Variant report

Variant	nsv542002
Chromosome Location	chr14:24930993-24990765
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:441)
CpG islands
(count:185)
Chromatin interactive
region (count:19)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:441 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24950760-24951183	HepG2	liver:	n/a	n/a
2	ATF2	chr14:24932426-24932919	GM12878	blood:	n/a	n/a
3	BCLAF1	chr14:24932394-24932853	GM12878	blood:	n/a	chr14:24932495-24932504
4	BHLHE40	chr14:24950873-24951083	GM12878	blood:	n/a	n/a
5	BHLHE40	chr14:24988161-24988425	GM12878	blood:	n/a	chr14:24988285-24988298 chr14:24988287-24988296 chr14:24988287-24988296 chr14:24988288-24988297
6	BHLHE40	chr14:24950918-24951048	K562	blood:	n/a	n/a
7	BHLHE40	chr14:24977363-24977725	GM12878	blood:	n/a	n/a
8	CEBPB	chr14:24933358-24933637	IMR90	lung:	n/a	chr14:24933477-24933488
9	CEBPB	chr14:24933380-24933633	A549	lung:	n/a	chr14:24933477-24933488
10	CEBPB	chr14:24961288-24961606	HepG2	liver:	n/a	n/a
11	CEBPB	chr14:24984093-24984194	HepG2	liver:	n/a	chr14:24984150-24984161
12	CEBPB	chr14:24933331-24933629	HepG2	liver:	n/a	chr14:24933477-24933488
13	CEBPB	chr14:24936556-24936597	IMR90	lung:	n/a	chr14:24936570-24936581
14	CEBPB	chr14:24985169-24985265	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:24961363-24961489	HepG2	liver:	n/a	n/a
16	CEBPB	chr14:24933322-24933646	K562	blood:	n/a	chr14:24933477-24933488
17	CEBPB	chr14:24961460-24961471	A549	lung:	n/a	n/a
18	CEBPB	chr14:24936466-24936680	HepG2	liver:	n/a	chr14:24936570-24936581
19	CEBPB	chr14:24961365-24961539	MCF-7	breast:	n/a	n/a
20	CEBPB	chr14:24961253-24961544	HepG2	liver:	n/a	n/a
21	CHD2	chr14:24950846-24951061	HepG2	liver:	n/a	n/a
22	CHD2	chr14:24950790-24951053	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr14:24953109-24953480	GM12878	blood:	n/a	n/a
24	CREB1	chr14:24934957-24935508	GM12878	blood:	n/a	n/a
25	CREB1	chr14:24935061-24935433	GM12878	blood:	n/a	n/a
26	CTCF	chr14:24950880-24951030	K562	blood:	n/a	chr14:24950940-24950958
27	CTCF	chr14:24950857-24951043	GM20000	blood:	n/a	chr14:24950940-24950958
28	CTCF	chr14:24950860-24951010	Hela-S3	cervix:	n/a	chr14:24950940-24950958
29	CTCF	chr14:24974780-24974930	GM06990	blood:	n/a	n/a
30	CTCF	chr14:24950652-24951196	MCF-7	breast:	n/a	chr14:24950940-24950958
31	CTCF	chr14:24950860-24951010	GM12875	blood:	n/a	chr14:24950940-24950958
32	CTCF	chr14:24950860-24951010	GM12874	blood:	n/a	chr14:24950940-24950958
33	CTCF	chr14:24950860-24951010	GM12871	blood:	n/a	chr14:24950940-24950958
34	CTCF	chr14:24950860-24951010	GM12870	blood:	n/a	chr14:24950940-24950958
35	CTCF	chr14:24950819-24951059	LNCaP	prostate:	n/a	chr14:24950940-24950958
36	CTCF	chr14:24950880-24951030	GM12866	blood:	n/a	chr14:24950940-24950958
37	CTCF	chr14:24950860-24951010	WERI-Rb-1	eye:	n/a	chr14:24950940-24950958
38	CTCF	chr14:24950880-24951030	GM12878	blood:	n/a	chr14:24950940-24950958
39	CTCF	chr14:24950880-24951030	GM12872	blood:	n/a	chr14:24950940-24950958
40	CTCF	chr14:24950860-24951010	MCF-7	breast:	n/a	chr14:24950940-24950958
41	CTCF	chr14:24950880-24951030	NHEK	skin:	n/a	chr14:24950940-24950958
42	CTCF	chr14:24950880-24951030	GM12873	blood:	n/a	chr14:24950940-24950958
43	CTCF	chr14:24950880-24951030	HCM	heart:	n/a	chr14:24950940-24950958
44	CTCF	chr14:24950860-24951010	RPTEC	kidney:	n/a	chr14:24950940-24950958
45	CTCF	chr14:24950860-24951010	GM12872	blood:	n/a	chr14:24950940-24950958
46	CTCF	chr14:24950860-24951010	HPF	lung:	n/a	chr14:24950940-24950958
47	CTCF	chr14:24950880-24951030	HEK293	kidney:	n/a	chr14:24950940-24950958
48	CTCF	chr14:24950880-24951030	HVMF	connective:	n/a	chr14:24950940-24950958
49	CTCF	chr14:24951260-24951410	HCT-116	colon:	n/a	n/a
50	CTCF	chr14:24950900-24951050	AG04450	lung:	n/a	chr14:24950940-24950958

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24977773-24977823	HepG2	liver:	n/a
2	chr14:24974804-24974854	HNPCEpiC	eye:	n/a
3	chr14:24977773-24977823	HepG2	liver:	n/a
