Variant report

Variant	nsv878588
Chromosome Location	chr4:8034772-8070793
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:362)
CpG islands
(count:427)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:8052351-8052437	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr4:8039082-8039561	GM12878	blood:	n/a	n/a
3	BCL3	chr4:8051772-8052024	GM12878	blood:	n/a	n/a
4	BCL3	chr4:8038912-8039504	GM12878	blood:	n/a	n/a
5	BCL3	chr4:8048544-8049032	GM12878	blood:	n/a	chr4:8049002-8049011
6	BCL3	chr4:8051760-8052130	GM12878	blood:	n/a	n/a
7	BCL3	chr4:8048580-8049026	GM12878	blood:	n/a	chr4:8049002-8049011
8	BHLHE40	chr4:8052473-8052834	HepG2	liver:	n/a	n/a
9	BHLHE40	chr4:8042425-8042692	HepG2	liver:	n/a	n/a
10	BHLHE40	chr4:8042424-8042710	K562	blood:	n/a	n/a
11	BHLHE40	chr4:8069388-8069707	K562	blood:	n/a	n/a
12	BHLHE40	chr4:8052547-8052963	HepG2	liver:	n/a	n/a
13	CBX3	chr4:8065798-8065980	K562	blood:	n/a	n/a
14	CBX3	chr4:8065639-8066235	HCT-116	colon:	n/a	n/a
15	CBX3	chr4:8065778-8066062	K562	blood:	n/a	n/a
16	CBX3	chr4:8065744-8066192	HCT-116	colon:	n/a	n/a
17	CEBPB	chr4:8034949-8035108	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:8055589-8055789	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:8058752-8058940	HepG2	liver:	n/a	chr4:8058881-8058892
20	CEBPB	chr4:8058783-8058947	HepG2	liver:	n/a	chr4:8058881-8058892
21	CEBPD	chr4:8052511-8052966	HepG2	liver:	n/a	n/a
22	CHD2	chr4:8048823-8048827	GM12878	blood:	n/a	n/a
23	CHD2	chr4:8049980-8049988	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr4:8052164-8052523	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr4:8060181-8060187	HepG2	liver:	n/a	n/a
26	CHD2	chr4:8051122-8051443	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr4:8039852-8039902	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr4:8047764-8047834	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr4:8036142-8036227	GM19239	blood:	n/a	n/a
30	CTCF	chr4:8047740-8047890	Caco-2	colon:	n/a	n/a
31	CTCF	chr4:8039881-8039913	HepG2	liver:	n/a	n/a
32	CTCF	chr4:8037240-8037390	NB4	blood:	n/a	n/a
33	CTCF	chr4:8047700-8047850	HepG2	liver:	n/a	n/a
34	CTCF	chr4:8041080-8041230	BE2_C	brain:	n/a	chr4:8041108-8041126
35	CTCF	chr4:8047680-8047830	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr4:8063010-8063107	H1-hESC	embryonic stem cell:	n/a	chr4:8063079-8063089
37	CTCF	chr4:8054280-8054430	HAc	cerebellar:	n/a	chr4:8054399-8054408
38	CTCF	chr4:8047705-8047903	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr4:8047720-8047870	A549	lung:	n/a	n/a
40	CTCF	chr4:8039820-8039944	GM12878	blood:	n/a	n/a
41	CTCF	chr4:8037349-8037405	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr4:8037280-8037430	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr4:8047758-8047824	A549	lung:	n/a	n/a
44	CTCF	chr4:8037260-8037410	HAc	cerebellar:	n/a	n/a
45	CTCF	chr4:8047760-8047910	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr4:8054240-8054390	HepG2	liver:	n/a	n/a
47	CTCF	chr4:8036787-8036833	GM19239	blood:	n/a	n/a
48	CTCF	chr4:8063880-8064030	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr4:8047740-8047890	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr4:8037260-8037410	HBMEC	blood vessel:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8062478-8062528	AG10803	skin:	n/a
2	chr4:8062541-8062591	BE2_C	brain:	n/a
