Variant report

Variant	nsv831520
Chromosome Location	chr9:15404866-15444447
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1005)
CpG islands
(count:610)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1005 , 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	ARID3A	chr9:15423654-15424033	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15426284-15426484	K562	blood:	n/a	n/a
3	ARID3A	chr9:15422587-15422682	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:15423509-15423900	K562	blood:	n/a	n/a
5	ARID3A	chr9:15422654-15422834	K562	blood:	n/a	n/a
6	ARID3A	chr9:15416889-15417137	HepG2	liver:	n/a	n/a
7	ATF1	chr9:15416926-15417228	K562	blood:	n/a	n/a
8	ATF2	chr9:15422425-15422861	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr9:15425980-15426551	GM12878	blood:	n/a	n/a
10	ATF2	chr9:15416815-15417288	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr9:15416859-15417296	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr9:15422346-15422848	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr9:15422403-15423034	GM12878	blood:	n/a	n/a
14	ATF2	chr9:15426044-15426358	GM12878	blood:	n/a	n/a
15	ATF3	chr9:15422610-15422838	K562	blood:	n/a	n/a
16	ATF3	chr9:15416909-15417257	K562	blood:	n/a	n/a
17	BATF	chr9:15426020-15426415	GM12878	blood:	n/a	n/a
18	BATF	chr9:15426063-15426425	GM12878	blood:	n/a	n/a
19	BATF	chr9:15424848-15425076	GM12878	blood:	n/a	chr9:15424968-15424977
20	BCL11A	chr9:15422429-15422805	GM12878	blood:	n/a	chr9:15422614-15422627
21	BCL11A	chr9:15422513-15422747	GM12878	blood:	n/a	chr9:15422614-15422627
22	BCL3	chr9:15422174-15423029	A549	lung:	n/a	chr9:15422414-15422423 chr9:15422614-15422627
23	BCLAF1	chr9:15422287-15423154	GM12878	blood:	n/a	chr9:15422414-15422423 chr9:15422614-15422627
24	BCLAF1	chr9:15425904-15426489	GM12878	blood:	n/a	n/a
25	BCLAF1	chr9:15422376-15423136	GM12878	blood:	n/a	chr9:15422414-15422423 chr9:15422614-15422627
26	BHLHE40	chr9:15422162-15423396	K562	blood:	n/a	n/a
27	BHLHE40	chr9:15426347-15426389	K562	blood:	n/a	n/a
28	BHLHE40	chr9:15422278-15423305	GM12878	blood:	n/a	n/a
29	BRCA1	chr9:15422537-15422940	HepG2	liver:	n/a	n/a
30	BRCA1	chr9:15422481-15422931	GM12878	blood:	n/a	n/a
31	BRCA1	chr9:15422422-15423005	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr9:15422502-15422911	H1-hESC	embryonic stem cell:	n/a	n/a
33	CBX3	chr9:15422380-15422745	K562	blood:	n/a	n/a
34	CCNT2	chr9:15422421-15423210	K562	blood:	n/a	n/a
35	CEBPB	chr9:15417053-15417070	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:15434145-15434324	HepG2	liver:	n/a	chr9:15434275-15434286
37	CEBPB	chr9:15422293-15422802	A549	lung:	n/a	n/a
38	CEBPB	chr9:15433217-15433476	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:15433260-15433477	A549	lung:	n/a	n/a
40	CEBPB	chr9:15422347-15422748	HepG2	liver:	n/a	n/a
41	CEBPD	chr9:15422416-15423009	HepG2	liver:	n/a	n/a
42	CHD1	chr9:15422447-15422941	GM12878	blood:	n/a	n/a
43	CHD1	chr9:15422908-15423217	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr9:15423142-15423320	GM12878	blood:	n/a	n/a
45	CHD2	chr9:15422450-15423067	HepG2	liver:	n/a	n/a
46	CHD2	chr9:15426399-15426441	K562	blood:	n/a	n/a
47	CHD2	chr9:15422304-15423438	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr9:15422206-15423224	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr9:15422057-15423116	GM12878	blood:	n/a	n/a
50	CHD2	chr9:15422425-15422939	K562	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15420564-15420614	PANC-1	pancreas:	n/a
2	chr9:15422993-15423043	MCF10A-Er-Src	breast:	n/a
3	chr9:15442613-15442663	HRPEpiC	eye:	n/a
4	chr9:15422376-15422426	IMR90	lung:	fetal
5	chr9:15423182-15423232	GM06990	blood:	n/a
6	chr9:15423618-15423668	HEK293	kidney:	embryo
7	chr9:15422769-15422819	MCF10A-Er-Src	breast:	n/a
8	chr9:15425935-15425985	Jurkat	blood:	n/a
9	chr9:15423618-15423668	K562	blood:	n/a
10	chr9:15423618-15423668	HEEpiC	esophagus:	n/a
11	chr9:15425935-15425985	AG10803	skin:	n/a
12	chr9:15425935-15425985	U87	brain:	n/a
13	chr9:15422769-15422819	BJ	skin:	n/a
14	chr9:15423618-15423668	ECC-1	luminal epithelium:	n/a
15	chr9:15422769-15422819	Jurkat	blood:	n/a
16	chr9:15422589-15422639	HNPCEpiC	eye:	n/a
17	chr9:15423182-15423232	K562	blood:	n/a
