Variant report

Variant	esv3378886
Chromosome Location	chr3:23846373-23849821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:589)
CpG islands
(count:732)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:23846044-23846438	K562	blood:	n/a	n/a
2	ATF2	chr3:23847243-23847664	GM12878	blood:	n/a	n/a
3	BACH1	chr3:23848521-23848904	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:23847048-23847622	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr3:23847347-23847591	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:23847337-23847629	GM12878	blood:	n/a	n/a
7	BCL3	chr3:23847315-23847925	GM12878	blood:	n/a	chr3:23847878-23847891
8	BCLAF1	chr3:23847259-23847625	GM12878	blood:	n/a	n/a
9	BCLAF1	chr3:23847184-23847768	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:23847053-23847799	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:23846641-23847043	A549	lung:	n/a	chr3:23846798-23846807
12	BHLHE40	chr3:23848496-23848696	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:23848959-23849272	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:23846628-23847665	K562	blood:	n/a	chr3:23846798-23846807
15	BHLHE40	chr3:23846605-23847174	HepG2	liver:	n/a	chr3:23846798-23846807
16	CBX3	chr3:23847303-23847625	K562	blood:	n/a	n/a
17	CCNT2	chr3:23847378-23848866	K562	blood:	n/a	chr3:23847925-23847934
18	CEBPB	chr3:23847344-23847587	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:23847396-23847595	K562	blood:	n/a	n/a
20	CHD1	chr3:23847118-23847583	GM12878	blood:	n/a	n/a
21	CHD1	chr3:23848444-23849462	GM12878	blood:	n/a	n/a
22	CHD2	chr3:23847141-23848459	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr3:23847336-23848315	K562	blood:	n/a	n/a
24	CHD2	chr3:23848566-23848956	GM12878	blood:	n/a	n/a
25	CHD2	chr3:23848210-23848605	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr3:23847434-23847481	HepG2	liver:	n/a	n/a
27	CHD2	chr3:23848022-23848241	GM12878	blood:	n/a	n/a
28	CHD2	chr3:23847062-23847796	GM12878	blood:	n/a	n/a
29	CREB1	chr3:23847162-23847775	GM12878	blood:	n/a	n/a
30	CREB1	chr3:23847083-23847600	A549	lung:	n/a	n/a
31	CTCF	chr3:23847160-23847310	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr3:23847440-23847590	GM12874	blood:	n/a	n/a
33	CTCF	chr3:23847140-23847290	BJ	skin:	n/a	n/a
34	CTCF	chr3:23847060-23847210	HRE	kidney:	n/a	chr3:23847105-23847113
35	CTCF	chr3:23847120-23847270	AG04449	skin:	n/a	n/a
36	CTCF	chr3:23847440-23847590	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr3:23847060-23847210	HAc	cerebellar:	n/a	chr3:23847105-23847113
38	CTCF	chr3:23847120-23847270	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr3:23847100-23847250	GM12874	blood:	n/a	chr3:23847105-23847113
40	CTCF	chr3:23847160-23847310	GM12864	blood:	n/a	n/a
41	CTCF	chr3:23847120-23847270	AG09319	gingival:	n/a	n/a
42	CTCF	chr3:23847401-23847592	GM12892	blood:	n/a	n/a
43	CTCF	chr3:23847120-23847270	HMF	breast:	n/a	n/a
44	CTCF	chr3:23847260-23847410	HCM	heart:	n/a	n/a
45	CTCF	chr3:23847415-23847453	GM12891	blood:	n/a	n/a
46	CTCF	chr3:23848640-23848790	HAc	cerebellar:	n/a	n/a
