Variant report

Variant	nsv1007910
Chromosome Location	chr1:72247302-72543998
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	chr1:72503489-72503650	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:72384415-72384667	HepG2	liver:	n/a	chr1:72384650-72384666
3	ATF1	chr1:72445759-72445819	K562	blood:	n/a	n/a
4	ATF2	chr1:72433342-72433674	GM12878	blood:	n/a	n/a
5	ATF2	chr1:72433360-72433766	GM12878	blood:	n/a	n/a
6	BATF	chr1:72433420-72433717	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:72433421-72433695	GM12878	blood:	n/a	n/a
8	BRCA1	chr1:72391047-72391054	GM12878	blood:	n/a	n/a
9	BRCA1	chr1:72519630-72519642	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr1:72378156-72378200	GM12878	blood:	n/a	n/a
11	CEBPB	chr1:72322163-72322385	HepG2	liver:	n/a	chr1:72322284-72322295
12	CEBPB	chr1:72396266-72396495	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:72290112-72290442	HepG2	liver:	n/a	chr1:72290286-72290297
14	CEBPB	chr1:72411635-72411888	IMR90	lung:	n/a	chr1:72411787-72411798
15	CEBPB	chr1:72290198-72290381	H1-hESC	embryonic stem cell:	n/a	chr1:72290286-72290297
16	CEBPB	chr1:72326678-72327071	IMR90	lung:	n/a	n/a
17	CEBPB	chr1:72353187-72353408	A549	lung:	n/a	chr1:72353242-72353253
18	CEBPB	chr1:72503347-72503641	HepG2	liver:	n/a	chr1:72503460-72503471 chr1:72503459-72503472
19	CEBPB	chr1:72474893-72475164	A549	lung:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073
20	CEBPB	chr1:72353163-72353392	HepG2	liver:	n/a	chr1:72353242-72353253
21	CEBPB	chr1:72326736-72327069	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr1:72407709-72407906	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:72353137-72353285	K562	blood:	n/a	chr1:72353242-72353253
24	CEBPB	chr1:72353101-72353423	IMR90	lung:	n/a	chr1:72353242-72353253
25	CEBPB	chr1:72290161-72290431	A549	lung:	n/a	chr1:72290286-72290297
26	CEBPB	chr1:72274296-72274496	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:72474908-72475232	HepG2	liver:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073
28	CEBPB	chr1:72396255-72396524	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:72294559-72294726	HepG2	liver:	n/a	chr1:72294674-72294685
30	CEBPB	chr1:72474879-72475236	IMR90	lung:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073 chr1:72474884-72474897
31	CEBPB	chr1:72290106-72290476	IMR90	lung:	n/a	chr1:72290286-72290297
32	CEBPB	chr1:72474965-72475177	K562	blood:	n/a	chr1:72475064-72475073 chr1:72475064-72475073 chr1:72475062-72475075 chr1:72475064-72475073
33	CEBPB	chr1:72490316-72490600	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:72411651-72411943	H1-hESC	embryonic stem cell:	n/a	chr1:72411787-72411798
35	CEBPB	chr1:72411685-72411897	HepG2	liver:	n/a	chr1:72411787-72411798
36	CEBPB	chr1:72290139-72290394	K562	blood:	n/a	chr1:72290286-72290297
37	CEBPZ	chr1:72395734-72395783	HepG2	liver:	n/a	n/a
38	CTCF	chr1:72503313-72503919	A549	lung:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
39	CTCF	chr1:72503520-72503711	HepG2	liver:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
40	CTCF	chr1:72503513-72503719	GM10266	blood:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
41	CTCF	chr1:72261840-72261990	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr1:72387980-72388130	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr1:72503560-72503710	HRE	kidney:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
44	CTCF	chr1:72261860-72262010	SAEC	small airway:	n/a	n/a
45	CTCF	chr1:72503520-72503670	HMEC	breast:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
46	CTCF	chr1:72439740-72439890	A549	lung:	n/a	n/a
47	CTCF	chr1:72503540-72503690	NHLF	lung:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627
48	CTCF	chr1:72387738-72387771	GM13976	blood:	n/a	n/a
49	CTCF	chr1:72525860-72526010	RPTEC	kidney:	n/a	n/a
50	CTCF	chr1:72503540-72503690	NB4	blood:	n/a	chr1:72503607-72503628 chr1:72503617-72503630 chr1:72503614-72503627 chr1:72503612-72503630 chr1:72503619-72503627

