Variant report

Variant	nsv1054784
Chromosome Location	chr9:96976419-97025515
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:541)
CpG islands
(count:306)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:97021239-97021729	K562	blood:	n/a	n/a
2	ARID3A	chr9:97018517-97018706	K562	blood:	n/a	n/a
3	ARID3A	chr9:97019229-97019305	K562	blood:	n/a	n/a
4	ATF1	chr9:97018366-97018736	K562	blood:	n/a	n/a
5	ATF2	chr9:97021344-97021598	GM12878	blood:	n/a	n/a
6	ATF3	chr9:97021410-97021656	K562	blood:	n/a	n/a
7	BACH1	chr9:97021395-97022034	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr9:97021349-97021823	GM12878	blood:	n/a	n/a
9	BCLAF1	chr9:97021278-97021779	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:97021352-97022053	GM12878	blood:	n/a	n/a
11	BHLHE40	chr9:97021368-97022134	HepG2	liver:	n/a	n/a
12	BHLHE40	chr9:97021412-97022057	K562	blood:	n/a	n/a
13	BRCA1	chr9:97021381-97021724	HepG2	liver:	n/a	n/a
14	BRCA1	chr9:97021483-97021839	GM12878	blood:	n/a	n/a
15	BRCA1	chr9:97025359-97025520	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr9:97007913-97008307	K562	blood:	n/a	n/a
17	CBX3	chr9:97021352-97021885	K562	blood:	n/a	n/a
18	CBX3	chr9:97007961-97008293	K562	blood:	n/a	n/a
19	CCNT2	chr9:97016386-97016577	K562	blood:	n/a	n/a
20	CCNT2	chr9:97000961-97001205	K562	blood:	n/a	n/a
21	CCNT2	chr9:97021383-97022018	K562	blood:	n/a	n/a
22	CEBPB	chr9:97025089-97025459	K562	blood:	n/a	chr9:97025278-97025289
23	CEBPB	chr9:97022093-97022275	K562	blood:	n/a	n/a
24	CEBPB	chr9:97021418-97021576	HepG2	liver:	n/a	n/a
25	CEBPB	chr9:97025144-97025452	K562	blood:	n/a	chr9:97025278-97025289
26	CEBPB	chr9:97025209-97025374	A549	lung:	n/a	chr9:97025278-97025289
27	CEBPB	chr9:97025164-97025424	HepG2	liver:	n/a	chr9:97025278-97025289
28	CEBPB	chr9:96985179-96985418	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr9:97021371-97021716	K562	blood:	n/a	n/a
30	CEBPB	chr9:97021352-97021686	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr9:97025184-97025340	Hela-S3	cervix:	n/a	chr9:97025278-97025289
32	CEBPB	chr9:97007459-97007502	K562	blood:	n/a	n/a
33	CEBPB	chr9:97021388-97021670	IMR90	lung:	n/a	n/a
34	CEBPD	chr9:97021552-97021837	HepG2	liver:	n/a	n/a
35	CHD1	chr9:97021714-97021997	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr9:97021782-97021954	GM12878	blood:	n/a	n/a
37	CHD2	chr9:97021391-97022138	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr9:97021369-97021759	K562	blood:	n/a	n/a
39	CHD2	chr9:97021367-97022013	HepG2	liver:	n/a	n/a
40	CHD2	chr9:97021359-97021840	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr9:97021304-97021818	GM12878	blood:	n/a	n/a
42	CREB1	chr9:97021234-97021924	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr9:97021349-97021856	HepG2	liver:	n/a	n/a
44	CREB1	chr9:97021287-97022089	HepG2	liver:	n/a	n/a
45	CREB1	chr9:97021342-97021867	K562	blood:	n/a	n/a
46	CREB1	chr9:97021297-97021833	GM12878	blood:	n/a	n/a
47	CREB1	chr9:97021360-97021884	A549	lung:	n/a	n/a
48	CREB1	chr9:97021371-97021652	A549	lung:	n/a	n/a
49	CREB1	chr9:97021393-97022071	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr9:97015189-97015235	GM20000	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:97021415-97021465	SK-N-SH	brain:	n/a
2	chr9:97021415-97021465	SK-N-SH	brain:	n/a
3	chr9:97021415-97021465	PANC-1	pancreas:	n/a
4	chr9:97021919-97021969	H1-hESC	embryonic stem cell:	embryo
5	chr9:97021919-97021969	SK-N-SH_RA	brain:	n/a
6	chr9:97020667-97020717	HUVEC	blood vessel:	n/a
7	chr9:97022269-97022319	Hepatocyte	liver:	n/a
8	chr9:97020667-97020717	NT2-D1	testis:	n/a
9	chr9:97021966-97022016	HRE	kidney:	n/a
10	chr9:97021966-97022016	HUVEC	blood vessel:	n/a
11	chr9:97020667-97020717	HRPEpiC	eye:	n/a
12	chr9:97022269-97022319	AG04449	skin:	fetal
13	chr9:97020667-97020717	BE2_C	brain:	n/a
14	chr9:97020667-97020717	AG04450	lung:	fetal
15	chr9:97021415-97021465	K562	blood:	n/a
16	chr9:97021415-97021465	RPTEC	kidney:	n/a
17	chr9:97020667-97020717	HEK293	kidney:	embryo
18	chr9:97021966-97022016	MCF-7	breast:	n/a
19	chr9:97021966-97022016	U87	brain:	n/a
