Variant report

Variant	esv1005399
Chromosome Location	chr4:8387281-8397983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:382)
CpG islands
(count:1099)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:382 , 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	ATF2	chr4:8393604-8394136	GM12878	blood:	n/a	n/a
2	ATF2	chr4:8393632-8394071	GM12878	blood:	n/a	n/a
3	ATF3	chr4:8394650-8394856	K562	blood:	n/a	n/a
4	BATF	chr4:8393671-8394070	GM12878	blood:	n/a	chr4:8393850-8393861
5	BATF	chr4:8393629-8394080	GM12878	blood:	n/a	chr4:8393850-8393861
6	BATF	chr4:8395274-8395671	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:8393709-8394001	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:8395270-8395502	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:8393722-8394039	GM12878	blood:	n/a	n/a
10	BCL3	chr4:8392791-8393336	GM12878	blood:	n/a	n/a
11	BCL3	chr4:8393673-8394086	GM12878	blood:	n/a	n/a
12	BCLAF1	chr4:8393699-8394095	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:8395256-8395626	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:8386788-8387307	K562	blood:	n/a	n/a
15	BHLHE40	chr4:8387010-8387297	HepG2	liver:	n/a	n/a
16	BHLHE40	chr4:8393674-8394053	GM12878	blood:	n/a	n/a
17	BRCA1	chr4:8392996-8393002	GM12878	blood:	n/a	n/a
18	CEBPB	chr4:8391611-8391979	K562	blood:	n/a	chr4:8391780-8391791
19	CEBPB	chr4:8395300-8395843	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:8391618-8392011	H1-hESC	embryonic stem cell:	n/a	chr4:8391780-8391791
21	CEBPB	chr4:8394317-8394537	IMR90	lung:	n/a	chr4:8394384-8394395
22	CEBPB	chr4:8391584-8391938	K562	blood:	n/a	chr4:8391780-8391791
23	CEBPB	chr4:8391609-8391978	A549	lung:	n/a	chr4:8391780-8391791
24	CEBPB	chr4:8393645-8394040	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:8391705-8391841	K562	blood:	n/a	chr4:8391780-8391791
26	CEBPB	chr4:8394377-8394428	HepG2	liver:	n/a	chr4:8394384-8394395
27	CEBPB	chr4:8393636-8393996	MCF-7	breast:	n/a	n/a
28	CEBPB	chr4:8389645-8389845	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:8391613-8392104	IMR90	lung:	n/a	chr4:8391780-8391791
30	CEBPB	chr4:8391613-8391995	HepG2	liver:	n/a	chr4:8391780-8391791
31	CHD2	chr4:8393388-8394189	GM12878	blood:	n/a	n/a
32	CHD2	chr4:8395313-8395713	GM12878	blood:	n/a	n/a
33	CREB1	chr4:8386771-8387294	K562	blood:	n/a	n/a
34	CREB1	chr4:8386774-8387339	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr4:8386798-8387339	HepG2	liver:	n/a	n/a
36	CREB1	chr4:8386815-8387389	K562	blood:	n/a	n/a
37	CREB1	chr4:8386843-8387302	HepG2	liver:	n/a	n/a
38	CREB1	chr4:8386778-8387347	GM12878	blood:	n/a	n/a
39	CREB1	chr4:8386769-8387369	GM12878	blood:	n/a	n/a
40	CTCF	chr4:8393880-8394030	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr4:8393920-8394070	GM12878	blood:	n/a	n/a
42	CTCF	chr4:8395480-8395630	HVMF	connective:	n/a	n/a
43	CTCF	chr4:8395520-8395670	WERI-Rb-1	eye:	n/a	chr4:8395662-8395670
44	CTCF	chr4:8395860-8396010	AG10803	skin:	n/a	n/a
45	CTCF	chr4:8395500-8395650	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr4:8393740-8393890	HVMF	connective:	n/a	n/a