18	chr9:15442613-15442663	NT2-D1	testis:	n/a
19	chr9:15422943-15422993	H1-hESC	embryonic stem cell:	embryo
20	chr9:15422943-15422993	AG09319	gingival:	n/a
21	chr9:15442613-15442663	K562	blood:	n/a
22	chr9:15423182-15423232	HRCEpiC	kidney:	n/a
23	chr9:15423618-15423668	HRPEpiC	eye:	n/a
24	chr9:15422993-15423043	HPAEpiC	pulmonary alveolar:	n/a
25	chr9:15422589-15422639	SK-N-MC	brain:	n/a
26	chr9:15422589-15422639	Jurkat	blood:	n/a
27	chr9:15420564-15420614	RPTEC	kidney:	n/a
28	chr9:15422376-15422426	AG10803	skin:	n/a
29	chr9:15422993-15423043	NH-A	brain:	n/a
30	chr9:15422993-15423043	Hepatocyte	liver:	n/a
31	chr9:15422943-15422993	PFSK-1	brain:	n/a
32	chr9:15423182-15423232	GM19239	blood:	n/a
33	chr9:15422769-15422819	AG09309	skin:	n/a
34	chr9:15423182-15423232	AoSMC	blood vessel:	n/a
35	chr9:15423182-15423232	H1-hESC	embryonic stem cell:	embryo
36	chr9:15422943-15422993	GM06990	blood:	n/a
37	chr9:15442613-15442663	CMK	blood:	n/a
38	chr9:15422993-15423043	HL-60	blood:	n/a
39	chr9:15425935-15425985	HMEC	breast:	n/a
40	chr9:15422769-15422819	A549	lung:	n/a
41	chr9:15442613-15442663	Hela-S3	cervix:	n/a
42	chr9:15420564-15420614	MCF-7	breast:	n/a
43	chr9:15425935-15425985	HCT-116	colon:	n/a
44	chr9:15422943-15422993	A549	lung:	n/a
45	chr9:15422943-15422993	HCF	heart:	n/a
46	chr9:15425935-15425985	SKMC	muscle:	n/a
47	chr9:15442613-15442663	HRE	kidney:	n/a
48	chr9:15425935-15425985	HRPEpiC	eye:	n/a
49	chr9:15422993-15423043	HEEpiC	esophagus:	n/a
50	chr9:15422769-15422819	GM19239	blood:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:217363452..217364033-chr9:15422219..15422852,2	HCT-116	colon:
2	chr1:159894793..159895333-chr9:15422180..15423023,2	Hela-S3	cervix:
3	chr9:15420915..15423147-chr9:15426389..15428949,2	K562	blood:
4	chr9:15305088..15306661-chr9:15415103..15416933,2	MCF-7	breast:
5	chr9:15418505..15420597-chr9:15421286..15424516,4	MCF-7	breast:
6	chr9:15305128..15307154-chr9:15417021..15419951,2	MCF-7	breast:
7	chr9:15415166..15416789-chr9:15420978..15423004,2	MCF-7	breast:
8	chr9:15422069..15423659-chr9:15430578..15433740,3	K562	blood:
9	chr9:15422934..15425831-chr9:15427630..15429287,2	K562	blood:
10	chr9:15422138..15423750-chr9:15430824..15433204,2	K562	blood:
11	chr9:15211245..15212139-chr9:15416585..15417547,5	MCF-7	breast:
12	chr9:15276373..15278004-chr9:15420785..15422574,2	MCF-7	breast:
13	chr1:205782053..205782858-chr9:15422168..15422987,2	HCT-116	colon:
14	chr9:15277682..15279519-chr9:15415467..15418240,3	MCF-7	breast:
15	chr9:15420090..15425077-chr9:15425243..15430966,9	MCF-7	breast:
16	chr12:7052754..7053671-chr9:15422600..15423100,2	Hela-S3	cervix:
17	chr11:71751691..71752198-chr9:15422276..15423243,2	HCT-116	colon:
18	chr9:15385459..15387196-chr9:15436159..15438276,2	K562	blood:
19	chr17:56083086..56085615-chr9:15422777..15425325,2	MCF-7	breast:
20	chr9:15277764..15278338-chr9:15416698..15417388,2	MCF-7	breast:
21	chr9:15414997..15416790-chr9:15421464..15423490,2	MCF-7	breast:
22	chr9:15421340..15424109-chr9:15510012..15511838,2	K562	blood:
23	chr9:15306135..15309581-chr9:15420818..15425516,6	MCF-7	breast:
24	chr9:15422138..15423750-chr9:15430824..15433204,2	K562	blood:
25	chr9:15414032..15416513-chr9:15421401..15423007,2	K562	blood:
26	chr9:15429263..15431513-chr9:15449169..15450709,2	K562	blood:
27	chr9:15352501..15354066-chr9:15419261..15422025,2	MCF-7	breast:
28	chr2:173940670..173941204-chr9:15422600..15423282,2	Hela-S3	cervix:
29	chr9:15420595..15424773-chr9:15424796..15433036,11	MCF-7	breast:
30	chr9:15422069..15423659-chr9:15430578..15433740,3	K562	blood:
31	chr9:15298942..15301605-chr9:15420446..15422025,2	MCF-7	breast:
32	chr9:15420595..15424773-chr9:15424796..15433036,11	MCF-7	breast:
33	chr9:15104624..15105430-chr9:15416660..15417504,2	MCF-7	breast:
34	chr1:11865371..11866248-chr9:15422460..15422973,2	Hela-S3	cervix:
35	chr9:15211153..15211795-chr9:15417051..15417568,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-319P	TF binding region
SNAPC3	TF binding region
RNU6-319P	CpG island
SNAPC3	CpG island
ENSG00000155158	chromatin interactions
ENSG00000011021	chromatin interactions
ENSG00000136450	chromatin interactions
ENSG00000158710	chromatin interactions
