Variant report

Variant	nsv432623
Chromosome Location	chr4:124780908-124851395
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	ARID3A	chr4:124791402-124791524	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:124791765-124791937	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:124814193-124814497	HepG2	liver:	n/a	n/a
4	BACH1	chr4:124811003-124811040	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr4:124789484-124789711	K562	blood:	n/a	chr4:124789534-124789545 chr4:124789569-124789580
6	CEBPB	chr4:124789402-124789663	A549	lung:	n/a	chr4:124789534-124789545 chr4:124789569-124789580
7	CEBPB	chr4:124789396-124789738	HepG2	liver:	n/a	chr4:124789534-124789545 chr4:124789569-124789580
8	CEBPB	chr4:124815586-124815883	ECC-1	luminal epithelium:	n/a	chr4:124815725-124815738
9	CEBPB	chr4:124789450-124789632	HepG2	liver:	n/a	chr4:124789534-124789545 chr4:124789569-124789580
10	CEBPB	chr4:124814203-124814489	MCF-7	breast:	n/a	chr4:124814266-124814277
11	CEBPB	chr4:124814141-124814448	Hela-S3	cervix:	n/a	chr4:124814266-124814277
12	CEBPB	chr4:124814094-124814457	HepG2	liver:	n/a	chr4:124814266-124814277
13	CEBPB	chr4:124789491-124789682	H1-hESC	embryonic stem cell:	n/a	chr4:124789534-124789545 chr4:124789569-124789580
14	CEBPB	chr4:124789398-124789751	IMR90	lung:	n/a	chr4:124789534-124789545 chr4:124789569-124789580
15	CEBPB	chr4:124789412-124789736	HepG2	liver:	n/a	chr4:124789534-124789545 chr4:124789569-124789580
16	CTCF	chr4:124803440-124803590	HepG2	liver:	n/a	n/a
17	CTCF	chr4:124816401-124816428	Pancreas_OC	pancreas:	n/a	n/a
18	CTCF	chr4:124803460-124803617	MCF-7	breast:	n/a	n/a
19	CTCF	chr4:124782300-124782450	WI-38	lung:	n/a	n/a
20	CTCF	chr4:124803510-124803575	MCF-7	breast:	n/a	n/a
21	CTCF	chr4:124803400-124803550	MCF-7	breast:	n/a	n/a
22	CTCF	chr4:124820900-124821050	GM12871	blood:	n/a	n/a
23	CTCF	chr4:124836394-124836450	GM13976	blood:	n/a	n/a
24	CTCF	chr4:124803440-124803590	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr4:124822760-124822910	HMEC	breast:	n/a	chr4:124822853-124822863
26	CTCF	chr4:124803517-124803569	HepG2	liver:	n/a	n/a
27	CTCF	chr4:124803478-124803589	Gliobla	brain:	n/a	n/a
28	CTCF	chr4:124803476-124803589	Fibrobl	skin:	n/a	n/a
29	CTCF	chr4:124822780-124822930	HPAF	blood vessel:	n/a	chr4:124822853-124822863
30	E2F4	chr4:124846924-124847047	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr4:124834284-124834631	MCF10A-Er-Src	breast:	n/a	chr4:124834390-124834399
32	E2F4	chr4:124830297-124830497	MCF10A-Er-Src	breast:	n/a	n/a
33	EP300	chr4:124843903-124844536	SK-N-SH	brain:	n/a	chr4:124844226-124844239 chr4:124844361-124844370 chr4:124844360-124844374 chr4:124844316-124844325
34	EP300	chr4:124810643-124811215	SK-N-SH	brain:	n/a	chr4:124810671-124810678 chr4:124810832-124810841 chr4:124810953-124810962
35	EP300	chr4:124813605-124813919	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr4:124842432-124842986	SK-N-SH_RA	brain:	n/a	n/a
37	EP300	chr4:124810570-124811232	SK-N-SH	brain:	n/a	chr4:124810671-124810678 chr4:124810832-124810841 chr4:124810953-124810962
38	EP300	chr4:124810325-124812135	SK-N-SH	brain:	n/a	chr4:124810671-124810678 chr4:124811934-124811943 chr4:124810832-124810841 chr4:124810953-124810962
39	EP300	chr4:124812869-124815514	SK-N-SH	brain:	n/a	chr4:124814508-124814522 chr4:124814490-124814504 chr4:124814114-124814128 chr4:124814747-124814761 chr4:124814267-124814281
40	EP300	chr4:124819932-124820219	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr4:124794499-124796343	SK-N-SH	brain:	n/a	chr4:124794756-124794766
42	EP300	chr4:124791639-124792040	HepG2	liver:	n/a	n/a
43	EP300	chr4:124795214-124795567	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr4:124814127-124814549	HepG2	liver:	n/a	chr4:124814508-124814522 chr4:124814490-124814504 chr4:124814267-124814281
45	EP300	chr4:124843938-124844385	SK-N-SH_RA	brain:	n/a	chr4:124844226-124844239 chr4:124844361-124844370 chr4:124844360-124844374 chr4:124844316-124844325
46	EP300	chr4:124841810-124843058	SK-N-SH	brain:	n/a	n/a
47	EP300	chr4:124814040-124814823	SK-N-SH_RA	brain:	n/a	chr4:124814508-124814522 chr4:124814490-124814504 chr4:124814114-124814128 chr4:124814747-124814761 chr4:124814267-124814281
48	EP300	chr4:124842337-124843011	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr4:124787959-124788337	SK-N-SH_RA	brain:	n/a	chr4:124788238-124788247
