Variant report

Variant	esv3384011
Chromosome Location	chr4:1287052-1291350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:74)
CpG islands
(count:183)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:74 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD1	chr4:1288193-1288335	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr4:1287340-1287490	GM12868	blood:	n/a	n/a
3	EBF1	chr4:1287446-1287699	GM12878	blood:	n/a	chr4:1287495-1287506
4	EBF1	chr4:1287354-1287723	GM12878	blood:	n/a	chr4:1287495-1287506
5	EBF1	chr4:1289571-1289819	GM12878	blood:	n/a	n/a
6	EBF1	chr4:1287349-1287702	GM12878	blood:	n/a	chr4:1287495-1287506
7	GATA1	chr4:1287819-1288356	PBDE	blood:	n/a	chr4:1288129-1288136 chr4:1288127-1288137
8	MYC	chr4:1289798-1289801	MCF-7	breast:	n/a	n/a
9	MYC	chr4:1289840-1289855	MCF-7	breast:	n/a	n/a
10	POLR2A	chr4:1290789-1292001	K562	blood:	n/a	n/a
11	POLR2A	chr4:1287842-1288170	K562	blood:	n/a	n/a
12	POLR2A	chr4:1290511-1290565	K562	blood:	n/a	n/a
13	POLR2A	chr4:1291162-1291164	K562	blood:	n/a	n/a
14	POLR2A	chr4:1289803-1290003	K562	blood:	n/a	n/a
15	POLR2A	chr4:1287203-1287404	K562	blood:	n/a	n/a
16	POLR2A	chr4:1288593-1289060	K562	blood:	n/a	n/a
17	POLR2A	chr4:1290576-1290608	K562	blood:	n/a	n/a
18	POLR2A	chr4:1288690-1289060	GM12891	blood:	n/a	n/a
19	POLR2A	chr4:1287317-1287941	GM12878	blood:	n/a	n/a
20	POLR2A	chr4:1290153-1290458	K562	blood:	n/a	n/a
21	POLR2A	chr4:1287907-1288283	K562	blood:	n/a	n/a
22	POLR2A	chr4:1287798-1287884	K562	blood:	n/a	n/a
23	POLR2A	chr4:1289669-1289795	GM12878	blood:	n/a	n/a
24	POLR2A	chr4:1289352-1289398	K562	blood:	n/a	n/a
25	POLR2A	chr4:1288592-1289068	GM12892	blood:	n/a	n/a
26	POLR2A	chr4:1290613-1290667	K562	blood:	n/a	n/a
27	POLR2A	chr4:1288600-1289797	K562	blood:	n/a	n/a
28	POLR2A	chr4:1287634-1287670	K562	blood:	n/a	n/a
29	POLR2A	chr4:1289945-1290008	ProgFib	skin:	n/a	n/a
30	POLR2A	chr4:1289931-1289990	HepG2	liver:	n/a	n/a
31	POLR2A	chr4:1287545-1287656	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr4:1287267-1288191	K562	blood:	n/a	n/a
33	POLR2A	chr4:1288857-1288877	K562	blood:	n/a	n/a
34	POLR2A	chr4:1288833-1288896	HepG2	liver:	n/a	n/a
35	POLR2A	chr4:1288197-1288559	K562	blood:	n/a	n/a
36	POLR2A	chr4:1289632-1290130	K562	blood:	n/a	n/a
37	POLR2A	chr4:1290893-1291068	GM12878	blood:	n/a	n/a
38	POLR2A	chr4:1287871-1287960	K562	blood:	n/a	n/a
39	POLR2A	chr4:1289261-1289322	K562	blood:	n/a	n/a
40	POLR2A	chr4:1287344-1287937	K562	blood:	n/a	n/a
41	POLR2A	chr4:1287458-1287877	GM12891	blood:	n/a	n/a
42	POLR2A	chr4:1288990-1289021	K562	blood:	n/a	n/a
43	POLR2A	chr4:1290939-1291735	GM12878	blood:	n/a	n/a
44	POLR2A	chr4:1287641-1287708	HepG2	liver:	n/a	n/a
45	POLR2A	chr4:1287523-1287545	K562	blood:	n/a	n/a
46	POLR2A	chr4:1289188-1289254	K562	blood:	n/a	n/a
47	POLR2A	chr4:1291180-1291237	K562	blood:	n/a	n/a
48	POLR2A	chr4:1290890-1291590	K562	blood:	n/a	n/a
49	POLR2A	chr4:1287386-1287388	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr4:1288584-1288931	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1290568-1290618	AG04450	lung:	fetal
2	chr4:1290568-1290618	HCT-116	colon:	n/a
3	chr4:1290568-1290618	AG09309	skin:	n/a