4	chr14:24974804-24974854	HNPCEpiC	eye:	n/a
5	chr14:24974804-24974854	HMEC	breast:	n/a
6	chr14:24978681-24978731	BE2_C	brain:	n/a
7	chr14:24978681-24978731	AoSMC	blood vessel:	n/a
8	chr14:24974804-24974854	GM19239	blood:	n/a
9	chr14:24977773-24977823	ECC-1	luminal epithelium:	n/a
10	chr14:24978681-24978731	GM12878	blood:	n/a
11	chr14:24978681-24978731	SKMC	muscle:	n/a
12	chr14:24974804-24974854	HCM	heart:	n/a
13	chr14:24974804-24974854	SAEC	small airway:	n/a
14	chr14:24974804-24974854	GM12878	blood:	n/a
15	chr14:24978681-24978731	HUVEC	blood vessel:	n/a
16	chr14:24978681-24978731	SK-N-MC	brain:	n/a
17	chr14:24974804-24974854	Caco-2	colon:	n/a
18	chr14:24974804-24974854	AG04450	lung:	fetal
19	chr14:24978681-24978731	HMEC	breast:	n/a
20	chr14:24977773-24977823	PANC-1	pancreas:	n/a
21	chr14:24974804-24974854	BE2_C	brain:	n/a
22	chr14:24974804-24974854	NH-A	brain:	n/a
23	chr14:24974804-24974854	ProgFib	skin:	n/a
24	chr14:24977773-24977823	A549	lung:	n/a
25	chr14:24977773-24977823	PFSK-1	brain:	n/a
26	chr14:24977773-24977823	HAEpiC	amniotic membrane:	n/a
27	chr14:24974804-24974854	Jurkat	blood:	n/a
28	chr14:24977773-24977823	HUVEC	blood vessel:	n/a
29	chr14:24977773-24977823	HCPEpiC	choroid plexus:	n/a
30	chr14:24974804-24974854	HIPEpiC	eye:	n/a
31	chr14:24977773-24977823	HEK293	kidney:	embryo
32	chr14:24977773-24977823	BJ	skin:	n/a
33	chr14:24977773-24977823	AG09309	skin:	n/a
34	chr14:24977773-24977823	IMR90	lung:	fetal
35	chr14:24978681-24978731	Hepatocyte	liver:	n/a
36	chr14:24978681-24978731	A549	lung:	n/a
37	chr14:24977773-24977823	AG04449	skin:	fetal
38	chr14:24974804-24974854	CMK	blood:	n/a
39	chr14:24977773-24977823	NB4	blood:	n/a
40	chr14:24974804-24974854	HRPEpiC	eye:	n/a
41	chr14:24974804-24974854	A549	lung:	n/a
42	chr14:24974804-24974854	HEEpiC	esophagus:	n/a
43	chr14:24978681-24978731	IMR90	lung:	fetal
44	chr14:24974804-24974854	PFSK-1	brain:	n/a
45	chr14:24977773-24977823	NT2-D1	testis:	n/a
46	chr14:24978681-24978731	HPAEpiC	pulmonary alveolar:	n/a
47	chr14:24978681-24978731	T-47D	breast:	n/a
48	chr14:24974804-24974854	RPTEC	kidney:	n/a
49	chr14:24974804-24974854	SK-N-SH	brain:	n/a
50	chr14:24977773-24977823	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:24940138..24941029-chr14:24952690..24953556,3	MCF-7	breast:
2	chr14:24952643..24955226-chr14:24957985..24960918,2	K562	blood:
3	chr14:24950901..24951428-chr14:25147948..25148704,2	K562	blood:
4	chr14:24950851..24951362-chr14:25074499..25075225,3	MCF-7	breast:
5	chr14:24977730..24979918-chr14:24980024..24982313,2	MCF-7	breast:
6	chr14:24941879..24943792-chr14:24944086..24946470,2	MCF-7	breast:
7	chr14:24950478..24951496-chr14:25147845..25148826,8	MCF-7	breast:
8	chr14:24925537..24927679-chr14:24931012..24933705,2	MCF-7	breast:
9	chr14:24940138..24941029-chr14:24952690..24953556,3	MCF-7	breast:
10	chr14:24950446..24951536-chr14:25147799..25148973,31	MCF-7	breast:
11	chr14:24952643..24955226-chr14:24957985..24960918,2	K562	blood:
12	chr14:24911704..24914258-chr14:24948506..24950947,2	MCF-7	breast:
13	chr14:24911430..24913240-chr14:24948207..24950557,2	K562	blood:
14	chr14:24941879..24943792-chr14:24944086..24946470,2	MCF-7	breast:
15	chr14:24987134..24988670-chr14:24989655..24991180,2	K562	blood:
16	chr14:24987134..24988670-chr14:24989655..24991180,2	K562	blood:
17	chr14:24960817..24963613-chr14:24965277..24968190,2	K562	blood:
18	chr14:24977730..24979918-chr14:24980024..24982313,2	MCF-7	breast:
19	chr14:24960817..24963613-chr14:24965277..24968190,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-80A15.1.1-1	chr14:24970766-24971403	NR_110032
2	lnc-RP11-80A15.1.1-1	chr14:24970766-24971403	ENSG00000251021

No data

Variant related genes	Relation type
CMA1	TF binding region
ENSG00000258744	TF binding region
CMA1	CpG island
ENSG00000258744	CpG island
ENSG00000100445	chromatin interactions
CYP2C8	miRNA target sites

Extended variants
