Variant report

Variant	nsv999098
Chromosome Location	chr4:87899091-88016048
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3779)
CpG islands
(count:2016)
Chromatin interactive
region (count:226)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3779 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:87938558-87939427	K562	blood:	n/a	chr4:87938800-87938816
2	ARID3A	chr4:87898802-87899331	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:87932639-87933603	K562	blood:	n/a	chr4:87932701-87932717
4	ARID3A	chr4:87921093-87921623	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:87927582-87929577	K562	blood:	n/a	n/a
6	ARID3A	chr4:87952208-87952802	K562	blood:	n/a	n/a
7	ARID3A	chr4:88010559-88011002	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:87940021-87940680	K562	blood:	n/a	n/a
9	ARID3A	chr4:87935533-87936014	K562	blood:	n/a	chr4:87935812-87935828
10	ARID3A	chr4:87915326-87915742	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:87965892-87966321	K562	blood:	n/a	n/a
12	ARID3A	chr4:88013775-88014187	K562	blood:	n/a	n/a
13	ARID3A	chr4:88014767-88014980	HepG2	liver:	n/a	n/a
14	ARID3A	chr4:87975236-87975921	K562	blood:	n/a	n/a
15	ARID3A	chr4:87913231-87913628	K562	blood:	n/a	n/a
16	ARID3A	chr4:87935074-87935218	K562	blood:	n/a	n/a
17	ARID3A	chr4:87979842-87980164	K562	blood:	n/a	n/a
18	ARID3A	chr4:87927594-87928471	HepG2	liver:	n/a	n/a
19	ARID3A	chr4:87936916-87937022	K562	blood:	n/a	n/a
20	ARID3A	chr4:87959365-87959550	K562	blood:	n/a	n/a
21	ARID3A	chr4:87937742-87937948	K562	blood:	n/a	n/a
22	ARID3A	chr4:88014625-88015045	K562	blood:	n/a	n/a
23	ATF1	chr4:87911609-87911825	K562	blood:	n/a	n/a
24	ATF1	chr4:87938761-87939138	K562	blood:	n/a	n/a
25	ATF1	chr4:87932832-87933165	K562	blood:	n/a	n/a
26	ATF1	chr4:87913189-87913809	K562	blood:	n/a	n/a
27	ATF2	chr4:87941072-87941508	GM12878	blood:	n/a	n/a
28	ATF2	chr4:87927775-87928438	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr4:87927398-87928598	GM12878	blood:	n/a	n/a
30	ATF2	chr4:87926407-87927272	GM12878	blood:	n/a	n/a
31	ATF2	chr4:87979527-87980095	GM12878	blood:	n/a	n/a
32	ATF2	chr4:87926704-87927330	GM12878	blood:	n/a	n/a
33	ATF2	chr4:87898883-87899349	GM12878	blood:	n/a	n/a
34	ATF2	chr4:88014613-88015300	GM12878	blood:	n/a	n/a
35	ATF2	chr4:87994805-87995786	GM12878	blood:	n/a	n/a
36	ATF2	chr4:87919187-87919776	GM12878	blood:	n/a	n/a
37	ATF2	chr4:87927479-87928289	GM12878	blood:	n/a	n/a
38	ATF2	chr4:87899778-87900244	GM12878	blood:	n/a	n/a
39	ATF2	chr4:87948056-87948859	GM12878	blood:	n/a	n/a
40	ATF2	chr4:88014672-88015206	GM12878	blood:	n/a	n/a
41	ATF2	chr4:87947952-87949127	GM12878	blood:	n/a	n/a
42	ATF2	chr4:87919162-87919815	GM12878	blood:	n/a	n/a
43	ATF2	chr4:87994389-87995700	GM12878	blood:	n/a	n/a
44	ATF2	chr4:87927840-87928294	H1-hESC	embryonic stem cell:	n/a	n/a
45	ATF2	chr4:87898738-87899276	GM12878	blood:	n/a	n/a
46	ATF3	chr4:87932709-87933154	K562	blood:	n/a	n/a
47	BACH1	chr4:87928724-87929275	K562	blood:	n/a	n/a
48	BACH1	chr4:87955084-87955479	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr4:87979867-87979968	K562	blood:	n/a	n/a
50	BACH1	chr4:87939029-87939146	K562	blood:	n/a	n/a

