Variant report

Variant	esv3584522
Chromosome Location	chr4:100432841-100467011
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:95)
CpG islands
(count:62)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:95 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:100458228-100458410	HepG2	liver:	n/a	n/a
2	CEBPB	chr4:100458878-100459118	HepG2	liver:	n/a	chr4:100459009-100459020 chr4:100459022-100459035 chr4:100459008-100459021
3	CEBPB	chr4:100450505-100450659	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr4:100450378-100450743	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr4:100446841-100446997	HepG2	liver:	n/a	n/a
6	CTCF	chr4:100446860-100447010	K562	blood:	n/a	n/a
7	CTCF	chr4:100446860-100447010	MCF-7	breast:	n/a	n/a
8	CTCF	chr4:100446798-100447002	K562	blood:	n/a	n/a
9	CTCF	chr4:100446888-100446957	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr4:100446840-100446990	Caco-2	colon:	n/a	n/a
11	CTCF	chr4:100446840-100446990	BE2_C	brain:	n/a	n/a
12	CTCF	chr4:100446822-100446989	MCF-7	breast:	n/a	n/a
13	CTCF	chr4:100446813-100447005	HepG2	liver:	n/a	n/a
14	CTCF	chr4:100446900-100447050	BE2_C	brain:	n/a	n/a
15	CTCF	chr4:100446840-100446990	HepG2	liver:	n/a	n/a
16	CTCF	chr4:100457009-100457116	Pancreas_OC	pancreas:	n/a	n/a
17	CTCF	chr4:100440995-100441133	K562	blood:	n/a	chr4:100441033-100441054 chr4:100441031-100441049
18	CTCF	chr4:100446855-100447002	K562	blood:	n/a	n/a
19	CTCF	chr4:100446813-100447003	MCF-7	breast:	n/a	n/a
20	CTCF	chr4:100446874-100446966	LNCaP	prostate:	n/a	n/a
21	CTCF	chr4:100446796-100447098	HepG2	liver:	n/a	n/a
22	CTCF	chr4:100446836-100446926	Fibrobl	skin:	n/a	n/a
23	CTCF	chr4:100458484-100458598	GM20000	blood:	n/a	n/a
24	CTCF	chr4:100446787-100447098	MCF-7	breast:	n/a	n/a
25	CTCF	chr4:100446797-100447002	MCF-7	breast:	n/a	n/a
26	CTCF	chr4:100446764-100447012	K562	blood:	n/a	n/a
27	CTCF	chr4:100446779-100447047	K562	blood:	n/a	n/a
28	CTCF	chr4:100446822-100446974	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:100446900-100447050	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr4:100446848-100446947	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:100446852-100446942	Gliobla	brain:	n/a	n/a
32	CTCF	chr4:100446780-100446930	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr4:100458483-100458536	GM10248	blood:	n/a	n/a
34	CTCF	chr4:100446819-100446991	MCF-7	breast:	n/a	n/a
35	EP300	chr4:100450413-100450770	Hela-S3	cervix:	n/a	chr4:100450668-100450675
36	EP300	chr4:100457989-100458430	HepG2	liver:	n/a	n/a
37	FOXA1	chr4:100457936-100458510	HepG2	liver:	n/a	n/a
38	FOXA1	chr4:100458034-100458437	HepG2	liver:	n/a	n/a
39	FOXA1	chr4:100457933-100458581	HepG2	liver:	n/a	n/a
40	FOXA1	chr4:100457977-100458451	HepG2	liver:	n/a	n/a
41	FOXA2	chr4:100458162-100458425	A549	lung:	n/a	n/a
42	FOXA2	chr4:100457966-100458520	HepG2	liver:	n/a	n/a
43	FOXA2	chr4:100458151-100458493	A549	lung:	n/a	n/a
44	FOXA2	chr4:100444119-100444318	HepG2	liver:	n/a	n/a
45	FOXA2	chr4:100457967-100458417	HepG2	liver:	n/a	n/a
46	GATA2	chr4:100442373-100442835	SH-SY5Y	brain:	n/a	n/a
47	GATA2	chr4:100438319-100438783	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr4:100442509-100442817	MCF-7	breast:	n/a	n/a
49	GATA3	chr4:100442675-100442846	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr4:100453218-100453282	SH-SY5Y	brain:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:100434274-100434324	NH-A	brain:	n/a
2	chr4:100434274-100434324	NH-A	brain:	n/a
3	chr4:100434274-100434324	HEK293	kidney:	embryo
