Variant report

Variant	nsv879840
Chromosome Location	chr4:120227419-120257417
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	BACH1	chr4:120236742-120236793	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr4:120230779-120231016	IMR90	lung:	n/a	n/a
3	CEBPB	chr4:120234416-120234739	A549	lung:	n/a	chr4:120234578-120234589
4	CEBPB	chr4:120234417-120234747	IMR90	lung:	n/a	chr4:120234578-120234589
5	CEBPB	chr4:120231976-120232267	IMR90	lung:	n/a	n/a
6	CEBPB	chr4:120243648-120243744	A549	lung:	n/a	n/a
7	CEBPB	chr4:120250151-120250390	HepG2	liver:	n/a	chr4:120250277-120250288
8	CEBPB	chr4:120239305-120239347	K562	blood:	n/a	n/a
9	CEBPB	chr4:120234421-120234752	HepG2	liver:	n/a	chr4:120234578-120234589
10	CTCF	chr4:120235580-120235730	BE2_C	brain:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
11	CTCF	chr4:120235302-120236082	SK-N-SH	brain:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
12	CTCF	chr4:120235558-120235851	Spleen_OC	spleen:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
13	CTCF	chr4:120235600-120235750	GM12878	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
14	CTCF	chr4:120235680-120235830	GM12864	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
15	CTCF	chr4:120235620-120235770	HMEC	breast:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
16	CTCF	chr4:120235660-120235810	HRE	kidney:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
17	CTCF	chr4:120235484-120235945	IMR90	lung:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
18	CTCF	chr4:120235540-120235690	HCM	heart:	n/a	n/a
19	CTCF	chr4:120235620-120235770	GM12871	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
20	CTCF	chr4:120235580-120235730	NHLF	lung:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
21	CTCF	chr4:120235624-120235790	GM10248	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
22	CTCF	chr4:120235660-120235810	GM12864	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
23	CTCF	chr4:120235600-120235750	HFF	foreskin:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
24	CTCF	chr4:120235600-120235750	GM12873	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
25	CTCF	chr4:120235620-120235770	HPF	lung:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
26	CTCF	chr4:120235640-120235790	HVMF	connective:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
27	CTCF	chr4:120235546-120235895	MCF-7	breast:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
28	CTCF	chr4:120235508-120235898	K562	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
29	CTCF	chr4:120235600-120235750	MCF-7	breast:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
30	CTCF	chr4:120235540-120235690	HCT-116	colon:	n/a	n/a
31	CTCF	chr4:120235640-120235790	GM12872	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
32	CTCF	chr4:120235626-120235789	GM20000	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
33	CTCF	chr4:120235620-120235770	GM06990	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
34	CTCF	chr4:120235660-120235810	SK-N-SH_RA	brain:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
35	CTCF	chr4:120235580-120235730	GM12869	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
36	CTCF	chr4:120235620-120235770	HEEpiC	esophagus:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
37	CTCF	chr4:120235640-120235790	GM12874	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
38	CTCF	chr4:120235420-120235570	WI-38	lung:	n/a	n/a
39	CTCF	chr4:120235620-120235770	Caco-2	colon:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
40	CTCF	chr4:120235620-120235770	HAc	cerebellar:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
41	CTCF	chr4:120235640-120235790	HBMEC	blood vessel:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
42	CTCF	chr4:120235640-120235790	WERI-Rb-1	eye:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
43	CTCF	chr4:120235620-120235770	HRPEpiC	eye:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
44	CTCF	chr4:120235660-120235810	NHEK	skin:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
45	CTCF	chr4:120235628-120235773	A549	lung:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
46	CTCF	chr4:120235660-120235810	GM12870	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
47	CTCF	chr4:120235600-120235750	HPAF	blood vessel:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
48	CTCF	chr4:120235564-120235961	MCF-7	breast:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721
49	CTCF	chr4:120235720-120235870	A549	lung:	n/a	n/a
50	CTCF	chr4:120235622-120235782	GM13976	blood:	n/a	chr4:120235704-120235722 chr4:120235706-120235727 chr4:120235705-120235721

