Variant report

Variant	nsv566156
Chromosome Location	chr14:105591377-105654606
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1536)
CpG islands
(count:4092)
Chromatin interactive
region (count:124)
LncRNA
region (count:2)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:1536 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105635551-105635751	K562	blood:	n/a	n/a
2	ARID3A	chr14:105646970-105647099	K562	blood:	n/a	n/a
3	ATF3	chr14:105647527-105647695	GM12878	blood:	n/a	n/a
4	ATF3	chr14:105647408-105647698	GM12878	blood:	n/a	n/a
5	ATF3	chr14:105647476-105647754	K562	blood:	n/a	n/a
6	ATF3	chr14:105633815-105634024	K562	blood:	n/a	n/a
7	BACH1	chr14:105634160-105634415	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr14:105650175-105650256	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:105635446-105635818	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:105647431-105647661	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr14:105647471-105647910	GM12878	blood:	n/a	chr14:105647556-105647572
12	BHLHE40	chr14:105647446-105647893	K562	blood:	n/a	chr14:105647556-105647572
13	BHLHE40	chr14:105633488-105634425	K562	blood:	n/a	chr14:105633626-105633642
14	BHLHE40	chr14:105635049-105635625	K562	blood:	n/a	n/a
15	BHLHE40	chr14:105641106-105641239	GM12878	blood:	n/a	n/a
16	BRCA1	chr14:105628806-105629067	HepG2	liver:	n/a	n/a
17	CBX3	chr14:105654397-105654814	K562	blood:	n/a	n/a
18	CBX3	chr14:105597533-105598007	HCT-116	colon:	n/a	n/a
19	CBX3	chr14:105607430-105607762	K562	blood:	n/a	n/a
20	CBX3	chr14:105654534-105654767	K562	blood:	n/a	n/a
21	CBX3	chr14:105606324-105606692	K562	blood:	n/a	n/a
22	CBX3	chr14:105597490-105598063	HCT-116	colon:	n/a	n/a
23	CBX3	chr14:105606276-105606713	K562	blood:	n/a	n/a
24	CBX3	chr14:105635458-105635833	K562	blood:	n/a	n/a
25	CCNT2	chr14:105647484-105647639	K562	blood:	n/a	n/a
26	CCNT2	chr14:105633598-105634394	K562	blood:	n/a	n/a
27	CCNT2	chr14:105634944-105635778	K562	blood:	n/a	chr14:105635426-105635435
28	CEBPB	chr14:105602020-105602475	A549	lung:	n/a	chr14:105602218-105602229
29	CEBPB	chr14:105646836-105646884	K562	blood:	n/a	n/a
30	CEBPB	chr14:105602051-105602404	K562	blood:	n/a	chr14:105602218-105602229
31	CEBPB	chr14:105602049-105602403	IMR90	lung:	n/a	chr14:105602218-105602229
32	CEBPB	chr14:105602070-105602404	HepG2	liver:	n/a	chr14:105602218-105602229
33	CEBPB	chr14:105602145-105602475	MCF-7	breast:	n/a	chr14:105602218-105602229
34	CEBPB	chr14:105602082-105602324	Hela-S3	cervix:	n/a	chr14:105602218-105602229
35	CEBPB	chr14:105631426-105631943	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr14:105602053-105602402	A549	lung:	n/a	chr14:105602218-105602229
37	CEBPB	chr14:105602202-105602233	H1-hESC	embryonic stem cell:	n/a	chr14:105602218-105602229
38	CHD2	chr14:105647556-105647857	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr14:105635288-105635741	K562	blood:	n/a	n/a
40	CHD2	chr14:105635003-105635186	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr14:105635604-105635860	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr14:105633690-105633737	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr14:105632638-105632642	K562	blood:	n/a	n/a
44	CHD2	chr14:105634239-105634449	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr14:105628806-105628928	HepG2	liver:	n/a	n/a
46	CREB1	chr14:105633974-105634413	A549	lung:	n/a	n/a
47	CREB1	chr14:105603330-105603686	K562	blood:	n/a	n/a
48	CREB1	chr14:105647357-105647807	A549	lung:	n/a	n/a
49	CREB1	chr14:105634956-105635290	A549	lung:	n/a	n/a
50	CTCF	chr14:105647440-105647590	GM12874	blood:	n/a	n/a

(count:4092 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105617080-105617130	GM12892	blood:	n/a
2	chr14:105648224-105648274	HUVEC	blood vessel:	n/a
3	chr14:105634387-105634437	AG04450	lung:	fetal
4	chr14:105609516-105609566	GM12878	blood:	n/a
5	chr14:105613783-105613833	AoSMC	blood vessel:	n/a
6	chr14:105617080-105617130	GM12892	blood:	n/a
7	chr14:105648224-105648274	HUVEC	blood vessel:	n/a
8	chr14:105634387-105634437	AG04450	lung:	fetal
9	chr14:105609516-105609566	GM12878	blood:	n/a
10	chr14:105613783-105613833	AoSMC	blood vessel:	n/a
11	chr14:105614818-105614868	PFSK-1	brain:	n/a
12	chr14:105603153-105603203	AG09319	gingival:	n/a
13	chr14:105615401-105615451	HPAEpiC	pulmonary alveolar:	n/a
14	chr14:105635081-105635131	ProgFib	skin:	n/a
15	chr14:105635708-105635758	HAEpiC	amniotic membrane:	n/a
16	chr14:105608567-105608617	Hela-S3	cervix:	n/a
17	chr14:105603986-105604036	AoSMC	blood vessel:	n/a
18	chr14:105649747-105649797	ProgFib	skin:	n/a
19	chr14:105612753-105612803	AG09309	skin:	n/a
20	chr14:105619511-105619561	HCPEpiC	choroid plexus:	n/a
21	chr14:105608260-105608310	LNCaP	prostate:	n/a
22	chr14:105634387-105634437	GM12878	blood:	n/a
23	chr14:105649747-105649797	Jurkat	blood:	n/a
24	chr14:105612787-105612837	HPAEpiC	pulmonary alveolar:	n/a
