Variant report

Variant	nsv1032667
Chromosome Location	chr9:2691667-2788242
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:797)
CpG islands
(count:733)
Chromatin interactive
region (count:20)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:2720014-2720751	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:2748593-2748730	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:2728099-2728328	K562	blood:	n/a	n/a
4	ARID3A	chr9:2749640-2749746	K562	blood:	n/a	n/a
5	ARID3A	chr9:2728083-2728402	HepG2	liver:	n/a	n/a
6	ATF1	chr9:2744096-2744412	K562	blood:	n/a	n/a
7	ATF1	chr9:2727987-2728385	K562	blood:	n/a	n/a
8	ATF2	chr9:2727920-2728426	GM12878	blood:	n/a	n/a
9	ATF2	chr9:2727983-2728444	GM12878	blood:	n/a	n/a
10	ATF3	chr9:2728084-2728311	K562	blood:	n/a	n/a
11	ATF3	chr9:2722681-2723102	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr9:2728063-2728376	HepG2	liver:	n/a	n/a
13	BHLHE40	chr9:2739889-2740087	GM12878	blood:	n/a	n/a
14	BHLHE40	chr9:2728009-2728483	GM12878	blood:	n/a	n/a
15	BHLHE40	chr9:2697445-2697801	GM12878	blood:	n/a	n/a
16	CCNT2	chr9:2771209-2771469	K562	blood:	n/a	n/a
17	CEBPB	chr9:2741880-2742130	A549	lung:	n/a	n/a
18	CEBPB	chr9:2771535-2772078	IMR90	lung:	n/a	chr9:2771591-2771604 chr9:2771593-2771604 chr9:2771901-2771912
19	CEBPB	chr9:2753133-2753460	IMR90	lung:	n/a	chr9:2753291-2753302
20	CEBPB	chr9:2771723-2772062	Hela-S3	cervix:	n/a	chr9:2771901-2771912
21	CEBPB	chr9:2771749-2772036	A549	lung:	n/a	chr9:2771901-2771912
22	CEBPB	chr9:2741817-2742144	HepG2	liver:	n/a	n/a
23	CEBPB	chr9:2741817-2742153	IMR90	lung:	n/a	n/a
24	CEBPB	chr9:2728004-2728344	K562	blood:	n/a	n/a
25	CEBPB	chr9:2728041-2728345	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:2720040-2720343	HepG2	liver:	n/a	n/a
27	CEBPB	chr9:2753145-2753435	K562	blood:	n/a	chr9:2753291-2753302
28	CEBPB	chr9:2763182-2763426	HepG2	liver:	n/a	chr9:2763309-2763320
29	CEBPB	chr9:2763266-2763398	K562	blood:	n/a	chr9:2763309-2763320
30	CEBPB	chr9:2715391-2715602	A549	lung:	n/a	chr9:2715565-2715576
31	CEBPB	chr9:2753142-2753466	HepG2	liver:	n/a	chr9:2753291-2753302
32	CEBPB	chr9:2753200-2753436	A549	lung:	n/a	chr9:2753291-2753302
33	CEBPB	chr9:2715500-2715698	HepG2	liver:	n/a	chr9:2715565-2715576
34	CEBPB	chr9:2741829-2742119	K562	blood:	n/a	n/a
35	CEBPB	chr9:2787057-2787431	IMR90	lung:	n/a	n/a
36	CEBPB	chr9:2701690-2701947	H1-hESC	embryonic stem cell:	n/a	chr9:2701846-2701859
37	CHD2	chr9:2697629-2697756	GM12878	blood:	n/a	n/a
38	CTCF	chr9:2728151-2728395	GM19239	blood:	n/a	n/a
39	CTCF	chr9:2728149-2728399	GM10248	blood:	n/a	n/a
40	CTCF	chr9:2748600-2748750	GM12872	blood:	n/a	n/a
41	CTCF	chr9:2728200-2728350	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr9:2728009-2728468	HCT-116	colon:	n/a	n/a
43	CTCF	chr9:2728200-2728350	GM06990	blood:	n/a	n/a
44	CTCF	chr9:2739200-2739350	Caco-2	colon:	n/a	n/a
45	CTCF	chr9:2748647-2748746	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr9:2739140-2739290	SAEC	small airway:	n/a	n/a
47	CTCF	chr9:2728025-2728505	GM12878	blood:	n/a	n/a
48	CTCF	chr9:2728039-2728455	T-47D	breast:	n/a	n/a
49	CTCF	chr9:2728133-2728428	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr9:2728178-2728371	GM12892	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2717146-2717196	GM12878	blood:	n/a
2	chr9:2717146-2717196	GM12878	blood:	n/a
3	chr9:2718456-2718506	LNCaP	prostate:	n/a
4	chr9:2717531-2717581	GM12878	blood:	n/a
5	chr9:2717946-2717996	HepG2	liver:	n/a
6	chr9:2717946-2717996	HIPEpiC	eye:	n/a
7	chr9:2718952-2719002	BJ	skin:	n/a
8	chr9:2718456-2718506	Hepatocyte	liver:	n/a
9	chr9:2718952-2719002	GM12878	blood:	n/a
10	chr9:2717531-2717581	A549	lung:	n/a
11	chr9:2726670-2726720	HEEpiC	esophagus:	n/a
12	chr9:2700667-2700717	ovcar-3	ovarian:	n/a
13	chr9:2700667-2700717	U87	brain:	n/a
14	chr9:2715487-2715537	GM06990	blood:	n/a
