Variant report

Variant	nsv1037823
Chromosome Location	chr14:46873171-47013125
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	BCLAF1	chr14:46959550-46960028	GM12878	blood:	n/a	n/a
2	CEBPB	chr14:46874424-46874880	ECC-1	luminal epithelium:	n/a	n/a
3	CEBPB	chr14:47007646-47007959	IMR90	lung:	n/a	chr14:47007809-47007820
4	CEBPB	chr14:46959424-46959778	HepG2	liver:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
5	CEBPB	chr14:46959392-46959846	MCF-7	breast:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
6	CEBPB	chr14:46887890-46888142	HepG2	liver:	n/a	chr14:46887964-46887975
7	CEBPB	chr14:46874491-46874834	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr14:47007729-47007887	K562	blood:	n/a	chr14:47007809-47007820
9	CEBPB	chr14:46922132-46922270	HepG2	liver:	n/a	chr14:46922172-46922183
10	CEBPB	chr14:46944327-46944520	HepG2	liver:	n/a	chr14:46944345-46944356
11	CEBPB	chr14:47007631-47007991	HepG2	liver:	n/a	chr14:47007809-47007820
12	CEBPB	chr14:46901890-46901905	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr14:46887921-46888002	K562	blood:	n/a	chr14:46887964-46887975
14	CEBPB	chr14:46959344-46959844	MCF-7	breast:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
15	CEBPB	chr14:46959463-46959768	A549	lung:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
16	CEBPB	chr14:47007725-47007946	H1-hESC	embryonic stem cell:	n/a	chr14:47007809-47007820
17	CEBPB	chr14:46874231-46874599	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr14:47007629-47007980	A549	lung:	n/a	chr14:47007809-47007820
19	CEBPB	chr14:46959438-46959906	H1-hESC	embryonic stem cell:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
20	CEBPB	chr14:46874550-46874834	MCF-7	breast:	n/a	n/a
21	CEBPB	chr14:46957289-46957481	HepG2	liver:	n/a	chr14:46957452-46957465 chr14:46957352-46957363 chr14:46957351-46957364
22	CEBPB	chr14:46889950-46890217	HepG2	liver:	n/a	chr14:46890121-46890134 chr14:46890122-46890133
23	CHD1	chr14:46921497-46921523	GM12878	blood:	n/a	n/a
24	CTCF	chr14:46959740-46959890	HEK293	kidney:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
25	CTCF	chr14:46959740-46959890	HBMEC	blood vessel:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
26	CTCF	chr14:46959720-46959870	GM12873	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
27	CTCF	chr14:46959690-46959923	Gliobla	brain:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
28	CTCF	chr14:47003620-47003770	BE2_C	brain:	n/a	n/a
29	CTCF	chr14:46959758-46959857	GM10266	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
30	CTCF	chr14:46959740-46959890	GM12875	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
31	CTCF	chr14:46959738-46959901	HepG2	liver:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
32	CTCF	chr14:46959700-46959850	GM12871	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
33	CTCF	chr14:46959699-46959924	GM13977	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
34	CTCF	chr14:46959740-46959890	RPTEC	kidney:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
35	CTCF	chr14:46959739-46959899	Pancreas_OC	pancreas:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
36	CTCF	chr14:46959800-46959950	HEK293	kidney:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834 chr14:46959936-46959944
37	CTCF	chr14:46959780-46959930	MCF-7	breast:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
38	CTCF	chr14:47003688-47003770	Medullo	brain:	n/a	n/a
39	CTCF	chr14:46959680-46959830	NHEK	skin:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828
40	CTCF	chr14:46959780-46959930	HCT-116	colon:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
41	CTCF	chr14:46959680-46959830	HMF	breast:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828
42	CTCF	chr14:46959699-46959933	MCF-7	breast:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
43	CTCF	chr14:46959720-46959870	GM12874	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
44	CTCF	chr14:46959760-46959910	HBMEC	blood vessel:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
45	CTCF	chr14:46959717-46959855	HepG2	liver:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
46	CTCF	chr14:46959720-46959870	HRE	kidney:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
47	CTCF	chr14:46959740-46959890	HEEpiC	esophagus:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
48	CTCF	chr14:46959716-46959892	Medullo	brain:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
49	CTCF	chr14:46933940-46934090	AG10803	skin:	n/a	n/a
50	CTCF	chr14:46959760-46959910	GM12867	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46916080-46916130	SK-N-SH	brain:	n/a
2	chr14:46874779-46874829	SK-N-SH_RA	brain:	n/a
3	chr14:46916528-46916578	GM06990	blood:	n/a
4	chr14:46916080-46916130	HepG2	liver:	n/a
5	chr14:46874779-46874829	AG09319	gingival:	n/a
6	chr14:46874779-46874829	HCF	heart:	n/a
7	chr14:46874779-46874829	SK-N-SH	brain:	n/a
8	chr14:46916528-46916578	AG09309	skin:	n/a
9	chr14:46916080-46916130	H1-hESC	embryonic stem cell:	embryo
10	chr14:46916080-46916130	BE2_C	brain:	n/a
11	chr14:46874779-46874829	Caco-2	colon:	n/a
12	chr14:46916080-46916130	MCF10A-Er-Src	breast:	n/a
13	chr14:46874779-46874829	AG09309	skin:	n/a
14	chr14:46916080-46916130	CMK	blood:	n/a
15	chr14:46874779-46874829	HUVEC	blood vessel:	n/a
16	chr14:46916080-46916130	GM12891	blood:	n/a
17	chr14:46916528-46916578	H1-hESC	embryonic stem cell:	embryo
18	chr14:46916528-46916578	NH-A	brain:	n/a
19	chr14:46916528-46916578	HCT-116	colon:	n/a
