Variant report

Variant	nsv830888
Chromosome Location	chr7:3577214-3776276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1259)
CpG islands
(count:610)
Chromatin interactive
region (count:42)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1259 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3635039-3635334	HepG2	liver:	n/a	chr7:3635139-3635155
2	BACH1	chr7:3657589-3657734	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:3713169-3713470	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:3731377-3731827	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr7:3636895-3637153	GM12878	blood:	n/a	n/a
6	BATF	chr7:3621741-3622079	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:3621641-3621866	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:3721967-3722323	HepG2	liver:	n/a	n/a
9	BHLHE40	chr7:3621621-3622000	HepG2	liver:	n/a	n/a
10	BHLHE40	chr7:3609848-3610033	K562	blood:	n/a	n/a
11	CBX3	chr7:3618108-3618346	K562	blood:	n/a	n/a
12	CCNT2	chr7:3662206-3662335	K562	blood:	n/a	n/a
13	CEBPB	chr7:3750353-3750572	IMR90	lung:	n/a	chr7:3750408-3750425
14	CEBPB	chr7:3632070-3632192	HepG2	liver:	n/a	n/a
15	CEBPB	chr7:3633614-3633989	K562	blood:	n/a	chr7:3633893-3633904
16	CEBPB	chr7:3603888-3604250	A549	lung:	n/a	chr7:3604071-3604082
17	CEBPB	chr7:3599007-3599412	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr7:3599043-3599360	A549	lung:	n/a	n/a
19	CEBPB	chr7:3603783-3604360	A549	lung:	n/a	chr7:3604071-3604082
20	CEBPB	chr7:3633733-3634004	A549	lung:	n/a	chr7:3633893-3633904
21	CEBPB	chr7:3625582-3625840	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:3689739-3690076	HepG2	liver:	n/a	chr7:3689906-3689917
23	CEBPB	chr7:3631968-3632350	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:3591680-3591787	K562	blood:	n/a	n/a
25	CEBPB	chr7:3689730-3690095	IMR90	lung:	n/a	chr7:3689906-3689917
26	CEBPB	chr7:3603892-3604257	HepG2	liver:	n/a	chr7:3604071-3604082
27	CEBPB	chr7:3774764-3775045	A549	lung:	n/a	chr7:3774879-3774890
28	CEBPB	chr7:3579181-3579258	A549	lung:	n/a	n/a
29	CEBPB	chr7:3722310-3722477	HepG2	liver:	n/a	chr7:3722426-3722437
30	CEBPB	chr7:3735440-3735874	A549	lung:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
31	CEBPB	chr7:3632048-3632246	A549	lung:	n/a	n/a
32	CEBPB	chr7:3603864-3604274	K562	blood:	n/a	chr7:3604071-3604082
33	CEBPB	chr7:3603921-3604218	K562	blood:	n/a	chr7:3604071-3604082
34	CEBPB	chr7:3750088-3750627	MCF-7	breast:	n/a	chr7:3750408-3750425
35	CEBPB	chr7:3603902-3604250	ECC-1	luminal epithelium:	n/a	chr7:3604071-3604082
36	CEBPB	chr7:3735439-3735877	K562	blood:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
37	CEBPB	chr7:3689783-3689977	H1-hESC	embryonic stem cell:	n/a	chr7:3689906-3689917
38	CEBPB	chr7:3603889-3604262	IMR90	lung:	n/a	chr7:3604071-3604082
39	CEBPB	chr7:3669159-3669429	HepG2	liver:	n/a	chr7:3669297-3669308
40	CEBPB	chr7:3735419-3735759	H1-hESC	embryonic stem cell:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716
41	CEBPB	chr7:3689734-3690090	A549	lung:	n/a	chr7:3689906-3689917
42	CEBPB	chr7:3603770-3604392	MCF-7	breast:	n/a	chr7:3604071-3604082
43	CEBPB	chr7:3732825-3733006	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:3666847-3666953	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:3615496-3615771	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:3750311-3750526	K562	blood:	n/a	chr7:3750408-3750425
47	CEBPB	chr7:3722392-3722443	IMR90	lung:	n/a	chr7:3722426-3722437
48	CEBPB	chr7:3632072-3632263	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr7:3603977-3604108	K562	blood:	n/a	chr7:3604071-3604082
50	CEBPB	chr7:3735387-3735863	HepG2	liver:	n/a	chr7:3735704-3735717 chr7:3735591-3735599 chr7:3735705-3735716

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3691268-3691318	HL-60	blood:	n/a
2	chr7:3723660-3723710	AG09319	gingival:	n/a
3	chr7:3632395-3632445	ProgFib	skin:	n/a
4	chr7:3588642-3588692	BE2_C	brain:	n/a
5	chr7:3613164-3613214	SK-N-SH_RA	brain:	n/a
6	chr7:3691268-3691318	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:3632395-3632445	HRE	kidney:	n/a
8	chr7:3727189-3727239	CMK	blood:	n/a
9	chr7:3727166-3727216	ProgFib	skin:	n/a
