Variant report

Variant	esv1792551
Chromosome Location	chr5:14180257-14202590
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:491)
CpG islands
(count:305)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:14190403-14190408	K562	blood:	n/a	n/a
2	BACH1	chr5:14196944-14197064	H1-hESC	embryonic stem cell:	n/a	chr5:14196970-14196984
3	BCL3	chr5:14190352-14190717	GM12878	blood:	n/a	n/a
4	BHLHE40	chr5:14187102-14187180	GM12878	blood:	n/a	n/a
5	BRCA1	chr5:14185657-14186572	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr5:14190249-14190968	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr5:14185419-14186799	HCT-116	colon:	n/a	n/a
8	CEBPB	chr5:14190224-14190894	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr5:14190196-14190817	IMR90	lung:	n/a	n/a
10	CEBPB	chr5:14190251-14190728	A549	lung:	n/a	n/a
11	CEBPB	chr5:14187933-14188119	A549	lung:	n/a	n/a
12	CEBPB	chr5:14191569-14191621	A549	lung:	n/a	n/a
13	CEBPB	chr5:14185761-14186244	A549	lung:	n/a	n/a
14	CEBPB	chr5:14185669-14186310	A549	lung:	n/a	n/a
15	CEBPB	chr5:14185834-14186176	IMR90	lung:	n/a	n/a
16	CEBPB	chr5:14190115-14190982	A549	lung:	n/a	n/a
17	CEBPB	chr5:14185694-14186545	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr5:14185799-14186176	A549	lung:	n/a	n/a
19	CHD2	chr5:14190390-14190843	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr5:14185606-14186595	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr5:14183039-14183205	HepG2	liver:	n/a	n/a
22	CREB1	chr5:14190501-14190832	A549	lung:	n/a	n/a
23	CTCF	chr5:14190380-14190530	AG04450	lung:	n/a	n/a
24	CTCF	chr5:14190280-14190430	AG04449	skin:	n/a	n/a
25	CTCF	chr5:14184340-14184490	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr5:14184280-14184430	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr5:14183019-14183069	H1-hESC	embryonic stem cell:	n/a	chr5:14183039-14183052
28	CTCF	chr5:14182920-14183070	HMEC	breast:	n/a	chr5:14183039-14183052
29	CTCF	chr5:14182880-14183030	HMEC	breast:	n/a	n/a
30	CTCF	chr5:14182960-14183110	NHEK	skin:	n/a	chr5:14183039-14183052
31	CTCF	chr5:14183008-14183100	NHEK	skin:	n/a	chr5:14183039-14183052
32	CTCF	chr5:14183020-14183170	SAEC	small airway:	n/a	chr5:14183039-14183052
33	CTCF	chr5:14199720-14199870	HPF	lung:	n/a	n/a
34	E2F4	chr5:14190217-14190812	MCF10A-Er-Src	breast:	n/a	n/a
35	EBF1	chr5:14183222-14183504	GM12878	blood:	n/a	chr5:14183382-14183393
36	ELK1	chr5:14185655-14186090	Hela-S3	cervix:	n/a	n/a
37	ELK1	chr5:14187187-14187204	GM12878	blood:	n/a	n/a
38	EP300	chr5:14193612-14194030	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr5:14181399-14181721	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr5:14190479-14190898	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr5:14181708-14181911	H1-hESC	embryonic stem cell:	n/a	chr5:14181888-14181902
42	EP300	chr5:14190128-14191100	SK-N-SH	brain:	n/a	chr5:14190887-14190901 chr5:14190465-14190479
43	EP300	chr5:14185672-14185981	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr5:14181448-14181708	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr5:14193670-14194025	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr5:14185691-14186032	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr5:14195763-14196088	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr5:14190108-14191109	A549	lung:	n/a	chr5:14190887-14190901 chr5:14190465-14190479
49	EP300	chr5:14190130-14190946	A549	lung:	n/a	chr5:14190887-14190901 chr5:14190465-14190479
50	EP300	chr5:14185527-14186776	SK-N-SH	brain:	n/a	chr5:14186520-14186534 chr5:14186423-14186432

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:14195757-14195807	HRPEpiC	eye:	n/a
2	chr5:14188039-14188089	AG04450	lung:	fetal
3	chr5:14195757-14195807	AoSMC	blood vessel:	n/a
4	chr5:14194251-14194301	GM06990	blood:	n/a
5	chr5:14192303-14192353	U87	brain:	n/a
6	chr5:14195757-14195807	GM12878	blood:	n/a
7	chr5:14192303-14192353	LNCaP	prostate:	n/a
8	chr5:14194251-14194301	GM12892	blood:	n/a
9	chr5:14192303-14192353	NB4	blood:	n/a