ENSG00000091436	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000197756	chromatin interactions
ENSG00000137497	chromatin interactions
ENSG00000251834	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000164975	chromatin interactions
ENSG00000232485	chromatin interactions
ENSG00000133065	chromatin interactions
ENSG00000164985	chromatin interactions
ENSG00000177000	chromatin interactions

Extended variants
information (count: 1589 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77329081	chr9:15404873-15404874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs577629048	chr9:15404895-15404896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76059779	chr9:15404917-15404918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541305179	chr9:15404929-15404930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374956749	chr9:15404939-15404940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558280707	chr9:15404974-15404975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560501863	chr9:15404998-15404999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2488960	chr9:15408003-15408004	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs571229552	chr9:15408096-15408097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542693845	chr9:15408098-15408099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs199579888	chr9:15408099-15408100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371178527	chr9:15408101-15408102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374115237	chr9:15408114-15408115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76461646	chr9:15408150-15408151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2490867	chr9:15408162-15408163	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs536055159	chr9:15408231-15408232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544912240	chr9:15408287-15408288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564703028	chr9:15408302-15408303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181247127	chr9:15408327-15408328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369773492	chr9:15408346-15408347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73413231	chr9:15408370-15408371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143803338	chr9:15408381-15408382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191022741	chr9:15408382-15408383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73413235	chr9:15408413-15408414	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs376970316	chr9:15408442-15408443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541551402	chr9:15408443-15408444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146351291	chr9:15408454-15408455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550237714	chr9:15408464-15408465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10962022	chr9:15408475-15408476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542063251	chr9:15408534-15408535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563832688	chr9:15408541-15408542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114370771	chr9:15408553-15408554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552876935	chr9:15408658-15408659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7041424	chr9:15408664-15408665	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs532001815	chr9:15408713-15408714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547516077	chr9:15408721-15408722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370285428	chr9:15408734-15408735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565641493	chr9:15408745-15408746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184072955	chr9:15408758-15408759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143619537	chr9:15414036-15414037	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs188273169	chr9:15414037-15414038	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs374090400	chr9:15414038-15414039	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs151006654	chr9:15414039-15414040	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs552236535	