Variant report

Variant	nsv830065
Chromosome Location	chr4:132134254-132338316
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	ATF2	chr4:132230758-132231240	GM12878	blood:	n/a	n/a
2	ATF3	chr4:132179544-132179772	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:132164565-132164579	K562	blood:	n/a	n/a
4	BACH1	chr4:132150946-132150962	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:132237834-132237865	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:132142159-132142343	K562	blood:	n/a	n/a
7	BATF	chr4:132269461-132269747	GM12878	blood:	n/a	n/a
8	BATF	chr4:132237297-132237506	GM12878	blood:	n/a	chr4:132237434-132237445
9	BATF	chr4:132269393-132269798	GM12878	blood:	n/a	n/a
10	BATF	chr4:132230807-132231142	GM12878	blood:	n/a	chr4:132230925-132230936
11	BATF	chr4:132230793-132231130	GM12878	blood:	n/a	chr4:132230925-132230936
12	BCL11A	chr4:132178348-132178643	GM12878	blood:	n/a	chr4:132178369-132178378
13	BCL11A	chr4:132178410-132178696	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:132230818-132231127	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:132178402-132178703	GM12878	blood:	n/a	n/a
16	CBX3	chr4:132209558-132210022	HCT-116	colon:	n/a	n/a
17	CCNT2	chr4:132300478-132300751	K562	blood:	n/a	n/a
18	CCNT2	chr4:132205064-132205471	K562	blood:	n/a	n/a
19	CEBPB	chr4:132334395-132334652	IMR90	lung:	n/a	chr4:132334512-132334525 chr4:132334513-132334524 chr4:132334514-132334523 chr4:132334512-132334525 chr4:132334512-132334523
20	CEBPB	chr4:132184264-132184515	HepG2	liver:	n/a	chr4:132184363-132184376 chr4:132184363-132184374 chr4:132184365-132184376
21	CEBPB	chr4:132179607-132179807	HepG2	liver:	n/a	chr4:132179698-132179709
22	CEBPB	chr4:132179537-132179884	ECC-1	luminal epithelium:	n/a	chr4:132179698-132179709
23	CEBPB	chr4:132300197-132300397	HepG2	liver:	n/a	chr4:132300269-132300282 chr4:132300270-132300281 chr4:132300256-132300267
24	CEBPB	chr4:132246562-132246885	IMR90	lung:	n/a	chr4:132246745-132246756
25	CEBPB	chr4:132246573-132246902	HepG2	liver:	n/a	chr4:132246745-132246756
26	CEBPB	chr4:132316111-132316328	HepG2	liver:	n/a	chr4:132316170-132316181 chr4:132316241-132316252 chr4:132316170-132316183 chr4:132316241-132316254 chr4:132316241-132316254
27	CEBPB	chr4:132334417-132334650	HepG2	liver:	n/a	chr4:132334512-132334525 chr4:132334513-132334524 chr4:132334514-132334523 chr4:132334512-132334525 chr4:132334512-132334523
28	CEBPB	chr4:132179571-132179733	A549	lung:	n/a	chr4:132179698-132179709
29	CEBPB	chr4:132334422-132334633	K562	blood:	n/a	chr4:132334512-132334525 chr4:132334513-132334524 chr4:132334514-132334523 chr4:132334512-132334525 chr4:132334512-132334523
30	CEBPB	chr4:132246621-132246930	K562	blood:	n/a	chr4:132246745-132246756
31	CEBPB	chr4:132179525-132179882	H1-hESC	embryonic stem cell:	n/a	chr4:132179698-132179709
32	CEBPB	chr4:132179496-132179815	ECC-1	luminal epithelium:	n/a	chr4:132179698-132179709
33	CEBPB	chr4:132299279-132299529	K562	blood:	n/a	n/a
34	CTCF	chr4:132314586-132314638	GM10248	blood:	n/a	n/a
35	CTCF	chr4:132223460-132223610	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr4:132223369-132223392	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr4:132223331-132223407	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:132223537-132223618	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:132223380-132223530	GM12865	blood:	n/a	n/a
40	CTCF	chr4:132300602-132300797	K562	blood:	n/a	n/a
41	CTCF	chr4:132159760-132159910	GM12867	blood:	n/a	n/a
42	CTCF	chr4:132168475-132168509	Lung_OC	lung:	n/a	n/a
43	CTCF	chr4:132223440-132223590	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr4:132300627-132300750	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr4:132223480-132223630	HMEC	breast:	n/a	n/a
46	CTCF	chr4:132223480-132223630	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:132223534-132223633	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:132223286-132223425	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:132274246-132274320	Fibrobl	skin:	n/a	n/a
50	CTCF	chr4:132223440-132223590	GM12865	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132300589-132300639	GM12891	blood:	n/a
2	chr4:132273830-132273880	NH-A	brain:	n/a
3	chr4:132300589-132300639	Hela-S3	cervix:	n/a
4	chr4:132273830-132273880	AG09319	gingival:	n/a
5	chr4:132273830-132273880	PrEC	prostate:	n/a
6	chr4:132273830-132273880	NB4	blood:	n/a
7	chr4:132273830-132273880	HRE	kidney:	n/a
8	chr4:132273830-132273880	SAEC	small airway:	n/a
9	chr4:132300589-132300639	K562	blood:	n/a
10	chr4:132273830-132273880	AG09309	skin:	n/a
11	chr4:132300589-132300639	MCF-7	breast:	n/a
12	chr4:132300589-132300639	HCPEpiC	choroid plexus:	n/a
13	chr4:132273830-132273880	A549	lung:	n/a
14	chr4:132273830-132273880	U87	brain:	n/a
15	chr4:132273830-132273880	BJ	skin:	n/a
16	chr4:132300589-132300639	SKMC	muscle:	n/a
17	chr4:132300589-132300639	CMK	blood:	n/a
18	chr4:132273830-132273880	GM12892	blood:	n/a
19	chr4:132273830-132273880	SKMC	muscle:	n/a
20	chr4:132273830-132273880	GM12891	blood:	n/a
21	chr4:132300589-132300639	NHBE	bronchial:	n/a
22	chr4:132273830-132273880	ProgFib	skin:	n/a
23	chr4:132273830-132273880	ovcar-3	ovarian:	n/a
24	chr4:132300589-132300639	HIPEpiC	eye:	n/a
