Variant report

Variant	nsv901595
Chromosome Location	chr14:32928634-32961434
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	chr14:32938606-32938955	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:32938725-32938910	K562	blood:	n/a	n/a
3	BACH1	chr14:32953383-32953584	K562	blood:	n/a	n/a
4	BATF	chr14:32953354-32954358	GM12878	blood:	n/a	n/a
5	BATF	chr14:32953337-32954435	GM12878	blood:	n/a	n/a
6	BCL11A	chr14:32953360-32954352	GM12878	blood:	n/a	n/a
7	BCL11A	chr14:32953284-32954370	GM12878	blood:	n/a	n/a
8	BHLHE40	chr14:32953340-32954372	HepG2	liver:	n/a	n/a
9	BHLHE40	chr14:32953211-32953584	K562	blood:	n/a	n/a
10	CEBPB	chr14:32942693-32942968	A549	lung:	n/a	n/a
11	CEBPB	chr14:32938157-32938467	A549	lung:	n/a	n/a
12	CEBPB	chr14:32942721-32942895	HepG2	liver:	n/a	n/a
13	CEBPB	chr14:32942543-32943156	MCF-7	breast:	n/a	n/a
14	CEBPB	chr14:32938112-32938927	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr14:32942654-32943060	MCF-7	breast:	n/a	n/a
16	CEBPB	chr14:32938123-32938524	IMR90	lung:	n/a	n/a
17	CEBPB	chr14:32938183-32938460	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:32941344-32943027	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr14:32942042-32942162	HepG2	liver:	n/a	n/a
20	CEBPB	chr14:32942577-32942991	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr14:32941994-32942278	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr14:32942703-32942960	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:32941928-32942312	IMR90	lung:	n/a	n/a
24	CEBPB	chr14:32942683-32942889	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPD	chr14:32953319-32954531	K562	blood:	n/a	n/a
26	CHD2	chr14:32953383-32953583	K562	blood:	n/a	n/a
27	CHD2	chr14:32942431-32942983	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr14:32938720-32938870	AG04449	skin:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
29	CTCF	chr14:32938614-32938996	GM12878	blood:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
30	CTCF	chr14:32938719-32938918	GM10248	blood:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
31	CTCF	chr14:32947600-32947750	BJ	skin:	n/a	n/a
32	CTCF	chr14:32941740-32941890	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr14:32938280-32938430	HMEC	breast:	n/a	n/a
34	CTCF	chr14:32938740-32938890	BE2_C	brain:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
35	CTCF	chr14:32938720-32938870	AG09319	gingival:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
36	CTCF	chr14:32938687-32938959	Medullo	brain:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
37	CTCF	chr14:32938700-32938850	NHEK	skin:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
38	CTCF	chr14:32938720-32938870	K562	blood:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
39	CTCF	chr14:32938700-32938850	HAc	cerebellar:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
40	CTCF	chr14:32947560-32947710	AG10803	skin:	n/a	n/a
41	CTCF	chr14:32930631-32930677	MCF-7	breast:	n/a	n/a
42	CTCF	chr14:32938578-32938908	MCF-7	breast:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
43	CTCF	chr14:32938340-32938490	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr14:32938660-32938810	WI-38	lung:	n/a	n/a
45	CTCF	chr14:32938720-32938870	GM12865	blood:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
46	CTCF	chr14:32938720-32938870	SAEC	small airway:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
47	CTCF	chr14:32938780-32938930	HVMF	connective:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819
48	CTCF	chr14:32947520-32947670	NHLF	lung:	n/a	n/a
49	CTCF	chr14:32941100-32941250	HFF-Myc	foreskin:	n/a	chr14:32941172-32941179
50	CTCF	chr14:32938700-32938850	SAEC	small airway:	n/a	chr14:32938802-32938820 chr14:32938797-32938818 chr14:32938803-32938819

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:32941841-32941891	SK-N-MC	brain:	n/a
2	chr14:32941841-32941891	PFSK-1	brain:	n/a
3	chr14:32941841-32941891	HNPCEpiC	eye:	n/a
4	chr14:32941841-32941891	MCF10A-Er-Src	breast:	n/a
5	chr14:32941841-32941891	HL-60	blood:	n/a
6	chr14:32941841-32941891	SK-N-SH	brain:	n/a
7	chr14:32941841-32941891	HEEpiC	esophagus:	n/a
8	chr14:32941841-32941891	NB4	blood:	n/a
9	chr14:32941841-32941891	NHBE	bronchial:	n/a
10	chr14:32941841-32941891	HUVEC	blood vessel:	n/a
11	chr14:32941841-32941891	HPAEpiC	pulmonary alveolar:	n/a
12	chr14:32941841-32941891	BJ	skin:	n/a
13	chr14:32941841-32941891	K562	blood:	n/a
14	chr14:32941841-32941891	ProgFib	skin:	n/a
15	chr14:32941841-32941891	NHDF-neo	bronchial:	n/a
16	chr14:32941841-32941891	ovcar-3	ovarian:	n/a
17	chr14:32941841-32941891	SKMC	muscle:	n/a
18	chr14:32941841-32941891	HRE	kidney:	n/a
19	chr14:32941841-32941891	GM19239	blood:	n/a
20	chr14:32941841-32941891	AG09319	gingival:	n/a
21	chr14:32941841-32941891	IMR90	lung:	fetal
22	chr14:32941841-32941891	AG04449	skin:	fetal
23	chr14:32941841-32941891	HRPEpiC	eye:	n/a
24	chr14:32941841-32941891	NT2-D1	testis:	n/a
25	chr14:32941841-32941891	T-47D	breast:	n/a
26	chr14:32941841-32941891	HepG2	liver:	n/a
