Variant report

Variant	nsv906890
Chromosome Location	chr16:70740707-70790831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1536)
CpG islands
(count:732)
Chromatin interactive
region (count:140)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1536 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70783430-70783434	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:70758177-70760063	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:70772338-70772610	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:70780639-70781200	K562	blood:	n/a	n/a
5	ARID3A	chr16:70779999-70781304	HepG2	liver:	n/a	n/a
6	ATF1	chr16:70780603-70781205	K562	blood:	n/a	n/a
7	ATF2	chr16:70771333-70771911	GM12878	blood:	n/a	n/a
8	ATF2	chr16:70771328-70771985	GM12878	blood:	n/a	n/a
9	ATF3	chr16:70780385-70781032	A549	lung:	n/a	n/a
10	ATF3	chr16:70780580-70780931	HepG2	liver:	n/a	n/a
11	ATF3	chr16:70748940-70749471	A549	lung:	n/a	n/a
12	ATF3	chr16:70780446-70781042	A549	lung:	n/a	n/a
13	ATF3	chr16:70780538-70780970	K562	blood:	n/a	n/a
14	BACH1	chr16:70760373-70760459	K562	blood:	n/a	n/a
15	BATF	chr16:70771501-70771754	GM12878	blood:	n/a	n/a
16	BATF	chr16:70771420-70771777	GM12878	blood:	n/a	n/a
17	BCL11A	chr16:70771343-70771810	GM12878	blood:	n/a	chr16:70771552-70771565 chr16:70771479-70771488
18	BCL11A	chr16:70771388-70771806	GM12878	blood:	n/a	chr16:70771552-70771565 chr16:70771479-70771488
19	BCL3	chr16:70779717-70780260	A549	lung:	n/a	n/a
20	BCL3	chr16:70779908-70780451	A549	lung:	n/a	n/a
21	BCL3	chr16:70748867-70749435	A549	lung:	n/a	n/a
22	BCL3	chr16:70779960-70780438	GM12878	blood:	n/a	n/a
23	BCL3	chr16:70749067-70749450	GM12878	blood:	n/a	n/a
24	BCL3	chr16:70780437-70781102	A549	lung:	n/a	chr16:70780788-70780797 chr16:70780789-70780798
25	BCL3	chr16:70780065-70780317	GM12878	blood:	n/a	n/a
26	BHLHE40	chr16:70779907-70781278	HepG2	liver:	n/a	n/a
27	BHLHE40	chr16:70779983-70780216	HepG2	liver:	n/a	n/a
28	BHLHE40	chr16:70758173-70760016	HepG2	liver:	n/a	n/a
29	BHLHE40	chr16:70782202-70782206	K562	blood:	n/a	n/a
30	BHLHE40	chr16:70779996-70780319	A549	lung:	n/a	n/a
31	BHLHE40	chr16:70772347-70772605	HepG2	liver:	n/a	n/a
32	BHLHE40	chr16:70748994-70749336	K562	blood:	n/a	n/a
33	BHLHE40	chr16:70770952-70772027	GM12878	blood:	n/a	chr16:70771488-70771497 chr16:70771272-70771288
34	BHLHE40	chr16:70780559-70780876	HepG2	liver:	n/a	n/a
35	BHLHE40	chr16:70772413-70772528	K562	blood:	n/a	n/a
36	BHLHE40	chr16:70779958-70780994	K562	blood:	n/a	n/a
37	BHLHE40	chr16:70749012-70749400	A549	lung:	n/a	n/a
38	BRCA1	chr16:70758191-70759764	HepG2	liver:	n/a	n/a
39	BRCA1	chr16:70740997-70741513	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr16:70780022-70780866	HepG2	liver:	n/a	n/a
41	CBX3	chr16:70780513-70781040	K562	blood:	n/a	n/a
42	CBX3	chr16:70780080-70780511	K562	blood:	n/a	n/a
43	CCNT2	chr16:70780556-70780888	K562	blood:	n/a	n/a
44	CEBPB	chr16:70780546-70780972	HepG2	liver:	n/a	n/a
45	CEBPB	chr16:70754903-70755141	HepG2	liver:	n/a	chr16:70754980-70754991
46	CEBPB	chr16:70747313-70747634	IMR90	lung:	n/a	chr16:70747469-70747482 chr16:70747470-70747481
47	CEBPB	chr16:70747375-70747579	A549	lung:	n/a	chr16:70747469-70747482 chr16:70747470-70747481
48	CEBPB	chr16:70780564-70781067	K562	blood:	n/a	n/a
49	CEBPB	chr16:70745207-70745632	HepG2	liver:	n/a	n/a
50	CEBPB	chr16:70754939-70755139	A549	lung:	n/a	chr16:70754980-70754991

