Variant report

Variant	nsv901636
Chromosome Location	chr14:37702799-37736054
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	ARID3A	chr14:37720992-37722152	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:37707129-37707415	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:37715436-37716157	HepG2	liver:	n/a	n/a
4	BHLHE40	chr14:37715661-37715909	HepG2	liver:	n/a	n/a
5	CEBPB	chr14:37733140-37733402	A549	lung:	n/a	chr14:37733285-37733296
6	CEBPB	chr14:37715843-37716172	ECC-1	luminal epithelium:	n/a	chr14:37715992-37716003 chr14:37715991-37716004 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715991-37716002
7	CEBPB	chr14:37715770-37716183	HepG2	liver:	n/a	chr14:37715992-37716003 chr14:37715991-37716004 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715991-37716002
8	CEBPB	chr14:37715604-37716054	HCT-116	colon:	n/a	chr14:37715992-37716003 chr14:37715991-37716004 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715991-37716002
9	CEBPB	chr14:37715790-37716169	IMR90	lung:	n/a	chr14:37715992-37716003 chr14:37715991-37716004 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715991-37716002
10	CEBPB	chr14:37715712-37716169	A549	lung:	n/a	chr14:37715992-37716003 chr14:37715991-37716004 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715991-37716002
11	CEBPB	chr14:37715683-37716298	MCF-7	breast:	n/a	chr14:37715992-37716003 chr14:37715991-37716004 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715991-37716002
12	CEBPB	chr14:37715595-37716171	Hela-S3	cervix:	n/a	chr14:37715992-37716003 chr14:37715991-37716004 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715991-37716002
13	CEBPB	chr14:37715602-37716165	H1-hESC	embryonic stem cell:	n/a	chr14:37715992-37716003 chr14:37715991-37716004 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715991-37716002
14	CEBPB	chr14:37715800-37716150	A549	lung:	n/a	chr14:37715992-37716003 chr14:37715991-37716004 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715991-37716002
15	CEBPB	chr14:37733108-37733417	HepG2	liver:	n/a	chr14:37733285-37733296
16	CEBPB	chr14:37715825-37716158	K562	blood:	n/a	chr14:37715992-37716003 chr14:37715991-37716004 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715991-37716002
17	CEBPB	chr14:37733073-37733456	IMR90	lung:	n/a	chr14:37733285-37733296 chr14:37733435-37733446 chr14:37733435-37733446
18	CEBPB	chr14:37726522-37726766	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:37715774-37716106	MCF-7	breast:	n/a	chr14:37715992-37716003 chr14:37715991-37716004 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715993-37716002 chr14:37715991-37716002
20	CEBPB	chr14:37733197-37733313	K562	blood:	n/a	chr14:37733285-37733296
21	CHD1	chr14:37723829-37724206	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr14:37715413-37715479	Medullo	brain:	n/a	n/a
23	CTCF	chr14:37720951-37721282	A549	lung:	n/a	chr14:37721152-37721173
24	CTCF	chr14:37721060-37721210	Caco-2	colon:	n/a	chr14:37721152-37721173
25	CTCF	chr14:37715660-37715810	AG04450	lung:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
26	CTCF	chr14:37715660-37715810	WERI-Rb-1	eye:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
27	CTCF	chr14:37721080-37721230	HMF	breast:	n/a	chr14:37721152-37721173
28	CTCF	chr14:37715660-37715810	RPTEC	kidney:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
29	CTCF	chr14:37721180-37721330	RPTEC	kidney:	n/a	n/a
30	CTCF	chr14:37715680-37715830	Caco-2	colon:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
31	CTCF	chr14:37715504-37715896	H1-hESC	embryonic stem cell:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
32	CTCF	chr14:37715620-37715770	HMEC	breast:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
33	CTCF	chr14:37715620-37715770	HCM	heart:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
34	CTCF	chr14:37715660-37715810	HepG2	liver:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
35	CTCF	chr14:37715660-37715810	BE2_C	brain:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
36	CTCF	chr14:37715640-37715790	Hela-S3	cervix:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
37	CTCF	chr14:37715607-37715884	Spleen_OC	spleen:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
38	CTCF	chr14:37715638-37715872	Hela-S3	cervix:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
