Variant report

Variant	nsv564932
Chromosome Location	chr14:65660502-65691545
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:802)
CpG islands
(count:123)
Chromatin interactive
region (count:32)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:65678125-65678490	K562	blood:	n/a	n/a
2	ATF1	chr14:65672237-65672405	K562	blood:	n/a	n/a
3	ATF1	chr14:65676877-65677224	K562	blood:	n/a	n/a
4	ATF1	chr14:65678101-65678411	K562	blood:	n/a	n/a
5	ATF1	chr14:65674949-65675149	K562	blood:	n/a	n/a
6	ATF2	chr14:65672774-65673886	GM12878	blood:	n/a	n/a
7	ATF2	chr14:65661603-65662344	GM12878	blood:	n/a	n/a
8	ATF2	chr14:65671841-65674132	GM12878	blood:	n/a	n/a
9	ATF2	chr14:65676588-65677170	GM12878	blood:	n/a	n/a
10	ATF2	chr14:65676522-65677325	GM12878	blood:	n/a	n/a
11	ATF2	chr14:65661647-65662291	GM12878	blood:	n/a	n/a
12	ATF2	chr14:65674669-65675610	GM12878	blood:	n/a	n/a
13	ATF2	chr14:65671966-65672572	GM12878	blood:	n/a	n/a
14	ATF3	chr14:65678113-65678420	K562	blood:	n/a	n/a
15	BATF	chr14:65661691-65662114	GM12878	blood:	n/a	n/a
16	BATF	chr14:65675229-65675482	GM12878	blood:	n/a	chr14:65675361-65675372
17	BATF	chr14:65672658-65674315	GM12878	blood:	n/a	n/a
18	BATF	chr14:65676813-65677146	GM12878	blood:	n/a	n/a
19	BATF	chr14:65672936-65673837	GM12878	blood:	n/a	n/a
20	BATF	chr14:65672149-65672545	GM12878	blood:	n/a	n/a
21	BATF	chr14:65676779-65677168	GM12878	blood:	n/a	n/a
22	BATF	chr14:65672135-65672469	GM12878	blood:	n/a	n/a
23	BATF	chr14:65661654-65662259	GM12878	blood:	n/a	n/a
24	BCL11A	chr14:65672061-65672527	GM12878	blood:	n/a	n/a
25	BCL11A	chr14:65672134-65672464	GM12878	blood:	n/a	n/a
26	BCL11A	chr14:65673514-65674055	GM12878	blood:	n/a	n/a
27	BCL11A	chr14:65672937-65674148	GM12878	blood:	n/a	chr14:65673142-65673151
28	BCL11A	chr14:65676815-65677169	GM12878	blood:	n/a	n/a
29	BCL11A	chr14:65661693-65662171	GM12878	blood:	n/a	n/a
30	BCL11A	chr14:65676725-65677215	GM12878	blood:	n/a	n/a
31	BCL3	chr14:65673002-65674310	GM12878	blood:	n/a	chr14:65673142-65673151
32	BCL3	chr14:65661694-65662237	GM12878	blood:	n/a	n/a
33	BCL3	chr14:65689121-65689514	GM12878	blood:	n/a	n/a
34	BCL3	chr14:65672100-65672502	GM12878	blood:	n/a	n/a
35	BCLAF1	chr14:65661675-65662239	GM12878	blood:	n/a	n/a
36	BCLAF1	chr14:65671922-65672552	GM12878	blood:	n/a	n/a
37	BCLAF1	chr14:65671882-65672664	GM12878	blood:	n/a	n/a
38	BCLAF1	chr14:65661520-65662254	GM12878	blood:	n/a	n/a
39	BCLAF1	chr14:65672670-65674137	GM12878	blood:	n/a	chr14:65673142-65673151
40	BCLAF1	chr14:65676694-65677395	GM12878	blood:	n/a	n/a
41	BHLHE40	chr14:65672988-65674024	GM12878	blood:	n/a	n/a
42	BHLHE40	chr14:65672066-65672554	GM12878	blood:	n/a	n/a
43	BHLHE40	chr14:65661818-65662176	GM12878	blood:	n/a	n/a
44	BHLHE40	chr14:65672249-65672462	K562	blood:	n/a	n/a
45	BHLHE40	chr14:65676767-65677105	GM12878	blood:	n/a	n/a
46	BRCA1	chr14:65689160-65689478	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr14:65689710-65689795	HepG2	liver:	n/a	n/a
48	CEBPB	chr14:65673493-65673846	GM12878	blood:	n/a	n/a
49	CEBPB	chr14:65678099-65678312	K562	blood:	n/a	chr14:65678224-65678235
50	CEBPB	chr14:65678093-65678465	A549	lung:	n/a	chr14:65678224-65678235

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:65681230-65681280	HRCEpiC	kidney:	n/a
2	chr14:65681230-65681280	HRCEpiC	kidney:	n/a
3	chr14:65681230-65681280	AoSMC	blood vessel:	n/a
4	chr14:65673646-65673696	HIPEpiC	eye:	n/a
5	chr14:65673646-65673696	NHBE	bronchial:	n/a
6	chr14:65673646-65673696	MCF10A-Er-Src	breast:	n/a
7	chr14:65673646-65673696	HCF	heart:	n/a
8	chr14:65673646-65673696	MCF-7	breast:	n/a
9	chr14:65681230-65681280	BE2_C	brain:	n/a
10	chr14:65673646-65673696	A549	lung:	n/a
11	chr14:65673646-65673696	SK-N-SH_RA	brain:	n/a
12	chr14:65673646-65673696	PANC-1	pancreas:	n/a
13	chr14:65673646-65673696	SK-N-MC	brain:	n/a
14	chr14:65673646-65673696	SKMC	muscle:	n/a
15	chr14:65673646-65673696	HRCEpiC	kidney:	n/a
16	chr14:65673646-65673696	GM12892	blood:	n/a
17	chr14:65681230-65681280	PFSK-1	brain:	n/a
18	chr14:65673646-65673696	Caco-2	colon:	n/a
19	chr14:65681230-65681280	ovcar-3	ovarian:	n/a
20	chr14:65673646-65673696	ovcar-3	ovarian:	n/a
21	chr14:65681230-65681280	HNPCEpiC	eye:	n/a
22	chr14:65681230-65681280	BJ	skin:	n/a
23	chr14:65673646-65673696	AG10803	skin:	n/a
