Variant report

Variant	nsv1047042
Chromosome Location	chr14:24484459-24513905
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	chr14:24505981-24506248	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:24502290-24502595	HepG2	liver:	n/a	n/a
3	ATF2	chr14:24505949-24506263	GM12878	blood:	n/a	n/a
4	BATF	chr14:24506432-24506750	GM12878	blood:	n/a	n/a
5	BATF	chr14:24506427-24506735	GM12878	blood:	n/a	n/a
6	BCL3	chr14:24505902-24506304	A549	lung:	n/a	n/a
7	BCL3	chr14:24502093-24502738	A549	lung:	n/a	n/a
8	BHLHE40	chr14:24505965-24506313	GM12878	blood:	n/a	n/a
9	BRCA1	chr14:24505981-24506214	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr14:24501866-24502194	K562	blood:	n/a	n/a
11	CBX3	chr14:24501883-24502114	K562	blood:	n/a	n/a
12	CEBPB	chr14:24503786-24503943	HepG2	liver:	n/a	n/a
13	CEBPB	chr14:24502095-24502733	A549	lung:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
14	CEBPB	chr14:24502288-24502568	K562	blood:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
15	CEBPB	chr14:24505883-24506354	Hela-S3	cervix:	n/a	chr14:24506174-24506185
16	CEBPB	chr14:24505959-24506192	HepG2	liver:	n/a	chr14:24506174-24506185
17	CEBPB	chr14:24505955-24506340	MCF-7	breast:	n/a	chr14:24506174-24506185
18	CEBPB	chr14:24505949-24506410	HepG2	liver:	n/a	chr14:24506174-24506185
19	CEBPB	chr14:24502325-24502567	HepG2	liver:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
20	CEBPB	chr14:24502247-24502669	HepG2	liver:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
21	CEBPB	chr14:24505530-24505585	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr14:24506005-24506217	HepG2	liver:	n/a	chr14:24506174-24506185
23	CEBPB	chr14:24503873-24504233	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:24504202-24504207	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr14:24502235-24502633	MCF-7	breast:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
26	CEBPB	chr14:24505953-24506379	MCF-7	breast:	n/a	chr14:24506174-24506185
27	CEBPB	chr14:24505928-24506341	A549	lung:	n/a	chr14:24506174-24506185
28	CEBPB	chr14:24502174-24502650	HepG2	liver:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
29	CEBPB	chr14:24506005-24506241	ECC-1	luminal epithelium:	n/a	chr14:24506174-24506185
30	CEBPB	chr14:24502292-24502624	K562	blood:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
31	CEBPB	chr14:24503705-24503975	MCF-7	breast:	n/a	n/a
32	CEBPB	chr14:24502240-24502694	Hela-S3	cervix:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
33	CEBPB	chr14:24502259-24502654	HepG2	liver:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
34	CEBPB	chr14:24504095-24504242	HepG2	liver:	n/a	n/a
35	CEBPB	chr14:24505832-24506370	GM12878	blood:	n/a	chr14:24506174-24506185
36	CEBPB	chr14:24502254-24502670	IMR90	lung:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
37	CEBPB	chr14:24502257-24502651	A549	lung:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
38	CEBPB	chr14:24502240-24502596	A549	lung:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
39	CEBPB	chr14:24503875-24503956	A549	lung:	n/a	n/a
40	CEBPB	chr14:24505919-24506258	H1-hESC	embryonic stem cell:	n/a	chr14:24506174-24506185
41	CEBPB	chr14:24505923-24506358	A549	lung:	n/a	chr14:24506174-24506185
42	CEBPD	chr14:24505874-24506366	HepG2	liver:	n/a	n/a
43	CEBPD	chr14:24505308-24505800	HepG2	liver:	n/a	n/a
44	CEBPD	chr14:24505867-24506262	HepG2	liver:	n/a	n/a
45	CEBPD	chr14:24502325-24502575	HepG2	liver:	n/a	chr14:24502435-24502446
46	CEBPD	chr14:24502317-24502638	HepG2	liver:	n/a	chr14:24502435-24502446
47	CHD1	chr14:24505868-24506176	GM12878	blood:	n/a	n/a
48	CHD2	chr14:24505969-24506247	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr14:24505991-24506252	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr14:24502364-24502617	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24505537-24505587	NH-A	brain:	n/a
2	chr14:24503311-24503361	GM19239	blood:	n/a
3	chr14:24505537-24505587	NH-A	brain:	n/a
4	chr14:24503311-24503361	GM19239	blood:	n/a
5	chr14:24505898-24505948	SAEC	small airway:	n/a
6	chr14:24505554-24505604	BE2_C	brain:	n/a
7	chr14:24505898-24505948	NHBE	bronchial:	n/a
8	chr14:24509703-24509753	AG09319	gingival:	n/a
9	chr14:24505898-24505948	BE2_C	brain:	n/a
10	chr14:24505554-24505604	AG10803	skin:	n/a
11	chr14:24505743-24505793	HNPCEpiC	eye:	n/a
12	chr14:24505743-24505793	RPTEC	kidney:	n/a
13	chr14:24505898-24505948	HAEpiC	amniotic membrane:	n/a
14	chr14:24503311-24503361	GM12892	blood:	n/a
15	chr14:24505537-24505587	HAEpiC	amniotic membrane:	n/a
16	chr14:24509703-24509753	NT2-D1	testis:	n/a
17	chr14:24505671-24505721	PANC-1	pancreas:	n/a
18	chr14:24505537-24505587	HCF	heart:	n/a
19	chr14:24505537-24505587	GM19239	blood:	n/a
20	chr14:24506241-24506291	A549	lung:	n/a
21	chr14:24506241-24506291	HEEpiC	esophagus:	n/a
22	chr14:24505554-24505604	PFSK-1	brain:	n/a
23	chr14:24505547-24505597	K562	blood:	n/a
24	chr14:24506241-24506291	AG10803	skin:	n/a
25	chr14:24503311-24503361	Hela-S3	cervix:	n/a
26	chr14:24505537-24505587	RPTEC	kidney:	n/a
