Variant report

Variant	nsv1035903
Chromosome Location	chr14:24929447-24981097
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:377)
CpG islands
(count:183)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr14:24977363-24977725	GM12878	blood:	n/a	n/a
5	BHLHE40	chr14:24950873-24951083	GM12878	blood:	n/a	n/a
6	BHLHE40	chr14:24950918-24951048	K562	blood:	n/a	n/a
7	CEBPB	chr14:24961363-24961489	HepG2	liver:	n/a	n/a
8	CEBPB	chr14:24961460-24961471	A549	lung:	n/a	n/a
9	CEBPB	chr14:24933380-24933633	A549	lung:	n/a	chr14:24933477-24933488
10	CEBPB	chr14:24933331-24933629	HepG2	liver:	n/a	chr14:24933477-24933488
11	CEBPB	chr14:24961253-24961544	HepG2	liver:	n/a	n/a
12	CEBPB	chr14:24936556-24936597	IMR90	lung:	n/a	chr14:24936570-24936581
13	CEBPB	chr14:24933358-24933637	IMR90	lung:	n/a	chr14:24933477-24933488
14	CEBPB	chr14:24961288-24961606	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:24933322-24933646	K562	blood:	n/a	chr14:24933477-24933488
16	CEBPB	chr14:24961365-24961539	MCF-7	breast:	n/a	n/a
17	CEBPB	chr14:24936466-24936680	HepG2	liver:	n/a	chr14:24936570-24936581
18	CHD2	chr14:24950790-24951053	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr14:24950846-24951061	HepG2	liver:	n/a	n/a
20	CREB1	chr14:24934957-24935508	GM12878	blood:	n/a	n/a
21	CREB1	chr14:24953109-24953480	GM12878	blood:	n/a	n/a
22	CREB1	chr14:24935061-24935433	GM12878	blood:	n/a	n/a
23	CTCF	chr14:24950820-24951104	MCF-7	breast:	n/a	chr14:24950940-24950958
24	CTCF	chr14:24950860-24951010	HMF	breast:	n/a	chr14:24950940-24950958
25	CTCF	chr14:24950900-24951050	HCT-116	colon:	n/a	chr14:24950940-24950958
26	CTCF	chr14:24950860-24951010	HFF	foreskin:	n/a	chr14:24950940-24950958
27	CTCF	chr14:24950940-24951090	A549	lung:	n/a	chr14:24950940-24950958
28	CTCF	chr14:24950832-24951070	Pancreas_OC	pancreas:	n/a	chr14:24950940-24950958
29	CTCF	chr14:24950719-24951201	H1-hESC	embryonic stem cell:	n/a	chr14:24950940-24950958
30	CTCF	chr14:24950200-24950350	HepG2	liver:	n/a	n/a
31	CTCF	chr14:24951380-24951530	GM12868	blood:	n/a	chr14:24951464-24951482
32	CTCF	chr14:24950787-24951103	T-47D	breast:	n/a	chr14:24950940-24950958
33	CTCF	chr14:24950860-24951010	BE2_C	brain:	n/a	chr14:24950940-24950958
34	CTCF	chr14:24950652-24951196	MCF-7	breast:	n/a	chr14:24950940-24950958
35	CTCF	chr14:24950880-24951030	HVMF	connective:	n/a	chr14:24950940-24950958
36	CTCF	chr14:24950829-24951075	HepG2	liver:	n/a	chr14:24950940-24950958
37	CTCF	chr14:24974780-24974930	GM06990	blood:	n/a	n/a
38	CTCF	chr14:24950860-24951010	HPF	lung:	n/a	chr14:24950940-24950958
39	CTCF	chr14:24950808-24951119	A549	lung:	n/a	chr14:24950940-24950958
40	CTCF	chr14:24950840-24950990	GM12875	blood:	n/a	chr14:24950940-24950958
41	CTCF	chr14:24950900-24951050	HFF-Myc	foreskin:	n/a	chr14:24950940-24950958
42	CTCF	chr14:24950860-24951010	SK-N-SH_RA	brain:	n/a	chr14:24950940-24950958
43	CTCF	chr14:24950825-24951083	H1-hESC	embryonic stem cell:	n/a	chr14:24950940-24950958
44	CTCF	chr14:24950900-24951050	SAEC	small airway:	n/a	chr14:24950940-24950958
45	CTCF	chr14:24950860-24951010	HBMEC	blood vessel:	n/a	chr14:24950940-24950958
46	CTCF	chr14:24950833-24951127	Fibrobl	skin:	n/a	chr14:24950940-24950958
47	CTCF	chr14:24950720-24950870	HAc	cerebellar:	n/a	n/a
48	CTCF	chr14:24950880-24951030	BJ	skin:	n/a	chr14:24950940-24950958
49	CTCF	chr14:24950716-24951155	K562	blood:	n/a	chr14:24950940-24950958
50	CTCF	chr14:24961380-24961530	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24974804-24974854	K562	blood:	n/a
2	chr14:24978681-24978731	RPTEC	kidney:	n/a
3	chr14:24977773-24977823	MCF-7	breast:	n/a
4	chr14:24974804-24974854	SAEC	small airway:	n/a
5	chr14:24974804-24974854	NH-A	brain:	n/a
6	chr14:24974804-24974854	NHDF-neo	bronchial:	n/a
7	chr14:24978681-24978731	A549	lung:	n/a
8	chr14:24978681-24978731	Hela-S3	cervix:	n/a
9	chr14:24978681-24978731	NH-A	brain:	n/a
