Variant report

Variant	esv3343459
Chromosome Location	chr9:102862156-102864304
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	chr9:102863902-102864233	K562	blood:	n/a	n/a
2	BHLHE40	chr9:102860565-102862280	K562	blood:	n/a	n/a
3	BHLHE40	chr9:102863953-102864247	K562	blood:	n/a	n/a
4	BRCA1	chr9:102861151-102862415	Hela-S3	cervix:	n/a	n/a
5	CCNT2	chr9:102863942-102864235	K562	blood:	n/a	n/a
6	CEBPB	chr9:102861846-102862517	A549	lung:	n/a	chr9:102862034-102862043 chr9:102862034-102862043
7	CEBPB	chr9:102861065-102862501	Hela-S3	cervix:	n/a	chr9:102862034-102862043 chr9:102862034-102862043
8	CEBPB	chr9:102861818-102862324	MCF-7	breast:	n/a	chr9:102862034-102862043 chr9:102862034-102862043
9	CEBPB	chr9:102861825-102862403	K562	blood:	n/a	chr9:102862034-102862043 chr9:102862034-102862043
10	CEBPB	chr9:102861626-102862551	HepG2	liver:	n/a	chr9:102862034-102862043 chr9:102862034-102862043
11	CEBPB	chr9:102861679-102862326	A549	lung:	n/a	chr9:102862034-102862043 chr9:102862034-102862043
12	CEBPD	chr9:102863811-102864280	K562	blood:	n/a	n/a
13	CEBPD	chr9:102863872-102864404	K562	blood:	n/a	n/a
14	CHD2	chr9:102860521-102862343	Hela-S3	cervix:	n/a	chr9:102861818-102861828 chr9:102862183-102862193
15	CREB1	chr9:102860419-102862237	HepG2	liver:	n/a	n/a
16	CTCF	chr9:102862080-102862230	AG04450	lung:	n/a	n/a
17	E2F4	chr9:102861279-102862394	MCF10A-Er-Src	breast:	n/a	n/a
18	ELF1	chr9:102860239-102862202	HCT-116	colon:	n/a	chr9:102861317-102861328 chr9:102861317-102861328 chr9:102861318-102861327
19	EP300	chr9:102863870-102864247	K562	blood:	n/a	n/a
20	EP300	chr9:102862639-102862784	K562	blood:	n/a	n/a
21	EP300	chr9:102861700-102862172	K562	blood:	n/a	n/a
22	GABPA	chr9:102863917-102864215	K562	blood:	n/a	n/a
23	GATA1	chr9:102863537-102864783	PBDE	blood:	n/a	n/a
24	GATA1	chr9:102863907-102864233	PBDEFetal	blood:	n/a	n/a
25	GATA2	chr9:102863919-102864312	K562	blood:	n/a	n/a
26	GATA3	chr9:102864061-102864262	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr9:102863590-102863769	SH-SY5Y	brain:	n/a	n/a
28	GTF2F1	chr9:102861047-102862240	Hela-S3	cervix:	n/a	n/a
29	HA-E2F1	chr9:102860811-102862324	MCF-7	breast:	n/a	n/a
30	HCFC1	chr9:102860568-102862258	K562	blood:	n/a	n/a
31	HCFC1	chr9:102860073-102862658	Hela-S3	cervix:	n/a	n/a
32	HDAC2	chr9:102863914-102864222	K562	blood:	n/a	n/a
33	HDAC2	chr9:102863879-102864248	K562	blood:	n/a	n/a
34	HEY1	chr9:102861978-102862206	HepG2	liver:	n/a	n/a
35	HEY1	chr9:102861006-102862187	HepG2	liver:	n/a	n/a
36	HNF4A	chr9:102861124-102862190	HepG2	liver:	n/a	n/a
37	HNF4A	chr9:102862601-102862804	HepG2	liver:	n/a	chr9:102862745-102862760 chr9:102862723-102862736 chr9:102862723-102862736 chr9:102862721-102862736 chr9:102862723-102862736 chr9:102862722-102862736 chr9:102862745-102862760 chr9:102862721-102862736 chr9:102862720-102862738 chr9:102862745-102862760 chr9:102862723-102862735 chr9:102862722-102862735
38	JUND	chr9:102863936-102864273	K562	blood:	n/a	n/a
39	KAP1	chr9:102860842-102862189	U2OS	brain:	n/a	n/a
40	KAP1	chr9:102860465-102862443	HEK293	kidney:	n/a	n/a
41	MAFK	chr9:102861164-102862367	Hela-S3	cervix:	n/a	n/a
42	MAX	chr9:102860560-102862251	K562	blood:	n/a	chr9:102861825-102861835
43	MAX	chr9:102861912-102862196	HepG2	liver:	n/a	n/a
44	MAX	chr9:102861059-102862282	SK-N-SH	brain:	n/a	chr9:102861825-102861835
45	MAX	chr9:102860939-102862192	K562	blood:	n/a	chr9:102861825-102861835
46	MAX	chr9:102860391-102862442	A549	lung:	n/a	chr9:102861825-102861835
47	MAX	chr9:102861085-102862384	ECC-1	luminal epithelium:	n/a	chr9:102861825-102861835
48	MAX	chr9:102860937-102862354	A549	lung:	n/a	chr9:102861825-102861835
49	MAX	chr9:102860295-102862353	MCF-7	breast:	n/a	chr9:102861825-102861835
50	MAX	chr9:102860976-102862239	SK-N-SH	brain:	n/a	chr9:102861825-102861835

