Variant report

Variant	nsv525719
Chromosome Location	chr4:187411297-187521037
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1133)
CpG islands
(count:3299)
Chromatin interactive
region (count:52)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1133 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187508528-187509011	K562	blood:	n/a	n/a
2	ARID3A	chr4:187508653-187508797	HepG2	liver:	n/a	n/a
3	ATF1	chr4:187421894-187422344	K562	blood:	n/a	n/a
4	ATF1	chr4:187420491-187420916	K562	blood:	n/a	n/a
5	ATF3	chr4:187421950-187422165	K562	blood:	n/a	n/a
6	BACH1	chr4:187476293-187476945	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:187487400-187487517	K562	blood:	n/a	n/a
8	BACH1	chr4:187459112-187459482	K562	blood:	n/a	n/a
9	BACH1	chr4:187487248-187487849	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:187467939-187468156	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:187422808-187423008	K562	blood:	n/a	n/a
12	BHLHE40	chr4:187491598-187491621	K562	blood:	n/a	n/a
13	BHLHE40	chr4:187421756-187422525	K562	blood:	n/a	n/a
14	BHLHE40	chr4:187442068-187442244	K562	blood:	n/a	n/a
15	BHLHE40	chr4:187475724-187475895	HepG2	liver:	n/a	n/a
16	BHLHE40	chr4:187475701-187476008	K562	blood:	n/a	n/a
17	BHLHE40	chr4:187458935-187459776	K562	blood:	n/a	n/a
18	BRCA1	chr4:187511473-187511598	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr4:187520434-187520442	HepG2	liver:	n/a	n/a
20	BRCA1	chr4:187475689-187475898	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr4:187459280-187459848	K562	blood:	n/a	n/a
22	CBX3	chr4:187503291-187503563	K562	blood:	n/a	n/a
23	CBX3	chr4:187503228-187503597	K562	blood:	n/a	n/a
24	CBX3	chr4:187421797-187422410	K562	blood:	n/a	n/a
25	CBX3	chr4:187458876-187459841	K562	blood:	n/a	n/a
26	CBX3	chr4:187411097-187411357	K562	blood:	n/a	n/a
27	CBX3	chr4:187457484-187457861	K562	blood:	n/a	n/a
28	CBX3	chr4:187421712-187422622	K562	blood:	n/a	n/a
29	CCNT2	chr4:187421964-187422263	K562	blood:	n/a	n/a
30	CCNT2	chr4:187459142-187459761	K562	blood:	n/a	n/a
31	CEBPB	chr4:187463059-187463241	K562	blood:	n/a	chr4:187463129-187463140
32	CEBPB	chr4:187506056-187506356	HepG2	liver:	n/a	chr4:187506188-187506199
33	CEBPB	chr4:187483137-187483363	HepG2	liver:	n/a	chr4:187483253-187483264
34	CEBPB	chr4:187432537-187432726	K562	blood:	n/a	chr4:187432667-187432678
35	CEBPB	chr4:187506068-187506341	A549	lung:	n/a	chr4:187506188-187506199
36	CEBPB	chr4:187432638-187432777	HepG2	liver:	n/a	chr4:187432667-187432678
37	CEBPB	chr4:187460389-187460582	K562	blood:	n/a	chr4:187460425-187460436
38	CEBPB	chr4:187473671-187473945	HepG2	liver:	n/a	n/a
39	CEBPB	chr4:187460400-187460586	A549	lung:	n/a	chr4:187460425-187460436
40	CEBPB	chr4:187476382-187476666	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:187459108-187459678	K562	blood:	n/a	n/a
42	CEBPB	chr4:187509008-187509087	A549	lung:	n/a	chr4:187509020-187509031
43	CEBPB	chr4:187474913-187475079	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr4:187462983-187463293	K562	blood:	n/a	chr4:187463129-187463140
45	CEBPB	chr4:187457597-187457841	H1-hESC	embryonic stem cell:	n/a	chr4:187457709-187457722
46	CEBPB	chr4:187463000-187463285	IMR90	lung:	n/a	chr4:187463129-187463140
47	CEBPB	chr4:187420609-187420949	K562	blood:	n/a	n/a
48	CEBPB	chr4:187478309-187478548	HepG2	liver:	n/a	chr4:187478413-187478424
49	CEBPB	chr4:187501408-187501628	HepG2	liver:	n/a	chr4:187501507-187501518
50	CEBPB	chr4:187481732-187481922	IMR90	lung:	n/a	n/a

