Variant report

Variant	nsv908570
Chromosome Location	chr17:45571502-45684651
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1234)
CpG islands
(count:488)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1234 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr17:45579678-45580209	GM12878	blood:	n/a	chr17:45580000-45580010
2	BATF	chr17:45578032-45578241	GM12878	blood:	n/a	n/a
3	BATF	chr17:45579872-45580148	GM12878	blood:	n/a	chr17:45580000-45580010
4	BCL11A	chr17:45579668-45580125	GM12878	blood:	n/a	chr17:45579999-45580008
5	BCL11A	chr17:45579757-45579928	GM12878	blood:	n/a	n/a
6	BCL11A	chr17:45609110-45609438	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
7	BCLAF1	chr17:45609125-45609498	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
8	BHLHE40	chr17:45605793-45605974	HepG2	liver:	n/a	n/a
9	BHLHE40	chr17:45610659-45610881	HepG2	liver:	n/a	n/a
10	BRCA1	chr17:45682094-45682251	HepG2	liver:	n/a	n/a
11	BRCA1	chr17:45579916-45580110	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr17:45577979-45578350	K562	blood:	n/a	n/a
13	CBX3	chr17:45609185-45609788	K562	blood:	n/a	n/a
14	CCNT2	chr17:45608329-45608370	K562	blood:	n/a	n/a
15	CEBPB	chr17:45616172-45616360	K562	blood:	n/a	chr17:45616275-45616286
16	CEBPB	chr17:45665732-45665756	K562	blood:	n/a	n/a
17	CEBPB	chr17:45644646-45644894	Hela-S3	cervix:	n/a	chr17:45644788-45644801
18	CEBPB	chr17:45616239-45616426	H1-hESC	embryonic stem cell:	n/a	chr17:45616275-45616286
19	CEBPB	chr17:45589395-45589618	K562	blood:	n/a	n/a
20	CEBPB	chr17:45616218-45616423	HepG2	liver:	n/a	chr17:45616275-45616286
21	CEBPB	chr17:45632282-45632410	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr17:45609557-45609591	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr17:45579926-45580036	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr17:45665580-45665831	IMR90	lung:	n/a	n/a
25	CEBPB	chr17:45665566-45665892	A549	lung:	n/a	n/a
26	CEBPB	chr17:45616205-45616431	K562	blood:	n/a	chr17:45616275-45616286
27	CEBPB	chr17:45580366-45580376	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr17:45616089-45616461	K562	blood:	n/a	chr17:45616275-45616286
29	CEBPB	chr17:45616208-45616423	IMR90	lung:	n/a	chr17:45616275-45616286
30	CEBPB	chr17:45616203-45616429	Hela-S3	cervix:	n/a	chr17:45616275-45616286
31	CEBPB	chr17:45665734-45665763	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr17:45589310-45589646	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr17:45665577-45665788	HepG2	liver:	n/a	n/a
34	CEBPB	chr17:45593807-45594016	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr17:45665734-45665783	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr17:45579500-45579717	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr17:45596411-45596603	IMR90	lung:	n/a	n/a
38	CEBPD	chr17:45580257-45580571	K562	blood:	n/a	n/a
39	CEBPD	chr17:45608348-45608658	HepG2	liver:	n/a	n/a
40	CHD2	chr17:45608171-45608525	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr17:45608212-45608501	HepG2	liver:	n/a	n/a
42	CREB1	chr17:45608212-45608653	A549	lung:	n/a	n/a
43	CTCF	chr17:45578200-45578350	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr17:45608670-45608672	MCF-7	breast:	n/a	n/a
45	CTCF	chr17:45578060-45578350	BJ	skin:	n/a	chr17:45578156-45578177 chr17:45578154-45578172 chr17:45578159-45578167 chr17:45578155-45578171
