Variant report

Variant	nsv878562
Chromosome Location	chr4:7414226-7438352
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	BACH1	chr4:7431462-7431555	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr4:7415403-7415635	GM12878	blood:	n/a	n/a
3	BCL3	chr4:7418400-7418837	GM12878	blood:	n/a	n/a
4	BCL3	chr4:7418462-7418837	GM12878	blood:	n/a	n/a
5	BCL3	chr4:7418098-7418400	GM12878	blood:	n/a	n/a
6	BRCA1	chr4:7436571-7436572	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:7433508-7433674	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr4:7433460-7433830	MCF-7	breast:	n/a	n/a
9	CEBPB	chr4:7433501-7433762	MCF-7	breast:	n/a	n/a
10	CEBPB	chr4:7437595-7437783	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:7437550-7437908	HepG2	liver:	n/a	n/a
12	CHD2	chr4:7436619-7436861	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr4:7432316-7432365	MCF-7	breast:	n/a	n/a
14	CTCF	chr4:7433640-7433790	HMEC	breast:	n/a	n/a
15	CTCF	chr4:7420320-7420470	GM12872	blood:	n/a	chr4:7420353-7420371 chr4:7420355-7420368
16	CTCF	chr4:7420260-7420410	NB4	blood:	n/a	chr4:7420353-7420371 chr4:7420355-7420368
17	CTCF	chr4:7426274-7426421	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr4:7420040-7420190	HAc	cerebellar:	n/a	n/a
19	CTCF	chr4:7435308-7435402	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr4:7432260-7432410	HMEC	breast:	n/a	n/a
21	CTCF	chr4:7426660-7426810	WERI-Rb-1	eye:	n/a	chr4:7426696-7426709
22	CTCF	chr4:7420220-7420370	HEK293	kidney:	n/a	chr4:7420355-7420368
23	CTCF	chr4:7432400-7432550	HRE	kidney:	n/a	n/a
24	CTCF	chr4:7420320-7420470	HMF	breast:	n/a	chr4:7420353-7420371 chr4:7420355-7420368
25	CTCF	chr4:7426304-7426367	K562	blood:	n/a	n/a
26	CTCF	chr4:7435240-7435390	AG04449	skin:	n/a	n/a
27	CTCF	chr4:7420260-7420410	GM12873	blood:	n/a	chr4:7420353-7420371 chr4:7420355-7420368
28	CTCF	chr4:7432240-7432390	NHEK	skin:	n/a	n/a
29	CTCF	chr4:7432277-7432412	NHEK	skin:	n/a	n/a
30	CTCF	chr4:7435260-7435410	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr4:7418441-7418584	GM19239	blood:	n/a	n/a
32	CTCF	chr4:7426260-7426410	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr4:7436683-7436741	LNCaP	prostate:	n/a	chr4:7436701-7436719
34	E2F4	chr4:7436626-7436856	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F6	chr4:7427199-7427591	H1-hESC	embryonic stem cell:	n/a	n/a
36	EGR1	chr4:7433472-7433889	MCF-7	breast:	n/a	n/a
37	FOS	chr4:7436578-7436862	MCF10A-Er-Src	breast:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
38	FOS	chr4:7433600-7433663	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr4:7436572-7436866	MCF10A-Er-Src	breast:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
40	FOS	chr4:7436573-7436878	MCF10A-Er-Src	breast:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
41	FOS	chr4:7436597-7436862	MCF10A-Er-Src	breast:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
42	FOSL2	chr4:7436508-7436891	HepG2	liver:	n/a	chr4:7436730-7436738 chr4:7436729-7436740
43	FOXA2	chr4:7437238-7437500	HepG2	liver:	n/a	n/a
44	FOXA2	chr4:7433240-7433711	A549	lung:	n/a	n/a
45	FOXA2	chr4:7433379-7433710	A549	lung:	n/a	n/a
46	HCFC1	chr4:7421743-7421982	K562	blood:	n/a	n/a
47	HMGN3	chr4:7423984-7424064	K562	blood:	n/a	n/a
48	IRF1	chr4:7426982-7427302	K562	blood:	n/a	chr4:7427133-7427147 chr4:7427127-7427144 chr4:7427132-7427145 chr4:7427130-7427144 chr4:7427131-7427145 chr4:7427132-7427145 chr4:7427132-7427145 chr4:7427131-7427151 chr4:7427131-7427141 chr4:7427131-7427142 chr4:7427132-7427146 chr4:7427132-7427144 chr4:7427132-7427143 chr4:7427131-7427144 chr4:7427129-7427146
49	JUND	chr4:7436533-7436871	A549	lung:	n/a	chr4:7436730-7436738 chr4:7436728-7436739 chr4:7436729-7436740
50	JUND	chr4:7436677-7436865	HepG2	liver:	n/a	chr4:7436730-7436738 chr4:7436728-7436739 chr4:7436729-7436740

