Variant report

Variant	esv3339520
Chromosome Location	chr14:21741166-21806074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:814)
CpG islands
(count:733)
Chromatin interactive
region (count:73)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:814 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21776279-21777397	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:21776552-21777534	K562	blood:	n/a	n/a
3	ARID3A	chr14:21747410-21747610	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:21766152-21766244	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:21788216-21788219	K562	blood:	n/a	n/a
6	ARID3A	chr14:21766716-21766742	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:21770673-21771067	HepG2	liver:	n/a	n/a
8	ATF1	chr14:21776699-21777288	K562	blood:	n/a	n/a
9	ATF1	chr14:21785645-21785927	K562	blood:	n/a	n/a
10	ATF2	chr14:21776636-21777278	GM12878	blood:	n/a	n/a
11	ATF2	chr14:21785532-21786027	GM12878	blood:	n/a	n/a
12	ATF2	chr14:21776687-21777400	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr14:21775817-21777333	GM12878	blood:	n/a	n/a
14	BATF	chr14:21776769-21777023	GM12878	blood:	n/a	n/a
15	BCLAF1	chr14:21776618-21777336	GM12878	blood:	n/a	n/a
16	BHLHE40	chr14:21776314-21777235	HepG2	liver:	n/a	n/a
17	BHLHE40	chr14:21785724-21785902	K562	blood:	n/a	n/a
18	BHLHE40	chr14:21776700-21777231	GM12878	blood:	n/a	n/a
19	BHLHE40	chr14:21747457-21747741	HepG2	liver:	n/a	n/a
20	BHLHE40	chr14:21776625-21776987	K562	blood:	n/a	n/a
21	BHLHE40	chr14:21788208-21788349	K562	blood:	n/a	n/a
22	BHLHE40	chr14:21788917-21789244	K562	blood:	n/a	n/a
23	CEBPB	chr14:21766498-21766756	K562	blood:	n/a	chr14:21766609-21766620
24	CEBPB	chr14:21788118-21788449	A549	lung:	n/a	n/a
25	CEBPB	chr14:21781767-21781966	HepG2	liver:	n/a	chr14:21781897-21781908
26	CEBPB	chr14:21766410-21766864	MCF-7	breast:	n/a	chr14:21766609-21766620
27	CEBPB	chr14:21804093-21804303	HepG2	liver:	n/a	chr14:21804215-21804226 chr14:21804214-21804225 chr14:21804214-21804227 chr14:21804216-21804225
28	CEBPB	chr14:21788161-21788368	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:21781742-21782025	HepG2	liver:	n/a	chr14:21781897-21781908
30	CEBPB	chr14:21766460-21766895	Hela-S3	cervix:	n/a	chr14:21766609-21766620
31	CEBPB	chr14:21795289-21795494	K562	blood:	n/a	n/a
32	CEBPB	chr14:21747349-21747647	HepG2	liver:	n/a	chr14:21747467-21747478
33	CEBPB	chr14:21804201-21804255	Hela-S3	cervix:	n/a	chr14:21804215-21804226 chr14:21804214-21804225 chr14:21804214-21804227 chr14:21804216-21804225
34	CEBPB	chr14:21788108-21788432	K562	blood:	n/a	n/a
35	CEBPB	chr14:21777105-21777108	A549	lung:	n/a	n/a
36	CEBPB	chr14:21747455-21747537	IMR90	lung:	n/a	chr14:21747467-21747478
37	CEBPB	chr14:21741659-21741772	HepG2	liver:	n/a	chr14:21741695-21741706
38	CEBPB	chr14:21750063-21750281	HepG2	liver:	n/a	chr14:21750204-21750215
39	CEBPB	chr14:21805629-21805763	HepG2	liver:	n/a	chr14:21805656-21805667
40	CEBPB	chr14:21788087-21788462	K562	blood:	n/a	n/a
41	CEBPB	chr14:21795165-21795572	MCF-7	breast:	n/a	chr14:21795491-21795499
42	CEBPB	chr14:21795276-21795502	HepG2	liver:	n/a	chr14:21795491-21795499
43	CEBPB	chr14:21781731-21782019	HepG2	liver:	n/a	chr14:21781897-21781908
44	CEBPB	chr14:21805626-21805765	K562	blood:	n/a	chr14:21805656-21805667
45	CEBPB	chr14:21766599-21766687	H1-hESC	embryonic stem cell:	n/a	chr14:21766609-21766620
46	CEBPB	chr14:21765207-21765474	HepG2	liver:	n/a	chr14:21765308-21765319
47	CEBPB	chr14:21766530-21766803	A549	lung:	n/a	chr14:21766609-21766620
48	CEBPB	chr14:21795259-21795456	A549	lung:	n/a	n/a
49	CEBPB	chr14:21789587-21789653	HepG2	liver:	n/a	n/a
50	CEBPB	chr14:21765141-21765485	K562	blood:	n/a	chr14:21765308-21765319

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21756040-21756090	AG10803	skin:	n/a
2	chr14:21756040-21756090	AG10803	skin:	n/a
3	chr14:21765313-21765363	SKMC	muscle:	n/a
4	chr14:21755658-21755708	RPTEC	kidney:	n/a
5	chr14:21772854-21772904	SAEC	small airway:	n/a
6	chr14:21755658-21755708	SK-N-SH_RA	brain:	n/a
7	chr14:21769176-21769226	BJ	skin:	n/a
8	chr14:21765313-21765363	PANC-1	pancreas:	n/a
9	chr14:21756231-21756281	SK-N-MC	brain:	n/a
10	chr14:21769379-21769429	PFSK-1	brain:	n/a
11	chr14:21755798-21755848	HEEpiC	esophagus:	n/a
12	chr14:21765313-21765363	ProgFib	skin:	n/a
13	chr14:21769176-21769226	NHBE	bronchial:	n/a
14	chr14:21765313-21765363	PFSK-1	brain:	n/a
15	chr14:21772854-21772904	ProgFib	skin:	n/a
