Variant report

Variant	nsv536930
Chromosome Location	chr4:45682-123867
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1563)
CpG islands
(count:1344)
Chromatin interactive
region (count:68)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1563 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:55074-62562	K562	blood:	n/a	chr4:59934-59950 chr4:59538-59554
2	ARID3A	chr4:50859-54863	K562	blood:	n/a	n/a
3	ATF1	chr4:50536-53493	K562	blood:	n/a	n/a
4	ATF1	chr4:59954-63212	K562	blood:	n/a	n/a
5	ATF1	chr4:63649-65225	K562	blood:	n/a	n/a
6	ATF1	chr4:47552-48360	K562	blood:	n/a	n/a
7	ATF1	chr4:46422-47217	K562	blood:	n/a	n/a
8	ATF1	chr4:58355-59701	K562	blood:	n/a	n/a
9	ATF1	chr4:49243-50168	K562	blood:	n/a	n/a
10	ATF1	chr4:53699-58079	K562	blood:	n/a	n/a
11	ATF1	chr4:66516-66787	K562	blood:	n/a	n/a
12	ATF2	chr4:51468-52077	GM12878	blood:	n/a	n/a
13	ATF3	chr4:51522-52289	K562	blood:	n/a	n/a
14	BACH1	chr4:55097-61002	K562	blood:	n/a	n/a
15	BACH1	chr4:52750-53412	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:61301-63322	K562	blood:	n/a	n/a
17	BACH1	chr4:63639-64801	K562	blood:	n/a	n/a
18	BACH1	chr4:107111-107177	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr4:50515-54873	K562	blood:	n/a	n/a
20	BACH1	chr4:46413-47194	K562	blood:	n/a	n/a
21	BACH1	chr4:47659-50155	K562	blood:	n/a	n/a
22	BCL11A	chr4:51522-52034	GM12878	blood:	n/a	n/a
23	BCL3	chr4:67986-68640	K562	blood:	n/a	n/a
24	BCL3	chr4:58347-59453	K562	blood:	n/a	n/a
25	BCL3	chr4:64661-65243	K562	blood:	n/a	n/a
26	BCL3	chr4:64244-64642	K562	blood:	n/a	n/a
27	BCL3	chr4:61959-62618	K562	blood:	n/a	n/a
28	BCL3	chr4:57268-58100	K562	blood:	n/a	n/a
29	BCL3	chr4:51572-51881	GM12878	blood:	n/a	n/a
30	BCL3	chr4:65559-65938	K562	blood:	n/a	n/a
31	BCLAF1	chr4:54975-57752	K562	blood:	n/a	n/a
32	BDP1	chr4:57211-58198	Hela-S3	cervix:	n/a	n/a
33	BDP1	chr4:55568-56251	Hela-S3	cervix:	n/a	n/a
34	BDP1	chr4:61261-63046	Hela-S3	cervix:	n/a	n/a
35	BDP1	chr4:47688-48887	Hela-S3	cervix:	n/a	n/a
36	BDP1	chr4:65547-67327	Hela-S3	cervix:	n/a	n/a
37	BDP1	chr4:54340-59681	K562	blood:	n/a	chr4:55208-55217
38	BDP1	chr4:50490-52141	Hela-S3	cervix:	n/a	n/a
39	BDP1	chr4:46325-47270	Hela-S3	cervix:	n/a	n/a
40	BHLHE40	chr4:46726-47198	K562	blood:	n/a	n/a
41	BHLHE40	chr4:63551-65025	K562	blood:	n/a	n/a
42	BHLHE40	chr4:52234-52309	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:55414-56046	GM12878	blood:	n/a	n/a
44	BHLHE40	chr4:51105-52007	GM12878	blood:	n/a	n/a
45	BHLHE40	chr4:47562-48904	K562	blood:	n/a	n/a
46	BHLHE40	chr4:50478-61077	K562	blood:	n/a	chr4:53473-53489 chr4:53481-53497
47	BHLHE40	chr4:49218-50150	K562	blood:	n/a	n/a
48	BRCA1	chr4:50494-52206	GM12878	blood:	n/a	n/a
49	BRCA1	chr4:47596-48353	GM12878	blood:	n/a	n/a
50	BRCA1	chr4:58487-59194	GM12878	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:106702-106752	GM12891	blood:	n/a
2	chr4:53362-53412	NH-A	brain:	n/a
3	chr4:106702-106752	GM12891	blood:	n/a
4	chr4:53362-53412	NH-A	brain:	n/a
5	chr4:106702-106752	HRCEpiC	kidney:	n/a
6	chr4:53233-53283	Hepatocyte	liver:	n/a
7	chr4:53146-53196	BE2_C	brain:	n/a
8	chr4:53010-53060	IMR90	lung:	fetal
9	chr4:53109-53159	HUVEC	blood vessel:	n/a
10	chr4:53146-53196	HCT-116	colon:	n/a
11	chr4:107725-107775	HL-60	blood:	n/a
12	chr4:53548-53598	PrEC	prostate:	n/a
13	chr4:53548-53598	HCT-116	colon:	n/a
14	chr4:107725-107775	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:53025-53075	GM12891	blood:	n/a
16	chr4:121568-121618	SK-N-MC	brain:	n/a
17	chr4:106750-106800	HL-60	blood:	n/a
18	chr4:110130-110180	HCM	heart:	n/a
19	chr4:55967-56017	HNPCEpiC	eye:	n/a
20	chr4:53115-53165	PrEC	prostate:	n/a
21	chr4:53362-53412	MCF10A-Er-Src	breast:	n/a
22	chr4:53025-53075	AG09309	skin:	n/a
23	chr4:55967-56017	SK-N-SH_RA	brain:	n/a
24	chr4:53109-53159	PFSK-1	brain:	n/a
25	chr4:50006-50056	CMK	blood:	n/a
26	chr4:53010-53060	A549	lung:	n/a
27	chr4:53146-53196	ovcar-3	ovarian:	n/a
28	chr4:53270-53320	GM19239	blood:	n/a
29	chr4:53270-53320	IMR90	lung:	fetal
30	chr4:50006-50056	NT2-D1	testis:	n/a
31	chr4:106750-106800	Jurkat	blood:	n/a
32	chr4:53264-53314	HMEC	breast:	n/a
