Variant report

Variant	nsv525540
Chromosome Location	chr4:119279098-119303024
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	CEBPB	chr4:119281330-119281636	IMR90	lung:	n/a	chr4:119281590-119281598 chr4:119281492-119281503
2	CEBPB	chr4:119293193-119293304	IMR90	lung:	n/a	n/a
3	CEBPB	chr4:119288580-119288812	IMR90	lung:	n/a	n/a
4	CEBPB	chr4:119294969-119295325	IMR90	lung:	n/a	n/a
5	CEBPB	chr4:119281401-119281624	A549	lung:	n/a	chr4:119281590-119281598 chr4:119281492-119281503
6	CTCF	chr4:119279660-119279810	HMEC	breast:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
7	CTCF	chr4:119279631-119279782	K562	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
8	CTCF	chr4:119279580-119279730	GM12873	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
9	CTCF	chr4:119291099-119291152	Fibrobl	skin:	n/a	n/a
10	CTCF	chr4:119300670-119300740	Lung_OC	lung:	n/a	n/a
11	CTCF	chr4:119279560-119279710	GM12874	blood:	n/a	n/a
12	CTCF	chr4:119279620-119279770	HCFaa	heart:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
13	CTCF	chr4:119279620-119279770	HMF	breast:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
14	CTCF	chr4:119279660-119279810	GM12878	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
15	CTCF	chr4:119279683-119279770	GM12878	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
16	CTCF	chr4:119279460-119279610	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr4:119279600-119279750	HEEpiC	esophagus:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
18	CTCF	chr4:119279640-119279790	HEK293	kidney:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
19	CTCF	chr4:119279600-119279750	AoAF	blood vessel:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
20	CTCF	chr4:119279660-119279810	HCPEpiC	choroid plexus:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
21	CTCF	chr4:119279602-119279838	K562	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
22	CTCF	chr4:119279640-119279790	GM06990	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
23	CTCF	chr4:119279720-119279870	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr4:119279660-119279810	GM06990	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
25	CTCF	chr4:119279600-119279750	GM12875	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
26	CTCF	chr4:119279560-119279710	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr4:119279700-119279753	Hela-S3	cervix:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
28	CTCF	chr4:119279620-119279770	GM12872	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
29	CTCF	chr4:119279600-119279750	HCT-116	colon:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
30	CTCF	chr4:119279601-119279832	IMR90	lung:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
31	CTCF	chr4:119279640-119279790	WERI-Rb-1	eye:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
32	CTCF	chr4:119279660-119279810	HVMF	connective:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
33	CTCF	chr4:119279640-119279790	AG09309	skin:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
34	CTCF	chr4:119279640-119279790	HVMF	connective:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
35	CTCF	chr4:119279600-119279750	NHEK	skin:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
36	CTCF	chr4:119279600-119279750	GM12872	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
37	CTCF	chr4:119279560-119279710	HMEC	breast:	n/a	n/a
38	CTCF	chr4:119288458-119288510	GM10266	blood:	n/a	n/a
39	CTCF	chr4:119279580-119279730	K562	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
40	CTCF	chr4:119279640-119279790	GM12868	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
41	CTCF	chr4:119279620-119279770	GM12873	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
42	CTCF	chr4:119279660-119279810	GM12866	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
43	CTCF	chr4:119279680-119279830	RPTEC	kidney:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
44	CTCF	chr4:119279660-119279810	NHLF	lung:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
45	CTCF	chr4:119279694-119279722	GM13977	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
46	CTCF	chr4:119279640-119279790	MCF-7	breast:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
47	CTCF	chr4:119279541-119279880	GM12878	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
48	CTCF	chr4:119297289-119297362	Fibrobl	skin:	n/a	n/a
49	CTCF	chr4:119279532-119279811	H1-hESC	embryonic stem cell:	n/a	chr4:119279707-119279716 chr4:119279704-119279722
50	CTCF	chr4:119279620-119279770	NB4	blood:	n/a	chr4:119279707-119279716 chr4:119279704-119279722

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:119282020-119282070	SKMC	muscle:	n/a
2	chr4:119295633-119295683	ProgFib	skin:	n/a
3	chr4:119295633-119295683	HEEpiC	esophagus:	n/a
4	chr4:119282020-119282070	NT2-D1	testis:	n/a
5	chr4:119284446-119284496	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:119284446-119284496	AG04450	lung:	fetal
7	chr4:119282020-119282070	PrEC	prostate:	n/a
8	chr4:119282020-119282070	IMR90	lung:	fetal
9	chr4:119284446-119284496	HCF	heart:	n/a
10	chr4:119295633-119295683	NT2-D1	testis:	n/a
11	chr4:119282020-119282070	NB4	blood:	n/a
12	chr4:119284446-119284496	HL-60	blood:	n/a