47	CTCF	chr3:23848620-23848770	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr3:23847040-23847190	GM12870	blood:	n/a	chr3:23847105-23847113
49	CTCF	chr3:23847400-23847550	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr3:23847204-23847251	A549	lung:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:23846810-23846860	Hela-S3	cervix:	n/a
2	chr3:23847480-23847530	HMEC	breast:	n/a
3	chr3:23847020-23847070	NH-A	brain:	n/a
4	chr3:23849114-23849164	HepG2	liver:	n/a
5	chr3:23847297-23847347	HCT-116	colon:	n/a
6	chr3:23847480-23847530	PFSK-1	brain:	n/a
7	chr3:23847480-23847530	AoSMC	blood vessel:	n/a
8	chr3:23848132-23848182	PANC-1	pancreas:	n/a
9	chr3:23846692-23846742	H1-hESC	embryonic stem cell:	embryo
10	chr3:23849114-23849164	HMEC	breast:	n/a
11	chr3:23848132-23848182	GM06990	blood:	n/a
12	chr3:23846692-23846742	Hela-S3	cervix:	n/a
13	chr3:23848132-23848182	HAEpiC	amniotic membrane:	n/a
14	chr3:23848512-23848562	AG10803	skin:	n/a
15	chr3:23846692-23846742	GM12892	blood:	n/a
16	chr3:23847295-23847345	HEK293	kidney:	embryo
17	chr3:23847297-23847347	Hela-S3	cervix:	n/a
18	chr3:23849114-23849164	H1-hESC	embryonic stem cell:	embryo
19	chr3:23847297-23847347	HRPEpiC	eye:	n/a
20	chr3:23847295-23847345	GM06990	blood:	n/a
21	chr3:23846692-23846742	GM19239	blood:	n/a
22	chr3:23846692-23846742	HMEC	breast:	n/a
23	chr3:23847297-23847347	PrEC	prostate:	n/a
24	chr3:23849114-23849164	HIPEpiC	eye:	n/a
25	chr3:23846692-23846742	SK-N-SH_RA	brain:	n/a
26	chr3:23849114-23849164	T-47D	breast:	n/a
27	chr3:23847480-23847530	PANC-1	pancreas:	n/a
28	chr3:23847480-23847530	SK-N-MC	brain:	n/a
29	chr3:23846810-23846860	A549	lung:	n/a
30	chr3:23849114-23849164	CMK	blood:	n/a
31	chr3:23846810-23846860	NHDF-neo	bronchial:	n/a
32	chr3:23846810-23846860	LNCaP	prostate:	n/a
33	chr3:23847297-23847347	BE2_C	brain:	n/a
34	chr3:23847297-23847347	GM12878	blood:	n/a
35	chr3:23846810-23846860	MCF-7	breast:	n/a
36	chr3:23847990-23848040	BJ	skin:	n/a
37	chr3:23847295-23847345	AG10803	skin:	n/a
38	chr3:23848512-23848562	Caco-2	colon:	n/a
39	chr3:23848563-23848613	NB4	blood:	n/a
40	chr3:23848512-23848562	GM19239	blood:	n/a
41	chr3:23848512-23848562	Jurkat	blood:	n/a
42	chr3:23847480-23847530	BJ	skin:	n/a
43	chr3:23847020-23847070	SAEC	small airway:	n/a
44	chr3:23847295-23847345	CMK	blood:	n/a
45	chr3:23848512-23848562	NB4	blood:	n/a
46	chr3:23849114-23849164	BJ	skin:	n/a
47	chr3:23847990-23848040	NB4	blood:	n/a
48	chr3:23846810-23846860	ECC-1	luminal epithelium:	n/a
49	chr3:23849114-23849164	HCM	heart:	n/a
50	chr3:23847295-23847345	GM12892	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:23845112..23848622-chr3:23958029..23961906,4	K562	blood:
2	chr3:23846193..23848940-chr3:24535065..24537255,2	K562	blood:
3	chr3:23849778..23851567-chr3:23881436..23883574,2	K562	blood:
4	chr3:23846531..23848270-chr3:23987055..23988984,2	MCF-7	breast:
5	chr3:23243031..23244851-chr3:23845499..23848237,2	MCF-7	breast:
6	chr3:23845393..23848355-chr3:23958587..23960710,4	K562	blood:
7	chr3:23848988..23853074-chr3:23957156..23960234,5	K562	blood:
8	chr1:166868912..166869506-chr3:23849255..23849755,2	MCF-7	breast:
9	chr3:23846380..23850116-chr3:23956700..23960461,6	MCF-7	breast:

