Variant report

Variant	nsv533129
Chromosome Location	chr14:56568535-56819234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2401)
CpG islands
(count:2380)
Chromatin interactive
region (count:115)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2401 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:56691703-56692006	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:56800461-56800677	K562	blood:	n/a	n/a
3	ARID3A	chr14:56806804-56807128	K562	blood:	n/a	n/a
4	ARID3A	chr14:56665885-56666474	K562	blood:	n/a	n/a
5	ARID3A	chr14:56686570-56687188	K562	blood:	n/a	n/a
6	ARID3A	chr14:56809150-56809372	K562	blood:	n/a	n/a
7	ATF1	chr14:56686637-56687110	K562	blood:	n/a	n/a
8	ATF1	chr14:56583325-56583525	K562	blood:	n/a	n/a
9	ATF1	chr14:56807700-56807903	K562	blood:	n/a	n/a
10	ATF1	chr14:56800409-56800721	K562	blood:	n/a	n/a
11	ATF1	chr14:56639364-56639740	K562	blood:	n/a	n/a
12	ATF1	chr14:56809054-56809355	K562	blood:	n/a	n/a
13	ATF2	chr14:56665738-56666295	GM12878	blood:	n/a	n/a
14	ATF2	chr14:56709881-56710234	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr14:56709812-56710211	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr14:56639328-56639606	K562	blood:	n/a	n/a
17	ATF3	chr14:56686636-56687053	K562	blood:	n/a	n/a
18	BACH1	chr14:56806595-56807064	K562	blood:	n/a	n/a
19	BACH1	chr14:56780639-56780839	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr14:56665925-56666397	K562	blood:	n/a	n/a
21	BACH1	chr14:56585687-56585943	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr14:56665938-56666306	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr14:56584490-56585294	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr14:56613083-56613223	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr14:56806610-56807116	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr14:56686724-56687159	K562	blood:	n/a	n/a
27	BATF	chr14:56668960-56669292	GM12878	blood:	n/a	chr14:56669144-56669155
28	BATF	chr14:56668951-56669300	GM12878	blood:	n/a	chr14:56669144-56669155
29	BATF	chr14:56710627-56711110	GM12878	blood:	n/a	n/a
30	BATF	chr14:56806756-56807027	GM12878	blood:	n/a	chr14:56806866-56806877 chr14:56806867-56806877
31	BCL3	chr14:56691544-56692069	A549	lung:	n/a	n/a
32	BCL3	chr14:56648261-56648865	A549	lung:	n/a	n/a
33	BCLAF1	chr14:56683632-56684216	K562	blood:	n/a	n/a
34	BCLAF1	chr14:56683643-56684304	K562	blood:	n/a	n/a
35	BHLHE40	chr14:56665179-56665462	K562	blood:	n/a	n/a
36	BHLHE40	chr14:56649490-56649839	K562	blood:	n/a	n/a
37	BHLHE40	chr14:56691606-56692075	HepG2	liver:	n/a	n/a
38	BHLHE40	chr14:56806727-56807145	K562	blood:	n/a	n/a
39	BHLHE40	chr14:56762527-56762767	K562	blood:	n/a	n/a
40	BHLHE40	chr14:56674631-56674900	K562	blood:	n/a	n/a
41	BHLHE40	chr14:56686476-56687340	K562	blood:	n/a	n/a
42	BHLHE40	chr14:56780626-56780753	K562	blood:	n/a	n/a
43	BHLHE40	chr14:56639253-56639682	K562	blood:	n/a	n/a
44	BHLHE40	chr14:56665827-56666230	K562	blood:	n/a	n/a
45	BHLHE40	chr14:56601852-56602029	K562	blood:	n/a	n/a
46	BHLHE40	chr14:56574478-56574643	HepG2	liver:	n/a	n/a
47	BHLHE40	chr14:56662401-56662938	GM12878	blood:	n/a	n/a
48	BHLHE40	chr14:56666910-56667245	GM12878	blood:	n/a	n/a
49	BHLHE40	chr14:56792219-56792416	K562	blood:	n/a	n/a
50	BHLHE40	chr14:56584494-56585224	K562	blood:	n/a	n/a