13	chr4:119284446-119284496	ECC-1	luminal epithelium:	n/a
14	chr4:119295633-119295683	HRPEpiC	eye:	n/a
15	chr4:119295633-119295683	T-47D	breast:	n/a
16	chr4:119295633-119295683	MCF-7	breast:	n/a
17	chr4:119284446-119284496	RPTEC	kidney:	n/a
18	chr4:119282020-119282070	GM12891	blood:	n/a
19	chr4:119295633-119295683	GM12878	blood:	n/a
20	chr4:119284446-119284496	IMR90	lung:	fetal
21	chr4:119282020-119282070	RPTEC	kidney:	n/a
22	chr4:119284446-119284496	HCT-116	colon:	n/a
23	chr4:119295633-119295683	GM19239	blood:	n/a
24	chr4:119284446-119284496	NB4	blood:	n/a
25	chr4:119284446-119284496	BE2_C	brain:	n/a
26	chr4:119295633-119295683	BJ	skin:	n/a
27	chr4:119295633-119295683	U87	brain:	n/a
28	chr4:119295633-119295683	BE2_C	brain:	n/a
29	chr4:119282020-119282070	AG09309	skin:	n/a
30	chr4:119282020-119282070	AG04449	skin:	fetal
31	chr4:119282020-119282070	K562	blood:	n/a
32	chr4:119284446-119284496	PFSK-1	brain:	n/a
33	chr4:119295633-119295683	HepG2	liver:	n/a
34	chr4:119284446-119284496	H1-hESC	embryonic stem cell:	embryo
35	chr4:119284446-119284496	HUVEC	blood vessel:	n/a
36	chr4:119282020-119282070	LNCaP	prostate:	n/a
37	chr4:119282020-119282070	PANC-1	pancreas:	n/a
38	chr4:119284446-119284496	HIPEpiC	eye:	n/a
39	chr4:119295633-119295683	A549	lung:	n/a
40	chr4:119284446-119284496	HCM	heart:	n/a
41	chr4:119284446-119284496	GM12878	blood:	n/a
42	chr4:119284446-119284496	CMK	blood:	n/a
43	chr4:119295633-119295683	AG09319	gingival:	n/a
44	chr4:119284446-119284496	A549	lung:	n/a
45	chr4:119295633-119295683	HCPEpiC	choroid plexus:	n/a
46	chr4:119295633-119295683	Jurkat	blood:	n/a
47	chr4:119282020-119282070	HEK293	kidney:	embryo
48	chr4:119295633-119295683	HPAEpiC	pulmonary alveolar:	n/a
49	chr4:119282020-119282070	HL-60	blood:	n/a
50	chr4:119282020-119282070	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:119204030..119205775-chr4:119295374..119296879,2	K562	blood:
2	chr4:119297227..119299368-chr4:119300296..119302370,2	K562	blood:
3	chr4:119202015..119204587-chr4:119283908..119285983,2	K562	blood:
4	chr4:119292842..119294538-chr4:119297260..119300160,2	MCF-7	breast:
5	chr4:119297227..119299368-chr4:119300296..119302370,2	K562	blood:
6	chr4:119199772..119201389-chr4:119276128..119279305,3	MCF-7	breast:
7	chr4:119292842..119294538-chr4:119297260..119300160,2	MCF-7	breast:
8	chr4:119201789..119203327-chr4:119280623..119282185,2	K562	blood:
9	chr4:119198677..119205956-chr4:119272273..119279963,18	MCF-7	breast:
10	chr4:119199853..119201646-chr4:119293860..119297820,3	MCF-7	breast:

Variant related genes	Relation type
PRSS12	TF binding region
PRSS12	CpG island
ENSG00000269893	chromatin interactions

Extended variants
information (count: 491 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1514657	chr4:119279098-119279099	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572072485	chr4:119279112-119279113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs187420920	chr4:119279137-119279138	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs561150715	chr4:119279162-119279163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530045750	chr4:119279177-119279178	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs549998143	chr4:119279188-119279189	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs192321878	chr4:119279243-119279244	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs137945562	chr4:119279326-119279327	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs561134607	chr4:119279347-119279348	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs116767700	chr4:119279378-119279379	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs114741164	chr4:119279387-119279388	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs528443672	chr4:119279395-119279396	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs142942879	chr4:119279415-119279416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs13124454	chr4:119279431-119279432	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs77657370	chr4:119279441-119279442	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs368537965	chr4:119279554-119279555	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529639753	chr4:119279574-119279575	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs377612618	chr4:119279611-119279612	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs556096120	chr4:119279630-119279631	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs557121753	chr4:119279638-119279639	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570670327	chr4:119279721-119279722	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540025827	chr4:119279797-119279798	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs372794719	chr4:119279905-119279906	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs558340983	chr4:119279913-119279914	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184784709	chr4:119279930-119279931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs540648658	chr4:119279961-119279962	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs554653573	chr4:119280058-119280059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535092252	chr4:119280059-119280060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574776375	