Variant report

Variant	nsv904345
Chromosome Location	chr15:74458181-74526596
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1668)
CpG islands
(count:2442)
Chromatin interactive
region (count:86)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1668 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:74507718-74507872	HepG2	liver:	n/a	n/a
2	ATF1	chr15:74502533-74502830	K562	blood:	n/a	n/a
3	ATF1	chr15:74485874-74486026	K562	blood:	n/a	n/a
4	ATF2	chr15:74506325-74506657	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr15:74516142-74516531	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr15:74494985-74495663	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:74494889-74495592	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr15:74517335-74517547	K562	blood:	n/a	n/a
9	ATF3	chr15:74488366-74488824	A549	lung:	n/a	n/a
10	ATF3	chr15:74492667-74493149	A549	lung:	n/a	n/a
11	BACH1	chr15:74521267-74521353	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:74496082-74496694	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:74470313-74470353	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:74494893-74495685	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr15:74516256-74516452	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr15:74504375-74504439	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr15:74485585-74485896	GM12878	blood:	n/a	chr15:74485884-74485894 chr15:74485742-74485753
18	BATF	chr15:74492765-74493061	GM12878	blood:	n/a	chr15:74492924-74492935
19	BATF	chr15:74486777-74487103	GM12878	blood:	n/a	n/a
20	BATF	chr15:74485565-74485981	GM12878	blood:	n/a	chr15:74485884-74485894 chr15:74485742-74485753
21	BCL3	chr15:74488346-74488987	A549	lung:	n/a	n/a
22	BCL3	chr15:74469937-74470889	A549	lung:	n/a	chr15:74470402-74470411
23	BCL3	chr15:74477076-74477507	GM12878	blood:	n/a	n/a
24	BCL3	chr15:74488487-74488992	A549	lung:	n/a	n/a
25	BCL3	chr15:74467360-74467828	A549	lung:	n/a	n/a
26	BCL3	chr15:74492637-74493293	A549	lung:	n/a	chr15:74492969-74492978
27	BCL3	chr15:74477172-74477415	GM12878	blood:	n/a	n/a
28	BCL3	chr15:74492626-74493188	A549	lung:	n/a	chr15:74492969-74492978
29	BHLHE40	chr15:74473297-74473479	HepG2	liver:	n/a	n/a
30	BHLHE40	chr15:74506104-74506388	K562	blood:	n/a	n/a
31	BHLHE40	chr15:74473300-74473513	GM12878	blood:	n/a	n/a
32	BHLHE40	chr15:74494772-74494865	K562	blood:	n/a	n/a
33	BHLHE40	chr15:74515801-74516117	HepG2	liver:	n/a	chr15:74515954-74515963 chr15:74515954-74515963 chr15:74515953-74515962
34	BHLHE40	chr15:74519595-74519733	K562	blood:	n/a	n/a
35	BHLHE40	chr15:74473238-74473591	K562	blood:	n/a	n/a
36	BHLHE40	chr15:74515777-74516104	K562	blood:	n/a	chr15:74515954-74515963 chr15:74515954-74515963 chr15:74515953-74515962
37	BRCA1	chr15:74470248-74470590	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr15:74494960-74495467	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr15:74504795-74504804	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr15:74488286-74488926	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr15:74471698-74472168	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr15:74470197-74470675	IMR90	lung:	n/a	n/a
43	CEBPB	chr15:74485562-74486010	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr15:74492740-74493117	A549	lung:	n/a	n/a
45	CEBPB	chr15:74492746-74493094	HepG2	liver:	n/a	n/a
46	CEBPB	chr15:74492662-74493110	GM12878	blood:	n/a	n/a
47	CEBPB	chr15:74464644-74464748	K562	blood:	n/a	chr15:74464667-74464678
48	CEBPB	chr15:74502489-74502881	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr15:74507612-74507975	IMR90	lung:	n/a	chr15:74507788-74507799
50	CEBPB	chr15:74495012-74495601	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2442 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74501771-74501821	H1-hESC	embryonic stem cell:	embryo
2	chr15:74494861-74494911	SAEC	small airway:	n/a
3	chr15:74501771-74501821	H1-hESC	embryonic stem cell:	embryo
