Variant report

Variant	esv3327752
Chromosome Location	chr4:8507302-8509800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:55)
CpG islands
(count:62)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:55 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:8508063-8508360	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr4:8507994-8508447	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr4:8507900-8508050	AG04449	skin:	n/a	n/a
4	CTCF	chr4:8507937-8508005	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr4:8507980-8508130	BJ	skin:	n/a	n/a
6	CTCF	chr4:8507940-8508090	HMEC	breast:	n/a	n/a
7	CTCF	chr4:8507960-8508110	AG04449	skin:	n/a	n/a
8	CTCF	chr4:8508120-8508270	HCPEpiC	choroid plexus:	n/a	chr4:8508168-8508181
9	CTCF	chr4:8507880-8508030	AG09319	gingival:	n/a	n/a
10	CTCF	chr4:8507940-8508090	AG10803	skin:	n/a	n/a
11	CTCF	chr4:8508040-8508190	AoAF	blood vessel:	n/a	chr4:8508168-8508181
12	CTCF	chr4:8507900-8508050	AG10803	skin:	n/a	n/a
13	CTCF	chr4:8508020-8508170	NHDF-neo	bronchial:	n/a	n/a
14	CTCF	chr4:8508820-8508970	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr4:8508100-8508250	BJ	skin:	n/a	chr4:8508168-8508181
16	CTCF	chr4:8507986-8508022	GM12892	blood:	n/a	n/a
17	CTCF	chr4:8507925-8508025	K562	blood:	n/a	n/a
18	CTCF	chr4:8508100-8508250	HAc	cerebellar:	n/a	chr4:8508168-8508181
19	CTCF	chr4:8508040-8508190	NHDF-neo	bronchial:	n/a	chr4:8508168-8508181
20	CTCF	chr4:8507940-8508090	Caco-2	colon:	n/a	n/a
21	CTCF	chr4:8508200-8508350	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr4:8508420-8508570	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr4:8507940-8508090	HMF	breast:	n/a	n/a
24	CTCF	chr4:8507980-8508130	AG09309	skin:	n/a	n/a
25	CTCF	chr4:8507960-8508110	NHLF	lung:	n/a	n/a
26	CTCF	chr4:8508680-8508830	BJ	skin:	n/a	n/a
27	CTCF	chr4:8507920-8508070	AG09319	gingival:	n/a	n/a
28	CTCF	chr4:8508008-8508228	IMR90	lung:	n/a	chr4:8508168-8508181
29	GABPA	chr4:8508026-8508363	H1-hESC	embryonic stem cell:	n/a	n/a
30	GTF2F1	chr4:8508808-8508986	H1-hESC	embryonic stem cell:	n/a	n/a
31	GTF2F1	chr4:8508186-8508270	H1-hESC	embryonic stem cell:	n/a	n/a
32	HMGN3	chr4:8508288-8508583	K562	blood:	n/a	n/a
33	JUND	chr4:8508025-8508245	H1-hESC	embryonic stem cell:	n/a	n/a
34	MAX	chr4:8507926-8508334	H1-hESC	embryonic stem cell:	n/a	chr4:8507956-8507966 chr4:8507958-8507968 chr4:8507957-8507968 chr4:8507960-8507976 chr4:8507958-8507967 chr4:8507959-8507966
35	MAX	chr4:8507872-8508585	H1-hESC	embryonic stem cell:	n/a	chr4:8508449-8508458 chr4:8507956-8507966 chr4:8507958-8507968 chr4:8507957-8507968 chr4:8507960-8507976 chr4:8507958-8507967 chr4:8507959-8507966
36	MAX	chr4:8507898-8508019	NB4	blood:	n/a	chr4:8507956-8507966 chr4:8507958-8507968 chr4:8507957-8507968 chr4:8507960-8507976 chr4:8507958-8507967 chr4:8507959-8507966
37	MXI1	chr4:8508323-8508347	H1-hESC	embryonic stem cell:	n/a	n/a
38	MXI1	chr4:8508196-8509158	IMR90	lung:	n/a	n/a
39	MYC	chr4:8507950-8508232	H1-hESC	embryonic stem cell:	n/a	chr4:8507956-8507966 chr4:8507958-8507968 chr4:8507957-8507968 chr4:8507960-8507976 chr4:8507958-8507967 chr4:8507959-8507966
40	POLR2A	chr4:8509002-8509215	U87	brain:	n/a	n/a
41	POLR2A	chr4:8509626-8510274	K562	blood:	n/a	n/a
