Variant report

Variant	esv10993
Chromosome Location	chr1:214774207-214778763
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:631)
CpG islands
(count:855)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:631 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:214776193-214776604	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:214775385-214776694	K562	blood:	n/a	chr1:214776181-214776197
3	ATF1	chr1:214775849-214776633	K562	blood:	n/a	n/a
4	ATF2	chr1:214776112-214776528	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:214776092-214776570	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr1:214776187-214776471	K562	blood:	n/a	n/a
7	ATF3	chr1:214776040-214776750	A549	lung:	n/a	n/a
8	BACH1	chr1:214776810-214776944	K562	blood:	n/a	n/a
9	BCL3	chr1:214776022-214776582	A549	lung:	n/a	n/a
10	BCL3	chr1:214775803-214776680	A549	lung:	n/a	n/a
11	BHLHE40	chr1:214776157-214776612	HepG2	liver:	n/a	n/a
12	BHLHE40	chr1:214776180-214777012	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:214776025-214777003	K562	blood:	n/a	n/a
14	BRCA1	chr1:214776981-214777087	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr1:214776253-214776672	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr1:214776002-214776567	K562	blood:	n/a	n/a
17	CBX3	chr1:214775015-214775414	K562	blood:	n/a	n/a
18	CBX3	chr1:214775878-214777027	K562	blood:	n/a	n/a
19	CCNT2	chr1:214776206-214776787	K562	blood:	n/a	n/a
20	CEBPB	chr1:214775952-214776555	K562	blood:	n/a	n/a
21	CEBPB	chr1:214775923-214776457	K562	blood:	n/a	n/a
22	CEBPD	chr1:214775926-214776784	K562	blood:	n/a	n/a
23	CHD1	chr1:214776688-214777031	GM12878	blood:	n/a	n/a
24	CHD1	chr1:214776203-214776437	GM12878	blood:	n/a	n/a
25	CHD1	chr1:214776116-214777652	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr1:214776086-214776704	HepG2	liver:	n/a	n/a
27	CHD2	chr1:214776106-214777013	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr1:214776161-214776969	GM12878	blood:	n/a	n/a
29	CHD2	chr1:214776163-214776938	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr1:214777318-214777600	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr1:214775831-214777032	K562	blood:	n/a	n/a
32	CREB1	chr1:214776054-214776898	HepG2	liver:	n/a	n/a
33	CREB1	chr1:214776264-214776662	A549	lung:	n/a	n/a
34	CREB1	chr1:214776088-214776720	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr1:214776183-214776853	A549	lung:	n/a	n/a
36	CREB1	chr1:214776006-214776885	K562	blood:	n/a	n/a
37	CREB1	chr1:214775850-214776964	K562	blood:	n/a	n/a
38	CTCF	chr1:214776320-214776470	GM12871	blood:	n/a	n/a
39	CTCF	chr1:214776328-214776473	GM12892	blood:	n/a	n/a
40	CTCF	chr1:214776220-214776370	HMEC	breast:	n/a	n/a
41	CTCF	chr1:214776104-214776585	K562	blood:	n/a	n/a
42	CTCF	chr1:214776260-214776410	GM12866	blood:	n/a	n/a
43	CTCF	chr1:214776300-214776450	Caco-2	colon:	n/a	n/a
44	CTCF	chr1:214776320-214776470	GM12865	blood:	n/a	n/a
45	CTCF	chr1:214776260-214776410	GM12874	blood:	n/a	n/a
46	CTCF	chr1:214776317-214776434	ProgFib	skin:	n/a	n/a
47	CTCF	chr1:214776300-214776450	HMEC	breast:	n/a	n/a