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70745992-70746042	BJ	skin:	n/a
2	chr16:70759994-70760044	AG09309	skin:	n/a
3	chr16:70749564-70749614	ProgFib	skin:	n/a
4	chr16:70784519-70784569	RPTEC	kidney:	n/a
5	chr16:70745992-70746042	NHDF-neo	bronchial:	n/a
6	chr16:70749564-70749614	AG09319	gingival:	n/a
7	chr16:70749564-70749614	NHBE	bronchial:	n/a
8	chr16:70749564-70749614	PANC-1	pancreas:	n/a
9	chr16:70784519-70784569	NB4	blood:	n/a
10	chr16:70745992-70746042	IMR90	lung:	fetal
11	chr16:70760142-70760192	RPTEC	kidney:	n/a
12	chr16:70749564-70749614	HEK293	kidney:	embryo
13	chr16:70749564-70749614	HRPEpiC	eye:	n/a
14	chr16:70759914-70759964	HUVEC	blood vessel:	n/a
15	chr16:70759095-70759145	GM19239	blood:	n/a
16	chr16:70770604-70770654	SAEC	small airway:	n/a
17	chr16:70759095-70759145	SK-N-SH	brain:	n/a
18	chr16:70760142-70760192	Caco-2	colon:	n/a
19	chr16:70787597-70787647	GM06990	blood:	n/a
20	chr16:70771142-70771192	SKMC	muscle:	n/a
21	chr16:70787597-70787647	AG04449	skin:	fetal
22	chr16:70748321-70748371	Hepatocyte	liver:	n/a
23	chr16:70760142-70760192	SAEC	small airway:	n/a
24	chr16:70760142-70760192	HCT-116	colon:	n/a
25	chr16:70759914-70759964	MCF10A-Er-Src	breast:	n/a
26	chr16:70759994-70760044	Jurkat	blood:	n/a
27	chr16:70784519-70784569	HRPEpiC	eye:	n/a
28	chr16:70770604-70770654	MCF10A-Er-Src	breast:	n/a
29	chr16:70770604-70770654	SK-N-SH	brain:	n/a
30	chr16:70759994-70760044	GM06990	blood:	n/a
31	chr16:70770604-70770654	PANC-1	pancreas:	n/a
32	chr16:70749564-70749614	Hela-S3	cervix:	n/a
33	chr16:70784519-70784569	NHBE	bronchial:	n/a
34	chr16:70748321-70748371	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:70759994-70760044	HCF	heart:	n/a
36	chr16:70771142-70771192	GM06990	blood:	n/a
37	chr16:70759914-70759964	AoSMC	blood vessel:	n/a
38	chr16:70748321-70748371	NB4	blood:	n/a
39	chr16:70771142-70771192	H1-hESC	embryonic stem cell:	embryo
40	chr16:70771142-70771192	IMR90	lung:	fetal
41	chr16:70759095-70759145	BE2_C	brain:	n/a
42	chr16:70749564-70749614	SAEC	small airway:	n/a
43	chr16:70749564-70749614	SK-N-SH	brain:	n/a
44	chr16:70784519-70784569	AG09309	skin:	n/a
45	chr16:70783744-70783794	A549	lung:	n/a
46	chr16:70759914-70759964	HCM	heart:	n/a
47	chr16:70759914-70759964	AG04449	skin:	fetal
48	chr16:70760142-70760192	LNCaP	prostate:	n/a
49	chr16:70748321-70748371	SAEC	small airway:	n/a
50	chr16:70759914-70759964	ProgFib	skin:	n/a