4	chr4:100434274-100434324	AG09309	skin:	n/a
5	chr4:100434274-100434324	T-47D	breast:	n/a
6	chr4:100434274-100434324	SK-N-SH	brain:	n/a
7	chr4:100434274-100434324	ovcar-3	ovarian:	n/a
8	chr4:100434274-100434324	GM06990	blood:	n/a
9	chr4:100434274-100434324	GM12892	blood:	n/a
10	chr4:100434274-100434324	HCM	heart:	n/a
11	chr4:100434274-100434324	NHBE	bronchial:	n/a
12	chr4:100434274-100434324	Hela-S3	cervix:	n/a
13	chr4:100434274-100434324	Jurkat	blood:	n/a
14	chr4:100434274-100434324	SK-N-SH_RA	brain:	n/a
15	chr4:100434274-100434324	HL-60	blood:	n/a
16	chr4:100434274-100434324	GM19239	blood:	n/a
17	chr4:100434274-100434324	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:100434274-100434324	HRPEpiC	eye:	n/a
19	chr4:100434274-100434324	HCT-116	colon:	n/a
20	chr4:100434274-100434324	Caco-2	colon:	n/a
21	chr4:100434274-100434324	MCF-7	breast:	n/a
22	chr4:100434274-100434324	AG04450	lung:	fetal
23	chr4:100434274-100434324	PFSK-1	brain:	n/a
24	chr4:100434274-100434324	PANC-1	pancreas:	n/a
25	chr4:100434274-100434324	LNCaP	prostate:	n/a
26	chr4:100434274-100434324	HIPEpiC	eye:	n/a
27	chr4:100434274-100434324	SAEC	small airway:	n/a
28	chr4:100434274-100434324	CMK	blood:	n/a
29	chr4:100434274-100434324	RPTEC	kidney:	n/a
30	chr4:100434274-100434324	HRE	kidney:	n/a
31	chr4:100434274-100434324	SKMC	muscle:	n/a
32	chr4:100434274-100434324	BJ	skin:	n/a
33	chr4:100434274-100434324	HMEC	breast:	n/a
34	chr4:100434274-100434324	SK-N-MC	brain:	n/a
35	chr4:100434274-100434324	A549	lung:	n/a
36	chr4:100434274-100434324	NHDF-neo	bronchial:	n/a
37	chr4:100434274-100434324	IMR90	lung:	fetal
38	chr4:100434274-100434324	MCF10A-Er-Src	breast:	n/a
39	chr4:100434274-100434324	AG04449	skin:	fetal
40	chr4:100434274-100434324	HRCEpiC	kidney:	n/a
41	chr4:100434274-100434324	HUVEC	blood vessel:	n/a
42	chr4:100434274-100434324	HCPEpiC	choroid plexus:	n/a
43	chr4:100434274-100434324	U87	brain:	n/a
44	chr4:100434274-100434324	BE2_C	brain:	n/a
45	chr4:100434274-100434324	HAEpiC	amniotic membrane:	n/a
46	chr4:100434274-100434324	PrEC	prostate:	n/a
47	chr4:100434274-100434324	AoSMC	blood vessel:	n/a
48	chr4:100434274-100434324	ECC-1	luminal epithelium:	n/a
49	chr4:100434274-100434324	ProgFib	skin:	n/a
50	chr4:100434274-100434324	HEEpiC	esophagus:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:100446974..100449213-chr4:100450825..100453764,2	MCF-7	breast:
2	chr4:100458736..100461686-chr4:100868132..100870522,2	K562	blood:
3	chr4:100433956..100434757-chr5:13844267..13844959,2	MCF-7	breast:
4	chr4:100442006..100443922-chr4:100445466..100447568,2	K562	blood:
5	chr4:100446974..100449213-chr4:100450825..100453764,2	MCF-7	breast:
6	chr4:100442006..100443922-chr4:100445466..100447568,2	K562	blood:
7	chr4:100452738..100454334-chr4:100458012..100459573,2	K562	blood:
8	chr4:100457175..100460170-chr4:100461778..100463584,2	K562	blood:
9	chr4:100457175..100460170-chr4:100461778..100463584,2	K562	blood:
10	chr4:100452738..100454334-chr4:100458012..100459573,2	K562	blood:
11	chr20:52481362..52483334-chr4:100456733..100459317,2	MCF-7	breast:
12	chr4:100459336..100463167-chr4:100464703..100466787,3	K562	blood:
13	chr4:100449160..100451370-chr4:100870396..100872457,2	K562	blood:
14	chr4:100459336..100463167-chr4:100464703..100466787,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTTP-1	chr4:100440649-100441494	l_2693_chr4:100440424-100441494_placenta
2	lnc-MTTP-1	chr4:100440425-100440550	l_2693_chr4:100440424-100441494_placenta

