Variant report

Variant	nsv892637
Chromosome Location	chr9:15926508-16060746
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1011)
CpG islands
(count:183)
Chromatin interactive
region (count:4)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1011 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:16060647-16061176	GM12878	blood:	n/a	n/a
2	ATF2	chr9:16030527-16030923	GM12878	blood:	n/a	n/a
3	BATF	chr9:16030529-16030841	GM12878	blood:	n/a	chr9:16030712-16030722
4	BATF	chr9:16030503-16030837	GM12878	blood:	n/a	chr9:16030712-16030722
5	BATF	chr9:16060743-16061148	GM12878	blood:	n/a	n/a
6	BATF	chr9:16046711-16046966	GM12878	blood:	n/a	n/a
7	BCL11A	chr9:16030497-16030868	GM12878	blood:	n/a	chr9:16030711-16030720
8	BCL11A	chr9:16030563-16030805	GM12878	blood:	n/a	chr9:16030711-16030720
9	BHLHE40	chr9:16030533-16030834	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:16060676-16061037	GM12878	blood:	n/a	n/a
11	BRCA1	chr9:15972021-15972038	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr9:16030498-16031118	HCT-116	colon:	n/a	n/a
13	CBX3	chr9:16030378-16031078	HCT-116	colon:	n/a	n/a
14	CEBPB	chr9:16049018-16049283	Hela-S3	cervix:	n/a	chr9:16049185-16049196
15	CEBPB	chr9:15985970-15986263	HepG2	liver:	n/a	chr9:15986112-15986123 chr9:15986111-15986122 chr9:15986111-15986124
16	CEBPB	chr9:16049057-16049343	HepG2	liver:	n/a	chr9:16049185-16049196
17	CEBPB	chr9:16040364-16040850	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr9:15999599-16000359	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:16029202-16029509	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:16053187-16053402	HepG2	liver:	n/a	chr9:16053306-16053317
21	CEBPB	chr9:16025750-16026221	A549	lung:	n/a	chr9:16025870-16025881
22	CEBPB	chr9:15999094-15999227	HepG2	liver:	n/a	chr9:15999159-15999170
23	CEBPB	chr9:15999666-16000309	A549	lung:	n/a	n/a
24	CEBPB	chr9:15985947-15986280	A549	lung:	n/a	chr9:15986112-15986123 chr9:15986111-15986122 chr9:15986111-15986124
25	CEBPB	chr9:16026885-16027334	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:16002836-16003245	IMR90	lung:	n/a	chr9:16003091-16003102
27	CEBPB	chr9:15965805-15966042	H1-hESC	embryonic stem cell:	n/a	chr9:15965897-15965909
28	CEBPB	chr9:16049066-16049267	IMR90	lung:	n/a	chr9:16049185-16049196
29	CEBPB	chr9:16025738-16026208	HepG2	liver:	n/a	chr9:16025870-16025881
30	CEBPB	chr9:16058124-16058404	IMR90	lung:	n/a	n/a
31	CEBPB	chr9:15965806-15966055	Hela-S3	cervix:	n/a	chr9:15965897-15965909
32	CEBPB	chr9:16025734-16026185	IMR90	lung:	n/a	chr9:16025870-16025881
33	CEBPB	chr9:15965736-15966099	A549	lung:	n/a	chr9:15965897-15965909
34	CEBPB	chr9:16014658-16014823	IMR90	lung:	n/a	n/a
35	CEBPB	chr9:15965743-15966089	HepG2	liver:	n/a	chr9:15965897-15965909
36	CEBPB	chr9:15965726-15966104	IMR90	lung:	n/a	chr9:15965897-15965909
37	CEBPB	chr9:16012589-16012880	IMR90	lung:	n/a	n/a
38	CEBPB	chr9:16053308-16053347	A549	lung:	n/a	n/a
39	CEBPB	chr9:16049017-16049349	A549	lung:	n/a	chr9:16049185-16049196
40	CEBPB	chr9:15999013-15999317	IMR90	lung:	n/a	chr9:15999159-15999170
41	CHD2	chr9:16040292-16040680	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr9:16030674-16030777	GM12878	blood:	n/a	n/a
43	CHD2	chr9:15999712-16000044	Hela-S3	cervix:	n/a	n/a
44	CTBP2	chr9:16040059-16040654	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr9:16058440-16058498	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr9:16039480-16039630	NB4	blood:	n/a	n/a
47	CTCF	chr9:15967200-15967350	MCF-7	breast:	n/a	chr9:15967233-15967254
48	CTCF	chr9:16053160-16053310	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr9:16039520-16039670	GM12867	blood:	n/a	n/a
50	CTCF	chr9:15967213-15967281	MCF-7	breast:	n/a	chr9:15967233-15967254

