Variant report

Variant	nsv9270
Chromosome Location	chr15:56686946-56760420
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:600)
CpG islands
(count:917)
Chromatin interactive
region (count:18)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:56757183-56757342	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:56757439-56757589	K562	blood:	n/a	n/a
3	ARID3A	chr15:56721089-56721405	K562	blood:	n/a	n/a
4	ATF1	chr15:56701414-56701616	K562	blood:	n/a	n/a
5	ATF2	chr15:56757025-56757555	GM12878	blood:	n/a	n/a
6	BACH1	chr15:56757137-56757703	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr15:56757918-56757978	K562	blood:	n/a	n/a
8	BCL3	chr15:56757103-56757795	A549	lung:	n/a	n/a
9	BCL3	chr15:56757037-56757647	GM12878	blood:	n/a	n/a
10	BCLAF1	chr15:56757083-56757625	GM12878	blood:	n/a	n/a
11	BHLHE40	chr15:56704886-56704981	GM12878	blood:	n/a	n/a
12	BHLHE40	chr15:56757184-56757611	K562	blood:	n/a	chr15:56757254-56757270
13	BHLHE40	chr15:56757494-56757730	HepG2	liver:	n/a	n/a
14	CBX3	chr15:56757309-56757702	K562	blood:	n/a	n/a
15	CBX3	chr15:56757101-56757760	K562	blood:	n/a	n/a
16	CCNT2	chr15:56757151-56757524	K562	blood:	n/a	n/a
17	CEBPB	chr15:56748579-56748651	A549	lung:	n/a	n/a
18	CEBPB	chr15:56706437-56706660	A549	lung:	n/a	n/a
19	CEBPB	chr15:56715699-56715899	IMR90	lung:	n/a	n/a
20	CEBPB	chr15:56687195-56687330	HepG2	liver:	n/a	chr15:56687247-56687258
21	CEBPB	chr15:56708065-56708209	HepG2	liver:	n/a	n/a
22	CEBPB	chr15:56715740-56715857	A549	lung:	n/a	n/a
23	CEBPB	chr15:56757311-56757566	K562	blood:	n/a	n/a
24	CEBPB	chr15:56724617-56724796	H1-hESC	embryonic stem cell:	n/a	chr15:56724724-56724735
25	CEBPB	chr15:56752307-56752555	K562	blood:	n/a	n/a
26	CEBPB	chr15:56701741-56701793	K562	blood:	n/a	n/a
27	CEBPB	chr15:56724457-56724851	A549	lung:	n/a	chr15:56724724-56724735
28	CEBPB	chr15:56724449-56724866	HepG2	liver:	n/a	chr15:56724724-56724735
29	CEBPB	chr15:56708105-56708119	IMR90	lung:	n/a	n/a
30	CEBPB	chr15:56724404-56724778	IMR90	lung:	n/a	chr15:56724724-56724735
31	CHD1	chr15:56756836-56757173	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr15:56757109-56757659	H1-hESC	embryonic stem cell:	n/a	chr15:56757214-56757224
33	CHD2	chr15:56757151-56757631	K562	blood:	n/a	chr15:56757214-56757224
34	CHD2	chr15:56757172-56757543	HepG2	liver:	n/a	chr15:56757214-56757224
35	CHD2	chr15:56731171-56731196	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr15:56757084-56757599	GM12878	blood:	n/a	chr15:56757214-56757224
37	CREB1	chr15:56757090-56757700	A549	lung:	n/a	n/a
38	CTCF	chr15:56721200-56721350	HMEC	breast:	n/a	n/a
39	CTCF	chr15:56721200-56721350	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr15:56721100-56721250	K562	blood:	n/a	n/a
41	CTCF	chr15:56721180-56721330	K562	blood:	n/a	n/a
42	CTCF	chr15:56721180-56721330	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr15:56721140-56721290	GM12867	blood:	n/a	n/a
44	CTCF	chr15:56757290-56757407	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr15:56757500-56757650	K562	blood:	n/a	n/a
46	CTCF	chr15:56756840-56756990	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr15:56721177-56721330	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:56721260-56721410	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr15:56720879-56721521	HCT-116	colon:	n/a	n/a
50	CTCF	chr15:56721520-56721670	AG10803	skin:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56757325-56757375	GM06990	blood:	n/a
2	chr15:56759655-56759705	AG09319	gingival:	n/a
3	chr15:56757325-56757375	GM06990	blood:	n/a
4	chr15:56759655-56759705	AG09319	gingival:	n/a
5	chr15:56757625-56757675	SK-N-MC	brain:	n/a
