Variant report

Variant	esv2754445
Chromosome Location	chr4:36568-116981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1764)
CpG islands
(count:1284)
Chromatin interactive
region (count:66)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1764 , 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	chr4:36835-37141	K562	blood:	n/a	n/a
2	ARID3A	chr4:50859-54863	K562	blood:	n/a	n/a
3	ARID3A	chr4:55074-62562	K562	blood:	n/a	chr4:59934-59950 chr4:59538-59554
4	ARID3A	chr4:40826-41573	K562	blood:	n/a	n/a
5	ATF1	chr4:58355-59701	K562	blood:	n/a	n/a
6	ATF1	chr4:63649-65225	K562	blood:	n/a	n/a
7	ATF1	chr4:42873-44116	K562	blood:	n/a	n/a
8	ATF1	chr4:50536-53493	K562	blood:	n/a	n/a
9	ATF1	chr4:59954-63212	K562	blood:	n/a	n/a
10	ATF1	chr4:53699-58079	K562	blood:	n/a	n/a
11	ATF1	chr4:44475-45429	K562	blood:	n/a	n/a
12	ATF1	chr4:47552-48360	K562	blood:	n/a	n/a
13	ATF1	chr4:36709-37394	K562	blood:	n/a	n/a
14	ATF1	chr4:40925-41405	K562	blood:	n/a	n/a
15	ATF1	chr4:46422-47217	K562	blood:	n/a	n/a
16	ATF1	chr4:49243-50168	K562	blood:	n/a	n/a
17	ATF1	chr4:66516-66787	K562	blood:	n/a	n/a
18	ATF2	chr4:51468-52077	GM12878	blood:	n/a	n/a
19	ATF3	chr4:51522-52289	K562	blood:	n/a	n/a
20	BACH1	chr4:52750-53412	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr4:47659-50155	K562	blood:	n/a	n/a
22	BACH1	chr4:46413-47194	K562	blood:	n/a	n/a
23	BACH1	chr4:107111-107177	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr4:36885-37510	K562	blood:	n/a	n/a
25	BACH1	chr4:50515-54873	K562	blood:	n/a	n/a
26	BACH1	chr4:55097-61002	K562	blood:	n/a	n/a
27	BACH1	chr4:40109-40248	K562	blood:	n/a	n/a
28	BACH1	chr4:61301-63322	K562	blood:	n/a	n/a
29	BACH1	chr4:63639-64801	K562	blood:	n/a	n/a
30	BACH1	chr4:36609-36633	K562	blood:	n/a	n/a
31	BCL11A	chr4:51522-52034	GM12878	blood:	n/a	n/a
32	BCL3	chr4:67986-68640	K562	blood:	n/a	n/a
33	BCL3	chr4:51572-51881	GM12878	blood:	n/a	n/a
34	BCL3	chr4:65559-65938	K562	blood:	n/a	n/a
35	BCL3	chr4:58347-59453	K562	blood:	n/a	n/a
36	BCL3	chr4:61959-62618	K562	blood:	n/a	n/a
37	BCL3	chr4:57268-58100	K562	blood:	n/a	n/a
38	BCL3	chr4:64661-65243	K562	blood:	n/a	n/a
39	BCL3	chr4:64244-64642	K562	blood:	n/a	n/a
40	BCLAF1	chr4:54975-57752	K562	blood:	n/a	n/a
41	BDP1	chr4:54340-59681	K562	blood:	n/a	chr4:55208-55217
42	BDP1	chr4:65547-67327	Hela-S3	cervix:	n/a	n/a
43	BDP1	chr4:50490-52141	Hela-S3	cervix:	n/a	n/a
44	BDP1	chr4:57211-58198	Hela-S3	cervix:	n/a	n/a
45	BDP1	chr4:55568-56251	Hela-S3	cervix:	n/a	n/a
46	BDP1	chr4:61261-63046	Hela-S3	cervix:	n/a	n/a
47	BDP1	chr4:47688-48887	Hela-S3	cervix:	n/a	n/a
48	BDP1	chr4:42890-44145	Hela-S3	cervix:	n/a	n/a
49	BDP1	chr4:46325-47270	Hela-S3	cervix:	n/a	n/a
50	BHLHE40	chr4:51105-52007	GM12878	blood:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:53146-53196	IMR90	lung:	fetal
2	chr4:55967-56017	AoSMC	blood vessel:	n/a
3	chr4:107897-107947	U87	brain:	n/a
4	chr4:53146-53196	IMR90	lung:	fetal
5	chr4:55967-56017	AoSMC	blood vessel:	n/a
6	chr4:107897-107947	U87	brain:	n/a
7	chr4:107176-107226	Caco-2	colon:	n/a
8	chr4:53025-53075	MCF10A-Er-Src	breast:	n/a
9	chr4:107897-107947	LNCaP	prostate:	n/a
10	chr4:53010-53060	ProgFib	skin:	n/a
11	chr4:53025-53075	PrEC	prostate:	n/a
12	chr4:106702-106752	Hela-S3	cervix:	n/a
13	chr4:53264-53314	IMR90	lung:	fetal
14	chr4:53362-53412	ProgFib	skin:	n/a
15	chr4:53115-53165	NB4	blood:	n/a
16	chr4:53264-53314	GM12878	blood:	n/a
17	chr4:50006-50056	AG09309	skin:	n/a
18	chr4:55967-56017	GM12891	blood:	n/a
19	chr4:53115-53165	HCM	heart:	n/a
20	chr4:50006-50056	SK-N-SH	brain:	n/a
21	chr4:50006-50056	HL-60	blood:	n/a
22	chr4:107995-108045	AoSMC	blood vessel:	n/a
23	chr4:110130-110180	U87	brain:	n/a
24	chr4:106525-106575	HAEpiC	amniotic membrane:	n/a
25	chr4:53025-53075	HNPCEpiC	eye:	n/a
26	chr4:106702-106752	SK-N-MC	brain:	n/a
27	chr4:53548-53598	ProgFib	skin:	n/a
28	chr4:53362-53412	H1-hESC	embryonic stem cell:	embryo
29	chr4:53362-53412	SK-N-SH	brain:	n/a
30	chr4:106525-106575	LNCaP	prostate:	n/a
31	chr4:107176-107226	HRPEpiC	eye:	n/a
32	chr4:50006-50056	Caco-2	colon:	n/a
33	chr4:110130-110180	GM12891	blood:	n/a
34	chr4:107725-107775	AG04450	lung:	fetal
35	chr4:53010-53060	HCM	heart:	n/a
