Variant report

Variant	nsv563854
Chromosome Location	chr14:22391433-22393388
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	CTCF	chr14:22392827-22392955	MCF-7	breast:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
2	CTCF	chr14:22392780-22392930	GM12868	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
3	CTCF	chr14:22392720-22392870	NHEK	skin:	n/a	n/a
4	CTCF	chr14:22392800-22392950	GM12869	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
5	CTCF	chr14:22392840-22392990	GM12872	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
6	CTCF	chr14:22392829-22392947	MCF-7	breast:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
7	CTCF	chr14:22392780-22392930	Caco-2	colon:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
8	CTCF	chr14:22392800-22392981	GM12892	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
9	CTCF	chr14:22392760-22392910	GM12871	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
10	CTCF	chr14:22392860-22393010	HBMEC	blood vessel:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
11	CTCF	chr14:22392825-22392971	MCF-7	breast:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
12	CTCF	chr14:22392824-22392942	GM12891	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
13	CTCF	chr14:22392780-22392930	GM12875	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
14	CTCF	chr14:22392834-22392921	MCF-7	breast:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
15	CTCF	chr14:22392800-22392950	GM12864	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
16	CTCF	chr14:22392800-22392950	GM12873	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
17	CTCF	chr14:22392840-22392990	GM12870	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
18	CTCF	chr14:22392800-22392950	GM12868	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
19	CTCF	chr14:22392780-22392930	GM12872	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
20	CTCF	chr14:22392760-22392910	GM12864	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
21	CTCF	chr14:22392740-22392890	HepG2	liver:	n/a	n/a
22	CTCF	chr14:22392680-22392830	A549	lung:	n/a	n/a
23	CTCF	chr14:22392800-22392950	GM12865	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
24	CTCF	chr14:22392840-22392990	Caco-2	colon:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
25	CTCF	chr14:22392820-22392970	GM12872	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
26	CTCF	chr14:22392840-22392987	GM12878	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
27	CTCF	chr14:22392820-22392970	GM12871	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
28	CTCF	chr14:22392780-22392930	GM12866	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
29	CTCF	chr14:22392780-22392930	GM12873	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
30	CTCF	chr14:22392820-22392970	GM12869	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
31	CTCF	chr14:22392800-22392950	HUVEC	blood vessel:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
32	CTCF	chr14:22392826-22392984	Spleen_OC	spleen:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
33	CTCF	chr14:22392820-22392970	HEK293	kidney:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
34	CTCF	chr14:22392720-22392870	GM06990	blood:	n/a	n/a
35	CTCF	chr14:22392880-22393030	GM06990	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901
36	CTCF	chr14:22392772-22392992	GM19238	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
37	CTCF	chr14:22392832-22392959	MCF-7	breast:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
38	CTCF	chr14:22392813-22392956	H1-hESC	embryonic stem cell:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
39	CTCF	chr14:22392827-22392905	HepG2	liver:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
40	CTCF	chr14:22392831-22392955	GM19239	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
41	CTCF	chr14:22392840-22392990	GM12867	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
42	CTCF	chr14:22392700-22392850	GM12867	blood:	n/a	n/a
43	CTCF	chr14:22392847-22392972	GM19240	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
44	CTCF	chr14:22392820-22392970	GM12875	blood:	n/a	chr14:22392890-22392898 chr14:22392883-22392901 chr14:22392878-22392899
45	E2F6	chr14:22392752-22393106	H1-hESC	embryonic stem cell:	n/a	chr14:22392908-22392915 chr14:22392907-22392916 chr14:22392904-22392916 chr14:22392908-22392915 chr14:22392908-22392915
46	E2F6	chr14:22392816-22392951	K562	blood:	n/a	chr14:22392908-22392915 chr14:22392907-22392916 chr14:22392904-22392916 chr14:22392908-22392915 chr14:22392908-22392915
47	E2F6	chr14:22392783-22393171	H1-hESC	embryonic stem cell:	n/a	chr14:22392908-22392915 chr14:22392907-22392916 chr14:22392904-22392916 chr14:22392908-22392915 chr14:22392908-22392915
48	EBF1	chr14:22392831-22392955	GM12878	blood:	n/a	chr14:22392863-22392874
49	EBF1	chr14:22392721-22393005	GM12878	blood:	n/a	chr14:22392863-22392874
50	EBF1	chr14:22392721-22392999	GM12878	blood:	n/a	chr14:22392863-22392874

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22392573-22392623	PANC-1	pancreas:	n/a
2	chr14:22392573-22392623	HEEpiC	esophagus:	n/a
3	chr14:22392573-22392623	AoSMC	blood vessel:	n/a
4	chr14:22392573-22392623	PFSK-1	brain:	n/a
5	chr14:22392573-22392623	GM12891	blood:	n/a
6	chr14:22392573-22392623	GM12878	blood:	n/a
7	chr14:22392573-22392623	HepG2	liver:	n/a
8	chr14:22392573-22392623	SK-N-MC	brain:	n/a
9	chr14:22392573-22392623	PrEC	prostate:	n/a
10	chr14:22392573-22392623	HRCEpiC	kidney:	n/a
