Variant report

Variant	nsv982625
Chromosome Location	chr9:94702344-94712887
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:701)
CpG islands
(count:490)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:94710383-94710964	K562	blood:	n/a	n/a
2	ARID3A	chr9:94706132-94706682	K562	blood:	n/a	n/a
3	ARID3A	chr9:94707375-94708666	K562	blood:	n/a	n/a
4	ARID3A	chr9:94712529-94712598	K562	blood:	n/a	n/a
5	ATF1	chr9:94706177-94706583	K562	blood:	n/a	n/a
6	ATF1	chr9:94707597-94708122	K562	blood:	n/a	n/a
7	ATF3	chr9:94706209-94706598	K562	blood:	n/a	n/a
8	BACH1	chr9:94711162-94711495	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:94712501-94712871	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr9:94712258-94712984	K562	blood:	n/a	chr9:94712633-94712649 chr9:94712636-94712652
11	BHLHE40	chr9:94707056-94708939	K562	blood:	n/a	n/a
12	BHLHE40	chr9:94710423-94710707	K562	blood:	n/a	n/a
13	BHLHE40	chr9:94711063-94711373	K562	blood:	n/a	chr9:94711166-94711182
14	CBX3	chr9:94710994-94711464	K562	blood:	n/a	n/a
15	CCNT2	chr9:94708333-94709085	K562	blood:	n/a	n/a
16	CCNT2	chr9:94706364-94706494	K562	blood:	n/a	n/a
17	CCNT2	chr9:94710887-94712937	K562	blood:	n/a	chr9:94711693-94711702 chr9:94711618-94711627 chr9:94711360-94711369
18	CCNT2	chr9:94707619-94707907	K562	blood:	n/a	n/a
19	CEBPB	chr9:94706128-94706681	K562	blood:	n/a	chr9:94706365-94706376
20	CEBPB	chr9:94710337-94710859	K562	blood:	n/a	n/a
21	CEBPB	chr9:94706265-94706463	HepG2	liver:	n/a	chr9:94706365-94706376
22	CEBPB	chr9:94709276-94709448	A549	lung:	n/a	n/a
23	CEBPB	chr9:94706194-94706514	IMR90	lung:	n/a	chr9:94706365-94706376
24	CEBPB	chr9:94712556-94712630	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr9:94710359-94710884	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:94710744-94710944	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr9:94706195-94706452	K562	blood:	n/a	chr9:94706365-94706376
28	CEBPB	chr9:94706229-94706494	Hela-S3	cervix:	n/a	chr9:94706365-94706376
29	CEBPB	chr9:94706068-94706680	K562	blood:	n/a	chr9:94706365-94706376
30	CEBPB	chr9:94706216-94706498	A549	lung:	n/a	chr9:94706365-94706376
31	CEBPD	chr9:94707521-94707882	K562	blood:	n/a	n/a
32	CHD1	chr9:94712777-94712847	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr9:94710494-94710729	K562	blood:	n/a	n/a
34	CHD2	chr9:94711573-94711773	K562	blood:	n/a	n/a
35	CHD2	chr9:94707530-94707904	K562	blood:	n/a	n/a
36	CHD2	chr9:94707600-94707874	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr9:94712243-94712348	K562	blood:	n/a	n/a
38	CHD2	chr9:94711517-94711563	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr9:94710941-94711305	K562	blood:	n/a	chr9:94711172-94711182
40	CHD2	chr9:94710555-94710586	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr9:94712387-94712587	H1-hESC	embryonic stem cell:	n/a	chr9:94712539-94712549
42	CREB1	chr9:94706065-94706592	K562	blood:	n/a	n/a
43	CREB1	chr9:94706013-94706670	K562	blood:	n/a	n/a
44	CREB1	chr9:94712395-94712789	A549	lung:	n/a	n/a
45	CTBP2	chr9:94710859-94712998	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr9:94711240-94711390	K562	blood:	n/a	n/a
47	CTCF	chr9:94712520-94712670	HCT-116	colon:	n/a	n/a
48	CTCF	chr9:94712472-94712704	MCF-7	breast:	n/a	n/a
49	CTCF	chr9:94711057-94711434	K562	blood:	n/a	chr9:94711213-94711226 chr9:94711211-94711229
