Variant report

Variant	nsv904246
Chromosome Location	chr15:56665827-56732192
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:289)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:289 , 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	ARID3A	chr15:56721089-56721405	K562	blood:	n/a	n/a
2	ATF1	chr15:56701414-56701616	K562	blood:	n/a	n/a
3	BHLHE40	chr15:56704886-56704981	GM12878	blood:	n/a	n/a
4	CEBPB	chr15:56724404-56724778	IMR90	lung:	n/a	chr15:56724724-56724735
5	CEBPB	chr15:56687195-56687330	HepG2	liver:	n/a	chr15:56687247-56687258
6	CEBPB	chr15:56715740-56715857	A549	lung:	n/a	n/a
7	CEBPB	chr15:56724617-56724796	H1-hESC	embryonic stem cell:	n/a	chr15:56724724-56724735
8	CEBPB	chr15:56701741-56701793	K562	blood:	n/a	n/a
9	CEBPB	chr15:56708065-56708209	HepG2	liver:	n/a	n/a
10	CEBPB	chr15:56708105-56708119	IMR90	lung:	n/a	n/a
11	CEBPB	chr15:56706437-56706660	A549	lung:	n/a	n/a
12	CEBPB	chr15:56715699-56715899	IMR90	lung:	n/a	n/a
13	CEBPB	chr15:56724457-56724851	A549	lung:	n/a	chr15:56724724-56724735
14	CEBPB	chr15:56683119-56683285	A549	lung:	n/a	n/a
15	CEBPB	chr15:56724449-56724866	HepG2	liver:	n/a	chr15:56724724-56724735
16	CHD2	chr15:56731171-56731196	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr15:56720879-56721521	HCT-116	colon:	n/a	n/a
18	CTCF	chr15:56721135-56721336	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr15:56721160-56721310	AG04449	skin:	n/a	n/a
20	CTCF	chr15:56721015-56721388	A549	lung:	n/a	n/a
21	CTCF	chr15:56721140-56721290	HMEC	breast:	n/a	n/a
22	CTCF	chr15:56721001-56721460	MCF-7	breast:	n/a	n/a
23	CTCF	chr15:56721220-56721370	GM12878	blood:	n/a	n/a
24	CTCF	chr15:56721160-56721310	GM12874	blood:	n/a	n/a
25	CTCF	chr15:56721180-56721330	GM12865	blood:	n/a	n/a
26	CTCF	chr15:56721100-56721250	GM12865	blood:	n/a	n/a
27	CTCF	chr15:56721200-56721350	HPF	lung:	n/a	n/a
28	CTCF	chr15:56721160-56721310	GM12872	blood:	n/a	n/a
29	CTCF	chr15:56720979-56721442	K562	blood:	n/a	n/a
30	CTCF	chr15:56709345-56709384	LNCaP	prostate:	n/a	n/a
31	CTCF	chr15:56721200-56721350	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr15:56721180-56721330	GM12875	blood:	n/a	n/a
33	CTCF	chr15:56721156-56721323	GM10266	blood:	n/a	n/a
34	CTCF	chr15:56721160-56721310	GM12871	blood:	n/a	n/a
35	CTCF	chr15:56721180-56721330	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr15:56721140-56721290	BJ	skin:	n/a	n/a
37	CTCF	chr15:56721140-56721290	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr15:56721040-56721190	HCT-116	colon:	n/a	n/a
39	CTCF	chr15:56721180-56721330	K562	blood:	n/a	n/a
40	CTCF	chr15:56721160-56721310	GM12865	blood:	n/a	n/a
41	CTCF	chr15:56721140-56721290	AG09319	gingival:	n/a	n/a
42	CTCF	chr15:56721100-56721250	K562	blood:	n/a	n/a
43	CTCF	chr15:56721080-56721230	RPTEC	kidney:	n/a	n/a
44	CTCF	chr15:56721100-56721250	RPTEC	kidney:	n/a	n/a
45	CTCF	chr15:56721133-56721374	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr15:56721120-56721270	GM12864	blood:	n/a	n/a
47	CTCF	chr15:56721140-56721290	GM12869	blood:	n/a	n/a
48	CTCF	chr15:56721180-56721330	AG09319	gingival:	n/a	n/a
49	CTCF	chr15:56721046-56721416	K562	blood:	n/a	n/a
50	CTCF	chr15:56721177-56721330	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56725876-56725926	SK-N-SH_RA	brain:	n/a
2	chr15:56725876-56725926	CMK	blood:	n/a
3	chr15:56725876-56725926	GM12878	blood:	n/a
4	chr15:56725876-56725926	A549	lung:	n/a
5	chr15:56725876-56725926	HIPEpiC	eye:	n/a
6	chr15:56725876-56725926	HCT-116	colon:	n/a