information (count: 1757 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1757 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559855184	chr14:24931016-24931017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs528808221	chr14:24931083-24931084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7152718	chr14:24931088-24931089	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs56376004	chr14:24931110-24931111	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs543040515	chr14:24931131-24931132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs57361547	chr14:24931143-24931144	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs10150240	chr14:24931151-24931152	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs59266025	chr14:24931192-24931193	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs57096613	chr14:24931203-24931204	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs12890665	chr14:24931234-24931235	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs572965948	chr14:24931254-24931255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148300426	chr14:24931265-24931266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371656573	chr14:24931287-24931288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141320589	chr14:24931288-24931289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145577116	chr14:24931324-24931325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533007124	chr14:24931328-24931329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs80196978	chr14:24931345-24931346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557274541	chr14:24931418-24931419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190856290	chr14:24931442-24931443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551141446	chr14:24931457-24931458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138159125	chr14:24931463-24931464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528720662	chr14:24931482-24931483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142038777	chr14:24931591-24931592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529040921	chr14:24931592-24931593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71119079	chr14:24931600-24931601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12895684	chr14:24931601-24931602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566464023	chr14:24931643-24931644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs8014706	chr14:24931655-24931656	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs549231454	chr14:24931703-24931704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565628561	chr14:24931711-24931712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531185173	chr14:24931720-24931721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs57928011	chr14:24931739-24931740	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs373337352	chr14:24931746-24931747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529775004	chr14:24931747-24931748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546704417	chr14:24931749-24931750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs58791058	chr14:24931806-24931807	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs149273802	chr14:24931823-24931824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs61463716	chr14:24931830-24931831	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs568813002	chr14:24931841-24931842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182922350	chr14:24931858-24931859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111732704	chr14:24931870-24931871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557090352	chr14:24931894-24931895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573948037	chr14:24931928-24931929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542632156	chr14:24932000-24932001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4981525	chr14:24932002-24932003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4982928	chr14:24932058-24932059	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs76416393	chr14:24932107-24932108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185686442	chr14:24932111-24932112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545623641	chr14:24932126-24932127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565439512	chr14:24932155-24932156	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24912800-24950800	Weak transcription	Gastric	stomach
