Variant report

Variant	esv1793428
Chromosome Location	chr4:110340134-110355591
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1195)
CpG islands
(count:673)
Chromatin interactive
region (count:31)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1195 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:110354211-110354931	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:110343605-110343884	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:110343526-110343824	K562	blood:	n/a	n/a
4	ATF2	chr4:110354473-110355010	GM12878	blood:	n/a	n/a
5	ATF3	chr4:110354491-110354811	A549	lung:	n/a	n/a
6	ATF3	chr4:110354590-110355029	K562	blood:	n/a	n/a
7	BACH1	chr4:110354710-110354946	K562	blood:	n/a	n/a
8	BACH1	chr4:110355512-110355621	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:110354432-110355016	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:110345493-110345985	GM12878	blood:	n/a	n/a
11	BCLAF1	chr4:110354481-110355062	GM12878	blood:	n/a	chr4:110354645-110354658 chr4:110354725-110354738 chr4:110354752-110354765
12	BCLAF1	chr4:110354396-110355310	GM12878	blood:	n/a	chr4:110354645-110354658 chr4:110354725-110354738 chr4:110354752-110354765
13	BHLHE40	chr4:110355545-110356014	GM12878	blood:	n/a	chr4:110355801-110355817
14	BHLHE40	chr4:110345646-110345989	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:110354543-110355029	GM12878	blood:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
16	BHLHE40	chr4:110354288-110355032	K562	blood:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
17	BHLHE40	chr4:110355440-110355810	HepG2	liver:	n/a	n/a
18	BHLHE40	chr4:110343674-110343895	K562	blood:	n/a	n/a
19	BHLHE40	chr4:110354627-110354827	A549	lung:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
20	BHLHE40	chr4:110345644-110346005	K562	blood:	n/a	n/a
21	BHLHE40	chr4:110354469-110355120	HepG2	liver:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
22	BRCA1	chr4:110354768-110354947	GM12878	blood:	n/a	n/a
23	BRCA1	chr4:110354583-110354804	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr4:110354689-110354889	HepG2	liver:	n/a	n/a
25	BRCA1	chr4:110343541-110343886	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr4:110354275-110355033	K562	blood:	n/a	n/a
27	CCNT2	chr4:110354501-110355331	K562	blood:	n/a	n/a
28	CEBPB	chr4:110353487-110353788	HepG2	liver:	n/a	chr4:110353616-110353627 chr4:110353617-110353628 chr4:110353616-110353629 chr4:110353618-110353627
29	CEBPB	chr4:110340917-110341272	K562	blood:	n/a	n/a
30	CEBPB	chr4:110353435-110354161	IMR90	lung:	n/a	chr4:110353616-110353627 chr4:110353617-110353628 chr4:110353616-110353629 chr4:110353618-110353627 chr4:110353881-110353892
31	CEBPB	chr4:110340837-110341268	K562	blood:	n/a	n/a
32	CEBPB	chr4:110346450-110346457	K562	blood:	n/a	n/a
33	CEBPB	chr4:110353476-110354386	Hela-S3	cervix:	n/a	chr4:110353616-110353627 chr4:110353617-110353628 chr4:110353616-110353629 chr4:110353618-110353627 chr4:110353881-110353892
34	CEBPB	chr4:110340941-110341246	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:110354600-110354908	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr4:110353478-110354091	A549	lung:	n/a	chr4:110353616-110353627 chr4:110353617-110353628 chr4:110353616-110353629 chr4:110353618-110353627 chr4:110353881-110353892
37	CEBPB	chr4:110344197-110344320	K562	blood:	n/a	n/a
38	CEBPB	chr4:110343643-110344318	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr4:110353519-110354064	K562	blood:	n/a	chr4:110353616-110353627 chr4:110353617-110353628 chr4:110353616-110353629 chr4:110353618-110353627 chr4:110353881-110353892
40	CEBPB	chr4:110354588-110355000	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:110340905-110341249	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPD	chr4:110354505-110355207	HepG2	liver:	n/a	n/a
43	CHD1	chr4:110355474-110355809	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr4:110354216-110354720	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr4:110354529-110354915	GM12878	blood:	n/a	n/a
46	CHD2	chr4:110343622-110343823	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr4:110354323-110355067	HepG2	liver:	n/a	n/a
48	CHD2	chr4:110345370-110345383	HepG2	liver:	n/a	n/a
49	CHD2	chr4:110354553-110355068	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr4:110354495-110354992	H1-hESC	embryonic stem cell:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:110354354-110354404	AG04449	skin:	fetal
2	chr4:110354896-110354946	HAEpiC	amniotic membrane:	n/a
3	chr4:110354354-110354404	AG04449	skin:	fetal
4	chr4:110354896-110354946	HAEpiC	amniotic membrane:	n/a
5	chr4:110354674-110354724	HEEpiC	esophagus:	n/a
6	chr4:110352980-110353030	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:110354820-110354870	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:110355525-110355575	BJ	skin:	n/a
