Variant report

Variant	esv3410057
Chromosome Location	chr16:46663476-46666024
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	CEBPB	chr16:46663360-46663531	Hela-S3	cervix:	n/a	chr16:46663464-46663476
2	CTCF	chr16:46663400-46663550	GM12873	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
3	CTCF	chr16:46663460-46663610	HCT-116	colon:	n/a	n/a
4	CTCF	chr16:46663360-46663510	HepG2	liver:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
5	CTCF	chr16:46663340-46663490	A549	lung:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
6	CTCF	chr16:46663322-46663569	Gliobla	brain:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
7	CTCF	chr16:46663343-46663563	HUVEC	blood vessel:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
8	CTCF	chr16:46663420-46663570	GM12875	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
9	CTCF	chr16:46663420-46663570	GM06990	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
10	CTCF	chr16:46663360-46663510	NHEK	skin:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
11	CTCF	chr16:46663700-46663850	HRE	kidney:	n/a	n/a
12	CTCF	chr16:46663400-46663550	GM12871	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
13	CTCF	chr16:46663242-46663660	K562	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
14	CTCF	chr16:46663960-46664110	AG09319	gingival:	n/a	n/a
15	CTCF	chr16:46663340-46663490	MCF-7	breast:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
16	CTCF	chr16:46663380-46663530	SAEC	small airway:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
17	CTCF	chr16:46663344-46663498	A549	lung:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
18	CTCF	chr16:46663380-46663530	HCM	heart:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
19	CTCF	chr16:46663483-46663508	GM13976	blood:	n/a	n/a
20	CTCF	chr16:46663380-46663530	HEEpiC	esophagus:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
21	CTCF	chr16:46663320-46663567	MCF-7	breast:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
22	CTCF	chr16:46663266-46663585	K562	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
23	CTCF	chr16:46663360-46663510	HBMEC	blood vessel:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
24	CTCF	chr16:46663360-46663510	AG10803	skin:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
25	CTCF	chr16:46663356-46663533	MCF-7	breast:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
26	CTCF	chr16:46663366-46663494	Fibrobl	skin:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
27	CTCF	chr16:46663360-46663510	HMF	breast:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
28	CTCF	chr16:46663096-46664179	A549	lung:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
29	CTCF	chr16:46663340-46663490	GM12872	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
30	CTCF	chr16:46663420-46663570	K562	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
31	CTCF	chr16:46663380-46663530	BJ	skin:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
32	CTCF	chr16:46663380-46663530	SK-N-SH_RA	brain:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
33	CTCF	chr16:46663380-46663530	AG09319	gingival:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
34	CTCF	chr16:46663380-46663530	HVMF	connective:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
35	CTCF	chr16:46663780-46663930	GM12872	blood:	n/a	n/a
36	CTCF	chr16:46663640-46663790	AG04449	skin:	n/a	n/a
37	CTCF	chr16:46663340-46663490	HCM	heart:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
38	CTCF	chr16:46663520-46663670	K562	blood:	n/a	n/a
39	CTCF	chr16:46663420-46663540	GM20000	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
40	CTCF	chr16:46663540-46663690	A549	lung:	n/a	n/a
41	CTCF	chr16:46663400-46663550	HVMF	connective:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
42	CTCF	chr16:46663340-46663490	AG09309	skin:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
43	CTCF	chr16:46663380-46663530	RPTEC	kidney:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
44	CTCF	chr16:46663400-46663550	GM12864	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
45	CTCF	chr16:46663309-46663619	GM12892	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
46	CTCF	chr16:46663340-46663490	Hela-S3	cervix:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
47	CTCF	chr16:46663206-46663700	MCF-7	breast:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
48	CTCF	chr16:46663270-46663632	GM12878	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
49	CTCF	chr16:46663400-46663550	GM12878	blood:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461
50	CTCF	chr16:46663163-46663741	HCT-116	colon:	n/a	chr16:46663446-46663459 chr16:46663445-46663466 chr16:46663444-46663460 chr16:46663448-46663456 chr16:46663443-46663461

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:46663534-46663584	PFSK-1	brain:	n/a
2	chr16:46663534-46663584	MCF10A-Er-Src	breast:	n/a
3	chr16:46663534-46663584	SAEC	small airway:	n/a
4	chr16:46663534-46663584	SKMC	muscle:	n/a
5	chr16:46663534-46663584	HIPEpiC	eye:	n/a
6	chr16:46663534-46663584	CMK	blood:	n/a
7	chr16:46663534-46663584	HepG2	liver:	n/a
8	chr16:46663534-46663584	Hepatocyte	liver:	n/a
9	chr16:46663534-46663584	U87	brain:	n/a
10	chr16:46663534-46663584	ECC-1	luminal epithelium:	n/a
11	chr16:46663534-46663584	HEEpiC	esophagus:	n/a
