Variant report

Variant	esv1793600
Chromosome Location	chr4:74046221-74116012
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:762)
CpG islands
(count:305)
Chromatin interactive
region (count:92)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:74088179-74089111	K562	blood:	n/a	chr4:74088412-74088428
2	ARID3A	chr4:74098327-74098361	K562	blood:	n/a	n/a
3	ARID3A	chr4:74053144-74053255	K562	blood:	n/a	n/a
4	ARID3A	chr4:74055386-74055525	K562	blood:	n/a	n/a
5	ARID3A	chr4:74096860-74097556	K562	blood:	n/a	n/a
6	ARID3A	chr4:74088637-74088954	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:74111830-74112051	K562	blood:	n/a	n/a
8	ATF1	chr4:74088642-74089046	K562	blood:	n/a	n/a
9	ATF2	chr4:74088448-74089073	GM12878	blood:	n/a	n/a
10	ATF2	chr4:74088491-74089048	GM12878	blood:	n/a	n/a
11	ATF3	chr4:74088565-74089120	K562	blood:	n/a	n/a
12	BACH1	chr4:74078840-74079040	K562	blood:	n/a	n/a
13	BATF	chr4:74088639-74088976	GM12878	blood:	n/a	n/a
14	BCLAF1	chr4:74046849-74047376	GM12878	blood:	n/a	n/a
15	BCLAF1	chr4:74088420-74089071	K562	blood:	n/a	n/a
16	BHLHE40	chr4:74088555-74089111	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:74088715-74089013	HepG2	liver:	n/a	n/a
18	BHLHE40	chr4:74088581-74089061	K562	blood:	n/a	n/a
19	BRCA1	chr4:74088635-74089113	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr4:74090500-74090501	GM12878	blood:	n/a	n/a
21	CBX3	chr4:74088578-74089172	HCT-116	colon:	n/a	n/a
22	CBX3	chr4:74111569-74112016	K562	blood:	n/a	n/a
23	CBX3	chr4:74088575-74089030	K562	blood:	n/a	n/a
24	CBX3	chr4:74055032-74055417	K562	blood:	n/a	n/a
25	CBX3	chr4:74088641-74089117	HCT-116	colon:	n/a	n/a
26	CBX3	chr4:74069559-74069966	K562	blood:	n/a	n/a
27	CBX3	chr4:74088524-74089058	K562	blood:	n/a	n/a
28	CCNT2	chr4:74088629-74088829	K562	blood:	n/a	n/a
29	CCNT2	chr4:74046840-74047040	K562	blood:	n/a	n/a
30	CCNT2	chr4:74087518-74087724	K562	blood:	n/a	n/a
31	CCNT2	chr4:74111518-74112034	K562	blood:	n/a	n/a
32	CCNT2	chr4:74058936-74059136	K562	blood:	n/a	n/a
33	CCNT2	chr4:74059942-74060113	K562	blood:	n/a	n/a
34	CCNT2	chr4:74097005-74097205	K562	blood:	n/a	n/a
35	CEBPB	chr4:74092435-74092522	IMR90	lung:	n/a	chr4:74092486-74092497
36	CEBPB	chr4:74063003-74063307	K562	blood:	n/a	n/a
37	CEBPB	chr4:74088136-74088291	K562	blood:	n/a	chr4:74088218-74088229 chr4:74088218-74088231
38	CEBPB	chr4:74059460-74059730	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:74055921-74056073	K562	blood:	n/a	n/a
40	CEBPB	chr4:74059430-74059779	A549	lung:	n/a	n/a
41	CEBPB	chr4:74059374-74059787	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:74063037-74063275	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr4:74059439-74059782	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:74100579-74100647	IMR90	lung:	n/a	n/a
45	CEBPB	chr4:74059408-74059789	K562	blood:	n/a	n/a
46	CEBPB	chr4:74059358-74059776	A549	lung:	n/a	n/a