3	chr4:8062541-8062591	GM12878	blood:	n/a
4	chr4:8062590-8062640	GM12892	blood:	n/a
5	chr4:8062541-8062591	HL-60	blood:	n/a
6	chr4:8062590-8062640	AG04450	lung:	fetal
7	chr4:8062541-8062591	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:8062541-8062591	GM12891	blood:	n/a
9	chr4:8046547-8046597	HEK293	kidney:	embryo
10	chr4:8046547-8046597	HNPCEpiC	eye:	n/a
11	chr4:8046547-8046597	IMR90	lung:	fetal
12	chr4:8037325-8037375	MCF-7	breast:	n/a
13	chr4:8062541-8062591	MCF10A-Er-Src	breast:	n/a
14	chr4:8062478-8062528	NH-A	brain:	n/a
15	chr4:8062590-8062640	SK-N-MC	brain:	n/a
16	chr4:8046793-8046843	RPTEC	kidney:	n/a
17	chr4:8046547-8046597	NT2-D1	testis:	n/a
18	chr4:8050781-8050831	GM06990	blood:	n/a
19	chr4:8062590-8062640	PFSK-1	brain:	n/a
20	chr4:8062478-8062528	RPTEC	kidney:	n/a
21	chr4:8046547-8046597	HRE	kidney:	n/a
22	chr4:8046547-8046597	HEEpiC	esophagus:	n/a
23	chr4:8062541-8062591	ECC-1	luminal epithelium:	n/a
24	chr4:8062478-8062528	LNCaP	prostate:	n/a
25	chr4:8062478-8062528	H1-hESC	embryonic stem cell:	embryo
26	chr4:8062541-8062591	GM12892	blood:	n/a
27	chr4:8062478-8062528	HAEpiC	amniotic membrane:	n/a
28	chr4:8037325-8037375	AoSMC	blood vessel:	n/a
29	chr4:8062478-8062528	SKMC	muscle:	n/a
30	chr4:8062590-8062640	GM19239	blood:	n/a
31	chr4:8050781-8050831	HEK293	kidney:	embryo
32	chr4:8062541-8062591	MCF-7	breast:	n/a
33	chr4:8062590-8062640	Hepatocyte	liver:	n/a
34	chr4:8046547-8046597	AG10803	skin:	n/a
35	chr4:8037325-8037375	HCPEpiC	choroid plexus:	n/a
36	chr4:8037325-8037375	SKMC	muscle:	n/a
37	chr4:8050781-8050831	H1-hESC	embryonic stem cell:	embryo
38	chr4:8062590-8062640	MCF10A-Er-Src	breast:	n/a
39	chr4:8046547-8046597	RPTEC	kidney:	n/a
40	chr4:8050781-8050831	ECC-1	luminal epithelium:	n/a
41	chr4:8037325-8037375	A549	lung:	n/a
42	chr4:8062541-8062591	RPTEC	kidney:	n/a
43	chr4:8062478-8062528	HMEC	breast:	n/a
44	chr4:8046547-8046597	MCF10A-Er-Src	breast:	n/a
45	chr4:8062590-8062640	HCT-116	colon:	n/a
46	chr4:8050781-8050831	CMK	blood:	n/a
47	chr4:8037325-8037375	NB4	blood:	n/a
48	chr4:8050781-8050831	GM19239	blood:	n/a
49	chr4:8046547-8046597	NHDF-neo	bronchial:	n/a
50	chr4:8062478-8062528	GM12891	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8048107..8050691-chr4:8051962..8053661,2	K562	blood:
2	chr4:8039157..8040706-chr4:8050002..8052437,2	K562	blood:
3	chr4:8048107..8050691-chr4:8051962..8053661,2	K562	blood:
4	chr4:8055317..8057478-chr4:8062900..8065450,3	MCF-7	breast:
5	chr4:8039157..8040706-chr4:8050002..8052437,2	K562	blood:
6	chr4:8055317..8057478-chr4:8062900..8065450,3	MCF-7	breast:
7	chr4:8034679..8036492-chr4:8044258..8047037,2	K562	blood:
8	chr4:8033575..8035551-chr4:8063220..8065289,2	K562	blood:
9	chr4:8024330..8026063-chr4:8034890..8037450,2	MCF-7	breast:
10	chr4:8034679..8036492-chr4:8044258..8047037,2	K562	blood:
11	chr4:8030886..8034532-chr4:8039153..8041983,3	MCF-7	breast:
12	chr4:8033575..8035551-chr4:8063220..8065289,2	K562	blood:
13	chr4:8034585..8036214-chr4:8037779..8039313,2	MCF-7	breast:
14	chr4:8030441..8032567-chr4:8033404..8037009,3	K562	blood:
15	chr4:8019333..8020892-chr4:8033325..8035259,2	MCF-7	breast:
16	chr4:8034585..8036214-chr4:8037779..8039313,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3TC1-2	chr4:8068255-8068448	ENSG00000251460.1
2	lnc-SH3TC1-2	chr4:8068787-8069451	ENSG00000251460.1