(count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:87927706-87927756	HL-60	blood:	n/a
2	chr4:87928911-87928961	BJ	skin:	n/a
3	chr4:87966326-87966376	SK-N-SH_RA	brain:	n/a
4	chr4:87927706-87927756	HL-60	blood:	n/a
5	chr4:87928911-87928961	BJ	skin:	n/a
6	chr4:87966326-87966376	SK-N-SH_RA	brain:	n/a
7	chr4:87968922-87968972	A549	lung:	n/a
8	chr4:87927884-87927934	U87	brain:	n/a
9	chr4:87959251-87959301	GM19239	blood:	n/a
10	chr4:87945786-87945836	AG04449	skin:	fetal
11	chr4:87974092-87974142	SK-N-SH	brain:	n/a
12	chr4:87938832-87938882	HCM	heart:	n/a
13	chr4:87928170-87928220	GM12891	blood:	n/a
14	chr4:87980297-87980347	GM12878	blood:	n/a
15	chr4:87999314-87999364	AG04450	lung:	fetal
16	chr4:87932378-87932428	GM12892	blood:	n/a
17	chr4:87966326-87966376	HCF	heart:	n/a
18	chr4:87974092-87974142	U87	brain:	n/a
19	chr4:87968922-87968972	NH-A	brain:	n/a
20	chr4:87928170-87928220	SAEC	small airway:	n/a
21	chr4:87928911-87928961	HMEC	breast:	n/a
22	chr4:87965259-87965309	GM12878	blood:	n/a
23	chr4:87928170-87928220	NT2-D1	testis:	n/a
24	chr4:87928110-87928160	AG10803	skin:	n/a
25	chr4:87999314-87999364	HNPCEpiC	eye:	n/a
26	chr4:87958903-87958953	HAEpiC	amniotic membrane:	n/a
27	chr4:87959251-87959301	Jurkat	blood:	n/a
28	chr4:87928530-87928580	ovcar-3	ovarian:	n/a
29	chr4:87927706-87927756	SK-N-SH	brain:	n/a
30	chr4:87993109-87993159	GM19239	blood:	n/a
31	chr4:88014081-88014131	HUVEC	blood vessel:	n/a
32	chr4:87938832-87938882	GM12891	blood:	n/a
33	chr4:87966326-87966376	PFSK-1	brain:	n/a
34	chr4:87938832-87938882	A549	lung:	n/a
35	chr4:87923929-87923979	GM12891	blood:	n/a
36	chr4:87921477-87921527	SK-N-SH_RA	brain:	n/a
37	chr4:87945786-87945836	Hela-S3	cervix:	n/a
38	chr4:88014081-88014131	H1-hESC	embryonic stem cell:	embryo
39	chr4:87932378-87932428	GM12891	blood:	n/a
40	chr4:87952173-87952223	LNCaP	prostate:	n/a
41	chr4:87928590-87928640	SKMC	muscle:	n/a
42	chr4:87928911-87928961	CMK	blood:	n/a
43	chr4:87945786-87945836	HCT-116	colon:	n/a
44	chr4:87968922-87968972	HCT-116	colon:	n/a
45	chr4:87927884-87927934	PrEC	prostate:	n/a
46	chr4:87928110-87928160	HMEC	breast:	n/a
47	chr4:87966326-87966376	HAEpiC	amniotic membrane:	n/a
48	chr4:87927975-87928025	Caco-2	colon:	n/a
49	chr4:87923929-87923979	Hela-S3	cervix:	n/a
50	chr4:87968922-87968972	HMEC	breast:	n/a

