Variant report

Variant	nsv538662
Chromosome Location	chr7:3348458-3554820
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1414)
CpG islands
(count:732)
Chromatin interactive
region (count:93)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1414 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3418058-3418349	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:3419747-3420059	HepG2	liver:	n/a	n/a
3	ATF1	chr7:3385311-3385328	K562	blood:	n/a	n/a
4	ATF2	chr7:3439424-3439867	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:3515387-3515402	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:3356180-3356380	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:3420718-3420741	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:3370227-3370294	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr7:3439465-3439755	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr7:3519977-3520319	K562	blood:	n/a	n/a
11	BHLHE40	chr7:3418024-3418475	HepG2	liver:	n/a	n/a
12	BRCA1	chr7:3522141-3522202	GM12878	blood:	n/a	n/a
13	CEBPB	chr7:3478986-3479323	HepG2	liver:	n/a	chr7:3479156-3479167
14	CEBPB	chr7:3533231-3533366	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:3427134-3427430	A549	lung:	n/a	chr7:3427395-3427408
16	CEBPB	chr7:3522292-3522669	IMR90	lung:	n/a	chr7:3522481-3522492
17	CEBPB	chr7:3393443-3393652	A549	lung:	n/a	chr7:3393579-3393590
18	CEBPB	chr7:3522096-3522799	A549	lung:	n/a	chr7:3522481-3522492
19	CEBPB	chr7:3410002-3410305	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr7:3444003-3444489	MCF-7	breast:	n/a	n/a
21	CEBPB	chr7:3534870-3535070	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:3478893-3479425	A549	lung:	n/a	chr7:3479156-3479167
23	CEBPB	chr7:3478988-3479368	ECC-1	luminal epithelium:	n/a	chr7:3479156-3479167
24	CEBPB	chr7:3526587-3526825	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:3533031-3533530	A549	lung:	n/a	n/a
26	CEBPB	chr7:3533116-3533450	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr7:3443878-3444610	MCF-7	breast:	n/a	n/a
28	CEBPB	chr7:3515394-3515623	A549	lung:	n/a	n/a
29	CEBPB	chr7:3471268-3471422	HepG2	liver:	n/a	chr7:3471347-3471358
30	CEBPB	chr7:3420050-3420246	A549	lung:	n/a	n/a
31	CEBPB	chr7:3522175-3522675	A549	lung:	n/a	chr7:3522481-3522492
32	CEBPB	chr7:3478943-3479301	ECC-1	luminal epithelium:	n/a	chr7:3479156-3479167
33	CEBPB	chr7:3481954-3482057	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr7:3486445-3486801	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:3478840-3479385	IMR90	lung:	n/a	chr7:3479156-3479167
36	CEBPB	chr7:3478751-3479563	A549	lung:	n/a	chr7:3479156-3479167
37	CEBPB	chr7:3479036-3479317	K562	blood:	n/a	chr7:3479156-3479167
38	CEBPB	chr7:3551480-3551693	K562	blood:	n/a	chr7:3551564-3551575
39	CEBPB	chr7:3471229-3471499	HepG2	liver:	n/a	chr7:3471347-3471358
40	CEBPB	chr7:3522183-3522654	H1-hESC	embryonic stem cell:	n/a	chr7:3522481-3522492
41	CEBPB	chr7:3533115-3533486	IMR90	lung:	n/a	n/a
42	CEBPB	chr7:3457543-3457997	H1-hESC	embryonic stem cell:	n/a	chr7:3457585-3457598 chr7:3457585-3457598
43	CEBPB	chr7:3478791-3479549	MCF-7	breast:	n/a	chr7:3479156-3479167
44	CEBPB	chr7:3522143-3522706	MCF-7	breast:	n/a	chr7:3522481-3522492
45	CEBPB	chr7:3522164-3522619	HCT-116	colon:	n/a	chr7:3522481-3522492
46	CEBPB	chr7:3515429-3515566	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr7:3475773-3476125	HepG2	liver:	n/a	chr7:3475940-3475949 chr7:3475939-3475950 chr7:3475940-3475949
48	CEBPB	chr7:3478910-3479342	MCF-7	breast:	n/a	chr7:3479156-3479167
49	CEBPB	chr7:3475761-3476128	IMR90	lung:	n/a	chr7:3475940-3475949 chr7:3475939-3475950 chr7:3475940-3475949
50	CEBPB	chr7:3393401-3393650	HepG2	liver:	n/a	chr7:3393579-3393590

