Variant report

Variant	nsv1038492
Chromosome Location	chr14:24452689-24489426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:831)
CpG islands
(count:1162)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:831 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24483172-24483507	K562	blood:	n/a	n/a
2	ARID3A	chr14:24483175-24483522	HepG2	liver:	n/a	n/a
3	ATF2	chr14:24458816-24459305	GM12878	blood:	n/a	n/a
4	BACH1	chr14:24476252-24476312	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr14:24458105-24458174	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr14:24458871-24459266	GM12878	blood:	n/a	n/a
7	BATF	chr14:24458905-24459223	GM12878	blood:	n/a	n/a
8	BHLHE40	chr14:24456162-24456216	HepG2	liver:	n/a	n/a
9	BHLHE40	chr14:24475943-24476541	HepG2	liver:	n/a	n/a
10	BHLHE40	chr14:24483227-24483438	K562	blood:	n/a	n/a
11	BHLHE40	chr14:24483187-24483465	GM12878	blood:	n/a	n/a
12	BRCA1	chr14:24483351-24483423	GM12878	blood:	n/a	n/a
13	CBX3	chr14:24483227-24483553	K562	blood:	n/a	n/a
14	CBX3	chr14:24483218-24483539	K562	blood:	n/a	n/a
15	CBX3	chr14:24476155-24476416	K562	blood:	n/a	n/a
16	CEBPB	chr14:24454143-24454908	A549	lung:	n/a	chr14:24454690-24454701
17	CEBPB	chr14:24454258-24454790	MCF-7	breast:	n/a	chr14:24454690-24454701
18	CEBPB	chr14:24482978-24483461	A549	lung:	n/a	n/a
19	CEBPB	chr14:24454491-24454833	Hela-S3	cervix:	n/a	chr14:24454690-24454701
20	CEBPB	chr14:24454165-24454464	MCF-7	breast:	n/a	n/a
21	CEBPB	chr14:24454542-24454918	MCF-7	breast:	n/a	chr14:24454690-24454701
22	CEBPB	chr14:24454350-24454830	A549	lung:	n/a	chr14:24454690-24454701
23	CEBPB	chr14:24454237-24454396	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:24454506-24454789	A549	lung:	n/a	chr14:24454690-24454701
25	CEBPB	chr14:24454359-24454892	IMR90	lung:	n/a	chr14:24454690-24454701
26	CEBPB	chr14:24454306-24454822	HepG2	liver:	n/a	chr14:24454690-24454701
27	CEBPB	chr14:24456316-24456341	HepG2	liver:	n/a	n/a
28	CEBPD	chr14:24475992-24476248	HepG2	liver:	n/a	n/a
29	CEBPD	chr14:24457723-24458280	HepG2	liver:	n/a	n/a
30	CEBPD	chr14:24457835-24458170	HepG2	liver:	n/a	n/a
31	CEBPD	chr14:24455859-24456293	HepG2	liver:	n/a	n/a
32	CHD1	chr14:24483316-24483498	GM12878	blood:	n/a	n/a
33	CHD2	chr14:24483281-24483447	GM12878	blood:	n/a	n/a
34	CHD2	chr14:24457926-24458005	Hela-S3	cervix:	n/a	chr14:24457984-24457994
35	CTCF	chr14:24489360-24489510	HCT-116	colon:	n/a	n/a
36	CTCF	chr14:24489140-24489290	GM12870	blood:	n/a	n/a
37	CTCF	chr14:24483280-24483430	GM06990	blood:	n/a	n/a
38	CTCF	chr14:24489380-24489530	GM12872	blood:	n/a	n/a
39	CTCF	chr14:24489140-24489290	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr14:24489262-24489497	MCF-7	breast:	n/a	n/a
41	CTCF	chr14:24483280-24483430	GM12865	blood:	n/a	n/a
42	CTCF	chr14:24454260-24454410	SAEC	small airway:	n/a	n/a
43	CTCF	chr14:24483160-24483511	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr14:24483064-24483503	A549	lung:	n/a	n/a
45	CTCF	chr14:24454240-24454390	SAEC	small airway:	n/a	n/a
46	CTCF	chr14:24483300-24483450	A549	lung:	n/a	n/a
47	CTCF	chr14:24457655-24457707	GM10248	blood:	n/a	chr14:24457659-24457668
48	CTCF	chr14:24483280-24483430	GM12870	blood:	n/a	n/a
49	CTCF	chr14:24454260-24454410	A549	lung:	n/a	n/a
50	CTCF	chr14:24489380-24489530	RPTEC	kidney:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24458014-24458064	BJ	skin:	n/a
2	chr14:24458014-24458064	U87	brain:	n/a
3	chr14:24476082-24476132	NHDF-neo	bronchial:	n/a
4	chr14:24458014-24458064	BJ	skin:	n/a
5	chr14:24458014-24458064	U87	brain:	n/a
6	chr14:24476082-24476132	NHDF-neo	bronchial:	n/a
7	chr14:24475906-24475956	MCF-7	breast:	n/a
8	chr14:24458299-24458349	SKMC	muscle:	n/a
9	chr14:24458208-24458258	HUVEC	blood vessel:	n/a
10	chr14:24458004-24458054	A549	lung:	n/a
11	chr14:24457509-24457559	SAEC	small airway:	n/a
12	chr14:24458299-24458349	HEEpiC	esophagus:	n/a
13	chr14:24475053-24475103	GM12891	blood:	n/a
14	chr14:24458014-24458064	MCF10A-Er-Src	breast:	n/a
15	chr14:24473832-24473882	GM12891	blood:	n/a
16	chr14:24475906-24475956	SK-N-SH_RA	brain:	n/a
17	chr14:24458208-24458258	MCF-7	breast:	n/a
18	chr14:24457509-24457559	SK-N-MC	brain:	n/a
19	chr14:24478620-24478670	Caco-2	colon:	n/a
20	chr14:24458004-24458054	HRCEpiC	kidney:	n/a
21	chr14:24458000-24458050	HRCEpiC	kidney:	n/a
22	chr14:24458014-24458064	HCPEpiC	choroid plexus:	n/a
23	chr14:24457509-24457559	MCF-7	breast:	n/a
24	chr14:24457993-24458043	Hepatocyte	liver:	n/a
25	chr14:24475053-24475103	PANC-1	pancreas:	n/a
26	chr14:24457993-24458043	HEEpiC	esophagus:	n/a
27	chr14:24458004-24458054	GM12878	blood:	n/a
28	chr14:24475906-24475956	HEK293	kidney:	embryo
29	chr14:24475053-24475103	HepG2	liver:	n/a
30	chr14:24476559-24476609	PANC-1	pancreas:	n/a
31	chr14:24476559-24476609	Caco-2	colon:	n/a
32	chr14:24458004-24458054	SKMC	muscle:	n/a
33	chr14:24476082-24476132	HPAEpiC	pulmonary alveolar:	n/a
34	chr14:24473832-24473882	CMK	blood:	n/a
35	chr14:24475906-24475956	HNPCEpiC	eye:	n/a
36	chr14:24458345-24458395	NT2-D1	testis:	n/a
