Variant report

Variant	nsv1014911
Chromosome Location	chr2:9863969-9905959
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:963)
CpG islands
(count:427)
Chromatin interactive
region (count:72)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:9905759-9906088	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:9903798-9904137	K562	blood:	n/a	n/a
3	ARID3A	chr2:9893333-9893592	K562	blood:	n/a	n/a
4	ATF1	chr2:9900214-9900455	K562	blood:	n/a	n/a
5	ATF1	chr2:9903764-9904095	K562	blood:	n/a	n/a
6	ATF2	chr2:9888714-9889291	GM12878	blood:	n/a	n/a
7	ATF2	chr2:9892636-9893134	GM12878	blood:	n/a	n/a
8	ATF2	chr2:9893214-9893700	GM12878	blood:	n/a	n/a
9	ATF2	chr2:9893195-9893756	GM12878	blood:	n/a	n/a
10	ATF3	chr2:9900151-9900484	K562	blood:	n/a	n/a
11	ATF3	chr2:9903763-9904096	K562	blood:	n/a	n/a
12	BACH1	chr2:9903801-9904037	K562	blood:	n/a	n/a
13	BATF	chr2:9894355-9894756	GM12878	blood:	n/a	n/a
14	BATF	chr2:9894384-9894701	GM12878	blood:	n/a	n/a
15	BATF	chr2:9893229-9893775	GM12878	blood:	n/a	chr2:9893467-9893478
16	BATF	chr2:9904505-9904797	GM12878	blood:	n/a	n/a
17	BATF	chr2:9878679-9879016	GM12878	blood:	n/a	n/a
18	BATF	chr2:9892661-9893121	GM12878	blood:	n/a	chr2:9892919-9892929
19	BATF	chr2:9893245-9893716	GM12878	blood:	n/a	chr2:9893467-9893478
20	BATF	chr2:9888898-9889202	GM12878	blood:	n/a	n/a
21	BCL11A	chr2:9893336-9893728	GM12878	blood:	n/a	chr2:9893680-9893689 chr2:9893462-9893471
22	BCL11A	chr2:9894435-9894704	GM12878	blood:	n/a	n/a
23	BCL11A	chr2:9892734-9893001	GM12878	blood:	n/a	n/a
24	BCL11A	chr2:9893330-9893647	GM12878	blood:	n/a	chr2:9893462-9893471
25	BCL3	chr2:9892544-9893897	A549	lung:	n/a	chr2:9893680-9893689 chr2:9893462-9893471
26	BCL3	chr2:9903767-9904068	GM12878	blood:	n/a	n/a
27	BCL3	chr2:9905927-9906348	GM12878	blood:	n/a	n/a
28	BCL3	chr2:9893294-9893744	GM12878	blood:	n/a	chr2:9893680-9893689 chr2:9893462-9893471
29	BCL3	chr2:9888749-9889158	GM12878	blood:	n/a	chr2:9889030-9889039
30	BCLAF1	chr2:9893172-9893750	GM12878	blood:	n/a	chr2:9893680-9893689 chr2:9893462-9893471
31	BCLAF1	chr2:9888734-9889132	GM12878	blood:	n/a	chr2:9889030-9889039
32	BHLHE40	chr2:9892878-9893025	K562	blood:	n/a	n/a
33	BHLHE40	chr2:9903883-9904364	K562	blood:	n/a	n/a
34	BHLHE40	chr2:9905808-9905961	K562	blood:	n/a	n/a
35	BHLHE40	chr2:9878527-9878675	GM12878	blood:	n/a	n/a
36	BHLHE40	chr2:9901609-9901903	K562	blood:	n/a	n/a
37	BHLHE40	chr2:9891187-9891237	GM12878	blood:	n/a	n/a
38	BHLHE40	chr2:9895509-9895538	K562	blood:	n/a	n/a
39	BHLHE40	chr2:9893245-9893765	K562	blood:	n/a	n/a
40	BHLHE40	chr2:9893321-9893742	GM12878	blood:	n/a	n/a
41	BHLHE40	chr2:9894360-9894794	GM12878	blood:	n/a	n/a
42	BRCA1	chr2:9880701-9881166	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr2:9892770-9893757	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr2:9874493-9874803	K562	blood:	n/a	n/a
45	CBX3	chr2:9900189-9900621	K562	blood:	n/a	n/a
46	CBX3	chr2:9874445-9874808	K562	blood:	n/a	n/a
47	CBX3	chr2:9893218-9893773	K562	blood:	n/a	n/a
48	CCNT2	chr2:9893424-9893678	K562	blood:	n/a	n/a
49	CCNT2	chr2:9903814-9904069	K562	blood:	n/a	n/a
50	CEBPB	chr2:9866931-9867150	Hela-S3	cervix:	n/a	chr2:9867008-9867019

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:9893528-9893578	SK-N-SH_RA	brain:	n/a
2	chr2:9865398-9865448	GM06990	blood:	n/a
3	chr2:9878816-9878866	HRPEpiC	eye:	n/a
4	chr2:9865398-9865448	HRPEpiC	eye:	n/a
5	chr2:9894335-9894385	PrEC	prostate:	n/a
6	chr2:9865398-9865448	ECC-1	luminal epithelium:	n/a
7	chr2:9894335-9894385	RPTEC	kidney:	n/a
8	chr2:9893528-9893578	AG04449	skin:	fetal
9	chr2:9893528-9893578	ovcar-3	ovarian:	n/a
10	chr2:9894335-9894385	AoSMC	blood vessel:	n/a
11	chr2:9893528-9893578	NT2-D1	testis:	n/a
12	chr2:9865477-9865527	PFSK-1	brain:	n/a
13	chr2:9865398-9865448	T-47D	breast:	n/a
14	chr2:9878816-9878866	A549	lung:	n/a
15	chr2:9893528-9893578	HEEpiC	esophagus:	n/a
16	chr2:9893528-9893578	AG09309	skin:	n/a
17	chr2:9865477-9865527	HCPEpiC	choroid plexus:	n/a
18	chr2:9865398-9865448	SK-N-MC	brain:	n/a
19	chr2:9894335-9894385	HRPEpiC	eye:	n/a
20	chr2:9865398-9865448	BJ	skin:	n/a
21	chr2:9893528-9893578	HIPEpiC	eye:	n/a
22	chr2:9865477-9865527	RPTEC	kidney:	n/a
23	chr2:9898228-9898278	AG10803	skin:	n/a
24	chr2:9893528-9893578	HL-60	blood:	n/a
