Variant report

Variant	nsv431026
Chromosome Location	chr14:97079926-97163106
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:421)
CpG islands
(count:1221)
Chromatin interactive
region (count:66)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:97113854-97114026	K562	blood:	n/a	n/a
2	ARID3A	chr14:97126507-97126797	K562	blood:	n/a	n/a
3	ATF1	chr14:97102247-97102558	K562	blood:	n/a	n/a
4	ATF1	chr14:97151485-97151654	K562	blood:	n/a	n/a
5	ATF1	chr14:97148684-97148746	K562	blood:	n/a	n/a
6	ATF1	chr14:97126481-97126798	K562	blood:	n/a	n/a
7	ATF3	chr14:97129932-97130110	K562	blood:	n/a	n/a
8	ATF3	chr14:97154975-97155235	K562	blood:	n/a	n/a
9	BACH1	chr14:97093553-97093561	K562	blood:	n/a	n/a
10	BHLHE40	chr14:97092811-97093615	K562	blood:	n/a	n/a
11	BHLHE40	chr14:97082434-97082636	K562	blood:	n/a	n/a
12	BHLHE40	chr14:97129978-97130201	K562	blood:	n/a	n/a
13	BHLHE40	chr14:97127039-97127064	K562	blood:	n/a	n/a
14	BRCA1	chr14:97083897-97083954	HepG2	liver:	n/a	n/a
15	CBX3	chr14:97129917-97130313	K562	blood:	n/a	n/a
16	CBX3	chr14:97129812-97130286	K562	blood:	n/a	n/a
17	CCNT2	chr14:97126335-97126729	K562	blood:	n/a	chr14:97126450-97126459
18	CEBPB	chr14:97155026-97155256	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr14:97151472-97151769	K562	blood:	n/a	chr14:97151605-97151616
20	CEBPB	chr14:97123014-97123254	K562	blood:	n/a	chr14:97123165-97123176
21	CEBPB	chr14:97151475-97151726	IMR90	lung:	n/a	chr14:97151605-97151616
22	CEBPB	chr14:97123038-97123338	IMR90	lung:	n/a	chr14:97123165-97123176
23	CEBPB	chr14:97082927-97083127	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:97155011-97155246	K562	blood:	n/a	n/a
25	CEBPB	chr14:97154971-97155303	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr14:97148250-97148491	HepG2	liver:	n/a	chr14:97148310-97148321
27	CEBPB	chr14:97099041-97099257	HepG2	liver:	n/a	n/a
28	CEBPB	chr14:97151432-97151767	HepG2	liver:	n/a	chr14:97151605-97151616
29	CEBPB	chr14:97149037-97149375	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr14:97123007-97123330	HepG2	liver:	n/a	chr14:97123165-97123176
31	CEBPB	chr14:97151461-97151738	A549	lung:	n/a	chr14:97151605-97151616
32	CEBPB	chr14:97123015-97123332	A549	lung:	n/a	chr14:97123165-97123176
33	CEBPD	chr14:97126470-97126782	K562	blood:	n/a	n/a
34	CEBPD	chr14:97132151-97132601	K562	blood:	n/a	n/a
35	CHD2	chr14:97129970-97130133	K562	blood:	n/a	n/a
36	CTCF	chr14:97132602-97132723	MCF-7	breast:	n/a	n/a
37	CTCF	chr14:97137524-97137962	MCF-7	breast:	n/a	chr14:97137729-97137747 chr14:97137730-97137746 chr14:97137724-97137745
38	CTCF	chr14:97155594-97155677	MCF-7	breast:	n/a	n/a
39	CTCF	chr14:97145460-97145610	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr14:97145533-97145608	HepG2	liver:	n/a	n/a
41	CTCF	chr14:97145360-97145510	GM12872	blood:	n/a	n/a
42	CTCF	chr14:97145518-97145621	GM19239	blood:	n/a	n/a
43	CTCF	chr14:97132540-97132690	GM12873	blood:	n/a	n/a
44	CTCF	chr14:97132560-97132710	A549	lung:	n/a	n/a
45	CTCF	chr14:97155583-97155671	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:97132437-97132906	MCF-7	breast:	n/a	n/a
47	CTCF	chr14:97132438-97132912	HCT-116	colon:	n/a	n/a
48	CTCF	chr14:97132453-97132841	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr14:97145320-97145470	GM06990	blood:	n/a	n/a
50	CTCF	chr14:97132560-97132710	MCF-7	breast:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:97081208-97081258	IMR90	lung:	fetal
2	chr14:97081208-97081258	IMR90	lung:	fetal
3	chr14:97129577-97129627	GM12892	blood:	n/a
4	chr14:97091489-97091539	ProgFib	skin:	n/a
5	chr14:97081655-97081705	SK-N-SH_RA	brain:	n/a
6	chr14:97090212-97090262	HNPCEpiC	eye:	n/a
7	chr14:97090367-97090417	AG04449	skin:	fetal
8	chr14:97090367-97090417	RPTEC	kidney:	n/a
9	chr14:97089082-97089132	AG10803	skin:	n/a
10	chr14:97091489-97091539	GM12892	blood:	n/a
11	chr14:97091520-97091570	ProgFib	skin:	n/a
12	chr14:97091520-97091570	CMK	blood:	n/a
13	chr14:97089082-97089132	HEK293	kidney:	embryo
14	chr14:97091520-97091570	K562	blood:	n/a
15	chr14:97091520-97091570	HCF	heart:	n/a
16	chr14:97092096-97092146	HepG2	liver:	n/a
17	chr14:97091902-97091952	HepG2	liver:	n/a
18	chr14:97091520-97091570	HCM	heart:	n/a
19	chr14:97127338-97127388	MCF10A-Er-Src	breast:	n/a
20	chr14:97091489-97091539	GM19239	blood:	n/a
21	chr14:97089420-97089470	Caco-2	colon:	n/a
22	chr14:97135129-97135179	HNPCEpiC	eye:	n/a
23	chr14:97082103-97082153	HRCEpiC	kidney:	n/a
