Variant report

Variant	nsv916783
Chromosome Location	chr1:72196061-72707953
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:72707055-72707441	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:72700492-72701236	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:72695593-72695955	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:72652447-72652641	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:72503489-72503650	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:72384415-72384667	HepG2	liver:	n/a	chr1:72384650-72384666
7	ATF1	chr1:72445759-72445819	K562	blood:	n/a	n/a
8	ATF2	chr1:72433342-72433674	GM12878	blood:	n/a	n/a
9	ATF2	chr1:72433360-72433766	GM12878	blood:	n/a	n/a
10	BACH1	chr1:72616564-72616622	H1-hESC	embryonic stem cell:	n/a	chr1:72616581-72616595
11	BATF	chr1:72246439-72246725	GM12878	blood:	n/a	chr1:72246586-72246597 chr1:72246587-72246597
12	BATF	chr1:72433420-72433717	GM12878	blood:	n/a	n/a
13	BATF	chr1:72246451-72246721	GM12878	blood:	n/a	chr1:72246586-72246597 chr1:72246587-72246597
14	BCL11A	chr1:72433421-72433695	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:72563429-72563467	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:72205203-72205242	GM12878	blood:	n/a	n/a
17	BRCA1	chr1:72378156-72378200	GM12878	blood:	n/a	n/a
18	BRCA1	chr1:72519630-72519642	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr1:72391047-72391054	GM12878	blood:	n/a	n/a
20	CEBPB	chr1:72230483-72230683	Hela-S3	cervix:	n/a	chr1:72230589-72230600
21	CEBPB	chr1:72230467-72230667	H1-hESC	embryonic stem cell:	n/a	chr1:72230589-72230600
22	CEBPB	chr1:72326736-72327069	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:72568541-72568867	HepG2	liver:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
24	CEBPB	chr1:72396266-72396495	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:72683845-72684065	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:72663467-72663765	H1-hESC	embryonic stem cell:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
27	CEBPB	chr1:72568532-72568868	IMR90	lung:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
28	CEBPB	chr1:72230432-72230774	A549	lung:	n/a	chr1:72230589-72230600
29	CEBPB	chr1:72649995-72650046	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:72663573-72663744	HepG2	liver:	n/a	chr1:72663648-72663659 chr1:72663646-72663657 chr1:72663646-72663659 chr1:72663648-72663657
31	CEBPB	chr1:72290161-72290431	A549	lung:	n/a	chr1:72290286-72290297
32	CEBPB	chr1:72568547-72568841	A549	lung:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
33	CEBPB	chr1:72353163-72353392	HepG2	liver:	n/a	chr1:72353242-72353253
34	CEBPB	chr1:72240165-72240391	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr1:72474965-72475177	K562	blood:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073
36	CEBPB	chr1:72396255-72396524	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr1:72407709-72407906	HepG2	liver:	n/a	n/a
38	CEBPB	chr1:72707111-72707491	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr1:72707137-72707455	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr1:72490316-72490600	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:72707179-72707470	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr1:72294559-72294726	HepG2	liver:	n/a	chr1:72294674-72294685
43	CEBPB	chr1:72353187-72353408	A549	lung:	n/a	chr1:72353242-72353253
44	CEBPB	chr1:72230419-72230782	HepG2	liver:	n/a	chr1:72230589-72230600
45	CEBPB	chr1:72568659-72568859	K562	blood:	n/a	chr1:72568711-72568722 chr1:72568710-72568723 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721 chr1:72568712-72568721
46	CEBPB	chr1:72474908-72475232	HepG2	liver:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073
47	CEBPB	chr1:72290106-72290476	IMR90	lung:	n/a	chr1:72290286-72290297
48	CEBPB	chr1:72411651-72411943	H1-hESC	embryonic stem cell:	n/a	chr1:72411787-72411798
49	CEBPB	chr1:72707099-72707502	HepG2	liver:	n/a	n/a
50	CEBPB	chr1:72411685-72411897	HepG2	liver:	n/a	chr1:72411787-72411798

