Variant report

Variant	nsv1044082
Chromosome Location	chr15:39693241-39750193
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:921)
CpG islands
(count:246)
Chromatin interactive
region (count:53)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:921 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:39740665-39740941	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:39747583-39748662	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:39746918-39747168	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:39747732-39747957	K562	blood:	n/a	n/a
5	ARID3A	chr15:39726993-39727601	HepG2	liver:	n/a	n/a
6	ATF1	chr15:39697043-39697457	K562	blood:	n/a	n/a
7	ATF1	chr15:39695823-39696026	K562	blood:	n/a	n/a
8	ATF1	chr15:39746636-39746643	K562	blood:	n/a	n/a
9	ATF2	chr15:39722020-39722552	GM12878	blood:	n/a	n/a
10	ATF2	chr15:39703805-39704253	GM12878	blood:	n/a	n/a
11	ATF2	chr15:39745878-39746319	GM12878	blood:	n/a	n/a
12	ATF2	chr15:39703840-39704314	GM12878	blood:	n/a	n/a
13	ATF2	chr15:39719232-39719822	GM12878	blood:	n/a	n/a
14	ATF2	chr15:39745859-39746251	GM12878	blood:	n/a	n/a
15	ATF2	chr15:39719284-39719792	GM12878	blood:	n/a	n/a
16	ATF3	chr15:39697207-39697400	K562	blood:	n/a	n/a
17	BACH1	chr15:39747633-39748029	K562	blood:	n/a	n/a
18	BACH1	chr15:39747639-39747989	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr15:39747620-39747876	GM12878	blood:	n/a	n/a
20	BATF	chr15:39745912-39746230	GM12878	blood:	n/a	n/a
21	BATF	chr15:39722126-39722419	GM12878	blood:	n/a	n/a
22	BATF	chr15:39719291-39719713	GM12878	blood:	n/a	n/a
23	BATF	chr15:39719251-39719741	GM12878	blood:	n/a	n/a
24	BATF	chr15:39745906-39746252	GM12878	blood:	n/a	n/a
25	BATF	chr15:39736093-39736339	GM12878	blood:	n/a	n/a
26	BATF	chr15:39703837-39704269	GM12878	blood:	n/a	n/a
27	BATF	chr15:39721949-39722530	GM12878	blood:	n/a	n/a
28	BCL11A	chr15:39703839-39704204	GM12878	blood:	n/a	n/a
29	BCL11A	chr15:39719215-39719727	GM12878	blood:	n/a	n/a
30	BCL11A	chr15:39703767-39704164	GM12878	blood:	n/a	n/a
31	BCL11A	chr15:39719378-39719719	GM12878	blood:	n/a	n/a
32	BCL11A	chr15:39745906-39746214	GM12878	blood:	n/a	n/a
33	BCL11A	chr15:39745955-39746242	GM12878	blood:	n/a	n/a
34	BCL3	chr15:39719267-39719762	GM12878	blood:	n/a	n/a
35	BCL3	chr15:39696961-39697356	A549	lung:	n/a	n/a
36	BCL3	chr15:39719289-39719739	GM12878	blood:	n/a	n/a
37	BCLAF1	chr15:39719224-39719849	GM12878	blood:	n/a	n/a
38	BCLAF1	chr15:39703772-39704302	GM12878	blood:	n/a	n/a
39	BCLAF1	chr15:39719244-39719771	GM12878	blood:	n/a	n/a
40	BHLHE40	chr15:39745934-39746244	GM12878	blood:	n/a	n/a
41	BHLHE40	chr15:39719389-39719800	K562	blood:	n/a	n/a
42	BHLHE40	chr15:39698744-39699063	GM12878	blood:	n/a	n/a
43	BHLHE40	chr15:39721937-39722434	GM12878	blood:	n/a	n/a
44	BHLHE40	chr15:39703781-39704328	GM12878	blood:	n/a	n/a
45	BHLHE40	chr15:39719077-39719993	GM12878	blood:	n/a	n/a
46	BRCA1	chr15:39726897-39726974	H1-hESC	embryonic stem cell:	n/a	n/a
47	BRCA1	chr15:39722260-39722519	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr15:39695714-39696300	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr15:39696566-39697547	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr15:39708416-39708869	K562	blood:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:39696638-39696688	Caco-2	colon:	n/a
2	chr15:39726997-39727047	SK-N-MC	brain:	n/a
3	chr15:39696638-39696688	Caco-2	colon:	n/a
4	chr15:39726997-39727047	SK-N-MC	brain:	n/a
5	chr15:39742079-39742129	AG09309	skin:	n/a
6	chr15:39742079-39742129	BJ	skin:	n/a
7	chr15:39726997-39727047	CMK	blood:	n/a
8	chr15:39713049-39713099	HCM	heart:	n/a
9	chr15:39742079-39742129	HCF	heart:	n/a
10	chr15:39696638-39696688	NH-A	brain:	n/a
11	chr15:39742079-39742129	HNPCEpiC	eye:	n/a
12	chr15:39696638-39696688	AG04449	skin:	fetal
13	chr15:39696638-39696688	HPAEpiC	pulmonary alveolar:	n/a
14	chr15:39726997-39727047	K562	blood:	n/a
15	chr15:39726997-39727047	AoSMC	blood vessel:	n/a
16	chr15:39713049-39713099	IMR90	lung:	fetal
17	chr15:39713049-39713099	K562	blood:	n/a
18	chr15:39713049-39713099	HIPEpiC	eye:	n/a
19	chr15:39742079-39742129	HEEpiC	esophagus:	n/a
20	chr15:39726997-39727047	NHDF-neo	bronchial:	n/a
21	chr15:39742079-39742129	HCM	heart:	n/a
22	chr15:39713049-39713099	NHDF-neo	bronchial:	n/a
23	chr15:39713049-39713099	NH-A	brain:	n/a
24	chr15:39726997-39727047	GM06990	blood:	n/a
25	chr15:39726997-39727047	AG10803	skin:	n/a
26	chr15:39713049-39713099	LNCaP	prostate:	n/a
27	chr15:39726997-39727047	GM12878	blood:	n/a
