Variant report

Variant	nsv595606
Chromosome Location	chr4:143631691-143729595
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr4:143723168-143723634	HCT-116	colon:	n/a	n/a
2	CBX3	chr4:143664207-143665012	HCT-116	colon:	n/a	n/a
3	CBX3	chr4:143640947-143641624	HCT-116	colon:	n/a	n/a
4	CEBPB	chr4:143647576-143647849	IMR90	lung:	n/a	chr4:143647716-143647729
5	CEBPB	chr4:143664214-143664470	HepG2	liver:	n/a	chr4:143664319-143664330
6	CEBPB	chr4:143647708-143647757	K562	blood:	n/a	chr4:143647716-143647729
7	CEBPB	chr4:143699270-143699405	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:143698743-143698867	A549	lung:	n/a	n/a
9	CEBPB	chr4:143652895-143653164	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:143652977-143653126	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr4:143664206-143664406	A549	lung:	n/a	chr4:143664319-143664330
12	CEBPB	chr4:143664062-143664720	HCT-116	colon:	n/a	chr4:143664319-143664330
13	CEBPB	chr4:143664141-143664514	IMR90	lung:	n/a	chr4:143664319-143664330
14	CEBPB	chr4:143698596-143698950	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:143698657-143698909	HepG2	liver:	n/a	n/a
16	CTCF	chr4:143663322-143663429	Gliobla	brain:	n/a	n/a
17	CTCF	chr4:143673560-143673710	HPAF	blood vessel:	n/a	n/a
18	CTCF	chr4:143641380-143641530	GM06990	blood:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
19	CTCF	chr4:143663240-143663390	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr4:143663180-143663330	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr4:143641400-143641550	Hela-S3	cervix:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
22	CTCF	chr4:143673600-143673750	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr4:143641340-143641490	GM12869	blood:	n/a	n/a
24	CTCF	chr4:143641440-143641590	SAEC	small airway:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
25	CTCF	chr4:143641420-143641570	HMF	breast:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
26	CTCF	chr4:143663280-143663430	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr4:143641097-143641783	HCT-116	colon:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
28	CTCF	chr4:143641407-143641601	Kidney_OC	kidney:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
29	CTCF	chr4:143673680-143673830	MCF-7	breast:	n/a	n/a
30	CTCF	chr4:143663280-143663430	BE2_C	brain:	n/a	n/a
31	CTCF	chr4:143663256-143663436	LNCaP	prostate:	n/a	n/a
32	CTCF	chr4:143663300-143663450	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr4:143663260-143663410	NHLF	lung:	n/a	n/a
34	CTCF	chr4:143641313-143641679	MCF-7	breast:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
35	CTCF	chr4:143641276-143641702	IMR90	lung:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
36	CTCF	chr4:143641380-143641530	GM12874	blood:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
37	CTCF	chr4:143641420-143641570	HRE	kidney:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
38	CTCF	chr4:143641400-143641550	GM12878	blood:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
39	CTCF	chr4:143641440-143641590	AoAF	blood vessel:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
40	CTCF	chr4:143641380-143641530	NHDF-neo	bronchial:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
41	CTCF	chr4:143641480-143641630	RPTEC	kidney:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
42	CTCF	chr4:143641400-143641550	HPF	lung:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
43	CTCF	chr4:143641440-143641590	BE2_C	brain:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
44	CTCF	chr4:143663220-143663370	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:143673580-143673730	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr4:143718243-143718278	Lung_OC	lung:	n/a	n/a
47	CTCF	chr4:143641460-143641610	GM12873	blood:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
48	CTCF	chr4:143641420-143641570	SK-N-SH_RA	brain:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513
49	CTCF	chr4:143663180-143663330	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr4:143641400-143641613	Pancreas_OC	pancreas:	n/a	chr4:143641490-143641511 chr4:143641496-143641512 chr4:143641495-143641513