27	chr14:32941841-32941891	A549	lung:	n/a
28	chr14:32941841-32941891	PrEC	prostate:	n/a
29	chr14:32941841-32941891	HAEpiC	amniotic membrane:	n/a
30	chr14:32941841-32941891	HIPEpiC	eye:	n/a
31	chr14:32941841-32941891	NH-A	brain:	n/a
32	chr14:32941841-32941891	SAEC	small airway:	n/a
33	chr14:32941841-32941891	Jurkat	blood:	n/a
34	chr14:32941841-32941891	U87	brain:	n/a
35	chr14:32941841-32941891	GM12892	blood:	n/a
36	chr14:32941841-32941891	Hela-S3	cervix:	n/a
37	chr14:32941841-32941891	ECC-1	luminal epithelium:	n/a
38	chr14:32941841-32941891	HCM	heart:	n/a
39	chr14:32941841-32941891	HCF	heart:	n/a
40	chr14:32941841-32941891	Caco-2	colon:	n/a
41	chr14:32941841-32941891	HCPEpiC	choroid plexus:	n/a
42	chr14:32941841-32941891	GM06990	blood:	n/a
43	chr14:32941841-32941891	AG04450	lung:	fetal
44	chr14:32941841-32941891	RPTEC	kidney:	n/a
45	chr14:32941841-32941891	AoSMC	blood vessel:	n/a
46	chr14:32941841-32941891	CMK	blood:	n/a
47	chr14:32941841-32941891	PANC-1	pancreas:	n/a
48	chr14:32941841-32941891	SK-N-SH_RA	brain:	n/a
49	chr14:32941841-32941891	HRCEpiC	kidney:	n/a
50	chr14:32941841-32941891	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr14:32938979..32940480-chr14:32942478..32945273,2	K562	blood:
2	chr14:32941433..32942936-chr14:32946433..32948525,2	MCF-7	breast:
3	chr14:32943721..32945692-chr14:32947594..32949862,2	MCF-7	breast:
4	chr14:32936100..32938638-chr14:32940941..32943770,2	K562	blood:
5	chr14:32394986..32395973-chr14:32938340..32938867,2	K562	blood:
6	chr14:32942791..32945014-chr14:32949857..32951632,2	MCF-7	breast:
7	chr14:32960517..32962763-chr14:32965947..32968898,2	MCF-7	breast:
8	chr14:32947699..32950524-chr14:32951801..32954077,2	K562	blood:
9	chr14:32943721..32945692-chr14:32947594..32949862,2	MCF-7	breast:
10	chr14:32941433..32942936-chr14:32946433..32948525,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000259045	TF binding region
AKAP6	TF binding region
ENSG00000259045	CpG island
AKAP6	CpG island
ENSG00000151320	chromatin interactions
ENSG00000259045	chromatin interactions

Extended variants
information (count: 1365 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1365 , 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	rs941749	chr14:32928634-32928635	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575444600	chr14:32928668-32928669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189186706	chr14:32928674-32928675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558039227	chr14:32928696-32928697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548855055	chr14:32928710-32928711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540251829	chr14:32928765-32928766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565100727	chr14:32928784-32928785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6571521	chr14:32928828-32928829	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs192878811	chr14:32928865-32928866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185464092	chr14:32928910-32928911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs71432056	chr14:32928947-32928948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs386381044	chr14:32928948-32928949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78238264	chr14:32928958-32928959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563726938	chr14:32928977-32928978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531146091	chr14:32928997-32928998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189394187	chr14:32928999-32929000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs61981159	chr14:32929036-32929037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560007294	chr14:32929079-32929080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530225312	chr14:32929095-32929096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149580129	chr14:32929103-32929104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528788807	chr14:32929171-32929172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546576358	chr14:32929176-32929177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548399105	chr14:32929214-32929215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569393175	chr14:32929251-32929252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181240641	chr14:32929261-32929262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557433835	chr14:32929300-32929301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183512209	chr14:32929339-32929340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1957023	chr14:32929362-32929363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539634688	chr14:32929393-32929394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116754849	chr14:32929405-32929406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200303678	chr14:32929431-32929432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1957024	chr14:32929441-32929442	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs11625399	chr14:32929449-32929450	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs144350791	