Variant report

Variant	nsv827916
Chromosome Location	chr17:20379830-20442445
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:296)
CpG islands
(count:305)
Chromatin interactive
region (count:0)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr17:20388438-20388633	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr17:20438566-20438789	GM12878	blood:	n/a	n/a
3	CEBPB	chr17:20388357-20388509	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr17:20432902-20433054	IMR90	lung:	n/a	chr17:20432946-20432955 chr17:20432944-20432957 chr17:20432944-20432955
5	CEBPB	chr17:20432878-20433065	A549	lung:	n/a	chr17:20432946-20432955 chr17:20432944-20432957 chr17:20432944-20432955
6	CEBPB	chr17:20428677-20428912	K562	blood:	n/a	n/a
7	CEBPB	chr17:20432904-20432946	K562	blood:	n/a	n/a
8	CHD1	chr17:20434510-20434553	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr17:20404993-20405007	Gliobla	brain:	n/a	n/a
10	CTCF	chr17:20405365-20405464	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr17:20420837-20421005	GM13977	blood:	n/a	n/a
12	CTCF	chr17:20420840-20420990	GM12873	blood:	n/a	n/a
13	CTCF	chr17:20435634-20435680	Pancreas_OC	pancreas:	n/a	n/a
14	CTCF	chr17:20405380-20405430	GM13977	blood:	n/a	n/a
15	CTCF	chr17:20405381-20405461	MCF-7	breast:	n/a	n/a
16	CTCF	chr17:20399521-20399538	GM10248	blood:	n/a	n/a
17	CTCF	chr17:20405502-20405620	GM10266	blood:	n/a	n/a
18	CTCF	chr17:20420800-20420950	GM12873	blood:	n/a	chr17:20420800-20420813
19	CTCF	chr17:20405332-20405549	A549	lung:	n/a	n/a
20	CTCF	chr17:20409682-20409752	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr17:20405179-20405592	A549	lung:	n/a	n/a
22	CTCF	chr17:20405301-20405510	LNCaP	prostate:	n/a	n/a
23	CTCF	chr17:20411841-20412098	K562	blood:	n/a	n/a
24	CTCF	chr17:20404566-20404651	Lung_OC	lung:	n/a	n/a
25	CTCF	chr17:20405316-20405539	A549	lung:	n/a	n/a
26	CTCF	chr17:20406418-20406482	A549	lung:	n/a	n/a
27	CTCF	chr17:20440911-20440950	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr17:20399541-20399560	GM10248	blood:	n/a	n/a
29	CTCF	chr17:20380718-20380769	Lung_OC	lung:	n/a	n/a
30	CTCF	chr17:20405080-20405230	RPTEC	kidney:	n/a	n/a
31	CTCF	chr17:20405281-20405489	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr17:20405320-20405470	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr17:20405320-20405470	SAEC	small airway:	n/a	n/a
34	CTCF	chr17:20405320-20405470	HEK293	kidney:	n/a	n/a
35	CTCF	chr17:20402776-20402828	GM10266	blood:	n/a	n/a
36	CTCF	chr17:20411842-20412144	A549	lung:	n/a	n/a
37	CTCF	chr17:20393678-20393752	GM20000	blood:	n/a	n/a
38	CTCF	chr17:20405260-20405410	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr17:20405344-20405485	GM10266	blood:	n/a	n/a
40	CTCF	chr17:20420883-20420946	GM20000	blood:	n/a	n/a
41	CTCF	chr17:20395438-20395742	NHEK	skin:	n/a	chr17:20395527-20395536
42	CTCF	chr17:20405232-20405518	K562	blood:	n/a	n/a