25	chr14:105622454-105622504	NHBE	bronchial:	n/a
26	chr14:105600994-105601044	RPTEC	kidney:	n/a
27	chr14:105619634-105619684	HCT-116	colon:	n/a
28	chr14:105617839-105617889	NH-A	brain:	n/a
29	chr14:105617173-105617223	RPTEC	kidney:	n/a
30	chr14:105608567-105608617	U87	brain:	n/a
31	chr14:105622454-105622504	HRCEpiC	kidney:	n/a
32	chr14:105635236-105635286	HepG2	liver:	n/a
33	chr14:105608973-105609023	AG10803	skin:	n/a
34	chr14:105647734-105647784	U87	brain:	n/a
35	chr14:105619701-105619751	NHBE	bronchial:	n/a
36	chr14:105619634-105619684	HEEpiC	esophagus:	n/a
37	chr14:105635236-105635286	BJ	skin:	n/a
38	chr14:105619701-105619751	Hepatocyte	liver:	n/a
39	chr14:105635769-105635819	A549	lung:	n/a
40	chr14:105617080-105617130	HRCEpiC	kidney:	n/a
41	chr14:105635706-105635756	HMEC	breast:	n/a
42	chr14:105618816-105618866	ovcar-3	ovarian:	n/a
43	chr14:105603460-105603510	HRCEpiC	kidney:	n/a
44	chr14:105619511-105619561	HepG2	liver:	n/a
45	chr14:105608567-105608617	HEEpiC	esophagus:	n/a
46	chr14:105633697-105633747	GM12892	blood:	n/a
47	chr14:105647510-105647560	K562	blood:	n/a
48	chr14:105614564-105614614	HPAEpiC	pulmonary alveolar:	n/a
49	chr14:105617839-105617889	IMR90	lung:	fetal
50	chr14:105635706-105635756	SAEC	small airway:	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:105615698..105618053-chr14:105622347..105625638,3	MCF-7	breast:
2	chr14:105605892..105608252-chr14:105621955..105625449,3	K562	blood:
3	chr14:105635593..105636402-chr14:105818301..105819224,3	K562	blood:
4	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:
5	chr14:105611401..105614212-chr14:105625101..105627298,2	MCF-7	breast:
6	chr14:105605014..105607392-chr14:105623375..105626287,2	K562	blood:
7	chr14:105615014..105617239-chr14:105619145..105622136,2	K562	blood:
8	chr14:105268465..105270651-chr14:105635461..105637238,2	K562	blood:
9	chr14:105649547..105651849-chr14:105660128..105661657,2	MCF-7	breast:
10	chr14:105644378..105646118-chr14:105647825..105650297,2	MCF-7	breast:
11	chr14:105563166..105566144-chr14:105593732..105596034,2	MCF-7	breast:
12	chr14:105635176..105636125-chr14:105747875..105748809,5	K562	blood:
13	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:
14	chr14:105640130..105641650-chr6:31587480..31589137,3	K562	blood:
15	chr14:105450462..105452951-chr14:105633617..105637647,3	MCF-7	breast:
16	chr14:105559890..105560867-chr14:105633779..105634301,2	MCF-7	breast:
17	chr14:105633273..105637288-chr14:105642227..105645314,5	MCF-7	breast:
18	chr14:105583616..105585913-chr14:105629918..105634007,5	MCF-7	breast:
19	chr14:105647019..105649589-chr14:105780411..105782070,2	MCF-7	breast:
20	chr14:105597394..105599153-chr14:105603205..105605036,2	K562	blood:
21	chr14:105613142..105616306-chr14:105622290..105625169,3	K562	blood:
22	chr14:105586207..105587794-chr14:105595383..105596914,2	MCF-7	breast:
23	chr14:105611629..105615687-chr14:105625576..105630230,4	K562	blood:
24	chr14:105617835..105619717-chr14:105620167..105621698,2	MCF-7	breast:
25	chr14:105556904..105557457-chr14:105630667..105631594,2	MCF-7	breast:
26	chr14:105619466..105621170-chr14:105628840..105630613,2	MCF-7	breast:
27	chr14:105627527..105629912-chr14:105632611..105634539,3	MCF-7	breast:
28	chr14:105635244..105636129-chr14:105665708..105667054,3	K562	blood:
29	chr14:105599383..105601359-chr14:105605338..105607216,2	MCF-7	breast:
30	chr14:105433467..105435387-chr14:105640925..105642715,2	MCF-7	breast:
31	chr14:105511711..105512332-chr14:105633666..105634346,2	MCF-7	breast:
32	chr14:105619466..105621170-chr14:105628840..105630613,2	MCF-7	breast:
33	chr14:105631482..105635033-chr14:105765939..105767661,3	K562	blood:
34	chr14:105557263..105559202-chr14:105649515..105651192,2	MCF-7	breast:
35	chr14:105618086..105620322-chr14:105622917..105625684,2	MCF-7	breast:
36	chr14:105539437..105542411-chr14:105625371..105627547,2	K562	blood:
37	chr14:105647774..105650762-chr14:105651625..105655733,5	MCF-7	breast:
38	chr14:105633273..105637288-chr14:105642227..105645314,5	MCF-7	breast:
39	chr14:105647226..105648734-chr14:105780236..105782314,2	MCF-7	breast:
40	chr14:105610604..105613096-chr14:105619107..105620769,2	K562	blood:
41	chr14:105632765..105635152-chr14:105864248..105866641,2	K562	blood:
42	chr14:105632764..105636922-chr14:105637769..105642057,5	MCF-7	breast:
43	chr14:105556509..105557265-chr14:105631240..105632200,2	MCF-7	breast:
44	chr14:105645461..105647244-chr14:105649629..105652172,2	MCF-7	breast:
45	chr14:105581813..105588921-chr14:105589522..105595491,7	MCF-7	breast:
46	chr14:105646332..105648438-chr14:105653932..105656621,2	K562	blood:
47	chr14:105556907..105557905-chr14:105631981..105632717,2	MCF-7	breast:
48	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
49	chr14:105556861..105558363-chr14:105628903..105631842,2	K562	blood:
50	chr14:105618156..105621334-chr14:105628329..105630360,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTBD6-1	chr14:105639787-105640155	ENSG00000257816.1
2	lnc-BTBD6-1	chr14:105639541-105639584	ENSG00000257816.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6765-3p	chr14:105617115-105617135	MIMAT0027431
hsa-miR-6765-5p	chr14:105617177-105617201	MIMAT0027430

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	JAG2	hsa-miR-124-3p	chr14:105608227-105608246
2	JAG2	hsa-miR-124-3p	chr14:105608233-105608227

Variant related genes	Relation type
JAG2	TF binding region
ENSG00000257622	TF binding region
NUDT14	TF binding region
JAG2	CpG island
ENSG00000257622	CpG island
NUDT14	CpG island
ENSG00000185567	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000257622	chromatin interactions
ENSG00000257556	chromatin interactions
ENSG00000184916	chromatin interactions
ENSG00000256498	chromatin interactions
ENSG00000204469	chromatin interactions
ENSG00000140104	chromatin interactions
ENSG00000183828	chromatin interactions
ENSG00000170779	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000185347	chromatin interactions
ENSG00000184887	chromatin interactions
ENSG00000170027	chromatin interactions
ENSG00000226174	chromatin interactions

Extended variants
information (count: 2655 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:2655 , 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	rs4399485	chr14:105591377-105591378	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs187455580	chr14:105591462-105591463	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs587715502	chr14:105591465-105591466	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs587770955	chr14:105591497-105591498	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs587645765	chr14:105591556-105591557	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs117075418	chr14:105591563-105591564	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs4983398	chr14:105591666-105591667	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs376730799	chr14:105591811-105591812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190775447	chr14:105591812-105591813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs587718847	chr14:105591848-105591849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182297433	chr14:105591855-105591856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185028401	chr14:105591887-105591888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs59715822	chr14:105591950-105591951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs587724364	chr14:105591971-105591972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs398057475	chr14:105591974-105591975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142889817	chr14:105591975-105591976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs587728194	chr14:105591977-105591978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190276916	chr14:105592020-105592021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs587600081	chr14:105592021-105592022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs587658972	chr14:105592033-105592034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111631326	chr14:105592102-105592103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs386382415	chr14:105592103-105592104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs386382416	chr14:105592112-105592113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs57994662	chr14:105592114-105592115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369201552	chr14:105592115-105592116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587707908	chr14:105592118-105592119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587612056	chr14:105592122-105592123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77228776	chr14:105592176-105592177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2735811	chr14:105592191-105592192	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs140764213	chr14:105592222-105592223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs587594961	chr14:105592223-105592224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs587690840	chr14:105592229-105592230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374219664	chr14:105592243-105592244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs587747933	chr14:105592258-105592259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2735810	chr14:105592259-105592260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113157419	chr14:105592275-105592276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs587736340	chr14:105592280-105592281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113203583	chr14:105592294-105592295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147326343	chr14:105592329-105592330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs111470638	