20	chr9:97020667-97020717	HCM	heart:	n/a
21	chr9:97021966-97022016	HMEC	breast:	n/a
22	chr9:97021919-97021969	HIPEpiC	eye:	n/a
23	chr9:97021966-97022016	BJ	skin:	n/a
24	chr9:97021966-97022016	HRCEpiC	kidney:	n/a
25	chr9:97022269-97022319	PFSK-1	brain:	n/a
26	chr9:97020667-97020717	HCT-116	colon:	n/a
27	chr9:97021966-97022016	HepG2	liver:	n/a
28	chr9:97021415-97021465	BJ	skin:	n/a
29	chr9:97021966-97022016	AG04449	skin:	fetal
30	chr9:97022269-97022319	T-47D	breast:	n/a
31	chr9:97021415-97021465	SK-N-MC	brain:	n/a
32	chr9:97020667-97020717	NHDF-neo	bronchial:	n/a
33	chr9:97022269-97022319	GM12878	blood:	n/a
34	chr9:97020667-97020717	GM12892	blood:	n/a
35	chr9:97021415-97021465	IMR90	lung:	fetal
36	chr9:97022269-97022319	HMEC	breast:	n/a
37	chr9:97021415-97021465	HEK293	kidney:	embryo
38	chr9:97021919-97021969	HPAEpiC	pulmonary alveolar:	n/a
39	chr9:97022269-97022319	HEK293	kidney:	embryo
40	chr9:97022269-97022319	HepG2	liver:	n/a
41	chr9:97021415-97021465	HPAEpiC	pulmonary alveolar:	n/a
42	chr9:97021966-97022016	SK-N-SH_RA	brain:	n/a
43	chr9:97021966-97022016	AG10803	skin:	n/a
44	chr9:97021966-97022016	Hela-S3	cervix:	n/a
45	chr9:97021415-97021465	ECC-1	luminal epithelium:	n/a
46	chr9:97021415-97021465	LNCaP	prostate:	n/a
47	chr9:97020667-97020717	ovcar-3	ovarian:	n/a
48	chr9:97022269-97022319	HEEpiC	esophagus:	n/a
49	chr9:97020667-97020717	HMEC	breast:	n/a
50	chr9:97021919-97021969	GM12878	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:97017106..97019746-chr9:97019872..97021495,2	K562	blood:
2	chr9:97007341..97009316-chr9:97013277..97015921,2	MCF-7	breast:
3	chr9:96796176..96798166-chr9:96993062..96994935,2	MCF-7	breast:
4	chr9:97021249..97023395-chr9:97039780..97042509,4	MCF-7	breast:
5	chr9:97021406..97023043-chr9:97038524..97041223,2	K562	blood:
6	chr9:97011802..97014770-chr9:97055516..97058379,2	K562	blood:
7	chr9:96936846..96939200-chr9:96984254..96986208,2	K562	blood:
8	chr9:96975962..96978942-chr9:96988831..96990467,2	MCF-7	breast:
9	chr9:97000881..97002624-chr9:97017487..97019622,2	K562	blood:
10	chr9:96773554..96776449-chr9:96974238..96977177,2	MCF-7	breast:
11	chr9:97021611..97023203-chr9:97065025..97066542,2	K562	blood:
12	chr9:97020053..97021567-chr9:97135095..97137937,2	MCF-7	breast:
13	chr9:96727836..96728378-chr9:96975555..96976476,2	MCF-7	breast:
14	chr9:96928568..96930309-chr9:97024360..97026072,2	K562	blood:
15	chr9:97015612..97017858-chr9:97018523..97020622,2	MCF-7	breast:
16	chr9:96827200..96828396-chr9:96975283..96976482,6	MCF-7	breast:
17	chr9:96927406..96930148-chr9:97007636..97010398,2	MCF-7	breast:
18	chr9:97017627..97019343-chr9:97026034..97028389,2	K562	blood:
19	chr9:96789976..96794362-chr9:96971656..96977390,6	MCF-7	breast:
20	chr9:96725158..96725897-chr9:96975460..96976466,4	K562	blood:
21	chr9:96792428..96794821-chr9:96985023..96987291,2	K562	blood:
22	chr9:97021632..97023442-chr9:97057310..97060089,2	MCF-7	breast:
23	chr9:97000881..97002624-chr9:97017487..97019622,2	K562	blood:
24	chr9:96975962..96978942-chr9:96988831..96990467,2	MCF-7	breast:
25	chr9:97017106..97019746-chr9:97019872..97021495,2	K562	blood:
26	chr9:96776018..96777153-chr9:96975464..96976521,5	MCF-7	breast:
27	chr9:96776042..96777028-chr9:96975491..96976419,9	MCF-7	breast:
28	chr9:96989595..96992075-chr9:96994817..96996695,2	K562	blood:
29	chr9:97015612..97017858-chr9:97018523..97020622,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIATL1-13	chr9:97021603-97021627	NONHSAT133303

No data

Variant related genes	Relation type
RNU6-677P	TF binding region
ZNF169	TF binding region
ENSG00000238792	TF binding region
RNU6-677P	CpG island
ZNF169	CpG island
ENSG00000238792	CpG island
ENSG00000199165	chromatin interactions
ENSG00000238792	chromatin interactions
ENSG00000148110	chromatin interactions
ENSG00000199072	chromatin interactions
ENSG00000269929	chromatin interactions
ENSG00000175787	chromatin interactions
ENSG00000269946	chromatin interactions
ENSG00000252723	chromatin interactions
ENSG00000158079	chromatin interactions

Extended variants