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:143633738-143633788	AG04450	lung:	fetal
2	chr4:143633738-143633788	MCF-7	breast:	n/a
3	chr4:143633738-143633788	GM12892	blood:	n/a
4	chr4:143633738-143633788	BE2_C	brain:	n/a
5	chr4:143633738-143633788	Hela-S3	cervix:	n/a
6	chr4:143633738-143633788	NHBE	bronchial:	n/a
7	chr4:143633738-143633788	HEK293	kidney:	embryo
8	chr4:143633738-143633788	GM12878	blood:	n/a
9	chr4:143633738-143633788	PrEC	prostate:	n/a
10	chr4:143633738-143633788	AG09309	skin:	n/a
11	chr4:143633738-143633788	NHDF-neo	bronchial:	n/a
12	chr4:143633738-143633788	HCT-116	colon:	n/a
13	chr4:143633738-143633788	NH-A	brain:	n/a
14	chr4:143633738-143633788	AG09319	gingival:	n/a
15	chr4:143633738-143633788	SKMC	muscle:	n/a
16	chr4:143633738-143633788	HRPEpiC	eye:	n/a
17	chr4:143633738-143633788	NT2-D1	testis:	n/a
18	chr4:143633738-143633788	HL-60	blood:	n/a
19	chr4:143633738-143633788	RPTEC	kidney:	n/a
20	chr4:143633738-143633788	Jurkat	blood:	n/a
21	chr4:143633738-143633788	HCF	heart:	n/a
22	chr4:143633738-143633788	SAEC	small airway:	n/a
23	chr4:143633738-143633788	GM19239	blood:	n/a
24	chr4:143633738-143633788	AG04449	skin:	fetal
25	chr4:143633738-143633788	Hepatocyte	liver:	n/a
26	chr4:143633738-143633788	SK-N-MC	brain:	n/a
27	chr4:143633738-143633788	SK-N-SH_RA	brain:	n/a
28	chr4:143633738-143633788	IMR90	lung:	fetal
29	chr4:143633738-143633788	T-47D	breast:	n/a
30	chr4:143633738-143633788	NB4	blood:	n/a
31	chr4:143633738-143633788	HepG2	liver:	n/a
32	chr4:143633738-143633788	AoSMC	blood vessel:	n/a
33	chr4:143633738-143633788	K562	blood:	n/a
34	chr4:143633738-143633788	HRCEpiC	kidney:	n/a
35	chr4:143633738-143633788	HRE	kidney:	n/a
36	chr4:143633738-143633788	PANC-1	pancreas:	n/a
37	chr4:143633738-143633788	U87	brain:	n/a
38	chr4:143633738-143633788	H1-hESC	embryonic stem cell:	embryo
39	chr4:143633738-143633788	PFSK-1	brain:	n/a
40	chr4:143633738-143633788	Caco-2	colon:	n/a
41	chr4:143633738-143633788	HCM	heart:	n/a
42	chr4:143633738-143633788	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:143633738-143633788	GM06990	blood:	n/a
44	chr4:143633738-143633788	HMEC	breast:	n/a
45	chr4:143633738-143633788	HUVEC	blood vessel:	n/a
46	chr4:143633738-143633788	ECC-1	luminal epithelium:	n/a
47	chr4:143633738-143633788	HEEpiC	esophagus:	n/a
48	chr4:143633738-143633788	HAEpiC	amniotic membrane:	n/a
49	chr4:143633738-143633788	ovcar-3	ovarian:	n/a
50	chr4:143633738-143633788	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:143646473..143648911-chr4:143650261..143652367,2	MCF-7	breast:
2	chr4:143637297..143639595-chr4:143640905..143643324,3	MCF-7	breast:
3	chr4:143629918..143632766-chr4:143633001..143634713,2	MCF-7	breast:
4	chr4:143728679..143731015-chr4:143735952..143738151,2	MCF-7	breast:
5	chr4:143394255..143395855-chr4:143697810..143700529,2	MCF-7	breast:
6	chr4:143391122..143393717-chr4:143678959..143680972,2	MCF-7	breast:
7	chr4:143637297..143639595-chr4:143640905..143643324,3	MCF-7	breast:
8	chr4:143629918..143632766-chr4:143633001..143634713,2	MCF-7	breast:
9	chr4:143682400..143684805-chr4:143686793..143689462,3	K562	blood:
10	chr4:143726994..143729226-chr4:144104406..144106843,2	K562	blood:
11	chr4:143634044..143636846-chr4:143637396..143641073,3	MCF-7	breast:
12	chr4:143535273..143539133-chr4:143641663..143644812,3	MCF-7	breast:
13	chr4:143653633..143656587-chr4:143659661..143662244,2	MCF-7	breast:
14	chr4:143728789..143731644-chr4:143731660..143733720,2	MCF-7	breast:
15	chr4:143536517..143538495-chr4:143637512..143640289,2	MCF-7	breast:
16	chr4:143646473..143648911-chr4:143650261..143652367,2	MCF-7	breast:
17	chr4:143644944..143646737-chr4:143768301..143769914,2	MCF-7	breast:
18	chr4:143634044..143636846-chr4:143637396..143641073,3	MCF-7	breast:
19	chr4:143393131..143399799-chr4:143636317..143645681,15	MCF-7	breast:
20	chr4:143651955..143654079-chr4:143655734..143658142,2	MCF-7	breast:
21	chr4:143401960..143404960-chr4:143637401..143640738,3	MCF-7	breast:
22	chr4:143651955..143654079-chr4:143655734..143658142,2	MCF-7	breast:
23	chr4:143724161..143726942-chr4:143730485..143732877,2	K562	blood:
24	chr4:143393465..143396592-chr4:143631239..143633455,3	MCF-7	breast:
25	chr4:143392644..143398601-chr4:143638137..143645320,14	MCF-7	breast:
26	chr4:143653633..143656587-chr4:143659661..143662244,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FREM3-8	chr4:143687891-143687990	NONHSAT098541
2	lnc-FREM3-8	chr4:143687891-143688005	NONHSAT098540
3	lnc-FREM3-8	chr4:143687027-143687156	NONHSAT098540
4	lnc-FREM3-8	chr4:143688985-143689007	NONHSAT098540
5	lnc-FREM3-8	chr4:143688742-143688814	NONHSAT098540
6	lnc-FREM3-8	chr4:143687891-143687972	NONHSAT098539
7	lnc-FREM3-7	chr4:143716305-143716766	NONHSAT098542
8	lnc-FREM3-8	chr4:143688985-143689122	NONHSAT098541
9	lnc-FREM3-8	chr4:143646992-143647054	NONHSAT098539

