Variant report

Variant	nsv872156
Chromosome Location	chr1:112886545-112927912
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	chr1:112912327-112912611	HepG2	liver:	n/a	n/a
2	ATF3	chr1:112912288-112912565	K562	blood:	n/a	n/a
3	ATF3	chr1:112912209-112912620	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:112901538-112901767	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:112897404-112897456	K562	blood:	n/a	n/a
6	BCLAF1	chr1:112912277-112912621	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:112901441-112901751	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:112887457-112887469	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:112922460-112922583	GM12878	blood:	n/a	chr1:112922503-112922512 chr1:112922497-112922518 chr1:112922503-112922512 chr1:112922504-112922513
10	BHLHE40	chr1:112912298-112912620	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:112912262-112912624	K562	blood:	n/a	n/a
12	BHLHE40	chr1:112922452-112922651	K562	blood:	n/a	chr1:112922503-112922512 chr1:112922497-112922518 chr1:112922503-112922512 chr1:112922504-112922513
13	BHLHE40	chr1:112901416-112901667	K562	blood:	n/a	n/a
14	BRCA1	chr1:112912340-112912650	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr1:112912402-112912476	HepG2	liver:	n/a	n/a
16	BRCA1	chr1:112912293-112912658	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr1:112902848-112903195	HepG2	liver:	n/a	chr1:112903024-112903035
18	CEBPB	chr1:112890123-112890303	K562	blood:	n/a	chr1:112890155-112890172
19	CEBPB	chr1:112902841-112903216	IMR90	lung:	n/a	chr1:112903024-112903035
20	CEBPB	chr1:112916499-112916596	K562	blood:	n/a	n/a
21	CEBPB	chr1:112902876-112903182	H1-hESC	embryonic stem cell:	n/a	chr1:112903024-112903035
22	CEBPB	chr1:112912276-112912634	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:112890073-112890295	HepG2	liver:	n/a	chr1:112890155-112890172
24	CHD1	chr1:112887365-112887448	GM12878	blood:	n/a	n/a
25	CHD2	chr1:112901607-112901616	K562	blood:	n/a	n/a
26	CHD2	chr1:112887434-112887579	GM12878	blood:	n/a	n/a
27	CHD2	chr1:112912289-112912624	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr1:112912410-112912543	HepG2	liver:	n/a	n/a
29	CTCF	chr1:112901520-112901670	GM12874	blood:	n/a	chr1:112901591-112901604 chr1:112901590-112901611 chr1:112901588-112901606
30	CTCF	chr1:112887680-112887830	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr1:112912304-112912640	MCF-7	breast:	n/a	chr1:112912475-112912493 chr1:112912482-112912490 chr1:112912477-112912490 chr1:112912477-112912490
32	CTCF	chr1:112901500-112901650	GM12872	blood:	n/a	chr1:112901591-112901604 chr1:112901590-112901611 chr1:112901588-112901606
33	CTCF	chr1:112901500-112901650	HEK293	kidney:	n/a	chr1:112901591-112901604 chr1:112901590-112901611 chr1:112901588-112901606
34	CTCF	chr1:112912284-112912598	SK-N-SH_RA	brain:	n/a	chr1:112912475-112912493 chr1:112912482-112912490 chr1:112912477-112912490 chr1:112912477-112912490
35	CTCF	chr1:112912380-112912530	MCF-7	breast:	n/a	chr1:112912475-112912493 chr1:112912482-112912490 chr1:112912477-112912490 chr1:112912477-112912490
36	CTCF	chr1:112912400-112912550	HL-60	blood:	n/a	chr1:112912475-112912493 chr1:112912482-112912490 chr1:112912477-112912490 chr1:112912477-112912490
37	CTCF	chr1:112912400-112912550	GM12875	blood:	n/a	chr1:112912475-112912493 chr1:112912482-112912490 chr1:112912477-112912490 chr1:112912477-112912490
38	CTCF	chr1:112887540-112887690	HMEC	breast:	n/a	n/a
39	CTCF	chr1:112912420-112912570	HEK293	kidney:	n/a	chr1:112912475-112912493 chr1:112912482-112912490 chr1:112912477-112912490 chr1:112912477-112912490
40	CTCF	chr1:112912420-112912570	AG09309	skin:	n/a	chr1:112912475-112912493 chr1:112912482-112912490 chr1:112912477-112912490 chr1:112912477-112912490
41	CTCF	chr1:112902340-112902490	AG04450	lung:	n/a	n/a
42	CTCF	chr1:112901540-112901690	HCFaa	heart:	n/a	chr1:112901591-112901604 chr1:112901590-112901611 chr1:112901588-112901606
43	CTCF	chr1:112912079-112912927	HCT-116	colon:	n/a	chr1:112912475-112912493 chr1:112912482-112912490 chr1:112912477-112912490 chr1:112912477-112912490
44	CTCF	chr1:112912400-112912550	HepG2	liver:	n/a	chr1:112912475-112912493 chr1:112912482-112912490 chr1:112912477-112912490 chr1:112912477-112912490
45	CTCF	chr1:112901444-112901758	MCF-7	breast:	n/a	chr1:112901591-112901604 chr1:112901590-112901611 chr1:112901588-112901606