15	chr9:2717621-2717671	HRE	kidney:	n/a
16	chr9:2717146-2717196	GM19239	blood:	n/a
17	chr9:2717146-2717196	AG04450	lung:	fetal
18	chr9:2717946-2717996	HL-60	blood:	n/a
19	chr9:2717946-2717996	HRPEpiC	eye:	n/a
20	chr9:2717621-2717671	HepG2	liver:	n/a
21	chr9:2717338-2717388	ovcar-3	ovarian:	n/a
22	chr9:2717621-2717671	NT2-D1	testis:	n/a
23	chr9:2715487-2715537	SKMC	muscle:	n/a
24	chr9:2718738-2718788	HEEpiC	esophagus:	n/a
25	chr9:2718456-2718506	AoSMC	blood vessel:	n/a
26	chr9:2717338-2717388	PANC-1	pancreas:	n/a
27	chr9:2717621-2717671	HRCEpiC	kidney:	n/a
28	chr9:2718738-2718788	H1-hESC	embryonic stem cell:	embryo
29	chr9:2717146-2717196	IMR90	lung:	fetal
30	chr9:2717146-2717196	NHDF-neo	bronchial:	n/a
31	chr9:2717338-2717388	A549	lung:	n/a
32	chr9:2717146-2717196	HCF	heart:	n/a
33	chr9:2715487-2715537	T-47D	breast:	n/a
34	chr9:2718456-2718506	AG09309	skin:	n/a
35	chr9:2717946-2717996	NT2-D1	testis:	n/a
36	chr9:2717325-2717375	HRPEpiC	eye:	n/a
37	chr9:2718738-2718788	AoSMC	blood vessel:	n/a
38	chr9:2717146-2717196	SAEC	small airway:	n/a
39	chr9:2718738-2718788	ProgFib	skin:	n/a
40	chr9:2700667-2700717	NHDF-neo	bronchial:	n/a
41	chr9:2718738-2718788	NH-A	brain:	n/a
42	chr9:2700667-2700717	GM12891	blood:	n/a
43	chr9:2717946-2717996	MCF-7	breast:	n/a
44	chr9:2700667-2700717	SK-N-MC	brain:	n/a
45	chr9:2718456-2718506	AG09319	gingival:	n/a
46	chr9:2700667-2700717	HRCEpiC	kidney:	n/a
47	chr9:2718738-2718788	GM12891	blood:	n/a
48	chr9:2700667-2700717	GM06990	blood:	n/a
49	chr9:2726670-2726720	HNPCEpiC	eye:	n/a
50	chr9:2717621-2717671	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:2697672..2699456-chr9:2700934..2702755,2	MCF-7	breast:
2	chr9:2787135..2789034-chr9:2791407..2793364,2	K562	blood:
3	chr9:2748687..2751294-chr9:2757879..2760318,3	MCF-7	breast:
4	chr9:2321723..2322570-chr9:2728160..2728820,2	MCF-7	breast:
5	chr9:2729748..2733202-chr9:2733269..2736748,3	MCF-7	breast:
6	chr9:2739072..2739783-chr9:2800448..2801064,2	MCF-7	breast:
7	chr9:2708882..2710546-chr9:2712571..2714429,2	K562	blood:
8	chr9:2335749..2336338-chr9:2727775..2728597,3	MCF-7	breast:
9	chr9:2758593..2762360-chr9:2765303..2768910,5	K562	blood:
10	chr9:2748687..2751294-chr9:2757879..2760318,3	MCF-7	breast:
11	chr9:2767181..2768946-chr9:2770729..2772819,2	K562	blood:
12	chr9:2767181..2768946-chr9:2770729..2772819,2	K562	blood:
13	chr9:2695521..2698232-chr9:3222806..3225730,2	K562	blood:
14	chr9:2717251..2720244-chr9:2720440..2722938,2	MCF-7	breast:
15	chr9:2729748..2733202-chr9:2733269..2736748,3	MCF-7	breast:
16	chr9:2776529..2778337-chr9:2809907..2812711,2	K562	blood:
17	chr9:2697672..2699456-chr9:2700934..2702755,2	MCF-7	breast:
18	chr9:2708882..2710546-chr9:2712571..2714429,2	K562	blood:
19	chr9:2758593..2762360-chr9:2765303..2768910,5	K562	blood:
20	chr9:2787061..2789950-chr9:2798613..2800282,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA0020-4	chr9:2704045-2704737	NONHSAT130005
2	lnc-KCNV2-4	chr9:2763773-2763907	NONHSAT130009
3	lnc-KCNV2-4	chr9:2769007-2769707	NONHSAT130009
4	lnc-RFX3-3	chr9:2783674-2784301	NONHSAT130010
5	lnc-RFX3-3	chr9:2783604-2783616	NONHSAT130010
6	lnc-RFX3-3	chr9:2785525-2786518	NONHSAT130010
7	lnc-RFX3-3	chr9:2779834-2780490	NONHSAT130010
8	lnc-KCNV2-4	chr9:2770480-2771317	NONHSAT130009
9	lnc-RFX3-4	chr9:2759256-2760832	NONHSAT130008
10	lnc-KIAA0020-4	chr9:2697878-2698075	NONHSAT130005
11	lnc-KIAA0020-4	chr9:2700367-2700587	NONHSAT130005

No data

Variant related genes	Relation type
KCNV2	TF binding region
KCNV2	CpG island
ENSG00000168263	chromatin interactions

Extended variants
