Variant report

Variant	nsv539104
Chromosome Location	chr7:121069455-121143942
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:724)
CpG islands
(count:183)
Chromatin interactive
region (count:65)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:724 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:121115224-121115242	K562	blood:	n/a	n/a
2	ARID3A	chr7:121077898-121078751	K562	blood:	n/a	n/a
3	ATF1	chr7:121124269-121124282	K562	blood:	n/a	n/a
4	ATF1	chr7:121106594-121106973	K562	blood:	n/a	n/a
5	ATF1	chr7:121108732-121108836	K562	blood:	n/a	n/a
6	ATF1	chr7:121143862-121143930	K562	blood:	n/a	n/a
7	ATF1	chr7:121078557-121078820	K562	blood:	n/a	n/a
8	ATF2	chr7:121140726-121141000	GM12878	blood:	n/a	n/a
9	BATF	chr7:121072589-121072929	GM12878	blood:	n/a	n/a
10	BATF	chr7:121140731-121141068	GM12878	blood:	n/a	chr7:121140908-121140919
11	BATF	chr7:121072659-121072930	GM12878	blood:	n/a	n/a
12	BATF	chr7:121140685-121141108	GM12878	blood:	n/a	chr7:121140908-121140919
13	BCL11A	chr7:121140792-121141017	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:121140706-121141079	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:121078559-121078630	K562	blood:	n/a	n/a
16	BHLHE40	chr7:121111370-121111376	K562	blood:	n/a	n/a
17	BHLHE40	chr7:121088228-121088300	K562	blood:	n/a	n/a
18	BHLHE40	chr7:121072735-121072838	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:121080992-121081288	K562	blood:	n/a	n/a
20	BHLHE40	chr7:121072202-121072228	K562	blood:	n/a	n/a
21	CBX3	chr7:121137600-121137956	K562	blood:	n/a	n/a
22	CBX3	chr7:121089318-121089813	HCT-116	colon:	n/a	n/a
23	CBX3	chr7:121078346-121078975	K562	blood:	n/a	n/a
24	CBX3	chr7:121076652-121077218	K562	blood:	n/a	n/a
25	CBX3	chr7:121137628-121137908	K562	blood:	n/a	n/a
26	CBX3	chr7:121078412-121078872	K562	blood:	n/a	n/a
27	CCNT2	chr7:121078573-121078770	K562	blood:	n/a	n/a
28	CEBPB	chr7:121101592-121101856	HepG2	liver:	n/a	chr7:121101749-121101760
29	CEBPB	chr7:121133358-121133459	HepG2	liver:	n/a	chr7:121133376-121133387
30	CEBPB	chr7:121088560-121088864	K562	blood:	n/a	n/a
31	CEBPB	chr7:121130374-121130739	K562	blood:	n/a	chr7:121130555-121130566 chr7:121130554-121130567 chr7:121130556-121130565 chr7:121130554-121130567 chr7:121130554-121130565
32	CEBPB	chr7:121101630-121101913	A549	lung:	n/a	chr7:121101749-121101760
33	CEBPB	chr7:121114464-121114673	K562	blood:	n/a	chr7:121114526-121114537
34	CEBPB	chr7:121124227-121124722	HepG2	liver:	n/a	chr7:121124331-121124344
35	CEBPB	chr7:121134700-121135247	IMR90	lung:	n/a	n/a
36	CEBPB	chr7:121101634-121101845	Hela-S3	cervix:	n/a	chr7:121101749-121101760
37	CEBPB	chr7:121070662-121070998	K562	blood:	n/a	n/a
38	CEBPB	chr7:121119850-121119875	A549	lung:	n/a	n/a
39	CEBPB	chr7:121142548-121142728	K562	blood:	n/a	n/a
40	CEBPB	chr7:121114357-121114661	IMR90	lung:	n/a	chr7:121114526-121114537
41	CEBPB	chr7:121086624-121086997	MCF-7	breast:	n/a	n/a
42	CEBPB	chr7:121130389-121130741	HepG2	liver:	n/a	chr7:121130555-121130566 chr7:121130554-121130567 chr7:121130556-121130565 chr7:121130554-121130567 chr7:121130554-121130565
43	CEBPB	chr7:121086627-121086995	MCF-7	breast:	n/a	n/a
44	CEBPB	chr7:121106750-121107006	A549	lung:	n/a	chr7:121106910-121106919 chr7:121106910-121106919 chr7:121106908-121106919
45	CEBPB	chr7:121085267-121085500	K562	blood:	n/a	n/a
46	CEBPB	chr7:121106885-121107008	HepG2	liver:	n/a	chr7:121106910-121106919 chr7:121106910-121106919 chr7:121106908-121106919
47	CEBPB	chr7:121114390-121114658	HepG2	liver:	n/a	chr7:121114526-121114537
48	CEBPB	chr7:121069875-121070201	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr7:121099236-121099520	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr7:121078690-121078713	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:121128867-121128917	HRE	kidney:	n/a
2	chr7:121128867-121128917	HCT-116	colon:	n/a
3	chr7:121128867-121128917	A549	lung:	n/a
4	chr7:121078303-121078353	PFSK-1	brain:	n/a
5	chr7:121120431-121120481	HRCEpiC	kidney:	n/a
6	chr7:121120431-121120481	HCPEpiC	choroid plexus:	n/a
7	chr7:121128867-121128917	SK-N-SH_RA	brain:	n/a
8	chr7:121120431-121120481	SAEC	small airway:	n/a
9	chr7:121078303-121078353	SK-N-SH_RA	brain:	n/a
10	chr7:121120431-121120481	IMR90	lung:	fetal
11	chr7:121120431-121120481	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:121128867-121128917	MCF10A-Er-Src	breast:	n/a
13	chr7:121128867-121128917	SKMC	muscle:	n/a
14	chr7:121128867-121128917	BE2_C	brain:	n/a
15	chr7:121078303-121078353	SK-N-MC	brain:	n/a
16	chr7:121128867-121128917	HUVEC	blood vessel:	n/a