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:102863959-102864009	PrEC	prostate:	n/a
2	chr9:102863959-102864009	RPTEC	kidney:	n/a
3	chr9:102863959-102864009	HMEC	breast:	n/a
4	chr9:102863959-102864009	PANC-1	pancreas:	n/a
5	chr9:102863959-102864009	SK-N-SH_RA	brain:	n/a
6	chr9:102863959-102864009	AG09309	skin:	n/a
7	chr9:102863959-102864009	HNPCEpiC	eye:	n/a
8	chr9:102863959-102864009	HRE	kidney:	n/a
9	chr9:102863959-102864009	HRPEpiC	eye:	n/a
10	chr9:102863959-102864009	SKMC	muscle:	n/a
11	chr9:102863959-102864009	AG04450	lung:	fetal
12	chr9:102863959-102864009	ECC-1	luminal epithelium:	n/a
13	chr9:102863959-102864009	AoSMC	blood vessel:	n/a
14	chr9:102863959-102864009	HCM	heart:	n/a
15	chr9:102863959-102864009	GM12878	blood:	n/a
16	chr9:102863959-102864009	Jurkat	blood:	n/a
17	chr9:102863959-102864009	HCF	heart:	n/a
18	chr9:102863959-102864009	BE2_C	brain:	n/a
19	chr9:102863959-102864009	AG04449	skin:	fetal
20	chr9:102863959-102864009	HAEpiC	amniotic membrane:	n/a
21	chr9:102863959-102864009	HepG2	liver:	n/a
22	chr9:102863959-102864009	HCT-116	colon:	n/a
23	chr9:102863959-102864009	HRCEpiC	kidney:	n/a
24	chr9:102863959-102864009	H1-hESC	embryonic stem cell:	embryo
25	chr9:102863959-102864009	SK-N-SH	brain:	n/a
26	chr9:102863959-102864009	NHBE	bronchial:	n/a
27	chr9:102863959-102864009	HIPEpiC	eye:	n/a
28	chr9:102863959-102864009	MCF-7	breast:	n/a
29	chr9:102863959-102864009	ProgFib	skin:	n/a
30	chr9:102863959-102864009	Caco-2	colon:	n/a
31	chr9:102863959-102864009	AG10803	skin:	n/a
32	chr9:102863959-102864009	SAEC	small airway:	n/a
33	chr9:102863959-102864009	GM12892	blood:	n/a
34	chr9:102863959-102864009	K562	blood:	n/a
35	chr9:102863959-102864009	T-47D	breast:	n/a
36	chr9:102863959-102864009	Hepatocyte	liver:	n/a
37	chr9:102863959-102864009	NH-A	brain:	n/a
38	chr9:102863959-102864009	GM19239	blood:	n/a
39	chr9:102863959-102864009	CMK	blood:	n/a
40	chr9:102863959-102864009	U87	brain:	n/a
41	chr9:102863959-102864009	HEK293	kidney:	embryo
42	chr9:102863959-102864009	Hela-S3	cervix:	n/a
43	chr9:102863959-102864009	NT2-D1	testis:	n/a
44	chr9:102863959-102864009	NB4	blood:	n/a
45	chr9:102863959-102864009	HCPEpiC	choroid plexus:	n/a
46	chr9:102863959-102864009	LNCaP	prostate:	n/a
47	chr9:102863959-102864009	HL-60	blood:	n/a
48	chr9:102863959-102864009	HEEpiC	esophagus:	n/a
49	chr9:102863959-102864009	HUVEC	blood vessel:	n/a
50	chr9:102863959-102864009	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:102860210..102863951-chr9:102865614..102871017,5	K562	blood:
2	chr9:102861067..102864152-chr9:102881091..102884307,4	K562	blood:
3	chr15:45003558..45004176-chr9:102861994..102862803,2	Hela-S3	cervix:
4	chr9:102859693..102862029-chr9:102863024..102865040,3	MCF-7	breast:
5	chr9:102667836..102670748-chr9:102860445..102862735,2	K562	blood:
6	chr9:102581254..102583712-chr9:102860113..102863116,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STX17-2	chr9:102863583-102864299	NONHSAT133707

Variant related genes	Relation type
ERP44	TF binding region
RN7SL75P	TF binding region
INVS	TF binding region
ERP44	CpG island
RN7SL75P	CpG island
INVS	CpG island
ENSG00000023318	chromatin interactions
ENSG00000119509	chromatin interactions
ENSG00000255145	chromatin interactions
ENSG00000166710	chromatin interactions
ENSG00000136874	chromatin interactions
ENSG00000270995	chromatin interactions
ENSG00000237461	chromatin interactions

