Variant report

Variant	esv3427988
Chromosome Location	chr15:58356685-58359533
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58357749-58357751	K562	blood:	n/a	n/a
2	ARID3A	chr15:58358634-58358800	K562	blood:	n/a	n/a
3	ARID3A	chr15:58357164-58357177	K562	blood:	n/a	n/a
4	ATF1	chr15:58357118-58357128	K562	blood:	n/a	n/a
5	ATF3	chr15:58357915-58358171	K562	blood:	n/a	chr15:58358044-58358053
6	BACH1	chr15:58358059-58358350	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr15:58357508-58358003	K562	blood:	n/a	chr15:58357980-58357993
8	BCLAF1	chr15:58358424-58358973	K562	blood:	n/a	n/a
9	BHLHE40	chr15:58358494-58358828	K562	blood:	n/a	n/a
10	BHLHE40	chr15:58357209-58357396	K562	blood:	n/a	n/a
11	CBX3	chr15:58358482-58358944	K562	blood:	n/a	n/a
12	CCNT2	chr15:58356876-58358872	K562	blood:	n/a	chr15:58358513-58358522
13	CHD1	chr15:58357405-58357503	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr15:58358549-58358710	K562	blood:	n/a	n/a
15	CHD2	chr15:58358037-58358236	K562	blood:	n/a	n/a
16	CHD2	chr15:58358551-58358879	HepG2	liver:	n/a	n/a
17	CREB1	chr15:58358478-58358805	A549	lung:	n/a	n/a
18	CTCF	chr15:58358700-58358850	RPTEC	kidney:	n/a	n/a
19	CTCF	chr15:58358900-58359050	K562	blood:	n/a	chr15:58358986-58358994
20	CTCF	chr15:58358620-58358770	HUVEC	blood vessel:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
21	CTCF	chr15:58358580-58358730	GM12869	blood:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
22	CTCF	chr15:58358580-58358730	GM12871	blood:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
23	CTCF	chr15:58359240-58359390	AG04449	skin:	n/a	n/a
24	CTCF	chr15:58358554-58358827	GM19240	blood:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
25	CTCF	chr15:58358528-58358829	Spleen_OC	spleen:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
26	CTCF	chr15:58358640-58358790	SK-N-SH_RA	brain:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
27	CTCF	chr15:58358520-58358670	GM12865	blood:	n/a	n/a
28	CTCF	chr15:58358640-58358790	GM12866	blood:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
29	CTCF	chr15:58358640-58358790	K562	blood:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
30	CTCF	chr15:58357573-58358079	K562	blood:	n/a	n/a
31	CTCF	chr15:58358620-58358770	HL-60	blood:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
32	CTCF	chr15:58358530-58358837	MCF-7	breast:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
33	CTCF	chr15:58358571-58358812	GM13976	blood:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
34	CTCF	chr15:58358660-58358810	BJ	skin:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
35	CTCF	chr15:58358580-58358730	GM12865	blood:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
36	CTCF	chr15:58358457-58358822	K562	blood:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
37	CTCF	chr15:58358620-58358770	NHLF	lung:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
38	CTCF	chr15:58358545-58358836	MCF-7	breast:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
39	CTCF	chr15:58358620-58358770	HPF	lung:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
40	CTCF	chr15:58358572-58358818	ECC-1	luminal epithelium:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
41	CTCF	chr15:58358660-58358810	BE2_C	brain:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
42	CTCF	chr15:58358640-58358790	HCFaa	heart:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
43	CTCF	chr15:58358660-58358810	HCM	heart:	n/a	chr15:58358676-58358694 chr15:58358678-58358691
44	CTCF	chr15:58358368-58358857	K562	blood:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
45	CTCF	chr15:58358510-58358821	HepG2	liver:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
46	CTCF	chr15:58358554-58358818	Pancreas_OC	pancreas:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
47	CTCF	chr15:58358526-58358829	NHEK	skin:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
48	CTCF	chr15:58358940-58359090	HPF	lung:	n/a	chr15:58358986-58358994
49	CTCF	chr15:58358581-58358848	GM20000	blood:	n/a	chr15:58358678-58358691 chr15:58358676-58358694
50	CTCF	chr15:58358580-58358730	GM12866	blood:	n/a	chr15:58358678-58358691 chr15:58358676-58358694

