Variant report

Variant	nsv520527
Chromosome Location	chr15:75108636-75122856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:570)
CpG islands
(count:915)
Chromatin interactive
region (count:73)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:75110995-75111370	K562	blood:	n/a	n/a
2	ATF3	chr15:75110967-75111349	K562	blood:	n/a	n/a
3	ATF3	chr15:75110990-75111359	K562	blood:	n/a	n/a
4	ATF3	chr15:75118705-75118869	K562	blood:	n/a	n/a
5	BACH1	chr15:75118906-75119134	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr15:75121909-75122199	GM12878	blood:	n/a	n/a
7	BHLHE40	chr15:75110979-75111416	K562	blood:	n/a	n/a
8	BHLHE40	chr15:75111016-75111433	HepG2	liver:	n/a	n/a
9	BHLHE40	chr15:75119351-75119564	K562	blood:	n/a	n/a
10	BHLHE40	chr15:75118758-75118820	K562	blood:	n/a	n/a
11	BRCA1	chr15:75110993-75111439	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr15:75110895-75111349	K562	blood:	n/a	n/a
13	CEBPB	chr15:75110858-75111310	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr15:75121899-75122145	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr15:75110975-75111303	HepG2	liver:	n/a	n/a
16	CEBPB	chr15:75113881-75113915	HepG2	liver:	n/a	n/a
17	CEBPB	chr15:75113718-75114065	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr15:75110995-75111353	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr15:75109108-75109129	K562	blood:	n/a	n/a
20	CTCF	chr15:75109640-75109790	GM06990	blood:	n/a	n/a
21	CTCF	chr15:75113566-75113695	GM12878	blood:	n/a	n/a
22	CTCF	chr15:75109720-75109870	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr15:75109644-75109969	T-47D	breast:	n/a	n/a
24	CTCF	chr15:75109000-75109150	WERI-Rb-1	eye:	n/a	chr15:75109121-75109130 chr15:75109071-75109084 chr15:75109121-75109134 chr15:75109118-75109136
25	CTCF	chr15:75109730-75109883	GM19239	blood:	n/a	n/a
26	CTCF	chr15:75109640-75109790	NHEK	skin:	n/a	n/a
27	CTCF	chr15:75109755-75109863	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr15:75109720-75109870	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr15:75109720-75109870	GM12873	blood:	n/a	n/a
30	CTCF	chr15:75109645-75109917	IMR90	lung:	n/a	n/a
31	CTCF	chr15:75109100-75109250	HRPEpiC	eye:	n/a	chr15:75109121-75109130 chr15:75109121-75109134 chr15:75109118-75109136
32	CTCF	chr15:75109080-75109230	BJ	skin:	n/a	chr15:75109121-75109130 chr15:75109121-75109134 chr15:75109118-75109136
33	CTCF	chr15:75111760-75111910	A549	lung:	n/a	n/a
34	CTCF	chr15:75109740-75109890	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr15:75109740-75109890	GM12871	blood:	n/a	n/a
36	CTCF	chr15:75109703-75109913	Fibrobl	skin:	n/a	n/a
37	CTCF	chr15:75109720-75109870	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr15:75109660-75109810	GM12865	blood:	n/a	n/a
39	CTCF	chr15:75109131-75109156	K562	blood:	n/a	n/a
40	CTCF	chr15:75120092-75120247	K562	blood:	n/a	chr15:75120167-75120185 chr15:75120162-75120183
41	CTCF	chr15:75109701-75109892	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr15:75109040-75109190	K562	blood:	n/a	chr15:75109121-75109130 chr15:75109071-75109084 chr15:75109121-75109134 chr15:75109118-75109136
43	CTCF	chr15:75109689-75109940	MCF-7	breast:	n/a	n/a
44	CTCF	chr15:75109060-75109210	HCFaa	heart:	n/a	chr15:75109121-75109130 chr15:75109071-75109084 chr15:75109121-75109134 chr15:75109118-75109136
45	CTCF	chr15:75109720-75109870	AG04450	lung:	n/a	n/a
46	CTCF	chr15:75120120-75120233	GM12892	blood:	n/a	chr15:75120167-75120185 chr15:75120162-75120183
47	CTCF	chr15:75109691-75109919	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:75109760-75109910	MCF-7	breast:	n/a	n/a
49	CTCF	chr15:75109720-75109870	GM12865	blood:	n/a	n/a
50	CTCF	chr15:75109000-75109150	AG04449	skin:	n/a	chr15:75109121-75109130 chr15:75109071-75109084 chr15:75109121-75109134 chr15:75109118-75109136