36	chr4:107995-108045	NHDF-neo	bronchial:	n/a
37	chr4:110130-110180	K562	blood:	n/a
38	chr4:53025-53075	HCPEpiC	choroid plexus:	n/a
39	chr4:107897-107947	HEK293	kidney:	embryo
40	chr4:106750-106800	ovcar-3	ovarian:	n/a
41	chr4:53548-53598	T-47D	breast:	n/a
42	chr4:53109-53159	BJ	skin:	n/a
43	chr4:107995-108045	PANC-1	pancreas:	n/a
44	chr4:107176-107226	HMEC	breast:	n/a
45	chr4:106750-106800	HRPEpiC	eye:	n/a
46	chr4:53362-53412	T-47D	breast:	n/a
47	chr4:53233-53283	AG09319	gingival:	n/a
48	chr4:53362-53412	GM12892	blood:	n/a
49	chr4:106702-106752	SK-N-SH	brain:	n/a
50	chr4:55967-56017	AG09309	skin:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:66579..68102-chr4:88093..90808,2	K562	blood:
2	chr4:64276..66692-chr4:71520..73135,2	MCF-7	breast:
3	chr4:113981..116306-chr4:118455..121404,2	MCF-7	breast:
4	chr4:49240..50788-chr4:51565..54254,2	MCF-7	breast:
5	chr4:53379..54171-chr4:206857..207651,2	K562	blood:
6	chr4:101653..105420-chr4:105846..108846,4	MCF-7	breast:
7	chr4:72577..74516-chr4:132936..135427,2	K562	blood:
8	chr4:54876..56789-chr4:65058..66668,2	MCF-7	breast:
9	chr4:54683..57001-chr4:109535..111840,2	K562	blood:
10	chr22:29136936..29138528-chr4:45551..48161,2	MCF-7	breast:
11	chr4:42552..45424-chr4:49559..51220,2	MCF-7	breast:
12	chr4:89325..91239-chr4:93291..94849,2	K562	blood:
13	chr4:74721..76642-chr4:78877..81572,2	K562	blood:
14	chr4:74721..76904-chr4:78146..80377,2	K562	blood:
15	chr4:67382..69502-chr4:124091..125813,2	MCF-7	breast:
16	chr4:46489..48476-chr4:152002..154876,2	K562	blood:
17	chr4:54683..57001-chr4:109535..111840,2	K562	blood:
18	chr4:100612..102987-chr4:123401..125060,2	MCF-7	breast:
19	chr4:41249..43391-chr4:46700..48279,2	K562	blood:
20	chr4:49240..50788-chr4:51565..54254,2	MCF-7	breast:
21	chr4:65052..66687-chr4:71710..74435,2	K562	blood:
22	chr4:74721..76642-chr4:78877..81572,2	K562	blood:
23	chr4:35278..37660-chr4:45954..48345,2	K562	blood:
24	chr4:58315..60128-chr6:30582159..30584362,2	K562	blood:
25	chr13:115098696..115100218-chr4:35677..37893,2	K562	blood:
26	chr4:70042..72884-chr4:73758..76524,4	K562	blood:
27	chr4:35105..37664-chr4:54869..57777,2	K562	blood:
28	chr4:107591..110237-chr4:118674..121659,2	MCF-7	breast:
29	chr4:53253..54771-chr4:331507..334328,2	MCF-7	breast:
30	chr4:56714..58749-chr8:129715262..129716946,2	MCF-7	breast:
31	chr4:54381..56089-chr4:130547..133394,2	MCF-7	breast:
32	chr4:66452..69014-chr4:71272..74410,4	K562	blood:
33	chr4:52592..54684-chr4:123109..125181,3	MCF-7	breast:
34	chr4:93074..95113-chr4:96141..98752,2	K562	blood:
35	chr4:26589..30670-chr4:53416..55763,3	K562	blood:
36	chr4:65052..66687-chr4:71710..74435,2	K562	blood:
37	chr4:41249..43391-chr4:46700..48279,2	K562	blood:
38	chr4:74721..76904-chr4:78146..80377,2	K562	blood:
39	chr4:66452..69014-chr4:71272..74410,4	K562	blood:
40	chr4:102775..104891-chr4:123526..125879,2	MCF-7	breast:
41	chr4:62303..64481-chr4:269727..272605,2	MCF-7	breast:
42	chr4:35278..37660-chr4:45954..48345,2	K562	blood:
43	chr4:66579..68102-chr4:88093..90808,2	K562	blood:
44	chr4:106774..108697-chr4:111039..113755,2	MCF-7	breast:
45	chr4:63202..65856-chr4:67720..70578,3	MCF-7	breast:
46	chr4:40027..42645-chr4:43576..46121,2	MCF-7	breast:
47	chr4:51557..54446-chr4:122221..124926,2	K562	blood:
48	chr4:61389..64231-chr4:132497..135116,2	K562	blood:
49	chr4:89325..91239-chr4:93291..94849,2	K562	blood:
50	chr4:47548..51523-chr4:51547..55504,6	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF732-9	chr4:75488-75675	NONHSAT094499
2	lnc-ZNF732-9	chr4:59869-59956	NONHSAT094499
3	lnc-ZNF732-9	chr4:49163-49618	NONHSAT094499
4	lnc-ZNF732-9	chr4:50562-50619	NONHSAT094499
5	lnc-ZNF732-9	chr4:75049-75288	NONHSAT094503
6	lnc-ZNF732-9	chr4:73409-74416	NONHSAT094503
7	lnc-ZNF732-9	chr4:85378-85550	NONHSAT094503
8	lnc-ZNF732-9	chr4:49448-50018	NONHSAT094500
9	lnc-ZNF732-9	chr4:48991-49850	NONHSAT094498
10	lnc-ZNF732-9	chr4:88200-88375	NONHSAT094499
11	lnc-ZNF732-8	chr4:105845-107000	NONHSAT094506
12	lnc-ZNF732-9	chr4:75049-75288	NONHSAT094499

No data

Variant related genes	Relation type
ENSG00000255436	TF binding region
ZNF595	TF binding region
ENSG00000207643	TF binding region
