Variant report

Variant	nsv879848
Chromosome Location	chr4:120408931-120433807
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:369)
CpG islands
(count:184)
Chromatin interactive
region (count:12)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:120422798-120423435	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:120425516-120426323	HepG2	liver:	n/a	n/a
3	BHLHE40	chr4:120433767-120433871	K562	blood:	n/a	n/a
4	CEBPB	chr4:120427610-120427828	IMR90	lung:	n/a	n/a
5	CEBPB	chr4:120423072-120423114	HepG2	liver:	n/a	n/a
6	CEBPB	chr4:120430181-120430494	IMR90	lung:	n/a	n/a
7	CEBPB	chr4:120431841-120432178	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:120419686-120420123	IMR90	lung:	n/a	n/a
9	CTCF	chr4:120411640-120411790	BJ	skin:	n/a	n/a
10	CTCF	chr4:120411660-120411810	GM12864	blood:	n/a	n/a
11	CTCF	chr4:120411680-120411830	HCM	heart:	n/a	n/a
12	CTCF	chr4:120414760-120414910	AG09319	gingival:	n/a	chr4:120414761-120414779
13	CTCF	chr4:120411660-120411810	WI-38	lung:	n/a	n/a
14	CTCF	chr4:120411581-120411814	MCF-7	breast:	n/a	n/a
15	CTCF	chr4:120414720-120414870	HMEC	breast:	n/a	chr4:120414756-120414777 chr4:120414761-120414779
16	CTCF	chr4:120411640-120411790	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr4:120414640-120414930	AG09319	gingival:	n/a	chr4:120414756-120414777 chr4:120414761-120414779
18	CTCF	chr4:120414723-120414859	GM12878	blood:	n/a	chr4:120414756-120414777 chr4:120414761-120414779
19	CTCF	chr4:120411680-120411830	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr4:120411620-120411770	AG09319	gingival:	n/a	n/a
21	CTCF	chr4:120411562-120411778	HepG2	liver:	n/a	n/a
22	CTCF	chr4:120411500-120411650	HFF	foreskin:	n/a	n/a
23	CTCF	chr4:120411560-120411710	BE2_C	brain:	n/a	n/a
24	CTCF	chr4:120411660-120411810	Caco-2	colon:	n/a	n/a
25	CTCF	chr4:120414640-120414790	HCFaa	heart:	n/a	chr4:120414756-120414777 chr4:120414761-120414779
26	CTCF	chr4:120414640-120414790	HEEpiC	esophagus:	n/a	chr4:120414756-120414777 chr4:120414761-120414779
27	CTCF	chr4:120411480-120411630	HA-sp	spinal cord:	n/a	n/a
28	CTCF	chr4:120411640-120411790	GM12865	blood:	n/a	n/a
29	CTCF	chr4:120411640-120411790	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr4:120411549-120411827	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:120411649-120411767	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr4:120411582-120411784	K562	blood:	n/a	n/a
33	CTCF	chr4:120411640-120411790	HPF	lung:	n/a	n/a
34	CTCF	chr4:120415060-120415210	HPF	lung:	n/a	n/a
35	CTCF	chr4:120414714-120414843	Hela-S3	cervix:	n/a	chr4:120414756-120414777 chr4:120414761-120414779
36	CTCF	chr4:120411640-120411790	HMF	breast:	n/a	n/a
37	CTCF	chr4:120411600-120411750	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr4:120411580-120411730	SAEC	small airway:	n/a	n/a
39	CTCF	chr4:120414880-120415030	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr4:120414920-120414925	Medullo	brain:	n/a	n/a
41	CTCF	chr4:120414680-120414830	HBMEC	blood vessel:	n/a	chr4:120414756-120414777 chr4:120414761-120414779
42	CTCF	chr4:120411592-120411802	Medullo	brain:	n/a	n/a
43	CTCF	chr4:120414718-120414828	Pancreas_OC	pancreas:	n/a	chr4:120414756-120414777 chr4:120414761-120414779
44	CTCF	chr4:120411627-120411742	LNCaP	prostate:	n/a	n/a
45	CTCF	chr4:120411640-120411790	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr4:120411600-120411750	NHEK	skin:	n/a	n/a
47	CTCF	chr4:120414800-120414950	RPTEC	kidney:	n/a	n/a
48	CTCF	chr4:120411640-120411790	GM12873	blood:	n/a	n/a
49	CTCF	chr4:120411600-120411750	GM12875	blood:	n/a	n/a
50	CTCF	chr4:120414680-120414830	HCPEpiC	choroid plexus:	n/a	chr4:120414756-120414777 chr4:120414761-120414779

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120419485-120419535	HL-60	blood:	n/a
2	chr4:120419485-120419535	HL-60	blood:	n/a
3	chr4:120428634-120428684	T-47D	breast:	n/a
4	chr4:120428634-120428684	U87	brain:	n/a
5	chr4:120419485-120419535	HCT-116	colon:	n/a
6	chr4:120433619-120433669	ProgFib	skin:	n/a
7	chr4:120419485-120419535	NHDF-neo	bronchial:	n/a
8	chr4:120433619-120433669	SK-N-MC	brain:	n/a
9	chr4:120419485-120419535	AG09319	gingival:	n/a
10	chr4:120433619-120433669	HAEpiC	amniotic membrane:	n/a
11	chr4:120419485-120419535	ProgFib	skin:	n/a
12	chr4:120428634-120428684	HEEpiC	esophagus:	n/a
13	chr4:120433619-120433669	BE2_C	brain:	n/a
