Variant report

Variant	nsv542218
Chromosome Location	chr14:104771655-104912436
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1091)
CpG islands
(count:4340)
Chromatin interactive
region (count:87)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1091 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:104853315-104853690	GM12878	blood:	n/a	n/a
2	BACH1	chr14:104910308-104910836	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr14:104873533-104873737	GM12878	blood:	n/a	chr14:104873580-104873591 chr14:104873618-104873629
4	BATF	chr14:104873436-104873767	GM12878	blood:	n/a	chr14:104873580-104873591 chr14:104873618-104873629
5	BATF	chr14:104853348-104853593	GM12878	blood:	n/a	n/a
6	BATF	chr14:104882766-104882975	GM12878	blood:	n/a	chr14:104882870-104882881
7	BCL11A	chr14:104853356-104853621	GM12878	blood:	n/a	chr14:104853461-104853470
8	BCL3	chr14:104906905-104907311	GM12878	blood:	n/a	n/a
9	BCL3	chr14:104792253-104792517	GM12878	blood:	n/a	n/a
10	BCL3	chr14:104792028-104792354	GM12878	blood:	n/a	n/a
11	BCL3	chr14:104910404-104910832	GM12878	blood:	n/a	n/a
12	BCL3	chr14:104850572-104850917	GM12878	blood:	n/a	chr14:104850648-104850657
13	BCL3	chr14:104850568-104850914	GM12878	blood:	n/a	chr14:104850648-104850657
14	BCL3	chr14:104790507-104790824	GM12878	blood:	n/a	n/a
15	BCL3	chr14:104906971-104907201	GM12878	blood:	n/a	n/a
16	BCL3	chr14:104910462-104910720	GM12878	blood:	n/a	n/a
17	BCL3	chr14:104853374-104853619	GM12878	blood:	n/a	chr14:104853461-104853470
18	BCLAF1	chr14:104853385-104853683	GM12878	blood:	n/a	chr14:104853461-104853470
19	BHLHE40	chr14:104891140-104891268	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:104891142-104891342	K562	blood:	n/a	n/a
21	BHLHE40	chr14:104789191-104789192	K562	blood:	n/a	n/a
22	BHLHE40	chr14:104811740-104811940	HepG2	liver:	n/a	n/a
23	BHLHE40	chr14:104811665-104811782	GM12878	blood:	n/a	n/a
24	CBX3	chr14:104808070-104808820	HCT-116	colon:	n/a	n/a
25	CEBPB	chr14:104836980-104837263	A549	lung:	n/a	n/a
26	CEBPB	chr14:104817900-104818104	HepG2	liver:	n/a	chr14:104818065-104818076
27	CEBPB	chr14:104862712-104862901	Hela-S3	cervix:	n/a	chr14:104862810-104862823
28	CEBPB	chr14:104837024-104837262	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:104862743-104862899	A549	lung:	n/a	chr14:104862810-104862823
30	CEBPB	chr14:104862645-104863007	H1-hESC	embryonic stem cell:	n/a	chr14:104862810-104862823
31	CEBPB	chr14:104862635-104863004	MCF-7	breast:	n/a	chr14:104862810-104862823
32	CEBPB	chr14:104862673-104862964	HepG2	liver:	n/a	chr14:104862810-104862823
33	CHD2	chr14:104836616-104836682	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr14:104808370-104808676	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr14:104909120-104909319	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr14:104808207-104808588	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr14:104886313-104886828	GM12878	blood:	n/a	n/a
38	CREB1	chr14:104808384-104808562	A549	lung:	n/a	n/a
39	CREB1	chr14:104886256-104886838	GM12878	blood:	n/a	n/a
40	CTCF	chr14:104798320-104798470	GM12874	blood:	n/a	n/a
41	CTCF	chr14:104808400-104808550	HUVEC	blood vessel:	n/a	chr14:104808472-104808488 chr14:104808480-104808493 chr14:104808478-104808486 chr14:104808466-104808487 chr14:104808471-104808489 chr14:104808473-104808486
42	CTCF	chr14:104798360-104798510	GM12872	blood:	n/a	n/a
43	CTCF	chr14:104798260-104798410	NHEK	skin:	n/a	n/a
44	CTCF	chr14:104798120-104798270	NHEK	skin:	n/a	chr14:104798242-104798255
45	CTCF	chr14:104836694-104836826	GM19239	blood:	n/a	chr14:104836752-104836773 chr14:104836759-104836772 chr14:104836789-104836797 chr14:104836757-104836775 chr14:104836758-104836774
46	CTCF	chr14:104808340-104808490	HPAF	blood vessel:	n/a	chr14:104808472-104808488 chr14:104808478-104808486 chr14:104808466-104808487 chr14:104808471-104808489 chr14:104808473-104808486