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:16040625-16040675	U87	brain:	n/a
2	chr9:16040625-16040675	H1-hESC	embryonic stem cell:	embryo
3	chr9:16040625-16040675	NB4	blood:	n/a
4	chr9:16039921-16039971	GM12892	blood:	n/a
5	chr9:16040625-16040675	AG04449	skin:	fetal
6	chr9:16044344-16044394	BE2_C	brain:	n/a
7	chr9:16044344-16044394	T-47D	breast:	n/a
8	chr9:16044344-16044394	GM12891	blood:	n/a
9	chr9:16044344-16044394	LNCaP	prostate:	n/a
10	chr9:16044344-16044394	MCF10A-Er-Src	breast:	n/a
11	chr9:16039921-16039971	GM12878	blood:	n/a
12	chr9:16039921-16039971	SAEC	small airway:	n/a
13	chr9:16039921-16039971	HCT-116	colon:	n/a
14	chr9:16044344-16044394	GM06990	blood:	n/a
15	chr9:16044344-16044394	GM12878	blood:	n/a
16	chr9:16044344-16044394	HMEC	breast:	n/a
17	chr9:16044344-16044394	HCF	heart:	n/a
18	chr9:16039921-16039971	RPTEC	kidney:	n/a
19	chr9:16040625-16040675	A549	lung:	n/a
20	chr9:16040625-16040675	AG04450	lung:	fetal
21	chr9:16044344-16044394	SAEC	small airway:	n/a
22	chr9:16040625-16040675	HCM	heart:	n/a
23	chr9:16039921-16039971	AG09309	skin:	n/a
24	chr9:16039921-16039971	AG04450	lung:	fetal
25	chr9:16039921-16039971	NHDF-neo	bronchial:	n/a
26	chr9:16044344-16044394	AG04449	skin:	fetal
27	chr9:16044344-16044394	AG09319	gingival:	n/a
28	chr9:16040625-16040675	NHBE	bronchial:	n/a
29	chr9:16039921-16039971	AG04449	skin:	fetal
30	chr9:16039921-16039971	HCF	heart:	n/a
31	chr9:16039921-16039971	HUVEC	blood vessel:	n/a
32	chr9:16039921-16039971	AG09319	gingival:	n/a
33	chr9:16039921-16039971	Jurkat	blood:	n/a
34	chr9:16040625-16040675	SK-N-SH	brain:	n/a
35	chr9:16040625-16040675	BE2_C	brain:	n/a
36	chr9:16039921-16039971	PFSK-1	brain:	n/a
37	chr9:16044344-16044394	Jurkat	blood:	n/a
38	chr9:16040625-16040675	HCPEpiC	choroid plexus:	n/a
39	chr9:16040625-16040675	HPAEpiC	pulmonary alveolar:	n/a
40	chr9:16039921-16039971	HAEpiC	amniotic membrane:	n/a
41	chr9:16039921-16039971	H1-hESC	embryonic stem cell:	embryo
42	chr9:16039921-16039971	PANC-1	pancreas:	n/a
43	chr9:16040625-16040675	HRPEpiC	eye:	n/a
44	chr9:16039921-16039971	ProgFib	skin:	n/a
45	chr9:16039921-16039971	HRCEpiC	kidney:	n/a
46	chr9:16040625-16040675	SAEC	small airway:	n/a
47	chr9:16039921-16039971	K562	blood:	n/a
48	chr9:16040625-16040675	HMEC	breast:	n/a
49	chr9:16040625-16040675	T-47D	breast:	n/a
50	chr9:16040625-16040675	IMR90	lung:	fetal

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:16032646..16033464-chr9:16130747..16131983,3	MCF-7	breast:
2	chr9:16039127..16039773-chr9:16131360..16131916,2	MCF-7	breast:
3	chr9:16032565..16033224-chr9:16133403..16134072,3	MCF-7	breast:
4	chr9:16039283..16040078-chr9:16131109..16131609,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-1	chr9:16060644-16060851	XLOC_007290
2	lnc-SNAPC3-1	chr9:16042796-16042918	XLOC_007290
3	lnc-SNAPC3-1	chr9:16060644-16061855	XLOC_007290
4	lnc-SNAPC3-1	chr9:16035455-16035523	NONHSAT130279
5	lnc-SNAPC3-1	chr9:16036091-16036204	XLOC_007290
6	lnc-SNAPC3-1	chr9:16060644-16061661	NONHSAT130279
7	lnc-SNAPC3-1	chr9:16060644-16061318	NONHSAT130282
8	lnc-SNAPC3-1	chr9:16042796-16042918	XLOC_007290
9	lnc-SNAPC3-1	chr9:16022330-16022583	NONHSAT130279
10	lnc-SNAPC3-1	chr9:16020587-16020792	NONHSAT130279
11	lnc-SNAPC3-1	chr9:16035383-16035523	XLOC_007290
12	lnc-SNAPC3-1	chr9:16036091-16036204	NONHSAT130279
13	lnc-SNAPC3-1	chr9:16042796-16042884	NONHSAT130282
14	lnc-SNAPC3-1	chr9:16042796-16042918	NONHSAT130279
15	lnc-SNAPC3-1	chr9:16022737-16022906	NONHSAT130279
16	lnc-SNAPC3-1	chr9:16036091-16036204	XLOC_007290

