Variant report

Variant	nsv1026157
Chromosome Location	chr4:189377762-189587590
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:654)
CpG islands
(count:1403)
Chromatin interactive
region (count:5)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:654 , 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	ARID3A	chr4:189499935-189500273	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:189455499-189455789	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:189527693-189528168	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:189456095-189456482	HepG2	liver:	n/a	n/a
5	BACH1	chr4:189580313-189580512	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr4:189527879-189528027	HepG2	liver:	n/a	n/a
7	BHLHE40	chr4:189539576-189539609	K562	blood:	n/a	n/a
8	BHLHE40	chr4:189456176-189456442	HepG2	liver:	n/a	n/a
9	BRCA1	chr4:189404735-189404847	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr4:189424045-189424347	HepG2	liver:	n/a	chr4:189424047-189424059 chr4:189424170-189424181
11	CEBPB	chr4:189551807-189551980	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:189533974-189534058	A549	lung:	n/a	n/a
13	CEBPB	chr4:189493631-189493895	A549	lung:	n/a	chr4:189493776-189493787
14	CEBPB	chr4:189516061-189516240	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:189514348-189514658	HepG2	liver:	n/a	chr4:189514490-189514501 chr4:189514359-189514372 chr4:189514489-189514500
16	CEBPB	chr4:189433899-189434105	HepG2	liver:	n/a	chr4:189433976-189433987
17	CEBPB	chr4:189514320-189514661	IMR90	lung:	n/a	chr4:189514490-189514501 chr4:189514359-189514372 chr4:189514489-189514500
18	CEBPB	chr4:189581873-189582175	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:189517237-189517434	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:189584445-189584963	A549	lung:	n/a	n/a
21	CEBPB	chr4:189437762-189437878	HepG2	liver:	n/a	chr4:189437793-189437804
22	CEBPB	chr4:189493638-189493884	IMR90	lung:	n/a	chr4:189493776-189493787
23	CEBPB	chr4:189495393-189495495	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:189584550-189585193	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:189549147-189549347	A549	lung:	n/a	n/a
26	CEBPB	chr4:189493605-189493919	HepG2	liver:	n/a	chr4:189493776-189493787
27	CEBPB	chr4:189456046-189456370	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:189514350-189514601	A549	lung:	n/a	chr4:189514490-189514501 chr4:189514359-189514372 chr4:189514489-189514500
29	CEBPB	chr4:189424052-189424344	IMR90	lung:	n/a	chr4:189424170-189424181
30	CEBPB	chr4:189560668-189561000	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:189380428-189380719	HepG2	liver:	n/a	chr4:189380547-189380558
32	CEBPB	chr4:189584573-189585174	A549	lung:	n/a	n/a
33	CEBPB	chr4:189584550-189585245	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:189385467-189385594	IMR90	lung:	n/a	n/a
35	CEBPB	chr4:189527875-189528128	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:189560668-189560998	IMR90	lung:	n/a	n/a
37	CEBPB	chr4:189549174-189549466	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:189560699-189560954	A549	lung:	n/a	n/a
39	CEBPB	chr4:189560714-189560941	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr4:189549105-189549301	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:189584536-189584848	A549	lung:	n/a	n/a
42	CREB1	chr4:189456053-189456493	HepG2	liver:	n/a	n/a
43	CTCF	chr4:189549222-189549253	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr4:189379680-189379830	K562	blood:	n/a	chr4:189379740-189379761 chr4:189379751-189379760 chr4:189379746-189379762 chr4:189379745-189379763
45	CTCF	chr4:189580311-189580553	H1-hESC	embryonic stem cell:	n/a	chr4:189580407-189580420 chr4:189580435-189580443 chr4:189580455-189580468
46	CTCF	chr4:189580220-189580370	HVMF	connective:	n/a	n/a
47	CTCF	chr4:189379620-189379770	WERI-Rb-1	eye:	n/a	chr4:189379740-189379761 chr4:189379751-189379760 chr4:189379746-189379762 chr4:189379745-189379763
48	CTCF	chr4:189379680-189379830	HCT-116	colon:	n/a	chr4:189379740-189379761 chr4:189379751-189379760 chr4:189379746-189379762 chr4:189379745-189379763
49	CTCF	chr4:189549150-189549295	HepG2	liver:	n/a	n/a
50	CTCF	chr4:189580192-189580563	H1-hESC	embryonic stem cell:	n/a	chr4:189580407-189580420 chr4:189580435-189580443 chr4:189580455-189580468