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75118021-75118071	GM12891	blood:	n/a
2	chr15:75117658-75117708	NB4	blood:	n/a
3	chr15:75119018-75119068	AG09309	skin:	n/a
4	chr15:75119324-75119374	GM19239	blood:	n/a
5	chr15:75119335-75119385	NHBE	bronchial:	n/a
6	chr15:75108826-75108876	A549	lung:	n/a
7	chr15:75117658-75117708	A549	lung:	n/a
8	chr15:75118456-75118506	PrEC	prostate:	n/a
9	chr15:75118021-75118071	A549	lung:	n/a
10	chr15:75119335-75119385	HRCEpiC	kidney:	n/a
11	chr15:75118021-75118071	HEK293	kidney:	embryo
12	chr15:75117708-75117758	SAEC	small airway:	n/a
13	chr15:75118021-75118071	RPTEC	kidney:	n/a
14	chr15:75119335-75119385	K562	blood:	n/a
15	chr15:75119324-75119374	BE2_C	brain:	n/a
16	chr15:75118021-75118071	NHBE	bronchial:	n/a
17	chr15:75119324-75119374	HEEpiC	esophagus:	n/a
18	chr15:75117708-75117758	GM12891	blood:	n/a
19	chr15:75118714-75118764	HPAEpiC	pulmonary alveolar:	n/a
20	chr15:75117708-75117758	GM12892	blood:	n/a
21	chr15:75117708-75117758	LNCaP	prostate:	n/a
22	chr15:75108826-75108876	AG04449	skin:	fetal
23	chr15:75117069-75117119	AG04449	skin:	fetal
24	chr15:75118427-75118477	NHBE	bronchial:	n/a
25	chr15:75119018-75119068	HIPEpiC	eye:	n/a
26	chr15:75118714-75118764	GM12892	blood:	n/a
27	chr15:75118427-75118477	U87	brain:	n/a
28	chr15:75119018-75119068	IMR90	lung:	fetal
29	chr15:75117658-75117708	ProgFib	skin:	n/a
30	chr15:75119018-75119068	NB4	blood:	n/a
31	chr15:75118714-75118764	AG09319	gingival:	n/a
32	chr15:75117069-75117119	IMR90	lung:	fetal
33	chr15:75108859-75108909	SK-N-SH_RA	brain:	n/a
34	chr15:75118821-75118871	PFSK-1	brain:	n/a
35	chr15:75108826-75108876	CMK	blood:	n/a
36	chr15:75119324-75119374	HRE	kidney:	n/a
37	chr15:75108859-75108909	H1-hESC	embryonic stem cell:	embryo
38	chr15:75117658-75117708	Hepatocyte	liver:	n/a
39	chr15:75108859-75108909	Caco-2	colon:	n/a
40	chr15:75118021-75118071	PFSK-1	brain:	n/a
41	chr15:75117033-75117083	HRE	kidney:	n/a
42	chr15:75117069-75117119	K562	blood:	n/a
43	chr15:75118427-75118477	HRE	kidney:	n/a
44	chr15:75117033-75117083	HRPEpiC	eye:	n/a
45	chr15:75119018-75119068	AG04450	lung:	fetal
46	chr15:75117708-75117758	NH-A	brain:	n/a
47	chr15:75108826-75108876	SK-N-MC	brain:	n/a
48	chr15:75119335-75119385	HNPCEpiC	eye:	n/a
49	chr15:75118456-75118506	BJ	skin:	n/a
50	chr15:75117033-75117083	LNCaP	prostate:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:75116807..75119405-chr15:75229123..75231541,2	K562	blood:
2	chr15:75108356..75114001-chr15:75126388..75130558,9	MCF-7	breast:
3	chr15:75120331..75122019-chr15:75133523..75135622,3	K562	blood:
4	chr15:75105168..75109047-chr15:75134120..75137766,4	K562	blood:
5	chr15:75121491..75123430-chr15:75173569..75176195,2	MCF-7	breast:
6	chr15:75081323..75082242-chr15:75109443..75110385,9	MCF-7	breast:
7	chr15:75110223..75112810-chr15:75165268..75167627,2	MCF-7	breast:
8	chr15:75109188..75110335-chr15:75127274..75128567,6	MCF-7	breast:
9	chr15:75074148..75076667-chr15:75119485..75121788,2	K562	blood:
10	chr15:75112798..75114870-chr15:75119173..75121348,2	K562	blood:
11	chr15:75112517..75114870-chr15:75115640..75117170,2	MCF-7	breast:
12	chr15:75093545..75095294-chr15:75111184..75112969,2	K562	blood:
13	chr15:75109449..75112132-chr15:75112266..75114045,2	MCF-7	breast:
14	chr15:75109533..75111240-chr15:75228886..75230754,2	MCF-7	breast:
15	chr15:75113859..75115829-chr15:75135120..75137203,2	MCF-7	breast:
16	chr15:75063364..75063990-chr15:75109881..75110560,2	MCF-7	breast:
17	chr15:75111167..75114133-chr15:75116068..75118230,2	K562	blood:
18	chr15:75072350..75078841-chr15:75107920..75114107,12	MCF-7	breast:
19	chr15:75117625..75119967-chr15:75247068..75249643,2	K562	blood:
20	chr15:75109469..75110121-chr15:75139541..75140329,6	MCF-7	breast:
21	chr15:75109529..75110053-chr15:75194068..75194696,2	MCF-7	breast:
22	chr15:75110559..75112836-chr15:75746524..75748233,2	K562	blood:
23	chr15:75062932..75063974-chr15:75109427..75110335,6	MCF-7	breast:
24	chr15:75116359..75118172-chr15:75182130..75184765,2	MCF-7	breast:
25	chr15:75074461..75076806-chr15:75112062..75114585,2	K562	blood:
26	chr15:75109403..75110158-chr15:75139541..75140351,8	MCF-7	breast:
27	chr15:75108017..75109912-chr15:75114230..75116710,2	MCF-7	breast:
28	chr15:75081235..75085402-chr15:75108223..75111318,4	MCF-7	breast:
29	chr15:75109533..75110332-chr15:75134854..75135663,2	MCF-7	breast:
30	chr15:75062932..75063974-chr15:75109427..75110288,5	MCF-7	breast:
31	chr15:75072740..75076753-chr15:75116483..75119304,4	MCF-7	breast:
32	chr15:75090919..75095080-chr15:75105772..75108722,6	MCF-7	breast:
33	chr15:75074174..75075858-chr15:75112738..75114767,2	MCF-7	breast:
34	chr15:75106165..75113668-chr15:75132311..75136608,10	MCF-7	breast:
35	chr15:75113543..75115731-chr15:75122217..75124290,2	K562	blood:
36	chr15:75115096..75116793-chr15:75116936..75121281,3	K562	blood:
37	chr15:75107962..75109830-chr15:75247955..75249471,2	K562	blood:
38	chr15:75074126..75076948-chr15:75116903..75120530,4	MCF-7	breast:
39	chr15:75109719..75111456-chr15:75185022..75186522,2	MCF-7	breast:
40	chr15:75081065..75082080-chr15:75109443..75110385,9	MCF-7	breast:
41	chr15:75120576..75122611-chr15:75248587..75251052,2	MCF-7	breast:
42	chr15:75109829..75110505-chr15:75121077..75121887,4	MCF-7	breast:
43	chr15:75109649..75110485-chr15:75229607..75230565,5	MCF-7	breast:
44	chr15:75099365..75100320-chr15:75120145..75120900,2	MCF-7	breast:
45	chr15:75106841..75109332-chr15:75121089..75123309,4	MCF-7	breast:
46	chr15:75113543..75115731-chr15:75122217..75124290,2	K562	blood:
47	chr15:75073853..75076173-chr15:75120593..75122828,2	MCF-7	breast:
48	chr15:75074156..75079604-chr15:75107384..75112501,9	MCF-7	breast:
49	chr15:75110563..75112666-chr15:75119398..75122234,2	K562	blood:
50	chr15:75118890..75121057-chr15:75121173..75124170,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LMAN1L-1	chr15:75114170-75114241	NONHSAT047272
2	lnc-LMAN1L-1	chr15:75114983-75115050	NONHSAT047272
3	lnc-LMAN1L-1	chr15:75111808-75113108	NONHSAT047272
4	lnc-LMAN1L-1	chr15:75117814-75118095	NONHSAT047272
5	lnc-LMAN1L-1	chr15:75113416-75113567	NONHSAT047272
6	lnc-LMAN1L-1	chr15:75115900-75116819	NONHSAT047272

No data

Variant related genes	Relation type
ENSG00000261606	TF binding region
CPLX3	TF binding region
LMAN1L	TF binding region
ENSG00000261606	CpG island
CPLX3	CpG island
LMAN1L	CpG island
ENSG00000247240	chromatin interactions
ENSG00000178741	chromatin interactions
ENSG00000264386	chromatin interactions
ENSG00000178761	chromatin interactions
ENSG00000178802	chromatin interactions
ENSG00000261606	chromatin interactions
ENSG00000169375	chromatin interactions
ENSG00000140474	chromatin interactions
ENSG00000140506	chromatin interactions
ENSG00000198794	chromatin interactions
ENSG00000103653	chromatin interactions
ENSG00000140497	chromatin interactions
ENSG00000138629	chromatin interactions
ENSG00000260919	chromatin interactions
ENSG00000179335	chromatin interactions
ENSG00000178718	chromatin interactions
ENSG00000213578	chromatin interactions
ENSG00000167196	chromatin interactions

Extended variants
information (count: 626 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:626 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3803568	chr15:75108636-75108637	Weak transcription Enhancers Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374270623	chr15:75108677-75108678	Weak transcription Enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs376568108	chr15:75108682-75108683	Weak transcription Enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs201549948	chr15:75108683-75108684	Weak transcription Enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs369651898	chr15:75108700-75108701	Weak transcription Enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs372903974	chr15:75108715-75108716	Weak transcription Enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs563585989	chr15:75108770-75108771	Weak transcription Enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs376132416	chr15:75108771-75108772	Weak transcription Enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs369158387	chr15:75108782-75108783	Weak transcription Enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs372530929	chr15:75108803-75108804	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs151233715	chr15:75108814-75108815	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs530685001	chr15:75108840-75108841	Enhancers Weak transcription Bivalent Enhancer Active TSS	CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs377071600	chr15:75108886-75108887	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs552522947	chr15:75108904-75108905	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs370022093	chr15:75108912-75108913	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs200794545	chr15:75108928-75108929	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs374529748	chr15:75108940-75108941	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs369165871	chr15:75108943-75108944	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs372486040	chr15:75108948-75108949	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs370635758	chr15:75108962-75108963	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs201975832	chr15:75108980-75108981	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs568109724	chr15:75108988-75108989	Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs535407762	chr15:75109005-75109006	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs200522014	chr15:75109042-75109043	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs568848871	chr15:75109089-75109090	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs191127849	chr15:75109093-75109094	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs182868784	chr15:75109094-75109095	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs573093031	chr15:75109128-75109129	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs540472717	chr15:75109132-75109133	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs559901317	chr15:75109145-75109146	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs574086662	chr15:75109148-75109149	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs398088814	chr15:75109156-75109157	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs28397782	chr15:75109157-75109158	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs112467575	chr15:75109180-75109181	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs562713682	chr15:75109184-75109185	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs533364148	chr15:75109190-75109191	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs546076655	chr15:75109235-75109236	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs28577988	chr15:75109250-75109251	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs528288813	chr15:75109273-75109274	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs546844219	chr15:75109287-75109288	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs74320710	chr15:75109316-75109317	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs531161442	chr15:75109334-75109335	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs114286395	chr15:75109337-75109338	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs550907999	chr15:75109363-75109364	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs568721246	chr15:75109368-75109369	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs539088450	chr15:75109374-75109375	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs558027637	chr15:75109425-75109426	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs566852279	chr15:75109443-75109444	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs534114838	chr15:75109477-75109478	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs77995001	chr15:75109515-75109516	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75096000-75109000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr15:75096200-75109600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr15:75096800-75109000	Weak transcription	Fetal Intestine Large	intestine