43	CTCF	chr17:20405332-20405337	GM13976	blood:	n/a	n/a
44	CTCF	chr17:20418549-20418655	Medullo	brain:	n/a	n/a
45	CTCF	chr17:20405320-20405470	AG04449	skin:	n/a	n/a
46	CTCF	chr17:20381895-20381977	GM10248	blood:	n/a	n/a
47	CTCF	chr17:20405360-20405510	A549	lung:	n/a	n/a
48	CTCF	chr17:20405320-20405470	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr17:20405108-20405598	A549	lung:	n/a	n/a
50	CTCF	chr17:20380888-20380960	Spleen_OC	spleen:	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	chr17:20433187-20433237	PFSK-1	brain:	n/a
2	chr17:20433187-20433237	HAEpiC	amniotic membrane:	n/a
3	chr17:20433187-20433237	ovcar-3	ovarian:	n/a
4	chr17:20433187-20433237	AG09319	gingival:	n/a
5	chr17:20409125-20409175	NT2-D1	testis:	n/a
6	chr17:20433187-20433237	HRCEpiC	kidney:	n/a
7	chr17:20433187-20433237	GM12878	blood:	n/a
8	chr17:20408647-20408697	SK-N-SH_RA	brain:	n/a
9	chr17:20405382-20405432	HAEpiC	amniotic membrane:	n/a
10	chr17:20433187-20433237	H1-hESC	embryonic stem cell:	embryo
11	chr17:20408772-20408822	NH-A	brain:	n/a
12	chr17:20405382-20405432	ovcar-3	ovarian:	n/a
13	chr17:20433187-20433237	NH-A	brain:	n/a
14	chr17:20405382-20405432	SK-N-SH_RA	brain:	n/a
15	chr17:20409125-20409175	GM06990	blood:	n/a
16	chr17:20405382-20405432	MCF10A-Er-Src	breast:	n/a
17	chr17:20433187-20433237	HUVEC	blood vessel:	n/a
18	chr17:20409125-20409175	Hela-S3	cervix:	n/a
19	chr17:20409125-20409175	NH-A	brain:	n/a
20	chr17:20405382-20405432	ProgFib	skin:	n/a
21	chr17:20408772-20408822	SK-N-MC	brain:	n/a
22	chr17:20409125-20409175	AG04450	lung:	fetal
23	chr17:20409125-20409175	T-47D	breast:	n/a
24	chr17:20408772-20408822	K562	blood:	n/a
25	chr17:20408772-20408822	MCF10A-Er-Src	breast:	n/a
26	chr17:20433187-20433237	HCF	heart:	n/a
27	chr17:20409125-20409175	HAEpiC	amniotic membrane:	n/a
28	chr17:20405382-20405432	HepG2	liver:	n/a
29	chr17:20408772-20408822	HCPEpiC	choroid plexus:	n/a
30	chr17:20405382-20405432	ECC-1	luminal epithelium:	n/a
31	chr17:20409125-20409175	HRPEpiC	eye:	n/a
32	chr17:20405382-20405432	HCM	heart:	n/a
33	chr17:20408647-20408697	SKMC	muscle:	n/a
34	chr17:20408647-20408697	SK-N-MC	brain:	n/a
35	chr17:20408647-20408697	GM12892	blood:	n/a
36	chr17:20433187-20433237	HCT-116	colon:	n/a
37	chr17:20408772-20408822	GM06990	blood:	n/a
38	chr17:20405382-20405432	SK-N-SH	brain:	n/a
39	chr17:20433187-20433237	PrEC	prostate:	n/a
40	chr17:20405382-20405432	GM12891	blood:	n/a
41	chr17:20405382-20405432	HRE	kidney:	n/a
42	chr17:20408772-20408822	HL-60	blood:	n/a
43	chr17:20408772-20408822	SKMC	muscle:	n/a
44	chr17:20409125-20409175	NHBE	bronchial:	n/a
45	chr17:20433187-20433237	HepG2	liver:	n/a
46	chr17:20409125-20409175	PrEC	prostate:	n/a
47	chr17:20405382-20405432	HL-60	blood:	n/a
48	chr17:20409125-20409175	HRCEpiC	kidney:	n/a
49	chr17:20433187-20433237	AG04449	skin:	fetal
50	chr17:20433187-20433237	Jurkat	blood:	n/a