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3385318-3385368	IMR90	lung:	fetal
2	chr7:3358214-3358264	GM12878	blood:	n/a
3	chr7:3411503-3411553	LNCaP	prostate:	n/a
4	chr7:3488816-3488866	HRE	kidney:	n/a
5	chr7:3470434-3470484	AoSMC	blood vessel:	n/a
6	chr7:3549961-3550011	SK-N-SH	brain:	n/a
7	chr7:3536689-3536739	SK-N-SH	brain:	n/a
8	chr7:3470434-3470484	HCM	heart:	n/a
9	chr7:3549961-3550011	ECC-1	luminal epithelium:	n/a
10	chr7:3470434-3470484	HRPEpiC	eye:	n/a
11	chr7:3358214-3358264	GM19239	blood:	n/a
12	chr7:3478077-3478127	PANC-1	pancreas:	n/a
13	chr7:3385318-3385368	PrEC	prostate:	n/a
14	chr7:3375859-3375909	HIPEpiC	eye:	n/a
15	chr7:3470434-3470484	HL-60	blood:	n/a
16	chr7:3488816-3488866	AG04449	skin:	fetal
17	chr7:3358214-3358264	CMK	blood:	n/a
18	chr7:3375859-3375909	AG04450	lung:	fetal
19	chr7:3549961-3550011	LNCaP	prostate:	n/a
20	chr7:3470434-3470484	MCF-7	breast:	n/a
21	chr7:3385318-3385368	GM06990	blood:	n/a
22	chr7:3375859-3375909	HNPCEpiC	eye:	n/a
23	chr7:3533958-3534008	NH-A	brain:	n/a
24	chr7:3375859-3375909	HMEC	breast:	n/a
25	chr7:3411503-3411553	SAEC	small airway:	n/a
26	chr7:3536689-3536739	HRCEpiC	kidney:	n/a
27	chr7:3375859-3375909	HEEpiC	esophagus:	n/a
28	chr7:3385318-3385368	HRE	kidney:	n/a
29	chr7:3358214-3358264	LNCaP	prostate:	n/a
30	chr7:3478077-3478127	HRCEpiC	kidney:	n/a
31	chr7:3411356-3411406	PrEC	prostate:	n/a
32	chr7:3385318-3385368	HNPCEpiC	eye:	n/a
33	chr7:3385318-3385368	MCF-7	breast:	n/a
34	chr7:3536689-3536739	HCF	heart:	n/a
35	chr7:3385318-3385368	PANC-1	pancreas:	n/a
36	chr7:3549961-3550011	GM12878	blood:	n/a
37	chr7:3385318-3385368	HCPEpiC	choroid plexus:	n/a
38	chr7:3478077-3478127	HCM	heart:	n/a
39	chr7:3385318-3385368	U87	brain:	n/a
40	chr7:3419305-3419355	H1-hESC	embryonic stem cell:	embryo
41	chr7:3375859-3375909	AG10803	skin:	n/a
42	chr7:3419305-3419355	SKMC	muscle:	n/a
43	chr7:3533958-3534008	NT2-D1	testis:	n/a
44	chr7:3549961-3550011	CMK	blood:	n/a
45	chr7:3536689-3536739	BE2_C	brain:	n/a
46	chr7:3375859-3375909	NHBE	bronchial:	n/a
47	chr7:3419305-3419355	HMEC	breast:	n/a
48	chr7:3536689-3536739	GM12891	blood:	n/a
49	chr7:3385318-3385368	HRPEpiC	eye:	n/a
50	chr7:3358214-3358264	HNPCEpiC	eye:	n/a

