Variant report

Variant	nsv1015296
Chromosome Location	chr7:3381813-3560401
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1310)
CpG islands
(count:610)
Chromatin interactive
region (count:85)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1310 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3419747-3420059	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:3418058-3418349	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	chr7:3420718-3420741	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:3515387-3515402	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr7:3439465-3439755	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr7:3519977-3520319	K562	blood:	n/a	n/a
9	BHLHE40	chr7:3418024-3418475	HepG2	liver:	n/a	n/a
10	BRCA1	chr7:3522141-3522202	GM12878	blood:	n/a	n/a
11	CEBPB	chr7:3393401-3393650	HepG2	liver:	n/a	chr7:3393579-3393590
12	CEBPB	chr7:3420050-3420246	A549	lung:	n/a	n/a
13	CEBPB	chr7:3478893-3479425	A549	lung:	n/a	chr7:3479156-3479167
14	CEBPB	chr7:3478938-3479358	Hela-S3	cervix:	n/a	chr7:3479156-3479167
15	CEBPB	chr7:3486445-3486801	IMR90	lung:	n/a	n/a
16	CEBPB	chr7:3478943-3479301	ECC-1	luminal epithelium:	n/a	chr7:3479156-3479167
17	CEBPB	chr7:3475791-3476051	A549	lung:	n/a	chr7:3475940-3475949 chr7:3475939-3475950 chr7:3475940-3475949
18	CEBPB	chr7:3478751-3479563	A549	lung:	n/a	chr7:3479156-3479167
19	CEBPB	chr7:3522096-3522799	A549	lung:	n/a	chr7:3522481-3522492
20	CEBPB	chr7:3522089-3522651	Hela-S3	cervix:	n/a	chr7:3522481-3522492
21	CEBPB	chr7:3515347-3515593	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:3551499-3551703	HepG2	liver:	n/a	chr7:3551564-3551575
23	CEBPB	chr7:3533115-3533486	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:3551459-3551660	H1-hESC	embryonic stem cell:	n/a	chr7:3551564-3551575
25	CEBPB	chr7:3417979-3418421	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:3551480-3551693	K562	blood:	n/a	chr7:3551564-3551575
27	CEBPB	chr7:3526587-3526825	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:3521976-3522775	MCF-7	breast:	n/a	chr7:3522481-3522492
29	CEBPB	chr7:3534870-3535070	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:3410009-3410230	K562	blood:	n/a	n/a
31	CEBPB	chr7:3478840-3479385	IMR90	lung:	n/a	chr7:3479156-3479167
32	CEBPB	chr7:3478791-3479549	MCF-7	breast:	n/a	chr7:3479156-3479167
33	CEBPB	chr7:3471268-3471422	HepG2	liver:	n/a	chr7:3471347-3471358
34	CEBPB	chr7:3533231-3533366	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:3444003-3444489	MCF-7	breast:	n/a	n/a
36	CEBPB	chr7:3419990-3420315	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:3478910-3479342	MCF-7	breast:	n/a	chr7:3479156-3479167
38	CEBPB	chr7:3475773-3476125	HepG2	liver:	n/a	chr7:3475940-3475949 chr7:3475939-3475950 chr7:3475940-3475949
39	CEBPB	chr7:3533116-3533450	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr7:3540105-3540112	K562	blood:	n/a	n/a
41	CEBPB	chr7:3533031-3533530	A549	lung:	n/a	n/a
42	CEBPB	chr7:3522143-3522706	MCF-7	breast:	n/a	chr7:3522481-3522492
43	CEBPB	chr7:3481954-3482057	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr7:3476192-3476839	A549	lung:	n/a	n/a
45	CEBPB	chr7:3522361-3522623	K562	blood:	n/a	chr7:3522481-3522492
46	CEBPB	chr7:3443878-3444610	MCF-7	breast:	n/a	n/a
47	CEBPB	chr7:3522183-3522654	H1-hESC	embryonic stem cell:	n/a	chr7:3522481-3522492
48	CEBPB	chr7:3515364-3515642	IMR90	lung:	n/a	n/a
49	CEBPB	chr7:3479036-3479317	K562	blood:	n/a	chr7:3479156-3479167
50	CEBPB	chr7:3478874-3479351	A549	lung:	n/a	chr7:3479156-3479167