46	CTCF	chr1:112887640-112887790	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr1:112901580-112901730	HRE	kidney:	n/a	chr1:112901591-112901604 chr1:112901590-112901611 chr1:112901588-112901606
48	CTCF	chr1:112901520-112901670	GM12867	blood:	n/a	chr1:112901591-112901604 chr1:112901590-112901611 chr1:112901588-112901606
49	CTCF	chr1:112901463-112901718	GM13977	blood:	n/a	chr1:112901591-112901604 chr1:112901590-112901611 chr1:112901588-112901606
50	CTCF	chr1:112912380-112912530	HA-sp	spinal cord:	n/a	chr1:112912475-112912493 chr1:112912482-112912490 chr1:112912477-112912490 chr1:112912477-112912490

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:112902215-112902265	Jurkat	blood:	n/a
2	chr1:112902215-112902265	AG04450	lung:	fetal
3	chr1:112902215-112902265	BJ	skin:	n/a
4	chr1:112902215-112902265	HepG2	liver:	n/a
5	chr1:112902215-112902265	SK-N-SH	brain:	n/a
6	chr1:112902215-112902265	NHDF-neo	bronchial:	n/a
7	chr1:112902215-112902265	HRCEpiC	kidney:	n/a
8	chr1:112902215-112902265	NH-A	brain:	n/a
9	chr1:112902215-112902265	HEEpiC	esophagus:	n/a
10	chr1:112902215-112902265	GM06990	blood:	n/a
11	chr1:112902215-112902265	SKMC	muscle:	n/a
12	chr1:112902215-112902265	NHBE	bronchial:	n/a
13	chr1:112902215-112902265	HCPEpiC	choroid plexus:	n/a
14	chr1:112902215-112902265	NB4	blood:	n/a
15	chr1:112902215-112902265	LNCaP	prostate:	n/a
16	chr1:112902215-112902265	K562	blood:	n/a
17	chr1:112902215-112902265	CMK	blood:	n/a
18	chr1:112902215-112902265	MCF10A-Er-Src	breast:	n/a
19	chr1:112902215-112902265	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:112902215-112902265	HMEC	breast:	n/a
21	chr1:112902215-112902265	U87	brain:	n/a
22	chr1:112902215-112902265	AG04449	skin:	fetal
23	chr1:112902215-112902265	AG09319	gingival:	n/a
24	chr1:112902215-112902265	AG09309	skin:	n/a
25	chr1:112902215-112902265	Caco-2	colon:	n/a
26	chr1:112902215-112902265	T-47D	breast:	n/a
27	chr1:112902215-112902265	GM12878	blood:	n/a
28	chr1:112902215-112902265	HRPEpiC	eye:	n/a
29	chr1:112902215-112902265	ProgFib	skin:	n/a
30	chr1:112902215-112902265	GM12891	blood:	n/a
31	chr1:112902215-112902265	AoSMC	blood vessel:	n/a
32	chr1:112902215-112902265	GM12892	blood:	n/a
33	chr1:112902215-112902265	AG10803	skin:	n/a
34	chr1:112902215-112902265	ovcar-3	ovarian:	n/a
35	chr1:112902215-112902265	IMR90	lung:	fetal
36	chr1:112902215-112902265	HRE	kidney:	n/a
37	chr1:112902215-112902265	BE2_C	brain:	n/a
38	chr1:112902215-112902265	HCF	heart:	n/a
39	chr1:112902215-112902265	HL-60	blood:	n/a
40	chr1:112902215-112902265	HEK293	kidney:	embryo
41	chr1:112902215-112902265	HAEpiC	amniotic membrane:	n/a
42	chr1:112902215-112902265	SAEC	small airway:	n/a
43	chr1:112902215-112902265	SK-N-SH_RA	brain:	n/a
44	chr1:112902215-112902265	Hela-S3	cervix:	n/a
45	chr1:112902215-112902265	H1-hESC	embryonic stem cell:	embryo
46	chr1:112902215-112902265	PFSK-1	brain:	n/a
47	chr1:112902215-112902265	HCT-116	colon:	n/a
48	chr1:112902215-112902265	PANC-1	pancreas:	n/a
49	chr1:112902215-112902265	HCM	heart:	n/a
50	chr1:112902215-112902265	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:112900465..112902593-chr1:112911954..112912991,20	MCF-7	breast:
2	chr1:112911288..112915007-chr1:112915833..112919531,4	K562	blood:
3	chr1:112922435..112924282-chr1:112955267..112957859,2	MCF-7	breast:
4	chr1:112911695..112912372-chr1:112924781..112925385,2	MCF-7	breast:
5	chr1:112905552..112907554-chr1:112910893..112912600,2	MCF-7	breast:
6	chr1:112880187..112882790-chr1:112887781..112889675,2	K562	blood:
7	chr1:112895643..112897677-chr1:112897797..112899950,2	K562	blood:
8	chr1:112912009..112912593-chr1:113044548..113045085,2	MCF-7	breast:
9	chr1:112914121..112916776-chr1:112921538..112923263,2	K562	blood:
10	chr1:112895643..112897677-chr1:112897797..112899950,2	K562	blood:
11	chr1:112841241..112841818-chr1:112912086..112912921,2	MCF-7	breast:
12	chr1:112840939..112841965-chr1:112911561..112912931,5	K562	blood:
13	chr1:112840708..112841508-chr1:112911801..112912878,3	MCF-7	breast:
14	chr1:112911695..112912372-chr1:112924781..112925385,2	MCF-7	breast:
15	chr1:112332371..112333211-chr1:112912263..112912927,2	MCF-7	breast:
16	chr1:112911281..112914240-chr1:112915410..112919234,5	K562	blood:
17	chr1:112920907..112923373-chr1:112930498..112932173,2	K562	blood:
18	chr1:112914121..112916776-chr1:112921538..112923263,2	K562	blood:
19	chr1:112900465..112902593-chr1:112911954..112912991,20	MCF-7	breast:
20	chr1:112900992..112901946-chr1:113008887..113009414,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST7L-2	chr1:112902984-112903150	ENSG00000231246
2	lnc-CTTNBP2NL-3	chr1:112905903-112906203	NONHSAT005228

Variant related genes	Relation type
ENSG00000238761	TF binding region
ENSG00000231246	TF binding region
TXNP3	TF binding region
ENSG00000238761	CpG island
ENSG00000231246	CpG island
TXNP3	CpG island
ENSG00000234388	chromatin interactions
ENSG00000134245	chromatin interactions
ENSG00000143079	chromatin interactions
ENSG00000238761	chromatin interactions

Extended variants
information (count: 1576 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1576 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2995765	chr1:112886545-112886546	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs3005781	chr1:112886561-112886562	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574955073	chr1:112886592-112886593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568703398	chr1:112886676-112886677	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs114438783	chr1:112886689-112886690	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs190982465	chr1:112886753-112886754	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs570512283	chr1:112886876-112886877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539449362	chr1:112886893-112886894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555926918	chr1:112886928-112886929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575985361	chr1:112886939-112886940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182962622	chr1:112886958-112886959	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144677087	chr1:112887039-112887040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1936048	chr1:112887053-112887054	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs540799653	chr1:112887055-112887056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187670201	chr1:112887166-112887167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543748478	chr1:112887199-112887200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540716422	chr1:112887231-112887232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148074567	chr1:112887254-112887255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs57998860	chr1:112887334-112887335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141844533	chr1:112887337-112887338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562337685	chr1:112887351-112887352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527888177	chr1:112887356-112887357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150632066	chr1:112887424-112887425	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571047219	chr1:112887435-112887436	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539203708	chr1:112887458-112887459	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140087856	chr1:112887475-112887476	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569585277	chr1:112887492-112887493	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535397480	chr1:112887508-112887509	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538116109	chr1:112887522-112887523	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555984856	chr1:112887684-112887685	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115330562	chr1:112887694-112887695	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560663674	chr1:112887703-112887704	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200543853	chr1:112887704-112887705	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143776039	chr1:112887709-112887710	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577415405	chr1:112887719-112887720	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546011107	chr1:112887769-112887770	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146374331	chr1:112887796-112887797	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576378943	chr1:112887801-112887802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34576479	chr1:112887813-112887814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542156342	chr1:112887857-112887858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562375669	