Variant report

Variant	esv2757779
Chromosome Location	chr1:246407146-246740944
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4446)
CpG islands
(count:3788)
Chromatin interactive
region (count:155)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4446 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:246729530-246729980	K562	blood:	n/a	n/a
2	ARID3A	chr1:246732646-246733496	K562	blood:	n/a	n/a
3	ARID3A	chr1:246472537-246472962	K562	blood:	n/a	n/a
4	ARID3A	chr1:246409804-246409947	K562	blood:	n/a	n/a
5	ARID3A	chr1:246729459-246729909	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:246476713-246476913	K562	blood:	n/a	n/a
7	ARID3A	chr1:246614048-246614417	K562	blood:	n/a	chr1:246614110-246614126
8	ARID3A	chr1:246536567-246536576	K562	blood:	n/a	n/a
9	ARID3A	chr1:246740073-246740316	K562	blood:	n/a	n/a
10	ARID3A	chr1:246495436-246495765	K562	blood:	n/a	n/a
11	ARID3A	chr1:246468839-246469426	K562	blood:	n/a	n/a
12	ARID3A	chr1:246670516-246670577	HepG2	liver:	n/a	n/a
13	ARID3A	chr1:246469874-246470465	K562	blood:	n/a	n/a
14	ARID3A	chr1:246587912-246588291	K562	blood:	n/a	n/a
15	ARID3A	chr1:246591789-246592119	K562	blood:	n/a	n/a
16	ARID3A	chr1:246660564-246660991	K562	blood:	n/a	n/a
17	ARID3A	chr1:246729043-246729235	HepG2	liver:	n/a	n/a
18	ARID3A	chr1:246739546-246739738	K562	blood:	n/a	n/a
19	ARID3A	chr1:246443886-246444158	K562	blood:	n/a	n/a
20	ARID3A	chr1:246730285-246730981	K562	blood:	n/a	n/a
21	ARID3A	chr1:246514223-246514241	K562	blood:	n/a	n/a
22	ARID3A	chr1:246660581-246660971	HepG2	liver:	n/a	n/a
23	ARID3A	chr1:246444896-246445377	HepG2	liver:	n/a	n/a
24	ARID3A	chr1:246740858-246741585	K562	blood:	n/a	chr1:246741392-246741408 chr1:246741393-246741409
25	ARID3A	chr1:246614088-246614383	HepG2	liver:	n/a	chr1:246614110-246614126
26	ATF1	chr1:246501515-246501774	K562	blood:	n/a	n/a
27	ATF1	chr1:246591887-246592268	K562	blood:	n/a	n/a
28	ATF1	chr1:246507966-246508030	K562	blood:	n/a	n/a
29	ATF1	chr1:246495450-246495686	K562	blood:	n/a	n/a
30	ATF1	chr1:246445017-246445192	K562	blood:	n/a	n/a
31	ATF1	chr1:246514087-246514345	K562	blood:	n/a	n/a
32	ATF1	chr1:246740536-246740756	K562	blood:	n/a	n/a
33	ATF1	chr1:246589653-246589853	K562	blood:	n/a	n/a
34	ATF1	chr1:246561390-246561724	K562	blood:	n/a	n/a
35	ATF1	chr1:246469981-246470295	K562	blood:	n/a	n/a
36	ATF1	chr1:246732872-246733329	K562	blood:	n/a	n/a
37	ATF1	chr1:246588435-246588914	K562	blood:	n/a	n/a
38	ATF1	chr1:246730636-246730930	K562	blood:	n/a	n/a
39	ATF2	chr1:246729326-246729950	GM12878	blood:	n/a	n/a
40	ATF2	chr1:246492949-246493723	GM12878	blood:	n/a	n/a
41	ATF2	chr1:246729048-246729793	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF2	chr1:246501723-246502313	GM12878	blood:	n/a	n/a
43	ATF2	chr1:246729219-246729717	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF2	chr1:246598868-246599249	H1-hESC	embryonic stem cell:	n/a	n/a
45	ATF2	chr1:246729298-246730096	GM12878	blood:	n/a	n/a
46	ATF2	chr1:246493100-246493631	GM12878	blood:	n/a	n/a
47	ATF3	chr1:246729163-246730103	A549	lung:	n/a	n/a
48	ATF3	chr1:246734658-246735052	K562	blood:	n/a	n/a
49	ATF3	chr1:246729333-246729841	A549	lung:	n/a	n/a
50	BACH1	chr1:246669921-246670862	H1-hESC	embryonic stem cell:	n/a	n/a