33	chr4:55967-56017	PANC-1	pancreas:	n/a
34	chr4:55967-56017	HCM	heart:	n/a
35	chr4:53109-53159	NHBE	bronchial:	n/a
36	chr4:107995-108045	PrEC	prostate:	n/a
37	chr4:110130-110180	HAEpiC	amniotic membrane:	n/a
38	chr4:106750-106800	SAEC	small airway:	n/a
39	chr4:53010-53060	ovcar-3	ovarian:	n/a
40	chr4:106702-106752	H1-hESC	embryonic stem cell:	embryo
41	chr4:53025-53075	Jurkat	blood:	n/a
42	chr4:106525-106575	HCM	heart:	n/a
43	chr4:107725-107775	HIPEpiC	eye:	n/a
44	chr4:53025-53075	SK-N-SH_RA	brain:	n/a
45	chr4:53115-53165	HRPEpiC	eye:	n/a
46	chr4:106525-106575	PrEC	prostate:	n/a
47	chr4:107176-107226	AG09319	gingival:	n/a
48	chr4:53010-53060	Hela-S3	cervix:	n/a
49	chr4:50006-50056	HEK293	kidney:	embryo
50	chr4:107725-107775	HEK293	kidney:	embryo

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:51557..54446-chr4:122221..124926,2	K562	blood:
2	chr4:58315..60128-chr6:30582159..30584362,2	K562	blood:
3	chr4:53253..54771-chr4:331507..334328,2	MCF-7	breast:
4	chr4:51861..55604-chr4:123095..126398,4	K562	blood:
5	chr4:68372..71217-chr4:81265..84111,2	K562	blood:
6	chr4:56572..58810-chr4:85301..87608,2	K562	blood:
7	chr4:93074..95113-chr4:96141..98752,2	K562	blood:
8	chr4:100612..102987-chr4:123401..125060,2	MCF-7	breast:
9	chr4:65052..66687-chr4:71710..74435,2	K562	blood:
10	chr4:101653..105420-chr4:105846..108846,4	MCF-7	breast:
11	chr4:53379..54171-chr4:206857..207651,2	K562	blood:
12	chr4:63202..65856-chr4:67720..70578,3	MCF-7	breast:
13	chr4:52592..54684-chr4:123109..125181,3	MCF-7	breast:
14	chr4:107591..110237-chr4:118674..121659,2	MCF-7	breast:
15	chr4:74721..76642-chr4:78877..81572,2	K562	blood:
16	chr4:105793..108047-chr4:122631..124537,2	MCF-7	breast:
17	chr4:56714..58749-chr8:129715262..129716946,2	MCF-7	breast:
18	chr4:70042..72884-chr4:73758..76524,4	K562	blood:
19	chr4:35278..37660-chr4:45954..48345,2	K562	blood:
20	chr4:113981..116306-chr4:118455..121404,2	MCF-7	breast:
21	chr4:66579..68102-chr4:88093..90808,2	K562	blood:
22	chr4:72577..74516-chr4:132936..135427,2	K562	blood:
23	chr4:102775..104891-chr4:123526..125879,2	MCF-7	breast:
24	chr4:51557..54446-chr4:122221..124926,2	K562	blood:
25	chr4:41249..43391-chr4:46700..48279,2	K562	blood:
26	chr4:113742..117319-chr4:123301..126989,4	MCF-7	breast:
27	chr4:52592..54684-chr4:123109..125181,3	MCF-7	breast:
28	chr4:107591..110237-chr4:118674..121659,2	MCF-7	breast:
29	chr4:70042..72884-chr4:73758..76524,4	K562	blood:
30	chr4:66579..68102-chr4:88093..90808,2	K562	blood:
31	chr4:114377..117349-chr4:123456..126203,3	MCF-7	breast:
32	chr4:54683..57001-chr4:109535..111840,2	K562	blood:
33	chr4:89325..91239-chr4:93291..94849,2	K562	blood:
34	chr4:85805..88516-chr4:153649..156824,3	K562	blood:
35	chr4:54876..56789-chr4:65058..66668,2	MCF-7	breast:
36	chr4:68372..71217-chr4:81265..84111,2	K562	blood:
37	chr4:35105..37664-chr4:54869..57777,2	K562	blood:
38	chr4:65052..66687-chr4:71710..74435,2	K562	blood:
39	chr4:46489..48476-chr4:152002..154876,2	K562	blood:
40	chr22:29136936..29138528-chr4:45551..48161,2	MCF-7	breast:
41	chr4:66452..69014-chr4:71272..74410,4	K562	blood:
42	chr4:49240..50788-chr4:51565..54254,2	MCF-7	breast:
43	chr4:52960..55808-chr4:61632..64740,3	MCF-7	breast:
44	chr4:123317..126012-chr4:128877..131305,3	MCF-7	breast:
45	chr4:61389..64231-chr4:132497..135116,2	K562	blood:
46	chr4:64276..66692-chr4:71520..73135,2	MCF-7	breast:
47	chr4:123751..126430-chr4:128432..130835,2	K562	blood:
48	chr4:117597..121763-chr4:123049..126351,6	K562	blood:
49	chr4:113981..116306-chr4:118455..121404,2	MCF-7	breast:
50	chr4:106774..108697-chr4:111039..113755,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
ENSG00000255436	TF binding region
ZNF718	TF binding region
ZNF595	TF binding region
ENSG00000207643	TF binding region
ENSG00000248302	TF binding region
ENSG00000250238	TF binding region
ENSG00000255436	CpG island
ZNF718	CpG island
ZNF595	CpG island
ENSG00000207643	CpG island
ENSG00000248302	CpG island
ENSG00000250238	CpG island
ENSG00000256143	chromatin interactions
ENSG00000211553	chromatin interactions
ENSG00000100209	chromatin interactions