39	CTCF	chr14:37715640-37715790	GM12869	blood:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
40	CTCF	chr14:37721060-37721210	HMEC	breast:	n/a	chr14:37721152-37721173
41	CTCF	chr14:37715380-37715530	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr14:37721020-37721170	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr14:37715620-37715770	HPF	lung:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
44	CTCF	chr14:37715377-37715457	GM12878	blood:	n/a	n/a
45	CTCF	chr14:37706180-37706330	HepG2	liver:	n/a	n/a
46	CTCF	chr14:37721134-37721162	K562	blood:	n/a	n/a
47	CTCF	chr14:37715640-37715790	HUVEC	blood vessel:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
48	CTCF	chr14:37715660-37715810	HRE	kidney:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747
49	CTCF	chr14:37721080-37721230	HepG2	liver:	n/a	chr14:37721152-37721173
50	CTCF	chr14:37715676-37715815	MCF-7	breast:	n/a	chr14:37715731-37715752 chr14:37715732-37715745 chr14:37715729-37715747

No.	Distal block	Cell Line	Cell type
1	chr14:37706094..37707784-chr14:37708938..37711000,2	K562	blood:
2	chr14:37700806..37703619-chr14:37711035..37714311,4	MCF-7	breast:
3	chr14:37720959..37721697-chr14:38343187..38344314,3	MCF-7	breast:
4	chr14:37720865..37721694-chr14:38063366..38064030,2	MCF-7	breast:
5	chr14:37713823..37721404-chr14:38030834..38039698,13	MCF-7	breast:
6	chr14:37713685..37715695-chr14:37718418..37720705,2	K562	blood:
7	chr14:37722315..37724544-chr14:38070398..38072993,2	MCF-7	breast:
8	chr14:37724973..37727829-chr14:37731230..37733021,2	MCF-7	breast:
9	chr14:37720431..37722161-chr14:37725187..37727828,2	MCF-7	breast:
10	chr14:37723949..37726058-chr14:37737860..37739770,2	MCF-7	breast:
11	chr14:37710312..37712829-chr14:37714356..37716232,3	MCF-7	breast:
12	chr14:37717816..37720206-chr14:38145329..38146961,2	K562	blood:
13	chr14:37720748..37721511-chr14:38034504..38035461,3	MCF-7	breast:
14	chr14:37714570..37718771-chr14:37719606..37724141,5	MCF-7	breast:
15	chr14:37715349..37716204-chr14:38063509..38064571,3	MCF-7	breast:
16	chr14:37723784..37725511-chr14:37726243..37728327,2	MCF-7	breast:
17	chr14:37715456..37719212-chr14:38032266..38035206,4	MCF-7	breast:
18	chr14:37715577..37716109-chr14:38062848..38063529,2	MCF-7	breast:
19	chr14:37699123..37701373-chr14:37712703..37714358,2	K562	blood:
20	chr14:37715448..37716190-chr14:38343588..38344540,3	MCF-7	breast:
21	chr14:37723534..37725938-chr14:37730959..37732560,2	K562	blood:
22	chr14:37724973..37727829-chr14:37731230..37733021,2	MCF-7	breast:
23	chr14:37665370..37667151-chr14:37702519..37705426,2	MCF-7	breast:
24	chr14:37715320..37716132-chr14:38343587..38344326,2	MCF-7	breast:
25	chr14:37711608..37713623-chr14:38177380..38180362,2	MCF-7	breast:
26	chr14:37719816..37722174-chr14:38034571..38037096,4	MCF-7	breast:
27	chr14:37724664..37726988-chr14:38331777..38333562,2	MCF-7	breast:
28	chr14:37703862..37705867-chr14:38056619..38058843,2	MCF-7	breast:
29	chr14:37720026..37722656-chr14:38040517..38043861,3	MCF-7	breast:
30	chr14:37710312..37712829-chr14:37714356..37716232,3	MCF-7	breast:
31	chr14:37731472..37733246-chr14:38060600..38063260,2	MCF-7	breast:
32	chr14:37713685..37715772-chr14:37718261..37720705,2	K562	blood:
33	chr14:37709149..37730989-chr14:38048141..38067789,135	MCF-7	breast:
34	chr14:37730985..37733871-chr14:37737549..37739404,2	MCF-7	breast:
35	chr14:37713685..37715695-chr14:37718418..37720705,2	K562	blood:
36	chr14:37715306..37715938-chr14:38034662..38035728,3	MCF-7	breast:
37	chr14:37720431..37722161-chr14:37725187..37727828,2	MCF-7	breast:
38	chr14:37713685..37715772-chr14:37718261..37720705,2	K562	blood:
39	chr14:37698096..37705480-chr14:38061309..38066013,13	MCF-7	breast:
40	chr14:37729389..37731109-chr14:38029582..38031383,2	MCF-7	breast:
41	chr13:21961882..21963808-chr14:37714535..37717476,2	MCF-7	breast:
42	chr14:37709403..37711519-chr14:37714565..37716617,2	K562	blood:
43	chr14:37708906..37733371-chr14:38048131..38068843,170	MCF-7	breast:
44	chr14:37723534..37725938-chr14:37730959..37732560,2	K562	blood:
45	chr1:45187178..45188919-chr14:37715615..37718367,2	MCF-7	breast:
46	chr14:37697269..37708885-chr14:38056043..38068163,30	MCF-7	breast:
47	chr14:37699430..37701952-chr14:37706278..37708031,2	MCF-7	breast:
48	chr14:37704717..37707352-chr14:38053028..38056563,4	MCF-7	breast:
49	chr14:37718130..37720442-chr14:38122398..38124870,2	MCF-7	breast:
50	chr14:37704955..37707594-chr14:37708330..37711962,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-537P22.1.1-1	chr14:37732158-37732474	l_969_chr14:37729807-37741737_76bGuttman_hES
2	lnc-RP11-537P22.1.1-1	chr14:37717034-37717112	NONHSAT036456
3	lnc-RP11-537P22.1.1-1	chr14:37709629-37709774	NONHSAT036456
4	lnc-RP11-537P22.1.1-1	chr14:37734270-37737659	l_969_chr14:37729807-37741737_76bGuttman_hES
5	lnc-RP11-537P22.1.1-1	chr14:37727929-37730334	NONHSAT036457
6	lnc-RP11-537P22.1.1-1	chr14:37716308-37716445	NONHSAT036456
7	lnc-RP11-537P22.1.1-1	chr14:37729808-37730221	l_969_chr14:37729807-37741737_76bGuttman_hES

Variant related genes	Relation type
MIPOL1	TF binding region
ENSG00000139865	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000151338	chromatin interactions
ENSG00000258414	chromatin interactions
ENSG00000259087	chromatin interactions

Extended variants
information (count: 1130 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2093119	chr14:37702799-37702800	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563186490	chr14:37702811-37702812	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs374907425	chr14:37702823-37702824	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs189294167	chr14:37702843-37702844	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs180820221	chr14:37702857-37702858	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs2092790	chr14:37702863-37702864	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs528775452	chr14:37702901-37702902	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs548848215	chr14:37702938-37702939	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs530275749	chr14:37702941-37702942	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs145071346	chr14:37702943-37702944	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs568276796	chr14:37702972-37702973	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs186269345	chr14:37702996-37702997	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs535286666	chr14:37703022-37703023	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs537601299	chr14:37703076-37703077	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs189485825	chr14:37703079-37703080	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs181386892	chr14:37703127-37703128	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs536754296	chr14:37703151-37703152	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs377669147	chr14:37703155-37703156	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs557262133	chr14:37703166-37703167	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs539855435	chr14:37703210-37703211	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs553068726	chr14:37703211-37703212	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs572053779	chr14:37703237-37703238	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs185959695	chr14:37703250-37703251	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs554400604	chr14:37703285-37703286	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs190724068	chr14:37703304-37703305	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs147139411	chr14:37703318-37703319	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs563414915	chr14:37703339-37703340	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs545643764	chr14:37703406-37703407	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs557352766	chr14:37703463-37703464	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs201446881	chr14:37703468-37703469	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs559389047	chr14:37703537-37703538	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs183226165	chr14:37703541-37703542	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs534855428	chr14:37703566-37703567	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs113984470	chr14:37703567-37703568	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs199902674	chr14:37703571-37703572	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs3061899	chr14:37703579-37703580	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs562321455	chr14:37703598-37703599	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs187230961	chr14:37703601-37703602	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs550879246	chr14:37703634-37703635	