Variant report

Variant	nsv1060132
Chromosome Location	chr16:76640155-77057830
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1961)
CpG islands
(count:366)
Chromatin interactive
region (count:53)
LncRNA
region (count:14)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1961 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:76980885-76981085	K562	blood:	n/a	n/a
2	ARID3A	chr16:76934165-76934485	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:76673948-76674099	K562	blood:	n/a	n/a
4	ARID3A	chr16:76913373-76913653	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:76668888-76668938	K562	blood:	n/a	n/a
6	ARID3A	chr16:76687350-76687721	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:76684292-76684820	HepG2	liver:	n/a	n/a
8	ATF1	chr16:76668805-76669470	K562	blood:	n/a	n/a
9	ATF1	chr16:76789952-76789998	K562	blood:	n/a	n/a
10	ATF1	chr16:76687134-76687664	K562	blood:	n/a	n/a
11	ATF2	chr16:77010103-77010377	GM12878	blood:	n/a	n/a
12	ATF2	chr16:76839037-76839302	GM12878	blood:	n/a	n/a
13	ATF3	chr16:77003970-77004466	A549	lung:	n/a	n/a
14	ATF3	chr16:76980721-76981225	A549	lung:	n/a	n/a
15	ATF3	chr16:76980774-76981124	K562	blood:	n/a	n/a
16	ATF3	chr16:76980737-76981284	A549	lung:	n/a	n/a
17	ATF3	chr16:76668818-76669064	K562	blood:	n/a	n/a
18	ATF3	chr16:76687346-76687640	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr16:76703299-76703491	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr16:77057336-77057341	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr16:76980722-76981230	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr16:76980807-76981126	K562	blood:	n/a	n/a
23	BATF	chr16:76838975-76839411	GM12878	blood:	n/a	n/a
24	BATF	chr16:76850433-76850727	GM12878	blood:	n/a	chr16:76850562-76850573
25	BATF	chr16:76980831-76981097	GM12878	blood:	n/a	chr16:76980965-76980976
26	BATF	chr16:76966490-76966773	GM12878	blood:	n/a	chr16:76966611-76966622 chr16:76966612-76966622
27	BATF	chr16:76856327-76856649	GM12878	blood:	n/a	n/a
28	BATF	chr16:76850471-76850665	GM12878	blood:	n/a	chr16:76850562-76850573
29	BATF	chr16:76838952-76839361	GM12878	blood:	n/a	n/a
30	BATF	chr16:76980823-76981049	GM12878	blood:	n/a	chr16:76980965-76980976
31	BATF	chr16:76856386-76856604	GM12878	blood:	n/a	n/a
32	BATF	chr16:76966506-76966724	GM12878	blood:	n/a	chr16:76966611-76966622 chr16:76966612-76966622
33	BCL11A	chr16:76839121-76839299	GM12878	blood:	n/a	chr16:76839215-76839224 chr16:76839226-76839235
34	BCL11A	chr16:77010106-77010349	GM12878	blood:	n/a	n/a
35	BCL11A	chr16:76839015-76839347	GM12878	blood:	n/a	chr16:76839215-76839224 chr16:76839226-76839235
36	BCL3	chr16:76980667-76981333	A549	lung:	n/a	n/a
37	BHLHE40	chr16:76704362-76704737	K562	blood:	n/a	chr16:76704597-76704606
38	BHLHE40	chr16:76668642-76669184	K562	blood:	n/a	n/a
39	BHLHE40	chr16:76937293-76937310	HepG2	liver:	n/a	n/a
40	BHLHE40	chr16:76981970-76981973	HepG2	liver:	n/a	n/a
41	BHLHE40	chr16:76968723-76968754	HepG2	liver:	n/a	n/a
42	BHLHE40	chr16:76980800-76981182	K562	blood:	n/a	n/a
43	CBX3	chr16:76668672-76669213	K562	blood:	n/a	n/a
44	CBX3	chr16:76668556-76669332	K562	blood:	n/a	n/a
45	CCNT2	chr16:76668739-76669178	K562	blood:	n/a	n/a
46	CCNT2	chr16:76980827-76981168	K562	blood:	n/a	n/a
47	CEBPB	chr16:76640194-76640523	K562	blood:	n/a	chr16:76640353-76640364
