Variant report

Variant	nsv1015163
Chromosome Location	chr7:47734913-47832389
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2119)
CpG islands
(count:915)
Chromatin interactive
region (count:46)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2119 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:47773729-47774859	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:47827490-47827716	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:47820195-47820538	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:47817560-47818252	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:47755265-47755779	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:47802606-47803648	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:47822887-47823953	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:47828539-47828706	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:47825875-47826884	HepG2	liver:	n/a	n/a
10	ATF2	chr7:47764166-47764569	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:47764122-47764606	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:47754580-47755209	GM12878	blood:	n/a	n/a
13	ATF3	chr7:47823230-47824019	A549	lung:	n/a	n/a
14	ATF3	chr7:47802645-47803677	A549	lung:	n/a	n/a
15	ATF3	chr7:47825903-47826813	A549	lung:	n/a	chr7:47826184-47826197
16	ATF3	chr7:47825771-47826990	A549	lung:	n/a	chr7:47826184-47826197
17	ATF3	chr7:47823447-47824013	A549	lung:	n/a	n/a
18	ATF3	chr7:47802727-47803697	A549	lung:	n/a	n/a
19	BACH1	chr7:47826206-47826462	H1-hESC	embryonic stem cell:	n/a	chr7:47826333-47826347
20	BACH1	chr7:47783843-47784043	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr7:47754825-47755145	GM12878	blood:	n/a	n/a
22	BCL3	chr7:47764881-47765484	A549	lung:	n/a	chr7:47765211-47765220 chr7:47765212-47765221
23	BCL3	chr7:47817618-47818325	A549	lung:	n/a	n/a
24	BCL3	chr7:47802544-47803831	A549	lung:	n/a	chr7:47802944-47802953
25	BCL3	chr7:47823087-47824066	A549	lung:	n/a	n/a
26	BCL3	chr7:47825499-47827050	A549	lung:	n/a	n/a
27	BCL3	chr7:47823464-47823996	A549	lung:	n/a	n/a
28	BCL3	chr7:47764888-47765489	A549	lung:	n/a	chr7:47765211-47765220 chr7:47765212-47765221
29	BCL3	chr7:47802221-47803718	A549	lung:	n/a	chr7:47802944-47802953
30	BCL3	chr7:47825718-47827088	A549	lung:	n/a	n/a
31	BHLHE40	chr7:47760347-47760635	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:47817802-47818157	HepG2	liver:	n/a	n/a
33	BHLHE40	chr7:47773549-47773641	K562	blood:	n/a	n/a
34	BHLHE40	chr7:47826029-47826776	HepG2	liver:	n/a	chr7:47826407-47826423 chr7:47826413-47826429
35	BHLHE40	chr7:47773801-47774315	HepG2	liver:	n/a	chr7:47774079-47774088 chr7:47774079-47774088 chr7:47774077-47774090 chr7:47774073-47774094 chr7:47774078-47774087
36	BHLHE40	chr7:47802685-47803591	HepG2	liver:	n/a	n/a
37	BHLHE40	chr7:47773969-47774225	K562	blood:	n/a	chr7:47774079-47774088 chr7:47774079-47774088 chr7:47774077-47774090 chr7:47774073-47774094 chr7:47774078-47774087
38	BHLHE40	chr7:47755427-47755706	HepG2	liver:	n/a	n/a
39	BHLHE40	chr7:47778249-47778478	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:47773453-47774513	HepG2	liver:	n/a	chr7:47774079-47774088 chr7:47774079-47774088 chr7:47774077-47774090 chr7:47774073-47774094 chr7:47774078-47774087
41	BRCA1	chr7:47826023-47827179	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr7:47823373-47823966	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr7:47824988-47825276	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr7:47802926-47803566	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr7:47823382-47824041	HCT-116	colon:	n/a	n/a
46	CBX3	chr7:47825903-47826807	HCT-116	colon:	n/a	n/a
47	CEBPB	chr7:47764259-47764590	IMR90	lung:	n/a	n/a
48	CEBPB	chr7:47774542-47774667	IMR90	lung:	n/a	n/a
49	CEBPB	chr7:47778474-47778813	HepG2	liver:	n/a	chr7:47778624-47778635
50	CEBPB	chr7:47825965-47826589	MCF-7	breast:	n/a	chr7:47826220-47826229 chr7:47826218-47826231 chr7:47826220-47826229 chr7:47826220-47826229

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:47797675-47797725	GM06990	blood:	n/a
2	chr7:47749519-47749569	RPTEC	kidney:	n/a
3	chr7:47783848-47783898	U87	brain:	n/a
4	chr7:47783668-47783718	AoSMC	blood vessel:	n/a
5	chr7:47764246-47764296	HMEC	breast:	n/a
6	chr7:47783848-47783898	HRE	kidney:	n/a
7	chr7:47783949-47783999	HIPEpiC	eye:	n/a
8	chr7:47826387-47826437	SK-N-SH_RA	brain:	n/a
9	chr7:47764246-47764296	SAEC	small airway:	n/a
10	chr7:47783949-47783999	NH-A	brain:	n/a
11	chr7:47797675-47797725	HCF	heart:	n/a
12	chr7:47749519-47749569	BJ	skin:	n/a
