Variant report

Variant	nsv510662
Chromosome Location	chr15:56686353-56735547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:257)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:257 , 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	chr15:56708065-56708209	HepG2	liver:	n/a	n/a
5	CEBPB	chr15:56708105-56708119	IMR90	lung:	n/a	n/a
6	CEBPB	chr15:56724449-56724866	HepG2	liver:	n/a	chr15:56724724-56724735
7	CEBPB	chr15:56715699-56715899	IMR90	lung:	n/a	n/a
8	CEBPB	chr15:56701741-56701793	K562	blood:	n/a	n/a
9	CEBPB	chr15:56715740-56715857	A549	lung:	n/a	n/a
10	CEBPB	chr15:56724457-56724851	A549	lung:	n/a	chr15:56724724-56724735
11	CEBPB	chr15:56724617-56724796	H1-hESC	embryonic stem cell:	n/a	chr15:56724724-56724735
12	CEBPB	chr15:56724404-56724778	IMR90	lung:	n/a	chr15:56724724-56724735
13	CEBPB	chr15:56687195-56687330	HepG2	liver:	n/a	chr15:56687247-56687258
14	CEBPB	chr15:56706437-56706660	A549	lung:	n/a	n/a
15	CHD2	chr15:56731171-56731196	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr15:56721040-56721190	AG04450	lung:	n/a	n/a
17	CTCF	chr15:56721159-56721297	HepG2	liver:	n/a	n/a
18	CTCF	chr15:56721015-56721388	A549	lung:	n/a	n/a
19	CTCF	chr15:56721180-56721330	HepG2	liver:	n/a	n/a
20	CTCF	chr15:56721140-56721290	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr15:56721160-56721310	GM12871	blood:	n/a	n/a
22	CTCF	chr15:56721140-56721290	GM06990	blood:	n/a	n/a
23	CTCF	chr15:56721240-56721390	Caco-2	colon:	n/a	n/a
24	CTCF	chr15:56721180-56721330	GM12865	blood:	n/a	n/a
25	CTCF	chr15:56721200-56721350	WI-38	lung:	n/a	n/a
26	CTCF	chr15:56721180-56721330	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr15:56721143-56721307	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr15:56721160-56721310	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr15:56721260-56721410	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr15:56721167-56721336	LNCaP	prostate:	n/a	n/a
31	CTCF	chr15:56721220-56721370	GM12871	blood:	n/a	n/a
32	CTCF	chr15:56721140-56721290	HRE	kidney:	n/a	n/a
33	CTCF	chr15:56721220-56721370	HEK293	kidney:	n/a	n/a
34	CTCF	chr15:56721180-56721330	NHLF	lung:	n/a	n/a
35	CTCF	chr15:56721260-56721410	HVMF	connective:	n/a	n/a
36	CTCF	chr15:56721280-56721430	HCT-116	colon:	n/a	n/a
37	CTCF	chr15:56721180-56721330	K562	blood:	n/a	n/a
38	CTCF	chr15:56721260-56721410	BE2_C	brain:	n/a	n/a
39	CTCF	chr15:56720554-56721667	A549	lung:	n/a	n/a
40	CTCF	chr15:56721500-56721650	Caco-2	colon:	n/a	n/a
41	CTCF	chr15:56721200-56721350	SAEC	small airway:	n/a	n/a
42	CTCF	chr15:56721125-56721379	HepG2	liver:	n/a	n/a
43	CTCF	chr15:56721156-56721323	GM10266	blood:	n/a	n/a
44	CTCF	chr15:56721046-56721416	K562	blood:	n/a	n/a
45	CTCF	chr15:56721100-56721250	RPTEC	kidney:	n/a	n/a
46	CTCF	chr15:56721080-56721346	ECC-1	luminal epithelium:	n/a	n/a
47	CTCF	chr15:56721111-56721362	A549	lung:	n/a	n/a
48	CTCF	chr15:56721200-56721350	HVMF	connective:	n/a	n/a
49	CTCF	chr15:56721160-56721310	MCF-7	breast:	n/a	n/a
50	CTCF	chr15:56721059-56721433	IMR90	lung:	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	BJ	skin:	n/a
2	chr15:56725876-56725926	GM12891	blood:	n/a
3	chr15:56725876-56725926	SKMC	muscle:	n/a
4	chr15:56725876-56725926	Hela-S3	cervix:	n/a
5	chr15:56725876-56725926	RPTEC	kidney:	n/a
6	chr15:56725876-56725926	T-47D	breast:	n/a
7	chr15:56725876-56725926	Jurkat	blood:	n/a
8	chr15:56725876-56725926	NH-A	brain:	n/a
9	chr15:56725876-56725926	HEK293	kidney:	embryo
10	chr15:56725876-56725926	AG09319	gingival:	n/a
11	chr15:56725876-56725926	HRCEpiC	kidney:	n/a
12	chr15:56725876-56725926	AG04450	lung:	fetal
13	chr15:56725876-56725926	NHDF-neo	bronchial:	n/a
14	chr15:56725876-56725926	H1-hESC	embryonic stem cell:	embryo
15	chr15:56725876-56725926	PANC-1	pancreas:	n/a
16	chr15:56725876-56725926	HUVEC	blood vessel:	n/a
17	chr15:56725876-56725926	ovcar-3	ovarian:	n/a
18	chr15:56725876-56725926	HRE	kidney:	n/a
19	chr15:56725876-56725926	HMEC	breast:	n/a
20	chr15:56725876-56725926	CMK	blood:	n/a
21	chr15:56725876-56725926	PrEC	prostate:	n/a
22	chr15:56725876-56725926	AG09309	skin:	n/a
23	chr15:56725876-56725926	U87	brain:	n/a
24	chr15:56725876-56725926	HIPEpiC	eye:	n/a
25	chr15:56725876-56725926	MCF10A-Er-Src	breast:	n/a
26	chr15:56725876-56725926	GM12878	blood:	n/a
27	chr15:56725876-56725926	SK-N-SH_RA	brain:	n/a
28	chr15:56725876-56725926	AG10803	skin:	n/a
