Variant report

Variant	esv3366813
Chromosome Location	chr9:102657446-102670065
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:482)
CpG islands
(count:244)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:102668983-102669193	HepG2	liver:	n/a	n/a
2	ATF2	chr9:102669128-102669452	GM12878	blood:	n/a	n/a
3	ATF3	chr9:102668865-102669027	K562	blood:	n/a	chr9:102668924-102668933
4	BACH1	chr9:102669316-102669460	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr9:102668939-102669619	GM12878	blood:	n/a	n/a
6	BHLHE40	chr9:102669071-102669590	K562	blood:	n/a	n/a
7	BRCA1	chr9:102669305-102669503	HepG2	liver:	n/a	n/a
8	BRCA1	chr9:102669497-102669560	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr9:102668887-102669180	K562	blood:	n/a	n/a
10	CBX3	chr9:102669192-102669798	K562	blood:	n/a	n/a
11	CCNT2	chr9:102668801-102669536	K562	blood:	n/a	n/a
12	CEBPB	chr9:102667677-102667922	HepG2	liver:	n/a	n/a
13	CEBPB	chr9:102667784-102667961	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr9:102666018-102666351	HepG2	liver:	n/a	chr9:102666090-102666102
15	CEBPB	chr9:102667731-102667995	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:102668120-102668894	MCF-7	breast:	n/a	n/a
17	CEBPB	chr9:102667704-102667942	K562	blood:	n/a	n/a
18	CEBPB	chr9:102666063-102666297	IMR90	lung:	n/a	chr9:102666090-102666102
19	CEBPB	chr9:102668271-102669123	Hela-S3	cervix:	n/a	n/a
20	CEBPD	chr9:102668761-102669156	HepG2	liver:	n/a	n/a
21	CHD1	chr9:102669090-102669613	GM12878	blood:	n/a	n/a
22	CHD2	chr9:102668661-102669629	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr9:102669066-102669370	K562	blood:	n/a	n/a
24	CHD2	chr9:102669039-102669468	HepG2	liver:	n/a	n/a
25	CHD2	chr9:102668220-102668627	HepG2	liver:	n/a	n/a
26	CHD2	chr9:102668707-102669483	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr9:102669004-102669492	GM12878	blood:	n/a	n/a
28	CREB1	chr9:102668838-102669485	A549	lung:	n/a	n/a
29	CREB1	chr9:102668565-102669698	HepG2	liver:	n/a	n/a
30	CTCF	chr9:102668580-102668730	GM12864	blood:	n/a	n/a
31	CTCF	chr9:102669286-102669468	MCF-7	breast:	n/a	n/a
32	CTCF	chr9:102669040-102669190	Caco-2	colon:	n/a	n/a
33	CTCF	chr9:102669055-102669142	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr9:102668792-102668814	Lung_OC	lung:	n/a	n/a
35	CTCF	chr9:102669369-102669459	GM12892	blood:	n/a	n/a
36	CTCF	chr9:102668759-102668835	GM12878	blood:	n/a	n/a
37	CTCF	chr9:102669435-102669440	GM19239	blood:	n/a	n/a
38	CTCF	chr9:102668840-102668990	GM12874	blood:	n/a	n/a
39	CTCF	chr9:102668980-102669130	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr9:102668720-102668870	GM12868	blood:	n/a	n/a
41	CTCF	chr9:102669000-102669150	HMEC	breast:	n/a	n/a
42	CTCF	chr9:102669140-102669290	GM06990	blood:	n/a	n/a
43	CTCF	chr9:102668640-102668790	GM12872	blood:	n/a	n/a
44	CTCF	chr9:102669000-102669150	GM12873	blood:	n/a	n/a
45	CTCF	chr9:102668940-102669090	SAEC	small airway:	n/a	n/a
46	CTCF	chr9:102668700-102668850	GM12878	blood:	n/a	n/a
47	CTCF	chr9:102669000-102669150	AG04449	skin:	n/a	n/a
48	CTCF	chr9:102668757-102668824	GM10248	blood:	n/a	n/a
49	CTCF	chr9:102669376-102669428	GM19239	blood:	n/a	n/a
50	CTCF	chr9:102668720-102668870	AG04449	skin:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:102669115-102669165	K562	blood:	n/a
2	chr9:102669115-102669165	HL-60	blood:	n/a
3	chr9:102669472-102669522	NH-A	brain:	n/a
4	chr9:102669472-102669522	NHBE	bronchial:	n/a
5	chr9:102669613-102669663	RPTEC	kidney:	n/a
6	chr9:102669472-102669522	NHDF-neo	bronchial:	n/a
7	chr9:102668725-102668775	LNCaP	prostate:	n/a
8	chr9:102669613-102669663	HEEpiC	esophagus:	n/a
9	chr9:102669613-102669663	CMK	blood:	n/a
10	chr9:102668725-102668775	MCF-7	breast:	n/a
11	chr9:102669613-102669663	NHDF-neo	bronchial:	n/a
12	chr9:102669115-102669165	NH-A	brain:	n/a
13	chr9:102668725-102668775	ECC-1	luminal epithelium:	n/a
14	chr9:102668725-102668775	GM12878	blood:	n/a
15	chr9:102669613-102669663	SK-N-MC	brain:	n/a
16	chr9:102669115-102669165	ProgFib	skin:	n/a
17	chr9:102668725-102668775	RPTEC	kidney:	n/a
18	chr9:102669472-102669522	HCF	heart:	n/a
19	chr9:102668725-102668775	HCF	heart:	n/a