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120235615-120235665	AG04450	lung:	fetal
2	chr4:120235615-120235665	AG04450	lung:	fetal
3	chr4:120235615-120235665	GM12892	blood:	n/a
4	chr4:120239158-120239208	PrEC	prostate:	n/a
5	chr4:120243252-120243302	PFSK-1	brain:	n/a
6	chr4:120243555-120243605	MCF-7	breast:	n/a
7	chr4:120239158-120239208	ECC-1	luminal epithelium:	n/a
8	chr4:120243555-120243605	AG04449	skin:	fetal
9	chr4:120235615-120235665	Caco-2	colon:	n/a
10	chr4:120235615-120235665	ProgFib	skin:	n/a
11	chr4:120243311-120243361	HepG2	liver:	n/a
12	chr4:120235615-120235665	NHDF-neo	bronchial:	n/a
13	chr4:120243555-120243605	Jurkat	blood:	n/a
14	chr4:120243311-120243361	HCPEpiC	choroid plexus:	n/a
15	chr4:120243555-120243605	H1-hESC	embryonic stem cell:	embryo
16	chr4:120243555-120243605	NH-A	brain:	n/a
17	chr4:120243311-120243361	HEK293	kidney:	embryo
18	chr4:120235615-120235665	HAEpiC	amniotic membrane:	n/a
19	chr4:120243311-120243361	NHBE	bronchial:	n/a
20	chr4:120243252-120243302	ovcar-3	ovarian:	n/a
21	chr4:120243311-120243361	NB4	blood:	n/a
22	chr4:120235615-120235665	BJ	skin:	n/a
23	chr4:120243252-120243302	AG10803	skin:	n/a
24	chr4:120235615-120235665	ECC-1	luminal epithelium:	n/a
25	chr4:120235615-120235665	HL-60	blood:	n/a
26	chr4:120243555-120243605	HEEpiC	esophagus:	n/a
27	chr4:120243555-120243605	HEK293	kidney:	embryo
28	chr4:120243555-120243605	HL-60	blood:	n/a
29	chr4:120235615-120235665	MCF10A-Er-Src	breast:	n/a
30	chr4:120243555-120243605	HCT-116	colon:	n/a
31	chr4:120235615-120235665	AG10803	skin:	n/a
32	chr4:120243252-120243302	AG09309	skin:	n/a
33	chr4:120243555-120243605	ovcar-3	ovarian:	n/a
34	chr4:120243311-120243361	ECC-1	luminal epithelium:	n/a
35	chr4:120243252-120243302	A549	lung:	n/a
36	chr4:120239158-120239208	HepG2	liver:	n/a
37	chr4:120243252-120243302	AG04450	lung:	fetal
38	chr4:120239158-120239208	HCT-116	colon:	n/a
39	chr4:120235615-120235665	Jurkat	blood:	n/a
40	chr4:120243311-120243361	HCT-116	colon:	n/a
41	chr4:120243311-120243361	LNCaP	prostate:	n/a
42	chr4:120239158-120239208	AG09319	gingival:	n/a
43	chr4:120235615-120235665	BE2_C	brain:	n/a
44	chr4:120243252-120243302	H1-hESC	embryonic stem cell:	embryo
45	chr4:120243311-120243361	NHDF-neo	bronchial:	n/a
46	chr4:120243555-120243605	AG09309	skin:	n/a
47	chr4:120243252-120243302	NHBE	bronchial:	n/a
48	chr4:120243311-120243361	AG09319	gingival:	n/a
49	chr4:120243252-120243302	Caco-2	colon:	n/a
50	chr4:120243311-120243361	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:120234842..120237819-chr4:120239424..120241485,2	K562	blood:
2	chr4:120235624..120236167-chr4:120970907..120971659,2	K562	blood:
3	chr4:120235330..120235847-chr4:120411289..120411806,2	MCF-7	breast:
4	chr4:120235306..120236113-chr4:120548177..120548693,2	MCF-7	breast:
5	chr4:120234892..120236203-chr4:120548295..120548927,3	K562	blood:
6	chr4:120230931..120233394-chr4:120986011..120987625,2	K562	blood:
7	chr4:120235248..120235905-chr4:120414247..120414953,2	MCF-7	breast:
8	chr4:120249451..120251294-chr4:120987361..120988915,2	K562	blood:
9	chr4:120234842..120237819-chr4:120239424..120241485,2	K562	blood:
10	chr4:120235208..120236116-chr4:122017267..122018044,2	K562	blood:

Variant related genes	Relation type
FABP2	TF binding region
KLHL2P1	TF binding region
C4orf3	TF binding region
FABP2	CpG island
KLHL2P1	CpG island
C4orf3	CpG island
ENSG00000164109	chromatin interactions
ENSG00000250938	chromatin interactions
ENSG00000138735	chromatin interactions

