Variant report

Variant	nsv892088
Chromosome Location	chr9:3019383-3215842
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:775)
CpG islands
(count:366)
Chromatin interactive
region (count:5)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:775 , 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	chr9:3151777-3152598	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:3177356-3177704	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:3150159-3150316	HepG2	liver:	n/a	n/a
4	ATF2	chr9:3032872-3033291	GM12878	blood:	n/a	n/a
5	ATF2	chr9:3032977-3033245	GM12878	blood:	n/a	n/a
6	BACH1	chr9:3181571-3181959	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr9:3032986-3033270	GM12878	blood:	n/a	n/a
8	BATF	chr9:3032883-3033333	GM12878	blood:	n/a	n/a
9	BCL11A	chr9:3032888-3033295	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:3199072-3199094	A549	lung:	n/a	n/a
11	BHLHE40	chr9:3039378-3039580	K562	blood:	n/a	n/a
12	BRCA1	chr9:3181672-3181872	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr9:3039382-3039534	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr9:3120588-3120776	IMR90	lung:	n/a	chr9:3120682-3120693
15	CEBPB	chr9:3190854-3191011	A549	lung:	n/a	chr9:3190978-3190989 chr9:3190978-3190991
16	CEBPB	chr9:3047995-3048234	IMR90	lung:	n/a	n/a
17	CEBPB	chr9:3100550-3100731	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr9:3048009-3048274	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr9:3170780-3170873	K562	blood:	n/a	chr9:3170829-3170840
20	CEBPB	chr9:3100982-3101195	A549	lung:	n/a	chr9:3101069-3101082 chr9:3101069-3101080
21	CEBPB	chr9:3181702-3182017	MCF-7	breast:	n/a	n/a
22	CEBPB	chr9:3104444-3104652	HepG2	liver:	n/a	chr9:3104530-3104541 chr9:3104508-3104519
23	CEBPB	chr9:3200523-3200878	IMR90	lung:	n/a	n/a
24	CEBPB	chr9:3190953-3190956	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr9:3215236-3215317	A549	lung:	n/a	n/a
26	CEBPB	chr9:3125851-3126031	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr9:3170867-3171186	MCF-7	breast:	n/a	chr9:3171102-3171115 chr9:3171029-3171040 chr9:3171029-3171042
28	CEBPB	chr9:3125776-3126477	A549	lung:	n/a	chr9:3126307-3126318
29	CEBPB	chr9:3155717-3155852	HepG2	liver:	n/a	chr9:3155778-3155789
30	CEBPB	chr9:3087894-3088447	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr9:3043175-3043437	A549	lung:	n/a	n/a
32	CEBPB	chr9:3126342-3126432	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr9:3073535-3073772	HepG2	liver:	n/a	chr9:3073648-3073659 chr9:3073622-3073633
34	CEBPB	chr9:3170691-3171059	A549	lung:	n/a	chr9:3171029-3171040 chr9:3170829-3170840 chr9:3171029-3171042
35	CEBPB	chr9:3116254-3116374	HepG2	liver:	n/a	chr9:3116302-3116313
36	CEBPB	chr9:3126137-3126460	HepG2	liver:	n/a	chr9:3126307-3126318
37	CEBPB	chr9:3100940-3101140	HepG2	liver:	n/a	chr9:3101069-3101082 chr9:3101069-3101080
38	CEBPB	chr9:3170663-3171095	HepG2	liver:	n/a	chr9:3171029-3171040 chr9:3170829-3170840 chr9:3171029-3171042
39	CEBPB	chr9:3035690-3035980	MCF-7	breast:	n/a	chr9:3035735-3035747
40	CEBPB	chr9:3190567-3191066	HepG2	liver:	n/a	chr9:3190846-3190857 chr9:3190978-3190989 chr9:3190978-3190991 chr9:3190844-3190857
41	CEBPB	chr9:3039378-3039444	K562	blood:	n/a	n/a
42	CEBPB	chr9:3037652-3037824	HepG2	liver:	n/a	chr9:3037739-3037750
43	CEBPB	chr9:3035662-3035958	A549	lung:	n/a	chr9:3035735-3035747
44	CEBPB	chr9:3035663-3035905	HepG2	liver:	n/a	chr9:3035735-3035747
45	CEBPB	chr9:3126173-3126446	IMR90	lung:	n/a	chr9:3126307-3126318
46	CEBPB	chr9:3181646-3182042	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr9:3073580-3073780	A549	lung:	n/a	chr9:3073648-3073659 chr9:3073622-3073633
48	CEBPB	chr9:3137269-3137464	IMR90	lung:	n/a	chr9:3137373-3137384
49	CEBPB	chr9:3177376-3177660	HepG2	liver:	n/a	n/a