Extended variants
information (count: 130 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:130 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551530083	chr9:102862188-102862189	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs73656935	chr9:102862230-102862231	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs573054474	chr9:102862266-102862267	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs113042850	chr9:102862268-102862269	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs547328462	chr9:102862279-102862280	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs145149972	chr9:102862283-102862284	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs188106650	chr9:102862306-102862307	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs143943894	chr9:102862331-102862332	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs576187046	chr9:102862350-102862351	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs538401063	chr9:102862352-102862353	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs562967567	chr9:102862354-102862355	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs559096255	chr9:102862355-102862356	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs572503537	chr9:102862419-102862420	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs541613551	chr9:102862434-102862435	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs556371534	chr9:102862507-102862508	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs202094766	chr9:102862519-102862520	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs540941656	chr9:102862520-102862521	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs192938252	chr9:102862521-102862522	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs10988972	chr9:102862539-102862540	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs563368900	chr9:102862546-102862547	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs532630266	chr9:102862547-102862548	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs552350923	chr9:102862555-102862556	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs559800894	chr9:102862612-102862613	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs527467527	chr9:102862643-102862644	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs142061022	chr9:102862741-102862742	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs370437263	chr9:102862754-102862755	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs567554014	chr9:102862766-102862767	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs199529570	chr9:102862867-102862868	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs574259684	chr9:102862871-102862872	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs200504352	chr9:102862878-102862879	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs59637286	chr9:102862881-102862882	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs549802070	chr9:102862882-102862883	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs569706638	chr9:102862886-102862887	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs538635515	chr9:102862899-102862900	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs71503729	chr9:102862905-102862906	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs558318676	chr9:102862923-102862924	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs377177996	chr9:102862931-102862932	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs71370979	chr9:102862937-102862938	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs71498728	chr9:102862944-102862945	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs13288877	chr9:102862945-102862946	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs13293164	chr9:102862946-102862947	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs370614711	chr9:102862947-102862948	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs57032191	chr9:102862957-102862958	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs565786489	chr9:102862963-102862964	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs13288894	chr9:102862971-102862972	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs558817741	chr9:102862972-102862973	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs34351574	chr9:102862973-102862974	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs67592817	chr9:102862978-102862979	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs376899033	chr9:102862983-102862984	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs540643602	chr9:102862989-102862990	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:102859200-102862400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:102859200-102862600	Active TSS	GM12878-XiMat	blood
3	chr9:102859200-102862600	Active TSS	K562	blood
4	chr9:102859600-102862800	Active TSS	NHLF	lung
5	chr9:102859800-102862200	Active TSS	iPS-18 Cell Line	embryonic stem cell
6	chr9:102860000-102862200	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr9:102860000-102862600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr9:102860000-102862600	Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr9:102860000-102862600	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr9:102860000-102862600	Active TSS	NHDF-Ad	bronchial
11	chr9:102860000-102862800	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr9:102860000-102862800	Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr9:102860200-102862200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr9:102860200-102862200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:102860200-102862200	Active TSS	Esophagus	oesophagus
16	chr9:102860200-102862200	Active TSS	Gastric	stomach
17	chr9:102860200-102862200	Active TSS	Lung	lung
18	chr9:102860200-102862400	Active TSS	H1 Cell Line	embryonic stem cell
19	chr9:102860200-102862400	Active TSS	H9 Cell Line	embryonic stem cell
20	chr9:102860200-102862400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr9:102860200-102862400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr9:102860200-102862400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr9:102860200-102862400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr9:102860200-102862400	Active TSS	Aorta	Aorta
25	chr9:102860200-102862400	Active TSS	Fetal Muscle Trunk	muscle
26	chr9:102860200-102862400	Active TSS	Left Ventricle	heart
27	chr9:102860200-102862400	Active TSS	Ovary	ovary
28	chr9:102860200-102862400	Active TSS	Thymus	Thymus
29	chr9:102860200-102862600	Active TSS	Right Atrium	heart
30	chr9:102860200-102862600	Active TSS	A549	lung
31	chr9:102860200-102862800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr9:102860200-102862800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr9:102860200-102862800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr9:102860200-102862800	Active TSS	Right Ventricle	heart
35	chr9:102860400-102862200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr9:102860400-102862200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr9:102860400-102862200	Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr9:102860400-102862200	Active TSS	Fetal Intestine Large	intestine
39	chr9:102860400-102862200	Active TSS	Fetal Intestine Small	intestine
40	chr9:102860400-102862400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
41	chr9:102860400-102862400	Bivalent/Poised TSS	HepG2	liver
42	chr9:102860400-102862400	Active TSS	NHEK	skin
43	chr9:102860400-102862600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr9:102860400-102862600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr9:102860400-102862600	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr9:102860400-102862600	Active TSS	HMEC	breast
47	chr9:102860400-102862800	Active TSS	Psoas Muscle	Psoas
48	chr9:102860600-102862200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr9:102860600-102862200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr9:102860600-102862200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood

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