7	chr15:56725876-56725926	PANC-1	pancreas:	n/a
8	chr15:56725876-56725926	SAEC	small airway:	n/a
9	chr15:56725876-56725926	NHDF-neo	bronchial:	n/a
10	chr15:56725876-56725926	AG04449	skin:	fetal
11	chr15:56725876-56725926	Jurkat	blood:	n/a
12	chr15:56725876-56725926	T-47D	breast:	n/a
13	chr15:56725876-56725926	HCF	heart:	n/a
14	chr15:56725876-56725926	MCF-7	breast:	n/a
15	chr15:56725876-56725926	AG10803	skin:	n/a
16	chr15:56725876-56725926	PFSK-1	brain:	n/a
17	chr15:56725876-56725926	HMEC	breast:	n/a
18	chr15:56725876-56725926	Hepatocyte	liver:	n/a
19	chr15:56725876-56725926	GM06990	blood:	n/a
20	chr15:56725876-56725926	HNPCEpiC	eye:	n/a
21	chr15:56725876-56725926	IMR90	lung:	fetal
22	chr15:56725876-56725926	HRPEpiC	eye:	n/a
23	chr15:56725876-56725926	NH-A	brain:	n/a
24	chr15:56725876-56725926	NHBE	bronchial:	n/a
25	chr15:56725876-56725926	U87	brain:	n/a
26	chr15:56725876-56725926	SK-N-MC	brain:	n/a
27	chr15:56725876-56725926	PrEC	prostate:	n/a
28	chr15:56725876-56725926	K562	blood:	n/a
29	chr15:56725876-56725926	MCF10A-Er-Src	breast:	n/a
30	chr15:56725876-56725926	H1-hESC	embryonic stem cell:	embryo
31	chr15:56725876-56725926	HPAEpiC	pulmonary alveolar:	n/a
32	chr15:56725876-56725926	ovcar-3	ovarian:	n/a
33	chr15:56725876-56725926	GM12891	blood:	n/a
34	chr15:56725876-56725926	HEEpiC	esophagus:	n/a
35	chr15:56725876-56725926	HCM	heart:	n/a
36	chr15:56725876-56725926	SKMC	muscle:	n/a
37	chr15:56725876-56725926	BE2_C	brain:	n/a
38	chr15:56725876-56725926	AG09309	skin:	n/a
39	chr15:56725876-56725926	AG09319	gingival:	n/a
40	chr15:56725876-56725926	HAEpiC	amniotic membrane:	n/a
41	chr15:56725876-56725926	BJ	skin:	n/a
42	chr15:56725876-56725926	AoSMC	blood vessel:	n/a
43	chr15:56725876-56725926	HRE	kidney:	n/a
44	chr15:56725876-56725926	RPTEC	kidney:	n/a
45	chr15:56725876-56725926	HCPEpiC	choroid plexus:	n/a
46	chr15:56725876-56725926	GM12892	blood:	n/a
47	chr15:56725876-56725926	ECC-1	luminal epithelium:	n/a
48	chr15:56725876-56725926	LNCaP	prostate:	n/a
49	chr15:56725876-56725926	AG04450	lung:	fetal
50	chr15:56725876-56725926	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr15:56537725..56539025-chr15:56720287..56722326,16	MCF-7	breast:
2	chr15:56696715..56699099-chr15:56700955..56702991,2	MCF-7	breast:
3	chr15:56537986..56539019-chr15:56720847..56721772,4	K562	blood:
4	chr15:56540966..56543133-chr15:56718827..56720916,2	MCF-7	breast:
5	chr15:56540398..56542023-chr15:56720800..56721752,16	MCF-7	breast:
6	chr15:55940442..55941185-chr15:56720975..56721740,2	K562	blood:
7	chr15:56714747..56716284-chr15:56716589..56718483,2	MCF-7	breast:
8	chr15:56587524..56588313-chr15:56720286..56721333,4	MCF-7	breast:
9	chr15:56066629..56067204-chr15:56720771..56721659,2	K562	blood:
10	chr15:56541012..56541917-chr15:56720826..56721341,2	K562	blood:
11	chr15:56662303..56664925-chr15:56669257..56671232,2	MCF-7	breast:
12	chr15:56536734..56539507-chr15:56718886..56721172,2	MCF-7	breast:
13	chr15:56541018..56541999-chr15:56720733..56721455,3	MCF-7	breast:
14	chr15:56697956..56699869-chr15:56701440..56703984,2	MCF-7	breast:
15	chr15:56714747..56716284-chr15:56716589..56718483,2	MCF-7	breast:
16	chr15:56538080..56538849-chr15:56720711..56721356,4	MCF-7	breast:
17	chr15:56731142..56732969-chr15:56736651..56738760,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MNS1-1	chr15:56700681-56701128	ENSG00000261823.1
2	lnc-TCF12-5	chr15:56666352-56666821	NONHSAT044018
3	lnc-MNS1-1	chr15:56701994-56702384	ENSG00000261823.1