50	EP300	chr4:124813421-124815165	SK-N-SH_RA	brain:	n/a	chr4:124814508-124814522 chr4:124814490-124814504 chr4:124814114-124814128 chr4:124814747-124814761 chr4:124814267-124814281

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:124814442-124814492	HRE	kidney:	n/a
2	chr4:124791563-124791613	HRPEpiC	eye:	n/a
3	chr4:124791563-124791613	K562	blood:	n/a
4	chr4:124820603-124820653	SAEC	small airway:	n/a
5	chr4:124820603-124820653	HUVEC	blood vessel:	n/a
6	chr4:124791563-124791613	GM06990	blood:	n/a
7	chr4:124791563-124791613	HRCEpiC	kidney:	n/a
8	chr4:124820603-124820653	SK-N-SH	brain:	n/a
9	chr4:124791563-124791613	Hepatocyte	liver:	n/a
10	chr4:124814442-124814492	HNPCEpiC	eye:	n/a
11	chr4:124820603-124820653	HIPEpiC	eye:	n/a
12	chr4:124814442-124814492	NH-A	brain:	n/a
13	chr4:124820603-124820653	AoSMC	blood vessel:	n/a
14	chr4:124791563-124791613	H1-hESC	embryonic stem cell:	embryo
15	chr4:124820603-124820653	A549	lung:	n/a
16	chr4:124814442-124814492	GM12892	blood:	n/a
17	chr4:124814442-124814492	HepG2	liver:	n/a
18	chr4:124820603-124820653	HRCEpiC	kidney:	n/a
19	chr4:124820603-124820653	T-47D	breast:	n/a
20	chr4:124791563-124791613	A549	lung:	n/a
21	chr4:124820603-124820653	HCF	heart:	n/a
22	chr4:124814442-124814492	NHDF-neo	bronchial:	n/a
23	chr4:124820603-124820653	PFSK-1	brain:	n/a
24	chr4:124820603-124820653	MCF-7	breast:	n/a
25	chr4:124814442-124814492	SKMC	muscle:	n/a
26	chr4:124791563-124791613	MCF-7	breast:	n/a
27	chr4:124814442-124814492	NB4	blood:	n/a
28	chr4:124814442-124814492	IMR90	lung:	fetal
29	chr4:124814442-124814492	K562	blood:	n/a
30	chr4:124814442-124814492	SK-N-SH	brain:	n/a
31	chr4:124820603-124820653	AG04450	lung:	fetal
32	chr4:124814442-124814492	BJ	skin:	n/a
33	chr4:124820603-124820653	CMK	blood:	n/a
34	chr4:124814442-124814492	PANC-1	pancreas:	n/a
35	chr4:124820603-124820653	AG09319	gingival:	n/a
36	chr4:124814442-124814492	HCT-116	colon:	n/a
37	chr4:124814442-124814492	U87	brain:	n/a
38	chr4:124791563-124791613	HCT-116	colon:	n/a
39	chr4:124791563-124791613	HUVEC	blood vessel:	n/a
40	chr4:124791563-124791613	AG04449	skin:	fetal
41	chr4:124820603-124820653	ProgFib	skin:	n/a
42	chr4:124820603-124820653	HCT-116	colon:	n/a
43	chr4:124814442-124814492	Hela-S3	cervix:	n/a
44	chr4:124820603-124820653	HAEpiC	amniotic membrane:	n/a
45	chr4:124814442-124814492	HCF	heart:	n/a
46	chr4:124814442-124814492	HRPEpiC	eye:	n/a
47	chr4:124791563-124791613	AG09319	gingival:	n/a
48	chr4:124791563-124791613	HNPCEpiC	eye:	n/a
49	chr4:124791563-124791613	PrEC	prostate:	n/a
50	chr4:124814442-124814492	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:124797782..124800401-chr4:124803423..124805795,2	K562	blood:
2	chr4:124830712..124832385-chr4:124840886..124843472,2	K562	blood:
3	chr4:124807453..124810257-chr4:124819316..124821753,2	K562	blood:
4	chr4:124830712..124832385-chr4:124840886..124843472,2	K562	blood:
5	chr4:124797782..124800401-chr4:124803423..124805795,2	K562	blood:
6	chr4:124807453..124810257-chr4:124819316..124821753,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPRY1-2	chr4:124846339-124846492	ENSG00000249464
2	lnc-SPRY1-2	chr4:124846339-124846492	NONHSAT098199
3	lnc-SPRY1-7	chr4:124802358-124802438	l_2723_chr4:124790799-124802989_ovary
4	lnc-SPRY1-7	chr4:124802927-124802989	l_2723_chr4:124790799-124802989_ovary
5	lnc-SPRY1-7	chr4:124793392-124793507	l_2723_chr4:124790799-124802989_ovary
6	lnc-SPRY1-2	chr4:124850942-124851365	NONHSAT098194
7	lnc-SPRY1-2	chr4:124828696-124829244	NONHSAT098194
8	lnc-SPRY1-2	chr4:124807004-124807375	NONHSAT098194
9	lnc-SPRY1-2	chr4:124806122-124806861	NONHSAT098194
10	lnc-SPRY1-2	chr4:124846337-124846492	NONHSAT098205
11	lnc-SPRY1-7	chr4:124790800-124790937	l_2723_chr4:124790799-124802989_ovary
12	lnc-SPRY1-2	chr4:124817328-124818022	NONHSAT098194
13	lnc-SPRY1-2	chr4:124846339-124846492	ENSG00000249464
14	lnc-SPRY1-2	chr4:124815914-124815975	NONHSAT098194
15	lnc-SPRY1-2	chr4:124784730-124786730	NONHSAT098201
16	lnc-SPRY1-2	chr4:124846339-124846492	NONHSAT098194
17	lnc-SPRY1-2	chr4:124850922-124851883	NONHSAT098205
18	lnc-SPRY1-2	chr4:124784729-124785198	NONHSAT098194
19	lnc-SPRY1-2	chr4:124786276-124786730	NONHSAT098194
20	lnc-SPRY1-2	chr4:124784730-124786728	ENSG00000249464

