Variant report

Variant	nsv1030624
Chromosome Location	chr7:100991433-101137314
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2170)
CpG islands
(count:1649)
Chromatin interactive
region (count:74)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2170 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101034275-101034431	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:100995557-100996013	K562	blood:	n/a	n/a
3	ARID3A	chr7:101041212-101041406	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:101029701-101030402	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:100995510-100995986	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:101054542-101054748	HepG2	liver:	n/a	n/a
7	ATF1	chr7:100995667-100996035	K562	blood:	n/a	n/a
8	ATF2	chr7:101045113-101045819	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:101054507-101054909	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:101045260-101045884	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:101034206-101034498	GM12878	blood:	n/a	n/a
12	ATF2	chr7:101034154-101034562	GM12878	blood:	n/a	n/a
13	ATF2	chr7:101007153-101007579	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr7:101005691-101006042	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr7:101083791-101083930	K562	blood:	n/a	n/a
16	ATF3	chr7:100995608-100996147	K562	blood:	n/a	n/a
17	BACH1	chr7:101080560-101080609	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:101054392-101054843	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:101006969-101007517	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:101006064-101006399	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:101045151-101045712	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:101042008-101042270	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:101083766-101083964	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL11A	chr7:101034127-101034558	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:101045447-101045692	H1-hESC	embryonic stem cell:	n/a	chr7:101045565-101045572 chr7:101045573-101045582
26	BCL3	chr7:101071831-101072136	GM12878	blood:	n/a	n/a
27	BCL3	chr7:101085919-101086314	GM12878	blood:	n/a	n/a
28	BCL3	chr7:101045252-101045835	A549	lung:	n/a	chr7:101045565-101045572 chr7:101045573-101045582 chr7:101045420-101045433
29	BCL3	chr7:101085899-101086361	GM12878	blood:	n/a	n/a
30	BCL3	chr7:101071768-101072139	GM12878	blood:	n/a	n/a
31	BCL3	chr7:101045065-101045790	A549	lung:	n/a	chr7:101045565-101045572 chr7:101045573-101045582 chr7:101045420-101045433
32	BCL3	chr7:100995430-100996053	A549	lung:	n/a	chr7:100995867-100995874
33	BCL3	chr7:101034235-101034520	GM12878	blood:	n/a	n/a
34	BCL3	chr7:100995424-100996093	A549	lung:	n/a	chr7:100995867-100995874
35	BCL3	chr7:101006990-101007617	A549	lung:	n/a	chr7:101007240-101007249 chr7:101007424-101007437
36	BHLHE40	chr7:101083725-101083894	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:100995649-100996149	K562	blood:	n/a	n/a
38	BHLHE40	chr7:101006937-101007505	HepG2	liver:	n/a	n/a
39	BHLHE40	chr7:101034158-101034493	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:101054571-101054732	K562	blood:	n/a	n/a
41	BHLHE40	chr7:101007069-101007443	K562	blood:	n/a	n/a
42	BHLHE40	chr7:101007335-101007606	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:101085990-101086330	K562	blood:	n/a	n/a
44	BHLHE40	chr7:100995806-100995888	HepG2	liver:	n/a	n/a
45	BRCA1	chr7:101034269-101034281	HepG2	liver:	n/a	n/a
46	BRCA1	chr7:101030201-101030430	HepG2	liver:	n/a	n/a
47	BRCA1	chr7:100996299-100996395	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr7:101034222-101034342	GM12878	blood:	n/a	n/a
49	CBX3	chr7:101053258-101053574	K562	blood:	n/a	n/a
50	CBX3	chr7:101053212-101053473	K562	blood:	n/a	n/a

