Variant report

Variant	esv3325727
Chromosome Location	chr4:150998027-151001275
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:317)
CpG islands
(count:733)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:150999880-151000018	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:150999232-150999272	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:151000262-151000541	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:151000571-151000648	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:150999039-150999353	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr4:151001032-151001104	HepG2	liver:	n/a	chr4:151001044-151001055
7	CEBPB	chr4:151000454-151000685	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr4:151000898-151001193	A549	lung:	n/a	chr4:151001044-151001055
9	CEBPB	chr4:151000880-151001192	IMR90	lung:	n/a	chr4:151001044-151001055
10	CHD2	chr4:150999159-151000788	Hela-S3	cervix:	n/a	chr4:150999727-150999737 chr4:150999722-150999732 chr4:150999363-150999373
11	CREB1	chr4:150999115-150999474	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr4:150999068-150999492	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr4:150999094-150999572	A549	lung:	n/a	n/a
14	CTBP2	chr4:150999878-151000831	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr4:151000620-151000770	GM12865	blood:	n/a	chr4:151000638-151000651
16	CTCF	chr4:150999440-150999590	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr4:151000560-151000710	WERI-Rb-1	eye:	n/a	chr4:151000638-151000651
18	CTCF	chr4:151000560-151000710	GM12871	blood:	n/a	chr4:151000638-151000651
19	CTCF	chr4:151000520-151000670	HRE	kidney:	n/a	chr4:151000638-151000651
20	CTCF	chr4:151000510-151000709	Hela-S3	cervix:	n/a	chr4:151000638-151000651
21	CTCF	chr4:151000602-151000615	GM12891	blood:	n/a	n/a
22	CTCF	chr4:151000500-151000650	GM12872	blood:	n/a	n/a
23	CTCF	chr4:151000560-151000710	GM12875	blood:	n/a	chr4:151000638-151000651
24	CTCF	chr4:151000405-151000725	IMR90	lung:	n/a	chr4:151000638-151000651
25	CTCF	chr4:151000380-151000530	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr4:151000520-151000670	AG04450	lung:	n/a	chr4:151000638-151000651
27	CTCF	chr4:150999460-150999610	AG04449	skin:	n/a	n/a
28	CTCF	chr4:151000500-151000650	AG09319	gingival:	n/a	n/a
29	CTCF	chr4:151000420-151000570	BJ	skin:	n/a	n/a
30	CTCF	chr4:151000615-151000640	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr4:150999442-150999649	IMR90	lung:	n/a	n/a
32	CTCF	chr4:151000580-151000730	SK-N-SH_RA	brain:	n/a	chr4:151000638-151000651
33	CTCF	chr4:151000520-151000670	RPTEC	kidney:	n/a	chr4:151000638-151000651
34	CTCF	chr4:151000340-151000490	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr4:151000520-151000670	Caco-2	colon:	n/a	chr4:151000638-151000651
36	CTCF	chr4:151000580-151000730	GM06990	blood:	n/a	chr4:151000638-151000651
37	CTCF	chr4:151000500-151000650	GM12865	blood:	n/a	n/a
38	CTCF	chr4:151000527-151000730	MCF-7	breast:	n/a	chr4:151000638-151000651
39	CTCF	chr4:151000680-151000830	HRE	kidney:	n/a	n/a
40	CTCF	chr4:151000460-151000610	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr4:151000420-151000570	HRE	kidney:	n/a	n/a
42	CTCF	chr4:151000400-151000550	HPF	lung:	n/a	n/a
43	CTCF	chr4:151000490-151000750	MCF-7	breast:	n/a	chr4:151000638-151000651
44	CTCF	chr4:151000520-151000670	AG04449	skin:	n/a	chr4:151000638-151000651
45	CTCF	chr4:151000580-151000730	HRPEpiC	eye:	n/a	chr4:151000638-151000651
46	CTCF	chr4:151000420-151000710	GM12870	blood:	n/a	chr4:151000638-151000651
47	CTCF	chr4:151000000-151000150	HRE	kidney:	n/a	n/a
48	CTCF	chr4:151000340-151000490	GM12865	blood:	n/a	n/a
49	CTCF	chr4:151000580-151000730	AoAF	blood vessel:	n/a	chr4:151000638-151000651
50	CTCF	chr4:151000580-151000728	GM19238	blood:	n/a	chr4:151000638-151000651