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58357891-58357941	HL-60	blood:	n/a
2	chr15:58358775-58358825	GM12892	blood:	n/a
3	chr15:58357891-58357941	HL-60	blood:	n/a
4	chr15:58358775-58358825	GM12892	blood:	n/a
5	chr15:58357922-58357972	GM12892	blood:	n/a
6	chr15:58357891-58357941	BJ	skin:	n/a
7	chr15:58357204-58357254	ECC-1	luminal epithelium:	n/a
8	chr15:58358879-58358929	MCF-7	breast:	n/a
9	chr15:58358775-58358825	NB4	blood:	n/a
10	chr15:58357987-58358037	SK-N-SH	brain:	n/a
11	chr15:58357987-58358037	NHDF-neo	bronchial:	n/a
12	chr15:58357204-58357254	HAEpiC	amniotic membrane:	n/a
13	chr15:58357989-58358039	NHDF-neo	bronchial:	n/a
14	chr15:58357989-58358039	SK-N-MC	brain:	n/a
15	chr15:58358811-58358861	SK-N-SH	brain:	n/a
16	chr15:58358879-58358929	HCPEpiC	choroid plexus:	n/a
17	chr15:58358879-58358929	SAEC	small airway:	n/a
18	chr15:58358384-58358434	GM19239	blood:	n/a
19	chr15:58357879-58357929	ProgFib	skin:	n/a
20	chr15:58357319-58357369	Hepatocyte	liver:	n/a
21	chr15:58357922-58357972	SK-N-MC	brain:	n/a
22	chr15:58358775-58358825	NH-A	brain:	n/a
23	chr15:58357922-58357972	BE2_C	brain:	n/a
24	chr15:58358811-58358861	U87	brain:	n/a
25	chr15:58357922-58357972	HNPCEpiC	eye:	n/a
26	chr15:58358775-58358825	HEK293	kidney:	embryo
27	chr15:58357989-58358039	ECC-1	luminal epithelium:	n/a
28	chr15:58358811-58358861	T-47D	breast:	n/a
29	chr15:58357987-58358037	CMK	blood:	n/a
30	chr15:58357879-58357929	NH-A	brain:	n/a
31	chr15:58357989-58358039	HCM	heart:	n/a
32	chr15:58358775-58358825	BE2_C	brain:	n/a
33	chr15:58357874-58357924	NHBE	bronchial:	n/a
34	chr15:58357987-58358037	BJ	skin:	n/a
35	chr15:58358384-58358434	SK-N-MC	brain:	n/a
36	chr15:58357922-58357972	H1-hESC	embryonic stem cell:	embryo
37	chr15:58357204-58357254	SK-N-SH_RA	brain:	n/a
38	chr15:58357891-58357941	NT2-D1	testis:	n/a
39	chr15:58357989-58358039	T-47D	breast:	n/a
40	chr15:58357204-58357254	HRCEpiC	kidney:	n/a
41	chr15:58358811-58358861	BJ	skin:	n/a
42	chr15:58357874-58357924	SK-N-SH	brain:	n/a
43	chr15:58357874-58357924	Hela-S3	cervix:	n/a
44	chr15:58358879-58358929	HEEpiC	esophagus:	n/a
45	chr15:58357204-58357254	HNPCEpiC	eye:	n/a
46	chr15:58357891-58357941	IMR90	lung:	fetal
47	chr15:58357922-58357972	HIPEpiC	eye:	n/a
48	chr15:58357879-58357929	HEEpiC	esophagus:	n/a
49	chr15:58357922-58357972	HMEC	breast:	n/a
50	chr15:58357987-58358037	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:58306217..58308259-chr15:58356597..58358737,2	K562	blood:
2	chr15:58299490..58302063-chr15:58354314..58356908,2	K562	blood:
3	chr15:58328560..58331091-chr15:58356467..58358929,2	K562	blood:
4	chr15:58356974..58359469-chr15:60688408..60691704,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AQP9-1	chr15:58357401-58357405	NONHSAT044091
2	lnc-AQP9-1	chr15:58357428-58357940	NONHSAT044091
3	lnc-AQP9-1	chr15:58357423-58357940	ENSG00000259285.1
4	lnc-AQP9-1	chr15:58359013-58359132	ENSG00000259285.1
5	lnc-AQP9-1	chr15:58359013-58359132	NONHSAT044091
6	lnc-AQP9-1	chr15:58359013-58359132	ENSG00000245722
7	lnc-AQP9-1	chr15:58357423-58357940	ENSG00000245722

Variant related genes	Relation type
ENSG00000259285	TF binding region
ALDH1A2	TF binding region
ENSG00000259285	CpG island
ALDH1A2	CpG island
ENSG00000128918	chromatin interactions
ENSG00000182718	chromatin interactions
PRDM1	miRNA target sites

