Variant report

Variant	nsv833058
Chromosome Location	chr15:77235895-77393640
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3288)
CpG islands
(count:2565)
Chromatin interactive
region (count:141)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3288 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:77324454-77324600	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:77360322-77360620	K562	blood:	n/a	n/a
3	ARID3A	chr15:77359749-77360087	K562	blood:	n/a	n/a
4	ARID3A	chr15:77356962-77357653	K562	blood:	n/a	n/a
5	ARID3A	chr15:77357124-77357218	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:77359696-77360073	HepG2	liver:	n/a	n/a
7	ATF1	chr15:77356868-77357302	K562	blood:	n/a	n/a
8	ATF1	chr15:77377561-77377886	K562	blood:	n/a	n/a
9	ATF2	chr15:77306145-77306892	GM12878	blood:	n/a	n/a
10	ATF2	chr15:77306056-77307216	GM12878	blood:	n/a	n/a
11	ATF2	chr15:77280450-77281122	GM12878	blood:	n/a	n/a
12	ATF2	chr15:77314306-77314560	GM12878	blood:	n/a	n/a
13	ATF2	chr15:77316619-77316962	GM12878	blood:	n/a	n/a
14	ATF2	chr15:77314226-77314800	GM12878	blood:	n/a	n/a
15	ATF2	chr15:77280492-77281189	GM12878	blood:	n/a	n/a
16	ATF3	chr15:77345998-77346388	K562	blood:	n/a	n/a
17	BACH1	chr15:77386788-77387162	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:77362785-77363076	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:77363295-77363664	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:77320425-77320611	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr15:77377554-77377837	K562	blood:	n/a	n/a
22	BATF	chr15:77306056-77306497	GM12878	blood:	n/a	chr15:77306290-77306300 chr15:77306289-77306300 chr15:77306286-77306296
23	BATF	chr15:77306094-77306473	GM12878	blood:	n/a	chr15:77306290-77306300 chr15:77306289-77306300 chr15:77306286-77306296
24	BATF	chr15:77377594-77378131	GM12878	blood:	n/a	n/a
25	BATF	chr15:77268877-77269183	GM12878	blood:	n/a	n/a
26	BATF	chr15:77290050-77290368	GM12878	blood:	n/a	chr15:77290281-77290290
27	BATF	chr15:77280672-77281099	GM12878	blood:	n/a	n/a
28	BATF	chr15:77377687-77378083	GM12878	blood:	n/a	n/a
29	BATF	chr15:77290041-77290431	GM12878	blood:	n/a	chr15:77290281-77290290
30	BATF	chr15:77280368-77281177	GM12878	blood:	n/a	n/a
31	BATF	chr15:77312280-77312501	GM12878	blood:	n/a	n/a
32	BCL11A	chr15:77280639-77281215	GM12878	blood:	n/a	n/a
33	BCL11A	chr15:77306811-77307122	GM12878	blood:	n/a	n/a
34	BCL11A	chr15:77290034-77290413	GM12878	blood:	n/a	chr15:77290214-77290223
35	BCL11A	chr15:77280649-77281093	GM12878	blood:	n/a	n/a
36	BCL11A	chr15:77306807-77307126	GM12878	blood:	n/a	n/a
37	BCL3	chr15:77383019-77383407	GM12878	blood:	n/a	n/a
38	BCL3	chr15:77325651-77326184	A549	lung:	n/a	n/a
39	BCL3	chr15:77359613-77360283	A549	lung:	n/a	n/a
40	BCL3	chr15:77327427-77328043	A549	lung:	n/a	n/a
41	BCL3	chr15:77326463-77328028	A549	lung:	n/a	n/a
42	BCL3	chr15:77280656-77281077	GM12878	blood:	n/a	n/a
43	BCL3	chr15:77325266-77325980	A549	lung:	n/a	n/a
44	BCL3	chr15:77326777-77327284	A549	lung:	n/a	n/a
45	BCL3	chr15:77319696-77320041	GM12878	blood:	n/a	n/a
46	BCL3	chr15:77319746-77319961	GM12878	blood:	n/a	n/a
47	BCLAF1	chr15:77280280-77281228	GM12878	blood:	n/a	n/a
48	BCLAF1	chr15:77306496-77307260	GM12878	blood:	n/a	n/a
49	BCLAF1	chr15:77265609-77265941	GM12878	blood:	n/a	chr15:77265853-77265861
50	BHLHE40	chr15:77386829-77386924	K562	blood:	n/a	n/a

(count:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77324758-77324808	HepG2	liver:	n/a
2	chr15:77289047-77289097	BE2_C	brain:	n/a
3	chr15:77324607-77324657	HAEpiC	amniotic membrane:	n/a
4	chr15:77324758-77324808	HepG2	liver:	n/a
5	chr15:77289047-77289097	BE2_C	brain:	n/a
6	chr15:77324607-77324657	HAEpiC	amniotic membrane:	n/a
7	chr15:77286232-77286282	HL-60	blood:	n/a
8	chr15:77320787-77320837	GM12878	blood:	n/a