25	chr4:132273830-132273880	HCT-116	colon:	n/a
26	chr4:132273830-132273880	H1-hESC	embryonic stem cell:	embryo
27	chr4:132273830-132273880	T-47D	breast:	n/a
28	chr4:132300589-132300639	A549	lung:	n/a
29	chr4:132300589-132300639	AG10803	skin:	n/a
30	chr4:132273830-132273880	PFSK-1	brain:	n/a
31	chr4:132273830-132273880	SK-N-SH	brain:	n/a
32	chr4:132300589-132300639	HEEpiC	esophagus:	n/a
33	chr4:132300589-132300639	T-47D	breast:	n/a
34	chr4:132300589-132300639	BE2_C	brain:	n/a
35	chr4:132273830-132273880	Caco-2	colon:	n/a
36	chr4:132273830-132273880	HEEpiC	esophagus:	n/a
37	chr4:132273830-132273880	SK-N-SH_RA	brain:	n/a
38	chr4:132300589-132300639	AG04450	lung:	fetal
39	chr4:132273830-132273880	LNCaP	prostate:	n/a
40	chr4:132300589-132300639	BJ	skin:	n/a
41	chr4:132300589-132300639	PrEC	prostate:	n/a
42	chr4:132300589-132300639	PANC-1	pancreas:	n/a
43	chr4:132300589-132300639	AG09319	gingival:	n/a
44	chr4:132273830-132273880	RPTEC	kidney:	n/a
45	chr4:132273830-132273880	SK-N-MC	brain:	n/a
46	chr4:132273830-132273880	NHDF-neo	bronchial:	n/a
47	chr4:132273830-132273880	HRPEpiC	eye:	n/a
48	chr4:132273830-132273880	IMR90	lung:	fetal
49	chr4:132300589-132300639	NHDF-neo	bronchial:	n/a
50	chr4:132300589-132300639	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:
2	chr4:132287444..132289970-chr4:132292320..132294677,2	K562	blood:
3	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:
4	chr4:132208528..132210188-chr4:132213412..132215740,2	MCF-7	breast:
5	chr4:132287444..132289970-chr4:132292320..132294677,2	K562	blood:
6	chr4:132149758..132152174-chr4:132152925..132155789,2	MCF-7	breast:
7	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:
8	chr4:132208528..132210188-chr4:132213412..132215740,2	MCF-7	breast:
9	chr4:132149758..132152174-chr4:132152925..132155789,2	MCF-7	breast:
10	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH10-7	chr4:132301168-132301496	ENSG00000250102.1
2	lnc-PCDH10-7	chr4:132300925-132301522	NONHSAT098311

Variant related genes	Relation type
RNU6-224P	TF binding region
ENSG00000250102	TF binding region
RNU6-224P	CpG island
ENSG00000250102	CpG island

Extended variants
information (count: 980 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536633268	chr4:132153420-132153421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs189805523	chr4:132153532-132153533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566968656	chr4:132153538-132153539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539178748	chr4:132153545-132153546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs34696537	chr4:132153559-132153560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558794930	chr4:132153574-132153575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116121294	chr4:132153607-132153608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539312844	chr4:132153651-132153652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555226117	chr4:132153659-132153660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551362491	chr4:132153758-132153759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368321957	chr4:132153770-132153771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182104699	chr4:132153787-132153788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188019630	chr4:132153798-132153799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558960979	chr4:132153839-132153840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572515007	chr4:132153862-132153863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544657445	chr4:132153864-132153865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534128196	chr4:132153870-132153871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564850123	chr4:132153878-132153879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375221600	chr4:132153883-132153884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558854661	chr4:132153913-132153914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550537119	chr4:132153918-132153919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191294342	chr4:132153984-132153985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554008342	chr4:132155205-132155206	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs144295759	chr4:132155231-132155232	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs538608537	chr4:132155277-132155278	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs558316681	chr4:132155285-132155286	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs191284742	chr4:132155305-132155306	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs377425545	chr4:132155318-132155319	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs543931534	chr4:132155347-132155348	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs376198585	chr4:132155355-132155356	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs554710842	chr4:132155356-132155357	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs574660652	chr4:132155360-132155361	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs540450052	chr4:132155399-132155400	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs540567029	chr4:132155418-132155419	