10	chr5:14188039-14188089	NHDF-neo	bronchial:	n/a
11	chr5:14194251-14194301	SK-N-MC	brain:	n/a
12	chr5:14195757-14195807	Caco-2	colon:	n/a
13	chr5:14192303-14192353	HRCEpiC	kidney:	n/a
14	chr5:14195757-14195807	Jurkat	blood:	n/a
15	chr5:14188039-14188089	GM12878	blood:	n/a
16	chr5:14194251-14194301	HAEpiC	amniotic membrane:	n/a
17	chr5:14188039-14188089	HCF	heart:	n/a
18	chr5:14183868-14183918	BE2_C	brain:	n/a
19	chr5:14194251-14194301	HCPEpiC	choroid plexus:	n/a
20	chr5:14183868-14183918	HCT-116	colon:	n/a
21	chr5:14194251-14194301	MCF-7	breast:	n/a
22	chr5:14194251-14194301	HMEC	breast:	n/a
23	chr5:14183868-14183918	AG04449	skin:	fetal
24	chr5:14183868-14183918	GM12892	blood:	n/a
25	chr5:14183868-14183918	GM12878	blood:	n/a
26	chr5:14195757-14195807	MCF-7	breast:	n/a
27	chr5:14188039-14188089	Jurkat	blood:	n/a
28	chr5:14188039-14188089	NHBE	bronchial:	n/a
29	chr5:14183868-14183918	SKMC	muscle:	n/a
30	chr5:14183868-14183918	RPTEC	kidney:	n/a
31	chr5:14188039-14188089	HEEpiC	esophagus:	n/a
32	chr5:14192303-14192353	A549	lung:	n/a
33	chr5:14194251-14194301	Hela-S3	cervix:	n/a
34	chr5:14188039-14188089	AoSMC	blood vessel:	n/a
35	chr5:14183868-14183918	NH-A	brain:	n/a
36	chr5:14195757-14195807	H1-hESC	embryonic stem cell:	embryo
37	chr5:14183868-14183918	CMK	blood:	n/a
38	chr5:14188039-14188089	LNCaP	prostate:	n/a
39	chr5:14188039-14188089	MCF10A-Er-Src	breast:	n/a
40	chr5:14194251-14194301	NHDF-neo	bronchial:	n/a
41	chr5:14183868-14183918	SK-N-SH	brain:	n/a
42	chr5:14194251-14194301	NH-A	brain:	n/a
43	chr5:14192303-14192353	SK-N-SH_RA	brain:	n/a
44	chr5:14194251-14194301	ProgFib	skin:	n/a
45	chr5:14183868-14183918	HRPEpiC	eye:	n/a
46	chr5:14192303-14192353	AoSMC	blood vessel:	n/a
47	chr5:14195757-14195807	AG04450	lung:	fetal
48	chr5:14195757-14195807	GM12891	blood:	n/a
49	chr5:14194251-14194301	MCF10A-Er-Src	breast:	n/a
50	chr5:14194251-14194301	HCT-116	colon:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:14193728..14196151-chr5:14263145..14265627,2	MCF-7	breast:
2	chr5:14188839..14190409-chr5:14192288..14195221,2	MCF-7	breast:
3	chr5:14142296..14145562-chr5:14179804..14183456,3	MCF-7	breast:
4	chr5:14201198..14203758-chr5:14208446..14210570,2	K562	blood:
5	chr5:14143107..14145345-chr5:14183034..14185852,4	MCF-7	breast:
6	chr5:14188839..14190409-chr5:14192288..14195221,2	MCF-7	breast:
7	chr5:14186990..14191289-chr5:14196188..14199111,4	MCF-7	breast:
8	chr5:14172374..14175679-chr5:14185951..14189494,3	MCF-7	breast:
9	chr5:14190934..14193452-chr5:14204987..14206665,2	K562	blood:
10	chr5:14142390..14144382-chr5:14192692..14194445,2	MCF-7	breast:
11	chr5:14190314..14192078-chr5:14242022..14244161,2	MCF-7	breast:
12	chr5:14147688..14150262-chr5:14179544..14182482,2	MCF-7	breast:
13	chr5:14142056..14144734-chr5:14202359..14205545,3	MCF-7	breast:
14	chr5:14186990..14191289-chr5:14196188..14199111,4	MCF-7	breast:
15	chr5:14156677..14158288-chr5:14179472..14181137,2	MCF-7	breast:
16	chr5:14179684..14181395-chr5:14181871..14184690,2	MCF-7	breast:
17	chr5:14143292..14145490-chr5:14185700..14188808,3	MCF-7	breast:
18	chr5:14166623..14168657-chr5:14184854..14187549,2	MCF-7	breast:
19	chr5:14176923..14179557-chr5:14181390..14183679,4	MCF-7	breast:
20	chr5:14190950..14193183-chr5:14195167..14198577,4	MCF-7	breast:
21	chr5:14179287..14181889-chr5:14185448..14187309,2	MCF-7	breast:
22	chr5:14190950..14193183-chr5:14195167..14198577,4	MCF-7	breast:
23	chr5:14184247..14187128-chr5:14363897..14366486,2	K562	blood:
24	chr5:14147282..14149095-chr5:14192990..14194827,2	MCF-7	breast:
25	chr5:14173022..14175208-chr5:14181474..14183850,2	MCF-7	breast:
26	chr5:14175254..14177607-chr5:14178876..14181098,2	MCF-7	breast:
27	chr5:14143338..14144978-chr5:14188286..14191627,3	MCF-7	breast:
28	chr5:14179287..14181889-chr5:14185448..14187309,2	MCF-7	breast:

No data

Variant related genes	Relation type
TRIO	TF binding region
TRIO	CpG island
ENSG00000038382	chromatin interactions

Extended variants