10	chr7:3613164-3613214	GM12891	blood:	n/a
11	chr7:3723660-3723710	ProgFib	skin:	n/a
12	chr7:3632395-3632445	HNPCEpiC	eye:	n/a
13	chr7:3762272-3762322	HCT-116	colon:	n/a
14	chr7:3713348-3713398	Caco-2	colon:	n/a
15	chr7:3762272-3762322	HRCEpiC	kidney:	n/a
16	chr7:3713348-3713398	LNCaP	prostate:	n/a
17	chr7:3691268-3691318	GM19239	blood:	n/a
18	chr7:3762272-3762322	AG10803	skin:	n/a
19	chr7:3691268-3691318	HRE	kidney:	n/a
20	chr7:3727166-3727216	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:3727189-3727239	NT2-D1	testis:	n/a
22	chr7:3723660-3723710	NB4	blood:	n/a
23	chr7:3713348-3713398	HEK293	kidney:	embryo
24	chr7:3727189-3727239	Jurkat	blood:	n/a
25	chr7:3632395-3632445	HCF	heart:	n/a
26	chr7:3613164-3613214	HAEpiC	amniotic membrane:	n/a
27	chr7:3713348-3713398	AG10803	skin:	n/a
28	chr7:3723660-3723710	IMR90	lung:	fetal
29	chr7:3762272-3762322	GM12878	blood:	n/a
30	chr7:3762272-3762322	SAEC	small airway:	n/a
31	chr7:3723660-3723710	AG04450	lung:	fetal
32	chr7:3691268-3691318	RPTEC	kidney:	n/a
33	chr7:3713348-3713398	BE2_C	brain:	n/a
34	chr7:3632395-3632445	HL-60	blood:	n/a
35	chr7:3723660-3723710	AG10803	skin:	n/a
36	chr7:3588642-3588692	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:3691268-3691318	HUVEC	blood vessel:	n/a
38	chr7:3613164-3613214	U87	brain:	n/a
39	chr7:3632395-3632445	HEEpiC	esophagus:	n/a
40	chr7:3727166-3727216	A549	lung:	n/a
41	chr7:3632395-3632445	HIPEpiC	eye:	n/a
42	chr7:3632395-3632445	HMEC	breast:	n/a
43	chr7:3723660-3723710	HCM	heart:	n/a
44	chr7:3762272-3762322	NT2-D1	testis:	n/a
45	chr7:3713348-3713398	HUVEC	blood vessel:	n/a
46	chr7:3613164-3613214	NHDF-neo	bronchial:	n/a
47	chr7:3727166-3727216	HAEpiC	amniotic membrane:	n/a
48	chr7:3713348-3713398	HepG2	liver:	n/a
49	chr7:3710628-3710678	GM06990	blood:	n/a
50	chr7:3613164-3613214	AoSMC	blood vessel:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3726774..3729602-chr7:3732139..3735055,2	K562	blood:
2	chr7:3608810..3611760-chr7:3613102..3614702,2	MCF-7	breast:
3	chr7:3577804..3580555-chr7:3590884..3593146,2	MCF-7	breast:
4	chr7:3757251..3758935-chr7:3765168..3767703,2	MCF-7	breast:
5	chr7:3650446..3652502-chr7:3655244..3656781,2	MCF-7	breast:
6	chr7:3726774..3729602-chr7:3732139..3735055,2	K562	blood:
7	chr7:3675585..3677733-chr7:3691127..3693566,2	K562	blood:
8	chr7:3727791..3730295-chr7:3732130..3734302,2	MCF-7	breast:
9	chr7:3670051..3672841-chr7:3673465..3675022,2	MCF-7	breast:
10	chr7:3757251..3758935-chr7:3765168..3767703,2	MCF-7	breast:
11	chr7:3650446..3652502-chr7:3655244..3656781,2	MCF-7	breast:
12	chr7:3750817..3752407-chr7:3752998..3754553,2	K562	blood:
13	chr7:3596799..3598779-chr7:3598841..3601044,2	K562	blood:
14	chr7:3596799..3598779-chr7:3598841..3601044,2	K562	blood:
15	chr7:3734945..3735889-chr7:3936899..3937757,3	MCF-7	breast:
16	chr7:3624042..3625672-chr7:3626577..3628999,2	MCF-7	breast:
17	chr7:3624042..3625672-chr7:3626577..3628999,2	MCF-7	breast:
18	chr7:3598045..3599826-chr7:3607481..3609986,2	K562	blood:
19	chr7:3609002..3610756-chr7:3616407..3619133,2	MCF-7	breast:
20	chr7:3577804..3580555-chr7:3590884..3593146,2	MCF-7	breast:
21	chr7:3522949..3523470-chr7:3687761..3688597,2	MCF-7	breast:
22	chr7:3727791..3730295-chr7:3732130..3734302,2	MCF-7	breast:
23	chr7:3727225..3728784-chr7:3739798..3742268,2	K562	blood:
24	chr7:3670051..3672841-chr7:3673465..3675022,2	MCF-7	breast:
25	chr4:37757943..37758649-chr7:3694176..3695010,2	MCF-7	breast:
26	chr7:3598045..3599826-chr7:3607481..3609986,2	K562	blood:
27	chr7:3609002..3610756-chr7:3616407..3619133,2	MCF-7	breast:
28	chr7:3675585..3677733-chr7:3691127..3693566,2	K562	blood:
29	chr7:3521755..3523053-chr7:3688631..3689551,7	MCF-7	breast:
30	chr7:3521696..3522495-chr7:3631928..3632648,2	MCF-7	breast:
31	chr7:3610768..3613073-chr7:3628327..3630622,2	MCF-7	breast:
32	chr7:3581196..3583334-chr7:3583848..3586419,2	K562	blood:
33	chr7:3657416..3659816-chr7:3660917..3663637,2	K562	blood:
34	chr7:3681955..3684927-chr7:3685128..3688064,3	K562	blood:
35	chr7:3750817..3752407-chr7:3752998..3754553,2	K562	blood:
36	chr7:3666241..3668989-chr7:3678664..3681539,2	MCF-7	breast:
37	chr7:3727225..3728784-chr7:3739798..3742268,2	K562	blood:
38	chr7:3657416..3659816-chr7:3660917..3663637,2	K562	blood:
39	chr7:3610768..3613073-chr7:3628327..3630622,2	MCF-7	breast:
40	chr7:3666241..3668989-chr7:3678664..3681539,2	MCF-7	breast:
41	chr7:3581196..3583334-chr7:3583848..3586419,2	K562	blood:
42	chr7:3608810..3611760-chr7:3613102..3614702,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC091801.1.1-7	chr7:3683098-3683416	ENSG00000236510.1
2	lnc-AC091801.1.1-7	chr7:3682447-3682983	ENSG00000236510.1

No data

Variant related genes	Relation type
ENSG00000236510	TF binding region
ENSG00000236510	CpG island
ENSG00000236510	chromatin interactions

Extended variants
information (count: 12433 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:12433 , 50 per page) page: 1 2 3 4 5 6 7 ... 249

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552076619	chr7:3577218-3577219	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs527358223	chr7:3577223-3577224	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs541064168	chr7:3577227-3577228	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs373174208	chr7:3577231-3577232	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs560719569	chr7:3577251-3577252	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs140696961	chr7:3577260-3577261	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs376402186	chr7:3577269-3577270	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs369379276	chr7:3577285-3577286	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs529966175	chr7:3577314-3577315	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs113788824	chr7:3577324-3577325	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs183423069	chr7:3577327-3577328	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs532177003	chr7:3577355-3577356	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs552044481	chr7:3577361-3577362	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs138393590	chr7:3577369-3577370	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs142473635	chr7:3577370-3577371	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs554162332	chr7:3577398-3577399	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs567645997	chr7:3577403-3577404	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536613681	chr7:3577422-3577423	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74623428	chr7:3577451-3577452	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373049241	chr7:3577475-3577476	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576765988	chr7:3577478-3577479	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73036002	chr7:3577488-3577489	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs558878537	chr7:3577502-3577503	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370414103	chr7:3577504-3577505	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572155829	chr7:3577518-3577519	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540747963	chr7:3577526-3577527	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542973143	chr7:3577531-3577532	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560585193	chr7:3577573-3577574	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574112422	chr7:3577588-3577589	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542987153	chr7:3577590-3577591	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138432356	chr7:3577603-3577604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532263909	chr7:3577644-3577645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552393763	chr7:3577654-3577655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559258689	chr7:3577659-3577660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527817018	chr7:3577663-3577664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10238783	chr7:3577665-3577666	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs567732243	chr7:3577673-3577674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187297592	chr7:3577678-3577679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549314783	chr7:3577690-3577691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191976789	