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7435639-7435689	NHBE	bronchial:	n/a
2	chr4:7435639-7435689	NHBE	bronchial:	n/a
3	chr4:7427195-7427245	HL-60	blood:	n/a
4	chr4:7435357-7435407	HUVEC	blood vessel:	n/a
5	chr4:7427313-7427363	HCF	heart:	n/a
6	chr4:7436874-7436924	SK-N-SH_RA	brain:	n/a
7	chr4:7437156-7437206	HCM	heart:	n/a
8	chr4:7435463-7435513	HL-60	blood:	n/a
9	chr4:7436701-7436751	ProgFib	skin:	n/a
10	chr4:7430936-7430986	SKMC	muscle:	n/a
11	chr4:7427313-7427363	AG09319	gingival:	n/a
12	chr4:7437156-7437206	AG09309	skin:	n/a
13	chr4:7435639-7435689	LNCaP	prostate:	n/a
14	chr4:7427313-7427363	K562	blood:	n/a
15	chr4:7430936-7430986	MCF10A-Er-Src	breast:	n/a
16	chr4:7417336-7417386	NHBE	bronchial:	n/a
17	chr4:7437812-7437862	IMR90	lung:	fetal
18	chr4:7436199-7436249	LNCaP	prostate:	n/a
19	chr4:7437812-7437862	HRPEpiC	eye:	n/a
20	chr4:7427446-7427496	GM12892	blood:	n/a
21	chr4:7435357-7435407	RPTEC	kidney:	n/a
22	chr4:7436199-7436249	SAEC	small airway:	n/a
23	chr4:7436874-7436924	HCF	heart:	n/a
24	chr4:7436259-7436309	HIPEpiC	eye:	n/a
25	chr4:7437156-7437206	HIPEpiC	eye:	n/a
26	chr4:7435357-7435407	HRCEpiC	kidney:	n/a
27	chr4:7437156-7437206	PFSK-1	brain:	n/a
28	chr4:7427195-7427245	GM12878	blood:	n/a
29	chr4:7435639-7435689	GM12878	blood:	n/a
30	chr4:7436239-7436289	AG09319	gingival:	n/a
31	chr4:7437027-7437077	PrEC	prostate:	n/a
32	chr4:7435639-7435689	H1-hESC	embryonic stem cell:	embryo
33	chr4:7436693-7436743	HAEpiC	amniotic membrane:	n/a
34	chr4:7436701-7436751	MCF10A-Er-Src	breast:	n/a
35	chr4:7436199-7436249	SK-N-SH_RA	brain:	n/a
36	chr4:7435639-7435689	CMK	blood:	n/a
37	chr4:7430936-7430986	HNPCEpiC	eye:	n/a
38	chr4:7427313-7427363	IMR90	lung:	fetal
39	chr4:7434754-7434804	NH-A	brain:	n/a
40	chr4:7436259-7436309	Hela-S3	cervix:	n/a
41	chr4:7436701-7436751	Caco-2	colon:	n/a
42	chr4:7427446-7427496	K562	blood:	n/a
43	chr4:7435357-7435407	AG09309	skin:	n/a
44	chr4:7436199-7436249	IMR90	lung:	fetal
45	chr4:7427313-7427363	MCF-7	breast:	n/a
46	chr4:7436693-7436743	HRPEpiC	eye:	n/a
47	chr4:7427446-7427496	AG09309	skin:	n/a
48	chr4:7436199-7436249	HRCEpiC	kidney:	n/a
49	chr4:7436861-7436911	HEEpiC	esophagus:	n/a
50	chr4:7436701-7436751	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:7426666..7428188-chr4:7440042..7442576,2	MCF-7	breast:
2	chr4:7421765..7423604-chr4:7439157..7441831,2	K562	blood:
3	chr4:7410518..7413253-chr4:7418283..7420136,2	K562	blood:
4	chr4:7430206..7433720-chr4:7434978..7437884,3	K562	blood:
5	chr4:7430997..7432542-chr4:7435254..7438169,2	MCF-7	breast:
6	chr4:7412059..7414681-chr4:7420210..7422240,3	MCF-7	breast:
7	chr4:7428532..7430154-chr4:7431457..7433548,3	K562	blood:
8	chr4:7420470..7422077-chr4:7425743..7427334,2	MCF-7	breast:
9	chr4:7420470..7422077-chr4:7425743..7427334,2	MCF-7	breast:
10	chr4:7412059..7414681-chr4:7420210..7422240,3	MCF-7	breast:
11	chr4:7368964..7371820-chr4:7419661..7422236,2	K562	blood:
12	chr4:7432269..7435967-chr4:7438458..7442398,4	MCF-7	breast:
13	chr4:7421842..7424756-chr4:7435320..7437360,2	MCF-7	breast:
14	chr4:7428532..7430154-chr4:7431457..7433548,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSAPL1-1	chr4:7432021-7433304	NONHSAT095056

Variant related genes	Relation type
PSAPL1	TF binding region
PSAPL1	CpG island
ENSG00000178597	chromatin interactions

