Variant report

Variant	esv1803011
Chromosome Location	chr1:145214080-145368848
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2138)
CpG islands
(count:305)
Chromatin interactive
region (count:27)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:145289928-145289938	K562	blood:	n/a	n/a
2	ARID3A	chr1:145253698-145253898	K562	blood:	n/a	n/a
3	ARID3A	chr1:145293424-145293644	K562	blood:	n/a	n/a
4	ARID3A	chr1:145254404-145254507	K562	blood:	n/a	n/a
5	ARID3A	chr1:145246167-145246562	HepG2	liver:	n/a	n/a
6	ATF1	chr1:145216140-145216326	K562	blood:	n/a	n/a
7	ATF1	chr1:145292274-145292564	K562	blood:	n/a	n/a
8	ATF1	chr1:145293304-145293510	K562	blood:	n/a	n/a
9	ATF1	chr1:145254447-145254481	K562	blood:	n/a	n/a
10	ATF2	chr1:145291190-145292070	GM12878	blood:	n/a	n/a
11	ATF2	chr1:145233655-145233883	GM12878	blood:	n/a	n/a
12	BACH1	chr1:145292365-145292516	K562	blood:	n/a	n/a
13	BACH1	chr1:145253854-145253876	K562	blood:	n/a	n/a
14	BACH1	chr1:145254230-145254652	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr1:145254231-145254659	K562	blood:	n/a	n/a
16	BATF	chr1:145356362-145356521	GM12878	blood:	n/a	n/a
17	BATF	chr1:145293025-145293677	GM12878	blood:	n/a	n/a
18	BATF	chr1:145233237-145234045	GM12878	blood:	n/a	n/a
19	BATF	chr1:145310440-145310923	GM12878	blood:	n/a	chr1:145310669-145310677
20	BATF	chr1:145260188-145260447	GM12878	blood:	n/a	n/a
21	BATF	chr1:145342174-145342333	GM12878	blood:	n/a	n/a
22	BATF	chr1:145304748-145305052	GM12878	blood:	n/a	n/a
23	BATF	chr1:145368329-145368784	GM12878	blood:	n/a	n/a
24	BATF	chr1:145234968-145235329	GM12878	blood:	n/a	n/a
25	BATF	chr1:145362622-145362781	GM12878	blood:	n/a	n/a
26	BATF	chr1:145351628-145351787	GM12878	blood:	n/a	n/a
27	BATF	chr1:145259491-145259713	GM12878	blood:	n/a	chr1:145259620-145259631
28	BATF	chr1:145323297-145323456	GM12878	blood:	n/a	n/a
29	BATF	chr1:145285189-145285435	GM12878	blood:	n/a	n/a
30	BATF	chr1:145233198-145234079	GM12878	blood:	n/a	n/a
31	BATF	chr1:145281369-145281733	GM12878	blood:	n/a	n/a
32	BATF	chr1:145234411-145234753	GM12878	blood:	n/a	n/a
33	BATF	chr1:145296560-145296816	GM12878	blood:	n/a	n/a
34	BATF	chr1:145346898-145347057	GM12878	blood:	n/a	n/a
35	BATF	chr1:145296892-145297102	GM12878	blood:	n/a	n/a
36	BATF	chr1:145218967-145219192	GM12878	blood:	n/a	chr1:145218977-145218990
37	BATF	chr1:145234955-145235323	GM12878	blood:	n/a	n/a
38	BATF	chr1:145291553-145291993	GM12878	blood:	n/a	n/a
39	BATF	chr1:145291523-145292252	GM12878	blood:	n/a	n/a
40	BATF	chr1:145277155-145277522	GM12878	blood:	n/a	n/a
41	BATF	chr1:145368315-145369169	GM12878	blood:	n/a	n/a
42	BATF	chr1:145293193-145293698	GM12878	blood:	n/a	n/a
43	BATF	chr1:145304760-145305106	GM12878	blood:	n/a	n/a
44	BATF	chr1:145297112-145297381	GM12878	blood:	n/a	n/a