information (count: 1056 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1056 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181414682	chr9:96976462-96976463	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs556603309	chr9:96976524-96976525	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529552746	chr9:96976553-96976554	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs577989870	chr9:96976555-96976556	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150981967	chr9:96976563-96976564	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564226598	chr9:96976573-96976574	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs186229192	chr9:96976630-96976631	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs140660773	chr9:96976666-96976667	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs71366210	chr9:96976682-96976683	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2542761	chr9:96976743-96976744	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs545426144	chr9:96976808-96976809	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs529030645	chr9:96976830-96976831	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs144471936	chr9:96976849-96976850	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568933366	chr9:96976851-96976852	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs191328108	chr9:96976878-96976879	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113369103	chr9:96976886-96976887	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs180988360	chr9:96976942-96976943	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs147774877	chr9:96976946-96976947	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs556075563	chr9:96976956-96976957	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs567894291	chr9:96977020-96977021	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538423306	chr9:96977152-96977153	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs570571802	chr9:96977155-96977156	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs201055820	chr9:96977187-96977188	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs58937522	chr9:96977188-96977189	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371909608	chr9:96977189-96977190	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs141092212	chr9:96977204-96977205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs545079205	chr9:96977242-96977243	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs150290871	chr9:96977266-96977267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs572820475	chr9:96977289-96977290	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs13284558	chr9:96977297-96977298	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs10993097	chr9:96977298-96977299	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs529102021	chr9:96977316-96977317	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs544349579	chr9:96977319-96977320	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs562455326	chr9:96977329-96977330	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs2717489	chr9:96977377-96977378	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs551112579	chr9:96977390-96977391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370453665	chr9:96977402-96977403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185282965	chr9:96977435-96977436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527264035	chr9:96977487-96977488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549737257	chr9:96977505-96977506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374506597	chr9:96977521-96977522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538058303	chr9:96977548-96977549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550308632	chr9:96977588-96977589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571662529	chr9:96977605-96977606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554135977	chr9:96977630-96977631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10739973	chr9:96977650-96977651	