Variant report

Variant	esv1817837
Chromosome Location	chr16:31301125-31331958
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	chr16:31310490-31310492	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:31313480-31313682	K562	blood:	n/a	n/a
3	BHLHE40	chr16:31309652-31309852	K562	blood:	n/a	n/a
4	CEBPB	chr16:31313362-31313721	IMR90	lung:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
5	CEBPB	chr16:31301525-31301764	HepG2	liver:	n/a	chr16:31301651-31301662
6	CEBPB	chr16:31313355-31313735	HepG2	liver:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
7	CEBPB	chr16:31313183-31313715	MCF-7	breast:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
8	CEBPB	chr16:31313362-31313736	H1-hESC	embryonic stem cell:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
9	CEBPB	chr16:31313408-31313735	HCT-116	colon:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
10	CEBPB	chr16:31313395-31313730	ECC-1	luminal epithelium:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
11	CEBPB	chr16:31313411-31313713	HepG2	liver:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
12	CEBPB	chr16:31313413-31313708	A549	lung:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
13	CEBPB	chr16:31313372-31313730	A549	lung:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
14	CEBPB	chr16:31313349-31313865	A549	lung:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
15	CEBPB	chr16:31313322-31313687	K562	blood:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
16	CEBPB	chr16:31301521-31301737	K562	blood:	n/a	chr16:31301651-31301662
17	CEBPB	chr16:31313466-31313654	HepG2	liver:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
18	CEBPB	chr16:31313446-31313668	HepG2	liver:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
19	CEBPB	chr16:31301554-31301725	H1-hESC	embryonic stem cell:	n/a	chr16:31301651-31301662
20	CEBPB	chr16:31313386-31313693	K562	blood:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
21	CEBPB	chr16:31313250-31313753	K562	blood:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
22	CEBPB	chr16:31313357-31313781	Hela-S3	cervix:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
23	CEBPB	chr16:31313380-31313696	MCF-7	breast:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
24	CEBPB	chr16:31301529-31301801	IMR90	lung:	n/a	chr16:31301651-31301662
25	CEBPB	chr16:31313242-31313728	HCT-116	colon:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
26	CEBPB	chr16:31313304-31313712	GM12878	blood:	n/a	chr16:31313536-31313549 chr16:31313538-31313547 chr16:31313537-31313548
27	CEBPD	chr16:31313386-31313657	K562	blood:	n/a	chr16:31313536-31313547
28	CEBPD	chr16:31313343-31313764	K562	blood:	n/a	chr16:31313536-31313547
29	CTCF	chr16:31313540-31313690	NHEK	skin:	n/a	n/a
30	CTCF	chr16:31310413-31310537	Lung_OC	lung:	n/a	n/a
31	CTCF	chr16:31310380-31310530	SAEC	small airway:	n/a	n/a
32	CTCF	chr16:31310360-31310510	GM06990	blood:	n/a	n/a
33	CTCF	chr16:31310400-31310550	Caco-2	colon:	n/a	n/a
34	CTCF	chr16:31313540-31313690	GM12874	blood:	n/a	n/a
35	CTCF	chr16:31310440-31310590	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr16:31310420-31310570	GM12870	blood:	n/a	n/a
37	CTCF	chr16:31310420-31310570	K562	blood:	n/a	n/a
38	CTCF	chr16:31310460-31310610	GM12878	blood:	n/a	n/a
39	CTCF	chr16:31310422-31310583	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr16:31310424-31310582	GM10248	blood:	n/a	n/a
41	CTCF	chr16:31310293-31310680	GM12878	blood:	n/a	chr16:31310334-31310342
42	CTCF	chr16:31310420-31310570	GM12868	blood:	n/a	n/a
43	CTCF	chr16:31310387-31310598	LNCaP	prostate:	n/a	n/a
44	CTCF	chr16:31310245-31310615	MCF-7	breast:	n/a	chr16:31310334-31310342
45	CTCF	chr16:31310440-31310590	GM12866	blood:	n/a	n/a
46	CTCF	chr16:31310375-31310571	K562	blood:	n/a	n/a
47	CTCF	chr16:31313500-31313650	GM12864	blood:	n/a	n/a
48	CTCF	chr16:31310401-31310587	Medullo	brain:	n/a	n/a
49	CTCF	chr16:31313440-31313590	MCF-7	breast:	n/a	n/a
50	CTCF	chr16:31313511-31313671	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:31198262..31200598-chr16:31310110..31313227,3	K562	blood:
2	chr16:31326402..31329084-chr16:31335600..31338483,2	K562	blood:
3	chr16:31302537..31304453-chr16:31307896..31310538,2	MCF-7	breast:
4	chr16:31190554..31193108-chr16:31310541..31313194,2	K562	blood:
5	chr16:31302537..31304453-chr16:31307896..31310538,2	MCF-7	breast:
6	chr16:31330986..31333685-chr16:31334773..31336947,2	K562	blood:
7	chr16:31306439..31308367-chr16:31312122..31314629,2	K562	blood:
8	chr16:31330219..31332365-chr16:31451597..31454168,2	K562	blood:
9	chr16:30995967..30996872-chr16:31309965..31310532,2	K562	blood:
10	chr16:31191061..31193614-chr16:31307269..31309911,4	MCF-7	breast:
11	chr16:31331494..31335412-chr16:31342610..31345111,3	K562	blood:
12	chr16:31127178..31129343-chr16:31311883..31313531,2	MCF-7	breast:
13	chr16:31313279..31315111-chr16:31315474..31317506,2	MCF-7	breast:
14	chr16:31327344..31330164-chr16:31471037..31472860,2	MCF-7	breast:
15	chr16:31227286..31229689-chr16:31304037..31306749,2	MCF-7	breast:
16	chr16:31190510..31192547-chr16:31304719..31307544,2	K562	blood:
17	chr16:31212793..31214907-chr16:31311577..31313966,2	MCF-7	breast:
18	chr16:31226931..31229900-chr16:31308283..31311766,3	MCF-7	breast:
19	chr16:31307209..31309080-chr16:31463373..31465636,2	MCF-7	breast:
20	chr16:31308392..31310591-chr16:31341817..31344039,2	K562	blood:
21	chr16:31122825..31124997-chr16:31308822..31311698,2	K562	blood:
22	chr16:31306439..31308367-chr16:31312122..31314629,2	K562	blood:
23	chr16:31313279..31315111-chr16:31315474..31317506,2	MCF-7	breast:
24	chr16:31199558..31201465-chr16:31328647..31330678,2	K562	blood:
25	chr16:31200877..31205446-chr16:31331682..31336266,5	K562	blood:

