Variant report

Variant	nsv965602
Chromosome Location	chr5:42767568-42889585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1762)
CpG islands
(count:733)
Chromatin interactive
region (count:51)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1762 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:42881492-42881891	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:42879503-42879715	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:42817121-42817150	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:42876305-42877134	K562	blood:	n/a	n/a
5	ARID3A	chr5:42811658-42812667	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:42874824-42876277	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:42802038-42802681	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:42889399-42889783	HepG2	liver:	n/a	chr5:42889752-42889768
9	ARID3A	chr5:42848854-42849034	K562	blood:	n/a	n/a
10	ARID3A	chr5:42767683-42767688	K562	blood:	n/a	n/a
11	ARID3A	chr5:42854769-42855471	HepG2	liver:	n/a	n/a
12	ARID3A	chr5:42847601-42848233	HepG2	liver:	n/a	n/a
13	ARID3A	chr5:42858197-42858662	HepG2	liver:	n/a	n/a
14	ARID3A	chr5:42846913-42847308	HepG2	liver:	n/a	n/a
15	ARID3A	chr5:42799374-42800208	HepG2	liver:	n/a	n/a
16	ARID3A	chr5:42843886-42844426	HepG2	liver:	n/a	chr5:42844138-42844154
17	ARID3A	chr5:42824136-42825046	HepG2	liver:	n/a	n/a
18	ARID3A	chr5:42853105-42853305	K562	blood:	n/a	n/a
19	ATF1	chr5:42778759-42778959	K562	blood:	n/a	n/a
20	ATF1	chr5:42858236-42858519	K562	blood:	n/a	n/a
21	ATF1	chr5:42879581-42879781	K562	blood:	n/a	n/a
22	ATF1	chr5:42831034-42831299	K562	blood:	n/a	n/a
23	ATF1	chr5:42872929-42873290	K562	blood:	n/a	n/a
24	ATF1	chr5:42881684-42881869	K562	blood:	n/a	n/a
25	ATF1	chr5:42876514-42877027	K562	blood:	n/a	n/a
26	ATF1	chr5:42889452-42889862	K562	blood:	n/a	n/a
27	ATF1	chr5:42811906-42812363	K562	blood:	n/a	n/a
28	ATF1	chr5:42853123-42853231	K562	blood:	n/a	n/a
29	ATF2	chr5:42811934-42812648	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr5:42813610-42814039	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr5:42813694-42813986	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr5:42811935-42812557	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr5:42804933-42805035	K562	blood:	n/a	n/a
34	BACH1	chr5:42813760-42814032	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr5:42831093-42831259	K562	blood:	n/a	n/a
36	BATF	chr5:42813967-42814491	GM12878	blood:	n/a	n/a
37	BATF	chr5:42834654-42834934	GM12878	blood:	n/a	n/a
38	BATF	chr5:42813972-42814543	GM12878	blood:	n/a	n/a
39	BATF	chr5:42854875-42855101	GM12878	blood:	n/a	n/a
40	BATF	chr5:42817484-42817653	GM12878	blood:	n/a	n/a
41	BCL11A	chr5:42813964-42814490	GM12878	blood:	n/a	n/a
42	BCL11A	chr5:42812358-42812594	H1-hESC	embryonic stem cell:	n/a	n/a
43	BHLHE40	chr5:42811932-42812096	GM12878	blood:	n/a	n/a
44	BHLHE40	chr5:42811828-42812581	HepG2	liver:	n/a	n/a
45	BHLHE40	chr5:42858416-42858507	HepG2	liver:	n/a	n/a
46	BHLHE40	chr5:42876493-42877049	K562	blood:	n/a	n/a
47	BHLHE40	chr5:42858850-42859186	HepG2	liver:	n/a	n/a
48	BHLHE40	chr5:42875780-42876118	K562	blood:	n/a	n/a
49	BHLHE40	chr5:42811823-42812549	K562	blood:	n/a	n/a
50	BHLHE40	chr5:42811875-42812245	HepG2	liver:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:42858327-42858377	AG10803	skin:	n/a
2	chr5:42858327-42858377	AG10803	skin:	n/a
3	chr5:42813842-42813892	LNCaP	prostate:	n/a
4	chr5:42812334-42812384	AG10803	skin:	n/a
5	chr5:42811952-42812002	MCF-7	breast:	n/a
6	chr5:42813937-42813987	HMEC	breast:	n/a
7	chr5:42812844-42812894	A549	lung:	n/a
8	chr5:42767749-42767799	CMK	blood:	n/a
9	chr5:42812334-42812384	A549	lung:	n/a
10	chr5:42840698-42840748	H1-hESC	embryonic stem cell:	embryo
11	chr5:42811952-42812002	BE2_C	brain:	n/a
12	chr5:42812334-42812384	AG04449	skin:	fetal
13	chr5:42812509-42812559	NHDF-neo	bronchial:	n/a
14	chr5:42812509-42812559	AG09319	gingival:	n/a
15	chr5:42813896-42813946	CMK	blood:	n/a
16	chr5:42800967-42801017	HRPEpiC	eye:	n/a
17	chr5:42812244-42812294	SK-N-SH	brain:	n/a
18	chr5:42811952-42812002	Hepatocyte	liver:	n/a
19	chr5:42813842-42813892	Hepatocyte	liver:	n/a
20	chr5:42813842-42813892	SAEC	small airway:	n/a
21	chr5:42813937-42813987	A549	lung:	n/a
22	chr5:42812844-42812894	HMEC	breast:	n/a
23	chr5:42800967-42801017	A549	lung:	n/a
24	chr5:42813896-42813946	PANC-1	pancreas:	n/a
25	chr5:42800967-42801017	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:42813896-42813946	Hepatocyte	liver:	n/a
