Variant report

Variant	nsv879652
Chromosome Location	chr4:99125659-99303633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1237)
CpG islands
(count:855)
Chromatin interactive
region (count:98)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1237 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:99183740-99183927	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:99153553-99153558	K562	blood:	n/a	n/a
3	ARID3A	chr4:99174738-99175080	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:99182185-99182418	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:99182631-99182760	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:99239639-99239936	HepG2	liver:	n/a	n/a
7	ATF1	chr4:99153376-99153775	K562	blood:	n/a	n/a
8	ATF2	chr4:99181655-99182496	GM12878	blood:	n/a	n/a
9	ATF3	chr4:99153348-99153854	HCT-116	colon:	n/a	n/a
10	ATF3	chr4:99153321-99153783	K562	blood:	n/a	n/a
11	BACH1	chr4:99208547-99208551	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:99181738-99183321	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr4:99184897-99185129	GM12878	blood:	n/a	chr4:99185019-99185030
14	BATF	chr4:99125451-99125672	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:99125383-99125694	GM12878	blood:	n/a	chr4:99125514-99125523
16	BHLHE40	chr4:99182746-99183481	HepG2	liver:	n/a	n/a
17	BHLHE40	chr4:99183157-99183490	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:99181212-99182502	HepG2	liver:	n/a	chr4:99182283-99182299
19	BHLHE40	chr4:99181201-99182493	K562	blood:	n/a	chr4:99182283-99182299
20	BHLHE40	chr4:99183263-99183566	A549	lung:	n/a	n/a
21	BHLHE40	chr4:99182696-99183494	K562	blood:	n/a	n/a
22	BHLHE40	chr4:99153453-99153676	K562	blood:	n/a	n/a
23	BHLHE40	chr4:99124431-99125689	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:99182731-99182932	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:99181174-99182504	GM12878	blood:	n/a	chr4:99182283-99182299
26	BRCA1	chr4:99181324-99181506	GM12878	blood:	n/a	n/a
27	BRCA1	chr4:99181865-99182364	HepG2	liver:	n/a	n/a
28	BRCA1	chr4:99182106-99182317	GM12878	blood:	n/a	n/a
29	BRCA1	chr4:99182012-99182213	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr4:99181842-99182337	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr4:99289199-99289529	K562	blood:	n/a	n/a
32	CBX3	chr4:99205616-99206414	HCT-116	colon:	n/a	n/a
33	CBX3	chr4:99182060-99183452	K562	blood:	n/a	n/a
34	CBX3	chr4:99254923-99255312	HCT-116	colon:	n/a	n/a
35	CBX3	chr4:99181213-99181825	K562	blood:	n/a	n/a
36	CCNT2	chr4:99295425-99295560	K562	blood:	n/a	n/a
37	CCNT2	chr4:99181456-99183396	K562	blood:	n/a	chr4:99182920-99182929
38	CEBPB	chr4:99153384-99153746	HepG2	liver:	n/a	chr4:99153553-99153564
39	CEBPB	chr4:99153417-99153751	MCF-7	breast:	n/a	chr4:99153553-99153564
40	CEBPB	chr4:99260200-99260397	HepG2	liver:	n/a	chr4:99260288-99260299 chr4:99260288-99260299 chr4:99260286-99260297
41	CEBPB	chr4:99180548-99180687	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:99148245-99148444	K562	blood:	n/a	n/a
43	CEBPB	chr4:99279819-99280069	HepG2	liver:	n/a	chr4:99279982-99279993
44	CEBPB	chr4:99180569-99180661	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr4:99183284-99183740	A549	lung:	n/a	n/a
46	CEBPB	chr4:99265140-99265282	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:99153274-99153808	K562	blood:	n/a	chr4:99153553-99153564
48	CEBPB	chr4:99184546-99184762	HepG2	liver:	n/a	n/a
49	CEBPB	chr4:99153372-99153737	A549	lung:	n/a	chr4:99153553-99153564
50	CEBPB	chr4:99153414-99153726	H1-hESC	embryonic stem cell:	n/a	chr4:99153553-99153564

