Variant report

Variant	nsv901511
Chromosome Location	chr14:25505085-25588029
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:607)
CpG islands
(count:671)
Chromatin interactive
region (count:13)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:607 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:25519099-25519144	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:25517182-25517745	K562	blood:	n/a	n/a
3	ARID3A	chr14:25507001-25507029	HepG2	liver:	n/a	n/a
4	ATF1	chr14:25517415-25517757	K562	blood:	n/a	n/a
5	ATF3	chr14:25517401-25517686	K562	blood:	n/a	n/a
6	BACH1	chr14:25562557-25562633	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr14:25529777-25530004	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr14:25512084-25512541	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:25519180-25519718	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:25517483-25517764	K562	blood:	n/a	n/a
11	BATF	chr14:25525970-25526204	GM12878	blood:	n/a	n/a
12	BHLHE40	chr14:25518980-25519578	HepG2	liver:	n/a	chr14:25519094-25519110 chr14:25519236-25519252
13	BHLHE40	chr14:25510800-25511004	K562	blood:	n/a	n/a
14	BHLHE40	chr14:25518960-25519311	GM12878	blood:	n/a	chr14:25519094-25519110 chr14:25519236-25519252
15	CCNT2	chr14:25519078-25519498	K562	blood:	n/a	chr14:25519458-25519467 chr14:25519465-25519474 chr14:25519270-25519279
16	CCNT2	chr14:25516822-25517806	K562	blood:	n/a	n/a
17	CEBPB	chr14:25583392-25583698	HepG2	liver:	n/a	chr14:25583532-25583543
18	CEBPB	chr14:25532730-25532995	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:25524312-25524649	HepG2	liver:	n/a	chr14:25524492-25524505
20	CEBPB	chr14:25550807-25551261	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr14:25517347-25517638	K562	blood:	n/a	n/a
22	CEBPB	chr14:25572564-25572774	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:25531155-25531503	HepG2	liver:	n/a	chr14:25531321-25531332 chr14:25531320-25531333 chr14:25531320-25531333
24	CEBPB	chr14:25583480-25583583	K562	blood:	n/a	chr14:25583532-25583543
25	CEBPB	chr14:25511617-25511909	IMR90	lung:	n/a	chr14:25511633-25511645
26	CEBPB	chr14:25518728-25518987	HepG2	liver:	n/a	chr14:25518797-25518814
27	CEBPB	chr14:25563377-25563729	IMR90	lung:	n/a	n/a
28	CEBPB	chr14:25550651-25551292	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr14:25511761-25511940	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr14:25548632-25548741	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:25518649-25518910	H1-hESC	embryonic stem cell:	n/a	chr14:25518797-25518814
32	CEBPB	chr14:25518635-25518960	IMR90	lung:	n/a	chr14:25518797-25518814
33	CEBPB	chr14:25511683-25511903	K562	blood:	n/a	n/a
34	CEBPB	chr14:25531178-25531509	A549	lung:	n/a	chr14:25531321-25531332 chr14:25531320-25531333 chr14:25531320-25531333
35	CEBPB	chr14:25531156-25531512	IMR90	lung:	n/a	chr14:25531321-25531332 chr14:25531320-25531333 chr14:25531320-25531333
36	CEBPB	chr14:25572595-25572849	IMR90	lung:	n/a	n/a
37	CEBPB	chr14:25511626-25511923	HepG2	liver:	n/a	chr14:25511633-25511645
38	CEBPB	chr14:25580134-25580914	IMR90	lung:	n/a	n/a
39	CEBPB	chr14:25525397-25526089	IMR90	lung:	n/a	n/a
40	CEBPD	chr14:25517310-25517711	K562	blood:	n/a	n/a
41	CEBPD	chr14:25519167-25519522	HepG2	liver:	n/a	n/a
42	CEBPD	chr14:25518938-25519662	HepG2	liver:	n/a	n/a
43	CHD2	chr14:25519681-25519725	HepG2	liver:	n/a	n/a
44	CHD2	chr14:25518664-25519075	HepG2	liver:	n/a	chr14:25519065-25519075
45	CHD2	chr14:25518701-25518764	GM12878	blood:	n/a	n/a
46	CTBP2	chr14:25517904-25519875	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr14:25512220-25512370	AG09309	skin:	n/a	chr14:25512279-25512300 chr14:25512290-25512299 chr14:25512287-25512297
48	CTCF	chr14:25512200-25512350	HUVEC	blood vessel:	n/a	chr14:25512279-25512300 chr14:25512290-25512299 chr14:25512287-25512297
49	CTCF	chr14:25543503-25543526	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:25573197-25573358	GM12878	blood:	n/a	chr14:25573236-25573249 chr14:25573234-25573252 chr14:25573229-25573250

