Variant report

Variant	nsv878965
Chromosome Location	chr4:41994645-42082479
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:341)
CpG islands
(count:61)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:41995297-41995500	K562	blood:	n/a	n/a
2	BACH1	chr4:42003406-42003497	K562	blood:	n/a	n/a
3	BATF	chr4:42080235-42080546	GM12878	blood:	n/a	n/a
4	BRCA1	chr4:42050387-42050834	Hela-S3	cervix:	n/a	n/a
5	CCNT2	chr4:42030007-42030203	K562	blood:	n/a	n/a
6	CEBPB	chr4:42069322-42069745	K562	blood:	n/a	chr4:42069342-42069359 chr4:42069478-42069489
7	CEBPB	chr4:42069404-42069608	H1-hESC	embryonic stem cell:	n/a	chr4:42069478-42069489
8	CEBPB	chr4:42017553-42017721	K562	blood:	n/a	chr4:42017663-42017676 chr4:42017663-42017676 chr4:42017663-42017674
9	CEBPB	chr4:42025305-42025513	K562	blood:	n/a	n/a
10	CEBPB	chr4:42017535-42017844	H1-hESC	embryonic stem cell:	n/a	chr4:42017663-42017676 chr4:42017663-42017676 chr4:42017663-42017674
11	CEBPB	chr4:42017511-42017842	Hela-S3	cervix:	n/a	chr4:42017663-42017676 chr4:42017663-42017676 chr4:42017663-42017674
12	CEBPB	chr4:42017488-42017858	IMR90	lung:	n/a	chr4:42017663-42017676 chr4:42017663-42017676 chr4:42017663-42017674
13	CEBPB	chr4:42069349-42069533	A549	lung:	n/a	chr4:42069478-42069489
14	CEBPB	chr4:42069298-42069641	HepG2	liver:	n/a	chr4:42069342-42069359 chr4:42069478-42069489
15	CEBPB	chr4:42050416-42050781	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr4:42017506-42017856	HepG2	liver:	n/a	chr4:42017663-42017676 chr4:42017663-42017676 chr4:42017663-42017674
17	CEBPB	chr4:42065030-42065230	HepG2	liver:	n/a	chr4:42065100-42065111
18	CEBPB	chr4:42017515-42017828	A549	lung:	n/a	chr4:42017663-42017676 chr4:42017663-42017676 chr4:42017663-42017674
19	CEBPB	chr4:42069323-42069624	MCF-7	breast:	n/a	chr4:42069342-42069359 chr4:42069478-42069489
20	CEBPB	chr4:42050452-42050805	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:41996162-41996207	K562	blood:	n/a	n/a
22	CEBPB	chr4:42025305-42025482	A549	lung:	n/a	n/a
23	CEBPB	chr4:42069311-42069671	IMR90	lung:	n/a	chr4:42069342-42069359 chr4:42069478-42069489
24	CEBPB	chr4:42017472-42017852	K562	blood:	n/a	chr4:42017663-42017676 chr4:42017663-42017676 chr4:42017663-42017674
25	CEBPB	chr4:42064957-42065272	K562	blood:	n/a	chr4:42065100-42065111
26	CHD2	chr4:42080090-42080440	GM12878	blood:	n/a	n/a
27	CTCF	chr4:42020618-42020671	Medullo	brain:	n/a	n/a
28	CTCF	chr4:42059131-42059306	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr4:41996560-41996710	GM12867	blood:	n/a	n/a
30	CTCF	chr4:41996620-41996770	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr4:41997825-41997867	GM12891	blood:	n/a	n/a
32	CTCF	chr4:41996820-41996970	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr4:42059154-42059282	MCF-7	breast:	n/a	n/a
34	CTCF	chr4:42053036-42053104	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:42052936-42053235	GM12878	blood:	n/a	n/a
36	CTCF	chr4:42053047-42053144	NHEK	skin:	n/a	n/a
37	CTCF	chr4:42053020-42053170	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr4:41996540-41996690	BE2_C	brain:	n/a	n/a
39	CTCF	chr4:42059164-42059251	MCF-7	breast:	n/a	n/a
40	CTCF	chr4:42059200-42059350	Caco-2	colon:	n/a	n/a
41	CTCF	chr4:41996500-41996650	BJ	skin:	n/a	chr4:41996503-41996511
42	CTCF	chr4:42059180-42059330	HEK293	kidney:	n/a	n/a
43	CTCF	chr4:42082160-42082310	GM12872	blood:	n/a	n/a
44	CTCF	chr4:42053037-42053136	Fibrobl	skin:	n/a	n/a
45	CTCF	chr4:41996660-41996810	GM12864	blood:	n/a	n/a
46	CTCF	chr4:41996780-41996930	GM12864	blood:	n/a	n/a
47	CTCF	chr4:41996520-41996670	HVMF	connective:	n/a	n/a
48	CTCF	chr4:42053017-42053175	LNCaP	prostate:	n/a	n/a
49	CTCF	chr4:41996720-41996870	GM06990	blood:	n/a	n/a
50	CTCF	chr4:41996640-41996790	GM12872	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:41996723-41996773	HepG2	liver:	n/a
2	chr4:41996723-41996773	K562	blood:	n/a
3	chr4:41996723-41996773	SK-N-SH	brain:	n/a
4	chr4:41996723-41996773	H1-hESC	embryonic stem cell:	embryo
5	chr4:41996723-41996773	SK-N-SH_RA	brain:	n/a
6	chr4:41996723-41996773	NHBE	bronchial:	n/a
7	chr4:41996723-41996773	BE2_C	brain:	n/a
8	chr4:41996723-41996773	GM12892	blood:	n/a
9	chr4:41996723-41996773	U87	brain:	n/a
10	chr4:41996723-41996773	IMR90	lung:	fetal
11	chr4:41996723-41996773	CMK	blood:	n/a
12	chr4:41996723-41996773	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:41996723-41996773	AG09319	gingival:	n/a
14	chr4:41996723-41996773	Hela-S3	cervix:	n/a
15	chr4:41996723-41996773	HMEC	breast:	n/a