ENSG00000248302	TF binding region
ENSG00000250238	TF binding region
ENSG00000255436	CpG island
ZNF595	CpG island
ENSG00000207643	CpG island
ENSG00000248302	CpG island
ENSG00000250238	CpG island
ENSG00000248564	chromatin interactions
ENSG00000183765	chromatin interactions
ENSG00000250238	chromatin interactions
ENSG00000255436	chromatin interactions
ENSG00000197701	chromatin interactions
ENSG00000131127	chromatin interactions
ENSG00000100209	chromatin interactions
ENSG00000248302	chromatin interactions
ENSG00000229723	chromatin interactions
ENSG00000256143	chromatin interactions
ENSG00000250312	chromatin interactions
ENSG00000207643	chromatin interactions
ENSG00000222894	chromatin interactions

Extended variants
information (count: 3229 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3229 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1988520	chr4:36568-36569	ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs58232829	chr4:36667-36668	ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs4087043	chr4:36721-36722	ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs377301918	chr4:36750-36751	ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs58707166	chr4:36798-36799	ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369909144	chr4:36800-36801	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2859181	chr4:36877-36878	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs535629131	chr4:36920-36921	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs2859182	chr4:36958-36959	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs28706059	chr4:36975-36976	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs6821151	chr4:36989-36990	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs2859183	chr4:37018-37019	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554341974	chr4:37057-37058	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs58506903	chr4:37106-37107	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572078824	chr4:37120-37121	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs4097896	chr4:37177-37178	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539517035	chr4:37263-37264	ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs557808052	chr4:37265-37266	ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs3864123	chr4:37338-37339	ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs576072769	chr4:37385-37386	ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs543746833	chr4:37394-37395	ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs3884776	chr4:37399-37400	ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs1961922	chr4:37448-37449	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs9715808	chr4:37534-37535	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs376984172	chr4:37549-37550	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs60321032	chr4:37551-37552	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs7670122	chr4:37552-37553	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs3952228	chr4:37625-37626	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs4690170	chr4:37665-37666	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs4021987	chr4:37711-37712	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs56155921	chr4:37734-37735	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs4690245	chr4:37740-37741	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs9715650	chr4:37789-37790	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs573311687	chr4:37801-37802	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs61186592	chr4:37803-37804	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185128054	chr4:37808-37809	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs55756906	chr4:37822-37823	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs555323225	chr4:37868-37869	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs10452289	chr4:37908-37909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4021986	chr4:37913-37914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4029737	chr4:37940-37941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144070671	