11	chr14:22392573-22392623	AG09319	gingival:	n/a
12	chr14:22392573-22392623	HMEC	breast:	n/a
13	chr14:22392573-22392623	ECC-1	luminal epithelium:	n/a
14	chr14:22392573-22392623	NT2-D1	testis:	n/a
15	chr14:22392573-22392623	AG04449	skin:	fetal
16	chr14:22392573-22392623	U87	brain:	n/a
17	chr14:22392573-22392623	T-47D	breast:	n/a
18	chr14:22392573-22392623	A549	lung:	n/a
19	chr14:22392573-22392623	RPTEC	kidney:	n/a
20	chr14:22392573-22392623	SAEC	small airway:	n/a
21	chr14:22392573-22392623	HCM	heart:	n/a
22	chr14:22392573-22392623	BE2_C	brain:	n/a
23	chr14:22392573-22392623	H1-hESC	embryonic stem cell:	embryo
24	chr14:22392573-22392623	NHDF-neo	bronchial:	n/a
25	chr14:22392573-22392623	HL-60	blood:	n/a
26	chr14:22392573-22392623	NB4	blood:	n/a
27	chr14:22392573-22392623	MCF10A-Er-Src	breast:	n/a
28	chr14:22392573-22392623	ProgFib	skin:	n/a
29	chr14:22392573-22392623	Hela-S3	cervix:	n/a
30	chr14:22392573-22392623	CMK	blood:	n/a
31	chr14:22392573-22392623	GM12892	blood:	n/a
32	chr14:22392573-22392623	ovcar-3	ovarian:	n/a
33	chr14:22392573-22392623	HCPEpiC	choroid plexus:	n/a
34	chr14:22392573-22392623	BJ	skin:	n/a
35	chr14:22392573-22392623	LNCaP	prostate:	n/a
36	chr14:22392573-22392623	AG09309	skin:	n/a
37	chr14:22392573-22392623	HAEpiC	amniotic membrane:	n/a
38	chr14:22392573-22392623	HIPEpiC	eye:	n/a
39	chr14:22392573-22392623	HNPCEpiC	eye:	n/a
40	chr14:22392573-22392623	NH-A	brain:	n/a
41	chr14:22392573-22392623	NHBE	bronchial:	n/a
42	chr14:22392573-22392623	AG04450	lung:	fetal
43	chr14:22392573-22392623	HEK293	kidney:	embryo
44	chr14:22392573-22392623	K562	blood:	n/a
45	chr14:22392573-22392623	AG10803	skin:	n/a
46	chr14:22392573-22392623	HUVEC	blood vessel:	n/a
47	chr14:22392573-22392623	HCT-116	colon:	n/a
48	chr14:22392573-22392623	HRPEpiC	eye:	n/a
49	chr14:22392573-22392623	GM19239	blood:	n/a
50	chr14:22392573-22392623	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:22384435..22387181-chr14:22391820..22393820,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AE000662.92.1-10	chr14:22392628-22392831	NONHSAT035716
2	lnc-AE000662.92.1-10	chr14:22392662-22392811	NONHSAT035718
3	lnc-AE000662.92.1-10	chr14:22392607-22392811	NONHSAT035715
4	lnc-AE000662.92.1-10	chr14:22392658-22392811	NONHSAT035717

Variant related genes	Relation type
TRAV14DV4	TF binding region
TRAV14DV4	CpG island
ENSG00000211791	chromatin interactions

Extended variants
information (count: 119 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:119 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs723879	chr14:22391433-22391434	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537453382	chr14:22391438-22391439	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs567466245	chr14:22391459-22391460	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs74035430	chr14:22391461-22391462	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs147105898	chr14:22391475-22391476	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs148092102	chr14:22391484-22391485	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs573064617	chr14:22391485-22391486	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs189632503	chr14:22391499-22391500	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs557809151	chr14:22391504-22391505	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs193014939	chr14:22391509-22391510	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs536015356	chr14:22391512-22391513	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs530481689	chr14:22391516-22391517	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs723880	chr14:22391539-22391540	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs528898160	chr14:22391573-22391574	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs185207007	chr14:22391580-22391581	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs559719225	chr14:22391591-22391592	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs528274267	chr14:22391637-22391638	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs145699418	chr14:22391643-22391644	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs189705029	chr14:22391714-22391715	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs563895822	chr14:22391721-22391722	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs140909939	chr14:22391725-22391726	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs530872061	chr14:22391757-22391758	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs181202289	chr14:22391762-22391763	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs150220866	chr14:22391784-22391785	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs12434370	chr14:22391790-22391791	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185607738	chr14:22391836-22391837	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188122397	chr14:22391840-22391841	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs138844845	chr14:22391888-22391889	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs377472835	chr14:22391926-22391927	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs115398891	chr14:22391928-22391929	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs575804213	chr14:22391949-22391950	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs142037113	chr14:22391970-22391971	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs557036810	chr14:22391995-22391996	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs181020796	chr14:22392009-22392010	