Variant report

Variant	nsv471403
Chromosome Location	chr17:45608444-45700642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45693174-45693540	K562	blood:	n/a	n/a
2	ARID3A	chr17:45697829-45698241	HepG2	liver:	n/a	n/a
3	BACH1	chr17:45688020-45688343	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr17:45688008-45688377	K562	blood:	n/a	n/a
5	BATF	chr17:45688022-45688356	GM12878	blood:	n/a	chr17:45688193-45688204
6	BATF	chr17:45688037-45688336	GM12878	blood:	n/a	chr17:45688193-45688204
7	BCL11A	chr17:45609110-45609438	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
8	BCLAF1	chr17:45609125-45609498	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
9	BHLHE40	chr17:45610659-45610881	HepG2	liver:	n/a	n/a
10	BRCA1	chr17:45682094-45682251	HepG2	liver:	n/a	n/a
11	CBX3	chr17:45609185-45609788	K562	blood:	n/a	n/a
12	CBX3	chr17:45697551-45698344	HCT-116	colon:	n/a	n/a
13	CEBPB	chr17:45687122-45687636	A549	lung:	n/a	chr17:45687274-45687285
14	CEBPB	chr17:45687144-45687531	IMR90	lung:	n/a	chr17:45687274-45687285
15	CEBPB	chr17:45616208-45616423	IMR90	lung:	n/a	chr17:45616275-45616286
16	CEBPB	chr17:45616218-45616423	HepG2	liver:	n/a	chr17:45616275-45616286
17	CEBPB	chr17:45616205-45616431	K562	blood:	n/a	chr17:45616275-45616286
18	CEBPB	chr17:45665580-45665831	IMR90	lung:	n/a	n/a
19	CEBPB	chr17:45665577-45665788	HepG2	liver:	n/a	n/a
20	CEBPB	chr17:45687180-45687630	A549	lung:	n/a	chr17:45687274-45687285
21	CEBPB	chr17:45609557-45609591	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr17:45687284-45687544	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr17:45665566-45665892	A549	lung:	n/a	n/a
24	CEBPB	chr17:45687287-45687525	K562	blood:	n/a	n/a
25	CEBPB	chr17:45665734-45665783	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr17:45616203-45616429	Hela-S3	cervix:	n/a	chr17:45616275-45616286
27	CEBPB	chr17:45632282-45632410	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr17:45644646-45644894	Hela-S3	cervix:	n/a	chr17:45644788-45644801
29	CEBPB	chr17:45616239-45616426	H1-hESC	embryonic stem cell:	n/a	chr17:45616275-45616286
30	CEBPB	chr17:45616172-45616360	K562	blood:	n/a	chr17:45616275-45616286
31	CEBPB	chr17:45665732-45665756	K562	blood:	n/a	n/a
32	CEBPB	chr17:45616089-45616461	K562	blood:	n/a	chr17:45616275-45616286
33	CEBPB	chr17:45665734-45665763	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr17:45687159-45687596	HepG2	liver:	n/a	chr17:45687274-45687285
35	CEBPB	chr17:45687378-45687406	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPD	chr17:45608348-45608658	HepG2	liver:	n/a	n/a
37	CHD1	chr17:45693022-45693789	IMR90	lung:	n/a	n/a
38	CHD2	chr17:45699153-45699444	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr17:45608212-45608501	HepG2	liver:	n/a	n/a
40	CHD2	chr17:45608171-45608525	Hela-S3	cervix:	n/a	n/a
41	CREB1	chr17:45608212-45608653	A549	lung:	n/a	n/a
42	CTCF	chr17:45693620-45693770	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr17:45693278-45693476	LNCaP	prostate:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
44	CTCF	chr17:45693340-45693490	GM12871	blood:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
45	CTCF	chr17:45693269-45693507	A549	lung:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
46	CTCF	chr17:45695700-45695850	GM12864	blood:	n/a	n/a
47	CTCF	chr17:45693320-45693470	GM12873	blood:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
48	CTCF	chr17:45693340-45693490	NHDF-neo	bronchial:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388
49	CTCF	chr17:45655360-45655510	K562	blood:	n/a	n/a
50	CTCF	chr17:45693300-45693450	NHLF	lung:	n/a	chr17:45693377-45693385 chr17:45693372-45693390 chr17:45693373-45693389 chr17:45693367-45693388

