Variant report

Variant	nsv879525
Chromosome Location	chr4:87964363-88033352
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1774)
CpG islands
(count:856)
Chromatin interactive
region (count:134)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1774 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:87975236-87975921	K562	blood:	n/a	n/a
2	ARID3A	chr4:88013775-88014187	K562	blood:	n/a	n/a
3	ARID3A	chr4:88024791-88025203	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:88010559-88011002	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:88026072-88026801	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:87979842-87980164	K562	blood:	n/a	n/a
7	ARID3A	chr4:87965892-87966321	K562	blood:	n/a	n/a
8	ARID3A	chr4:88033310-88033619	K562	blood:	n/a	n/a
9	ARID3A	chr4:88014625-88015045	K562	blood:	n/a	n/a
10	ARID3A	chr4:88014767-88014980	HepG2	liver:	n/a	n/a
11	ATF1	chr4:88033199-88033731	K562	blood:	n/a	n/a
12	ATF2	chr4:88014672-88015206	GM12878	blood:	n/a	n/a
13	ATF2	chr4:87994389-87995700	GM12878	blood:	n/a	n/a
14	ATF2	chr4:88014613-88015300	GM12878	blood:	n/a	n/a
15	ATF2	chr4:87994805-87995786	GM12878	blood:	n/a	n/a
16	ATF2	chr4:87979527-87980095	GM12878	blood:	n/a	n/a
17	BACH1	chr4:87979867-87979968	K562	blood:	n/a	n/a
18	BATF	chr4:87995340-87995719	GM12878	blood:	n/a	chr4:87995390-87995399
19	BATF	chr4:87979392-87979911	GM12878	blood:	n/a	chr4:87979530-87979539
20	BATF	chr4:87982142-87982381	GM12878	blood:	n/a	chr4:87982243-87982254 chr4:87982244-87982254
21	BATF	chr4:87982103-87982461	GM12878	blood:	n/a	chr4:87982243-87982254 chr4:87982244-87982254
22	BATF	chr4:87994789-87995274	GM12878	blood:	n/a	chr4:87995069-87995079 chr4:87995068-87995079
23	BATF	chr4:87979641-87979957	GM12878	blood:	n/a	n/a
24	BATF	chr4:87994726-87995286	GM12878	blood:	n/a	chr4:87995069-87995079 chr4:87995068-87995079
25	BCL11A	chr4:87995376-87995655	GM12878	blood:	n/a	n/a
26	BCL3	chr4:87994762-87995699	GM12878	blood:	n/a	n/a
27	BCLAF1	chr4:87979235-87980075	GM12878	blood:	n/a	chr4:87979494-87979503 chr4:87979669-87979678 chr4:87979493-87979502
28	BCLAF1	chr4:87994425-87995792	GM12878	blood:	n/a	chr4:87994470-87994479
29	BCLAF1	chr4:87994230-87995752	GM12878	blood:	n/a	chr4:87994470-87994479
30	BCLAF1	chr4:88014619-88015200	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:87973692-87974256	K562	blood:	n/a	n/a
32	BHLHE40	chr4:88004298-88004498	GM12878	blood:	n/a	n/a
33	BHLHE40	chr4:88014712-88015100	GM12878	blood:	n/a	n/a
34	BHLHE40	chr4:87964371-87964391	GM12878	blood:	n/a	n/a
35	BHLHE40	chr4:88014001-88014119	GM12878	blood:	n/a	n/a
36	BHLHE40	chr4:87975450-87975946	K562	blood:	n/a	n/a
37	BHLHE40	chr4:87995005-87995273	K562	blood:	n/a	n/a
38	BHLHE40	chr4:87965842-87966629	K562	blood:	n/a	n/a
39	BHLHE40	chr4:87994302-87996107	GM12878	blood:	n/a	n/a
40	BHLHE40	chr4:88018449-88018603	K562	blood:	n/a	n/a
41	BHLHE40	chr4:87979329-87979857	GM12878	blood:	n/a	n/a
42	BHLHE40	chr4:88014732-88015022	K562	blood:	n/a	n/a
43	BHLHE40	chr4:88013893-88014431	K562	blood:	n/a	n/a
44	BHLHE40	chr4:87979842-87980495	K562	blood:	n/a	n/a
45	BHLHE40	chr4:88001207-88001441	K562	blood:	n/a	n/a
46	BHLHE40	chr4:88029359-88029362	K562	blood:	n/a	n/a
47	BHLHE40	chr4:88033233-88033667	K562	blood:	n/a	n/a
48	BHLHE40	chr4:87979411-87979596	A549	lung:	n/a	n/a
49	BRCA1	chr4:87994903-87995343	GM12878	blood:	n/a	n/a
50	BRCA1	chr4:88013685-88014241	Hela-S3	cervix:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:88008667-88008717	AG10803	skin:	n/a
2	chr4:87968922-87968972	A549	lung:	n/a
3	chr4:88008667-88008717	AG10803	skin:	n/a
4	chr4:87968922-87968972	A549	lung:	n/a
5	chr4:87999314-87999364	NT2-D1	testis:	n/a
6	chr4:87989696-87989746	HEEpiC	esophagus:	n/a
7	chr4:88008667-88008717	Hela-S3	cervix:	n/a
8	chr4:87968922-87968972	IMR90	lung:	fetal
9	chr4:87989696-87989746	GM06990	blood:	n/a
10	chr4:87965259-87965309	HAEpiC	amniotic membrane:	n/a
11	chr4:87993109-87993159	NH-A	brain:	n/a
12	chr4:87999314-87999364	HCM	heart:	n/a
13	chr4:88000269-88000319	PANC-1	pancreas:	n/a
14	chr4:88014081-88014131	NHBE	bronchial:	n/a
15	chr4:87966326-87966376	AG09319	gingival:	n/a
16	chr4:88014081-88014131	IMR90	lung:	fetal
17	chr4:87980297-87980347	HIPEpiC	eye:	n/a
18	chr4:87980297-87980347	HNPCEpiC	eye:	n/a
19	chr4:88008667-88008717	HCM	heart:	n/a
20	chr4:88014081-88014131	T-47D	breast:	n/a
