Variant report

Variant	nsv470663
Chromosome Location	chr14:97092803-97127431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:125)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:125 , 50 per page) page: 1 2 3

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	chr14:97126481-97126798	K562	blood:	n/a	n/a
5	BACH1	chr14:97093553-97093561	K562	blood:	n/a	n/a
6	BHLHE40	chr14:97127039-97127064	K562	blood:	n/a	n/a
7	BHLHE40	chr14:97092811-97093615	K562	blood:	n/a	n/a
8	CCNT2	chr14:97126335-97126729	K562	blood:	n/a	chr14:97126450-97126459
9	CEBPB	chr14:97123038-97123338	IMR90	lung:	n/a	chr14:97123165-97123176
10	CEBPB	chr14:97123015-97123332	A549	lung:	n/a	chr14:97123165-97123176
11	CEBPB	chr14:97099041-97099257	HepG2	liver:	n/a	n/a
12	CEBPB	chr14:97123007-97123330	HepG2	liver:	n/a	chr14:97123165-97123176
13	CEBPB	chr14:97123014-97123254	K562	blood:	n/a	chr14:97123165-97123176
14	CEBPD	chr14:97126470-97126782	K562	blood:	n/a	n/a
15	CTCF	chr14:97109374-97109423	Kidney_OC	kidney:	n/a	n/a
16	E2F4	chr14:97108022-97108207	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr14:97101062-97101293	MCF10A-Er-Src	breast:	n/a	chr14:97101160-97101169
18	EBF1	chr14:97116241-97116544	GM12878	blood:	n/a	n/a
19	EP300	chr14:97127031-97127125	GM12878	blood:	n/a	chr14:97127115-97127124
20	EP300	chr14:97126447-97126858	K562	blood:	n/a	chr14:97126808-97126822
21	FOS	chr14:97098452-97098557	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr14:97098453-97098628	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr14:97098453-97098517	MCF10A-Er-Src	breast:	n/a	n/a
24	FOXA1	chr14:97127156-97127451	T-47D	breast:	n/a	n/a
25	FOXA1	chr14:97127126-97127384	T-47D	breast:	n/a	n/a
26	GABPA	chr14:97093845-97094041	Hela-S3	cervix:	n/a	n/a
27	GABPA	chr14:97093844-97094016	Hela-S3	cervix:	n/a	n/a
28	GABPA	chr14:97102189-97102461	K562	blood:	n/a	n/a
29	GATA1	chr14:97126117-97127106	PBDE	blood:	n/a	chr14:97126652-97126661
30	GATA1	chr14:97125943-97127088	K562	blood:	n/a	chr14:97126652-97126661
31	GATA2	chr14:97126462-97126749	SH-SY5Y	brain:	n/a	chr14:97126652-97126661
32	GATA2	chr14:97098757-97099067	SH-SY5Y	brain:	n/a	chr14:97098853-97098863 chr14:97098854-97098861 chr14:97098854-97098863
33	GATA2	chr14:97126406-97126805	K562	blood:	n/a	chr14:97126652-97126661
34	JUND	chr14:97098324-97098676	K562	blood:	n/a	n/a
35	JUND	chr14:97102260-97102364	HepG2	liver:	n/a	chr14:97102348-97102359
36	JUND	chr14:97102256-97102416	K562	blood:	n/a	chr14:97102348-97102359
37	JUND	chr14:97126490-97126825	K562	blood:	n/a	n/a
38	MAFF	chr14:97126044-97126244	HepG2	liver:	n/a	chr14:97126112-97126130
39	MAFF	chr14:97093484-97093715	K562	blood:	n/a	n/a
40	MAFF	chr14:97126105-97126150	K562	blood:	n/a	chr14:97126112-97126130
41	MAFK	chr14:97118784-97118787	HepG2	liver:	n/a	n/a
42	MAFK	chr14:97101134-97101354	HepG2	liver:	n/a	n/a
43	MAFK	chr14:97093474-97093679	K562	blood:	n/a	n/a
44	MAFK	chr14:97126006-97126208	HepG2	liver:	n/a	chr14:97126115-97126126 chr14:97126091-97126105 chr14:97126115-97126126 chr14:97126088-97126104 chr14:97126113-97126127
45	MAFK	chr14:97101150-97101275	HepG2	liver:	n/a	n/a
46	MAX	chr14:97115130-97115314	NB4	blood:	n/a	chr14:97115264-97115274
47	MAZ	chr14:97093017-97093351	K562	blood:	n/a	n/a
48	MAZ	chr14:97102391-97102425	K562	blood:	n/a	n/a
49	MYC	chr14:97114986-97115110	H1-hESC	embryonic stem cell:	n/a	n/a
50	MYC	chr14:97126464-97126741	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:97127338-97127388	HPAEpiC	pulmonary alveolar:	n/a
2	chr14:97127338-97127388	HUVEC	blood vessel:	n/a
3	chr14:97127338-97127388	HepG2	liver:	n/a
4	chr14:97127338-97127388	MCF-7	breast:	n/a
5	chr14:97127338-97127388	HCM	heart:	n/a
6	chr14:97127338-97127388	HIPEpiC	eye:	n/a
7	chr14:97127338-97127388	RPTEC	kidney:	n/a
8	chr14:97127338-97127388	ECC-1	luminal epithelium:	n/a
9	chr14:97127338-97127388	AG10803	skin:	n/a
10	chr14:97127338-97127388	HEEpiC	esophagus:	n/a
