Variant report

Variant	nsv902359
Chromosome Location	chr14:104699495-104769149
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:584)
CpG islands
(count:1649)
Chromatin interactive
region (count:34)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:104766727-104766924	K562	blood:	n/a	n/a
2	BCL11A	chr14:104717532-104718237	GM12878	blood:	n/a	n/a
3	BCL3	chr14:104754712-104755473	GM12878	blood:	n/a	n/a
4	BCL3	chr14:104733046-104733417	GM12878	blood:	n/a	n/a
5	BCL3	chr14:104733500-104733914	GM12878	blood:	n/a	n/a
6	BCL3	chr14:104754737-104756137	GM12878	blood:	n/a	chr14:104756045-104756058
7	BCL3	chr14:104713332-104713671	GM12878	blood:	n/a	n/a
8	BCL3	chr14:104733084-104733421	GM12878	blood:	n/a	n/a
9	BCL3	chr14:104755490-104755662	GM12878	blood:	n/a	n/a
10	BCL3	chr14:104733530-104733887	GM12878	blood:	n/a	n/a
11	BCL3	chr14:104755664-104755989	GM12878	blood:	n/a	n/a
12	BHLHE40	chr14:104733203-104733312	K562	blood:	n/a	n/a
13	BRCA1	chr14:104760931-104761615	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr14:104762913-104763304	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr14:104755929-104756620	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr14:104741821-104742162	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr14:104711995-104712385	HCT-116	colon:	n/a	n/a
18	CBX3	chr14:104712001-104712378	HCT-116	colon:	n/a	n/a
19	CEBPB	chr14:104721659-104721859	HepG2	liver:	n/a	chr14:104721796-104721807
20	CEBPB	chr14:104759885-104761832	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr14:104741273-104742573	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr14:104748127-104748195	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:104721710-104721853	A549	lung:	n/a	chr14:104721796-104721807
24	CEBPB	chr14:104762929-104763352	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr14:104721705-104721905	K562	blood:	n/a	chr14:104721796-104721807
26	CEBPB	chr14:104745687-104746247	Hela-S3	cervix:	n/a	chr14:104745796-104745807
27	CEBPB	chr14:104766604-104766963	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr14:104755978-104756796	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr14:104738331-104738554	HepG2	liver:	n/a	chr14:104738399-104738410
30	CEBPB	chr14:104738332-104738532	IMR90	lung:	n/a	chr14:104738399-104738410
31	CEBPB	chr14:104713013-104713344	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr14:104738254-104738516	A549	lung:	n/a	chr14:104738399-104738410
33	CHD2	chr14:104760913-104761660	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr14:104734458-104734543	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr14:104756031-104756587	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr14:104762980-104763598	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr14:104760514-104760678	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr14:104759827-104760202	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr14:104742073-104742481	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr14:104706780-104707033	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr14:104760550-104760705	A549	lung:	n/a	chr14:104760653-104760666 chr14:104760648-104760666 chr14:104760650-104760663
42	CTCF	chr14:104760560-104760710	HCM	heart:	n/a	chr14:104760653-104760666 chr14:104760648-104760666 chr14:104760650-104760663
43	CTCF	chr14:104760560-104760710	GM12864	blood:	n/a	chr14:104760653-104760666 chr14:104760648-104760666 chr14:104760650-104760663
44	CTCF	chr14:104761420-104761562	MCF-7	breast:	n/a	chr14:104761479-104761492 chr14:104761477-104761495
45	CTCF	chr14:104761402-104761589	MCF-7	breast:	n/a	chr14:104761479-104761492 chr14:104761477-104761495
46	CTCF	chr14:104760586-104760719	HepG2	liver:	n/a	chr14:104760653-104760666 chr14:104760648-104760666 chr14:104760650-104760663
47	CTCF	chr14:104760600-104760750	GM12864	blood:	n/a	chr14:104760653-104760666 chr14:104760648-104760666 chr14:104760650-104760663
48	CTCF	chr14:104760580-104760730	HUVEC	blood vessel:	n/a	chr14:104760653-104760666 chr14:104760648-104760666 chr14:104760650-104760663
49	CTCF	chr14:104733683-104733711	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:104760621-104760624	Kidney_OC	kidney:	n/a	n/a

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104762027-104762077	HCPEpiC	choroid plexus:	n/a
2	chr14:104734475-104734525	HepG2	liver:	n/a
3	chr14:104762027-104762077	HCPEpiC	choroid plexus:	n/a
4	chr14:104734475-104734525	HepG2	liver:	n/a
5	chr14:104741786-104741836	U87	brain:	n/a
6	chr14:104762027-104762077	HRE	kidney:	n/a
7	chr14:104761941-104761991	HEK293	kidney:	embryo
8	chr14:104742172-104742222	HRCEpiC	kidney:	n/a
9	chr14:104762027-104762077	HCF	heart:	n/a