48	CTCF	chr1:214776366-214776424	LNCaP	prostate:	n/a	n/a
49	CTCF	chr1:214776358-214776388	GM10266	blood:	n/a	n/a
50	CTCF	chr1:214776280-214776430	GM12865	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:214776613-214776663	Jurkat	blood:	n/a
2	chr1:214776613-214776663	Jurkat	blood:	n/a
3	chr1:214776453-214776503	AG10803	skin:	n/a
4	chr1:214776475-214776525	HCM	heart:	n/a
5	chr1:214776286-214776336	HRE	kidney:	n/a
6	chr1:214776304-214776354	GM06990	blood:	n/a
7	chr1:214776304-214776354	T-47D	breast:	n/a
8	chr1:214776469-214776519	AG09319	gingival:	n/a
9	chr1:214776469-214776519	HNPCEpiC	eye:	n/a
10	chr1:214776286-214776336	GM19239	blood:	n/a
11	chr1:214776469-214776519	HepG2	liver:	n/a
12	chr1:214776764-214776814	GM06990	blood:	n/a
13	chr1:214776613-214776663	BE2_C	brain:	n/a
14	chr1:214776286-214776336	ProgFib	skin:	n/a
15	chr1:214776469-214776519	NB4	blood:	n/a
16	chr1:214776326-214776376	HNPCEpiC	eye:	n/a
17	chr1:214776313-214776363	A549	lung:	n/a
18	chr1:214776477-214776527	SK-N-SH_RA	brain:	n/a
19	chr1:214776313-214776363	BE2_C	brain:	n/a
20	chr1:214776475-214776525	HepG2	liver:	n/a
21	chr1:214776475-214776525	LNCaP	prostate:	n/a
22	chr1:214777596-214777646	Caco-2	colon:	n/a
23	chr1:214776286-214776336	LNCaP	prostate:	n/a
24	chr1:214776764-214776814	HEK293	kidney:	embryo
25	chr1:214776475-214776525	SK-N-MC	brain:	n/a
26	chr1:214776613-214776663	GM12892	blood:	n/a
27	chr1:214776475-214776525	GM12892	blood:	n/a
28	chr1:214776469-214776519	HCF	heart:	n/a
29	chr1:214776286-214776336	PFSK-1	brain:	n/a
30	chr1:214776326-214776376	GM12878	blood:	n/a
31	chr1:214776790-214776840	HCPEpiC	choroid plexus:	n/a
32	chr1:214776313-214776363	AoSMC	blood vessel:	n/a
33	chr1:214776304-214776354	HRPEpiC	eye:	n/a
34	chr1:214776475-214776525	AG10803	skin:	n/a
35	chr1:214776790-214776840	PANC-1	pancreas:	n/a
36	chr1:214777596-214777646	BJ	skin:	n/a
37	chr1:214776477-214776527	HCT-116	colon:	n/a
38	chr1:214776286-214776336	A549	lung:	n/a
39	chr1:214776286-214776336	IMR90	lung:	fetal
40	chr1:214776304-214776354	HUVEC	blood vessel:	n/a
41	chr1:214776286-214776336	HCF	heart:	n/a
42	chr1:214776326-214776376	AoSMC	blood vessel:	n/a
43	chr1:214776613-214776663	NH-A	brain:	n/a
44	chr1:214776477-214776527	BE2_C	brain:	n/a
45	chr1:214776475-214776525	HMEC	breast:	n/a
46	chr1:214776790-214776840	HUVEC	blood vessel:	n/a
47	chr1:214776469-214776519	HRPEpiC	eye:	n/a
48	chr1:214776469-214776519	H1-hESC	embryonic stem cell:	embryo
49	chr1:214776613-214776663	PFSK-1	brain:	n/a
50	chr1:214777596-214777646	AG09309	skin:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:214777666..214779180-chr1:214780715..214782314,2	K562	blood:
2	chr1:214774784..214777425-chr1:214779446..214783969,6	K562	blood:
3	chr1:214723767..214726550-chr1:214774637..214776348,2	MCF-7	breast:
4	chr1:214773067..214775005-chr1:215239783..215241407,2	K562	blood:
5	chr1:214773497..214776791-chr1:214785798..214789572,5	K562	blood:
6	chr1:214452363..214455450-chr1:214775239..214777636,3	K562	blood:
7	chr1:214777011..214779791-chr1:214784551..214787409,3	K562	blood:

No data

Variant related genes	Relation type
CENPF	TF binding region
CENPF	CpG island
ENSG00000152104	chromatin interactions
ENSG00000143499	chromatin interactions
ENSG00000224584	chromatin interactions
ENSG00000250536	chromatin interactions

Extended variants
information (count: 145 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:145 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11120366	chr1:214774210-214774211	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186961517	chr1:214774212-214774213	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs191756269	chr1:214774290-214774291	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs561585583	chr1:214774395-214774396	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs11806558	chr1:214774522-214774523	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs544943544	chr1:214774565-214774566	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs563242025	chr1:214774634-214774635	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528881326	chr1:214774678-214774679	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs145139105	chr1:214774717-214774718	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs140607876	chr1:214774793-214774794	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs371580382	chr1:214774797-214774798	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs565765906	chr1:214774803-214774804	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs370811566	chr1:214774850-214774851	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs17792674	chr1:214774867-214774868	Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs571759156	chr1:214774904-214774905	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs571371648	chr1:214774912-214774913	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs536909356	chr1:214774913-214774914	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs149082959	chr1:214774975-214774976	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs183526975	chr1:214775039-214775040	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs536241392	chr1:214775053-214775054	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs553131869	chr1:214775067-214775068	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs112146178	chr1:214775085-214775086	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs144732943	chr1:214775097-214775098	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs76338942	chr1:214775116-214775117	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs61533924	chr1:214775172-214775173	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs141243208	chr1:214775195-214775196	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs141605957	chr1:214775234-214775235	Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs561545857	chr1:214775241-214775242	Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs145383273	chr1:214775247-214775248	Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs80000883	chr1:214775270-214775271	Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs147975556	chr1:214775317-214775318	Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs528158372	chr1:214775334-214775335	Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs551200380	chr1:214775364-214775365	Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs571042076	chr1:214775426-214775427	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs375688447	chr1:214775487-214775488	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs75049844	chr1:214775539-214775540	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs532388640	chr1:214775559-214775560	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs2362215	chr1:214775560-214775561	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs567212155	chr1:214775616-214775617	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs61820736	chr1:214775630-214775631	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs536165506	chr1:214775660-214775661	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs113322874	chr1:214775709-214775710	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs193214728	chr1:214775807-214775808	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs141655029	chr1:214775816-214775817	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs539089388	chr1:214775819-214775820	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs558768331	chr1:214775887-214775888	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs575838035	chr1:214775935-214775936	Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs565613080	chr1:214776057-214776058	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs185522269	chr1:214776097-214776098	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs150902681	chr1:214776112-214776113	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22522925	CNVD
Primary hepatocellular	22912832	CNVD

Chromatin state (count:464 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:214774200-214776000	Enhancers	HepG2	liver
2	chr1:214774600-214775400	Enhancers	A549	lung
3	chr1:214774800-214775400	Enhancers	K562	blood
4	chr1:214775200-214775600	Enhancers	Dnd41	blood
5	chr1:214775400-214775600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr1:214775400-214775600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr1:214775400-214775600	Flanking Active TSS	A549	lung
8	chr1:214775400-214775600	Enhancers	NHEK	skin
9	chr1:214775400-214775800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:214775400-214776000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr1:214775400-214776200	Flanking Active TSS	K562	blood
12	chr1:214775600-214775800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr1:214775600-214775800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr1:214775600-214775800	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr1:214775600-214775800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr1:214775600-214775800	Enhancers	Primary hematopoietic stem cells	blood
17	chr1:214775600-214775800	Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr1:214775600-214775800	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr1:214775600-214775800	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr1:214775600-214775800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr1:214775600-214775800	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr1:214775600-214775800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:214775600-214775800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:214775600-214775800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:214775600-214775800	Enhancers	Adipose Nuclei	Adipose
26	chr1:214775600-214775800	Enhancers	Fetal Kidney	kidney
27	chr1:214775600-214775800	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr1:214775600-214775800	Enhancers	Fetal Lung	lung
29	chr1:214775600-214775800	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr1:214775600-214775800	Enhancers	HMEC	breast
31	chr1:214775600-214775800	Enhancers	HUVEC	blood vessel
32	chr1:214775600-214775800	Enhancers	NHDF-Ad	bronchial
33	chr1:214775600-214776000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr1:214775600-214776000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
35	chr1:214775600-214776200	Flanking Active TSS	NHEK	skin
36	chr1:214775600-214776400	Flanking Active TSS	Dnd41	blood
37	chr1:214775600-214776800	Active TSS	Stomach Smooth Muscle	stomach
38	chr1:214775600-214777000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr1:214775600-214777200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:214775600-214777400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:214775600-214777800	Active TSS	A549	lung
42	chr1:214775800-214776000	Enhancers	H1 Cell Line	embryonic stem cell
43	chr1:214775800-214776000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr1:214775800-214776000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr1:214775800-214776000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr1:214775800-214776000	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr1:214775800-214776000	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr1:214775800-214776000	Enhancers	Primary B cells from peripheral blood	blood
49	chr1:214775800-214776000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr1:214775800-214776000	Enhancers	Primary T helper cells PMA-I stimulated	--

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