6	chr15:56757382-56757432	AG10803	skin:	n/a
7	chr15:56757312-56757362	PrEC	prostate:	n/a
8	chr15:56757806-56757856	SK-N-MC	brain:	n/a
9	chr15:56757314-56757364	GM06990	blood:	n/a
10	chr15:56757290-56757340	MCF10A-Er-Src	breast:	n/a
11	chr15:56757552-56757602	SKMC	muscle:	n/a
12	chr15:56757517-56757567	RPTEC	kidney:	n/a
13	chr15:56758270-56758320	AG09319	gingival:	n/a
14	chr15:56757325-56757375	SK-N-SH	brain:	n/a
15	chr15:56757625-56757675	HRE	kidney:	n/a
16	chr15:56757312-56757362	GM12891	blood:	n/a
17	chr15:56759655-56759705	SAEC	small airway:	n/a
18	chr15:56757312-56757362	T-47D	breast:	n/a
19	chr15:56757108-56757158	H1-hESC	embryonic stem cell:	embryo
20	chr15:56757290-56757340	PANC-1	pancreas:	n/a
21	chr15:56757312-56757362	K562	blood:	n/a
22	chr15:56757625-56757675	AG04449	skin:	fetal
23	chr15:56758270-56758320	HEEpiC	esophagus:	n/a
24	chr15:56757314-56757364	MCF10A-Er-Src	breast:	n/a
25	chr15:56757325-56757375	HCT-116	colon:	n/a
26	chr15:56725876-56725926	NT2-D1	testis:	n/a
27	chr15:56758270-56758320	SKMC	muscle:	n/a
28	chr15:56757108-56757158	HAEpiC	amniotic membrane:	n/a
29	chr15:56757180-56757230	MCF-7	breast:	n/a
30	chr15:56757382-56757432	HCPEpiC	choroid plexus:	n/a
31	chr15:56725876-56725926	Jurkat	blood:	n/a
32	chr15:56757552-56757602	K562	blood:	n/a
33	chr15:56757290-56757340	HCT-116	colon:	n/a
34	chr15:56757314-56757364	GM12891	blood:	n/a
35	chr15:56759655-56759705	PFSK-1	brain:	n/a
36	chr15:56757312-56757362	LNCaP	prostate:	n/a
37	chr15:56757312-56757362	GM19239	blood:	n/a
38	chr15:56757517-56757567	Hela-S3	cervix:	n/a
39	chr15:56757312-56757362	HRCEpiC	kidney:	n/a
40	chr15:56725876-56725926	AG04450	lung:	fetal
41	chr15:56757325-56757375	GM12891	blood:	n/a
42	chr15:56757314-56757364	AG09309	skin:	n/a
43	chr15:56757314-56757364	AG04449	skin:	fetal
44	chr15:56757180-56757230	NHDF-neo	bronchial:	n/a
45	chr15:56757290-56757340	HRE	kidney:	n/a
46	chr15:56757325-56757375	HUVEC	blood vessel:	n/a
47	chr15:56757180-56757230	HMEC	breast:	n/a
48	chr15:56757806-56757856	PFSK-1	brain:	n/a
49	chr15:56757180-56757230	HRE	kidney:	n/a
50	chr15:56757108-56757158	Jurkat	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:56536734..56539507-chr15:56718886..56721172,2	MCF-7	breast:
2	chr15:56537987..56538847-chr15:56756234..56756979,2	MCF-7	breast:
3	chr15:56731142..56732969-chr15:56736651..56738760,2	K562	blood:
4	chr15:56540398..56542023-chr15:56720800..56721752,16	MCF-7	breast:
5	chr15:55940442..55941185-chr15:56720975..56721740,2	K562	blood:
6	chr15:56541018..56541999-chr15:56720733..56721455,3	MCF-7	breast:
7	chr15:56714747..56716284-chr15:56716589..56718483,2	MCF-7	breast:
8	chr15:56541012..56541917-chr15:56720826..56721341,2	K562	blood:
9	chr15:56697956..56699869-chr15:56701440..56703984,2	MCF-7	breast:
10	chr15:56537986..56539019-chr15:56720847..56721772,4	K562	blood:
11	chr15:56696715..56699099-chr15:56700955..56702991,2	MCF-7	breast:
12	chr15:56540966..56543133-chr15:56718827..56720916,2	MCF-7	breast:
13	chr15:56066629..56067204-chr15:56720771..56721659,2	K562	blood:
14	chr15:56714747..56716284-chr15:56716589..56718483,2	MCF-7	breast:
15	chr15:56731142..56732969-chr15:56736651..56738760,2	K562	blood:
16	chr15:56587524..56588313-chr15:56720286..56721333,4	MCF-7	breast:
17	chr15:56538080..56538849-chr15:56720711..56721356,4	MCF-7	breast:
18	chr15:56537725..56539025-chr15:56720287..56722326,16	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MNS1-1	chr15:56701994-56702384	ENSG00000261823.1
2	lnc-ZNF280D-2	chr15:56757168-56757283	NONHSAT044023
3	lnc-ZNF280D-2	chr15:56755978-56756445	NONHSAT044023
4	lnc-MNS1-1	chr15:56700681-56701128	ENSG00000261823.1