No data

Variant related genes	Relation type
CCDC171	TF binding region
CCDC171	CpG island
PEMT	miRNA target sites
CDC42EP3	miRNA target sites
MLL3	miRNA target sites
RAB6A	miRNA target sites
DACT1	miRNA target sites

Extended variants
information (count: 5778 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5778 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3008682	chr9:15926508-15926509	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541239038	chr9:15926529-15926530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570237051	chr9:15926582-15926583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560796326	chr9:15926607-15926608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570041574	chr9:15926665-15926666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535414502	chr9:15926676-15926677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549863797	chr9:15926693-15926694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2987064	chr9:15926698-15926699	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs142826156	chr9:15926716-15926717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553820116	chr9:15926781-15926782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs735962	chr9:15926796-15926797	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs536084005	chr9:15926798-15926799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369422596	chr9:15926877-15926878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs77229828	chr9:15926894-15926895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554363962	chr9:15926929-15926930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189191267	chr9:15926934-15926935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543519394	chr9:15926973-15926974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs151040693	chr9:15927007-15927008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181671199	chr9:15927012-15927013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541401001	chr9:15927032-15927033	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140009287	chr9:15927057-15927058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540913810	chr9:15927058-15927059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373075489	chr9:15927088-15927089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542509512	chr9:15927106-15927107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143697451	chr9:15927114-15927115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557557201	chr9:15927119-15927120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531077175	chr9:15927138-15927139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185965664	chr9:15927149-15927150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146804358	chr9:15927158-15927159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532044332	chr9:15927183-15927184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547347237	chr9:15927231-15927232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543541088	chr9:15927280-15927281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191226413	chr9:15927297-15927298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181335971	chr9:15927320-15927321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548040410	chr9:15927360-15927361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186110914	chr9:15927366-15927367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563192682	chr9:15927367-15927368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140367316	chr9:15927409-15927410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190969511	chr9:15927484-15927485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150344562	chr9:15927491-15927492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62548687	chr9:15927507-15927508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528884435	chr9:15927522-15927523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76215968	chr9:15927536-15927537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145128765	chr9:15927546-15927547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542616480	chr9:15927611-15927612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542546109	chr9:15927710-15927711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563965986	chr9:15927718-15927719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1410446	chr9:15927795-15927796	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs79387099	chr9:15927796-15927797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369399273	chr9:15927812-15927813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	19835627	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15918200-15930800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr9:15920000-15936000	Weak transcription	Ovary	ovary
3	chr9:15922800-15930800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:15922800-15931600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr9:15923000-15929600	Weak transcription	Primary hematopoietic stem cells	blood
6	chr9:15926400-15928000	Enhancers	Muscle Satellite Cultured Cells	--
7	chr9:15926400-15928200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr9:15926400-15928400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:15926600-15927600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr9:15926800-15927800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr9:15926800-15927800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr9:15927000-15927600	Enhancers	Osteobl	bone
13	chr9:15927200-15927400	Enhancers	HSMM	muscle
14	chr9:15927200-15928000	Enhancers	NHDF-Ad	bronchial
15	chr9:15927400-15934800	Weak transcription	HSMM	muscle
16	chr9:15928000-15932600	Weak transcription	NHDF-Ad	bronchial
17	chr9:15930400-15938600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr9:15930800-15931600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr9:15930800-15933200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr9:15931400-15931800	Weak transcription	Primary hematopoietic stem cells	blood
21	chr9:15931600-15933200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr9:15932600-15933200	ZNF genes & repeats	NHDF-Ad	bronchial
23	chr9:15933200-15934200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr9:15933200-15934400	Weak transcription	NHDF-Ad	bronchial
25	chr9:15933200-15951400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:15934200-15936800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr9:15934400-15935800	Enhancers	NHDF-Ad	bronchial
28	chr9:15934600-15935400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr9:15934600-15938000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr9:15934800-15935000	Enhancers	Fetal Kidney	kidney
31	chr9:15934800-15935200	Genic enhancers	HSMM	muscle
32	chr9:15934800-15936000	Enhancers	Muscle Satellite Cultured Cells	--
33	chr9:15934800-15936600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr9:15934800-15937200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:15934800-15937800	Enhancers	Osteobl	bone
36	chr9:15935000-15936000	Weak transcription	Fetal Kidney	kidney
37	chr9:15935000-15936800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr9:15935200-15937000	Enhancers	HSMM	muscle
39	chr9:15935200-15937200	Enhancers	Brain Germinal Matrix	brain
40	chr9:15935200-15937200	Enhancers	NHLF	lung
41	chr9:15935400-15935800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr9:15935800-15936800	Enhancers	Adipose Nuclei	Adipose
43	chr9:15935800-15936800	Enhancers	NH-A	brain
44	chr9:15935800-15937000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr9:15935800-15937000	Enhancers	Fetal Lung	lung
46	chr9:15935800-15937000	Flanking Active TSS	NHDF-Ad	bronchial
47	chr9:15936000-15936200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr9:15936000-15936400	Enhancers	Fetal Kidney	kidney
49	chr9:15936000-15936600	Enhancers	HSMMtube	muscle
50	chr9:15936000-15936800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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