(count:3299 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187475891-187475941	ovcar-3	ovarian:	n/a
2	chr4:187491428-187491478	U87	brain:	n/a
3	chr4:187475891-187475941	GM12878	blood:	n/a
4	chr4:187476326-187476376	NT2-D1	testis:	n/a
5	chr4:187455559-187455609	SK-N-MC	brain:	n/a
6	chr4:187475891-187475941	ovcar-3	ovarian:	n/a
7	chr4:187491428-187491478	U87	brain:	n/a
8	chr4:187475891-187475941	GM12878	blood:	n/a
9	chr4:187476326-187476376	NT2-D1	testis:	n/a
10	chr4:187455559-187455609	SK-N-MC	brain:	n/a
11	chr4:187422119-187422169	U87	brain:	n/a
12	chr4:187476608-187476658	HAEpiC	amniotic membrane:	n/a
13	chr4:187422895-187422945	GM12892	blood:	n/a
14	chr4:187422114-187422164	Jurkat	blood:	n/a
15	chr4:187509785-187509835	AG10803	skin:	n/a
16	chr4:187473490-187473540	HEK293	kidney:	embryo
17	chr4:187517939-187517989	AoSMC	blood vessel:	n/a
18	chr4:187510183-187510233	ECC-1	luminal epithelium:	n/a
19	chr4:187473490-187473540	HL-60	blood:	n/a
20	chr4:187509603-187509653	ProgFib	skin:	n/a
21	chr4:187459415-187459465	IMR90	lung:	fetal
22	chr4:187475669-187475719	HepG2	liver:	n/a
23	chr4:187517939-187517989	MCF-7	breast:	n/a
24	chr4:187422341-187422391	AG09309	skin:	n/a
25	chr4:187491428-187491478	HEK293	kidney:	embryo
26	chr4:187422895-187422945	MCF10A-Er-Src	breast:	n/a
27	chr4:187499458-187499508	NHDF-neo	bronchial:	n/a
28	chr4:187455304-187455354	AG10803	skin:	n/a
29	chr4:187475891-187475941	LNCaP	prostate:	n/a
30	chr4:187491428-187491478	ovcar-3	ovarian:	n/a
31	chr4:187475891-187475941	AG10803	skin:	n/a
32	chr4:187422341-187422391	HMEC	breast:	n/a
33	chr4:187475669-187475719	HCM	heart:	n/a
34	chr4:187476543-187476593	HCF	heart:	n/a
35	chr4:187476608-187476658	BE2_C	brain:	n/a
36	chr4:187422895-187422945	HEEpiC	esophagus:	n/a
37	chr4:187473490-187473540	HepG2	liver:	n/a
38	chr4:187507476-187507526	AG09319	gingival:	n/a
39	chr4:187455830-187455880	HEK293	kidney:	embryo
40	chr4:187476837-187476887	GM12892	blood:	n/a
41	chr4:187475891-187475941	H1-hESC	embryonic stem cell:	embryo
42	chr4:187476608-187476658	AG04449	skin:	fetal
43	chr4:187510183-187510233	IMR90	lung:	fetal
44	chr4:187422895-187422945	HRPEpiC	eye:	n/a
45	chr4:187422895-187422945	RPTEC	kidney:	n/a
46	chr4:187476703-187476753	AG04449	skin:	fetal
47	chr4:187477065-187477115	HNPCEpiC	eye:	n/a
48	chr4:187459449-187459499	HEK293	kidney:	embryo
49	chr4:187422005-187422055	AG09309	skin:	n/a
50	chr4:187459415-187459465	MCF10A-Er-Src	breast:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:187507521..187509715-chr4:187510958..187513013,2	K562	blood:
2	chr4:187500135..187502809-chr4:187503552..187505975,2	MCF-7	breast:
3	chr4:187448150..187450256-chr4:187458216..187460408,2	K562	blood:
4	chr4:187516733..187519515-chr4:187519671..187523118,3	K562	blood:
5	chr4:187458318..187460106-chr4:187464822..187466767,2	K562	blood:
6	chr4:187422105..187424397-chr4:187432409..187434171,2	K562	blood:
7	chr11:62608697..62609221-chr4:187449246..187449766,2	Hela-S3	cervix:
8	chr4:187450978..187452522-chr4:187454014..187456071,2	K562	blood:
9	chr4:187425444..187427113-chr4:187432314..187434673,2	K562	blood:
10	chr17:41464198..41466205-chr4:187449246..187450766,2	MCF-7	breast:
11	chr4:187500880..187503976-chr4:187505788..187508799,3	K562	blood:
12	chr4:187458073..187459669-chr4:187489557..187491261,2	K562	blood:
13	chr4:187420835..187422454-chr4:187508241..187510216,2	K562	blood:
14	chr4:187414357..187416175-chr4:187420876..187423477,2	MCF-7	breast:
15	chr4:187516733..187519515-chr4:187519671..187523118,3	K562	blood:
16	chr4:187487952..187490198-chr4:187492658..187494283,2	K562	blood:
17	chr4:187500880..187503976-chr4:187505788..187508799,3	K562	blood:
18	chr4:187121686..187123375-chr4:187456206..187458817,2	K562	blood:
19	chr4:187425444..187427113-chr4:187432314..187434673,2	K562	blood:
20	chr4:187458073..187459669-chr4:187489557..187491261,2	K562	blood:
21	chr4:187421353..187422936-chr4:187501423..187503458,2	K562	blood:
22	chr4:187216645..187219482-chr4:187510341..187512353,2	K562	blood:
23	chr4:187448150..187450256-chr4:187458216..187460408,2	K562	blood:
24	chr4:187394154..187394722-chr4:187508267..187509221,2	K562	blood:
25	chr4:187424618..187426617-chr4:187440828..187442815,2	MCF-7	breast:
26	chr4:187463972..187466236-chr4:187470397..187471997,2	K562	blood:
27	chr4:187500135..187502809-chr4:187503552..187505975,2	MCF-7	breast:
28	chr4:187419835..187422222-chr4:187436024..187437802,2	K562	blood:
29	chr4:187487952..187490198-chr4:187492658..187494283,2	K562	blood:
30	chr4:187447764..187449411-chr4:187453319..187455061,2	K562	blood:
31	chr4:187464736..187466287-chr4:187469928..187471897,2	K562	blood:
32	chr4:187468016..187470329-chr4:187475852..187477420,2	MCF-7	breast:
33	chr4:187393785..187394637-chr4:187475328..187475950,2	MCF-7	breast:
34	chr4:187454593..187456201-chr4:187457410..187459187,2	K562	blood:
35	chr4:187217859..187218927-chr4:187508295..187509239,10	K562	blood:
36	chr4:187454593..187456201-chr4:187457410..187459187,2	K562	blood:
37	chr4:187463972..187466236-chr4:187470397..187471997,2	K562	blood:
38	chr4:187512892..187514461-chr4:187519314..187520852,2	MCF-7	breast:
39	chr4:187418143..187425298-chr4:187427395..187434877,12	K562	blood:
40	chr4:187450978..187452522-chr4:187454014..187456071,2	K562	blood:
41	chr4:187477233..187480575-chr4:187481254..187484237,4	K562	blood:
42	chr4:187447764..187449411-chr4:187453319..187455061,2	K562	blood:
43	chr4:187449413..187452478-chr4:187454571..187457368,4	K562	blood:
44	chr4:187477233..187480575-chr4:187481254..187484237,4	K562	blood:
45	chr4:187424618..187426617-chr4:187440828..187442815,2	MCF-7	breast:
46	chr4:187421685..187424267-chr4:187426709..187429265,2	MCF-7	breast:
47	chr4:187394348..187396815-chr4:187456742..187459587,2	K562	blood:
48	chr4:187458318..187460106-chr4:187464822..187466767,2	K562	blood:
49	chr4:187507521..187509715-chr4:187510958..187513013,2	K562	blood:
50	chr4:187464736..187466287-chr4:187469928..187471897,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTNR1A-1	chr4:187421999-187422151	ENSG00000251165.1
2	lnc-F11-8	chr4:187500098-187503339	NONHSAT099666
3	lnc-MTNR1A-1	chr4:187421999-187422212	NONHSAT099658
4	lnc-MTNR1A-1	chr4:187421999-187422151	ENSG00000251165.1

