Variant report

Variant	esv3439168
Chromosome Location	chr16:30345276-30348024
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:30347086-30347705	HepG2	liver:	n/a	n/a
2	BACH1	chr16:30346844-30346929	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr16:30345581-30346438	GM12878	blood:	n/a	n/a
4	BATF	chr16:30346553-30346767	GM12878	blood:	n/a	n/a
5	BATF	chr16:30345526-30345994	GM12878	blood:	n/a	n/a
6	BATF	chr16:30346999-30347227	GM12878	blood:	n/a	chr16:30347130-30347141
7	BCL11A	chr16:30345807-30346438	GM12878	blood:	n/a	chr16:30346062-30346075 chr16:30346128-30346141 chr16:30346402-30346411 chr16:30346412-30346425
8	BCL11A	chr16:30345524-30345790	GM12878	blood:	n/a	n/a
9	BCL11A	chr16:30345530-30346057	GM12878	blood:	n/a	n/a
10	BCL11A	chr16:30346091-30346345	GM12878	blood:	n/a	chr16:30346128-30346141
11	BCL11A	chr16:30346533-30346769	GM12878	blood:	n/a	chr16:30346716-30346729 chr16:30346712-30346725 chr16:30346718-30346727 chr16:30346723-30346732 chr16:30346709-30346722
12	BHLHE40	chr16:30344945-30345285	HepG2	liver:	n/a	n/a
13	BHLHE40	chr16:30346030-30346389	HepG2	liver:	n/a	chr16:30346048-30346064
14	BHLHE40	chr16:30346642-30346654	K562	blood:	n/a	n/a
15	BHLHE40	chr16:30346643-30346649	GM12878	blood:	n/a	n/a
16	BHLHE40	chr16:30345786-30345945	HepG2	liver:	n/a	n/a
17	BHLHE40	chr16:30345805-30346046	GM12878	blood:	n/a	n/a
18	CBX3	chr16:30345551-30346243	K562	blood:	n/a	n/a
19	CBX3	chr16:30346374-30346944	K562	blood:	n/a	n/a
20	CCNT2	chr16:30346687-30346800	K562	blood:	n/a	n/a
21	CEBPB	chr16:30347378-30347708	HepG2	liver:	n/a	n/a
22	CEBPB	chr16:30347402-30347588	HepG2	liver:	n/a	n/a
23	CEBPB	chr16:30345552-30346100	GM12878	blood:	n/a	n/a
24	CEBPB	chr16:30347278-30347684	HepG2	liver:	n/a	n/a
25	CEBPD	chr16:30347321-30347668	HepG2	liver:	n/a	n/a
26	CEBPD	chr16:30346387-30346829	HepG2	liver:	n/a	n/a
27	CEBPD	chr16:30346530-30346884	K562	blood:	n/a	n/a
28	CEBPD	chr16:30347129-30347764	HepG2	liver:	n/a	n/a
29	CEBPD	chr16:30345889-30346235	HepG2	liver:	n/a	n/a
30	CHD2	chr16:30346681-30346831	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr16:30346655-30346758	GM12878	blood:	n/a	n/a
32	CHD2	chr16:30347275-30347305	HepG2	liver:	n/a	n/a
33	CREB1	chr16:30346389-30346981	A549	lung:	n/a	n/a
34	CTCF	chr16:30347440-30347590	HepG2	liver:	n/a	chr16:30347515-30347533 chr16:30347518-30347531
35	CTCF	chr16:30346689-30346814	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr16:30347440-30347590	Caco-2	colon:	n/a	chr16:30347515-30347533 chr16:30347518-30347531
37	CTCF	chr16:30346155-30346194	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chr16:30346137-30346146	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr16:30347455-30347547	HepG2	liver:	n/a	chr16:30347515-30347533 chr16:30347518-30347531
40	CTCF	chr16:30347440-30347590	HRPEpiC	eye:	n/a	chr16:30347515-30347533 chr16:30347518-30347531
41	CTCF	chr16:30346659-30346712	GM10248	blood:	n/a	n/a
42	CTCF	chr16:30347411-30347595	HepG2	liver:	n/a	chr16:30347515-30347533 chr16:30347415-30347424 chr16:30347518-30347531
43	CTCF	chr16:30347460-30347610	Caco-2	colon:	n/a	chr16:30347515-30347533 chr16:30347518-30347531
44	CTCF	chr16:30346480-30346630	SAEC	small airway:	n/a	n/a
45	CTCF	chr16:30347420-30347570	HepG2	liver:	n/a	chr16:30347515-30347533 chr16:30347518-30347531
46	E2F4	chr16:30346660-30346766	MCF10A-Er-Src	breast:	n/a	chr16:30346699-30346708 chr16:30346721-30346730 chr16:30346696-30346708
47	E2F6	chr16:30346457-30346822	K562	blood:	n/a	chr16:30346699-30346708 chr16:30346721-30346730 chr16:30346696-30346708
48	EBF1	chr16:30346893-30347267	GM12878	blood:	n/a	n/a
49	EBF1	chr16:30345598-30345827	GM12878	blood:	n/a	n/a
50	EBF1	chr16:30346971-30347180	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:30346812-30346862	PANC-1	pancreas:	n/a
2	chr16:30346812-30346862	PANC-1	pancreas:	n/a
3	chr16:30346812-30346862	AG04450	lung:	fetal
4	chr16:30347078-30347128	HCT-116	colon:	n/a
5	chr16:30346368-30346418	HCT-116	colon:	n/a