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:25511763-25511813	HCPEpiC	choroid plexus:	n/a
2	chr14:25516343-25516393	RPTEC	kidney:	n/a
3	chr14:25516343-25516393	Caco-2	colon:	n/a
4	chr14:25517974-25518024	PrEC	prostate:	n/a
5	chr14:25519778-25519828	HUVEC	blood vessel:	n/a
6	chr14:25516343-25516393	SK-N-MC	brain:	n/a
7	chr14:25516343-25516393	T-47D	breast:	n/a
8	chr14:25511763-25511813	GM12878	blood:	n/a
9	chr14:25519611-25519661	HAEpiC	amniotic membrane:	n/a
10	chr14:25512111-25512161	Caco-2	colon:	n/a
11	chr14:25517974-25518024	T-47D	breast:	n/a
12	chr14:25522307-25522357	GM06990	blood:	n/a
13	chr14:25516343-25516393	SKMC	muscle:	n/a
14	chr14:25511763-25511813	GM06990	blood:	n/a
15	chr14:25526434-25526484	AG09319	gingival:	n/a
16	chr14:25511763-25511813	SKMC	muscle:	n/a
17	chr14:25511763-25511813	SK-N-SH_RA	brain:	n/a
18	chr14:25526434-25526484	MCF10A-Er-Src	breast:	n/a
19	chr14:25519611-25519661	AG09309	skin:	n/a
20	chr14:25520721-25520771	BE2_C	brain:	n/a
21	chr14:25526434-25526484	SK-N-MC	brain:	n/a
22	chr14:25519484-25519534	HNPCEpiC	eye:	n/a
23	chr14:25516343-25516393	Hela-S3	cervix:	n/a
24	chr14:25519611-25519661	HRCEpiC	kidney:	n/a
25	chr14:25519611-25519661	AG10803	skin:	n/a
26	chr14:25511763-25511813	NHBE	bronchial:	n/a
27	chr14:25519611-25519661	Hela-S3	cervix:	n/a
28	chr14:25511763-25511813	NB4	blood:	n/a
29	chr14:25517974-25518024	HNPCEpiC	eye:	n/a
30	chr14:25522307-25522357	HCF	heart:	n/a
31	chr14:25517974-25518024	MCF10A-Er-Src	breast:	n/a
32	chr14:25519611-25519661	MCF10A-Er-Src	breast:	n/a
33	chr14:25518624-25518674	AG10803	skin:	n/a
34	chr14:25511763-25511813	ProgFib	skin:	n/a
35	chr14:25520721-25520771	Caco-2	colon:	n/a
36	chr14:25520721-25520771	GM12892	blood:	n/a
37	chr14:25519778-25519828	Jurkat	blood:	n/a
38	chr14:25519778-25519828	CMK	blood:	n/a
39	chr14:25526434-25526484	BE2_C	brain:	n/a
40	chr14:25519778-25519828	AoSMC	blood vessel:	n/a
41	chr14:25511763-25511813	PFSK-1	brain:	n/a
42	chr14:25520721-25520771	MCF10A-Er-Src	breast:	n/a
43	chr14:25518624-25518674	K562	blood:	n/a
44	chr14:25522307-25522357	PrEC	prostate:	n/a
45	chr14:25512111-25512161	HMEC	breast:	n/a
46	chr14:25512111-25512161	BJ	skin:	n/a
47	chr14:25512111-25512161	U87	brain:	n/a
48	chr14:25519484-25519534	HEEpiC	esophagus:	n/a
49	chr14:25519484-25519534	HL-60	blood:	n/a
50	chr14:25526434-25526484	HRCEpiC	kidney:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:25517771..25520520-chr14:25522589..25526544,3	MCF-7	breast:
2	chr14:25179326..25179885-chr14:25512037..25512719,2	MCF-7	breast:
3	chr14:25542344..25543253-chr14:25601699..25602268,2	MCF-7	breast:
4	chr14:25275348..25276037-chr14:25510991..25511724,2	MCF-7	breast:
5	chr14:25286735..25287246-chr14:25511793..25512726,2	MCF-7	breast:
6	chr14:25542516..25543294-chr14:25601722..25602419,2	MCF-7	breast:
7	chr14:25274769..25276064-chr14:25511769..25512775,13	MCF-7	breast:
8	chr14:25286732..25287686-chr14:25511790..25512486,5	MCF-7	breast:
9	chr14:25422370..25423189-chr14:25504381..25505293,2	MCF-7	breast:
10	chr14:25516181..25518992-chr14:25521102..25522786,2	K562	blood:
11	chr14:25511682..25512314-chr14:25602148..25602701,2	MCF-7	breast:
12	chr14:24834687..24835397-chr14:25511870..25512753,2	MCF-7	breast:
13	chr14:25203732..25204545-chr14:25511727..25512593,3	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STXBP6-1	chr14:25587727-25587877	NONHSAT036073
2	lnc-RP11-80A15.1.1-3	chr14:25564556-25564798	XLOC_010773
3	lnc-RP11-80A15.1.1-4	chr14:25581978-25582066	XLOC_010774
4	lnc-STXBP6-1	chr14:25571251-25571467	NONHSAT036073
5	lnc-RP11-80A15.1.1-3	chr14:25571262-25571468	XLOC_010773
6	lnc-STXBP6-1	chr14:25571045-25571467	XLOC_010978
7	lnc-STXBP6-1	chr14:25581978-25582064	NONHSAT036073
8	lnc-STXBP6-1	chr14:25581978-25582063	XLOC_010978
9	lnc-STXBP6-1	chr14:25571098-25571467	XLOC_010978

No data

Variant related genes	Relation type
STXBP6	TF binding region
STXBP6	CpG island
ENSG00000100968	chromatin interactions
ENSG00000168952	chromatin interactions
GCFC1	miRNA target sites

Extended variants