10	chr14:104705443-104705493	GM12891	blood:	n/a
11	chr14:104746527-104746577	PFSK-1	brain:	n/a
12	chr14:104742172-104742222	Hela-S3	cervix:	n/a
13	chr14:104717528-104717578	AG09319	gingival:	n/a
14	chr14:104742009-104742059	NB4	blood:	n/a
15	chr14:104734475-104734525	GM19239	blood:	n/a
16	chr14:104705443-104705493	NHDF-neo	bronchial:	n/a
17	chr14:104746687-104746737	NB4	blood:	n/a
18	chr14:104768421-104768471	AG04450	lung:	fetal
19	chr14:104758477-104758527	A549	lung:	n/a
20	chr14:104705443-104705493	BJ	skin:	n/a
21	chr14:104741786-104741836	CMK	blood:	n/a
22	chr14:104705293-104705343	HL-60	blood:	n/a
23	chr14:104741448-104741498	BJ	skin:	n/a
24	chr14:104735644-104735694	PANC-1	pancreas:	n/a
25	chr14:104705443-104705493	GM12878	blood:	n/a
26	chr14:104721657-104721707	GM06990	blood:	n/a
27	chr14:104758477-104758527	AoSMC	blood vessel:	n/a
28	chr14:104761941-104761991	PANC-1	pancreas:	n/a
29	chr14:104742009-104742059	GM12892	blood:	n/a
30	chr14:104721657-104721707	GM12878	blood:	n/a
31	chr14:104746559-104746609	BJ	skin:	n/a
32	chr14:104721657-104721707	HIPEpiC	eye:	n/a
33	chr14:104746527-104746577	BJ	skin:	n/a
34	chr14:104741786-104741836	BE2_C	brain:	n/a
35	chr14:104746687-104746737	GM12878	blood:	n/a
36	chr14:104743900-104743950	PANC-1	pancreas:	n/a
37	chr14:104742009-104742059	HRCEpiC	kidney:	n/a
38	chr14:104768316-104768366	NHBE	bronchial:	n/a
39	chr14:104735644-104735694	NB4	blood:	n/a
40	chr14:104762027-104762077	CMK	blood:	n/a
41	chr14:104761941-104761991	Caco-2	colon:	n/a
42	chr14:104761941-104761991	NB4	blood:	n/a
43	chr14:104741448-104741498	HEEpiC	esophagus:	n/a
44	chr14:104734475-104734525	AG09309	skin:	n/a
45	chr14:104741786-104741836	ProgFib	skin:	n/a
46	chr14:104736574-104736624	H1-hESC	embryonic stem cell:	embryo
47	chr14:104762027-104762077	AG09319	gingival:	n/a
48	chr14:104743900-104743950	HRE	kidney:	n/a
49	chr14:104758477-104758527	NH-A	brain:	n/a
50	chr14:104735644-104735694	SAEC	small airway:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:104603676..104604415-chr14:104760235..104760804,2	MCF-7	breast:
2	chr14:104600334..104603089-chr14:104739484..104741726,2	MCF-7	breast:
3	chr14:104750633..104755093-chr14:104756730..104760416,4	MCF-7	breast:
4	chr14:104722882..104724563-chr14:104724745..104727407,2	MCF-7	breast:
5	chr14:104760654..104761549-chr14:104836417..104836978,2	MCF-7	breast:
6	chr14:104723993..104726216-chr14:104758223..104760086,2	K562	blood:
7	chr14:104768093..104769693-chr14:104774112..104776117,2	MCF-7	breast:
8	chr14:104603795..104604545-chr14:104760161..104761480,5	MCF-7	breast:
9	chr14:104575830..104578279-chr14:104758176..104760324,2	MCF-7	breast:
10	chr14:104747853..104750552-chr14:104755271..104758240,2	MCF-7	breast:
11	chr14:104756389..104758056-chr14:104758774..104761093,2	MCF-7	breast:
12	chr14:104746362..104748538-chr14:104754609..104757132,3	MCF-7	breast:
13	chr14:104756422..104758689-chr14:104761247..104763793,2	MCF-7	breast:
14	chr14:104747853..104750552-chr14:104755271..104758240,2	MCF-7	breast:
15	chr14:104603438..104604496-chr14:104718718..104719807,9	MCF-7	breast:
16	chr14:104750633..104755093-chr14:104756730..104760416,4	MCF-7	breast:
17	chr14:104603553..104604461-chr14:104718749..104719349,2	MCF-7	breast:
18	chr14:104723993..104726216-chr14:104758223..104760086,2	K562	blood:
19	chr14:104698677..104700498-chr14:104705265..104708074,2	MCF-7	breast:
20	chr14:104651259..104651765-chr14:104760560..104761404,2	MCF-7	breast:
21	chr14:104762292..104764129-chr14:104770564..104772247,2	MCF-7	breast:
22	chr14:104736178..104738016-chr14:104740822..104743657,2	MCF-7	breast:
23	chr14:104746362..104748538-chr14:104754609..104757132,3	MCF-7	breast:
24	chr14:104728779..104730960-chr14:104733381..104735361,2	K562	blood:
25	chr14:104756389..104758056-chr14:104758774..104761093,2	MCF-7	breast:
26	chr14:104728779..104730960-chr14:104733381..104735361,2	K562	blood:
27	chr14:104747907..104749438-chr14:104962689..104965288,2	K562	blood:
28	chr14:104617545..104619541-chr14:104760413..104762032,2	MCF-7	breast:
29	chr14:104698677..104700498-chr14:104705265..104708074,2	MCF-7	breast:
30	chr14:104736178..104738016-chr14:104740822..104743657,2	MCF-7	breast:
31	chr14:104623348..104624079-chr14:104760154..104761091,2	MCF-7	breast:
32	chr14:104722882..104724563-chr14:104724745..104727407,2	MCF-7	breast:
33	chr14:104709839..104712329-chr14:104712351..104715124,2	MCF-7	breast:
34	chr14:104756422..104758689-chr14:104761247..104763793,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf144-1	chr14:104753823-104753890	ENSG00000258913
2	lnc-RP11-614O9.3.1-3	chr14:104755902-104756432	NONHSAT040255
3	lnc-C14orf144-1	chr14:104754171-104754406	ENSG00000258913