11	chr14:97127338-97127388	HRPEpiC	eye:	n/a
12	chr14:97127338-97127388	HRCEpiC	kidney:	n/a
13	chr14:97127338-97127388	HL-60	blood:	n/a
14	chr14:97127338-97127388	AG04450	lung:	fetal
15	chr14:97127338-97127388	LNCaP	prostate:	n/a
16	chr14:97127338-97127388	Hepatocyte	liver:	n/a
17	chr14:97127338-97127388	MCF10A-Er-Src	breast:	n/a
18	chr14:97127338-97127388	BJ	skin:	n/a
19	chr14:97127338-97127388	HEK293	kidney:	embryo
20	chr14:97127338-97127388	T-47D	breast:	n/a
21	chr14:97127338-97127388	BE2_C	brain:	n/a
22	chr14:97127338-97127388	AG04449	skin:	fetal
23	chr14:97127338-97127388	SK-N-SH	brain:	n/a
24	chr14:97127338-97127388	AG09309	skin:	n/a
25	chr14:97127338-97127388	HCF	heart:	n/a
26	chr14:97127338-97127388	PrEC	prostate:	n/a
27	chr14:97127338-97127388	HMEC	breast:	n/a
28	chr14:97127338-97127388	H1-hESC	embryonic stem cell:	embryo
29	chr14:97127338-97127388	NHDF-neo	bronchial:	n/a
30	chr14:97127338-97127388	GM06990	blood:	n/a
31	chr14:97127338-97127388	HAEpiC	amniotic membrane:	n/a
32	chr14:97127338-97127388	SKMC	muscle:	n/a
33	chr14:97127338-97127388	CMK	blood:	n/a
34	chr14:97127338-97127388	GM12892	blood:	n/a
35	chr14:97127338-97127388	IMR90	lung:	fetal
36	chr14:97127338-97127388	NB4	blood:	n/a
37	chr14:97127338-97127388	HRE	kidney:	n/a
38	chr14:97127338-97127388	GM12891	blood:	n/a
39	chr14:97127338-97127388	Jurkat	blood:	n/a
40	chr14:97127338-97127388	ProgFib	skin:	n/a
41	chr14:97127338-97127388	U87	brain:	n/a
42	chr14:97127338-97127388	SK-N-MC	brain:	n/a
43	chr14:97127338-97127388	HCT-116	colon:	n/a
44	chr14:97127338-97127388	AG09319	gingival:	n/a
45	chr14:97127338-97127388	PFSK-1	brain:	n/a
46	chr14:97127338-97127388	ovcar-3	ovarian:	n/a
47	chr14:97127338-97127388	AoSMC	blood vessel:	n/a
48	chr14:97127338-97127388	NH-A	brain:	n/a
49	chr14:97127338-97127388	GM19239	blood:	n/a
50	chr14:97127338-97127388	HCPEpiC	choroid plexus:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:97093078..97095980-chr14:97096287..97099015,3	MCF-7	breast:
2	chr14:97098302..97100960-chr14:97102875..97104630,2	K562	blood:
3	chr14:97085374..97088173-chr14:97091908..97094865,2	K562	blood:
4	chr14:97125727..97128111-chr14:97129743..97131813,3	K562	blood:
5	chr14:97100553..97101432-chr14:97126836..97127804,5	MCF-7	breast:
6	chr14:97125727..97127557-chr14:97130189..97131813,2	K562	blood:
7	chr14:97093078..97095980-chr14:97096287..97099015,3	MCF-7	breast:
8	chr14:97040398..97040962-chr14:97100553..97101449,2	MCF-7	breast:
9	chr14:97121918..97124905-chr14:97127753..97129733,2	K562	blood:
10	chr14:97040333..97042090-chr14:97100526..97101489,19	MCF-7	breast:
11	chr14:97096962..97100936-chr14:97101885..97104048,3	K562	blood:
12	chr14:97047039..97047841-chr14:97100546..97101485,3	MCF-7	breast:
13	chr14:97100866..97101454-chr14:97138053..97138598,2	MCF-7	breast:
14	chr14:97047308..97047841-chr14:97100928..97101485,2	MCF-7	breast:
15	chr14:97096962..97100936-chr14:97101885..97104048,3	K562	blood:
16	chr14:97091981..97093780-chr14:97101556..97103907,3	MCF-7	breast:
17	chr14:93483695..93484309-chr14:97100592..97101400,2	MCF-7	breast:
18	chr14:97040936..97041835-chr14:97100556..97101428,4	MCF-7	breast:
19	chr14:97084192..97086627-chr14:97090861..97093279,2	MCF-7	breast:
20	chr14:97091981..97093780-chr14:97101556..97103907,3	MCF-7	breast:
21	chr14:97105478..97107756-chr14:97114890..97116903,2	MCF-7	breast:
22	chr14:97105478..97107756-chr14:97114890..97116903,2	MCF-7	breast:
23	chr14:97100553..97101432-chr14:97126836..97127804,5	MCF-7	breast:
24	chr14:97098302..97100960-chr14:97102875..97104630,2	K562	blood:
25	chr14:97041013..97042090-chr14:97100546..97101489,8	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

Extended variants
