Variant report

Variant	esv3490802
Chromosome Location	chr14:25560793-25675699
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:707)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:707 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:25620187-25620459	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:25667033-25667379	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:25602072-25602412	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:25620155-25620373	K562	blood:	n/a	n/a
5	ARID3A	chr14:25591062-25591237	HepG2	liver:	n/a	n/a
6	BACH1	chr14:25602060-25602357	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr14:25562557-25562633	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr14:25590974-25591358	K562	blood:	n/a	chr14:25591164-25591178 chr14:25591100-25591114
9	BACH1	chr14:25590914-25591590	H1-hESC	embryonic stem cell:	n/a	chr14:25591164-25591178 chr14:25591100-25591114
10	BATF	chr14:25591995-25592363	GM12878	blood:	n/a	n/a
11	BCL3	chr14:25629964-25630301	GM12878	blood:	n/a	n/a
12	BCL3	chr14:25621001-25621255	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:25602014-25602358	GM12878	blood:	n/a	n/a
14	BHLHE40	chr14:25602003-25602344	K562	blood:	n/a	n/a
15	BRCA1	chr14:25601956-25602253	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr14:25602081-25602287	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:25593665-25593984	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:25591539-25591800	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:25667032-25667428	HepG2	liver:	n/a	chr14:25667233-25667244
20	CEBPB	chr14:25590913-25591193	HepG2	liver:	n/a	chr14:25591008-25591019 chr14:25591010-25591019
21	CEBPB	chr14:25572564-25572774	HepG2	liver:	n/a	n/a
22	CEBPB	chr14:25667001-25667429	HepG2	liver:	n/a	chr14:25667233-25667244
23	CEBPB	chr14:25583480-25583583	K562	blood:	n/a	chr14:25583532-25583543
24	CEBPB	chr14:25667024-25667456	HepG2	liver:	n/a	chr14:25667233-25667244
25	CEBPB	chr14:25590824-25591251	MCF-7	breast:	n/a	chr14:25591008-25591019 chr14:25591010-25591019
26	CEBPB	chr14:25563377-25563729	IMR90	lung:	n/a	n/a
27	CEBPB	chr14:25572595-25572849	IMR90	lung:	n/a	n/a
28	CEBPB	chr14:25667053-25667379	HepG2	liver:	n/a	chr14:25667233-25667244
29	CEBPB	chr14:25583392-25583698	HepG2	liver:	n/a	chr14:25583532-25583543
30	CEBPB	chr14:25580134-25580914	IMR90	lung:	n/a	n/a
31	CEBPB	chr14:25590817-25591847	IMR90	lung:	n/a	chr14:25591008-25591019 chr14:25591010-25591019
32	CEBPD	chr14:25667005-25667415	HepG2	liver:	n/a	n/a
33	CEBPD	chr14:25667086-25667322	HepG2	liver:	n/a	n/a
34	CHD2	chr14:25602004-25602329	HepG2	liver:	n/a	n/a
35	CREB1	chr14:25602034-25602315	A549	lung:	n/a	n/a
36	CTCF	chr14:25620200-25620350	GM12878	blood:	n/a	chr14:25620316-25620334 chr14:25620317-25620333 chr14:25620322-25620331 chr14:25620311-25620332
37	CTCF	chr14:25620220-25620370	HUVEC	blood vessel:	n/a	chr14:25620316-25620334 chr14:25620317-25620333 chr14:25620322-25620331 chr14:25620311-25620332
38	CTCF	chr14:25602055-25602346	NHEK	skin:	n/a	n/a
39	CTCF	chr14:25602140-25602290	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr14:25620202-25620430	MCF-7	breast:	n/a	chr14:25620316-25620334 chr14:25620317-25620333 chr14:25620322-25620331 chr14:25620311-25620332
41	CTCF	chr14:25620220-25620370	GM12871	blood:	n/a	chr14:25620316-25620334 chr14:25620317-25620333 chr14:25620322-25620331 chr14:25620311-25620332
42	CTCF	chr14:25620780-25620930	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr14:25620215-25620431	LNCaP	prostate:	n/a	chr14:25620316-25620334 chr14:25620317-25620333 chr14:25620322-25620331 chr14:25620311-25620332
44	CTCF	chr14:25620220-25620370	GM12870	blood:	n/a	chr14:25620316-25620334 chr14:25620317-25620333 chr14:25620322-25620331 chr14:25620311-25620332
45	CTCF	chr14:25620220-25620370	GM12867	blood:	n/a	chr14:25620316-25620334 chr14:25620317-25620333 chr14:25620322-25620331 chr14:25620311-25620332
46	CTCF	chr14:25602140-25602290	HEK293	kidney:	n/a	n/a
47	CTCF	chr14:25602085-25602340	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr14:25620585-25620694	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr14:25601875-25601904	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr14:25602140-25602290	GM12866	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:25591076-25591126	NB4	blood:	n/a
2	chr14:25591076-25591126	NH-A	brain:	n/a
3	chr14:25591076-25591126	HL-60	blood:	n/a
4	chr14:25591076-25591126	GM06990	blood:	n/a
5	chr14:25591076-25591126	H1-hESC	embryonic stem cell:	embryo