48	CEBPB	chr16:76687293-76687724	K562	blood:	n/a	n/a
49	CEBPB	chr16:76696611-76696792	HepG2	liver:	n/a	chr16:76696685-76696698 chr16:76696686-76696697 chr16:76696685-76696696
50	CEBPB	chr16:76734183-76734406	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76668836-76668886	T-47D	breast:	n/a
2	chr16:76668836-76668886	ovcar-3	ovarian:	n/a
3	chr16:76708064-76708114	HRCEpiC	kidney:	n/a
4	chr16:76669151-76669201	GM12891	blood:	n/a
5	chr16:76670197-76670247	HCT-116	colon:	n/a
6	chr16:76670197-76670247	AG09319	gingival:	n/a
7	chr16:76666860-76666910	GM06990	blood:	n/a
8	chr16:76665665-76665715	PrEC	prostate:	n/a
9	chr16:76669151-76669201	AG09319	gingival:	n/a
10	chr16:76708064-76708114	GM06990	blood:	n/a
11	chr16:76666860-76666910	IMR90	lung:	fetal
12	chr16:76670197-76670247	Hela-S3	cervix:	n/a
13	chr16:76670197-76670247	IMR90	lung:	fetal
14	chr16:76708064-76708114	LNCaP	prostate:	n/a
15	chr16:76668836-76668886	PrEC	prostate:	n/a
16	chr16:76665665-76665715	SK-N-MC	brain:	n/a
17	chr16:76668836-76668886	RPTEC	kidney:	n/a
18	chr16:76670197-76670247	HRE	kidney:	n/a
19	chr16:76668836-76668886	AG09319	gingival:	n/a
20	chr16:76669151-76669201	Hepatocyte	liver:	n/a
21	chr16:76669151-76669201	A549	lung:	n/a
22	chr16:76669151-76669201	SAEC	small airway:	n/a
23	chr16:76670197-76670247	NB4	blood:	n/a
24	chr16:76668836-76668886	SK-N-SH	brain:	n/a
25	chr16:76669151-76669201	K562	blood:	n/a
26	chr16:76708064-76708114	GM12892	blood:	n/a
27	chr16:76670197-76670247	HRCEpiC	kidney:	n/a
28	chr16:76669151-76669201	BE2_C	brain:	n/a
29	chr16:76666860-76666910	SK-N-SH	brain:	n/a
30	chr16:76669151-76669201	HEEpiC	esophagus:	n/a
31	chr16:76670197-76670247	HMEC	breast:	n/a
32	chr16:76668836-76668886	SAEC	small airway:	n/a
33	chr16:76669151-76669201	AG10803	skin:	n/a
34	chr16:76669151-76669201	LNCaP	prostate:	n/a
35	chr16:76666860-76666910	CMK	blood:	n/a
36	chr16:76708064-76708114	Hela-S3	cervix:	n/a
37	chr16:76665665-76665715	AG10803	skin:	n/a
38	chr16:76668836-76668886	SK-N-SH_RA	brain:	n/a
39	chr16:76670197-76670247	HL-60	blood:	n/a
40	chr16:76668836-76668886	GM12878	blood:	n/a
41	chr16:76668836-76668886	U87	brain:	n/a
42	chr16:76666860-76666910	PFSK-1	brain:	n/a
43	chr16:76665665-76665715	GM12891	blood:	n/a
44	chr16:76669151-76669201	HCT-116	colon:	n/a
45	chr16:76666860-76666910	GM19239	blood:	n/a
46	chr16:76670197-76670247	NH-A	brain:	n/a
47	chr16:76669151-76669201	HRE	kidney:	n/a
48	chr16:76670197-76670247	Hepatocyte	liver:	n/a
49	chr16:76669151-76669201	HRCEpiC	kidney:	n/a
50	chr16:76708064-76708114	NB4	blood:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:76846196..76848121-chr16:76848521..76851117,2	MCF-7	breast:
2	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
3	chr16:76817240..76820216-chr16:76820936..76823507,2	K562	blood:
4	chr16:76773881..76775450-chr16:76881262..76882791,2	MCF-7	breast:
5	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
6	chr16:76878928..76880909-chr16:76882753..76884640,2	K562	blood:
7	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
8	chr16:75835108..75835786-chr16:76687075..76687822,2	MCF-7	breast:
9	chr16:76972133..76974493-chr16:76974679..76976840,2	MCF-7	breast:
10	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
11	chr16:76665227..76667688-chr16:76668445..76671290,2	K562	blood:
12	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
13	chr16:76887394..76888672-chr16:77203188..77204165,5	MCF-7	breast:
14	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
15	chr16:76881611..76883954-chr16:76887729..76889678,2	MCF-7	breast:
16	chr16:76878928..76880909-chr16:76882753..76884640,2	K562	blood:
17	chr16:76846196..76848121-chr16:76848521..76851117,2	MCF-7	breast:
18	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
19	chr16:77044641..77046687-chr16:77049304..77051697,2	K562	blood:
20	chr16:76886880..76887748-chr16:77077328..77078325,2	MCF-7	breast:
21	chr16:76856883..76857419-chr16:77076804..77077643,2	MCF-7	breast:
22	chr16:76887878..76888800-chr16:77205307..77205910,4	MCF-7	breast:
23	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
24	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
25	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
26	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
27	chr16:76887896..76888842-chr16:77076469..77077719,11	MCF-7	breast:
28	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
29	chr16:76699506..76700441-chr16:77205329..77206242,3	MCF-7	breast:
30	chr16:76773881..76775450-chr16:76881262..76882791,2	MCF-7	breast:
31	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
32	chr16:76972133..76974493-chr16:76974679..76976840,2	MCF-7	breast:
33	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
34	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
35	chr16:76844876..76847420-chr19:45599129..45600971,2	MCF-7	breast:
36	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
37	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
38	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
39	chr16:76881611..76883954-chr16:76887729..76889678,2	MCF-7	breast:
40	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
41	chr16:76312365..76313607-chr16:76673596..76674287,4	MCF-7	breast:
42	chr16:76887924..76888465-chr16:77203271..77204023,2	MCF-7	breast:
43	chr16:75834944..75835823-chr16:76687371..76688062,3	MCF-7	breast:
44	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:
45	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
46	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
47	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
48	chr16:77044641..77046687-chr16:77049304..77051697,2	K562	blood:
49	chr16:76817240..76820216-chr16:76820936..76823507,2	K562	blood:
50	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-58C22.1.1-3	chr16:76803213-76803278	XLOC_011793
2	lnc-ADAMTS18-2	chr16:77042061-77042204	XLOC_012014
3	lnc-RP11-58C22.1.1-2	chr16:76733678-76734033	XLOC_011792
4	lnc-RP11-58C22.1.1-4	chr16:76770239-76770376	ENSG00000259995.1
5	lnc-RP11-58C22.1.1-3	chr16:76806570-76806959	XLOC_011793
6	lnc-RP11-58C22.1.1-4	chr16:76961793-76962066	ENSG00000259995.1
7	lnc-RP11-58C22.1.1-1	chr16:76690565-76692375	ENSG00000250514
8	lnc-ADAMTS18-8	chr16:76912171-76912833	NONHSAT143788
9	lnc-RP11-58C22.1.1-4	chr16:76946252-76946305	ENSG00000259995.1
10	lnc-RP11-58C22.1.1-1	chr16:76669394-76669520	ENSG00000250514
11	lnc-RP11-58C22.1.1-2	chr16:76737141-76737172	XLOC_011792
12	lnc-RP11-58C22.1.1-1	chr16:76689454-76689561	ENSG00000250514
13	lnc-ADAMTS18-2	chr16:77028205-77028433	XLOC_012014
14	lnc-RP11-58C22.1.1-1	chr16:76668895-76669046	ENSG00000250514