information (count: 5106 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:5106 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10122524	chr9:2691667-2691668	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547968429	chr9:2691686-2691687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78079285	chr9:2691695-2691696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75276731	chr9:2691696-2691697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536515833	chr9:2691743-2691744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142095881	chr9:2691749-2691750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527709461	chr9:2691766-2691767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547866693	chr9:2691799-2691800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150750810	chr9:2691800-2691801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139107821	chr9:2691832-2691833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570946827	chr9:2691846-2691847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188921355	chr9:2691862-2691863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540731962	chr9:2691895-2691896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554316724	chr9:2691933-2691934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10122587	chr9:2691951-2691952	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs145010955	chr9:2691975-2691976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568989278	chr9:2692019-2692020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563630852	chr9:2692038-2692039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7864223	chr9:2692069-2692070	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs193270427	chr9:2692080-2692081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76732515	chr9:2692100-2692101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547932169	chr9:2692110-2692111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144930855	chr9:2692132-2692133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145793461	chr9:2692162-2692163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550185741	chr9:2692169-2692170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570368915	chr9:2692195-2692196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538973591	chr9:2692208-2692209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551710693	chr9:2692212-2692213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565360079	chr9:2692243-2692244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534381927	chr9:2692265-2692266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148985759	chr9:2692288-2692289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184204581	chr9:2692311-2692312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533551916	chr9:2692313-2692314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537301580	chr9:2692317-2692318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374751287	chr9:2692320-2692321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143696729	chr9:2692326-2692327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189468395	chr9:2692347-2692348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11788193	chr9:2692393-2692394	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs111378947	chr9:2692397-2692398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572488011	chr9:2692402-2692403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541520625	chr9:2692405-2692406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576529035	chr9:2692423-2692424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530227897	chr9:2692448-2692449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539175116	chr9:2692468-2692469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2375982	chr9:2692473-2692474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181119945	chr9:2692530-2692531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563733366	chr9:2692536-2692537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532639971	chr9:2692552-2692553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184334265	chr9:2692572-2692573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565323400	chr9:2692577-2692578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Gastric cancer	16715143	CNVD