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:189583617-189583667	HEK293	kidney:	embryo
2	chr4:189476745-189476795	HAEpiC	amniotic membrane:	n/a
3	chr4:189433040-189433090	NHDF-neo	bronchial:	n/a
4	chr4:189476613-189476663	K562	blood:	n/a
5	chr4:189552622-189552672	PrEC	prostate:	n/a
6	chr4:189554990-189555040	HAEpiC	amniotic membrane:	n/a
7	chr4:189552339-189552389	HCM	heart:	n/a
8	chr4:189580633-189580683	BE2_C	brain:	n/a
9	chr4:189572647-189572697	PFSK-1	brain:	n/a
10	chr4:189552622-189552672	HIPEpiC	eye:	n/a
11	chr4:189552677-189552727	HepG2	liver:	n/a
12	chr4:189580798-189580848	HUVEC	blood vessel:	n/a
13	chr4:189583617-189583667	AG09319	gingival:	n/a
14	chr4:189485260-189485310	AG04449	skin:	fetal
15	chr4:189541174-189541224	GM12891	blood:	n/a
16	chr4:189580633-189580683	HIPEpiC	eye:	n/a
17	chr4:189551752-189551802	H1-hESC	embryonic stem cell:	embryo
18	chr4:189580596-189580646	CMK	blood:	n/a
19	chr4:189554990-189555040	HCT-116	colon:	n/a
20	chr4:189552386-189552436	IMR90	lung:	fetal
21	chr4:189395410-189395460	AG10803	skin:	n/a
22	chr4:189551752-189551802	HL-60	blood:	n/a
23	chr4:189554990-189555040	AG04450	lung:	fetal
24	chr4:189548707-189548757	AG09319	gingival:	n/a
25	chr4:189552386-189552436	SK-N-SH_RA	brain:	n/a
26	chr4:189552386-189552436	HEK293	kidney:	embryo
27	chr4:189541174-189541224	GM12892	blood:	n/a
28	chr4:189541174-189541224	NB4	blood:	n/a
29	chr4:189552386-189552436	MCF-7	breast:	n/a
30	chr4:189476745-189476795	HIPEpiC	eye:	n/a
31	chr4:189553390-189553440	NT2-D1	testis:	n/a
32	chr4:189485260-189485310	SK-N-SH_RA	brain:	n/a
33	chr4:189485260-189485310	HCPEpiC	choroid plexus:	n/a
34	chr4:189433040-189433090	AG04449	skin:	fetal
35	chr4:189552677-189552727	MCF-7	breast:	n/a
36	chr4:189580798-189580848	NH-A	brain:	n/a
37	chr4:189578842-189578892	HRCEpiC	kidney:	n/a
38	chr4:189577711-189577761	ovcar-3	ovarian:	n/a
39	chr4:189580507-189580557	HepG2	liver:	n/a
40	chr4:189476613-189476663	SK-N-MC	brain:	n/a
41	chr4:189551752-189551802	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:189552622-189552672	NHBE	bronchial:	n/a
43	chr4:189580596-189580646	HEEpiC	esophagus:	n/a
44	chr4:189580507-189580557	GM19239	blood:	n/a
45	chr4:189548707-189548757	HRCEpiC	kidney:	n/a
46	chr4:189580596-189580646	AG04450	lung:	fetal
47	chr4:189552386-189552436	NHBE	bronchial:	n/a
48	chr4:189552339-189552389	LNCaP	prostate:	n/a
49	chr4:189476745-189476795	CMK	blood:	n/a
50	chr4:189476745-189476795	T-47D	breast:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:189510385..189513322-chr4:189513349..189516296,2	MCF-7	breast:
2	chr4:189390737..189392481-chr4:189394126..189396910,2	K562	blood:
3	chr4:189390737..189392481-chr4:189394126..189396910,2	K562	blood:
4	chr4:189510385..189513322-chr4:189513349..189516296,2	MCF-7	breast:
5	chr4:189427438..189430236-chr6:107435359..107438052,2	MCF-7	breast:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
2	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
3	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099745
4	lnc-TRIML1-3	chr4:189398792-189399066	NONHSAT099746
5	lnc-TRIML1-3	chr4:189397852-189397910	NONHSAT099746
6	lnc-TRIML1-3	chr4:189377818-189377916	NONHSAT099745
7	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
8	lnc-TRIML1-3	chr4:189377846-189377916	XLOC_003834
9	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
10	lnc-TRIML1-3	chr4:189377818-189377916	ENSG00000249378
11	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
12	lnc-TRIML1-3	chr4:189377818-189377916	NONHSAT099746
13	lnc-TRIML1-3	chr4:189457889-189459706	XLOC_003834
14	lnc-TRIML1-3	chr4:189406933-189407028	XLOC_003834
15	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
16	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
17	lnc-TRIML1-3	chr4:189398906-189399066	NONHSAT099749
18	lnc-TRIML1-3	chr4:189406933-189407076	NONHSAT099746
19	lnc-TRIML1-3	chr4:189522922-189523025	NONHSAT099749
20	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
21	lnc-TRIML1-3	chr4:189522922-189523062	NONHSAT099745
22	lnc-TRIML1-3	chr4:189406933-189407011	XLOC_003834
23	lnc-TRIML1-3	chr4:189398792-189399066	XLOC_003834
24	lnc-TRIML1-3	chr4:189397852-189397910	NONHSAT099745
25	lnc-TRIML1-3	chr4:189522922-189523060	XLOC_003834
26	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
27	lnc-TRIML1-3	chr4:189397852-189397910	ENSG00000249378
28	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
29	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
30	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099749
31	lnc-TRIML1-3	chr4:189522922-189523062	ENSG00000249378
32	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
33	lnc-TRIML1-3	chr4:189398792-189399066	ENSG00000249378
34	lnc-TRIML1-3	chr4:189397852-189397910	ENSG00000249378