(count:140 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr16:70739016..70741749-chr16:70743376..70745387,3	K562	blood:
2	chr16:70747966..70750643-chr16:70785979..70788271,2	MCF-7	breast:
3	chr16:70743274..70745698-chr16:70747282..70749621,3	K562	blood:
4	chr16:70737871..70744107-chr16:70778676..70782524,8	MCF-7	breast:
5	chr16:70741732..70744635-chr16:70754684..70756403,2	K562	blood:
6	chr16:70761517..70763051-chr16:70766034..70768582,2	K562	blood:
7	chr16:70775857..70777622-chr16:70780014..70781795,2	K562	blood:
8	chr16:70745613..70748451-chr16:70833649..70836455,2	K562	blood:
9	chr16:70773737..70776366-chr16:70784353..70786152,2	K562	blood:
10	chr16:70763729..70766674-chr16:70767583..70772048,4	K562	blood:
11	chr16:70747879..70752178-chr16:70754716..70759017,5	MCF-7	breast:
12	chr16:70749284..70751657-chr16:70760367..70762394,2	MCF-7	breast:
13	chr16:70749039..70749860-chr16:70771950..70772652,2	MCF-7	breast:
14	chr16:70713628..70714432-chr16:70772096..70772602,2	MCF-7	breast:
15	chr16:70748975..70750633-chr16:70770017..70771781,2	MCF-7	breast:
16	chr16:70747047..70751292-chr16:70770500..70773277,5	MCF-7	breast:
17	chr16:70753099..70755239-chr16:70768073..70771716,3	MCF-7	breast:
18	chr16:70737857..70741498-chr16:70742534..70745125,3	K562	blood:
19	chr16:70781821..70783701-chr16:70789924..70792216,3	K562	blood:
20	chr1:116519198..116522073-chr16:70780439..70782175,2	MCF-7	breast:
21	chr16:70728939..70732766-chr16:70778342..70782420,7	MCF-7	breast:
22	chr16:70782914..70785498-chr16:70796849..70798570,2	K562	blood:
23	chr16:70731044..70733238-chr16:70775632..70778039,2	MCF-7	breast:
24	chr16:70729407..70732134-chr16:70745492..70747752,2	K562	blood:
25	chr16:70761517..70763051-chr16:70766034..70768582,2	K562	blood:
26	chr16:70713469..70715146-chr16:70778729..70780747,2	MCF-7	breast:
27	chr16:70747788..70750728-chr16:70794954..70796850,2	MCF-7	breast:
28	chr16:70745639..70748512-chr16:70770742..70772516,3	MCF-7	breast:
29	chr16:70767547..70769820-chr16:70770075..70772238,2	K562	blood:
30	chr16:70765832..70768076-chr16:70774273..70775782,2	MCF-7	breast:
31	chr16:70740784..70746452-chr16:70747278..70752169,9	K562	blood:
32	chr16:70758547..70760441-chr16:70762170..70763955,2	K562	blood:
33	chr16:70716977..70720923-chr16:70779925..70783515,4	K562	blood:
34	chr16:70769869..70777910-chr16:70778144..70784375,13	MCF-7	breast:
35	chr16:70748975..70750633-chr16:70770017..70771781,2	MCF-7	breast:
36	chr16:70777980..70780022-chr16:70780577..70783431,2	K562	blood:
37	chr16:70749284..70751657-chr16:70760367..70762394,2	MCF-7	breast:
38	chr16:70785497..70787699-chr16:70811654..70814215,2	MCF-7	breast:
39	chr16:70771954..70772860-chr16:70804324..70805624,4	MCF-7	breast:
40	chr16:70717727..70720159-chr16:70744271..70745985,2	K562	blood:
41	chr16:70741732..70744635-chr16:70754684..70756403,2	K562	blood:
42	chr16:70715424..70721545-chr16:70778213..70783786,16	MCF-7	breast:
43	chr16:70733046..70734873-chr16:70779967..70781686,2	MCF-7	breast:
44	chr16:70760849..70763441-chr16:70769230..70771713,2	MCF-7	breast:
45	chr16:70717596..70719954-chr16:70769240..70771432,3	K562	blood:
46	chr16:70736848..70738799-chr16:70767007..70768655,2	MCF-7	breast:
47	chr16:70777980..70780022-chr16:70780577..70783431,2	K562	blood:
48	chr16:70735575..70742322-chr16:70778614..70782532,8	MCF-7	breast:
49	chr16:70772019..70772938-chr16:70804684..70805569,3	MCF-7	breast:
50	chr16:70753099..70755239-chr16:70768073..70771716,3	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL34-2	chr16:70789001-70789152	ENSG00000214353.3
2	lnc-IL34-2	chr16:70788963-70789152	NONHSAT143446
3	lnc-IL34-2	chr16:70789916-70789990	ENSG00000214353.3
4	lnc-IL34-2	chr16:70789916-70789990	NONHSAT143445
5	lnc-IL34-2	chr16:70789916-70789990	ENSG00000214353.3
6	lnc-IL34-2	chr16:70788863-70789152	NONHSAT143445
7	lnc-IL34-2	chr16:70789916-70789990	NONHSAT143446
8	lnc-IL34-2	chr16:70789036-70789152	ENSG00000214353.3

No data

Variant related genes	Relation type
VAC14	TF binding region
VAC14-AS1	TF binding region
ENSG00000260156	TF binding region
VAC14	CpG island
VAC14-AS1	CpG island
ENSG00000260156	CpG island
ENSG00000262890	chromatin interactions
ENSG00000132613	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000260156	chromatin interactions
ENSG00000163393	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000103051	chromatin interactions
ENSG00000103043	chromatin interactions
ENSG00000214353	chromatin interactions
ENSG00000157368	chromatin interactions

