Variant report

Variant	nsv593224
Chromosome Location	chr4:812598-862156
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:662)
CpG islands
(count:4216)
Chromatin interactive
region (count:64)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:662 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:833628-834116	GM12878	blood:	n/a	n/a
2	BACH1	chr4:839116-839212	K562	blood:	n/a	n/a
3	BACH1	chr4:819446-819522	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr4:849972-850190	GM12878	blood:	n/a	n/a
5	BCL3	chr4:847182-847471	GM12878	blood:	n/a	n/a
6	BCL3	chr4:847123-847521	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:843107-843184	K562	blood:	n/a	n/a
8	BHLHE40	chr4:819894-819984	K562	blood:	n/a	n/a
9	BHLHE40	chr4:815716-815913	K562	blood:	n/a	n/a
10	BHLHE40	chr4:819415-819463	K562	blood:	n/a	n/a
11	CBX3	chr4:825728-826011	K562	blood:	n/a	n/a
12	CBX3	chr4:838116-838393	K562	blood:	n/a	n/a
13	CBX3	chr4:831506-831745	K562	blood:	n/a	n/a
14	CBX3	chr4:831594-831878	K562	blood:	n/a	n/a
15	CBX3	chr4:825446-826136	K562	blood:	n/a	n/a
16	CCNT2	chr4:819353-819529	K562	blood:	n/a	n/a
17	CCNT2	chr4:819783-819973	K562	blood:	n/a	chr4:819957-819966
18	CEBPB	chr4:849655-849965	HepG2	liver:	n/a	chr4:849823-849834
19	CEBPB	chr4:849683-850000	A549	lung:	n/a	chr4:849823-849834
20	CEBPB	chr4:822668-822978	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr4:849746-849956	Hela-S3	cervix:	n/a	chr4:849823-849834
22	CEBPB	chr4:849671-849978	IMR90	lung:	n/a	chr4:849823-849834
23	CEBPB	chr4:831676-831904	K562	blood:	n/a	n/a
24	CEBPB	chr4:849715-849972	K562	blood:	n/a	chr4:849823-849834
25	CHD2	chr4:819901-820071	Hela-S3	cervix:	n/a	chr4:819955-819965
26	CHD2	chr4:820804-820813	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr4:822480-822935	Hela-S3	cervix:	n/a	n/a
28	CREB1	chr4:819784-820055	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr4:819832-820160	HepG2	liver:	n/a	n/a
30	CREB1	chr4:819757-820087	K562	blood:	n/a	n/a
31	CTBP2	chr4:820592-820908	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr4:818452-819542	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr4:849812-849912	Lung_OC	lung:	n/a	n/a
34	CTCF	chr4:818220-818370	HMEC	breast:	n/a	n/a
35	CTCF	chr4:822793-822978	Fibrobl	skin:	n/a	n/a
36	CTCF	chr4:818118-818236	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr4:822796-822959	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:822740-822890	HFF	foreskin:	n/a	n/a
39	CTCF	chr4:822760-822910	MCF-7	breast:	n/a	n/a
40	CTCF	chr4:822760-822910	AG04449	skin:	n/a	n/a
41	CTCF	chr4:855321-855402	GM10248	blood:	n/a	n/a
42	CTCF	chr4:822720-822870	GM12874	blood:	n/a	n/a
43	CTCF	chr4:822800-822950	AG04450	lung:	n/a	n/a
44	CTCF	chr4:822800-822950	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr4:822760-822910	GM12875	blood:	n/a	n/a
46	CTCF	chr4:818640-818790	SK-N-SH_RA	brain:	n/a	chr4:818691-818701
47	CTCF	chr4:848060-848210	GM12864	blood:	n/a	n/a
48	CTCF	chr4:818300-818550	GM06990	blood:	n/a	n/a
49	CTCF	chr4:818240-818390	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr4:822880-823030	GM06990	blood:	n/a	n/a

(count:4216 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:841315-841365	NHBE	bronchial:	n/a
2	chr4:829753-829803	NB4	blood:	n/a
3	chr4:828281-828331	AG09309	skin:	n/a
4	chr4:845572-845622	HRPEpiC	eye:	n/a
5	chr4:816935-816985	HRE	kidney:	n/a
6	chr4:845829-845879	NT2-D1	testis:	n/a
7	chr4:852566-852616	IMR90	lung:	fetal
8	chr4:841315-841365	NHBE	bronchial:	n/a
9	chr4:829753-829803	NB4	blood:	n/a
10	chr4:828281-828331	AG09309	skin:	n/a
11	chr4:845572-845622	HRPEpiC	eye:	n/a
12	chr4:816935-816985	HRE	kidney:	n/a
13	chr4:845829-845879	NT2-D1	testis:	n/a
14	chr4:852566-852616	IMR90	lung:	fetal
15	chr4:854474-854524	SK-N-SH	brain:	n/a
16	chr4:816935-816985	AoSMC	blood vessel:	n/a
17	chr4:844329-844379	BJ	skin:	n/a
18	chr4:860838-860888	NHBE	bronchial:	n/a
19	chr4:853036-853086	CMK	blood:	n/a
20	chr4:841315-841365	GM19239	blood:	n/a
21	chr4:858299-858349	SKMC	muscle:	n/a
22	chr4:828098-828148	CMK	blood:	n/a
23	chr4:819927-819977	HRCEpiC	kidney:	n/a
24	chr4:815269-815319	HepG2	liver:	n/a
25	chr4:851793-851843	BE2_C	brain:	n/a
26	chr4:854474-854524	HIPEpiC	eye:	n/a
27	chr4:854688-854738	GM19239	blood:	n/a
28	chr4:847310-847360	NH-A	brain:	n/a