29	chr15:56725876-56725926	PFSK-1	brain:	n/a
30	chr15:56725876-56725926	HRPEpiC	eye:	n/a
31	chr15:56725876-56725926	GM06990	blood:	n/a
32	chr15:56725876-56725926	IMR90	lung:	fetal
33	chr15:56725876-56725926	SK-N-MC	brain:	n/a
34	chr15:56725876-56725926	AoSMC	blood vessel:	n/a
35	chr15:56725876-56725926	AG04449	skin:	fetal
36	chr15:56725876-56725926	BE2_C	brain:	n/a
37	chr15:56725876-56725926	ProgFib	skin:	n/a
38	chr15:56725876-56725926	HepG2	liver:	n/a
39	chr15:56725876-56725926	SAEC	small airway:	n/a
40	chr15:56725876-56725926	LNCaP	prostate:	n/a
41	chr15:56725876-56725926	NT2-D1	testis:	n/a
42	chr15:56725876-56725926	HL-60	blood:	n/a
43	chr15:56725876-56725926	HCM	heart:	n/a
44	chr15:56725876-56725926	HCF	heart:	n/a
45	chr15:56725876-56725926	SK-N-SH	brain:	n/a
46	chr15:56725876-56725926	HPAEpiC	pulmonary alveolar:	n/a
47	chr15:56725876-56725926	NHBE	bronchial:	n/a
48	chr15:56725876-56725926	K562	blood:	n/a
49	chr15:56725876-56725926	HEEpiC	esophagus:	n/a
50	chr15:56725876-56725926	ECC-1	luminal epithelium:	n/a

(count:16 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MNS1-1	chr15:56701994-56702384	ENSG00000261823.1
2	lnc-MNS1-1	chr15:56700681-56701128	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: 2046 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2046 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140451868	chr15:56686388-56686389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181383242	chr15:56686401-56686402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371032774	chr15:56686402-56686403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565639097	chr15:56686413-56686414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534573646	chr15:56686471-56686472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553767735	chr15:56686486-56686487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567359738	chr15:56686506-56686507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536629742	chr15:56686507-56686508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542695863	chr15:56686574-56686575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562895817	chr15:56686652-56686653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111659492	chr15:56686714-56686715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112488937	chr15:56686722-56686723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556430827	chr15:56686734-56686735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369534235	chr15:56686739-56686740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576473018	chr15:56686755-56686756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113221317	chr15:56686760-56686761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545282612	chr15:56686764-56686765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559061673	chr15:56686784-56686785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149233382	chr15:56686788-56686789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574333266	chr15:56686812-56686813	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs199758113	chr15:56686831-56686832	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs372468345	chr15:56686849-56686850	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs200910908	chr15:56686861-56686862	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs143792290	chr15:56686884-56686885	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs561542184	chr15:56686886-56686887	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs538223285	chr15:56686898-56686899	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs201935835	chr15:56686899-56686900	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs376603848	chr15:56686913-56686914	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs373647702	chr15:56686924-56686925	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs145621344	chr15:56686931-56686932	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs576486868	chr15:56686953-56686954	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs79299042	chr15:56686989-56686990	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs541441008	chr15:56686990-56686991	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs148168860	chr15:56686999-56687000	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs375726251	