Variant report

Variant	nsv579861
Chromosome Location	chr19:45309972-45314395
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	chr19:45311305-45311475	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:45310601-45310612	HepG2	liver:	n/a	n/a
3	ATF2	chr19:45311188-45311983	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr19:45311211-45311597	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr19:45310251-45310780	A549	lung:	n/a	n/a
6	BCL3	chr19:45311038-45312314	A549	lung:	n/a	chr19:45312244-45312257 chr19:45311679-45311692
7	BHLHE40	chr19:45310340-45310764	HepG2	liver:	n/a	chr19:45310514-45310535
8	BHLHE40	chr19:45312088-45312151	K562	blood:	n/a	chr19:45312124-45312140
9	BHLHE40	chr19:45310251-45310772	HepG2	liver:	n/a	chr19:45310514-45310535
10	BHLHE40	chr19:45311227-45311704	HepG2	liver:	n/a	n/a
11	BHLHE40	chr19:45311358-45311508	K562	blood:	n/a	n/a
12	BHLHE40	chr19:45310328-45310702	HepG2	liver:	n/a	chr19:45310514-45310535
13	BHLHE40	chr19:45310387-45310678	K562	blood:	n/a	chr19:45310514-45310535
14	BHLHE40	chr19:45310353-45310721	A549	lung:	n/a	chr19:45310514-45310535
15	BRCA1	chr19:45311278-45311478	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr19:45311981-45311985	HepG2	liver:	n/a	n/a
17	CCNT2	chr19:45311883-45312513	K562	blood:	n/a	n/a
18	CEBPD	chr19:45311800-45312626	HepG2	liver:	n/a	n/a
19	CEBPD	chr19:45312272-45312522	HepG2	liver:	n/a	n/a
20	CEBPD	chr19:45311160-45311701	HepG2	liver:	n/a	n/a
21	CHD2	chr19:45311664-45311841	HepG2	liver:	n/a	n/a
22	CHD2	chr19:45312515-45312609	HepG2	liver:	n/a	n/a
23	CHD2	chr19:45311191-45312492	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTBP2	chr19:45311164-45312186	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr19:45311620-45311770	GM12878	blood:	n/a	n/a
26	CTCF	chr19:45311278-45311483	GM10248	blood:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
27	CTCF	chr19:45311260-45311410	HPF	lung:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
28	CTCF	chr19:45311300-45311450	GM12871	blood:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
29	CTCF	chr19:45310600-45310750	K562	blood:	n/a	n/a
30	CTCF	chr19:45311260-45311543	GM10266	blood:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
31	CTCF	chr19:45311168-45311626	H1-hESC	embryonic stem cell:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
32	CTCF	chr19:45311320-45311470	AG10803	skin:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
33	CTCF	chr19:45311280-45311430	HMEC	breast:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
34	CTCF	chr19:45311500-45311650	WI-38	lung:	n/a	n/a
35	CTCF	chr19:45311252-45311552	GM19238	blood:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
36	CTCF	chr19:45311280-45311430	GM12872	blood:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
37	CTCF	chr19:45311046-45311684	K562	blood:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
38	CTCF	chr19:45311255-45311526	HUVEC	blood vessel:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
39	CTCF	chr19:45311340-45311490	GM06990	blood:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
40	CTCF	chr19:45311260-45311410	GM12864	blood:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
41	CTCF	chr19:45311320-45311470	HCT-116	colon:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
42	CTCF	chr19:45311240-45311532	K562	blood:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
43	CTCF	chr19:45311280-45311430	Hela-S3	cervix:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
44	CTCF	chr19:45311302-45311480	GM13976	blood:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
45	CTCF	chr19:45311279-45311494	HepG2	liver:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
46	CTCF	chr19:45310852-45312815	A549	lung:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
47	CTCF	chr19:45311336-45311461	LNCaP	prostate:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
48	CTCF	chr19:45311280-45311430	HEK293	kidney:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387
49	CTCF	chr19:45311780-45312030	GM12874	blood:	n/a	n/a
50	CTCF	chr19:45311320-45311470	BJ	skin:	n/a	chr19:45311365-45311386 chr19:45311370-45311388 chr19:45311371-45311387

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:45312060-45312110	AG10803	skin:	n/a
2	chr19:45312525-45312575	SKMC	muscle:	n/a
3	chr19:45311781-45311831	NH-A	brain:	n/a
4	chr19:45311997-45312047	SK-N-SH_RA	brain:	n/a
5	chr19:45312525-45312575	AG04449	skin:	fetal
6	chr19:45312525-45312575	HAEpiC	amniotic membrane:	n/a
7	chr19:45312525-45312575	HIPEpiC	eye:	n/a
8	chr19:45311781-45311831	AG04450	lung:	fetal
9	chr19:45311781-45311831	RPTEC	kidney:	n/a
10	chr19:45312060-45312110	AG09319	gingival:	n/a
11	chr19:45311781-45311831	IMR90	lung:	fetal
12	chr19:45311868-45311918	SAEC	small airway:	n/a
13	chr19:45312060-45312110	GM19239	blood:	n/a
14	chr19:45312060-45312110	ProgFib	skin:	n/a
15	chr19:45312525-45312575	HCM	heart:	n/a
16	chr19:45312525-45312575	HRCEpiC	kidney:	n/a
17	chr19:45312060-45312110	Caco-2	colon:	n/a
18	chr19:45312525-45312575	NHBE	bronchial:	n/a
19	chr19:45312060-45312110	MCF-7	breast:	n/a
20	chr19:45312060-45312110	AoSMC	blood vessel:	n/a
21	chr19:45311781-45311831	H1-hESC	embryonic stem cell:	embryo
22	chr19:45311781-45311831	HL-60	blood:	n/a
23	chr19:45311997-45312047	U87	brain:	n/a
24	chr19:45311781-45311831	GM19239	blood:	n/a
25	chr19:45312060-45312110	GM12891	blood:	n/a
26	chr19:45312060-45312110	ovcar-3	ovarian:	n/a