16	chr4:41996723-41996773	NB4	blood:	n/a
17	chr4:41996723-41996773	HNPCEpiC	eye:	n/a
18	chr4:41996723-41996773	AG10803	skin:	n/a
19	chr4:41996723-41996773	ProgFib	skin:	n/a
20	chr4:41996723-41996773	HRCEpiC	kidney:	n/a
21	chr4:41996723-41996773	HL-60	blood:	n/a
22	chr4:41996723-41996773	NHDF-neo	bronchial:	n/a
23	chr4:41996723-41996773	AG04449	skin:	fetal
24	chr4:41996723-41996773	SAEC	small airway:	n/a
25	chr4:41996723-41996773	HUVEC	blood vessel:	n/a
26	chr4:41996723-41996773	NH-A	brain:	n/a
27	chr4:41996723-41996773	Jurkat	blood:	n/a
28	chr4:41996723-41996773	PrEC	prostate:	n/a
29	chr4:41996723-41996773	HEEpiC	esophagus:	n/a
30	chr4:41996723-41996773	HAEpiC	amniotic membrane:	n/a
31	chr4:41996723-41996773	SK-N-MC	brain:	n/a
32	chr4:41996723-41996773	ECC-1	luminal epithelium:	n/a
33	chr4:41996723-41996773	BJ	skin:	n/a
34	chr4:41996723-41996773	A549	lung:	n/a
35	chr4:41996723-41996773	GM19239	blood:	n/a
36	chr4:41996723-41996773	PANC-1	pancreas:	n/a
37	chr4:41996723-41996773	AG09309	skin:	n/a
38	chr4:41996723-41996773	T-47D	breast:	n/a
39	chr4:41996723-41996773	ovcar-3	ovarian:	n/a
40	chr4:41996723-41996773	AG04450	lung:	fetal
41	chr4:41996723-41996773	RPTEC	kidney:	n/a
42	chr4:41996723-41996773	AoSMC	blood vessel:	n/a
43	chr4:41996723-41996773	MCF10A-Er-Src	breast:	n/a
44	chr4:41996723-41996773	HCPEpiC	choroid plexus:	n/a
45	chr4:41996723-41996773	NT2-D1	testis:	n/a
46	chr4:41996723-41996773	HEK293	kidney:	embryo
47	chr4:41996723-41996773	HCT-116	colon:	n/a
48	chr4:41996723-41996773	Caco-2	colon:	n/a
49	chr4:41996723-41996773	HCF	heart:	n/a
50	chr4:41996723-41996773	GM12891	blood:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:42011205..42014126-chr4:42020911..42023639,2	K562	blood:
2	chr4:42026942..42028800-chr4:42029372..42031931,2	K562	blood:
3	chr4:42038623..42041228-chr4:42042869..42044413,2	K562	blood:
4	chr4:41992163..41993821-chr4:42022560..42024648,2	K562	blood:
5	chr4:42038193..42040123-chr4:42041446..42044369,2	K562	blood:
6	chr4:42018542..42021669-chr4:42023389..42027080,3	K562	blood:
7	chr4:42069229..42071395-chr4:42075246..42078006,3	K562	blood:
8	chr4:41992513..41996601-chr4:41997656..42002108,5	MCF-7	breast:
9	chr4:42023494..42025122-chr4:42025564..42028163,2	K562	blood:
10	chr4:42016806..42018575-chr4:42023149..42025017,2	MCF-7	breast:
11	chr4:41992181..41994658-chr4:42071184..42074034,2	K562	blood:
12	chr4:41934812..41937174-chr4:41992334..41995460,3	K562	blood:
13	chr4:41994046..41996601-chr4:41998237..42000990,3	K562	blood:
14	chr4:42018542..42021669-chr4:42023389..42027080,3	K562	blood:
15	chr4:41999852..42002669-chr4:42004694..42009087,4	K562	blood:
16	chr4:42006407..42008883-chr4:42009649..42011329,2	K562	blood:
17	chr4:41993044..41995026-chr4:41995476..41997833,3	K562	blood:
18	chr4:41990916..41993721-chr4:41994706..41998074,4	MCF-7	breast:
19	chr4:41996432..41997069-chr4:42521628..42522155,2	MCF-7	breast:
20	chr4:41999852..42002669-chr4:42004694..42009087,4	K562	blood:
21	chr4:42011205..42014126-chr4:42020911..42023639,2	K562	blood:
22	chr4:41996658..41999244-chr4:42017003..42019806,3	K562	blood:
23	chr4:42023494..42025122-chr4:42025564..42028163,2	K562	blood:
24	chr4:41951021..41953726-chr4:42021389..42023042,2	MCF-7	breast:
25	chr4:41990033..41992916-chr4:41994522..41996079,2	K562	blood:
26	chr4:41992389..41994567-chr4:42004462..42008051,3	MCF-7	breast:
27	chr4:41993509..41995425-chr4:42026760..42028592,2	K562	blood:
28	chr4:41992181..41994658-chr4:42071184..42074034,2	K562	blood:
29	chr4:41995450..41997547-chr4:42070955..42072678,2	K562	blood:
30	chr4:42016806..42018575-chr4:42023149..42025017,2	MCF-7	breast:
31	chr4:42006407..42008883-chr4:42009649..42011329,2	K562	blood:
32	chr4:41993044..41995026-chr4:41995476..41997833,3	K562	blood:
33	chr4:42067632..42069574-chr4:42070825..42073422,2	K562	blood:
34	chr4:41990679..41993655-chr4:41998083..42000258,2	K562	blood:
35	chr4:42069229..42071395-chr4:42075246..42078006,3	K562	blood:
36	chr4:41937967..41940239-chr4:41997714..41999924,2	K562	blood:
37	chr4:41987599..41990079-chr4:41996650..41999014,2	K562	blood:
38	chr4:41993898..41995601-chr4:42014935..42017753,2	K562	blood:
39	chr4:41990036..41992683-chr4:42060465..42062452,2	MCF-7	breast:
40	chr4:41993898..41995601-chr4:42014935..42017753,2	K562	blood:
41	chr4:42081198..42083799-chr4:42083920..42086074,2	K562	blood:
42	chr4:41992505..41997448-chr4:42002221..42006998,7	K562	blood:
43	chr4:42038623..42041228-chr4:42042869..42044413,2	K562	blood:
44	chr4:41996658..41999244-chr4:42017003..42019806,3	K562	blood:
45	chr4:42038193..42040123-chr4:42041446..42044369,2	K562	blood:
46	chr4:41991262..41994134-chr4:41999382..42001290,3	MCF-7	breast:
47	chr4:41993509..41995425-chr4:42026760..42028592,2	K562	blood:
48	chr4:41994046..41996601-chr4:41998237..42000990,3	K562	blood:

No data

Variant related genes	Relation type
ATP1B1P1	TF binding region
ENSG00000272862	TF binding region
SLC30A9	TF binding region
ATP1B1P1	CpG island
ENSG00000272862	CpG island
SLC30A9	CpG island
ENSG00000272862	chromatin interactions
ENSG00000109133	chromatin interactions
ENSG00000014824	chromatin interactions
ENSG00000249212	chromatin interactions

Extended variants
information (count: 3329 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3329 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2660346	chr4:41994645-41994646	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573264488	chr4:41994662-41994663	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs191176127	chr4:41994680-41994681	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs527699324	chr4:41994692-41994693	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs201959708	chr4:41994704-41994705	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs73810453	chr4:41994707-41994708	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs567529923	chr4:41994719-41994720	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs540222970	chr4:41994770-41994771	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs564983016	chr4:41994795-41994796	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs183339796	chr4:41994799-41994800	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs141275806	chr4:41994844-41994845	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs538398037	chr4:41995021-41995022	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs532643826	chr4:41995049-41995050	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs73810455	chr4:41995074-41995075	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs534594381	chr4:41995113-41995114	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs554599424	chr4:41995114-41995115	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs2581431	chr4:41995159-41995160	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs537153006	chr4:41995180-41995181	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs73810456	chr4:41995186-41995187	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs74795820	chr4:41995288-41995289	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs548502639	chr4:41995319-41995320	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs185498266	chr4:41995324-41995325	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs190848739	chr4:41995347-41995348	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs565320665	chr4:41995446-41995447	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs34652351	chr4:41995460-41995461	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs572725339	chr4:41995516-41995517	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs541356579	chr4:41995521-41995522	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs183042131	chr4:41995522-41995523	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs188123730	chr4:41995531-41995532	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs191669782	chr4:41995541-41995542	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs141530055	chr4:41995607-41995608	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs6830050	chr4:41995635-41995636	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs369429823	chr4:41995642-41995643	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533885124	chr4:41995660-41995661	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs373280336	chr4:41995664-41995665	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs551983978	chr4:41995797-41995798	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs2660345	chr4:41995812-41995813	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs534960468	chr4:41995828-41995829	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs182975180	chr4:41995844-41995845	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs57504228	chr4:41995875-41995876	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs537016528	chr4:41995879-41995880	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs557109943	chr4:41995911-41995912	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs187306938	