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101055912-101055962	HMEC	breast:	n/a
2	chr7:101063331-101063381	PrEC	prostate:	n/a
3	chr7:101055912-101055962	HMEC	breast:	n/a
4	chr7:101063331-101063381	PrEC	prostate:	n/a
5	chr7:101007603-101007653	HRCEpiC	kidney:	n/a
6	chr7:101017354-101017404	HRE	kidney:	n/a
7	chr7:101006089-101006139	AG10803	skin:	n/a
8	chr7:101007603-101007653	NT2-D1	testis:	n/a
9	chr7:101079617-101079667	HNPCEpiC	eye:	n/a
10	chr7:101006573-101006623	AG09319	gingival:	n/a
11	chr7:101006035-101006085	HCPEpiC	choroid plexus:	n/a
12	chr7:101017354-101017404	CMK	blood:	n/a
13	chr7:101006019-101006069	HCM	heart:	n/a
14	chr7:101017354-101017404	LNCaP	prostate:	n/a
15	chr7:101006019-101006069	AG09319	gingival:	n/a
16	chr7:101006363-101006413	HNPCEpiC	eye:	n/a
17	chr7:101055912-101055962	RPTEC	kidney:	n/a
18	chr7:101079617-101079667	BJ	skin:	n/a
19	chr7:101063331-101063381	AG10803	skin:	n/a
20	chr7:100993034-100993084	LNCaP	prostate:	n/a
21	chr7:101006573-101006623	PANC-1	pancreas:	n/a
22	chr7:101006035-101006085	HEEpiC	esophagus:	n/a
23	chr7:101049300-101049350	U87	brain:	n/a
24	chr7:101006052-101006102	GM12891	blood:	n/a
25	chr7:101006035-101006085	MCF-7	breast:	n/a
26	chr7:101063331-101063381	U87	brain:	n/a
27	chr7:101049372-101049422	NHDF-neo	bronchial:	n/a
28	chr7:101007072-101007122	MCF-7	breast:	n/a
29	chr7:101007190-101007240	LNCaP	prostate:	n/a
30	chr7:101007603-101007653	HAEpiC	amniotic membrane:	n/a
31	chr7:101079617-101079667	SKMC	muscle:	n/a
32	chr7:101055912-101055962	AG09309	skin:	n/a
33	chr7:101007190-101007240	Caco-2	colon:	n/a
34	chr7:101049372-101049422	AoSMC	blood vessel:	n/a
35	chr7:101007190-101007240	HCT-116	colon:	n/a
36	chr7:101007603-101007653	GM06990	blood:	n/a
37	chr7:101055912-101055962	LNCaP	prostate:	n/a
38	chr7:101005846-101005896	HepG2	liver:	n/a
39	chr7:101006063-101006113	H1-hESC	embryonic stem cell:	embryo
40	chr7:101055912-101055962	BJ	skin:	n/a
41	chr7:100993034-100993084	SK-N-MC	brain:	n/a
42	chr7:101079617-101079667	SK-N-SH	brain:	n/a
43	chr7:101006963-101007013	RPTEC	kidney:	n/a
44	chr7:101005846-101005896	BE2_C	brain:	n/a
45	chr7:101054654-101054704	MCF-7	breast:	n/a
46	chr7:100993034-100993084	AG09309	skin:	n/a
47	chr7:101054654-101054704	HCF	heart:	n/a
48	chr7:101006052-101006102	HNPCEpiC	eye:	n/a
49	chr7:101006308-101006358	ECC-1	luminal epithelium:	n/a
50	chr7:101006052-101006102	H1-hESC	embryonic stem cell:	embryo