information (count: 2904 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2904 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10141316	chr14:25505085-25505086	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185243590	chr14:25505102-25505103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563940839	chr14:25505107-25505108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573378255	chr14:25505118-25505119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542358984	chr14:25505183-25505184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558911803	chr14:25505206-25505207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11159041	chr14:25505217-25505218	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs189564314	chr14:25505252-25505253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140168039	chr14:25505253-25505254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150315525	chr14:25505293-25505294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546062542	chr14:25505347-25505348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564154367	chr14:25505371-25505372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531895593	chr14:25505385-25505386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529403780	chr14:25505408-25505409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs199687196	chr14:25505413-25505414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549539728	chr14:25505415-25505416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559433301	chr14:25505421-25505422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144953536	chr14:25505449-25505450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534987944	chr14:25505490-25505491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558147433	chr14:25505504-25505505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540207989	chr14:25505536-25505537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538898133	chr14:25505601-25505602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs17109515	chr14:25505604-25505605	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs141918006	chr14:25505620-25505621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529522348	chr14:25505631-25505632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557267909	chr14:25505653-25505654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10142533	chr14:25505657-25505658	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs542819492	chr14:25505670-25505671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117586340	chr14:25505684-25505685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558489985	chr14:25505688-25505689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372297719	chr14:25505689-25505690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544645960	chr14:25505732-25505733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182470546	chr14:25505788-25505789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10133967	chr14:25505804-25505805	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs553781813	chr14:25505810-25505811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560917385	chr14:25505831-25505832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529873992	chr14:25505840-25505841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187036691	chr14:25505890-25505891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561972477	chr14:25505901-25505902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145817743	chr14:25505916-25505917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs58640442	chr14:25505931-25505932	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs191923423	chr14:25505934-25505935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183247351	chr14:25505940-25505941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs111496439	chr14:25505967-25505968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113133261	chr14:25505981-25505982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185666897	chr14:25505991-25505992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11626799	chr14:25506035-25506036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs144133486	chr14:25506040-25506041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368109850	chr14:25506050-25506051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549439602	chr14:25506062-25506063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Breast cancer	16272173	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