45	BATF	chr1:145310436-145310883	GM12878	blood:	n/a	chr1:145310669-145310677
46	BATF	chr1:145231709-145232035	GM12878	blood:	n/a	n/a
47	BATF	chr1:145299644-145300057	GM12878	blood:	n/a	n/a
48	BATF	chr1:145219743-145220000	GM12878	blood:	n/a	n/a
49	BATF	chr1:145337454-145337613	GM12878	blood:	n/a	n/a
50	BATF	chr1:145290357-145290900	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145301948-145301998	SK-N-SH	brain:	n/a
2	chr1:145366536-145366586	HNPCEpiC	eye:	n/a
3	chr1:145301948-145301998	HCPEpiC	choroid plexus:	n/a
4	chr1:145366524-145366574	SK-N-SH	brain:	n/a
5	chr1:145366536-145366586	AG09319	gingival:	n/a
6	chr1:145302551-145302601	H1-hESC	embryonic stem cell:	embryo
7	chr1:145366524-145366574	HUVEC	blood vessel:	n/a
8	chr1:145366536-145366586	GM06990	blood:	n/a
9	chr1:145302551-145302601	SKMC	muscle:	n/a
10	chr1:145302551-145302601	AG09309	skin:	n/a
11	chr1:145366536-145366586	Jurkat	blood:	n/a
12	chr1:145250914-145250964	RPTEC	kidney:	n/a
13	chr1:145366524-145366574	AG10803	skin:	n/a
14	chr1:145250914-145250964	SAEC	small airway:	n/a
15	chr1:145366524-145366574	T-47D	breast:	n/a
16	chr1:145366536-145366586	ovcar-3	ovarian:	n/a
17	chr1:145302551-145302601	ECC-1	luminal epithelium:	n/a
18	chr1:145366524-145366574	HMEC	breast:	n/a
19	chr1:145302551-145302601	SAEC	small airway:	n/a
20	chr1:145302551-145302601	HRE	kidney:	n/a
21	chr1:145302551-145302601	BE2_C	brain:	n/a
22	chr1:145366536-145366586	HPAEpiC	pulmonary alveolar:	n/a
23	chr1:145366536-145366586	AoSMC	blood vessel:	n/a
24	chr1:145366536-145366586	BE2_C	brain:	n/a
25	chr1:145366536-145366586	HIPEpiC	eye:	n/a
26	chr1:145250914-145250964	HMEC	breast:	n/a
27	chr1:145366536-145366586	Hela-S3	cervix:	n/a
28	chr1:145366536-145366586	HAEpiC	amniotic membrane:	n/a
29	chr1:145366524-145366574	AoSMC	blood vessel:	n/a
30	chr1:145302551-145302601	NH-A	brain:	n/a
31	chr1:145366524-145366574	GM12892	blood:	n/a
32	chr1:145366536-145366586	Caco-2	colon:	n/a
33	chr1:145366536-145366586	CMK	blood:	n/a
34	chr1:145301948-145301998	A549	lung:	n/a
35	chr1:145366524-145366574	Caco-2	colon:	n/a
36	chr1:145301948-145301998	HEK293	kidney:	embryo
37	chr1:145301948-145301998	GM12891	blood:	n/a
38	chr1:145302551-145302601	NHDF-neo	bronchial:	n/a
39	chr1:145301948-145301998	SK-N-SH_RA	brain:	n/a
40	chr1:145366524-145366574	SK-N-MC	brain:	n/a
41	chr1:145250914-145250964	K562	blood:	n/a
42	chr1:145366524-145366574	Hepatocyte	liver:	n/a
43	chr1:145366536-145366586	NT2-D1	testis:	n/a
44	chr1:145250914-145250964	ProgFib	skin:	n/a
45	chr1:145302551-145302601	AoSMC	blood vessel:	n/a
46	chr1:145301948-145301998	MCF10A-Er-Src	breast:	n/a
47	chr1:145250914-145250964	HepG2	liver:	n/a
48	chr1:145250914-145250964	HUVEC	blood vessel:	n/a
49	chr1:145366524-145366574	HepG2	liver:	n/a
50	chr1:145301948-145301998	AG04449	skin:	fetal