37	chr14:24454443-24454493	A549	lung:	n/a
38	chr14:24458299-24458349	ovcar-3	ovarian:	n/a
39	chr14:24458345-24458395	BE2_C	brain:	n/a
40	chr14:24458004-24458054	GM12892	blood:	n/a
41	chr14:24458299-24458349	NHDF-neo	bronchial:	n/a
42	chr14:24473832-24473882	NH-A	brain:	n/a
43	chr14:24458345-24458395	HAEpiC	amniotic membrane:	n/a
44	chr14:24458000-24458050	HepG2	liver:	n/a
45	chr14:24475053-24475103	PFSK-1	brain:	n/a
46	chr14:24457915-24457965	NHDF-neo	bronchial:	n/a
47	chr14:24457993-24458043	HUVEC	blood vessel:	n/a
48	chr14:24458014-24458064	NHBE	bronchial:	n/a
49	chr14:24458004-24458054	H1-hESC	embryonic stem cell:	embryo
50	chr14:24457893-24457943	HMEC	breast:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24483262..24483795-chr14:24906005..24906586,2	K562	blood:
2	chr14:24452194..24454763-chr14:24457643..24460471,2	MCF-7	breast:
3	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
4	chr14:24482840..24483718-chr14:24710880..24711620,2	MCF-7	breast:
5	chr14:24421533..24423333-chr14:24480435..24482151,2	K562	blood:
6	chr14:24482858..24483785-chr14:24559502..24560237,2	K562	blood:
7	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
8	chr14:24483165..24483827-chr14:24559565..24560642,4	MCF-7	breast:
9	chr14:24476695..24479385-chr14:24563251..24564763,2	MCF-7	breast:
10	chr14:24482802..24483800-chr14:24505642..24506553,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRL-1	chr14:24457938-24458048	ENSG00000215256.3

No data

Variant related genes	Relation type
DHRS4L2	TF binding region
DHRS4-AS1	TF binding region
DHRS4L2	CpG island
DHRS4-AS1	CpG island
ENSG00000100889	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000092330	chromatin interactions
ENSG00000187630	chromatin interactions
ENSG00000225766	chromatin interactions
ENSG00000215256	chromatin interactions
ENSG00000129535	chromatin interactions

Extended variants
information (count: 1863 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1863 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370053988	chr14:24452714-24452715	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs571457609	chr14:24452726-24452727	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs140700708	chr14:24452730-24452731	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs112663076	chr14:24452731-24452732	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs567613330	chr14:24452751-24452752	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536575101	chr14:24452780-24452781	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs111367260	chr14:24452789-24452790	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs189820550	chr14:24452790-24452791	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs527588747	chr14:24452800-24452801	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs183593528	chr14:24452831-24452832	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs542860603	chr14:24452866-24452867	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs558629216	chr14:24452883-24452884	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs35165896	chr14:24452938-24452939	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs187809637	chr14:24452975-24452976	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs538036890	chr14:24453014-24453015	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs554833505	chr14:24453015-24453016	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs574770345	chr14:24453020-24453021	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs544465631	chr14:24453060-24453061	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540538755	chr14:24453077-24453078	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs559462270	chr14:24453082-24453083	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs72680450	chr14:24453083-24453084	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs192020593	chr14:24453105-24453106	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs183303411	chr14:24453111-24453112	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs77404835	chr14:24453132-24453133	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs78557923	chr14:24453142-24453143	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs188272519	chr14:24453146-24453147	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs1957677	chr14:24453147-24453148	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs35666932	chr14:24453161-24453162	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs112932501	chr14:24453167-24453168	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs77853015	chr14:24453169-24453170	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs530295208	chr14:24453178-24453179	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs192553167	chr14:24453205-24453206	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs566298089	chr14:24453215-24453216	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs549493945	chr14:24453239-24453240	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs1957679	