17	chr7:121078303-121078353	ProgFib	skin:	n/a
18	chr7:121120431-121120481	LNCaP	prostate:	n/a
19	chr7:121120431-121120481	AG09309	skin:	n/a
20	chr7:121078303-121078353	AG04449	skin:	fetal
21	chr7:121128867-121128917	GM12878	blood:	n/a
22	chr7:121128867-121128917	SAEC	small airway:	n/a
23	chr7:121078303-121078353	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:121128867-121128917	NHDF-neo	bronchial:	n/a
25	chr7:121078303-121078353	BJ	skin:	n/a
26	chr7:121078303-121078353	LNCaP	prostate:	n/a
27	chr7:121078303-121078353	HEEpiC	esophagus:	n/a
28	chr7:121120431-121120481	SK-N-SH	brain:	n/a
29	chr7:121078303-121078353	Hela-S3	cervix:	n/a
30	chr7:121128867-121128917	AG04449	skin:	fetal
31	chr7:121078303-121078353	GM12892	blood:	n/a
32	chr7:121078303-121078353	GM19239	blood:	n/a
33	chr7:121128867-121128917	HEEpiC	esophagus:	n/a
34	chr7:121128867-121128917	SK-N-MC	brain:	n/a
35	chr7:121078303-121078353	MCF-7	breast:	n/a
36	chr7:121078303-121078353	HCPEpiC	choroid plexus:	n/a
37	chr7:121120431-121120481	HCT-116	colon:	n/a
38	chr7:121128867-121128917	HMEC	breast:	n/a
39	chr7:121120431-121120481	HUVEC	blood vessel:	n/a
40	chr7:121128867-121128917	HAEpiC	amniotic membrane:	n/a
41	chr7:121128867-121128917	IMR90	lung:	fetal
42	chr7:121078303-121078353	NT2-D1	testis:	n/a
43	chr7:121078303-121078353	T-47D	breast:	n/a
44	chr7:121120431-121120481	Hepatocyte	liver:	n/a
45	chr7:121120431-121120481	HL-60	blood:	n/a
46	chr7:121128867-121128917	K562	blood:	n/a
47	chr7:121078303-121078353	Jurkat	blood:	n/a
48	chr7:121120431-121120481	A549	lung:	n/a
49	chr7:121120431-121120481	NHBE	bronchial:	n/a
50	chr7:121128867-121128917	HRCEpiC	kidney:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:120994398..120996999-chr7:121076063..121078486,2	K562	blood:
2	chr7:121115674..121118298-chr7:121118953..121120473,2	K562	blood:
3	chr7:121034392..121036621-chr7:121133511..121136433,2	K562	blood:
4	chr7:121071062..121073741-chr7:121077858..121079960,2	MCF-7	breast:
5	chr7:121034606..121036453-chr7:121075396..121077581,2	MCF-7	breast:
6	chr7:121115674..121117973-chr7:121118973..121121252,2	K562	blood:
7	chr7:121124175..121126190-chr7:121129210..121131009,2	K562	blood:
8	chr7:121063601..121065601-chr7:121068374..121070365,2	MCF-7	breast:
9	chr7:121084429..121087093-chr7:121100657..121103964,3	K562	blood:
10	chr7:121073008..121075987-chr7:121081368..121083333,2	K562	blood:
11	chr7:121127158..121128841-chr7:121137205..121139311,2	K562	blood:
12	chr7:121089158..121090017-chr7:121187411..121188046,2	MCF-7	breast:
13	chr7:121082501..121084474-chr7:121087406..121089640,2	MCF-7	breast:
14	chr7:121082938..121085924-chr7:121112606..121114729,2	K562	blood:
15	chr7:121082501..121084474-chr7:121087406..121089640,2	MCF-7	breast:
16	chr7:121115674..121117973-chr7:121118973..121121252,2	K562	blood:
17	chr7:121096657..121099226-chr7:121099333..121101212,2	MCF-7	breast:
18	chr7:121127158..121128841-chr7:121137205..121139311,2	K562	blood:
19	chr7:121091244..121093923-chr7:121101767..121103790,2	MCF-7	breast:
20	chr5:43040736..43042911-chr7:121084118..121086879,2	MCF-7	breast:
21	chr7:121084590..121086129-chr7:121087840..121089417,2	K562	blood:
22	chr7:121069870..121071528-chr7:121071586..121073268,2	K562	blood:
23	chr7:121035002..121037392-chr7:121079786..121082049,2	K562	blood:
24	chr7:121028108..121030349-chr7:121074356..121077552,3	K562	blood:
25	chr7:121035082..121037539-chr7:121077999..121080365,3	MCF-7	breast:
26	chr7:120946416..120948519-chr7:121124006..121127005,2	K562	blood:
27	chr7:121124175..121126190-chr7:121129210..121131009,2	K562	blood:
28	chr7:121031531..121033758-chr7:121126191..121127906,2	K562	blood:
29	chr7:121017884..121020146-chr7:121086694..121088827,2	K562	blood:
30	chr7:121125137..121127628-chr7:121130797..121133318,2	MCF-7	breast:
31	chr7:121069870..121071528-chr7:121071586..121073268,2	K562	blood:
32	chr7:121036043..121037977-chr7:121125686..121127316,2	MCF-7	breast:
33	chr7:121035131..121037238-chr7:121077312..121078831,2	K562	blood:
34	chr7:121007820..121010026-chr7:121078337..121080058,2	K562	blood:
35	chr7:121122074..121124983-chr7:121126769..121129080,3	K562	blood:
36	chr7:121122074..121126190-chr7:121126769..121131009,4	K562	blood:
37	chr7:121072404..121074478-chr7:121078211..121080066,2	K562	blood:
38	chr7:121073008..121075987-chr7:121081368..121083333,2	K562	blood:
39	chr7:121122074..121124983-chr7:121126769..121129080,3	K562	blood:
40	chr7:121084429..121087093-chr7:121100657..121103964,3	K562	blood:
41	chr7:121119950..121122804-chr7:121124054..121125979,2	K562	blood:
42	chr7:121084590..121086129-chr7:121087840..121089417,2	K562	blood:
43	chr7:121082938..121085924-chr7:121112606..121114729,2	K562	blood:
44	chr7:121096657..121099226-chr7:121099333..121101212,2	MCF-7	breast:
45	chr7:121086464..121088878-chr7:121090558..121092067,2	K562	blood:
46	chr7:121103901..121106297-chr7:121111081..121113849,2	K562	blood:
47	chr7:121071062..121073741-chr7:121077858..121079960,2	MCF-7	breast:
48	chr7:121125137..121127628-chr7:121130797..121133318,2	MCF-7	breast:
49	chr7:121119950..121122804-chr7:121124054..121125979,2	K562	blood:
50	chr7:121084438..121087093-chr7:121100657..121102565,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM3C-3	chr7:121126349-121126553	NONHSAT123008
2	lnc-FAM3C-3	chr7:121091087-121091247	NONHSAT123008

No data

Variant related genes	Relation type
ENSG00000234985	TF binding region
ENSG00000234985	CpG island
ENSG00000215068	chromatin interactions
ENSG00000196937	chromatin interactions

Extended variants
information (count: 3025 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3025 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573519339	chr7:121069461-121069462	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs115938916	chr7:121069478-121069479	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569332453	chr7:121069504-121069505	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369947195	chr7:121069534-121069535	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189694465	chr7:121069562-121069563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs544213851	chr7:121069570-121069571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs181232332	chr7:121069617-121069618	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs568492785	chr7:121069652-121069653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs549912574	chr7:121069667-121069668	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs553740779	chr7:121069728-121069729	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs201262947	chr7:121069745-121069746	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs386411148	chr7:121069746-121069747	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs386411149	chr7:121069756-121069757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs202006604	chr7:121069758-121069759	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185917401	chr7:121069800-121069801	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190376380	chr7:121069803-121069804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558400457	chr7:121069806-121069807	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs35426959	chr7:121069810-121069811	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs575462613	chr7:121069862-121069863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs544356128	chr7:121069883-121069884	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373832895	chr7:121069887-121069888	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs560929977	chr7:121069942-121069943	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs111741831	chr7:121069947-121069948	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs2697167	chr7:121069949-121069950	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs374273015	chr7:121069951-121069952	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs186095137	chr7:121069968-121069969	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528995638	chr7:121070073-121070074	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs115034530	chr7:121070112-121070113	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs2463646	chr7:121070146-121070147	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs368912222	chr7:121070155-121070156	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs566249996	chr7:121070181-121070182	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs71931782	chr7:121070189-121070190	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558451968	chr7:121070195-121070196	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200604737	chr7:121070206-121070207	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs377275159	chr7:121070208-121070209	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs2463647	chr7:121070246-121070247	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs148973059	chr7:121070261-121070262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs143826775	chr7:121070262-121070263	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534012135	chr7:121070322-121070323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs571556431	