12	chr16:46663534-46663584	BJ	skin:	n/a
13	chr16:46663534-46663584	HEK293	kidney:	embryo
14	chr16:46663534-46663584	NB4	blood:	n/a
15	chr16:46663534-46663584	A549	lung:	n/a
16	chr16:46663534-46663584	PrEC	prostate:	n/a
17	chr16:46663534-46663584	K562	blood:	n/a
18	chr16:46663534-46663584	Hela-S3	cervix:	n/a
19	chr16:46663534-46663584	ovcar-3	ovarian:	n/a
20	chr16:46663534-46663584	HAEpiC	amniotic membrane:	n/a
21	chr16:46663534-46663584	NHBE	bronchial:	n/a
22	chr16:46663534-46663584	HRCEpiC	kidney:	n/a
23	chr16:46663534-46663584	HMEC	breast:	n/a
24	chr16:46663534-46663584	HCF	heart:	n/a
25	chr16:46663534-46663584	GM06990	blood:	n/a
26	chr16:46663534-46663584	NT2-D1	testis:	n/a
27	chr16:46663534-46663584	LNCaP	prostate:	n/a
28	chr16:46663534-46663584	Jurkat	blood:	n/a
29	chr16:46663534-46663584	Caco-2	colon:	n/a
30	chr16:46663534-46663584	GM12891	blood:	n/a
31	chr16:46663534-46663584	HNPCEpiC	eye:	n/a
32	chr16:46663534-46663584	GM12878	blood:	n/a
33	chr16:46663534-46663584	BE2_C	brain:	n/a
34	chr16:46663534-46663584	AG09309	skin:	n/a
35	chr16:46663534-46663584	IMR90	lung:	fetal
36	chr16:46663534-46663584	GM12892	blood:	n/a
37	chr16:46663534-46663584	MCF-7	breast:	n/a
38	chr16:46663534-46663584	HRPEpiC	eye:	n/a
39	chr16:46663534-46663584	RPTEC	kidney:	n/a
40	chr16:46663534-46663584	T-47D	breast:	n/a
41	chr16:46663534-46663584	H1-hESC	embryonic stem cell:	embryo
42	chr16:46663534-46663584	AG04449	skin:	fetal
43	chr16:46663534-46663584	HCT-116	colon:	n/a
44	chr16:46663534-46663584	AG04450	lung:	fetal
45	chr16:46663534-46663584	HCM	heart:	n/a
46	chr16:46663534-46663584	PANC-1	pancreas:	n/a
47	chr16:46663534-46663584	HCPEpiC	choroid plexus:	n/a
48	chr16:46663534-46663584	NH-A	brain:	n/a
49	chr16:46663534-46663584	HRE	kidney:	n/a
50	chr16:46663534-46663584	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:46663117..46663909-chr16:46963648..46964236,2	MCF-7	breast:
2	chr16:46663477..46665810-chr16:46674721..46676333,2	K562	blood:
3	chr16:46663178..46663960-chr16:46723479..46724005,2	K562	blood:
4	chr16:46588378..46588920-chr16:46662972..46663507,2	K562	blood:
5	chr16:46651769..46655217-chr16:46661271..46664188,4	K562	blood:

Variant related genes	Relation type
RAB43P1	TF binding region
RAB43P1	CpG island
ENSG00000091651	chromatin interactions

Extended variants
information (count: 82 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192908240	chr16:46663487-46663488	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs556925950	chr16:46663497-46663498	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs538815414	chr16:46663505-46663506	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs144608851	chr16:46663523-46663524	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs62060522	chr16:46663606-46663607	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs575375971	chr16:46663642-46663643	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs118085222	chr16:46663673-46663674	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs554226511	chr16:46663716-46663717	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs572788331	chr16:46663717-46663718	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs539894798	chr16:46663765-46663766	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs559973687	chr16:46663786-46663787	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs4966603	chr16:46663790-46663791	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs563558495	chr16:46663791-46663792	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs530863659	chr16:46663885-46663886	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs549468458	chr16:46663896-46663897	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs368322200	chr16:46663927-46663928	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs561269350	chr16:46663964-46663965	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs532195948	chr16:46663968-46663969	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs201000466	chr16:46663994-46663995	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs528484841	chr16:46664129-46664130	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs546708128	chr16:46664146-46664147	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs9935497	chr16:46664160-46664161	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs185119374	chr16:46664214-46664215	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs139002121	chr16:46664237-46664238	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs142277971	chr16:46664255-46664256	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs190444206	chr16:46664273-46664274	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs554646366	chr16:46664317-46664318	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs112832054	chr16:46664354-46664355	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs374662116	chr16:46664364-46664365	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs572878502	chr16:46664385-46664386	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs34106723	chr16:46664491-46664492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12933750	chr16:46664493-46664494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35012767	chr16:46664495-46664496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35124275	chr16:46664497-46664498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs36065841	chr16:46664499-46664500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs56309128	chr16:46664527-46664528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs55720456	chr16:46664529-46664530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs3932852	chr16:46664535-46664536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
