Variant report

Variant	nsv832765
Chromosome Location	chr14:33188170-33367348
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:540)
CpG islands
(count:184)
Chromatin interactive
region (count:19)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:33366213-33367307	HepG2	liver:	n/a	n/a
2	BATF	chr14:33346539-33346763	GM12878	blood:	n/a	chr14:33346685-33346696
3	CEBPB	chr14:33269525-33269914	A549	lung:	n/a	chr14:33269767-33269778
4	CEBPB	chr14:33263630-33263823	H1-hESC	embryonic stem cell:	n/a	chr14:33263716-33263727
5	CEBPB	chr14:33269496-33269891	IMR90	lung:	n/a	chr14:33269767-33269778
6	CEBPB	chr14:33269477-33269946	HepG2	liver:	n/a	chr14:33269767-33269778
7	CEBPB	chr14:33194011-33194349	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr14:33249132-33249399	HepG2	liver:	n/a	chr14:33249276-33249287
9	CEBPB	chr14:33292076-33292518	HepG2	liver:	n/a	chr14:33292363-33292374
10	CEBPB	chr14:33190138-33190462	HepG2	liver:	n/a	chr14:33190269-33190282 chr14:33190279-33190290 chr14:33190277-33190288 chr14:33190277-33190290
11	CEBPB	chr14:33269522-33269891	Hela-S3	cervix:	n/a	chr14:33269767-33269778
12	CEBPB	chr14:33305163-33305423	HepG2	liver:	n/a	chr14:33305325-33305338
13	CEBPB	chr14:33310199-33310292	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:33194945-33195145	A549	lung:	n/a	chr14:33195066-33195077
15	CEBPB	chr14:33205664-33205802	A549	lung:	n/a	chr14:33205729-33205742 chr14:33205729-33205740 chr14:33205731-33205742
16	CEBPB	chr14:33205573-33205754	H1-hESC	embryonic stem cell:	n/a	chr14:33205729-33205742 chr14:33205729-33205740 chr14:33205731-33205742
17	CEBPB	chr14:33269647-33269872	K562	blood:	n/a	chr14:33269767-33269778
18	CEBPB	chr14:33306361-33306546	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:33263630-33263772	HepG2	liver:	n/a	chr14:33263716-33263727
20	CEBPB	chr14:33366932-33367270	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:33249127-33249381	IMR90	lung:	n/a	chr14:33249276-33249287
22	CEBPB	chr14:33194937-33195189	HepG2	liver:	n/a	chr14:33195066-33195077
23	CEBPB	chr14:33205644-33205846	HepG2	liver:	n/a	chr14:33205729-33205742 chr14:33205729-33205740 chr14:33205731-33205742
24	CEBPB	chr14:33306332-33306463	A549	lung:	n/a	n/a
25	CEBPB	chr14:33193933-33194811	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr14:33230593-33230961	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr14:33283437-33283656	HepG2	liver:	n/a	chr14:33283530-33283541
28	CHD2	chr14:33362916-33362924	GM12878	blood:	n/a	n/a
29	CHD2	chr14:33290816-33290910	HepG2	liver:	n/a	n/a
30	CREB1	chr14:33194083-33194802	ECC-1	luminal epithelium:	n/a	n/a
31	CTCF	chr14:33296127-33296175	LNCaP	prostate:	n/a	n/a
32	CTCF	chr14:33296020-33296170	HFF	foreskin:	n/a	n/a
33	CTCF	chr14:33296060-33296210	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr14:33295960-33296110	HVMF	connective:	n/a	n/a
35	CTCF	chr14:33214784-33215034	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:33296040-33296190	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr14:33295980-33296130	RPTEC	kidney:	n/a	n/a
38	CTCF	chr14:33296080-33296230	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr14:33296060-33296210	HMF	breast:	n/a	n/a
40	CTCF	chr14:33296060-33296210	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr14:33296060-33296210	HVMF	connective:	n/a	n/a
42	CTCF	chr14:33296100-33296250	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr14:33296040-33296190	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr14:33296036-33296219	MCF-7	breast:	n/a	n/a
45	CTCF	chr14:33238114-33238136	GM20000	blood:	n/a	n/a
46	CTCF	chr14:33214760-33214910	HMEC	breast:	n/a	n/a
47	CTCF	chr14:33296029-33296252	MCF-7	breast:	n/a	n/a
48	CTCF	chr14:33295811-33296406	SK-N-SH	brain:	n/a	n/a
49	CTCF	chr14:33296020-33296170	AG10803	skin:	n/a	n/a
50	CTCF	chr14:33295835-33296350	MCF-7	breast:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:33244107-33244157	PFSK-1	brain:	n/a
2	chr14:33244107-33244157	PFSK-1	brain:	n/a
3	chr14:33296030-33296080	ECC-1	luminal epithelium:	n/a