47	CTCF	chr4:8393940-8394090	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr4:8395540-8395690	AG04449	skin:	n/a	chr4:8395662-8395670
49	CTCF	chr4:8395447-8395804	IMR90	lung:	n/a	chr4:8395662-8395670
50	CTCF	chr4:8393920-8394070	HPF	lung:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8396410-8396460	HMEC	breast:	n/a
2	chr4:8396410-8396460	HMEC	breast:	n/a
3	chr4:8389845-8389895	NT2-D1	testis:	n/a
4	chr4:8388503-8388553	A549	lung:	n/a
5	chr4:8396502-8396552	T-47D	breast:	n/a
6	chr4:8389808-8389858	HIPEpiC	eye:	n/a
7	chr4:8388438-8388488	HIPEpiC	eye:	n/a
8	chr4:8390244-8390294	AoSMC	blood vessel:	n/a
9	chr4:8389845-8389895	AG09319	gingival:	n/a
10	chr4:8389845-8389895	AG10803	skin:	n/a
11	chr4:8395941-8395991	SK-N-SH_RA	brain:	n/a
12	chr4:8396410-8396460	SAEC	small airway:	n/a
13	chr4:8390837-8390887	Jurkat	blood:	n/a
14	chr4:8388503-8388553	HL-60	blood:	n/a
15	chr4:8389770-8389820	NB4	blood:	n/a
16	chr4:8389770-8389820	ovcar-3	ovarian:	n/a
17	chr4:8396163-8396213	GM06990	blood:	n/a
18	chr4:8396410-8396460	LNCaP	prostate:	n/a
19	chr4:8389770-8389820	CMK	blood:	n/a
20	chr4:8390193-8390243	BE2_C	brain:	n/a
21	chr4:8388503-8388553	NB4	blood:	n/a
22	chr4:8396410-8396460	PrEC	prostate:	n/a
23	chr4:8396502-8396552	GM06990	blood:	n/a
24	chr4:8396163-8396213	SAEC	small airway:	n/a
25	chr4:8396300-8396350	HMEC	breast:	n/a
26	chr4:8389467-8389517	PFSK-1	brain:	n/a
27	chr4:8396300-8396350	K562	blood:	n/a
28	chr4:8389097-8389147	Hela-S3	cervix:	n/a
29	chr4:8389770-8389820	HEK293	kidney:	embryo
30	chr4:8390193-8390243	GM12891	blood:	n/a
31	chr4:8389770-8389820	AG09309	skin:	n/a
32	chr4:8390148-8390198	HUVEC	blood vessel:	n/a
33	chr4:8388670-8388720	PFSK-1	brain:	n/a
34	chr4:8390244-8390294	ProgFib	skin:	n/a
35	chr4:8389467-8389517	ovcar-3	ovarian:	n/a
36	chr4:8390148-8390198	HCT-116	colon:	n/a
37	chr4:8388438-8388488	AG09319	gingival:	n/a
38	chr4:8389097-8389147	RPTEC	kidney:	n/a
39	chr4:8390193-8390243	Hepatocyte	liver:	n/a
40	chr4:8388438-8388488	GM12891	blood:	n/a
41	chr4:8390244-8390294	GM12878	blood:	n/a
42	chr4:8389808-8389858	HUVEC	blood vessel:	n/a
43	chr4:8390837-8390887	NT2-D1	testis:	n/a
44	chr4:8390193-8390243	SK-N-MC	brain:	n/a
45	chr4:8396502-8396552	U87	brain:	n/a
46	chr4:8390193-8390243	NH-A	brain:	n/a
47	chr4:8389770-8389820	SK-N-SH_RA	brain:	n/a
48	chr4:8390244-8390294	HCM	heart:	n/a
49	chr4:8390244-8390294	NHDF-neo	bronchial:	n/a
50	chr4:8390148-8390198	LNCaP	prostate:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8385368..8387475-chr4:8389606..8391227,2	MCF-7	breast:
2	chr4:8383597..8386239-chr4:8397040..8399494,2	K562	blood:
3	chr4:8380860..8383722-chr4:8386573..8388850,2	K562	blood:
4	chr4:8385799..8388766-chr4:8429513..8431932,2	K562	blood:
5	chr4:8359754..8361327-chr4:8385821..8388152,2	MCF-7	breast:
6	chr4:8385368..8387475-chr4:8389606..8391227,2	MCF-7	breast:
7	chr4:8247640..8250580-chr4:8396679..8398196,2	K562	blood:
8	chr4:8385149..8387717-chr4:8393140..8395716,2	K562	blood:
9	chr4:8389242..8391252-chr4:8392488..8394168,2	MCF-7	breast:
10	chr4:8389242..8391252-chr4:8392488..8394168,2	MCF-7	breast:

No data

Variant related genes	Relation type
ACOX3	TF binding region
RNA5SP152	TF binding region
ACOX3	CpG island
RNA5SP152	CpG island
ENSG00000087008	chromatin interactions
ENSG00000202054	chromatin interactions
ENSG00000251615	chromatin interactions

Extended variants
information (count: 616 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62286006	chr4:8387297-8387298	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs532275621	chr4:8387298-8387299	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs376000107	chr4:8387363-8387364	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs541102259	chr4:8387405-8387406	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs80061499	chr4:8387454-8387455	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs370606916	chr4:8387460-8387461	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs187407201	chr4:8387501-8387502	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs530275693	chr4:8387506-8387507	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs17194220	chr4:8387509-8387510	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs147495857	chr4:8387520-8387521	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs191798546	chr4:8387536-8387537	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs552181766	chr4:8387583-8387584	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs570484389	chr4:8387590-8387591	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs534806654	chr4:8387623-8387624	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs536458096	chr4:8387627-8387628	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs181707654	chr4:8387697-8387698	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs536491628	chr4:8387732-8387733	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs371403745	chr4:8387849-8387850	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs554455437	chr4:8387854-8387855	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs576436939	chr4:8387858-8387859	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs112171962	chr4:8387860-8387861	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs556054510	chr4:8387949-8387950	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs185619728	chr4:8388005-8388006	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs368538993	chr4:8388015-8388016	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs558609986	chr4:8388019-8388020	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576875180	chr4:8388020-8388021	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs190334432	chr4:8388021-8388022	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs371199897	chr4:8388031-8388032	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs574447027	chr4:8388038-8388039	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs149973324	chr4:8388051-8388052	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs145203919	chr4:8388060-8388061	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs182148527	chr4:8388064-8388065	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs186828960	chr4:8388075-8388076	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs574098655	chr4:8388086-8388087	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs191806447	chr4:8388089-8388090	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs538229324	chr4:8388090-8388091	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs556817659	chr4:8388099-8388100	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577525845	chr4:8388102-8388103	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs113596957	chr4:8388110-8388111	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs568578503	chr4:8388121-8388122	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs10938710	chr4:8388133-8388134	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs184048191	chr4:8388149-8388150	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs188947734	chr4:8388150-8388151	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs537360920	chr4:8388153-8388154	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs375900926	chr4:8388186-8388187	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs193084509	chr4:8388198-8388199	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs577895918	chr4:8388209-8388210	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs545271127	chr4:8388211-8388212	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs143932454	chr4:8388220-8388221	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs528915300	chr4:8388247-8388248	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

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

Chromatin state (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8360400-8394000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:8360400-8395600	Weak transcription	NHEK	skin
3	chr4:8362000-8395400	Weak transcription	Fetal Brain Male	brain
4	chr4:8364000-8388600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr4:8364800-8392400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:8365600-8388800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr4:8366400-8411600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr4:8366800-8390000	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr4:8368400-8388400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:8368800-8388800	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr4:8372600-8389800	Strong transcription	Esophagus	oesophagus
12	chr4:8373000-8388200	Weak transcription	Osteobl	bone
13	chr4:8373400-8401600	Strong transcription	Fetal Intestine Small	intestine
14	chr4:8375000-8401600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr4:8377000-8388800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr4:8378000-8391800	Strong transcription	Fetal Brain Female	brain
17	chr4:8378600-8398600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr4:8378600-8398800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr4:8378800-8397800	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr4:8379000-8395400	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr4:8379400-8392000	Strong transcription	Brain Hippocampus Middle	brain
22	chr4:8379600-8388400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr4:8381000-8393800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr4:8381200-8387600	Genic enhancers	Fetal Muscle Trunk	muscle
25	chr4:8381600-8392400	Strong transcription	Brain Cingulate Gyrus	brain
26	chr4:8381800-8394400	Strong transcription	Brain Germinal Matrix	brain
27	chr4:8381800-8398600	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr4:8382400-8401600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:8383200-8388000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr4:8383200-8388200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr4:8383400-8388200	Weak transcription	Brain Substantia Nigra	brain
32	chr4:8383600-8387600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr4:8383800-8419000	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr4:8384000-8387600	Genic enhancers	Placenta	Placenta
35	chr4:8384000-8388400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr4:8384000-8394600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:8384000-8395600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr4:8384000-8399600	Strong transcription	Spleen	Spleen
39	chr4:8384800-8387600	Enhancers	Left Ventricle	heart
40	chr4:8384800-8390000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:8384800-8391000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr4:8384800-8392000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr4:8384800-8401600	Strong transcription	Thymus	Thymus
44	chr4:8384800-8418600	Strong transcription	Primary T cells from cord blood	blood
45	chr4:8385000-8387400	Enhancers	Fetal Heart	heart
46	chr4:8385000-8387800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr4:8385000-8387800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr4:8385000-8388400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr4:8385200-8387400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr4:8385200-8395200	Weak transcription	Fetal Kidney	kidney

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links