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72382645-72382695	SAEC	small airway:	n/a
2	chr1:72302970-72303020	PFSK-1	brain:	n/a
3	chr1:72382835-72382885	HCT-116	colon:	n/a
4	chr1:72500866-72500916	PANC-1	pancreas:	n/a
5	chr1:72382645-72382695	K562	blood:	n/a
6	chr1:72500866-72500916	K562	blood:	n/a
7	chr1:72302970-72303020	SK-N-SH	brain:	n/a
8	chr1:72302970-72303020	T-47D	breast:	n/a
9	chr1:72382645-72382695	HEEpiC	esophagus:	n/a
10	chr1:72382645-72382695	ECC-1	luminal epithelium:	n/a
11	chr1:72500866-72500916	ProgFib	skin:	n/a
12	chr1:72382835-72382885	HMEC	breast:	n/a
13	chr1:72382645-72382695	MCF10A-Er-Src	breast:	n/a
14	chr1:72500866-72500916	GM12892	blood:	n/a
15	chr1:72382645-72382695	NHDF-neo	bronchial:	n/a
16	chr1:72382835-72382885	T-47D	breast:	n/a
17	chr1:72382835-72382885	HRCEpiC	kidney:	n/a
18	chr1:72354156-72354206	MCF-7	breast:	n/a
19	chr1:72302970-72303020	NHDF-neo	bronchial:	n/a
20	chr1:72382645-72382695	HMEC	breast:	n/a
21	chr1:72382835-72382885	HIPEpiC	eye:	n/a
22	chr1:72500866-72500916	GM19239	blood:	n/a
23	chr1:72382645-72382695	HCF	heart:	n/a
24	chr1:72382645-72382695	HL-60	blood:	n/a
25	chr1:72354156-72354206	HMEC	breast:	n/a
26	chr1:72382835-72382885	AoSMC	blood vessel:	n/a
27	chr1:72302970-72303020	HIPEpiC	eye:	n/a
28	chr1:72382835-72382885	Hepatocyte	liver:	n/a
29	chr1:72302970-72303020	NH-A	brain:	n/a
30	chr1:72500866-72500916	U87	brain:	n/a
31	chr1:72382645-72382695	HRCEpiC	kidney:	n/a
32	chr1:72382645-72382695	H1-hESC	embryonic stem cell:	embryo
33	chr1:72382645-72382695	Caco-2	colon:	n/a
34	chr1:72354156-72354206	H1-hESC	embryonic stem cell:	embryo
35	chr1:72354156-72354206	AG04449	skin:	fetal
36	chr1:72500866-72500916	SK-N-SH	brain:	n/a
37	chr1:72382645-72382695	RPTEC	kidney:	n/a
38	chr1:72354156-72354206	HCT-116	colon:	n/a
39	chr1:72500866-72500916	AG09319	gingival:	n/a
40	chr1:72382835-72382885	AG10803	skin:	n/a
41	chr1:72382645-72382695	Jurkat	blood:	n/a
42	chr1:72302970-72303020	SK-N-MC	brain:	n/a
43	chr1:72382645-72382695	HNPCEpiC	eye:	n/a
44	chr1:72500866-72500916	H1-hESC	embryonic stem cell:	embryo
45	chr1:72382645-72382695	HepG2	liver:	n/a
46	chr1:72354156-72354206	NHBE	bronchial:	n/a
47	chr1:72500866-72500916	HCT-116	colon:	n/a
48	chr1:72302970-72303020	HRCEpiC	kidney:	n/a
49	chr1:72500866-72500916	HL-60	blood:	n/a
50	chr1:72382645-72382695	CMK	blood:	n/a

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

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

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

Extended variants
information (count: 8526 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:8526 , 50 per page) page: 1 2 3 4 5 6 7 ... 171