9	chr15:77287338-77287388	SK-N-SH_RA	brain:	n/a
10	chr15:77363627-77363677	HCT-116	colon:	n/a
11	chr15:77327887-77327937	HMEC	breast:	n/a
12	chr15:77364801-77364851	GM12892	blood:	n/a
13	chr15:77320211-77320261	NH-A	brain:	n/a
14	chr15:77366214-77366264	PrEC	prostate:	n/a
15	chr15:77376250-77376300	NH-A	brain:	n/a
16	chr15:77320384-77320434	CMK	blood:	n/a
17	chr15:77324526-77324576	NHBE	bronchial:	n/a
18	chr15:77362853-77362903	NHDF-neo	bronchial:	n/a
19	chr15:77363192-77363242	A549	lung:	n/a
20	chr15:77324758-77324808	HNPCEpiC	eye:	n/a
21	chr15:77287762-77287812	K562	blood:	n/a
22	chr15:77364890-77364940	PFSK-1	brain:	n/a
23	chr15:77324526-77324576	NHDF-neo	bronchial:	n/a
24	chr15:77320261-77320311	NHDF-neo	bronchial:	n/a
25	chr15:77324751-77324801	Hepatocyte	liver:	n/a
26	chr15:77320211-77320261	HRCEpiC	kidney:	n/a
27	chr15:77314406-77314456	Hepatocyte	liver:	n/a
28	chr15:77271730-77271780	NHBE	bronchial:	n/a
29	chr15:77320787-77320837	AoSMC	blood vessel:	n/a
30	chr15:77347405-77347455	HCT-116	colon:	n/a
31	chr15:77364519-77364569	AoSMC	blood vessel:	n/a
32	chr15:77289047-77289097	Hela-S3	cervix:	n/a
33	chr15:77336938-77336988	RPTEC	kidney:	n/a
34	chr15:77363192-77363242	HRCEpiC	kidney:	n/a
35	chr15:77289047-77289097	PFSK-1	brain:	n/a
36	chr15:77324526-77324576	HCPEpiC	choroid plexus:	n/a
37	chr15:77271602-77271652	CMK	blood:	n/a
38	chr15:77376250-77376300	GM12891	blood:	n/a
39	chr15:77364890-77364940	BE2_C	brain:	n/a
40	chr15:77287762-77287812	HAEpiC	amniotic membrane:	n/a
41	chr15:77320672-77320722	U87	brain:	n/a
42	chr15:77364801-77364851	NHDF-neo	bronchial:	n/a
43	chr15:77363627-77363677	GM12892	blood:	n/a
44	chr15:77364519-77364569	AG04450	lung:	fetal
45	chr15:77362853-77362903	MCF10A-Er-Src	breast:	n/a
46	chr15:77287762-77287812	SK-N-MC	brain:	n/a
47	chr15:77271730-77271780	A549	lung:	n/a
48	chr15:77287656-77287706	AG09319	gingival:	n/a
49	chr15:77314406-77314456	HRPEpiC	eye:	n/a
50	chr15:77324526-77324576	SAEC	small airway:	n/a

(count:141 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:77358517..77361012-chr15:77366540..77368906,2	MCF-7	breast:
2	chr15:77390348..77392249-chr15:77393054..77395788,2	K562	blood:
3	chr15:77251144..77253865-chr15:77265251..77267565,2	K562	blood:
4	chr15:77359065..77361270-chr15:77362713..77364449,3	K562	blood:
5	chr15:77259410..77261761-chr15:77265771..77267804,2	MCF-7	breast:
6	chr15:77230977..77234854-chr15:77238676..77241282,3	MCF-7	breast:
7	chr15:77237726..77240574-chr15:77240909..77244202,4	K562	blood:
8	chr15:77337852..77340867-chr15:77357569..77361333,3	K562	blood:
9	chr15:77352302..77353897-chr15:77355148..77357991,2	MCF-7	breast:
10	chr15:77254684..77256252-chr15:77267880..77270200,2	K562	blood:
11	chr15:77283555..77285967-chr15:77287143..77289785,2	K562	blood:
12	chr15:77338266..77341370-chr15:77362139..77364149,3	K562	blood:
13	chr15:77361652..77364359-chr15:77387490..77390012,2	K562	blood:
14	chr15:77315639..77319825-chr15:77322811..77328362,7	MCF-7	breast:
15	chr15:77357220..77360797-chr15:77361367..77364060,6	MCF-7	breast:
16	chr15:77305426..77307546-chr15:77319169..77320927,2	K562	blood:
17	chr15:77257686..77261263-chr15:77264226..77266694,3	K562	blood:
18	chr15:77282963..77284982-chr15:77290568..77292460,2	K562	blood:
19	chr15:77265408..77266372-chr15:77316053..77316927,2	MCF-7	breast:
20	chr15:77280526..77282215-chr15:77292098..77294137,2	K562	blood:
21	chr15:77257244..77258840-chr15:77260404..77262433,2	K562	blood:
22	chr15:77335018..77337209-chr15:77378015..77379661,2	K562	blood:
23	chr15:77340819..77342632-chr15:77355039..77357924,2	K562	blood:
24	chr15:77238595..77241384-chr15:77923976..77926830,2	MCF-7	breast:
25	chr15:77224081..77226260-chr15:77238341..77240662,2	MCF-7	breast:
26	chr15:77345051..77347065-chr15:77356720..77358399,2	MCF-7	breast:
27	chr15:77237875..77240141-chr15:77253920..77256491,2	MCF-7	breast:
28	chr15:77334559..77338244-chr15:77361377..77364599,4	K562	blood:
29	chr15:77327141..77328063-chr15:77362386..77363086,2	MCF-7	breast:
30	chr15:77316379..77317255-chr15:77925626..77926458,2	MCF-7	breast:
31	chr15:77257244..77260342-chr15:77260767..77262433,3	K562	blood:
32	chr15:77320639..77324428-chr15:77362244..77364696,3	K562	blood:
33	chr15:77328280..77330879-chr15:77355103..77356921,2	K562	blood:
34	chr12:52607550..52609312-chr15:77270485..77271990,2	MCF-7	breast:
35	chr15:77241922..77243546-chr15:77246521..77248557,2	MCF-7	breast:
36	chr15:77245562..77247184-chr15:77254642..77256229,2	K562	blood:
37	chr15:77280561..77283110-chr15:77283637..77286723,3	MCF-7	breast:
38	chr15:77361764..77363824-chr15:77378016..77379591,2	MCF-7	breast:
39	chr15:77327656..77329511-chr15:77332033..77335172,3	K562	blood:
40	chr15:77283310..77284980-chr15:77285061..77287100,2	MCF-7	breast:
41	chr15:77344875..77348110-chr15:77358726..77362054,4	MCF-7	breast:
42	chr15:77334649..77338471-chr15:77361377..77364899,5	K562	blood:
43	chr15:77390348..77392249-chr15:77393054..77395788,2	K562	blood:
44	chr15:77333192..77335092-chr15:77340971..77343309,2	MCF-7	breast:
45	chr15:77240619..77242509-chr15:77252756..77255459,2	MCF-7	breast:
46	chr15:77333192..77335092-chr15:77340971..77343309,2	MCF-7	breast:
47	chr15:77343568..77346165-chr15:77350645..77352262,2	K562	blood:
48	chr15:77334649..77338471-chr15:77361377..77364899,5	K562	blood:
49	chr15:77311951..77316312-chr15:77325010..77329080,4	K562	blood:
50	chr15:77366731..77368356-chr15:77373004..77374845,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN3-3	chr15:77269258-77269551	NONHSAT047417
2	lnc-PEAK1.1-3	chr15:77362209-77362400	NONHSAT047422
3	lnc-SCAPER-2	chr15:77243537-77243916	NONHSAT047416
4	lnc-PSTPIP1-1	chr15:77336022-77336179	ENSG00000259652.1
5	lnc-TSPAN3-1	chr15:77333726-77333740	NONHSAT047418
6	lnc-PEAK1.1-4	chr15:77359996-77360667	ENSG00000269951.1
7	lnc-PEAK1.1-3	chr15:77363234-77363434	NONHSAT047422
8	lnc-TSPAN3-1	chr15:77334178-77335533	ENSG00000260787.1
9	lnc-TSPAN3-1	chr15:77334178-77335144	NONHSAT047418
10	lnc-PSTPIP1-1	chr15:77337397-77337502	ENSG00000259652.1

No data

Variant related genes	Relation type
RN7SL278P	TF binding region
PSTPIP1	TF binding region
ENSG00000260787	TF binding region
KRT8P23	TF binding region
ENSG00000269951	TF binding region
TSPAN3	TF binding region
ENSG00000259652	TF binding region
RN7SL278P	CpG island
PSTPIP1	CpG island
ENSG00000260787	CpG island
KRT8P23	CpG island
ENSG00000269951	CpG island
TSPAN3	CpG island
ENSG00000259652	CpG island
ENSG00000169783	chromatin interactions
ENSG00000259652	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000117906	chromatin interactions
ENSG00000140374	chromatin interactions
ENSG00000145332	chromatin interactions
ENSG00000243365	chromatin interactions
ENSG00000140368	chromatin interactions
ENSG00000140386	chromatin interactions
ENSG00000269951	chromatin interactions
ENSG00000260787	chromatin interactions
ENSG00000140391	chromatin interactions
ENSG00000212694	chromatin interactions

Extended variants
information (count: 6206 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:6206 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75116689	chr15:77235901-77235902	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs543979622	chr15:77235982-77235983	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs181911802	chr15:77236040-77236041	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs75550048	chr15:77236041-77236042	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs186289825	chr15:77236082-77236083	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs78925049	chr15:77236104-77236105	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs142859413	