chr4:119280071-119280072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540242532	chr4:119280085-119280086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559759469	chr4:119280146-119280147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189044363	chr4:119280157-119280158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs7661210	chr4:119280167-119280168	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs192785713	chr4:119280169-119280170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs367745364	chr4:119280225-119280226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs532182468	chr4:119280282-119280283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7435677	chr4:119280288-119280289	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs559573771	chr4:119280289-119280290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528612441	chr4:119280297-119280298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs554881300	chr4:119280300-119280301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548285144	chr4:119280366-119280367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184665165	chr4:119280369-119280370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530821269	chr4:119280376-119280377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs71608367	chr4:119280452-119280453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550814440	chr4:119280454-119280455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190033678	chr4:119280458-119280459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1113677	chr4:119280513-119280514	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs539611691	chr4:119280516-119280517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181574626	chr4:119280576-119280577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566255426	chr4:119280577-119280578	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
Autism	19246517	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119275200-119284200	Weak transcription	NHDF-Ad	bronchial
2	chr4:119276200-119283000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr4:119276200-119283000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr4:119277400-119283200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:119278600-119279400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:119278600-119283200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr4:119278800-119281800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:119278800-119283200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:119279000-119279400	Weak transcription	Fetal Brain Female	brain
10	chr4:119279000-119279400	Enhancers	Fetal Lung	lung
11	chr4:119279000-119282200	Enhancers	Fetal Brain Male	brain
12	chr4:119279400-119279600	Enhancers	Fetal Brain Female	brain
13	chr4:119279400-119280200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:119279400-119281200	Weak transcription	Fetal Lung	lung
15	chr4:119279600-119280600	Weak transcription	Fetal Brain Female	brain
16	chr4:119280200-119280600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:119280600-119282400	Enhancers	Fetal Brain Female	brain
18	chr4:119280800-119281000	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr4:119281200-119281600	Enhancers	Fetal Lung	lung
20	chr4:119281800-119283200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr4:119282400-119282600	Enhancers	Duodenum Smooth Muscle	Duodenum
22	chr4:119283000-119284600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr4:119283000-119284600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr4:119283000-119284600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr4:119283200-119284600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr4:119283200-119284600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:119283200-119285400	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr4:119283400-119284400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr4:119283600-119284400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr4:119283600-119284400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr4:119284200-119284600	Enhancers	NHDF-Ad	bronchial
32	chr4:119284600-119289000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr4:119284600-119289000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:119289000-119289400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:119289000-119289600	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr4:119294400-119294800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr4:119294400-119295000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr4:119294400-119296400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:119294600-119295800	Enhancers	Muscle Satellite Cultured Cells	--
40	chr4:119294800-119295200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:119295200-119295400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr4:119295400-119295600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr4:119295600-119295800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr4:119296400-119297800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr4:119297800-119298000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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