Variant report

Variant	nsv978315
Chromosome Location	chr16:31198121-31203785
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:347)
CpG islands
(count:0)
Chromatin interactive
region (count:33)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr16:31199221-31199644	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr16:31197646-31199600	K562	blood:	n/a	n/a
3	BCL3	chr16:31202102-31205638	K562	blood:	n/a	chr16:31204643-31204652
4	BCL3	chr16:31199277-31200217	K562	blood:	n/a	chr16:31199763-31199772
5	BCL3	chr16:31199686-31202004	K562	blood:	n/a	chr16:31199763-31199772 chr16:31200745-31200752
6	BCLAF1	chr16:31201935-31202669	K562	blood:	n/a	n/a
7	BCLAF1	chr16:31198510-31199075	K562	blood:	n/a	n/a
8	BCLAF1	chr16:31198223-31199201	K562	blood:	n/a	n/a
9	BCLAF1	chr16:31203088-31203785	GM12878	blood:	n/a	n/a
10	BHLHE40	chr16:31199187-31199717	A549	lung:	n/a	n/a
11	BRCA1	chr16:31198506-31198705	H1-hESC	embryonic stem cell:	n/a	n/a
12	CCNT2	chr16:31203191-31203459	K562	blood:	n/a	n/a
13	CCNT2	chr16:31199155-31199473	K562	blood:	n/a	n/a
14	CHD2	chr16:31201106-31201110	HepG2	liver:	n/a	n/a
15	CHD2	chr16:31198683-31198776	K562	blood:	n/a	n/a
16	CHD2	chr16:31198401-31200333	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr16:31198397-31198597	HepG2	liver:	n/a	n/a
18	CHD2	chr16:31199288-31199298	HepG2	liver:	n/a	n/a
19	CHD2	chr16:31203269-31203669	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr16:31199380-31199530	K562	blood:	n/a	n/a
21	CTCF	chr16:31201480-31201630	GM12864	blood:	n/a	n/a
22	CTCF	chr16:31199361-31199389	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr16:31199280-31199430	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr16:31199320-31199470	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr16:31202201-31202449	T-47D	breast:	n/a	n/a
26	CTCF	chr16:31202716-31202877	T-47D	breast:	n/a	n/a
27	CUX1	chr16:31198861-31199056	K562	blood:	n/a	n/a
28	CUX1	chr16:31198554-31198607	K562	blood:	n/a	n/a
29	CUX1	chr16:31202856-31203283	GM12878	blood:	n/a	n/a
30	ELK1	chr16:31202496-31202806	K562	blood:	n/a	n/a
31	GTF2F1	chr16:31198771-31198808	K562	blood:	n/a	n/a
32	GTF2F1	chr16:31198360-31198445	K562	blood:	n/a	n/a
33	HEY1	chr16:31201417-31201727	K562	blood:	n/a	n/a
34	HEY1	chr16:31195960-31200674	K562	blood:	n/a	chr16:31196925-31196934
35	HEY1	chr16:31200744-31202294	HepG2	liver:	n/a	n/a
36	HEY1	chr16:31198103-31198830	K562	blood:	n/a	n/a
37	HEY1	chr16:31199889-31200100	K562	blood:	n/a	n/a
38	HEY1	chr16:31199200-31199474	K562	blood:	n/a	n/a
39	HEY1	chr16:31202327-31203875	HepG2	liver:	n/a	n/a
40	HEY1	chr16:31200875-31201299	HepG2	liver:	n/a	n/a
41	HEY1	chr16:31198076-31199047	HepG2	liver:	n/a	n/a
42	HEY1	chr16:31203042-31203884	HepG2	liver:	n/a	n/a
43	HEY1	chr16:31200824-31205952	K562	blood:	n/a	n/a
44	HEY1	chr16:31196422-31200740	HepG2	liver:	n/a	chr16:31196925-31196934
45	MAFF	chr16:31203026-31203300	HepG2	liver:	n/a	n/a
46	MAFF	chr16:31201092-31201572	HepG2	liver:	n/a	chr16:31201253-31201271
47	MAFK	chr16:31203041-31203659	K562	blood:	n/a	n/a
48	MAFK	chr16:31199078-31199169	K562	blood:	n/a	n/a
49	MAFK	chr16:31203040-31203215	HepG2	liver:	n/a	n/a
50	MAFK	chr16:31201112-31201386	HepG2	liver:	n/a	chr16:31201259-31201270 chr16:31201258-31201269 chr16:31201257-31201271 chr16:31201254-31201269 chr16:31201254-31201270