6	chr14:25591076-25591126	GM19239	blood:	n/a
7	chr14:25591076-25591126	ovcar-3	ovarian:	n/a
8	chr14:25591076-25591126	NHBE	bronchial:	n/a
9	chr14:25591076-25591126	U87	brain:	n/a
10	chr14:25591076-25591126	ECC-1	luminal epithelium:	n/a
11	chr14:25591076-25591126	HRCEpiC	kidney:	n/a
12	chr14:25591076-25591126	HCPEpiC	choroid plexus:	n/a
13	chr14:25591076-25591126	Hepatocyte	liver:	n/a
14	chr14:25591076-25591126	K562	blood:	n/a
15	chr14:25591076-25591126	AG09309	skin:	n/a
16	chr14:25591076-25591126	AoSMC	blood vessel:	n/a
17	chr14:25591076-25591126	HCM	heart:	n/a
18	chr14:25591076-25591126	IMR90	lung:	fetal
19	chr14:25591076-25591126	PANC-1	pancreas:	n/a
20	chr14:25591076-25591126	Jurkat	blood:	n/a
21	chr14:25591076-25591126	SKMC	muscle:	n/a
22	chr14:25591076-25591126	GM12878	blood:	n/a
23	chr14:25591076-25591126	HPAEpiC	pulmonary alveolar:	n/a
24	chr14:25591076-25591126	HMEC	breast:	n/a
25	chr14:25591076-25591126	RPTEC	kidney:	n/a
26	chr14:25591076-25591126	MCF-7	breast:	n/a
27	chr14:25591076-25591126	SK-N-MC	brain:	n/a
28	chr14:25591076-25591126	HEK293	kidney:	embryo
29	chr14:25591076-25591126	SAEC	small airway:	n/a
30	chr14:25591076-25591126	HNPCEpiC	eye:	n/a
31	chr14:25591076-25591126	HRE	kidney:	n/a
32	chr14:25591076-25591126	AG04449	skin:	fetal
33	chr14:25591076-25591126	HUVEC	blood vessel:	n/a
34	chr14:25591076-25591126	SK-N-SH	brain:	n/a
35	chr14:25591076-25591126	GM12891	blood:	n/a
36	chr14:25591076-25591126	NHDF-neo	bronchial:	n/a
37	chr14:25591076-25591126	SK-N-SH_RA	brain:	n/a
38	chr14:25591076-25591126	ProgFib	skin:	n/a
39	chr14:25591076-25591126	A549	lung:	n/a
40	chr14:25591076-25591126	BE2_C	brain:	n/a
41	chr14:25591076-25591126	HCF	heart:	n/a
42	chr14:25591076-25591126	AG04450	lung:	fetal
43	chr14:25591076-25591126	NT2-D1	testis:	n/a
44	chr14:25591076-25591126	Hela-S3	cervix:	n/a
45	chr14:25591076-25591126	LNCaP	prostate:	n/a
46	chr14:25591076-25591126	AG10803	skin:	n/a
47	chr14:25591076-25591126	HCT-116	colon:	n/a
48	chr14:25591076-25591126	GM12892	blood:	n/a
49	chr14:25591076-25591126	T-47D	breast:	n/a
50	chr14:25591076-25591126	PrEC	prostate:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:25275145..25275846-chr14:25601792..25602797,3	K562	blood:
2	chr14:25663713..25666461-chr14:25668359..25670561,2	MCF-7	breast:
3	chr14:25275176..25276196-chr14:25601801..25602663,4	MCF-7	breast:
4	chr14:25286771..25287566-chr14:25619855..25620690,2	MCF-7	breast:
5	chr14:25286776..25287734-chr14:25601846..25602711,3	MCF-7	breast:
6	chr14:25511682..25512314-chr14:25602148..25602701,2	MCF-7	breast:
7	chr14:25179769..25180290-chr14:25601765..25602552,2	K562	blood:
8	chr14:25275205..25275993-chr14:25619860..25620768,3	MCF-7	breast:
9	chr14:25321574..25322086-chr14:25619974..25620739,2	MCF-7	breast:
10	chr14:25501777..25502348-chr14:25601749..25602573,2	MCF-7	breast:
11	chr14:25663713..25666461-chr14:25668359..25670561,2	MCF-7	breast:
12	chr14:25203987..25204775-chr14:25619881..25620710,3	MCF-7	breast:
13	chr14:25203927..25204680-chr14:25601779..25602586,4	MCF-7	breast:
14	chr14:25275324..25276030-chr14:25620025..25620602,2	K562	blood:
15	chr14:25275628..25276165-chr14:25620088..25620783,2	MCF-7	breast:
16	chr14:25542344..25543253-chr14:25601699..25602268,2	MCF-7	breast:
17	chr14:25275544..25276429-chr14:25600109..25600712,2	MCF-7	breast:
18	chr14:25286870..25287678-chr14:25619872..25620704,2	MCF-7	breast:
19	chr14:25542516..25543294-chr14:25601722..25602419,2	MCF-7	breast:
20	chr14:25662784..25663292-chr14:25869923..25870533,2	MCF-7	breast:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STXBP6-1	chr14:25581978-25582064	NONHSAT036073
2	lnc-STXBP6-1	chr14:25593693-25593896	ENSG00000258098
3	lnc-STXBP6-1	chr14:25571098-25571467	XLOC_010978
4	lnc-STXBP6-1	chr14:25587727-25587877	NONHSAT036073
5	lnc-STXBP6-1	chr14:25591046-25591222	NONHSAT036073
6	lnc-STXBP6-1	chr14:25581978-25582063	XLOC_010978
7	lnc-RP11-80A15.1.1-3	chr14:25564556-25564798	XLOC_010773
8	lnc-STXBP6-1	chr14:25596124-25596488	XLOC_010978
9	lnc-STXBP6-1	chr14:25591048-25591222	XLOC_010978
10	lnc-RP11-80A15.1.1-4	chr14:25591048-25591222	XLOC_010774
11	lnc-STXBP6-1	chr14:25593715-25593896	NONHSAT036077
12	lnc-STXBP6-1	chr14:25625394-25625439	NONHSAT036073
13	lnc-RP11-80A15.1.1-4	chr14:25581978-25582066	XLOC_010774
14	lnc-STXBP6-1	chr14:25614608-25614748	NONHSAT036073
15	lnc-STXBP6-1	chr14:25614608-25614748	NONHSAT036077
16	lnc-RP11-80A15.1.1-3	chr14:25571262-25571468	XLOC_010773
17	lnc-STXBP6-1	chr14:25571045-25571467	XLOC_010978