4	chr15:75096800-75109200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr15:75096800-75109400	Weak transcription	HUVEC	blood vessel
6	chr15:75096800-75109800	Weak transcription	NH-A	brain
7	chr15:75097000-75109200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr15:75097000-75109400	Weak transcription	Brain Anterior Caudate	brain
9	chr15:75097200-75109400	Weak transcription	Lung	lung
10	chr15:75097600-75111000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:75097800-75109200	Weak transcription	Brain Germinal Matrix	brain
12	chr15:75101200-75109000	Weak transcription	HMEC	breast
13	chr15:75101800-75109200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr15:75101800-75113200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr15:75102000-75108800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr15:75102600-75109600	Weak transcription	NHLF	lung
17	chr15:75107000-75112200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr15:75107200-75108800	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr15:75107200-75109000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr15:75107200-75109600	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr15:75107200-75110000	Enhancers	Colon Smooth Muscle	Colon
22	chr15:75107200-75111200	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr15:75107200-75111400	Enhancers	Esophagus	oesophagus
24	chr15:75107200-75111800	Enhancers	Colonic Mucosa	Colon
25	chr15:75107200-75112400	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr15:75107200-75114400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr15:75107600-75109000	Enhancers	Primary B cells from peripheral blood	blood
28	chr15:75107600-75109200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr15:75107800-75108800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr15:75107800-75109000	Weak transcription	Brain Cingulate Gyrus	brain
31	chr15:75107800-75109000	Weak transcription	Fetal Brain Male	brain
32	chr15:75107800-75109800	Weak transcription	A549	lung
33	chr15:75108000-75109000	Weak transcription	Placenta	Placenta
34	chr15:75108000-75109200	Weak transcription	Duodenum Mucosa	Duodenum
35	chr15:75108000-75109400	Weak transcription	Stomach Smooth Muscle	stomach
36	chr15:75108000-75109600	Weak transcription	Pancreas	Pancrea
37	chr15:75108000-75109800	Weak transcription	Liver	Liver
38	chr15:75108000-75113000	Weak transcription	Right Atrium	heart
39	chr15:75108200-75109200	Weak transcription	Fetal Heart	heart
40	chr15:75108200-75109200	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr15:75108200-75109400	Weak transcription	Stomach Mucosa	stomach
42	chr15:75108200-75111000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr15:75108200-75111000	Weak transcription	GM12878-XiMat	blood
44	chr15:75108200-75111400	Weak transcription	HSMMtube	muscle
45	chr15:75108400-75109400	Weak transcription	Right Ventricle	heart
46	chr15:75108400-75109600	Weak transcription	Rectal Smooth Muscle	rectum
47	chr15:75108400-75110400	Weak transcription	Gastric	stomach
48	chr15:75108400-75110600	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr15:75108600-75108800	Enhancers	Left Ventricle	heart
50	chr15:75108600-75109000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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