ENSG00000248302	chromatin interactions
ENSG00000183765	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000248564	chromatin interactions
ENSG00000197701	chromatin interactions
ENSG00000250312	chromatin interactions
ENSG00000255436	chromatin interactions
ENSG00000207643	chromatin interactions
ENSG00000250238	chromatin interactions
ENSG00000131127	chromatin interactions

Extended variants
information (count: 3217 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3217 , 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	rs555784085	chr4:45686-45687	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs79053523	chr4:45759-45760	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs6599328	chr4:45791-45792	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs372974577	chr4:45819-45820	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs528416331	chr4:45890-45891	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs4021988	chr4:45899-45900	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs2859204	chr4:46044-46045	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs7688850	chr4:46102-46103	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs2859205	chr4:46119-46120	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs12642103	chr4:46157-46158	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs574043712	chr4:46159-46160	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs541475503	chr4:46169-46170	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs2859206	chr4:46171-46172	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs10446880	chr4:46186-46187	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs10446881	chr4:46193-46194	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs6852014	chr4:46206-46207	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs11946661	chr4:46207-46208	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs6846977	chr4:46238-46239	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs10446882	chr4:46245-46246	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs559766513	chr4:46246-46247	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs111230928	chr4:46249-46250	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs6830180	chr4:46277-46278	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs12503943	chr4:46316-46317	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs112413281	chr4:46338-46339	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs575953342	chr4:46382-46383	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs78028533	chr4:46384-46385	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs74786301	chr4:46386-46387	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs71654576	chr4:46398-46399	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs56955260	chr4:46399-46400	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs35786872	chr4:46400-46401	ZNF genes & repeats Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs571964481	chr4:46401-46402	ZNF genes & repeats Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs112217882	chr4:46473-46474	ZNF genes & repeats Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs7694212	chr4:46498-46499	ZNF genes & repeats Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs207464221	chr4:46516-46517	ZNF genes & repeats Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs12650945	chr4:46557-46558	ZNF genes & repeats Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs12499600	chr4:46623-46624	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs578256605	chr4:46632-46633	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs11946853	chr4:46691-46692	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs58963610	chr4:46729-46730	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs544909003	chr4:46814-46815	ZNF genes & repeats Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs545691051	chr4:46835-46836	ZNF genes & repeats Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs112633385	chr4:46921-46922	ZNF genes & repeats Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs112362902	