Extended variants
information (count: 1146 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1146 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1858285	chr4:120227419-120227420	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs187778421	chr4:120227426-120227427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527869386	chr4:120227497-120227498	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs548304774	chr4:120227498-120227499	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs549057379	chr4:120227503-120227504	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs569241068	chr4:120227516-120227517	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs191345570	chr4:120227596-120227597	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs184297506	chr4:120227621-120227622	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs546755921	chr4:120227695-120227696	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs9985932	chr4:120227701-120227702	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs79069195	chr4:120227709-120227710	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs187045106	chr4:120227720-120227721	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs542117193	chr4:120227746-120227747	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs555032628	chr4:120227771-120227772	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs192248634	chr4:120227826-120227827	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs543952045	chr4:120227828-120227829	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs535484541	chr4:120227835-120227836	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs185008944	chr4:120227843-120227844	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs533339151	chr4:120227855-120227856	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs375156073	chr4:120227944-120227945	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs200330467	chr4:120228024-120228025	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs7656644	chr4:120228035-120228036	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs190200167	chr4:120228077-120228078	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs71595362	chr4:120228083-120228084	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs529518083	chr4:120228164-120228165	Weak transcription Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs373382726	chr4:120228237-120228238	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs560553511	chr4:120228240-120228241	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs549666668	chr4:120228278-120228279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569128360	chr4:120228295-120228296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531758831	chr4:120228307-120228308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551888536	chr4:120228326-120228327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537783668	chr4:120228378-120228379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147777731	chr4:120228395-120228396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143278478	chr4:120228396-120228397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs150281570	chr4:120228397-120228398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs56344202	chr4:120228425-120228426	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs534291870	chr4:120228520-120228521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577461724	chr4:120228541-120228542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs193147947	chr4:120228549-120228550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77558897	chr4:120228560-120228561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566675714	chr4:120228585-120228586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542009181	chr4:120228616-120228617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535361980	chr4:120228626-120228627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4834768	chr4:120228641-120228642	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs185593528	chr4:120228654-120228655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188281358	chr4:120228769-120228770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553511399	chr4:120228814-120228815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs180715652	chr4:120228824-120228825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs372483556	chr4:120228833-120228834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141580883	chr4:120228915-120228916	Weak transcription Enhancers	n/a	n/a	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
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
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120222000-120251000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr4:120222200-120244600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:120222400-120227800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr4:120222400-120229000	Weak transcription	Duodenum Mucosa	Duodenum
5	chr4:120222400-120240800	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr4:120222800-120240800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr4:120223200-120227800	Weak transcription	Fetal Intestine Large	intestine
8	chr4:120225000-120238800	Weak transcription	Fetal Intestine Small	intestine
9	chr4:120227800-120228200	ZNF genes & repeats	Fetal Intestine Large	intestine
10	chr4:120228000-120228200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr4:120228000-120228400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr4:120228000-120228600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr4:120228000-120229200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr4:120228200-120238600	Weak transcription	Fetal Intestine Large	intestine
15	chr4:120228400-120232400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr4:120229000-120229200	Enhancers	Duodenum Mucosa	Duodenum
17	chr4:120229200-120238400	Weak transcription	Duodenum Mucosa	Duodenum
18	chr4:120231200-120233000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:120231400-120231600	Enhancers	NHDF-Ad	bronchial
20	chr4:120231800-120232800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr4:120232000-120232600	Enhancers	NH-A	brain
22	chr4:120232000-120232800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:120232000-120232800	Enhancers	Osteobl	bone
24	chr4:120232200-120232800	Enhancers	HUVEC	blood vessel
25	chr4:120232800-120234200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:120232800-120235200	Weak transcription	Osteobl	bone
27	chr4:120232800-120235400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr4:120232800-120235400	Weak transcription	NHDF-Ad	bronchial
29	chr4:120233000-120235000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:120234000-120236800	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr4:120234200-120234600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:120234200-120237600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr4:120234400-120234600	Enhancers	Primary hematopoietic stem cells	blood
34	chr4:120234400-120235000	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr4:120234600-120235800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr4:120235000-120239400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr4:120235200-120235400	Enhancers	Psoas Muscle	Psoas
38	chr4:120235200-120237200	Enhancers	Osteobl	bone
39	chr4:120235400-120236000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr4:120235400-120238000	Enhancers	NHDF-Ad	bronchial
41	chr4:120235600-120251000	Weak transcription	Left Ventricle	heart
42	chr4:120235800-120236200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr4:120235800-120236400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:120235800-120236600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:120235800-120236600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr4:120235800-120237000	Enhancers	NHLF	lung
47	chr4:120235800-120237200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:120235800-120237200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr4:120235800-120241800	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr4:120236000-120236400	Enhancers	HUES48 Cell Line	embryonic stem cell

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