20	chr9:102669613-102669663	HAEpiC	amniotic membrane:	n/a
21	chr9:102669472-102669522	CMK	blood:	n/a
22	chr9:102669613-102669663	HCT-116	colon:	n/a
23	chr9:102669115-102669165	HNPCEpiC	eye:	n/a
24	chr9:102668725-102668775	HepG2	liver:	n/a
25	chr9:102669613-102669663	Jurkat	blood:	n/a
26	chr9:102669115-102669165	GM06990	blood:	n/a
27	chr9:102669472-102669522	SAEC	small airway:	n/a
28	chr9:102668725-102668775	PrEC	prostate:	n/a
29	chr9:102668725-102668775	HEK293	kidney:	embryo
30	chr9:102669472-102669522	SK-N-SH	brain:	n/a
31	chr9:102669115-102669165	HRE	kidney:	n/a
32	chr9:102668725-102668775	HCPEpiC	choroid plexus:	n/a
33	chr9:102669613-102669663	HUVEC	blood vessel:	n/a
34	chr9:102669115-102669165	HEEpiC	esophagus:	n/a
35	chr9:102669613-102669663	NB4	blood:	n/a
36	chr9:102669613-102669663	AG09309	skin:	n/a
37	chr9:102669472-102669522	HCPEpiC	choroid plexus:	n/a
38	chr9:102669115-102669165	Hepatocyte	liver:	n/a
39	chr9:102668725-102668775	HUVEC	blood vessel:	n/a
40	chr9:102669472-102669522	K562	blood:	n/a
41	chr9:102669613-102669663	AG04449	skin:	fetal
42	chr9:102669613-102669663	GM12891	blood:	n/a
43	chr9:102668725-102668775	GM12892	blood:	n/a
44	chr9:102668725-102668775	Hepatocyte	liver:	n/a
45	chr9:102669613-102669663	MCF-7	breast:	n/a
46	chr9:102669613-102669663	HPAEpiC	pulmonary alveolar:	n/a
47	chr9:102669472-102669522	HAEpiC	amniotic membrane:	n/a
48	chr9:102669115-102669165	ovcar-3	ovarian:	n/a
49	chr9:102669472-102669522	LNCaP	prostate:	n/a
50	chr9:102669613-102669663	U87	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:102650412..102654067-chr9:102659447..102661891,3	MCF-7	breast:
2	chr19:33793735..33796057-chr9:102667838..102669482,2	MCF-7	breast:
3	chr9:102667836..102670748-chr9:102860445..102862735,2	K562	blood:
4	chr9:102659571..102663302-chr9:102667954..102670638,4	MCF-7	breast:
5	chr9:102580667..102584355-chr9:102667685..102671328,3	K562	blood:
6	chr9:102655317..102659100-chr9:102666802..102669789,3	MCF-7	breast:
7	chr9:102668724..102670876-chr9:102691785..102694126,2	MCF-7	breast:
8	chr9:102655013..102658748-chr9:102659114..102662823,3	K562	blood:
9	chr3:39424870..39425746-chr9:102668917..102669582,2	Hela-S3	cervix:
10	chr19:56631872..56632543-chr9:102669033..102669852,2	Hela-S3	cervix:
11	chr3:183353868..183354472-chr9:102668593..102669387,2	Hela-S3	cervix:
12	chr9:102665635..102667758-chr9:102670222..102671965,2	K562	blood:
13	chr9:102670054..102672961-chr9:102682119..102683745,2	MCF-7	breast:
14	chr10:33293935..33294887-chr9:102668937..102669750,2	Hela-S3	cervix:
15	chr9:102655013..102658748-chr9:102659114..102662823,3	K562	blood:
16	chr9:102580574..102584384-chr9:102666062..102670667,9	K562	blood:
17	chr9:102656589..102660265-chr9:102668420..102672852,5	MCF-7	breast:
18	chr9:102580482..102589062-chr9:102666380..102672134,16	MCF-7	breast:
19	chr6:133135395..133135910-chr9:102668805..102669502,2	MCF-7	breast:
20	chr9:101982798..101985464-chr9:102669885..102671484,2	MCF-7	breast:
21	chr9:102580555..102587852-chr9:102667958..102670918,11	MCF-7	breast:
22	chr9:102668815..102670753-chr9:102697540..102700821,3	K562	blood:
23	chr9:102665503..102667135-chr9:102668839..102671722,2	K562	blood:
24	chr9:102668815..102670753-chr9:102698922..102700821,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERP44-2	chr9:102668836-102668883	ENSG00000255145.1
2	lnc-ERP44-2	chr9:102668836-102668883	NONHSAT133701

No data

Variant related genes	Relation type
ENSG00000255145	TF binding region
STX17	TF binding region
ENSG00000255145	CpG island
STX17	CpG island
ENSG00000114796	chromatin interactions
ENSG00000112306	chromatin interactions
ENSG00000150093	chromatin interactions
ENSG00000237461	chromatin interactions
ENSG00000119523	chromatin interactions
ENSG00000106803	chromatin interactions
ENSG00000119509	chromatin interactions
ENSG00000267296	chromatin interactions
ENSG00000119508	chromatin interactions
ENSG00000255145	chromatin interactions
ENSG00000178863	chromatin interactions
ENSG00000144659	chromatin interactions
ENSG00000023318	chromatin interactions
ENSG00000267130	chromatin interactions
ENSG00000254571	chromatin interactions
ENSG00000136874	chromatin interactions