27	chr19:45312060-45312110	HUVEC	blood vessel:	n/a
28	chr19:45311997-45312047	HEK293	kidney:	embryo
29	chr19:45311868-45311918	PrEC	prostate:	n/a
30	chr19:45311781-45311831	Hepatocyte	liver:	n/a
31	chr19:45311868-45311918	HL-60	blood:	n/a
32	chr19:45311868-45311918	NHBE	bronchial:	n/a
33	chr19:45311781-45311831	AG04449	skin:	fetal
34	chr19:45311868-45311918	GM19239	blood:	n/a
35	chr19:45312060-45312110	ECC-1	luminal epithelium:	n/a
36	chr19:45311868-45311918	Caco-2	colon:	n/a
37	chr19:45311781-45311831	T-47D	breast:	n/a
38	chr19:45311997-45312047	ProgFib	skin:	n/a
39	chr19:45311781-45311831	HPAEpiC	pulmonary alveolar:	n/a
40	chr19:45311868-45311918	T-47D	breast:	n/a
41	chr19:45311997-45312047	HepG2	liver:	n/a
42	chr19:45311997-45312047	Hela-S3	cervix:	n/a
43	chr19:45312060-45312110	AG09309	skin:	n/a
44	chr19:45311781-45311831	HEEpiC	esophagus:	n/a
45	chr19:45311868-45311918	HRE	kidney:	n/a
46	chr19:45312525-45312575	AG10803	skin:	n/a
47	chr19:45312525-45312575	Caco-2	colon:	n/a
48	chr19:45312525-45312575	AG04450	lung:	fetal
49	chr19:45312525-45312575	SK-N-MC	brain:	n/a
50	chr19:45312060-45312110	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:45305840..45308889-chr19:45308989..45312130,4	MCF-7	breast:
2	chr19:45258326..45260627-chr19:45310152..45311875,2	MCF-7	breast:
3	chr19:45256385..45258826-chr19:45310390..45312154,2	MCF-7	breast:
4	chr19:45147379..45150123-chr19:45308817..45312008,3	MCF-7	breast:
5	chr19:45298818..45303552-chr19:45309335..45312129,4	MCF-7	breast:
6	chr19:45227043..45229115-chr19:45309849..45311993,3	MCF-7	breast:
7	chr19:45310566..45312166-chr19:45318337..45320547,2	K562	blood:
8	chr19:45249129..45253567-chr19:45309146..45313529,6	MCF-7	breast:
9	chr19:45308884..45313334-chr19:45345353..45351688,18	MCF-7	breast:
10	chr19:45287462..45288194-chr19:45311126..45311751,2	MCF-7	breast:
11	chr19:45223983..45225752-chr19:45308635..45310345,2	MCF-7	breast:
12	chr19:45311083..45313001-chr19:45347399..45349440,2	K562	blood:
13	chr19:45308022..45312966-chr19:45346579..45352259,11	MCF-7	breast:
14	chr19:45309587..45312322-chr19:45456957..45459370,2	MCF-7	breast:
15	chr19:45309744..45311644-chr19:45324913..45327057,2	MCF-7	breast:
16	chr19:45250785..45254453-chr19:45309921..45313662,4	MCF-7	breast:
17	chr19:45314362..45315171-chr19:45348110..45348929,2	K562	blood:

Variant related genes	Relation type
BCAM	TF binding region
BCAM	CpG island
ENSG00000104853	chromatin interactions
ENSG00000073008	chromatin interactions
ENSG00000267114	chromatin interactions
ENSG00000069399	chromatin interactions
ENSG00000130202	chromatin interactions

Extended variants
information (count: 177 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:177 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28399594	chr19:45309972-45309973	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs370853867	chr19:45309975-45309976	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs373474000	chr19:45309979-45309980	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs201928310	chr19:45309980-45309981	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs28399595	chr19:45309981-45309982	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs398034759	chr19:45309998-45309999	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs28399596	chr19:45310035-45310036	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs558463500	chr19:45310059-45310060	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs578254459	chr19:45310134-45310135	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs540816195	chr19:45310137-45310138	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs2968181	chr19:45310164-45310165	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs574049671	chr19:45310173-45310174	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs183782745	chr19:45310174-45310175	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs562848855	chr19:45310234-45310235	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs28399597	chr19:45310245-45310246	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs545020815	chr19:45310263-45310264	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs564004361	chr19:45310265-45310266	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs533089646	chr19:45310268-45310269	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs34970872	chr19:45310272-45310273	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs546367736	chr19:45310275-45310276	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs2965161	chr19:45310319-45310320	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs370204088	chr19:45310357-45310358	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs549016358	chr19:45310401-45310402	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs568882046	chr19:45310419-45310420	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs578097718	chr19:45310435-45310436	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs537815136	chr19:45310618-45310619	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs551432808	chr19:45310656-45310657	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs80002675	chr19:45310666-45310667	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs545511692	chr19:45310679-45310680	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs571950806	chr19:45310719-45310720	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs534548342	chr19:45310723-45310724	