information (count: 917 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189389980	chr5:14180264-14180265	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs114318244	chr5:14180272-14180273	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs556013182	chr5:14180279-14180280	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs114938754	chr5:14180389-14180390	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs33028	chr5:14180433-14180434	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs552968721	chr5:14180523-14180524	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577720265	chr5:14180554-14180555	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs553950788	chr5:14180580-14180581	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs145808614	chr5:14180617-14180618	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs116265252	chr5:14180626-14180627	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs529499671	chr5:14180683-14180684	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs138390142	chr5:14180708-14180709	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs529294704	chr5:14180709-14180710	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs528346238	chr5:14180712-14180713	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs33027	chr5:14180743-14180744	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs534173663	chr5:14180780-14180781	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs369061502	chr5:14180809-14180810	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs192933269	chr5:14180816-14180817	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs73055570	chr5:14180828-14180829	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs569548874	chr5:14180861-14180862	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs373681709	chr5:14180869-14180870	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551452668	chr5:14180871-14180872	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs114274449	chr5:14180890-14180891	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs537632771	chr5:14180933-14180934	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs201462431	chr5:14180956-14180957	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs200051060	chr5:14180957-14180958	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs555654355	chr5:14180961-14180962	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs398083935	chr5:14180967-14180968	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558153731	chr5:14180974-14180975	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs566706306	chr5:14180992-14180993	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs567866858	chr5:14180996-14180997	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs539873823	chr5:14181024-14181025	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs368683883	chr5:14181034-14181035	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs534963513	chr5:14181053-14181054	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs553705087	chr5:14181073-14181074	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs577705638	chr5:14181086-14181087	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs538675345	chr5:14181158-14181159	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs540017653	chr5:14181167-14181168	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs557077262	chr5:14181176-14181177	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs575272019	chr5:14181181-14181182	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs542727903	chr5:14181193-14181194	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs367573266	chr5:14181194-14181195	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs572997758	chr5:14181196-14181197	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs35461923	chr5:14181198-14181199	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs397933097	chr5:14181207-14181208	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs200988297	