chr7:121070351-121070352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570631306	chr7:121070412-121070413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192248921	chr7:121070420-121070421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537006549	chr7:121070430-121070431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182753648	chr7:121070458-121070459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575450866	chr7:121070490-121070491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537801725	chr7:121070491-121070492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554742654	chr7:121070568-121070569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148155962	chr7:121070636-121070637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371544788	chr7:121070663-121070664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556925591	chr7:121070681-121070682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute monocytic leukemia	16498392	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121067600-121070000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr7:121068800-121069600	Enhancers	Muscle Satellite Cultured Cells	--
3	chr7:121068800-121069600	Enhancers	Osteobl	bone
4	chr7:121068800-121069800	Enhancers	Fetal Kidney	kidney
5	chr7:121069000-121069600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:121069000-121073400	Weak transcription	Placenta	Placenta
7	chr7:121069200-121069600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:121069200-121077600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:121069400-121074400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr7:121069800-121078000	Weak transcription	Fetal Kidney	kidney
11	chr7:121070800-121072400	Enhancers	Fetal Intestine Small	intestine
12	chr7:121071200-121072400	Enhancers	Fetal Intestine Large	intestine
13	chr7:121072000-121073000	Enhancers	GM12878-XiMat	blood
14	chr7:121072200-121077600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:121072400-121074000	Weak transcription	Fetal Intestine Large	intestine
16	chr7:121072400-121074200	Weak transcription	Fetal Intestine Small	intestine
17	chr7:121073000-121074400	Flanking Active TSS	GM12878-XiMat	blood
18	chr7:121073400-121073600	Enhancers	Placenta	Placenta
19	chr7:121073400-121073800	Enhancers	Primary B cells from peripheral blood	blood
20	chr7:121073600-121074000	Weak transcription	Placenta	Placenta
21	chr7:121073600-121074400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:121073800-121076800	Weak transcription	Primary B cells from peripheral blood	blood
23	chr7:121074000-121074600	Enhancers	Fetal Intestine Large	intestine
24	chr7:121074000-121074600	Enhancers	Placenta	Placenta
25	chr7:121074200-121074400	Enhancers	Pancreas	Pancrea
26	chr7:121074200-121074600	Enhancers	Fetal Intestine Small	intestine
27	chr7:121074400-121074600	Enhancers	GM12878-XiMat	blood
28	chr7:121074400-121077400	Enhancers	Placenta Amnion	Placenta Amnion
29	chr7:121074400-121078000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:121074400-121080800	Weak transcription	Pancreas	Pancrea
31	chr7:121074600-121076000	Weak transcription	Fetal Intestine Large	intestine
32	chr7:121074600-121076000	Weak transcription	Placenta	Placenta
33	chr7:121074600-121077400	Weak transcription	Fetal Intestine Small	intestine
34	chr7:121074600-121077800	Weak transcription	GM12878-XiMat	blood
35	chr7:121075800-121076600	Enhancers	HUVEC	blood vessel
36	chr7:121076000-121078200	Enhancers	Fetal Intestine Large	intestine
37	chr7:121076000-121079000	Enhancers	Placenta	Placenta
38	chr7:121076200-121076600	Enhancers	NHEK	skin
39	chr7:121076200-121076800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr7:121076200-121077800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr7:121076400-121076600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr7:121076400-121076600	Enhancers	Esophagus	oesophagus
43	chr7:121076400-121076800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr7:121076400-121077200	Enhancers	H1 Cell Line	embryonic stem cell
45	chr7:121076400-121077200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr7:121076400-121077800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr7:121076400-121078400	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr7:121076600-121077600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr7:121076600-121077600	Weak transcription	Esophagus	oesophagus
50	chr7:121076600-121077600	Weak transcription	NHEK	skin

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