Variant report

Variant	nsv905759
Chromosome Location	chr16:31565597-31647754
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:170)
CpG islands
(count:1040)
Chromatin interactive
region (count:7)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:170 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:31639711-31639822	HepG2	liver:	n/a	n/a
2	ATF1	chr16:31593151-31593199	K562	blood:	n/a	n/a
3	BHLHE40	chr16:31639614-31639804	HepG2	liver:	n/a	n/a
4	CBX3	chr16:31588768-31589075	K562	blood:	n/a	n/a
5	CBX3	chr16:31588835-31589018	K562	blood:	n/a	n/a
6	CEBPB	chr16:31620908-31621218	HepG2	liver:	n/a	chr16:31621045-31621056
7	CEBPB	chr16:31620982-31621195	A549	lung:	n/a	chr16:31621045-31621056
8	CEBPB	chr16:31591338-31591399	HepG2	liver:	n/a	chr16:31591372-31591383
9	CEBPB	chr16:31620971-31621116	IMR90	lung:	n/a	chr16:31621045-31621056
10	CTCF	chr16:31591460-31591610	GM12873	blood:	n/a	n/a
11	CTCF	chr16:31580281-31580383	Spleen_OC	spleen:	n/a	n/a
12	CTCF	chr16:31580183-31580504	K562	blood:	n/a	n/a
13	CTCF	chr16:31591526-31591567	GM12892	blood:	n/a	n/a
14	CTCF	chr16:31580248-31580403	Lung_OC	lung:	n/a	n/a
15	CTCF	chr16:31631227-31631322	Pancreas_OC	pancreas:	n/a	n/a
16	CTCF	chr16:31591440-31591590	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr16:31580200-31580378	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr16:31580280-31580430	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr16:31600528-31600591	Fibrobl	skin:	n/a	n/a
20	CTCF	chr16:31580240-31580390	HRE	kidney:	n/a	n/a
21	CTCF	chr16:31580187-31580453	K562	blood:	n/a	n/a
22	CTCF	chr16:31580220-31580370	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr16:31580234-31580418	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr16:31580275-31580293	Fibrobl	skin:	n/a	n/a
25	CTCF	chr16:31640195-31640231	MCF-7	breast:	n/a	n/a
26	CTCF	chr16:31580194-31580418	K562	blood:	n/a	n/a
27	CTCF	chr16:31591516-31591567	MCF-7	breast:	n/a	n/a
28	CTCF	chr16:31591545-31591564	A549	lung:	n/a	n/a
29	CTCF	chr16:31580246-31580387	NHEK	skin:	n/a	n/a
30	CTCF	chr16:31580254-31580404	K562	blood:	n/a	n/a
31	CTCF	chr16:31580242-31580402	IMR90	lung:	n/a	n/a
32	CTCF	chr16:31591460-31591610	HepG2	liver:	n/a	n/a
33	CTCF	chr16:31580220-31580370	AG04449	skin:	n/a	n/a
34	CTCF	chr16:31570248-31570297	Lung_OC	lung:	n/a	n/a
35	CTCF	chr16:31628612-31628648	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr16:31591521-31591524	GM12892	blood:	n/a	n/a
37	CTCF	chr16:31591760-31591910	HepG2	liver:	n/a	n/a
38	CTCF	chr16:31603780-31603930	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr16:31568417-31568463	K562	blood:	n/a	n/a
40	CTCF	chr16:31591460-31591610	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr16:31607297-31607367	Gliobla	brain:	n/a	n/a
42	CTCF	chr16:31591480-31591642	HepG2	liver:	n/a	n/a
43	CTCF	chr16:31591440-31591590	HEK293	kidney:	n/a	n/a
44	CTCF	chr16:31635769-31635813	MCF-7	breast:	n/a	n/a
45	CTCF	chr16:31600140-31600290	HepG2	liver:	n/a	n/a
46	CTCF	chr16:31591380-31591530	K562	blood:	n/a	n/a
47	CTCF	chr16:31600080-31600230	HEK293	kidney:	n/a	n/a
48	CTCF	chr16:31580259-31580390	ProgFib	skin:	n/a	n/a
49	CTCF	chr16:31600410-31600442	GM20000	blood:	n/a	n/a
50	CTCF	chr16:31600446-31600451	GM20000	blood:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:31580424-31580474	GM12892	blood:	n/a
2	chr16:31581268-31581318	A549	lung:	n/a
3	chr16:31579805-31579855	HRPEpiC	eye:	n/a
4	chr16:31580424-31580474	GM12892	blood:	n/a
5	chr16:31581268-31581318	A549	lung:	n/a
6	chr16:31579805-31579855	HRPEpiC	eye:	n/a
7	chr16:31580590-31580640	AG10803	skin:	n/a
8	chr16:31579647-31579697	PFSK-1	brain:	n/a
9	chr16:31580590-31580640	GM12891	blood:	n/a
10	chr16:31579647-31579697	HCPEpiC	choroid plexus:	n/a
11	chr16:31580560-31580610	Caco-2	colon:	n/a
12	chr16:31580989-31581039	AG09309	skin:	n/a
13	chr16:31579647-31579697	PANC-1	pancreas:	n/a
14	chr16:31576339-31576389	HUVEC	blood vessel:	n/a
15	chr16:31581150-31581200	PFSK-1	brain:	n/a
16	chr16:31579805-31579855	LNCaP	prostate:	n/a
17	chr16:31576872-31576922	AG10803	skin:	n/a
18	chr16:31580560-31580610	AG10803	skin:	n/a
19	chr16:31580153-31580203	NB4	blood:	n/a