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs542673679	chr14:22392033-22392034	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs559682548	chr14:22392046-22392047	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs28583314	chr14:22392142-22392143	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs34663669	chr14:22392185-22392186	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs564885969	chr14:22392207-22392208	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs528694366	chr14:22392234-22392235	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs17182937	chr14:22392250-22392251	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs117602924	chr14:22392257-22392258	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs28501628	chr14:22392283-22392284	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs530012256	chr14:22392284-22392285	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546633543	chr14:22392285-22392286	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs34365759	chr14:22392304-22392305	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs33998628	chr14:22392312-22392313	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs376381841	chr14:22392314-22392315	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs552837149	chr14:22392343-22392344	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs369000440	chr14:22392347-22392348	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	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
Developmental delay	21147756	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
Barrett''s syndrome	19417022	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22387000-22392000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
2	chr14:22387200-22391600	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr14:22389200-22395200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr14:22390200-22392200	Enhancers	Primary T cells from cord blood	blood
5	chr14:22390200-22392200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
6	chr14:22390200-22392600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr14:22390400-22392000	Enhancers	Primary B cells from cord blood	blood
8	chr14:22390400-22392200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr14:22390800-22392200	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr14:22391000-22391800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr14:22391000-22392200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr14:22391000-22392400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr14:22391200-22392200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr14:22391200-22392400	Enhancers	Primary B cells from peripheral blood	blood
15	chr14:22391200-22392400	Enhancers	Primary hematopoietic stem cells	blood
16	chr14:22391200-22392400	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr14:22391200-22392400	Enhancers	Dnd41	blood
18	chr14:22391400-22392200	Enhancers	Primary T cells fromperipheralblood	blood
19	chr14:22391400-22392200	Enhancers	Thymus	Thymus
20	chr14:22391400-22392400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr14:22391400-22392400	Enhancers	Fetal Thymus	thymus
22	chr14:22391400-22392600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr14:22391400-22393200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
24	chr14:22391400-22393400	Enhancers	HUVEC	blood vessel
25	chr14:22391600-22392800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
26	chr14:22391800-22393200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr14:22392000-22392800	Flanking Active TSS	Primary B cells from cord blood	blood
28	chr14:22392000-22392800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
29	chr14:22392000-22393000	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr14:22392200-22392600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
31	chr14:22392200-22392800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
32	chr14:22392200-22392800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
33	chr14:22392200-22392800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr14:22392200-22392800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
35	chr14:22392200-22393000	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr14:22392200-22393000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
37	chr14:22392200-22393000	Flanking Active TSS	Thymus	Thymus
38	chr14:22392200-22393200	Flanking Active TSS	Primary T cells from cord blood	blood
39	chr14:22392400-22392800	Flanking Active TSS	Primary B cells from peripheral blood	blood
40	chr14:22392400-22392800	Flanking Active TSS	Primary hematopoietic stem cells	blood
41	chr14:22392400-22392800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
42	chr14:22392400-22392800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
43	chr14:22392400-22392800	Flanking Active TSS	Fetal Thymus	thymus
44	chr14:22392400-22392800	Flanking Active TSS	Dnd41	blood
45	chr14:22392400-22393000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr14:22392400-22393000	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr14:22392600-22392800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr14:22392600-22393000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr14:22392600-22394200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr14:22392800-22393600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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