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72382645-72382695	HCF	heart:	n/a
2	chr1:72382645-72382695	HMEC	breast:	n/a
3	chr1:72566690-72566740	AG09319	gingival:	n/a
4	chr1:72382835-72382885	NB4	blood:	n/a
5	chr1:72302970-72303020	RPTEC	kidney:	n/a
6	chr1:72382645-72382695	NB4	blood:	n/a
7	chr1:72382645-72382695	Jurkat	blood:	n/a
8	chr1:72354156-72354206	GM12878	blood:	n/a
9	chr1:72354156-72354206	HMEC	breast:	n/a
10	chr1:72566690-72566740	HCT-116	colon:	n/a
11	chr1:72382835-72382885	NT2-D1	testis:	n/a
12	chr1:72500866-72500916	AG09319	gingival:	n/a
13	chr1:72302970-72303020	AG04450	lung:	fetal
14	chr1:72566690-72566740	HEK293	kidney:	embryo
15	chr1:72500866-72500916	AG09309	skin:	n/a
16	chr1:72566690-72566740	NHDF-neo	bronchial:	n/a
17	chr1:72382835-72382885	SKMC	muscle:	n/a
18	chr1:72566690-72566740	PFSK-1	brain:	n/a
19	chr1:72566690-72566740	AG10803	skin:	n/a
20	chr1:72382645-72382695	IMR90	lung:	fetal
21	chr1:72354156-72354206	NHBE	bronchial:	n/a
22	chr1:72566690-72566740	Caco-2	colon:	n/a
23	chr1:72500866-72500916	AoSMC	blood vessel:	n/a
24	chr1:72500866-72500916	GM12878	blood:	n/a
25	chr1:72566690-72566740	BE2_C	brain:	n/a
26	chr1:72354156-72354206	NB4	blood:	n/a
27	chr1:72382645-72382695	NHBE	bronchial:	n/a
28	chr1:72500866-72500916	SK-N-SH_RA	brain:	n/a
29	chr1:72566690-72566740	CMK	blood:	n/a
30	chr1:72354156-72354206	ECC-1	luminal epithelium:	n/a
31	chr1:72500866-72500916	NHBE	bronchial:	n/a
32	chr1:72382835-72382885	K562	blood:	n/a
33	chr1:72382835-72382885	GM19239	blood:	n/a
34	chr1:72354156-72354206	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:72354156-72354206	Jurkat	blood:	n/a
36	chr1:72500866-72500916	AG04450	lung:	fetal
37	chr1:72382835-72382885	BE2_C	brain:	n/a
38	chr1:72354156-72354206	BE2_C	brain:	n/a
39	chr1:72302970-72303020	Jurkat	blood:	n/a
40	chr1:72500866-72500916	NHDF-neo	bronchial:	n/a
41	chr1:72302970-72303020	SAEC	small airway:	n/a
42	chr1:72500866-72500916	RPTEC	kidney:	n/a
43	chr1:72500866-72500916	ovcar-3	ovarian:	n/a
44	chr1:72302970-72303020	HEEpiC	esophagus:	n/a
45	chr1:72566690-72566740	SK-N-SH	brain:	n/a
46	chr1:72354156-72354206	U87	brain:	n/a
47	chr1:72382835-72382885	GM12891	blood:	n/a
48	chr1:72500866-72500916	HCPEpiC	choroid plexus:	n/a
49	chr1:72354156-72354206	HRCEpiC	kidney:	n/a
50	chr1:72354156-72354206	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:72399874..72402263-chr1:72409207..72411359,2	K562	blood:
2	chr1:72399874..72402263-chr1:72409207..72411359,2	K562	blood:
3	chr1:71559221..71560259-chr1:72503170..72503778,3	MCF-7	breast:
4	chr1:72210098..72212560-chr1:72216356..72218852,2	K562	blood:
5	chr1:72497090..72498877-chr1:72501866..72504493,2	K562	blood:
6	chr1:72511431..72513999-chr1:72515087..72517593,2	K562	blood:
7	chr1:72381957..72383996-chr1:72389950..72392631,2	K562	blood:
8	chr1:72497090..72498877-chr1:72501866..72504493,2	K562	blood:
9	chr1:72488016..72488819-chr1:72503014..72503883,2	K562	blood:
10	chr1:72495707..72498590-chr1:72500903..72503366,2	K562	blood:
11	chr1:72487764..72489951-chr1:72495667..72497783,2	K562	blood:
12	chr1:72483188..72484849-chr1:72487728..72489377,2	K562	blood:
13	chr1:72467998..72470410-chr1:72472067..72474561,2	K562	blood:
14	chr1:72495707..72498590-chr1:72500903..72503366,2	K562	blood:
15	chr1:72381957..72383996-chr1:72389950..72392631,2	K562	blood:
16	chr1:72483188..72484849-chr1:72487728..72489377,2	K562	blood:
17	chr1:72472788..72474801-chr1:72492789..72495541,2	K562	blood:
18	chr1:72210098..72212560-chr1:72216356..72218852,2	K562	blood:
19	chr1:72463115..72465700-chr1:72466215..72468715,2	K562	blood:
20	chr1:72467998..72470410-chr1:72472067..72474561,2	K562	blood:
21	chr1:72472788..72474801-chr1:72492789..72495541,2	K562	blood:
22	chr1:72488016..72488819-chr1:72503014..72503883,2	K562	blood:
23	chr1:72053665..72054637-chr1:72503102..72503767,2	MCF-7	breast:
24	chr1:72487764..72489951-chr1:72495667..72497783,2	K562	blood:
25	chr1:72463115..72465700-chr1:72466215..72468715,2	K562	blood:
26	chr1:72511431..72513999-chr1:72515087..72517593,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZRANB2-1	chr1:72302663-72302695	ENSG00000228853.1
2	lnc-ZRANB2-1	chr1:72259915-72260219	ENSG00000228853.1
3	lnc-ZRANB2-1	chr1:72263758-72263953	ENSG00000228853.1