chr15:56687017-56687018	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs141149800	chr15:56687032-56687033	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs376888794	chr15:56687035-56687036	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs371507729	chr15:56687044-56687045	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs374626306	chr15:56687049-56687050	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs367699476	chr15:56687051-56687052	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs16976896	chr15:56687065-56687066	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs368059447	chr15:56687069-56687070	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs568013131	chr15:56687087-56687088	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs188428419	chr15:56687116-56687117	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs147360195	chr15:56687173-56687174	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs570056647	chr15:56687198-56687199	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs565493422	chr15:56687220-56687221	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs368806944	chr15:56687225-56687226	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs180889430	chr15:56687251-56687252	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs137999336	chr15:56687270-56687271	Weak transcription ZNF genes & repeats	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:236 , 50 per page) page: 1 2 3 4 5

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	chr15:56684600-56686800	Weak transcription	GM12878-XiMat	blood
14	chr15:56686000-56734600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr15:56686200-56691400	Weak transcription	Duodenum Mucosa	Duodenum
16	chr15:56686400-56689000	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr15:56686600-56686800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr15:56686800-56691000	ZNF genes & repeats	GM12878-XiMat	blood
19	chr15:56687000-56687800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr15:56687000-56687800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr15:56687800-56690000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr15:56687800-56691400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr15:56689000-56689200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
24	chr15:56689400-56695000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr15:56690000-56690400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr15:56690000-56690800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
27	chr15:56690000-56692400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr15:56690000-56717400	Weak transcription	Dnd41	blood
29	chr15:56690000-56737800	Weak transcription	Stomach Mucosa	stomach
30	chr15:56690400-56691800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr15:56690400-56692800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr15:56690800-56692000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr15:56691000-56692200	Strong transcription	Fetal Stomach	stomach
34	chr15:56691400-56692400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr15:56691600-56692000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
36	chr15:56691600-56692000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr15:56691800-56692200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr15:56692200-56694600	Weak transcription	Fetal Stomach	stomach
39	chr15:56692400-56692600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr15:56692600-56693800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr15:56699000-56706000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr15:56699200-56717800	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr15:56701400-56705200	Weak transcription	Small Intestine	intestine
44	chr15:56701800-56706800	Weak transcription	Primary hematopoietic stem cells	blood
45	chr15:56702000-56704000	Enhancers	GM12878-XiMat	blood
46	chr15:56702800-56703200	Enhancers	Fetal Stomach	stomach
47	chr15:56702800-56703800	Enhancers	Fetal Brain Male	brain
48	chr15:56703200-56703400	Weak transcription	Fetal Stomach	stomach
49	chr15:56703400-56703600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr15:56703400-56703800	Enhancers	Fetal Stomach	stomach

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