Variant report

Variant	esv3402031
Chromosome Location	chr17:19769585-19772133
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	ATF2	chr17:19771194-19771530	H1-hESC	embryonic stem cell:	n/a	chr17:19771258-19771272
2	ATF3	chr17:19770941-19771557	A549	lung:	n/a	chr17:19771017-19771030
3	BACH1	chr17:19771055-19771481	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr17:19770164-19770705	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr17:19770070-19770837	A549	lung:	n/a	chr17:19770760-19770773
6	BCL3	chr17:19770958-19771458	A549	lung:	n/a	chr17:19770968-19770981 chr17:19771174-19771183 chr17:19771197-19771210 chr17:19771175-19771188 chr17:19771284-19771297 chr17:19771202-19771211 chr17:19771339-19771352 chr17:19771418-19771431 chr17:19771000-19771013 chr17:19771395-19771408
7	BCLAF1	chr17:19771023-19771415	GM12878	blood:	n/a	chr17:19771174-19771183 chr17:19771197-19771210 chr17:19771175-19771188 chr17:19771284-19771297 chr17:19771202-19771211 chr17:19771339-19771352 chr17:19771395-19771408
8	BHLHE40	chr17:19770223-19770419	A549	lung:	n/a	n/a
9	BRCA1	chr17:19771132-19771411	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr17:19769827-19770473	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr17:19770985-19771568	HCT-116	colon:	n/a	n/a
12	CEBPB	chr17:19769796-19770190	A549	lung:	n/a	chr17:19769955-19769972 chr17:19769958-19769970
13	CEBPB	chr17:19769830-19770167	IMR90	lung:	n/a	chr17:19769955-19769972 chr17:19769958-19769970
14	CEBPB	chr17:19769839-19770224	A549	lung:	n/a	chr17:19769955-19769972 chr17:19769958-19769970
15	CEBPB	chr17:19769762-19770632	A549	lung:	n/a	chr17:19769955-19769972 chr17:19769958-19769970
16	CEBPB	chr17:19769719-19770553	Hela-S3	cervix:	n/a	chr17:19769955-19769972 chr17:19769958-19769970
17	CEBPB	chr17:19769864-19770147	H1-hESC	embryonic stem cell:	n/a	chr17:19769955-19769972 chr17:19769958-19769970
18	CEBPB	chr17:19769855-19770132	HepG2	liver:	n/a	chr17:19769955-19769972 chr17:19769958-19769970
19	CEBPB	chr17:19771226-19771381	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr17:19769785-19770202	ECC-1	luminal epithelium:	n/a	chr17:19769955-19769972 chr17:19769958-19769970
21	CHD1	chr17:19770865-19771041	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr17:19769825-19770733	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr17:19771041-19771500	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr17:19770409-19770790	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr17:19770524-19770724	HepG2	liver:	n/a	n/a
26	CREB1	chr17:19770865-19771535	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr17:19770164-19771597	A549	lung:	n/a	n/a
28	CREB1	chr17:19771091-19771375	A549	lung:	n/a	n/a
29	CREB1	chr17:19770889-19771553	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTBP2	chr17:19770220-19771829	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr17:19770326-19770531	Fibrobl	skin:	n/a	n/a
32	CTCF	chr17:19771060-19771210	GM12874	blood:	n/a	n/a
33	CTCF	chr17:19770686-19770793	MCF-7	breast:	n/a	n/a
34	CTCF	chr17:19771043-19771291	ProgFib	skin:	n/a	n/a
35	CTCF	chr17:19771380-19771530	GM12868	blood:	n/a	chr17:19771481-19771494
36	CTCF	chr17:19771160-19771218	GM12878	blood:	n/a	n/a
37	CTCF	chr17:19770325-19770592	GM12878	blood:	n/a	n/a
38	CTCF	chr17:19771046-19771273	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr17:19771440-19771590	AoAF	blood vessel:	n/a	chr17:19771520-19771533 chr17:19771481-19771494
40	CTCF	chr17:19770326-19770569	GM19240	blood:	n/a	n/a
41	CTCF	chr17:19771111-19771252	GM10248	blood:	n/a	n/a
42	CTCF	chr17:19770336-19770485	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr17:19771460-19771610	HCM	heart:	n/a	chr17:19771520-19771533 chr17:19771481-19771494
44	CTCF	chr17:19770660-19770810	GM12868	blood:	n/a	n/a
45	CTCF	chr17:19770300-19770450	GM12865	blood:	n/a	n/a
46	CTCF	chr17:19770340-19770490	GM12870	blood:	n/a	n/a
47	CTCF	chr17:19770380-19770530	HEK293	kidney:	n/a	n/a
48	CTCF	chr17:19770980-19771130	HCT-116	colon:	n/a	n/a
49	CTCF	chr17:19771001-19771325	MCF-7	breast:	n/a	chr17:19771299-19771312
50	CTCF	chr17:19770332-19770522	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:19771548-19771598	IMR90	lung:	fetal
2	chr17:19771548-19771598	IMR90	lung:	fetal
3	chr17:19771612-19771662	SK-N-SH_RA	brain:	n/a
4	chr17:19771783-19771833	HPAEpiC	pulmonary alveolar:	n/a
5	chr17:19771783-19771833	K562	blood:	n/a
6	chr17:19771783-19771833	RPTEC	kidney:	n/a
7	chr17:19771612-19771662	HRPEpiC	eye:	n/a
8	chr17:19771364-19771414	BE2_C	brain:	n/a
9	chr17:19771612-19771662	NHDF-neo	bronchial:	n/a
10	chr17:19770448-19770498	MCF10A-Er-Src	breast:	n/a
11	chr17:19770910-19770960	HCM	heart:	n/a
12	chr17:19770448-19770498	BJ	skin:	n/a
13	chr17:19771708-19771758	HAEpiC	amniotic membrane:	n/a
14	chr17:19770443-19770493	MCF-7	breast:	n/a
15	chr17:19771360-19771410	ECC-1	luminal epithelium:	n/a
16	chr17:19770443-19770493	T-47D	breast:	n/a
17	chr17:19770910-19770960	GM06990	blood:	n/a
18	chr17:19771813-19771863	HRPEpiC	eye:	n/a
19	chr17:19771360-19771410	HIPEpiC	eye:	n/a
20	chr17:19771360-19771410	AG04449	skin:	fetal
21	chr17:19771612-19771662	HRE	kidney:	n/a
22	chr17:19770448-19770498	HNPCEpiC	eye:	n/a
23	chr17:19771708-19771758	HEEpiC	esophagus:	n/a