50	CEBPB	chr9:3035636-3035931	H1-hESC	embryonic stem cell:	n/a	chr9:3035735-3035747

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:3180869-3180919	HPAEpiC	pulmonary alveolar:	n/a
2	chr9:3181659-3181709	SAEC	small airway:	n/a
3	chr9:3180869-3180919	HepG2	liver:	n/a
4	chr9:3181772-3181822	AG09309	skin:	n/a
5	chr9:3181659-3181709	SKMC	muscle:	n/a
6	chr9:3181007-3181057	Jurkat	blood:	n/a
7	chr9:3181007-3181057	NB4	blood:	n/a
8	chr9:3183159-3183209	HNPCEpiC	eye:	n/a
9	chr9:3180374-3180424	HRPEpiC	eye:	n/a
10	chr9:3181772-3181822	HRCEpiC	kidney:	n/a
11	chr9:3180869-3180919	K562	blood:	n/a
12	chr9:3181007-3181057	AG04450	lung:	fetal
13	chr9:3180869-3180919	HEK293	kidney:	embryo
14	chr9:3181772-3181822	AG10803	skin:	n/a
15	chr9:3181772-3181822	GM06990	blood:	n/a
16	chr9:3181007-3181057	SK-N-SH_RA	brain:	n/a
17	chr9:3181007-3181057	GM12891	blood:	n/a
18	chr9:3181007-3181057	HepG2	liver:	n/a
19	chr9:3181772-3181822	H1-hESC	embryonic stem cell:	embryo
20	chr9:3180374-3180424	HNPCEpiC	eye:	n/a
21	chr9:3181007-3181057	PFSK-1	brain:	n/a
22	chr9:3180374-3180424	HCT-116	colon:	n/a
23	chr9:3181007-3181057	MCF10A-Er-Src	breast:	n/a
24	chr9:3181007-3181057	HRPEpiC	eye:	n/a
25	chr9:3181659-3181709	ovcar-3	ovarian:	n/a
26	chr9:3181007-3181057	MCF-7	breast:	n/a
27	chr9:3180869-3180919	ECC-1	luminal epithelium:	n/a
28	chr9:3181007-3181057	HNPCEpiC	eye:	n/a
29	chr9:3181007-3181057	NHDF-neo	bronchial:	n/a
30	chr9:3183159-3183209	GM12892	blood:	n/a
31	chr9:3180374-3180424	HRE	kidney:	n/a
32	chr9:3180374-3180424	HEEpiC	esophagus:	n/a
33	chr9:3180869-3180919	MCF10A-Er-Src	breast:	n/a
34	chr9:3181659-3181709	K562	blood:	n/a
35	chr9:3180374-3180424	U87	brain:	n/a
36	chr9:3180869-3180919	T-47D	breast:	n/a
37	chr9:3181007-3181057	HCPEpiC	choroid plexus:	n/a
38	chr9:3180869-3180919	ProgFib	skin:	n/a
39	chr9:3181772-3181822	HMEC	breast:	n/a
40	chr9:3180374-3180424	GM19239	blood:	n/a
41	chr9:3183159-3183209	GM12878	blood:	n/a
42	chr9:3180869-3180919	HMEC	breast:	n/a
43	chr9:3181659-3181709	Hepatocyte	liver:	n/a
44	chr9:3181772-3181822	HUVEC	blood vessel:	n/a
45	chr9:3183159-3183209	MCF10A-Er-Src	breast:	n/a
46	chr9:3181659-3181709	HEK293	kidney:	embryo
47	chr9:3180374-3180424	PFSK-1	brain:	n/a
48	chr9:3181659-3181709	HNPCEpiC	eye:	n/a
49	chr9:3181007-3181057	AG10803	skin:	n/a
50	chr9:3181007-3181057	Hela-S3	cervix:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:3189825..3191620-chr9:3192425..3195414,2	MCF-7	breast:
2	chr9:3153271..3155559-chr9:3163455..3165401,2	K562	blood:
3	chr1:62477919..62478756-chr9:3062250..3062792,2	MCF-7	breast:
4	chr9:3153271..3155559-chr9:3163455..3165401,2	K562	blood:
5	chr9:3189825..3191620-chr9:3192425..3195414,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV2-6	chr9:3176918-3177035	NONHSAT130016
2	lnc-KCNV2-2	chr9:3181589-3181889	XLOC_007268
3	lnc-KCNV2-2	chr9:3198186-3198924	NONHSAT130017
4	lnc-KCNV2-6	chr9:3171589-3171889	NONHSAT130016
5	lnc-KCNV2-2	chr9:3186918-3187035	NONHSAT130017
6	lnc-KCNV2-2	chr9:3181589-3181889	NONHSAT130017
7	lnc-KCNV2-2	chr9:3186918-3187035	XLOC_007268
8	lnc-KCNV2-6	chr9:3183460-3183594	NONHSAT130016
9	lnc-KCNV2-2	chr9:3193460-3193594	NONHSAT130017
10	lnc-RFX3-1	chr9:3213829-3214127	expReg_chr9_150_-
11	lnc-KCNV2-2	chr9:3193460-3193594	XLOC_007268
12	lnc-KCNV2-2	chr9:3198186-3198517	XLOC_007268
13	lnc-KCNV2-2	chr9:3200300-3200500	NONHSAT130017
14	lnc-KCNV2-6	chr9:3188186-3188517	NONHSAT130016

No data

Variant related genes	Relation type
CARM1P1	TF binding region
ENSG00000236511	TF binding region
CARM1P1	CpG island
ENSG00000236511	CpG island
RAG1	miRNA target sites
CNOT6L	miRNA target sites

Extended variants