4	chr14:33279138-33279188	ProgFib	skin:	n/a
5	chr14:33296030-33296080	HNPCEpiC	eye:	n/a
6	chr14:33244107-33244157	ovcar-3	ovarian:	n/a
7	chr14:33296030-33296080	MCF-7	breast:	n/a
8	chr14:33244107-33244157	MCF-7	breast:	n/a
9	chr14:33279138-33279188	HIPEpiC	eye:	n/a
10	chr14:33296030-33296080	HEEpiC	esophagus:	n/a
11	chr14:33244107-33244157	T-47D	breast:	n/a
12	chr14:33244107-33244157	Hepatocyte	liver:	n/a
13	chr14:33279138-33279188	Hepatocyte	liver:	n/a
14	chr14:33244107-33244157	GM12878	blood:	n/a
15	chr14:33296030-33296080	HRE	kidney:	n/a
16	chr14:33296030-33296080	CMK	blood:	n/a
17	chr14:33296030-33296080	NB4	blood:	n/a
18	chr14:33279138-33279188	NHBE	bronchial:	n/a
19	chr14:33244107-33244157	H1-hESC	embryonic stem cell:	embryo
20	chr14:33279138-33279188	GM12892	blood:	n/a
21	chr14:33244107-33244157	AG09309	skin:	n/a
22	chr14:33244107-33244157	Hela-S3	cervix:	n/a
23	chr14:33244107-33244157	HMEC	breast:	n/a
24	chr14:33296030-33296080	GM06990	blood:	n/a
25	chr14:33244107-33244157	HepG2	liver:	n/a
26	chr14:33296030-33296080	H1-hESC	embryonic stem cell:	embryo
27	chr14:33279138-33279188	GM12878	blood:	n/a
28	chr14:33296030-33296080	NH-A	brain:	n/a
29	chr14:33279138-33279188	MCF-7	breast:	n/a
30	chr14:33296030-33296080	AG04450	lung:	fetal
31	chr14:33279138-33279188	HUVEC	blood vessel:	n/a
32	chr14:33296030-33296080	HPAEpiC	pulmonary alveolar:	n/a
33	chr14:33244107-33244157	GM12891	blood:	n/a
34	chr14:33279138-33279188	NB4	blood:	n/a
35	chr14:33296030-33296080	ProgFib	skin:	n/a
36	chr14:33279138-33279188	GM12891	blood:	n/a
37	chr14:33279138-33279188	U87	brain:	n/a
38	chr14:33279138-33279188	CMK	blood:	n/a
39	chr14:33296030-33296080	SK-N-MC	brain:	n/a
40	chr14:33279138-33279188	BJ	skin:	n/a
41	chr14:33279138-33279188	HRPEpiC	eye:	n/a
42	chr14:33296030-33296080	PrEC	prostate:	n/a
43	chr14:33244107-33244157	AG04450	lung:	fetal
44	chr14:33296030-33296080	SK-N-SH	brain:	n/a
45	chr14:33244107-33244157	AoSMC	blood vessel:	n/a
46	chr14:33244107-33244157	HNPCEpiC	eye:	n/a
47	chr14:33279138-33279188	GM06990	blood:	n/a
48	chr14:33296030-33296080	A549	lung:	n/a
49	chr14:33279138-33279188	AoSMC	blood vessel:	n/a
50	chr14:33244107-33244157	ProgFib	skin:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:33056882..33058698-chr14:33290959..33292706,2	MCF-7	breast:
2	chr14:33237236..33239475-chr14:33240396..33242556,2	MCF-7	breast:
3	chr14:33287174..33289754-chr14:33290856..33293809,2	K562	blood:
4	chr14:33180317..33181019-chr14:33295661..33296988,3	MCF-7	breast:
5	chr14:33279893..33283166-chr14:33285562..33288346,3	K562	blood:
6	chr14:33180083..33180602-chr14:33295763..33296544,2	MCF-7	breast:
7	chr14:33190851..33193807-chr14:33195720..33198266,2	MCF-7	breast:
8	chr14:33240420..33240920-chr6:82461989..82462603,2	Hela-S3	cervix:
9	chr14:33279893..33283166-chr14:33285562..33288346,3	K562	blood:
10	chr14:33201447..33204366-chr14:33204778..33206779,2	MCF-7	breast:
11	chr14:33201447..33204366-chr14:33204778..33206779,2	MCF-7	breast:
12	chr14:33190851..33193807-chr14:33195720..33198266,2	MCF-7	breast:
13	chr14:33294467..33296146-chr14:33298470..33300795,2	MCF-7	breast:
14	chr14:33287174..33289754-chr14:33290856..33293809,2	K562	blood:
15	chr14:33294467..33296146-chr14:33298470..33300795,2	MCF-7	breast:
16	chr14:33237236..33239475-chr14:33240396..33242556,2	MCF-7	breast:
17	chr14:33194408..33197099-chr14:33297873..33299696,2	MCF-7	breast:
18	chr14:33194408..33197099-chr14:33297873..33299696,2	MCF-7	breast:
19	chr14:33364204..33365918-chr14:33372502..33375369,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPAS3-4	chr14:33192368-33192580	uc_369_+
2	lnc-NPAS3-3	chr14:33245370-33246860	NONHSAT036308
3	lnc-AKAP6-1	chr14:33348452-33349081	NONHSAT036311
4	lnc-EGLN3-4	chr14:33272322-33272714	uc_370_-
5	lnc-EGLN3-5	chr14:33192368-33192580	uc_369_-
6	lnc-NPAS3-2	chr14:33272322-33272714	uc_370_+
7	lnc-AKAP6-1	chr14:33349087-33352036	NONHSAT036311

No data

Variant related genes	Relation type
AKAP6	TF binding region
AKAP6	CpG island
