Variant report

Variant	esv1793036
Chromosome Location	chr14:96983291-97023059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:176)
CpG islands
(count:61)
Chromatin interactive
region (count:41)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:176 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:96996751-96996882	HepG2	liver:	n/a	chr14:96996779-96996790
2	CTCF	chr14:97012982-97013004	Kidney_OC	kidney:	n/a	n/a
3	EBF1	chr14:97020793-97021020	GM12878	blood:	n/a	n/a
4	EBF1	chr14:96984054-96984080	GM12878	blood:	n/a	n/a
5	EBF1	chr14:96986461-96986474	GM12878	blood:	n/a	n/a
6	EBF1	chr14:96983978-96984298	GM12878	blood:	n/a	n/a
7	EP300	chr14:97017942-97017944	K562	blood:	n/a	n/a
8	EP300	chr14:96991843-96992071	SK-N-SH_RA	brain:	n/a	n/a
9	FOS	chr14:96991876-96991967	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr14:97004819-97005331	MCF10A-Er-Src	breast:	n/a	chr14:97005181-97005190 chr14:97005177-97005188
11	FOS	chr14:97005077-97005278	MCF10A-Er-Src	breast:	n/a	chr14:97005181-97005190 chr14:97005177-97005188
12	FOS	chr14:97005023-97005333	MCF10A-Er-Src	breast:	n/a	chr14:97005181-97005190 chr14:97005177-97005188
13	FOS	chr14:97020819-97020838	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr14:97005018-97005332	MCF10A-Er-Src	breast:	n/a	chr14:97005181-97005190 chr14:97005177-97005188
15	FOSL2	chr14:97004923-97005405	SK-N-SH	brain:	n/a	chr14:97005181-97005190 chr14:97005177-97005188
16	FOSL2	chr14:97004837-97005484	A549	lung:	n/a	chr14:97005181-97005190 chr14:97005177-97005188
17	FOSL2	chr14:97004999-97005343	A549	lung:	n/a	chr14:97005181-97005190 chr14:97005177-97005188
18	FOXA1	chr14:97005180-97005803	HepG2	liver:	n/a	n/a
19	GATA3	chr14:97006006-97006208	SH-SY5Y	brain:	n/a	n/a
20	GATA3	chr14:96999165-96999231	SH-SY5Y	brain:	n/a	n/a
21	GATA3	chr14:97007935-97008021	MCF-7	breast:	n/a	n/a
22	IRF1	chr14:97011795-97011883	K562	blood:	n/a	n/a
23	IRF1	chr14:97010705-97010799	K562	blood:	n/a	n/a
24	IRF1	chr14:96996555-96996574	K562	blood:	n/a	n/a
25	JUND	chr14:96991755-96992317	SK-N-SH	brain:	n/a	n/a
26	MAFF	chr14:97003179-97003528	HepG2	liver:	n/a	chr14:97003330-97003348
27	MAFF	chr14:97003206-97003510	K562	blood:	n/a	chr14:97003330-97003348
28	MAFK	chr14:97003162-97003527	HepG2	liver:	n/a	chr14:97003332-97003347
29	MAFK	chr14:97003169-97003514	IMR90	lung:	n/a	chr14:97003332-97003347
30	MAFK	chr14:97003182-97003524	Hela-S3	cervix:	n/a	chr14:97003332-97003347
31	MAFK	chr14:97003199-97003480	K562	blood:	n/a	chr14:97003332-97003347
32	MAFK	chr14:97003179-97003526	HepG2	liver:	n/a	chr14:97003332-97003347
33	MAZ	chr14:97016756-97016769	GM12878	blood:	n/a	n/a
34	MXI1	chr14:97005229-97005266	H1-hESC	embryonic stem cell:	n/a	n/a
35	MYC	chr14:96990175-96990251	H1-hESC	embryonic stem cell:	n/a	n/a
36	MYC	chr14:96990915-96990925	MCF-7	breast:	n/a	n/a
37	NRF1	chr14:97000701-97000709	H1-hESC	embryonic stem cell:	n/a	n/a
38	PBX3	chr14:97004974-97005449	SK-N-SH	brain:	n/a	n/a
39	PBX3	chr14:97005024-97005342	SK-N-SH	brain:	n/a	n/a
40	PBX3	chr14:96991746-96992090	SK-N-SH	brain:	n/a	n/a
41	POLR2A	chr14:96993362-96994216	HepG2	liver:	n/a	n/a
42	POLR2A	chr14:97019710-97019824	MCF-7	breast:	n/a	n/a
43	POLR2A	chr14:97004239-97004273	MCF-7	breast:	n/a	n/a
44	POLR2A	chr14:97002124-97002518	GM12878	blood:	n/a	n/a
45	POLR2A	chr14:97003443-97004478	HepG2	liver:	n/a	n/a
46	POLR2A	chr14:97010327-97010351	MCF-7	breast:	n/a	n/a
47	POLR2A	chr14:97005065-97005316	GM12878	blood:	n/a	n/a
48	POLR2A	chr14:96992699-96992827	Gliobla	brain:	n/a	n/a
49	POLR2A	chr14:97000683-97000979	GM12892	blood:	n/a	n/a
50	POLR2A	chr14:97010881-97011184	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:97019527-97019577	Caco-2	colon:	n/a
2	chr14:97019527-97019577	GM12891	blood:	n/a
3	chr14:97019527-97019577	PFSK-1	brain:	n/a
4	chr14:97019527-97019577	ProgFib	skin:	n/a
5	chr14:97019527-97019577	HCT-116	colon:	n/a
6	chr14:97019527-97019577	H1-hESC	embryonic stem cell:	embryo
7	chr14:97019527-97019577	HIPEpiC	eye:	n/a
8	chr14:97019527-97019577	GM19239	blood:	n/a
9	chr14:97019527-97019577	PrEC	prostate:	n/a
10	chr14:97019527-97019577	ovcar-3	ovarian:	n/a
11	chr14:97019527-97019577	SKMC	muscle:	n/a
12	chr14:97019527-97019577	NT2-D1	testis:	n/a
13	chr14:97019527-97019577	HCPEpiC	choroid plexus:	n/a
14	chr14:97019527-97019577	K562	blood:	n/a
15	chr14:97019527-97019577	NHBE	bronchial:	n/a
16	chr14:97019527-97019577	HEEpiC	esophagus:	n/a