24	chr14:65681230-65681280	HCPEpiC	choroid plexus:	n/a
25	chr14:65681230-65681280	AG09319	gingival:	n/a
26	chr14:65673646-65673696	GM06990	blood:	n/a
27	chr14:65681230-65681280	HCT-116	colon:	n/a
28	chr14:65681230-65681280	MCF-7	breast:	n/a
29	chr14:65673646-65673696	IMR90	lung:	fetal
30	chr14:65681230-65681280	HRE	kidney:	n/a
31	chr14:65681230-65681280	SAEC	small airway:	n/a
32	chr14:65681230-65681280	SK-N-MC	brain:	n/a
33	chr14:65681230-65681280	AG09309	skin:	n/a
34	chr14:65673646-65673696	HMEC	breast:	n/a
35	chr14:65673646-65673696	HCPEpiC	choroid plexus:	n/a
36	chr14:65673646-65673696	H1-hESC	embryonic stem cell:	embryo
37	chr14:65673646-65673696	AG09309	skin:	n/a
38	chr14:65673646-65673696	NB4	blood:	n/a
39	chr14:65681230-65681280	PANC-1	pancreas:	n/a
40	chr14:65673646-65673696	HRE	kidney:	n/a
41	chr14:65681230-65681280	HL-60	blood:	n/a
42	chr14:65681230-65681280	CMK	blood:	n/a
43	chr14:65673646-65673696	HCM	heart:	n/a
44	chr14:65681230-65681280	HPAEpiC	pulmonary alveolar:	n/a
45	chr14:65673646-65673696	HL-60	blood:	n/a
46	chr14:65673646-65673696	HCT-116	colon:	n/a
47	chr14:65673646-65673696	NH-A	brain:	n/a
48	chr14:65673646-65673696	CMK	blood:	n/a
49	chr14:65681230-65681280	LNCaP	prostate:	n/a
50	chr14:65673646-65673696	U87	brain:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:65682951..65699539-chr14:65874873..65882779,51	MCF-7	breast:
2	chr14:65647388..65649639-chr14:65690929..65693608,3	MCF-7	breast:
3	chr14:65672466..65675216-chr14:65679164..65681633,2	MCF-7	breast:
4	chr14:65689122..65691456-chr14:65806206..65809002,2	MCF-7	breast:
5	chr10:24512569..24513529-chr14:65673481..65674224,2	MCF-7	breast:
6	chr14:65685682..65688470-chr14:65691307..65693933,2	MCF-7	breast:
7	chr14:65663873..65666764-chr14:65668430..65671209,2	MCF-7	breast:
8	chr14:65665995..65668443-chr14:65670507..65672680,2	K562	blood:
9	chr14:65672206..65674878-chr14:65876967..65879221,2	MCF-7	breast:
10	chr14:65631009..65633878-chr14:65689261..65691263,2	MCF-7	breast:
11	chr14:65688460..65689522-chr14:65878564..65879464,3	MCF-7	breast:
12	chr14:65687538..65689210-chr14:65800729..65803430,2	MCF-7	breast:
13	chr14:65665995..65668443-chr14:65670507..65672680,2	K562	blood:
14	chr14:65685385..65700060-chr14:65874568..65884730,76	MCF-7	breast:
15	chr14:65687978..65690881-chr14:65733392..65735746,2	MCF-7	breast:
16	chr14:65670192..65672045-chr14:65675137..65676974,2	K562	blood:
17	chr14:65689494..65692237-chr14:65695472..65698101,2	K562	blood:
18	chr14:65665649..65668443-chr14:65670507..65672924,2	K562	blood:
19	chr14:65685682..65688470-chr14:65691307..65693933,2	MCF-7	breast:
20	chr14:65672466..65675216-chr14:65679164..65681633,2	MCF-7	breast:
21	chr14:65663873..65666764-chr14:65668430..65671209,2	MCF-7	breast:
22	chr14:65658486..65660530-chr14:65878624..65880179,2	MCF-7	breast:
23	chr14:65684066..65685787-chr14:65691739..65693406,2	MCF-7	breast:
24	chr14:65630590..65631461-chr14:65667717..65668463,3	MCF-7	breast:
25	chr14:65674009..65676655-chr14:65879335..65881090,2	MCF-7	breast:
26	chr14:65670192..65672045-chr14:65675137..65676974,2	K562	blood:
27	chr14:65681059..65683272-chr14:65691597..65694149,3	MCF-7	breast:
28	chr14:65689238..65689806-chr14:65721908..65722565,2	MCF-7	breast:
29	chr14:65677692..65679763-chr14:65878183..65880174,3	MCF-7	breast:
30	chr14:65689123..65699940-chr14:65718655..65726829,32	MCF-7	breast:
31	chr14:65665649..65668443-chr14:65670507..65672924,2	K562	blood:
32	chr14:65681195..65684359-chr14:65877909..65881383,4	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAX-1	chr14:65684419-65684508	XLOC_011053
2	lnc-MAX-5	chr14:65670172-65670684	NONHSAT037375
3	lnc-MAX-1	chr14:65679611-65680644	ENSG00000255002
4	lnc-CHURC1-FNTB-3	chr14:65663433-65663557	l_1001_chr14:65648002-65665287_testes
5	lnc-MAX-1	chr14:65684419-65684508	ENSG00000255002
6	lnc-MAX-1	chr14:65688937-65689065	ENSG00000255002
7	lnc-CHURC1-FNTB-3	chr14:65664226-65665287	l_1001_chr14:65648002-65665287_testes
8	lnc-CHURC1-FNTB-3	chr14:65662938-65662980	l_1001_chr14:65648002-65665287_testes
9	lnc-MAX-1	chr14:65688937-65689065	XLOC_011053
10	lnc-MAX-1	chr14:65685225-65685413	ENSG00000255002
11	lnc-CHURC1-FNTB-3	chr14:65663644-65663673	l_1001_chr14:65648002-65665287_testes
12	lnc-MAX-1	chr14:65679612-65680644	XLOC_011053