chr4:37967-37968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373321922	chr4:37973-37974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs9637724	chr4:37975-37976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375639575	chr4:37976-37977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4413906	chr4:37985-37986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149807174	chr4:37994-37995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6811365	chr4:38095-38096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4480240	chr4:38119-38120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56349226	chr4:38136-38137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Autism	22495309	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Williams Syndrome	20824207	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:1632 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:35600-37400	ZNF genes & repeats	Primary B cells from peripheral blood	blood
2	chr4:35600-37600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:35600-37600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr4:35600-37600	ZNF genes & repeats	Dnd41	blood
5	chr4:35800-37200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr4:35800-37400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:35800-37400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
8	chr4:35800-37400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
9	chr4:35800-37400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:35800-37400	ZNF genes & repeats	Aorta	Aorta
11	chr4:35800-37400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
12	chr4:35800-37400	ZNF genes & repeats	Fetal Brain Male	brain
13	chr4:35800-37400	Active TSS	Fetal Heart	heart
14	chr4:35800-37600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
15	chr4:35800-37600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:36000-37400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:36400-37400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
18	chr4:36600-37200	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
19	chr4:36600-37400	Bivalent Enhancer	Adipose Nuclei	Adipose
20	chr4:36600-37400	ZNF genes & repeats	Liver	Liver
21	chr4:36600-37400	ZNF genes & repeats	Thymus	Thymus
22	chr4:36800-37200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr4:36800-37400	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
24	chr4:36800-37400	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
25	chr4:37200-37400	Bivalent Enhancer	Ovary	ovary
26	chr4:37400-40400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:37400-40600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr4:37600-39000	Weak transcription	Dnd41	blood
29	chr4:38600-92000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:39000-46600	ZNF genes & repeats	Dnd41	blood
31	chr4:39800-71000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:39800-92200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
33	chr4:40200-41000	Enhancers	K562	blood
34	chr4:40200-41200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:40200-43200	ZNF genes & repeats	Liver	Liver
36	chr4:40200-45400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
37	chr4:40200-91800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
38	chr4:40400-42600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:40400-45200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
40	chr4:40400-72200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
41	chr4:40600-41200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:40600-41600	ZNF genes & repeats	Fetal Brain Male	brain
43	chr4:40600-42000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr4:40600-60600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr4:40800-41800	ZNF genes & repeats	Primary B cells from cord blood	blood
46	chr4:41000-41400	Flanking Active TSS	K562	blood
47	chr4:41000-43400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr4:41400-42200	Enhancers	K562	blood
49	chr4:41400-72400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
50	chr4:41800-42000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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