Variant report

Variant	nsv595686
Chromosome Location	chr4:149794284-149903982
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:278)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr4:149803382-149803778	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr4:149803432-149803719	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr4:149896761-149897011	HepG2	liver:	n/a	n/a
4	CEBPB	chr4:149812954-149813132	HepG2	liver:	n/a	chr4:149813000-149813011
5	CEBPB	chr4:149812990-149813128	A549	lung:	n/a	chr4:149813000-149813011
6	CEBPB	chr4:149819586-149819774	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr4:149803274-149804251	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr4:149795680-149795830	NHEK	skin:	n/a	n/a
9	CTCF	chr4:149864568-149864592	Lung_OC	lung:	n/a	n/a
10	CTCF	chr4:149801864-149801898	GM20000	blood:	n/a	n/a
11	CTCF	chr4:149795660-149795810	GM12869	blood:	n/a	n/a
12	CTCF	chr4:149795654-149795766	HUVEC	blood vessel:	n/a	n/a
13	CTCF	chr4:149795643-149795805	LNCaP	prostate:	n/a	n/a
14	CTCF	chr4:149822340-149822490	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr4:149795698-149795760	GM12892	blood:	n/a	n/a
16	CTCF	chr4:149795714-149795752	GM19238	blood:	n/a	n/a
17	CTCF	chr4:149795600-149795750	RPTEC	kidney:	n/a	n/a
18	CTCF	chr4:149851934-149851993	GM10248	blood:	n/a	n/a
19	CTCF	chr4:149795640-149795790	NHEK	skin:	n/a	n/a
20	CTCF	chr4:149795640-149795790	HRE	kidney:	n/a	n/a
21	CTCF	chr4:149795620-149795770	Caco-2	colon:	n/a	n/a
22	CTCF	chr4:149822342-149822524	GM12878	blood:	n/a	n/a
23	CTCF	chr4:149795698-149795792	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:149795660-149795810	SAEC	small airway:	n/a	n/a
25	CTCF	chr4:149795660-149795810	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr4:149795840-149795990	AG10803	skin:	n/a	n/a
27	CTCF	chr4:149828000-149828150	NHEK	skin:	n/a	chr4:149828107-149828125 chr4:149828113-149828122
28	CTCF	chr4:149795625-149795813	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr4:149795729-149795803	Lung_OC	lung:	n/a	n/a
30	CTCF	chr4:149829255-149829310	LNCaP	prostate:	n/a	n/a
31	CTCF	chr4:149795628-149795832	NHEK	skin:	n/a	n/a
32	CTCF	chr4:149822360-149822510	RPTEC	kidney:	n/a	n/a
33	CTCF	chr4:149822415-149822450	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr4:149850137-149850194	Lung_OC	lung:	n/a	n/a
35	CTCF	chr4:149795674-149795780	Medullo	brain:	n/a	n/a
36	CTCF	chr4:149795660-149795810	HMEC	breast:	n/a	n/a
37	CTCF	chr4:149795640-149795790	SAEC	small airway:	n/a	n/a
38	CTCF	chr4:149795640-149795790	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr4:149795581-149795779	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr4:149795640-149795790	GM12875	blood:	n/a	n/a
41	CTCF	chr4:149795681-149795790	Gliobla	brain:	n/a	n/a
42	CTCF	chr4:149795540-149795690	RPTEC	kidney:	n/a	n/a
43	CTCF	chr4:149795680-149795830	BE2_C	brain:	n/a	n/a
44	CTCF	chr4:149795600-149795750	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr4:149795687-149795771	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr4:149822300-149822450	BE2_C	brain:	n/a	n/a
47	CTCF	chr4:149795700-149795850	HMEC	breast:	n/a	n/a
48	CTCF	chr4:149818323-149818353	GM13976	blood:	n/a	n/a
49	CTCF	chr4:149795678-149795764	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:149902144-149902214	LNCaP	prostate:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:149794611-149794661	NHDF-neo	bronchial:	n/a
2	chr4:149822936-149822986	NH-A	brain:	n/a
3	chr4:149822936-149822986	HRCEpiC	kidney:	n/a
4	chr4:149822936-149822986	NB4	blood:	n/a
5	chr4:149822936-149822986	SKMC	muscle:	n/a
6	chr4:149822936-149822986	GM12891	blood:	n/a
7	chr4:149794611-149794661	K562	blood:	n/a
8	chr4:149794611-149794661	HCT-116	colon:	n/a
9	chr4:149822936-149822986	AG09319	gingival:	n/a
10	chr4:149794611-149794661	MCF10A-Er-Src	breast:	n/a
11	chr4:149822936-149822986	AG09309	skin:	n/a
12	chr4:149794611-149794661	AoSMC	blood vessel:	n/a
13	chr4:149822936-149822986	GM12878	blood:	n/a
14	chr4:149794611-149794661	ProgFib	skin:	n/a
15	chr4:149794611-149794661	AG10803	skin:	n/a
16	chr4:149794611-149794661	Hepatocyte	liver:	n/a
17	chr4:149794611-149794661	GM12878	blood:	n/a
18	chr4:149794611-149794661	MCF-7	breast:	n/a
19	chr4:149822936-149822986	AoSMC	blood vessel:	n/a
20	chr4:149794611-149794661	NHBE	bronchial:	n/a
21	chr4:149822936-149822986	T-47D	breast:	n/a
22	chr4:149822936-149822986	HRE	kidney:	n/a
23	chr4:149822936-149822986	NHDF-neo	bronchial:	n/a
24	chr4:149822936-149822986	Hepatocyte	liver:	n/a
25	chr4:149794611-149794661	HUVEC	blood vessel:	n/a
26	chr4:149794611-149794661	NT2-D1	testis:	n/a
27	chr4:149794611-149794661	RPTEC	kidney:	n/a
28	chr4:149794611-149794661	Jurkat	blood:	n/a
29	chr4:149794611-149794661	HCM	heart:	n/a
30	chr4:149794611-149794661	HPAEpiC	pulmonary alveolar:	n/a
31	chr4:149822936-149822986	IMR90	lung:	fetal
32	chr4:149794611-149794661	BJ	skin:	n/a
33	chr4:149822936-149822986	SK-N-SH_RA	brain:	n/a
34	chr4:149794611-149794661	HCPEpiC	choroid plexus:	n/a
35	chr4:149794611-149794661	NH-A	brain:	n/a