13	lnc-CHURC1-FNTB-3	chr14:65662240-65662362	l_1001_chr14:65648002-65665287_testes
14	lnc-MAX-1	chr14:65685225-65685413	XLOC_011053

No data

Variant related genes	Relation type
ENSG00000255002	TF binding region
ENSG00000255002	CpG island
ENSG00000266740	chromatin interactions
ENSG00000214759	chromatin interactions
ENSG00000033170	chromatin interactions
ENSG00000258613	chromatin interactions

Extended variants
information (count: 1165 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1165 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12588672	chr14:65660502-65660503	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140776058	chr14:65660543-65660544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142079571	chr14:65660565-65660566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs180924262	chr14:65660567-65660568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs766907	chr14:65660568-65660569	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs186152286	chr14:65660616-65660617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576874324	chr14:65660617-65660618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545589164	chr14:65660634-65660635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs17102477	chr14:65660644-65660645	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs542955703	chr14:65660702-65660703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572711907	chr14:65660733-65660734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs116179693	chr14:65660762-65660763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377762426	chr14:65660780-65660781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561667018	chr14:65660803-65660804	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs530003474	chr14:65660841-65660842	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs543804466	chr14:65660844-65660845	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs1679876	chr14:65660923-65660924	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs201847432	chr14:65660941-65660942	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs151113770	chr14:65660955-65660956	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs565518737	chr14:65660973-65660974	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs528314150	chr14:65660982-65660983	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs548068469	chr14:65661045-65661046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147044763	chr14:65661055-65661056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188256742	chr14:65661080-65661081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141121534	chr14:65661147-65661148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35196405	chr14:65661154-65661155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148077203	chr14:65661217-65661218	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs150271166	chr14:65661241-65661242	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs532087406	chr14:65661291-65661292	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs551797605	chr14:65661311-65661312	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs570416914	chr14:65661320-65661321	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs539524809	chr14:65661323-65661324	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs553132297	chr14:65661361-65661362	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs116742597	chr14:65661380-65661381	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs541654821	chr14:65661423-65661424	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs571876227	chr14:65661534-65661535	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs554918956	chr14:65661537-65661538	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs575099936	chr14:65661538-65661539	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs534152788	chr14:65661543-65661544	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs139201949	chr14:65661570-65661571	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs111887101	chr14:65661617-65661618	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs553926558	chr14:65661650-65661651	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs182036985	