Variant report

Variant	esv3427017
Chromosome Location	chr4:100200905-100232354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:87)
CpG islands
(count:244)
Chromatin interactive
region (count:5)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:87 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:100221944-100222479	MCF-7	breast:	n/a	n/a
2	CEBPB	chr4:100222100-100222264	HepG2	liver:	n/a	n/a
3	CEBPB	chr4:100222024-100222886	IMR90	lung:	n/a	n/a
4	CEBPB	chr4:100222069-100222783	HepG2	liver:	n/a	n/a
5	CEBPB	chr4:100222053-100222429	MCF-7	breast:	n/a	n/a
6	CTCF	chr4:100218247-100218279	Lung_OC	lung:	n/a	n/a
7	CTCF	chr4:100205135-100205258	GM20000	blood:	n/a	n/a
8	CTCF	chr4:100204020-100204170	GM12868	blood:	n/a	n/a
9	CTCF	chr4:100205771-100205783	LNCaP	prostate:	n/a	n/a
10	ELF1	chr4:100221930-100222371	MCF-7	breast:	n/a	n/a
11	FOS	chr4:100222189-100222404	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr4:100222106-100222588	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr4:100222090-100222604	MCF10A-Er-Src	breast:	n/a	n/a
14	FOXA1	chr4:100222061-100222403	HepG2	liver:	n/a	n/a
15	FOXA1	chr4:100208703-100208953	HepG2	liver:	n/a	chr4:100208828-100208840
16	FOXA1	chr4:100222030-100222336	HepG2	liver:	n/a	n/a
17	FOXA1	chr4:100222025-100222375	HepG2	liver:	n/a	n/a
18	FOXA2	chr4:100222042-100222312	HepG2	liver:	n/a	n/a
19	FOXA2	chr4:100213308-100213498	HepG2	liver:	n/a	n/a
20	FOXA2	chr4:100208747-100208938	HepG2	liver:	n/a	chr4:100208828-100208840
21	FOXP2	chr4:100222026-100222368	SK-N-MC	brain:	n/a	n/a
22	GATA3	chr4:100209310-100209505	SH-SY5Y	brain:	n/a	n/a
23	GATA3	chr4:100221910-100222445	MCF-7	breast:	n/a	n/a
24	HDAC2	chr4:100222037-100222307	MCF-7	breast:	n/a	n/a
25	MAFF	chr4:100228218-100228272	HepG2	liver:	n/a	chr4:100228227-100228245
26	MAFF	chr4:100222111-100223032	HepG2	liver:	n/a	chr4:100222591-100222609
27	MAFF	chr4:100222565-100222786	K562	blood:	n/a	chr4:100222591-100222609
28	MAFF	chr4:100227644-100227781	HepG2	liver:	n/a	n/a
29	MAFK	chr4:100222437-100223121	HepG2	liver:	n/a	chr4:100222593-100222608
30	MAFK	chr4:100222098-100223126	IMR90	lung:	n/a	chr4:100222593-100222608
31	MAFK	chr4:100227613-100227863	HepG2	liver:	n/a	n/a
32	MAFK	chr4:100228199-100228344	HepG2	liver:	n/a	n/a
33	MAFK	chr4:100228120-100228323	HepG2	liver:	n/a	n/a
34	MAFK	chr4:100227623-100227811	IMR90	lung:	n/a	n/a
35	MAFK	chr4:100222558-100222716	K562	blood:	n/a	chr4:100222593-100222608
36	MAFK	chr4:100227631-100227815	HepG2	liver:	n/a	n/a
37	MAFK	chr4:100222468-100223014	HepG2	liver:	n/a	chr4:100222593-100222608
38	MAFK	chr4:100222216-100222221	HepG2	liver:	n/a	n/a
39	MAX	chr4:100207952-100208210	NB4	blood:	n/a	chr4:100208103-100208113
40	MAZ	chr4:100210803-100210851	HepG2	liver:	n/a	n/a
41	MYC	chr4:100228998-100229062	HUVEC	blood vessel:	n/a	n/a
42	MYC	chr4:100221995-100222800	MCF10A-Er-Src	breast:	n/a	n/a
43	MYC	chr4:100221991-100222901	MCF10A-Er-Src	breast:	n/a	n/a
44	MYC	chr4:100223182-100223251	MCF10A-Er-Src	breast:	n/a	n/a
45	NFIC	chr4:100221959-100222370	HepG2	liver:	n/a	n/a
46	NFIC	chr4:100221955-100222460	ECC-1	luminal epithelium:	n/a	n/a
47	NFIC	chr4:100221996-100222512	SK-N-SH	brain:	n/a	n/a
48	NFIC	chr4:100221965-100222332	SK-N-SH	brain:	n/a	n/a
49	NFIC	chr4:100221847-100222519	ECC-1	luminal epithelium:	n/a	n/a
50	POLR2A	chr4:100229966-100229980	MCF10A-Er-Src	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:100212502-100212552	HL-60	blood:	n/a
2	chr4:100222470-100222520	IMR90	lung:	fetal
3	chr4:100228660-100228710	AG09319	gingival:	n/a
4	chr4:100222470-100222520	HL-60	blood:	n/a
5	chr4:100212536-100212586	SK-N-SH_RA	brain:	n/a
6	chr4:100212536-100212586	ECC-1	luminal epithelium:	n/a
7	chr4:100212502-100212552	AG09319	gingival:	n/a