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:99182328-99182378	HUVEC	blood vessel:	n/a
2	chr4:99182328-99182378	HUVEC	blood vessel:	n/a
3	chr4:99186446-99186496	HCF	heart:	n/a
4	chr4:99181393-99181443	Jurkat	blood:	n/a
5	chr4:99181393-99181443	A549	lung:	n/a
6	chr4:99159401-99159451	ProgFib	skin:	n/a
7	chr4:99159401-99159451	SK-N-SH	brain:	n/a
8	chr4:99182416-99182466	NHBE	bronchial:	n/a
9	chr4:99181920-99181970	NH-A	brain:	n/a
10	chr4:99181393-99181443	ProgFib	skin:	n/a
11	chr4:99186446-99186496	HEEpiC	esophagus:	n/a
12	chr4:99186446-99186496	AG04450	lung:	fetal
13	chr4:99182555-99182605	HCF	heart:	n/a
14	chr4:99186446-99186496	NB4	blood:	n/a
15	chr4:99182798-99182848	HRCEpiC	kidney:	n/a
16	chr4:99159401-99159451	HEK293	kidney:	embryo
17	chr4:99182555-99182605	T-47D	breast:	n/a
18	chr4:99182416-99182466	NB4	blood:	n/a
19	chr4:99186446-99186496	MCF10A-Er-Src	breast:	n/a
20	chr4:99235909-99235959	Hela-S3	cervix:	n/a
21	chr4:99159401-99159451	PFSK-1	brain:	n/a
22	chr4:99181393-99181443	HRCEpiC	kidney:	n/a
23	chr4:99298930-99298980	SKMC	muscle:	n/a
24	chr4:99181920-99181970	GM19239	blood:	n/a
25	chr4:99183198-99183248	SK-N-SH_RA	brain:	n/a
26	chr4:99181393-99181443	ovcar-3	ovarian:	n/a
27	chr4:99182422-99182472	HIPEpiC	eye:	n/a
28	chr4:99182328-99182378	AoSMC	blood vessel:	n/a
29	chr4:99182422-99182472	NB4	blood:	n/a
30	chr4:99181393-99181443	GM12892	blood:	n/a
31	chr4:99182555-99182605	HRCEpiC	kidney:	n/a
32	chr4:99181920-99181970	BE2_C	brain:	n/a
33	chr4:99178293-99178343	Jurkat	blood:	n/a
34	chr4:99181393-99181443	NHDF-neo	bronchial:	n/a
35	chr4:99178293-99178343	HRCEpiC	kidney:	n/a
36	chr4:99178293-99178343	AG10803	skin:	n/a
37	chr4:99182555-99182605	AG04449	skin:	fetal
38	chr4:99182416-99182466	HCPEpiC	choroid plexus:	n/a
39	chr4:99182242-99182292	Caco-2	colon:	n/a
40	chr4:99182416-99182466	Caco-2	colon:	n/a
41	chr4:99181920-99181970	NT2-D1	testis:	n/a
42	chr4:99182328-99182378	NHBE	bronchial:	n/a
43	chr4:99186446-99186496	BE2_C	brain:	n/a
44	chr4:99183198-99183248	A549	lung:	n/a
45	chr4:99183198-99183248	HMEC	breast:	n/a
46	chr4:99182555-99182605	GM12891	blood:	n/a
47	chr4:99181393-99181443	K562	blood:	n/a
48	chr4:99182555-99182605	AoSMC	blood vessel:	n/a
49	chr4:99182328-99182378	MCF10A-Er-Src	breast:	n/a
50	chr4:99182242-99182292	AG09309	skin:	n/a