24	chr17:19770908-19770958	PrEC	prostate:	n/a
25	chr17:19771708-19771758	Caco-2	colon:	n/a
26	chr17:19771813-19771863	K562	blood:	n/a
27	chr17:19771360-19771410	GM19239	blood:	n/a
28	chr17:19771548-19771598	GM12892	blood:	n/a
29	chr17:19771364-19771414	GM12892	blood:	n/a
30	chr17:19771548-19771598	ProgFib	skin:	n/a
31	chr17:19770443-19770493	GM12891	blood:	n/a
32	chr17:19771360-19771410	SK-N-MC	brain:	n/a
33	chr17:19770443-19770493	Hepatocyte	liver:	n/a
34	chr17:19771783-19771833	NB4	blood:	n/a
35	chr17:19771708-19771758	LNCaP	prostate:	n/a
36	chr17:19771708-19771758	U87	brain:	n/a
37	chr17:19770234-19770284	H1-hESC	embryonic stem cell:	embryo
38	chr17:19770443-19770493	AG04450	lung:	fetal
39	chr17:19770908-19770958	Hela-S3	cervix:	n/a
40	chr17:19771548-19771598	HNPCEpiC	eye:	n/a
41	chr17:19771813-19771863	HCM	heart:	n/a
42	chr17:19771783-19771833	GM12891	blood:	n/a
43	chr17:19770448-19770498	HAEpiC	amniotic membrane:	n/a
44	chr17:19770443-19770493	HCF	heart:	n/a
45	chr17:19770443-19770493	HUVEC	blood vessel:	n/a
46	chr17:19770443-19770493	NT2-D1	testis:	n/a
47	chr17:19771783-19771833	AG10803	skin:	n/a
48	chr17:19771364-19771414	K562	blood:	n/a
49	chr17:19771612-19771662	HAEpiC	amniotic membrane:	n/a
50	chr17:19770443-19770493	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:19752348..19754374-chr17:19768940..19771870,2	MCF-7	breast:
2	chr17:19770561..19771488-chr4:140374749..140375509,2	HCT-116	colon:
3	chr17:19769588..19772074-chr17:19879592..19882526,4	MCF-7	breast:
4	chr17:19770311..19771954-chr17:19910328..19912594,2	MCF-7	breast:
5	chr17:19769802..19772027-chr17:19799780..19804333,4	MCF-7	breast:
6	chr17:19769754..19773058-chr17:19878983..19882883,4	MCF-7	breast:

Variant related genes	Relation type
ULK2	TF binding region
ULK2	CpG island
ENSG00000083290	chromatin interactions
ENSG00000261033	chromatin interactions
ENSG00000273247	chromatin interactions
ENSG00000270091	chromatin interactions
ENSG00000172007	chromatin interactions
ENSG00000108599	chromatin interactions

Extended variants
information (count: 101 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:101 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557178388	chr17:19769633-19769634	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs573956940	chr17:19769638-19769639	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs557559781	chr17:19769658-19769659	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs201836052	chr17:19769664-19769665	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs539649804	chr17:19769676-19769677	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs182246419	chr17:19769682-19769683	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs576322498	chr17:19769730-19769731	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs575349861	chr17:19769734-19769735	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs556459175	chr17:19769759-19769760	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs569950482	chr17:19769766-19769767	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs544882516	chr17:19769783-19769784	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs562763958	chr17:19769822-19769823	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs374031111	chr17:19769823-19769824	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs564761982	chr17:19769846-19769847	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs185254684	chr17:19769864-19769865	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs573305451	chr17:19769866-19769867	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs72841969	chr17:19769907-19769908	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs540736277	chr17:19770002-19770003	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs560993951	chr17:19770127-19770128	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs529751003	chr17:19770130-19770131	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs555367217	chr17:19770139-19770140	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs116818674	chr17:19770159-19770160	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs572028090	chr17:19770167-19770168	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs540024566	chr17:19770191-19770192	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs9914323	chr17:19770198-19770199	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs532072078	chr17:19770204-19770205	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs552074634	chr17:19770205-19770206	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs189035844	chr17:19770216-19770217	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs181477493	chr17:19770227-19770228	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs373671397	chr17:19770315-19770316	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs534347295	chr17:19770352-19770353	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs553976435	chr17:19770357-19770358	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs567791711	chr17:19770393-19770394	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs536335311	chr17:19770437-19770438	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs556550188	