21	chr4:87993109-87993159	MCF-7	breast:	n/a
22	chr4:88020856-88020906	K562	blood:	n/a
23	chr4:87974092-87974142	BE2_C	brain:	n/a
24	chr4:88008667-88008717	GM12878	blood:	n/a
25	chr4:87999314-87999364	Caco-2	colon:	n/a
26	chr4:88020856-88020906	HCT-116	colon:	n/a
27	chr4:87989696-87989746	NHDF-neo	bronchial:	n/a
28	chr4:87999314-87999364	AoSMC	blood vessel:	n/a
29	chr4:88023169-88023219	ProgFib	skin:	n/a
30	chr4:88023169-88023219	AG10803	skin:	n/a
31	chr4:87968922-87968972	HEK293	kidney:	embryo
32	chr4:87999314-87999364	HCT-116	colon:	n/a
33	chr4:88029472-88029522	HepG2	liver:	n/a
34	chr4:87965259-87965309	HIPEpiC	eye:	n/a
35	chr4:87993109-87993159	HepG2	liver:	n/a
36	chr4:87993109-87993159	SK-N-MC	brain:	n/a
37	chr4:87999314-87999364	IMR90	lung:	fetal
38	chr4:88014081-88014131	K562	blood:	n/a
39	chr4:87965259-87965309	HCPEpiC	choroid plexus:	n/a
40	chr4:87966326-87966376	BJ	skin:	n/a
41	chr4:88000269-88000319	HRE	kidney:	n/a
42	chr4:87966326-87966376	HCM	heart:	n/a
43	chr4:88029472-88029522	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:87974092-87974142	HepG2	liver:	n/a
45	chr4:87993109-87993159	ECC-1	luminal epithelium:	n/a
46	chr4:87989696-87989746	NHBE	bronchial:	n/a
47	chr4:87999314-87999364	GM12892	blood:	n/a
48	chr4:87968922-87968972	GM12892	blood:	n/a
49	chr4:88008667-88008717	BE2_C	brain:	n/a
50	chr4:87989696-87989746	K562	blood:	n/a

(count:134 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:87963142..87968842-chr4:87969641..87976222,9	K562	blood:
2	chr4:88024626..88027340-chr4:88034144..88035743,2	MCF-7	breast:
3	chr4:87973947..87977443-chr4:87977698..87982276,5	K562	blood:
4	chr4:87931438..87933105-chr4:87978302..87980723,2	K562	blood:
5	chr4:87927611..87929346-chr4:87974999..87977042,2	MCF-7	breast:
6	chr4:88016859..88019570-chr4:88023284..88025236,3	MCF-7	breast:
7	chr4:87945681..87948538-chr4:88025074..88026618,2	MCF-7	breast:
8	chr4:87980531..87986351-chr4:87988282..87991075,4	K562	blood:
9	chr4:87991257..87994898-chr4:87995752..87998471,3	MCF-7	breast:
10	chr4:87969507..87971822-chr4:87975846..87977390,2	K562	blood:
11	chr4:88005383..88008853-chr4:88008930..88010972,3	K562	blood:
12	chr4:87973183..87975185-chr4:87980947..87982650,2	MCF-7	breast:
13	chr4:87812118..87814923-chr4:88028471..88030564,2	K562	blood:
14	chr4:87965986..87967736-chr4:87989394..87991945,2	K562	blood:
15	chr4:87963284..87965045-chr4:87965190..87967797,2	K562	blood:
16	chr4:87951686..87953695-chr4:87963099..87965280,2	K562	blood:
17	chr4:88004411..88007536-chr4:88008930..88011901,3	K562	blood:
18	chr4:87926823..87929290-chr4:87998316..87999990,2	K562	blood:
19	chr4:87926976..87930331-chr4:87978377..87981328,6	K562	blood:
20	chr4:87849195..87851661-chr4:88027634..88030050,2	MCF-7	breast:
21	chr4:87843821..87845327-chr4:88013319..88016028,2	MCF-7	breast:
22	chr4:87926587..87929393-chr4:88014126..88017404,4	MCF-7	breast:
23	chr4:88013784..88016288-chr4:88023619..88027731,5	MCF-7	breast:
24	chr4:87854883..87857377-chr4:88013074..88015993,4	MCF-7	breast:
25	chr4:88005383..88008853-chr4:88008930..88010972,3	K562	blood:
26	chr4:88021442..88026056-chr4:88026505..88030511,4	MCF-7	breast:
27	chr4:87926137..87929773-chr4:88012891..88016296,3	K562	blood:
28	chr4:87926465..87928087-chr4:88020560..88022641,2	K562	blood:
29	chr4:87979844..87982158-chr4:87983072..87985121,2	K562	blood:
30	chr4:88022117..88024925-chr4:88027985..88030710,2	K562	blood:
31	chr4:87969741..87972043-chr4:88141021..88142542,2	MCF-7	breast:
32	chr4:87980531..87984297-chr4:87985969..87990791,4	K562	blood:
33	chr4:87991629..87993752-chr4:87994519..87997259,3	K562	blood:
34	chr4:87965986..87967736-chr4:87989394..87991945,2	K562	blood:
35	chr4:87842585..87845353-chr4:87979775..87981630,2	K562	blood:
36	chr4:87980531..87984297-chr4:87985969..87990791,4	K562	blood:
37	chr4:87969835..87971822-chr4:87974907..87977346,2	K562	blood:
38	chr4:88002713..88005662-chr4:88048003..88049629,2	K562	blood:
39	chr4:87854450..87858445-chr4:88020078..88026757,11	MCF-7	breast:
40	chr4:87856199..87857891-chr4:87995074..87997725,3	MCF-7	breast:
41	chr4:87856843..87858663-chr4:87996123..87998357,2	MCF-7	breast:
42	chr4:87973947..87977443-chr4:87977698..87982276,5	K562	blood:
43	chr4:87927007..87928738-chr4:87968800..87971824,3	K562	blood:
44	chr4:87843288..87844189-chr4:88013665..88015393,4	K562	blood:
45	chr4:87966822..87969393-chr4:87974722..87976813,3	K562	blood:
46	chr4:87843422..87844230-chr4:88014418..88015268,4	MCF-7	breast:
47	chr4:87880122..87883120-chr4:87994863..87997796,2	K562	blood:
48	chr4:87963284..87965045-chr4:87965190..87967797,2	K562	blood:
49	chr4:88011101..88013841-chr4:88036538..88039018,2	MCF-7	breast:
50	chr4:87980531..87986351-chr4:87988282..87991075,4	K562	blood:

No data

Variant related genes	Relation type
AFF1	TF binding region
AFF1	CpG island
ENSG00000145332	chromatin interactions
ENSG00000163633	chromatin interactions
ENSG00000172493	chromatin interactions

Extended variants
information (count: 2811 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2811 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6839933	chr4:87964363-87964364	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558989469	chr4:87964372-87964373	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs72877948	chr4:87964389-87964390	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs539785305	chr4:87964423-87964424	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs534679787	chr4:87964425-87964426	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376710684	chr4:87964427-87964428	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs529579172	chr4:87964433-87964434	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs184960343	chr4:87964498-87964499	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs574461192	chr4:87964545-87964546	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541978835	chr4:87964611-87964612	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs188899038	chr4:87964614-87964615	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs138992949	chr4:87964640-87964641	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs77941570	chr4:87964658-87964659	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs557657083	chr4:87964734-87964735	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs564235123	chr4:87964749-87964750	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577829760	chr4:87964757-87964758	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs141546429	chr4:87964807-87964808	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs12506102	chr4:87964814-87964815	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs559350249	chr4:87964830-87964831	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530022213	chr4:87964831-87964832	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548293222	chr4:87964841-87964842	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs570107836	chr4:87964859-87964860	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs181645546	chr4:87964903-87964904	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs150712073	chr4:87964929-87964930	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs553253804	chr4:87964962-87964963	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs200300495	chr4:87964977-87964978	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs67037333	chr4:87964978-87964979	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs570953937	chr4:87964979-87964980	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs535356585	chr4:87964981-87964982	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs79273864	chr4:87964988-87964989	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs201734422	chr4:87964989-87964990	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs139108872	chr4:87964993-87964994	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs114701347	chr4:87965001-87965002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371294651	chr4:87965002-87965003	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs557093726	chr4:87965003-87965004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs186150998	chr4:87965004-87965005	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs149901483	chr4:87965007-87965008	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs111601302	chr4:87965015-87965016	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs557981408	chr4:87965054-87965055	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs7659244	chr4:87965115-87965116	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs144083257	chr4:87965122-87965123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs547664991	chr4:87965170-87965171	