27	chr5:42800967-42801017	HMEC	breast:	n/a
28	chr5:42813896-42813946	MCF-7	breast:	n/a
29	chr5:42813896-42813946	SAEC	small airway:	n/a
30	chr5:42812244-42812294	GM12878	blood:	n/a
31	chr5:42812509-42812559	PrEC	prostate:	n/a
32	chr5:42812509-42812559	HCT-116	colon:	n/a
33	chr5:42813896-42813946	K562	blood:	n/a
34	chr5:42813896-42813946	HRPEpiC	eye:	n/a
35	chr5:42813896-42813946	HRCEpiC	kidney:	n/a
36	chr5:42811952-42812002	PrEC	prostate:	n/a
37	chr5:42812334-42812384	SK-N-SH	brain:	n/a
38	chr5:42811952-42812002	HPAEpiC	pulmonary alveolar:	n/a
39	chr5:42813842-42813892	Caco-2	colon:	n/a
40	chr5:42813842-42813892	ECC-1	luminal epithelium:	n/a
41	chr5:42840698-42840748	PANC-1	pancreas:	n/a
42	chr5:42812334-42812384	NT2-D1	testis:	n/a
43	chr5:42767749-42767799	MCF10A-Er-Src	breast:	n/a
44	chr5:42812244-42812294	ProgFib	skin:	n/a
45	chr5:42840698-42840748	GM12892	blood:	n/a
46	chr5:42813896-42813946	SK-N-SH	brain:	n/a
47	chr5:42840698-42840748	Hela-S3	cervix:	n/a
48	chr5:42812334-42812384	GM12892	blood:	n/a
49	chr5:42813896-42813946	U87	brain:	n/a
50	chr5:42813896-42813946	BE2_C	brain:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:42849114..42851312-chr5:42872827..42874820,2	MCF-7	breast:
2	chr5:42668135..42668954-chr5:42889373..42890051,2	MCF-7	breast:
3	chr5:42849114..42851312-chr5:42872827..42874820,2	MCF-7	breast:
4	chr5:42876153..42877710-chr5:42880139..42881887,2	K562	blood:
5	chr5:42853973..42857038-chr5:42873699..42877054,3	K562	blood:
6	chr5:42767982..42769578-chr5:43064219..43066603,2	K562	blood:
7	chr5:42767269..42768214-chr5:42889107..42889727,3	MCF-7	breast:
8	chr5:42881977..42885731-chr5:42887904..42891094,4	K562	blood:
9	chr5:42881977..42885731-chr5:42887904..42891094,4	K562	blood:
10	chr5:42767269..42768214-chr5:42889107..42889727,3	MCF-7	breast:
11	chr5:42804005..42807994-chr5:42809581..42813463,4	K562	blood:
12	chr5:42057339..42057915-chr5:42889168..42890099,2	K562	blood:
13	chr5:42800716..42803612-chr5:42804755..42806774,2	K562	blood:
14	chr5:42755862..42758340-chr5:42772497..42774222,2	K562	blood:
15	chr5:42871730..42873375-chr5:42874311..42877246,2	K562	blood:
16	chr5:42849318..42851714-chr5:42853312..42856268,2	K562	blood:
17	chr5:42796821..42798465-chr5:42802403..42805335,2	K562	blood:
18	chr5:42849318..42851714-chr5:42853312..42856268,2	K562	blood:
19	chr5:41903042..41905905-chr5:42874785..42876524,2	K562	blood:
20	chr5:42874819..42877698-chr5:42883856..42886524,3	K562	blood:
21	chr5:42874819..42877698-chr5:42883856..42886524,3	K562	blood:
22	chr5:42798391..42799940-chr5:42801692..42804127,2	K562	blood:
23	chr5:42745610..42746111-chr5:42889125..42890106,2	K562	blood:
24	chr5:41843679..41844304-chr5:42767097..42767879,2	MCF-7	breast:
25	chr5:42788274..42790445-chr5:42792719..42794547,2	K562	blood:
26	chr5:42812021..42814105-chr5:42817037..42818822,2	K562	blood:
27	chr5:42853973..42857038-chr5:42873699..42877054,3	K562	blood:
28	chr5:42774126..42776512-chr5:42779653..42781578,2	K562	blood:
29	chr5:42583006..42583706-chr5:42767773..42768316,2	MCF-7	breast:
30	chr5:42876153..42877710-chr5:42880139..42881887,2	K562	blood:
31	chr5:42889184..42890160-chr5:42904939..42905716,2	K562	blood:
32	chr5:42825774..42827829-chr5:42829137..42831240,2	MCF-7	breast:
33	chr5:42822767..42827233-chr5:42829501..42832610,4	K562	blood:
34	chr5:42798391..42799940-chr5:42801692..42804127,2	K562	blood:
35	chr5:42774206..42775075-chr5:42889129..42889866,2	K562	blood:
36	chr5:42804005..42807710-chr5:42809581..42813463,4	K562	blood:
37	chr5:42796821..42798465-chr5:42802403..42805335,2	K562	blood:
38	chr5:42879448..42882053-chr5:42991985..42994094,2	K562	blood:
39	chr5:42879999..42882103-chr5:43040168..43041691,2	K562	blood:
40	chr5:42774126..42776512-chr5:42779653..42781578,2	K562	blood:
41	chr5:42851174..42853504-chr5:42855107..42856666,2	K562	blood:
42	chr5:42788274..42790445-chr5:42792719..42794547,2	K562	blood:
43	chr5:42774206..42775075-chr5:42889129..42889866,2	K562	blood:
44	chr5:42874757..42877271-chr5:42884816..42887879,3	K562	blood:
45	chr5:42804005..42807710-chr5:42809581..42813463,4	K562	blood:
46	chr5:42871730..42873375-chr5:42874311..42877246,2	K562	blood:
47	chr5:42804005..42807994-chr5:42809581..42813463,4	K562	blood:
48	chr5:42808126..42809697-chr5:42810037..42813024,2	K562	blood:
49	chr5:42808126..42809697-chr5:42810037..42813024,2	K562	blood:
50	chr5:41856747..41857414-chr5:42767289..42768219,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GHR-4	chr5:42769700-42769767	NONHSAT101224
2	lnc-C5orf39-8	chr5:42806998-42807400	NONHSAT101226
3	lnc-CCDC152-3	chr5:42813783-42814021	NONHSAT101231
4	lnc-GHR-4	chr5:42796932-42796997	NONHSAT101224
5	lnc-CCDC152-2	chr5:42806496-42807099	ENSG00000272234.1
6	lnc-C5orf39-8	chr5:42811938-42811991	NONHSAT101228
7	lnc-GHR-4	chr5:42783577-42783678	NONHSAT101224
8	lnc-C5orf39-8	chr5:42804758-42804875	NONHSAT101226
9	lnc-C5orf39-8	chr5:42806685-42807210	NONHSAT101228
10	lnc-C5orf39-8	chr5:42801302-42801433	NONHSAT101226
11	lnc-GHR-4	chr5:42779561-42779624	NONHSAT101224

No data

Variant related genes	Relation type
SEPP1	TF binding region
ENSG00000272234	TF binding region
SEPP1	CpG island
ENSG00000272234	CpG island
ENSG00000272234	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000198865	chromatin interactions
ENSG00000250722	chromatin interactions
ENSG00000215068	chromatin interactions
ENSG00000083720	chromatin interactions
ENSG00000205765	chromatin interactions

Extended variants
information (count: 4616 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4616 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536394779	chr5:42767616-42767617	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs554361255	chr5:42767690-42767691	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs58096119	chr5:42767720-42767721	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs533535559	chr5:42767761-42767762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs111701544	chr5:42767784-42767785	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs553725516	chr5:42767790-42767791	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs190104075	chr5:42767850-42767851	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs545627969	chr5:42767923-42767924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563826721	chr5:42767925-42767926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142833983	chr5:42767937-42767938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182747129	chr5:42767944-42767945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369901407	chr5:42767954-42767955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528507928	chr5:42768023-42768024	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs546551914	chr5:42768052-42768053	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs530464699	chr5:42768124-42768125	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532224943	chr5:42768159-42768160	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs7734918	chr5:42768180-42768181	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs75454874	chr5:42768191-42768192	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536046022	chr5:42768207-42768208	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs548296367	chr5:42768277-42768278	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs146100889	chr5:42768307-42768308	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535400136	chr5:42768353-42768354	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs55828406	chr5:42768362-42768363	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs578251110	chr5:42768363-42768364	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs187365996	chr5:42768371-42768372	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557671018	chr5:42768375-42768376	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs192188860	chr5:42768386-42768387	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs183328444	chr5:42768450-42768451	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs6451643	chr5:42768454-42768455	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs2910860	chr5:42768469-42768470	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs377511176	chr5:42768488-42768489	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201638299	chr5:42768490-42768491	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs10627477	chr5:42768491-42768492	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs140123904	chr5:42768657-42768658	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs564983060	chr5:42768665-42768666	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs532364635	chr5:42768677-42768678	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550497762	chr5:42768684-42768685	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs562621585	chr5:42768694-42768695	