Variant report

Variant	nsv999152
Chromosome Location	chr4:119001143-119138322
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:331)
CpG islands
(count:123)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:331 , 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	BHLHE40	chr4:119034526-119034599	GM12878	blood:	n/a	n/a
2	CBX3	chr4:119007354-119007992	HCT-116	colon:	n/a	n/a
3	CEBPB	chr4:119074634-119074699	HepG2	liver:	n/a	chr4:119074679-119074690
4	CEBPB	chr4:119006659-119006859	HepG2	liver:	n/a	chr4:119006661-119006669
5	CEBPB	chr4:119060525-119060719	A549	lung:	n/a	chr4:119060644-119060655 chr4:119060646-119060657 chr4:119060646-119060655
6	CEBPB	chr4:119075171-119075389	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:119094331-119094615	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:119075130-119075301	A549	lung:	n/a	n/a
9	CEBPB	chr4:119074583-119074757	IMR90	lung:	n/a	chr4:119074679-119074690
10	CEBPB	chr4:119060489-119060807	IMR90	lung:	n/a	chr4:119060644-119060655 chr4:119060646-119060657 chr4:119060646-119060655
11	CEBPB	chr4:119041524-119041823	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr4:119012317-119012451	HepG2	liver:	n/a	chr4:119012361-119012372
13	CEBPB	chr4:119060500-119060779	HepG2	liver:	n/a	chr4:119060644-119060655 chr4:119060646-119060657 chr4:119060646-119060655
14	CTCF	chr4:119099671-119099811	HepG2	liver:	n/a	n/a
15	CTCF	chr4:119062540-119062690	NB4	blood:	n/a	n/a
16	CTCF	chr4:119062494-119062595	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr4:119032260-119032410	AG04449	skin:	n/a	n/a
18	CTCF	chr4:119099760-119099910	AG04450	lung:	n/a	n/a
19	CTCF	chr4:119082640-119082790	GM12865	blood:	n/a	n/a
20	CTCF	chr4:119099700-119099850	HMEC	breast:	n/a	n/a
21	CTCF	chr4:119002660-119002810	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr4:119099697-119099817	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr4:119074766-119074798	GM13976	blood:	n/a	n/a
24	CTCF	chr4:119062320-119062470	HCT-116	colon:	n/a	n/a
25	CTCF	chr4:119108985-119109033	Lung_OC	lung:	n/a	n/a
26	CTCF	chr4:119062440-119062590	HEK293	kidney:	n/a	n/a
27	CTCF	chr4:119104060-119104210	NHLF	lung:	n/a	n/a
28	CTCF	chr4:119109035-119109038	Lung_OC	lung:	n/a	n/a
29	CTCF	chr4:119099709-119099849	GM10266	blood:	n/a	n/a
30	CTCF	chr4:119099761-119099786	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr4:119065334-119065372	GM20000	blood:	n/a	n/a
32	CTCF	chr4:119099766-119099794	HepG2	liver:	n/a	n/a
33	CTCF	chr4:119099680-119099830	HMF	breast:	n/a	n/a
34	CTCF	chr4:119099500-119099650	HVMF	connective:	n/a	n/a
35	CTCF	chr4:119099660-119099810	HCT-116	colon:	n/a	n/a
36	CTCF	chr4:119002700-119002850	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr4:119062500-119062650	AG09309	skin:	n/a	n/a
38	CTCF	chr4:119002700-119002850	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr4:119062460-119062610	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr4:119099702-119099862	GM12878	blood:	n/a	n/a
41	CTCF	chr4:119062500-119062650	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr4:119002620-119002770	HPF	lung:	n/a	n/a
43	CTCF	chr4:119062480-119062630	GM12873	blood:	n/a	n/a
44	CTCF	chr4:119080360-119080510	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr4:119095200-119095350	AG04450	lung:	n/a	n/a
46	CTCF	chr4:119099720-119099870	BJ	skin:	n/a	n/a
47	CTCF	chr4:119121361-119121425	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr4:119099680-119099830	AG10803	skin:	n/a	n/a