Glioblastoma multiforme	22286061	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Ovarian cancer	22355333	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2679400-2692400	Weak transcription	Psoas Muscle	Psoas
2	chr9:2687200-2693200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr9:2688600-2702400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr9:2689200-2692200	Enhancers	Fetal Heart	heart
5	chr9:2689600-2691800	Weak transcription	Ovary	ovary
6	chr9:2689800-2700200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:2690000-2692600	Enhancers	HUVEC	blood vessel
8	chr9:2690000-2702600	Weak transcription	Primary T cells from cord blood	blood
9	chr9:2690600-2718000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr9:2690800-2700600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr9:2691200-2692200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:2691200-2692200	Enhancers	Placenta Amnion	Placenta Amnion
13	chr9:2691200-2710600	Weak transcription	Left Ventricle	heart
14	chr9:2691400-2692000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:2691400-2692200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr9:2691400-2692600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr9:2691600-2692200	Enhancers	Muscle Satellite Cultured Cells	--
18	chr9:2692000-2709600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr9:2692200-2693200	Weak transcription	Fetal Heart	heart
20	chr9:2693200-2694000	Enhancers	Fetal Heart	heart
21	chr9:2696600-2700600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr9:2697200-2698600	Enhancers	GM12878-XiMat	blood
23	chr9:2697200-2722800	Weak transcription	HSMM	muscle
24	chr9:2697600-2698200	Enhancers	Adipose Nuclei	Adipose
25	chr9:2697800-2698000	Enhancers	Esophagus	oesophagus
26	chr9:2697800-2698200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr9:2698000-2717600	Weak transcription	Esophagus	oesophagus
28	chr9:2698200-2700400	Weak transcription	Adipose Nuclei	Adipose
29	chr9:2699000-2702200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr9:2699200-2701400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr9:2699400-2702200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr9:2699600-2700400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr9:2699800-2700000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr9:2699800-2700600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr9:2699800-2701000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr9:2699800-2701600	Enhancers	H1 Cell Line	embryonic stem cell
37	chr9:2699800-2702000	Enhancers	H9 Cell Line	embryonic stem cell
38	chr9:2700000-2701000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr9:2700000-2701400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr9:2700000-2701600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr9:2700200-2700600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr9:2700200-2701400	Enhancers	Fetal Heart	heart
43	chr9:2700200-2701800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr9:2700400-2701200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr9:2700400-2701200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr9:2700400-2701600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr9:2700400-2701600	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr9:2700400-2702200	Enhancers	Adipose Nuclei	Adipose
49	chr9:2700600-2701200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr9:2700600-2701400	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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