4	lnc-RP11-614O9.3.1-3	chr14:104753936-104755057	NONHSAT040254
5	lnc-C14orf144-1	chr14:104709434-104709704	XLOC_010948
6	lnc-RP11-614O9.3.1-3	chr14:104755476-104756432	NONHSAT040254
7	lnc-C14orf144-1	chr14:104747468-104747661	NONHSAT040253
8	lnc-C14orf144-1	chr14:104756355-104756432	NONHSAT040253
9	lnc-C14orf144-1	chr14:104709434-104710084	ENSG00000258913
10	lnc-C14orf144-1	chr14:104753823-104753890	NONHSAT040253
11	lnc-C14orf144-1	chr14:104741681-104741966	ENSG00000258913

No data

Variant related genes	Relation type
C14orf144	TF binding region
C14orf144	CpG island
ENSG00000258748	chromatin interactions
ENSG00000166183	chromatin interactions
ENSG00000228032	chromatin interactions
BRWD1	miRNA target sites

Extended variants
information (count: 3414 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:3414 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4906423	chr14:104699495-104699496	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191943822	chr14:104699501-104699502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561943098	chr14:104699517-104699518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs59991447	chr14:104699557-104699558	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs182320921	chr14:104699604-104699605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185151660	chr14:104699642-104699643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146428407	chr14:104699657-104699658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77156402	chr14:104699658-104699659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116165758	chr14:104699663-104699664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569534168	chr14:104699679-104699680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189569712	chr14:104699704-104699705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527700860	chr14:104699727-104699728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373874539	chr14:104699734-104699735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534082954	chr14:104699755-104699756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553935097	chr14:104699768-104699769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76516601	chr14:104699778-104699779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112101832	chr14:104699781-104699782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539730531	chr14:104699783-104699784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs17868959	chr14:104699794-104699795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112660138	chr14:104699850-104699851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576333628	chr14:104699864-104699865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542314571	chr14:104699871-104699872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555537944	chr14:104699873-104699874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113732387	chr14:104699897-104699898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35082822	chr14:104700011-104700012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540188065	chr14:104700095-104700096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541276059	chr14:104700109-104700110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142049930	chr14:104700116-104700117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117182892	chr14:104700143-104700144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182549614	chr14:104700162-104700163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111691487	chr14:104700166-104700167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528833582	chr14:104700179-104700180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532271309	chr14:104700186-104700187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549069717	chr14:104700194-104700195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565477466	chr14:104700234-104700235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs151129085	chr14:104700269-104700270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187788767	chr14:104700372-104700373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141076301	chr14:104700391-104700392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146769121	chr14:104700412-104700413	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550163489	chr14:104700471-104700472	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147922419	chr14:104700488-104700489	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141662435	chr14:104700506-104700507	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs193199733	chr14:104700521-104700522	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147070773	chr14:104700531-104700532	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76697193	chr14:104700554-104700555	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71419813	chr14:104700558-104700559	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs80110980	chr14:104700571-104700572	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530290375	chr14:104700624-104700625	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577884143	chr14:104700639-104700640	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114415174	chr14:104700651-104700652	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