24	chr14:97092205-97092255	HAEpiC	amniotic membrane:	n/a
25	chr14:97089082-97089132	T-47D	breast:	n/a
26	chr14:97091489-97091539	NHDF-neo	bronchial:	n/a
27	chr14:97135129-97135179	CMK	blood:	n/a
28	chr14:97092150-97092200	SK-N-SH	brain:	n/a
29	chr14:97129577-97129627	NH-A	brain:	n/a
30	chr14:97082103-97082153	NH-A	brain:	n/a
31	chr14:97091067-97091117	U87	brain:	n/a
32	chr14:97081558-97081608	Hepatocyte	liver:	n/a
33	chr14:97092150-97092200	HPAEpiC	pulmonary alveolar:	n/a
34	chr14:97127338-97127388	GM12878	blood:	n/a
35	chr14:97135129-97135179	AG04450	lung:	fetal
36	chr14:97127338-97127388	ECC-1	luminal epithelium:	n/a
37	chr14:97090367-97090417	SK-N-SH_RA	brain:	n/a
38	chr14:97081655-97081705	GM06990	blood:	n/a
39	chr14:97091067-97091117	ECC-1	luminal epithelium:	n/a
40	chr14:97127338-97127388	SAEC	small airway:	n/a
41	chr14:97129452-97129502	NB4	blood:	n/a
42	chr14:97092205-97092255	SK-N-MC	brain:	n/a
43	chr14:97089420-97089470	ProgFib	skin:	n/a
44	chr14:97081899-97081949	U87	brain:	n/a
45	chr14:97082103-97082153	SK-N-MC	brain:	n/a
46	chr14:97091067-97091117	PrEC	prostate:	n/a
47	chr14:97089082-97089132	Jurkat	blood:	n/a
48	chr14:97092205-97092255	HCT-116	colon:	n/a
49	chr14:97092205-97092255	NB4	blood:	n/a
50	chr14:97082103-97082153	CMK	blood:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:97058853..97060564-chr14:97080580..97083238,2	K562	blood:
2	chr14:97100553..97101432-chr14:97126836..97127804,5	MCF-7	breast:
3	chr14:97098302..97100960-chr14:97102875..97104630,2	K562	blood:
4	chr14:97133535..97135440-chr14:97140308..97142145,2	MCF-7	breast:
5	chr14:97075091..97077466-chr14:97079393..97081183,2	MCF-7	breast:
6	chr14:97040398..97040962-chr14:97100553..97101449,2	MCF-7	breast:
7	chr14:97050566..97051176-chr14:97145157..97145895,3	MCF-7	breast:
8	chr14:97151757..97153903-chr14:97156739..97159660,2	K562	blood:
9	chr14:97040333..97042090-chr14:97100526..97101489,19	MCF-7	breast:
10	chr14:97125727..97127557-chr14:97130189..97131813,2	K562	blood:
11	chr14:97050109..97051246-chr14:97131819..97133058,6	MCF-7	breast:
12	chr14:97049843..97051026-chr14:97131982..97133064,8	MCF-7	breast:
13	chr14:97091981..97093780-chr14:97101556..97103907,3	MCF-7	breast:
14	chr14:97079988..97082344-chr14:97083126..97085624,2	MCF-7	breast:
15	chr14:97047039..97047841-chr14:97100546..97101485,3	MCF-7	breast:
16	chr14:97100866..97101454-chr14:97138053..97138598,2	MCF-7	breast:
17	chr14:97040936..97041835-chr14:97100556..97101428,4	MCF-7	breast:
18	chr14:97084192..97086627-chr14:97090861..97093279,2	MCF-7	breast:
19	chr14:97137196..97139523-chr14:97142703..97145275,2	MCF-7	breast:
20	chr14:97091981..97093780-chr14:97101556..97103907,3	MCF-7	breast:
21	chr14:97140314..97141902-chr14:97154245..97156779,2	K562	blood:
22	chr14:97125727..97128111-chr14:97129743..97131813,3	K562	blood:
23	chr14:97084192..97086627-chr14:97090861..97093279,2	MCF-7	breast:
24	chr14:97050265..97051308-chr14:97136874..97138151,3	MCF-7	breast:
25	chr14:97127931..97131812-chr14:97133536..97135209,3	K562	blood:
26	chr14:97137196..97139523-chr14:97142703..97145275,2	MCF-7	breast:
27	chr14:97136763..97139575-chr14:97158044..97160413,2	MCF-7	breast:
28	chr14:97098302..97100960-chr14:97102875..97104630,2	K562	blood:
29	chr14:97135759..97137328-chr14:97140118..97143356,3	MCF-7	breast:
30	chr14:97074081..97075800-chr14:97155879..97157935,2	MCF-7	breast:
31	chr14:97127931..97131812-chr14:97133536..97135209,3	K562	blood:
32	chr14:97125727..97128111-chr14:97129743..97131813,3	K562	blood:
33	chr14:97147561..97149240-chr14:97151523..97153558,2	K562	blood:
34	chr14:97100553..97101432-chr14:97126836..97127804,5	MCF-7	breast:
35	chr14:97050772..97051636-chr14:97147130..97147711,2	MCF-7	breast:
36	chr14:97041013..97042090-chr14:97100546..97101489,8	MCF-7	breast:
37	chr14:97127690..97129431-chr14:97133268..97135036,2	K562	blood:
38	chr14:97100866..97101454-chr14:97138053..97138598,2	MCF-7	breast:
39	chr14:97079988..97082344-chr14:97083126..97085624,2	MCF-7	breast:
40	chr14:97147561..97149240-chr14:97151523..97153558,2	K562	blood:
41	chr14:97050324..97051208-chr14:97145144..97146022,4	MCF-7	breast:
42	chr14:97085374..97088173-chr14:97091908..97094865,2	K562	blood:
43	chr14:97105478..97107756-chr14:97114890..97116903,2	MCF-7	breast:
44	chr14:97105478..97107756-chr14:97114890..97116903,2	MCF-7	breast:
45	chr14:97121918..97124905-chr14:97127753..97129733,2	K562	blood:
46	chr14:97080445..97082633-chr14:97084397..97086531,2	K562	blood:
47	chr14:97047308..97047841-chr14:97100928..97101485,2	MCF-7	breast:
48	chr14:97127690..97129431-chr14:97133268..97135036,2	K562	blood:
49	chr14:97133535..97135440-chr14:97140308..97142145,2	MCF-7	breast:
50	chr14:97093078..97095980-chr14:97096287..97099015,3	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG2B-8	chr14:97104524-97104851	NONHSAT039549

No data

Variant related genes	Relation type
RN7SKP108	TF binding region
RN7SKP108	CpG island
ENSG00000258702	chromatin interactions

Extended variants
information (count: 3076 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3076 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12435870	chr14:97079926-97079927	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144977759	chr14:97079971-97079972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529697482	chr14:97080002-97080003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs57092075	chr14:97080016-97080017	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs566399189	chr14:97080047-97080048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533911306	chr14:97080055-97080056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77653270	chr14:97080056-97080057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182827106	chr14:97080088-97080089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12892353	chr14:97080116-97080117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556534868	chr14:97080132-97080133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574790894	chr14:97080149-97080150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148957708	chr14:97080150-97080151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528643303	chr14:97080155-97080156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs369773689	chr14:97080165-97080166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs28637204	chr14:97080212-97080213	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs532970939	chr14:97080232-97080233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565162794	chr14:97080259-97080260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142853596	chr14:97080267-97080268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573221289	chr14:97080303-97080304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs77501656	chr14:97080336-97080337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539804192	chr14:97080345-97080346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112441848	chr14:97080354-97080355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78823290	chr14:97080389-97080390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs61983124	chr14:97080396-97080397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544494041	chr14:97080408-97080409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74522470	chr14:97080460-97080461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530426207	chr14:97080480-97080481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs17094199	chr14:97080571-97080572	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs550900596	chr14:97080599-97080600	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs234600	chr14:97080601-97080602	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs114451020	chr14:97080607-97080608	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs79519839	chr14:97080612-97080613	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs234599	chr14:97080633-97080634	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs8019595	chr14:97080664-97080665	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs372390936	chr14:97080701-97080702	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs550001938	chr14:97080703-97080704	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568234468	chr14:97080704-97080705	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs234598	chr14:97080722-97080723	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs554649176	chr14:97080731-97080732	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573217575	chr14:97080746-97080747	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs34488830	chr14:97080759-97080760	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs139345141	chr14:97080777-97080778	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs17094206	chr14:97080836-97080837	