No data

Variant related genes	Relation type
ENSG00000259941	TF binding region
MNS1	TF binding region
TEX9	TF binding region
ENSG00000261823	TF binding region
ENSG00000259941	CpG island
MNS1	CpG island
TEX9	CpG island
ENSG00000261823	CpG island
ENSG00000261823	chromatin interactions

Extended variants
information (count: 2696 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2696 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8026111	chr15:56665827-56665828	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79166246	chr15:56665843-56665844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs144160324	chr15:56665847-56665848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574652996	chr15:56665902-56665903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148709685	chr15:56665911-56665912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554669415	chr15:56665985-56665986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562761812	chr15:56666064-56666065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531695638	chr15:56666091-56666092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373618068	chr15:56666126-56666127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367729261	chr15:56666203-56666204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551344216	chr15:56666207-56666208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116746392	chr15:56666216-56666217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527775087	chr15:56666217-56666218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570538512	chr15:56666290-56666291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117906767	chr15:56666292-56666293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536568154	chr15:56666350-56666351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187337975	chr15:56666398-56666399	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs550418794	chr15:56666419-56666420	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
19	rs570240620	chr15:56666430-56666431	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
20	rs77651209	chr15:56666441-56666442	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
21	rs538667370	chr15:56666469-56666470	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
22	rs2682038	chr15:56666500-56666501	Weak transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs572212730	chr15:56666611-56666612	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
24	rs534665522	chr15:56666618-56666619	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
25	rs117675823	chr15:56666622-56666623	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
26	rs190664314	chr15:56666627-56666628	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
27	rs147472386	chr15:56666628-56666629	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
28	rs563634752	chr15:56666717-56666718	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
29	rs551974125	chr15:56666769-56666770	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
30	rs577037687	chr15:56666796-56666797	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
31	rs182942808	chr15:56666807-56666808	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs187241504	chr15:56666813-56666814	ZNF genes & repeats Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs74472048	chr15:56666854-56666855	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145548813	chr15:56666886-56666887	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566984098	chr15:56666891-56666892	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561341406	chr15:56666898-56666899	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530355494	chr15:56666920-56666921	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550087438	chr15:56666924-56666925	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76505104	chr15:56666936-56666937	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532847507	chr15:56666940-56666941	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190388139	chr15:56666946-56666947	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77772253	chr15:56666982-56666983	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2682039	chr15:56666996-56666997	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs549614280	chr15:56667021-56667022	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569808292	chr15:56667035-56667036	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554614021	chr15:56667054-56667055	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183190411	chr15:56667069-56667070	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537276595	chr15:56667098-56667099	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111735267	chr15:56667173-56667174	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576765691	chr15:56667174-56667175	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	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:262 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56658200-56675400	Weak transcription	Pancreas	Pancrea
2	chr15:56658800-56669600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr15:56659400-56666800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr15:56659600-56675400	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr15:56660400-56674400	Weak transcription	Hela-S3	cervix
6	chr15:56661000-56671000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr15:56661800-56668400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr15:56662000-56666800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr15:56664400-56667600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr15:56664400-56669400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr15:56664400-56669600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr15:56664400-56685200	Weak transcription	Duodenum Mucosa	Duodenum
13	chr15:56665200-56733400	Weak transcription	Fetal Kidney	kidney
14	chr15:56665800-56666000	Enhancers	GM12878-XiMat	blood
15	chr15:56666000-56666200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr15:56666000-56666400	Weak transcription	GM12878-XiMat	blood
17	chr15:56666400-56667200	ZNF genes & repeats	GM12878-XiMat	blood
18	chr15:56666800-56667200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr15:56666800-56667200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
20	chr15:56667200-56668400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr15:56667200-56670400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr15:56670400-56672000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr15:56670600-56673000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr15:56670800-56671000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr15:56671000-56671200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr15:56671000-56672000	ZNF genes & repeats	GM12878-XiMat	blood
27	chr15:56671000-56676800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr15:56671400-56676200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr15:56671800-56672000	ZNF genes & repeats	Ovary	ovary
30	chr15:56672000-56673600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr15:56672000-56694600	Weak transcription	Ovary	ovary
32	chr15:56672400-56674000	Weak transcription	Thymus	Thymus
33	chr15:56672400-56677400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr15:56673000-56678000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr15:56673200-56677000	Weak transcription	Gastric	stomach
36	chr15:56673400-56675800	Weak transcription	Fetal Intestine Large	intestine
37	chr15:56673400-56676600	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr15:56673600-56675200	ZNF genes & repeats	GM12878-XiMat	blood
39	chr15:56673600-56675400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr15:56673600-56675400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr15:56673800-56674000	ZNF genes & repeats	Fetal Intestine Small	intestine
42	chr15:56673800-56676800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr15:56674000-56675000	Strong transcription	Fetal Intestine Small	intestine
44	chr15:56674000-56675400	ZNF genes & repeats	Fetal Stomach	stomach
45	chr15:56674000-56675400	Strong transcription	Thymus	Thymus
46	chr15:56674200-56675000	Weak transcription	Fetal Lung	lung
47	chr15:56674800-56675600	Enhancers	HMEC	breast
48	chr15:56675000-56675200	ZNF genes & repeats	Fetal Lung	lung
49	chr15:56675000-56675800	Enhancers	Stomach Mucosa	stomach
50	chr15:56675000-56685000	Weak transcription	Fetal Intestine Small	intestine

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