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs138415270	chr19:45310743-45310744	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs554399834	chr19:45310786-45310787	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs374011742	chr19:45310840-45310841	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs557031906	chr19:45310870-45310871	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs574134936	chr19:45310934-45310935	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs536446875	chr19:45310947-45310948	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs556590938	chr19:45310965-45310966	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs187007475	chr19:45311083-45311084	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs140824606	chr19:45311084-45311085	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs191914779	chr19:45311114-45311115	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs73048258	chr19:45311144-45311145	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs149626525	chr19:45311153-45311154	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs577511423	chr19:45311172-45311173	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs374289380	chr19:45311187-45311188	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs79060456	chr19:45311272-45311273	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs529057621	chr19:45311288-45311289	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs199801493	chr19:45311298-45311299	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs200936382	chr19:45311306-45311307	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs560898656	chr19:45311310-45311311	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Cancer	20164920	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Adrenocortical carcinoma	18281524	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Muscular dystrophy	17160897	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:45281400-45311400	Weak transcription	Right Atrium	heart
2	chr19:45284800-45311400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr19:45294200-45311600	Weak transcription	Small Intestine	intestine
4	chr19:45296200-45310600	Weak transcription	Colonic Mucosa	Colon
5	chr19:45296800-45311000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr19:45297000-45311800	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr19:45298200-45310200	Weak transcription	Gastric	stomach
8	chr19:45299200-45310200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr19:45300600-45310400	Weak transcription	Stomach Mucosa	stomach
10	chr19:45300600-45311400	Weak transcription	Psoas Muscle	Psoas
11	chr19:45303800-45310600	Weak transcription	Hela-S3	cervix
12	chr19:45304000-45310400	Weak transcription	Esophagus	oesophagus
13	chr19:45304000-45310400	Weak transcription	Pancreas	Pancrea
14	chr19:45307400-45310400	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr19:45307400-45311200	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr19:45307600-45310200	Weak transcription	Liver	Liver
17	chr19:45307600-45310200	Weak transcription	Fetal Intestine Large	intestine
18	chr19:45307600-45310400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr19:45307600-45310600	Weak transcription	Fetal Stomach	stomach
20	chr19:45307600-45310600	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr19:45307600-45311200	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr19:45307600-45311200	Weak transcription	Spleen	Spleen
23	chr19:45307600-45311400	Weak transcription	Lung	lung
24	chr19:45307800-45311400	Weak transcription	Duodenum Mucosa	Duodenum
25	chr19:45308000-45310200	Weak transcription	Fetal Intestine Small	intestine
26	chr19:45309400-45311200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr19:45309400-45311800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr19:45309600-45310400	Enhancers	A549	lung
29	chr19:45309600-45310400	Enhancers	HepG2	liver
30	chr19:45309600-45311200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
31	chr19:45309600-45311400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr19:45309600-45311800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr19:45309600-45311800	Enhancers	Placenta	Placenta
34	chr19:45309600-45311800	Enhancers	HMEC	breast
35	chr19:45309600-45311800	Enhancers	NHEK	skin
36	chr19:45309800-45310000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr19:45309800-45310000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr19:45309800-45310000	Enhancers	NHLF	lung
39	chr19:45309800-45310600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
40	chr19:45309800-45310600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
41	chr19:45309800-45311200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr19:45309800-45311400	Enhancers	H9 Cell Line	embryonic stem cell
43	chr19:45309800-45311400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr19:45309800-45311400	Enhancers	Fetal Heart	heart
45	chr19:45309800-45312000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr19:45310000-45311200	Weak transcription	NHLF	lung
47	chr19:45310000-45311600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr19:45310200-45310400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr19:45310200-45310400	Bivalent Enhancer	Fetal Brain Male	brain
50	chr19:45310200-45310800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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