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs113583157	chr4:132155440-132155441	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs532347916	chr4:132155443-132155444	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs184273828	chr4:132155537-132155538	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs377292900	chr4:132155543-132155544	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs562696742	chr4:132155563-132155564	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs531733427	chr4:132155564-132155565	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs141285552	chr4:132155575-132155576	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs189637268	chr4:132155611-132155612	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs527862120	chr4:132155693-132155694	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs547613935	chr4:132155772-132155773	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs570807566	chr4:132155773-132155774	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs34936034	chr4:132155795-132155796	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs182325822	chr4:132167429-132167430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs28605768	chr4:132167432-132167433	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs79319713	chr4:132167440-132167441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs116742051	chr4:132167459-132167460	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
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
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
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132153400-132154000	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr4:132155200-132155800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:132167400-132167800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:132169600-132170000	Enhancers	Dnd41	blood
5	chr4:132178600-132178800	Enhancers	Brain Substantia Nigra	brain
6	chr4:132178800-132179600	Weak transcription	Brain Substantia Nigra	brain
7	chr4:132179000-132180000	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr4:132179400-132180400	Enhancers	Brain Hippocampus Middle	brain
9	chr4:132179600-132180000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr4:132179600-132180400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr4:132179600-132180600	Enhancers	Brain Cingulate Gyrus	brain
12	chr4:132179600-132180600	Enhancers	Brain Substantia Nigra	brain
13	chr4:132208400-132210400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:132211600-132211800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
15	chr4:132211600-132211800	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr4:132211600-132211800	Flanking Bivalent TSS/Enh	HSMM	muscle
17	chr4:132211600-132211800	Enhancers	HSMMtube	muscle
18	chr4:132211600-132211800	ZNF genes & repeats	HUVEC	blood vessel
19	chr4:132211600-132211800	ZNF genes & repeats	K562	blood
20	chr4:132211600-132211800	Flanking Bivalent TSS/Enh	NH-A	brain
21	chr4:132211600-132211800	Flanking Bivalent TSS/Enh	NHEK	skin
22	chr4:132211600-132211800	Flanking Bivalent TSS/Enh	NHLF	lung
23	chr4:132211600-132211800	Enhancers	Osteobl	bone
24	chr4:132211600-132212000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr4:132211600-132212000	ZNF genes & repeats	Primary T cells from cord blood	blood
26	chr4:132211600-132212000	ZNF genes & repeats	GM12878-XiMat	blood
27	chr4:132211600-132212000	Active TSS	HMEC	breast
28	chr4:132211800-132212000	Active TSS	HSMM	muscle
29	chr4:132211800-132212000	Bivalent/Poised TSS	NHEK	skin
30	chr4:132214600-132214800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:132215200-132215400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:132223600-132223800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:132223800-132224800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr4:132237000-132238600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr4:132265600-132266600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr4:132265800-132269800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr4:132265800-132269800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr4:132266000-132266200	Enhancers	H9 Cell Line	embryonic stem cell
39	chr4:132266000-132266400	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr4:132266000-132266600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr4:132266000-132266800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr4:132266000-132266800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr4:132266000-132268800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr4:132266600-132267600	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr4:132266600-132267600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr4:132266800-132267800	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr4:132266800-132267800	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr4:132267600-132268600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr4:132267600-132269800	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr4:132267800-132268200	Enhancers	H9 Cell Line	embryonic stem cell

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