10	chr14:24977773-24977823	HCF	heart:	n/a
11	chr14:24974804-24974854	HL-60	blood:	n/a
12	chr14:24974804-24974854	GM12891	blood:	n/a
13	chr14:24974804-24974854	HRE	kidney:	n/a
14	chr14:24977773-24977823	PFSK-1	brain:	n/a
15	chr14:24977773-24977823	GM12891	blood:	n/a
16	chr14:24978681-24978731	HEEpiC	esophagus:	n/a
17	chr14:24974804-24974854	BE2_C	brain:	n/a
18	chr14:24974804-24974854	A549	lung:	n/a
19	chr14:24977773-24977823	HRE	kidney:	n/a
20	chr14:24978681-24978731	GM19239	blood:	n/a
21	chr14:24974804-24974854	IMR90	lung:	fetal
22	chr14:24974804-24974854	GM06990	blood:	n/a
23	chr14:24978681-24978731	PANC-1	pancreas:	n/a
24	chr14:24974804-24974854	Caco-2	colon:	n/a
25	chr14:24977773-24977823	PrEC	prostate:	n/a
26	chr14:24974804-24974854	MCF10A-Er-Src	breast:	n/a
27	chr14:24974804-24974854	HEEpiC	esophagus:	n/a
28	chr14:24974804-24974854	AG09319	gingival:	n/a
29	chr14:24974804-24974854	ProgFib	skin:	n/a
30	chr14:24978681-24978731	HEK293	kidney:	embryo
31	chr14:24977773-24977823	ECC-1	luminal epithelium:	n/a
32	chr14:24978681-24978731	HMEC	breast:	n/a
33	chr14:24978681-24978731	NHBE	bronchial:	n/a
34	chr14:24974804-24974854	HNPCEpiC	eye:	n/a
35	chr14:24977773-24977823	HL-60	blood:	n/a
36	chr14:24974804-24974854	AG04450	lung:	fetal
37	chr14:24974804-24974854	RPTEC	kidney:	n/a
38	chr14:24978681-24978731	GM06990	blood:	n/a
39	chr14:24978681-24978731	SK-N-SH_RA	brain:	n/a
40	chr14:24977773-24977823	Jurkat	blood:	n/a
41	chr14:24977773-24977823	IMR90	lung:	fetal
42	chr14:24977773-24977823	HepG2	liver:	n/a
43	chr14:24977773-24977823	ProgFib	skin:	n/a
44	chr14:24974804-24974854	SKMC	muscle:	n/a
45	chr14:24977773-24977823	HAEpiC	amniotic membrane:	n/a
46	chr14:24974804-24974854	AoSMC	blood vessel:	n/a
47	chr14:24978681-24978731	GM12878	blood:	n/a
48	chr14:24978681-24978731	K562	blood:	n/a
49	chr14:24977773-24977823	AG10803	skin:	n/a
50	chr14:24974804-24974854	MCF-7	breast:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24950851..24951362-chr14:25074499..25075225,3	MCF-7	breast:
2	chr14:24910451..24913467-chr14:24926014..24930297,6	MCF-7	breast:
3	chr14:24911430..24913240-chr14:24948207..24950557,2	K562	blood:
4	chr14:24940138..24941029-chr14:24952690..24953556,3	MCF-7	breast:
5	chr14:24952643..24955226-chr14:24957985..24960918,2	K562	blood:
6	chr14:24960817..24963613-chr14:24965277..24968190,2	K562	blood:
7	chr14:24929358..24930887-chr8:102503029..102505102,2	MCF-7	breast:
8	chr14:24911704..24914258-chr14:24948506..24950947,2	MCF-7	breast:
9	chr14:24950446..24951536-chr14:25147799..25148973,31	MCF-7	breast:
10	chr14:24925537..24927679-chr14:24931012..24933705,2	MCF-7	breast:
11	chr14:24941879..24943792-chr14:24944086..24946470,2	MCF-7	breast:
12	chr14:24941879..24943792-chr14:24944086..24946470,2	MCF-7	breast:
13	chr14:24923545..24925251-chr14:24928583..24930504,2	MCF-7	breast:
14	chr14:24977730..24979918-chr14:24980024..24982313,2	MCF-7	breast:
15	chr14:24960817..24963613-chr14:24965277..24968190,2	K562	blood:
16	chr14:24940138..24941029-chr14:24952690..24953556,3	MCF-7	breast:
17	chr14:24977730..24979918-chr14:24980024..24982313,2	MCF-7	breast:
18	chr14:24952643..24955226-chr14:24957985..24960918,2	K562	blood:
19	chr14:24950901..24951428-chr14:25147948..25148704,2	K562	blood:
20	chr14:24950478..24951496-chr14:25147845..25148826,8	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
CMA1	TF binding region
ENSG00000258744	TF binding region
CMA1	CpG island
ENSG00000258744	CpG island
ENSG00000100445	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000254024	chromatin interactions
CYP2C8	miRNA target sites

Extended variants