ENSG00000151320	chromatin interactions
ENSG00000112773	chromatin interactions

Extended variants
information (count: 5945 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:5945 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550295212	chr14:33188354-33188355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs3837677	chr14:33188369-33188370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs397829956	chr14:33188377-33188378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76003156	chr14:33188418-33188419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149756680	chr14:33188481-33188482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575467542	chr14:33188483-33188484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147847008	chr14:33188521-33188522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116129292	chr14:33188527-33188528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs17099482	chr14:33188568-33188569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs375586245	chr14:33188590-33188591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564049169	chr14:33188591-33188592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572394828	chr14:33188593-33188594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542823179	chr14:33188598-33188599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568546695	chr14:33188625-33188626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139905110	chr14:33188662-33188663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543869848	chr14:33188732-33188733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145358335	chr14:33188756-33188757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117678309	chr14:33188764-33188765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147656231	chr14:33188935-33188936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528254668	chr14:33188970-33188971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369482834	chr14:33189083-33189084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369237930	chr14:33189110-33189111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528761559	chr14:33189205-33189206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547040881	chr14:33189235-33189236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149165237	chr14:33189250-33189251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143287606	chr14:33189256-33189257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551045852	chr14:33189261-33189262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs569246908	chr14:33189275-33189276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs151310391	chr14:33189327-33189328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557651587	chr14:33189343-33189344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566785840	chr14:33189411-33189412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533816773	chr14:33189420-33189421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11622735	chr14:33189449-33189450	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs573255349	chr14:33189471-33189472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112639772	chr14:33189472-33189473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7149061	chr14:33189526-33189527	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs140542613	chr14:33189630-33189631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577650573	chr14:33189640-33189641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546407964	chr14:33189662-33189663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs376864915	chr14:33189725-33189726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564496573	chr14:33189768-33189769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574094197	chr14:33189804-33189805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533915969	chr14:33189919-33189920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs117779541	chr14:33189920-33189921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184668701	