097722-97097723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548974782	chr14:97097745-97097746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182608588	chr14:97097788-97097789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559553647	chr14:97097789-97097790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528748262	chr14:97097790-97097791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375099547	chr14:97097798-97097799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117462046	chr14:97097800-97097801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373524189	chr14:97097803-97097804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs58737714	chr14:97097807-97097808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs115916499	chr14:97097850-97097851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186472889	chr14:97097885-97097886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs199920052	chr14:97097920-97097921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs55754303	chr14:97097951-97097952	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs11621885	chr14:97097970-97097971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192365916	chr14:97097996-97097997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551702040	chr14:97098010-97098011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111673876	chr14:97098012-97098013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs17094246	chr14:97098013-97098014	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs185644892	chr14:97098053-97098054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560354226	chr14:97098064-97098065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527812721	chr14:97098065-97098066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537461783	chr14:97098113-97098114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552476499	chr14:97098114-97098115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs74089313	chr14:97098139-97098140	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs190569162	chr14:97098142-97098143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs17094250	chr14:97098149-97098150	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs568778869	chr14:97098155-97098156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535072402	chr14:97098173-97098174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553758129	chr14:97098183-97098184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs17094253	chr14:97098185-97098186	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs145029707	chr14:97098186-97098187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557527152	chr14:97098212-97098213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575786819	chr14:97098241-97098242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs17094256	chr14:97098244-97098245	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs555741283	chr14:97098268-97098269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573903586	chr14:97098304-97098305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541834050	chr14:97098305-97098306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs193065072	chr14:97098325-97098326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12435587	chr14:97098357-97098358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs546366082	chr14:97098359-97098360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564574031	chr14:97098375-97098376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531900410	chr14:97098404-97098405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555530090	chr14:97098424-97098425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147552217	chr14:97098438-97098439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550412026	chr14:97098446-97098447	Weak transcription	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:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97097000-97098000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:97098000-97098400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:97098400-97100600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:97100600-97101400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:97101200-97101600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr14:97101400-97115000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:97101600-97106000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr14:97102400-97102600	Enhancers	Spleen	Spleen
9	chr14:97102600-97103800	Weak transcription	Spleen	Spleen
10	chr14:97103800-97104200	Active TSS	Spleen	Spleen
11	chr14:97106000-97106400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr14:97115000-97115200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:97115200-97116400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:97116400-97129600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:97120000-97120600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr14:97124800-97125400	Enhancers	Duodenum Mucosa	Duodenum
17	chr14:97124800-97129600	Enhancers	Fetal Intestine Large	intestine
18	chr14:97124800-97129800	Enhancers	Fetal Intestine Small	intestine
19	chr14:97125000-97125800	Enhancers	NHEK	skin
20	chr14:97125200-97125400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:97125200-97125400	Enhancers	Stomach Mucosa	stomach
22	chr14:97125200-97125600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr14:97125200-97127200	Enhancers	K562	blood
24	chr14:97125400-97125600	Flanking Active TSS	Duodenum Mucosa	Duodenum
25	chr14:97125400-97125600	Enhancers	Pancreas	Pancrea
26	chr14:97125400-97127000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr14:97125400-97127400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr14:97125600-97126400	Weak transcription	Pancreas	Pancrea
29	chr14:97125600-97126600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr14:97126200-97127400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr14:97126200-97129800	Enhancers	H1 Cell Line	embryonic stem cell
32	chr14:97126400-97128600	Enhancers	Brain Germinal Matrix	brain
33	chr14:97126400-97129000	Enhancers	Pancreas	Pancrea
34	chr14:97126600-97127400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr14:97126600-97127600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr14:97126600-97128000	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr14:97126800-97127600	Enhancers	GM12878-XiMat	blood
38	chr14:97126800-97128000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr14:97126800-97130000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr14:97127000-97127400	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr14:97127000-97128000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr14:97127000-97128000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr14:97127000-97128200	Bivalent Enhancer	Fetal Muscle Leg	muscle
44	chr14:97127000-97129000	Enhancers	Placenta	Placenta
45	chr14:97127200-97127400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr14:97127200-97129400	Weak transcription	K562	blood
47	chr14:97127200-97129800	Enhancers	Esophagus	oesophagus
48	chr14:97127400-97128000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr14:97127400-97132000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr14:97127600-97128600	Enhancers	Fetal Brain Female	brain

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