16	chr14:21769240-21769290	ECC-1	luminal epithelium:	n/a
17	chr14:21769332-21769382	HNPCEpiC	eye:	n/a
18	chr14:21755658-21755708	MCF10A-Er-Src	breast:	n/a
19	chr14:21755798-21755848	AG04449	skin:	fetal
20	chr14:21755820-21755870	A549	lung:	n/a
21	chr14:21756231-21756281	MCF-7	breast:	n/a
22	chr14:21769240-21769290	HCPEpiC	choroid plexus:	n/a
23	chr14:21769379-21769429	HCF	heart:	n/a
24	chr14:21756231-21756281	SK-N-SH	brain:	n/a
25	chr14:21765313-21765363	NHBE	bronchial:	n/a
26	chr14:21755798-21755848	BE2_C	brain:	n/a
27	chr14:21756040-21756090	HL-60	blood:	n/a
28	chr14:21765313-21765363	HCM	heart:	n/a
29	chr14:21756231-21756281	HL-60	blood:	n/a
30	chr14:21769176-21769226	NHDF-neo	bronchial:	n/a
31	chr14:21756040-21756090	T-47D	breast:	n/a
32	chr14:21765313-21765363	ECC-1	luminal epithelium:	n/a
33	chr14:21769379-21769429	LNCaP	prostate:	n/a
34	chr14:21755820-21755870	HRCEpiC	kidney:	n/a
35	chr14:21769176-21769226	LNCaP	prostate:	n/a
36	chr14:21769176-21769226	AG04450	lung:	fetal
37	chr14:21765313-21765363	HUVEC	blood vessel:	n/a
38	chr14:21765313-21765363	HCT-116	colon:	n/a
39	chr14:21755798-21755848	CMK	blood:	n/a
40	chr14:21772854-21772904	RPTEC	kidney:	n/a
41	chr14:21755798-21755848	Jurkat	blood:	n/a
42	chr14:21769240-21769290	AG09309	skin:	n/a
43	chr14:21756231-21756281	H1-hESC	embryonic stem cell:	embryo
44	chr14:21756231-21756281	HEK293	kidney:	embryo
45	chr14:21756231-21756281	K562	blood:	n/a
46	chr14:21769176-21769226	HEK293	kidney:	embryo
47	chr14:21769332-21769382	HCT-116	colon:	n/a
48	chr14:21772854-21772904	Caco-2	colon:	n/a
49	chr14:21769240-21769290	Hela-S3	cervix:	n/a
50	chr14:21765313-21765363	GM12878	blood:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:21776403..21778650-chr14:21847769..21849405,2	K562	blood:
2	chr14:21770316..21772335-chr14:21774235..21777152,2	K562	blood:
3	chr14:21788541..21790958-chr14:21804803..21806582,2	MCF-7	breast:
4	chr14:21783367..21785383-chr14:21850388..21852879,2	MCF-7	breast:
5	chr14:21777189..21779079-chr14:21786297..21788417,2	MCF-7	breast:
6	chr14:21735883..21738830-chr14:21774715..21778854,7	MCF-7	breast:
7	chr14:21736080..21739636-chr14:21765775..21769584,7	MCF-7	breast:
8	chr14:21736447..21738561-chr14:21758872..21762321,3	MCF-7	breast:
9	chr14:21736832..21738818-chr14:21756962..21758604,2	MCF-7	breast:
10	chr14:21725317..21729371-chr14:21774547..21778706,6	K562	blood:
11	chr14:21775315..21780588-chr14:21785592..21789606,7	K562	blood:
12	chr14:21751576..21753820-chr14:21765651..21767514,2	MCF-7	breast:
13	chr14:21793702..21795777-chr14:21799796..21801612,2	MCF-7	breast:
14	chr14:21776722..21779291-chr14:21780222..21782831,3	K562	blood:
15	chr14:21774301..21777973-chr14:21828099..21831298,3	K562	blood:
16	chr14:21770316..21772335-chr14:21774235..21777152,2	K562	blood:
17	chr14:21785391..21787053-chr14:21851556..21854033,2	K562	blood:
18	chr14:21736417..21739908-chr14:21744669..21746956,5	MCF-7	breast:
19	chr14:21731095..21732813-chr14:21767081..21768936,2	K562	blood:
20	chr14:21732486..21734251-chr14:21742553..21744073,2	MCF-7	breast:
21	chr14:21786246..21790945-chr14:21792270..21796637,5	MCF-7	breast:
22	chr14:21731798..21735401-chr14:21775005..21778167,4	MCF-7	breast:
23	chr14:21793702..21795777-chr14:21799796..21801612,2	MCF-7	breast:
24	chr14:21730115..21732637-chr14:21776169..21779224,3	MCF-7	breast:
25	chr14:21715916..21717624-chr14:21774839..21777114,2	MCF-7	breast:
26	chr14:21733893..21736248-chr14:21775936..21778469,3	K562	blood:
27	chr14:21732976..21734644-chr14:21771387..21772893,2	MCF-7	breast:
28	chr14:21698305..21701103-chr14:21775340..21777251,2	MCF-7	breast:
29	chr14:21768791..21773432-chr14:21775011..21777048,5	MCF-7	breast:
30	chr14:21731325..21733922-chr14:21791322..21794128,2	MCF-7	breast:
31	chr14:21673277..21675794-chr14:21775419..21778094,2	MCF-7	breast:
32	chr14:21775799..21777853-chr14:21792862..21795336,2	MCF-7	breast:
33	chr14:21751576..21753820-chr14:21765651..21767514,2	MCF-7	breast:
34	chr14:21735133..21741012-chr14:21774869..21780347,13	MCF-7	breast:
35	chr14:21729912..21732388-chr14:21794121..21797950,3	K562	blood:
36	chr14:21732396..21736856-chr14:21795995..21798414,4	K562	blood:
37	chr14:21757631..21759281-chr14:21771209..21774120,2	K562	blood:
38	chr14:21786246..21790945-chr14:21792270..21796637,5	MCF-7	breast:
39	chr14:21775706..21777351-chr14:21851149..21853404,2	MCF-7	breast:
40	chr14:21783845..21785729-chr14:21787728..21789358,2	K562	blood:
41	chr14:21729752..21732364-chr14:21780119..21782538,3	K562	blood:
42	chr14:21802656..21804899-chr14:21816429..21817981,2	K562	blood:
43	chr14:21736279..21738855-chr14:21774365..21778910,7	K562	blood:
44	chr14:21736078..21738930-chr14:21751792..21754705,3	MCF-7	breast:
45	chr14:21734081..21737638-chr14:21753111..21756446,3	K562	blood:
46	chr14:21738165..21739837-chr14:21745511..21747672,2	K562	blood:
47	chr14:21733164..21734781-chr14:21745082..21746648,2	MCF-7	breast:
48	chr14:21757631..21759281-chr14:21771209..21774120,2	K562	blood:
49	chr14:21776722..21779782-chr14:21780222..21783756,4	K562	blood:
50	chr14:21783698..21785345-chr14:21786663..21789358,2	K562	blood:

No data

Variant related genes	Relation type
HNRNPC	TF binding region
RPGRIP1	TF binding region
HNRNPC	CpG island
RPGRIP1	CpG island
ENSG00000092199	chromatin interactions
ENSG00000258441	chromatin interactions
ENSG00000260830	chromatin interactions
ENSG00000092200	chromatin interactions
ENSG00000092201	chromatin interactions

Extended variants
information (count: 2551 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2551 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183003668	chr14:21741178-21741179	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs566208695	chr14:21741221-21741222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs543169670	chr14:21741258-21741259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs188757163	chr14:21741276-21741277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs191140290	chr14:21741278-21741279	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs551920402	chr14:21741285-21741286	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs527664792	chr14:21741301-21741302	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs571848280	chr14:21741307-21741308	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531280064	chr14:21741319-21741320	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs115890965	chr14:21741395-21741396	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs550037561	chr14:21741477-21741478	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs535069572	chr14:21741482-21741483	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555059537	chr14:21741496-21741497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs565409873	chr14:21741514-21741515	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs534512258	chr14:21741558-21741559	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs549455217	chr14:21741572-21741573	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557894827	chr14:21741609-21741610	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs561625351	chr14:21741612-21741613	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs182979482	chr14:21741618-21741619	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs150041697	chr14:21741623-21741624	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs187560505	chr14:21741666-21741667	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs574115731	chr14:21741723-21741724	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs543007026	chr14:21741729-21741730	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs559905922	chr14:21741740-21741741	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs528545572	chr14:21741776-21741777	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs545278486	chr14:21741778-21741779	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs145395631	chr14:21741805-21741806	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565522708	chr14:21741827-21741828	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531815237	chr14:21741842-21741843	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs8008748	chr14:21741941-21741942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs72678659	chr14:21741946-21741947	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs528880380	chr14:21741948-21741949	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs548523926	chr14:21742029-21742030	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565447019	chr14:21742040-21742041	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs534756060	chr14:21742073-21742074	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533031877	chr14:21742077-21742078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs557563914	chr14:21742083-21742084	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs571447620	