49	CTCF	chr4:119099680-119099830	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr4:119062480-119062630	BE2_C	brain:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:119095240-119095290	SAEC	small airway:	n/a
2	chr4:119095240-119095290	SAEC	small airway:	n/a
3	chr4:119095240-119095290	RPTEC	kidney:	n/a
4	chr4:119093021-119093071	GM12878	blood:	n/a
5	chr4:119093021-119093071	SK-N-SH_RA	brain:	n/a
6	chr4:119095240-119095290	HIPEpiC	eye:	n/a
7	chr4:119093021-119093071	AG04450	lung:	fetal
8	chr4:119093021-119093071	NHBE	bronchial:	n/a
9	chr4:119093021-119093071	SKMC	muscle:	n/a
10	chr4:119095240-119095290	Hela-S3	cervix:	n/a
11	chr4:119093021-119093071	HEEpiC	esophagus:	n/a
12	chr4:119093021-119093071	GM12892	blood:	n/a
13	chr4:119095240-119095290	HL-60	blood:	n/a
14	chr4:119093021-119093071	AG10803	skin:	n/a
15	chr4:119095240-119095290	AG04450	lung:	fetal
16	chr4:119095240-119095290	GM12878	blood:	n/a
17	chr4:119093021-119093071	U87	brain:	n/a
18	chr4:119095240-119095290	HCF	heart:	n/a
19	chr4:119093021-119093071	NHDF-neo	bronchial:	n/a
20	chr4:119095240-119095290	NT2-D1	testis:	n/a
21	chr4:119095240-119095290	HUVEC	blood vessel:	n/a
22	chr4:119095240-119095290	GM19239	blood:	n/a
23	chr4:119095240-119095290	HepG2	liver:	n/a
24	chr4:119093021-119093071	PANC-1	pancreas:	n/a
25	chr4:119093021-119093071	HCM	heart:	n/a
26	chr4:119095240-119095290	HRCEpiC	kidney:	n/a
27	chr4:119093021-119093071	Caco-2	colon:	n/a
28	chr4:119095240-119095290	HNPCEpiC	eye:	n/a
29	chr4:119095240-119095290	GM12891	blood:	n/a
30	chr4:119093021-119093071	BE2_C	brain:	n/a
31	chr4:119095240-119095290	GM12892	blood:	n/a
32	chr4:119095240-119095290	AG09309	skin:	n/a
33	chr4:119093021-119093071	T-47D	breast:	n/a
34	chr4:119093021-119093071	HIPEpiC	eye:	n/a
35	chr4:119093021-119093071	H1-hESC	embryonic stem cell:	embryo
36	chr4:119093021-119093071	HNPCEpiC	eye:	n/a
37	chr4:119095240-119095290	Caco-2	colon:	n/a
38	chr4:119093021-119093071	AoSMC	blood vessel:	n/a
39	chr4:119095240-119095290	U87	brain:	n/a
40	chr4:119093021-119093071	GM19239	blood:	n/a
41	chr4:119095240-119095290	NH-A	brain:	n/a
42	chr4:119095240-119095290	HAEpiC	amniotic membrane:	n/a
43	chr4:119093021-119093071	Hela-S3	cervix:	n/a
44	chr4:119095240-119095290	NHBE	bronchial:	n/a
45	chr4:119095240-119095290	HCM	heart:	n/a
46	chr4:119093021-119093071	HAEpiC	amniotic membrane:	n/a
47	chr4:119093021-119093071	HRCEpiC	kidney:	n/a
48	chr4:119093021-119093071	HEK293	kidney:	embryo
49	chr4:119095240-119095290	HCT-116	colon:	n/a
50	chr4:119093021-119093071	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr4:119038066..119040119-chr4:119044894..119047706,2	K562	blood:
2	chr4:119014582..119016836-chr4:119018455..119021400,2	K562	blood:
3	chr4:118998999..119001085-chr4:119002906..119004997,2	MCF-7	breast:
4	chr4:119103980..119104963-chr9:127026146..127026708,2	MCF-7	breast:
5	chr4:119038066..119040119-chr4:119044894..119047706,2	K562	blood:
6	chr4:119002654..119004598-chr4:119011337..119014286,2	K562	blood:
7	chr4:119063256..119065719-chr4:119066386..119068420,2	MCF-7	breast:
8	chr4:119002654..119004598-chr4:119011337..119014286,2	K562	blood:
9	chr4:119071407..119073017-chr4:119079096..119080736,2	K562	blood:
10	chr4:119014582..119016836-chr4:119018455..119021400,2	K562	blood:
11	chr4:119071407..119073017-chr4:119079096..119080736,2	K562	blood:
12	chr4:119063256..119065719-chr4:119066386..119068420,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDST3-6	chr4:119010062-119010551	NONHSAT097969