14	chr4:120433619-120433669	HIPEpiC	eye:	n/a
15	chr4:120419485-120419535	HRPEpiC	eye:	n/a
16	chr4:120433619-120433669	ovcar-3	ovarian:	n/a
17	chr4:120428634-120428684	AG09309	skin:	n/a
18	chr4:120433619-120433669	PrEC	prostate:	n/a
19	chr4:120428634-120428684	HCPEpiC	choroid plexus:	n/a
20	chr4:120428634-120428684	HEK293	kidney:	embryo
21	chr4:120428634-120428684	AoSMC	blood vessel:	n/a
22	chr4:120419485-120419535	MCF10A-Er-Src	breast:	n/a
23	chr4:120419485-120419535	HIPEpiC	eye:	n/a
24	chr4:120419485-120419535	GM12891	blood:	n/a
25	chr4:120433619-120433669	K562	blood:	n/a
26	chr4:120419485-120419535	NB4	blood:	n/a
27	chr4:120419485-120419535	IMR90	lung:	fetal
28	chr4:120428634-120428684	CMK	blood:	n/a
29	chr4:120419485-120419535	HPAEpiC	pulmonary alveolar:	n/a
30	chr4:120428634-120428684	SK-N-SH	brain:	n/a
31	chr4:120428634-120428684	IMR90	lung:	fetal
32	chr4:120428634-120428684	GM19239	blood:	n/a
33	chr4:120433619-120433669	AG04450	lung:	fetal
34	chr4:120419485-120419535	AG09309	skin:	n/a
35	chr4:120428634-120428684	Hepatocyte	liver:	n/a
36	chr4:120428634-120428684	HNPCEpiC	eye:	n/a
37	chr4:120433619-120433669	AG10803	skin:	n/a
38	chr4:120433619-120433669	RPTEC	kidney:	n/a
39	chr4:120428634-120428684	Jurkat	blood:	n/a
40	chr4:120433619-120433669	NH-A	brain:	n/a
41	chr4:120428634-120428684	HepG2	liver:	n/a
42	chr4:120433619-120433669	HNPCEpiC	eye:	n/a
43	chr4:120433619-120433669	NHBE	bronchial:	n/a
44	chr4:120419485-120419535	PrEC	prostate:	n/a
45	chr4:120433619-120433669	BJ	skin:	n/a
46	chr4:120428634-120428684	GM12891	blood:	n/a
47	chr4:120433619-120433669	HRCEpiC	kidney:	n/a
48	chr4:120428634-120428684	NT2-D1	testis:	n/a
49	chr4:120433619-120433669	Caco-2	colon:	n/a
50	chr4:120433619-120433669	HPAEpiC	pulmonary alveolar:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:120415776..120419919-chr4:120421483..120424125,5	K562	blood:
2	chr4:120426318..120428351-chr4:120986302..120988038,2	K562	blood:
3	chr4:120235248..120235905-chr4:120414247..120414953,2	MCF-7	breast:
4	chr4:120428240..120430118-chr4:120439870..120442381,2	K562	blood:
5	chr4:120235330..120235847-chr4:120411289..120411806,2	MCF-7	breast:
6	chr4:120418959..120421709-chr4:120435895..120438263,2	MCF-7	breast:
7	chr4:120417192..120419085-chr4:120422435..120424125,2	K562	blood:
8	chr4:120417192..120419085-chr4:120422435..120424125,2	K562	blood:
9	chr4:120415776..120419919-chr4:120421483..120424125,5	K562	blood:
10	chr4:120427480..120429953-chr4:120431995..120434202,3	K562	blood:
11	chr4:120431226..120433152-chr4:120441758..120443501,2	K562	blood:
12	chr4:120422211..120423883-chr4:120441121..120442797,2	K562	blood:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC110373.1-8	chr4:120414488-120414592	NONHSAT098079
2	lnc-AC110373.1-8	chr4:120420716-120420848	NONHSAT098081
3	lnc-AC110373.1-8	chr4:120418817-120419182	NONHSAT098087
4	lnc-AC110373.1-8	chr4:120418966-120419058	NONHSAT098079
5	lnc-AC110373.1-8	chr4:120415641-120415678	NONHSAT147297
6	lnc-AC110373.1-8	chr4:120433506-120433665	NONHSAT098079
7	lnc-AC110373.1-8	chr4:120433512-120433619	NONHSAT098091
8	lnc-AC110373.1-8	chr4:120409798-120409872	NONHSAT098085
9	lnc-AC110373.1-8	chr4:120414488-120414592	NONHSAT098081
10	lnc-AC110373.1-8	chr4:120414488-120414592	NONHSAT098085
11	lnc-AC110373.1-8	chr4:120418966-120419058	NONHSAT098086
12	lnc-AC110373.1-8	chr4:120418966-120419142	NONHSAT098082
13	lnc-AC110373.1-8	chr4:120415588-120415678	NONHSAT098081
14	lnc-AC110373.1-8	chr4:120415588-120415678	NONHSAT098085
15	lnc-AC110373.1-8	chr4:120418966-120419058	NONHSAT098085
16	lnc-AC110373.1-8	chr4:120433506-120433619	NONHSAT098085
17	lnc-AC110373.1-8	chr4:120433512-120433619	NONHSAT147298
18	lnc-AC110373.1-8	chr4:120418966-120419058	NONHSAT147297
19	lnc-AC110373.1-8	chr4:120433512-120433619	NONHSAT098090
20	lnc-AC110373.1-8	chr4:120415588-120415678	NONHSAT098082
21	lnc-AC110373.1-8	chr4:120414488-120414592	NONHSAT098082
22	lnc-AC110373.1-8	chr4:120420716-120421434	NONHSAT147297
23	lnc-AC110373.1-8	chr4:120433506-120433619	NONHSAT098089
24	lnc-AC110373.1-8	chr4:120418966-120419058	NONHSAT098081
25	lnc-AC110373.1-8	chr4:120433506-120433619	NONHSAT098086
26	lnc-AC110373.1-8	chr4:120415588-120415678	NONHSAT098079
27	lnc-AC110373.1-8	chr4:120409800-120409872	NONHSAT098084