Extended variants
information (count: 401 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:401 , 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	rs190864089	chr9:102657511-102657512	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs113643958	chr9:102657599-102657600	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs6478986	chr9:102657626-102657627	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs560420834	chr9:102657653-102657654	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs557667180	chr9:102657670-102657671	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs7040578	chr9:102657673-102657674	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs143850018	chr9:102657691-102657692	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs552559409	chr9:102657733-102657734	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs553140080	chr9:102657739-102657740	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs116637958	chr9:102657811-102657812	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs564411115	chr9:102657820-102657821	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs573492173	chr9:102657826-102657827	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs541928949	chr9:102657883-102657884	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs554308752	chr9:102657947-102657948	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs7850043	chr9:102657986-102657987	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs180884461	chr9:102658014-102658015	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs370164960	chr9:102658043-102658044	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs532342866	chr9:102658066-102658067	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs550795158	chr9:102658077-102658078	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs548129674	chr9:102658082-102658083	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs114993518	chr9:102658085-102658086	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs569541950	chr9:102658104-102658105	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs528145081	chr9:102658131-102658132	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs184905393	chr9:102658154-102658155	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs150188889	chr9:102658189-102658190	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs569113141	chr9:102658268-102658269	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs113201152	chr9:102658395-102658396	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs531113833	chr9:102658487-102658488	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs115606825	chr9:102658496-102658497	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs372598258	chr9:102658515-102658516	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs367783716	chr9:102658603-102658604	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs377530778	chr9:102658619-102658620	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs571123477	chr9:102658680-102658681	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs537197338	chr9:102658681-102658682	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs190154836	chr9:102658682-102658683	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs370311670	chr9:102658687-102658688	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs574822649	chr9:102658777-102658778	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs555419525	chr9:102658802-102658803	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs138102054	chr9:102658839-102658840	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs543201885	chr9:102658931-102658932	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs183128973	chr9:102658968-102658969	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs577018651	chr9:102659018-102659019	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs149534463	chr9:102659021-102659022	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs559276556	chr9:102659025-102659026	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs528072706	chr9:102659033-102659034	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs148665407	chr9:102659035-102659036	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs561758337	chr9:102659073-102659074	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs558669199	chr9:102659106-102659107	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs530672712	chr9:102659117-102659118	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs577528575	chr9:102659159-102659160	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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