29	chr4:854474-854524	NB4	blood:	n/a
30	chr4:858299-858349	AG10803	skin:	n/a
31	chr4:853036-853086	RPTEC	kidney:	n/a
32	chr4:841569-841619	AG09309	skin:	n/a
33	chr4:851793-851843	SK-N-SH	brain:	n/a
34	chr4:828281-828331	HCT-116	colon:	n/a
35	chr4:819151-819201	AG04449	skin:	fetal
36	chr4:843637-843687	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:829373-829423	SKMC	muscle:	n/a
38	chr4:820756-820806	BE2_C	brain:	n/a
39	chr4:841315-841365	AG09309	skin:	n/a
40	chr4:821075-821125	NHBE	bronchial:	n/a
41	chr4:828198-828248	Hela-S3	cervix:	n/a
42	chr4:859471-859521	HL-60	blood:	n/a
43	chr4:828198-828248	Jurkat	blood:	n/a
44	chr4:851935-851985	ovcar-3	ovarian:	n/a
45	chr4:846732-846782	HepG2	liver:	n/a
46	chr4:855988-856038	ECC-1	luminal epithelium:	n/a
47	chr4:845829-845879	HCF	heart:	n/a
48	chr4:859328-859378	HRCEpiC	kidney:	n/a
49	chr4:829373-829423	SAEC	small airway:	n/a
50	chr4:847411-847461	HMEC	breast:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:832836..834891-chr4:838449..840859,2	K562	blood:
2	chr4:848413..850023-chr4:852591..855386,3	K562	blood:
3	chr4:829544..831715-chr4:924978..927589,2	MCF-7	breast:
4	chr4:853767..855933-chr4:865699..868669,2	K562	blood:
5	chr4:758761..760317-chr4:841497..843378,2	K562	blood:
6	chr4:723282..726108-chr4:810901..813432,2	K562	blood:
7	chr4:813190..814907-chr4:985263..987918,2	MCF-7	breast:
8	chr4:770559..774303-chr4:822047..825549,3	MCF-7	breast:
9	chr4:810119..812562-chr4:817081..819359,3	MCF-7	breast:
10	chr4:822237..824857-chr4:826820..829457,3	MCF-7	breast:
11	chr4:812550..814672-chr4:1242293..1245103,2	K562	blood:
12	chr4:814287..815828-chr4:819004..820949,2	MCF-7	breast:
13	chr4:831253..832902-chr4:836853..838473,2	K562	blood:
14	chr4:779184..781836-chr4:815756..818416,2	MCF-7	breast:
15	chr4:837032..839261-chr4:841910..844601,2	MCF-7	breast:
16	chr4:852977..854762-chr4:857237..859475,3	K562	blood:
17	chr4:782997..785390-chr4:814047..817037,2	K562	blood:
18	chr4:832058..834845-chr4:1004120..1005952,2	MCF-7	breast:
19	chr4:821558..823207-chr4:827876..830795,2	MCF-7	breast:
20	chr4:835693..839507-chr4:843140..845149,3	K562	blood:
21	chr4:832836..834891-chr4:838449..840859,2	K562	blood:
22	chr4:857086..858882-chr4:868913..870778,2	MCF-7	breast:
23	chr4:675798..677554-chr4:822582..825253,2	K562	blood:
24	chr4:811397..815674-chr4:816390..820314,6	K562	blood:
25	chr4:809375..810958-chr4:813347..815488,2	MCF-7	breast:
26	chr4:774090..776323-chr4:847875..849767,2	K562	blood:
27	chr4:815070..817280-chr4:1004466..1007388,2	K562	blood:
28	chr4:851167..852931-chr4:994797..996823,2	K562	blood:
29	chr4:858604..860545-chr4:870716..872818,3	K562	blood:
30	chr4:775742..777793-chr4:821294..823838,2	MCF-7	breast:
31	chr4:782165..784382-chr4:833187..836148,2	MCF-7	breast:
32	chr4:767045..769488-chr4:820601..823147,2	K562	blood:
33	chr4:835693..839507-chr4:843140..845149,3	K562	blood:
34	chr4:848413..850023-chr4:852591..855386,3	K562	blood:
35	chr4:837032..839261-chr4:841910..844601,2	MCF-7	breast:
36	chr4:800740..802863-chr4:815216..816948,2	K562	blood:
37	chr4:837167..839761-chr4:843838..845758,2	K562	blood:
38	chr4:774284..777559-chr4:817781..820963,6	MCF-7	breast:
39	chr4:849056..851800-chr4:859991..861903,3	K562	blood:
40	chr4:841841..844172-chr4:851691..854143,3	K562	blood:
41	chr4:835499..837438-chr4:837585..839240,2	MCF-7	breast:
42	chr4:831253..832902-chr4:836853..838473,2	K562	blood:
43	chr4:820499..822225-chr4:975841..977924,2	K562	blood:
44	chr4:699605..701232-chr4:847515..849852,2	K562	blood:
45	chr4:829399..831025-chr4:842323..844372,2	MCF-7	breast:
46	chr4:846749..848551-chr4:850245..851895,3	K562	blood:
47	chr4:855613..858404-chr4:873095..876275,3	K562	blood:
48	chr4:814299..816163-chr4:965905..968513,2	MCF-7	breast:
49	chr4:841841..845277-chr4:851298..854143,3	K562	blood:
50	chr4:813382..814362-chr8:22941603..22942165,2	HCT-116	colon:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPLX1-1	chr4:830300-831012	ENSG00000260262.1
2	lnc-CPLX1-10	chr4:850179-850600	NONHSAT094624
3	lnc-CPLX1-10	chr4:849805-849945	NONHSAT094624

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GAK	hsa-miR-1	chr4:843294-843288
2	GAK	hsa-miR-1	chr4:843289-843310

Variant related genes	Relation type
ENSG00000260262	TF binding region
