Variant report

Variant	nsv1035212
Chromosome Location	chr15:52995637-53030603
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:53027711-53028005	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:53025336-53025762	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:53001404-53001641	HepG2	liver:	n/a	n/a
4	ATF3	chr15:53027706-53027979	K562	blood:	n/a	n/a
5	BATF	chr15:53027744-53028040	GM12878	blood:	n/a	chr15:53027945-53027954
6	BHLHE40	chr15:53027714-53028030	K562	blood:	n/a	n/a
7	BHLHE40	chr15:53027701-53028165	GM12878	blood:	n/a	n/a
8	BHLHE40	chr15:53022411-53022779	K562	blood:	n/a	chr15:53022550-53022559 chr15:53022550-53022559
9	BHLHE40	chr15:53022151-53022783	GM12878	blood:	n/a	chr15:53022550-53022559 chr15:53022550-53022559
10	BHLHE40	chr15:53022405-53022675	HepG2	liver:	n/a	chr15:53022550-53022559 chr15:53022550-53022559
11	BRCA1	chr15:53021054-53021493	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr15:53003829-53003910	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr15:53027739-53028160	A549	lung:	n/a	n/a
14	CEBPB	chr15:53025408-53025729	K562	blood:	n/a	chr15:53025567-53025578
15	CEBPB	chr15:53001333-53001688	Hela-S3	cervix:	n/a	chr15:53001493-53001504 chr15:53001527-53001538
16	CEBPB	chr15:53012270-53012669	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr15:53021130-53021481	IMR90	lung:	n/a	n/a
18	CEBPB	chr15:53001361-53001671	IMR90	lung:	n/a	chr15:53001493-53001504 chr15:53001527-53001538
19	CEBPB	chr15:53025384-53025753	HepG2	liver:	n/a	chr15:53025567-53025578
20	CEBPB	chr15:53015982-53016146	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr15:53007378-53007639	HepG2	liver:	n/a	n/a
22	CEBPB	chr15:53025362-53025763	Hela-S3	cervix:	n/a	chr15:53025567-53025578
23	CEBPB	chr15:53001315-53001704	HepG2	liver:	n/a	chr15:53001493-53001504 chr15:53001527-53001538
24	CEBPB	chr15:53025415-53025697	HepG2	liver:	n/a	chr15:53025567-53025578
25	CEBPB	chr15:53001375-53001589	HepG2	liver:	n/a	chr15:53001493-53001504 chr15:53001527-53001538
26	CEBPB	chr15:53012468-53012470	A549	lung:	n/a	n/a
27	CEBPB	chr15:53015920-53016153	A549	lung:	n/a	n/a
28	CEBPB	chr15:53025447-53025711	HepG2	liver:	n/a	chr15:53025567-53025578
29	CEBPB	chr15:53025372-53025801	HepG2	liver:	n/a	chr15:53025567-53025578
30	CEBPB	chr15:53021098-53021506	Hela-S3	cervix:	n/a	n/a
31	CEBPD	chr15:53025449-53025682	HepG2	liver:	n/a	chr15:53025568-53025579
32	CTCF	chr15:53026040-53026190	AG04449	skin:	n/a	n/a
33	CTCF	chr15:53027820-53027970	SK-N-SH_RA	brain:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
34	CTCF	chr15:53009579-53009640	GM20000	blood:	n/a	n/a
35	CTCF	chr15:53027800-53027950	AG04449	skin:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
36	CTCF	chr15:53022514-53022630	Lung_OC	lung:	n/a	n/a
37	CTCF	chr15:53022540-53022690	GM12868	blood:	n/a	n/a
38	CTCF	chr15:53027800-53027950	GM12878	blood:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
39	CTCF	chr15:53027820-53027970	Caco-2	colon:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
40	CTCF	chr15:53027800-53027950	HUVEC	blood vessel:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
41	CTCF	chr15:53027760-53027910	NHEK	skin:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
42	CTCF	chr15:53022485-53022624	NHEK	skin:	n/a	n/a
43	CTCF	chr15:53027800-53027950	BJ	skin:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
44	CTCF	chr15:53022460-53022610	GM12873	blood:	n/a	n/a
45	CTCF	chr15:53027527-53028121	GM12878	blood:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
46	CTCF	chr15:53027840-53027990	HA-sp	spinal cord:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
47	CTCF	chr15:53027800-53027950	HPAF	blood vessel:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882
48	CTCF	chr15:53022504-53022647	GM13977	blood:	n/a	n/a
49	CTCF	chr15:53022480-53022630	GM12875	blood:	n/a	n/a
50	CTCF	chr15:53027760-53027910	HRE	kidney:	n/a	chr15:53027866-53027879 chr15:53027859-53027880 chr15:53027865-53027881 chr15:53027864-53027882

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:53001117-53001167	AG09319	gingival:	n/a
2	chr15:53001117-53001167	AG09309	skin:	n/a
3	chr15:53001117-53001167	RPTEC	kidney:	n/a
4	chr15:53001117-53001167	AG10803	skin:	n/a
5	chr15:53001117-53001167	HRCEpiC	kidney:	n/a
6	chr15:53001117-53001167	AoSMC	blood vessel:	n/a
7	chr15:53001117-53001167	H1-hESC	embryonic stem cell:	embryo
8	chr15:53001117-53001167	GM12878	blood:	n/a
9	chr15:53001117-53001167	IMR90	lung:	fetal
10	chr15:53001117-53001167	NHBE	bronchial:	n/a