Variant related genes	Relation type
NEGR1-IT1	TF binding region
NEGR1	TF binding region
ENSG00000271618	TF binding region
NEGR1-IT1	CpG island
NEGR1	CpG island
ENSG00000271618	CpG island

Extended variants
information (count: 14560 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:14560 , 50 per page) page: 1 2 3 4 5 6 7 ... 292

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371177950	chr1:72196155-72196156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532967288	chr1:72196195-72196196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189956360	chr1:72196206-72196207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370694117	chr1:72196252-72196253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs71686030	chr1:72196253-72196254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182902866	chr1:72196254-72196255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528825832	chr1:72196275-72196276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs56382019	chr1:72196276-72196277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373002721	chr1:72196354-72196355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548688680	chr1:72196358-72196359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556240152	chr1:72196370-72196371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187281940	chr1:72196431-72196432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140198394	chr1:72196441-72196442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191016143	chr1:72196547-72196548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571018312	chr1:72196555-72196556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371353763	chr1:72196561-72196562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562441741	chr1:72196607-72196608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533065324	chr1:72196612-72196613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545139778	chr1:72196617-72196618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540042698	chr1:72196640-72196641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557549987	chr1:72196705-72196706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553668217	chr1:72196843-72196844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573560769	chr1:72196905-72196906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536173597	chr1:72196912-72196913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560108625	chr1:72196997-72196998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs375111858	chr1:72197013-72197014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555474224	chr1:72197037-72197038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs17091695	chr1:72197053-72197054	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs74782184	chr1:72197134-72197135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564605525	chr1:72197145-72197146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112440210	chr1:72197226-72197227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540055469	chr1:72197267-72197268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559951824	chr1:72197273-72197274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529131943	chr1:72197281-72197282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548788008	chr1:72197303-72197304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375043651	chr1:72197309-72197310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562334716	chr1:72197314-72197315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531346916	chr1:72197362-72197363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574816800	chr1:72197473-72197474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183777458	chr1:72197474-72197475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188041936	chr1:72197489-72197490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146437993	chr1:72197492-72197493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547193456	chr1:72197549-72197550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567115636	chr1:72197594-72197595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368012883	chr1:72197600-72197601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535764099	chr1:72197673-72197674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556031835	chr1:72197701-72197702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4649942	chr1:72197704-72197705	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs192267917	chr1:72197723-72197724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557794258	chr1:72197727-72197728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	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
Melanoma	17363583	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
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
body mass index	19812545	CNVD
Obesity	20935630	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD
Attention deficit hyperactivity disorder	22138692	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cancer	21272361	CNVD
Obesity	21131291	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:1369 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72189400-72197000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr1:72189600-72197600	Weak transcription	Thymus	Thymus
3	chr1:72191400-72198800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr1:72195800-72196400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:72195800-72197800	Enhancers	Dnd41	blood
6	chr1:72196400-72196800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:72196800-72199400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:72197000-72199200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr1:72197200-72200000	Enhancers	Fetal Thymus	thymus
10	chr1:72197400-72199200	Enhancers	Primary hematopoietic stem cells	blood
11	chr1:72197600-72200000	Enhancers	Thymus	Thymus
12	chr1:72197800-72198200	Enhancers	Left Ventricle	heart
13	chr1:72197800-72199000	Flanking Active TSS	Dnd41	blood
14	chr1:72198000-72198800	Enhancers	Primary T cells from cord blood	blood
15	chr1:72198800-72199000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr1:72198800-72199200	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr1:72199000-72201200	Enhancers	Dnd41	blood
18	chr1:72199200-72200400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr1:72200400-72200600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr1:72200400-72200800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr1:72200400-72200800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr1:72200400-72200800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr1:72200800-72202000	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr1:72200800-72202000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr1:72200800-72202200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr1:72200800-72203200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr1:72201200-72203800	Weak transcription	Dnd41	blood
28	chr1:72202000-72204400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr1:72202000-72204800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr1:72202200-72202400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr1:72202200-72204600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr1:72202200-72204800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr1:72202600-72203600	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr1:72202600-72204200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr1:72202800-72205200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr1:72203000-72204600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr1:72203200-72204800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr1:72203400-72204000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:72203600-72204200	Enhancers	H1 Cell Line	embryonic stem cell
40	chr1:72203600-72204400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr1:72203600-72204800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr1:72203800-72204200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr1:72203800-72204200	Enhancers	Dnd41	blood
44	chr1:72203800-72204400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr1:72204000-72204400	Enhancers	Gastric	stomach
46	chr1:72207000-72208800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr1:72212400-72212800	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr1:72215600-72219400	Weak transcription	Thymus	Thymus
49	chr1:72217400-72218000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:72218000-72221000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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