(count:2380 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:56711197-56711247	BE2_C	brain:	n/a
2	chr14:56711197-56711247	BE2_C	brain:	n/a
3	chr14:56584647-56584697	HRCEpiC	kidney:	n/a
4	chr14:56663411-56663461	HUVEC	blood vessel:	n/a
5	chr14:56645376-56645426	HEK293	kidney:	embryo
6	chr14:56604516-56604566	SKMC	muscle:	n/a
7	chr14:56672508-56672558	Jurkat	blood:	n/a
8	chr14:56672508-56672558	LNCaP	prostate:	n/a
9	chr14:56585486-56585536	MCF-7	breast:	n/a
10	chr14:56645376-56645426	HL-60	blood:	n/a
11	chr14:56800153-56800203	NT2-D1	testis:	n/a
12	chr14:56777251-56777301	HPAEpiC	pulmonary alveolar:	n/a
13	chr14:56584702-56584752	GM06990	blood:	n/a
14	chr14:56690625-56690675	HIPEpiC	eye:	n/a
15	chr14:56616059-56616109	AG04449	skin:	fetal
16	chr14:56586522-56586572	LNCaP	prostate:	n/a
17	chr14:56645376-56645426	ProgFib	skin:	n/a
18	chr14:56766873-56766923	HRCEpiC	kidney:	n/a
19	chr14:56615077-56615127	HRPEpiC	eye:	n/a
20	chr14:56711197-56711247	PANC-1	pancreas:	n/a
21	chr14:56666067-56666117	Caco-2	colon:	n/a
22	chr14:56584702-56584752	MCF-7	breast:	n/a
23	chr14:56649615-56649665	HIPEpiC	eye:	n/a
24	chr14:56584647-56584697	CMK	blood:	n/a
25	chr14:56740867-56740917	A549	lung:	n/a
26	chr14:56672508-56672558	PFSK-1	brain:	n/a
27	chr14:56755262-56755312	SKMC	muscle:	n/a
28	chr14:56585092-56585142	GM12892	blood:	n/a
29	chr14:56585102-56585152	HepG2	liver:	n/a
30	chr14:56808483-56808533	PrEC	prostate:	n/a
31	chr14:56808483-56808533	RPTEC	kidney:	n/a
32	chr14:56663411-56663461	HCT-116	colon:	n/a
33	chr14:56766873-56766923	HEK293	kidney:	embryo
34	chr14:56659945-56659995	A549	lung:	n/a
35	chr14:56645376-56645426	SAEC	small airway:	n/a
36	chr14:56584987-56585037	HRE	kidney:	n/a
37	chr14:56800153-56800203	NH-A	brain:	n/a
38	chr14:56645829-56645879	H1-hESC	embryonic stem cell:	embryo
39	chr14:56663411-56663461	Caco-2	colon:	n/a
40	chr14:56584647-56584697	HCPEpiC	choroid plexus:	n/a
41	chr14:56766873-56766923	AoSMC	blood vessel:	n/a
42	chr14:56585486-56585536	SK-N-SH	brain:	n/a
43	chr14:56659945-56659995	ProgFib	skin:	n/a
44	chr14:56663411-56663461	HL-60	blood:	n/a
45	chr14:56615077-56615127	ProgFib	skin:	n/a
46	chr14:56591902-56591952	A549	lung:	n/a
47	chr14:56755226-56755276	HRE	kidney:	n/a
48	chr14:56740867-56740917	Hela-S3	cervix:	n/a
49	chr14:56777251-56777301	AG04450	lung:	fetal
50	chr14:56645376-56645426	IMR90	lung:	fetal