20	chr14:46916528-46916578	PrEC	prostate:	n/a
21	chr14:46916080-46916130	SK-N-MC	brain:	n/a
22	chr14:46874779-46874829	HCM	heart:	n/a
23	chr14:46916528-46916578	AG10803	skin:	n/a
24	chr14:46916528-46916578	HCM	heart:	n/a
25	chr14:46874779-46874829	HEEpiC	esophagus:	n/a
26	chr14:46916080-46916130	HCM	heart:	n/a
27	chr14:46874779-46874829	HEK293	kidney:	embryo
28	chr14:46874779-46874829	HMEC	breast:	n/a
29	chr14:46916528-46916578	AG04449	skin:	fetal
30	chr14:46874779-46874829	NHBE	bronchial:	n/a
31	chr14:46916528-46916578	MCF10A-Er-Src	breast:	n/a
32	chr14:46874779-46874829	SAEC	small airway:	n/a
33	chr14:46916528-46916578	HL-60	blood:	n/a
34	chr14:46916528-46916578	SK-N-SH_RA	brain:	n/a
35	chr14:46916528-46916578	SKMC	muscle:	n/a
36	chr14:46916528-46916578	IMR90	lung:	fetal
37	chr14:46874779-46874829	A549	lung:	n/a
38	chr14:46874779-46874829	AoSMC	blood vessel:	n/a
39	chr14:46874779-46874829	HepG2	liver:	n/a
40	chr14:46916080-46916130	NHDF-neo	bronchial:	n/a
41	chr14:46874779-46874829	MCF-7	breast:	n/a
42	chr14:46874779-46874829	GM12878	blood:	n/a
43	chr14:46916528-46916578	HRCEpiC	kidney:	n/a
44	chr14:46916080-46916130	HAEpiC	amniotic membrane:	n/a
45	chr14:46916080-46916130	A549	lung:	n/a
46	chr14:46916080-46916130	HEK293	kidney:	embryo
47	chr14:46916080-46916130	HCPEpiC	choroid plexus:	n/a
48	chr14:46916080-46916130	Hepatocyte	liver:	n/a
49	chr14:46916080-46916130	T-47D	breast:	n/a
50	chr14:46916080-46916130	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
2	chr14:46984156..46986673-chr14:46987478..46989928,2	K562	blood:
3	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
4	chr14:46984156..46986673-chr14:46987478..46989928,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-6	chr14:46940562-46940714	NONHSAT036681
2	lnc-FANCM-6	chr14:46970510-46971026	ENSG00000258700
3	lnc-FANCM-6	chr14:46919111-46919157	ENSG00000258700
4	lnc-FANCM-6	chr14:46916512-46916578	ENSG00000258700
5	lnc-FANCM-6	chr14:46970510-46971104	NONHSAT036681
6	lnc-FANCM-6	chr14:46970510-46971104	NONHSAT036680
7	lnc-FANCM-6	chr14:46959395-46959490	ENSG00000258700
8	lnc-FANCM-6	chr14:46940562-46940714	ENSG00000258700
9	lnc-FANCM-6	chr14:46919111-46919157	NONHSAT036678
10	lnc-FANCM-6	chr14:46970510-46970814	ENSG00000258700
11	lnc-FANCM-6	chr14:46915388-46915429	ENSG00000258700
12	lnc-FANCM-6	chr14:46970510-46970814	ENSG00000258700
13	lnc-FANCM-6	chr14:46907384-46907453	NONHSAT036678
14	lnc-FANCM-6	chr14:46907384-46907453	ENSG00000258700
15	lnc-FANCM-6	chr14:46959395-46959490	NONHSAT036681
16	lnc-FANCM-6	chr14:46970510-46971104	NONHSAT036679
17	lnc-FANCM-6	chr14:46940562-46940714	NONHSAT036680
18	lnc-FANCM-6	chr14:46940564-46940714	ENSG00000258700
19	lnc-FANCM-6	chr14:46970510-46971104	NONHSAT036678

Variant related genes	Relation type
LINC00871	TF binding region
LINC00871	CpG island

Extended variants
information (count: 2213 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2213 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567224646	chr14:46873175-46873176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534610725	chr14:46873188-46873189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114681463	chr14:46873194-46873195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183838152	chr14:46873204-46873205	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539999417	chr14:46873218-46873219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187327065	chr14:46873243-46873244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4379984	chr14:46873257-46873258	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs543506805	chr14:46873259-46873260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537616622	chr14:46873299-46873300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116022906	chr14:46873304-46873305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561858853	chr14:46873306-46873307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4533179	chr14:46873328-46873329	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs541075151	chr14:46873402-46873403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559201359	chr14:46873446-46873447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs61991023	chr14:46873450-46873451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551670113	chr14:46873464-46873465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10131183	chr14:46873474-46873475	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs530733920	chr14:46873584-46873585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549058338	chr14:46873597-46873598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567408387	chr14:46873598-46873599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77803374	chr14:46873611-46873612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191911409	chr14:46873619-46873620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78080512	chr14:46873622-46873623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183994366	chr14:46873632-46873633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572220671	chr14:46873731-46873732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576521533	chr14:46873753-46873754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2415984	chr14:46873776-46873777	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs138332861	chr14:46873784-46873785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs72672810	chr14:46873833-46873834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs61991024	