chr5:14181208-14181209	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs201936754	chr5:14181209-14181210	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs200090837	chr5:14181281-14181282	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs201247714	chr5:14181282-14181283	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs140060058	chr5:14181285-14181286	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Intracranial aneurysm	16715129	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:1240 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14164600-14181600	Weak transcription	Esophagus	oesophagus
2	chr5:14169200-14180400	Enhancers	HepG2	liver
3	chr5:14174400-14183400	Weak transcription	Fetal Lung	lung
4	chr5:14174400-14184400	Weak transcription	Colonic Mucosa	Colon
5	chr5:14174600-14183000	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr5:14174800-14181400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr5:14174800-14181400	Weak transcription	Thymus	Thymus
8	chr5:14174800-14184000	Weak transcription	Fetal Kidney	kidney
9	chr5:14175000-14181400	Weak transcription	Primary B cells from peripheral blood	blood
10	chr5:14175000-14184000	Weak transcription	Stomach Mucosa	stomach
11	chr5:14175000-14191600	Weak transcription	Primary hematopoietic stem cells	blood
12	chr5:14175200-14186400	Weak transcription	Primary B cells from cord blood	blood
13	chr5:14175600-14181000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr5:14175800-14181800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr5:14176600-14182800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr5:14177000-14180600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr5:14177200-14189400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr5:14177400-14180800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:14177400-14181800	Enhancers	NHEK	skin
20	chr5:14177400-14191800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr5:14177800-14183000	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr5:14178000-14184400	Weak transcription	Brain Cingulate Gyrus	brain
23	chr5:14178400-14182000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr5:14178600-14183000	Weak transcription	Gastric	stomach
25	chr5:14178600-14183800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr5:14178600-14187000	Enhancers	Left Ventricle	heart
27	chr5:14178800-14180800	Weak transcription	Aorta	Aorta
28	chr5:14178800-14182400	Weak transcription	Brain Anterior Caudate	brain
29	chr5:14178800-14183000	Weak transcription	Brain Substantia Nigra	brain
30	chr5:14178800-14183400	Enhancers	NHDF-Ad	bronchial
31	chr5:14178800-14184000	Enhancers	NH-A	brain
32	chr5:14179000-14180400	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr5:14179000-14180800	Enhancers	Lung	lung
34	chr5:14179000-14181000	Enhancers	Placenta	Placenta
35	chr5:14179000-14181000	Weak transcription	HUVEC	blood vessel
36	chr5:14179000-14181600	Weak transcription	Colon Smooth Muscle	Colon
37	chr5:14179000-14183000	Weak transcription	Spleen	Spleen
38	chr5:14179000-14184800	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr5:14179200-14180400	Enhancers	HSMM	muscle
40	chr5:14179200-14180800	Weak transcription	HMEC	breast
41	chr5:14179200-14181400	Weak transcription	Brain Angular Gyrus	brain
42	chr5:14179200-14181400	Weak transcription	Brain Germinal Matrix	brain
43	chr5:14179200-14181400	Weak transcription	Fetal Heart	heart
44	chr5:14179200-14181400	Weak transcription	Right Ventricle	heart
45	chr5:14179200-14181400	Weak transcription	GM12878-XiMat	blood
46	chr5:14179200-14181600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:14179200-14181600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr5:14179200-14181600	Weak transcription	Psoas Muscle	Psoas
49	chr5:14179200-14181800	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr5:14179200-14182200	Enhancers	Muscle Satellite Cultured Cells	--

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