Variant report

Variant	nsv516137
Chromosome Location	chr1:94404238-94504545
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1323)
CpG islands
(count:550)
Chromatin interactive
region (count:68)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1323 , 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	chr1:94493716-94494030	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:94445268-94445807	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:94429256-94429440	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:94426183-94426458	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:94412693-94412890	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:94430303-94430558	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:94499450-94499799	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:94446053-94446344	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:94470598-94470614	K562	blood:	n/a	n/a
10	ATF1	chr1:94434003-94434014	K562	blood:	n/a	n/a
11	ATF1	chr1:94465335-94466291	K562	blood:	n/a	n/a
12	ATF1	chr1:94443039-94443057	K562	blood:	n/a	n/a
13	ATF1	chr1:94484900-94485186	K562	blood:	n/a	n/a
14	ATF1	chr1:94441840-94442276	K562	blood:	n/a	n/a
15	ATF1	chr1:94480375-94480974	K562	blood:	n/a	n/a
16	ATF2	chr1:94502216-94502800	GM12878	blood:	n/a	n/a
17	ATF2	chr1:94502907-94503870	GM12878	blood:	n/a	n/a
18	ATF2	chr1:94503219-94503842	GM12878	blood:	n/a	n/a
19	ATF2	chr1:94430116-94430553	GM12878	blood:	n/a	n/a
20	ATF3	chr1:94430283-94430511	HepG2	liver:	n/a	n/a
21	ATF3	chr1:94430166-94430636	A549	lung:	n/a	n/a
22	ATF3	chr1:94480451-94481047	K562	blood:	n/a	chr1:94480831-94480844
23	BACH1	chr1:94478399-94478418	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr1:94470748-94470768	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr1:94430230-94430552	GM12878	blood:	n/a	n/a
26	BATF	chr1:94503172-94503714	GM12878	blood:	n/a	n/a
27	BCL3	chr1:94503004-94503788	GM12878	blood:	n/a	chr1:94503155-94503164
28	BHLHE40	chr1:94489728-94490046	K562	blood:	n/a	n/a
29	BHLHE40	chr1:94503381-94503667	GM12878	blood:	n/a	n/a
30	BHLHE40	chr1:94480403-94481020	K562	blood:	n/a	n/a
31	BHLHE40	chr1:94478253-94478593	HepG2	liver:	n/a	chr1:94478467-94478483
32	BHLHE40	chr1:94441966-94442079	K562	blood:	n/a	n/a
33	BHLHE40	chr1:94477679-94477822	K562	blood:	n/a	n/a
34	BHLHE40	chr1:94491636-94491739	HepG2	liver:	n/a	n/a
35	BHLHE40	chr1:94445446-94445622	K562	blood:	n/a	n/a
36	BHLHE40	chr1:94477578-94477941	HepG2	liver:	n/a	n/a
37	BHLHE40	chr1:94496749-94497115	HepG2	liver:	n/a	chr1:94496946-94496955 chr1:94496939-94496960 chr1:94496945-94496954 chr1:94496943-94496956 chr1:94496945-94496954 chr1:94496944-94496953
38	BHLHE40	chr1:94491311-94491320	K562	blood:	n/a	n/a
39	BHLHE40	chr1:94478242-94479148	K562	blood:	n/a	chr1:94478467-94478483
40	BHLHE40	chr1:94496846-94497080	K562	blood:	n/a	chr1:94496946-94496955 chr1:94496939-94496960 chr1:94496945-94496954 chr1:94496943-94496956 chr1:94496945-94496954 chr1:94496944-94496953
41	BHLHE40	chr1:94445312-94445671	HepG2	liver:	n/a	n/a
42	BHLHE40	chr1:94445284-94445799	HepG2	liver:	n/a	n/a
43	BHLHE40	chr1:94465366-94465494	K562	blood:	n/a	n/a
44	BHLHE40	chr1:94496899-94497101	GM12878	blood:	n/a	chr1:94496946-94496955 chr1:94496939-94496960 chr1:94496945-94496954 chr1:94496943-94496956 chr1:94496945-94496954 chr1:94496944-94496953
45	BHLHE40	chr1:94445288-94445622	HepG2	liver:	n/a	n/a
46	BRCA1	chr1:94486448-94487167	Hela-S3	cervix:	n/a	n/a
47	CBX3	chr1:94421383-94421686	K562	blood:	n/a	n/a
48	CBX3	chr1:94417651-94417795	K562	blood:	n/a	n/a
49	CBX3	chr1:94421399-94421684	HCT-116	colon:	n/a	n/a
50	CBX3	chr1:94421464-94421680	K562	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:94483746-94483796	GM12878	blood:	n/a
2	chr1:94483746-94483796	GM12878	blood:	n/a
3	chr1:94445292-94445342	AG04449	skin:	fetal
4	chr1:94431058-94431108	HCPEpiC	choroid plexus:	n/a
5	chr1:94431058-94431108	PFSK-1	brain:	n/a
6	chr1:94445292-94445342	Hela-S3	cervix:	n/a
7	chr1:94454989-94455039	AG04449	skin:	fetal
8	chr1:94454989-94455039	HAEpiC	amniotic membrane:	n/a
9	chr1:94458645-94458695	HAEpiC	amniotic membrane:	n/a
10	chr1:94477653-94477703	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:94445292-94445342	K562	blood:	n/a
12	chr1:94458645-94458695	NH-A	brain:	n/a
13	chr1:94489791-94489841	SK-N-SH	brain:	n/a
14	chr1:94477653-94477703	AG09319	gingival:	n/a
