Variant report

Variant	esv1840396
Chromosome Location	chr9:71733603-71743100
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:665)
CpG islands
(count:549)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71735292-71735927	HepG2	liver:	n/a	n/a
2	ATF2	chr9:71737566-71738148	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr9:71735106-71735934	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr9:71737258-71738069	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:71735153-71736138	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:71735251-71735859	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:71737585-71738101	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr9:71735576-71735811	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr9:71735558-71735835	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr9:71736571-71737127	GM12878	blood:	n/a	n/a
11	BHLHE40	chr9:71737647-71738054	HepG2	liver:	n/a	n/a
12	BRCA1	chr9:71736246-71736410	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr9:71736719-71737059	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr9:71735568-71735826	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr9:71735672-71735688	HepG2	liver:	n/a	n/a
16	CEBPB	chr9:71735281-71735937	MCF-7	breast:	n/a	n/a
17	CEBPB	chr9:71735584-71736233	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr9:71735281-71735626	HepG2	liver:	n/a	n/a
19	CEBPB	chr9:71735135-71736002	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr9:71735476-71735947	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr9:71737217-71738032	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr9:71735933-71736104	HepG2	liver:	n/a	n/a
23	CEBPB	chr9:71735697-71735833	HepG2	liver:	n/a	n/a
24	CEBPD	chr9:71735539-71735956	HepG2	liver:	n/a	n/a
25	CEBPD	chr9:71735430-71736087	HepG2	liver:	n/a	n/a
26	CHD1	chr9:71735356-71736142	H1-hESC	embryonic stem cell:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
27	CHD1	chr9:71734666-71735025	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr9:71736356-71738055	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr9:71736643-71737207	GM12878	blood:	n/a	n/a
30	CHD2	chr9:71735257-71736978	H1-hESC	embryonic stem cell:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
31	CHD2	chr9:71735572-71736125	HepG2	liver:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
32	CHD2	chr9:71736772-71736958	HepG2	liver:	n/a	n/a
33	CHD2	chr9:71735590-71737998	Hela-S3	cervix:	n/a	chr9:71735872-71735882 chr9:71735875-71735885
34	CREB1	chr9:71735173-71736321	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTBP2	chr9:71736458-71737761	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTBP2	chr9:71735145-71736239	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr9:71736820-71736970	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr9:71736436-71736449	LNCaP	prostate:	n/a	n/a
39	CTCF	chr9:71736761-71737032	GM12891	blood:	n/a	n/a
40	CTCF	chr9:71736800-71736950	HepG2	liver:	n/a	n/a
41	CTCF	chr9:71737200-71737350	RPTEC	kidney:	n/a	n/a
42	CTCF	chr9:71736752-71737034	MCF-7	breast:	n/a	n/a
43	CTCF	chr9:71736060-71736210	GM12867	blood:	n/a	n/a
44	CTCF	chr9:71736793-71736994	MCF-7	breast:	n/a	n/a
45	CTCF	chr9:71736840-71736990	HCM	heart:	n/a	n/a
46	CTCF	chr9:71736800-71736950	AG09319	gingival:	n/a	n/a
47	CTCF	chr9:71735640-71735790	GM12865	blood:	n/a	n/a
48	CTCF	chr9:71736900-71737050	SAEC	small airway:	n/a	n/a
49	CTCF	chr9:71736800-71736950	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr9:71736820-71736970	RPTEC	kidney:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71737258-71737308	HRE	kidney:	n/a
2	chr9:71736999-71737049	HCT-116	colon:	n/a
3	chr9:71737204-71737254	ovcar-3	ovarian:	n/a
4	chr9:71736854-71736904	Jurkat	blood:	n/a
5	chr9:71735648-71735698	SAEC	small airway:	n/a
6	chr9:71737756-71737806	HPAEpiC	pulmonary alveolar:	n/a