42	POLR2A	chr4:8507701-8508402	K562	blood:	n/a	n/a
43	POLR2A	chr4:8507864-8507915	H1-hESC	embryonic stem cell:	n/a	n/a
44	RAD21	chr4:8507869-8508217	H1-hESC	embryonic stem cell:	n/a	n/a
45	RAD21	chr4:8507766-8508439	H1-hESC	embryonic stem cell:	n/a	chr4:8508416-8508430
46	RAD21	chr4:8508541-8508786	IMR90	lung:	n/a	n/a
47	RAD21	chr4:8507904-8508347	H1-hESC	embryonic stem cell:	n/a	n/a
48	RCOR1	chr4:8508093-8509345	IMR90	lung:	n/a	n/a
49	RXRA	chr4:8508062-8508475	H1-hESC	embryonic stem cell:	n/a	n/a
50	RXRA	chr4:8508041-8508473	H1-hESC	embryonic stem cell:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8508604-8508654	HCM	heart:	n/a
2	chr4:8508604-8508654	HCM	heart:	n/a
3	chr4:8508604-8508654	BE2_C	brain:	n/a
4	chr4:8508604-8508654	HNPCEpiC	eye:	n/a
5	chr4:8508604-8508654	HUVEC	blood vessel:	n/a
6	chr4:8508604-8508654	GM12892	blood:	n/a
7	chr4:8508604-8508654	ovcar-3	ovarian:	n/a
8	chr4:8508604-8508654	GM12891	blood:	n/a
9	chr4:8508604-8508654	HCF	heart:	n/a
10	chr4:8508604-8508654	H1-hESC	embryonic stem cell:	embryo
11	chr4:8508604-8508654	BJ	skin:	n/a
12	chr4:8508604-8508654	SAEC	small airway:	n/a
13	chr4:8508604-8508654	NHDF-neo	bronchial:	n/a
14	chr4:8508604-8508654	HepG2	liver:	n/a
15	chr4:8508604-8508654	NB4	blood:	n/a
16	chr4:8508604-8508654	K562	blood:	n/a
17	chr4:8508604-8508654	HEEpiC	esophagus:	n/a
18	chr4:8508604-8508654	SK-N-SH	brain:	n/a
19	chr4:8508604-8508654	AG09319	gingival:	n/a
20	chr4:8508604-8508654	IMR90	lung:	fetal
21	chr4:8508604-8508654	AG10803	skin:	n/a
22	chr4:8508604-8508654	MCF-7	breast:	n/a
23	chr4:8508604-8508654	SK-N-MC	brain:	n/a
24	chr4:8508604-8508654	Hela-S3	cervix:	n/a
25	chr4:8508604-8508654	HRCEpiC	kidney:	n/a
26	chr4:8508604-8508654	PANC-1	pancreas:	n/a
27	chr4:8508604-8508654	SKMC	muscle:	n/a
28	chr4:8508604-8508654	HCPEpiC	choroid plexus:	n/a
29	chr4:8508604-8508654	MCF10A-Er-Src	breast:	n/a
30	chr4:8508604-8508654	RPTEC	kidney:	n/a
31	chr4:8508604-8508654	HL-60	blood:	n/a
32	chr4:8508604-8508654	HEK293	kidney:	embryo
33	chr4:8508604-8508654	AG04449	skin:	fetal
34	chr4:8508604-8508654	Jurkat	blood:	n/a
35	chr4:8508604-8508654	Caco-2	colon:	n/a
36	chr4:8508604-8508654	AG09309	skin:	n/a
37	chr4:8508604-8508654	LNCaP	prostate:	n/a
38	chr4:8508604-8508654	SK-N-SH_RA	brain:	n/a
39	chr4:8508604-8508654	U87	brain:	n/a
40	chr4:8508604-8508654	NH-A	brain:	n/a
41	chr4:8508604-8508654	PrEC	prostate:	n/a
42	chr4:8508604-8508654	Hepatocyte	liver:	n/a
43	chr4:8508604-8508654	A549	lung:	n/a
44	chr4:8508604-8508654	ProgFib	skin:	n/a
45	chr4:8508604-8508654	HMEC	breast:	n/a
46	chr4:8508604-8508654	GM12878	blood:	n/a
47	chr4:8508604-8508654	HRPEpiC	eye:	n/a
48	chr4:8508604-8508654	AG04450	lung:	fetal
49	chr4:8508604-8508654	GM06990	blood:	n/a
50	chr4:8508604-8508654	HPAEpiC	pulmonary alveolar:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8479557..8483754-chr4:8505033..8507334,3	K562	blood:
2	chr4:8498123..8500167-chr4:8506357..8507950,2	MCF-7	breast:
3	chr4:8507896..8508408-chr4:8595816..8596778,2	MCF-7	breast:
4	chr4:8506167..8508857-chr4:8582205..8583898,2	MCF-7	breast:
5	chr4:8500499..8503047-chr4:8505239..8508077,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METTL19-1	chr4:8508555-8509234	ENSG00000205959.3