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:150999899-150999949	HNPCEpiC	eye:	n/a
2	chr4:150999899-150999949	HNPCEpiC	eye:	n/a
3	chr4:151000084-151000134	ovcar-3	ovarian:	n/a
4	chr4:150999042-150999092	Hela-S3	cervix:	n/a
5	chr4:150999905-150999955	ovcar-3	ovarian:	n/a
6	chr4:150999911-150999961	HCF	heart:	n/a
7	chr4:150999042-150999092	LNCaP	prostate:	n/a
8	chr4:150999251-150999301	LNCaP	prostate:	n/a
9	chr4:150999899-150999949	HCM	heart:	n/a
10	chr4:151000014-151000064	HAEpiC	amniotic membrane:	n/a
11	chr4:150999911-150999961	GM19239	blood:	n/a
12	chr4:151000235-151000285	GM06990	blood:	n/a
13	chr4:150999899-150999949	NH-A	brain:	n/a
14	chr4:151000684-151000734	HAEpiC	amniotic membrane:	n/a
15	chr4:150999949-150999999	CMK	blood:	n/a
16	chr4:151000084-151000134	GM12891	blood:	n/a
17	chr4:150999911-150999961	ECC-1	luminal epithelium:	n/a
18	chr4:150999905-150999955	SKMC	muscle:	n/a
19	chr4:151000684-151000734	AG04449	skin:	fetal
20	chr4:151000235-151000285	AG09309	skin:	n/a
21	chr4:150999547-150999597	HEEpiC	esophagus:	n/a
22	chr4:151000684-151000734	HCT-116	colon:	n/a
23	chr4:151000235-151000285	Caco-2	colon:	n/a
24	chr4:151000014-151000064	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:150999911-150999961	AG09319	gingival:	n/a
26	chr4:150999911-150999961	BJ	skin:	n/a
27	chr4:150999899-150999949	Hela-S3	cervix:	n/a
28	chr4:151000235-151000285	MCF10A-Er-Src	breast:	n/a
29	chr4:150999923-150999973	SK-N-SH	brain:	n/a
30	chr4:151000684-151000734	HCPEpiC	choroid plexus:	n/a
31	chr4:150999042-150999092	HRCEpiC	kidney:	n/a
32	chr4:151000084-151000134	HCT-116	colon:	n/a
33	chr4:150999923-150999973	Hepatocyte	liver:	n/a
34	chr4:150999251-150999301	HPAEpiC	pulmonary alveolar:	n/a
35	chr4:150999949-150999999	NHDF-neo	bronchial:	n/a
36	chr4:150999911-150999961	HCPEpiC	choroid plexus:	n/a
37	chr4:150999547-150999597	PANC-1	pancreas:	n/a
38	chr4:151000235-151000285	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:150999547-150999597	ovcar-3	ovarian:	n/a
40	chr4:151000014-151000064	NHDF-neo	bronchial:	n/a
41	chr4:150999911-150999961	SK-N-SH	brain:	n/a
42	chr4:151000235-151000285	Hela-S3	cervix:	n/a
43	chr4:151000235-151000285	GM12891	blood:	n/a
44	chr4:151000684-151000734	ovcar-3	ovarian:	n/a
45	chr4:151000684-151000734	HCM	heart:	n/a
46	chr4:151000014-151000064	BJ	skin:	n/a
47	chr4:151000684-151000734	BE2_C	brain:	n/a
48	chr4:151000084-151000134	ProgFib	skin:	n/a
49	chr4:151000684-151000734	SK-N-SH_RA	brain:	n/a
50	chr4:151000084-151000134	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:42758633..42759495-chr4:150999375..150999897,2	Hela-S3	cervix:
2	chr4:151000698..151001437-chr4:151130301..151131200,2	MCF-7	breast:

No data

Variant related genes	Relation type
DCLK2	TF binding region
DCLK2	CpG island
ENSG00000238721	chromatin interactions
ENSG00000268643	chromatin interactions
ENSG00000105722	chromatin interactions