Chromatin state (count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:102648800-102667800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr9:102657000-102657600	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr9:102657000-102657800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr9:102657000-102657800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr9:102657200-102657600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr9:102657200-102658000	Enhancers	H9 Cell Line	embryonic stem cell
7	chr9:102657400-102657600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr9:102657400-102657600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr9:102657400-102668200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr9:102657600-102658200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr9:102657800-102658600	Enhancers	Lung	lung
12	chr9:102658200-102658400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr9:102661000-102668200	Weak transcription	Aorta	Aorta
14	chr9:102666200-102666400	Enhancers	HepG2	liver
15	chr9:102666200-102666600	Enhancers	Fetal Intestine Large	intestine
16	chr9:102666600-102668400	Weak transcription	Fetal Intestine Large	intestine
17	chr9:102667000-102668000	Weak transcription	HepG2	liver
18	chr9:102667800-102668000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr9:102667800-102668200	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr9:102667800-102668200	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr9:102668000-102668200	Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr9:102668000-102668200	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr9:102668000-102668200	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr9:102668000-102668200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr9:102668000-102668200	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr9:102668000-102668200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr9:102668000-102668200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr9:102668000-102668200	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr9:102668000-102668200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr9:102668000-102668200	Enhancers	Liver	Liver
31	chr9:102668000-102668200	Enhancers	Brain Anterior Caudate	brain
32	chr9:102668000-102668200	Enhancers	Brain Cingulate Gyrus	brain
33	chr9:102668000-102668200	Enhancers	Brain Hippocampus Middle	brain
34	chr9:102668000-102668200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr9:102668000-102668200	Enhancers	Brain Substantia Nigra	brain
36	chr9:102668000-102668200	Enhancers	Duodenum Mucosa	Duodenum
37	chr9:102668000-102668200	Enhancers	Duodenum Smooth Muscle	Duodenum
38	chr9:102668000-102668200	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr9:102668000-102668200	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr9:102668000-102668200	Enhancers	Hela-S3	cervix
41	chr9:102668000-102668200	Enhancers	HepG2	liver
42	chr9:102668000-102668200	Enhancers	HSMMtube	muscle
43	chr9:102668000-102668200	Enhancers	K562	blood
44	chr9:102668000-102668400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr9:102668000-102668400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
46	chr9:102668000-102668400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr9:102668000-102668400	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr9:102668000-102668400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr9:102668000-102668400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr9:102668000-102668400	Enhancers	Fetal Stomach	stomach

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