18	lnc-STXBP6-1	chr14:25624974-25625034	NONHSAT036073
19	lnc-STXBP6-1	chr14:25596124-25596487	XLOC_010978
20	lnc-STXBP6-1	chr14:25593712-25593896	XLOC_010978
21	lnc-STXBP6-1	chr14:25596124-25596204	ENSG00000258098
22	lnc-STXBP6-1	chr14:25624974-25625034	NONHSAT036077
23	lnc-STXBP6-1	chr14:25614608-25614750	XLOC_010978
24	lnc-STXBP6-1	chr14:25614608-25614751	XLOC_010978
25	lnc-STXBP6-1	chr14:25614608-25614751	XLOC_010978
26	lnc-STXBP6-1	chr14:25596124-25596487	NONHSAT036077
27	lnc-STXBP6-1	chr14:25591046-25591222	XLOC_010978
28	lnc-STXBP6-1	chr14:25625394-25625439	NONHSAT036077
29	lnc-STXBP6-1	chr14:25571251-25571467	NONHSAT036073
30	lnc-STXBP6-1	chr14:25593712-25593896	XLOC_010978

No data

Variant related genes	Relation type
ENSG00000258098	TF binding region
ENSG00000258098	CpG island
SOX9	miRNA target sites
C5orf41	miRNA target sites
ADO	miRNA target sites
SECISBP2	miRNA target sites
ARF4	miRNA target sites
GCFC1	miRNA target sites

Extended variants
information (count: 2691 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2691 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528926898	chr14:25560812-25560813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs200403447	chr14:25560813-25560814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572524789	chr14:25560822-25560823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559726514	chr14:25560823-25560824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528292849	chr14:25560824-25560825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148081920	chr14:25560831-25560832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77040052	chr14:25560856-25560857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576490131	chr14:25560891-25560892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370672349	chr14:25560894-25560895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs61979906	chr14:25560903-25560904	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs533240242	chr14:25560971-25560972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562609586	chr14:25560996-25560997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148808204	chr14:25561028-25561029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569697723	chr14:25561069-25561070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535496241	chr14:25561076-25561077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555635427	chr14:25561113-25561114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191596565	chr14:25561153-25561154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535333327	chr14:25561215-25561216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558038275	chr14:25561228-25561229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561648814	chr14:25561257-25561258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs578142449	chr14:25561264-25561265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181865452	chr14:25561267-25561268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs557128647	chr14:25561297-25561298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186513210	chr14:25561328-25561329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542692272	chr14:25561331-25561332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142396200	chr14:25561340-25561341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528334155	chr14:25561342-25561343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545309629	chr14:25561344-25561345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564908527	chr14:25561372-25561373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1958387	chr14:25561403-25561404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111417884	chr14:25561404-25561405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190054156	chr14:25561421-25561422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1958388	chr14:25561456-25561457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182300544	chr14:25561469-25561470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548922025	chr14:25561510-25561511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186735569	chr14:25561537-25561538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565749350	chr14:25561549-25561550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534981379	chr14:25561593-25561594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552082358	chr14:25561623-25561624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571734502	