Variant report

Variant	esv1812629
Chromosome Location	chr17:16730223-16764972
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:227)
CpG islands
(count:305)
Chromatin interactive
region (count:1)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:227 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr17:16764549-16764560	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr17:16764555-16764730	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr17:16764004-16764108	HepG2	liver:	n/a	chr17:16764008-16764019
4	CEBPB	chr17:16763876-16764183	Hela-S3	cervix:	n/a	chr17:16764008-16764019
5	CEBPB	chr17:16763881-16764076	A549	lung:	n/a	chr17:16764008-16764019
6	CHD2	chr17:16764544-16764744	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr17:16733701-16733826	ProgFib	skin:	n/a	n/a
8	CTCF	chr17:16764560-16764710	NHEK	skin:	n/a	n/a
9	CTCF	chr17:16733445-16733489	A549	lung:	n/a	n/a
10	CTCF	chr17:16750972-16751068	Spleen_OC	spleen:	n/a	n/a
11	CTCF	chr17:16733626-16733923	A549	lung:	n/a	n/a
12	CTCF	chr17:16742689-16742755	Medullo	brain:	n/a	n/a
13	CTCF	chr17:16753626-16753711	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr17:16733647-16733833	A549	lung:	n/a	n/a
15	CTCF	chr17:16764660-16764810	HMEC	breast:	n/a	n/a
16	CTCF	chr17:16733620-16733770	HCT-116	colon:	n/a	n/a
17	CTCF	chr17:16764620-16764770	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr17:16732189-16732220	GM10266	blood:	n/a	n/a
19	CTCF	chr17:16752504-16752573	GM19240	blood:	n/a	n/a
20	CTCF	chr17:16740288-16740357	GM10248	blood:	n/a	n/a
21	CTCF	chr17:16742054-16742198	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr17:16764569-16764769	K562	blood:	n/a	n/a
23	CTCF	chr17:16752351-16752402	Lung_OC	lung:	n/a	n/a
24	CTCF	chr17:16733720-16733870	HepG2	liver:	n/a	n/a
25	CTCF	chr17:16733660-16733810	GM12864	blood:	n/a	n/a
26	CTCF	chr17:16764580-16764730	HFF-Myc	foreskin:	n/a	n/a
27	CTCF	chr17:16733563-16733841	GM10248	blood:	n/a	n/a
28	CTCF	chr17:16764600-16764750	HCT-116	colon:	n/a	n/a
29	CTCF	chr17:16733600-16733750	HCFaa	heart:	n/a	n/a
30	CTCF	chr17:16752664-16752728	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr17:16733653-16733834	NHEK	skin:	n/a	n/a
32	CTCF	chr17:16764620-16764770	HRE	kidney:	n/a	n/a
33	CTCF	chr17:16733526-16733849	K562	blood:	n/a	n/a
34	CTCF	chr17:16764620-16764770	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr17:16755109-16755234	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr17:16753766-16753829	GM13977	blood:	n/a	n/a
37	CTCF	chr17:16733677-16733842	MCF-7	breast:	n/a	n/a
38	CTCF	chr17:16732536-16732650	LNCaP	prostate:	n/a	n/a
39	CTCF	chr17:16764600-16764750	Caco-2	colon:	n/a	n/a
40	CTCF	chr17:16764570-16764841	NHEK	skin:	n/a	n/a
41	CTCF	chr17:16763960-16764110	SAEC	small airway:	n/a	n/a
42	CTCF	chr17:16733699-16733830	GM19239	blood:	n/a	n/a
43	CTCF	chr17:16733647-16733851	K562	blood:	n/a	n/a
44	CTCF	chr17:16733624-16733833	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr17:16749302-16749401	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr17:16749233-16749287	LNCaP	prostate:	n/a	n/a