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs561615720	chr4:87965185-87965186	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs530059300	chr4:87965189-87965190	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7659431	chr4:87965203-87965204	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs113670795	chr4:87965215-87965216	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs113167444	chr4:87965216-87965217	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs147853160	chr4:87965226-87965227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs13129172	chr4:87965234-87965235	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs115130619	chr4:87965260-87965261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	20952505	CNVD
Breast cancer	22522925	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:4168 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:87952400-87967000	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr4:87952600-87968000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:87953400-87965800	Weak transcription	Primary T cells from cord blood	blood
4	chr4:87953400-87967600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr4:87954600-87965800	Enhancers	Colon Smooth Muscle	Colon
6	chr4:87955600-87964800	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr4:87958600-87965800	Weak transcription	Fetal Intestine Small	intestine
8	chr4:87958800-87968000	Weak transcription	Esophagus	oesophagus
9	chr4:87959200-87967000	Weak transcription	Dnd41	blood
10	chr4:87959400-87966400	Enhancers	Left Ventricle	heart
11	chr4:87959600-87967200	Enhancers	Psoas Muscle	Psoas
12	chr4:87959800-87966000	Weak transcription	Aorta	Aorta
13	chr4:87960000-87964800	Enhancers	Right Atrium	heart
14	chr4:87960400-87965600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:87960400-87965800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr4:87960400-87968000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr4:87960400-87975400	Weak transcription	Brain Germinal Matrix	brain
18	chr4:87960600-87965000	Enhancers	Brain Cingulate Gyrus	brain
19	chr4:87960600-87965000	Enhancers	Brain Hippocampus Middle	brain
20	chr4:87960600-87965600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr4:87960800-87965400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr4:87960800-87965400	Weak transcription	Fetal Stomach	stomach
23	chr4:87960800-87965400	Weak transcription	NHLF	lung
24	chr4:87960800-87965600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr4:87960800-87965600	Weak transcription	NH-A	brain
26	chr4:87960800-87965800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr4:87960800-87966000	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr4:87960800-87968000	Weak transcription	HSMM	muscle
29	chr4:87961000-87965000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr4:87961000-87965200	Weak transcription	NHEK	skin
31	chr4:87961000-87979200	Weak transcription	HSMMtube	muscle
32	chr4:87961200-87964600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr4:87961200-87967800	Weak transcription	Fetal Muscle Trunk	muscle
34	chr4:87961600-87964400	Weak transcription	Fetal Lung	lung
35	chr4:87961600-87966000	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr4:87961800-87964400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:87961800-87966000	Weak transcription	Thymus	Thymus
38	chr4:87962000-87964800	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr4:87962200-87964600	Enhancers	Primary T cells fromperipheralblood	blood
40	chr4:87962200-87964600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr4:87962200-87964800	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr4:87962200-87964800	Enhancers	Liver	Liver
43	chr4:87962200-87965000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr4:87962200-87966400	Enhancers	Adipose Nuclei	Adipose
45	chr4:87962400-87964600	Enhancers	Primary B cells from peripheral blood	blood
46	chr4:87962400-87964600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr4:87962400-87964600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr4:87962400-87964600	Enhancers	Placenta	Placenta
49	chr4:87962400-87965600	Enhancers	K562	blood
50	chr4:87962400-87966200	Enhancers	Primary neutrophils fromperipheralblood	blood

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