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:3388931..3391698-chr7:3393863..3395884,2	K562	blood:
2	chr7:3349072..3350762-chr7:3354639..3356462,2	K562	blood:
3	chr7:3424678..3427459-chr7:3437708..3440654,2	MCF-7	breast:
4	chr7:3441889..3444490-chr7:3452543..3454242,2	MCF-7	breast:
5	chr7:3379742..3382229-chr7:3382243..3386040,3	K562	blood:
6	chr7:3388931..3391698-chr7:3393863..3395884,2	K562	blood:
7	chr7:3424678..3427459-chr7:3437708..3440654,2	MCF-7	breast:
8	chr7:3467584..3469607-chr7:3473579..3476455,2	MCF-7	breast:
9	chr7:3421160..3422732-chr7:3429225..3430935,2	MCF-7	breast:
10	chr7:3521823..3522640-chr7:3807742..3808264,2	MCF-7	breast:
11	chr7:3438230..3440428-chr7:3448766..3450871,2	MCF-7	breast:
12	chr7:3349154..3351811-chr7:3384855..3387148,2	MCF-7	breast:
13	chr7:3425023..3426589-chr7:3427708..3429646,2	MCF-7	breast:
14	chr7:3354663..3356940-chr7:3364964..3367662,2	K562	blood:
15	chr7:3444122..3444632-chr7:3471439..3472016,2	MCF-7	breast:
16	chr7:3425641..3430182-chr7:3430225..3435357,4	MCF-7	breast:
17	chr7:3340063..3340822-chr7:3439252..3440083,5	MCF-7	breast:
18	chr7:3537080..3539372-chr7:3543955..3546696,2	MCF-7	breast:
19	chr7:3551947..3554691-chr7:3562735..3565041,2	MCF-7	breast:
20	chr7:3537080..3539372-chr7:3543955..3546696,2	MCF-7	breast:
21	chr7:3438230..3440428-chr7:3448766..3450871,2	MCF-7	breast:
22	chr7:3425023..3426589-chr7:3427708..3429646,2	MCF-7	breast:
23	chr7:3435622..3438009-chr7:3442617..3444470,2	MCF-7	breast:
24	chr7:3340385..3341337-chr7:3439295..3440058,3	MCF-7	breast:
25	chr7:3385347..3387289-chr7:3389084..3391687,2	K562	blood:
26	chr7:3351745..3355702-chr7:3356161..3359964,4	K562	blood:
27	chr7:3427962..3429690-chr7:3438000..3440152,2	K562	blood:
28	chr7:3444047..3446365-chr7:3452049..3455174,3	MCF-7	breast:
29	chr7:3443032..3445719-chr7:3938528..3940389,2	MCF-7	breast:
30	chr7:3342709..3344229-chr7:3346065..3349002,2	K562	blood:
31	chr7:3441889..3444490-chr7:3452543..3454242,2	MCF-7	breast:
32	chr7:3553060..3555067-chr7:3563741..3566106,2	MCF-7	breast:
33	chr7:3425641..3430182-chr7:3430225..3435357,4	MCF-7	breast:
34	chr7:3452987..3455737-chr7:3457417..3460056,3	MCF-7	breast:
35	chr7:3444122..3444632-chr7:3471439..3472016,2	MCF-7	breast:
36	chr7:3381518..3384288-chr7:3389563..3392329,2	MCF-7	breast:
37	chr7:3525893..3527972-chr7:3528761..3530519,2	K562	blood:
38	chr7:3194262..3194922-chr7:3439333..3439841,2	MCF-7	breast:
39	chr7:3444047..3446365-chr7:3452049..3455174,3	MCF-7	breast:
40	chr7:3528452..3531258-chr7:3533365..3536191,2	MCF-7	breast:
41	chr7:3439202..3440208-chr7:3521793..3522518,3	MCF-7	breast:
42	chr7:3521340..3522302-chr7:4671144..4671918,2	MCF-7	breast:
43	chr7:3528452..3531258-chr7:3533365..3536191,2	MCF-7	breast:
44	chr7:3419417..3422397-chr7:3422583..3424637,2	K562	blood:
45	chr7:3341947..3342585-chr7:3439297..3440029,2	MCF-7	breast:
46	chr7:3521755..3523053-chr7:3688631..3689551,7	MCF-7	breast:
47	chr7:3525893..3527972-chr7:3528761..3530519,2	K562	blood:
48	chr7:3521696..3522495-chr7:3631928..3632648,2	MCF-7	breast:
49	chr7:3463184..3466150-chr7:3469039..3471328,2	MCF-7	breast:
50	chr7:3385347..3387289-chr7:3389084..3391687,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMZ1-7	chr7:3377521-3378121	NONHSAT118850
2	lnc-AMZ1-7	chr7:3377758-3378233	NONHSAT118851

No data

Variant related genes	Relation type
ENSG00000224593	TF binding region
ENSG00000211544	TF binding region
ENSG00000224593	CpG island
ENSG00000211544	CpG island
ENSG00000236708	chromatin interactions
ENSG00000146555	chromatin interactions
ENSG00000211544	chromatin interactions