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372025700	chr1:72247327-72247328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527682435	chr1:72247331-72247332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs144955713	chr1:72247362-72247363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567723026	chr1:72247393-72247394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs1380484	chr1:72247412-72247413	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs191328691	chr1:72247431-72247432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371929749	chr1:72247437-72247438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148601294	chr1:72247445-72247446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142063067	chr1:72247492-72247493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183473027	chr1:72247508-72247509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572057619	chr1:72247560-72247561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545112166	chr1:72247598-72247599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534274565	chr1:72247599-72247600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188595622	chr1:72247669-72247670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574419360	chr1:72247718-72247719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543483492	chr1:72247737-72247738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181128400	chr1:72247758-72247759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147783756	chr1:72247774-72247775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141428198	chr1:72247812-72247813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560331600	chr1:72247826-72247827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533881780	chr1:72247832-72247833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565530346	chr1:72247851-72247852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527281039	chr1:72247883-72247884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542649282	chr1:72247888-72247889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561359021	chr1:72247902-72247903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530069650	chr1:72247964-72247965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147018871	chr1:72247969-72247970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562204431	chr1:72247976-72247977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147608850	chr1:72248032-72248033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs55847536	chr1:72248052-72248053	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs79700936	chr1:72248054-72248055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114580855	chr1:72248055-72248056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534623639	chr1:72248056-72248057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35898505	chr1:72248066-72248067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140840575	chr1:72248115-72248116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116522612	chr1:72248140-72248141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574358611	chr1:72248162-72248163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533381982	chr1:72248174-72248175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557624206	chr1:72248181-72248182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557012564	chr1:72248201-72248202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115834641	chr1:72248208-72248209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372474287	chr1:72248221-72248222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545576535	chr1:72248241-72248242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185272915	chr1:72248297-72248298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545755468	chr1:72248419-72248420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201372557	chr1:72248450-72248451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572750342	chr1:72248469-72248470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541727286	chr1:72248573-72248574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs72678955	chr1:72248631-72248632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561462258	chr1:72248657-72248658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

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
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
Non-syndromic sensorineural hearing loss	21293372	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

Chromatin state (count:933 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72239000-72252600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:72239600-72251200	Weak transcription	Fetal Stomach	stomach
3	chr1:72240000-72248600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr1:72240600-72256600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr1:72240800-72247400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:72245600-72249800	Enhancers	Dnd41	blood
7	chr1:72246400-72247400	Enhancers	Thymus	Thymus
8	chr1:72247000-72254400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr1:72247200-72247400	Enhancers	Colon Smooth Muscle	Colon
10	chr1:72247400-72248600	Weak transcription	Colon Smooth Muscle	Colon
11	chr1:72247400-72248800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:72247400-72251200	Weak transcription	Thymus	Thymus
13	chr1:72248400-72249800	Enhancers	Rectal Smooth Muscle	rectum
14	chr1:72248600-72249200	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr1:72248600-72251600	Enhancers	Colon Smooth Muscle	Colon
16	chr1:72248800-72249000	Enhancers	Adipose Nuclei	Adipose
17	chr1:72248800-72249200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:72248800-72249600	Enhancers	Primary hematopoietic stem cells	blood
19	chr1:72249200-72249600	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr1:72249200-72254000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:72249600-72251000	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr1:72249600-72257000	Weak transcription	Primary hematopoietic stem cells	blood
23	chr1:72249800-72250400	Weak transcription	Rectal Smooth Muscle	rectum
24	chr1:72250200-72252400	Enhancers	Fetal Lung	lung
25	chr1:72250400-72251600	Enhancers	Fetal Kidney	kidney
26	chr1:72250400-72251600	Enhancers	Rectal Smooth Muscle	rectum
27	chr1:72250600-72251400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:72250800-72251000	Enhancers	Pancreas	Pancrea
29	chr1:72250800-72251400	Enhancers	Gastric	stomach
30	chr1:72250800-72251400	Enhancers	Stomach Smooth Muscle	stomach
31	chr1:72250800-72251600	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr1:72250800-72251600	Enhancers	Aorta	Aorta
33	chr1:72250800-72251600	Enhancers	Right Atrium	heart
34	chr1:72250800-72251600	Enhancers	Right Ventricle	heart
35	chr1:72250800-72251800	Enhancers	Adipose Nuclei	Adipose
36	chr1:72251000-72252200	Weak transcription	Pancreas	Pancrea
37	chr1:72251000-72256000	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr1:72251200-72251400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:72251200-72251600	Enhancers	Fetal Stomach	stomach
40	chr1:72251200-72251600	Enhancers	Thymus	Thymus
41	chr1:72251200-72252800	Enhancers	Fetal Heart	heart
42	chr1:72251200-72252800	Enhancers	Fetal Muscle Leg	muscle
43	chr1:72251400-72252400	Weak transcription	Stomach Smooth Muscle	stomach
44	chr1:72251600-72252400	Weak transcription	Right Ventricle	heart
45	chr1:72251600-72254600	Weak transcription	Rectal Smooth Muscle	rectum
46	chr1:72251600-72254800	Weak transcription	Colon Smooth Muscle	Colon
47	chr1:72252200-72252400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr1:72252200-72253600	Enhancers	Pancreas	Pancrea
49	chr1:72252600-72252800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:72252600-72252800	Enhancers	Right Ventricle	heart

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