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4719	chr16:76902885-76902906	MIMAT0019832

No data

Variant related genes	Relation type
ENSG00000260797	TF binding region
ENSG00000259995	TF binding region
MIR4719	TF binding region
ENSG00000250514	TF binding region
ENSG00000260797	CpG island
ENSG00000259995	CpG island
MIR4719	CpG island
ENSG00000250514	CpG island
ENSG00000250514	chromatin interactions
SPRYD3	miRNA target sites
DDX3Y	miRNA target sites
PYGO2	miRNA target sites
CDV3	miRNA target sites
QARS	miRNA target sites
CDKN1A	miRNA target sites

Extended variants
information (count: 10434 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:10434 , 50 per page) page: 1 2 3 4 5 6 7 ... 209

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556362359	chr16:76645614-76645615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548208898	chr16:76645634-76645635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568362075	chr16:76645648-76645649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75593087	chr16:76645662-76645663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570279014	chr16:76645684-76645685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553003038	chr16:76645701-76645702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147227844	chr16:76645711-76645712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs117626792	chr16:76645726-76645727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187182983	chr16:76645732-76645733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs193028194	chr16:76645736-76645737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544302799	chr16:76645753-76645754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554595301	chr16:76645758-76645759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574340570	chr16:76645782-76645783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563232439	chr16:76646428-76646429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34071157	chr16:76646457-76646458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528272682	chr16:76646458-76646459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545688351	chr16:76646476-76646477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577148883	chr16:76646483-76646484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191673796	chr16:76646488-76646489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562783849	chr16:76646533-76646534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531800044	chr16:76646541-76646542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562391572	chr16:76646543-76646544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542363622	chr16:76646598-76646599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562064350	chr16:76646630-76646631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142177881	chr16:76646694-76646695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559094593	chr16:76646723-76646724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183817766	chr16:76646818-76646819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547509379	chr16:76646846-76646847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528385834	chr16:76646880-76646881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564451092	chr16:76646907-76646908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56686940	chr16:76646966-76646967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567819239	chr16:76646967-76646968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189628710	chr16:76646968-76646969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181669030	chr16:76646974-76646975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs397701813	chr16:76646975-76646976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373006323	chr16:76646976-76646977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567351608	chr16:76646978-76646979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569131345	chr16:76646981-76646982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201468243	chr16:76646992-76646993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371248239	chr16:76646993-76646994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs397740364	chr16:76646994-76646995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199774100	chr16:76646995-76646996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200726468	chr16:76646996-76646997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201710731	chr16:76646997-76646998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370861741	chr16:76647006-76647007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548335357	chr16:76647018-76647019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568075246	chr16:76647027-76647028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550292275	chr16:76647032-76647033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12447210	chr16:76647066-76647067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs553537079	chr16:76647078-76647079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Lung cancer	24585490	CNVD
Cancer	20164919	CNVD
Neuroblastoma	18923524	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20581869	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76645600-76645800	Enhancers	Placenta Amnion	Placenta Amnion
2	chr16:76646400-76647400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr16:76647200-76650000	Enhancers	Brain Germinal Matrix	brain
4	chr16:76647400-76647800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr16:76647400-76647800	Enhancers	Placenta Amnion	Placenta Amnion
6	chr16:76647600-76648800	Enhancers	Brain Substantia Nigra	brain
7	chr16:76647800-76648200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr16:76647800-76649000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr16:76647800-76649400	Enhancers	Fetal Brain Female	brain
10	chr16:76648000-76648600	Enhancers	Brain Hippocampus Middle	brain
11	chr16:76648000-76649200	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr16:76648000-76649800	Enhancers	Fetal Brain Male	brain
13	chr16:76648000-76650000	Enhancers	Fetal Lung	lung
14	chr16:76648200-76649000	Enhancers	Brain Cingulate Gyrus	brain
15	chr16:76648200-76649000	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr16:76648200-76649200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr16:76648400-76649000	Enhancers	Brain Angular Gyrus	brain
18	chr16:76648400-76649200	Enhancers	Fetal Stomach	stomach
19	chr16:76649000-76649200	Enhancers	Placenta Amnion	Placenta Amnion
20	chr16:76649200-76650000	Weak transcription	Fetal Stomach	stomach
21	chr16:76650000-76650200	Enhancers	Fetal Stomach	stomach
22	chr16:76653600-76653800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr16:76653600-76653800	Enhancers	Pancreas	Pancrea
24	chr16:76653800-76654000	ZNF genes & repeats	Pancreas	Pancrea
25	chr16:76656000-76659000	Enhancers	Fetal Lung	lung
26	chr16:76657000-76657600	Enhancers	Fetal Brain Male	brain
27	chr16:76657200-76657800	Enhancers	Fetal Brain Female	brain
28	chr16:76660400-76660800	Enhancers	K562	blood
29	chr16:76668600-76668800	Enhancers	Pancreas	Pancrea
30	chr16:76668600-76669800	Active TSS	K562	blood
31	chr16:76668800-76669200	Active TSS	Gastric	stomach
32	chr16:76668800-76669200	Flanking Active TSS	Pancreas	Pancrea
33	chr16:76669000-76669400	Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr16:76669000-76669400	Active TSS	Duodenum Mucosa	Duodenum
35	chr16:76673400-76674600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr16:76673600-76674000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
37	chr16:76673800-76674400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr16:76684400-76685200	Flanking Active TSS	A549	lung
39	chr16:76684600-76685200	Enhancers	HepG2	liver
40	chr16:76685200-76685400	Enhancers	A549	lung
41	chr16:76686600-76687000	Enhancers	Fetal Brain Male	brain
42	chr16:76687200-76687800	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr16:76687200-76688000	Enhancers	Brain Substantia Nigra	brain
44	chr16:76687200-76688200	Enhancers	Fetal Lung	lung
45	chr16:76687600-76688200	Enhancers	Brain Hippocampus Middle	brain
46	chr16:76687600-76689600	Enhancers	Brain Germinal Matrix	brain
47	chr16:76688200-76690600	Weak transcription	Fetal Lung	lung
48	chr16:76689600-76690400	Weak transcription	Brain Germinal Matrix	brain
49	chr16:76690000-76692000	Enhancers	Primary hematopoietic stem cells	blood
50	chr16:76690400-76692000	Enhancers	Brain Germinal Matrix	brain

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