Variant report

Variant	nsv831518
Chromosome Location	chr9:14760638-14953501
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14908366-14908878	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:14913278-14913856	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:14882074-14882476	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:14899812-14900038	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:14925038-14925148	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:14893420-14893599	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:14888518-14888791	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:14768583-14768889	K562	blood:	n/a	n/a
9	ARID3A	chr9:14868526-14869963	HepG2	liver:	n/a	chr9:14869168-14869184 chr9:14869167-14869183
10	ATF1	chr9:14779539-14779966	K562	blood:	n/a	n/a
11	ATF1	chr9:14797561-14797747	K562	blood:	n/a	n/a
12	ATF1	chr9:14926973-14927434	K562	blood:	n/a	n/a
13	ATF3	chr9:14846813-14847157	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr9:14779743-14779981	K562	blood:	n/a	n/a
15	BCL3	chr9:14812818-14813170	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:14770538-14770679	K562	blood:	n/a	n/a
17	BHLHE40	chr9:14831736-14831957	K562	blood:	n/a	n/a
18	BHLHE40	chr9:14779512-14779982	K562	blood:	n/a	n/a
19	BHLHE40	chr9:14822708-14823063	GM12878	blood:	n/a	n/a
20	CCNT2	chr9:14926887-14927432	K562	blood:	n/a	n/a
21	CEBPB	chr9:14799060-14799419	K562	blood:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
22	CEBPB	chr9:14945585-14945795	HepG2	liver:	n/a	chr9:14945603-14945614
23	CEBPB	chr9:14905488-14905648	HepG2	liver:	n/a	chr9:14905524-14905535
24	CEBPB	chr9:14779706-14780011	K562	blood:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
25	CEBPB	chr9:14799087-14799406	A549	lung:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
26	CEBPB	chr9:14799090-14799366	MCF-7	breast:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
27	CEBPB	chr9:14777095-14777393	HepG2	liver:	n/a	chr9:14777345-14777356 chr9:14777261-14777272 chr9:14777124-14777135 chr9:14777124-14777135 chr9:14777345-14777356
28	CEBPB	chr9:14877121-14877303	HepG2	liver:	n/a	n/a
29	CEBPB	chr9:14799070-14799407	IMR90	lung:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
30	CEBPB	chr9:14799109-14799362	H1-hESC	embryonic stem cell:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
31	CEBPB	chr9:14924869-14925229	Hela-S3	cervix:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
32	CEBPB	chr9:14799112-14799348	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
33	CEBPB	chr9:14782726-14783009	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr9:14782789-14783062	MCF-7	breast:	n/a	n/a
35	CEBPB	chr9:14899811-14900187	HepG2	liver:	n/a	chr9:14899992-14900003
36	CEBPB	chr9:14779747-14779985	A549	lung:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
37	CEBPB	chr9:14941573-14941825	HepG2	liver:	n/a	chr9:14941720-14941731 chr9:14941718-14941731 chr9:14941718-14941729 chr9:14941720-14941729
38	CEBPB	chr9:14799137-14799326	Hela-S3	cervix:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
39	CEBPB	chr9:14777093-14777293	A549	lung:	n/a	chr9:14777261-14777272 chr9:14777124-14777135 chr9:14777124-14777135
40	CEBPB	chr9:14924863-14925268	HepG2	liver:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
41	CEBPB	chr9:14782802-14783000	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr9:14799044-14799407	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
43	CEBPB	chr9:14899873-14900096	HepG2	liver:	n/a	chr9:14899992-14900003
44	CEBPB	chr9:14924866-14925231	IMR90	lung:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
45	CEBPB	chr9:14949391-14949419	K562	blood:	n/a	n/a
46	CEBPB	chr9:14782745-14783078	MCF-7	breast:	n/a	n/a
47	CEBPB	chr9:14827709-14827960	HepG2	liver:	n/a	chr9:14827827-14827838
48	CEBPB	chr9:14924936-14925115	K562	blood:	n/a	chr9:14925029-14925040 chr9:14925086-14925097
49	CEBPB	chr9:14827792-14827904	IMR90	lung:	n/a	chr9:14827827-14827838