6	chr16:30347240-30347290	PrEC	prostate:	n/a
7	chr16:30346208-30346258	MCF10A-Er-Src	breast:	n/a
8	chr16:30346834-30346884	HRCEpiC	kidney:	n/a
9	chr16:30347078-30347128	MCF-7	breast:	n/a
10	chr16:30346834-30346884	AG09309	skin:	n/a
11	chr16:30347078-30347128	Jurkat	blood:	n/a
12	chr16:30346368-30346418	HRE	kidney:	n/a
13	chr16:30346834-30346884	SK-N-SH	brain:	n/a
14	chr16:30347333-30347383	LNCaP	prostate:	n/a
15	chr16:30347078-30347128	HNPCEpiC	eye:	n/a
16	chr16:30346834-30346884	Hepatocyte	liver:	n/a
17	chr16:30347333-30347383	NT2-D1	testis:	n/a
18	chr16:30347240-30347290	PFSK-1	brain:	n/a
19	chr16:30346208-30346258	NT2-D1	testis:	n/a
20	chr16:30347333-30347383	HCF	heart:	n/a
21	chr16:30347078-30347128	HRPEpiC	eye:	n/a
22	chr16:30346812-30346862	GM19239	blood:	n/a
23	chr16:30346834-30346884	GM12892	blood:	n/a
24	chr16:30346208-30346258	IMR90	lung:	fetal
25	chr16:30347333-30347383	A549	lung:	n/a
26	chr16:30346834-30346884	K562	blood:	n/a
27	chr16:30347240-30347290	AG04449	skin:	fetal
28	chr16:30347333-30347383	HMEC	breast:	n/a
29	chr16:30346208-30346258	GM12878	blood:	n/a
30	chr16:30346812-30346862	HIPEpiC	eye:	n/a
31	chr16:30346368-30346418	ProgFib	skin:	n/a
32	chr16:30346834-30346884	HCPEpiC	choroid plexus:	n/a
33	chr16:30346812-30346862	MCF10A-Er-Src	breast:	n/a
34	chr16:30346812-30346862	Hela-S3	cervix:	n/a
35	chr16:30346834-30346884	ProgFib	skin:	n/a
36	chr16:30346208-30346258	CMK	blood:	n/a
37	chr16:30346834-30346884	SKMC	muscle:	n/a
38	chr16:30347333-30347383	SK-N-SH	brain:	n/a
39	chr16:30346368-30346418	HMEC	breast:	n/a
40	chr16:30347240-30347290	A549	lung:	n/a
41	chr16:30346834-30346884	HNPCEpiC	eye:	n/a
42	chr16:30347333-30347383	GM06990	blood:	n/a
43	chr16:30346812-30346862	HRPEpiC	eye:	n/a
44	chr16:30346812-30346862	PrEC	prostate:	n/a
45	chr16:30346208-30346258	ECC-1	luminal epithelium:	n/a
46	chr16:30346208-30346258	PFSK-1	brain:	n/a
47	chr16:30346208-30346258	PANC-1	pancreas:	n/a
48	chr16:30346834-30346884	HRE	kidney:	n/a
49	chr16:30346834-30346884	SAEC	small airway:	n/a
50	chr16:30347240-30347290	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:30346170..30348596-chr16:30376800..30378752,2	MCF-7	breast:
2	chr16:30347166..30350893-chr16:30361521..30367279,6	K562	blood:
3	chr16:30345604..30348863-chr16:30403977..30407853,5	MCF-7	breast:
4	chr16:30345336..30346987-chr16:30364992..30366777,2	K562	blood:
5	chr16:30347893..30349482-chr16:30349670..30352076,2	K562	blood:
6	chr16:30346222..30347053-chr6:2999778..3000588,2	Hela-S3	cervix:
7	chr16:30344696..30347636-chr16:30378058..30380333,2	MCF-7	breast:
8	chr16:30345346..30347194-chr16:30364689..30366452,2	MCF-7	breast:
9	chr16:30347434..30350400-chr16:30361325..30364299,2	K562	blood:
10	chr16:30346164..30346852-chrX:118109757..118110705,2	Hela-S3	cervix:
11	chr16:30345814..30348548-chr16:30669791..30672071,2	MCF-7	breast:
12	chr16:30347495..30351048-chr16:30363113..30367497,5	MCF-7	breast:
13	chr16:30345231..30348064-chr16:30583285..30585199,2	MCF-7	breast:
14	chr12:56211453..56212433-chr16:30346609..30347165,2	Hela-S3	cervix:
15	chr16:30346820..30348778-chr16:30708252..30710060,2	K562	blood:

Variant related genes	Relation type
ENSG00000183604	TF binding region
ENSG00000183604	CpG island
ENSG00000180096	chromatin interactions
ENSG00000169217	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000260219	chromatin interactions
ENSG00000239791	chromatin interactions
ENSG00000229809	chromatin interactions
ENSG00000205323	chromatin interactions
ENSG00000124588	chromatin interactions
ENSG00000080603	chromatin interactions
ENSG00000169221	chromatin interactions
ENSG00000123353	chromatin interactions
ENSG00000175556	chromatin interactions
ENSG00000156860	chromatin interactions

Extended variants