20	chr16:31584046-31584096	PrEC	prostate:	n/a
21	chr16:31580889-31580939	CMK	blood:	n/a
22	chr16:31580889-31580939	AG09319	gingival:	n/a
23	chr16:31579805-31579855	CMK	blood:	n/a
24	chr16:31580889-31580939	Hepatocyte	liver:	n/a
25	chr16:31579805-31579855	K562	blood:	n/a
26	chr16:31581150-31581200	HEK293	kidney:	embryo
27	chr16:31580560-31580610	HepG2	liver:	n/a
28	chr16:31581309-31581359	IMR90	lung:	fetal
29	chr16:31580424-31580474	HAEpiC	amniotic membrane:	n/a
30	chr16:31580560-31580610	NT2-D1	testis:	n/a
31	chr16:31580153-31580203	PrEC	prostate:	n/a
32	chr16:31576872-31576922	AG09309	skin:	n/a
33	chr16:31580889-31580939	HCF	heart:	n/a
34	chr16:31580299-31580349	AG10803	skin:	n/a
35	chr16:31580889-31580939	HL-60	blood:	n/a
36	chr16:31580560-31580610	HCT-116	colon:	n/a
37	chr16:31580299-31580349	Jurkat	blood:	n/a
38	chr16:31580560-31580610	HIPEpiC	eye:	n/a
39	chr16:31576339-31576389	HMEC	breast:	n/a
40	chr16:31580560-31580610	H1-hESC	embryonic stem cell:	embryo
41	chr16:31580964-31581014	AG09309	skin:	n/a
42	chr16:31581268-31581318	HRCEpiC	kidney:	n/a
43	chr16:31581309-31581359	HRCEpiC	kidney:	n/a
44	chr16:31580150-31580200	HRPEpiC	eye:	n/a
45	chr16:31576872-31576922	HAEpiC	amniotic membrane:	n/a
46	chr16:31581150-31581200	HL-60	blood:	n/a
47	chr16:31584046-31584096	Hepatocyte	liver:	n/a
48	chr16:31580590-31580640	HAEpiC	amniotic membrane:	n/a
49	chr16:31580560-31580610	BE2_C	brain:	n/a
50	chr16:31580150-31580200	HCF	heart:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:31563997..31565923-chr16:31567034..31569130,2	K562	blood:
2	chr16:31629167..31631052-chr16:31633702..31636647,2	K562	blood:
3	chr16:31519671..31522254-chr16:31566727..31568830,2	MCF-7	breast:
4	chr16:31566968..31568774-chr16:31592560..31594234,2	MCF-7	breast:
5	chr16:31566968..31568774-chr16:31592560..31594234,2	MCF-7	breast:
6	chr16:31629167..31631052-chr16:31633702..31636647,2	K562	blood:
7	chr16:31556967..31559890-chr16:31567945..31570238,2	K562	blood:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C16orf58-6	chr16:31575897-31576029	NONHSAT141937
2	lnc-C16orf58-6	chr16:31574506-31574955	NONHSAT141936
3	lnc-AHSP-4	chr16:31628780-31629709	expReg_chr16_4904_+
4	lnc-C16orf58-6	chr16:31574403-31574920	NONHSAT141935
5	lnc-C16orf58-7	chr16:31612914-31614852	NONHSAT141940
6	lnc-AHSP-2	chr16:31565426-31566233	NONHSAT141933
7	lnc-AHSP-3	chr16:31625243-31625276	NONHSAT141942
8	lnc-AHSP-3	chr16:31624494-31624840	NONHSAT141941
9	lnc-C16orf58-6	chr16:31574154-31574955	NONHSAT141934
10	lnc-AHSP-3	chr16:31624492-31624614	NONHSAT141942
11	lnc-AHSP-3	chr16:31624171-31624294	NONHSAT141941
12	lnc-C16orf58-6	chr16:31575929-31576029	NONHSAT141936
13	lnc-C16orf58-6	chr16:31578695-31579037	NONHSAT141936
14	lnc-AHSP-3	chr16:31625713-31626173	NONHSAT141942
15	lnc-C16orf58-6	chr16:31578695-31579197	NONHSAT141937
16	lnc-AHSP-3	chr16:31624712-31624816	NONHSAT141942
17	lnc-C16orf58-6	chr16:31575924-31576104	NONHSAT141935
18	lnc-C16orf58-6	chr16:31575246-31575322	NONHSAT141936
19	lnc-C16orf58-6	chr16:31575929-31576029	NONHSAT141934
20	lnc-C16orf58-6	chr16:31579707-31580796	NONHSAT141939
21	lnc-AHSP-3	chr16:31623102-31623212	NONHSAT141941
22	lnc-C16orf58-6	chr16:31575246-31575322	NONHSAT141934
23	lnc-C16orf58-6	chr16:31575246-31575322	NONHSAT141935
24	lnc-C16orf58-6	chr16:31575556-31575606	NONHSAT141935
25	lnc-C16orf58-6	chr16:31579088-31580845	NONHSAT141938
26	lnc-C16orf58-6	chr16:31602915-31602937	NONHSAT141934

No data

Variant related genes	Relation type
ZNF720P1	TF binding region
ENSG00000261741	TF binding region
ENSG00000261475	TF binding region
YBX3P1	TF binding region
ZNF720P1	CpG island
ENSG00000261741	CpG island
ENSG00000261475	CpG island
YBX3P1	CpG island
ENSG00000261475	chromatin interactions
ENSG00000140688	chromatin interactions
ENSG00000213547	chromatin interactions
ENSG00000260883	chromatin interactions
ENSG00000261648	chromatin interactions
ENSG00000260625	chromatin interactions

Extended variants