8	chr4:100212502-100212552	NT2-D1	testis:	n/a
9	chr4:100212536-100212586	MCF-7	breast:	n/a
10	chr4:100228660-100228710	SKMC	muscle:	n/a
11	chr4:100222470-100222520	H1-hESC	embryonic stem cell:	embryo
12	chr4:100222470-100222520	HIPEpiC	eye:	n/a
13	chr4:100228660-100228710	HAEpiC	amniotic membrane:	n/a
14	chr4:100228660-100228710	GM12892	blood:	n/a
15	chr4:100212502-100212552	LNCaP	prostate:	n/a
16	chr4:100222470-100222520	Jurkat	blood:	n/a
17	chr4:100228660-100228710	GM06990	blood:	n/a
18	chr4:100212536-100212586	RPTEC	kidney:	n/a
19	chr4:100212502-100212552	HAEpiC	amniotic membrane:	n/a
20	chr4:100212502-100212552	A549	lung:	n/a
21	chr4:100228660-100228710	BE2_C	brain:	n/a
22	chr4:100212536-100212586	MCF10A-Er-Src	breast:	n/a
23	chr4:100212536-100212586	GM12891	blood:	n/a
24	chr4:100222470-100222520	A549	lung:	n/a
25	chr4:100222470-100222520	NT2-D1	testis:	n/a
26	chr4:100212502-100212552	SK-N-MC	brain:	n/a
27	chr4:100222470-100222520	NHBE	bronchial:	n/a
28	chr4:100212502-100212552	HUVEC	blood vessel:	n/a
29	chr4:100228660-100228710	NHBE	bronchial:	n/a
30	chr4:100222470-100222520	HAEpiC	amniotic membrane:	n/a
31	chr4:100212502-100212552	HRE	kidney:	n/a
32	chr4:100228660-100228710	AG09309	skin:	n/a
33	chr4:100228660-100228710	ProgFib	skin:	n/a
34	chr4:100212502-100212552	HNPCEpiC	eye:	n/a
35	chr4:100212536-100212586	NT2-D1	testis:	n/a
36	chr4:100212502-100212552	GM12891	blood:	n/a
37	chr4:100212502-100212552	CMK	blood:	n/a
38	chr4:100222470-100222520	K562	blood:	n/a
39	chr4:100228660-100228710	HCT-116	colon:	n/a
40	chr4:100212502-100212552	HepG2	liver:	n/a
41	chr4:100222470-100222520	GM12878	blood:	n/a
42	chr4:100228660-100228710	AG10803	skin:	n/a
43	chr4:100228660-100228710	PrEC	prostate:	n/a
44	chr4:100212502-100212552	HCM	heart:	n/a
45	chr4:100222470-100222520	PANC-1	pancreas:	n/a
46	chr4:100212502-100212552	HRCEpiC	kidney:	n/a
47	chr4:100228660-100228710	AoSMC	blood vessel:	n/a
48	chr4:100222470-100222520	AG04449	skin:	fetal
49	chr4:100222470-100222520	HNPCEpiC	eye:	n/a
50	chr4:100228660-100228710	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:100201270..100203218-chr4:100206334..100208825,2	K562	blood:
2	chr4:100231557..100233908-chr4:100237578..100239506,2	K562	blood:
3	chr4:100201270..100203218-chr4:100206334..100208825,2	K562	blood:
4	chr4:100226234..100228316-chr4:100230420..100232273,2	K562	blood:
5	chr4:100226234..100228316-chr4:100230420..100232273,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METAP1-3	chr4:100212094-100212105	ENSG00000246090
2	lnc-METAP1-3	chr4:100222108-100222455	ENSG00000246090
3	lnc-METAP1-3	chr4:100221626-100221812	ENSG00000246090
4	lnc-METAP1-3	chr4:100209823-100209942	ENSG00000246090
5	lnc-METAP1-3	chr4:100222108-100222513	ENSG00000246090
6	lnc-METAP1-3	chr4:100221456-100221527	ENSG00000246090
7	lnc-METAP1-3	chr4:100212093-100212162	ENSG00000246090
8	lnc-METAP1-3	chr4:100221626-100221812	ENSG00000246090
9	lnc-METAP1-3	chr4:100221456-100221527	ENSG00000246090
10	lnc-C4orf17-3	chr4:100229214-100229458	l_2691_chr4:100229213-100242580_adipose
11	lnc-METAP1-3	chr4:100202339-100202398	ENSG00000246090
12	lnc-METAP1-3	chr4:100207952-100208190	ENSG00000246090

No data

Variant related genes	Relation type
ADH1A	TF binding region
ENSG00000246090	TF binding region
ADH1A	CpG island
ENSG00000246090	CpG island

Extended variants