chr14:33189941-33189942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529350551	chr14:33189979-33189980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150490252	chr14:33189981-33189982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569367192	chr14:33189992-33189993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2057122	chr14:33190028-33190029	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs138490799	chr14:33190040-33190041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1219 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:33172600-33191600	Weak transcription	Psoas Muscle	Psoas
2	chr14:33173200-33194800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr14:33178800-33191600	Weak transcription	Right Ventricle	heart
4	chr14:33179000-33193400	Weak transcription	HSMMtube	muscle
5	chr14:33180400-33193400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:33180600-33191800	Weak transcription	Left Ventricle	heart
7	chr14:33180600-33193800	Weak transcription	Fetal Stomach	stomach
8	chr14:33180800-33194600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr14:33181000-33188200	Weak transcription	Brain Angular Gyrus	brain
10	chr14:33181000-33193000	Weak transcription	Brain Substantia Nigra	brain
11	chr14:33183400-33190000	Weak transcription	Brain Hippocampus Middle	brain
12	chr14:33183400-33193000	Weak transcription	Brain Anterior Caudate	brain
13	chr14:33183600-33194000	Weak transcription	Aorta	Aorta
14	chr14:33186200-33189000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr14:33186200-33196200	Enhancers	Fetal Heart	heart
16	chr14:33186400-33188600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:33187800-33188400	Weak transcription	Fetal Muscle Leg	muscle
18	chr14:33188200-33188400	Enhancers	Brain Angular Gyrus	brain
19	chr14:33188400-33188600	Enhancers	Fetal Muscle Leg	muscle
20	chr14:33188400-33188800	Weak transcription	Brain Angular Gyrus	brain
21	chr14:33188600-33189800	Weak transcription	Fetal Muscle Leg	muscle
22	chr14:33188600-33193000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr14:33188800-33189000	Enhancers	Brain Angular Gyrus	brain
24	chr14:33189000-33189200	Enhancers	Fetal Brain Female	brain
25	chr14:33189000-33190200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr14:33189000-33193600	Weak transcription	Brain Angular Gyrus	brain
27	chr14:33189200-33198000	Weak transcription	Fetal Brain Female	brain
28	chr14:33189800-33190200	Enhancers	Fetal Muscle Leg	muscle
29	chr14:33189800-33190600	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr14:33190000-33190400	Enhancers	Brain Hippocampus Middle	brain
31	chr14:33190000-33190600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr14:33190200-33190600	Enhancers	NHDF-Ad	bronchial
33	chr14:33190200-33191000	Weak transcription	Fetal Muscle Leg	muscle
34	chr14:33190200-33196600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr14:33190400-33190600	Enhancers	HSMM	muscle
36	chr14:33190400-33190600	Enhancers	Osteobl	bone
37	chr14:33190400-33193000	Weak transcription	Brain Hippocampus Middle	brain
38	chr14:33190600-33193400	Weak transcription	HSMM	muscle
39	chr14:33190600-33193400	Weak transcription	NHDF-Ad	bronchial
40	chr14:33190600-33194400	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr14:33190800-33191000	Enhancers	Brain Cingulate Gyrus	brain
42	chr14:33190800-33193600	Weak transcription	Osteobl	bone
43	chr14:33191000-33192200	Enhancers	Fetal Muscle Leg	muscle
44	chr14:33191200-33193200	Weak transcription	Brain Cingulate Gyrus	brain
45	chr14:33191600-33191800	Enhancers	Psoas Muscle	Psoas
46	chr14:33191600-33192200	Enhancers	Right Ventricle	heart
47	chr14:33191600-33192400	Enhancers	Fetal Muscle Trunk	muscle
48	chr14:33191800-33192400	Enhancers	Left Ventricle	heart
49	chr14:33192000-33192200	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr14:33192200-33193600	Weak transcription	Brain Inferior Temporal Lobe	brain

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