4	chr4:1290568-1290618	Caco-2	colon:	n/a
5	chr4:1287888-1287938	SK-N-MC	brain:	n/a
6	chr4:1290568-1290618	NHDF-neo	bronchial:	n/a
7	chr4:1287888-1287938	NHBE	bronchial:	n/a
8	chr4:1291076-1291126	HL-60	blood:	n/a
9	chr4:1291076-1291126	PrEC	prostate:	n/a
10	chr4:1291076-1291126	BE2_C	brain:	n/a
11	chr4:1291076-1291126	SKMC	muscle:	n/a
12	chr4:1291076-1291126	HUVEC	blood vessel:	n/a
13	chr4:1290568-1290618	AoSMC	blood vessel:	n/a
14	chr4:1290568-1290618	NT2-D1	testis:	n/a
15	chr4:1291076-1291126	Jurkat	blood:	n/a
16	chr4:1291076-1291126	MCF-7	breast:	n/a
17	chr4:1290568-1290618	U87	brain:	n/a
18	chr4:1290568-1290618	PFSK-1	brain:	n/a
19	chr4:1290568-1290618	Hela-S3	cervix:	n/a
20	chr4:1291076-1291126	U87	brain:	n/a
21	chr4:1287888-1287938	GM19239	blood:	n/a
22	chr4:1287888-1287938	Caco-2	colon:	n/a
23	chr4:1287888-1287938	AG04449	skin:	fetal
24	chr4:1291076-1291126	AG04449	skin:	fetal
25	chr4:1291076-1291126	BJ	skin:	n/a
26	chr4:1291076-1291126	HNPCEpiC	eye:	n/a
27	chr4:1290568-1290618	ovcar-3	ovarian:	n/a
28	chr4:1291076-1291126	PANC-1	pancreas:	n/a
29	chr4:1291076-1291126	Hepatocyte	liver:	n/a
30	chr4:1291076-1291126	HPAEpiC	pulmonary alveolar:	n/a
31	chr4:1287888-1287938	A549	lung:	n/a
32	chr4:1291076-1291126	K562	blood:	n/a
33	chr4:1290568-1290618	BJ	skin:	n/a
34	chr4:1287888-1287938	BE2_C	brain:	n/a
35	chr4:1291076-1291126	GM06990	blood:	n/a
36	chr4:1290568-1290618	Jurkat	blood:	n/a
37	chr4:1290568-1290618	AG10803	skin:	n/a
38	chr4:1290568-1290618	HRPEpiC	eye:	n/a
39	chr4:1287888-1287938	BJ	skin:	n/a
40	chr4:1290568-1290618	SK-N-MC	brain:	n/a
41	chr4:1290568-1290618	HNPCEpiC	eye:	n/a
42	chr4:1290568-1290618	IMR90	lung:	fetal
43	chr4:1287888-1287938	NHDF-neo	bronchial:	n/a
44	chr4:1291076-1291126	HMEC	breast:	n/a
45	chr4:1291076-1291126	NHBE	bronchial:	n/a
46	chr4:1287888-1287938	HCPEpiC	choroid plexus:	n/a
47	chr4:1291076-1291126	NB4	blood:	n/a
48	chr4:1287888-1287938	RPTEC	kidney:	n/a
49	chr4:1287888-1287938	ProgFib	skin:	n/a
50	chr4:1287888-1287938	PANC-1	pancreas:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1287434..1290416-chr4:1342936..1345119,2	K562	blood:
2	chr4:1284419..1287813-chr4:1334118..1338051,4	MCF-7	breast:
3	chr4:1236833..1250005-chr4:1276188..1292579,54	MCF-7	breast:
4	chr4:1280807..1287593-chr4:1339102..1342185,6	K562	blood:
5	chr4:1240745..1244252-chr4:1285454..1287557,3	MCF-7	breast:
6	chr4:1265257..1267082-chr4:1285469..1287790,2	K562	blood:
7	chr4:1036618..1039246-chr4:1287884..1290247,2	K562	blood:
8	chr4:1225914..1229092-chr4:1286494..1288303,3	K562	blood:
9	chr4:1286127..1289218-chr4:1332032..1335159,3	K562	blood:
10	chr4:1288933..1290698-chr4:1333775..1336445,2	K562	blood:
11	chr4:1241391..1244976-chr4:1289369..1292052,3	MCF-7	breast:
12	chr4:1280977..1287340-chr4:1335495..1344055,33	MCF-7	breast:
13	chr4:1242309..1244859-chr4:1287604..1289236,2	MCF-7	breast:
14	chr4:1238004..1246805-chr4:1279798..1288475,25	K562	blood:
15	chr4:1289122..1291329-chr4:1338444..1340407,2	MCF-7	breast:
16	chr4:1287223..1288934-chr4:1342789..1345119,2	K562	blood:
17	chr4:1282437..1287650-chr4:1338224..1344043,13	MCF-7	breast:

No data

Variant related genes	Relation type
MAEA	TF binding region
MAEA	CpG island
ENSG00000196810	chromatin interactions
ENSG00000163945	chromatin interactions
ENSG00000159692	chromatin interactions

Extended variants
information (count: 260 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541200509	chr4:1287127-1287128	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs184781350	chr4:1287129-1287130	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs78147894	chr4:1287136-1287137	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs112712932	chr4:1287149-1287150	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs147893865	chr4:1287171-1287172	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs112492605	chr4:1287203-1287204	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs189643680	chr4:1287209-1287210	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs548969411	chr4:1287222-1287223	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs568366640	chr4:1287242-1287243	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs551599157	chr4:1287266-1287267	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs57461362	chr4:1287286-1287287	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs180790571	chr4:1287291-1287292	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs148934330	chr4:1287292-1287293	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs10012539	chr4:1287322-1287323	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs527932794	chr4:1287345-1287346	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs4974589	chr4:1287352-1287353	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs545209724	chr4:1287383-1287384	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs555755389	chr4:1287392-1287393	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs4974590	chr4:1287477-1287478	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs541370987	chr4:1287510-1287511	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs559565613	chr4:1287568-1287569	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs60410862	chr4:1287597-1287598	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs545075856	chr4:1287620-1287621	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs140569422	chr4:1287628-1287629	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs35708350	chr4:1287629-1287630	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs397748711	chr4:1287631-1287632	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs200497960	chr4:1287632-1287633	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs189319519	chr4:1287654-1287655	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs530630772	chr4:1287664-1287665	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs142822536	chr4:1287665-1287666	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs560585571	chr4:1287690-1287691	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs76625675	chr4:1287697-1287698	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs151032336	chr4:1287701-1287702	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs565927948	chr4:1287712-1287713	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs182015334	chr4:1287751-1287752	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs59669372	chr4:1287773-1287774	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs570025072	chr4:1287785-1287786	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs1344300	chr4:1287790-1287791	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs187186479	chr4:1287826-1287827	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs539630448	chr4:1287855-1287856	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs557941068	chr4:1287857-1287858	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs372722961	chr4:1287880-1287881	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs574109492	chr4:1287889-1287890	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs534913129	chr4:1287911-1287912	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs553344747	chr4:1287925-1287926	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs78233882	chr4:1287928-1287929	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs550219650	chr4:1287931-1287932	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs73069979	chr4:1287978-1287979	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs563518453	chr4:1287980-1287981	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs540502884	chr4:1287999-1288000	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
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
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Type 2 diabetes	21754918	CNVD

Chromatin state (count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1284600-1290200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:1284800-1288400	Enhancers	Primary B cells from peripheral blood	blood
3	chr4:1285000-1287600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:1285000-1289400	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr4:1285200-1287400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:1285200-1287600	Enhancers	Primary T cells fromperipheralblood	blood
7	chr4:1285200-1287800	Enhancers	Right Ventricle	heart
8	chr4:1285200-1290200	Weak transcription	Aorta	Aorta
9	chr4:1285200-1293800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr4:1285200-1303400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:1285400-1287400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr4:1285400-1287400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr4:1285400-1287400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr4:1285400-1287400	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr4:1285400-1287600	Weak transcription	NH-A	brain
16	chr4:1285400-1288400	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr4:1285400-1289200	Enhancers	Colon Smooth Muscle	Colon
18	chr4:1285400-1289400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr4:1285400-1290200	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr4:1285400-1290600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr4:1285400-1291200	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr4:1285400-1291200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr4:1285400-1293400	Weak transcription	A549	lung
24	chr4:1285400-1294200	Weak transcription	HSMMtube	muscle
25	chr4:1285400-1294200	Weak transcription	HUVEC	blood vessel
26	chr4:1285400-1302400	Weak transcription	Fetal Kidney	kidney
27	chr4:1285600-1287400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr4:1285600-1287600	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr4:1285600-1287800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:1285600-1289400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
31	chr4:1285600-1290200	Weak transcription	Fetal Lung	lung
32	chr4:1285600-1290600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr4:1285600-1291400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr4:1285800-1287400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr4:1285800-1289200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr4:1285800-1296000	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr4:1285800-1302200	Weak transcription	NHDF-Ad	bronchial
38	chr4:1286000-1287400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr4:1286000-1287400	Weak transcription	Osteobl	bone
40	chr4:1286000-1287600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr4:1286000-1288200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr4:1286000-1288800	Weak transcription	Primary hematopoietic stem cells	blood
43	chr4:1286000-1288800	Weak transcription	Rectal Smooth Muscle	rectum
44	chr4:1286000-1289400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:1286000-1289400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr4:1286000-1295200	Strong transcription	Thymus	Thymus
47	chr4:1286200-1287200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr4:1286200-1287400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr4:1286200-1287400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr4:1286200-1287400	Weak transcription	Rectal Mucosa Donor 29	rectum

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