information (count: 1444 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1444 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs234584	chr14:97092803-97092804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs147003678	chr14:97092809-97092810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138141983	chr14:97092856-97092857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534059868	chr14:97092862-97092863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552721859	chr14:97092875-97092876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34048492	chr14:97092880-97092881	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs552014829	chr14:97092887-97092888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191203726	chr14:97092917-97092918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556846694	chr14:97092935-97092936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143616391	chr14:97092959-97092960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs367759588	chr14:97092996-97092997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs113876277	chr14:97093015-97093016	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs553823621	chr14:97093040-97093041	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs527961389	chr14:97093041-97093042	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs545622772	chr14:97093098-97093099	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
16	rs17214379	chr14:97093113-97093114	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs368110022	chr14:97093151-97093152	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
18	rs576112248	chr14:97093169-97093170	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs183753192	chr14:97093170-97093171	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
20	rs145397164	chr14:97093177-97093178	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs370750248	chr14:97093178-97093179	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs369489595	chr14:97093255-97093256	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs372765115	chr14:97093291-97093292	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs188215993	chr14:97093302-97093303	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
25	rs529173179	chr14:97093342-97093343	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs192386732	chr14:97093358-97093359	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs150863151	chr14:97093421-97093422	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
28	rs527775570	chr14:97093439-97093440	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
29	rs552437014	chr14:97093473-97093474	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
30	rs527992561	chr14:97093505-97093506	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
31	rs570927887	chr14:97093518-97093519	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
32	rs185570525	chr14:97093526-97093527	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
33	rs550409999	chr14:97093542-97093543	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
34	rs541333702	chr14:97093545-97093546	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
35	rs531782381	chr14:97093568-97093569	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
36	rs550000429	chr14:97093594-97093595	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
37	rs79173552	chr14:97093636-97093637	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs4905510	chr14:97093659-97093660	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs138221190	chr14:97093666-97093667	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs11847868	chr14:97093680-97093681	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs149578448	chr14:97093692-97093693	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs17094229	chr14:97093700-97093701	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs79746329	chr14:97093731-97093732	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs555172018	chr14:97093735-97093736	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs573581677	chr14:97093739-97093740	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs144244012	