Extended variants
information (count: 143 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:143 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7668293	chr4:150998079-150998080	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564419020	chr4:150998089-150998090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181716199	chr4:150998159-150998160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148988934	chr4:150998190-150998191	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs143804642	chr4:150998218-150998219	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs185849039	chr4:150998241-150998242	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs562123258	chr4:150998288-150998289	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs566045775	chr4:150998314-150998315	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs534843495	chr4:150998341-150998342	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs548657377	chr4:150998349-150998350	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs531823880	chr4:150998409-150998410	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568310804	chr4:150998410-150998411	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34144863	chr4:150998464-150998465	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537246598	chr4:150998468-150998469	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557152981	chr4:150998471-150998472	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200712204	chr4:150998472-150998473	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577227901	chr4:150998476-150998477	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539696332	chr4:150998488-150998489	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148171953	chr4:150998508-150998509	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572786747	chr4:150998524-150998525	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10003178	chr4:150998544-150998545	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs561448326	chr4:150998554-150998555	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs141127848	chr4:150998564-150998565	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs565902666	chr4:150998608-150998609	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs79202291	chr4:150998635-150998636	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs543621912	chr4:150998644-150998645	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs563509011	chr4:150998671-150998672	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs111996967	chr4:150998674-150998675	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs533336487	chr4:150998733-150998734	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs79788742	chr4:150998760-150998761	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs372157848	chr4:150998870-150998871	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs552820907	chr4:150998878-150998879	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs150719061	chr4:150998898-150998899	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs528485065	chr4:150998910-150998911	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs72730319	chr4:150998937-150998938	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs568577431	chr4:150999029-150999030	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs199544269	chr4:150999035-150999036	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs550817125	chr4:150999047-150999048	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs76774998	chr4:150999062-150999063	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs539390704	chr4:150999066-150999067	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs374492582	chr4:150999100-150999101	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs10005992	chr4:150999112-150999113	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs573006374	chr4:150999145-150999146	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs10028598	chr4:150999167-150999168	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs535438558	chr4:150999187-150999188	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs112573840	chr4:150999217-150999218	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs376837887	chr4:150999218-150999219	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs575015426	chr4:150999258-150999259	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs543880212	chr4:150999264-150999265	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs563576595	chr4:150999285-150999286	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD

Chromatin state (count:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:150989800-150998400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:150994000-150999000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:150994400-150998800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr4:150994600-150998800	Weak transcription	HSMM	muscle
5	chr4:150994800-150998600	Weak transcription	Brain Angular Gyrus	brain
6	chr4:150994800-150998800	Weak transcription	Adipose Nuclei	Adipose
7	chr4:150994800-150998800	Weak transcription	Colon Smooth Muscle	Colon
8	chr4:150995000-150998400	Weak transcription	Brain Anterior Caudate	brain
9	chr4:150995000-150998600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:150995000-150998800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:150995000-150998800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr4:150995000-150998800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:150995000-150998800	Weak transcription	HSMMtube	muscle
14	chr4:150995000-150998800	Weak transcription	NH-A	brain
15	chr4:150995000-150998800	Weak transcription	NHDF-Ad	bronchial
16	chr4:150995000-150998800	Weak transcription	NHLF	lung
17	chr4:150995200-150998800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr4:150995400-150998800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:150995400-150998800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr4:150995400-150998800	Weak transcription	Osteobl	bone
21	chr4:150997000-150998600	Enhancers	A549	lung
22	chr4:150997600-150998400	Enhancers	Brain Germinal Matrix	brain
23	chr4:150998200-150998400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:150998200-150998400	Enhancers	Brain Cingulate Gyrus	brain
25	chr4:150998200-150998400	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr4:150998200-150998600	Enhancers	Fetal Brain Male	brain
27	chr4:150998200-150998600	Enhancers	Fetal Brain Female	brain
28	chr4:150998200-150998600	Enhancers	Stomach Smooth Muscle	stomach
29	chr4:150998200-150998800	Enhancers	Fetal Heart	heart
30	chr4:150998400-150998600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr4:150998400-150998600	Enhancers	Brain Anterior Caudate	brain
32	chr4:150998400-150998600	Enhancers	Brain Hippocampus Middle	brain
33	chr4:150998400-150998600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
34	chr4:150998400-150998800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
35	chr4:150998400-150998800	Enhancers	Brain Substantia Nigra	brain
36	chr4:150998400-150998800	Enhancers	Left Ventricle	heart
37	chr4:150998400-150998800	Enhancers	Ovary	ovary
38	chr4:150998400-150998800	Enhancers	Rectal Smooth Muscle	rectum
39	chr4:150998400-150999000	Flanking Active TSS	Brain Cingulate Gyrus	brain
40	chr4:150998400-150999000	Flanking Active TSS	Brain Germinal Matrix	brain
41	chr4:150998400-150999200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr4:150998400-150999400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:150998400-151000400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:150998400-151001800	Active TSS	Fetal Kidney	kidney
45	chr4:150998400-151002400	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr4:150998600-150998800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr4:150998600-150998800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr4:150998600-150998800	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr4:150998600-150998800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr4:150998600-150998800	Flanking Active TSS	Brain Angular Gyrus	brain

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