47	CTCF	chr14:104836646-104836895	LNCaP	prostate:	n/a	chr14:104836752-104836773 chr14:104836759-104836772 chr14:104836789-104836797 chr14:104836757-104836775 chr14:104836758-104836774
48	CTCF	chr14:104811720-104811870	Caco-2	colon:	n/a	chr14:104811805-104811813
49	CTCF	chr14:104900260-104900410	GM12870	blood:	n/a	chr14:104900373-104900391
50	CTCF	chr14:104858340-104858490	Hela-S3	cervix:	n/a	n/a

(count:4340 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104854940-104854990	HAEpiC	amniotic membrane:	n/a
2	chr14:104862680-104862730	BE2_C	brain:	n/a
3	chr14:104895709-104895759	HAEpiC	amniotic membrane:	n/a
4	chr14:104856667-104856717	SK-N-SH	brain:	n/a
5	chr14:104909505-104909555	MCF10A-Er-Src	breast:	n/a
6	chr14:104834222-104834272	HMEC	breast:	n/a
7	chr14:104800445-104800495	HPAEpiC	pulmonary alveolar:	n/a
8	chr14:104808516-104808566	ProgFib	skin:	n/a
9	chr14:104889005-104889055	MCF10A-Er-Src	breast:	n/a
10	chr14:104854940-104854990	HAEpiC	amniotic membrane:	n/a
11	chr14:104862680-104862730	BE2_C	brain:	n/a
12	chr14:104895709-104895759	HAEpiC	amniotic membrane:	n/a
13	chr14:104856667-104856717	SK-N-SH	brain:	n/a
14	chr14:104909505-104909555	MCF10A-Er-Src	breast:	n/a
15	chr14:104834222-104834272	HMEC	breast:	n/a
16	chr14:104800445-104800495	HPAEpiC	pulmonary alveolar:	n/a
17	chr14:104808516-104808566	ProgFib	skin:	n/a
18	chr14:104889005-104889055	MCF10A-Er-Src	breast:	n/a
19	chr14:104800568-104800618	HCF	heart:	n/a
20	chr14:104789371-104789421	U87	brain:	n/a
21	chr14:104801102-104801152	NH-A	brain:	n/a
22	chr14:104852104-104852154	HCM	heart:	n/a
23	chr14:104854790-104854840	NHDF-neo	bronchial:	n/a
24	chr14:104854940-104854990	HCT-116	colon:	n/a
25	chr14:104842040-104842090	BJ	skin:	n/a
26	chr14:104897068-104897118	AG09319	gingival:	n/a
27	chr14:104862680-104862730	HCM	heart:	n/a
28	chr14:104842040-104842090	IMR90	lung:	fetal
29	chr14:104834222-104834272	T-47D	breast:	n/a
30	chr14:104837541-104837591	SKMC	muscle:	n/a
31	chr14:104864723-104864773	HPAEpiC	pulmonary alveolar:	n/a
32	chr14:104854711-104854761	HCM	heart:	n/a
33	chr14:104789524-104789574	SAEC	small airway:	n/a
34	chr14:104900453-104900503	HEK293	kidney:	embryo
35	chr14:104824020-104824070	Hepatocyte	liver:	n/a
36	chr14:104787656-104787706	AoSMC	blood vessel:	n/a
37	chr14:104799486-104799536	SK-N-SH	brain:	n/a
38	chr14:104799486-104799536	IMR90	lung:	fetal
39	chr14:104897608-104897658	HPAEpiC	pulmonary alveolar:	n/a
40	chr14:104808474-104808524	U87	brain:	n/a
41	chr14:104789371-104789421	HNPCEpiC	eye:	n/a
42	chr14:104808652-104808702	AG09309	skin:	n/a
43	chr14:104800445-104800495	K562	blood:	n/a
44	chr14:104850405-104850455	ovcar-3	ovarian:	n/a
45	chr14:104896758-104896808	LNCaP	prostate:	n/a
46	chr14:104784005-104784055	SKMC	muscle:	n/a
47	chr14:104896001-104896051	AG04450	lung:	fetal
48	chr14:104898358-104898408	U87	brain:	n/a
49	chr14:104789524-104789574	GM19239	blood:	n/a
50	chr14:104824020-104824070	MCF10A-Er-Src	breast:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:104808137..104810517-chr14:104838226..104840189,2	MCF-7	breast:
2	chr14:104890275..104892805-chr14:104894264..104895980,2	MCF-7	breast:
3	chr14:104828202..104830108-chr14:104833873..104835498,2	K562	blood:
4	chr14:104654764..104655392-chr14:104812527..104813058,2	MCF-7	breast:
5	chr14:104818033..104822202-chr14:104826990..104831579,5	MCF-7	breast:
6	chr14:104846626..104850072-chr14:104851431..104854716,4	MCF-7	breast:
7	chr14:104890951..104893457-chr14:104909378..104911636,2	MCF-7	breast:
8	chr14:104902006..104903971-chr14:104906199..104909973,3	MCF-7	breast:
9	chr14:104604366..104607521-chr14:104837580..104840047,4	MCF-7	breast:
10	chr14:104841247..104842926-chr14:104851671..104854407,2	MCF-7	breast:
11	chr14:104808040..104808889-chr14:104836311..104836990,2	MCF-7	breast:
12	chr14:104809922..104812049-chr14:104902257..104904031,2	MCF-7	breast:
13	chr14:104907597..104909438-chr14:105077013..105079589,2	K562	blood:
14	chr14:104827640..104830097-chr14:104849702..104851434,2	MCF-7	breast:
15	chr14:104841247..104842926-chr14:104851671..104854407,2	MCF-7	breast:
16	chr14:104808137..104810517-chr14:104838226..104840189,2	MCF-7	breast:
17	chr14:104890951..104893457-chr14:104909378..104911636,2	MCF-7	breast:
18	chr14:104602116..104607691-chr14:104807710..104814314,8	MCF-7	breast:
19	chr14:104575835..104578265-chr14:104818122..104819690,2	MCF-7	breast:
20	chr14:104890275..104892805-chr14:104894264..104895980,2	MCF-7	breast:
21	chr14:104810225..104812544-chr14:104838511..104840510,3	MCF-7	breast:
22	chr14:104893761..104895389-chr14:104914243..104917076,2	MCF-7	breast:
23	chr14:104808612..104811334-chr14:105028919..105032790,3	MCF-7	breast:
24	chr14:104808000..104808682-chr3:120279791..120280680,2	MCF-7	breast:
25	chr14:104827640..104830097-chr14:104849702..104851434,2	MCF-7	breast:
26	chr14:104769312..104770225-chr14:104779545..104780136,2	MCF-7	breast:
27	chr14:104596286..104598130-chr14:104827828..104829835,2	MCF-7	breast:
28	chr14:104816456..104819206-chr14:104822482..104825637,3	MCF-7	breast:
29	chr14:104842421..104844937-chr14:104846124..104848778,2	K562	blood:
30	chr14:104634157..104636948-chr14:104811497..104813606,2	MCF-7	breast:
31	chr14:104894876..104896838-chr14:104897650..104900830,3	MCF-7	breast:
32	chr14:104860512..104862041-chr14:104863587..104866008,2	K562	blood:
33	chr14:104839152..104841523-chr14:104843087..104845999,3	MCF-7	breast:
34	chr14:104862114..104865269-chr14:104866594..104868712,3	MCF-7	breast:
35	chr14:104890913..104893677-chr14:104894092..104896751,2	MCF-7	breast:
36	chr14:104803247..104805895-chr14:104810944..104812693,2	MCF-7	breast:
37	chr14:104890913..104893677-chr14:104894092..104896751,2	MCF-7	breast:
38	chr14:104837762..104840619-chr14:104842293..104845118,2	MCF-7	breast:
39	chr14:104903421..104906757-chr14:104907729..104911933,3	MCF-7	breast:
40	chr14:104772029..104774740-chr14:104807798..104809607,2	K562	blood:
41	chr14:104760654..104761549-chr14:104836417..104836978,2	MCF-7	breast:
42	chr14:104792609..104796456-chr14:104799877..104802767,4	MCF-7	breast:
43	chr14:104820971..104823040-chr14:104824214..104826295,2	MCF-7	breast:
44	chr14:104903421..104906757-chr14:104907729..104911933,3	MCF-7	breast:
45	chr14:104852349..104854257-chr14:104854522..104857044,2	MCF-7	breast:
46	chr14:104572503..104574382-chr14:104808640..104810339,2	MCF-7	breast:
47	chr14:104797978..104799771-chr14:104802827..104805475,2	MCF-7	breast:
48	chr10:27147488..27149216-chr14:104802775..104805122,2	MCF-7	breast:
49	chr14:104816456..104819206-chr14:104822482..104825637,3	MCF-7	breast:
50	chr14:104894876..104896838-chr14:104897650..104900830,3	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-614O9.3.1-1	chr14:104845218-104845288	ENSG00000258598
2	lnc-RP11-614O9.3.1-1	chr14:104842867-104843033	ENSG00000258598
3	lnc-RP11-614O9.3.1-2	chr14:104824919-104825367	NONHSAT040256
4	lnc-RP11-614O9.3.1-2	chr14:104828079-104828393	NONHSAT040256
5	lnc-RP11-614O9.3.1-1	chr14:104843878-104844157	ENSG00000258598

No data

Variant related genes	Relation type
CEND1P1	TF binding region
RNU6-684P	TF binding region
ENSG00000258598	TF binding region
CEND1P1	CpG island
RNU6-684P	CpG island
ENSG00000258598	CpG island
ENSG00000258986	chromatin interactions
ENSG00000258748	chromatin interactions
ENSG00000184640	chromatin interactions
ENSG00000258598	chromatin interactions
ENSG00000222761	chromatin interactions
ENSG00000066735	chromatin interactions
ENSG00000166183	chromatin interactions

Extended variants