chr14:32929501-32929502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573725520	chr14:32929509-32929510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544276459	chr14:32929545-32929546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559003270	chr14:32929547-32929548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562618876	chr14:32929600-32929601	Weak transcription Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148778788	chr14:32929611-32929612	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12323684	chr14:32929661-32929662	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372080401	chr14:32929697-32929698	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143784900	chr14:32929702-32929703	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs180948375	chr14:32929728-32929729	Enhancers Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114488380	chr14:32929807-32929808	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111606752	chr14:32929899-32929900	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190798137	chr14:32929952-32929953	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529261472	chr14:32929984-32929985	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550760934	chr14:32930024-32930025	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534629559	chr14:32930068-32930069	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569353334	chr14:32930103-32930104	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:519 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32920800-32930200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr14:32923800-32929600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:32923800-32929600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr14:32923800-32936400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr14:32926800-32936800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr14:32927000-32929600	Weak transcription	Aorta	Aorta
7	chr14:32927200-32929800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr14:32928200-32929400	Weak transcription	Fetal Heart	heart
9	chr14:32928400-32929600	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr14:32928600-32929600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr14:32929400-32930800	Enhancers	Fetal Heart	heart
12	chr14:32929600-32929800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr14:32929600-32930000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr14:32929600-32930600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr14:32929600-32930600	Strong transcription	Aorta	Aorta
16	chr14:32929600-32930600	Enhancers	Placenta	Placenta
17	chr14:32929600-32930600	Enhancers	Left Ventricle	heart
18	chr14:32929600-32930600	Enhancers	Right Ventricle	heart
19	chr14:32929600-32931000	Enhancers	Placenta Amnion	Placenta Amnion
20	chr14:32929800-32930000	Enhancers	Stomach Smooth Muscle	stomach
21	chr14:32929800-32930600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr14:32930000-32930600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr14:32930200-32931000	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr14:32930600-32936800	Weak transcription	Aorta	Aorta
25	chr14:32930600-32937400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr14:32931000-32931600	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr14:32931000-32941400	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr14:32932800-32933000	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr14:32936200-32936400	Enhancers	Brain Angular Gyrus	brain
30	chr14:32936200-32937400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr14:32936200-32937600	Enhancers	Fetal Heart	heart
32	chr14:32936200-32942800	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr14:32936200-32942800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:32936400-32937000	Weak transcription	Brain Angular Gyrus	brain
35	chr14:32936400-32937000	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr14:32936400-32938400	Enhancers	NHEK	skin
37	chr14:32936400-32943200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:32936400-32944800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr14:32936600-32939400	Enhancers	Colon Smooth Muscle	Colon
40	chr14:32936600-32941800	Enhancers	HMEC	breast
41	chr14:32936800-32937000	Enhancers	Brain Cingulate Gyrus	brain
42	chr14:32936800-32937000	Enhancers	Brain Substantia Nigra	brain
43	chr14:32936800-32937000	Enhancers	Rectal Smooth Muscle	rectum
44	chr14:32936800-32937000	Enhancers	HSMMtube	muscle
45	chr14:32936800-32937400	Enhancers	Aorta	Aorta
46	chr14:32936800-32941200	Enhancers	Brain Anterior Caudate	brain
47	chr14:32936800-32942200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr14:32936800-32944000	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr14:32937000-32937200	Enhancers	Brain Angular Gyrus	brain
50	chr14:32937000-32937600	Enhancers	Brain Hippocampus Middle	brain

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