13	chr7:47811084-47811134	ovcar-3	ovarian:	n/a
14	chr7:47783644-47783694	HL-60	blood:	n/a
15	chr7:47783644-47783694	SK-N-MC	brain:	n/a
16	chr7:47783603-47783653	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:47749519-47749569	HCT-116	colon:	n/a
18	chr7:47814633-47814683	HL-60	blood:	n/a
19	chr7:47783644-47783694	HRE	kidney:	n/a
20	chr7:47784660-47784710	BE2_C	brain:	n/a
21	chr7:47814633-47814683	HCF	heart:	n/a
22	chr7:47783949-47783999	Hepatocyte	liver:	n/a
23	chr7:47778880-47778930	GM12892	blood:	n/a
24	chr7:47778880-47778930	HMEC	breast:	n/a
25	chr7:47797675-47797725	Hepatocyte	liver:	n/a
26	chr7:47784660-47784710	CMK	blood:	n/a
27	chr7:47783668-47783718	GM06990	blood:	n/a
28	chr7:47826387-47826437	AG09309	skin:	n/a
29	chr7:47783644-47783694	NB4	blood:	n/a
30	chr7:47814633-47814683	HIPEpiC	eye:	n/a
31	chr7:47814633-47814683	HCPEpiC	choroid plexus:	n/a
32	chr7:47783668-47783718	HEEpiC	esophagus:	n/a
33	chr7:47783603-47783653	HL-60	blood:	n/a
34	chr7:47783603-47783653	Caco-2	colon:	n/a
35	chr7:47784660-47784710	AG10803	skin:	n/a
36	chr7:47783949-47783999	HL-60	blood:	n/a
37	chr7:47783668-47783718	SK-N-SH	brain:	n/a
38	chr7:47797675-47797725	Jurkat	blood:	n/a
39	chr7:47780844-47780894	HCPEpiC	choroid plexus:	n/a
40	chr7:47797675-47797725	AoSMC	blood vessel:	n/a
41	chr7:47826387-47826437	HNPCEpiC	eye:	n/a
42	chr7:47778880-47778930	AG04449	skin:	fetal
43	chr7:47783668-47783718	HCT-116	colon:	n/a
44	chr7:47814633-47814683	SAEC	small airway:	n/a
45	chr7:47780844-47780894	MCF10A-Er-Src	breast:	n/a
46	chr7:47811084-47811134	PFSK-1	brain:	n/a
47	chr7:47784660-47784710	Hela-S3	cervix:	n/a
48	chr7:47749519-47749569	AG10803	skin:	n/a
49	chr7:47826387-47826437	MCF10A-Er-Src	breast:	n/a
50	chr7:47811084-47811134	MCF10A-Er-Src	breast:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:47802480..47806239-chr7:47808296..47811941,4	MCF-7	breast:
2	chr7:47620351..47622930-chr7:47803514..47805956,2	MCF-7	breast:
3	chr7:47615873..47619377-chr7:47823257..47826592,4	MCF-7	breast:
4	chr7:47732465..47733984-chr7:47739980..47741778,2	MCF-7	breast:
5	chr7:47672004..47676377-chr7:47825197..47828520,6	MCF-7	breast:
6	chr7:47581328..47582282-chr7:47783520..47784378,2	MCF-7	breast:
7	chr7:47478891..47481808-chr7:47825195..47826977,2	MCF-7	breast:
8	chr7:47640494..47642144-chr7:47748546..47750324,2	MCF-7	breast:
9	chr7:47810003..47811923-chr7:47819425..47821850,2	MCF-7	breast:
10	chr7:47513598..47515664-chr7:47748978..47751641,2	MCF-7	breast:
11	chr7:47674844..47676482-chr7:47831154..47832832,2	MCF-7	breast:
12	chr7:47773818..47776003-chr7:47781051..47783557,2	MCF-7	breast:
13	chr7:47731657..47733270-chr7:47740448..47743349,2	MCF-7	breast:
14	chr7:47811123..47812959-chr7:47824881..47826552,2	MCF-7	breast:
15	chr7:47788868..47790580-chr7:47796478..47799163,2	MCF-7	breast:
16	chr7:47817549..47819162-chr7:47820902..47823876,2	MCF-7	breast:
17	chr7:47730789..47733579-chr7:47824840..47827791,2	MCF-7	breast:
18	chr7:47673413..47676550-chr7:47822059..47827530,9	MCF-7	breast:
19	chr7:47817549..47819162-chr7:47820902..47823876,2	MCF-7	breast:
20	chr7:47760936..47761875-chr7:47847263..47848045,2	MCF-7	breast:
21	chr7:47811123..47812959-chr7:47824881..47826552,2	MCF-7	breast:
22	chr7:47814103..47816415-chr7:47816480..47819252,2	K562	blood:
23	chr7:47758562..47761407-chr7:47764047..47766786,2	MCF-7	breast:
24	chr7:47620160..47622417-chr7:47828049..47831688,3	MCF-7	breast:
25	chr7:47758562..47761407-chr7:47764047..47766786,2	MCF-7	breast:
26	chr7:47733692..47735989-chr7:47787740..47790017,2	MCF-7	breast:
27	chr7:47673447..47675801-chr7:47812685..47814844,2	MCF-7	breast:
28	chr7:47619271..47621011-chr7:47774897..47776657,2	MCF-7	breast:
29	chr7:47814103..47816415-chr7:47816480..47819252,2	K562	blood:
30	chr7:47802975..47804848-chr7:47806029..47808822,2	MCF-7	breast:
31	chr7:47802975..47804848-chr7:47806029..47808822,2	MCF-7	breast:
32	chr7:47789337..47791664-chr7:47815360..47817822,2	MCF-7	breast:
33	chr7:47789337..47791664-chr7:47815360..47817822,2	MCF-7	breast:
34	chr7:47624955..47626619-chr7:47816230..47818018,2	MCF-7	breast:
35	chr7:47672522..47676333-chr7:47822222..47824169,3	MCF-7	breast:
36	chr7:47788868..47790580-chr7:47796478..47799163,2	MCF-7	breast:
37	chr7:47832164..47833007-chr7:47847350..47848005,2	MCF-7	breast:
38	chr7:47773818..47776003-chr7:47781051..47783557,2	MCF-7	breast:
39	chr7:47646097..47647972-chr7:47737601..47739251,2	MCF-7	breast:
40	chr7:47751987..47752487-chr8:103822998..103823507,2	K562	blood:
41	chr7:47620215..47623501-chr7:47821573..47827272,7	MCF-7	breast:
42	chr7:47810003..47811923-chr7:47819425..47821850,2	MCF-7	breast:
43	chr7:47619426..47621699-chr7:47736196..47738585,2	MCF-7	breast:
44	chr7:47731019..47733171-chr7:47747681..47749285,2	MCF-7	breast:
45	chr7:47615532..47617126-chr7:47757928..47759519,2	MCF-7	breast:
46	chr7:47733692..47735989-chr7:47787740..47790017,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf69-3	chr7:47769496-47769701	ucscGeneNc_uc003tnx_2
2	lnc-C7orf69-1	chr7:47802947-47803176	ENSG00000146666.4
3	lnc-C7orf69-1	chr7:47805427-47806369	ENSG00000146666.4
4	lnc-C7orf69-1	chr7:47802971-47803176	ENSG00000146666.4
5	lnc-C7orf69-1	chr7:47805427-47806370	ENSG00000146666.4
6	lnc-C7orf69-3	chr7:47767599-47767636	ucscGeneNc_uc003tnx_2
7	lnc-C7orf69-3	chr7:47771952-47772894	ucscGeneNc_uc003tnx_2
8	lnc-C7orf69-1	chr7:47801074-47801111	ENSG00000146666.4

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PKD1L1	hsa-miR-1	chr7:47814336-47814357

Variant related genes	Relation type
LINC00525	TF binding region
C7orf69	TF binding region
LINC00525	CpG island
C7orf69	CpG island
ENSG00000136205	chromatin interactions
ENSG00000146666	chromatin interactions

Extended variants
information (count: 4343 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:4343 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186697880	chr7:47734977-47734978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73107256	chr7:47735041-47735042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs191178747	chr7:47735057-47735058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569993932	chr7:47735060-47735061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183827929	chr7:47735076-47735077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200456807	chr7:47735104-47735105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149240879	chr7:47735112-47735113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146670754	chr7:47735113-47735114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146769132	chr7:47735115-47735116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200424284	chr7:47735125-47735126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530688092	chr7:47735127-47735128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201603328	chr7:47735129-47735130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530828192	chr7:47735134-47735135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564283803	chr7:47735153-47735154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372559376	chr7:47735198-47735199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs13437880	chr7:47735207-47735208	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs549625960	chr7:47735307-47735308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147064117	chr7:47735308-47735309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183286393	chr7:47735323-47735324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560547919	chr7:47735413-47735414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529547837	chr7:47735447-47735448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571394974	chr7:47735454-47735455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34199067	chr7:47735476-47735477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141905938	chr7:47735482-47735483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143819686	chr7:47735491-47735492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538436037	chr7:47735514-47735515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553969414	chr7:47735532-47735533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12702365	chr7:47735537-47735538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540372269	chr7:47735542-47735543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570397110	chr7:47735547-47735548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148156307	chr7:47735554-47735555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552825417	chr7:47735577-47735578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572568333	chr7:47735587-47735588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535287419	chr7:47735591-47735592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373239979	chr7:47735595-47735596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371590657	chr7:47735636-47735637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141848813	chr7:47735676-47735677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376469884	chr7:47735709-47735710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544221513	