25	chr2:9893528-9893578	HepG2	liver:	n/a
26	chr2:9865477-9865527	HL-60	blood:	n/a
27	chr2:9865477-9865527	K562	blood:	n/a
28	chr2:9865398-9865448	SKMC	muscle:	n/a
29	chr2:9898228-9898278	K562	blood:	n/a
30	chr2:9898228-9898278	HRCEpiC	kidney:	n/a
31	chr2:9865477-9865527	HCM	heart:	n/a
32	chr2:9894335-9894385	HCF	heart:	n/a
33	chr2:9878816-9878866	HCPEpiC	choroid plexus:	n/a
34	chr2:9865398-9865448	NH-A	brain:	n/a
35	chr2:9894335-9894385	HUVEC	blood vessel:	n/a
36	chr2:9865477-9865527	ProgFib	skin:	n/a
37	chr2:9865398-9865448	NT2-D1	testis:	n/a
38	chr2:9898228-9898278	NT2-D1	testis:	n/a
39	chr2:9878816-9878866	BJ	skin:	n/a
40	chr2:9893528-9893578	BE2_C	brain:	n/a
41	chr2:9865398-9865448	NHBE	bronchial:	n/a
42	chr2:9865398-9865448	HCM	heart:	n/a
43	chr2:9878816-9878866	Caco-2	colon:	n/a
44	chr2:9865477-9865527	BJ	skin:	n/a
45	chr2:9894335-9894385	IMR90	lung:	fetal
46	chr2:9878816-9878866	RPTEC	kidney:	n/a
47	chr2:9865398-9865448	AG04449	skin:	fetal
48	chr2:9894165-9894215	PrEC	prostate:	n/a
49	chr2:9878816-9878866	Jurkat	blood:	n/a
50	chr2:9898228-9898278	SKMC	muscle:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:9851071..9852686-chr2:9893395..9896154,2	K562	blood:
2	chr2:9843332..9845543-chr2:9887968..9890552,2	K562	blood:
3	chr2:9891910..9893733-chr2:9895279..9898420,3	MCF-7	breast:
4	chr2:9892015..9894940-chr2:9904744..9907619,3	K562	blood:
5	chr2:9883472..9885352-chr2:9885421..9887800,2	MCF-7	breast:
6	chr2:9780247..9783706-chr2:9899815..9903353,3	K562	blood:
7	chr2:9695083..9696978-chr2:9901909..9904289,2	K562	blood:
8	chr2:9881645..9885042-chr2:9886477..9889282,3	K562	blood:
9	chr2:9897831..9899412-chr2:9902196..9904626,2	MCF-7	breast:
10	chr2:9899081..9899639-chr3:43902591..43903091,2	MCF-7	breast:
11	chr2:9897830..9899713-chr2:9900837..9903744,2	K562	blood:
12	chr2:9772230..9774093-chr2:9892101..9894340,2	MCF-7	breast:
13	chr2:9845748..9848155-chr2:9867890..9870403,2	K562	blood:
14	chr2:9904753..9906453-chr2:9909403..9911953,2	MCF-7	breast:
15	chr2:9841151..9843890-chr2:9865033..9866985,2	K562	blood:
16	chr2:9881091..9883145-chr2:9887782..9890192,2	K562	blood:
17	chr2:9871478..9874528-chr2:9876144..9879356,3	K562	blood:
18	chr15:79058374..79058894-chr2:9877496..9878033,2	MCF-7	breast:
19	chr2:9893434..9894306-chr6:31619956..31620466,2	Hela-S3	cervix:
20	chr2:9842465..9843983-chr2:9901077..9903005,2	K562	blood:
21	chr2:9891163..9893022-chr2:9896031..9898454,2	K562	blood:
22	chr2:9769153..9773017-chr2:9899930..9902488,4	K562	blood:
23	chr2:9902911..9905269-chr2:9908747..9910675,2	K562	blood:
24	chr1:245493743..245494253-chr2:9877159..9877996,2	MCF-7	breast:
25	chr2:9877856..9880099-chr2:9889992..9892399,2	K562	blood:
26	chr2:9888046..9890254-chr2:9893584..9895138,2	K562	blood:
27	chr2:9694952..9697993-chr2:9876014..9878927,3	MCF-7	breast:
28	chr2:9892015..9895829-chr2:9904744..9907713,4	K562	blood:
29	chr2:9897831..9899412-chr2:9902196..9904626,2	MCF-7	breast:
30	chr2:9893059..9895633-chr2:9899321..9902671,3	K562	blood:
31	chr2:9877832..9879861-chr2:9884355..9886742,3	K562	blood:
32	chr2:9887703..9890322-chr2:9895249..9898241,2	MCF-7	breast:
33	chr2:9881091..9883145-chr2:9887782..9890192,2	K562	blood:
34	chr2:9891910..9893733-chr2:9895279..9898420,3	MCF-7	breast:
35	chr2:9870027..9872978-chr2:9873410..9875751,2	K562	blood:
36	chr2:9881447..9883906-chr2:9890191..9892636,2	MCF-7	breast:
37	chr2:9897830..9899713-chr2:9900837..9903744,2	K562	blood:
38	chr2:9877856..9880099-chr2:9889992..9892399,2	K562	blood:
39	chr2:9891163..9893022-chr2:9896031..9898454,2	K562	blood:
40	chr2:9901768..9906137-chr2:9907161..9912624,7	K562	blood:
41	chr2:9900453..9903358-chr2:9916510..9918074,2	K562	blood:
42	chr2:9881447..9883906-chr2:9890191..9892636,2	MCF-7	breast:
43	chr2:9870027..9872978-chr2:9873410..9875751,2	K562	blood:
44	chr2:9877764..9878356-chr9:21674606..21675106,2	Hela-S3	cervix:
45	chr2:9845674..9847302-chr2:9868513..9870809,2	MCF-7	breast:
46	chr2:9892798..9893661-chr3:149530498..149531325,2	Hela-S3	cervix:
47	chr2:9892015..9894940-chr2:9904744..9907619,3	K562	blood:
48	chr2:9877830..9880619-chr2:9884575..9886353,2	MCF-7	breast:
49	chr2:9888046..9890254-chr2:9893584..9895138,2	K562	blood:
50	chr2:9769789..9771364-chr2:9892124..9894482,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-YWHAQ-1	chr2:9897625-9899428	XLOC_001982

No data

Variant related genes	Relation type
ENSG00000240960	TF binding region
RNU4-73P	TF binding region
ENSG00000240960	CpG island
RNU4-73P	CpG island
ENSG00000134308	chromatin interactions
ENSG00000243491	chromatin interactions
ENSG00000271855	chromatin interactions
ENSG00000240960	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000082996	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000180628	chromatin interactions
ENSG00000151694	chromatin interactions

Extended variants
information (count: 1910 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1910 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12466375	chr2:9863969-9863970	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73152934	chr2:9864055-9864056	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs78921586	chr2:9864121-9864122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572423574	chr2:9864144-9864145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142522730	chr2:9864145-9864146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73152935	chr2:9864157-9864158	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs150517355	chr2:9864170-9864171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73152940	chr2:9864182-9864183	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs563380987	chr2:9864202-9864203	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs532348438	chr2:9864207-9864208	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs73152941	chr2:9864220-9864221	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs559046119	chr2:9864223-9864224	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs139508728	chr2:9864225-9864226	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs73913179	chr2:9864307-9864308	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs571398851	chr2:9864312-9864313	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs118046039	chr2:9864326-9864327	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs377450563	chr2:9864331-9864332	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs536590763	chr2:9864335-9864336	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs73152943	chr2:9864349-9864350	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs537157209	chr2:9864367-9864368	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs570108941	chr2:9864391-9864392	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs11695437	chr2:9864392-9864393	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs146725632	chr2:9864418-9864419	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs377318405	chr2:9864429-9864430	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs534998214	chr2:9864460-9864461	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs567759359	chr2:9864492-9864493	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs555030022	chr2:9864498-9864499	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs73152945	chr2:9864501-9864502	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs543390634	chr2:9864541-9864542	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs372647225	chr2:9864558-9864559	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs576938121	chr2:9864568-9864569	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs189959556	chr2:9864579-9864580	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs192657737	chr2:9864588-9864589	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs184743150	chr2:9864687-9864688	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140345025	chr2:9864697-9864698	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561570639	chr2:9864713-9864714	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs188236767	chr2:9864726-9864727	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550159473	chr2:9864739-9864740	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs113683238	chr2:9864766-9864767	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs111738807	chr2:9864771-9864772	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs116389828	chr2:9864783-9864784	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs114447480	chr2:9864796-9864797	