47	CTCF	chr17:16733676-16733830	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr17:16733664-16733837	GM12892	blood:	n/a	n/a
49	CTCF	chr17:16764623-16764825	Gliobla	brain:	n/a	n/a
50	CTCF	chr17:16733620-16733770	GM12869	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:16757356-16757406	MCF-7	breast:	n/a
2	chr17:16757356-16757406	BJ	skin:	n/a
3	chr17:16734819-16734869	Jurkat	blood:	n/a
4	chr17:16757305-16757355	HRE	kidney:	n/a
5	chr17:16737096-16737146	U87	brain:	n/a
6	chr17:16737096-16737146	AG04449	skin:	fetal
7	chr17:16757356-16757406	ProgFib	skin:	n/a
8	chr17:16757356-16757406	NT2-D1	testis:	n/a
9	chr17:16757356-16757406	HRCEpiC	kidney:	n/a
10	chr17:16737096-16737146	K562	blood:	n/a
11	chr17:16757356-16757406	RPTEC	kidney:	n/a
12	chr17:16736463-16736513	H1-hESC	embryonic stem cell:	embryo
13	chr17:16736463-16736513	NHBE	bronchial:	n/a
14	chr17:16737096-16737146	ovcar-3	ovarian:	n/a
15	chr17:16734819-16734869	CMK	blood:	n/a
16	chr17:16757356-16757406	HNPCEpiC	eye:	n/a
17	chr17:16736463-16736513	Hepatocyte	liver:	n/a
18	chr17:16757356-16757406	PrEC	prostate:	n/a
19	chr17:16757305-16757355	SKMC	muscle:	n/a
20	chr17:16757356-16757406	NHBE	bronchial:	n/a
21	chr17:16737096-16737146	T-47D	breast:	n/a
22	chr17:16757356-16757406	AG09319	gingival:	n/a
23	chr17:16757305-16757355	AG10803	skin:	n/a
24	chr17:16737096-16737146	SAEC	small airway:	n/a
25	chr17:16757356-16757406	HCPEpiC	choroid plexus:	n/a
26	chr17:16757305-16757355	MCF10A-Er-Src	breast:	n/a
27	chr17:16734819-16734869	NHBE	bronchial:	n/a
28	chr17:16737096-16737146	AG09319	gingival:	n/a
29	chr17:16757356-16757406	U87	brain:	n/a
30	chr17:16737096-16737146	NHDF-neo	bronchial:	n/a
31	chr17:16734819-16734869	HCPEpiC	choroid plexus:	n/a
32	chr17:16737096-16737146	HCF	heart:	n/a
33	chr17:16757356-16757406	H1-hESC	embryonic stem cell:	embryo
34	chr17:16736463-16736513	SK-N-MC	brain:	n/a
35	chr17:16757356-16757406	GM12878	blood:	n/a
36	chr17:16757305-16757355	ovcar-3	ovarian:	n/a
37	chr17:16736463-16736513	BE2_C	brain:	n/a
38	chr17:16734819-16734869	Hela-S3	cervix:	n/a
39	chr17:16757356-16757406	AG10803	skin:	n/a
40	chr17:16757356-16757406	AG04449	skin:	fetal
41	chr17:16734819-16734869	LNCaP	prostate:	n/a
42	chr17:16737096-16737146	ProgFib	skin:	n/a
43	chr17:16757356-16757406	T-47D	breast:	n/a
44	chr17:16736463-16736513	HRCEpiC	kidney:	n/a
45	chr17:16734819-16734869	NH-A	brain:	n/a
46	chr17:16734819-16734869	T-47D	breast:	n/a
47	chr17:16737096-16737146	GM19239	blood:	n/a
48	chr17:16734819-16734869	MCF10A-Er-Src	breast:	n/a
49	chr17:16734819-16734869	PFSK-1	brain:	n/a
50	chr17:16734819-16734869	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:16756059..16758999-chr17:16760586..16763495,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRT17P1-2	chr17:16750949-16751252	NONHSAT146019
2	lnc-KRT17P1-2	chr17:16751411-16751727	NONHSAT146019
3	lnc-CCDC144A-4	chr17:16735634-16735881	NONHSAT146016
4	lnc-CCDC144A-4	chr17:16734662-16734742	NONHSAT146016