28	lnc-AC110373.1-8	chr4:120415620-120415678	NONHSAT098087
29	lnc-AC110373.1-8	chr4:120415581-120415678	NONHSAT098086

No data

Variant related genes	Relation type
PDE5A	TF binding region
ENSG00000245958	TF binding region
PDE5A	CpG island
ENSG00000245958	CpG island
ENSG00000164109	chromatin interactions
ENSG00000138735	chromatin interactions
ENSG00000245958	chromatin interactions

Extended variants
information (count: 1059 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1059 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10006525	chr4:120408931-120408932	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532632098	chr4:120409021-120409022	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs549347086	chr4:120409050-120409051	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs372847320	chr4:120409092-120409093	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs541169312	chr4:120409107-120409108	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs569438486	chr4:120409131-120409132	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs10006706	chr4:120409152-120409153	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs533285745	chr4:120409154-120409155	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs11940549	chr4:120409201-120409202	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs572561702	chr4:120409232-120409233	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs183123820	chr4:120409243-120409244	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs79330381	chr4:120409345-120409346	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs574756855	chr4:120409347-120409348	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs111613314	chr4:120409419-120409420	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs559382362	chr4:120409435-120409436	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs543832946	chr4:120409451-120409452	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs563653682	chr4:120409452-120409453	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs149173984	chr4:120409493-120409494	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs533175773	chr4:120409503-120409504	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs143277610	chr4:120409535-120409536	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs6849171	chr4:120409549-120409550	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs566479309	chr4:120409560-120409561	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs114818005	chr4:120409643-120409644	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs72920619	chr4:120409668-120409669	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs187501664	chr4:120409693-120409694	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs6849561	chr4:120409694-120409695	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs368792629	chr4:120409729-120409730	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs193264843	chr4:120409769-120409770	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs138075780	chr4:120409820-120409821	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs140997584	chr4:120409830-120409831	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs555504281	chr4:120409867-120409868	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs183654917	chr4:120409889-120409890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372703030	chr4:120409952-120409953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs13145352	chr4:120409963-120409964	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs187965448	chr4:120410043-120410044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538430688	chr4:120410049-120410050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554849458	chr4:120410073-120410074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558420944	chr4:120410085-120410086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575105783	chr4:120410150-120410151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144891038	chr4:120410167-120410168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557399832	chr4:120410213-120410214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs75539164	chr4:120410245-120410246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192199779	chr4:120410299-120410300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559850120	