17	chr14:97019527-97019577	HNPCEpiC	eye:	n/a
18	chr14:97019527-97019577	HMEC	breast:	n/a
19	chr14:97019527-97019577	SK-N-SH	brain:	n/a
20	chr14:97019527-97019577	HEK293	kidney:	embryo
21	chr14:97019527-97019577	AG10803	skin:	n/a
22	chr14:97019527-97019577	HAEpiC	amniotic membrane:	n/a
23	chr14:97019527-97019577	HRPEpiC	eye:	n/a
24	chr14:97019527-97019577	HCM	heart:	n/a
25	chr14:97019527-97019577	AoSMC	blood vessel:	n/a
26	chr14:97019527-97019577	NH-A	brain:	n/a
27	chr14:97019527-97019577	CMK	blood:	n/a
28	chr14:97019527-97019577	Hela-S3	cervix:	n/a
29	chr14:97019527-97019577	SK-N-SH_RA	brain:	n/a
30	chr14:97019527-97019577	BE2_C	brain:	n/a
31	chr14:97019527-97019577	LNCaP	prostate:	n/a
32	chr14:97019527-97019577	Hepatocyte	liver:	n/a
33	chr14:97019527-97019577	AG04449	skin:	fetal
34	chr14:97019527-97019577	RPTEC	kidney:	n/a
35	chr14:97019527-97019577	MCF10A-Er-Src	breast:	n/a
36	chr14:97019527-97019577	MCF-7	breast:	n/a
37	chr14:97019527-97019577	NB4	blood:	n/a
38	chr14:97019527-97019577	AG09309	skin:	n/a
39	chr14:97019527-97019577	GM12878	blood:	n/a
40	chr14:97019527-97019577	T-47D	breast:	n/a
41	chr14:97019527-97019577	ECC-1	luminal epithelium:	n/a
42	chr14:97019527-97019577	A549	lung:	n/a
43	chr14:97019527-97019577	AG09319	gingival:	n/a
44	chr14:97019527-97019577	BJ	skin:	n/a
45	chr14:97019527-97019577	HUVEC	blood vessel:	n/a
46	chr14:97019527-97019577	HepG2	liver:	n/a
47	chr14:97019527-97019577	SAEC	small airway:	n/a
48	chr14:97019527-97019577	AG04450	lung:	fetal
49	chr14:97019527-97019577	HCF	heart:	n/a
50	chr14:97019527-97019577	HPAEpiC	pulmonary alveolar:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:96985630..96987652-chr14:97013134..97015914,2	MCF-7	breast:
2	chr14:96984347..96986683-chr14:97013576..97015718,2	K562	blood:
3	chr14:96968318..96970026-chr14:96990174..96992851,2	K562	blood:
4	chr14:96989700..96992252-chr14:96995292..96996938,2	MCF-7	breast:
5	chr14:96973732..96976070-chr14:96984297..96985956,2	K562	blood:
6	chr14:96968041..96970064-chr14:96987625..96989616,3	MCF-7	breast:
7	chr14:96998656..97003736-chr14:97006318..97010679,5	MCF-7	breast:
8	chr14:96999522..97003460-chr14:97003745..97007468,4	K562	blood:
9	chr14:96966203..96970615-chr14:96984362..96986675,5	MCF-7	breast:
10	chr14:96997411..96999330-chr14:97015854..97017598,2	MCF-7	breast:
11	chr14:96991877..96993555-chr14:97010853..97012624,2	MCF-7	breast:
12	chr14:96967059..96970873-chr14:97003621..97006595,4	K562	blood:
13	chr14:96965294..96968379-chr14:96992362..96994561,3	MCF-7	breast:
14	chr14:96992168..96995386-chr14:96999762..97002036,3	MCF-7	breast:
15	chr14:96992168..96995386-chr14:96999762..97002036,3	MCF-7	breast:
16	chr14:96968706..96970870-chr14:96989041..96991198,2	MCF-7	breast:
17	chr14:96967041..96969469-chr14:97004339..97006247,2	MCF-7	breast:
18	chr14:97010400..97013410-chr14:97024824..97026785,3	K562	blood:
19	chr14:96997411..96999330-chr14:97015854..97017598,2	MCF-7	breast:
20	chr14:96989613..96991388-chr14:96992755..96994484,2	K562	blood:
21	chr14:96968572..96970585-chr14:96987828..96990250,2	K562	blood:
22	chr14:96985630..96987652-chr14:97013134..97015914,2	MCF-7	breast:
23	chr14:96967004..96969133-chr14:97009562..97011863,2	MCF-7	breast:
24	chr14:96967059..96968706-chr14:97003755..97006595,2	K562	blood:
25	chr14:96998941..97001776-chr14:97003511..97005211,2	MCF-7	breast:
26	chr14:96947839..96950152-chr14:96988315..96991118,2	K562	blood:
27	chr14:96998656..97003736-chr14:97006318..97010679,5	MCF-7	breast:
28	chr14:97007480..97011210-chr14:97011511..97014615,3	K562	blood:
29	chr14:96977217..96979586-chr14:96982926..96984761,2	MCF-7	breast:
30	chr14:96967956..96970809-chr14:96981741..96983595,3	MCF-7	breast:
31	chr14:96968950..96970471-chr14:97010412..97012390,2	MCF-7	breast:
32	chr14:96980357..96982346-chr14:96989639..96991890,2	MCF-7	breast:
33	chr14:96988073..96990786-chr14:96992864..96995262,2	MCF-7	breast:
34	chr14:96989700..96992252-chr14:96995292..96996938,2	MCF-7	breast:
35	chr14:97006749..97008466-chr14:97026369..97029131,2	MCF-7	breast:
36	chr14:97011141..97013270-chr14:97015044..97017205,2	K562	blood:
37	chr14:97011141..97013270-chr14:97015044..97017205,2	K562	blood:
38	chr14:97018033..97019612-chr14:97020291..97022357,2	K562	blood:
39	chr14:97007480..97011210-chr14:97011511..97014615,3	K562	blood:
40	chr14:96967194..96972735-chr14:96975570..96985371,13	K562	blood:
41	chr14:97018033..97019612-chr14:97020291..97022357,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAPOLA-2	chr14:96999722-97000248	ucscGeneNc_uc001yfu_2
2	lnc-PAPOLA-2	chr14:96997894-96998422	ucscGeneNc_uc001yfu_2
3	lnc-PAPOLA-2	chr14:96994960-96995017	ucscGeneNc_uc001yfu_2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PAPOLA	hsa-miR-155-5p	chr14:96998551-96998571

Variant related genes	Relation type
PAPOLA	TF binding region
PAPOLA	CpG island
ENSG00000260806	chromatin interactions
ENSG00000090060	chromatin interactions
ENSG00000140057	chromatin interactions

Extended variants
information (count: 1468 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28718054	chr14:96983291-96983292	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534963292	chr14:96983354-96983355	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs553290635	chr14:96983404-96983405	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs147017147	chr14:96983463-96983464	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs538283960	chr14:96983480-96983481	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs185520992	chr14:96983493-96983494	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138190914	chr14:96983505-96983506	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs190431107	chr14:96983568-96983569	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs560878811	chr14:96983578-96983579	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs143678062	chr14:96983581-96983582	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs36034232	chr14:96983637-96983638	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs538078174	chr14:96983650-96983651	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs540531560	chr14:96983655-96983656	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs565205740	chr14:96983674-96983675	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs150563611	chr14:96983700-96983701	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs117381787	chr14:96983711-96983712	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs76592159	chr14:96983721-96983722	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs28600893	chr14:96983765-96983766	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs549462547	chr14:96983781-96983782	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs117914283	chr14:96983797-96983798	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs535265493	chr14:96983831-96983832	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs546876153	chr14:96983894-96983895	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs563558381	chr14:96983901-96983902	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs149592846	chr14:96983905-96983906	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs553899481	chr14:96983907-96983908	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs556493236	chr14:96984003-96984004	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs375760047	chr14:96984036-96984037	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs577376011	chr14:96984104-96984105	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs180829048	chr14:96984118-96984119	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs539924981	chr14:96984143-96984144	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs572929966	chr14:96984144-96984145	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs186225801	chr14:96984234-96984235	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs565091454	chr14:96984285-96984286	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs191901416	chr14:96984321-96984322	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs183945380	chr14:96984328-96984329	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs544519775	chr14:96984341-96984342	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs563491472	chr14:96984382-96984383	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs577990640	chr14:96984415-96984416	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs76434381	chr14:96984427-96984428	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs549204388	chr14:96984428-96984429	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs561469078	chr14:96984481-96984482	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs187828590	chr14:96984582-96984583	