information (count: 6158 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:6158 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139595849	chr14:104771722-104771723	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566507183	chr14:104771723-104771724	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4906438	chr14:104771729-104771730	Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs560411649	chr14:104771732-104771733	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532468182	chr14:104771744-104771745	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs55793068	chr14:104771759-104771760	Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs144433102	chr14:104771779-104771780	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs59132453	chr14:104771786-104771787	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs80102079	chr14:104771797-104771798	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369600090	chr14:104771799-104771800	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554853353	chr14:104771800-104771801	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569990457	chr14:104771801-104771802	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547365094	chr14:104771831-104771832	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147814931	chr14:104771844-104771845	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539497530	chr14:104771874-104771875	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559196640	chr14:104771905-104771906	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs117539607	chr14:104771909-104771910	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372524417	chr14:104771932-104771933	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554998229	chr14:104771933-104771934	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190962449	chr14:104771963-104771964	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78939597	chr14:104771994-104771995	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560530213	chr14:104772050-104772051	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs199978326	chr14:104772082-104772083	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs59446655	chr14:104772136-104772137	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371335054	chr14:104772141-104772142	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs61576185	chr14:104772144-104772145	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74425368	chr14:104772149-104772150	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76260788	chr14:104772152-104772153	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145160233	chr14:104772166-104772167	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562367558	chr14:104772173-104772174	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs60637655	chr14:104772191-104772192	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs117398011	chr14:104772192-104772193	Genic enhancers Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs117830657	chr14:104772228-104772229	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs527572607	chr14:104772229-104772230	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183260460	chr14:104772250-104772251	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547084400	chr14:104772265-104772266	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570414478	chr14:104772273-104772274	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533081051	chr14:104772275-104772276	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4255721	chr14:104772276-104772277	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs569752156	chr14:104772288-104772289	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs116773346	chr14:104772289-104772290	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs114659130	chr14:104772341-104772342	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374353156	chr14:104772396-104772397	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs568701154	chr14:104772397-104772398	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs117005594	chr14:104772400-104772401	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561730187	chr14:104772454-104772455	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34146341	chr14:104772491-104772492	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112346968	chr14:104772502-104772503	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12436200	chr14:104772534-104772535	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs576801793	chr14:104772584-104772585	Genic enhancers ZNF genes & repeats Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	20932292	CNVD