11	chr15:53001117-53001167	NHDF-neo	bronchial:	n/a
12	chr15:53001117-53001167	ProgFib	skin:	n/a
13	chr15:53001117-53001167	U87	brain:	n/a
14	chr15:53001117-53001167	A549	lung:	n/a
15	chr15:53001117-53001167	Hepatocyte	liver:	n/a
16	chr15:53001117-53001167	PrEC	prostate:	n/a
17	chr15:53001117-53001167	HUVEC	blood vessel:	n/a
18	chr15:53001117-53001167	Jurkat	blood:	n/a
19	chr15:53001117-53001167	NT2-D1	testis:	n/a
20	chr15:53001117-53001167	HEEpiC	esophagus:	n/a
21	chr15:53001117-53001167	NH-A	brain:	n/a
22	chr15:53001117-53001167	K562	blood:	n/a
23	chr15:53001117-53001167	GM06990	blood:	n/a
24	chr15:53001117-53001167	HCM	heart:	n/a
25	chr15:53001117-53001167	PANC-1	pancreas:	n/a
26	chr15:53001117-53001167	SK-N-SH_RA	brain:	n/a
27	chr15:53001117-53001167	HRE	kidney:	n/a
28	chr15:53001117-53001167	HNPCEpiC	eye:	n/a
29	chr15:53001117-53001167	ECC-1	luminal epithelium:	n/a
30	chr15:53001117-53001167	MCF10A-Er-Src	breast:	n/a
31	chr15:53001117-53001167	HAEpiC	amniotic membrane:	n/a
32	chr15:53001117-53001167	SAEC	small airway:	n/a
33	chr15:53001117-53001167	BJ	skin:	n/a
34	chr15:53001117-53001167	GM19239	blood:	n/a
35	chr15:53001117-53001167	HepG2	liver:	n/a
36	chr15:53001117-53001167	HCPEpiC	choroid plexus:	n/a
37	chr15:53001117-53001167	Hela-S3	cervix:	n/a
38	chr15:53001117-53001167	SK-N-SH	brain:	n/a
39	chr15:53001117-53001167	Caco-2	colon:	n/a
40	chr15:53001117-53001167	SK-N-MC	brain:	n/a
41	chr15:53001117-53001167	HMEC	breast:	n/a
42	chr15:53001117-53001167	HRPEpiC	eye:	n/a
43	chr15:53001117-53001167	HCT-116	colon:	n/a
44	chr15:53001117-53001167	MCF-7	breast:	n/a
45	chr15:53001117-53001167	AG04450	lung:	fetal
46	chr15:53001117-53001167	SKMC	muscle:	n/a
47	chr15:53001117-53001167	GM12891	blood:	n/a
48	chr15:53001117-53001167	HL-60	blood:	n/a
49	chr15:53001117-53001167	GM12892	blood:	n/a
50	chr15:53001117-53001167	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:53002359..53006038-chr15:53007315..53009805,4	K562	blood:
2	chr15:52970779..52973636-chr15:53016610..53018142,2	MCF-7	breast:
3	chr15:53022444..53024405-chr15:53025609..53027744,2	MCF-7	breast:
4	chr15:53020211..53022742-chr15:53022811..53024880,2	MCF-7	breast:
5	chr15:52969340..52972976-chr15:53024542..53030044,12	MCF-7	breast:
6	chr15:53020023..53021825-chr15:53025584..53028001,2	MCF-7	breast:
7	chr15:52942373..52946105-chr15:53022429..53026141,4	MCF-7	breast:
8	chr15:52965949..52968646-chr15:53025332..53028243,3	MCF-7	breast:
9	chr15:52849763..52852458-chr15:53021230..53022756,2	MCF-7	breast:
10	chr15:52508008..52509939-chr15:53026331..53028847,2	MCF-7	breast:
11	chr15:52548546..52549086-chr15:53027357..53028249,2	MCF-7	breast:
12	chr15:52509083..52509697-chr15:53027309..53027962,2	MCF-7	breast:
13	chr15:52987035..52988935-chr15:53020479..53022010,2	MCF-7	breast:
14	chr15:52979304..52981911-chr15:53011644..53013861,2	MCF-7	breast:
15	chr15:52623157..52624688-chr15:53027206..53029012,2	MCF-7	breast:
16	chr15:52587244..52588799-chr15:53018696..53021344,2	MCF-7	breast:
17	chr15:53008460..53014321-chr15:53016290..53019599,5	MCF-7	breast:
18	chr15:52998097..53002621-chr15:53002876..53006188,5	K562	blood:
19	chr15:53017085..53018702-chr15:53021319..53022831,2	MCF-7	breast:
20	chr15:52623330..52624257-chr15:53027398..53028338,3	K562	blood:
21	chr15:52859015..52862196-chr15:53026182..53028979,3	MCF-7	breast:
22	chr15:52978223..52981172-chr15:53005234..53007666,2	MCF-7	breast:
23	chr15:53020023..53021825-chr15:53025584..53028001,2	MCF-7	breast:
24	chr15:52970614..52972574-chr15:53011299..53014236,2	MCF-7	breast:
25	chr15:52820586..52822979-chr15:53024504..53027126,2	MCF-7	breast:
26	chr15:53001798..53003547-chr15:53015558..53017626,2	MCF-7	breast:
27	chr15:53017085..53018702-chr15:53021319..53022831,2	MCF-7	breast:
28	chr15:53014375..53016603-chr15:53017308..53019885,2	MCF-7	breast:
29	chr15:52548200..52549159-chr15:53027337..53028329,9	MCF-7	breast:
30	chr15:52860064..52861646-chr15:53023947..53025473,2	MCF-7	breast:
31	chr15:52623345..52624286-chr15:53022394..53023020,2	MCF-7	breast:
32	chr15:52820704..52821409-chr15:53027435..53028340,2	K562	blood:
33	chr15:53008460..53014321-chr15:53016290..53019599,5	MCF-7	breast:
34	chr15:53006205..53008987-chr15:53009449..53012016,3	MCF-7	breast:
35	chr15:52973784..52977367-chr15:53024530..53026901,4	MCF-7	breast:
36	chr15:53006205..53008987-chr15:53009449..53012016,3	MCF-7	breast:
37	chr15:52969966..52973260-chr15:53007866..53011792,4	MCF-7	breast:
38	chr15:53001338..53004194-chr15:53026134..53027960,2	MCF-7	breast:
39	chr15:52968259..52973250-chr15:52997483..53005703,18	MCF-7	breast:
40	chr15:52844953..52847640-chr15:53010163..53013098,2	MCF-7	breast:
41	chr15:52628155..52629955-chr15:53015410..53018106,2	MCF-7	breast:
42	chr15:52967780..52973455-chr15:53015921..53024493,22	MCF-7	breast:
43	chr15:53002359..53006038-chr15:53007315..53009805,4	K562	blood:
44	chr15:52548183..52549192-chr15:53027141..53028320,9	K562	blood:
45	chr15:52623110..52623924-chr15:53027427..53028267,4	MCF-7	breast:
46	chr15:52981751..52983702-chr15:52997065..52999540,2	MCF-7	breast:
47	chr15:52509089..52509941-chr15:53027516..53028325,2	MCF-7	breast:
48	chr15:53022444..53024405-chr15:53025609..53027744,2	MCF-7	breast:
49	chr15:52968697..52973342-chr15:53018163..53028590,24	MCF-7	breast:
50	chr15:52991504..52994033-chr15:53002922..53004759,2	MCF-7	breast:

Variant related genes	Relation type
FAM214A	TF binding region
FAM214A	CpG island
ENSG00000128833	chromatin interactions
ENSG00000197535	chromatin interactions
ENSG00000128989	chromatin interactions
ENSG00000047346	chromatin interactions

Extended variants
information (count: 1387 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1387 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577001909	chr15:52995663-52995664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73409638	chr15:52995670-52995671	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs114687560	chr15:52995707-52995708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529698117	chr15:52995734-52995735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371379512	chr15:52995787-52995788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547806773	chr15:52995792-52995793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34632155	chr15:52995796-52995797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562974271	chr15:52995825-52995826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79787378	chr15:52995837-52995838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550249606	chr15:52995863-52995864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78348244	chr15:52995884-52995885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35700617	chr15:52995893-52995894	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs370554661	chr15:52995895-52995896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147642018	chr15:52995911-52995912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111682315	chr15:52995937-52995938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536714621	chr15:52995944-52995945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555077292	chr15:52995963-52995964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576392731	chr15:52995978-52995979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144423726	chr15:52995997-52995998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538961886	chr15:52996004-52996005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553801927	chr15:52996014-52996015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558623579	chr15:52996037-52996038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577018403	chr15:52996074-52996075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186550082	chr15:52996112-52996113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2899494	chr15:52996138-52996139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs574273426	chr15:52996160-52996161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557592125	chr15:52996171-52996172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7179250	chr15:52996227-52996228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577429426	chr15:52996254-52996255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190792212	chr15:52996256-52996257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181913253	chr15:52996261-52996262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563037197	chr15:52996334-52996335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186376383	chr15:52996355-52996356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530471147	chr15:52996406-52996407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145496367	chr15:52996414-52996415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs55970486	chr15:52996446-52996447	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs185421563	chr15:52996497-52996498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148857271	chr15:52996522-52996523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189784400	