Variant report

Variant	nsv429811
Chromosome Location	chr7:127857891-127889049
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	ATF1	chr7:127876915-127877457	K562	blood:	n/a	n/a
2	ATF3	chr7:127862045-127862344	K562	blood:	n/a	n/a
3	BACH1	chr7:127887842-127888056	K562	blood:	n/a	n/a
4	BACH1	chr7:127877271-127877311	K562	blood:	n/a	n/a
5	BACH1	chr7:127887928-127888127	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:127862104-127862273	K562	blood:	n/a	n/a
7	BACH1	chr7:127869506-127869599	K562	blood:	n/a	n/a
8	BACH1	chr7:127862036-127862281	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr7:127862100-127862409	K562	blood:	n/a	n/a
10	BHLHE40	chr7:127876976-127877461	K562	blood:	n/a	n/a
11	BHLHE40	chr7:127858489-127858893	K562	blood:	n/a	n/a
12	BHLHE40	chr7:127887959-127887994	K562	blood:	n/a	n/a
13	BRCA1	chr7:127861828-127862245	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr7:127887605-127888188	K562	blood:	n/a	n/a
15	CBX3	chr7:127878910-127879546	K562	blood:	n/a	n/a
16	CBX3	chr7:127879018-127879517	K562	blood:	n/a	n/a
17	CBX3	chr7:127876814-127877569	K562	blood:	n/a	n/a
18	CBX3	chr7:127879164-127879492	HCT-116	colon:	n/a	n/a
19	CCNT2	chr7:127877155-127877436	K562	blood:	n/a	n/a
20	CCNT2	chr7:127880936-127881080	K562	blood:	n/a	n/a
21	CEBPB	chr7:127877007-127877405	A549	lung:	n/a	chr7:127877088-127877096
22	CEBPB	chr7:127869706-127869935	K562	blood:	n/a	chr7:127869798-127869809
23	CEBPB	chr7:127881146-127881337	HepG2	liver:	n/a	chr7:127881276-127881285 chr7:127881276-127881285 chr7:127881274-127881287 chr7:127881276-127881285 chr7:127881276-127881285
24	CEBPB	chr7:127876954-127877461	IMR90	lung:	n/a	chr7:127877088-127877096
25	CEBPB	chr7:127874612-127874914	MCF-7	breast:	n/a	chr7:127874727-127874740 chr7:127874728-127874739
26	CEBPB	chr7:127881052-127881500	A549	lung:	n/a	chr7:127881276-127881285 chr7:127881276-127881285 chr7:127881274-127881287 chr7:127881276-127881285 chr7:127881276-127881285
27	CEBPB	chr7:127876977-127877338	Hela-S3	cervix:	n/a	chr7:127877088-127877096
28	CEBPB	chr7:127881225-127881365	H1-hESC	embryonic stem cell:	n/a	chr7:127881276-127881285 chr7:127881276-127881285 chr7:127881274-127881287 chr7:127881276-127881285 chr7:127881276-127881285
29	CEBPB	chr7:127877024-127877338	HepG2	liver:	n/a	chr7:127877088-127877096
30	CEBPB	chr7:127876965-127877363	K562	blood:	n/a	chr7:127877088-127877096
31	CEBPB	chr7:127880993-127881451	HepG2	liver:	n/a	chr7:127881276-127881285 chr7:127881276-127881285 chr7:127881274-127881287 chr7:127881276-127881285 chr7:127881276-127881285
32	CEBPB	chr7:127881179-127881418	A549	lung:	n/a	chr7:127881276-127881285 chr7:127881276-127881285 chr7:127881274-127881287 chr7:127881276-127881285 chr7:127881276-127881285
33	CEBPB	chr7:127877064-127877208	HepG2	liver:	n/a	chr7:127877088-127877096
34	CEBPB	chr7:127887741-127888142	K562	blood:	n/a	n/a
35	CEBPB	chr7:127874725-127874744	IMR90	lung:	n/a	chr7:127874727-127874740 chr7:127874728-127874739
36	CEBPB	chr7:127877001-127877275	K562	blood:	n/a	chr7:127877088-127877096
37	CEBPB	chr7:127876932-127877339	K562	blood:	n/a	chr7:127877088-127877096
38	CEBPB	chr7:127869646-127869933	HepG2	liver:	n/a	chr7:127869798-127869809
39	CEBPB	chr7:127881115-127881383	K562	blood:	n/a	chr7:127881276-127881285 chr7:127881276-127881285 chr7:127881274-127881287 chr7:127881276-127881285 chr7:127881276-127881285
40	CEBPB	chr7:127876977-127877339	A549	lung:	n/a	chr7:127877088-127877096
41	CEBPB	chr7:127876946-127877437	MCF-7	breast:	n/a	chr7:127877088-127877096
42	CEBPB	chr7:127881098-127881463	K562	blood:	n/a	chr7:127881276-127881285 chr7:127881276-127881285 chr7:127881274-127881287 chr7:127881276-127881285 chr7:127881276-127881285
43	CEBPB	chr7:127881118-127881395	IMR90	lung:	n/a	chr7:127881276-127881285 chr7:127881276-127881285 chr7:127881274-127881287 chr7:127881276-127881285 chr7:127881276-127881285
44	CEBPB	chr7:127874590-127874917	HepG2	liver:	n/a	chr7:127874727-127874740 chr7:127874728-127874739
45	CEBPB	chr7:127861732-127862327	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr7:127887860-127888158	K562	blood:	n/a	n/a
47	CHD2	chr7:127887885-127887890	K562	blood:	n/a	n/a
48	CHD2	chr7:127861986-127862394	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr7:127858480-127858630	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr7:127858520-127858670	GM12873	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:127881269-127881319	RPTEC	kidney:	n/a