39	rs200671251	chr16:46664536-46664537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs3932851	chr16:46664537-46664538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113107364	chr16:46664547-46664548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540715457	chr16:46664610-46664611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533764492	chr16:46664645-46664646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs8057277	chr16:46664715-46664716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183885796	chr16:46664750-46664751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562089864	chr16:46664785-46664786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188217827	chr16:46664820-46664821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs8053364	chr16:46664853-46664854	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs181391907	chr16:46664888-46664889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs377641718	chr16:46664903-46664904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
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
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	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
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:135 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46655600-46672600	Weak transcription	Esophagus	oesophagus
2	chr16:46655600-46694200	Weak transcription	Right Ventricle	heart
3	chr16:46655800-46663600	Weak transcription	HUVEC	blood vessel
4	chr16:46656000-46663600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr16:46658000-46663800	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr16:46659200-46672200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr16:46662800-46663600	Enhancers	Brain Cingulate Gyrus	brain
8	chr16:46662800-46664200	Enhancers	K562	blood
9	chr16:46663000-46663600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr16:46663000-46663600	Enhancers	Brain Anterior Caudate	brain
11	chr16:46663000-46663800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr16:46663000-46663800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr16:46663000-46663800	Enhancers	Brain Hippocampus Middle	brain
14	chr16:46663000-46663800	Enhancers	NHLF	lung
15	chr16:46663000-46664000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr16:46663000-46664000	Enhancers	GM12878-XiMat	blood
17	chr16:46663000-46664200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr16:46663000-46664400	Flanking Active TSS	HepG2	liver
19	chr16:46663000-46666800	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr16:46663200-46663600	Enhancers	Fetal Brain Female	brain
21	chr16:46663200-46663800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr16:46663200-46663800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr16:46663200-46663800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr16:46663200-46663800	Enhancers	Adipose Nuclei	Adipose
25	chr16:46663200-46663800	Enhancers	Brain Germinal Matrix	brain
26	chr16:46663200-46663800	Enhancers	Duodenum Mucosa	Duodenum
27	chr16:46663200-46664000	Enhancers	H1 Cell Line	embryonic stem cell
28	chr16:46663200-46664000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr16:46663200-46664000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr16:46663200-46664000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr16:46663200-46664000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr16:46663200-46664000	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr16:46663200-46664000	Enhancers	Fetal Intestine Small	intestine
34	chr16:46663200-46664000	Enhancers	Fetal Muscle Trunk	muscle
35	chr16:46663200-46664200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr16:46663200-46664200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr16:46663200-46664200	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr16:46663200-46664200	Enhancers	Fetal Lung	lung
39	chr16:46663200-46664200	Enhancers	Fetal Stomach	stomach
40	chr16:46663200-46664400	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr16:46663400-46663600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr16:46663400-46663600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr16:46663400-46663600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr16:46663400-46663600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr16:46663400-46663600	Active TSS	Brain Substantia Nigra	brain
46	chr16:46663400-46663600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr16:46663400-46663600	Enhancers	Stomach Smooth Muscle	stomach
48	chr16:46663400-46663600	Active TSS	Hela-S3	cervix
49	chr16:46663400-46663600	Enhancers	HMEC	breast
50	chr16:46663400-46663800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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