No data

Variant related genes	Relation type
ABLIM2	TF binding region
ENSG00000251460	TF binding region
ABLIM2	CpG island
ENSG00000251460	CpG island
ENSG00000273267	chromatin interactions

Extended variants
information (count: 1867 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1867 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6857972	chr4:8034772-8034773	Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555139032	chr4:8034776-8034777	Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187711031	chr4:8034781-8034782	Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573511175	chr4:8034800-8034801	Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116516751	chr4:8034832-8034833	Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553644037	chr4:8034839-8034840	Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541875639	chr4:8034854-8034855	Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542397235	chr4:8034856-8034857	Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190984670	chr4:8034857-8034858	Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576055886	chr4:8034863-8034864	Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371267010	chr4:8034871-8034872	Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73798927	chr4:8034892-8034893	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs564878811	chr4:8034893-8034894	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs4696733	chr4:8034908-8034909	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs547297171	chr4:8034915-8034916	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559172913	chr4:8034919-8034920	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs116376102	chr4:8034943-8034944	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs548329084	chr4:8034988-8034989	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145390669	chr4:8035016-8035017	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs537529181	chr4:8035057-8035058	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs552336592	chr4:8035067-8035068	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs116361750	chr4:8035076-8035077	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs112066917	chr4:8035089-8035090	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs4696734	chr4:8035102-8035103	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs564355351	chr4:8035129-8035130	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs553707326	chr4:8035171-8035172	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs543377074	chr4:8035200-8035201	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs568743759	chr4:8035208-8035209	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536074100	chr4:8035226-8035227	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs557517634	chr4:8035273-8035274	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs114001141	chr4:8035320-8035321	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182826496	chr4:8035342-8035343	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558324942	chr4:8035349-8035350	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112669925	chr4:8035386-8035387	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs540593742	chr4:8035387-8035388	Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112643397	chr4:8035414-8035415	Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559236587	chr4:8035460-8035461	Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs547360192	chr4:8035480-8035481	Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs142301826	chr4:8035486-8035487	Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs145946237	chr4:8035487-8035488	Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs563494589	chr4:8035488-8035489	Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187180046	chr4:8035611-8035612	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs139603845	chr4:8035640-8035641	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs191636901	chr4:8035706-8035707	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs528519034	chr4:8035736-8035737	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs539193191	chr4:8035743-8035744	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs546983051	chr4:8035787-8035788	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs568807241	chr4:8035802-8035803	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs34790115	chr4:8035817-8035818	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs183093597	chr4:8035828-8035829	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Sezary syndrome	18413736	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:614 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8010600-8052000	Weak transcription	Left Ventricle	heart
2	chr4:8012400-8039000	Weak transcription	Gastric	stomach
3	chr4:8012800-8035000	Weak transcription	Pancreas	Pancrea
4	chr4:8013000-8036600	Weak transcription	Right Ventricle	heart
5	chr4:8017400-8040400	Weak transcription	Right Atrium	heart
6	chr4:8022000-8037600	Weak transcription	Lung	lung
7	chr4:8022200-8040600	Weak transcription	Fetal Brain Female	brain
8	chr4:8022400-8035400	Weak transcription	Brain Anterior Caudate	brain
9	chr4:8022400-8039000	Weak transcription	Brain Angular Gyrus	brain
10	chr4:8023200-8039600	Weak transcription	Brain Germinal Matrix	brain
11	chr4:8023200-8041000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr4:8023800-8037200	Weak transcription	Brain Cingulate Gyrus	brain
13	chr4:8023800-8041200	Weak transcription	Brain Substantia Nigra	brain
14	chr4:8028800-8035600	Weak transcription	Stomach Smooth Muscle	stomach
15	chr4:8029200-8035400	Strong transcription	Spleen	Spleen
16	chr4:8029800-8046600	Weak transcription	Brain Hippocampus Middle	brain
17	chr4:8030400-8039200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr4:8030800-8037600	Weak transcription	Fetal Intestine Small	intestine
19	chr4:8031200-8052000	Weak transcription	Psoas Muscle	Psoas
20	chr4:8033000-8035400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:8033000-8035400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr4:8033000-8036800	Strong transcription	Skeletal Muscle Male	skeletal muscle
23	chr4:8033200-8035400	Weak transcription	Esophagus	oesophagus
24	chr4:8033200-8035600	Weak transcription	Aorta	Aorta
25	chr4:8033400-8036800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr4:8033400-8037000	Strong transcription	Skeletal Muscle Female	skeletal muscle
27	chr4:8034600-8035000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr4:8034600-8036000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr4:8034600-8039000	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr4:8035000-8039400	Strong transcription	Pancreas	Pancrea
31	chr4:8035200-8036000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr4:8035400-8035600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:8035400-8035800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr4:8035400-8036200	Enhancers	Brain Anterior Caudate	brain
35	chr4:8035400-8036200	Strong transcription	Esophagus	oesophagus
36	chr4:8035400-8038000	Genic enhancers	Spleen	Spleen
37	chr4:8035600-8035800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:8035600-8036000	Bivalent Enhancer	Fetal Muscle Leg	muscle
39	chr4:8035600-8036000	Strong transcription	Stomach Smooth Muscle	stomach
40	chr4:8035600-8038000	Strong transcription	Aorta	Aorta
41	chr4:8035800-8036000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr4:8035800-8036000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:8035800-8036800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr4:8036000-8036200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:8036000-8036200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr4:8036000-8036800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr4:8036000-8036800	Weak transcription	Stomach Smooth Muscle	stomach
48	chr4:8036200-8037000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:8036200-8040800	Weak transcription	Brain Anterior Caudate	brain
50	chr4:8036200-8045000	Weak transcription	Esophagus	oesophagus

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