No data

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:31199383..31201639-chr16:31463370..31465464,2	K562	blood:
2	chr16:31085155..31087268-chr16:31196940..31199413,2	K562	blood:
3	chr16:31123268..31127557-chr16:31200577..31203158,3	K562	blood:
4	chr16:31085251..31088144-chr16:31197291..31199789,2	MCF-7	breast:
5	chr16:31083121..31087142-chr16:31201423..31205329,4	K562	blood:
6	chr16:31202771..31204452-chr16:31233343..31235697,2	K562	blood:
7	chr16:31198823..31201315-chr16:31470098..31472818,2	K562	blood:
8	chr16:31203543..31204044-chr17:62161100..62161600,2	Hela-S3	cervix:
9	chr16:31135542..31139152-chr16:31197024..31199898,3	K562	blood:
10	chr16:31198655..31200900-chr17:56735001..56737984,2	K562	blood:
11	chr16:31202583..31204612-chr16:31229217..31230740,2	K562	blood:
12	chr16:31203117..31206112-chr16:31465658..31467942,3	K562	blood:
13	chr16:31151687..31162079-chr16:31189046..31201898,43	K562	blood:
14	chr16:31042749..31045217-chr16:31199190..31201398,2	K562	blood:
15	chr16:31127872..31130849-chr16:31201012..31203039,2	K562	blood:
16	chr16:31141207..31143921-chr16:31201382..31203908,3	MCF-7	breast:
17	chr16:31200877..31205446-chr16:31331682..31336266,5	K562	blood:
18	chr16:31119811..31122617-chr16:31200745..31202517,2	K562	blood:
19	chr16:31127731..31129409-chr16:31203290..31205242,2	K562	blood:
20	chr16:31149707..31163529-chr16:31187237..31198825,44	K562	blood:
21	chr16:31116825..31119866-chr16:31203052..31206563,4	K562	blood:
22	chr16:31127717..31129231-chr16:31203742..31205961,2	K562	blood:
23	chr16:31084050..31087268-chr16:31196940..31199413,3	K562	blood:
24	chr16:30969131..30970956-chr16:31201908..31204585,2	MCF-7	breast:
25	chr16:31201969..31203831-chr16:31454344..31455907,2	K562	blood:
26	chr16:31137652..31139439-chr16:31197304..31198969,2	K562	blood:
27	chr16:31117742..31119780-chr16:31197007..31199693,2	MCF-7	breast:
28	chr16:31149322..31163059-chr16:31188531..31198512,46	MCF-7	breast:
29	chr16:31141772..31145245-chr16:31195885..31201101,4	MCF-7	breast:
30	chr16:31083053..31084601-chr16:31201158..31202703,2	MCF-7	breast:
31	chr16:30994262..30997879-chr16:31200586..31204219,3	K562	blood:
32	chr16:30959999..30961967-chr16:31197956..31199862,2	K562	blood:
33	chr16:30996900..30998531-chr16:31196842..31199686,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM72-2	chr16:31200986-31201016	NONHSAT141885
2	lnc-TRIM72-2	chr16:31199788-31200547	NONHSAT141885

No data

Variant related genes	Relation type
ENSG00000260304	TF binding region
ENSG00000260060	TF binding region
FUS	TF binding region
ENSG00000202077	chromatin interactions
ENSG00000167394	chromatin interactions
ENSG00000140691	chromatin interactions
ENSG00000167395	chromatin interactions
ENSG00000103507	chromatin interactions
ENSG00000262766	chromatin interactions
ENSG00000268863	chromatin interactions
ENSG00000178226	chromatin interactions
ENSG00000261385	chromatin interactions
ENSG00000176723	chromatin interactions
ENSG00000103510	chromatin interactions
ENSG00000169896	chromatin interactions
ENSG00000252809	chromatin interactions
ENSG00000103496	chromatin interactions
ENSG00000261474	chromatin interactions
ENSG00000260267	chromatin interactions
ENSG00000099377	chromatin interactions
ENSG00000175938	chromatin interactions