chr14:46873856-46873857	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs542911524	chr14:46873872-46873873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371866892	chr14:46873873-46873874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111984102	chr14:46873890-46873891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577986506	chr14:46874001-46874002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186901921	chr14:46874016-46874017	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544926003	chr14:46874077-46874078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144139565	chr14:46874099-46874100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192747702	chr14:46874106-46874107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531801790	chr14:46874155-46874156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375618671	chr14:46874159-46874160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551922424	chr14:46874161-46874162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570481717	chr14:46874230-46874231	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs369713445	chr14:46874254-46874255	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs549243991	chr14:46874262-46874263	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs574565720	chr14:46874362-46874363	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs146903762	chr14:46874396-46874397	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs184262852	chr14:46874398-46874399	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs533031095	chr14:46874406-46874407	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs571112360	chr14:46874425-46874426	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs373990650	chr14:46874426-46874427	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	19907438	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46869200-46874200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr14:46871600-46874400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr14:46871800-46874200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr14:46871800-46874400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr14:46871800-46875200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr14:46871800-46877200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr14:46872000-46875000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr14:46872200-46877800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr14:46872800-46875000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr14:46873000-46873600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr14:46873000-46876200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr14:46873200-46873600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr14:46873200-46874400	Enhancers	Fetal Lung	lung
14	chr14:46873200-46876000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr14:46873400-46874200	Enhancers	Fetal Kidney	kidney
16	chr14:46873400-46876000	Enhancers	Brain Germinal Matrix	brain
17	chr14:46873600-46874000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr14:46873600-46874800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr14:46874000-46874200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr14:46874000-46874200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr14:46874200-46874600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr14:46874200-46874600	Active TSS	Brain Anterior Caudate	brain
23	chr14:46874200-46874600	Enhancers	Placenta Amnion	Placenta Amnion
24	chr14:46874200-46874800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr14:46874200-46874800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr14:46874200-46874800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr14:46874200-46874800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr14:46874200-46874800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr14:46874200-46874800	Flanking Active TSS	Fetal Kidney	kidney
30	chr14:46874200-46875000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr14:46874200-46875000	Enhancers	Adipose Nuclei	Adipose
32	chr14:46874200-46875000	Enhancers	Brain Substantia Nigra	brain
33	chr14:46874200-46875000	Enhancers	Colon Smooth Muscle	Colon
34	chr14:46874200-46875000	Enhancers	Fetal Intestine Large	intestine
35	chr14:46874200-46875000	Enhancers	Fetal Intestine Small	intestine
36	chr14:46874400-46874600	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr14:46874400-46874800	Enhancers	H9 Cell Line	embryonic stem cell
38	chr14:46874400-46874800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr14:46874400-46874800	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr14:46874400-46874800	Enhancers	Brain Hippocampus Middle	brain
41	chr14:46874400-46874800	Flanking Active TSS	Fetal Lung	lung
42	chr14:46874400-46874800	Enhancers	Fetal Stomach	stomach
43	chr14:46874600-46875000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr14:46874600-46875000	Enhancers	Brain Anterior Caudate	brain
45	chr14:46874800-46875000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr14:46874800-46875000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr14:46874800-46875000	Enhancers	Fetal Lung	lung
48	chr14:46874800-46875200	Enhancers	Fetal Kidney	kidney
49	chr14:46874800-46875400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr14:46874800-46877400	Enhancers	iPS-18 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links