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45681383-45681433	AG04449	skin:	fetal
2	chr17:45681383-45681433	AG04449	skin:	fetal
3	chr17:45690396-45690446	ECC-1	luminal epithelium:	n/a
4	chr17:45690396-45690446	AoSMC	blood vessel:	n/a
5	chr17:45612338-45612388	LNCaP	prostate:	n/a
6	chr17:45609121-45609171	MCF-7	breast:	n/a
7	chr17:45609121-45609171	HL-60	blood:	n/a
8	chr17:45609121-45609171	PrEC	prostate:	n/a
9	chr17:45612338-45612388	HCPEpiC	choroid plexus:	n/a
10	chr17:45699322-45699372	GM19239	blood:	n/a
11	chr17:45699322-45699372	LNCaP	prostate:	n/a
12	chr17:45612338-45612388	AoSMC	blood vessel:	n/a
13	chr17:45699260-45699310	SK-N-MC	brain:	n/a
14	chr17:45681383-45681433	GM19239	blood:	n/a
15	chr17:45609121-45609171	GM06990	blood:	n/a
16	chr17:45690396-45690446	BJ	skin:	n/a
17	chr17:45681383-45681433	HUVEC	blood vessel:	n/a
18	chr17:45612338-45612388	Hepatocyte	liver:	n/a
19	chr17:45608823-45608873	SK-N-SH	brain:	n/a
20	chr17:45608823-45608873	HEEpiC	esophagus:	n/a
21	chr17:45612338-45612388	T-47D	breast:	n/a
22	chr17:45612338-45612388	HRCEpiC	kidney:	n/a
23	chr17:45608823-45608873	IMR90	lung:	fetal
24	chr17:45690396-45690446	H1-hESC	embryonic stem cell:	embryo
25	chr17:45681383-45681433	MCF-7	breast:	n/a
26	chr17:45612338-45612388	PANC-1	pancreas:	n/a
27	chr17:45609121-45609171	HCM	heart:	n/a
28	chr17:45612338-45612388	ECC-1	luminal epithelium:	n/a
29	chr17:45608823-45608873	MCF10A-Er-Src	breast:	n/a
30	chr17:45690396-45690446	BE2_C	brain:	n/a
31	chr17:45690396-45690446	HEEpiC	esophagus:	n/a
32	chr17:45608823-45608873	GM06990	blood:	n/a
33	chr17:45609121-45609171	BJ	skin:	n/a
34	chr17:45681383-45681433	GM06990	blood:	n/a
35	chr17:45699260-45699310	H1-hESC	embryonic stem cell:	embryo
36	chr17:45699260-45699310	HAEpiC	amniotic membrane:	n/a
37	chr17:45609121-45609171	HPAEpiC	pulmonary alveolar:	n/a
38	chr17:45681383-45681433	AG09319	gingival:	n/a
39	chr17:45699322-45699372	HEK293	kidney:	embryo
40	chr17:45690396-45690446	PANC-1	pancreas:	n/a
41	chr17:45699260-45699310	HPAEpiC	pulmonary alveolar:	n/a
42	chr17:45699322-45699372	Caco-2	colon:	n/a
43	chr17:45609121-45609171	RPTEC	kidney:	n/a
44	chr17:45612338-45612388	HepG2	liver:	n/a
45	chr17:45608823-45608873	BJ	skin:	n/a
46	chr17:45681383-45681433	T-47D	breast:	n/a
47	chr17:45609121-45609171	HMEC	breast:	n/a
48	chr17:45681383-45681433	GM12892	blood:	n/a
49	chr17:45699322-45699372	T-47D	breast:	n/a
50	chr17:45609121-45609171	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:45697869..45699408-chr17:45722972..45724595,2	K562	blood:
2	chr17:45700634..45703555-chr17:45708176..45711349,3	MCF-7	breast:
3	chr17:45679584..45682875-chr17:45684553..45688203,6	K562	blood:
4	chr17:45607951..45610083-chr17:45616920..45619918,2	MCF-7	breast:
5	chr17:45698425..45699322-chr17:45867182..45867731,2	MCF-7	breast:
6	chr17:45695726..45697562-chr17:45698247..45700833,3	K562	blood:
7	chr17:45694580..45697420-chr17:45726459..45728756,2	K562	blood:
8	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
9	chr17:45608528..45610827-chr17:45614421..45616919,2	MCF-7	breast:
10	chr17:45681295..45682836-chr17:45684602..45686967,2	MCF-7	breast:
11	chr17:45681295..45682836-chr17:45684602..45686967,2	MCF-7	breast:
12	chr17:45399473..45401724-chr17:45692079..45694320,2	K562	blood:
13	chr17:45695726..45697562-chr17:45698247..45700833,3	K562	blood:
14	chr14:38063458..38065003-chr17:45607681..45609442,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC040934.1-3	chr17:45699208-45699453	ENSG00000263766.1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NPEPPS	hsa-miR-122-5p	chr17:45699436-45699443
2	NPEPPS	hsa-miR-27b-3p	chr17:45699543-45699550
3	NPEPPS	hsa-miR-27b-3p	chr17:45699528-45699550
4	NPEPPS	hsa-miR-122-5p	chr17:45699574-45699594
5	NPEPPS	hsa-miR-122-5p	chr17:45699422-45699443

Variant related genes	Relation type
NPEPPS	TF binding region
ENSG00000206734	TF binding region
NPEPPS	CpG island
ENSG00000206734	CpG island
ENSG00000263766	chromatin interactions
ENSG00000228782	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000141279	chromatin interactions
ENSG00000263293	chromatin interactions
ENSG00000108424	chromatin interactions
ENSG00000178852	chromatin interactions