Extended variants
information (count: 298 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:298 , 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	rs547578383	chr16:31198127-31198128	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
2	rs144917373	chr16:31198146-31198147	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs374716753	chr16:31198170-31198171	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs565802108	chr16:31198298-31198299	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs112245972	chr16:31198325-31198326	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs60976516	chr16:31198336-31198337	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs551415027	chr16:31198347-31198348	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs145080653	chr16:31198404-31198405	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs538913233	chr16:31198462-31198463	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs537085937	chr16:31198519-31198520	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs555500490	chr16:31198538-31198539	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs567375321	chr16:31198549-31198550	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs540520385	chr16:31198562-31198563	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs534869047	chr16:31198567-31198568	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs147563969	chr16:31198571-31198572	Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs553850151	chr16:31198607-31198608	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs150172554	chr16:31198627-31198628	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs72550857	chr16:31198630-31198631	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs565658593	chr16:31198652-31198653	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs191770775	chr16:31198670-31198671	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs542614776	chr16:31198677-31198678	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs552804704	chr16:31198679-31198680	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs535971915	chr16:31198680-31198681	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
24	rs531972278	chr16:31198690-31198691	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
25	rs370786235	chr16:31198725-31198726	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs561005491	chr16:31198735-31198736	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
27	rs528578535	chr16:31198839-31198840	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
28	rs540839986	chr16:31198869-31198870	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
29	rs9938819	chr16:31199052-31199053	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
30	rs183595614	chr16:31199056-31199057	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
31	rs374614664	chr16:31199094-31199095	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
32	rs190845128	chr16:31199110-31199111	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
33	rs75418901	chr16:31199182-31199183	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
34	rs530472679	chr16:31199224-31199225	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
35	rs183447846	chr16:31199249-31199250	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
36	rs567338611	chr16:31199261-31199262	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
37	rs534690319	chr16:31199299-31199300	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
38	rs552825137	chr16:31199320-31199321	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
39	rs72550824	chr16:31199367-31199368	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
40	rs138631439	chr16:31199371-31199372	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
41	rs2550045	chr16:31199399-31199400	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
42	rs186678167	chr16:31199450-31199451	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
43	rs111719937	chr16:31199456-31199457	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
44	rs575574429	chr16:31199457-31199458	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs542596682	chr16:31199500-31199501	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
46	rs554572292	chr16:31199538-31199539	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs573178354	chr16:31199564-31199565	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs148885618	chr16:31199567-31199568	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs565243106	chr16:31199588-31199589	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs533101111	chr16:31199600-31199601	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Sezary syndrome	18413736	CNVD
Lung adenocarcinoma	21151896	CNVD

Chromatin state (count:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31193200-31200000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr16:31193400-31198600	Genic enhancers	Primary monocytes fromperipheralblood	blood
3	chr16:31194200-31198200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr16:31194200-31200000	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr16:31194200-31205800	Strong transcription	Small Intestine	intestine
6	chr16:31194200-31208000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr16:31194200-31208200	Strong transcription	Rectal Mucosa Donor 31	rectum
8	chr16:31194400-31199800	Genic enhancers	Thymus	Thymus
9	chr16:31194400-31200200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
10	chr16:31194400-31201200	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr16:31194400-31201800	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr16:31194400-31202600	Genic enhancers	Primary T cells fromperipheralblood	blood
13	chr16:31194400-31208200	Strong transcription	HSMMtube	muscle
14	chr16:31194400-31208400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
15	chr16:31194400-31211000	Strong transcription	Fetal Intestine Large	intestine
16	chr16:31194600-31199000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
17	chr16:31194600-31207000	Strong transcription	Aorta	Aorta
18	chr16:31194600-31207800	Strong transcription	Placenta Amnion	Placenta Amnion
19	chr16:31194600-31208400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr16:31194600-31208800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr16:31194600-31209000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr16:31194800-31198600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr16:31194800-31208000	Strong transcription	Brain Angular Gyrus	brain
24	chr16:31195000-31208000	Strong transcription	Esophagus	oesophagus
25	chr16:31195000-31208200	Strong transcription	NHEK	skin
26	chr16:31195000-31208400	Strong transcription	H9 Cell Line	embryonic stem cell
27	chr16:31195000-31208800	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr16:31195000-31208800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
29	chr16:31195000-31208800	Strong transcription	Rectal Mucosa Donor 29	rectum
30	chr16:31195000-31211000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr16:31195000-31211000	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr16:31195200-31199400	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr16:31195200-31206400	Strong transcription	Pancreatic Islets	Pancreatic Islet
34	chr16:31195200-31208000	Strong transcription	Fetal Kidney	kidney
35	chr16:31195200-31208400	Strong transcription	Fetal Lung	lung
36	chr16:31195400-31198400	Strong transcription	Brain Cingulate Gyrus	brain
37	chr16:31195400-31200200	Strong transcription	Gastric	stomach
38	chr16:31195400-31201400	Strong transcription	Spleen	Spleen
39	chr16:31195400-31202600	Strong transcription	Psoas Muscle	Psoas
40	chr16:31195400-31207400	Strong transcription	Colon Smooth Muscle	Colon
41	chr16:31195400-31208000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
42	chr16:31195400-31208000	Strong transcription	HUVEC	blood vessel
43	chr16:31195400-31208400	Strong transcription	Right Ventricle	heart
44	chr16:31195400-31208400	Strong transcription	HMEC	breast
45	chr16:31195400-31208600	Strong transcription	H1 Cell Line	embryonic stem cell
46	chr16:31195400-31208800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
47	chr16:31195400-31209000	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr16:31195400-31209200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr16:31195400-31210200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr16:31195400-31211200	Strong transcription	HUES6 Cell Line	embryonic stem cell

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