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:101006441..101008974-chr7:101023704..101025266,2	MCF-7	breast:
2	chr7:101112161..101112969-chr7:101150803..101151689,2	MCF-7	breast:
3	chr7:101083863..101087245-chr7:101089520..101092470,3	K562	blood:
4	chr7:101083863..101087245-chr7:101089520..101092470,3	K562	blood:
5	chr7:101006746..101007872-chr7:101054217..101055171,4	K562	blood:
6	chr7:101006530..101007875-chr7:101054200..101055148,9	MCF-7	breast:
7	chr7:101006838..101009123-chr7:101009732..101012047,2	K562	blood:
8	chr7:101006862..101007822-chr7:101083395..101084349,8	MCF-7	breast:
9	chr7:101016391..101018815-chr7:101033017..101035506,2	K562	blood:
10	chr7:101005587..101007184-chr7:101013675..101015580,2	MCF-7	breast:
11	chr7:101083724..101084446-chr7:101150709..101151315,2	MCF-7	breast:
12	chr7:101100597..101102046-chr7:101150673..101151702,7	MCF-7	breast:
13	chr7:101115888..101118705-chr7:101119430..101120969,2	MCF-7	breast:
14	chr7:101032377..101034733-chr7:101037402..101040388,2	MCF-7	breast:
15	chr7:101032377..101034733-chr7:101037402..101040388,2	MCF-7	breast:
16	chr7:101016391..101018815-chr7:101033017..101035506,2	K562	blood:
17	chr7:101012360..101015108-chr7:101017249..101019175,2	K562	blood:
18	chr7:101012941..101015108-chr7:101017148..101018749,2	K562	blood:
19	chr7:101054544..101055233-chr7:101150595..101151343,2	K562	blood:
20	chr7:101054216..101055052-chr7:101150685..101151359,3	MCF-7	breast:
21	chr7:101015968..101018340-chr7:101024306..101026455,2	MCF-7	breast:
22	chr7:101006510..101007838-chr7:101150604..101151700,15	MCF-7	breast:
23	chr7:101023195..101025977-chr7:101028738..101030293,2	K562	blood:
24	chr7:100964942..100967208-chr7:101081876..101083958,2	MCF-7	breast:
25	chr7:101006908..101008057-chr7:101150804..101151679,7	MCF-7	breast:
26	chr7:101006838..101009123-chr7:101009732..101012047,2	K562	blood:
27	chr7:100949900..100952097-chr7:100994165..100995851,2	MCF-7	breast:
28	chr7:100989055..100991707-chr7:100994198..100995736,2	MCF-7	breast:
29	chr7:101006939..101007476-chr7:101083770..101084337,2	K562	blood:
30	chr7:101115888..101118705-chr7:101119430..101120969,2	MCF-7	breast:
31	chr7:101068095..101068916-chr7:101150848..101151469,2	MCF-7	breast:
32	chr7:101037193..101039012-chr7:101045881..101047459,2	MCF-7	breast:
33	chr7:101012941..101015108-chr7:101017148..101018749,2	K562	blood:
34	chr7:101084569..101086934-chr7:101141583..101143364,2	MCF-7	breast:
35	chr7:101041365..101043542-chr7:101048323..101050814,2	MCF-7	breast:
36	chr7:101006811..101007905-chr7:101150693..101151800,11	K562	blood:
37	chr7:101131107..101133497-chr7:101133742..101135419,2	K562	blood:
38	chr7:101006966..101007850-chr7:101054283..101055103,3	MCF-7	breast:
39	chr7:100964710..100967141-chr7:101003077..101007417,4	MCF-7	breast:
40	chr7:101031371..101033701-chr7:101034998..101036873,2	K562	blood:
41	chr7:101131107..101133497-chr7:101133742..101135419,2	K562	blood:
42	chr7:101043147..101045492-chr7:101051053..101052921,2	K562	blood:
43	chr7:101007762..101011060-chr7:101013667..101017793,3	K562	blood:
44	chr7:100963124..100966014-chr7:101122778..101124584,2	MCF-7	breast:
45	chr7:101006746..101007872-chr7:101054217..101055171,4	K562	blood:
46	chr7:101022613..101024114-chr7:101025793..101027679,2	MCF-7	breast:
47	chr7:101006995..101008302-chr7:101082934..101084354,6	MCF-7	breast:
48	chr7:101023195..101026718-chr7:101028403..101030293,3	K562	blood:
49	chr7:101117670..101118572-chr7:101150768..101151530,2	MCF-7	breast:
50	chr7:101043147..101045492-chr7:101051053..101052921,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RABL5-2	chr7:101032149-101032361	NONHSAT122467
2	lnc-RABL5-1	chr7:100995310-100996633	ucscGeneNc_uc003uyp_2
3	lnc-RABL5-1	chr7:100998850-100999006	ucscGeneNc_uc003uyp_2

No data

Variant related genes	Relation type
ENSG00000233683	TF binding region
COL26A1	TF binding region
ENSG00000233683	CpG island
COL26A1	CpG island
ENSG00000128581	chromatin interactions
ENSG00000160963	chromatin interactions
ENSG00000255992	chromatin interactions
ENSG00000232445	chromatin interactions
ENSG00000233683	chromatin interactions
ENSG00000177192	chromatin interactions