GAK	TF binding region
CPLX1	TF binding region
ENSG00000260262	CpG island
GAK	CpG island
CPLX1	CpG island
ENSG00000233799	chromatin interactions
ENSG00000173535	chromatin interactions
ENSG00000159692	chromatin interactions
ENSG00000145217	chromatin interactions
ENSG00000178950	chromatin interactions
ENSG00000196810	chromatin interactions
ENSG00000127419	chromatin interactions
ENSG00000260262	chromatin interactions
ENSG00000127418	chromatin interactions
ENSG00000185619	chromatin interactions
ENSG00000145214	chromatin interactions
ENSG00000168993	chromatin interactions
ENSG00000249592	chromatin interactions
ENSG00000127415	chromatin interactions

Extended variants
information (count: 2633 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2633 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11248042	chr4:812598-812599	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540500196	chr4:812603-812604	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs564776554	chr4:812612-812613	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs532126017	chr4:812623-812624	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs181556343	chr4:812634-812635	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs549497068	chr4:812636-812637	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs7687101	chr4:812679-812680	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs541805269	chr4:812716-812717	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs11248043	chr4:812753-812754	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs370005346	chr4:812861-812862	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs149026201	chr4:812874-812875	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs184058673	chr4:812878-812879	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs550419484	chr4:812879-812880	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs373362497	chr4:812940-812941	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs547266357	chr4:812978-812979	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs554743543	chr4:812981-812982	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs538979450	chr4:813012-813013	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs568825448	chr4:813065-813066	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs557058297	chr4:813099-813100	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs6816444	chr4:813126-813127	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs568978133	chr4:813176-813177	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs188042490	chr4:813179-813180	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs554372348	chr4:813203-813204	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs112906841	chr4:813205-813206	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs146867007	chr4:813232-813233	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs140713634	chr4:813237-813238	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs180854448	chr4:813243-813244	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs544198801	chr4:813244-813245	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs562585488	chr4:813252-813253	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs529849002	chr4:813253-813254	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs541923604	chr4:813299-813300	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs561368164	chr4:813304-813305	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs145822802	chr4:813314-813315	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs138401320	chr4:813315-813316	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs571860169	chr4:813349-813350	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs532389003	chr4:813363-813364	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs17165046	chr4:813393-813394	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	mRNA abundance