9	chr4:110355447-110355497	CMK	blood:	n/a
10	chr4:110355472-110355522	HEK293	kidney:	embryo
11	chr4:110354923-110354973	HepG2	liver:	n/a
12	chr4:110354923-110354973	H1-hESC	embryonic stem cell:	embryo
13	chr4:110355472-110355522	AG09309	skin:	n/a
14	chr4:110352891-110352941	AG09319	gingival:	n/a
15	chr4:110354354-110354404	HNPCEpiC	eye:	n/a
16	chr4:110354923-110354973	AG04449	skin:	fetal
17	chr4:110355472-110355522	HCF	heart:	n/a
18	chr4:110352980-110353030	HepG2	liver:	n/a
19	chr4:110355472-110355522	AG04450	lung:	fetal
20	chr4:110355472-110355522	MCF-7	breast:	n/a
21	chr4:110352980-110353030	PANC-1	pancreas:	n/a
22	chr4:110354443-110354493	Caco-2	colon:	n/a
23	chr4:110354896-110354946	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:110354896-110354946	H1-hESC	embryonic stem cell:	embryo
25	chr4:110354820-110354870	SK-N-SH	brain:	n/a
26	chr4:110352980-110353030	NHBE	bronchial:	n/a
27	chr4:110352891-110352941	HL-60	blood:	n/a
28	chr4:110354896-110354946	HRCEpiC	kidney:	n/a
29	chr4:110355525-110355575	CMK	blood:	n/a
30	chr4:110354820-110354870	HCT-116	colon:	n/a
31	chr4:110354923-110354973	HRCEpiC	kidney:	n/a
32	chr4:110354443-110354493	HMEC	breast:	n/a
33	chr4:110352891-110352941	ovcar-3	ovarian:	n/a
34	chr4:110355472-110355522	PANC-1	pancreas:	n/a
35	chr4:110352980-110353030	MCF-7	breast:	n/a
36	chr4:110355525-110355575	PrEC	prostate:	n/a
37	chr4:110354820-110354870	SK-N-SH_RA	brain:	n/a
38	chr4:110354923-110354973	Jurkat	blood:	n/a
39	chr4:110355447-110355497	HRCEpiC	kidney:	n/a
40	chr4:110354354-110354404	HAEpiC	amniotic membrane:	n/a
41	chr4:110354443-110354493	AG10803	skin:	n/a
42	chr4:110355472-110355522	SK-N-SH	brain:	n/a
43	chr4:110354443-110354493	MCF-7	breast:	n/a
44	chr4:110355525-110355575	HRE	kidney:	n/a
45	chr4:110352980-110353030	NH-A	brain:	n/a
46	chr4:110354820-110354870	MCF-7	breast:	n/a
47	chr4:110354674-110354724	CMK	blood:	n/a
48	chr4:110354674-110354724	HIPEpiC	eye:	n/a
49	chr4:110354820-110354870	HAEpiC	amniotic membrane:	n/a
50	chr4:110352980-110353030	GM12878	blood:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:110346840..110352517-chr4:110352798..110357196,11	MCF-7	breast:
2	chr4:110354421..110354923-chr7:44084218..44084744,2	Hela-S3	cervix:
3	chr4:110343261..110343867-chr4:110747612..110748494,2	K562	blood:
4	chr4:110343481..110344216-chr4:110495251..110496139,3	K562	blood:
5	chr4:110353323..110356452-chr4:110478874..110481567,4	MCF-7	breast:
6	chr4:110343664..110344216-chr4:111436112..111436708,2	K562	blood:
7	chr4:110343683..110344194-chr4:110898737..110899276,3	K562	blood:
8	chr4:110343690..110344246-chr4:110624228..110624826,2	K562	blood:
9	chr4:110351870..110353542-chr4:110355047..110357946,2	MCF-7	breast:
10	chr4:110349880..110352137-chr4:110747017..110748778,2	K562	blood:
11	chr4:110341049..110342014-chr4:110579969..110580500,2	MCF-7	breast:
12	chr4:110353826..110356085-chr4:110735938..110738635,3	MCF-7	breast:
13	chr4:110348791..110349300-chr4:110495675..110496212,2	MCF-7	breast:
14	chr4:110351870..110353542-chr4:110355047..110357946,2	MCF-7	breast:
15	chr4:110351897..110354482-chr4:110431012..110433361,3	MCF-7	breast:
16	chr4:110344454..110346906-chr4:110479620..110481792,2	MCF-7	breast:
17	chr4:109540362..109542277-chr4:110353620..110356489,2	K562	blood:
18	chr4:110354680..110356371-chr4:110650734..110652526,2	MCF-7	breast:
19	chr4:110343403..110344007-chr4:112552340..112552988,2	MCF-7	breast:
20	chr4:110343302..110344212-chr4:110573149..110574182,3	K562	blood:
21	chr4:110343313..110344215-chr4:111439563..111440337,2	K562	blood:
22	chr4:110348580..110349332-chr4:110747353..110748131,2	MCF-7	breast:
23	chr4:110346614..110351456-chr4:110352636..110356029,5	MCF-7	breast:
24	chr4:110352891..110355275-chr4:110649929..110651520,2	MCF-7	breast:
25	chr4:110350104..110352430-chr4:110610795..110612756,2	K562	blood:
26	chr4:110343609..110345169-chr4:110353025..110355277,2	K562	blood:
27	chr4:110353269..110354820-chr4:110577196..110580148,2	MCF-7	breast:
28	chr4:110348797..110349339-chr4:110495526..110496188,3	MCF-7	breast:
29	chr4:110343687..110344193-chr4:110796753..110797352,2	K562	blood:
30	chr4:110350104..110351990-chr4:110609862..110612756,2	K562	blood:
31	chr14:105261712..105263242-chr4:110355266..110356786,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL25A1-1	chr4:110353104-110353262	NONHSAT097782
2	lnc-COL25A1-1	chr4:110351838-110351936	NONHSAT097782
3	lnc-COL25A1-1	chr4:110352848-110352902	ENSG00000247950
4	lnc-COL25A1-1	chr4:110352848-110352902	ENSG00000247950
5	lnc-COL25A1-1	chr4:110352848-110352904	NONHSAT097782
6	lnc-COL25A1-1	chr4:110354890-110354920	ENSG00000247950