Variant related genes	Relation type
ENSG00000250458	TF binding region
ENSG00000250458	CpG island
PAPD5	miRNA target sites
LRRC1	miRNA target sites
C2orf44	miRNA target sites

Extended variants
information (count: 2268 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2268 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1433209	chr4:124780908-124780909	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs142643277	chr4:124780924-124780925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186176238	chr4:124780938-124780939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115441860	chr4:124780966-124780967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146044007	chr4:124780971-124780972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574679114	chr4:124780972-124780973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543548177	chr4:124780974-124780975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73846809	chr4:124780982-124780983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576930940	chr4:124780997-124780998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190320352	chr4:124781014-124781015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554876448	chr4:124781033-124781034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs397715132	chr4:124781060-124781061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374418047	chr4:124781084-124781085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148661740	chr4:124781144-124781145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114296438	chr4:124781163-124781164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373531841	chr4:124781201-124781202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541702195	chr4:124781210-124781211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182047220	chr4:124781212-124781213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530191198	chr4:124781213-124781214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368810325	chr4:124781214-124781215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549878383	chr4:124781232-124781233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79291522	chr4:124781313-124781314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115245839	chr4:124781321-124781322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552322240	chr4:124781392-124781393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113094901	chr4:124781397-124781398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75610339	chr4:124781434-124781435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371463551	chr4:124781446-124781447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs28736467	chr4:124781477-124781478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554855785	chr4:124781494-124781495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544078408	chr4:124781503-124781504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150772075	chr4:124781512-124781513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537211616	chr4:124781535-124781536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557116243	chr4:124781566-124781567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577042651	chr4:124781567-124781568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186080480	chr4:124781580-124781581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552735416	chr4:124781600-124781601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139076406	chr4:124781620-124781621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541364607	chr4:124781625-124781626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561211474	chr4:124781638-124781639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190452817	chr4:124781658-124781659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113709183	chr4:124781659-124781660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543635957	chr4:124781681-124781682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183058667	chr4:124781705-124781706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528047685	chr4:124781712-124781713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542942011	chr4:124781736-124781737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532536555	chr4:124781739-124781740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199922203	chr4:124781754-124781755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76219872	chr4:124781768-124781769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147557370	chr4:124781786-124781787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201190503	chr4:124781787-124781788	Weak transcription	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