chr9:15414070-15414071	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs564412165	chr9:15414073-15414074	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs140844219	chr9:15414112-15414113	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs547034506	chr9:15414135-15414136	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs568438101	chr9:15414187-15414188	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs182048803	chr9:15414224-15414225	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs144603999	chr9:15414262-15414263	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:1558 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15404000-15405000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr9:15408000-15408800	Enhancers	HepG2	liver
3	chr9:15416200-15416800	Enhancers	Fetal Intestine Small	intestine
4	chr9:15416600-15417000	Enhancers	HepG2	liver
5	chr9:15416800-15417000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:15416800-15417000	Enhancers	H9 Cell Line	embryonic stem cell
7	chr9:15416800-15417000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr9:15416800-15417000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr9:15416800-15417000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr9:15416800-15417000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:15416800-15417000	Enhancers	Esophagus	oesophagus
12	chr9:15416800-15417200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr9:15416800-15418000	Enhancers	Placenta	Placenta
14	chr9:15416800-15418400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr9:15417000-15417400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:15417000-15417600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr9:15417000-15417600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr9:15417000-15417800	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr9:15417000-15417800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr9:15417000-15421800	Weak transcription	HepG2	liver
21	chr9:15417000-15422000	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr9:15417000-15422000	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr9:15417000-15422200	Weak transcription	Esophagus	oesophagus
24	chr9:15417400-15417800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr9:15417600-15418200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr9:15417600-15418400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr9:15417800-15418000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr9:15417800-15418000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr9:15417800-15418200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr9:15417800-15418200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr9:15417800-15418400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr9:15418000-15419800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr9:15418000-15422000	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr9:15418200-15421400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr9:15418200-15422000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr9:15418200-15422200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr9:15418400-15421600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr9:15418400-15421800	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr9:15418400-15421800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr9:15420600-15422000	Weak transcription	Brain Cingulate Gyrus	brain
41	chr9:15420600-15422000	Enhancers	Osteobl	bone
42	chr9:15421200-15422000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr9:15421400-15421600	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr9:15421400-15421800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr9:15421400-15421800	Enhancers	Duodenum Mucosa	Duodenum
46	chr9:15421400-15422000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr9:15421400-15422000	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr9:15421400-15422200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr9:15421400-15422200	Enhancers	Fetal Intestine Small	intestine
50	chr9:15421600-15421800	Enhancers	Gastric	stomach

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