Extended variants
information (count: 11538 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:11538 , 50 per page) page: 1 2 3 4 5 6 7 ... 231

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183146416	chr7:3348484-3348485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557045107	chr7:3348490-3348491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576756950	chr7:3348508-3348509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139917994	chr7:3348540-3348541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80334747	chr7:3348541-3348542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546093236	chr7:3348542-3348543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185699456	chr7:3348615-3348616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10276190	chr7:3348663-3348664	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs530769016	chr7:3348670-3348671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549985368	chr7:3348746-3348747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566940570	chr7:3348747-3348748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs201405795	chr7:3348748-3348749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563853055	chr7:3348765-3348766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs149816254	chr7:3348799-3348800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556101188	chr7:3348846-3348847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552567169	chr7:3348852-3348853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190263849	chr7:3348854-3348855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73286353	chr7:3348883-3348884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574881290	chr7:3348884-3348885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1525555	chr7:3348903-3348904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs118112498	chr7:3348905-3348906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75935934	chr7:3348927-3348928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73286356	chr7:3348930-3348931	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs113320155	chr7:3348974-3348975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537694544	chr7:3348984-3348985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377519039	chr7:3348988-3348989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34437244	chr7:3349002-3349003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576416179	chr7:3349003-3349004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs61266092	chr7:3349010-3349011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs74580205	chr7:3349016-3349017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62437667	chr7:3349018-3349019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139515609	chr7:3349111-3349112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182133143	chr7:3349129-3349130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs71550397	chr7:3349156-3349157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs59762021	chr7:3349174-3349175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12700786	chr7:3349185-3349186	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs73286357	chr7:3349209-3349210	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs117710610	chr7:3349224-3349225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs541706086	chr7:3349239-3349240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs10276933	chr7:3349262-3349263	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs151128946	chr7:3349266-3349267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs193226262	chr7:3349319-3349320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544437978	chr7:3349323-3349324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs367676382	chr7:3349340-3349341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564138648	chr7:3349341-3349342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112109990	chr7:3349424-3349425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189198920	chr7:3349425-3349426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565550839	chr7:3349479-3349480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7807417	chr7:3349481-3349482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529659454	chr7:3349486-3349487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:985 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3343800-3357000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr7:3344600-3366600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:3344800-3354600	Weak transcription	Pancreas	Pancrea
4	chr7:3346200-3362400	Weak transcription	Aorta	Aorta
5	chr7:3347000-3350000	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr7:3347400-3349800	Weak transcription	Adipose Nuclei	Adipose
7	chr7:3347600-3349600	Weak transcription	Fetal Brain Male	brain
8	chr7:3349600-3350200	Enhancers	Fetal Brain Male	brain
9	chr7:3349800-3350000	Enhancers	Adipose Nuclei	Adipose
10	chr7:3350000-3350400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr7:3350200-3366800	Weak transcription	Fetal Brain Male	brain
12	chr7:3350400-3350600	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr7:3350600-3358800	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr7:3352000-3352600	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr7:3353800-3354800	Enhancers	Fetal Heart	heart
16	chr7:3354600-3355200	Enhancers	Pancreas	Pancrea
17	chr7:3356000-3356200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr7:3356200-3357200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr7:3357000-3357400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr7:3357000-3359400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:3357200-3357400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr7:3357200-3357800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr7:3357200-3358800	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr7:3357400-3358400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr7:3357800-3361000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr7:3358200-3358800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:3358400-3359000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr7:3358400-3359000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr7:3358400-3359200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr7:3358600-3359200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr7:3358600-3359200	Enhancers	Placenta Amnion	Placenta Amnion
32	chr7:3358800-3359000	Enhancers	Pancreas	Pancrea
33	chr7:3358800-3359200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr7:3358800-3360600	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr7:3358800-3360800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr7:3358800-3366800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:3359000-3359800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr7:3359000-3360600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr7:3359000-3385800	Weak transcription	Pancreas	Pancrea
40	chr7:3359200-3362400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr7:3360400-3361800	Enhancers	HepG2	liver
42	chr7:3360600-3361800	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr7:3360600-3364600	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr7:3360800-3361200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr7:3361000-3361200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:3361000-3361200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr7:3361200-3362200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr7:3361800-3362000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr7:3362200-3363000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr7:3362400-3362800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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