No data

Variant related genes	Relation type
ENSG00000205959	TF binding region
ENSG00000205959	CpG island
ENSG00000155269	chromatin interactions

Extended variants
information (count: 136 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:136 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113201725	chr4:8507302-8507303	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141718844	chr4:8507306-8507307	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs78265940	chr4:8507310-8507311	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs542294973	chr4:8507333-8507334	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569898103	chr4:8507386-8507387	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs561071156	chr4:8507411-8507412	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs531496288	chr4:8507412-8507413	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs549825940	chr4:8507437-8507438	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs368855035	chr4:8507439-8507440	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs565214694	chr4:8507504-8507505	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532292838	chr4:8507539-8507540	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs547412162	chr4:8507556-8507557	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs565335647	chr4:8507562-8507563	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs531054003	chr4:8507579-8507580	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs189663148	chr4:8507583-8507584	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs192527349	chr4:8507613-8507614	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs569932376	chr4:8507638-8507639	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs184383832	chr4:8507693-8507694	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368342605	chr4:8507759-8507760	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs530723274	chr4:8507778-8507779	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs571162858	chr4:8507807-8507808	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs545149943	chr4:8507849-8507850	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs373591769	chr4:8507855-8507856	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs574842880	chr4:8507859-8507860	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs542356378	chr4:8507902-8507903	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs557460940	chr4:8507908-8507909	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs377588601	chr4:8507927-8507928	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs543640366	chr4:8507931-8507932	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs370952683	chr4:8507962-8507963	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs150569243	chr4:8507986-8507987	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs540881267	chr4:8507990-8507991	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs374279657	chr4:8508015-8508016	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs558933787	chr4:8508056-8508057	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs529608888	chr4:8508095-8508096	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs16842416	chr4:8508108-8508109	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs569446468	chr4:8508172-8508173	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs530512109	chr4:8508173-8508174	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs552782033	chr4:8508178-8508179	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs570909078	chr4:8508180-8508181	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs2688240	chr4:8508231-8508232	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs553666614	chr4:8508261-8508262	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs546937628	chr4:8508272-8508273	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs6813502	chr4:8508274-8508275	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs6832505	chr4:8508315-8508316	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs6832668	chr4:8508334-8508335	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs61574335	chr4:8508338-8508339	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs189646336	chr4:8508344-8508345	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs73076290	chr4:8508370-8508371	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs568831097	chr4:8508383-8508384	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs558722666	chr4:8508386-8508387	Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	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
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8501600-8507400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr4:8501600-8507400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr4:8501600-8507600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:8501600-8507600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr4:8501600-8507600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr4:8501600-8507800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr4:8501600-8507800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:8501600-8507800	Weak transcription	Brain Angular Gyrus	brain
9	chr4:8501800-8510600	Enhancers	Ovary	ovary
10	chr4:8502800-8512800	Enhancers	Placenta	Placenta
11	chr4:8503600-8509400	Enhancers	Right Ventricle	heart
12	chr4:8503600-8509800	Enhancers	Adipose Nuclei	Adipose
13	chr4:8504200-8509000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr4:8504200-8509400	Enhancers	Right Atrium	heart
15	chr4:8504200-8510600	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr4:8504400-8507400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
17	chr4:8504600-8507600	Weak transcription	Fetal Kidney	kidney
18	chr4:8504600-8510800	Enhancers	Fetal Muscle Leg	muscle
19	chr4:8504800-8507800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:8505000-8508000	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr4:8505200-8507800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:8505200-8507800	Weak transcription	Brain Anterior Caudate	brain
23	chr4:8505200-8508000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr4:8505400-8507800	Weak transcription	HSMM	muscle
25	chr4:8505400-8509000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr4:8505600-8507800	Weak transcription	NHDF-Ad	bronchial
27	chr4:8505800-8507800	Weak transcription	Rectal Smooth Muscle	rectum
28	chr4:8505800-8509600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr4:8505800-8509800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:8506000-8507600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr4:8506000-8509000	Enhancers	Spleen	Spleen
32	chr4:8506200-8507400	Weak transcription	Stomach Smooth Muscle	stomach
33	chr4:8506200-8507600	Weak transcription	Fetal Brain Male	brain
34	chr4:8506200-8507800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr4:8506200-8507800	Weak transcription	Colonic Mucosa	Colon
36	chr4:8506200-8508200	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr4:8506200-8509600	Enhancers	HSMMtube	muscle
38	chr4:8506400-8507600	Weak transcription	Fetal Lung	lung
39	chr4:8506400-8507800	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr4:8506400-8507800	Weak transcription	Brain Substantia Nigra	brain
41	chr4:8506400-8507800	Weak transcription	Left Ventricle	heart
42	chr4:8506400-8508200	Weak transcription	Lung	lung
43	chr4:8506400-8509200	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr4:8506600-8507600	Weak transcription	Colon Smooth Muscle	Colon
45	chr4:8506600-8508200	Weak transcription	Pancreas	Pancrea
46	chr4:8506600-8508600	Weak transcription	Brain Cingulate Gyrus	brain
47	chr4:8506800-8507800	Weak transcription	Brain Hippocampus Middle	brain
48	chr4:8506800-8508200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:8507000-8509200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:8507000-8509800	Enhancers	H1 Cell Line	embryonic stem cell

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