No data

Variant related genes	Relation type
UBE2E1-AS1	TF binding region
UBE2E1	TF binding region
UBE2E1-AS1	CpG island
UBE2E1	CpG island
ENSG00000228791	chromatin interactions
ENSG00000197885	chromatin interactions
ENSG00000233153	chromatin interactions
ENSG00000174748	chromatin interactions
ENSG00000182247	chromatin interactions
ENSG00000151090	chromatin interactions
ENSG00000174738	chromatin interactions

Extended variants
information (count: 101 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:101 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532465043	chr3:23846396-23846397	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs534710965	chr3:23846495-23846496	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs115814373	chr3:23846549-23846550	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs554521909	chr3:23846551-23846552	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs565693834	chr3:23846624-23846625	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs73148287	chr3:23846679-23846680	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs554706663	chr3:23846692-23846693	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs569725070	chr3:23846703-23846704	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs536736250	chr3:23846715-23846716	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs3762768	chr3:23846724-23846725	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs145242772	chr3:23846740-23846741	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs556748157	chr3:23846893-23846894	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs578100638	chr3:23846939-23846940	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs17013751	chr3:23846940-23846941	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs181533347	chr3:23847003-23847004	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs374356146	chr3:23847081-23847082	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs572112168	chr3:23847100-23847101	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs557366452	chr3:23847119-23847120	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs3762767	chr3:23847211-23847212	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs545948688	chr3:23847223-23847224	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs543529408	chr3:23847233-23847234	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs374912841	chr3:23847300-23847301	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs565122049	chr3:23847312-23847313	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs567768679	chr3:23847373-23847374	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs368219911	chr3:23847374-23847375	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs532172314	chr3:23847393-23847394	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs547690251	chr3:23847495-23847496	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs7646772	chr3:23847670-23847671	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs529721842	chr3:23847709-23847710	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs111481071	chr3:23847849-23847850	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs569662435	chr3:23847852-23847853	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs537187155	chr3:23847857-23847858	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs558337065	chr3:23847930-23847931	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs571835829	chr3:23847968-23847969	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs538811625	chr3:23848073-23848074	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs554055116	chr3:23848154-23848155	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs572448077	chr3:23848280-23848281	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs542911394	chr3:23848291-23848292	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs72625887	chr3:23848336-23848337	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs576342260	chr3:23848359-23848360	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs543912040	chr3:23848416-23848417	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs565204868	chr3:23848418-23848419	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs367722984	chr3:23848457-23848458	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs576969080	chr3:23848476-23848477	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs191488086	chr3:23848512-23848513	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs151264152	chr3:23848523-23848524	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs530060259	chr3:23848530-23848531	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs548490620	chr3:23848567-23848568	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs563290643	chr3:23848569-23848570	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs76464485	chr3:23848584-23848585	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23840000-23847000	Weak transcription	Right Atrium	heart
2	chr3:23840200-23846800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr3:23840200-23846800	Weak transcription	GM12878-XiMat	blood
4	chr3:23843800-23846600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:23843800-23846800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr3:23844400-23846800	Enhancers	Fetal Intestine Small	intestine
7	chr3:23844400-23846800	Weak transcription	Small Intestine	intestine
8	chr3:23845400-23846600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:23845600-23846800	Weak transcription	Fetal Lung	lung
10	chr3:23845800-23846600	Enhancers	A549	lung
11	chr3:23846000-23846800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr3:23846000-23846800	Enhancers	Primary hematopoietic stem cells	blood
13	chr3:23846000-23846800	Enhancers	Fetal Intestine Large	intestine
14	chr3:23846000-23846800	Enhancers	K562	blood
15	chr3:23846000-23847000	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr3:23846200-23846400	Flanking Active TSS	Duodenum Mucosa	Duodenum
17	chr3:23846200-23846600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr3:23846200-23846600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr3:23846200-23846600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
20	chr3:23846200-23846600	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr3:23846200-23846800	Enhancers	Fetal Kidney	kidney
22	chr3:23846200-23847000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr3:23846200-23847600	Active TSS	Fetal Brain Male	brain
24	chr3:23846400-23846600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:23846400-23846800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr3:23846400-23846800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr3:23846400-23846800	Enhancers	Duodenum Mucosa	Duodenum
28	chr3:23846600-23846800	Active TSS	H1 Cell Line	embryonic stem cell
29	chr3:23846600-23846800	Flanking Active TSS	H9 Cell Line	embryonic stem cell
30	chr3:23846600-23846800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr3:23846600-23846800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr3:23846600-23846800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr3:23846600-23846800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
34	chr3:23846600-23846800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:23846600-23846800	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr3:23846600-23846800	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr3:23846600-23846800	Enhancers	Primary B cells from cord blood	blood
38	chr3:23846600-23846800	Enhancers	Primary B cells from peripheral blood	blood
39	chr3:23846600-23846800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr3:23846600-23846800	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr3:23846600-23846800	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr3:23846600-23846800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr3:23846600-23846800	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr3:23846600-23846800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr3:23846600-23846800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr3:23846600-23846800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr3:23846600-23846800	Enhancers	Fetal Brain Female	brain
48	chr3:23846600-23846800	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr3:23846600-23846800	Enhancers	Hela-S3	cervix
50	chr3:23846600-23846800	Bivalent Enhancer	HepG2	liver

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