Extended variants
information (count: 143 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:143 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192177767	chr15:58356745-58356746	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs35710482	chr15:58356746-58356747	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554288963	chr15:58356765-58356766	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs34972167	chr15:58356784-58356785	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs543069149	chr15:58356787-58356788	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs562545720	chr15:58356800-58356801	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs576269806	chr15:58356803-58356804	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs545354230	chr15:58356817-58356818	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs565155178	chr15:58356819-58356820	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs527329362	chr15:58356820-58356821	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs7171261	chr15:58356855-58356856	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs192897297	chr15:58356874-58356875	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs184537180	chr15:58356911-58356912	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs530504403	chr15:58356946-58356947	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs549818052	chr15:58356953-58356954	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs150644108	chr15:58356954-58356955	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs139743202	chr15:58356959-58356960	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs550352905	chr15:58356970-58356971	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs570716143	chr15:58357036-58357037	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs35270169	chr15:58357044-58357045	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs35365571	chr15:58357048-58357049	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs112697055	chr15:58357056-58357057	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs4646550	chr15:58357057-58357058	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs552702029	chr15:58357084-58357085	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs146856712	chr15:58357108-58357109	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs566349455	chr15:58357141-58357142	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs139678676	chr15:58357147-58357148	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs144551448	chr15:58357169-58357170	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs180725764	chr15:58357222-58357223	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs11637348	chr15:58357231-58357232	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs556603353	chr15:58357235-58357236	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs544328081	chr15:58357294-58357295	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs564998436	chr15:58357295-58357296	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs562664284	chr15:58357297-58357298	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs565218124	chr15:58357394-58357395	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs34346064	chr15:58357410-58357411	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs3840021	chr15:58357418-58357419	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs398027475	chr15:58357422-58357423	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs541270990	chr15:58357432-58357433	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs555423521	chr15:58357438-58357439	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs560742121	chr15:58357442-58357443	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs3803451	chr15:58357458-58357459	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs549647285	chr15:58357508-58357509	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs3803450	chr15:58357532-58357533	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs367573489	chr15:58357545-58357546	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs372345595	chr15:58357548-58357549	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs531834628	chr15:58357574-58357575	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs34804991	chr15:58357585-58357586	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs186496587	chr15:58357611-58357612	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs571467566	chr15:58357616-58357617	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58353400-58358800	Active TSS	K562	blood
2	chr15:58353600-58359000	Active TSS	Fetal Kidney	kidney
3	chr15:58354000-58356800	Flanking Active TSS	HUVEC	blood vessel
4	chr15:58354200-58358800	Active TSS	Ovary	ovary
5	chr15:58354400-58358800	Active TSS	Right Atrium	heart
6	chr15:58355800-58357200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
7	chr15:58355800-58357200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
8	chr15:58356000-58357400	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
9	chr15:58356400-58356800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
10	chr15:58356400-58357000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
11	chr15:58356600-58356800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
12	chr15:58356600-58356800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
13	chr15:58356600-58357000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr15:58356600-58357000	Active TSS	Fetal Stomach	stomach
15	chr15:58356800-58357000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
16	chr15:58356800-58357000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
17	chr15:58356800-58357000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
18	chr15:58356800-58357000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
19	chr15:58356800-58357200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
20	chr15:58356800-58357200	Active TSS	HUVEC	blood vessel
21	chr15:58357000-58357200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
22	chr15:58357000-58357200	Flanking Bivalent TSS/Enh	Fetal Lung	lung
23	chr15:58357000-58357200	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
24	chr15:58357000-58357200	Bivalent/Poised TSS	Fetal Stomach	stomach
25	chr15:58357000-58357200	Enhancers	Pancreas	Pancrea
26	chr15:58357000-58357400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
27	chr15:58357000-58357600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
28	chr15:58357000-58357600	Bivalent/Poised TSS	Primary neutrophils fromperipheralblood	blood
29	chr15:58357000-58357600	Bivalent/Poised TSS	Primary B cells from cord blood	blood
30	chr15:58357000-58358800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
31	chr15:58357200-58357400	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr15:58357200-58357400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr15:58357200-58357400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr15:58357200-58357400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
35	chr15:58357200-58357400	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
36	chr15:58357200-58357400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
37	chr15:58357200-58357400	Bivalent Enhancer	Primary T cells from cord blood	blood
38	chr15:58357200-58357400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
39	chr15:58357200-58357400	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
40	chr15:58357200-58357400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
41	chr15:58357200-58357400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr15:58357200-58357400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr15:58357200-58357400	Bivalent Enhancer	Brain Germinal Matrix	brain
44	chr15:58357200-58357400	Bivalent Enhancer	Colonic Mucosa	Colon
45	chr15:58357200-58357400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
46	chr15:58357200-58357400	Flanking Active TSS	Lung	lung
47	chr15:58357200-58357400	Bivalent/Poised TSS	Placenta Amnion	Placenta Amnion
48	chr15:58357200-58357400	Flanking Bivalent TSS/Enh	Sigmoid Colon	Sigmoid Colon
49	chr15:58357200-58357400	Bivalent/Poised TSS	Small Intestine	intestine
50	chr15:58357200-58357400	Bivalent Enhancer	Spleen	Spleen

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