(count:226 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr4:87944954..87950016-chr4:87950159..87955839,10	K562	blood:
2	chr4:87979844..87982158-chr4:87983072..87985121,2	K562	blood:
3	chr4:87946215..87948894-chr4:88011118..88013120,2	MCF-7	breast:
4	chr4:87933850..87935566-chr4:88140971..88143383,2	K562	blood:
5	chr4:87938501..87940925-chr4:87946524..87948135,2	K562	blood:
6	chr4:87997558..88001299-chr4:88002036..88005142,4	K562	blood:
7	chr4:87960365..87962821-chr4:87965345..87969600,5	K562	blood:
8	chr4:87925271..87928107-chr4:88005926..88008504,3	K562	blood:
9	chr4:87945681..87948538-chr4:88025074..88026618,2	MCF-7	breast:
10	chr4:87931438..87933105-chr4:87978302..87980723,2	K562	blood:
11	chr4:87928043..87929592-chr4:87976767..87978738,2	MCF-7	breast:
12	chr4:87980531..87984297-chr4:87985969..87990791,4	K562	blood:
13	chr4:87964446..87966356-chr4:87966393..87968677,2	MCF-7	breast:
14	chr4:87938324..87940317-chr4:87979217..87981960,2	K562	blood:
15	chr4:84376491..84377257-chr4:87927501..87928067,2	NB4	blood:
16	chr4:87964446..87966356-chr4:87966393..87968677,2	MCF-7	breast:
17	chr4:87927969..87930713-chr4:87984972..87986683,2	K562	blood:
18	chr4:88004411..88007536-chr4:88008930..88011901,3	K562	blood:
19	chr4:87897462..87900322-chr4:87922255..87924346,2	K562	blood:
20	chr4:88004411..88007536-chr4:88008930..88011901,3	K562	blood:
21	chr4:88014659..88016864-chr4:88019432..88023640,4	K562	blood:
22	chr4:87989325..87991682-chr4:87996204..87998737,2	K562	blood:
23	chr4:87858860..87860584-chr4:87909283..87910972,2	K562	blood:
24	chr4:87934960..87936958-chr4:87949259..87951055,2	MCF-7	breast:
25	chr4:87965986..87967736-chr4:87989394..87991945,2	K562	blood:
26	chr4:87965646..87968151-chr4:87970035..87972421,2	K562	blood:
27	chr4:87938324..87940317-chr4:87979217..87981960,2	K562	blood:
28	chr4:87880122..87883120-chr4:87994863..87997796,2	K562	blood:
29	chr4:87894580..87900721-chr4:87926553..87929375,8	MCF-7	breast:
30	chr4:87960294..87962501-chr4:87964781..87966501,2	K562	blood:
31	chr4:87855388..87857616-chr4:87927379..87929131,8	MCF-7	breast:
32	chr4:87855923..87858787-chr4:87983318..87985582,3	MCF-7	breast:
33	chr4:87977551..87981344-chr4:87982047..87984756,4	K562	blood:
34	chr4:87926997..87929078-chr4:88000294..88003614,4	K562	blood:
35	chr4:87867281..87868896-chr4:87929541..87932174,2	MCF-7	breast:
36	chr4:87929393..87932319-chr4:87992706..87994245,2	K562	blood:
37	chr4:87897075..87899882-chr4:87931733..87933801,2	K562	blood:
38	chr3:156392079..156392717-chr4:87927562..87928123,2	MCF-7	breast:
39	chr4:87854447..87858210-chr4:88013360..88015983,3	K562	blood:
40	chr4:87901681..87903384-chr4:87927694..87930144,3	MCF-7	breast:
41	chr4:87894083..87901163-chr4:87926378..87930735,13	K562	blood:
42	chr4:87925271..87927953-chr4:88006288..88008752,2	K562	blood:
43	chr4:87895920..87900923-chr4:87925411..87930708,9	MCF-7	breast:
44	chr4:87927772..87928405-chrX:153626454..153627118,2	Hela-S3	cervix:
45	chr4:87927619..87928120-chr6:108901137..108901637,2	NB4	blood:
46	chr4:87927030..87929816-chr4:88013244..88015675,3	MCF-7	breast:
47	chr4:87952663..87956832-chr4:87958320..87961763,4	K562	blood:
48	chr4:87988554..87990336-chr4:88011051..88012696,2	K562	blood:
49	chr4:87912671..87915829-chr4:87926237..87929506,4	MCF-7	breast:
50	chr4:87906047..87909235-chr4:87925490..87928515,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf36-1	chr4:87913620-87914833	ENSG00000249366
2	lnc-PTPN13-2	chr4:87963228-87963870	NONHSAT097297
3	lnc-C4orf36-1	chr4:87918346-87918913	ENSG00000249366

No data

Variant related genes	Relation type
AFF1	TF binding region
AFF1	CpG island
ENSG00000177352	chromatin interactions
ENSG00000166886	chromatin interactions
ENSG00000160746	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000004866	chromatin interactions
ENSG00000163659	chromatin interactions
ENSG00000163319	chromatin interactions
ENSG00000127399	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000214188	chromatin interactions
ENSG00000163312	chromatin interactions
ENSG00000161547	chromatin interactions
ENSG00000243926	chromatin interactions
ENSG00000124171	chromatin interactions
ENSG00000106526	chromatin interactions
ENSG00000235043	chromatin interactions
ENSG00000092931	chromatin interactions
ENSG00000163633	chromatin interactions
ENSG00000011198	chromatin interactions
ENSG00000166881	chromatin interactions
ENSG00000145332	chromatin interactions
ENSG00000147403	chromatin interactions
ENSG00000172493	chromatin interactions
CDK1	miRNA target sites
SATB2	miRNA target sites