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs546765751	chr14:96984652-96984653	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs571512277	chr14:96984653-96984654	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs538906599	chr14:96984697-96984698	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs550902583	chr14:96984704-96984705	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs555142641	chr14:96984727-96984728	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs74086703	chr14:96984739-96984740	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs370195512	chr14:96984752-96984753	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs397966631	chr14:96984763-96984764	Enhancers Weak transcription	Chromatin interactive region	2 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	18451855	CNVD

Chromatin state (count:1106 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:96970000-96984600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr14:96970000-96987000	Enhancers	Primary B cells from peripheral blood	blood
3	chr14:96970600-96984400	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr14:96970600-96987800	Weak transcription	Fetal Stomach	stomach
5	chr14:96970600-96990600	Weak transcription	NH-A	brain
6	chr14:96970600-96991200	Weak transcription	Fetal Kidney	kidney
7	chr14:96970800-96987400	Weak transcription	HSMM	muscle
8	chr14:96970800-96988400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr14:96971200-96987400	Weak transcription	Osteobl	bone
10	chr14:96971600-96989800	Weak transcription	NHLF	lung
11	chr14:96971800-96990800	Weak transcription	HMEC	breast
12	chr14:96971800-96991000	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr14:96972000-96984800	Enhancers	Primary T cells from cord blood	blood
14	chr14:96972200-96984200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr14:96972200-96986400	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr14:96972200-96986600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr14:96972200-96987800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:96972200-96988200	Weak transcription	Colonic Mucosa	Colon
19	chr14:96972400-96986200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr14:96972400-96986600	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr14:96972400-96987800	Weak transcription	Esophagus	oesophagus
22	chr14:96972400-96987800	Weak transcription	Spleen	Spleen
23	chr14:96973400-96986600	Weak transcription	Fetal Thymus	thymus
24	chr14:96974000-96984800	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr14:96974400-96985000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr14:96974600-96987800	Weak transcription	Gastric	stomach
27	chr14:96974600-96987800	Weak transcription	Lung	lung
28	chr14:96975000-96992400	Weak transcription	K562	blood
29	chr14:96975400-96989200	Weak transcription	Hela-S3	cervix
30	chr14:96975600-96985400	Weak transcription	Fetal Muscle Trunk	muscle
31	chr14:96975600-96986400	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr14:96975600-96987800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr14:96975600-96992200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr14:96976000-96987200	Weak transcription	NHDF-Ad	bronchial
35	chr14:96976200-96988000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr14:96976200-96992400	Weak transcription	NHEK	skin
37	chr14:96977000-96992600	Weak transcription	Fetal Brain Male	brain
38	chr14:96977200-96985400	Weak transcription	Right Atrium	heart
39	chr14:96977600-96987800	Weak transcription	Dnd41	blood
40	chr14:96977600-96988000	Weak transcription	Stomach Smooth Muscle	stomach
41	chr14:96977800-96986400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr14:96978000-97019400	Weak transcription	Aorta	Aorta
43	chr14:96978800-96984600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr14:96979200-96985800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr14:96979200-96986800	Enhancers	Primary B cells from cord blood	blood
46	chr14:96979400-96987800	Weak transcription	Brain Germinal Matrix	brain
47	chr14:96979400-96988000	Weak transcription	Brain Cingulate Gyrus	brain
48	chr14:96979400-96988800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr14:96979600-96983600	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr14:96979600-96983600	Enhancers	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links