50	CEBPB	chr9:14799051-14799431	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14910315-14910365	NB4	blood:	n/a
2	chr9:14838752-14838802	IMR90	lung:	fetal
3	chr9:14910315-14910365	Hepatocyte	liver:	n/a
4	chr9:14883945-14883995	MCF-7	breast:	n/a
5	chr9:14908132-14908182	HRCEpiC	kidney:	n/a
6	chr9:14883945-14883995	ovcar-3	ovarian:	n/a
7	chr9:14910689-14910739	AG09319	gingival:	n/a
8	chr9:14910689-14910739	CMK	blood:	n/a
9	chr9:14883945-14883995	HNPCEpiC	eye:	n/a
10	chr9:14910689-14910739	NHBE	bronchial:	n/a
11	chr9:14908132-14908182	Hepatocyte	liver:	n/a
12	chr9:14910689-14910739	U87	brain:	n/a
13	chr9:14908132-14908182	AG09309	skin:	n/a
14	chr9:14910689-14910739	PANC-1	pancreas:	n/a
15	chr9:14910689-14910739	HL-60	blood:	n/a
16	chr9:14838752-14838802	HMEC	breast:	n/a
17	chr9:14910689-14910739	HIPEpiC	eye:	n/a
18	chr9:14883945-14883995	AG04449	skin:	fetal
19	chr9:14838752-14838802	HPAEpiC	pulmonary alveolar:	n/a
20	chr9:14910315-14910365	GM19239	blood:	n/a
21	chr9:14883945-14883995	Hela-S3	cervix:	n/a
22	chr9:14908132-14908182	GM12891	blood:	n/a
23	chr9:14883945-14883995	AG09309	skin:	n/a
24	chr9:14883945-14883995	AG04450	lung:	fetal
25	chr9:14910315-14910365	SK-N-SH	brain:	n/a
26	chr9:14883945-14883995	HAEpiC	amniotic membrane:	n/a
27	chr9:14838752-14838802	Hepatocyte	liver:	n/a
28	chr9:14883945-14883995	HRCEpiC	kidney:	n/a
29	chr9:14883945-14883995	PFSK-1	brain:	n/a
30	chr9:14910315-14910365	BE2_C	brain:	n/a
31	chr9:14908132-14908182	A549	lung:	n/a
32	chr9:14910315-14910365	HUVEC	blood vessel:	n/a
33	chr9:14883945-14883995	NT2-D1	testis:	n/a
34	chr9:14910315-14910365	AG10803	skin:	n/a
35	chr9:14908132-14908182	NT2-D1	testis:	n/a
36	chr9:14883945-14883995	NHDF-neo	bronchial:	n/a
37	chr9:14910689-14910739	H1-hESC	embryonic stem cell:	embryo
38	chr9:14838752-14838802	ProgFib	skin:	n/a
39	chr9:14910689-14910739	AG09309	skin:	n/a
40	chr9:14910689-14910739	ECC-1	luminal epithelium:	n/a
41	chr9:14838752-14838802	GM12891	blood:	n/a
42	chr9:14910315-14910365	NHDF-neo	bronchial:	n/a
43	chr9:14910689-14910739	AG04450	lung:	fetal
44	chr9:14910315-14910365	U87	brain:	n/a
45	chr9:14883945-14883995	NHBE	bronchial:	n/a
46	chr9:14883945-14883995	HCPEpiC	choroid plexus:	n/a
47	chr9:14883945-14883995	HepG2	liver:	n/a
48	chr9:14908132-14908182	HCPEpiC	choroid plexus:	n/a
49	chr9:14910689-14910739	HNPCEpiC	eye:	n/a
50	chr9:14838752-14838802	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr9:14785127..14787393-chr9:14791653..14793787,2	MCF-7	breast:
2	chr9:14813259..14815238-chr9:14818255..14820615,2	K562	blood:
3	chr9:14897379..14899021-chr9:14903144..14904953,2	MCF-7	breast:
4	chr9:14616185..14616937-chr9:14768483..14769168,4	MCF-7	breast:
5	chr9:14778874..14780922-chr9:14784330..14786333,2	K562	blood:
6	chr9:14678774..14681640-chr9:14758881..14761517,2	MCF-7	breast:
7	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
8	chr9:14897379..14899021-chr9:14903144..14904953,2	MCF-7	breast:
9	chr9:14465013..14466518-chr9:14768250..14769873,6	MCF-7	breast:
10	chr9:14813259..14815238-chr9:14818255..14820615,2	K562	blood:
11	chr9:14846510..14847037-chr9:15142689..15143560,2	MCF-7	breast:
12	chr9:14914097..14915785-chr9:14923708..14925930,2	K562	blood:
13	chr9:14692712..14694901-chr9:14767288..14769707,2	MCF-7	breast:
14	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
15	chr9:14778874..14780922-chr9:14784330..14786333,2	K562	blood:
16	chr9:14914097..14915785-chr9:14923708..14925930,2	K562	blood:
17	chr20:52274228..52274993-chr9:14900093..14900641,2	MCF-7	breast:
18	chr9:14842932..14845441-chr9:14846633..14848951,2	K562	blood:
19	chr9:14693065..14694740-chr9:14764446..14767133,2	MCF-7	breast:
20	chr4:48089025..48089740-chr9:14788684..14789184,2	MCF-7	breast:
21	chr9:14850312..14853276-chr9:14856165..14857741,2	MCF-7	breast:
22	chr9:14691985..14694492-chr9:14845348..14847282,2	MCF-7	breast:
23	chr9:14441846..14442823-chr9:14768420..14769609,5	MCF-7	breast:
24	chr9:14842932..14845441-chr9:14846633..14848951,2	K562	blood:

Variant related genes	Relation type
LDHAP4	TF binding region
RNU6-1260P	TF binding region
FREM1	TF binding region
LDHAP4	CpG island
RNU6-1260P	CpG island
FREM1	CpG island
ENSG00000251960	chromatin interactions
ENSG00000164946	chromatin interactions
ENSG00000175893	chromatin interactions
ENSG00000199814	chromatin interactions

Extended variants
information (count: 9581 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:9581 , 50 per page) page: 1 2 3 4 5 6 7 ... 192

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79702127	chr9:14760657-14760658	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs568029229	chr9:14760684-14760685	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs187266448	chr9:14760700-14760701	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs144528016	chr9:14760715-14760716	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs540409339	chr9:14760722-14760723	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs566991991	chr9:14760732-14760733	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs148483457	chr9:14760795-14760796	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs558678040	chr9:14760797-14760798	Enhancers Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs72605694	chr9:14760880-14760881	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs574006673	chr9:14760903-14760904	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544272543	chr9:14760905-14760906	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34933596	chr9:14760907-14760908	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112803616	chr9:14760908-14760909	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141760840	chr9:14760916-14760917	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549578483	chr9:14760923-14760924	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574761583	chr9:14760965-14760966	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540201001	chr9:14760966-14760967	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545921549	chr9:14760988-14760989	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs13294547	chr9:14761002-14761003	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs34779302	chr9:14761008-14761009	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192731691	chr9:14761109-14761110	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546032287	chr9:14761168-14761169	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11790664	chr9:14761175-14761176	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs16932262	chr9:14761181-14761182	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs116717417	chr9:14761200-14761201	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1724	chr9:14761226-14761227	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs530354453	chr9:14761249-14761250	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10124839	chr9:14761260-14761261	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs547026861	chr9:14761262-14761263	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79207813	chr9:14761285-14761286	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563492331	chr9:14761299-14761300	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538922738	chr9:14761362-14761363	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184698833	chr9:14761364-14761365	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569087639	chr9:14761371-14761372	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538588211	chr9:14761431-14761432	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573932426	chr9:14761456-14761457	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs117817404	chr9:14761476-14761477	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554633538	chr9:14761503-14761504	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574785427	chr9:14761507-14761508	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370357758	chr9:14761519-14761520	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369958095	chr9:14761543-14761544	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189560612	chr9:14761562-14761563	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539083326	chr9:14761600-14761601	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577080034	chr9:14761646-14761647	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140338620	chr9:14761659-14761660	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373491382	chr9:14761676-14761677	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562703822	chr9:14761679-14761680	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568884553	chr9:14761684-14761685	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537868975	chr9:14761685-14761686	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576290961	chr9:14761730-14761731	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1616 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14730800-14764400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:14745000-14809800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:14748800-14775600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:14748800-14775800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr9:14748800-14790000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr9:14752800-14775800	Weak transcription	Duodenum Mucosa	Duodenum
7	chr9:14755400-14768400	Weak transcription	Colon Smooth Muscle	Colon
8	chr9:14755600-14765200	Weak transcription	Adipose Nuclei	Adipose
9	chr9:14755800-14766000	Weak transcription	Fetal Intestine Large	intestine
10	chr9:14755800-14775600	Weak transcription	Fetal Stomach	stomach
11	chr9:14755800-14812400	Weak transcription	Pancreas	Pancrea
12	chr9:14756400-14766400	Weak transcription	Fetal Muscle Leg	muscle
13	chr9:14757000-14771800	Strong transcription	Fetal Kidney	kidney
14	chr9:14758200-14766400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr9:14758400-14793400	Weak transcription	Aorta	Aorta
16	chr9:14759400-14765800	Weak transcription	HepG2	liver
17	chr9:14759600-14760800	Strong transcription	Fetal Lung	lung
18	chr9:14760000-14775200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr9:14760200-14760800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr9:14760600-14761400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr9:14760800-14761800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr9:14760800-14763000	Weak transcription	Fetal Lung	lung
23	chr9:14761400-14763000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr9:14761800-14762200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr9:14762200-14762600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr9:14762600-14763800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr9:14763000-14763200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr9:14763000-14770800	Strong transcription	Fetal Lung	lung
29	chr9:14763800-14764200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr9:14764200-14764400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:14764400-14764800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:14764400-14765200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:14764800-14809600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr9:14765200-14765400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr9:14765200-14767200	Strong transcription	Adipose Nuclei	Adipose
36	chr9:14765400-14765600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr9:14765600-14766000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr9:14765800-14768000	Strong transcription	HepG2	liver
39	chr9:14766000-14766400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr9:14766000-14766600	Enhancers	Fetal Intestine Large	intestine
41	chr9:14766400-14766800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr9:14766400-14767200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr9:14766400-14767400	Strong transcription	Fetal Muscle Leg	muscle
44	chr9:14766600-14766800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr9:14766600-14787400	Weak transcription	Fetal Intestine Large	intestine
46	chr9:14766800-14768400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr9:14766800-14775400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr9:14767200-14769200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr9:14767200-14779200	Weak transcription	Adipose Nuclei	Adipose
50	chr9:14767400-14779000	Weak transcription	Fetal Muscle Leg	muscle

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