4	chr15:74494861-74494911	SAEC	small airway:	n/a
5	chr15:74501771-74501821	BJ	skin:	n/a
6	chr15:74496040-74496090	K562	blood:	n/a
7	chr15:74467891-74467941	AG09319	gingival:	n/a
8	chr15:74501549-74501599	HL-60	blood:	n/a
9	chr15:74467158-74467208	NHDF-neo	bronchial:	n/a
10	chr15:74466933-74466983	SAEC	small airway:	n/a
11	chr15:74467158-74467208	AG04449	skin:	fetal
12	chr15:74489089-74489139	HL-60	blood:	n/a
13	chr15:74465558-74465608	GM19239	blood:	n/a
14	chr15:74466704-74466754	HUVEC	blood vessel:	n/a
15	chr15:74496576-74496626	K562	blood:	n/a
16	chr15:74514346-74514396	SKMC	muscle:	n/a
17	chr15:74466910-74466960	HEK293	kidney:	embryo
18	chr15:74466794-74466844	AG10803	skin:	n/a
19	chr15:74467047-74467097	ovcar-3	ovarian:	n/a
20	chr15:74466794-74466844	HEK293	kidney:	embryo
21	chr15:74466704-74466754	HAEpiC	amniotic membrane:	n/a
22	chr15:74496040-74496090	HCF	heart:	n/a
23	chr15:74494854-74494904	PrEC	prostate:	n/a
24	chr15:74525447-74525497	NH-A	brain:	n/a
25	chr15:74467432-74467482	HRE	kidney:	n/a
26	chr15:74487890-74487940	HCT-116	colon:	n/a
27	chr15:74495637-74495687	BE2_C	brain:	n/a
28	chr15:74494900-74494950	HAEpiC	amniotic membrane:	n/a
29	chr15:74496040-74496090	A549	lung:	n/a
30	chr15:74502200-74502250	NT2-D1	testis:	n/a
31	chr15:74494781-74494831	HRCEpiC	kidney:	n/a
32	chr15:74471974-74472024	HepG2	liver:	n/a
33	chr15:74495637-74495687	LNCaP	prostate:	n/a
34	chr15:74465888-74465938	Hela-S3	cervix:	n/a
35	chr15:74466794-74466844	ECC-1	luminal epithelium:	n/a
36	chr15:74471974-74472024	GM12878	blood:	n/a
37	chr15:74466794-74466844	AoSMC	blood vessel:	n/a
38	chr15:74466933-74466983	AoSMC	blood vessel:	n/a
39	chr15:74466910-74466960	ProgFib	skin:	n/a
40	chr15:74466704-74466754	AG04449	skin:	fetal
41	chr15:74467709-74467759	BJ	skin:	n/a
42	chr15:74467047-74467097	NHBE	bronchial:	n/a
43	chr15:74489089-74489139	HEK293	kidney:	embryo
44	chr15:74495603-74495653	Hela-S3	cervix:	n/a
45	chr15:74495109-74495159	HMEC	breast:	n/a
46	chr15:74495603-74495653	SK-N-SH_RA	brain:	n/a
47	chr15:74495354-74495404	BE2_C	brain:	n/a
48	chr15:74501549-74501599	GM06990	blood:	n/a
49	chr15:74501771-74501821	HL-60	blood:	n/a
50	chr15:74465888-74465938	AoSMC	blood vessel:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:74483505..74486452-chr15:74486727..74489080,2	MCF-7	breast:
2	chr15:74473995..74476347-chr15:74479894..74482391,2	K562	blood:
3	chr15:74465289..74467713-chr15:74468699..74473006,4	MCF-7	breast:
4	chr15:74525463..74526963-chr17:41465876..41467879,2	K562	blood:
5	chr15:74489985..74491760-chr15:74513574..74516077,2	MCF-7	breast:
6	chr15:74465639..74467443-chr15:74467856..74470686,2	MCF-7	breast:
7	chr15:74515195..74518052-chr15:74528039..74529707,2	K562	blood:
8	chr15:74494408..74497236-chr15:74500706..74502894,2	MCF-7	breast:
9	chr15:74473602..74475447-chr15:74485969..74488494,2	MCF-7	breast:
10	chr15:74494443..74497074-chr15:74501503..74504271,2	K562	blood:
11	chr15:74492912..74495035-chr15:74502031..74504562,2	MCF-7	breast:
12	chr15:74468916..74471772-chr15:74477049..74479874,2	MCF-7	breast:
13	chr15:74495756..74498011-chr15:74498578..74500648,2	K562	blood:
14	chr15:74483505..74486452-chr15:74486727..74489080,2	MCF-7	breast:
15	chr1:247553460..247553986-chr15:74497052..74497552,2	MCF-7	breast:
16	chr15:74478980..74480513-chr15:74491993..74494403,2	MCF-7	breast:
17	chr15:74516668..74519200-chr15:74524275..74526738,2	MCF-7	breast:
18	chr15:74449618..74451381-chr15:74459821..74462700,2	K562	blood:
19	chr15:74490081..74492588-chr15:74507681..74510665,2	MCF-7	breast:
20	chr15:74473995..74476347-chr15:74479894..74482391,2	K562	blood:
21	chr15:74489184..74491442-chr15:74495568..74497527,4	MCF-7	breast:
22	chr15:74489028..74490850-chr15:74509672..74512569,2	MCF-7	breast:
23	chr15:74477830..74479940-chr15:74481480..74483032,2	MCF-7	breast:
24	chr15:74421502..74423343-chr15:74491775..74494417,2	MCF-7	breast:
25	chr15:74474607..74476974-chr15:74483546..74486134,2	K562	blood:
26	chr15:74513953..74515786-chr15:74517220..74519970,2	K562	blood:
27	chr15:74465310..74466081-chr15:74488442..74489174,2	K562	blood:
28	chr15:74426280..74428473-chr15:74476788..74479441,2	MCF-7	breast:
29	chr15:74519618..74521200-chr15:74525359..74527344,2	K562	blood:
30	chr15:74466286..74468382-chr15:74470933..74472488,2	MCF-7	breast:
31	chr15:74474607..74476974-chr15:74483546..74486134,2	K562	blood:
32	chr15:74488727..74491632-chr15:74492213..74494817,3	MCF-7	breast:
33	chr15:74489028..74490850-chr15:74509672..74512569,2	MCF-7	breast:
34	chr15:74464539..74466553-chr15:74477409..74479282,2	MCF-7	breast:
35	chr15:74489985..74491760-chr15:74513574..74516077,2	MCF-7	breast:
36	chr15:74516266..74518836-chr15:74583231..74585495,2	MCF-7	breast:
37	chr15:74522433..74524879-chr15:74525973..74529290,3	K562	blood:
38	chr15:74471188..74474733-chr15:74480852..74485546,5	MCF-7	breast:
39	chr15:74466900..74472029-chr15:74474380..74478364,5	K562	blood:
40	chr15:74467637..74470186-chr15:74471128..74474134,3	K562	blood:
41	chr15:74471188..74474733-chr15:74480852..74485546,5	MCF-7	breast:
42	chr15:74494443..74497074-chr15:74501503..74504271,2	K562	blood:
43	chr15:74466900..74472644-chr15:74474380..74478364,5	K562	blood:
44	chr15:74466286..74468382-chr15:74470933..74472488,2	MCF-7	breast:
45	chr15:74516668..74519200-chr15:74524275..74526738,2	MCF-7	breast:
46	chr15:74495538..74499115-chr15:74503082..74506667,3	MCF-7	breast:
47	chr15:74447963..74450953-chr15:74457628..74460185,2	K562	blood:
48	chr15:74507650..74508397-chr6:26216677..26217335,2	Hela-S3	cervix:
49	chr15:74503151..74507416-chr15:74511304..74513886,3	MCF-7	breast:
50	chr15:74481853..74488513-chr15:74489689..74497281,13	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC33-1	chr15:74495391-74495439	ENSG00000259264.1
2	lnc-CCDC33-1	chr15:74495351-74495439	ENSG00000259264.1
3	lnc-CCDC33-1	chr15:74505609-74505829	ENSG00000259264.1
4	lnc-RP11-247C2.2.1-5	chr15:74483226-74483584	NONHSAT047211
5	lnc-CCDC33-1	chr15:74501729-74501875	ENSG00000259264.1
6	lnc-CCDC33-1	chr15:74504487-74504618	ENSG00000259264.1
7	lnc-CCDC33-1	chr15:74504487-74504618	ENSG00000259264.1
8	lnc-CCDC33-1	chr15:74501729-74501875	ENSG00000259264.1
9	lnc-CCDC33-1	chr15:74501729-74501875	ENSG00000259264.1
10	lnc-RP11-247C2.2.1-3	chr15:74474684-74475219	NONHSAT047210
11	lnc-RP11-247C2.2.1-5	chr15:74483765-74483832	NONHSAT047211
12	lnc-RP11-247C2.2.1-6	chr15:74494496-74494746	NONHSAT047214
13	lnc-RP11-247C2.2.1-5	chr15:74483982-74484349	NONHSAT047211
14	lnc-STRA6-1	chr15:74471497-74471567	ENSG00000261543.1
15	lnc-RP11-247C2.2.1-3	chr15:74474568-74474603	NONHSAT047210
16	lnc-CCDC33-1	chr15:74510838-74511202	ENSG00000259264.1
17	lnc-CCDC33-1	chr15:74513591-74513896	ENSG00000259264.1
18	lnc-CCDC33-1	chr15:74504823-74505314	ENSG00000259264.1
19	lnc-RP11-247C2.2.1-6	chr15:74487672-74488016	NONHSAT047214
20	lnc-CCDC33-1	chr15:74495046-74495439	ENSG00000259264.1
21	lnc-CCDC33-1	chr15:74504487-74504618	ENSG00000259264.1

No data

Variant related genes	Relation type
ISLR	TF binding region
ENSG00000259264	TF binding region
ENSG00000261543	TF binding region
CCDC33	TF binding region
STRA6	TF binding region
ISLR	CpG island
ENSG00000259264	CpG island
ENSG00000261543	CpG island
CCDC33	CpG island
STRA6	CpG island
ENSG00000129009	chromatin interactions
ENSG00000167178	chromatin interactions
ENSG00000248540	chromatin interactions
ENSG00000261543	chromatin interactions
ENSG00000137868	chromatin interactions
ENSG00000168274	chromatin interactions
ENSG00000140481	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000259264	chromatin interactions

Extended variants