chr1:112887916-112887917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528032424	chr1:112887923-112887924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs5777102	chr1:112887927-112887928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573897953	chr1:112887949-112887950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541743523	chr1:112887950-112887951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541197498	chr1:112887957-112887958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1105184	chr1:112887982-112887983	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs369426096	chr1:112888086-112888087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs1105183	chr1:112888105-112888106	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs1105182	chr1:112888147-112888148	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:112880000-112889600	Weak transcription	Right Atrium	heart
2	chr1:112880200-112886600	Weak transcription	Esophagus	oesophagus
3	chr1:112885600-112887600	Weak transcription	Adipose Nuclei	Adipose
4	chr1:112886000-112889400	Weak transcription	Fetal Stomach	stomach
5	chr1:112886400-112886600	Enhancers	Thymus	Thymus
6	chr1:112886400-112888200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr1:112886600-112886800	ZNF genes & repeats	Esophagus	oesophagus
8	chr1:112886600-112886800	Enhancers	Pancreas	Pancrea
9	chr1:112886600-112887000	Enhancers	Fetal Thymus	thymus
10	chr1:112886600-112887200	Weak transcription	Thymus	Thymus
11	chr1:112886600-112887400	Enhancers	Primary T cells from cord blood	blood
12	chr1:112886600-112887800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr1:112886600-112888000	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr1:112886600-112888200	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr1:112886600-112888400	Enhancers	Primary T cells fromperipheralblood	blood
16	chr1:112886600-112888400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr1:112886600-112888800	Enhancers	Dnd41	blood
18	chr1:112886800-112889200	Weak transcription	Esophagus	oesophagus
19	chr1:112886800-112901400	Weak transcription	Pancreas	Pancrea
20	chr1:112887000-112887400	Weak transcription	Fetal Thymus	thymus
21	chr1:112887000-112888000	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr1:112887000-112888200	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr1:112887000-112888400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr1:112887200-112887400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:112887200-112888000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr1:112887200-112888200	Enhancers	Thymus	Thymus
27	chr1:112887400-112887800	Flanking Active TSS	Primary T cells from cord blood	blood
28	chr1:112887400-112887800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr1:112887400-112887800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:112887400-112888000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:112887400-112888000	Enhancers	Primary B cells from peripheral blood	blood
32	chr1:112887400-112888000	Enhancers	Primary hematopoietic stem cells	blood
33	chr1:112887400-112888000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:112887400-112888200	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr1:112887400-112888400	Enhancers	Fetal Thymus	thymus
36	chr1:112887400-112888600	Enhancers	HMEC	breast
37	chr1:112887600-112887800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr1:112887600-112888000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr1:112887600-112888000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr1:112887600-112888000	Enhancers	Adipose Nuclei	Adipose
41	chr1:112887800-112888000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:112887800-112888200	Enhancers	Primary T cells from cord blood	blood
43	chr1:112887800-112888200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:112887800-112889400	Enhancers	Spleen	Spleen
45	chr1:112888000-112889000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr1:112889000-112889800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr1:112889000-112890200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:112889200-112889400	Enhancers	Esophagus	oesophagus
49	chr1:112889200-112890400	Enhancers	Stomach Smooth Muscle	stomach
50	chr1:112889400-112889600	Enhancers	Right Ventricle	heart

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