chr7:47735713-47735714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564404010	chr7:47735747-47735748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113942340	chr7:47735766-47735767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540607503	chr7:47735782-47735783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560586409	chr7:47735808-47735809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529381097	chr7:47735819-47735820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549604957	chr7:47735820-47735821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201777355	chr7:47735822-47735823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75139002	chr7:47735835-47735836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563113249	chr7:47735884-47735885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531927148	chr7:47735924-47735925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567843270	chr7:47735949-47735950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	17237825	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Abnormal phenotypes	18644119	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD

Chromatin state (count:1151 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:47731200-47741600	Weak transcription	Right Atrium	heart
2	chr7:47732800-47737800	Weak transcription	HSMMtube	muscle
3	chr7:47732800-47739000	Weak transcription	Pancreas	Pancrea
4	chr7:47733000-47737600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:47733000-47750000	Weak transcription	Aorta	Aorta
6	chr7:47733200-47741400	Weak transcription	A549	lung
7	chr7:47734000-47748600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr7:47734200-47739000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:47734600-47739400	Weak transcription	Fetal Kidney	kidney
10	chr7:47734600-47748200	Weak transcription	Fetal Stomach	stomach
11	chr7:47737200-47738200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr7:47737400-47737800	Enhancers	Fetal Heart	heart
13	chr7:47737400-47738400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:47737600-47738200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:47737600-47738200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr7:47737600-47738200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr7:47737600-47738200	Enhancers	HMEC	breast
18	chr7:47737800-47738200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:47737800-47738400	Enhancers	HSMMtube	muscle
20	chr7:47738000-47738200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr7:47738400-47741600	Weak transcription	HSMMtube	muscle
22	chr7:47739000-47739200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:47739000-47739600	Genic enhancers	Pancreas	Pancrea
24	chr7:47739200-47739400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:47739400-47740000	ZNF genes & repeats	Fetal Kidney	kidney
26	chr7:47739600-47740000	Enhancers	Pancreas	Pancrea
27	chr7:47740000-47744800	Weak transcription	Fetal Kidney	kidney
28	chr7:47740000-47744800	Weak transcription	Pancreas	Pancrea
29	chr7:47741400-47742000	Enhancers	A549	lung
30	chr7:47741600-47742000	Enhancers	HepG2	liver
31	chr7:47741600-47742800	Enhancers	HSMMtube	muscle
32	chr7:47742000-47748600	Weak transcription	A549	lung
33	chr7:47744800-47745400	Enhancers	Fetal Kidney	kidney
34	chr7:47745400-47748600	Weak transcription	Fetal Kidney	kidney
35	chr7:47747200-47747400	Enhancers	Fetal Intestine Small	intestine
36	chr7:47747200-47749200	Enhancers	Primary B cells from peripheral blood	blood
37	chr7:47747400-47755200	Weak transcription	Fetal Intestine Small	intestine
38	chr7:47748200-47750400	Enhancers	Fetal Stomach	stomach
39	chr7:47748400-47749000	Enhancers	GM12878-XiMat	blood
40	chr7:47748400-47750800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr7:47748600-47748800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:47748600-47749000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr7:47748600-47749000	Enhancers	Fetal Kidney	kidney
44	chr7:47748600-47749200	Enhancers	Spleen	Spleen
45	chr7:47748600-47749400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr7:47748600-47750400	Enhancers	Stomach Smooth Muscle	stomach
47	chr7:47748600-47750400	Enhancers	A549	lung
48	chr7:47748600-47750600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:47748800-47755000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:47749000-47749200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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