information (count: 2929 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2929 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17326524	chr15:74458181-74458182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186914184	chr15:74458193-74458194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540878836	chr15:74458221-74458222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559540729	chr15:74458279-74458280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529846263	chr15:74458315-74458316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555805742	chr15:74458403-74458404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541756814	chr15:74458442-74458443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563207033	chr15:74458485-74458486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143398060	chr15:74458499-74458500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11637108	chr15:74458558-74458559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562550287	chr15:74458569-74458570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533163277	chr15:74458570-74458571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551709105	chr15:74458576-74458577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570220601	chr15:74458578-74458579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138600676	chr15:74458623-74458624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373604534	chr15:74458677-74458678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546372751	chr15:74458680-74458681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568668090	chr15:74458698-74458699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577272674	chr15:74458712-74458713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191389984	chr15:74458723-74458724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569546632	chr15:74458724-74458725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539846291	chr15:74458734-74458735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558143738	chr15:74458736-74458737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142695283	chr15:74458767-74458768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112923651	chr15:74458793-74458794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184960030	chr15:74458806-74458807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574932855	chr15:74458829-74458830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200020935	chr15:74458851-74458852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368028007	chr15:74458935-74458936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540447538	chr15:74458936-74458937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112889458	chr15:74458938-74458939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189853265	chr15:74458949-74458950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541596507	chr15:74458974-74458975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370618235	chr15:74459015-74459016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563244906	chr15:74459083-74459084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530674334	chr15:74459125-74459126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545680459	chr15:74459145-74459146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564154438	chr15:74459265-74459266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528051484	chr15:74459281-74459282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546710882	chr15:74459300-74459301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561595995	chr15:74459315-74459316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529515105	chr15:74459352-74459353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181133119	chr15:74459366-74459367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560179652	chr15:74459373-74459374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185351517	chr15:74459374-74459375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540176538	chr15:74459377-74459378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529161739	chr15:74459405-74459406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111578756	chr15:74459413-74459414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566886669	chr15:74459424-74459425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533906418	chr15:74459475-74459476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Lung cancer	18438408	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