38	rs564058741	chr4:813403-813404	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs17165051	chr4:813428-813429	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs12504575	chr4:813438-813439	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs376912978	chr4:813439-813440	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs566559725	chr4:813444-813445	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs533942285	chr4:813445-813446	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs79822067	chr4:813450-813451	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs558601033	chr4:813481-813482	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs577032970	chr4:813576-813577	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs544501765	chr4:813630-813631	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs186101327	chr4:813652-813653	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs556222797	chr4:813663-813664	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs58372555	chr4:813689-813690	Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1226 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:789600-816800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr4:809400-817200	Weak transcription	Brain Angular Gyrus	brain
3	chr4:811600-813800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr4:813800-814400	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
5	chr4:814400-815800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:814800-815000	Bivalent Enhancer	Placenta	Placenta
7	chr4:815400-819200	Bivalent Enhancer	Fetal Brain Male	brain
8	chr4:815600-816000	Bivalent Enhancer	Brain Germinal Matrix	brain
9	chr4:815800-816000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:815800-816000	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
11	chr4:815800-816000	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
12	chr4:816000-816200	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
13	chr4:816000-817000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr4:816000-817200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
15	chr4:816200-816400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
16	chr4:816200-816800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr4:816200-817000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
18	chr4:816200-817000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
19	chr4:816600-816800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr4:816600-816800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:816600-816800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr4:816600-816800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr4:816800-817000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr4:816800-817000	Bivalent Enhancer	NH-A	brain
25	chr4:816800-817400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr4:816800-817600	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr4:816800-818400	Bivalent Enhancer	Brain Anterior Caudate	brain
28	chr4:817000-817200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr4:817000-817200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:817000-817600	Bivalent Enhancer	Fetal Brain Female	brain
31	chr4:817200-817400	Enhancers	Brain Angular Gyrus	brain
32	chr4:817200-817400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
33	chr4:817200-817600	Bivalent Enhancer	HMEC	breast
34	chr4:817200-818400	Bivalent Enhancer	Brain Germinal Matrix	brain
35	chr4:817200-818600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr4:817200-819800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
37	chr4:817200-819800	Bivalent Enhancer	Placenta	Placenta
38	chr4:817400-817600	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
39	chr4:817400-817800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr4:817600-817800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:817600-818600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:817600-818800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:817600-819200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:817800-818000	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
45	chr4:817800-818000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr4:817800-818000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr4:817800-818200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr4:817800-818200	Bivalent/Poised TSS	Fetal Brain Female	brain
49	chr4:817800-818200	Enhancers	Pancreas	Pancrea
50	chr4:817800-818400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland

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