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1276 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25479400-25508600	Weak transcription	Brain Anterior Caudate	brain
2	chr14:25481200-25507400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr14:25492400-25517600	Weak transcription	Psoas Muscle	Psoas
4	chr14:25495400-25507400	Weak transcription	Fetal Lung	lung
5	chr14:25497200-25515200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr14:25503400-25505200	Enhancers	Fetal Intestine Large	intestine
7	chr14:25503400-25505600	Enhancers	Stomach Mucosa	stomach
8	chr14:25503600-25505600	Enhancers	Fetal Intestine Small	intestine
9	chr14:25503800-25515800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr14:25504000-25511000	Weak transcription	Small Intestine	intestine
11	chr14:25504200-25506200	Weak transcription	Left Ventricle	heart
12	chr14:25504600-25505400	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr14:25504600-25505800	Enhancers	Right Ventricle	heart
14	chr14:25504600-25509200	Weak transcription	Pancreas	Pancrea
15	chr14:25504800-25506200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr14:25504800-25507400	Enhancers	HepG2	liver
17	chr14:25505000-25505200	Enhancers	Duodenum Mucosa	Duodenum
18	chr14:25505000-25507000	Enhancers	Placenta Amnion	Placenta Amnion
19	chr14:25505200-25510400	Weak transcription	Fetal Intestine Large	intestine
20	chr14:25505400-25508600	Weak transcription	Duodenum Mucosa	Duodenum
21	chr14:25505400-25509400	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr14:25505600-25506600	Weak transcription	Stomach Mucosa	stomach
23	chr14:25505600-25509200	Weak transcription	Fetal Intestine Small	intestine
24	chr14:25505800-25506200	Weak transcription	Right Ventricle	heart
25	chr14:25506200-25506400	Enhancers	Right Ventricle	heart
26	chr14:25506200-25506600	Enhancers	Left Ventricle	heart
27	chr14:25506200-25506600	Enhancers	Lung	lung
28	chr14:25506200-25506600	Enhancers	Right Atrium	heart
29	chr14:25506200-25506800	Enhancers	Brain Angular Gyrus	brain
30	chr14:25506200-25507000	Enhancers	Colon Smooth Muscle	Colon
31	chr14:25506200-25507000	Enhancers	Stomach Smooth Muscle	stomach
32	chr14:25506200-25507200	Enhancers	Fetal Heart	heart
33	chr14:25506200-25509400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr14:25506400-25507000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr14:25506400-25507200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr14:25506400-25508600	Weak transcription	Right Ventricle	heart
37	chr14:25506600-25506800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr14:25506600-25506800	Enhancers	Brain Hippocampus Middle	brain
39	chr14:25506600-25506800	Enhancers	HSMMtube	muscle
40	chr14:25506600-25507000	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr14:25506600-25507000	Enhancers	Stomach Mucosa	stomach
42	chr14:25506600-25508600	Weak transcription	Left Ventricle	heart
43	chr14:25506600-25508800	Weak transcription	Lung	lung
44	chr14:25506600-25511400	Weak transcription	Right Atrium	heart
45	chr14:25506800-25510800	Weak transcription	Brain Hippocampus Middle	brain
46	chr14:25506800-25511200	Weak transcription	Brain Angular Gyrus	brain
47	chr14:25507000-25508600	Weak transcription	Stomach Mucosa	stomach
48	chr14:25507000-25510800	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr14:25507000-25510800	Weak transcription	HSMMtube	muscle
50	chr14:25507000-25511000	Weak transcription	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links