chr4:120410302-120410303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573237911	chr4:120410381-120410382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540941471	chr4:120410416-120410417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375052759	chr4:120410424-120410425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35869650	chr4:120410453-120410454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560921387	chr4:120410485-120410486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553844682	chr4:120410498-120410499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:659 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120376400-120471600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:120376600-120419200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr4:120377000-120416000	Weak transcription	Colon Smooth Muscle	Colon
4	chr4:120377200-120415600	Weak transcription	Brain Substantia Nigra	brain
5	chr4:120377200-120416200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr4:120377200-120419600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr4:120377200-120433800	Weak transcription	Gastric	stomach
8	chr4:120377400-120415200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr4:120377400-120416200	Weak transcription	Rectal Smooth Muscle	rectum
10	chr4:120377400-120439000	Weak transcription	Small Intestine	intestine
11	chr4:120377400-120439000	Weak transcription	Spleen	Spleen
12	chr4:120377600-120441000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr4:120377600-120501200	Weak transcription	Pancreas	Pancrea
14	chr4:120384400-120439200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr4:120384600-120416200	Weak transcription	Fetal Brain Male	brain
16	chr4:120390400-120409400	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr4:120390600-120409200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr4:120390800-120419800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr4:120391600-120415600	Weak transcription	HUVEC	blood vessel
20	chr4:120393200-120419800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr4:120393800-120409800	Weak transcription	NH-A	brain
22	chr4:120394800-120415200	Weak transcription	NHEK	skin
23	chr4:120397600-120415000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr4:120397800-120416400	Weak transcription	HSMMtube	muscle
25	chr4:120397800-120442600	Weak transcription	Hela-S3	cervix
26	chr4:120398200-120419600	Weak transcription	Fetal Stomach	stomach
27	chr4:120398800-120420000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:120399200-120431200	Weak transcription	Fetal Heart	heart
29	chr4:120401000-120415000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr4:120401200-120416200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:120401400-120414400	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr4:120401400-120419600	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr4:120401400-120419800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:120401600-120409400	Weak transcription	Left Ventricle	heart
35	chr4:120401600-120413200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:120401600-120414800	Weak transcription	Brain Hippocampus Middle	brain
37	chr4:120401600-120415200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr4:120401600-120416000	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr4:120401600-120416000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr4:120401600-120419400	Weak transcription	Brain Angular Gyrus	brain
41	chr4:120401600-120433800	Weak transcription	Right Ventricle	heart
42	chr4:120401800-120409400	Weak transcription	Thymus	Thymus
43	chr4:120401800-120409400	Weak transcription	HepG2	liver
44	chr4:120401800-120409800	Weak transcription	HMEC	breast
45	chr4:120401800-120414800	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr4:120401800-120415000	Weak transcription	Primary B cells from peripheral blood	blood
47	chr4:120401800-120415000	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr4:120401800-120415200	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr4:120401800-120416200	Weak transcription	Aorta	Aorta
50	chr4:120401800-120416200	Weak transcription	Stomach Smooth Muscle	stomach

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