chr4:46966-46967	ZNF genes & repeats Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs2859207	chr4:46967-46968	ZNF genes & repeats Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs368488367	chr4:47005-47006	ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs529202100	chr4:47030-47031	ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs368098932	chr4:47031-47032	ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs563890437	chr4:47038-47039	ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs531095230	chr4:47091-47092	ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs10446883	chr4:47127-47128	ZNF genes & repeats Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	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
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1732 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:38600-92000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:39000-46600	ZNF genes & repeats	Dnd41	blood
3	chr4:39800-71000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:39800-92200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr4:40200-91800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr4:40400-72200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
7	chr4:40600-60600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:41400-72400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
9	chr4:42600-46800	ZNF genes & repeats	Primary T cells from cord blood	blood
10	chr4:42600-48400	ZNF genes & repeats	Fetal Heart	heart
11	chr4:42600-48800	ZNF genes & repeats	Primary B cells from cord blood	blood
12	chr4:42800-69800	ZNF genes & repeats	Fetal Brain Male	brain
13	chr4:43600-48200	ZNF genes & repeats	Aorta	Aorta
14	chr4:44200-48400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:44800-46200	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
16	chr4:45400-46800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:45400-47600	Enhancers	K562	blood
18	chr4:46400-46600	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
19	chr4:46600-51000	Transcr. at gene 5' and 3'	Dnd41	blood
20	chr4:46600-59200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
21	chr4:46600-75600	ZNF genes & repeats	Fetal Brain Female	brain
22	chr4:46800-47000	Bivalent Enhancer	Esophagus	oesophagus
23	chr4:46800-47200	ZNF genes & repeats	Spleen	Spleen
24	chr4:46800-48400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
25	chr4:46800-49800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:47000-48200	ZNF genes & repeats	Thymus	Thymus
27	chr4:47200-47800	Weak transcription	Spleen	Spleen
28	chr4:47600-47800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr4:47600-47800	Genic enhancers	K562	blood
30	chr4:47600-94200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
31	chr4:47800-48000	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
32	chr4:47800-48000	Active TSS	Spleen	Spleen
33	chr4:47800-48200	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr4:47800-48200	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
35	chr4:47800-48200	Transcr. at gene 5' and 3'	K562	blood
36	chr4:47800-50800	ZNF genes & repeats	Primary T cells from cord blood	blood
37	chr4:47800-55200	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
38	chr4:48000-48200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
39	chr4:48200-48400	Flanking Active TSS	K562	blood
40	chr4:48200-49400	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr4:48200-49400	Weak transcription	Aorta	Aorta
42	chr4:48400-48600	Active TSS	K562	blood
43	chr4:48400-49400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:48400-49400	Weak transcription	Fetal Heart	heart
45	chr4:48600-48800	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
46	chr4:48600-48800	Flanking Active TSS	K562	blood
47	chr4:48800-49400	Active TSS	K562	blood
48	chr4:49400-49600	Flanking Active TSS	K562	blood
49	chr4:49400-49800	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
50	chr4:49400-50000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood

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