chr15:52996530-52996531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576099993	chr15:52996643-52996644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182134660	chr15:52996655-52996656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570129002	chr15:52996661-52996662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185776380	chr15:52996678-52996679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377126957	chr15:52996713-52996714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537050291	chr15:52996737-52996738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190983183	chr15:52996744-52996745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543001466	chr15:52996803-52996804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564569649	chr15:52996846-52996847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147992479	chr15:52996866-52996867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183718116	chr15:52996872-52996873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:372 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52991400-52997800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr15:52994600-52995800	Enhancers	Liver	Liver
3	chr15:52995000-52999600	Weak transcription	Primary B cells from peripheral blood	blood
4	chr15:52995400-52995800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:52995800-52998200	Weak transcription	Liver	Liver
6	chr15:52995800-53001600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr15:52997800-52998800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr15:52998200-52998400	Enhancers	Liver	Liver
9	chr15:52998200-52998800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr15:52998200-52998800	Enhancers	NHEK	skin
11	chr15:52998200-52999200	Enhancers	Muscle Satellite Cultured Cells	--
12	chr15:52998200-52999400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr15:52998400-52998800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr15:52998400-52999000	Flanking Active TSS	Liver	Liver
15	chr15:52998400-52999000	Enhancers	HSMM	muscle
16	chr15:52998800-53000800	Enhancers	Primary B cells from cord blood	blood
17	chr15:52998800-53001000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr15:52998800-53001200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr15:52998800-53001600	Weak transcription	NHEK	skin
20	chr15:52998800-53002200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr15:52999000-52999200	Active TSS	Liver	Liver
22	chr15:52999200-52999400	Flanking Active TSS	Liver	Liver
23	chr15:52999400-52999800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr15:52999400-53000200	Active TSS	Liver	Liver
25	chr15:52999600-53001000	Enhancers	Primary B cells from peripheral blood	blood
26	chr15:52999800-53001200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr15:53000200-53000800	Flanking Active TSS	Liver	Liver
28	chr15:53000400-53000600	Enhancers	Adipose Nuclei	Adipose
29	chr15:53000400-53001200	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr15:53000400-53001200	Enhancers	HepG2	liver
31	chr15:53000600-53001000	Enhancers	Fetal Intestine Large	intestine
32	chr15:53000800-53001000	Active TSS	Liver	Liver
33	chr15:53000800-53001800	Weak transcription	Adipose Nuclei	Adipose
34	chr15:53000800-53002000	Flanking Active TSS	Primary B cells from cord blood	blood
35	chr15:53001000-53001200	Flanking Active TSS	Liver	Liver
36	chr15:53001000-53001200	Enhancers	Duodenum Mucosa	Duodenum
37	chr15:53001000-53001200	Flanking Active TSS	Fetal Intestine Large	intestine
38	chr15:53001000-53001200	Enhancers	Fetal Intestine Small	intestine
39	chr15:53001000-53001400	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr15:53001000-53001600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr15:53001000-53001600	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr15:53001000-53001800	Enhancers	GM12878-XiMat	blood
43	chr15:53001000-53002200	Flanking Active TSS	Primary B cells from peripheral blood	blood
44	chr15:53001200-53001600	Active TSS	Liver	Liver
45	chr15:53001200-53001800	Flanking Active TSS	Duodenum Mucosa	Duodenum
46	chr15:53001200-53002000	Active TSS	Fetal Intestine Large	intestine
47	chr15:53001200-53002000	Active TSS	Fetal Intestine Small	intestine
48	chr15:53001200-53002400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr15:53001200-53002600	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr15:53001200-53002800	Flanking Active TSS	HepG2	liver

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