chr14:97093752-97093753	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs71873019	chr14:97093773-97093774	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs77979618	chr14:97093797-97093798	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs75012727	chr14:97093815-97093816	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs531600278	chr14:97093834-97093835	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	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:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97084000-97096200	Weak transcription	Right Atrium	heart
2	chr14:97090000-97094600	Enhancers	Fetal Brain Male	brain
3	chr14:97090200-97093200	Weak transcription	Spleen	Spleen
4	chr14:97090400-97093000	Enhancers	Fetal Brain Female	brain
5	chr14:97091400-97093000	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr14:97092000-97095800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:97092400-97094400	Enhancers	Brain Germinal Matrix	brain
8	chr14:97092800-97093000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr14:97093000-97093200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
10	chr14:97093000-97093200	Enhancers	GM12878-XiMat	blood
11	chr14:97093000-97093200	Bivalent/Poised TSS	K562	blood
12	chr14:97093000-97093600	Flanking Bivalent TSS/Enh	NHEK	skin
13	chr14:97093000-97094000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr14:97093000-97094400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr14:97093200-97093400	Enhancers	Spleen	Spleen
16	chr14:97093200-97093600	Flanking Active TSS	GM12878-XiMat	blood
17	chr14:97093200-97093600	Flanking Bivalent TSS/Enh	K562	blood
18	chr14:97093200-97093800	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr14:97093400-97094200	Weak transcription	Spleen	Spleen
20	chr14:97093600-97093800	Bivalent/Poised TSS	K562	blood
21	chr14:97093600-97094000	Active TSS	GM12878-XiMat	blood
22	chr14:97094000-97094600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr14:97094200-97095000	Enhancers	Spleen	Spleen
24	chr14:97095800-97097000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr14:97096200-97096600	ZNF genes & repeats	Right Atrium	heart
26	chr14:97097000-97098000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr14:97098000-97098400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr14:97098400-97100600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr14:97100600-97101400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr14:97101200-97101600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr14:97101400-97115000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:97101600-97106000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr14:97102400-97102600	Enhancers	Spleen	Spleen
34	chr14:97102600-97103800	Weak transcription	Spleen	Spleen
35	chr14:97103800-97104200	Active TSS	Spleen	Spleen
36	chr14:97106000-97106400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr14:97115000-97115200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr14:97115200-97116400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr14:97116400-97129600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr14:97120000-97120600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr14:97124800-97125400	Enhancers	Duodenum Mucosa	Duodenum
42	chr14:97124800-97129600	Enhancers	Fetal Intestine Large	intestine
43	chr14:97124800-97129800	Enhancers	Fetal Intestine Small	intestine
44	chr14:97125000-97125800	Enhancers	NHEK	skin
45	chr14:97125200-97125400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr14:97125200-97125400	Enhancers	Stomach Mucosa	stomach
47	chr14:97125200-97125600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr14:97125200-97127200	Enhancers	K562	blood
49	chr14:97125400-97125600	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr14:97125400-97125600	Enhancers	Pancreas	Pancrea

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