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:56643693..56645416-chr14:56800419..56803265,2	K562	blood:
2	chr14:56608539..56610800-chr14:56613943..56615477,2	MCF-7	breast:
3	chr14:56652145..56654959-chr14:56655814..56657879,2	K562	blood:
4	chr14:56646170..56649121-chr14:56682750..56684520,2	K562	blood:
5	chr14:56660081..56671301-chr14:56679407..56688474,29	K562	blood:
6	chr14:56602302..56604892-chr14:56607961..56609487,2	MCF-7	breast:
7	chr14:56606632..56608561-chr14:56682094..56685625,3	K562	blood:
8	chr14:56684044..56686281-chr14:56718525..56720474,2	K562	blood:
9	chr14:56682968..56684539-chr14:56757092..56758766,2	K562	blood:
10	chr14:56642724..56645085-chr14:56645818..56648163,2	K562	blood:
11	chr14:56591173..56593665-chr14:56598218..56600855,2	MCF-7	breast:
12	chr14:56711133..56713005-chr14:56715491..56717445,2	MCF-7	breast:
13	chr14:56800511..56802640-chr14:56807027..56808554,2	K562	blood:
14	chr14:56653021..56655091-chr14:56684495..56686512,2	K562	blood:
15	chr14:56707205..56711139-chr14:56711153..56714589,3	K562	blood:
16	chr14:56583354..56586083-chr14:56598668..56601939,3	K562	blood:
17	chr14:56683693..56686050-chr14:56732906..56735340,3	K562	blood:
18	chr14:56682968..56684539-chr14:56757092..56758766,2	K562	blood:
19	chr14:56769713..56772001-chr14:56773071..56775429,2	K562	blood:
20	chr14:56649412..56651282-chr14:56653289..56655501,2	K562	blood:
21	chr14:56221789..56224702-chr14:56769776..56771612,2	K562	blood:
22	chr14:56675081..56677798-chr14:56689013..56691356,2	MCF-7	breast:
23	chr14:56636851..56638777-chr14:56670905..56672750,2	K562	blood:
24	chr14:56714179..56714751-chr14:56760641..56761350,3	MCF-7	breast:
25	chr14:56798962..56800809-chr14:56842457..56844323,2	K562	blood:
26	chr14:56664921..56668726-chr14:56673424..56676785,5	K562	blood:
27	chr14:56794620..56796149-chr14:56801330..56803015,2	K562	blood:
28	chr14:56649381..56651090-chr14:56683984..56685910,2	K562	blood:
29	chr14:56636851..56638777-chr14:56670905..56672750,2	K562	blood:
30	chr14:56643693..56645416-chr14:56800419..56803265,2	K562	blood:
31	chr14:56675081..56677798-chr14:56689013..56691356,2	MCF-7	breast:
32	chr14:56684475..56686514-chr14:56687367..56688980,2	MCF-7	breast:
33	chr14:56152134..56154942-chr14:56705477..56707691,2	K562	blood:
34	chr14:56584201..56586248-chr14:56600071..56602389,2	K562	blood:
35	chr14:56662437..56665407-chr14:56673840..56677281,3	K562	blood:
36	chr14:56637508..56640362-chr14:56648471..56651098,2	K562	blood:
37	chr14:56683722..56686050-chr14:56732906..56735340,2	K562	blood:
38	chr14:56643621..56646971-chr14:56684832..56688465,3	K562	blood:
39	chr14:56711133..56713005-chr14:56715491..56717445,2	MCF-7	breast:
40	chr14:56656212..56658616-chr14:56744495..56746783,2	K562	blood:
41	chr14:56802231..56804890-chr14:56805110..56807908,2	K562	blood:
42	chr14:56654435..56657114-chr14:56660451..56662666,2	K562	blood:
43	chr14:56667127..56669023-chr14:56670519..56672391,2	K562	blood:
44	chr14:56637508..56640362-chr14:56648471..56651098,2	K562	blood:
45	chr14:56602302..56604892-chr14:56607961..56609487,2	MCF-7	breast:
46	chr14:56713948..56714469-chr14:56948717..56949355,2	MCF-7	breast:
47	chr14:56713708..56714514-chr14:57783743..57784543,2	MCF-7	breast:
48	chr14:56667127..56669023-chr14:56670519..56672391,2	K562	blood:
49	chr14:56648236..56651090-chr14:56684410..56686125,2	K562	blood:
50	chr14:56713895..56714651-chr14:56940979..56941654,4	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PELI2-2	chr14:56788204-56788329	ENSG00000259719.1
2	lnc-PELI2-2	chr14:56811692-56811719	ENSG00000259719.1
3	lnc-RP11-1085N6.3.1-3	chr14:56776819-56776931	ENSG00000259483.1
4	lnc-PELI2-2	chr14:56811812-56812256	NONHSAT037041
5	lnc-PELI2-1	chr14:56776790-56776977	XLOC_010839
6	lnc-PELI2-2	chr14:56792822-56793190	NONHSAT037041
7	lnc-RP11-1085N6.3.1-3	chr14:56770208-56770387	ENSG00000259483.1
8	lnc-PELI2-2	chr14:56777654-56777820	ENSG00000259719.1
9	lnc-RP11-1085N6.3.1-3	chr14:56777427-56777479	ENSG00000259483.1
10	lnc-PELI2-2	chr14:56777598-56777820	ENSG00000259719.1
11	lnc-RP11-1085N6.3.1-3	chr14:56775457-56775627	ENSG00000259483.1
12	lnc-PELI2-2	chr14:56784610-56784804	ENSG00000259719.1
13	lnc-PELI2-2	chr14:56788204-56788329	NONHSAT037041
14	lnc-PELI2-2	chr14:56777598-56777820	NONHSAT037041
15	lnc-PELI2-2	chr14:56792898-56792926	ENSG00000259719.1
16	lnc-PELI2-1	chr14:56777422-56777445	XLOC_010839
17	lnc-PELI2-2	chr14:56788204-56788329	ENSG00000259719.1
18	lnc-PELI2-2	chr14:56794901-56795079	ENSG00000259719.1
19	lnc-PELI2-2	chr14:56797140-56797205	ENSG00000259719.1

No data

Variant related genes	Relation type
PELI2	TF binding region
ENSG00000259719	TF binding region
ENSG00000259483	TF binding region
PELI2	CpG island
ENSG00000259719	CpG island
ENSG00000259483	CpG island
ENSG00000070367	chromatin interactions
ENSG00000053770	chromatin interactions
ENSG00000139946	chromatin interactions