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs567646500	chr14:97080865-97080866	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs185721890	chr14:97080885-97080886	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs562765735	chr14:97081052-97081053	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs575000111	chr14:97081075-97081076	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs542545698	chr14:97081103-97081104	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs559874427	chr14:97081115-97081116	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs374691935	chr14:97081150-97081151	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Glioblastoma	21080181	CNVD
Cancer	20164920	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Breast cancer	21509527	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	17426248	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97075600-97080200	Weak transcription	Fetal Brain Male	brain
2	chr14:97079200-97080600	Enhancers	Fetal Brain Female	brain
3	chr14:97080200-97084000	Enhancers	Fetal Brain Male	brain
4	chr14:97080400-97082800	Enhancers	Brain Germinal Matrix	brain
5	chr14:97080600-97081400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:97080600-97081400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr14:97080600-97081400	Flanking Active TSS	Fetal Brain Female	brain
8	chr14:97080600-97083400	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr14:97080800-97081000	Enhancers	Brain Hippocampus Middle	brain
10	chr14:97080800-97081000	Bivalent Enhancer	Fetal Lung	lung
11	chr14:97080800-97081000	Bivalent Enhancer	HepG2	liver
12	chr14:97080800-97081400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
13	chr14:97081000-97081200	Flanking Active TSS	Brain Hippocampus Middle	brain
14	chr14:97081000-97081200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr14:97081000-97081200	Enhancers	Pancreas	Pancrea
16	chr14:97081000-97081600	Flanking Bivalent TSS/Enh	HepG2	liver
17	chr14:97081200-97081400	Bivalent Enhancer	Brain Angular Gyrus	brain
18	chr14:97081200-97081600	Active TSS	Brain Hippocampus Middle	brain
19	chr14:97081200-97081800	Enhancers	Spleen	Spleen
20	chr14:97081200-97082600	Weak transcription	Pancreas	Pancrea
21	chr14:97081400-97081600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr14:97081400-97083600	Enhancers	Fetal Brain Female	brain
23	chr14:97081600-97082000	Enhancers	Brain Hippocampus Middle	brain
24	chr14:97081600-97090200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr14:97081800-97082600	Active TSS	Spleen	Spleen
26	chr14:97082200-97083000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
27	chr14:97082200-97083000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr14:97082200-97083400	Enhancers	Fetal Intestine Small	intestine
29	chr14:97082400-97082600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
30	chr14:97082400-97082800	Enhancers	Fetal Intestine Large	intestine
31	chr14:97082400-97083200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
32	chr14:97082600-97082800	Bivalent Enhancer	Brain Angular Gyrus	brain
33	chr14:97082600-97083000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
34	chr14:97082600-97083000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
35	chr14:97082600-97083000	Active TSS	Duodenum Mucosa	Duodenum
36	chr14:97082600-97083000	Enhancers	Pancreas	Pancrea
37	chr14:97082600-97083200	Enhancers	Esophagus	oesophagus
38	chr14:97082800-97083000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr14:97082800-97083000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr14:97082800-97083200	Flanking Active TSS	Brain Germinal Matrix	brain
41	chr14:97083000-97083400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr14:97083000-97084000	Enhancers	Duodenum Mucosa	Duodenum
43	chr14:97083200-97083400	Enhancers	Brain Germinal Matrix	brain
44	chr14:97083400-97083600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr14:97084000-97090000	Weak transcription	Fetal Brain Male	brain
46	chr14:97084000-97096200	Weak transcription	Right Atrium	heart
47	chr14:97085400-97085800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:97088600-97088800	Enhancers	Brain Germinal Matrix	brain
49	chr14:97088800-97090600	Weak transcription	Brain Germinal Matrix	brain
50	chr14:97090000-97094600	Enhancers	Fetal Brain Male	brain

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