chr15:77236152-77236153	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs191064420	chr15:77236153-77236154	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs144772621	chr15:77236177-77236178	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374950090	chr15:77236198-77236199	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs147190935	chr15:77236205-77236206	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs530382435	chr15:77236239-77236240	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs369134932	chr15:77236241-77236242	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs548581323	chr15:77236244-77236245	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs12910059	chr15:77236259-77236260	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs201311990	chr15:77236260-77236261	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs569964687	chr15:77236263-77236264	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs111558646	chr15:77236267-77236268	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs74370819	chr15:77236269-77236270	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs115361828	chr15:77236274-77236275	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs12908880	chr15:77236289-77236290	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs1611866	chr15:77236291-77236292	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs7176638	chr15:77236295-77236296	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs12909309	chr15:77236306-77236307	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs12910232	chr15:77236311-77236312	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs75986807	chr15:77236312-77236313	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs376971699	chr15:77236321-77236322	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs75266588	chr15:77236326-77236327	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs78549251	chr15:77236344-77236345	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560237811	chr15:77236356-77236357	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs12909354	chr15:77236370-77236371	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs12909053	chr15:77236372-77236373	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs186169490	chr15:77236389-77236390	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs12910417	chr15:77236410-77236411	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs12909483	chr15:77236411-77236412	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs552900055	chr15:77236419-77236420	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs191081646	chr15:77236455-77236456	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs183436362	chr15:77236525-77236526	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs535768918	chr15:77236558-77236559	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs556971999	chr15:77236565-77236566	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs12909665	chr15:77236574-77236575	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs545980771	chr15:77236579-77236580	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs187594200	chr15:77236614-77236615	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs138749454	chr15:77236618-77236619	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs149347471	chr15:77236636-77236637	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559726851	chr15:77236668-77236669	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs375333451	chr15:77236690-77236691	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs530039293	chr15:77236699-77236700	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs548905743	chr15:77236711-77236712	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs369661030	chr15:77236788-77236789	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute myeloid leukemia	20962326	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:5028 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77224800-77243000	Weak transcription	Lung	lung