Variant related genes	Relation type
INPP4B	TF binding region
INPP4B	CpG island
ENSG00000109452	chromatin interactions
ENSG00000250326	chromatin interactions
ENSG00000170185	chromatin interactions

Extended variants
information (count: 3436 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3436 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1443187	chr4:143631691-143631692	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533174131	chr4:143631706-143631707	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs551339231	chr4:143631709-143631710	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs184812164	chr4:143631713-143631714	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs76643922	chr4:143631718-143631719	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs565194315	chr4:143631816-143631817	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs190562276	chr4:143631936-143631937	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs367667092	chr4:143632001-143632002	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs148808310	chr4:143632013-143632014	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs35660656	chr4:143632016-143632017	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs142455724	chr4:143632029-143632030	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs113190533	chr4:143632121-143632122	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs549871422	chr4:143632154-143632155	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371784573	chr4:143632186-143632187	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs181786243	chr4:143632217-143632218	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs376031279	chr4:143632257-143632258	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs569308266	chr4:143632279-143632280	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs151249681	chr4:143632289-143632290	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs558548233	chr4:143632293-143632294	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs558155215	chr4:143632397-143632398	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551773145	chr4:143632400-143632401	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573245408	chr4:143632453-143632454	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs72728615	chr4:143632464-143632465	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs185002156	chr4:143632620-143632621	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs573712365	chr4:143632655-143632656	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs190331350	chr4:143632718-143632719	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs181083117	chr4:143632728-143632729	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs75298256	chr4:143632734-143632735	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577722878	chr4:143632844-143632845	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545236048	chr4:143632869-143632870	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185615493	chr4:143632876-143632877	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs189640139	chr4:143632886-143632887	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs527621112	chr4:143632896-143632897	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs78814240	chr4:143632900-143632901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181017875	chr4:143632901-143632902	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs187356901	chr4:143632928-143632929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs549573631	chr4:143632979-143632980	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs191826555	chr4:143632999-143633000	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs539638178	chr4:143633006-143633007	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551584815	chr4:143633062-143633063	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs376336963	chr4:143633081-143633082	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144312900	chr4:143633085-143633086	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs112828387	chr4:143633086-143633087	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs62331902	chr4:143633094-143633095	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs570855300	chr4:143633096-143633097	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs975581	chr4:143633132-143633133	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs538581562	chr4:143633133-143633134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs556379048	chr4:143633176-143633177	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375852151	chr4:143633188-143633189	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs544861499	chr4:143633205-143633206	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Intellectual disability	22102821	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
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143620800-143642000	Weak transcription	Fetal Heart	heart
2	chr4:143625200-143641600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:143628800-143632000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
4	chr4:143629600-143634000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr4:143629800-143634400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr4:143630200-143640600	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr4:143630800-143650200	Weak transcription	Aorta	Aorta
8	chr4:143631000-143631800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr4:143631000-143632000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr4:143631400-143636800	Weak transcription	Primary hematopoietic stem cells	blood
11	chr4:143631600-143632000	Weak transcription	Dnd41	blood
12	chr4:143631600-143632200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:143631800-143632400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr4:143631800-143632600	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr4:143631800-143636600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr4:143632000-143632200	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr4:143632000-143632200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
18	chr4:143632000-143632200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr4:143632000-143632400	Enhancers	Dnd41	blood
20	chr4:143632000-143632600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr4:143632200-143632600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr4:143632200-143634000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr4:143632200-143634000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr4:143632200-143634200	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr4:143632200-143634800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:143632400-143632600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr4:143632400-143633400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr4:143632400-143634000	Weak transcription	Dnd41	blood
29	chr4:143632400-143640200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:143632600-143633800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr4:143632600-143634000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr4:143633400-143636800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr4:143633800-143636400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr4:143634000-143635600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr4:143634000-143635800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr4:143634000-143636200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr4:143634000-143636400	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr4:143634000-143636400	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr4:143634000-143636800	Enhancers	Dnd41	blood
40	chr4:143634000-143637200	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr4:143634200-143636000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
42	chr4:143634400-143636400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr4:143634400-143636600	Enhancers	Primary T cells from cord blood	blood
44	chr4:143634800-143635000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
45	chr4:143634800-143635000	Enhancers	Thymus	Thymus
46	chr4:143634800-143635200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr4:143634800-143635600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
48	chr4:143634800-143635600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
49	chr4:143634800-143635800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
50	chr4:143635000-143648200	Weak transcription	Thymus	Thymus

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