chr14:25561627-25561628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189589320	chr14:25561642-25561643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1958389	chr14:25561645-25561646	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs150886198	chr14:25561685-25561686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536362446	chr14:25561692-25561693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112893529	chr14:25561739-25561740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552970921	chr14:25561774-25561775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548661314	chr14:25561788-25561789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572822973	chr14:25561796-25561797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7141373	chr14:25561798-25561799	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs555214062	chr14:25561870-25561871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25547000-25561600	Weak transcription	Pancreas	Pancrea
2	chr14:25558200-25563600	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr14:25558600-25561800	Enhancers	HSMM	muscle
4	chr14:25559400-25560800	Enhancers	Osteobl	bone
5	chr14:25559600-25560800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr14:25559600-25560800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr14:25559600-25561000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr14:25559600-25561000	Enhancers	HSMMtube	muscle
9	chr14:25559600-25561800	Enhancers	Muscle Satellite Cultured Cells	--
10	chr14:25559600-25564200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr14:25560000-25560800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr14:25560000-25560800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr14:25560000-25561400	Enhancers	Fetal Intestine Small	intestine
14	chr14:25560400-25560800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr14:25560400-25561400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr14:25560400-25561400	Weak transcription	Left Ventricle	heart
17	chr14:25560400-25562400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr14:25560400-25565000	Weak transcription	Stomach Mucosa	stomach
19	chr14:25560600-25561400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr14:25560600-25561400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr14:25560600-25562400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr14:25560600-25563000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr14:25560600-25563000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:25560600-25563000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr14:25560600-25563000	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr14:25560600-25563400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr14:25560600-25563600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr14:25560600-25564600	Weak transcription	Fetal Intestine Large	intestine
29	chr14:25560600-25565000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr14:25560600-25565000	Weak transcription	Fetal Heart	heart
31	chr14:25560800-25562200	Enhancers	Placenta Amnion	Placenta Amnion
32	chr14:25560800-25562400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr14:25560800-25563400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr14:25561000-25561400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr14:25561000-25561600	Weak transcription	HSMMtube	muscle
36	chr14:25561400-25561600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr14:25561400-25561600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr14:25561400-25561600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr14:25561400-25561600	Enhancers	Left Ventricle	heart
40	chr14:25561400-25562000	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr14:25561400-25563400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr14:25561400-25564600	Weak transcription	Fetal Intestine Small	intestine
43	chr14:25561600-25561800	Enhancers	Pancreas	Pancrea
44	chr14:25561600-25561800	Enhancers	HSMMtube	muscle
45	chr14:25561600-25562800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr14:25561600-25563600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr14:25561800-25563000	Weak transcription	HSMM	muscle
48	chr14:25561800-25565200	Weak transcription	Pancreas	Pancrea
49	chr14:25562000-25562400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr14:25562200-25562600	Weak transcription	Placenta Amnion	Placenta Amnion

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