information (count: 879 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:879 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7190117	chr16:31565597-31565598	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538322522	chr16:31565601-31565602	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs189493918	chr16:31565632-31565633	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs574120496	chr16:31565671-31565672	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs542925685	chr16:31565694-31565695	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs55694990	chr16:31565724-31565725	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs61374523	chr16:31565780-31565781	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs540233095	chr16:31565784-31565785	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs565267279	chr16:31565807-31565808	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs532526911	chr16:31565859-31565860	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs58790407	chr16:31565867-31565868	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs563516114	chr16:31565881-31565882	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs112686174	chr16:31565889-31565890	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs114754718	chr16:31565894-31565895	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs549634669	chr16:31565903-31565904	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs528369691	chr16:31565906-31565907	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs550296711	chr16:31565952-31565953	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs201129264	chr16:31566021-31566022	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs8054784	chr16:31566029-31566030	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs571217616	chr16:31566128-31566129	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs538384178	chr16:31566154-31566155	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs8050193	chr16:31566206-31566207	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs531982674	chr16:31566225-31566226	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs79460391	chr16:31566729-31566730	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs576791547	chr16:31566773-31566774	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs60650248	chr16:31566888-31566889	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs571111519	chr16:31566915-31566916	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs546861158	chr16:31566957-31566958	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs369530434	chr16:31566961-31566962	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs531936742	chr16:31567031-31567032	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs550284694	chr16:31567051-31567052	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs182072051	chr16:31567096-31567097	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs374196832	chr16:31567134-31567135	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs185738406	chr16:31567176-31567177	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs190919023	chr16:31567202-31567203	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs567052004	chr16:31567242-31567243	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs534266259	chr16:31567255-31567256	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs117515579	chr16:31567286-31567287	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs114241387	chr16:31567315-31567316	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs368375119	chr16:31567350-31567351	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs140184668	chr16:31567372-31567373	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs370793547	chr16:31567386-31567387	Inactive region	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs562794197	chr16:31567396-31567397	Inactive region	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs538785385	chr16:31567412-31567413	Inactive region	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs553626121	chr16:31567486-31567487	Inactive region	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs542304165	chr16:31567558-31567559	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs560964411	chr16:31567568-31567569	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs572951457	chr16:31567573-31567574	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs540161625	chr16:31567574-31567575	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs538225787	chr16:31567591-31567592	Inactive region	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