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529924335	chr5:42768706-42768707	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs548046872	chr5:42768756-42768757	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566572150	chr5:42768788-42768789	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2973004	chr5:42768825-42768826	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs78583849	chr5:42768837-42768838	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570495602	chr5:42768850-42768851	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs189237955	chr5:42768894-42768895	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192227434	chr5:42768975-42768976	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs557656284	chr5:42769014-42769015	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs569415419	chr5:42769064-42769065	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs114854183	chr5:42769094-42769095	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs554816486	chr5:42769097-42769098	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42757800-42772200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr5:42758000-42767800	Weak transcription	Brain Hippocampus Middle	brain
3	chr5:42758000-42772200	Weak transcription	Brain Germinal Matrix	brain
4	chr5:42758200-42772600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr5:42758200-42772800	Weak transcription	NHDF-Ad	bronchial
6	chr5:42758200-42777600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr5:42765800-42770000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:42766400-42767600	Weak transcription	Liver	Liver
9	chr5:42767600-42769000	Enhancers	Liver	Liver
10	chr5:42767800-42768400	Enhancers	Brain Hippocampus Middle	brain
11	chr5:42767800-42769000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:42768000-42768600	Enhancers	HepG2	liver
13	chr5:42770000-42770800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr5:42770800-42784400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr5:42772000-42772800	Enhancers	Osteobl	bone
16	chr5:42772200-42772400	Enhancers	Adipose Nuclei	Adipose
17	chr5:42772200-42772600	Enhancers	NHEK	skin
18	chr5:42772200-42772800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:42772200-42773000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:42772200-42773000	Enhancers	HSMM	muscle
21	chr5:42772200-42773400	Enhancers	Hela-S3	cervix
22	chr5:42772400-42772600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr5:42772400-42772800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr5:42772400-42772800	Active TSS	Left Ventricle	heart
25	chr5:42772400-42772800	Active TSS	Rectal Mucosa Donor 29	rectum
26	chr5:42772400-42772800	Active TSS	Skeletal Muscle Male	skeletal muscle
27	chr5:42772400-42772800	Active TSS	Skeletal Muscle Female	skeletal muscle
28	chr5:42772400-42773200	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr5:42772600-42773000	Active TSS	Right Atrium	heart
30	chr5:42772600-42773200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr5:42772600-42773200	Active TSS	Muscle Satellite Cultured Cells	--
32	chr5:42772600-42773200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr5:42772600-42773200	Flanking Active TSS	NHEK	skin
34	chr5:42772800-42773000	Enhancers	NHDF-Ad	bronchial
35	chr5:42772800-42773200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr5:42772800-42773200	Bivalent Enhancer	Stomach Mucosa	stomach
37	chr5:42772800-42773200	Flanking Active TSS	Osteobl	bone
38	chr5:42772800-42773600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr5:42773000-42773400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr5:42773200-42773400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr5:42773200-42773400	Enhancers	Osteobl	bone
42	chr5:42773200-42777800	Weak transcription	Adipose Nuclei	Adipose
43	chr5:42773400-42773600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr5:42777600-42778600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr5:42777800-42778400	Enhancers	Adipose Nuclei	Adipose
46	chr5:42778000-42778400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr5:42778000-42778400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr5:42778000-42778400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr5:42778000-42778400	Enhancers	HUVEC	blood vessel
50	chr5:42778000-42778600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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