Variant report

Variant	esv3362881
Chromosome Location	chr3:48715948-48720546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:89)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:89 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:48717604-48717765	H1-hESC	embryonic stem cell:	n/a	chr3:48717680-48717694
2	BHLHE40	chr3:48717346-48717414	GM12878	blood:	n/a	n/a
3	EP300	chr3:48717390-48717391	GM12878	blood:	n/a	n/a
4	EP300	chr3:48717273-48717470	GM12878	blood:	n/a	chr3:48717328-48717342
5	IRF4	chr3:48717098-48717540	GM12878	blood:	n/a	n/a
6	JUND	chr3:48719803-48720036	HepG2	liver:	n/a	n/a
7	MAFK	chr3:48717647-48717764	H1-hESC	embryonic stem cell:	n/a	chr3:48717683-48717693 chr3:48717684-48717693
8	MAZ	chr3:48715398-48716095	IMR90	lung:	n/a	n/a
9	MAZ	chr3:48717280-48717439	GM12878	blood:	n/a	n/a
10	MXI1	chr3:48715125-48716052	IMR90	lung:	n/a	n/a
11	MXI1	chr3:48717413-48717423	GM12878	blood:	n/a	n/a
12	MYC	chr3:48717612-48717730	MCF-7	breast:	n/a	chr3:48717683-48717692
13	MYC	chr3:48719850-48719926	H1-hESC	embryonic stem cell:	n/a	n/a
14	MYC	chr3:48716984-48717120	MCF-7	breast:	n/a	n/a
15	MYC	chr3:48717624-48717680	H1-hESC	embryonic stem cell:	n/a	n/a
16	MYC	chr3:48717599-48717600	MCF-7	breast:	n/a	n/a
17	MYC	chr3:48717649-48717670	MCF-7	breast:	n/a	n/a
18	MYC	chr3:48717677-48717690	MCF-7	breast:	n/a	n/a
19	NFIC	chr3:48720435-48721241	SK-N-SH	brain:	n/a	chr3:48720803-48720819 chr3:48720803-48720820
20	NFIC	chr3:48720528-48721147	SK-N-SH	brain:	n/a	chr3:48720803-48720819 chr3:48720803-48720820
21	NRF1	chr3:48717324-48717343	GM12878	blood:	n/a	n/a
22	POLR2A	chr3:48715145-48716626	GM12878	blood:	n/a	n/a
23	POLR2A	chr3:48716665-48716723	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr3:48716844-48718670	GM12878	blood:	n/a	n/a
25	POLR2A	chr3:48717278-48717778	K562	blood:	n/a	n/a
26	POLR2A	chr3:48717239-48717260	GM12878	blood:	n/a	n/a
27	POLR2A	chr3:48717978-48718052	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr3:48717551-48717696	GM12878	blood:	n/a	n/a
29	POLR2A	chr3:48718115-48718367	K562	blood:	n/a	n/a
30	POLR2A	chr3:48719526-48719630	HepG2	liver:	n/a	n/a
31	POLR2A	chr3:48718498-48718640	HepG2	liver:	n/a	n/a
32	POLR2A	chr3:48717558-48717715	MCF-7	breast:	n/a	n/a
33	POLR2A	chr3:48718997-48719286	HepG2	liver:	n/a	n/a
34	POLR2A	chr3:48717926-48718078	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr3:48718144-48718412	K562	blood:	n/a	n/a
36	POLR2A	chr3:48719814-48720444	HepG2	liver:	n/a	n/a
37	POLR2A	chr3:48718058-48718254	MCF-7	breast:	n/a	n/a
38	POLR2A	chr3:48716056-48716089	K562	blood:	n/a	n/a
39	POLR2A	chr3:48716841-48717183	K562	blood:	n/a	n/a
40	POLR2A	chr3:48717866-48718062	K562	blood:	n/a	n/a
41	POLR2A	chr3:48717331-48717335	K562	blood:	n/a	n/a
42	POLR2A	chr3:48717899-48718429	K562	blood:	n/a	n/a
43	POLR2A	chr3:48717473-48717721	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr3:48719680-48719809	HepG2	liver:	n/a	n/a
45	POLR2A	chr3:48717457-48718119	K562	blood:	n/a	n/a
46	POLR2A	chr3:48718209-48718331	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr3:48717391-48717401	K562	blood:	n/a	n/a
48	POLR2A	chr3:48718351-48718489	HepG2	liver:	n/a	n/a
49	POLR2A	chr3:48717938-48718190	HepG2	liver:	n/a	n/a