15	chr1:94471306-94471356	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:94458645-94458695	HL-60	blood:	n/a
17	chr1:94486895-94486945	ProgFib	skin:	n/a
18	chr1:94431058-94431108	IMR90	lung:	fetal
19	chr1:94471306-94471356	ovcar-3	ovarian:	n/a
20	chr1:94445292-94445342	NHBE	bronchial:	n/a
21	chr1:94471306-94471356	HNPCEpiC	eye:	n/a
22	chr1:94483746-94483796	HEEpiC	esophagus:	n/a
23	chr1:94486895-94486945	Jurkat	blood:	n/a
24	chr1:94454989-94455039	RPTEC	kidney:	n/a
25	chr1:94431058-94431108	ProgFib	skin:	n/a
26	chr1:94483746-94483796	SKMC	muscle:	n/a
27	chr1:94486895-94486945	GM19239	blood:	n/a
28	chr1:94489791-94489841	SK-N-SH_RA	brain:	n/a
29	chr1:94471306-94471356	HMEC	breast:	n/a
30	chr1:94471306-94471356	H1-hESC	embryonic stem cell:	embryo
31	chr1:94477653-94477703	ovcar-3	ovarian:	n/a
32	chr1:94489791-94489841	BJ	skin:	n/a
33	chr1:94483746-94483796	HRCEpiC	kidney:	n/a
34	chr1:94454989-94455039	HCT-116	colon:	n/a
35	chr1:94489791-94489841	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:94471306-94471356	K562	blood:	n/a
37	chr1:94454989-94455039	Hela-S3	cervix:	n/a
38	chr1:94477653-94477703	CMK	blood:	n/a
39	chr1:94483746-94483796	SK-N-MC	brain:	n/a
40	chr1:94477653-94477703	NB4	blood:	n/a
41	chr1:94483746-94483796	A549	lung:	n/a
42	chr1:94483746-94483796	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:94471306-94471356	AG04449	skin:	fetal
44	chr1:94471306-94471356	IMR90	lung:	fetal
45	chr1:94486895-94486945	HNPCEpiC	eye:	n/a
46	chr1:94454989-94455039	AG10803	skin:	n/a
47	chr1:94489791-94489841	HCT-116	colon:	n/a
48	chr1:94477653-94477703	SK-N-MC	brain:	n/a
49	chr1:94471306-94471356	ECC-1	luminal epithelium:	n/a
50	chr1:94454989-94455039	U87	brain:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:94448780..94451908-chr1:94453061..94456181,3	K562	blood:
2	chr1:94439518..94440019-chr20:57225403..57225928,2	MCF-7	breast:
3	chr1:94495358..94496904-chr1:94499895..94502306,2	MCF-7	breast:
4	chr1:94448780..94451908-chr1:94453061..94456181,3	K562	blood:
5	chr1:94493808..94496136-chr1:94499478..94502103,2	K562	blood:
6	chr1:94478608..94480498-chr1:94484594..94486437,2	MCF-7	breast:
7	chr1:94483711..94487548-chr1:94487592..94490547,4	K562	blood:
8	chr1:94373743..94375409-chr1:94425249..94427408,2	MCF-7	breast:
9	chr1:94467932..94470358-chr1:94480661..94482981,2	K562	blood:
10	chr1:94448466..94451239-chr1:94453186..94455287,3	K562	blood:
11	chr1:94405857..94407993-chr1:94421477..94424032,2	K562	blood:
12	chr1:94422807..94425690-chr1:94438597..94441556,2	MCF-7	breast:
13	chr1:94373479..94375777-chr1:94457212..94459458,2	MCF-7	breast:
14	chr1:94459932..94461869-chr1:94465413..94468369,2	MCF-7	breast:
15	chr1:94491175..94491813-chr1:94510908..94511574,2	MCF-7	breast:
16	chr1:94430616..94432695-chr1:94432755..94434649,2	MCF-7	breast:
17	chr1:94502816..94505360-chr1:94694750..94697690,2	MCF-7	breast:
18	chr1:94442054..94445018-chr1:94467301..94469453,2	K562	blood:
19	chr1:94495358..94496904-chr1:94499895..94502306,2	MCF-7	breast:
20	chr1:94405857..94407993-chr1:94421477..94424032,2	K562	blood:
21	chr1:94471999..94474175-chr1:94483788..94486677,2	MCF-7	breast:
22	chr1:94340612..94342966-chr1:94406740..94409371,2	K562	blood:
23	chr1:94458162..94461024-chr1:94475606..94477649,2	K562	blood:
24	chr1:94430616..94432695-chr1:94432755..94434649,2	MCF-7	breast:
25	chr1:94448466..94451239-chr1:94453186..94455287,3	K562	blood:
26	chr1:94432732..94435204-chr1:94436211..94437948,2	K562	blood:
27	chr1:94491288..94492196-chr1:94801066..94801975,3	MCF-7	breast:
28	chr1:94486634..94489091-chr1:94489455..94492220,2	K562	blood:
29	chr1:94436933..94438891-chr1:94440239..94442187,2	K562	blood:
30	chr1:94454284..94456016-chr1:94463855..94465619,2	MCF-7	breast:
31	chr1:94431420..94433973-chr1:94440220..94443089,2	MCF-7	breast:
32	chr1:94424709..94427125-chr1:94437508..94439049,2	MCF-7	breast:
33	chr1:94372270..94376088-chr1:94480112..94484516,4	K562	blood:
34	chr1:94494107..94496556-chr1:94497405..94499346,2	K562	blood:
35	chr1:94491226..94491950-chr1:94505185..94505725,2	MCF-7	breast:
36	chr1:94474260..94476324-chr1:94481823..94483711,2	K562	blood:
37	chr1:94502330..94505107-chr1:94527585..94529424,2	MCF-7	breast:
38	chr1:94474072..94476669-chr1:94488321..94489901,2	MCF-7	breast:
39	chr1:94422807..94425690-chr1:94438597..94441556,2	MCF-7	breast:
40	chr1:94424709..94427125-chr1:94437508..94439049,2	MCF-7	breast:
41	chr1:94373717..94376146-chr1:94504477..94506025,2	MCF-7	breast:
42	chr1:94424138..94425931-chr1:94428683..94431238,2	K562	blood:
43	chr1:94494107..94496556-chr1:94497405..94499346,2	K562	blood:
44	chr1:94442054..94445018-chr1:94467301..94469453,2	K562	blood:
45	chr1:94490026..94492992-chr1:94500104..94503005,2	K562	blood:
46	chr1:94493808..94496136-chr1:94499478..94502103,2	K562	blood:
47	chr1:94475934..94477619-chr1:94484327..94486550,2	K562	blood:
48	chr1:94468902..94471857-chr1:94472562..94475051,2	MCF-7	breast:
49	chr1:94467932..94470358-chr1:94480661..94482981,2	K562	blood:
50	chr1:94491496..94492091-chr1:94526960..94527633,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCD3-8	chr1:94486052-94486183	NONHSAT004567
2	lnc-ABCD3-8	chr1:94487557-94487636	NONHSAT004567

No data

Variant related genes	Relation type
ENSG00000233129	TF binding region
ABCA4	TF binding region
ENSG00000233129	CpG island
ABCA4	CpG island
ENSG00000198691	chromatin interactions
ENSG00000023909	chromatin interactions

Extended variants
information (count: 4329 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:4329 , 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	rs6663218	chr1:94404238-94404239	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539495423	chr1:94404338-94404339	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs115083733	chr1:94404363-94404364	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs142934324	chr1:94404389-94404390	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs572868936	chr1:94404400-94404401	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs7514067	chr1:94404486-94404487	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs75964434	chr1:94404508-94404509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574968058	chr1:94404552-94404553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs75827099	chr1:94404579-94404580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185665712	chr1:94404648-94404649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575695358	chr1:94404654-94404655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs36118843	chr1:94404673-94404674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545850785	chr1:94404674-94404675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551646757	chr1:94404680-94404681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528462000	chr1:94404681-94404682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546516895	chr1:94404682-94404683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs59732296	chr1:94404683-94404684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368762605	chr1:94404692-94404693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190224272	chr1:94404748-94404749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529138965	chr1:94404785-94404786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550757656	chr1:94404822-94404823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568920481	chr1:94404826-94404827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539583945	chr1:94404839-94404840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149199181	chr1:94404842-94404843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143065941	chr1:94404860-94404861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2064765	chr1:94404872-94404873	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs527617568	chr1:94404875-94404876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192257280	chr1:94404882-94404883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183838319	chr1:94404889-94404890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535728125	chr1:94404940-94404941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533403032	chr1:94404942-94404943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557538498	chr1:94404954-94404955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547055576	chr1:94404986-94404987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575739399	chr1:94404998-94404999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545938398	chr1:94405013-94405014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7521934	chr1:94405041-94405042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs201330738	chr1:94405044-94405045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112995192	chr1:94405073-94405074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188563422	