Chromatin state (count:1125 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104770600-104773400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:104771800-104772800	Enhancers	Spleen	Spleen
3	chr14:104771800-104773200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
4	chr14:104772200-104774800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr14:104772600-104773400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr14:104772800-104773200	Active TSS	Spleen	Spleen
7	chr14:104773200-104773600	Weak transcription	Spleen	Spleen
8	chr14:104773200-104775200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr14:104773400-104773800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:104773600-104773800	Enhancers	Spleen	Spleen
11	chr14:104773800-104774800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr14:104774000-104774200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr14:104774600-104774800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr14:104774800-104776000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:104775600-104776400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr14:104775800-104776000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr14:104776000-104777200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr14:104776400-104776800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr14:104777000-104777200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr14:104777200-104780600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr14:104780600-104781000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr14:104780600-104781200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr14:104780600-104782400	Enhancers	Fetal Brain Male	brain
24	chr14:104780800-104782200	Enhancers	Fetal Brain Female	brain
25	chr14:104781000-104781400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr14:104781000-104782400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr14:104781200-104782000	Enhancers	Brain Germinal Matrix	brain
28	chr14:104781600-104785200	Weak transcription	Right Atrium	heart
29	chr14:104782000-104784600	Enhancers	Spleen	Spleen
30	chr14:104782000-104785000	Weak transcription	Brain Germinal Matrix	brain
31	chr14:104782200-104783000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
32	chr14:104782200-104783600	Enhancers	Colonic Mucosa	Colon
33	chr14:104782200-104785600	Weak transcription	Fetal Brain Female	brain
34	chr14:104782400-104782600	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr14:104782400-104782800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr14:104782400-104783200	Enhancers	Duodenum Mucosa	Duodenum
37	chr14:104782400-104784000	Weak transcription	Fetal Brain Male	brain
38	chr14:104782600-104783000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
39	chr14:104782600-104783000	Enhancers	Right Ventricle	heart
40	chr14:104782600-104783400	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr14:104782800-104785600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr14:104783000-104783400	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr14:104783000-104785000	Weak transcription	Right Ventricle	heart
44	chr14:104783400-104787000	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr14:104783800-104789400	Enhancers	Fetal Lung	lung
46	chr14:104784000-104784200	Enhancers	Fetal Brain Male	brain
47	chr14:104784200-104784600	Weak transcription	Fetal Brain Male	brain
48	chr14:104784600-104785800	Enhancers	Fetal Brain Male	brain
49	chr14:104784600-104787800	Weak transcription	Spleen	Spleen
50	chr14:104785000-104785600	Enhancers	Brain Germinal Matrix	brain

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