No data

Variant related genes	Relation type
ENSG00000259941	TF binding region
MNS1	TF binding region
ENSG00000261823	TF binding region
ENSG00000259941	CpG island
MNS1	CpG island
ENSG00000261823	CpG island
ENSG00000261823	chromatin interactions

Extended variants
information (count: 2976 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2976 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576486868	chr15:56686953-56686954	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs79299042	chr15:56686989-56686990	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs541441008	chr15:56686990-56686991	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs148168860	chr15:56686999-56687000	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs375726251	chr15:56687017-56687018	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs141149800	chr15:56687032-56687033	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs376888794	chr15:56687035-56687036	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs371507729	chr15:56687044-56687045	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs374626306	chr15:56687049-56687050	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs367699476	chr15:56687051-56687052	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs16976896	chr15:56687065-56687066	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs368059447	chr15:56687069-56687070	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs568013131	chr15:56687087-56687088	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs188428419	chr15:56687116-56687117	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs147360195	chr15:56687173-56687174	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs570056647	chr15:56687198-56687199	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs565493422	chr15:56687220-56687221	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs368806944	chr15:56687225-56687226	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs180889430	chr15:56687251-56687252	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs137999336	chr15:56687270-56687271	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs548110657	chr15:56687303-56687304	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs185192291	chr15:56687317-56687318	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs114763209	chr15:56687328-56687329	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs190776596	chr15:56687352-56687353	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs6493856	chr15:56687359-56687360	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs182575472	chr15:56687368-56687369	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs543051496	chr15:56687373-56687374	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs563265402	chr15:56687383-56687384	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs532121036	chr15:56687388-56687389	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs545920674	chr15:56687413-56687414	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs559004465	chr15:56687444-56687445	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs530410448	chr15:56687489-56687490	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs11853962	chr15:56687511-56687512	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs547974772	chr15:56687614-56687615	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs563213084	chr15:56687639-56687640	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs561658060	chr15:56687668-56687669	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs568815929	chr15:56687685-56687686	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs549929745	chr15:56687691-56687692	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs537269278	chr15:56687722-56687723	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs569999997	chr15:56687747-56687748	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs12164935	chr15:56687817-56687818	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs552750414	chr15:56687850-56687851	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs139544714	chr15:56687857-56687858	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs149722122	chr15:56687869-56687870	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs73413974	chr15:56687891-56687892	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs575174097	chr15:56687904-56687905	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs537712851	chr15:56687918-56687919	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs144600438	chr15:56687926-56687927	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs576803370	chr15:56688081-56688082	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs28408704	chr15:56688126-56688127	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	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
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:687 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56665200-56733400	Weak transcription	Fetal Kidney	kidney
2	chr15:56672000-56694600	Weak transcription	Ovary	ovary
3	chr15:56675400-56691000	Weak transcription	Fetal Stomach	stomach
4	chr15:56676400-56687400	Weak transcription	A549	lung
5	chr15:56677200-56691800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr15:56677600-56709600	Weak transcription	Fetal Lung	lung
7	chr15:56677800-56690800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr15:56677800-56726200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr15:56678600-56687000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr15:56678600-56690000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr15:56678600-56691800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr15:56678800-56689800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:56686000-56734600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr15:56686200-56691400	Weak transcription	Duodenum Mucosa	Duodenum
15	chr15:56686400-56689000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr15:56686800-56691000	ZNF genes & repeats	GM12878-XiMat	blood
17	chr15:56687000-56687800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr15:56687000-56687800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr15:56687800-56690000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr15:56687800-56691400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr15:56689000-56689200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
22	chr15:56689400-56695000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr15:56690000-56690400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr15:56690000-56690800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
25	chr15:56690000-56692400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr15:56690000-56717400	Weak transcription	Dnd41	blood
27	chr15:56690000-56737800	Weak transcription	Stomach Mucosa	stomach
28	chr15:56690400-56691800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr15:56690400-56692800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr15:56690800-56692000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr15:56691000-56692200	Strong transcription	Fetal Stomach	stomach
32	chr15:56691400-56692400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr15:56691600-56692000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
34	chr15:56691600-56692000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr15:56691800-56692200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr15:56692200-56694600	Weak transcription	Fetal Stomach	stomach
37	chr15:56692400-56692600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr15:56692600-56693800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr15:56699000-56706000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr15:56699200-56717800	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr15:56701400-56705200	Weak transcription	Small Intestine	intestine
42	chr15:56701800-56706800	Weak transcription	Primary hematopoietic stem cells	blood
43	chr15:56702000-56704000	Enhancers	GM12878-XiMat	blood
44	chr15:56702800-56703200	Enhancers	Fetal Stomach	stomach
45	chr15:56702800-56703800	Enhancers	Fetal Brain Male	brain
46	chr15:56703200-56703400	Weak transcription	Fetal Stomach	stomach
47	chr15:56703400-56703600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr15:56703400-56703800	Enhancers	Fetal Stomach	stomach
49	chr15:56703600-56704000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr15:56703600-56718000	Weak transcription	Fetal Intestine Large	intestine

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