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
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
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	18765545	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Hodgkin''s lymphoma	17606441	CNVD

Chromatin state (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124776400-124781400	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr4:124777200-124781000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr4:124778000-124781000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr4:124778600-124781400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:124778600-124791400	Weak transcription	Left Ventricle	heart
6	chr4:124778600-124791600	Weak transcription	Psoas Muscle	Psoas
7	chr4:124778600-124792400	Weak transcription	Right Atrium	heart
8	chr4:124778600-124797600	Weak transcription	Ovary	ovary
9	chr4:124778800-124784600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:124779600-124790800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr4:124779800-124791400	Weak transcription	Right Ventricle	heart
12	chr4:124780000-124789800	Weak transcription	Fetal Muscle Leg	muscle
13	chr4:124780000-124792600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:124780200-124784000	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr4:124780400-124783200	Weak transcription	Fetal Intestine Large	intestine
16	chr4:124780400-124784000	Weak transcription	Fetal Intestine Small	intestine
17	chr4:124780400-124784000	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr4:124780400-124784800	Weak transcription	Fetal Lung	lung
19	chr4:124780400-124790400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr4:124780800-124781000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr4:124780800-124781200	Enhancers	HSMM	muscle
22	chr4:124780800-124782600	Weak transcription	HepG2	liver
23	chr4:124781000-124782600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr4:124781400-124781600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:124782600-124783000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr4:124782600-124785400	Enhancers	HepG2	liver
27	chr4:124783000-124784000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr4:124783200-124783400	Enhancers	Fetal Intestine Large	intestine
29	chr4:124783400-124784000	Weak transcription	Fetal Intestine Large	intestine
30	chr4:124783600-124784200	Enhancers	NHEK	skin
31	chr4:124783800-124784400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:124784000-124784200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr4:124784000-124784400	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr4:124784000-124785000	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr4:124784000-124785600	Enhancers	Fetal Intestine Large	intestine
36	chr4:124784000-124785600	Enhancers	Fetal Intestine Small	intestine
37	chr4:124784600-124785000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:124784800-124785000	Enhancers	Fetal Lung	lung
39	chr4:124785000-124789400	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr4:124785000-124790400	Weak transcription	Fetal Lung	lung
41	chr4:124785400-124788200	Weak transcription	HepG2	liver
42	chr4:124788200-124788800	Enhancers	HepG2	liver
43	chr4:124788800-124789200	Weak transcription	HepG2	liver
44	chr4:124789200-124793200	Enhancers	HepG2	liver
45	chr4:124789400-124789600	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr4:124789600-124790000	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr4:124789600-124791600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:124789800-124793000	Enhancers	Fetal Muscle Leg	muscle
49	chr4:124790000-124791000	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr4:124790200-124791800	Enhancers	Cortex derived primary cultured neurospheres	brain

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