information (count: 5054 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:5054 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3847240	chr9:3019383-3019384	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs62533953	chr9:3019385-3019386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563143474	chr9:3019391-3019392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532091965	chr9:3019409-3019410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs5896002	chr9:3019414-3019415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374010300	chr9:3019482-3019483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559371456	chr9:3019509-3019510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183321256	chr9:3019513-3019514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186529865	chr9:3019514-3019515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189842446	chr9:3019521-3019522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568403325	chr9:3019577-3019578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147823019	chr9:3019581-3019582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377650210	chr9:3019596-3019597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550804803	chr9:3019601-3019602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146898950	chr9:3019633-3019634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201787960	chr9:3019635-3019636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368580631	chr9:3019636-3019637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199947563	chr9:3019645-3019646	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs78802662	chr9:3019658-3019659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74718850	chr9:3019659-3019660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371331367	chr9:3019664-3019665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182464838	chr9:3019666-3019667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541058027	chr9:3019690-3019691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs3847241	chr9:3019701-3019702	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs370775056	chr9:3019704-3019705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572183709	chr9:3019717-3019718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534929382	chr9:3019739-3019740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554740163	chr9:3019744-3019745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533098616	chr9:3019794-3019795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546446596	chr9:3019845-3019846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574076186	chr9:3019890-3019891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375338571	chr9:3019896-3019897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141362082	chr9:3019904-3019905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543716593	chr9:3019927-3019928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187914777	chr9:3019932-3019933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368597438	chr9:3019942-3019943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150319316	chr9:3019948-3019949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545763500	chr9:3019956-3019957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs137964727	chr9:3019957-3019958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149484787	chr9:3019959-3019960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs118023882	chr9:3019988-3019989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561865316	chr9:3019994-3019995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192596589	chr9:3019996-3019997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550616602	chr9:3020003-3020004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138548558	chr9:3020023-3020024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183316911	chr9:3020065-3020066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34816034	chr9:3020086-3020087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs397735691	chr9:3020087-3020088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142244608	chr9:3020137-3020138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552536397	chr9:3020138-3020139	Enhancers Weak transcription	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