No data

Variant related genes	Relation type
LINC01060	TF binding region
ENSG00000250523	TF binding region
LINC01060	CpG island
ENSG00000250523	CpG island
ENSG00000178409	chromatin interactions
KCNK1	miRNA target sites
PRNP	miRNA target sites
SHCBP1	miRNA target sites
TAPBP	miRNA target sites
RASSF2	miRNA target sites
BMPR2	miRNA target sites
FAM104A	miRNA target sites
PFN2	miRNA target sites

Extended variants
information (count: 10115 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:10115 , 50 per page) page: 1 2 3 4 5 6 7 ... 203

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182517286	chr4:189377814-189377815	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368914424	chr4:189377854-189377855	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs568558073	chr4:189377908-189377909	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs377635	chr4:189377991-189377992	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs562122175	chr4:189378056-189378057	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527522283	chr4:189378064-189378065	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371416778	chr4:189378100-189378101	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549440986	chr4:189378126-189378127	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200114551	chr4:189378186-189378187	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552956100	chr4:189378203-189378204	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs142661007	chr4:189378234-189378235	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564249093	chr4:189378272-189378273	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374902153	chr4:189378341-189378342	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56823981	chr4:189378342-189378343	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368614356	chr4:189378343-189378344	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553976222	chr4:189378353-189378354	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565919701	chr4:189378379-189378380	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569639046	chr4:189378394-189378395	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs380420	chr4:189378428-189378429	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs548712127	chr4:189378430-189378431	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565436456	chr4:189378452-189378453	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534151517	chr4:189378466-189378467	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547569700	chr4:189378492-189378493	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187518872	chr4:189378503-189378504	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192035026	chr4:189378548-189378549	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556531228	chr4:189378553-189378554	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144801324	chr4:189378590-189378591	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs398688	chr4:189378593-189378594	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs185058174	chr4:189378630-189378631	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185565954	chr4:189378632-189378633	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541261750	chr4:189378648-189378649	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147922517	chr4:189378654-189378655	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140559089	chr4:189378655-189378656	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150418417	chr4:189378656-189378657	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138220921	chr4:189378677-189378678	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528903366	chr4:189378681-189378682	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548548216	chr4:189378728-189378729	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs435948	chr4:189378853-189378854	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs189387017	chr4:189378914-189378915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530849187	chr4:189378915-189378916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551035401	chr4:189378918-189378919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571026203	chr4:189378929-189378930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539603624	chr4:189378949-189378950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552132868	chr4:189378962-189378963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116784115	chr4:189378966-189378967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570246960	chr4:189378992-189378993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564471974	chr4:189379016-189379017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs451526	chr4:189379097-189379098	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs555781672	chr4:189379114-189379115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572434619	chr4:189379117-189379118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Cognitive impairment	21505072	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Epilepsy	21635232	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:189366000-189415600	Weak transcription	Osteobl	bone
2	chr4:189371200-189378400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:189374200-189378200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:189374600-189377800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:189374600-189380600	Weak transcription	Brain Germinal Matrix	brain
6	chr4:189375600-189384800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
7	chr4:189375800-189377800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr4:189376000-189378600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:189376200-189379400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr4:189376400-189380600	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr4:189376800-189378400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:189376800-189416200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:189377000-189387000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:189377200-189384000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr4:189377600-189378000	Enhancers	A549	lung
16	chr4:189377600-189381400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr4:189377800-189378000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr4:189377800-189378000	Enhancers	HepG2	liver
19	chr4:189377800-189378600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr4:189377800-189384000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:189378200-189378400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:189378400-189378600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:189378400-189378600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr4:189378600-189378800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr4:189378600-189378800	Enhancers	H9 Cell Line	embryonic stem cell
26	chr4:189378600-189378800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:189378600-189378800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr4:189378600-189379400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr4:189378800-189379400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:189379200-189379400	Enhancers	Fetal Brain Male	brain
31	chr4:189379400-189379600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr4:189379400-189379600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr4:189379400-189380000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:189379600-189380800	Weak transcription	Fetal Brain Male	brain
35	chr4:189380000-189385000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr4:189380600-189381200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr4:189380600-189381200	Enhancers	Brain Germinal Matrix	brain
38	chr4:189380800-189381400	Enhancers	Fetal Brain Male	brain
39	chr4:189381400-189381800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
40	chr4:189381800-189383800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr4:189384000-189384400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:189384200-189385000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr4:189384400-189385000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr4:189384600-189385200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
45	chr4:189384800-189388000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr4:189385000-189385400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr4:189385000-189385600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:189385400-189415800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:189385600-189394800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr4:189386800-189387000	Enhancers	Brain Germinal Matrix	brain

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