Variant report

Variant	nsv570143
Chromosome Location	chr15:77993282-78017361
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:267)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:78004964-78005009	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr15:78011949-78012314	GM12878	blood:	n/a	n/a
3	BCL3	chr15:78008746-78009107	GM12878	blood:	n/a	n/a
4	BCL3	chr15:78008726-78009098	GM12878	blood:	n/a	n/a
5	CEBPB	chr15:78015519-78015716	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr15:78002959-78002977	K562	blood:	n/a	n/a
7	CEBPB	chr15:78001895-78002100	K562	blood:	n/a	n/a
8	CEBPB	chr15:78001873-78002076	HepG2	liver:	n/a	n/a
9	CHD1	chr15:77994110-77994188	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr15:77994868-77995200	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr15:78001941-78002128	K562	blood:	n/a	n/a
12	CTCF	chr15:78001900-78002050	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr15:78015040-78015190	A549	lung:	n/a	n/a
14	CTCF	chr15:78011840-78011904	K562	blood:	n/a	n/a
15	CTCF	chr15:78015209-78015399	H1-hESC	embryonic stem cell:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
16	CTCF	chr15:78015163-78015379	K562	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
17	CTCF	chr15:78001959-78002110	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr15:78015108-78015464	K562	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
19	CTCF	chr15:78015240-78015390	GM12871	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
20	CTCF	chr15:78002020-78002170	AG09309	skin:	n/a	n/a
21	CTCF	chr15:78015260-78015410	K562	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
22	CTCF	chr15:78015240-78015390	GM12873	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
23	CTCF	chr15:78015200-78015350	A549	lung:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
24	CTCF	chr15:78001900-78002050	HepG2	liver:	n/a	n/a
25	CTCF	chr15:77994880-77995030	MCF-7	breast:	n/a	n/a
26	CTCF	chr15:78001960-78002110	AG09309	skin:	n/a	n/a
27	CTCF	chr15:78015200-78015350	NB4	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
28	CTCF	chr15:78015220-78015370	GM06990	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
29	CTCF	chr15:78015237-78015372	K562	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
30	CTCF	chr15:78002009-78002051	Gliobla	brain:	n/a	n/a
31	CTCF	chr15:78015166-78015359	K562	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
32	CTCF	chr15:78015160-78015310	HCT-116	colon:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
33	CTCF	chr15:78015200-78015350	GM06990	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
34	CTCF	chr15:78009413-78009483	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr15:78009420-78009570	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr15:78004864-78005014	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr15:78001901-78002096	HepG2	liver:	n/a	n/a
38	CTCF	chr15:78001988-78002079	HepG2	liver:	n/a	n/a
39	CTCF	chr15:78015083-78015483	H1-hESC	embryonic stem cell:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
40	CTCF	chr15:78001980-78002130	K562	blood:	n/a	n/a
41	CTCF	chr15:78001871-78002194	K562	blood:	n/a	n/a
42	CTCF	chr15:78015118-78015491	H1-hESC	embryonic stem cell:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
43	CTCF	chr15:78015109-78015429	K562	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
44	CTCF	chr15:78015180-78015330	HFF-Myc	foreskin:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
45	CTCF	chr15:78001940-78002090	A549	lung:	n/a	n/a
46	CTCF	chr15:78001920-78002070	Caco-2	colon:	n/a	n/a
47	CTCF	chr15:78015260-78015410	HepG2	liver:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