(count:98 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:99169147..99171084-chr4:99176723..99180239,3	K562	blood:
2	chr4:99191861..99193936-chr4:99195305..99197274,2	K562	blood:
3	chr4:99187002..99188810-chr4:99194814..99197047,2	K562	blood:
4	chr4:99182748..99183661-chr6:89791487..89792153,2	Hela-S3	cervix:
5	chr4:99177447..99178988-chr4:99182434..99184206,2	K562	blood:
6	chr4:99166826..99169265-chr4:99180288..99182314,2	MCF-7	breast:
7	chr4:99062262..99068404-chr4:99178848..99183768,9	MCF-7	breast:
8	chr20:55837025..55838965-chr4:99178641..99181460,2	MCF-7	breast:
9	chr4:99171483..99174097-chr4:99174454..99176664,2	MCF-7	breast:
10	chr4:99211258..99213088-chr4:99217332..99219608,2	K562	blood:
11	chr4:99172163..99174911-chr4:99177261..99179829,2	K562	blood:
12	chr4:99171483..99174097-chr4:99174454..99176664,2	MCF-7	breast:
13	chr4:99183227..99185856-chr4:99306383..99308262,2	K562	blood:
14	chr4:99281508..99283161-chr4:99283275..99285281,2	MCF-7	breast:
15	chr4:99162667..99164867-chr4:99180598..99183232,2	K562	blood:
16	chr4:99190154..99192070-chr4:99204116..99206455,2	K562	blood:
17	chr4:99168522..99170647-chr4:99175545..99178223,2	K562	blood:
18	chr4:99180881..99185553-chr4:99191430..99194565,7	K562	blood:
19	chr4:99192442..99194622-chr4:99197664..99200193,4	K562	blood:
20	chr4:99284843..99287176-chr4:99294618..99297593,2	K562	blood:
21	chr4:99180881..99186469-chr4:99190114..99194249,6	K562	blood:
22	chr4:99275967..99278329-chr4:99281656..99283671,2	K562	blood:
23	chr4:99184237..99185798-chr4:99187404..99189518,2	K562	blood:
24	chr4:99118953..99122803-chr4:99123376..99126878,4	MCF-7	breast:
25	chr4:99063959..99066263-chr4:99181971..99183968,2	K562	blood:
26	chr4:99190517..99192752-chr4:99196803..99199545,2	MCF-7	breast:
27	chr4:99279969..99282662-chr4:99292297..99295112,2	K562	blood:
28	chr4:99181647..99184072-chr4:99579310..99582613,3	MCF-7	breast:
29	chr4:99190517..99192752-chr4:99196803..99199545,2	MCF-7	breast:
30	chr4:99181413..99182409-chr6:43737724..43738351,2	Hela-S3	cervix:
31	chr4:99181367..99183940-chr4:99249153..99251764,2	K562	blood:
32	chr4:99191861..99193936-chr4:99195305..99197274,2	K562	blood:
33	chr4:99235218..99237306-chr4:99238634..99241248,2	MCF-7	breast:
34	chr14:20923127..20923687-chr4:99285884..99286471,2	HCT-116	colon:
35	chr4:99173401..99175142-chr4:99176949..99179028,2	MCF-7	breast:
36	chr4:99126049..99128565-chr4:99168371..99171053,2	K562	blood:
37	chr4:99297214..99300431-chr4:99303291..99306046,3	K562	blood:
38	chr4:99180773..99182396-chr4:99197532..99199081,2	K562	blood:
39	chr4:99184237..99185798-chr4:99187404..99189518,2	K562	blood:
40	chr4:99179822..99184083-chr4:99191321..99196395,5	MCF-7	breast:
41	chr4:99211258..99213088-chr4:99217332..99219608,2	K562	blood:
42	chr4:99064189..99066561-chr4:99135372..99138314,2	MCF-7	breast:
43	chr4:99153861..99155781-chr4:99155970..99158168,2	K562	blood:
44	chr4:99177008..99180462-chr4:99180782..99182422,3	K562	blood:
45	chr4:99163747..99166432-chr4:99180932..99182707,2	MCF-7	breast:
46	chr4:99086672..99088660-chr4:99180652..99182426,2	MCF-7	breast:
47	chr4:99185202..99187066-chr4:99307470..99310118,2	K562	blood:
48	chr4:99166387..99172078-chr4:99179541..99183519,6	K562	blood:
49	chr19:47353883..47354410-chr4:99181779..99182612,2	HCT-116	colon:
50	chr4:99284843..99287176-chr4:99294618..99297593,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf37-2	chr4:99172839-99173156	ENSG00000214559.3
2	lnc-C4orf37-2	chr4:99182703-99182781	ENSG00000214559.3

No data

Variant related genes	Relation type
RAP1GDS1	TF binding region
ENSG00000214559	TF binding region
RAP1GDS1	CpG island
ENSG00000214559	CpG island
ENSG00000227220	chromatin interactions
ENSG00000146278	chromatin interactions
ENSG00000112715	chromatin interactions
ENSG00000103064	chromatin interactions
ENSG00000214559	chromatin interactions
ENSG00000101146	chromatin interactions
ENSG00000042753	chromatin interactions
ENSG00000168785	chromatin interactions
ENSG00000163116	chromatin interactions
ENSG00000260641	chromatin interactions
ENSG00000118523	chromatin interactions
ENSG00000184277	chromatin interactions
ENSG00000100823	chromatin interactions
ENSG00000138698	chromatin interactions
ENSG00000092094	chromatin interactions