Extended variants
information (count: 10024 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:10024 , 50 per page) page: 1 2 3 4 5 6 7 ... 201

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556267778	chr14:56568537-56568538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574128133	chr14:56568538-56568539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs59144258	chr14:56568540-56568541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182501456	chr14:56568551-56568552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554491660	chr14:56568581-56568582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572744000	chr14:56568709-56568710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145521555	chr14:56568799-56568800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148859684	chr14:56568805-56568806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs80277459	chr14:56568892-56568893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548887795	chr14:56568928-56568929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113367081	chr14:56568962-56568963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565423455	chr14:56568975-56568976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187142630	chr14:56568980-56568981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190504979	chr14:56568991-56568992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559334613	chr14:56568992-56568993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559792483	chr14:56569033-56569034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527551326	chr14:56569039-56569040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527535645	chr14:56569047-56569048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146438467	chr14:56569086-56569087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377372012	chr14:56569109-56569110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567341882	chr14:56569174-56569175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531582750	chr14:56569186-56569187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181676500	chr14:56569199-56569200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544108666	chr14:56569208-56569209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532888488	chr14:56569261-56569262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376868762	chr14:56569267-56569268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201234097	chr14:56569297-56569298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201601755	chr14:56569298-56569299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568795191	chr14:56569299-56569300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375192454	chr14:56569301-56569302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111430192	chr14:56569302-56569303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377588617	chr14:56569303-56569304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113046852	chr14:56569304-56569305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370529388	chr14:56569344-56569345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113449330	chr14:56569357-56569358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553774875	chr14:56569363-56569364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563422147	chr14:56569372-56569373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576973959	chr14:56569374-56569375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565683382	chr14:56569406-56569407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536906020	chr14:56569411-56569412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185900394	chr14:56569426-56569427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370400539	chr14:56569473-56569474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576556338	chr14:56569505-56569506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1812362	chr14:56569537-56569538	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs528734998	chr14:56569572-56569573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567337585	chr14:56569576-56569577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558765997	chr14:56569595-56569596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190274183	chr14:56569617-56569618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182629563	chr14:56569625-56569626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543350660	chr14:56569650-56569651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Autism	22495311	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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:4794 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56566000-56570600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:56566600-56572000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr14:56567600-56570400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr14:56568800-56569000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr14:56569400-56571000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr14:56569800-56570000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr14:56570000-56570200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr14:56570400-56570600	Enhancers	Fetal Kidney	kidney
9	chr14:56570400-56571000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr14:56570600-56571200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:56571000-56571200	Enhancers	Pancreas	Pancrea
12	chr14:56571000-56572800	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr14:56571200-56572800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:56572000-56573600	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr14:56572800-56573000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:56572800-56573200	Enhancers	Fetal Thymus	thymus
17	chr14:56572800-56573400	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr14:56573000-56573200	Enhancers	Primary B cells from cord blood	blood
19	chr14:56573200-56578800	Weak transcription	Primary B cells from cord blood	blood
20	chr14:56573400-56578600	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr14:56573600-56574000	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr14:56574000-56582600	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr14:56578600-56581000	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr14:56578800-56579000	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr14:56578800-56579400	Enhancers	Primary B cells from cord blood	blood
26	chr14:56579000-56579200	Enhancers	Primary B cells from peripheral blood	blood
27	chr14:56579000-56580200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr14:56579200-56580200	Enhancers	Primary T cells from cord blood	blood
29	chr14:56579400-56579600	Flanking Active TSS	Primary B cells from cord blood	blood
30	chr14:56579400-56579800	Weak transcription	Primary B cells from peripheral blood	blood
31	chr14:56579400-56579800	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr14:56579400-56580200	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr14:56579400-56580400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr14:56579600-56579800	Enhancers	Rectal Smooth Muscle	rectum
35	chr14:56579600-56580400	Enhancers	Primary B cells from cord blood	blood
36	chr14:56579800-56580000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
37	chr14:56579800-56582800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr14:56579800-56584200	Weak transcription	Rectal Smooth Muscle	rectum
39	chr14:56580200-56580600	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr14:56580200-56582000	Weak transcription	Primary T cells from cord blood	blood
41	chr14:56580200-56582600	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr14:56580200-56583200	Weak transcription	Primary B cells from peripheral blood	blood
43	chr14:56580400-56582200	Weak transcription	Primary B cells from cord blood	blood
44	chr14:56580400-56582600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr14:56580600-56581800	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr14:56580800-56581000	Enhancers	Fetal Brain Male	brain
47	chr14:56581000-56582000	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr14:56581000-56582000	Weak transcription	Fetal Brain Male	brain
49	chr14:56581800-56582200	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr14:56582000-56583200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links