Gastrointestinal stromal cancer	20877625	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2001 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74449400-74465600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr15:74450200-74460000	Weak transcription	HSMMtube	muscle
3	chr15:74450400-74460000	Weak transcription	Fetal Muscle Leg	muscle
4	chr15:74450600-74462400	Weak transcription	Fetal Brain Male	brain
5	chr15:74452800-74460000	Weak transcription	Fetal Heart	heart
6	chr15:74459400-74460200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr15:74460000-74461600	Enhancers	Rectal Smooth Muscle	rectum
8	chr15:74460000-74461600	Enhancers	HSMMtube	muscle
9	chr15:74460000-74462600	Enhancers	Fetal Heart	heart
10	chr15:74460000-74465600	Enhancers	Fetal Muscle Leg	muscle
11	chr15:74460200-74460400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr15:74460200-74460600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr15:74460200-74460600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr15:74460200-74461000	Enhancers	GM12878-XiMat	blood
15	chr15:74460200-74463800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr15:74460200-74465600	Enhancers	Ovary	ovary
17	chr15:74460200-74466000	Enhancers	Fetal Muscle Trunk	muscle
18	chr15:74460200-74466000	Enhancers	Fetal Stomach	stomach
19	chr15:74460200-74466400	Enhancers	Spleen	Spleen
20	chr15:74460400-74460600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr15:74460400-74460600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr15:74460400-74460600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
23	chr15:74460400-74460600	Enhancers	Pancreas	Pancrea
24	chr15:74460400-74461000	Enhancers	Lung	lung
25	chr15:74460400-74462000	Enhancers	Right Atrium	heart
26	chr15:74460400-74462200	Enhancers	Left Ventricle	heart
27	chr15:74460400-74462200	Enhancers	Right Ventricle	heart
28	chr15:74460400-74463400	Enhancers	Stomach Smooth Muscle	stomach
29	chr15:74460600-74461200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr15:74460600-74461400	Weak transcription	Pancreas	Pancrea
31	chr15:74460600-74461800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr15:74460600-74461800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr15:74460600-74463000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr15:74460600-74464600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr15:74460800-74462000	Enhancers	Adipose Nuclei	Adipose
36	chr15:74460800-74462000	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr15:74460800-74462000	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr15:74460800-74462400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr15:74460800-74462600	Enhancers	Colon Smooth Muscle	Colon
40	chr15:74461000-74461400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr15:74461000-74461400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr15:74461000-74461400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr15:74461000-74462800	Weak transcription	GM12878-XiMat	blood
44	chr15:74461000-74463400	Weak transcription	Lung	lung
45	chr15:74461000-74465600	Enhancers	Fetal Lung	lung
46	chr15:74461000-74465600	Enhancers	Placenta	Placenta
47	chr15:74461200-74461400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr15:74461200-74462000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
49	chr15:74461400-74461600	Weak transcription	Fetal Kidney	kidney
50	chr15:74461400-74461600	Enhancers	Pancreas	Pancrea

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