information (count: 79 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:79 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113233293	chr16:30345317-30345318	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs544511357	chr16:30345327-30345328	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs562496510	chr16:30345390-30345391	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs559102711	chr16:30345485-30345486	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs368953766	chr16:30345505-30345506	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs548382279	chr16:30345561-30345562	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs372256438	chr16:30345624-30345625	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs560614875	chr16:30345721-30345722	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs527662251	chr16:30345734-30345735	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs552635909	chr16:30345779-30345780	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs35715539	chr16:30345839-30345840	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs34489711	chr16:30345842-30345843	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs550455750	chr16:30345859-30345860	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs35932982	chr16:30345860-30345861	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs34998710	chr16:30345869-30345870	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs190602959	chr16:30345884-30345885	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs554367404	chr16:30345944-30345945	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs200271707	chr16:30345992-30345993	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs180913458	chr16:30346043-30346044	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs566259945	chr16:30346046-30346047	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs367900522	chr16:30346066-30346067	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs533530961	chr16:30346123-30346124	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs558095421	chr16:30346137-30346138	Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs576453285	chr16:30346184-30346185	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs544136417	chr16:30346243-30346244	Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs556462009	chr16:30346244-30346245	Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs6565177	chr16:30346248-30346249	Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs542035376	chr16:30346335-30346336	Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs560550006	chr16:30346358-30346359	Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs527749694	chr16:30346374-30346375	Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs546339446	chr16:30346389-30346390	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs564423903	chr16:30346410-30346411	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs531743406	chr16:30346485-30346486	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs550200399	chr16:30346498-30346499	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs528245702	chr16:30346507-30346508	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs568783521	chr16:30346514-30346515	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs529445739	chr16:30346527-30346528	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs62055454	chr16:30346560-30346561	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs551279114	chr16:30346634-30346635	Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
40	rs565950722	chr16:30346652-30346653	Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
41	rs146098127	chr16:30346692-30346693	Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	mRNA abundance
42	rs558238567	chr16:30346755-30346756	Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
43	rs570103376	chr16:30346762-30346763	Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
44	rs185675902	chr16:30346774-30346775	Active TSS Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
45	rs556162012	chr16:30346807-30346808	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