36	chr4:149794611-149794661	LNCaP	prostate:	n/a
37	chr4:149794611-149794661	HRCEpiC	kidney:	n/a
38	chr4:149794611-149794661	GM12892	blood:	n/a
39	chr4:149822936-149822986	K562	blood:	n/a
40	chr4:149822936-149822986	BJ	skin:	n/a
41	chr4:149794611-149794661	HepG2	liver:	n/a
42	chr4:149822936-149822986	SAEC	small airway:	n/a
43	chr4:149794611-149794661	HAEpiC	amniotic membrane:	n/a
44	chr4:149794611-149794661	GM19239	blood:	n/a
45	chr4:149822936-149822986	Caco-2	colon:	n/a
46	chr4:149822936-149822986	Jurkat	blood:	n/a
47	chr4:149822936-149822986	GM06990	blood:	n/a
48	chr4:149822936-149822986	U87	brain:	n/a
49	chr4:149794611-149794661	HRPEpiC	eye:	n/a
50	chr4:149822936-149822986	CMK	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:56988283..56990164-chr4:149864191..149866506,2	MCF-7	breast:
2	chr4:149855945..149858873-chr4:149859035..149861615,2	K562	blood:
3	chr4:149855945..149858873-chr4:149859035..149861615,2	K562	blood:
4	chr4:149789152..149791558-chr4:149797286..149799871,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NR3C2-2	chr4:149862101-149862239	ENSG00000249317
2	lnc-NR3C2-2	chr4:149862700-149862929	ENSG00000249317
3	lnc-ARHGAP10-4	chr4:149840726-149840925	l_2751_chr4:149833600-149840763_testes
4	lnc-NR3C2-2	chr4:149862809-149862994	XLOC_004118
5	lnc-NR3C2-2	chr4:149862093-149862239	XLOC_004118
6	lnc-NR3C2-2	chr4:149863494-149863530	XLOC_004118
7	lnc-ARHGAP10-4	chr4:149833601-149833859	l_2751_chr4:149833600-149840763_testes

No data

Variant related genes	Relation type
ENSG00000249317	TF binding region
ENSG00000249317	CpG island
GNG12	miRNA target sites
SETD7	miRNA target sites

Extended variants
information (count: 2400 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2400 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10003214	chr4:149794284-149794285	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185807656	chr4:149794396-149794397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76380281	chr4:149794461-149794462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528613157	chr4:149794467-149794468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs853705	chr4:149794550-149794551	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs568468448	chr4:149794553-149794554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190383977	chr4:149794566-149794567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557065821	chr4:149794584-149794585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571167116	chr4:149794623-149794624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539721220	chr4:149794636-149794637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79404920	chr4:149794639-149794640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567674296	chr4:149794640-149794641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374145022	chr4:149794656-149794657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573074905	chr4:149794657-149794658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541529198	chr4:149794704-149794705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555007182	chr4:149794707-149794708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575242376	chr4:149794790-149794791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147137186	chr4:149794804-149794805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140239814	chr4:149794871-149794872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565416769	chr4:149794877-149794878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533293678	chr4:149794932-149794933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540499218	chr4:149794949-149794950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560409267	chr4:149794956-149794957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143267036	chr4:149795025-149795026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200072264	chr4:149795042-149795043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs375580435	chr4:149795049-149795050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548709939	chr4:149795066-149795067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568580539	chr4:149795098-149795099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530903073	chr4:149795103-149795104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112234112	chr4:149795107-149795108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199799191	chr4:149795140-149795141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554037074	chr4:149795153-149795154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192790035	chr4:149795170-149795171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149196439	chr4:149795173-149795174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183623409	chr4:149795249-149795250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566735093	chr4:149795257-149795258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535694277	chr4:149795419-149795420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555541125	