Variant report

Variant	nsv878590
Chromosome Location	chr4:8047973-8075134
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:210)
CpG islands
(count:671)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:210 , 50 per page) page: 1 2 3 4 5

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	chr4:8051772-8052024	GM12878	blood:	n/a	n/a
3	BCL3	chr4:8048544-8049032	GM12878	blood:	n/a	chr4:8049002-8049011
4	BCL3	chr4:8048580-8049026	GM12878	blood:	n/a	chr4:8049002-8049011
5	BCL3	chr4:8051760-8052130	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:8052547-8052963	HepG2	liver:	n/a	n/a
7	BHLHE40	chr4:8069388-8069707	K562	blood:	n/a	n/a
8	BHLHE40	chr4:8052473-8052834	HepG2	liver:	n/a	n/a
9	CBX3	chr4:8065798-8065980	K562	blood:	n/a	n/a
10	CBX3	chr4:8065639-8066235	HCT-116	colon:	n/a	n/a
11	CBX3	chr4:8065778-8066062	K562	blood:	n/a	n/a
12	CBX3	chr4:8065744-8066192	HCT-116	colon:	n/a	n/a
13	CEBPB	chr4:8055589-8055789	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:8058783-8058947	HepG2	liver:	n/a	chr4:8058881-8058892
15	CEBPB	chr4:8058752-8058940	HepG2	liver:	n/a	chr4:8058881-8058892
16	CEBPD	chr4:8052511-8052966	HepG2	liver:	n/a	n/a
17	CHD2	chr4:8049980-8049988	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr4:8060181-8060187	HepG2	liver:	n/a	n/a
19	CHD2	chr4:8051122-8051443	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr4:8052164-8052523	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr4:8048823-8048827	GM12878	blood:	n/a	n/a
22	CTCF	chr4:8054380-8054530	HBMEC	blood vessel:	n/a	chr4:8054399-8054408
23	CTCF	chr4:8054280-8054430	HAc	cerebellar:	n/a	chr4:8054399-8054408
24	CTCF	chr4:8063010-8063107	H1-hESC	embryonic stem cell:	n/a	chr4:8063079-8063089
25	CTCF	chr4:8054365-8054447	H1-hESC	embryonic stem cell:	n/a	chr4:8054399-8054408
26	CTCF	chr4:8054320-8054470	K562	blood:	n/a	chr4:8054399-8054408
27	CTCF	chr4:8054240-8054390	HepG2	liver:	n/a	n/a
28	CTCF	chr4:8054120-8054270	HAc	cerebellar:	n/a	n/a
29	CTCF	chr4:8052520-8052670	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr4:8052720-8052870	HepG2	liver:	n/a	chr4:8052830-8052838
31	CTCF	chr4:8063880-8064030	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr4:8052660-8052810	SK-N-SH_RA	brain:	n/a	chr4:8052715-8052728
33	E2F4	chr4:8055096-8055148	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F6	chr4:8051998-8052652	H1-hESC	embryonic stem cell:	n/a	n/a
35	E2F6	chr4:8069384-8069529	K562	blood:	n/a	n/a
36	EBF1	chr4:8070511-8070905	GM12878	blood:	n/a	chr4:8070692-8070705 chr4:8070692-8070703
37	EGR1	chr4:8072595-8072758	K562	blood:	n/a	n/a
38	EGR1	chr4:8072584-8072796	K562	blood:	n/a	n/a
39	EP300	chr4:8052419-8052931	HepG2	liver:	n/a	n/a
40	EP300	chr4:8052330-8052956	HepG2	liver:	n/a	n/a
41	EP300	chr4:8052105-8052602	H1-hESC	embryonic stem cell:	n/a	n/a
42	EP300	chr4:8052394-8052790	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr4:8051024-8051546	H1-hESC	embryonic stem cell:	n/a	n/a