2	chr15:77224800-77256000	Weak transcription	Pancreas	Pancrea
3	chr15:77225000-77240400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr15:77225000-77240400	Weak transcription	Spleen	Spleen
5	chr15:77225000-77241000	Weak transcription	Colonic Mucosa	Colon
6	chr15:77225000-77242800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr15:77225000-77243000	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr15:77225000-77245200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr15:77225000-77245200	Weak transcription	Esophagus	oesophagus
10	chr15:77225000-77247000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr15:77225000-77254600	Weak transcription	Aorta	Aorta
12	chr15:77225000-77260200	Weak transcription	Right Ventricle	heart
13	chr15:77225200-77245200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr15:77225200-77246400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr15:77225400-77238000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr15:77225400-77238800	Weak transcription	Stomach Mucosa	stomach
17	chr15:77225400-77255400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr15:77225600-77243600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr15:77225800-77243800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr15:77225800-77244600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr15:77225800-77245000	Weak transcription	Fetal Heart	heart
22	chr15:77226000-77237000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr15:77226200-77247200	Weak transcription	Fetal Brain Male	brain
24	chr15:77227000-77236800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr15:77228200-77237200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr15:77228200-77243000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr15:77228200-77245600	Weak transcription	HMEC	breast
28	chr15:77229200-77240800	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr15:77229200-77243400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr15:77229200-77245200	Weak transcription	Small Intestine	intestine
31	chr15:77229200-77251600	Weak transcription	NHLF	lung
32	chr15:77229400-77236800	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr15:77229400-77237400	Weak transcription	Colon Smooth Muscle	Colon
34	chr15:77229400-77237800	Weak transcription	Rectal Smooth Muscle	rectum
35	chr15:77229400-77239800	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr15:77229400-77240200	Weak transcription	Hela-S3	cervix
37	chr15:77229400-77240600	Weak transcription	Stomach Smooth Muscle	stomach
38	chr15:77229400-77240800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr15:77229400-77243000	Weak transcription	Left Ventricle	heart
40	chr15:77229400-77243200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr15:77229400-77249000	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr15:77229400-77254400	Weak transcription	Psoas Muscle	Psoas
43	chr15:77229400-77255000	Weak transcription	Gastric	stomach
44	chr15:77229600-77236600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr15:77229600-77236600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr15:77229600-77237400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr15:77229600-77243600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr15:77230000-77236600	Weak transcription	Brain Germinal Matrix	brain
49	chr15:77230000-77236800	Weak transcription	HUVEC	blood vessel
50	chr15:77230200-77236600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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