No data

Variant related genes	Relation type
F11-AS1	TF binding region
RNU6-1055P	TF binding region
ENSG00000272297	TF binding region
FAT1	TF binding region
MTNR1A	TF binding region
F11-AS1	CpG island
RNU6-1055P	CpG island
ENSG00000272297	CpG island
FAT1	CpG island
MTNR1A	CpG island
ENSG00000168412	chromatin interactions
ENSG00000083857	chromatin interactions
ENSG00000212387	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000272297	chromatin interactions
ENSG00000251165	chromatin interactions

Extended variants
information (count: 4370 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4370 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11723176	chr4:187411297-187411298	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553056802	chr4:187411320-187411321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112921583	chr4:187411321-187411322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77838713	chr4:187411331-187411332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74663810	chr4:187411332-187411333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532345729	chr4:187411343-187411344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527478989	chr4:187411348-187411349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188857577	chr4:187411359-187411360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552140456	chr4:187411402-187411403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527685376	chr4:187411416-187411417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193117424	chr4:187411453-187411454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143718936	chr4:187411476-187411477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6831601	chr4:187411505-187411506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs536735073	chr4:187411506-187411507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs55641921	chr4:187411555-187411556	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs56031231	chr4:187411559-187411560	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184355140	chr4:187411600-187411601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6854525	chr4:187411620-187411621	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs115883422	chr4:187411673-187411674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552104303	chr4:187411674-187411675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189292639	chr4:187411677-187411678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7696757	chr4:187411684-187411685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554138868	chr4:187411698-187411699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565878887	chr4:187411759-187411760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574133335	chr4:187411782-187411783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs58064264	chr4:187411788-187411789	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs560196368	chr4:187411793-187411794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576932440	chr4:187411798-187411799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374151496	chr4:187411799-187411800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs921453	chr4:187411802-187411803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs80196405	chr4:187411824-187411825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181147991	chr4:187411841-187411842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76324095	chr4:187411852-187411853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs28420630	chr4:187411864-187411865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561226305	chr4:187411870-187411871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530122696	chr4:187411876-187411877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547091172	chr4:187411897-187411898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566973372	chr4:187411908-187411909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538792897	chr4:187411912-187411913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73022759	chr4:187411928-187411929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569395439	chr4:187412035-187412036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs80216625	chr4:187412040-187412041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554850174	chr4:187412117-187412118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574047148	chr4:187412159-187412160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533563773	chr4:187412172-187412173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553551383	chr4:187412207-187412208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs55716910	chr4:187412250-187412251	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559233944	chr4:187412251-187412252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs713223	chr4:187412263-187412264	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs562694460	chr4:187412264-187412265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
XY gonadal dysgenesis	20685758	CNVD

Chromatin state (count:942 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187395400-187413600	Weak transcription	K562	blood
2	chr4:187413600-187415600	Strong transcription	K562	blood
3	chr4:187415600-187416000	ZNF genes & repeats	K562	blood
4	chr4:187416000-187418600	Weak transcription	K562	blood
5	chr4:187419000-187420200	Weak transcription	K562	blood
6	chr4:187419800-187421000	Enhancers	Fetal Brain Male	brain
7	chr4:187420200-187420400	Flanking Active TSS	K562	blood
8	chr4:187420400-187420600	Active TSS	K562	blood
9	chr4:187420600-187420800	Flanking Active TSS	K562	blood
10	chr4:187420800-187421000	Active TSS	K562	blood
11	chr4:187421000-187421200	Flanking Active TSS	K562	blood
12	chr4:187421000-187433400	Weak transcription	Fetal Brain Male	brain
13	chr4:187421200-187422000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:187421200-187422600	Active TSS	K562	blood
15	chr4:187421800-187422600	Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr4:187422000-187422200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:187422000-187422400	Enhancers	H1 Cell Line	embryonic stem cell
18	chr4:187422000-187422400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr4:187422000-187422600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:187422000-187422600	Enhancers	Fetal Brain Female	brain
21	chr4:187422000-187423000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:187422200-187422400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:187422200-187422600	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr4:187422400-187423400	Enhancers	Fetal Intestine Large	intestine
25	chr4:187422600-187422800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
26	chr4:187422600-187423200	Flanking Active TSS	K562	blood
27	chr4:187422600-187423400	Enhancers	Fetal Intestine Small	intestine
28	chr4:187423000-187437400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr4:187423200-187423800	Enhancers	K562	blood
30	chr4:187423400-187423800	Weak transcription	Fetal Intestine Small	intestine
31	chr4:187423800-187424200	Enhancers	Fetal Intestine Small	intestine
32	chr4:187425200-187426000	Enhancers	Fetal Stomach	stomach
33	chr4:187432200-187432400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr4:187432600-187432800	Flanking Bivalent TSS/Enh	K562	blood
35	chr4:187432800-187433000	Bivalent Enhancer	K562	blood
36	chr4:187437400-187437800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:187437800-187442000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:187441800-187442000	Bivalent/Poised TSS	K562	blood
39	chr4:187442000-187442200	Flanking Bivalent TSS/Enh	K562	blood
40	chr4:187442000-187442400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:187442200-187442600	Active TSS	Spleen	Spleen
42	chr4:187442200-187442600	Bivalent Enhancer	K562	blood
43	chr4:187442400-187442800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr4:187452800-187455200	Weak transcription	Pancreas	Pancrea
45	chr4:187454200-187458800	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr4:187454600-187457600	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr4:187455200-187455800	Strong transcription	Pancreas	Pancrea
48	chr4:187455400-187455600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr4:187455600-187468400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:187455800-187459400	Weak transcription	Pancreas	Pancrea

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