44	EP300	chr4:8052655-8052855	HepG2	liver:	n/a	n/a
45	EP300	chr4:8052419-8052801	SK-N-SH_RA	brain:	n/a	n/a
46	FOS	chr4:8063353-8063507	MCF10A-Er-Src	breast:	n/a	n/a
47	FOXA1	chr4:8055578-8056014	HepG2	liver:	n/a	n/a
48	FOXA1	chr4:8055507-8056000	HepG2	liver:	n/a	n/a
49	FOXA1	chr4:8052320-8052899	HepG2	liver:	n/a	n/a
50	FOXA1	chr4:8055598-8056003	HepG2	liver:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8073804-8073854	NB4	blood:	n/a
2	chr4:8073790-8073840	SK-N-MC	brain:	n/a
3	chr4:8071486-8071536	ECC-1	luminal epithelium:	n/a
4	chr4:8071486-8071536	Hela-S3	cervix:	n/a
5	chr4:8062590-8062640	HCPEpiC	choroid plexus:	n/a
6	chr4:8071003-8071053	AG10803	skin:	n/a
7	chr4:8071486-8071536	H1-hESC	embryonic stem cell:	embryo
8	chr4:8073804-8073854	HIPEpiC	eye:	n/a
9	chr4:8071486-8071536	NH-A	brain:	n/a
10	chr4:8073790-8073840	GM12892	blood:	n/a
11	chr4:8062590-8062640	T-47D	breast:	n/a
12	chr4:8050781-8050831	BJ	skin:	n/a
13	chr4:8071486-8071536	PFSK-1	brain:	n/a
14	chr4:8062541-8062591	U87	brain:	n/a
15	chr4:8073790-8073840	NB4	blood:	n/a
16	chr4:8073790-8073840	HRPEpiC	eye:	n/a
17	chr4:8062590-8062640	NB4	blood:	n/a
18	chr4:8062541-8062591	AG09309	skin:	n/a
19	chr4:8073804-8073854	SK-N-SH_RA	brain:	n/a
20	chr4:8073804-8073854	NT2-D1	testis:	n/a
21	chr4:8074092-8074142	HAEpiC	amniotic membrane:	n/a
22	chr4:8050781-8050831	SKMC	muscle:	n/a
23	chr4:8050781-8050831	HCT-116	colon:	n/a
24	chr4:8071486-8071536	HEK293	kidney:	embryo
25	chr4:8062590-8062640	K562	blood:	n/a
26	chr4:8073804-8073854	AG04449	skin:	fetal
27	chr4:8073804-8073854	BE2_C	brain:	n/a
28	chr4:8074092-8074142	GM06990	blood:	n/a
29	chr4:8071202-8071252	BJ	skin:	n/a
30	chr4:8074092-8074142	CMK	blood:	n/a
31	chr4:8071003-8071053	Caco-2	colon:	n/a
32	chr4:8073804-8073854	SAEC	small airway:	n/a
33	chr4:8050781-8050831	MCF-7	breast:	n/a
34	chr4:8071003-8071053	NHDF-neo	bronchial:	n/a
35	chr4:8062590-8062640	HIPEpiC	eye:	n/a
36	chr4:8074192-8074242	SK-N-MC	brain:	n/a
37	chr4:8062590-8062640	ovcar-3	ovarian:	n/a
38	chr4:8071202-8071252	HCF	heart:	n/a
39	chr4:8071486-8071536	IMR90	lung:	fetal
40	chr4:8073790-8073840	RPTEC	kidney:	n/a
41	chr4:8071003-8071053	GM19239	blood:	n/a
42	chr4:8073804-8073854	ProgFib	skin:	n/a
43	chr4:8062541-8062591	ovcar-3	ovarian:	n/a
44	chr4:8071202-8071252	ovcar-3	ovarian:	n/a
45	chr4:8050781-8050831	NT2-D1	testis:	n/a
46	chr4:8073804-8073854	HRCEpiC	kidney:	n/a
47	chr4:8062590-8062640	BE2_C	brain:	n/a
48	chr4:8073804-8073854	PrEC	prostate:	n/a
49	chr4:8071202-8071252	AG09319	gingival:	n/a
50	chr4:8071003-8071053	LNCaP	prostate:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8055317..8057478-chr4:8062900..8065450,3	MCF-7	breast:
2	chr4:8048107..8050691-chr4:8051962..8053661,2	K562	blood:
3	chr4:8039157..8040706-chr4:8050002..8052437,2	K562	blood:
4	chr4:8048107..8050691-chr4:8051962..8053661,2	K562	blood:
5	chr4:8055317..8057478-chr4:8062900..8065450,3	MCF-7	breast:
6	chr4:8033575..8035551-chr4:8063220..8065289,2	K562	blood:

(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
ENSG00000251460	TF binding region
ABLIM2	TF binding region
ENSG00000251460	CpG island
ABLIM2	CpG island

Extended variants
information (count: 1402 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1402 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2385916	chr4:8047973-8047974	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550262406	chr4:8047984-8047985	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs13124344	chr4:8048052-8048053	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs547459143	chr4:8048057-8048058	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs60420862	chr4:8048077-8048078	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs7684537	chr4:8048096-8048097	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs34019254	chr4:8048116-8048117	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs548860627	chr4:8048142-8048143	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs188597300	chr4:8048152-8048153	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs537614723	chr4:8048181-8048182	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs556253360	chr4:8048231-8048232	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577652572	chr4:8048233-8048234	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538671977	chr4:8048258-8048259	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181089248	chr4:8048272-8048273	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143051024	chr4:8048276-8048277	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542520614	chr4:8048296-8048297	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368087033	chr4:8048310-8048311	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575851819	chr4:8048322-8048323	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543227303	chr4:8048334-8048335	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565411453	chr4:8048338-8048339	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532490854	chr4:8048354-8048355	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371871599	chr4:8048381-8048382	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146140874	chr4:8048399-8048400	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376483417	chr4:8048410-8048411	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530082918	chr4:8048440-8048441	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185969175	chr4:8048448-8048449	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148459022	chr4:8048531-8048532	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570342574	chr4:8048532-8048533	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552736154	chr4:8048533-8048534	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140181458	chr4:8048544-8048545	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372097209	chr4:8048596-8048597	Weak transcription Enhancers Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62290652	chr4:8048624-8048625	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs538360123	chr4:8048648-8048649	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553792383	chr4:8048649-8048650	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565350112	chr4:8048691-8048692	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534665568	chr4:8048699-8048700	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535815523	chr4:8048716-8048717	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546723772	chr4:8048719-8048720	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547219724	chr4:8048737-8048738	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575915020	chr4:8048753-8048754	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568036568	chr4:8048778-8048779	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565855792	chr4:8048780-8048781	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534016165	chr4:8048788-8048789	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149816740	chr4:8048830-8048831	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541183292	chr4:8048844-8048845	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145820339	chr4:8048858-8048859	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs56192722	chr4:8048870-8048871	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs542229511	chr4:8048890-8048891	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs564015010	chr4:8048899-8048900	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531110464	chr4:8048917-8048918	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	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
Sezary syndrome	18413736	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:500 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8010600-8052000	Weak transcription	Left Ventricle	heart
2	chr4:8031200-8052000	Weak transcription	Psoas Muscle	Psoas
3	chr4:8038000-8052000	Weak transcription	Right Ventricle	heart
4	chr4:8039200-8057000	Weak transcription	Gastric	stomach
5	chr4:8039400-8052400	Weak transcription	Pancreas	Pancrea
6	chr4:8039400-8056600	Weak transcription	Aorta	Aorta
7	chr4:8041200-8052400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:8041800-8049600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:8041800-8052000	Weak transcription	Adipose Nuclei	Adipose
10	chr4:8042000-8049200	Weak transcription	Brain Anterior Caudate	brain
11	chr4:8042000-8049200	Strong transcription	Skeletal Muscle Female	skeletal muscle
12	chr4:8043200-8049800	Strong transcription	Skeletal Muscle Male	skeletal muscle
13	chr4:8044400-8048000	Strong transcription	Spleen	Spleen
14	chr4:8045600-8052000	Weak transcription	Stomach Smooth Muscle	stomach
15	chr4:8046000-8050800	Weak transcription	Esophagus	oesophagus
16	chr4:8046400-8048200	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr4:8046600-8048000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr4:8046600-8052000	Weak transcription	Lung	lung
19	chr4:8046800-8051000	Weak transcription	Fetal Lung	lung
20	chr4:8047000-8048400	Weak transcription	Brain Cingulate Gyrus	brain
21	chr4:8047000-8050000	Weak transcription	Brain Angular Gyrus	brain
22	chr4:8047000-8050000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr4:8047000-8052000	Weak transcription	Brain Hippocampus Middle	brain
24	chr4:8047000-8052000	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr4:8047400-8048400	Weak transcription	Brain Germinal Matrix	brain
26	chr4:8047600-8048600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:8047800-8049600	Bivalent Enhancer	HepG2	liver
28	chr4:8047800-8052000	Weak transcription	Colonic Mucosa	Colon
29	chr4:8047800-8052200	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr4:8047800-8052200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr4:8047800-8054800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:8048000-8048200	Genic enhancers	Spleen	Spleen
33	chr4:8048200-8048400	Weak transcription	Spleen	Spleen
34	chr4:8048200-8049400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr4:8048200-8052000	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr4:8048400-8048600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr4:8048400-8048600	Enhancers	Brain Germinal Matrix	brain
38	chr4:8048400-8048800	Enhancers	Brain Cingulate Gyrus	brain
39	chr4:8048400-8048800	Strong transcription	Spleen	Spleen
40	chr4:8048600-8049000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:8048600-8052000	Weak transcription	Brain Germinal Matrix	brain
42	chr4:8048600-8054800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr4:8048800-8049000	Genic enhancers	Spleen	Spleen
44	chr4:8048800-8051200	Weak transcription	Brain Cingulate Gyrus	brain
45	chr4:8049000-8049200	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr4:8049000-8049400	Strong transcription	Spleen	Spleen
47	chr4:8049000-8053400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr4:8049200-8049800	Genic enhancers	Skeletal Muscle Female	skeletal muscle
49	chr4:8049200-8050400	Enhancers	Brain Anterior Caudate	brain
50	chr4:8049200-8052000	Enhancers	HUES6 Cell Line	embryonic stem cell

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