chr1:94405127-94405128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs180740549	chr1:94405207-94405208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561890239	chr1:94405245-94405246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186149835	chr1:94405271-94405272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4573532	chr1:94405290-94405291	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs189320634	chr1:94405351-94405352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533139629	chr1:94405386-94405387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551536651	chr1:94405391-94405392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566587222	chr1:94405411-94405412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527353193	chr1:94405426-94405427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548965432	chr1:94405427-94405428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs137946093	chr1:94405431-94405432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD

Chromatin state (count:1084 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94375600-94421200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:94408800-94409600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:94409000-94409200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr1:94409000-94409400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr1:94409000-94409400	Enhancers	NHEK	skin
6	chr1:94409000-94409800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:94409000-94411000	Enhancers	Placenta	Placenta
8	chr1:94409200-94410200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr1:94409600-94410000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr1:94409800-94415200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr1:94410000-94410800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr1:94410200-94411000	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr1:94410400-94410800	Enhancers	Placenta Amnion	Placenta Amnion
14	chr1:94412200-94413000	Enhancers	HepG2	liver
15	chr1:94413000-94413600	Enhancers	Liver	Liver
16	chr1:94415200-94416000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr1:94419400-94419800	Enhancers	HepG2	liver
18	chr1:94421200-94422200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr1:94422000-94422200	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr1:94422000-94422200	Enhancers	Liver	Liver
21	chr1:94422000-94422600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr1:94422200-94422400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr1:94422200-94422400	ZNF genes & repeats	Aorta	Aorta
24	chr1:94422200-94422600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr1:94422200-94422600	ZNF genes & repeats	Esophagus	oesophagus
26	chr1:94422200-94422800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:94422200-94423400	Weak transcription	Liver	Liver
28	chr1:94422400-94425200	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr1:94422400-94425800	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr1:94422600-94425000	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr1:94422600-94426200	Weak transcription	Esophagus	oesophagus
32	chr1:94422600-94445000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr1:94422800-94423600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:94423000-94423200	Weak transcription	Gastric	stomach
35	chr1:94423000-94423400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr1:94423000-94423600	Enhancers	HMEC	breast
37	chr1:94423000-94423600	Enhancers	NHEK	skin
38	chr1:94423000-94424000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr1:94423000-94424400	Enhancers	HepG2	liver
40	chr1:94423000-94427200	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr1:94423200-94423800	ZNF genes & repeats	Aorta	Aorta
42	chr1:94423400-94423600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr1:94423400-94423600	Enhancers	Pancreas	Pancrea
44	chr1:94423400-94424000	Enhancers	Liver	Liver
45	chr1:94423400-94426000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:94423600-94423800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr1:94423600-94423800	Enhancers	Fetal Intestine Large	intestine
48	chr1:94423600-94424000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr1:94423600-94425600	Weak transcription	HMEC	breast
50	chr1:94423600-94425600	Weak transcription	NHEK	skin

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