2	chr7:127881440-127881490	SK-N-SH_RA	brain:	n/a
3	chr7:127881001-127881051	K562	blood:	n/a
4	chr7:127881344-127881394	RPTEC	kidney:	n/a
5	chr7:127880932-127880982	H1-hESC	embryonic stem cell:	embryo
6	chr7:127861992-127862042	HRCEpiC	kidney:	n/a
7	chr7:127881001-127881051	GM12891	blood:	n/a
8	chr7:127883819-127883869	MCF-7	breast:	n/a
9	chr7:127880932-127880982	AG09319	gingival:	n/a
10	chr7:127880619-127880669	HEEpiC	esophagus:	n/a
11	chr7:127881440-127881490	HRCEpiC	kidney:	n/a
12	chr7:127881280-127881330	NT2-D1	testis:	n/a
13	chr7:127881440-127881490	K562	blood:	n/a
14	chr7:127883819-127883869	Caco-2	colon:	n/a
15	chr7:127880932-127880982	BE2_C	brain:	n/a
16	chr7:127880932-127880982	BJ	skin:	n/a
17	chr7:127881280-127881330	BE2_C	brain:	n/a
18	chr7:127876829-127876879	H1-hESC	embryonic stem cell:	embryo
19	chr7:127881280-127881330	PFSK-1	brain:	n/a
20	chr7:127881001-127881051	T-47D	breast:	n/a
21	chr7:127881344-127881394	AG04450	lung:	fetal
22	chr7:127861992-127862042	HNPCEpiC	eye:	n/a
23	chr7:127881298-127881348	PrEC	prostate:	n/a
24	chr7:127881269-127881319	GM19239	blood:	n/a
25	chr7:127881280-127881330	SAEC	small airway:	n/a
26	chr7:127881280-127881330	SK-N-MC	brain:	n/a
27	chr7:127881280-127881330	HCF	heart:	n/a
28	chr7:127881280-127881330	Caco-2	colon:	n/a
29	chr7:127861992-127862042	AG04449	skin:	fetal
30	chr7:127881269-127881319	HL-60	blood:	n/a
31	chr7:127880932-127880982	SKMC	muscle:	n/a
32	chr7:127881001-127881051	GM12878	blood:	n/a
33	chr7:127880932-127880982	HEEpiC	esophagus:	n/a
34	chr7:127881001-127881051	NHBE	bronchial:	n/a
35	chr7:127881344-127881394	NHBE	bronchial:	n/a
36	chr7:127881298-127881348	GM12878	blood:	n/a
37	chr7:127876829-127876879	AoSMC	blood vessel:	n/a
38	chr7:127880619-127880669	SK-N-SH_RA	brain:	n/a
39	chr7:127876829-127876879	AG09319	gingival:	n/a
40	chr7:127879920-127879970	SK-N-SH_RA	brain:	n/a
41	chr7:127876829-127876879	HRE	kidney:	n/a
42	chr7:127883819-127883869	AG10803	skin:	n/a
43	chr7:127881298-127881348	HAEpiC	amniotic membrane:	n/a
44	chr7:127880619-127880669	HEK293	kidney:	embryo
45	chr7:127880619-127880669	NHDF-neo	bronchial:	n/a
46	chr7:127883819-127883869	HUVEC	blood vessel:	n/a
47	chr7:127880932-127880982	HRPEpiC	eye:	n/a
48	chr7:127876829-127876879	HL-60	blood:	n/a
49	chr7:127880932-127880982	SK-N-MC	brain:	n/a
50	chr7:127876829-127876879	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:127874560..127877136-chr7:127888514..127890542,2	K562	blood:
2	chr7:127865874..127867760-chr7:127871525..127873172,2	K562	blood:
3	chr7:127863182..127865481-chr7:127873510..127875848,2	K562	blood:
4	chr7:127862647..127864792-chr7:127867370..127870104,2	K562	blood:
5	chr7:127862647..127864792-chr7:127867370..127870104,2	K562	blood:
6	chr7:127887971..127892049-chr7:127893662..127896900,5	MCF-7	breast:
7	chr7:127874560..127877136-chr7:127887540..127890542,3	K562	blood:
8	chr7:127804591..127807479-chr7:127875712..127877601,2	K562	blood:
9	chr7:127032256..127035129-chr7:127876340..127878786,2	K562	blood:
10	chr7:127873554..127876347-chr7:127879499..127882292,2	MCF-7	breast:
11	chr7:127861984..127865041-chr7:127865310..127867337,3	K562	blood:
12	chr7:127854529..127856623-chr7:127857622..127859528,2	MCF-7	breast:
13	chr7:127867634..127869490-chr7:127873026..127875409,2	MCF-7	breast:
14	chr7:127878986..127881459-chr7:127884838..127886744,2	MCF-7	breast:
15	chr7:127858029..127859044-chr7:127962044..127962840,5	MCF-7	breast:
16	chr7:127861984..127865041-chr7:127865310..127867337,3	K562	blood:
17	chr7:127847369..127850045-chr7:127881602..127884379,2	K562	blood:
18	chr7:127870227..127873605-chr7:127875454..127877245,3	K562	blood:
19	chr7:127882313..127884523-chr7:127888725..127892714,3	MCF-7	breast:
20	chr7:127883949..127886357-chr7:127899008..127901184,2	K562	blood:
21	chr7:127867634..127869490-chr7:127873026..127875409,2	MCF-7	breast:
22	chr7:127875949..127878533-chr7:127881337..127883773,2	K562	blood:
23	chr7:127882313..127884523-chr7:127888725..127892714,3	MCF-7	breast:
24	chr7:127872543..127874497-chr7:127956158..127958595,2	K562	blood:
25	chr7:127857539..127859442-chr7:127980846..127983357,2	K562	blood:
26	chr7:127654215..127656574-chr7:127869545..127871812,2	K562	blood:
27	chr7:127869772..127871626-chr7:127914672..127917131,2	K562	blood:
28	chr7:127870227..127873605-chr7:127875454..127877245,3	K562	blood:
29	chr7:127865874..127867760-chr7:127871525..127873172,2	K562	blood:
30	chr7:127885455..127887398-chr7:127907036..127909723,2	K562	blood:
31	chr7:127874560..127877136-chr7:127888514..127890542,2	K562	blood:
32	chr7:127849594..127850163-chr7:127861948..127862627,2	K562	blood:
33	chr7:127874763..127879327-chr7:127896549..127902097,6	MCF-7	breast:
34	chr7:127863182..127865481-chr7:127873510..127875848,2	K562	blood:
35	chr7:127874560..127877136-chr7:127887540..127890542,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBM28-2	chr7:127876311-127876469	XLOC_006597
2	lnc-LEP-2	chr7:127846774-127858291	NONHSAT123172
3	lnc-RBM28-2	chr7:127861457-127861593	XLOC_006597
4	lnc-LEP-2	chr7:127864086-127864945	NONHSAT123172

Variant related genes	Relation type
LEP	TF binding region
LEP	CpG island
ENSG00000048405	chromatin interactions
ENSG00000207705	chromatin interactions
ENSG00000174697	chromatin interactions

Extended variants
information (count: 1277 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1277 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2167289	chr7:127857891-127857892	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181442691	chr7:127857902-127857903	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs534147414	chr7:127857903-127857904	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
4	rs535271211	chr7:127857969-127857970	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
5	rs570981196	chr7:127857981-127857982	Enhancers Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
6	rs11764840	chr7:127858048-127858049	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs370073802	chr7:127858051-127858052	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
8	rs7785591	chr7:127858084-127858085	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs539324405	chr7:127858095-127858096	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
10	rs558009882	chr7:127858134-127858135	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
11	rs538378962	chr7:127858147-127858148	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
12	rs375935847	chr7:127858150-127858151	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
13	rs78332539	chr7:127858168-127858169	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
14	rs150415398	chr7:127858188-127858189	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
15	rs138210072	chr7:127858192-127858193	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
16	rs551673424	chr7:127858229-127858230	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
17	rs185777777	chr7:127858283-127858284	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
18	rs142889168	chr7:127858291-127858292	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
19	rs540056340	chr7:127858315-127858316	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs561781727	chr7:127858332-127858333	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs540224245	chr7:127858349-127858350	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs561812893	chr7:127858351-127858352	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs528971162	chr7:127858403-127858404	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs560127289	chr7:127858413-127858414	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs550694632	chr7:127858425-127858426	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs75374373	chr7:127858444-127858445	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs145993091	chr7:127858452-127858453	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs138696805	chr7:127858455-127858456	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs79567353	chr7:127858477-127858478	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs534088749	chr7:127858493-127858494	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs528679831	chr7:127858505-127858506	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs375001198	chr7:127858510-127858511	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs549304463	chr7:127858515-127858516	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs567895924	chr7:127858522-127858523	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs537930849	chr7:127858553-127858554	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs74729328	chr7:127858613-127858614	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs190101991	chr7:127858656-127858657	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs562672315	chr7:127858720-127858721	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs531817985	chr7:127858721-127858722	