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:145238836..145241577-chr1:145243504..145245771,2	K562	blood:
2	chr1:120561821..120563990-chr1:145256491..145258504,4	MCF-7	breast:
3	chr1:120555279..120557791-chr1:145264672..145267612,3	K562	blood:
4	chr1:120562041..120564945-chr1:145257130..145258905,2	K562	blood:
5	chr1:120602747..120604407-chr1:145216153..145218112,2	MCF-7	breast:
6	chr1:145238836..145241577-chr1:145243504..145245771,2	K562	blood:
7	chr1:145208945..145211572-chr1:145290799..145293780,3	MCF-7	breast:
8	chr1:145291510..145293949-chr1:149222418..149224230,2	K562	blood:
9	chr1:145287740..145289244-chr18:67226861..67228381,2	MCF-7	breast:
10	chr1:145257082..145259251-chr1:145260108..145261925,2	MCF-7	breast:
11	chr1:145130093..145132779-chr1:145291052..145292604,2	K562	blood:
12	chr1:145257082..145259251-chr1:145260108..145261925,2	MCF-7	breast:
13	chr1:145209133..145210911-chr1:145213297..145216185,2	MCF-7	breast:
14	chr1:120576520..120578439-chr1:145242059..145244929,2	MCF-7	breast:
15	chr1:145264618..145267295-chr1:145381743..145384010,2	K562	blood:
16	chr1:120574754..120575346-chr1:145245858..145246575,2	MCF-7	breast:
17	chr1:145290091..145292740-chr1:145382337..145384639,2	MCF-7	breast:
18	chr1:145258606..145260477-chr1:145381662..145384269,2	MCF-7	breast:
19	chr1:145110521..145113203-chr1:145271699..145274224,2	MCF-7	breast:
20	chr1:145289699..145292602-chr1:149222944..149224949,3	MCF-7	breast:
21	chr1:120573750..120576750-chr1:145244417..145247281,4	MCF-7	breast:
22	chr1:145288943..145293306-chr1:149221737..149224658,6	MCF-7	breast:
23	chr1:120562393..120564845-chr1:145256114..145258582,3	MCF-7	breast:
24	chr1:120533140..120534660-chr1:145287386..145288888,2	MCF-7	breast:
25	chr1:145207909..145210605-chr1:145214441..145216644,2	MCF-7	breast:
26	chr1:145246366..145248846-chr1:149222454..149225152,2	MCF-7	breast:
27	chr1:120565033..120566748-chr1:145252742..145255259,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOTCH2NL-2	chr1:145317406-145317457	NR_104217
2	lnc-NOTCH2NL-2	chr1:145304447-145304652	NR_104217
3	lnc-NOTCH2NL-2	chr1:145302649-145302868	NR_104217
4	lnc-NOTCH2NL-2	chr1:145316512-145316684	NR_104217
5	lnc-NOTCH2NL-2	chr1:145291855-145291972	NONHSAT005883
6	lnc-NOTCH2NL-2	chr1:145305945-145305996	NR_104217
7	lnc-NOTCH2NL-2	chr1:145319624-145319796	NR_104217
8	lnc-NOTCH2NL-2	chr1:145301720-145301817	NR_104217
9	lnc-NOTCH2NL-2	chr1:145309900-145310063	NR_104217
10	lnc-NOTCH2NL-2	chr1:145290781-145290850	NONHSAT005883
11	lnc-NOTCH2NL-2	chr1:145290422-145290511	NONHSAT005883
12	lnc-NOTCH2NL-2	chr1:145320511-145320619	NR_104217
13	lnc-NOTCH2NL-2	chr1:145290429-145290511	NR_104217
14	lnc-NOTCH2NL-2	chr1:145311103-145311154	NR_104217
15	lnc-NOTCH2NL-2	chr1:145293371-145293580	NR_104217
16	lnc-NOTCH2NL-2	chr1:145318936-145318987	NR_104217
17	lnc-NOTCH2NL-2	chr1:145289770-145289906	NR_104217
18	lnc-NOTCH2NL-2	chr1:145368441-145369446	NR_104217
19	lnc-NOTCH2NL-2	chr1:145318054-145318226	NR_104217
20	lnc-NOTCH2NL-2	chr1:145303910-145303982	NR_104217