Extended variants
information (count: 1517 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1517 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6446597	chr4:7414226-7414227	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372142424	chr4:7414255-7414256	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs374031675	chr4:7414272-7414273	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs573211646	chr4:7414290-7414291	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs533898128	chr4:7414299-7414300	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs555909980	chr4:7414301-7414302	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs368247936	chr4:7414303-7414304	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs372004331	chr4:7414325-7414326	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs544868803	chr4:7414339-7414340	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs563048276	chr4:7414366-7414367	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs6446598	chr4:7414368-7414369	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs112696090	chr4:7414380-7414381	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs370715507	chr4:7414406-7414407	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs6821852	chr4:7414407-7414408	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs560592898	chr4:7414409-7414410	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs372856212	chr4:7414413-7414414	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs186148869	chr4:7414420-7414421	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs139454797	chr4:7414424-7414425	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs376514535	chr4:7414425-7414426	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs189730621	chr4:7414428-7414429	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs564260146	chr4:7414465-7414466	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs550396961	chr4:7414471-7414472	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs531579167	chr4:7414542-7414543	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs561172702	chr4:7414562-7414563	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs557138265	chr4:7414588-7414589	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs112938125	chr4:7414622-7414623	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs569050114	chr4:7414625-7414626	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs4292335	chr4:7414630-7414631	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs534883023	chr4:7414686-7414687	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs551656651	chr4:7414690-7414691	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs114935055	chr4:7414727-7414728	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs373278411	chr4:7414733-7414734	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs370222889	chr4:7414739-7414740	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs375281720	chr4:7414743-7414744	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs545450687	chr4:7414778-7414779	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs555797668	chr4:7414795-7414796	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs574215705	chr4:7414830-7414831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538324250	chr4:7414838-7414839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556658816	chr4:7414847-7414848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369652691	chr4:7414858-7414859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146272473	chr4:7414896-7414897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545222943	chr4:7414905-7414906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554456427	chr4:7414930-7414931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572639538	chr4:7414941-7414942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539886892	chr4:7414945-7414946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549540404	chr4:7414985-7414986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372271324	chr4:7414987-7414988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528825638	chr4:7415014-7415015	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs543925770	chr4:7415022-7415023	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs4558873	chr4:7415038-7415039	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7411400-7414400	Enhancers	Colon Smooth Muscle	Colon
2	chr4:7411400-7415000	Enhancers	Fetal Brain Male	brain
3	chr4:7411800-7414400	Enhancers	Rectal Smooth Muscle	rectum
4	chr4:7412600-7415800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:7413000-7415000	Enhancers	Brain Germinal Matrix	brain
6	chr4:7413200-7414400	Enhancers	Brain Substantia Nigra	brain
7	chr4:7413400-7414400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr4:7413400-7414400	Enhancers	Fetal Brain Female	brain
9	chr4:7413400-7414600	Enhancers	Duodenum Smooth Muscle	Duodenum
10	chr4:7413600-7414400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr4:7413600-7414600	Bivalent Enhancer	Fetal Muscle Leg	muscle
12	chr4:7413600-7418200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:7413800-7414800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr4:7414000-7414400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr4:7414000-7414400	Enhancers	Fetal Heart	heart
16	chr4:7414000-7414600	Enhancers	Brain Hippocampus Middle	brain
17	chr4:7414000-7414600	Bivalent Enhancer	Fetal Stomach	stomach
18	chr4:7414200-7414600	Enhancers	Stomach Smooth Muscle	stomach
19	chr4:7414200-7418200	Weak transcription	Brain Anterior Caudate	brain
20	chr4:7414200-7421400	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr4:7414600-7422200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr4:7415000-7415200	Flanking Active TSS	Fetal Brain Male	brain
23	chr4:7415000-7415400	Weak transcription	Brain Germinal Matrix	brain
24	chr4:7415200-7415400	Enhancers	Fetal Brain Male	brain
25	chr4:7415200-7416000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:7415400-7415600	Flanking Active TSS	Fetal Brain Male	brain
27	chr4:7415400-7416000	Enhancers	Brain Germinal Matrix	brain
28	chr4:7415400-7416400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
29	chr4:7415600-7416000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr4:7415600-7416000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
31	chr4:7415600-7416200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
32	chr4:7415600-7416200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
33	chr4:7415600-7416200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:7415600-7416200	Enhancers	Fetal Brain Male	brain
35	chr4:7415600-7416400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
36	chr4:7415800-7416000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:7415800-7416200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
38	chr4:7415800-7417200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:7416000-7416200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
40	chr4:7416000-7417400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr4:7416200-7416800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
42	chr4:7416200-7418200	Weak transcription	Fetal Brain Male	brain
43	chr4:7416400-7417800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:7416600-7416800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
45	chr4:7416600-7417200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
46	chr4:7416800-7417000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
47	chr4:7416800-7417000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
48	chr4:7416800-7417200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
49	chr4:7416800-7417200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
50	chr4:7416800-7417200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell

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