chr4:149795430-149795431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75474533	chr4:149795434-149795435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34496860	chr4:149795435-149795436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs78713798	chr4:149795455-149795456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs397878353	chr4:149795456-149795457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200877088	chr4:149795457-149795458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76595014	chr4:149795458-149795459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142390258	chr4:149795467-149795468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537528613	chr4:149795526-149795527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557751933	chr4:149795558-149795559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577539678	chr4:149795560-149795561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs34334982	chr4:149795581-149795582	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs571591107	chr4:149795630-149795631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
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
Breast cancer	16272173	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:203 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:149794000-149794600	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr4:149794000-149794800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:149794000-149795000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:149794000-149795200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr4:149794200-149794800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr4:149794200-149794800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr4:149794200-149795600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:149794400-149794600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:149794800-149801400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr4:149794800-149802600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:149794800-149803000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr4:149795600-149801800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr4:149801200-149802800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr4:149801200-149804200	Enhancers	H1 Cell Line	embryonic stem cell
15	chr4:149801400-149801600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr4:149801400-149801600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:149801400-149801800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:149801400-149801800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:149801400-149802000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr4:149801400-149802000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr4:149801400-149804000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr4:149801400-149804200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr4:149801600-149802800	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr4:149801600-149802800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr4:149801800-149802000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr4:149801800-149803600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:149802000-149802200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:149802000-149802600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
29	chr4:149802000-149802800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr4:149802200-149802800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr4:149802600-149803200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr4:149802600-149804000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr4:149802800-149803000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr4:149802800-149803200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
35	chr4:149802800-149804200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr4:149802800-149804400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr4:149802800-149804800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr4:149803000-149804000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:149803000-149804000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr4:149803000-149804200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr4:149803200-149803400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr4:149803200-149803400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr4:149803200-149803600	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr4:149803400-149804200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr4:149803400-149805200	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr4:149803600-149804000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr4:149803800-149804200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr4:149804000-149804200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr4:149804000-149805200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr4:149804200-149805800	Weak transcription	H9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links