46	CTCF	chr17:45579440-45579590	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr17:45578060-45578210	GM12865	blood:	n/a	chr17:45578156-45578177 chr17:45578154-45578172 chr17:45578159-45578167 chr17:45578155-45578171
48	CTCF	chr17:45577991-45578282	MCF-7	breast:	n/a	chr17:45578156-45578177 chr17:45578154-45578172 chr17:45578159-45578167 chr17:45578155-45578171
49	CTCF	chr17:45578160-45578310	GM12878	blood:	n/a	n/a
50	CTCF	chr17:45639580-45639730	Hela-S3	cervix:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45609121-45609171	GM06990	blood:	n/a
2	chr17:45608823-45608873	NH-A	brain:	n/a
3	chr17:45681383-45681433	IMR90	lung:	fetal
4	chr17:45573695-45573745	HEEpiC	esophagus:	n/a
5	chr17:45573695-45573745	HRE	kidney:	n/a
6	chr17:45612338-45612388	SK-N-MC	brain:	n/a
7	chr17:45608315-45608365	Hepatocyte	liver:	n/a
8	chr17:45681383-45681433	HCM	heart:	n/a
9	chr17:45573695-45573745	NH-A	brain:	n/a
10	chr17:45608315-45608365	SK-N-SH	brain:	n/a
11	chr17:45612338-45612388	HRCEpiC	kidney:	n/a
12	chr17:45608823-45608873	PrEC	prostate:	n/a
13	chr17:45609121-45609171	HRPEpiC	eye:	n/a
14	chr17:45608114-45608164	U87	brain:	n/a
15	chr17:45608823-45608873	HCPEpiC	choroid plexus:	n/a
16	chr17:45609121-45609171	Jurkat	blood:	n/a
17	chr17:45681383-45681433	HPAEpiC	pulmonary alveolar:	n/a
18	chr17:45608114-45608164	GM12878	blood:	n/a
19	chr17:45609121-45609171	ECC-1	luminal epithelium:	n/a
20	chr17:45573695-45573745	HIPEpiC	eye:	n/a
21	chr17:45612338-45612388	RPTEC	kidney:	n/a
22	chr17:45681383-45681433	HRPEpiC	eye:	n/a
23	chr17:45612338-45612388	GM19239	blood:	n/a
24	chr17:45612338-45612388	HCPEpiC	choroid plexus:	n/a
25	chr17:45608823-45608873	GM12892	blood:	n/a
26	chr17:45573695-45573745	A549	lung:	n/a
27	chr17:45604514-45604564	HCT-116	colon:	n/a
28	chr17:45612338-45612388	HUVEC	blood vessel:	n/a
29	chr17:45612338-45612388	NH-A	brain:	n/a
30	chr17:45573695-45573745	HAEpiC	amniotic membrane:	n/a
31	chr17:45608823-45608873	U87	brain:	n/a
32	chr17:45612338-45612388	AG09319	gingival:	n/a
33	chr17:45608315-45608365	SK-N-SH_RA	brain:	n/a
34	chr17:45608823-45608873	HPAEpiC	pulmonary alveolar:	n/a
35	chr17:45609121-45609171	GM19239	blood:	n/a
36	chr17:45612338-45612388	HCT-116	colon:	n/a
37	chr17:45609121-45609171	HEEpiC	esophagus:	n/a
38	chr17:45609121-45609171	RPTEC	kidney:	n/a
39	chr17:45609121-45609171	ovcar-3	ovarian:	n/a
40	chr17:45573695-45573745	HPAEpiC	pulmonary alveolar:	n/a
41	chr17:45604514-45604564	HEK293	kidney:	embryo
42	chr17:45612338-45612388	Jurkat	blood:	n/a
43	chr17:45573695-45573745	SAEC	small airway:	n/a
44	chr17:45681383-45681433	HNPCEpiC	eye:	n/a
45	chr17:45608315-45608365	HepG2	liver:	n/a
46	chr17:45608823-45608873	GM12891	blood:	n/a
47	chr17:45608823-45608873	HRCEpiC	kidney:	n/a
48	chr17:45681383-45681433	T-47D	breast:	n/a
49	chr17:45608315-45608365	U87	brain:	n/a
50	chr17:45612338-45612388	HNPCEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45608528..45610827-chr17:45614421..45616919,2	MCF-7	breast:
2	chr17:45607951..45610083-chr17:45616920..45619918,2	MCF-7	breast:
3	chr17:45681295..45682836-chr17:45684602..45686967,2	MCF-7	breast:
4	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
5	chr17:45679584..45682875-chr17:45684553..45688203,6	K562	blood:
6	chr17:45681295..45682836-chr17:45684602..45686967,2	MCF-7	breast:
7	chr14:38063458..38065003-chr17:45607681..45609442,2	MCF-7	breast:
8	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:

No data

Variant related genes	Relation type
NPEPPS	TF binding region
MRPL45P2	TF binding region
ENSG00000206734	TF binding region
NPEPPS	CpG island
MRPL45P2	CpG island
ENSG00000206734	CpG island
ENSG00000141279	chromatin interactions
ENSG00000228782	chromatin interactions
ENSG00000129514	chromatin interactions

Extended variants
information (count: 3775 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:3775 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9900629	chr17:45571502-45571503	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs56191111	chr17:45571505-45571506	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs57336401	chr17:45571539-45571540	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs185873019	chr17:45571548-45571549	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs373166830	chr17:45571557-45571558	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs189993553	chr17:45571635-45571636	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs549511381	chr17:45571640-45571641	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs7405889	chr17:45571676-45571677	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs537110228	chr17:45571708-45571709	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs550683018	chr17:45571734-45571735	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs570491510	chr17:45571742-45571743	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs369372140	chr17:45571762-45571763	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs539439120	chr17:45571840-45571841	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs181252646	chr17:45571846-45571847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372696172	chr17:45571876-45571877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573052820	chr17:45571878-45571879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535294249	chr17:45571887-45571888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555509746	chr17:45571888-45571889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185992199	chr17:45571931-45571932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556291591	chr17:45572015-45572016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575348688	chr17:45572192-45572193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200426167	chr17:45572318-45572319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548481327	chr17:45572319-45572320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185024562	chr17:45572326-45572327	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs28645767	chr17:45572338-45572339	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs57492869	chr17:45572365-45572366	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs540609454	chr17:45572370-45572371	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs527471998	chr17:45572394-45572395	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs529565628	chr17:45572415-45572416	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs549328936	chr17:45572428-45572429	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs563134540	chr17:45572467-45572468	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs531921104	chr17:45572472-45572473	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs550743869	chr17:45572475-45572476	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs190556894	chr17:45572488-45572489	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs191140800	chr17:45572504-45572505	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs367896534	chr17:45572530-45572531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546528624	chr17:45572594-45572595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566675341	chr17:45572608-45572609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372474600	chr17:45572612-45572613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555357689	chr17:45572632-45572633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150749851	chr17:45572642-45572643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537645887	chr17:45572666-45572667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557867968	chr17:45572769-45572770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577671878	chr17:45572807-45572808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375492216	chr17:45572813-45572814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146217891	chr17:45572818-45572819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375987638	chr17:45572826-45572827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370201032	chr17:45572835-45572836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540292650	chr17:45572994-45572995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560507505	chr17:45573005-45573006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	21163964	CNVD
Epithelial cancer	20478067	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1660 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45569400-45571800	Active TSS	Placenta	Placenta
2	chr17:45569800-45579200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr17:45570400-45571800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr17:45570400-45579400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr17:45570600-45571600	Flanking Active TSS	HepG2	liver
6	chr17:45571600-45571800	Enhancers	HepG2	liver
7	chr17:45571800-45579200	Weak transcription	HepG2	liver
8	chr17:45574800-45575000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr17:45577000-45577600	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr17:45577400-45577600	Enhancers	Colonic Mucosa	Colon
11	chr17:45577600-45579400	Weak transcription	Colonic Mucosa	Colon
12	chr17:45577600-45579400	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr17:45577800-45578000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr17:45578000-45579400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr17:45578200-45578400	Enhancers	Muscle Satellite Cultured Cells	--
16	chr17:45578200-45578400	Enhancers	Fetal Stomach	stomach
17	chr17:45578200-45578400	Enhancers	NHDF-Ad	bronchial
18	chr17:45578400-45579000	Weak transcription	NHDF-Ad	bronchial
19	chr17:45578400-45579200	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr17:45578400-45579400	Weak transcription	Fetal Stomach	stomach
21	chr17:45578400-45579800	Enhancers	Placenta	Placenta
22	chr17:45578600-45578800	Weak transcription	Hela-S3	cervix
23	chr17:45578600-45580200	Enhancers	Fetal Muscle Leg	muscle
24	chr17:45578800-45579000	Weak transcription	GM12878-XiMat	blood
25	chr17:45578800-45579000	Enhancers	Hela-S3	cervix
26	chr17:45578800-45579400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr17:45578800-45579600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr17:45578800-45579800	Enhancers	Fetal Intestine Large	intestine
29	chr17:45579000-45579200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr17:45579000-45579200	Enhancers	GM12878-XiMat	blood
31	chr17:45579000-45579200	Enhancers	NHDF-Ad	bronchial
32	chr17:45579000-45579400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr17:45579000-45579600	Enhancers	Thymus	Thymus
34	chr17:45579000-45579800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr17:45579000-45579800	Flanking Active TSS	Hela-S3	cervix
36	chr17:45579000-45579800	Enhancers	HMEC	breast
37	chr17:45579000-45579800	Enhancers	HSMM	muscle
38	chr17:45579000-45579800	Enhancers	HSMMtube	muscle
39	chr17:45579000-45580200	Enhancers	Fetal Thymus	thymus
40	chr17:45579000-45580600	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr17:45579000-45580600	Enhancers	Dnd41	blood
42	chr17:45579200-45579400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr17:45579200-45579400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr17:45579200-45579400	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr17:45579200-45579400	Enhancers	Muscle Satellite Cultured Cells	--
46	chr17:45579200-45579400	Enhancers	Fetal Lung	lung
47	chr17:45579200-45579400	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr17:45579200-45579400	Enhancers	A549	lung
49	chr17:45579200-45579400	Enhancers	NH-A	brain
50	chr17:45579200-45579400	Enhancers	NHEK	skin

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