48	CTCF	chr15:78015180-78015330	Caco-2	colon:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
49	CTCF	chr15:78001973-78002103	A549	lung:	n/a	n/a
50	CTCF	chr15:78001960-78002110	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78015279-78015329	BE2_C	brain:	n/a
2	chr15:78015279-78015329	NB4	blood:	n/a
3	chr15:78004680-78004730	AG09309	skin:	n/a
4	chr15:78004680-78004730	HRPEpiC	eye:	n/a
5	chr15:78015279-78015329	HUVEC	blood vessel:	n/a
6	chr15:78015279-78015329	HAEpiC	amniotic membrane:	n/a
7	chr15:78004680-78004730	PANC-1	pancreas:	n/a
8	chr15:78004680-78004730	AG10803	skin:	n/a
9	chr15:78015279-78015329	NHBE	bronchial:	n/a
10	chr15:78015279-78015329	HL-60	blood:	n/a
11	chr15:78015279-78015329	Caco-2	colon:	n/a
12	chr15:78004680-78004730	SK-N-SH_RA	brain:	n/a
13	chr15:78004680-78004730	Jurkat	blood:	n/a
14	chr15:78004680-78004730	AG09319	gingival:	n/a
15	chr15:78004680-78004730	A549	lung:	n/a
16	chr15:78015279-78015329	BJ	skin:	n/a
17	chr15:78004680-78004730	HEK293	kidney:	embryo
18	chr15:78015279-78015329	LNCaP	prostate:	n/a
19	chr15:78015279-78015329	HEEpiC	esophagus:	n/a
20	chr15:78015279-78015329	GM12891	blood:	n/a
21	chr15:78004680-78004730	MCF10A-Er-Src	breast:	n/a
22	chr15:78004680-78004730	K562	blood:	n/a
23	chr15:78015279-78015329	SK-N-SH_RA	brain:	n/a
24	chr15:78015279-78015329	MCF-7	breast:	n/a
25	chr15:78015279-78015329	AG10803	skin:	n/a
26	chr15:78015279-78015329	SKMC	muscle:	n/a
27	chr15:78004680-78004730	GM06990	blood:	n/a
28	chr15:78015279-78015329	GM12878	blood:	n/a
29	chr15:78015279-78015329	PrEC	prostate:	n/a
30	chr15:78015279-78015329	HRPEpiC	eye:	n/a
31	chr15:78015279-78015329	NHDF-neo	bronchial:	n/a
32	chr15:78004680-78004730	Hela-S3	cervix:	n/a
33	chr15:78004680-78004730	HCF	heart:	n/a
34	chr15:78004680-78004730	GM12892	blood:	n/a
35	chr15:78015279-78015329	GM19239	blood:	n/a
36	chr15:78015279-78015329	HCF	heart:	n/a
37	chr15:78004680-78004730	ProgFib	skin:	n/a
38	chr15:78015279-78015329	HCT-116	colon:	n/a
39	chr15:78004680-78004730	NH-A	brain:	n/a
40	chr15:78015279-78015329	HMEC	breast:	n/a
41	chr15:78004680-78004730	U87	brain:	n/a
42	chr15:78004680-78004730	HCM	heart:	n/a
43	chr15:78015279-78015329	AG04449	skin:	fetal
44	chr15:78015279-78015329	IMR90	lung:	fetal
45	chr15:78015279-78015329	Jurkat	blood:	n/a
46	chr15:78004680-78004730	BJ	skin:	n/a
47	chr15:78004680-78004730	NHDF-neo	bronchial:	n/a
48	chr15:78004680-78004730	NB4	blood:	n/a
49	chr15:78015279-78015329	PANC-1	pancreas:	n/a
50	chr15:78004680-78004730	SK-N-MC	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:78006781..78008736-chr15:78010587..78012816,2	K562	blood:
2	chr15:78009070..78011036-chr15:78012914..78014777,2	K562	blood:
3	chr15:73923669..73926089-chr15:78010481..78013463,2	K562	blood:
4	chr15:78006143..78008281-chr15:78009901..78012087,2	K562	blood:
5	chr15:77986790..77988605-chr15:77991712..77993681,2	K562	blood:
6	chr15:77996121..77999450-chr15:78013163..78015366,3	K562	blood:
7	chr15:78008270..78009842-chr15:78011273..78013230,2	MCF-7	breast:
8	chr15:77993820..77996463-chr15:78016040..78017926,2	MCF-7	breast:
9	chr15:78006143..78008281-chr15:78009901..78012087,2	K562	blood:
10	chr15:77986790..77988861-chr15:77992181..77993938,2	K562	blood:
11	chr15:78004582..78006437-chr15:78057929..78059969,2	MCF-7	breast:
12	chr15:77993820..77996463-chr15:78016040..78017926,2	MCF-7	breast:
13	chr15:78006781..78008736-chr15:78010587..78012816,2	K562	blood:
14	chr15:78008224..78009963-chr15:78011351..78014041,3	MCF-7	breast:
15	chr15:77925750..77926474-chr15:78007678..78008229,2	MCF-7	breast:
16	chr15:77996121..77999450-chr15:78013163..78015366,3	K562	blood:
17	chr15:77988658..77990468-chr15:77993100..77994918,2	MCF-7	breast:

No data

Variant related genes	Relation type
LINGO1	TF binding region
LINGO1	CpG island
ENSG00000156642	chromatin interactions
ENSG00000169783	chromatin interactions

Extended variants
information (count: 1084 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1084 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11852429	chr15:77993282-77993283	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530696944	chr15:77993316-77993317	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569837130	chr15:77993328-77993329	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546227033	chr15:77993337-77993338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528179900	chr15:77993389-77993390	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs140959266	chr15:77993439-77993440	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs556706170	chr15:77993486-77993487	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs567809371	chr15:77993577-77993578	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs536888745	chr15:77993582-77993583	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs548479680	chr15:77993654-77993655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs570354583	chr15:77993666-77993667	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs367978929	chr15:77993681-77993682	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537316657	chr15:77993734-77993735	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs559002746	chr15:77993736-77993737	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185029288	chr15:77993779-77993780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535013117	chr15:77993783-77993784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs553545011	chr15:77993797-77993798	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs112437231	chr15:77993830-77993831	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145598987	chr15:77993857-77993858	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs528382176	chr15:77993858-77993859	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs78690315	chr15:77993906-77993907	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561906881	chr15:77993968-77993969	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs575513037	chr15:77993977-77993978	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs189440688	chr15:77994026-77994027	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563740361	chr15:77994032-77994033	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs180934516	chr15:77994036-77994037	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546176720	chr15:77994038-77994039	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs149143491	chr15:77994087-77994088	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528959457	chr15:77994088-77994089	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs377704753	chr15:77994125-77994126	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs573675489	chr15:77994126-77994127	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs72746412	chr15:77994130-77994131	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs143250794	chr15:77994131-77994132	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537744395	chr15:77994153-77994154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs148294467	chr15:77994159-77994160	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143150148	chr15:77994189-77994190	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs575156841	chr15:77994199-77994200	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550235696	chr15:77994254-77994255	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs79806869	chr15:77994255-77994256	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs147050659	chr15:77994266-77994267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535546231	chr15:77994285-77994286	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557131409	chr15:77994289-77994290	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs575296231	chr15:77994292-77994293	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs545588530	chr15:77994322-77994323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs564077917	chr15:77994344-77994345	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs138485029	chr15:77994347-77994348	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539870248	chr15:77994352-77994353	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570216481	chr15:77994364-77994365	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs553798229	chr15:77994367-77994368	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs183473249	chr15:77994390-77994391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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	22037309	CNVD

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77969200-78007600	Weak transcription	Right Atrium	heart
2	chr15:77992200-77993600	Weak transcription	Brain Substantia Nigra	brain
3	chr15:77992200-77993600	Weak transcription	Spleen	Spleen
4	chr15:77992200-77994600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr15:77992200-77994600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:77992200-77998800	Weak transcription	Brain Angular Gyrus	brain
7	chr15:77992200-77999200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr15:77992200-78002200	Weak transcription	Fetal Brain Male	brain
9	chr15:77993200-77993400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:77993400-77994600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr15:77993600-77993800	Enhancers	Spleen	Spleen
12	chr15:77994600-77994800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:77994600-77995400	Enhancers	H1 Cell Line	embryonic stem cell
14	chr15:77994600-77995400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:77994600-77995400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr15:77994800-78002000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr15:77995400-77996800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr15:77995400-78004200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr15:77996800-77997000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr15:77997000-77997200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr15:77997000-77997600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr15:77997200-77997400	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr15:77997600-77998200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr15:77998200-77999000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr15:77998800-77999800	Enhancers	Brain Angular Gyrus	brain
26	chr15:77999000-77999400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr15:77999200-78000200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr15:77999400-78003600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr15:77999800-78003600	Weak transcription	Brain Angular Gyrus	brain
30	chr15:78000200-78002200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr15:78002000-78002800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr15:78002000-78003600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr15:78002200-78002400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr15:78002200-78003400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr15:78002200-78003800	Enhancers	Fetal Brain Male	brain
36	chr15:78002400-78003400	Enhancers	Brain Germinal Matrix	brain
37	chr15:78002600-78003200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
38	chr15:78002600-78003400	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr15:78002600-78005200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr15:78002800-78004000	Enhancers	Brain Substantia Nigra	brain
41	chr15:78002800-78004200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr15:78003200-78003400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr15:78003200-78004000	Enhancers	Fetal Brain Female	brain
44	chr15:78003200-78004600	Weak transcription	Brain Cingulate Gyrus	brain
45	chr15:78003400-78003800	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr15:78003400-78005600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr15:78003400-78009600	Weak transcription	Brain Germinal Matrix	brain
48	chr15:78003600-78003800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr15:78003600-78004200	Enhancers	Brain Angular Gyrus	brain
50	chr15:78003600-78005400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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