50	CTCF	chr9:94712450-94712715	GM12892	blood:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:94712472-94712522	PrEC	prostate:	n/a
2	chr9:94711818-94711868	GM12878	blood:	n/a
3	chr9:94712472-94712522	PrEC	prostate:	n/a
4	chr9:94711818-94711868	GM12878	blood:	n/a
5	chr9:94712122-94712172	HL-60	blood:	n/a
6	chr9:94710553-94710603	ECC-1	luminal epithelium:	n/a
7	chr9:94712472-94712522	IMR90	lung:	fetal
8	chr9:94712122-94712172	HAEpiC	amniotic membrane:	n/a
9	chr9:94710553-94710603	GM12891	blood:	n/a
10	chr9:94711214-94711264	HCF	heart:	n/a
11	chr9:94712122-94712172	GM06990	blood:	n/a
12	chr9:94712472-94712522	HAEpiC	amniotic membrane:	n/a
13	chr9:94712780-94712830	BE2_C	brain:	n/a
14	chr9:94712122-94712172	AG09319	gingival:	n/a
15	chr9:94711647-94711697	HCF	heart:	n/a
16	chr9:94711214-94711264	CMK	blood:	n/a
17	chr9:94710553-94710603	Hepatocyte	liver:	n/a
18	chr9:94712472-94712522	MCF-7	breast:	n/a
19	chr9:94711818-94711868	Caco-2	colon:	n/a
20	chr9:94711214-94711264	A549	lung:	n/a
21	chr9:94712780-94712830	HUVEC	blood vessel:	n/a
22	chr9:94712122-94712172	U87	brain:	n/a
23	chr9:94710679-94710729	AG10803	skin:	n/a
24	chr9:94712122-94712172	HPAEpiC	pulmonary alveolar:	n/a
25	chr9:94711647-94711697	HepG2	liver:	n/a
26	chr9:94712780-94712830	HRE	kidney:	n/a
27	chr9:94711214-94711264	T-47D	breast:	n/a
28	chr9:94711818-94711868	HEEpiC	esophagus:	n/a
29	chr9:94710679-94710729	GM06990	blood:	n/a
30	chr9:94710553-94710603	U87	brain:	n/a
31	chr9:94711214-94711264	SKMC	muscle:	n/a
32	chr9:94712122-94712172	T-47D	breast:	n/a
33	chr9:94711647-94711697	HCT-116	colon:	n/a
34	chr9:94711647-94711697	NT2-D1	testis:	n/a
35	chr9:94711647-94711697	Jurkat	blood:	n/a
36	chr9:94712122-94712172	Jurkat	blood:	n/a
37	chr9:94712472-94712522	HCF	heart:	n/a
38	chr9:94712122-94712172	SK-N-MC	brain:	n/a
39	chr9:94712122-94712172	HCT-116	colon:	n/a
40	chr9:94710679-94710729	A549	lung:	n/a
41	chr9:94712122-94712172	HRPEpiC	eye:	n/a
42	chr9:94710679-94710729	SAEC	small airway:	n/a
43	chr9:94711818-94711868	HCM	heart:	n/a
44	chr9:94711214-94711264	LNCaP	prostate:	n/a
45	chr9:94710553-94710603	AG09319	gingival:	n/a
46	chr9:94711647-94711697	HPAEpiC	pulmonary alveolar:	n/a
47	chr9:94711647-94711697	GM12878	blood:	n/a
48	chr9:94710679-94710729	PFSK-1	brain:	n/a
49	chr9:94710553-94710603	GM06990	blood:	n/a
50	chr9:94711647-94711697	RPTEC	kidney:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:94700947..94708226-chr9:94708551..94712716,11	K562	blood:
2	chr9:94661900..94664292-chr9:94705248..94709269,4	K562	blood:
3	chr9:94696439..94698046-chr9:94704884..94707640,2	K562	blood:
4	chr9:94537481..94538450-chr9:94712230..94712819,2	MCF-7	breast:
5	chr9:94537694..94538378-chr9:94712239..94713033,2	K562	blood:
6	chr9:94702364..94705189-chr9:94709744..94712716,4	K562	blood:
7	chr9:94706769..94709242-chr9:94710784..94712955,2	MCF-7	breast:
8	chr9:94646595..94649139-chr9:94708273..94710120,2	K562	blood:
9	chr9:94708402..94710475-chr9:94715730..94717686,2	K562	blood:
10	chr9:94667534..94670775-chr9:94707582..94710553,5	K562	blood:
11	chr9:94533336..94534896-chr9:94707634..94709527,2	MCF-7	breast:
12	chr9:94706737..94709425-chr9:94709648..94712474,2	MCF-7	breast:
13	chr9:94537447..94538880-chr9:94712081..94713098,9	MCF-7	breast:
14	chr9:94496411..94497072-chr9:94712544..94713048,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPTLC1-6	chr9:94712149-94712188	NONHSAT133144
2	lnc-SPTLC1-6	chr9:94710889-94710997	NONHSAT133145