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
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
Cancer	20164920	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
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ependymoma	19289631	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:558 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104697000-104700200	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr14:104698800-104704000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr14:104699200-104700200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr14:104700400-104703200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
5	chr14:104702200-104705400	ZNF genes & repeats	Spleen	Spleen
6	chr14:104703200-104704600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr14:104703600-104704000	ZNF genes & repeats	Fetal Intestine Small	intestine
8	chr14:104703800-104704000	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
9	chr14:104703800-104704200	ZNF genes & repeats	Ovary	ovary
10	chr14:104704000-104705800	Weak transcription	Fetal Intestine Small	intestine
11	chr14:104704200-104704400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr14:104704200-104704400	Enhancers	Fetal Muscle Leg	muscle
13	chr14:104704200-104707000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr14:104704400-104705600	Weak transcription	Fetal Muscle Leg	muscle
15	chr14:104704600-104704800	Enhancers	Gastric	stomach
16	chr14:104704600-104705000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr14:104704800-104705800	Weak transcription	Gastric	stomach
18	chr14:104705000-104706600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr14:104705400-104706400	Weak transcription	Spleen	Spleen
20	chr14:104705600-104706600	Enhancers	Fetal Intestine Large	intestine
21	chr14:104705600-104706600	Enhancers	Stomach Mucosa	stomach
22	chr14:104705600-104706800	Enhancers	Colonic Mucosa	Colon
23	chr14:104705600-104707200	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr14:104705600-104707400	Enhancers	Fetal Muscle Leg	muscle
25	chr14:104705600-104707400	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr14:104705800-104706600	Enhancers	Duodenum Mucosa	Duodenum
27	chr14:104705800-104706600	Enhancers	Gastric	stomach
28	chr14:104705800-104706600	Enhancers	Pancreas	Pancrea
29	chr14:104705800-104707000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr14:104705800-104707400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:104705800-104707400	Enhancers	Fetal Intestine Small	intestine
32	chr14:104706200-104706600	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr14:104706200-104707000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr14:104706200-104707200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr14:104706200-104707200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr14:104706400-104706600	Bivalent Enhancer	Fetal Stomach	stomach
37	chr14:104706400-104707000	Enhancers	Spleen	Spleen
38	chr14:104706400-104707200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr14:104706400-104707200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr14:104706600-104707000	Enhancers	Primary B cells from peripheral blood	blood
41	chr14:104706600-104707200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr14:104706600-104707200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr14:104706600-104709200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr14:104707000-104707400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr14:104707000-104707400	Enhancers	Fetal Muscle Trunk	muscle
46	chr14:104707400-104708800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr14:104707400-104709400	Weak transcription	Fetal Muscle Trunk	muscle
48	chr14:104707400-104709600	Weak transcription	Fetal Muscle Leg	muscle
49	chr14:104708800-104709000	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
50	chr14:104708800-104709200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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