chr14:105592333-105592334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183276807	chr14:105592334-105592335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs587642834	chr14:105592385-105592386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187798556	chr14:105592444-105592445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs587761958	chr14:105592493-105592494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74876031	chr14:105592498-105592499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs587712816	chr14:105592623-105592624	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs193164839	chr14:105592630-105592631	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs117819661	chr14:105592665-105592666	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs143255606	chr14:105592666-105592667	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs74089811	chr14:105592668-105592669	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:113)

Disease	PMID	Source
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
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Recurrent pregnancy loss	19789632	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105588000-105592800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr14:105590400-105602600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:105590600-105591800	Enhancers	Primary hematopoietic stem cells	blood
4	chr14:105590800-105591400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
5	chr14:105590800-105591400	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr14:105590800-105591400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr14:105590800-105591400	Enhancers	Placenta	Placenta
8	chr14:105590800-105591600	Bivalent Enhancer	Fetal Muscle Leg	muscle
9	chr14:105590800-105593000	Enhancers	Fetal Intestine Large	intestine
10	chr14:105591000-105591400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
11	chr14:105591000-105591400	Flanking Active TSS	Duodenum Mucosa	Duodenum
12	chr14:105591000-105591600	Enhancers	Primary T cells from cord blood	blood
13	chr14:105591000-105591600	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr14:105591000-105591600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
15	chr14:105591200-105591400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr14:105591200-105591400	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
17	chr14:105591200-105591400	Flanking Bivalent TSS/Enh	HepG2	liver
18	chr14:105591200-105591400	Bivalent Enhancer	HSMMtube	muscle
19	chr14:105591200-105591600	Enhancers	Fetal Thymus	thymus
20	chr14:105591200-105592000	Enhancers	Fetal Intestine Small	intestine
21	chr14:105591400-105591600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
22	chr14:105591400-105591600	Bivalent Enhancer	HepG2	liver
23	chr14:105591400-105591800	Enhancers	Duodenum Mucosa	Duodenum
24	chr14:105591800-105592200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr14:105592200-105593400	Enhancers	Duodenum Mucosa	Duodenum
26	chr14:105592400-105593200	Enhancers	Esophagus	oesophagus
27	chr14:105592600-105593600	Enhancers	Fetal Intestine Small	intestine
28	chr14:105592600-105593800	Bivalent Enhancer	HepG2	liver
29	chr14:105592800-105593400	Enhancers	Brain Germinal Matrix	brain
30	chr14:105592800-105593600	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr14:105592800-105593600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr14:105593000-105593200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr14:105593000-105593600	Bivalent Enhancer	Fetal Intestine Large	intestine
34	chr14:105593200-105593400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr14:105593200-105593400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
36	chr14:105593200-105593400	Bivalent Enhancer	Stomach Mucosa	stomach
37	chr14:105593200-105593400	Bivalent Enhancer	K562	blood
38	chr14:105593400-105593600	Bivalent Enhancer	Fetal Muscle Leg	muscle
39	chr14:105593600-105596200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr14:105596000-105596400	Enhancers	A549	lung
41	chr14:105596200-105596400	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr14:105601000-105601400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr14:105601000-105601400	Enhancers	Pancreas	Pancrea
44	chr14:105601400-105605800	Weak transcription	Pancreas	Pancrea
45	chr14:105602600-105605200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr14:105602800-105603600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr14:105602800-105603600	Enhancers	Primary hematopoietic stem cells	blood
48	chr14:105602800-105629800	Weak transcription	K562	blood
49	chr14:105603000-105603600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr14:105603400-105603600	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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