Variant related genes	Relation type
ITGAM	TF binding region
ENSG00000261474	chromatin interactions
ENSG00000261359	chromatin interactions
ENSG00000099377	chromatin interactions
ENSG00000103510	chromatin interactions
ENSG00000140691	chromatin interactions
ENSG00000260267	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000169896	chromatin interactions
ENSG00000103490	chromatin interactions
ENSG00000169900	chromatin interactions

Extended variants
information (count: 1045 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:1045 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11150608	chr16:31301125-31301126	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373180110	chr16:31301133-31301134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532077266	chr16:31301142-31301143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551124862	chr16:31301147-31301148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569649511	chr16:31301190-31301191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536719590	chr16:31301208-31301209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12103025	chr16:31301220-31301221	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs567821320	chr16:31301234-31301235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535276653	chr16:31301261-31301262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184403616	chr16:31301317-31301318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs578211046	chr16:31301351-31301352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147743705	chr16:31301366-31301367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34079788	chr16:31301422-31301423	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141289502	chr16:31301423-31301424	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7190018	chr16:31301478-31301479	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs189158631	chr16:31301500-31301501	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542670398	chr16:31301521-31301522	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182014363	chr16:31301562-31301563	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs112716401	chr16:31301568-31301569	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201841730	chr16:31301575-31301576	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529050301	chr16:31301580-31301581	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536564951	chr16:31301600-31301601	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574081968	chr16:31301680-31301681	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142586236	chr16:31301703-31301704	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150246271	chr16:31301740-31301741	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533044502	chr16:31301819-31301820	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138870169	chr16:31301863-31301864	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149488037	chr16:31301901-31301902	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7190807	chr16:31301910-31301911	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs187617736	chr16:31301915-31301916	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567418220	chr16:31301951-31301952	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535213185	chr16:31301972-31301973	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558902436	chr16:31302012-31302013	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553567419	chr16:31302087-31302088	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577460595	chr16:31302103-31302104	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571830055	chr16:31302143-31302144	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116751121	chr16:31302184-31302185	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189155549	chr16:31302236-31302237	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375677949	chr16:31302249-31302250	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535303211	chr16:31302285-31302286	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143064736	chr16:31302319-31302320	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs57576899	chr16:31302404-31302405	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138543427	chr16:31302412-31302413	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573037661	chr16:31302416-31302417	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535071336	chr16:31302431-31302432	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377378774	chr16:31302463-31302464	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559254931	chr16:31302610-31302611	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577771355	chr16:31302619-31302620	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs180676967	chr16:31302620-31302621	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563643280	chr16:31302635-31302636	Weak transcription Strong transcription Enhancers	n/a	n/a	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
Sezary syndrome	18413736	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31290000-31301400	Weak transcription	Primary B cells from peripheral blood	blood
2	chr16:31290000-31310200	Weak transcription	Spleen	Spleen
3	chr16:31296800-31301200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr16:31296800-31308800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr16:31298000-31301600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr16:31298000-31303800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr16:31298400-31301800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr16:31299600-31301400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr16:31299800-31301400	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr16:31299800-31302800	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr16:31300800-31304200	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr16:31301400-31301600	Enhancers	Primary B cells from peripheral blood	blood
13	chr16:31301400-31303000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr16:31301400-31303200	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr16:31301600-31303000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr16:31301800-31302000	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr16:31302800-31303400	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr16:31303000-31303400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr16:31303000-31306600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr16:31303200-31305200	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr16:31303400-31304600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr16:31303400-31306000	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr16:31303800-31304000	Active TSS	Primary T killer memory cells from peripheral blood	blood
24	chr16:31304200-31307400	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr16:31304600-31313400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr16:31305000-31312800	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr16:31305200-31311600	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr16:31306000-31309200	Weak transcription	Primary B cells from cord blood	blood
29	chr16:31306000-31311600	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr16:31306600-31313800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr16:31307400-31312800	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr16:31308800-31309000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr16:31308800-31310200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr16:31309000-31309200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr16:31309200-31310000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr16:31309200-31310200	Strong transcription	Primary B cells from cord blood	blood
37	chr16:31310000-31310400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr16:31310000-31310400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr16:31310200-31310400	Active TSS	Spleen	Spleen
40	chr16:31310200-31313200	Weak transcription	Primary B cells from cord blood	blood
41	chr16:31310200-31326800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr16:31310400-31312600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr16:31310400-31313000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr16:31311400-31312800	Enhancers	GM12878-XiMat	blood
45	chr16:31311600-31312800	Genic enhancers	Primary monocytes fromperipheralblood	blood
46	chr16:31311600-31312800	Genic enhancers	Monocytes-CD14+_RO01746	blood
47	chr16:31312600-31313200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr16:31312600-31313800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr16:31312800-31313000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
50	chr16:31312800-31313000	Enhancers	Monocytes-CD14+_RO01746	blood

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