27	chr14:24505671-24505721	RPTEC	kidney:	n/a
28	chr14:24505743-24505793	U87	brain:	n/a
29	chr14:24505653-24505703	K562	blood:	n/a
30	chr14:24505537-24505587	HCT-116	colon:	n/a
31	chr14:24505671-24505721	GM06990	blood:	n/a
32	chr14:24505537-24505587	BJ	skin:	n/a
33	chr14:24505743-24505793	HCPEpiC	choroid plexus:	n/a
34	chr14:24503311-24503361	AG04449	skin:	fetal
35	chr14:24505671-24505721	AoSMC	blood vessel:	n/a
36	chr14:24505547-24505597	HCM	heart:	n/a
37	chr14:24505898-24505948	HCT-116	colon:	n/a
38	chr14:24503311-24503361	NB4	blood:	n/a
39	chr14:24506241-24506291	NB4	blood:	n/a
40	chr14:24505898-24505948	HCM	heart:	n/a
41	chr14:24505743-24505793	K562	blood:	n/a
42	chr14:24506241-24506291	HMEC	breast:	n/a
43	chr14:24505671-24505721	SK-N-SH_RA	brain:	n/a
44	chr14:24505671-24505721	BJ	skin:	n/a
45	chr14:24505554-24505604	HepG2	liver:	n/a
46	chr14:24505671-24505721	NH-A	brain:	n/a
47	chr14:24506241-24506291	MCF10A-Er-Src	breast:	n/a
48	chr14:24505653-24505703	NHBE	bronchial:	n/a
49	chr14:24505554-24505604	HMEC	breast:	n/a
50	chr14:24505743-24505793	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:24422701..24424551-chr14:24504249..24506129,2	MCF-7	breast:
2	chr14:24504090..24505966-chr14:24768791..24770568,2	MCF-7	breast:
3	chr14:24509893..24511543-chr14:24520701..24522909,2	MCF-7	breast:
4	chr14:24504490..24506127-chr14:24583788..24585514,2	MCF-7	breast:
5	chr14:24503791..24508058-chr14:24562194..24566408,5	MCF-7	breast:
6	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
7	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
8	chr14:24505124..24506975-chr14:24520204..24522367,2	MCF-7	breast:
9	chr14:24509752..24511803-chr14:24562900..24565443,2	MCF-7	breast:
10	chr14:24505359..24507247-chr14:24702110..24704400,2	MCF-7	breast:
11	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
12	chr14:24511940..24516638-chr14:24519281..24522769,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000225766	TF binding region
ENSG00000225766	CpG island
ENSG00000100889	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000157379	chromatin interactions
ENSG00000100938	chromatin interactions
ENSG00000186648	chromatin interactions
ENSG00000196943	chromatin interactions
ENSG00000215256	chromatin interactions
ENSG00000100897	chromatin interactions
ENSG00000157326	chromatin interactions

Extended variants
information (count: 1233 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1233 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10142648	chr14:24484459-24484460	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183329937	chr14:24484474-24484475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142910748	chr14:24484487-24484488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117036375	chr14:24484499-24484500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372890074	chr14:24484522-24484523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200347521	chr14:24484524-24484525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577004439	chr14:24484531-24484532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539334066	chr14:24484536-24484537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556468312	chr14:24484537-24484538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140973162	chr14:24484543-24484544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560242469	chr14:24484544-24484545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561317646	chr14:24484546-24484547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575007687	chr14:24484571-24484572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540795614	chr14:24484575-24484576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149801597	chr14:24484578-24484579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10142130	chr14:24484582-24484583	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs549566636	chr14:24484587-24484588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567815222	chr14:24484621-24484622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369543218	chr14:24484623-24484624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190544309	chr14:24484653-24484654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140506988	chr14:24484656-24484657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531166847	chr14:24484671-24484672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145660592	chr14:24484688-24484689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112972584	chr14:24484727-24484728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533629247	chr14:24484734-24484735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377567022	chr14:24484737-24484738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201815938	chr14:24484738-24484739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529423974	chr14:24484747-24484748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187668033	chr14:24484756-24484757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78234825	chr14:24484759-24484760	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