No data

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGALS9B-1	chr17:20433355-20434194	ENSG00000260907.1
2	lnc-LGALS9B-7	chr17:20410726-20412244	ENSG00000266925.1
3	lnc-LGALS9B-10	chr17:20435561-20436194	NONHSAT146584

No data

Variant related genes	Relation type
ENSG00000260907	TF binding region
YWHAEP3	TF binding region
ENSG00000266042	TF binding region
KRT16P5	TF binding region
ENSG00000266925	TF binding region
ENSG00000265916	TF binding region
ENSG00000205215	TF binding region
ENSG00000231645	TF binding region
KRT16P3	TF binding region
ENSG00000229586	TF binding region
ENSG00000260907	CpG island
YWHAEP3	CpG island
ENSG00000266042	CpG island
KRT16P5	CpG island
ENSG00000266925	CpG island
ENSG00000265916	CpG island
ENSG00000205215	CpG island
ENSG00000231645	CpG island
KRT16P3	CpG island
ENSG00000229586	CpG island

Extended variants
information (count: 1241 )
Associated
traits (count: 151 )

Variant overlapped rSNPs/rCNVs (count:1241 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371101352	chr17:20379849-20379850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs539485156	chr17:20379878-20379879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557810828	chr17:20379879-20379880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139967393	chr17:20379882-20379883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537240763	chr17:20379891-20379892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs9747101	chr17:20379893-20379894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144678227	chr17:20379894-20379895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
8	rs193069767	chr17:20379899-20379900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535021429	chr17:20379905-20379906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553661974	chr17:20379979-20379980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572047304	chr17:20379997-20379998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545862241	chr17:20380018-20380019	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs9890419	chr17:20380020-20380021	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs576214849	chr17:20380056-20380057	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113335715	chr17:20380122-20380123	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185393028	chr17:20380131-20380132	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs56204413	chr17:20380140-20380141	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs374070249	chr17:20380142-20380143	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529154089	chr17:20380159-20380160	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189017849	chr17:20380171-20380172	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112571509	chr17:20380262-20380263	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111630545	chr17:20380270-20380271	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533155331	chr17:20380304-20380305	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570610379	chr17:20380305-20380306	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539370004	chr17:20380336-20380337	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551405564	chr17:20380357-20380358	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145305246	chr17:20380366-20380367	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184024473	chr17:20380408-20380409	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs151017479	chr17:20380417-20380418	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72832534	chr17:20380453-20380454	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs150098474	chr17:20380486-20380487	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567740974	chr17:20380510-20380511	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535248419	chr17:20380515-20380516	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140289778	chr17:20380520-20380521	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578260099	chr17:20380537-20380538	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539399143	chr17:20380592-20380593	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138425110	chr17:20380593-20380594	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188364978	chr17:20380614-20380615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs9900286	chr17:20380622-20380623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9891859	chr17:20380656-20380657	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs543169950	chr17:20380677-20380678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561857510	chr17:20380700-20380701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573734545	chr17:20380715-20380716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535118688	chr17:20380724-20380725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559216362	chr17:20380757-20380758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533069525	chr17:20380800-20380801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551331977	chr17:20380830-20380831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9899693	chr17:20380919-20380920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113709227	chr17:20380954-20380955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530968075	chr17:20380992-20380993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:151)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Chronic lymphocytic leukemia	21546498	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
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
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
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
Acute lymphoblastic leukemia	21339820	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20369800-20380000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr17:20370800-20394800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr17:20379000-20396200	Weak transcription	NHEK	skin
4	chr17:20379800-20380600	Enhancers	Esophagus	oesophagus
5	chr17:20380000-20380600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr17:20380200-20380600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr17:20380600-20383600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr17:20381000-20381400	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr17:20383000-20383800	Enhancers	Stomach Mucosa	stomach
10	chr17:20383600-20384000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr17:20383600-20384400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr17:20384400-20384600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr17:20384600-20391800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr17:20388200-20388400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr17:20388200-20388600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr17:20388200-20388600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr17:20388200-20388600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr17:20388200-20388600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr17:20388200-20388600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr17:20388200-20388600	Enhancers	Muscle Satellite Cultured Cells	--
21	chr17:20388200-20388600	Active TSS	Hela-S3	cervix
22	chr17:20388200-20388600	Active TSS	Osteobl	bone
23	chr17:20388400-20388600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr17:20391800-20392400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr17:20392400-20394800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr17:20394800-20396200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr17:20394800-20397600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr17:20396200-20396400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr17:20396200-20396600	Flanking Active TSS	NHEK	skin
30	chr17:20396400-20397800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr17:20396600-20396800	Active TSS	NHEK	skin
32	chr17:20397600-20398200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr17:20397800-20398400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr17:20398200-20399200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr17:20420400-20421000	Active TSS	Fetal Thymus	thymus
36	chr17:20421000-20424800	Weak transcription	Fetal Thymus	thymus
37	chr17:20424800-20425200	Enhancers	Fetal Thymus	thymus
38	chr17:20432800-20433400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr17:20432800-20433800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr17:20433200-20434400	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr17:20433400-20433600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr17:20433400-20434400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr17:20433600-20433800	Enhancers	H1 Cell Line	embryonic stem cell
44	chr17:20433600-20433800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr17:20433600-20434000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr17:20433600-20434200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr17:20433600-20434400	Enhancers	Dnd41	blood
48	chr17:20433800-20434000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr17:20433800-20434200	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr17:20433800-20434400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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