No data

Variant related genes	Relation type
FKBP4P1	TF binding region
FKBP4P1	CpG island

Extended variants
information (count: 4716 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4716 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554194996	chr4:119001145-119001146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569322013	chr4:119001177-119001178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538291701	chr4:119001221-119001222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs151083563	chr4:119001260-119001261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141366980	chr4:119001291-119001292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145116963	chr4:119001309-119001310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191160807	chr4:119001311-119001312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574938720	chr4:119001324-119001325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139000536	chr4:119001326-119001327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183624616	chr4:119001431-119001432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186847321	chr4:119001433-119001434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191839054	chr4:119001434-119001435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72905204	chr4:119001447-119001448	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs2389513	chr4:119001513-119001514	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs72905206	chr4:119001567-119001568	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs561951517	chr4:119001625-119001626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529702294	chr4:119001627-119001628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75076651	chr4:119001664-119001665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112922942	chr4:119001672-119001673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185155916	chr4:119001700-119001701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190347102	chr4:119001722-119001723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182029899	chr4:119001775-119001776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79245218	chr4:119001921-119001922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565932144	chr4:119001922-119001923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562857546	chr4:119001936-119001937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534614029	chr4:119001973-119001974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554763854	chr4:119001978-119001979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568251402	chr4:119001989-119001990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537288971	chr4:119002004-119002005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373078787	chr4:119002028-119002029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577446221	chr4:119002133-119002134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185543982	chr4:119002134-119002135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553113260	chr4:119002171-119002172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200057249	chr4:119002172-119002173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114657318	chr4:119002183-119002184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562087996	chr4:119002187-119002188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77096271	chr4:119002189-119002190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544430850	chr4:119002207-119002208	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11098424	chr4:119002221-119002222	Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs532125090	chr4:119002227-119002228	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11098425	chr4:119002231-119002232	Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs565548510	chr4:119002311-119002312	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528128295	chr4:119002365-119002366	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548500083	chr4:119002369-119002370	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568392760	chr4:119002375-119002376	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537224148	chr4:119002376-119002377	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2389514	chr4:119002414-119002415	Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs36053074	chr4:119002478-119002479	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77904060	chr4:119002524-119002525	Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150391984	chr4:119002534-119002535	Genic 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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:118999000-119002200	Weak transcription	Dnd41	blood
2	chr4:119002200-119002600	Genic enhancers	Dnd41	blood
3	chr4:119002600-119002800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:119002600-119003200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:119002600-119007600	Strong transcription	Dnd41	blood
6	chr4:119003200-119003800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr4:119003200-119007200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr4:119003800-119007000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr4:119006800-119008600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:119006800-119008800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:119006800-119009000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr4:119006800-119009200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr4:119007000-119007400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:119007000-119007800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr4:119007000-119007800	Enhancers	H9 Cell Line	embryonic stem cell
16	chr4:119007000-119008600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr4:119007000-119008800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:119007000-119009000	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr4:119007000-119009200	Enhancers	HUVEC	blood vessel
20	chr4:119007200-119007400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr4:119007200-119007800	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr4:119007200-119008600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr4:119007400-119008000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr4:119007400-119008000	Enhancers	Osteobl	bone
25	chr4:119007400-119008200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr4:119007400-119008400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr4:119007600-119008000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr4:119007600-119008000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:119007600-119008000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr4:119007600-119008000	Enhancers	HMEC	breast
31	chr4:119007600-119008000	Enhancers	NHEK	skin
32	chr4:119007600-119008400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr4:119007600-119009000	Weak transcription	Dnd41	blood
34	chr4:119007800-119008600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr4:119007800-119008600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:119007800-119009000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr4:119008400-119008800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr4:119008600-119008800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr4:119008800-119013800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:119009000-119011200	Strong transcription	Dnd41	blood
41	chr4:119009200-119013800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr4:119009600-119009800	Enhancers	H9 Cell Line	embryonic stem cell
43	chr4:119011200-119014600	Weak transcription	Dnd41	blood
44	chr4:119013800-119014200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:119013800-119014200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr4:119014600-119019200	Strong transcription	Dnd41	blood
47	chr4:119018200-119019400	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr4:119019200-119020200	Weak transcription	Dnd41	blood
49	chr4:119019400-119020400	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr4:119020200-119020600	Strong transcription	Dnd41	blood

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