No data

Variant related genes	Relation type
ROR2	TF binding region
ROR2	CpG island
ENSG00000169071	chromatin interactions

Extended variants
information (count: 421 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372106177	chr9:94702375-94702376	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs565864641	chr9:94702432-94702433	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs79492899	chr9:94702433-94702434	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548635474	chr9:94702556-94702557	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs557043522	chr9:94702598-94702599	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537411282	chr9:94702600-94702601	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs547174043	chr9:94702601-94702602	Enhancers Weak transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558678828	chr9:94702614-94702615	Enhancers Weak transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs7022802	chr9:94702643-94702644	Enhancers Weak transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs536069754	chr9:94702654-94702655	Enhancers Weak transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73520889	chr9:94702701-94702702	Enhancers Weak transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs190745215	chr9:94702763-94702764	Enhancers Weak transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147645920	chr9:94702769-94702770	Enhancers Weak transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs148873501	chr9:94702839-94702840	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574666563	chr9:94702868-94702869	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570738211	chr9:94702877-94702878	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs183433854	chr9:94702884-94702885	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs200293150	chr9:94702890-94702891	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs554611559	chr9:94702929-94702930	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs568358825	chr9:94702974-94702975	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs71955954	chr9:94702987-94702988	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs368446555	chr9:94702994-94702995	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs74710025	chr9:94702996-94702997	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs185857451	chr9:94703036-94703037	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112363424	chr9:94703099-94703100	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs564714442	chr9:94703114-94703115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373488291	chr9:94703175-94703176	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs117369959	chr9:94703181-94703182	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs541311729	chr9:94703182-94703183	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs190610233	chr9:94703226-94703227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs529879963	chr9:94703252-94703253	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371606028	chr9:94703277-94703278	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs11321454	chr9:94703297-94703298	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs548090609	chr9:94703340-94703341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs569880142	chr9:94703348-94703349	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs183216306	chr9:94703366-94703367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs149678224	chr9:94703469-94703470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs527630534	chr9:94703470-94703471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534721698	chr9:94703480-94703481	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12551564	chr9:94703491-94703492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs377717817	chr9:94703515-94703516	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs568426115	chr9:94703558-94703559	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs536000476	chr9:94703635-94703636	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570794666	chr9:94703676-94703677	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs75076910	chr9:94703771-94703772	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs148858650	chr9:94703796-94703797	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs575833175	chr9:94703829-94703830	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs543133650	chr9:94703840-94703841	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs558643800	chr9:94703860-94703861	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs7871522	chr9:94703861-94703862	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:70)

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
Mental retardation	21693067	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
Breast cancer	21364760	CNVD

Chromatin state (count:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94695800-94702400	Enhancers	Fetal Lung	lung
2	chr9:94698000-94708200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:94698400-94707000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:94698400-94707600	Weak transcription	Fetal Intestine Small	intestine
5	chr9:94698600-94708200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:94698800-94702800	Weak transcription	Lung	lung
7	chr9:94700800-94707000	Weak transcription	Gastric	stomach
8	chr9:94701000-94702800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr9:94701000-94702800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr9:94701000-94703000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr9:94701400-94707800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr9:94701600-94702400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr9:94701600-94702800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr9:94701800-94702400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr9:94701800-94702400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr9:94701800-94702400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr9:94701800-94702400	Genic enhancers	K562	blood
18	chr9:94701800-94702600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr9:94701800-94702600	Flanking Active TSS	Stomach Smooth Muscle	stomach
20	chr9:94701800-94702800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr9:94701800-94703000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr9:94702000-94702400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr9:94702000-94702600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr9:94702000-94702600	Enhancers	Ovary	ovary
25	chr9:94702000-94702600	Enhancers	Rectal Smooth Muscle	rectum
26	chr9:94702000-94706200	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr9:94702200-94702400	Enhancers	Colon Smooth Muscle	Colon
28	chr9:94702200-94702400	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr9:94702200-94702400	Enhancers	Placenta	Placenta
30	chr9:94702200-94702400	Enhancers	Right Atrium	heart
31	chr9:94702200-94702600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr9:94702200-94702800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr9:94702200-94703000	Genic enhancers	Fetal Stomach	stomach
34	chr9:94702400-94702600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr9:94702400-94702600	Flanking Active TSS	Colon Smooth Muscle	Colon
36	chr9:94702400-94702800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr9:94702400-94702800	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr9:94702400-94702800	Weak transcription	Right Atrium	heart
39	chr9:94702400-94703200	Enhancers	K562	blood
40	chr9:94702400-94704800	Weak transcription	Fetal Lung	lung
41	chr9:94702400-94707200	Weak transcription	Placenta	Placenta
42	chr9:94702400-94707600	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr9:94702600-94702800	Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr9:94702600-94703400	Enhancers	Colon Smooth Muscle	Colon
45	chr9:94702600-94703600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr9:94702600-94704800	Weak transcription	Rectal Smooth Muscle	rectum
47	chr9:94702600-94705800	Weak transcription	Stomach Smooth Muscle	stomach
48	chr9:94702600-94707200	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr9:94702800-94703000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr9:94702800-94703000	Enhancers	Duodenum Smooth Muscle	Duodenum

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