2	chr14:24913000-24931600	Weak transcription	Fetal Kidney	kidney
3	chr14:24913000-24932400	Weak transcription	Primary B cells from cord blood	blood
4	chr14:24913000-24932800	Weak transcription	Primary T cells from cord blood	blood
5	chr14:24922200-24946000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr14:24922800-24951000	Weak transcription	Pancreas	Pancrea
7	chr14:24923200-24937400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr14:24923600-24932600	Weak transcription	Right Ventricle	heart
9	chr14:24924200-24932000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr14:24925800-24933400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr14:24926000-24936000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr14:24926400-24934200	Weak transcription	Lung	lung
13	chr14:24927600-24951000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:24928200-24934400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr14:24928200-24950400	Weak transcription	HepG2	liver
16	chr14:24928400-24936000	Weak transcription	Liver	Liver
17	chr14:24928600-24951000	Weak transcription	Placenta	Placenta
18	chr14:24928800-24951000	Weak transcription	Spleen	Spleen
19	chr14:24929800-24932400	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr14:24929800-24934600	Weak transcription	Aorta	Aorta
21	chr14:24930200-24931200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr14:24930600-24931200	Enhancers	HMEC	breast
23	chr14:24930600-24931200	Enhancers	NHEK	skin
24	chr14:24930800-24951000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr14:24932000-24933000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr14:24932200-24933000	Enhancers	GM12878-XiMat	blood
27	chr14:24932400-24936000	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr14:24932600-24935400	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr14:24932800-24933200	Enhancers	Fetal Thymus	thymus
30	chr14:24932800-24935000	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr14:24932800-24935400	Enhancers	Thymus	Thymus
32	chr14:24932800-24935600	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr14:24932800-24935800	Enhancers	Primary T cells from cord blood	blood
34	chr14:24933000-24933600	Flanking Active TSS	GM12878-XiMat	blood
35	chr14:24933000-24935200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr14:24933000-24935400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr14:24933000-24935600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr14:24933000-24951400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr14:24933200-24934400	Weak transcription	Fetal Thymus	thymus
40	chr14:24933200-24935600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr14:24933600-24934600	Enhancers	GM12878-XiMat	blood
42	chr14:24934000-24934400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
43	chr14:24934400-24934800	Enhancers	Primary T cells fromperipheralblood	blood
44	chr14:24934400-24934800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr14:24934400-24935400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr14:24934400-24935400	Enhancers	Fetal Thymus	thymus
47	chr14:24934600-24934800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr14:24935400-24948400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr14:24936000-24936200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr14:24937000-24937200	ZNF genes & repeats	Aorta	Aorta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links