information (count: 1774 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1774 , 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	rs543621316	chr14:24929452-24929453	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs1956892	chr14:24929481-24929482	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs111536428	chr14:24929532-24929533	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs544825582	chr14:24929548-24929549	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs151153841	chr14:24929549-24929550	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs141075707	chr14:24929554-24929555	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs1956891	chr14:24929564-24929565	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs371534469	chr14:24929579-24929580	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs149851932	chr14:24929639-24929640	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs75683693	chr14:24929640-24929641	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs116078555	chr14:24929647-24929648	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs8013354	chr14:24929648-24929649	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs543661616	chr14:24929708-24929709	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs74039010	chr14:24929715-24929716	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs75212143	chr14:24929748-24929749	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs147921928	chr14:24929749-24929750	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs541006821	chr14:24929765-24929766	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs190557812	chr14:24929768-24929769	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs549102240	chr14:24929777-24929778	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs192309930	chr14:24929786-24929787	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs563434305	chr14:24929787-24929788	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs547362958	chr14:24929789-24929790	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs4982924	chr14:24929798-24929799	Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs113033659	chr14:24929822-24929823	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs184373394	chr14:24929826-24929827	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs188678759	chr14:24929836-24929837	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs374270813	chr14:24929841-24929842	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs4982925	chr14:24929871-24929872	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs570651354	chr14:24929873-24929874	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs533211719	chr14:24929874-24929875	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs4982926	chr14:24929961-24929962	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs569885748	chr14:24929981-24929982	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs79635573	chr14:24930030-24930031	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs12884447	chr14:24930063-24930064	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs181156163	chr14:24930064-24930065	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs147096562	chr14:24930068-24930069	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs28692861	chr14:24930071-24930072	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs577824764	chr14:24930101-24930102	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs543498974	chr14:24930109-24930110	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs147693291	chr14:24930111-24930112	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs12882878	chr14:24930115-24930116	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs542783058	chr14:24930134-24930135	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs559433400	chr14:24930146-24930147	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs573081366	chr14:24930147-24930148	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs541032243	chr14:24930288-24930289	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs564100390	chr14:24930298-24930299	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs533266447	