Extended variants
information (count: 4794 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:4794 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543327423	chr4:87899111-87899112	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs144808496	chr4:87899128-87899129	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs533119809	chr4:87899160-87899161	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs138658322	chr4:87899205-87899206	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs17752307	chr4:87899285-87899286	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs66611183	chr4:87899309-87899310	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs555220529	chr4:87899310-87899311	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs398107603	chr4:87899312-87899313	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs202237411	chr4:87899314-87899315	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs71660105	chr4:87899329-87899330	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs10676975	chr4:87899344-87899345	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs78349081	chr4:87899354-87899355	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs548548657	chr4:87899404-87899405	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs559443913	chr4:87899411-87899412	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs377036102	chr4:87899412-87899413	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs561582740	chr4:87899423-87899424	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs527778820	chr4:87899460-87899461	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549593442	chr4:87899461-87899462	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs7658204	chr4:87899464-87899465	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs187399759	chr4:87899480-87899481	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs373615204	chr4:87899544-87899545	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs190982937	chr4:87899570-87899571	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs571274383	chr4:87899585-87899586	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs182697092	chr4:87899607-87899608	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs553801512	chr4:87899647-87899648	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs565810656	chr4:87899658-87899659	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs188161708	chr4:87899679-87899680	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs534028741	chr4:87899685-87899686	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs576126363	chr4:87899704-87899705	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs564198941	chr4:87899718-87899719	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs543325742	chr4:87899734-87899735	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs558388172	chr4:87899799-87899800	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs6815546	chr4:87899921-87899922	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs192742100	chr4:87900053-87900054	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs560104816	chr4:87900072-87900073	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs527820860	chr4:87900094-87900095	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs576896285	chr4:87900151-87900152	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs561547228	chr4:87900153-87900154	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs146272534	chr4:87900190-87900191	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs550498918	chr4:87900232-87900233	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs572020298	chr4:87900252-87900253	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs532847639	chr4:87900256-87900257	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113985017	chr4:87900286-87900287	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs4693796	chr4:87900288-87900289	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs536365966	chr4:87900310-87900311	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs111834846	chr4:87900333-87900334	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs569840881	chr4:87900335-87900336	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs6821413	chr4:87900375-87900376	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs142858101	chr4:87900399-87900400	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs576767520	chr4:87900411-87900412	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	20952505	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD

Chromatin state (count:6640 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:87872600-87926200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr4:87882600-87920200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr4:87882800-87912400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr4:87892000-87900400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr4:87892200-87907000	Weak transcription	Brain Anterior Caudate	brain
6	chr4:87892400-87920600	Weak transcription	Stomach Smooth Muscle	stomach
7	chr4:87892800-87909400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr4:87893200-87900200	Weak transcription	Esophagus	oesophagus
9	chr4:87894400-87911000	Weak transcription	Pancreas	Pancrea
10	chr4:87894600-87904200	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr4:87894600-87915600	Weak transcription	Lung	lung
12	chr4:87894600-87921000	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr4:87895200-87909400	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr4:87895400-87920000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr4:87895800-87899800	Weak transcription	Primary B cells from cord blood	blood
16	chr4:87896200-87902800	Weak transcription	Primary T cells from cord blood	blood
17	chr4:87896200-87916000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr4:87896200-87919200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr4:87896400-87899200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr4:87896400-87902800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr4:87896800-87918800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:87897200-87899200	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr4:87897200-87899200	Genic enhancers	Dnd41	blood
24	chr4:87897200-87900600	Enhancers	Primary hematopoietic stem cells	blood
25	chr4:87897200-87901000	Enhancers	Fetal Intestine Large	intestine
26	chr4:87897200-87902600	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr4:87897400-87899200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr4:87897400-87899200	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr4:87897600-87899200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr4:87897600-87915600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr4:87897800-87900000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:87897800-87900400	Enhancers	Fetal Intestine Small	intestine
33	chr4:87897800-87903000	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr4:87898000-87899200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr4:87898000-87899200	Enhancers	Hela-S3	cervix
36	chr4:87898000-87899200	Flanking Active TSS	NHEK	skin
37	chr4:87898000-87899800	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr4:87898000-87900000	Enhancers	Small Intestine	intestine
39	chr4:87898000-87900200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr4:87898000-87900200	Enhancers	HUVEC	blood vessel
41	chr4:87898000-87903000	Weak transcription	Thymus	Thymus
42	chr4:87898200-87899200	Enhancers	Stomach Mucosa	stomach
43	chr4:87898200-87915400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:87898400-87899200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr4:87898400-87899200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr4:87898400-87899200	Enhancers	Colon Smooth Muscle	Colon
47	chr4:87898400-87899200	Enhancers	Duodenum Mucosa	Duodenum
48	chr4:87898400-87899200	Genic enhancers	Fetal Thymus	thymus
49	chr4:87898400-87899200	Flanking Active TSS	GM12878-XiMat	blood
50	chr4:87898400-87899200	Enhancers	Osteobl	bone

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