Sezary syndrome	18413736	CNVD
Wilms tumour	21544195	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31568200-31568600	Flanking Active TSS	K562	blood
2	chr16:31568600-31568800	Active TSS	K562	blood
3	chr16:31572800-31573200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr16:31572800-31573400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr16:31573200-31579800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr16:31574400-31574600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr16:31579600-31580000	Enhancers	Gastric	stomach
8	chr16:31579600-31580400	ZNF genes & repeats	Lung	lung
9	chr16:31579600-31581000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
10	chr16:31579600-31581000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
11	chr16:31579600-31581400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
12	chr16:31579800-31580000	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr16:31579800-31580000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr16:31579800-31580000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr16:31579800-31580000	Enhancers	Pancreas	Pancrea
16	chr16:31579800-31580200	Bivalent/Poised TSS	Brain Anterior Caudate	brain
17	chr16:31579800-31581000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
18	chr16:31579800-31581000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
19	chr16:31579800-31581200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
20	chr16:31579800-31581400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
21	chr16:31579800-31581400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
22	chr16:31580000-31580200	Enhancers	Primary hematopoietic stem cells	blood
23	chr16:31580000-31580200	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr16:31580000-31580200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
25	chr16:31580000-31580200	Bivalent Enhancer	Fetal Stomach	stomach
26	chr16:31580000-31580200	Active TSS	Rectal Smooth Muscle	rectum
27	chr16:31580000-31580200	Active TSS	Right Atrium	heart
28	chr16:31580000-31580200	Active TSS	Right Ventricle	heart
29	chr16:31580000-31580200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
30	chr16:31580000-31580200	Bivalent Enhancer	Stomach Mucosa	stomach
31	chr16:31580000-31580200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
32	chr16:31580000-31580400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr16:31580000-31580400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
34	chr16:31580000-31580400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
35	chr16:31580000-31580400	Flanking Active TSS	Gastric	stomach
36	chr16:31580000-31580400	Flanking Active TSS	Pancreas	Pancrea
37	chr16:31580000-31580400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
38	chr16:31580000-31580600	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
39	chr16:31580000-31580600	Bivalent Enhancer	Fetal Heart	heart
40	chr16:31580000-31580600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
41	chr16:31580000-31580600	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr16:31580000-31580800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
43	chr16:31580000-31580800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr16:31580000-31580800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr16:31580000-31580800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr16:31580000-31580800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
47	chr16:31580000-31580800	Bivalent/Poised TSS	Brain Substantia Nigra	brain
48	chr16:31580000-31580800	Bivalent/Poised TSS	Left Ventricle	heart
49	chr16:31580000-31581000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr16:31580000-31581000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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