28	chr15:39726997-39727047	HRPEpiC	eye:	n/a
29	chr15:39742079-39742129	HUVEC	blood vessel:	n/a
30	chr15:39713049-39713099	NHBE	bronchial:	n/a
31	chr15:39742079-39742129	IMR90	lung:	fetal
32	chr15:39696638-39696688	Hela-S3	cervix:	n/a
33	chr15:39742079-39742129	NT2-D1	testis:	n/a
34	chr15:39742079-39742129	SKMC	muscle:	n/a
35	chr15:39742079-39742129	HL-60	blood:	n/a
36	chr15:39713049-39713099	ProgFib	skin:	n/a
37	chr15:39726997-39727047	SK-N-SH	brain:	n/a
38	chr15:39742079-39742129	HCT-116	colon:	n/a
39	chr15:39742079-39742129	Hepatocyte	liver:	n/a
40	chr15:39742079-39742129	T-47D	breast:	n/a
41	chr15:39696638-39696688	SAEC	small airway:	n/a
42	chr15:39713049-39713099	HRPEpiC	eye:	n/a
43	chr15:39696638-39696688	ovcar-3	ovarian:	n/a
44	chr15:39713049-39713099	HEK293	kidney:	embryo
45	chr15:39742079-39742129	A549	lung:	n/a
46	chr15:39742079-39742129	Caco-2	colon:	n/a
47	chr15:39696638-39696688	H1-hESC	embryonic stem cell:	embryo
48	chr15:39696638-39696688	AG09319	gingival:	n/a
49	chr15:39726997-39727047	MCF10A-Er-Src	breast:	n/a
50	chr15:39696638-39696688	U87	brain:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:39739352..39742846-chr15:39745277..39748876,4	MCF-7	breast:
2	chr15:39731790..39738265-chr15:39871818..39875275,7	MCF-7	breast:
3	chr15:39694348..39696610-chr15:39874084..39875864,2	MCF-7	breast:
4	chr15:39698653..39701088-chr15:39877017..39879720,2	MCF-7	breast:
5	chr15:39746552..39749195-chr15:39826550..39828305,2	MCF-7	breast:
6	chr15:39720867..39723371-chr15:39870394..39874925,5	MCF-7	breast:
7	chr15:39705799..39707909-chr15:39873297..39874835,2	MCF-7	breast:
8	chr15:39735362..39737088-chr15:39871158..39872700,2	MCF-7	breast:
9	chr15:39712002..39713506-chr15:39725005..39726661,2	MCF-7	breast:
10	chr15:39724781..39729630-chr15:39730304..39736268,5	MCF-7	breast:
11	chr15:39732986..39734871-chr9:127020115..127022303,2	MCF-7	breast:
12	chr15:39693251..39695685-chr15:39695839..39698387,3	K562	blood:
13	chr15:39744731..39747916-chr15:39873044..39877161,3	MCF-7	breast:
14	chr15:39728845..39734958-chr15:39871002..39874782,8	MCF-7	breast:
15	chr15:39693671..39697771-chr15:39871894..39873705,4	MCF-7	breast:
16	chr15:39560119..39564394-chr15:39727167..39731091,3	MCF-7	breast:
17	chr15:39694167..39696674-chr15:39698967..39702842,3	K562	blood:
18	chr15:39696668..39698687-chr15:39702884..39705384,2	MCF-7	breast:
19	chr15:39694167..39696674-chr15:39698967..39702842,3	K562	blood:
20	chr15:39733791..39736088-chr15:39738338..39740014,2	K562	blood:
21	chr15:39689591..39691834-chr15:39708077..39710104,2	K562	blood:
22	chr15:39693251..39695685-chr15:39695839..39698387,3	K562	blood:
23	chr15:39721562..39724453-chr15:39734811..39737253,2	MCF-7	breast:
24	chr15:39696668..39698687-chr15:39702884..39705384,2	MCF-7	breast:
25	chr15:39687930..39690603-chr15:39694421..39696812,2	MCF-7	breast:
26	chr15:39707618..39710570-chr15:40045505..40048143,2	K562	blood:
27	chr15:39739658..39743220-chr15:39872774..39876303,4	MCF-7	breast:
28	chr15:39693251..39695685-chr15:39695839..39697787,2	K562	blood:
29	chr15:39743414..39749749-chr15:39871400..39878085,10	MCF-7	breast:
30	chr15:39471065..39473001-chr15:39694678..39697568,2	MCF-7	breast:
31	chr15:39463804..39465395-chr15:39742405..39744124,2	MCF-7	breast:
32	chr15:39741167..39743297-chr15:39871792..39873904,2	MCF-7	breast:
33	chr15:39742666..39745111-chr15:39746881..39749174,2	K562	blood:
34	chr15:39704919..39707647-chr20:52293554..52295684,2	MCF-7	breast:
35	chr15:39723566..39727788-chr15:39872507..39874775,4	MCF-7	breast:
36	chr15:39464070..39465044-chr15:39730891..39731615,2	MCF-7	breast:
37	chr15:39693251..39695685-chr15:39695839..39697787,2	K562	blood:
38	chr15:39721051..39725636-chr15:39870055..39875310,7	MCF-7	breast:
39	chr15:39733381..39735588-chr15:39737180..39739166,2	MCF-7	breast:
40	chr15:39724781..39729630-chr15:39730304..39736268,5	MCF-7	breast:
41	chr15:39719354..39722131-chr15:39742373..39743921,2	K562	blood:
42	chr15:39724107..39725948-chr15:39841990..39843603,2	MCF-7	breast:
43	chr15:39464240..39465905-chr15:39723603..39725817,2	MCF-7	breast:
44	chr15:39745636..39749475-chr15:39752031..39754404,4	K562	blood:
45	chr15:39739352..39742846-chr15:39745277..39748876,4	MCF-7	breast:
46	chr15:39742666..39745111-chr15:39746881..39749174,2	K562	blood:
47	chr15:39462704..39465639-chr15:39730089..39732672,2	MCF-7	breast:
48	chr15:39733791..39736088-chr15:39738338..39740014,2	K562	blood:
49	chr15:39722154..39722685-chr15:39960642..39961199,2	MCF-7	breast:
50	chr15:39689811..39692581-chr15:39692665..39695062,3	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THBS1-2	chr15:39737149-39737401	NONHSAT041746
2	lnc-THBS1-2	chr15:39739845-39739940	NONHSAT041746
3	lnc-FSIP1-5	chr15:39713110-39713176	ENSG00000259345.1
4	lnc-THBS1-2	chr15:39739846-39739940	XLOC_011216
5	lnc-FSIP1-5	chr15:39711231-39711853	ENSG00000259345.1
6	lnc-FSIP1-5	chr15:39712745-39712910	ENSG00000259345.1
7	lnc-FSIP1-5	chr15:39719299-39719396	ENSG00000259345.1
8	lnc-THBS1-2	chr15:39737150-39737401	XLOC_011216
9	lnc-FSIP1-8	chr15:39699803-39700983	l_1148_chr15:39688871-39700983_testes

No data

Variant related genes	Relation type
ENSG00000259345	TF binding region
ENSG00000259345	CpG island
ENSG00000119408	chromatin interactions
ENSG00000137801	chromatin interactions
ENSG00000259345	chromatin interactions

Extended variants
information (count: 2280 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2280 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3973365	chr15:39693241-39693242	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536042366	chr15:39693254-39693255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs115402486	chr15:39693315-39693316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540659649	chr15:39693360-39693361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187725448	chr15:39693410-39693411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146532168	chr15:39693433-39693434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552710172	chr15:39693447-39693448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76160375	chr15:39693452-39693453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543855460	chr15:39693454-39693455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145832136	chr15:39693511-39693512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148975960	chr15:39693512-39693513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192685195	chr15:39693592-39693593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143749532	chr15:39693630-39693631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552965308	chr15:39693663-39693664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566368589	chr15:39693666-39693667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368807665	chr15:39693683-39693684	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs538683838	chr15:39693701-39693702	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs558379615	chr15:39693711-39693712	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs59068114	chr15:39693779-39693780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs538086089	chr15:39693801-39693802	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs35295323	chr15:39693817-39693818	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544824540	chr15:39693872-39693873	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs554882847	chr15:39693898-39693899	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs185698263	chr15:39693910-39693911	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs529781387	chr15:39693942-39693943	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs560509768	chr15:39693977-39693978	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577172365	chr15:39693999-39694000	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs546236703	chr15:39694002-39694003	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542273293	chr15:39694035-39694036	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs8033614	chr15:39694047-39694048	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs189010622	chr15:39694069-39694070	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs562026716	chr15:39694165-39694166	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs527942616	chr15:39694187-39694188	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs116418308	chr15:39694192-39694193	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566426408	chr15:39694220-39694221	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs538298533	chr15:39694238-39694239	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs531179795	chr15:39694239-39694240	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs569002125	chr15:39694248-39694249	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs143021386	chr15:39694259-39694260	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs77390002	chr15:39694353-39694354	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs3973349	