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3549961-3550011	RPTEC	kidney:	n/a
2	chr7:3411503-3411553	HCT-116	colon:	n/a
3	chr7:3533958-3534008	NB4	blood:	n/a
4	chr7:3411356-3411406	Hepatocyte	liver:	n/a
5	chr7:3536689-3536739	AoSMC	blood vessel:	n/a
6	chr7:3411356-3411406	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:3478077-3478127	NH-A	brain:	n/a
8	chr7:3536689-3536739	BE2_C	brain:	n/a
9	chr7:3478077-3478127	GM19239	blood:	n/a
10	chr7:3549961-3550011	PFSK-1	brain:	n/a
11	chr7:3419305-3419355	HRCEpiC	kidney:	n/a
12	chr7:3533958-3534008	HRPEpiC	eye:	n/a
13	chr7:3536689-3536739	HCF	heart:	n/a
14	chr7:3411503-3411553	AG04450	lung:	fetal
15	chr7:3470434-3470484	Jurkat	blood:	n/a
16	chr7:3411503-3411553	Hela-S3	cervix:	n/a
17	chr7:3385318-3385368	MCF10A-Er-Src	breast:	n/a
18	chr7:3533958-3534008	SK-N-MC	brain:	n/a
19	chr7:3549961-3550011	HCPEpiC	choroid plexus:	n/a
20	chr7:3536689-3536739	GM19239	blood:	n/a
21	chr7:3411356-3411406	NH-A	brain:	n/a
22	chr7:3549961-3550011	NT2-D1	testis:	n/a
23	chr7:3536689-3536739	HMEC	breast:	n/a
24	chr7:3411503-3411553	SAEC	small airway:	n/a
25	chr7:3549961-3550011	HepG2	liver:	n/a
26	chr7:3470434-3470484	IMR90	lung:	fetal
27	chr7:3536689-3536739	NT2-D1	testis:	n/a
28	chr7:3488816-3488866	NT2-D1	testis:	n/a
29	chr7:3411503-3411553	HIPEpiC	eye:	n/a
30	chr7:3536689-3536739	HAEpiC	amniotic membrane:	n/a
31	chr7:3385318-3385368	PrEC	prostate:	n/a
32	chr7:3385318-3385368	ProgFib	skin:	n/a
33	chr7:3536689-3536739	Caco-2	colon:	n/a
34	chr7:3470434-3470484	A549	lung:	n/a
35	chr7:3536689-3536739	HepG2	liver:	n/a
36	chr7:3411503-3411553	RPTEC	kidney:	n/a
37	chr7:3470434-3470484	MCF10A-Er-Src	breast:	n/a
38	chr7:3411503-3411553	Hepatocyte	liver:	n/a
39	chr7:3536689-3536739	SK-N-MC	brain:	n/a
40	chr7:3488816-3488866	RPTEC	kidney:	n/a
41	chr7:3411356-3411406	PFSK-1	brain:	n/a
42	chr7:3419305-3419355	MCF10A-Er-Src	breast:	n/a
43	chr7:3419305-3419355	BE2_C	brain:	n/a
44	chr7:3411356-3411406	ovcar-3	ovarian:	n/a
45	chr7:3419305-3419355	AG09319	gingival:	n/a
46	chr7:3549961-3550011	SKMC	muscle:	n/a
47	chr7:3419305-3419355	PANC-1	pancreas:	n/a
48	chr7:3411503-3411553	PrEC	prostate:	n/a
49	chr7:3478077-3478127	HRPEpiC	eye:	n/a
50	chr7:3478077-3478127	U87	brain:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:3425641..3430182-chr7:3430225..3435357,4	MCF-7	breast:
2	chr7:3444122..3444632-chr7:3471439..3472016,2	MCF-7	breast:
3	chr7:3444047..3446365-chr7:3452049..3455174,3	MCF-7	breast:
4	chr7:3385347..3387289-chr7:3389084..3391687,2	K562	blood:
5	chr7:3385347..3387562-chr7:3388126..3390584,2	K562	blood:
6	chr7:3452987..3455737-chr7:3457417..3460056,3	MCF-7	breast:
7	chr7:3444122..3444632-chr7:3471439..3472016,2	MCF-7	breast:
8	chr7:3537080..3539372-chr7:3543955..3546696,2	MCF-7	breast:
9	chr7:3435622..3438009-chr7:3442617..3444470,2	MCF-7	breast:
10	chr7:3442245..3445067-chr7:3448256..3450121,2	MCF-7	breast:
11	chr7:3528452..3531258-chr7:3533365..3536191,2	MCF-7	breast:
12	chr7:3381518..3384288-chr7:3389563..3392329,2	MCF-7	breast:
13	chr7:3390810..3392669-chr7:3397273..3399419,2	MCF-7	breast:
14	chr7:3463184..3466150-chr7:3469039..3471328,2	MCF-7	breast:
15	chr7:3525893..3527972-chr7:3528761..3530519,2	K562	blood:
16	chr7:3521696..3522495-chr7:3631928..3632648,2	MCF-7	breast:
17	chr7:3379742..3382229-chr7:3382243..3386040,3	K562	blood:
18	chr7:3435622..3438009-chr7:3442617..3444470,2	MCF-7	breast:
19	chr7:3436200..3438648-chr7:3443337..3445077,2	K562	blood:
20	chr7:3467584..3469607-chr7:3473579..3476455,2	MCF-7	breast:
21	chr7:3424678..3427459-chr7:3437708..3440654,2	MCF-7	breast:
22	chr7:3444047..3446365-chr7:3452049..3455174,3	MCF-7	breast:
23	chr7:3443032..3445719-chr7:3938528..3940389,2	MCF-7	breast:
24	chr7:3388931..3391698-chr7:3393863..3395884,2	K562	blood:
25	chr7:3525893..3527972-chr7:3528761..3530519,2	K562	blood:
26	chr7:3427962..3429690-chr7:3438000..3440152,2	K562	blood:
27	chr7:3194262..3194922-chr7:3439333..3439841,2	MCF-7	breast:
28	chr7:3441889..3444490-chr7:3452543..3454242,2	MCF-7	breast:
29	chr7:3467584..3469607-chr7:3473579..3476455,2	MCF-7	breast:
30	chr7:3553060..3555067-chr7:3563741..3566106,2	MCF-7	breast:
31	chr7:3379742..3382229-chr7:3382243..3386040,3	K562	blood:
32	chr7:3378023..3380579-chr7:3388510..3390019,2	MCF-7	breast:
33	chr7:3528452..3531258-chr7:3533365..3536191,2	MCF-7	breast:
34	chr7:3398782..3400855-chr7:3415548..3417886,2	MCF-7	breast:
35	chr7:3521823..3522640-chr7:3807742..3808264,2	MCF-7	breast:
36	chr7:3339718..3341766-chr7:3458306..3459954,2	K562	blood:
37	chr7:3421160..3422732-chr7:3429225..3430935,2	MCF-7	breast:
38	chr7:3555349..3557729-chr7:3560043..3561605,2	K562	blood:
39	chr7:3551543..3553743-chr7:3556409..3559283,2	MCF-7	breast:
40	chr7:3436200..3439462-chr7:3442138..3445077,3	K562	blood:
41	chr7:3546340..3548906-chr7:3559233..3561540,2	MCF-7	breast:
42	chr7:3463184..3466150-chr7:3469039..3471328,2	MCF-7	breast:
43	chr7:3436200..3439462-chr7:3442138..3445077,3	K562	blood:
44	chr7:3425023..3426589-chr7:3427708..3429646,2	MCF-7	breast:
45	chr7:3419417..3422397-chr7:3422583..3424637,2	K562	blood:
46	chr7:3421160..3422732-chr7:3429225..3430935,2	MCF-7	breast:
47	chr7:3381518..3384288-chr7:3389563..3392329,2	MCF-7	breast:
48	chr7:3385347..3387289-chr7:3389084..3391687,2	K562	blood:
49	chr7:3341947..3342585-chr7:3439297..3440029,2	MCF-7	breast:
50	chr7:3340063..3340822-chr7:3439252..3440083,5	MCF-7	breast:

No data

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

Extended variants
information (count: 10079 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:10079 , 50 per page) page: 1 2 3 4 5 6 7 ... 202

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553024971	chr7:3381828-3381829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573029552	chr7:3381837-3381838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541806214	chr7:3381850-3381851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562153772	chr7:3381854-3381855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149754433	chr7:3381877-3381878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188110671	chr7:3381908-3381909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564639681	chr7:3381942-3381943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113100763	chr7:3381948-3381949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191420403	chr7:3381955-3381956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566554771	chr7:3381959-3381960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568021327	chr7:3381980-3381981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373735003	chr7:3381986-3381987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182313172	chr7:3382010-3382011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187725845	chr7:3382034-3382035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192567607	chr7:3382038-3382039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199749667	chr7:3382047-3382048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557999764	chr7:3382048-3382049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529444449	chr7:3382076-3382077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571232511	chr7:3382081-3382082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533719611	chr7:3382124-3382125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553585230	chr7:3382135-3382136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572992782	chr7:3382155-3382156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184435819	chr7:3382168-3382169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369323397	chr7:3382174-3382175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555584661	chr7:3382175-3382176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575558767	chr7:3382190-3382191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544301683	chr7:3382197-3382198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547905197	chr7:3382207-3382208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573104285	chr7:3382220-3382221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566324086	chr7:3382241-3382242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10230321	chr7:3382246-3382247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10230335	chr7:3382275-3382276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140352311	chr7:3382287-3382288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540027974	chr7:3382337-3382338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529511894	chr7:3382350-3382351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549024383	chr7:3382353-3382354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144072721	chr7:3382375-3382376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115617732	chr7:3382393-3382394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4722705	chr7:3382408-3382409	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs190163443	chr7:3382431-3382432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573847156	chr7:3382470-3382471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192974690	chr7:3382477-3382478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547188094	chr7:3382482-3382483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184844074	chr7:3382503-3382504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189772539	chr7:3382517-3382518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs59031986	chr7:3382528-3382529	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs77332539	chr7:3382542-3382543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4722708	chr7:3382563-3382564	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs374008271	chr7:3382609-3382610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374342952	chr7:3382634-3382635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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	21293372	CNVD

Chromatin state (count:929 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3359000-3385800	Weak transcription	Pancreas	Pancrea
2	chr7:3376200-3385800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:3378600-3383200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:3383200-3384200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr7:3384200-3389800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr7:3385400-3385800	Enhancers	Brain Anterior Caudate	brain
7	chr7:3385800-3386000	Enhancers	Pancreas	Pancrea
8	chr7:3385800-3386200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:3386000-3388800	Weak transcription	Aorta	Aorta
10	chr7:3386000-3410400	Weak transcription	Pancreas	Pancrea
11	chr7:3386200-3408200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:3389800-3392400	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr7:3392400-3395400	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr7:3393600-3402600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:3395400-3396200	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr7:3395600-3396000	Enhancers	Colon Smooth Muscle	Colon
17	chr7:3396200-3402200	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr7:3397200-3397400	Enhancers	Aorta	Aorta
19	chr7:3397400-3398600	Weak transcription	Aorta	Aorta
20	chr7:3398000-3398800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr7:3398200-3399600	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr7:3398400-3398800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr7:3398400-3400200	Weak transcription	Right Ventricle	heart
24	chr7:3398600-3399000	Enhancers	Aorta	Aorta
25	chr7:3398600-3399600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:3398800-3403200	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr7:3399000-3402600	Weak transcription	Aorta	Aorta
28	chr7:3400200-3400400	Enhancers	Right Ventricle	heart
29	chr7:3401200-3403200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:3402200-3403000	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr7:3402600-3403400	Enhancers	Aorta	Aorta
32	chr7:3402600-3403600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr7:3403200-3403600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr7:3403200-3403600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr7:3403200-3403600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:3403200-3403600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr7:3403200-3403600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr7:3403200-3403600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr7:3403200-3403600	Enhancers	Fetal Brain Male	brain
40	chr7:3403400-3408200	Weak transcription	Aorta	Aorta
41	chr7:3403600-3407200	Weak transcription	Fetal Brain Male	brain
42	chr7:3406000-3406400	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr7:3406400-3409600	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr7:3407000-3407200	Enhancers	Colon Smooth Muscle	Colon
45	chr7:3407000-3408000	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr7:3407200-3407600	Enhancers	HSMMtube	muscle
47	chr7:3407200-3408200	Weak transcription	Colon Smooth Muscle	Colon
48	chr7:3407200-3411800	Enhancers	Fetal Brain Male	brain
49	chr7:3408000-3409600	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr7:3408200-3408400	Enhancers	Fetal Brain Female	brain

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