(count:3788 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:246728727-246728777	SK-N-SH	brain:	n/a
2	chr1:246613311-246613361	A549	lung:	n/a
3	chr1:246667857-246667907	AG04450	lung:	fetal
4	chr1:246622483-246622533	Jurkat	blood:	n/a
5	chr1:246451744-246451794	SAEC	small airway:	n/a
6	chr1:246668601-246668651	Caco-2	colon:	n/a
7	chr1:246728727-246728777	SK-N-SH	brain:	n/a
8	chr1:246613311-246613361	A549	lung:	n/a
9	chr1:246667857-246667907	AG04450	lung:	fetal
10	chr1:246622483-246622533	Jurkat	blood:	n/a
11	chr1:246451744-246451794	SAEC	small airway:	n/a
12	chr1:246668601-246668651	Caco-2	colon:	n/a
13	chr1:246728727-246728777	SKMC	muscle:	n/a
14	chr1:246728663-246728713	HCM	heart:	n/a
15	chr1:246729585-246729635	CMK	blood:	n/a
16	chr1:246729218-246729268	SK-N-SH	brain:	n/a
17	chr1:246646424-246646474	ProgFib	skin:	n/a
18	chr1:246415555-246415605	HRCEpiC	kidney:	n/a
19	chr1:246730185-246730235	GM06990	blood:	n/a
20	chr1:246622483-246622533	A549	lung:	n/a
21	chr1:246729218-246729268	HNPCEpiC	eye:	n/a
22	chr1:246670898-246670948	HCF	heart:	n/a
23	chr1:246415176-246415226	AG09319	gingival:	n/a
24	chr1:246613311-246613361	NH-A	brain:	n/a
25	chr1:246729572-246729622	HCF	heart:	n/a
26	chr1:246729345-246729395	NHDF-neo	bronchial:	n/a
27	chr1:246664003-246664053	HUVEC	blood vessel:	n/a
28	chr1:246730188-246730238	K562	blood:	n/a
29	chr1:246415214-246415264	AG09319	gingival:	n/a
30	chr1:246670898-246670948	Caco-2	colon:	n/a
31	chr1:246622633-246622683	PANC-1	pancreas:	n/a
32	chr1:246622633-246622683	HCT-116	colon:	n/a
33	chr1:246729585-246729635	PrEC	prostate:	n/a
34	chr1:246622662-246622712	HRCEpiC	kidney:	n/a
35	chr1:246415555-246415605	AG04450	lung:	fetal
36	chr1:246415568-246415618	ECC-1	luminal epithelium:	n/a
37	chr1:246518620-246518670	U87	brain:	n/a
38	chr1:246730188-246730238	NT2-D1	testis:	n/a
39	chr1:246414665-246414715	NHBE	bronchial:	n/a
40	chr1:246582035-246582085	SAEC	small airway:	n/a
41	chr1:246670217-246670267	T-47D	breast:	n/a
42	chr1:246466280-246466330	ovcar-3	ovarian:	n/a
43	chr1:246728663-246728713	AoSMC	blood vessel:	n/a
44	chr1:246581705-246581755	ovcar-3	ovarian:	n/a
45	chr1:246729669-246729719	HRPEpiC	eye:	n/a
46	chr1:246518620-246518670	CMK	blood:	n/a
47	chr1:246582071-246582121	HCM	heart:	n/a
48	chr1:246580717-246580767	HRE	kidney:	n/a
49	chr1:246667857-246667907	HRE	kidney:	n/a
50	chr1:246622662-246622712	BJ	skin:	n/a