information (count: 1039 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368331822	chr4:100200908-100200909	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557886481	chr4:100201013-100201014	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569964854	chr4:100201074-100201075	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs56098612	chr4:100201075-100201076	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377671214	chr4:100201093-100201094	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533797348	chr4:100201134-100201135	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537141225	chr4:100201136-100201137	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555866298	chr4:100201183-100201184	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573931946	chr4:100201190-100201191	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112637317	chr4:100201242-100201243	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541388819	chr4:100201249-100201250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553109363	chr4:100201250-100201251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28364331	chr4:100201295-100201296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142658552	chr4:100201346-100201347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150277869	chr4:100201365-100201366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371748133	chr4:100201384-100201385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138883026	chr4:100201385-100201386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372220406	chr4:100201386-100201387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149408684	chr4:100201388-100201389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199556184	chr4:100201426-100201427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561847120	chr4:100201450-100201451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201819088	chr4:100201453-100201454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375546922	chr4:100201458-100201459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370898699	chr4:100201468-100201469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs28364330	chr4:100201477-100201478	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs60357540	chr4:100201481-100201482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371792921	chr4:100201485-100201486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs28364329	chr4:100201508-100201509	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs569705560	chr4:100201532-100201533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576429117	chr4:100201544-100201545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185561592	chr4:100201585-100201586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571425384	chr4:100201586-100201587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549335166	chr4:100201623-100201624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567716412	chr4:100201625-100201626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs5860574	chr4:100201626-100201627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs975833	chr4:100201739-100201740	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs34362837	chr4:100201769-100201770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553286138	chr4:100201850-100201851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs28364327	chr4:100201869-100201870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190662513	chr4:100201872-100201873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374526222	chr4:100201881-100201882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377688433	chr4:100201957-100201958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182854129	chr4:100201994-100201995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576280414	chr4:100202007-100202008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538790391	chr4:100202042-100202043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543573711	chr4:100202062-100202063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1229976	chr4:100202078-100202079	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs28364326	chr4:100202084-100202085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540770076	chr4:100202126-100202127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187505296	chr4:100202139-100202140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	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