7	chr9:71735666-71735716	HIPEpiC	eye:	n/a
8	chr9:71737258-71737308	HNPCEpiC	eye:	n/a
9	chr9:71735666-71735716	HUVEC	blood vessel:	n/a
10	chr9:71737204-71737254	AG10803	skin:	n/a
11	chr9:71735701-71735751	HCM	heart:	n/a
12	chr9:71735666-71735716	K562	blood:	n/a
13	chr9:71735648-71735698	U87	brain:	n/a
14	chr9:71736854-71736904	HepG2	liver:	n/a
15	chr9:71737258-71737308	MCF10A-Er-Src	breast:	n/a
16	chr9:71735666-71735716	HAEpiC	amniotic membrane:	n/a
17	chr9:71737204-71737254	Hepatocyte	liver:	n/a
18	chr9:71736409-71736459	HCT-116	colon:	n/a
19	chr9:71736409-71736459	HRCEpiC	kidney:	n/a
20	chr9:71735648-71735698	HAEpiC	amniotic membrane:	n/a
21	chr9:71737258-71737308	CMK	blood:	n/a
22	chr9:71737204-71737254	AoSMC	blood vessel:	n/a
23	chr9:71737258-71737308	BE2_C	brain:	n/a
24	chr9:71737258-71737308	GM12878	blood:	n/a
25	chr9:71735648-71735698	BJ	skin:	n/a
26	chr9:71735666-71735716	AG09309	skin:	n/a
27	chr9:71735666-71735716	HMEC	breast:	n/a
28	chr9:71736854-71736904	SK-N-MC	brain:	n/a
29	chr9:71737756-71737806	NT2-D1	testis:	n/a
30	chr9:71736999-71737049	PANC-1	pancreas:	n/a
31	chr9:71736999-71737049	HCM	heart:	n/a
32	chr9:71737756-71737806	SK-N-SH	brain:	n/a
33	chr9:71737204-71737254	HAEpiC	amniotic membrane:	n/a
34	chr9:71735666-71735716	NHBE	bronchial:	n/a
35	chr9:71736409-71736459	HAEpiC	amniotic membrane:	n/a
36	chr9:71737756-71737806	SK-N-SH_RA	brain:	n/a
37	chr9:71737258-71737308	NB4	blood:	n/a
38	chr9:71735648-71735698	MCF10A-Er-Src	breast:	n/a
39	chr9:71736409-71736459	GM06990	blood:	n/a
40	chr9:71735701-71735751	NHBE	bronchial:	n/a
41	chr9:71737756-71737806	Hela-S3	cervix:	n/a
42	chr9:71737756-71737806	Caco-2	colon:	n/a
43	chr9:71735666-71735716	ECC-1	luminal epithelium:	n/a
44	chr9:71736999-71737049	HRCEpiC	kidney:	n/a
45	chr9:71735648-71735698	NHDF-neo	bronchial:	n/a
46	chr9:71737756-71737806	AoSMC	blood vessel:	n/a
47	chr9:71737258-71737308	MCF-7	breast:	n/a
48	chr9:71735648-71735698	MCF-7	breast:	n/a
49	chr9:71736999-71737049	HNPCEpiC	eye:	n/a
50	chr9:71737204-71737254	SK-N-SH	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:71727081..71728601-chr9:71737166..71739059,2	MCF-7	breast:
2	chr9:71732215..71735155-chr9:71735593..71737924,2	MCF-7	breast:
3	chr9:71733940..71739343-chr9:71741877..71748941,25	MCF-7	breast:
4	chr9:71736310..71738206-chr9:71797242..71798901,2	MCF-7	breast:
5	chr9:71735373..71738833-chr9:71764136..71766985,4	MCF-7	breast:
6	chr1:146555490..146556430-chr9:71736325..71736974,2	Hela-S3	cervix:
7	chr13:113241435..113242373-chr9:71735991..71736661,2	Hela-S3	cervix:
8	chr9:71696609..71699452-chr9:71736834..71738699,2	MCF-7	breast:
9	chr9:71736348..71739276-chr9:71751743..71753516,2	MCF-7	breast:
10	chr13:48611578..48612294-chr9:71736012..71736825,2	Hela-S3	cervix:
11	chr3:49066502..49067181-chr9:71736337..71736850,2	Hela-S3	cervix:
12	chr3:45017283..45018160-chr9:71735845..71736825,2	Hela-S3	cervix:
13	chr9:71649472..71654369-chr9:71735388..71737779,6	MCF-7	breast:
14	chr9:71733939..71735989-chr9:71814942..71816605,2	MCF-7	breast:
15	chr1:62208097..62208620-chr9:71736404..71737107,2	Hela-S3	cervix:
16	chr9:71734182..71738595-chr9:71741906..71745315,7	MCF-7	breast:
17	chr9:71734142..71739001-chr9:71788032..71795507,11	MCF-7	breast:
18	chr6:41040678..41041408-chr9:71735768..71736686,2	Hela-S3	cervix:
19	chr9:71720044..71724145-chr9:71733178..71738087,7	MCF-7	breast:
20	chr9:71733168..71738729-chr9:71786929..71793777,10	MCF-7	breast:
21	chr9:71736483..71737290-chr9:71808170..71808758,2	MCF-7	breast:
22	chr9:71680609..71683537-chr9:71732525..71735089,2	MCF-7	breast:
23	chr11:65666788..65667405-chr9:71737195..71738062,2	Hela-S3	cervix:
24	chr1:149223425..149225310-chr9:71736139..71738412,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TJP2-1	chr9:71736209-71736281	ENSG00000227410.1
2	lnc-TJP2-1	chr9:71736400-71737148	ENSG00000227410.1