31	rs538213609	chr14:24484781-24484782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192061248	chr14:24484795-24484796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574920421	chr14:24484800-24484801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540706392	chr14:24484816-24484817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185027334	chr14:24484836-24484837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373151422	chr14:24484843-24484844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143112808	chr14:24484862-24484863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562991851	chr14:24484863-24484864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35753952	chr14:24484890-24484891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148248806	chr14:24484903-24484904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189442602	chr14:24484909-24484910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200852406	chr14:24484934-24484935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11849560	chr14:24484935-24484936	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs547083681	chr14:24484958-24484959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570539536	chr14:24484961-24484962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs72692127	chr14:24485008-24485009	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs552004776	chr14:24485009-24485010	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs375276947	chr14:24485010-24485011	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs150322683	chr14:24485016-24485017	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs555165516	chr14:24485068-24485069	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24480400-24485000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr14:24480600-24486600	Weak transcription	Thymus	Thymus
3	chr14:24481200-24486400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr14:24483600-24485000	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr14:24483600-24485400	Weak transcription	Fetal Thymus	thymus
6	chr14:24483600-24485800	Weak transcription	Ovary	ovary
7	chr14:24483600-24486200	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr14:24483600-24486200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr14:24483600-24486800	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr14:24483800-24484800	Weak transcription	HepG2	liver
11	chr14:24483800-24485000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr14:24483800-24488200	Weak transcription	Dnd41	blood
13	chr14:24484800-24485400	Enhancers	HepG2	liver
14	chr14:24485000-24485200	Enhancers	Primary T cells fromperipheralblood	blood
15	chr14:24485000-24485200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr14:24485000-24485200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr14:24486800-24487200	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr14:24492800-24494600	Enhancers	HepG2	liver
19	chr14:24494000-24494600	Enhancers	Liver	Liver
20	chr14:24494400-24495600	Enhancers	Dnd41	blood
21	chr14:24495600-24500000	Weak transcription	Dnd41	blood
22	chr14:24500000-24500400	Enhancers	Dnd41	blood
23	chr14:24501200-24501400	Enhancers	A549	lung
24	chr14:24501400-24503000	Flanking Active TSS	A549	lung
25	chr14:24501600-24501800	Enhancers	Psoas Muscle	Psoas
26	chr14:24501800-24505200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr14:24501800-24505200	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr14:24502000-24502400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr14:24502000-24502600	Enhancers	Pancreas	Pancrea
30	chr14:24502000-24503000	Weak transcription	Psoas Muscle	Psoas
31	chr14:24502000-24503200	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr14:24502000-24503400	Enhancers	HepG2	liver
33	chr14:24502000-24503800	Enhancers	Placenta	Placenta
34	chr14:24502000-24504000	Enhancers	Liver	Liver
35	chr14:24502000-24504400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr14:24502000-24505200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr14:24502000-24505200	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr14:24502200-24502400	Enhancers	HMEC	breast
39	chr14:24502200-24502600	Enhancers	Osteobl	bone
40	chr14:24502200-24503000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr14:24502400-24502600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr14:24502400-24502600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr14:24502400-24502600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr14:24502400-24502600	Enhancers	Hela-S3	cervix
45	chr14:24502400-24502800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr14:24502400-24502800	Enhancers	NHDF-Ad	bronchial
47	chr14:24502400-24503000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr14:24502400-24505400	Weak transcription	HMEC	breast
49	chr14:24502600-24503400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr14:24502600-24504200	Weak transcription	Hela-S3	cervix

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