Autism	18414403	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100189400-100212400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:100192400-100205600	Weak transcription	Aorta	Aorta
3	chr4:100196200-100210800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:100197600-100205000	Strong transcription	Liver	Liver
5	chr4:100198000-100214600	Weak transcription	Fetal Intestine Small	intestine
6	chr4:100198800-100201200	Enhancers	Fetal Lung	lung
7	chr4:100201200-100202600	Weak transcription	Fetal Lung	lung
8	chr4:100202600-100203000	Enhancers	Fetal Lung	lung
9	chr4:100203000-100209200	Weak transcription	Fetal Lung	lung
10	chr4:100204000-100204200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:100204200-100214600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr4:100205000-100206000	Genic enhancers	Liver	Liver
13	chr4:100205600-100205800	ZNF genes & repeats	Aorta	Aorta
14	chr4:100205600-100205800	Enhancers	Ovary	ovary
15	chr4:100205800-100207400	Weak transcription	Aorta	Aorta
16	chr4:100205800-100208600	Weak transcription	Ovary	ovary
17	chr4:100206000-100207400	Strong transcription	Liver	Liver
18	chr4:100207200-100207600	Weak transcription	Pancreas	Pancrea
19	chr4:100207400-100208200	ZNF genes & repeats	Aorta	Aorta
20	chr4:100207400-100208800	Genic enhancers	Liver	Liver
21	chr4:100207600-100207800	Enhancers	Pancreas	Pancrea
22	chr4:100207600-100208000	Enhancers	Spleen	Spleen
23	chr4:100207800-100212400	Weak transcription	Pancreas	Pancrea
24	chr4:100208200-100212000	Weak transcription	Aorta	Aorta
25	chr4:100208800-100209000	Flanking Active TSS	Liver	Liver
26	chr4:100209000-100209200	Transcr. at gene 5' and 3'	Liver	Liver
27	chr4:100209200-100209600	Enhancers	Fetal Lung	lung
28	chr4:100209200-100209800	Flanking Active TSS	Liver	Liver
29	chr4:100209600-100213800	Weak transcription	Fetal Lung	lung
30	chr4:100209800-100210000	Active TSS	Liver	Liver
31	chr4:100210000-100210200	Flanking Active TSS	Liver	Liver
32	chr4:100210200-100212200	Active TSS	Liver	Liver
33	chr4:100210800-100211400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr4:100211400-100213400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr4:100212000-100213200	Strong transcription	Aorta	Aorta
36	chr4:100212000-100214800	Weak transcription	Esophagus	oesophagus
37	chr4:100212200-100213200	Flanking Active TSS	Liver	Liver
38	chr4:100212400-100212800	Enhancers	Pancreas	Pancrea
39	chr4:100212400-100214200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr4:100213200-100213800	Enhancers	Liver	Liver
41	chr4:100213200-100214800	Weak transcription	Aorta	Aorta
42	chr4:100213400-100214000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:100213800-100214400	Strong transcription	Fetal Lung	lung
44	chr4:100214000-100214400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:100214200-100216000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr4:100214400-100214600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:100214400-100215000	Enhancers	HMEC	breast
48	chr4:100214400-100216400	ZNF genes & repeats	Fetal Lung	lung
49	chr4:100214600-100215000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr4:100214600-100215200	ZNF genes & repeats	Fetal Intestine Small	intestine

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