50	POLR2A	chr3:48715588-48716324	SK-N-MC	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:48720378-48720428	AG04450	lung:	fetal
2	chr3:48720378-48720428	HL-60	blood:	n/a
3	chr3:48720378-48720428	PFSK-1	brain:	n/a
4	chr3:48716190-48716240	SK-N-SH	brain:	n/a
5	chr3:48720378-48720428	GM12878	blood:	n/a
6	chr3:48716190-48716240	GM12878	blood:	n/a
7	chr3:48716190-48716240	SK-N-SH_RA	brain:	n/a
8	chr3:48720378-48720428	SAEC	small airway:	n/a
9	chr3:48720378-48720428	HCM	heart:	n/a
10	chr3:48720378-48720428	LNCaP	prostate:	n/a
11	chr3:48720378-48720428	AG10803	skin:	n/a
12	chr3:48716190-48716240	H1-hESC	embryonic stem cell:	embryo
13	chr3:48716190-48716240	HCT-116	colon:	n/a
14	chr3:48720378-48720428	H1-hESC	embryonic stem cell:	embryo
15	chr3:48716190-48716240	IMR90	lung:	fetal
16	chr3:48720378-48720428	IMR90	lung:	fetal
17	chr3:48716190-48716240	Hepatocyte	liver:	n/a
18	chr3:48716190-48716240	AoSMC	blood vessel:	n/a
19	chr3:48716190-48716240	Hela-S3	cervix:	n/a
20	chr3:48720378-48720428	SK-N-SH_RA	brain:	n/a
21	chr3:48720378-48720428	HMEC	breast:	n/a
22	chr3:48716190-48716240	NH-A	brain:	n/a
23	chr3:48720378-48720428	HCF	heart:	n/a
24	chr3:48716190-48716240	HIPEpiC	eye:	n/a
25	chr3:48716190-48716240	GM12892	blood:	n/a
26	chr3:48720378-48720428	HEEpiC	esophagus:	n/a
27	chr3:48720378-48720428	BE2_C	brain:	n/a
28	chr3:48720378-48720428	BJ	skin:	n/a
29	chr3:48716190-48716240	HepG2	liver:	n/a
30	chr3:48720378-48720428	K562	blood:	n/a
31	chr3:48720378-48720428	HPAEpiC	pulmonary alveolar:	n/a
32	chr3:48720378-48720428	Caco-2	colon:	n/a
33	chr3:48716190-48716240	PANC-1	pancreas:	n/a
34	chr3:48716190-48716240	SKMC	muscle:	n/a
35	chr3:48716190-48716240	HMEC	breast:	n/a
36	chr3:48720378-48720428	T-47D	breast:	n/a
37	chr3:48720378-48720428	HEK293	kidney:	embryo
38	chr3:48716190-48716240	NT2-D1	testis:	n/a
39	chr3:48716190-48716240	HEEpiC	esophagus:	n/a
40	chr3:48716190-48716240	NB4	blood:	n/a
41	chr3:48720378-48720428	GM12891	blood:	n/a
42	chr3:48720378-48720428	MCF-7	breast:	n/a
43	chr3:48716190-48716240	AG10803	skin:	n/a
44	chr3:48716190-48716240	K562	blood:	n/a
45	chr3:48720378-48720428	U87	brain:	n/a
46	chr3:48720378-48720428	HIPEpiC	eye:	n/a
47	chr3:48716190-48716240	LNCaP	prostate:	n/a
48	chr3:48716190-48716240	AG04450	lung:	fetal
49	chr3:48720378-48720428	RPTEC	kidney:	n/a
50	chr3:48716190-48716240	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:48720189..48722244-chr3:48955560..48957238,2	MCF-7	breast:
2	chr3:48716233..48718830-chr3:48753340..48756269,2	K562	blood:
3	chr3:48717071..48719987-chr3:48721738..48723845,3	MCF-7	breast:
4	chr3:48713537..48717616-chr3:48720627..48724588,5	MCF-7	breast:
5	chr3:48709842..48711551-chr3:48717118..48719830,2	MCF-7	breast:
6	chr3:48593859..48595612-chr3:48717016..48718760,2	MCF-7	breast:
7	chr3:48699573..48703813-chr3:48719476..48724654,10	MCF-7	breast:
8	chr3:48698738..48703197-chr3:48713751..48717809,8	K562	blood:
9	chr3:48717662..48719232-chr3:48721596..48723446,2	MCF-7	breast:
10	chr3:48699299..48703873-chr3:48715927..48726939,20	MCF-7	breast:
11	chr3:48670681..48672886-chr3:48719551..48721875,2	K562	blood:
12	chr3:48720285..48722202-chr3:49057646..49059671,2	MCF-7	breast:

No data

Variant related genes	Relation type
NCKIPSD	TF binding region
NCKIPSD	CpG island
ENSG00000008300	chromatin interactions
ENSG00000228350	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000221883	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000199032	chromatin interactions
ENSG00000225697	chromatin interactions
ENSG00000213672	chromatin interactions
ENSG00000177479	chromatin interactions
ENSG00000271973	chromatin interactions
ENSG00000068745	chromatin interactions
ENSG00000114268	chromatin interactions
ENSG00000207605	chromatin interactions

Extended variants
information (count: 281 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546423953	chr3:48715963-48715964	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs568253385	chr3:48715979-48715980	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs529060187	chr3:48716000-48716001	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs141514245	chr3:48716006-48716007	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs550799052	chr3:48716014-48716015	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs368659411	chr3:48716015-48716016	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs569145688	chr3:48716020-48716021	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs371986166	chr3:48716021-48716022	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs147029935	chr3:48716028-48716029	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs36059909	chr3:48716029-48716030	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs375286046	chr3:48716034-48716035	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs142430903	chr3:48716065-48716066	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs367872973	chr3:48716074-48716075	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs114786792	chr3:48716075-48716076	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs150368865	chr3:48716077-48716078	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs550922203	chr3:48716087-48716088	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs140072076	chr3:48716088-48716089	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs371711887	chr3:48716093-48716094	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs368939900	chr3:48716100-48716101	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs34283811	chr3:48716111-48716112	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs35209367	chr3:48716119-48716120	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs144500544	chr3:48716120-48716121	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs142413952	chr3:48716130-48716131	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs140183576	chr3:48716134-48716135	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs147656098	chr3:48716139-48716140	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs78264164	chr3:48716148-48716149	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs375822241	chr3:48716153-48716154	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs138069597	chr3:48716157-48716158	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs369921862	chr3:48716187-48716188	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs200022611	chr3:48716191-48716192	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs557146289	chr3:48716200-48716201	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs376559115	chr3:48716208-48716209	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs575877995	chr3:48716239-48716240	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs546205952	chr3:48716258-48716259	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs564105629	chr3:48716261-48716262	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs375987916	chr3:48716286-48716287	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs201288471	chr3:48716288-48716289	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs372580180	chr3:48716299-48716300	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs11545752	chr3:48716353-48716354	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs142659579	chr3:48716361-48716362	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs201526411	chr3:48716362-48716363	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs138506843	chr3:48716373-48716374	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs561721255	chr3:48716374-48716375	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs370157632	chr3:48716390-48716391	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs529020504	chr3:48716415-48716416	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs201796592	chr3:48716416-48716417	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs375693229	chr3:48716423-48716424	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs370372783	chr3:48716435-48716436	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs184775250	chr3:48716443-48716444	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs376858235	chr3:48716446-48716447	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
abnormal development	18461090	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:48701200-48721000	Weak transcription	Fetal Brain Male	brain
2	chr3:48701600-48716800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr3:48701600-48718000	Weak transcription	NHDF-Ad	bronchial
4	chr3:48701600-48720800	Weak transcription	Right Atrium	heart
5	chr3:48701600-48720800	Weak transcription	HUVEC	blood vessel
6	chr3:48701800-48716800	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr3:48701800-48721400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr3:48702000-48716800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr3:48702000-48716800	Weak transcription	HSMMtube	muscle
10	chr3:48702000-48721400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr3:48702200-48717000	Weak transcription	K562	blood
12	chr3:48702800-48717000	Weak transcription	Fetal Heart	heart
13	chr3:48704400-48716000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr3:48705800-48720600	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr3:48707200-48721400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr3:48708200-48720200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr3:48708200-48720200	Strong transcription	Fetal Brain Female	brain
18	chr3:48708200-48720600	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr3:48708200-48720600	Strong transcription	Fetal Intestine Small	intestine
20	chr3:48708200-48720600	Strong transcription	Fetal Stomach	stomach
21	chr3:48708200-48721000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:48708400-48720400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr3:48708400-48720400	Strong transcription	Brain Germinal Matrix	brain
24	chr3:48708400-48720400	Strong transcription	Brain Inferior Temporal Lobe	brain
25	chr3:48708400-48720800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr3:48708400-48721000	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr3:48708600-48720600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
28	chr3:48708800-48720600	Strong transcription	H9 Cell Line	embryonic stem cell
29	chr3:48709000-48716800	Weak transcription	A549	lung
30	chr3:48709000-48721600	Weak transcription	Psoas Muscle	Psoas
31	chr3:48709200-48720200	Strong transcription	Fetal Muscle Trunk	muscle
32	chr3:48710200-48718000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr3:48710400-48719800	Strong transcription	Brain Cingulate Gyrus	brain
34	chr3:48710400-48721200	Strong transcription	HUES48 Cell Line	embryonic stem cell
35	chr3:48710600-48716800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr3:48710600-48720200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr3:48711000-48720200	Strong transcription	Left Ventricle	heart
38	chr3:48711000-48720400	Strong transcription	H1 Cell Line	embryonic stem cell
39	chr3:48711200-48720000	Strong transcription	Liver	Liver
40	chr3:48711200-48720000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr3:48711400-48717000	Strong transcription	GM12878-XiMat	blood
42	chr3:48711400-48717200	Strong transcription	Esophagus	oesophagus
43	chr3:48711400-48717200	Strong transcription	Spleen	Spleen
44	chr3:48711400-48717600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr3:48711400-48719200	Strong transcription	Brain Angular Gyrus	brain
46	chr3:48711400-48720000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr3:48711400-48720000	Strong transcription	Aorta	Aorta
48	chr3:48711400-48720000	Strong transcription	Brain Substantia Nigra	brain
49	chr3:48711400-48720000	Strong transcription	Fetal Muscle Leg	muscle
50	chr3:48711400-48720000	Strong transcription	Stomach Smooth Muscle	stomach

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