chr4:41995939-41995940	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs539516974	chr4:41995940-41995941	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs60210403	chr4:41995945-41995946	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs572538197	chr4:41995950-41995951	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs541716844	chr4:41995953-41995954	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs557192712	chr4:41995972-41995973	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs370823244	chr4:41996043-41996044	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs199612183	chr4:41996045-41996046	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	16616336	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Esophageal squamous carcinoma	18350619	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2078 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:41990800-41995000	Active TSS	HUES48 Cell Line	embryonic stem cell
2	chr4:41991800-41994800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:41993200-42025800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:41993400-41995000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr4:41993600-41995000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr4:41993600-41995800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr4:41993800-41994800	Enhancers	Liver	Liver
8	chr4:41993800-41995000	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr4:41993800-41995000	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr4:41993800-41995000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr4:41993800-41995000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr4:41993800-41995000	Enhancers	Fetal Brain Male	brain
13	chr4:41993800-41995400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr4:41993800-41995600	Enhancers	Fetal Intestine Large	intestine
15	chr4:41993800-41995800	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr4:41993800-42004200	Weak transcription	Primary B cells from cord blood	blood
17	chr4:41993800-42018400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr4:41993800-42020400	Weak transcription	Fetal Kidney	kidney
19	chr4:41993800-42023600	Weak transcription	Fetal Intestine Small	intestine
20	chr4:41993800-42025200	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr4:41993800-42025400	Weak transcription	Colonic Mucosa	Colon
22	chr4:41993800-42025600	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr4:41993800-42031000	Weak transcription	Thymus	Thymus
24	chr4:41994000-41995000	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr4:41994000-41995200	Enhancers	Primary T cells from cord blood	blood
26	chr4:41994000-42004200	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr4:41994200-41994800	Enhancers	Muscle Satellite Cultured Cells	--
28	chr4:41994200-41995000	Enhancers	Brain Anterior Caudate	brain
29	chr4:41994200-41995000	Enhancers	Colon Smooth Muscle	Colon
30	chr4:41994200-41995000	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr4:41994200-41995000	Enhancers	Hela-S3	cervix
32	chr4:41994200-41995600	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr4:41994200-41999800	Weak transcription	HSMM	muscle
34	chr4:41994200-42004200	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr4:41994200-42004200	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr4:41994200-42004600	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr4:41994200-42005600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr4:41994200-42007600	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr4:41994200-42007600	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr4:41994200-42008000	Weak transcription	Primary hematopoietic stem cells	blood
41	chr4:41994200-42008400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr4:41994200-42022600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:41994200-42023800	Weak transcription	Fetal Stomach	stomach
44	chr4:41994200-42024400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr4:41994200-42024600	Weak transcription	Brain Substantia Nigra	brain
46	chr4:41994200-42024600	Weak transcription	NHLF	lung
47	chr4:41994200-42025400	Weak transcription	HSMMtube	muscle
48	chr4:41994400-41995600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr4:41994400-42000000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:41994400-42000600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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