chr14:24453253-24453254	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs370615112	chr14:24453282-24453283	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs568952871	chr14:24453309-24453310	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs77613160	chr14:24453315-24453316	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs138247301	chr14:24453325-24453326	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs1957680	chr14:24453366-24453367	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs574710219	chr14:24453421-24453422	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs533802778	chr14:24453429-24453430	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs554041469	chr14:24453448-24453449	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs577100482	chr14:24453449-24453450	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs1028677	chr14:24453458-24453459	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs564964644	chr14:24453549-24453550	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs2008662	chr14:24453694-24453695	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs544315370	chr14:24453695-24453696	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs2008661	chr14:24453724-24453725	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs540510865	chr14:24453727-24453728	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	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:898 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24424000-24458000	Weak transcription	Primary T cells from cord blood	blood
2	chr14:24439400-24457600	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr14:24440000-24453600	Weak transcription	Dnd41	blood
4	chr14:24442800-24456000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr14:24445200-24454600	Weak transcription	Thymus	Thymus
6	chr14:24445200-24456200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr14:24446200-24458000	Weak transcription	Gastric	stomach
8	chr14:24446600-24457400	Weak transcription	Primary B cells from peripheral blood	blood
9	chr14:24448000-24457400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:24448400-24457400	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr14:24450400-24454200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr14:24450400-24457400	Weak transcription	Primary hematopoietic stem cells	blood
13	chr14:24450400-24457600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr14:24451400-24453800	Weak transcription	Fetal Intestine Small	intestine
15	chr14:24451400-24453800	Weak transcription	Fetal Thymus	thymus
16	chr14:24451400-24454400	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr14:24451600-24454600	Weak transcription	Duodenum Mucosa	Duodenum
18	chr14:24451800-24457400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr14:24452000-24455400	Weak transcription	Fetal Intestine Large	intestine
20	chr14:24452000-24455800	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr14:24452200-24454000	Weak transcription	HepG2	liver
22	chr14:24452600-24457600	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr14:24453600-24453800	Enhancers	Esophagus	oesophagus
24	chr14:24453600-24453800	Enhancers	Small Intestine	intestine
25	chr14:24453600-24457600	Enhancers	Dnd41	blood
26	chr14:24453800-24455200	Weak transcription	Esophagus	oesophagus
27	chr14:24453800-24456400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr14:24453800-24456400	Enhancers	Fetal Intestine Small	intestine
29	chr14:24453800-24457000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr14:24453800-24457000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr14:24453800-24457000	Enhancers	NHEK	skin
32	chr14:24453800-24457600	Enhancers	Fetal Thymus	thymus
33	chr14:24454000-24454200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr14:24454000-24455200	Enhancers	A549	lung
35	chr14:24454000-24455400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr14:24454000-24455800	Enhancers	HepG2	liver
37	chr14:24454000-24456000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr14:24454000-24456400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr14:24454200-24454400	Enhancers	NHLF	lung
40	chr14:24454200-24454600	Enhancers	Adipose Nuclei	Adipose
41	chr14:24454200-24454800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr14:24454200-24454800	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr14:24454200-24455000	Enhancers	HMEC	breast
44	chr14:24454200-24455000	Enhancers	HSMM	muscle
45	chr14:24454200-24455200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr14:24454200-24455200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr14:24454200-24455200	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr14:24454200-24455200	Enhancers	Osteobl	bone
49	chr14:24454200-24455400	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr14:24454200-24455800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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