No data

Variant related genes	Relation type
C4orf17	TF binding region
C4orf17	CpG island
ENSG00000164032	chromatin interactions
ENSG00000245322	chromatin interactions

Extended variants
information (count: 756 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:756 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550464551	chr4:100434240-100434241	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs568615017	chr4:100434241-100434242	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs139422953	chr4:100434253-100434254	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs112241691	chr4:100434259-100434260	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs142182271	chr4:100434263-100434264	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs554111966	chr4:100434285-100434286	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs201368502	chr4:100434303-100434304	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs150052319	chr4:100434321-100434322	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs201328109	chr4:100434323-100434324	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs539575720	chr4:100434333-100434334	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs200888528	chr4:100434365-100434366	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs367738210	chr4:100434370-100434371	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs576046439	chr4:100434376-100434377	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs145276985	chr4:100438198-100438199	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs11930574	chr4:100438329-100438330	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs571943561	chr4:100438365-100438366	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs532696911	chr4:100438394-100438395	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs140638276	chr4:100438422-100438423	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs190965540	chr4:100438431-100438432	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs530013592	chr4:100438441-100438442	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs549272522	chr4:100438475-100438476	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs567181421	chr4:100438480-100438481	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs2718686	chr4:100438486-100438487	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs113783060	chr4:100438510-100438511	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs546437047	chr4:100438512-100438513	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs376778231	chr4:100438526-100438527	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs35443703	chr4:100438570-100438571	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs571099422	chr4:100438576-100438577	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs182346230	chr4:100438600-100438601	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs556753363	chr4:100438625-100438626	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs74741645	chr4:100438628-100438629	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs535832722	chr4:100438646-100438647	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs114345807	chr4:100438657-100438658	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs573627773	chr4:100438672-100438673	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs141480312	chr4:100438701-100438702	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs71866040	chr4:100438709-100438710	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs74652291	chr4:100438735-100438736	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs398107724	chr4:100438741-100438742	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs540922378	chr4:100438748-100438749	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs546474013	chr4:100439254-100439255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548817753	chr4:100439313-100439314	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs182519803	chr4:100439316-100439317	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs532174406	chr4:100439326-100439327	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs376528288	chr4:100439357-100439358	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs368126276	chr4:100439361-100439362	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs115987346	chr4:100439365-100439366	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs114909098	chr4:100439406-100439407	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs188235280	chr4:100439433-100439434	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs111894116	chr4:100439458-100439459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548250048	chr4:100439490-100439491	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100434200-100434400	Active TSS	Gastric	stomach
2	chr4:100439200-100440800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr4:100439400-100439800	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr4:100439800-100440400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr4:100439800-100440400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr4:100440400-100440600	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr4:100449600-100451000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr4:100449800-100450600	Enhancers	Fetal Intestine Small	intestine
9	chr4:100449800-100451200	Enhancers	Fetal Intestine Large	intestine
10	chr4:100449800-100451200	Enhancers	Fetal Muscle Leg	muscle
11	chr4:100449800-100451200	Enhancers	HSMMtube	muscle
12	chr4:100449800-100451400	Enhancers	Fetal Lung	lung
13	chr4:100450200-100451000	Enhancers	HSMM	muscle
14	chr4:100450400-100451200	Enhancers	Colon Smooth Muscle	Colon
15	chr4:100451000-100451400	Enhancers	Stomach Mucosa	stomach
16	chr4:100451200-100457000	Weak transcription	Fetal Muscle Leg	muscle
17	chr4:100451200-100457200	Weak transcription	Fetal Intestine Large	intestine
18	chr4:100451400-100452600	Weak transcription	Stomach Mucosa	stomach
19	chr4:100452600-100452800	Enhancers	Stomach Mucosa	stomach
20	chr4:100457000-100457200	Enhancers	HepG2	liver
21	chr4:100457000-100458200	Enhancers	HSMM	muscle
22	chr4:100457000-100458200	Enhancers	HSMMtube	muscle
23	chr4:100457000-100458600	Enhancers	Fetal Muscle Leg	muscle
24	chr4:100457200-100457600	Bivalent Enhancer	HepG2	liver
25	chr4:100457200-100457800	Enhancers	Fetal Muscle Trunk	muscle
26	chr4:100457200-100460600	Enhancers	Fetal Intestine Small	intestine
27	chr4:100457200-100462200	Enhancers	Fetal Intestine Large	intestine
28	chr4:100457400-100457600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr4:100457400-100457800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:100457400-100457800	Enhancers	Fetal Lung	lung
31	chr4:100457600-100457800	Enhancers	HMEC	breast
32	chr4:100457600-100458000	Flanking Bivalent TSS/Enh	HepG2	liver
33	chr4:100457600-100458600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:100457600-100459600	Enhancers	Duodenum Mucosa	Duodenum
35	chr4:100457800-100459400	Enhancers	Liver	Liver
36	chr4:100458000-100459200	Enhancers	HepG2	liver
37	chr4:100458400-100459200	Enhancers	Small Intestine	intestine
38	chr4:100458600-100484000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:100459000-100459400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:100459200-100461800	Weak transcription	Small Intestine	intestine
41	chr4:100459400-100472200	Weak transcription	Liver	Liver
42	chr4:100459400-100477000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr4:100459600-100461400	Weak transcription	Duodenum Mucosa	Duodenum
44	chr4:100460200-100460600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr4:100460600-100461800	Weak transcription	Fetal Intestine Small	intestine
46	chr4:100460800-100462200	Enhancers	A549	lung
47	chr4:100461400-100462200	Enhancers	Duodenum Mucosa	Duodenum
48	chr4:100461800-100462000	Enhancers	Small Intestine	intestine
49	chr4:100461800-100462600	Enhancers	Fetal Intestine Small	intestine
50	chr4:100462000-100462200	Enhancers	Psoas Muscle	Psoas

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links