chr17:19770469-19770470	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs368182987	chr17:19770487-19770488	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs576004028	chr17:19770508-19770509	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs114872269	chr17:19770547-19770548	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs555513834	chr17:19770548-19770549	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs558390275	chr17:19770553-19770554	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs111389585	chr17:19770564-19770565	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs527784138	chr17:19770592-19770593	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs376905124	chr17:19770606-19770607	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs372759835	chr17:19770622-19770623	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs200274686	chr17:19770647-19770648	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs112009436	chr17:19770716-19770717	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs202233839	chr17:19770737-19770738	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs368856105	chr17:19770745-19770746	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs373948426	chr17:19770759-19770760	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs557926196	chr17:19770763-19770764	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:153)

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
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
Colorectal cancer	16774939	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
Autism	22543975	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:19673800-19769800	Weak transcription	NH-A	brain
2	chr17:19700800-19769800	Weak transcription	HSMMtube	muscle
3	chr17:19701000-19770000	Weak transcription	Colonic Mucosa	Colon
4	chr17:19703800-19769800	Weak transcription	Psoas Muscle	Psoas
5	chr17:19704400-19770000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr17:19706800-19769800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr17:19712400-19769800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr17:19727800-19769800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr17:19728000-19770000	Weak transcription	Esophagus	oesophagus
10	chr17:19728200-19769800	Weak transcription	HSMM	muscle
11	chr17:19728200-19770000	Weak transcription	Pancreas	Pancrea
12	chr17:19728600-19769800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr17:19737600-19769800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr17:19742800-19769800	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr17:19744000-19769800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr17:19744200-19770200	Weak transcription	Gastric	stomach
17	chr17:19747000-19769800	Weak transcription	NHDF-Ad	bronchial
18	chr17:19749600-19770000	Weak transcription	Right Ventricle	heart
19	chr17:19750000-19770000	Weak transcription	Left Ventricle	heart
20	chr17:19750200-19769800	Weak transcription	Duodenum Mucosa	Duodenum
21	chr17:19750200-19770000	Weak transcription	Aorta	Aorta
22	chr17:19750400-19769600	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr17:19750400-19769800	Weak transcription	Liver	Liver
24	chr17:19750400-19769800	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr17:19750800-19769600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr17:19750800-19770200	Weak transcription	Spleen	Spleen
27	chr17:19751400-19769800	Weak transcription	Osteobl	bone
28	chr17:19751600-19769800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr17:19752800-19769800	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr17:19755600-19770000	Weak transcription	Lung	lung
31	chr17:19757000-19769800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr17:19762800-19769600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr17:19763200-19769800	Weak transcription	Ovary	ovary
34	chr17:19763200-19770000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr17:19763200-19770200	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr17:19763400-19769800	Weak transcription	HMEC	breast
37	chr17:19763600-19769800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr17:19764400-19769800	Weak transcription	Fetal Kidney	kidney
39	chr17:19764600-19770000	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr17:19764800-19770000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr17:19765600-19769600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr17:19766400-19769800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr17:19766600-19769800	Weak transcription	Fetal Intestine Large	intestine
44	chr17:19767000-19769600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr17:19767000-19769800	Weak transcription	Stomach Smooth Muscle	stomach
46	chr17:19767200-19769800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr17:19767200-19769800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr17:19767600-19769800	Weak transcription	Fetal Stomach	stomach
49	chr17:19767800-19769800	Weak transcription	Fetal Intestine Small	intestine
50	chr17:19768200-19769800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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