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs180677980	chr2:9864878-9864879	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73152946	chr2:9864881-9864882	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs144129861	chr2:9864889-9864890	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76698717	chr2:9864892-9864893	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs76901261	chr2:9864920-9864921	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556945316	chr2:9864945-9864946	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186287030	chr2:9864976-9864977	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545572295	chr2:9864979-9864980	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Neuroblastoma	18923524	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1334 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:9861800-9864200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:9864200-9865000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:9864600-9865200	Enhancers	Esophagus	oesophagus
4	chr2:9865000-9865200	Bivalent Enhancer	HepG2	liver
5	chr2:9865200-9865400	Flanking Bivalent TSS/Enh	HepG2	liver
6	chr2:9865200-9865600	Enhancers	Duodenum Mucosa	Duodenum
7	chr2:9865200-9868200	Weak transcription	Esophagus	oesophagus
8	chr2:9865400-9865600	Bivalent Enhancer	HepG2	liver
9	chr2:9865600-9867200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr2:9866600-9867400	Enhancers	Fetal Intestine Large	intestine
11	chr2:9866600-9867400	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr2:9867000-9867600	Enhancers	Fetal Intestine Small	intestine
13	chr2:9867200-9867400	Enhancers	Duodenum Mucosa	Duodenum
14	chr2:9868000-9869400	Enhancers	Brain Germinal Matrix	brain
15	chr2:9868400-9868800	Enhancers	Fetal Brain Male	brain
16	chr2:9868400-9869000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr2:9868400-9869200	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr2:9868400-9869600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:9868800-9870400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr2:9869000-9869600	Enhancers	NHEK	skin
21	chr2:9869400-9869600	Enhancers	Fetal Thymus	thymus
22	chr2:9869400-9869800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:9869400-9870000	Enhancers	Primary T cells from cord blood	blood
24	chr2:9869600-9875800	Weak transcription	Fetal Thymus	thymus
25	chr2:9869800-9870400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr2:9869800-9871200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr2:9870000-9870400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr2:9870000-9870400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr2:9870400-9870600	Bivalent Enhancer	K562	blood
30	chr2:9870400-9870800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr2:9870400-9870800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr2:9870600-9870800	Enhancers	K562	blood
33	chr2:9871400-9871600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr2:9875000-9879200	Enhancers	Primary T cells fromperipheralblood	blood
35	chr2:9875000-9879200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr2:9875000-9879400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr2:9875000-9879400	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr2:9875200-9876800	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr2:9875200-9877400	Enhancers	HMEC	breast
40	chr2:9875200-9877600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr2:9875200-9877600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
42	chr2:9875200-9877800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr2:9875200-9878800	Weak transcription	Colon Smooth Muscle	Colon
44	chr2:9875200-9879000	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr2:9875200-9879000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr2:9875200-9879000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr2:9875200-9879000	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr2:9875200-9879400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr2:9875200-9879400	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr2:9875400-9879000	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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