Autism	20808228	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:3018200-3019800	Enhancers	Fetal Brain Male	brain
2	chr9:3018400-3019600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr9:3018600-3019600	Enhancers	Fetal Brain Female	brain
4	chr9:3018800-3020000	Enhancers	Psoas Muscle	Psoas
5	chr9:3019200-3028000	Weak transcription	Adipose Nuclei	Adipose
6	chr9:3019200-3028600	Weak transcription	Fetal Muscle Leg	muscle
7	chr9:3019600-3020400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr9:3019800-3020600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:3020000-3020400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr9:3020000-3020400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr9:3023400-3023800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:3023400-3024000	Enhancers	NHEK	skin
13	chr9:3025600-3025800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:3026000-3027200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr9:3026800-3029200	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr9:3026800-3029200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr9:3027000-3029200	Enhancers	Fetal Brain Male	brain
18	chr9:3027200-3027400	Enhancers	Psoas Muscle	Psoas
19	chr9:3027200-3027600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:3027200-3027600	Enhancers	Fetal Stomach	stomach
21	chr9:3027200-3027600	Enhancers	Stomach Smooth Muscle	stomach
22	chr9:3027400-3027800	Enhancers	Fetal Brain Female	brain
23	chr9:3027600-3028600	Weak transcription	Fetal Stomach	stomach
24	chr9:3027600-3029000	Weak transcription	Stomach Smooth Muscle	stomach
25	chr9:3027800-3028800	Weak transcription	Fetal Brain Female	brain
26	chr9:3028000-3029200	Enhancers	Adipose Nuclei	Adipose
27	chr9:3028200-3029200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr9:3028600-3029200	Enhancers	Psoas Muscle	Psoas
29	chr9:3028600-3029600	Enhancers	Fetal Muscle Leg	muscle
30	chr9:3028800-3029000	Enhancers	Fetal Stomach	stomach
31	chr9:3028800-3029200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr9:3028800-3029400	Enhancers	Fetal Brain Female	brain
33	chr9:3029000-3029200	Enhancers	Stomach Smooth Muscle	stomach
34	chr9:3029200-3035600	Weak transcription	Adipose Nuclei	Adipose
35	chr9:3029200-3035800	Weak transcription	Psoas Muscle	Psoas
36	chr9:3029600-3031800	Weak transcription	Fetal Muscle Leg	muscle
37	chr9:3030400-3030800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr9:3031200-3039200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr9:3031800-3032000	Enhancers	Fetal Muscle Leg	muscle
40	chr9:3032800-3033000	Enhancers	GM12878-XiMat	blood
41	chr9:3032800-3042200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr9:3035600-3036200	Enhancers	Adipose Nuclei	Adipose
43	chr9:3035800-3036200	Enhancers	Fetal Brain Male	brain
44	chr9:3035800-3036200	Enhancers	Fetal Muscle Leg	muscle
45	chr9:3035800-3036200	Enhancers	Psoas Muscle	Psoas
46	chr9:3038200-3038600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr9:3039200-3039400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr9:3039200-3039400	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
49	chr9:3039200-3039600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
50	chr9:3039200-3039600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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