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs572470870	chr14:37703636-37703637	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376648213	chr14:37703640-37703641	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs2899854	chr14:37703732-37703733	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs192477160	chr14:37703748-37703749	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs3861484	chr14:37703760-37703761	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs116852432	chr14:37703778-37703779	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs531254010	chr14:37703834-37703835	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs535409134	chr14:37703904-37703905	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs565449436	chr14:37703940-37703941	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs374516324	chr14:37703942-37703943	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs75653667	chr14:37703998-37703999	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37694800-37704800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr14:37694800-37756400	Weak transcription	Aorta	Aorta
3	chr14:37695400-37705200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr14:37696000-37715400	Weak transcription	Fetal Intestine Small	intestine
5	chr14:37696800-37706800	Weak transcription	Ovary	ovary
6	chr14:37702200-37710400	Weak transcription	K562	blood
7	chr14:37702400-37717000	Weak transcription	HUVEC	blood vessel
8	chr14:37702800-37703400	Enhancers	HepG2	liver
9	chr14:37703400-37706000	Weak transcription	HepG2	liver
10	chr14:37704800-37705000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr14:37705000-37705200	Enhancers	NHEK	skin
12	chr14:37705000-37705800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr14:37705200-37705800	Weak transcription	NHEK	skin
14	chr14:37705200-37706000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr14:37705800-37706200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr14:37705800-37706200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr14:37705800-37706400	Enhancers	NHEK	skin
18	chr14:37706000-37706400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr14:37706000-37706400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr14:37706000-37706600	Enhancers	HMEC	breast
21	chr14:37706000-37706800	Enhancers	HepG2	liver
22	chr14:37706200-37706600	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr14:37706400-37708800	Weak transcription	Rectal Smooth Muscle	rectum
24	chr14:37706400-37717000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr14:37706400-37717400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr14:37706400-37723200	Weak transcription	NHEK	skin
27	chr14:37706800-37707200	Enhancers	Ovary	ovary
28	chr14:37706800-37707200	Flanking Active TSS	HepG2	liver
29	chr14:37707200-37707800	Enhancers	HepG2	liver
30	chr14:37707200-37717200	Weak transcription	Ovary	ovary
31	chr14:37710000-37710400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr14:37710000-37710400	Enhancers	Stomach Mucosa	stomach
33	chr14:37710000-37710600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr14:37710000-37710600	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr14:37710200-37710600	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr14:37710200-37710600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr14:37710400-37710600	Enhancers	K562	blood
38	chr14:37710400-37710800	Enhancers	H1 Cell Line	embryonic stem cell
39	chr14:37710400-37715800	Weak transcription	Stomach Mucosa	stomach
40	chr14:37710400-37724000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr14:37710600-37722000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr14:37710600-37723800	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr14:37710800-37721200	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr14:37715200-37715600	Enhancers	Duodenum Mucosa	Duodenum
45	chr14:37715400-37715800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr14:37715400-37716000	Enhancers	Fetal Intestine Small	intestine
47	chr14:37715400-37716000	Enhancers	Fetal Lung	lung
48	chr14:37715600-37717200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr14:37715800-37716000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr14:37715800-37716000	Enhancers	Rectal Mucosa Donor 31	rectum

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