Extended variants
information (count: 2218 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:2218 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8059238	chr16:70740707-70740708	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370457623	chr16:70740710-70740711	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs187366120	chr16:70740738-70740739	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs550907368	chr16:70740781-70740782	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs563443660	chr16:70740791-70740792	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs141321478	chr16:70740806-70740807	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs374111604	chr16:70740816-70740817	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs548784488	chr16:70740835-70740836	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs567102073	chr16:70740855-70740856	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs534445265	chr16:70740869-70740870	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs546368625	chr16:70740884-70740885	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs571266739	chr16:70740895-70740896	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs192190574	chr16:70740987-70740988	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs145084422	chr16:70740988-70740989	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs71401828	chr16:70740997-70740998	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs560582783	chr16:70741045-70741046	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs146850731	chr16:70741111-70741112	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs536924125	chr16:70741129-70741130	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs555238884	chr16:70741191-70741192	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs140699107	chr16:70741194-70741195	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs79511906	chr16:70741213-70741214	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs184137309	chr16:70741216-70741217	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs201371749	chr16:70741255-70741256	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs577225159	chr16:70741387-70741388	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs75021004	chr16:70741393-70741394	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs12445557	chr16:70741432-70741433	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs530739276	chr16:70741446-70741447	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs542497899	chr16:70741462-70741463	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs573560373	chr16:70741483-70741484	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs188856842	chr16:70741563-70741564	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs546726839	chr16:70741578-70741579	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs143831796	chr16:70741611-70741612	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs532206427	chr16:70741658-70741659	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs199749177	chr16:70741704-70741705	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs550334532	chr16:70741707-70741708	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs568855667	chr16:70741732-70741733	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs148175227	chr16:70741741-70741742	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs544024010	chr16:70741744-70741745	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs564032192	chr16:70741755-70741756	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs555301905	chr16:70741786-70741787	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs567125571	chr16:70741801-70741802	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs2004103	chr16:70741838-70741839	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs150308343	chr16:70741842-70741843	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs577286435	chr16:70741897-70741898	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs544668738	chr16:70741939-70741940	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs556313641	chr16:70741980-70741981	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs371398915	chr16:70741982-70741983	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs77059773	chr16:70742033-70742034	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs560851388	chr16:70742053-70742054	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs528336735	chr16:70742082-70742083	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	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 myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	18923524	CNVD

Chromatin state (count:2848 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70720400-70753200	Weak transcription	Primary B cells from cord blood	blood
2	chr16:70727000-70770800	Weak transcription	GM12878-XiMat	blood
3	chr16:70731400-70755000	Weak transcription	Small Intestine	intestine
4	chr16:70732000-70746600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr16:70732200-70740800	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr16:70732800-70741000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr16:70732800-70744400	Enhancers	Fetal Muscle Trunk	muscle
8	chr16:70732800-70745000	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr16:70732800-70749600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr16:70733200-70759400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr16:70733400-70741000	Genic enhancers	Fetal Stomach	stomach
12	chr16:70733400-70742400	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr16:70733400-70743600	Enhancers	Placenta	Placenta
14	chr16:70733400-70754000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr16:70733600-70742400	Weak transcription	Primary B cells from peripheral blood	blood
16	chr16:70733800-70742000	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr16:70733800-70743400	Enhancers	Fetal Thymus	thymus
18	chr16:70733800-70744600	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr16:70733800-70753400	Weak transcription	Dnd41	blood
20	chr16:70734000-70741800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr16:70734000-70742000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr16:70734000-70742200	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr16:70734000-70742600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr16:70734000-70742600	Enhancers	Esophagus	oesophagus
25	chr16:70734200-70740800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr16:70734200-70741800	Enhancers	NHLF	lung
27	chr16:70734600-70743200	Enhancers	HSMMtube	muscle
28	chr16:70734600-70751200	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr16:70735000-70742000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr16:70735200-70742200	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr16:70735200-70743600	Weak transcription	Primary hematopoietic stem cells	blood
32	chr16:70735600-70741200	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr16:70735600-70744600	Enhancers	HSMM	muscle
34	chr16:70735800-70744400	Enhancers	Thymus	Thymus
35	chr16:70736000-70740800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr16:70736000-70741400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr16:70736000-70741400	Enhancers	Placenta Amnion	Placenta Amnion
38	chr16:70736000-70743600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr16:70736800-70741600	Genic enhancers	Fetal Intestine Small	intestine
40	chr16:70737000-70741000	Enhancers	Colon Smooth Muscle	Colon
41	chr16:70737000-70753800	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr16:70737200-70743600	Enhancers	Rectal Smooth Muscle	rectum
43	chr16:70737400-70741800	Enhancers	Osteobl	bone
44	chr16:70737400-70742200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr16:70737800-70740800	Enhancers	Hela-S3	cervix
46	chr16:70737800-70745600	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr16:70738000-70740800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr16:70738000-70741000	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr16:70738000-70741000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr16:70738000-70741000	Weak transcription	Lung	lung

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