(count:155 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:246719266..246723453-chr1:246727295..246731122,5	MCF-7	breast:
2	chr1:246693616..246696084-chr1:246696950..246700656,3	K562	blood:
3	chr1:246546236..246548052-chr1:246554234..246556624,2	MCF-7	breast:
4	chr1:246521302..246522820-chr1:246527857..246530408,2	K562	blood:
5	chr1:246660669..246662784-chr1:246700415..246702206,2	MCF-7	breast:
6	chr1:246699626..246702195-chr1:246706012..246708369,2	MCF-7	breast:
7	chr1:246665304..246668329-chr1:246668572..246671618,5	MCF-7	breast:
8	chr1:246675941..246677837-chr1:246690243..246691977,2	K562	blood:
9	chr1:246407877..246409674-chr1:246412098..246414077,2	K562	blood:
10	chr1:246175573..246176199-chr1:246409475..246409997,2	K562	blood:
11	chr1:246548799..246550495-chr1:246559308..246561111,2	K562	blood:
12	chr1:246729197..246730166-chr14:75745608..75746363,2	Hela-S3	cervix:
13	chr1:246601398..246602968-chr1:246608645..246610386,2	K562	blood:
14	chr1:246685591..246688881-chr1:246727054..246730014,3	K562	blood:
15	chr1:246594102..246596959-chr1:246598193..246600594,2	K562	blood:
16	chr1:246546236..246548052-chr1:246554234..246556624,2	MCF-7	breast:
17	chr1:246711201..246713601-chr1:246713604..246715628,2	K562	blood:
18	chr1:246643346..246644875-chr1:246651223..246652948,2	K562	blood:
19	chr1:246151420..246154131-chr1:246468233..246469966,2	K562	blood:
20	chr1:246458189..246460474-chr1:246462017..246465759,3	K562	blood:
21	chr1:246540059..246542497-chr1:246543085..246545736,2	K562	blood:
22	chr1:246699626..246702195-chr1:246706012..246708369,2	MCF-7	breast:
23	chr1:246489256..246490981-chr1:246569694..246571729,2	K562	blood:
24	chr1:245319905..245320442-chr1:246655652..246656156,2	K562	blood:
25	chr1:246697803..246699754-chr1:246703795..246706062,2	K562	blood:
26	chr1:246446720..246449077-chr1:246451672..246454637,2	K562	blood:
27	chr1:246738601..246740180-chr1:246754340..246756772,2	MCF-7	breast:
28	chr1:246497788..246499304-chr1:246499416..246501844,2	MCF-7	breast:
29	chr1:246444872..246446533-chr1:246597803..246600502,2	MCF-7	breast:
30	chr1:246692831..246695438-chr1:246704915..246707883,3	K562	blood:
31	chr1:246739822..246741667-chr1:246766063..246767788,2	K562	blood:
32	chr1:246694155..246697194-chr1:246698575..246701434,3	MCF-7	breast:
33	chr1:246643346..246644875-chr1:246651223..246652948,2	K562	blood:
34	chr1:246668302..246670787-chr1:246727323..246729930,4	MCF-7	breast:
35	chr1:246661655..246664160-chr1:246664640..246667505,3	K562	blood:
36	chr1:246685591..246688881-chr1:246727054..246730014,3	K562	blood:
37	chr1:246463275..246466123-chr1:246471236..246474164,2	MCF-7	breast:
38	chr1:246660290..246661312-chr1:246861799..246863185,8	K562	blood:
39	chr1:246666744..246667331-chr1:246771870..246772573,2	MCF-7	breast:
40	chr1:246446720..246449077-chr1:246451672..246454637,2	K562	blood:
41	chr1:246444872..246446533-chr1:246597803..246600502,2	MCF-7	breast:
42	chr1:246451778..246454398-chr1:246470226..246471898,2	K562	blood:
43	chr1:246679194..246683104-chr1:246689621..246693878,4	K562	blood:
44	chr1:246576999..246579498-chr1:246580594..246582855,2	K562	blood:
45	chr1:246464800..246467604-chr1:246470299..246472286,2	MCF-7	breast:
46	chr1:246480625..246484494-chr1:246484509..246487913,3	K562	blood:
47	chr1:246660387..246663593-chr1:246664027..246666681,4	MCF-7	breast:
48	chr1:246728909..246731573-chr1:246733348..246738076,5	MCF-7	breast:
49	chr1:246660548..246661305-chr1:246859828..246860357,2	K562	blood:
50	chr1:246658777..246661380-chr1:246664894..246666631,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFB2M-3	chr1:246691864-246692143	NONHSAT010709
2	lnc-SMYD3-4	chr1:246715093-246715408	NONHSAT010710
3	lnc-CNST-2	chr1:246691213-246691457	NONHSAT010708
4	lnc-TFB2M-2	chr1:246485586-246485740	ENSG00000230184.1
5	lnc-CNST-2	chr1:246690332-246690503	NONHSAT010708
6	lnc-SMYD3-4	chr1:246714169-246714819	NONHSAT010710
7	lnc-TFB2M-2	chr1:246484965-246485170	ENSG00000230184.1

No data

Variant related genes	Relation type
CNST	TF binding region
ENSG00000227728	TF binding region
TFB2M	TF binding region
ENSG00000229112	TF binding region
SMYD3	TF binding region
ENSG00000242042	TF binding region
SMYD3-IT1	TF binding region
ENSG00000230813	TF binding region
ENSG00000207326	TF binding region
CNST	CpG island
ENSG00000227728	CpG island
TFB2M	CpG island
ENSG00000229112	CpG island
SMYD3	CpG island
ENSG00000242042	CpG island
SMYD3-IT1	CpG island
ENSG00000230813	CpG island
ENSG00000207326	CpG island
ENSG00000162852	chromatin interactions
ENSG00000170345	chromatin interactions
ENSG00000207326	chromatin interactions
ENSG00000230184	chromatin interactions
ENSG00000166471	chromatin interactions
ENSG00000040487	chromatin interactions
ENSG00000225300	chromatin interactions
ENSG00000229112	chromatin interactions
ENSG00000227728	chromatin interactions
ENSG00000185420	chromatin interactions
ENSG00000143751	chromatin interactions
ENSG00000162851	chromatin interactions
ENSG00000242042	chromatin interactions
ENSG00000082996	chromatin interactions
ENSG00000230813	chromatin interactions
ENSG00000162714	chromatin interactions
ENSG00000260924	chromatin interactions