chr14:65661664-65661665	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs559459364	chr14:65661666-65661667	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs528229184	chr14:65661699-65661700	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs186370247	chr14:65661724-65661725	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs147055515	chr14:65661766-65661767	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs371422103	chr14:65661768-65661769	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs138419880	chr14:65661771-65661772	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs78592902	chr14:65661803-65661804	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65654800-65660600	Weak transcription	Primary B cells from peripheral blood	blood
2	chr14:65659800-65661400	Enhancers	Fetal Intestine Large	intestine
3	chr14:65660200-65661400	Enhancers	Fetal Intestine Small	intestine
4	chr14:65660400-65661200	Enhancers	GM12878-XiMat	blood
5	chr14:65660600-65660800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr14:65660600-65661200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr14:65660600-65661200	Enhancers	Brain Germinal Matrix	brain
8	chr14:65660600-65661200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr14:65660600-65661400	Enhancers	Brain Anterior Caudate	brain
10	chr14:65660600-65663000	Enhancers	Primary B cells from peripheral blood	blood
11	chr14:65660800-65661000	Bivalent Enhancer	HepG2	liver
12	chr14:65661000-65661400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr14:65661000-65661800	Enhancers	Brain Substantia Nigra	brain
14	chr14:65661000-65662200	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr14:65661000-65662600	Enhancers	HepG2	liver
16	chr14:65661200-65661800	Flanking Active TSS	GM12878-XiMat	blood
17	chr14:65661400-65662000	Weak transcription	Brain Anterior Caudate	brain
18	chr14:65661400-65665000	Weak transcription	Fetal Intestine Large	intestine
19	chr14:65661400-65665000	Weak transcription	Fetal Intestine Small	intestine
20	chr14:65661600-65663000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr14:65661800-65662200	Enhancers	Primary B cells from cord blood	blood
22	chr14:65661800-65662200	Active TSS	GM12878-XiMat	blood
23	chr14:65661800-65662400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr14:65661800-65662400	Weak transcription	Brain Substantia Nigra	brain
25	chr14:65661800-65663000	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr14:65661800-65663000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr14:65662000-65662200	Enhancers	Brain Anterior Caudate	brain
28	chr14:65662200-65662800	Flanking Active TSS	GM12878-XiMat	blood
29	chr14:65662400-65662600	Enhancers	Brain Substantia Nigra	brain
30	chr14:65662800-65663000	Enhancers	GM12878-XiMat	blood
31	chr14:65663000-65664400	Weak transcription	Primary B cells from peripheral blood	blood
32	chr14:65664400-65665000	Enhancers	Primary B cells from peripheral blood	blood
33	chr14:65664400-65665600	Enhancers	GM12878-XiMat	blood
34	chr14:65665000-65665600	Enhancers	Fetal Intestine Large	intestine
35	chr14:65665000-65665600	Enhancers	Fetal Intestine Small	intestine
36	chr14:65665000-65665600	Enhancers	HepG2	liver
37	chr14:65665000-65667600	Weak transcription	Primary B cells from peripheral blood	blood
38	chr14:65665200-65665600	Enhancers	Fetal Heart	heart
39	chr14:65665200-65665600	Enhancers	Fetal Muscle Leg	muscle
40	chr14:65665600-65667400	Weak transcription	Fetal Muscle Leg	muscle
41	chr14:65665600-65667600	Weak transcription	Fetal Intestine Large	intestine
42	chr14:65665600-65667800	Weak transcription	Fetal Intestine Small	intestine
43	chr14:65665600-65668000	Weak transcription	GM12878-XiMat	blood
44	chr14:65665600-65671000	Weak transcription	HepG2	liver
45	chr14:65667200-65667600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr14:65667400-65667600	Enhancers	Fetal Muscle Leg	muscle
47	chr14:65667600-65668000	Enhancers	Fetal Intestine Large	intestine
48	chr14:65667600-65668600	Enhancers	Primary B cells from peripheral blood	blood
49	chr14:65667600-65670400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr14:65667800-65668200	Enhancers	Fetal Intestine Small	intestine

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