chr14:21742085-21742086	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs79558585	chr14:21742097-21742098	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551479183	chr14:21742133-21742134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372493614	chr14:21742141-21742142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs142661347	chr14:21742195-21742196	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191627462	chr14:21742198-21742199	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs573952778	chr14:21742242-21742243	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs543045607	chr14:21742273-21742274	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146349102	chr14:21742303-21742304	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs8014450	chr14:21742338-21742339	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs184211458	chr14:21742340-21742341	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs565221120	chr14:21742346-21742347	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs76716627	chr14:21742416-21742417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ewing''s sarcoma	18628472	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21737800-21743400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:21738400-21743200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr14:21738600-21741800	Weak transcription	Placenta	Placenta
4	chr14:21738600-21741800	Weak transcription	HepG2	liver
5	chr14:21738600-21742600	Weak transcription	Thymus	Thymus
6	chr14:21738600-21743200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr14:21738600-21743400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr14:21738600-21743800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr14:21738800-21743400	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr14:21739000-21742600	Weak transcription	Dnd41	blood
11	chr14:21739000-21746600	Weak transcription	GM12878-XiMat	blood
12	chr14:21739200-21742600	Weak transcription	Fetal Thymus	thymus
13	chr14:21741800-21742000	Enhancers	HepG2	liver
14	chr14:21741800-21742200	Enhancers	Placenta	Placenta
15	chr14:21742000-21742600	Weak transcription	HepG2	liver
16	chr14:21742600-21743000	Enhancers	HepG2	liver
17	chr14:21742600-21743600	Enhancers	Thymus	Thymus
18	chr14:21742600-21745200	Enhancers	Fetal Thymus	thymus
19	chr14:21742600-21745400	Enhancers	Dnd41	blood
20	chr14:21743000-21743200	Weak transcription	HepG2	liver
21	chr14:21743200-21743800	Active TSS	HepG2	liver
22	chr14:21743200-21744000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr14:21743200-21744400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr14:21743400-21743600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr14:21743400-21743800	Enhancers	Primary T cells fromperipheralblood	blood
26	chr14:21743400-21744000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr14:21743600-21743800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr14:21743600-21744000	Active TSS	Thymus	Thymus
29	chr14:21743800-21744000	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr14:21743800-21744000	Enhancers	HepG2	liver
31	chr14:21743800-21744200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr14:21744000-21744400	Enhancers	Primary T cells fromperipheralblood	blood
33	chr14:21744000-21744600	Enhancers	Thymus	Thymus
34	chr14:21744000-21745200	Weak transcription	HepG2	liver
35	chr14:21744600-21746200	Weak transcription	Thymus	Thymus
36	chr14:21745200-21748800	Enhancers	HepG2	liver
37	chr14:21746600-21746800	Enhancers	GM12878-XiMat	blood
38	chr14:21746600-21747200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr14:21746800-21747400	Weak transcription	GM12878-XiMat	blood
40	chr14:21747400-21747600	Enhancers	GM12878-XiMat	blood
41	chr14:21749400-21751200	Enhancers	Placenta	Placenta
42	chr14:21756600-21758000	Enhancers	Primary B cells from peripheral blood	blood
43	chr14:21756800-21758000	Enhancers	GM12878-XiMat	blood
44	chr14:21757400-21757800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr14:21763800-21767600	Enhancers	Placenta	Placenta
46	chr14:21765800-21766200	Enhancers	HepG2	liver
47	chr14:21765800-21766600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr14:21765800-21766800	Enhancers	K562	blood
49	chr14:21766000-21766200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr14:21766000-21766600	Enhancers	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links