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs114827227	chr7:127858723-127858724	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs141817164	chr7:127858765-127858766	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs115403248	chr7:127858820-127858821	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs59464399	chr7:127858911-127858912	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs116390122	chr7:127858923-127858924	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs144621374	chr7:127858933-127858934	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs115747503	chr7:127858958-127858959	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs562257192	chr7:127858965-127858966	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs180986540	chr7:127858969-127858970	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs544616380	chr7:127859017-127859018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185858011	chr7:127859024-127859025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127844000-127875600	Weak transcription	Right Atrium	heart
2	chr7:127850000-127867400	Weak transcription	Spleen	Spleen
3	chr7:127854800-127858000	Enhancers	HSMMtube	muscle
4	chr7:127854800-127858800	Enhancers	Osteobl	bone
5	chr7:127855000-127858800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr7:127855000-127858800	Enhancers	Adipose Nuclei	Adipose
7	chr7:127855200-127858200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr7:127855200-127858600	Enhancers	Placenta	Placenta
9	chr7:127855800-127858600	Enhancers	Fetal Muscle Trunk	muscle
10	chr7:127856000-127863600	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr7:127856200-127859000	Enhancers	NHDF-Ad	bronchial
12	chr7:127856800-127858000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr7:127856800-127858200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:127856800-127858200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr7:127856800-127858800	Enhancers	NHEK	skin
16	chr7:127857000-127858400	Enhancers	NHLF	lung
17	chr7:127857000-127858600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr7:127857000-127858600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
19	chr7:127857000-127858600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr7:127857200-127858000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr7:127857200-127858000	Enhancers	Fetal Muscle Leg	muscle
22	chr7:127857200-127858400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:127857200-127858400	Enhancers	Hela-S3	cervix
24	chr7:127857400-127858400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:127857400-127858600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr7:127857400-127862200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:127857600-127858800	Enhancers	Primary B cells from cord blood	blood
28	chr7:127857800-127858200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr7:127857800-127858400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:127857800-127858400	Flanking Active TSS	HSMM	muscle
31	chr7:127857800-127858800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:127857800-127860000	Enhancers	HMEC	breast
33	chr7:127858000-127858400	Flanking Active TSS	HSMMtube	muscle
34	chr7:127858000-127859000	Bivalent Enhancer	Fetal Muscle Leg	muscle
35	chr7:127858000-127861800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr7:127858200-127858800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr7:127858400-127859000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr7:127858400-127860400	Enhancers	HSMM	muscle
39	chr7:127858400-127860600	Enhancers	HSMMtube	muscle
40	chr7:127858400-127860800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:127858400-127861200	Weak transcription	Hela-S3	cervix
42	chr7:127858400-127861400	Weak transcription	NHLF	lung
43	chr7:127858400-127861800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:127858600-127858800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr7:127858600-127859200	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr7:127858600-127860200	Enhancers	Muscle Satellite Cultured Cells	--
47	chr7:127858600-127861400	Weak transcription	Placenta	Placenta
48	chr7:127858600-127861400	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr7:127858800-127861400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr7:127858800-127861600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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