chr15:39694355-39694356	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs192741875	chr15:39694364-39694365	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs35824569	chr15:39694404-39694405	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs201221446	chr15:39694437-39694438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs532878563	chr15:39694443-39694444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs553791566	chr15:39694455-39694456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs575164640	chr15:39694525-39694526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs184627346	chr15:39694576-39694577	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs144628813	chr15:39694590-39694591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs3973348	chr15:39694652-39694653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:72)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21129771	CNVD
Breast cancer	21045282	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Ovarian cancer	21720365	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:969 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39690400-39696600	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr15:39690600-39696000	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr15:39691400-39697000	Weak transcription	Left Ventricle	heart
4	chr15:39692000-39693400	Enhancers	Placenta Amnion	Placenta Amnion
5	chr15:39692000-39693600	Enhancers	Osteobl	bone
6	chr15:39692200-39695400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr15:39692600-39695600	Enhancers	Fetal Heart	heart
8	chr15:39692800-39693600	Enhancers	K562	blood
9	chr15:39693000-39693400	Enhancers	NHDF-Ad	bronchial
10	chr15:39693000-39694200	Enhancers	Ovary	ovary
11	chr15:39693000-39695600	Weak transcription	NH-A	brain
12	chr15:39693000-39695800	Weak transcription	HepG2	liver
13	chr15:39693200-39693400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr15:39693200-39693600	Enhancers	Stomach Smooth Muscle	stomach
15	chr15:39693200-39693800	Enhancers	Colon Smooth Muscle	Colon
16	chr15:39693200-39694400	Enhancers	Rectal Smooth Muscle	rectum
17	chr15:39693200-39695400	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr15:39693200-39695600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr15:39693400-39693800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr15:39693400-39694000	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr15:39693400-39695400	Weak transcription	NHDF-Ad	bronchial
22	chr15:39693600-39695200	Weak transcription	Osteobl	bone
23	chr15:39693800-39694400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr15:39694000-39694200	Enhancers	Placenta Amnion	Placenta Amnion
25	chr15:39694000-39694200	Enhancers	Stomach Smooth Muscle	stomach
26	chr15:39694200-39696000	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr15:39694400-39696000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr15:39694800-39695200	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr15:39695200-39695600	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr15:39695200-39698000	Enhancers	Osteobl	bone
31	chr15:39695200-39699000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr15:39695400-39695600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr15:39695400-39697200	Enhancers	Fetal Lung	lung
34	chr15:39695400-39697600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr15:39695400-39698000	Enhancers	Hela-S3	cervix
36	chr15:39695400-39698000	Enhancers	K562	blood
37	chr15:39695400-39698800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr15:39695400-39699600	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr15:39695400-39700400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr15:39695400-39700400	Enhancers	NHDF-Ad	bronchial
41	chr15:39695600-39695800	Flanking Active TSS	Fetal Heart	heart
42	chr15:39695600-39696000	Enhancers	A549	lung
43	chr15:39695600-39696200	Enhancers	Duodenum Mucosa	Duodenum
44	chr15:39695600-39696200	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr15:39695600-39696400	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr15:39695600-39696400	Enhancers	Fetal Stomach	stomach
47	chr15:39695600-39697400	Enhancers	HUVEC	blood vessel
48	chr15:39695600-39697600	Enhancers	HSMM	muscle
49	chr15:39695600-39697600	Enhancers	NH-A	brain
50	chr15:39695600-39698000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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