No data

Variant related genes	Relation type
COTL1P1	TF binding region
ENSG00000205312	TF binding region
ENSG00000226145	TF binding region
KRT16P2	TF binding region
KRT17P1	TF binding region
COTL1P1	CpG island
ENSG00000205312	CpG island
ENSG00000226145	CpG island
KRT16P2	CpG island
KRT17P1	CpG island
ENSG00000229749	chromatin interactions
ENSG00000205312	chromatin interactions

Extended variants
information (count: 1039 )
Associated
traits (count: 159 )

Variant overlapped rSNPs/rCNVs (count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12601369	chr17:16730226-16730227	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7221681	chr17:16730264-16730265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547355437	chr17:16730315-16730316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567587221	chr17:16730335-16730336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535838176	chr17:16730424-16730425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555842819	chr17:16730463-16730464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569323633	chr17:16730470-16730471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539433028	chr17:16730489-16730490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150675693	chr17:16730492-16730493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558296524	chr17:16730506-16730507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs578126505	chr17:16730532-16730533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185791230	chr17:16730546-16730547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7221152	chr17:16730547-16730548	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs574322896	chr17:16730565-16730566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78605728	chr17:16730581-16730582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542169456	chr17:16730640-16730641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191045905	chr17:16730728-16730729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2688038	chr17:16730770-16730771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544727129	chr17:16730789-16730790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565023659	chr17:16730803-16730804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569807119	chr17:16730886-16730887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527481813	chr17:16730940-16730941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs659477	chr17:16730974-16730975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547607690	chr17:16730995-16730996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199802009	chr17:16731007-16731008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs3874879	chr17:16731042-16731043	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs555860830	chr17:16731054-16731055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530017074	chr17:16731098-16731099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs3955894	chr17:16731121-16731122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549354791	chr17:16731124-16731125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569288768	chr17:16731134-16731135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182096800	chr17:16731177-16731178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541792319	chr17:16731233-16731234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76989059	chr17:16731276-16731277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190569774	chr17:16731284-16731285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143167834	chr17:16731296-16731297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557949460	chr17:16731375-16731376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571746249	chr17:16731391-16731392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534127998	chr17:16731413-16731414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554347910	chr17:16731418-16731419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111945115	chr17:16731454-16731455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573957022	chr17:16731469-16731470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375888705	chr17:16731545-16731546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571894547	chr17:16731561-16731562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2656375	chr17:16731599-16731600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575611536	chr17:16731605-16731606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183133469	chr17:16731615-16731616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564822214	chr17:16731616-16731617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2386357	chr17:16731618-16731619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2688037	chr17:16731627-16731628	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:159)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric cancer	18160780	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Multiple myeloma	17550852	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16728200-16735600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr17:16734800-16735000	Enhancers	Esophagus	oesophagus
3	chr17:16735600-16735800	Enhancers	Esophagus	oesophagus
4	chr17:16735600-16736000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr17:16736000-16737600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr17:16737400-16737600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr17:16737600-16738000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr17:16737600-16739800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr17:16738000-16743000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr17:16738200-16739000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr17:16738200-16739600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr17:16738400-16738800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr17:16738800-16739000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr17:16738800-16739800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr17:16739000-16739400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr17:16739000-16739600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr17:16739000-16740200	Enhancers	NHEK	skin
18	chr17:16739400-16740200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr17:16739600-16740000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr17:16739600-16740200	Enhancers	H1 Cell Line	embryonic stem cell
21	chr17:16739600-16740200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
22	chr17:16739800-16740000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr17:16739800-16740000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr17:16739800-16740000	Enhancers	Adipose Nuclei	Adipose
25	chr17:16739800-16740200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr17:16739800-16740200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr17:16739800-16740200	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr17:16739800-16740200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr17:16739800-16740200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr17:16739800-16740200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
31	chr17:16739800-16740200	Enhancers	Fetal Thymus	thymus
32	chr17:16739800-16740600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr17:16740000-16740200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr17:16740200-16741600	Weak transcription	Fetal Thymus	thymus
35	chr17:16740200-16744000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr17:16741600-16742400	Enhancers	Fetal Thymus	thymus
37	chr17:16743000-16744200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr17:16744000-16744200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr17:16746000-16746200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
40	chr17:16747800-16748400	Active TSS	Fetal Thymus	thymus
41	chr17:16748400-16748800	Flanking Active TSS	Fetal Thymus	thymus
42	chr17:16754400-16754800	Enhancers	Stomach Mucosa	stomach
43	chr17:16754800-16761200	Weak transcription	Stomach Mucosa	stomach
44	chr17:16757600-16758000	Enhancers	Placenta	Placenta
45	chr17:16757600-16758200	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr17:16758000-16758200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr17:16758000-16758200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr17:16758200-16775200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr17:16758400-16760400	Enhancers	Fetal Intestine Large	intestine
50	chr17:16758400-16760600	Enhancers	Fetal Intestine Small	intestine

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