7	lnc-COL25A1-1	chr4:110351736-110351916	ENSG00000247950
8	lnc-COL25A1-1	chr4:110354890-110354973	ENSG00000247950
9	lnc-COL25A1-1	chr4:110351119-110351936	ENSG00000247950
10	lnc-COL25A1-1	chr4:110354890-110354939	ENSG00000247950
11	lnc-COL25A1-1	chr4:110352848-110352902	ENSG00000247950

No data

Variant related genes	Relation type
SEC24B-AS1	TF binding region
SEC24B	TF binding region
SEC24B-AS1	CpG island
SEC24B	CpG island
ENSG00000138794	chromatin interactions
ENSG00000138802	chromatin interactions
ENSG00000247950	chromatin interactions
ENSG00000234492	chromatin interactions
ENSG00000109534	chromatin interactions
ENSG00000123739	chromatin interactions
ENSG00000272795	chromatin interactions
ENSG00000109475	chromatin interactions
ENSG00000142208	chromatin interactions
ENSG00000136279	chromatin interactions
ENSG00000005059	chromatin interactions
PTK2B	miRNA target sites
PTK2	miRNA target sites
ITFG1	miRNA target sites
ATP6V1C1	miRNA target sites
CCNG1	miRNA target sites
PTP4A1	miRNA target sites
NCAPG	miRNA target sites
G3BP1	miRNA target sites

Extended variants
information (count: 497 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12648138	chr4:110340134-110340135	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529372654	chr4:110340221-110340222	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs547134840	chr4:110340269-110340270	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs536123142	chr4:110340273-110340274	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs538878576	chr4:110340336-110340337	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs558742154	chr4:110340337-110340338	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs186414849	chr4:110340341-110340342	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs80181412	chr4:110340363-110340364	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs138351277	chr4:110340376-110340377	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs78847884	chr4:110340386-110340387	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs374333850	chr4:110340420-110340421	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs118056361	chr4:110340504-110340505	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs540629339	chr4:110340601-110340602	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113930223	chr4:110340613-110340614	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9307330	chr4:110340642-110340643	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367759747	chr4:110340703-110340704	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533114282	chr4:110340706-110340707	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370189408	chr4:110340796-110340797	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546288506	chr4:110340798-110340799	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149215197	chr4:110340806-110340807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531361246	chr4:110340815-110340816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191579929	chr4:110340849-110340850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78256053	chr4:110340890-110340891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181626165	chr4:110340996-110340997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546970431	chr4:110340998-110340999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563703630	chr4:110340999-110341000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532885387	chr4:110341001-110341002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186707236	chr4:110341002-110341003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569442896	chr4:110341032-110341033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538046911	chr4:110341033-110341034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548911981	chr4:110341054-110341055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374648191	chr4:110341085-110341086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568637908	chr4:110341147-110341148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534220155	chr4:110341189-110341190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554226163	chr4:110341223-110341224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577283980	chr4:110341432-110341433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539945018	chr4:110341439-110341440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551710399	chr4:110341469-110341470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146884984	chr4:110341472-110341473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558101915	chr4:110341514-110341515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201468696	chr4:110341554-110341555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191209704	