46	rs560957403	chr16:30346844-30346845	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
47	rs62055455	chr16:30346865-30346866	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs549877131	chr16:30346900-30346901	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
49	rs553978914	chr16:30346975-30346976	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
50	rs572270377	chr16:30347014-30347015	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30286000-30345400	Weak transcription	Fetal Stomach	stomach
2	chr16:30324200-30345600	Weak transcription	Thymus	Thymus
3	chr16:30325800-30345800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr16:30326800-30345800	Weak transcription	Lung	lung
5	chr16:30329600-30345400	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr16:30336400-30345400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr16:30341600-30345800	Weak transcription	Small Intestine	intestine
8	chr16:30342200-30345400	Weak transcription	Liver	Liver
9	chr16:30343800-30345400	Enhancers	Primary B cells from cord blood	blood
10	chr16:30343800-30345800	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr16:30344000-30345600	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr16:30344000-30347000	Active TSS	GM12878-XiMat	blood
13	chr16:30344000-30347000	Active TSS	NHEK	skin
14	chr16:30344200-30345400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr16:30344200-30347600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr16:30344400-30345400	Weak transcription	Brain Substantia Nigra	brain
17	chr16:30344400-30347000	Weak transcription	Fetal Heart	heart
18	chr16:30344400-30347000	Active TSS	Hela-S3	cervix
19	chr16:30344400-30347000	Active TSS	HSMMtube	muscle
20	chr16:30344400-30347000	Active TSS	K562	blood
21	chr16:30344400-30347200	Active TSS	HepG2	liver
22	chr16:30344600-30346800	Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr16:30344600-30347000	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr16:30344600-30347000	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr16:30344600-30347000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr16:30344600-30347000	Active TSS	Primary hematopoietic stem cells short term culture	blood
27	chr16:30344600-30347000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr16:30344600-30347000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr16:30344600-30347200	Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr16:30344600-30347200	Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr16:30344600-30347200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr16:30344600-30347200	Active TSS	HMEC	breast
33	chr16:30344600-30347400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr16:30344800-30345400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr16:30344800-30345400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr16:30344800-30346800	Active TSS	Dnd41	blood
37	chr16:30344800-30347000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr16:30344800-30347000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr16:30344800-30347000	Active TSS	HUVEC	blood vessel
40	chr16:30344800-30347400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr16:30344800-30347600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr16:30345200-30345400	Enhancers	Primary B cells from peripheral blood	blood
43	chr16:30345200-30345400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr16:30345200-30345600	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr16:30345200-30345600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr16:30345200-30346800	Active TSS	H1 Cell Line	embryonic stem cell
47	chr16:30345200-30346800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr16:30345200-30346800	Active TSS	Fetal Thymus	thymus
49	chr16:30345200-30346800	Active TSS	Monocytes-CD14+_RO01746	blood
50	chr16:30345200-30347000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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