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs553824999	chr9:96977681-96977682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572140516	chr9:96977689-96977690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370718077	chr9:96977691-96977692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544450278	chr9:96977692-96977693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Bipolar disorder	18458673	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Effusion lymphoma	18079361	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:504 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96974400-96976600	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr9:96975400-96978400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:96979000-96979400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:96997000-96997600	Enhancers	Brain Germinal Matrix	brain
5	chr9:97000200-97000800	Enhancers	K562	blood
6	chr9:97000800-97001200	Flanking Active TSS	K562	blood
7	chr9:97001200-97001600	Active TSS	K562	blood
8	chr9:97001600-97001800	Flanking Active TSS	K562	blood
9	chr9:97011000-97011200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr9:97011200-97015800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr9:97012400-97013600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr9:97012600-97013000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr9:97012600-97013000	Enhancers	Hela-S3	cervix
14	chr9:97012600-97013400	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr9:97012600-97013400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr9:97012600-97013600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr9:97012600-97013600	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr9:97012600-97013600	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr9:97012600-97013800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr9:97012600-97013800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr9:97012800-97013000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:97012800-97013200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr9:97012800-97013200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr9:97012800-97013400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr9:97012800-97013400	Enhancers	Primary T cells from cord blood	blood
26	chr9:97012800-97013400	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr9:97012800-97013800	Enhancers	Primary T cells fromperipheralblood	blood
28	chr9:97013000-97013600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr9:97013400-97013800	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr9:97013800-97020800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr9:97015800-97016600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr9:97018000-97020800	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr9:97019200-97020800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr9:97020200-97020600	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr9:97020200-97020600	Enhancers	HepG2	liver
36	chr9:97020200-97021200	Enhancers	K562	blood
37	chr9:97020400-97020600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr9:97020400-97020600	Enhancers	Right Ventricle	heart
39	chr9:97020400-97021000	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr9:97020400-97021000	Enhancers	Ovary	ovary
41	chr9:97020400-97021000	Enhancers	A549	lung
42	chr9:97020400-97021200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr9:97020600-97020800	Flanking Active TSS	HepG2	liver
44	chr9:97020600-97021000	Enhancers	Placenta	Placenta
45	chr9:97020600-97021200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr9:97020800-97021000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr9:97020800-97021000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr9:97020800-97021000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr9:97020800-97021000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr9:97020800-97021000	Enhancers	Colon Smooth Muscle	Colon

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