chr7:3577694-3577695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373017478	chr7:3577701-3577702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149255304	chr7:3577729-3577730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185347449	chr7:3577760-3577761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187822824	chr7:3577806-3577807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs3946225	chr7:3577830-3577831	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs572532216	chr7:3577849-3577850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561234642	chr7:3577858-3577859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554267776	chr7:3577879-3577880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574153707	chr7:3577881-3577882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543054324	chr7:3577948-3577949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:989 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3567600-3579800	Weak transcription	Spleen	Spleen
2	chr7:3572600-3584600	Weak transcription	Pancreas	Pancrea
3	chr7:3576800-3577600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr7:3576800-3577600	Enhancers	HSMM	muscle
5	chr7:3576800-3577800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:3576800-3578400	Enhancers	Fetal Muscle Trunk	muscle
7	chr7:3577000-3577400	Enhancers	Fetal Brain Male	brain
8	chr7:3577000-3577600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:3577000-3577600	Enhancers	NH-A	brain
10	chr7:3577000-3577800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr7:3577000-3578800	Enhancers	Fetal Muscle Leg	muscle
12	chr7:3577000-3580000	Weak transcription	Fetal Kidney	kidney
13	chr7:3577200-3577400	Enhancers	Muscle Satellite Cultured Cells	--
14	chr7:3577200-3577600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:3577200-3577600	Flanking Active TSS	HSMMtube	muscle
16	chr7:3577200-3578800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:3577400-3577600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
18	chr7:3577400-3578200	Weak transcription	Fetal Brain Male	brain
19	chr7:3577600-3577800	Enhancers	Muscle Satellite Cultured Cells	--
20	chr7:3577600-3600200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr7:3578200-3581600	Enhancers	Fetal Brain Male	brain
22	chr7:3578400-3578600	Enhancers	Fetal Lung	lung
23	chr7:3578600-3578800	Enhancers	Aorta	Aorta
24	chr7:3578800-3580200	Weak transcription	Fetal Lung	lung
25	chr7:3578800-3588600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr7:3578800-3593200	Weak transcription	Aorta	Aorta
27	chr7:3579800-3580400	Enhancers	Spleen	Spleen
28	chr7:3580000-3580200	Enhancers	Fetal Kidney	kidney
29	chr7:3580200-3581000	Enhancers	Fetal Lung	lung
30	chr7:3580200-3581000	Enhancers	HUVEC	blood vessel
31	chr7:3581000-3581200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr7:3581600-3582600	Weak transcription	Fetal Brain Male	brain
33	chr7:3582600-3584600	Enhancers	Fetal Brain Female	brain
34	chr7:3582600-3585400	Enhancers	Fetal Brain Male	brain
35	chr7:3584200-3584600	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr7:3584200-3584600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:3584600-3584800	Enhancers	H1 Cell Line	embryonic stem cell
38	chr7:3584600-3584800	Enhancers	Pancreas	Pancrea
39	chr7:3584600-3587200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr7:3584800-3585200	Weak transcription	Pancreas	Pancrea
41	chr7:3584800-3588600	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr7:3585000-3588400	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr7:3585200-3585400	Enhancers	Pancreas	Pancrea
44	chr7:3585200-3586200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr7:3585400-3590000	Weak transcription	Pancreas	Pancrea
46	chr7:3586200-3586400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr7:3586400-3593400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr7:3587200-3587600	Enhancers	H9 Cell Line	embryonic stem cell
49	chr7:3587200-3588000	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr7:3587200-3588000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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