Extended variants
information (count: 13939 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:13939 , 50 per page) page: 1 2 3 4 5 6 7 ... 279

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1780808	chr1:246407443-246407444	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545039533	chr1:246407486-246407487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79656094	chr1:246407496-246407497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575293440	chr1:246407530-246407531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191181645	chr1:246407573-246407574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183841842	chr1:246407580-246407581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561031013	chr1:246407677-246407678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs12057323	chr1:246407678-246407679	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs150654422	chr1:246407686-246407687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12057327	chr1:246407730-246407731	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs189057927	chr1:246407791-246407792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528729654	chr1:246407829-246407830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1780807	chr1:246407842-246407843	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs12093226	chr1:246407857-246407858	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs530803311	chr1:246407908-246407909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377321272	chr1:246407909-246407910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2489737	chr1:246407925-246407926	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs567706558	chr1:246407974-246407975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12402506	chr1:246408013-246408014	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs115206058	chr1:246408019-246408020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566797434	chr1:246408074-246408075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10924612	chr1:246408172-246408173	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs556584590	chr1:246408195-246408196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78824150	chr1:246408197-246408198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537995847	chr1:246408221-246408222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78155299	chr1:246408266-246408267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574436242	chr1:246408285-246408286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566300519	chr1:246408296-246408297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542871587	chr1:246408326-246408327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1770003	chr1:246408356-246408357	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs1770004	chr1:246408360-246408361	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs545333114	chr1:246408361-246408362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565233916	chr1:246408379-246408380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76887915	chr1:246408421-246408422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74990711	chr1:246408422-246408423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201422984	chr1:246408423-246408424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs76051960	chr1:246408425-246408426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74335106	chr1:246408426-246408427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530817758	chr1:246408455-246408456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550913526	chr1:246408465-246408466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533783990	chr1:246408501-246408502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74528166	chr1:246408515-246408516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530181983	chr1:246408533-246408534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149017306	chr1:246408579-246408580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553467825	chr1:246408583-246408584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538829407	chr1:246408591-246408592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs386641698	chr1:246408622-246408623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1770008	chr1:246408635-246408636	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs77575757	chr1:246408653-246408654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554519763	chr1:246408678-246408679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	19805367	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Oral cancer	21386901	CNVD

Chromatin state (count:4067 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246407400-246407800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr1:246407400-246408600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:246407400-246409800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr1:246407400-246409800	Enhancers	Osteobl	bone
5	chr1:246407600-246408000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:246407600-246410200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr1:246407800-246411000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:246408600-246409000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:246408800-246409800	Enhancers	HUVEC	blood vessel
10	chr1:246409000-246409200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:246409200-246409800	Enhancers	NHDF-Ad	bronchial
12	chr1:246409200-246411400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:246409600-246409800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:246409600-246409800	Enhancers	HepG2	liver
15	chr1:246409800-246410400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:246409800-246411200	Weak transcription	Osteobl	bone
17	chr1:246410200-246411200	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr1:246410400-246410600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:246411000-246411400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:246411200-246411800	Enhancers	Muscle Satellite Cultured Cells	--
21	chr1:246411200-246411800	Enhancers	Osteobl	bone
22	chr1:246411400-246411800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:246411400-246411800	Enhancers	Fetal Intestine Small	intestine
24	chr1:246411400-246411800	Enhancers	Stomach Mucosa	stomach
25	chr1:246411400-246411800	Enhancers	HepG2	liver
26	chr1:246411800-246413000	Weak transcription	Fetal Intestine Small	intestine
27	chr1:246411800-246413200	Weak transcription	Stomach Mucosa	stomach
28	chr1:246411800-246425600	Weak transcription	Osteobl	bone
29	chr1:246413000-246414000	Enhancers	Fetal Intestine Small	intestine
30	chr1:246413200-246413800	Enhancers	Stomach Mucosa	stomach
31	chr1:246413200-246414600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:246416400-246417200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr1:246416600-246417200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:246418000-246425800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:246420600-246424000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:246421400-246421800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:246421800-246423000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:246421800-246423000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:246422400-246424400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:246422800-246423800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
41	chr1:246423000-246423400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:246423000-246423600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr1:246423000-246423600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:246423000-246423600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr1:246423000-246423600	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr1:246423200-246423400	ZNF genes & repeats	Aorta	Aorta
47	chr1:246423400-246428400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:246423400-246509000	Weak transcription	Aorta	Aorta
49	chr1:246423600-246423800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr1:246423600-246423800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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