No data

Variant related genes	Relation type
NOTCH2NL	TF binding region
NBPF10	TF binding region
NOTCH2NL	CpG island
NBPF10	CpG island
ENSG00000213240	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000255168	chromatin interactions
ENSG00000233396	chromatin interactions

Extended variants
information (count: 4311 )
Associated
traits (count: 173 )

Variant overlapped rSNPs/rCNVs (count:4311 , 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	rs75738504	chr1:145214084-145214085	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141567600	chr1:145214099-145214100	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs201409377	chr1:145214122-145214123	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs587615429	chr1:145214160-145214161	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587696990	chr1:145214165-145214166	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs587731847	chr1:145214179-145214180	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139054716	chr1:145214206-145214207	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs73002381	chr1:145214239-145214240	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200915305	chr1:145214259-145214260	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs374837279	chr1:145214260-145214261	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs587629704	chr1:145214279-145214280	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs201276276	chr1:145214283-145214284	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs587672325	chr1:145214397-145214398	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs587629605	chr1:145214409-145214410	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs3012020	chr1:145214480-145214481	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs200474127	chr1:145214786-145214787	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs3901521	chr1:145214917-145214918	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs61814525	chr1:145214945-145214946	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs2799234	chr1:145215006-145215007	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs61814552	chr1:145215009-145215010	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs587722244	chr1:145215091-145215092	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs367982617	chr1:145215102-145215103	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs201207937	chr1:145215122-145215123	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs368002939	chr1:145215123-145215124	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs111871027	chr1:145215207-145215208	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs540256488	chr1:145215208-145215209	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs587651539	chr1:145215218-145215219	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs113411004	chr1:145215283-145215284	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs587743199	chr1:145215284-145215285	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs587618120	chr1:145215299-145215300	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs587696149	chr1:145215462-145215463	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs61814553	chr1:145215468-145215469	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs373187108	chr1:145215621-145215622	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs61814554	chr1:145215828-145215829	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs112525300	chr1:145215835-145215836	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs61814555	chr1:145215854-145215855	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs200111184	chr1:145215952-145215953	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs200871201	chr1:145216047-145216048	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs587624981	chr1:145216285-145216286	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs587688094	chr1:145216295-145216296	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs587762655	chr1:145216310-145216311	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs587646517	chr1:145216330-145216331	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs28633534	chr1:145216365-145216366	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs587746166	chr1:145216412-145216413	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs587773107	chr1:145216419-145216420	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs71664071	chr1:145216441-145216442	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs372305487	chr1:145216467-145216468	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs587677019	chr1:145216514-145216515	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs201268151	chr1:145216536-145216537	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs587738071	chr1:145216685-145216686	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:173)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Autism	20858243	CNVD
Autism	22543975	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	20808228	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22102821	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:4414 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:145210200-145230400	Weak transcription	Spleen	Spleen
2	chr1:145210400-145215400	Weak transcription	Gastric	stomach
3	chr1:145210600-145214200	Enhancers	Fetal Heart	heart
4	chr1:145210600-145214600	Weak transcription	Esophagus	oesophagus
5	chr1:145210600-145214600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr1:145210600-145217000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr1:145210600-145217200	Enhancers	Primary B cells from peripheral blood	blood
8	chr1:145210600-145219200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr1:145210800-145215400	Weak transcription	K562	blood
10	chr1:145210800-145216000	Weak transcription	Placenta	Placenta
11	chr1:145210800-145216400	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr1:145210800-145220200	Weak transcription	Fetal Muscle Trunk	muscle
13	chr1:145210800-145220200	Weak transcription	Right Ventricle	heart
14	chr1:145211600-145215600	Weak transcription	Fetal Muscle Leg	muscle
15	chr1:145211600-145215800	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr1:145211600-145219800	Weak transcription	Brain Substantia Nigra	brain
17	chr1:145211600-145246400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr1:145211800-145214600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:145211800-145215000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr1:145211800-145215200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr1:145211800-145215200	Weak transcription	HUVEC	blood vessel
22	chr1:145211800-145219000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:145211800-145219200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:145211800-145219200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr1:145211800-145219200	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr1:145211800-145219200	Weak transcription	Right Atrium	heart
27	chr1:145211800-145220800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:145211800-145223400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:145212000-145218200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr1:145212200-145219200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr1:145212200-145221800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr1:145212400-145216400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr1:145212400-145230200	Weak transcription	Fetal Intestine Large	intestine
34	chr1:145212600-145215200	Weak transcription	Brain Anterior Caudate	brain
35	chr1:145212800-145215000	Weak transcription	Fetal Kidney	kidney
36	chr1:145212800-145217400	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr1:145212800-145219200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr1:145212800-145241600	Weak transcription	Fetal Stomach	stomach
39	chr1:145213200-145214400	Enhancers	Hela-S3	cervix
40	chr1:145213200-145216600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:145213200-145219200	Weak transcription	Thymus	Thymus
42	chr1:145213400-145214600	Weak transcription	Dnd41	blood
43	chr1:145213400-145214800	Weak transcription	A549	lung
44	chr1:145213400-145216400	Enhancers	NHEK	skin
45	chr1:145213400-145219000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr1:145213400-145219200	Weak transcription	NHLF	lung
47	chr1:145213400-145220200	Weak transcription	Small Intestine	intestine
48	chr1:145213600-145214600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr1:145213600-145214600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr1:145213600-145214600	Weak transcription	Liver	Liver

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