chr14:24930307-24930308	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs116206187	chr14:24930308-24930309	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs17104012	chr14:24930321-24930322	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs372720246	chr14:24930336-24930337	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	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:213 , 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	chr14:24913000-24930000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr14:24913000-24931600	Weak transcription	Fetal Kidney	kidney
4	chr14:24913000-24932400	Weak transcription	Primary B cells from cord blood	blood
5	chr14:24913000-24932800	Weak transcription	Primary T cells from cord blood	blood
6	chr14:24922200-24946000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr14:24922800-24951000	Weak transcription	Pancreas	Pancrea
8	chr14:24923200-24937400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr14:24923600-24932600	Weak transcription	Right Ventricle	heart
10	chr14:24924200-24932000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr14:24925200-24929600	Weak transcription	Fetal Stomach	stomach
12	chr14:24925800-24933400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr14:24926000-24936000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr14:24926400-24929600	Weak transcription	Aorta	Aorta
15	chr14:24926400-24930800	Weak transcription	Fetal Intestine Small	intestine
16	chr14:24926400-24934200	Weak transcription	Lung	lung
17	chr14:24926800-24929800	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr14:24927600-24930400	Weak transcription	Esophagus	oesophagus
19	chr14:24927600-24951000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:24928200-24934400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr14:24928200-24950400	Weak transcription	HepG2	liver
22	chr14:24928400-24936000	Weak transcription	Liver	Liver
23	chr14:24928600-24951000	Weak transcription	Placenta	Placenta
24	chr14:24928800-24951000	Weak transcription	Spleen	Spleen
25	chr14:24929600-24929800	ZNF genes & repeats	Aorta	Aorta
26	chr14:24929800-24932400	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr14:24929800-24934600	Weak transcription	Aorta	Aorta
28	chr14:24930200-24931200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr14:24930400-24930600	Enhancers	Esophagus	oesophagus
30	chr14:24930400-24930800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr14:24930600-24931200	Enhancers	HMEC	breast
32	chr14:24930600-24931200	Enhancers	NHEK	skin
33	chr14:24930800-24951000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr14:24932000-24933000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr14:24932200-24933000	Enhancers	GM12878-XiMat	blood
36	chr14:24932400-24936000	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr14:24932600-24935400	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr14:24932800-24933200	Enhancers	Fetal Thymus	thymus
39	chr14:24932800-24935000	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr14:24932800-24935400	Enhancers	Thymus	Thymus
41	chr14:24932800-24935600	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr14:24932800-24935800	Enhancers	Primary T cells from cord blood	blood
43	chr14:24933000-24933600	Flanking Active TSS	GM12878-XiMat	blood
44	chr14:24933000-24935200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr14:24933000-24935400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr14:24933000-24935600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr14:24933000-24951400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr14:24933200-24934400	Weak transcription	Fetal Thymus	thymus
49	chr14:24933200-24935600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr14:24933600-24934600	Enhancers	GM12878-XiMat	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links