Extended variants
information (count: 3243 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:3243 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552807092	chr17:45608511-45608512	Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs142358928	chr17:45608592-45608593	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs572926933	chr17:45608609-45608610	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs535178976	chr17:45608628-45608629	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs554988441	chr17:45608668-45608669	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs574882410	chr17:45608711-45608712	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs200065879	chr17:45608784-45608785	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs28482949	chr17:45608854-45608855	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs201212390	chr17:45608885-45608886	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs577785321	chr17:45608935-45608936	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs540389854	chr17:45608999-45609000	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs397833914	chr17:45609023-45609024	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs560077315	chr17:45609026-45609027	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs397833913	chr17:45609072-45609073	Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs529419960	chr17:45609251-45609252	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs62073968	chr17:45609270-45609271	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs562910611	chr17:45609332-45609333	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs531698989	chr17:45609333-45609334	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs552107332	chr17:45609354-45609355	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs571934663	chr17:45609435-45609436	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs73985167	chr17:45609454-45609455	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535575756	chr17:45609455-45609456	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs555000613	chr17:45609456-45609457	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs574894901	chr17:45609457-45609458	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs537418212	chr17:45609470-45609471	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs114696662	chr17:45609478-45609479	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577903898	chr17:45609483-45609484	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs527582417	chr17:45609521-45609522	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549258056	chr17:45609550-45609551	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs573746514	chr17:45609562-45609563	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs543153592	chr17:45609572-45609573	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs562924745	chr17:45609653-45609654	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs531761403	chr17:45609662-45609663	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs528812141	chr17:45609671-45609672	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs561167351	chr17:45609676-45609677	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs565110906	chr17:45609678-45609679	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs528035624	chr17:45609710-45609711	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs141674200	chr17:45609715-45609716	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs567854822	chr17:45609721-45609722	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs150542839	chr17:45609730-45609731	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs548687939	chr17:45609749-45609750	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs139459757	chr17:45609750-45609751	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs568580060	chr17:45609898-45609899	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs537533624	chr17:45609913-45609914	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs182224286	chr17:45609914-45609915	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs377270583	chr17:45609989-45609990	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372818375	chr17:45610048-45610049	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187541111	chr17:45610070-45610071	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192581402	chr17:45610129-45610130	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs553742699	chr17:45610141-45610142	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Epithelial cancer	20478067	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2084 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45607600-45609400	Active TSS	Primary neutrophils fromperipheralblood	blood
2	chr17:45607600-45610800	Active TSS	A549	lung
3	chr17:45607800-45609400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
4	chr17:45607800-45609800	Active TSS	Monocytes-CD14+_RO01746	blood
5	chr17:45607800-45610000	Active TSS	Colonic Mucosa	Colon
6	chr17:45607800-45610200	Active TSS	Rectal Mucosa Donor 31	rectum
7	chr17:45607800-45610400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr17:45608000-45609200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
9	chr17:45608000-45609200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
10	chr17:45608000-45609400	Active TSS	Primary hematopoietic stem cells	blood
11	chr17:45608000-45609400	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
12	chr17:45608000-45609400	Active TSS	Primary T helper cells PMA-I stimulated	--
13	chr17:45608000-45609400	Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr17:45608000-45609400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr17:45608000-45609400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr17:45608000-45609400	Active TSS	Liver	Liver
17	chr17:45608000-45609600	Active TSS	Primary T helper naive cells from peripheral blood	blood
18	chr17:45608000-45609600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
19	chr17:45608000-45609600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
20	chr17:45608000-45609600	Active TSS	Fetal Muscle Trunk	muscle
21	chr17:45608000-45609600	Active TSS	Fetal Thymus	thymus
22	chr17:45608000-45609800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr17:45608000-45609800	Active TSS	Primary T cells from cord blood	blood
24	chr17:45608000-45609800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr17:45608000-45609800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
26	chr17:45608000-45609800	Active TSS	Colon Smooth Muscle	Colon
27	chr17:45608000-45610000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr17:45608000-45610000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr17:45608000-45610000	Active TSS	Adipose Nuclei	Adipose
30	chr17:45608000-45610000	Active TSS	Brain Anterior Caudate	brain
31	chr17:45608000-45610000	Active TSS	Brain Substantia Nigra	brain
32	chr17:45608000-45610000	Active TSS	Fetal Stomach	stomach
33	chr17:45608000-45610000	Active TSS	Left Ventricle	heart
34	chr17:45608000-45610000	Active TSS	Ovary	ovary
35	chr17:45608000-45610000	Active TSS	Pancreas	Pancrea
36	chr17:45608000-45610200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr17:45608000-45610200	Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr17:45608000-45610200	Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr17:45608000-45610200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr17:45608000-45610200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr17:45608000-45610200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr17:45608000-45610200	Active TSS	Fetal Intestine Small	intestine
43	chr17:45608000-45610200	Active TSS	HepG2	liver
44	chr17:45608000-45610400	Active TSS	H9 Cell Line	embryonic stem cell
45	chr17:45608000-45610400	Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr17:45608000-45610400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr17:45608000-45610400	Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr17:45608000-45610400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr17:45608000-45610400	Active TSS	Brain Cingulate Gyrus	brain
50	chr17:45608000-45610400	Active TSS	Brain Germinal Matrix	brain

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