chr4:110341607-110341608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562047029	chr4:110341624-110341625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11098034	chr4:110341648-110341649	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs374519810	chr4:110341651-110341652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10709718	chr4:110341661-110341662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183297334	chr4:110341727-110341728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186921888	chr4:110341762-110341763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs10025781	chr4:110341780-110341781	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs189711510	chr4:110341783-110341784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	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
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Schizophrenia	19546859	CNVD
Colorectal cancer	16272173	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110328800-110353600	Weak transcription	Brain Germinal Matrix	brain
2	chr4:110332400-110340400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:110333200-110352800	Weak transcription	Fetal Intestine Small	intestine
4	chr4:110333400-110345400	Weak transcription	Fetal Stomach	stomach
5	chr4:110333800-110353400	Weak transcription	HSMM	muscle
6	chr4:110334400-110351600	Weak transcription	Fetal Muscle Leg	muscle
7	chr4:110334800-110340200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:110336200-110340200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr4:110336600-110340200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr4:110336600-110340400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr4:110336800-110340200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr4:110337400-110340200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:110337600-110340200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr4:110339600-110341600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr4:110339600-110341600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr4:110339800-110340200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:110339800-110341400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:110339800-110341400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:110340000-110341400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr4:110340000-110341400	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr4:110340200-110340800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:110340200-110340800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr4:110340200-110341000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr4:110340200-110341000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:110340200-110341600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr4:110340200-110341600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr4:110340200-110341800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr4:110340200-110341800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr4:110340200-110342600	Enhancers	H9 Cell Line	embryonic stem cell
30	chr4:110340200-110343800	Weak transcription	Right Atrium	heart
31	chr4:110340400-110340600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr4:110340400-110341000	Enhancers	Fetal Kidney	kidney
33	chr4:110340400-110341400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr4:110340600-110341000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr4:110340800-110342200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr4:110340800-110343800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:110341000-110341200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr4:110341000-110341400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr4:110341000-110343400	Weak transcription	Fetal Kidney	kidney
40	chr4:110341200-110341400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:110341200-110343800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr4:110341400-110341600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr4:110341400-110343000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr4:110341400-110343200	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr4:110341400-110343400	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr4:110341400-110343400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr4:110341400-110350000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:110341600-110343200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr4:110341600-110343400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr4:110341600-110343400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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