No data

Variant related genes	Relation type
TJP2	TF binding region
TJP2	CpG island
ENSG00000136159	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000163812	chromatin interactions
ENSG00000165060	chromatin interactions
ENSG00000270236	chromatin interactions
ENSG00000075914	chromatin interactions
ENSG00000126216	chromatin interactions
ENSG00000001167	chromatin interactions
ENSG00000136143	chromatin interactions
ENSG00000178035	chromatin interactions
ENSG00000272434	chromatin interactions
ENSG00000132849	chromatin interactions
ENSG00000119139	chromatin interactions

Extended variants
information (count: 312 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11145330	chr9:71733603-71733604	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575745851	chr9:71733609-71733610	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs564398271	chr9:71733610-71733611	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs7860277	chr9:71733650-71733651	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs146260126	chr9:71733679-71733680	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs183737309	chr9:71733690-71733691	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs199843449	chr9:71733724-71733725	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs188516361	chr9:71733751-71733752	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs539795333	chr9:71733814-71733815	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs561655863	chr9:71733842-71733843	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs149829744	chr9:71733852-71733853	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs550594529	chr9:71733878-71733879	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs562728860	chr9:71733907-71733908	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs191346764	chr9:71733943-71733944	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs183227571	chr9:71733973-71733974	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs187837668	chr9:71733974-71733975	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs10118087	chr9:71733980-71733981	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs535021200	chr9:71734018-71734019	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs544961746	chr9:71734028-71734029	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs200924387	chr9:71734041-71734042	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs569093264	chr9:71734042-71734043	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs200415168	chr9:71734043-71734044	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs184788021	chr9:71734044-71734045	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs151145562	chr9:71734055-71734056	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs536192101	chr9:71734057-71734058	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs112190272	chr9:71734065-71734066	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs187947708	chr9:71734075-71734076	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs539616167	chr9:71734172-71734173	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs10118146	chr9:71734198-71734199	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs144064312	chr9:71734232-71734233	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs539928734	chr9:71734244-71734245	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs146452226	chr9:71734253-71734254	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs192615787	chr9:71734255-71734256	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs544531889	chr9:71734297-71734298	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs140827895	chr9:71734325-71734326	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs10781425	chr9:71734346-71734347	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs77363868	chr9:71734351-71734352	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs12353531	chr9:71734378-71734379	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs370312208	chr9:71734414-71734415	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs144987993	chr9:71734426-71734427	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs528638209	chr9:71734445-71734446	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs547113729	chr9:71734470-71734471	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs568495224	chr9:71734471-71734472	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs535447339	chr9:71734477-71734478	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs199559570	chr9:71734529-71734530	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs185186873	chr9:71734538-71734539	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs569401826	chr9:71734542-71734543	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs11145339	chr9:71734574-71734575	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs377763529	chr9:71734614-71734615	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs34124928	chr9:71734654-71734655	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
Melanoma	22183965	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD

Chromatin state (count:562 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71701800-71735200	Weak transcription	Primary T cells from cord blood	blood
2	chr9:71712600-71735200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:71715000-71735000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:71720400-71735600	Weak transcription	Left Ventricle	heart
5	chr9:71720600-71735000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:71721400-71734600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr9:71727200-71735800	Weak transcription	Brain Substantia Nigra	brain
8	chr9:71729800-71745600	Weak transcription	K562	blood
9	chr9:71730000-71733800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr9:71730600-71734800	Weak transcription	Fetal Muscle Leg	muscle
11	chr9:71730600-71736000	Weak transcription	NHDF-Ad	bronchial
12	chr9:71731000-71734600	Weak transcription	Stomach Mucosa	stomach
13	chr9:71731000-71735400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr9:71731000-71736000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr9:71731000-71736000	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr9:71731200-71735400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr9:71733400-71734000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr9:71733600-71733800	Enhancers	H9 Cell Line	embryonic stem cell
19	chr9:71733600-71734600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr9:71733600-71735000	Enhancers	Placenta	Placenta
21	chr9:71733800-71734000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr9:71733800-71734600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr9:71733800-71735000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr9:71734000-71735000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr9:71734000-71735000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:71734200-71734400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr9:71734200-71734400	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr9:71734400-71734600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr9:71734400-71734600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr9:71734400-71734600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr9:71734400-71735000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr9:71734400-71735000	Enhancers	Fetal Intestine Large	intestine
33	chr9:71734400-71735600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
34	chr9:71734400-71735600	Enhancers	Fetal Lung	lung
35	chr9:71734600-71734800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr9:71734600-71734800	Enhancers	H9 Cell Line	embryonic stem cell
37	chr9:71734600-71734800	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr9:71734600-71735000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr9:71734600-71735000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr9:71734600-71735000	Weak transcription	Liver	Liver
41	chr9:71734600-71735000	Enhancers	Pancreas	Pancrea
42	chr9:71734600-71735200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr9:71734600-71735200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr9:71734600-71735200	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr9:71734600-71735400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr9:71734600-71735400	Enhancers	Stomach Mucosa	stomach
47	chr9:71734600-71735600	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr9:71734800-71735000	Enhancers	Fetal Intestine Small	intestine
49	chr9:71734800-71735200	Enhancers	Duodenum Mucosa	Duodenum
50	chr9:71734800-71735200	Enhancers	HepG2	liver

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