Extended variants
information (count: 6541 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6541 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572566303	chr7:100991462-100991463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574626115	chr7:100991485-100991486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73182913	chr7:100991491-100991492	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs563477683	chr7:100991576-100991577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12534704	chr7:100991596-100991597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112707635	chr7:100991642-100991643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs62465594	chr7:100991649-100991650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544221852	chr7:100991664-100991665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs36034015	chr7:100991676-100991677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs398005609	chr7:100991680-100991681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183289806	chr7:100991681-100991682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532382448	chr7:100991688-100991689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547808039	chr7:100991705-100991706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140349019	chr7:100991754-100991755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536348521	chr7:100991778-100991779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368568013	chr7:100991863-100991864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569930455	chr7:100991867-100991868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537280309	chr7:100991885-100991886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111481275	chr7:100991886-100991887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186864811	chr7:100991889-100991890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534315105	chr7:100991924-100991925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201348598	chr7:100991981-100991982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189984433	chr7:100992000-100992001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113651609	chr7:100992031-100992032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541970484	chr7:100992032-100992033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561386893	chr7:100992051-100992052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557160960	chr7:100992062-100992063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575498240	chr7:100992085-100992086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546010002	chr7:100992093-100992094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564213736	chr7:100992096-100992097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111571998	chr7:100992162-100992163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182192536	chr7:100992176-100992177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188166623	chr7:100992179-100992180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567949606	chr7:100992189-100992190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530098771	chr7:100992200-100992201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs58124971	chr7:100992205-100992206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192897318	chr7:100992219-100992220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369808873	chr7:100992245-100992246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569842233	chr7:100992250-100992251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185202866	chr7:100992253-100992254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552777837	chr7:100992342-100992343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571017226	chr7:100992361-100992362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs199640292	chr7:100992368-100992369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552667714	chr7:100992402-100992403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372867915	chr7:100992421-100992422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535479053	chr7:100992454-100992455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188471368	chr7:100992456-100992457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575460224	chr7:100992521-100992522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545636865	chr7:100992551-100992552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150587837	chr7:100992590-100992591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1934 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100991000-101006000	Weak transcription	Right Atrium	heart
2	chr7:100991400-100992800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:100991400-100993000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:100992800-100993000	Enhancers	Stomach Mucosa	stomach
5	chr7:100992800-100993200	Enhancers	K562	blood
6	chr7:100992800-100993400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:100992800-100993400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
8	chr7:100993000-100993200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:100993000-100994000	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr7:100993200-100993400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr7:100993200-100993400	Enhancers	HepG2	liver
12	chr7:100993200-100993400	Flanking Active TSS	K562	blood
13	chr7:100993400-100994800	Weak transcription	K562	blood
14	chr7:100993400-100995000	Weak transcription	HepG2	liver
15	chr7:100993400-100995600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr7:100993400-101005400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:100994000-100995600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr7:100994600-100995200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr7:100994800-100995400	Enhancers	A549	lung
20	chr7:100994800-100996000	Enhancers	Stomach Mucosa	stomach
21	chr7:100994800-100996400	Enhancers	K562	blood
22	chr7:100995000-100995200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr7:100995000-100995400	Enhancers	Hela-S3	cervix
24	chr7:100995000-100996400	Enhancers	Liver	Liver
25	chr7:100995000-100996400	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr7:100995000-100996600	Enhancers	HepG2	liver
27	chr7:100995200-101005600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr7:100995400-100995800	Enhancers	Fetal Intestine Large	intestine
29	chr7:100995400-100995800	Enhancers	Fetal Muscle Leg	muscle
30	chr7:100995400-100996000	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr7:100995400-100996000	Enhancers	Fetal Intestine Small	intestine
32	chr7:100995400-100996000	Flanking Active TSS	A549	lung
33	chr7:100995400-100996200	Flanking Active TSS	Hela-S3	cervix
34	chr7:100995600-100995800	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr7:100995600-100995800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr7:100995600-100996000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr7:100995600-100996000	Enhancers	Duodenum Mucosa	Duodenum
38	chr7:100995600-100996200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr7:100995800-100996000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr7:100996000-100996400	Enhancers	A549	lung
41	chr7:100996200-100996600	Enhancers	Hela-S3	cervix
42	chr7:100996400-101000200	Weak transcription	Liver	Liver
43	chr7:100996400-101000600	Weak transcription	A549	lung
44	chr7:100996600-101004000	Weak transcription	HepG2	liver
45	chr7:100996600-101007000	Weak transcription	Hela-S3	cervix
46	chr7:100997400-100998000	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr7:101000200-101001200	Enhancers	Liver	Liver
48	chr7:101000600-101001200	Enhancers	A549	lung
49	chr7:101000800-101001000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr7:101001200-101005600	Weak transcription	Liver	Liver

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