Extended variants
information (count: 5716 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:5716 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6820913	chr4:99125659-99125660	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530991902	chr4:99125680-99125681	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs146732449	chr4:99125687-99125688	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs6821608	chr4:99125722-99125723	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs79110024	chr4:99125769-99125770	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs535501922	chr4:99125823-99125824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs28603037	chr4:99125844-99125845	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs576264970	chr4:99125879-99125880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543592158	chr4:99125880-99125881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182678603	chr4:99125884-99125885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187103982	chr4:99125897-99125898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs28484692	chr4:99125912-99125913	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs575719704	chr4:99125916-99125917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs28612663	chr4:99125929-99125930	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs58954707	chr4:99125993-99125994	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs573822001	chr4:99126002-99126003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540928005	chr4:99126005-99126006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558881011	chr4:99126006-99126007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141467999	chr4:99126008-99126009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190103819	chr4:99126009-99126010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1228205	chr4:99126020-99126021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182750208	chr4:99126032-99126033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1214913	chr4:99126059-99126060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563224052	chr4:99126067-99126068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111556024	chr4:99126092-99126093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545817049	chr4:99126100-99126101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530648750	chr4:99126104-99126105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529647566	chr4:99126115-99126116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187350800	chr4:99126119-99126120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111800135	chr4:99126131-99126132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1310042	chr4:99126136-99126137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs71612616	chr4:99126161-99126162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1310041	chr4:99126162-99126163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs56924513	chr4:99126193-99126194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs58634916	chr4:99126202-99126203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547305521	chr4:99126219-99126220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572018580	chr4:99126225-99126226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539011095	chr4:99126366-99126367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs200133865	chr4:99126370-99126371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7670303	chr4:99126372-99126373	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs569217909	chr4:99126392-99126393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs74918716	chr4:99126408-99126409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555221402	chr4:99126461-99126462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192184337	chr4:99126468-99126469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372438880	chr4:99126485-99126486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564103576	chr4:99126486-99126487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs578229043	chr4:99126491-99126492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534545439	chr4:99126495-99126496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139189291	chr4:99126666-99126667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552844470	chr4:99126755-99126756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Schizophrenia	19197363	CNVD
Melanoma	20688739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	16891809	CNVD
Bipolar disorder	19114987	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2307 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99123200-99131400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr4:99124200-99125800	Flanking Active TSS	Primary B cells from cord blood	blood
3	chr4:99124200-99125800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr4:99124200-99125800	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr4:99124200-99126200	Enhancers	Primary hematopoietic stem cells	blood
6	chr4:99124400-99125800	Flanking Active TSS	GM12878-XiMat	blood
7	chr4:99124600-99125800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr4:99124600-99125800	Enhancers	Fetal Thymus	thymus
9	chr4:99124600-99126000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr4:99125000-99125800	Enhancers	Primary T cells from cord blood	blood
11	chr4:99125200-99129800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr4:99125400-99125800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr4:99125400-99126400	Enhancers	Primary B cells from peripheral blood	blood
14	chr4:99125600-99126000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr4:99125800-99126400	Enhancers	GM12878-XiMat	blood
16	chr4:99125800-99126600	Enhancers	Primary B cells from cord blood	blood
17	chr4:99129800-99130200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:99131200-99132200	Enhancers	Liver	Liver
19	chr4:99131400-99132200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr4:99135400-99136200	Enhancers	Primary T cells from cord blood	blood
21	chr4:99147400-99148800	Enhancers	Liver	Liver
22	chr4:99151800-99153000	Enhancers	Fetal Brain Male	brain
23	chr4:99152400-99154400	Enhancers	Dnd41	blood
24	chr4:99153000-99153800	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr4:99153400-99153800	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr4:99153400-99153800	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr4:99153400-99153800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr4:99153400-99153800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr4:99153600-99153800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:99153800-99163000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr4:99154400-99158000	Weak transcription	Dnd41	blood
32	chr4:99157400-99157800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:99157400-99157800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr4:99157400-99157800	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr4:99157600-99158800	Enhancers	Fetal Thymus	thymus
36	chr4:99158000-99159200	Enhancers	Dnd41	blood
37	chr4:99159000-99160000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr4:99159200-99159800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:99159400-99160000	Enhancers	H1 Cell Line	embryonic stem cell
40	chr4:99159600-99160000	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr4:99163000-99164400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:99163200-99163800	Enhancers	HMEC	breast
43	chr4:99163400-99163800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr4:99163600-99164000	Enhancers	Muscle Satellite Cultured Cells	--
45	chr4:99164400-99180600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:99167800-99168400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:99171400-99171600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr4:99171600-99172200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr4:99171600-99181000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr4:99174000-99174200	Active TSS	Liver	Liver

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