47	CEBPB	chr4:74059502-74059686	HepG2	liver:	n/a	n/a
48	CEBPB	chr4:74059435-74059738	MCF-7	breast:	n/a	n/a
49	CEBPB	chr4:74059433-74059785	IMR90	lung:	n/a	n/a
50	CEBPB	chr4:74063002-74063304	H1-hESC	embryonic stem cell:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:74065349-74065399	AG04449	skin:	fetal
2	chr4:74047370-74047420	PrEC	prostate:	n/a
3	chr4:74065349-74065399	GM12891	blood:	n/a
4	chr4:74103157-74103207	SAEC	small airway:	n/a
5	chr4:74103157-74103207	ovcar-3	ovarian:	n/a
6	chr4:74111455-74111505	Hela-S3	cervix:	n/a
7	chr4:74111455-74111505	T-47D	breast:	n/a
8	chr4:74047370-74047420	HEK293	kidney:	embryo
9	chr4:74088730-74088780	GM06990	blood:	n/a
10	chr4:74047370-74047420	CMK	blood:	n/a
11	chr4:74088730-74088780	HNPCEpiC	eye:	n/a
12	chr4:74065349-74065399	AG04450	lung:	fetal
13	chr4:74103157-74103207	AG04450	lung:	fetal
14	chr4:74065349-74065399	HRE	kidney:	n/a
15	chr4:74065349-74065399	HepG2	liver:	n/a
16	chr4:74111455-74111505	Caco-2	colon:	n/a
17	chr4:74103157-74103207	AG04449	skin:	fetal
18	chr4:74047370-74047420	HIPEpiC	eye:	n/a
19	chr4:74111455-74111505	HAEpiC	amniotic membrane:	n/a
20	chr4:74065349-74065399	HNPCEpiC	eye:	n/a
21	chr4:74103157-74103207	HIPEpiC	eye:	n/a
22	chr4:74103157-74103207	HRCEpiC	kidney:	n/a
23	chr4:74065349-74065399	K562	blood:	n/a
24	chr4:74047370-74047420	HEEpiC	esophagus:	n/a
25	chr4:74065349-74065399	PFSK-1	brain:	n/a
26	chr4:74103157-74103207	SK-N-SH	brain:	n/a
27	chr4:74065349-74065399	NT2-D1	testis:	n/a
28	chr4:74111455-74111505	AoSMC	blood vessel:	n/a
29	chr4:74111455-74111505	GM12878	blood:	n/a
30	chr4:74047370-74047420	NHBE	bronchial:	n/a
31	chr4:74088730-74088780	SKMC	muscle:	n/a
32	chr4:74111455-74111505	NHDF-neo	bronchial:	n/a
33	chr4:74065349-74065399	CMK	blood:	n/a
34	chr4:74111455-74111505	BJ	skin:	n/a
35	chr4:74088730-74088780	ovcar-3	ovarian:	n/a
36	chr4:74088730-74088780	MCF-7	breast:	n/a
37	chr4:74111455-74111505	ECC-1	luminal epithelium:	n/a
38	chr4:74065349-74065399	AG10803	skin:	n/a
39	chr4:74088730-74088780	AG09309	skin:	n/a
40	chr4:74088730-74088780	PFSK-1	brain:	n/a
41	chr4:74103157-74103207	GM12891	blood:	n/a
42	chr4:74047370-74047420	LNCaP	prostate:	n/a
43	chr4:74103157-74103207	HNPCEpiC	eye:	n/a
44	chr4:74103157-74103207	NT2-D1	testis:	n/a
45	chr4:74047370-74047420	RPTEC	kidney:	n/a
46	chr4:74065349-74065399	HCT-116	colon:	n/a
47	chr4:74088730-74088780	NH-A	brain:	n/a
48	chr4:74111455-74111505	BE2_C	brain:	n/a
49	chr4:74111455-74111505	ovcar-3	ovarian:	n/a
50	chr4:74088730-74088780	AG10803	skin:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:74086715..74092062-chr4:74122892..74125871,6	MCF-7	breast:
2	chr4:74060240..74062620-chr4:74065043..74067696,2	K562	blood:
3	chr4:74070251..74073029-chr4:74074120..74076871,2	MCF-7	breast:
4	chr4:74094205..74096174-chr4:74099236..74100932,2	MCF-7	breast:
5	chr4:74083507..74085941-chr4:74122682..74125492,2	MCF-7	breast:
6	chr4:74092974..74095435-chr4:74123584..74125368,2	K562	blood:
7	chr4:74048549..74051354-chr4:74053215..74054751,2	K562	blood:
8	chr4:74056365..74058810-chr4:74121522..74124421,2	K562	blood:
9	chr4:73983376..73985757-chr4:74044958..74047334,2	K562	blood:
10	chr4:74044444..74046783-chr4:74088415..74090635,2	K562	blood:
11	chr4:74066592..74068413-chr4:74122719..74124463,3	K562	blood:
12	chr4:74030007..74032415-chr4:74070930..74073778,2	K562	blood:
13	chr4:74050887..74052868-chr4:74066183..74068472,2	K562	blood:
14	chr4:74099672..74104982-chr4:74123482..74126181,5	MCF-7	breast:
15	chr4:74052583..74054936-chr4:74121603..74124404,2	K562	blood:
16	chr4:74052236..74053936-chr4:74063244..74066174,3	K562	blood:
17	chr4:74078580..74080113-chr4:74115423..74117254,2	K562	blood:
18	chr4:74086780..74089405-chr4:74114803..74116855,3	K562	blood:
19	chr4:74067827..74069350-chr4:74117043..74119731,2	K562	blood:
20	chr4:74103163..74106414-chr4:74122698..74126217,3	MCF-7	breast:
21	chr4:74046445..74048807-chr4:74084717..74087260,2	K562	blood:
22	chr4:74072374..74074564-chr4:74074721..74076887,2	K562	blood:
23	chr4:74094116..74095692-chr4:74117214..74119409,2	K562	blood:
24	chr4:74042864..74048117-chr4:74049066..74052625,5	K562	blood:
25	chr4:74042864..74048117-chr4:74049066..74052625,5	K562	blood:
26	chr4:74065951..74068812-chr4:74070946..74073291,3	K562	blood:
27	chr4:74044682..74047650-chr4:74072993..74074617,2	K562	blood:
28	chr4:74078580..74080113-chr4:74115423..74117254,2	K562	blood:
29	chr4:74099463..74102347-chr4:74103511..74105287,2	MCF-7	breast:
30	chr4:74094714..74099476-chr4:74109744..74111749,4	K562	blood:
31	chr4:74049747..74053903-chr4:74055413..74060187,5	K562	blood:
32	chr4:74096213..74098237-chr4:74123373..74125010,2	K562	blood:
33	chr4:74108645..74112551-chr4:74114263..74118175,3	MCF-7	breast:
34	chr4:74044682..74047650-chr4:74072993..74074617,2	K562	blood:
35	chr4:74030840..74033690-chr4:74081965..74083470,2	K562	blood:
36	chr4:74087106..74090351-chr4:74123421..74126445,9	K562	blood:
37	chr4:74085682..74087798-chr4:74091964..74093705,2	K562	blood:
38	chr4:74010850..74012963-chr4:74063750..74065280,2	MCF-7	breast:
39	chr4:74051359..74054338-chr4:74122904..74126621,3	K562	blood:
40	chr4:74084419..74090074-chr4:74102131..74108477,7	K562	blood:
41	chr4:74090826..74092875-chr4:74092966..74095699,2	MCF-7	breast:
42	chr4:74055545..74059425-chr4:74085647..74088678,3	K562	blood:
43	chr4:74048549..74051354-chr4:74053215..74054751,2	K562	blood:
44	chr4:74044912..74046496-chr4:74123417..74125726,2	K562	blood:
45	chr4:74107320..74110128-chr4:74122442..74124984,2	MCF-7	breast:
46	chr4:74003190..74004710-chr4:74112693..74114696,2	MCF-7	breast:
47	chr4:74041420..74044364-chr4:74048787..74051206,3	K562	blood:
48	chr4:74090826..74092875-chr4:74092966..74095699,2	MCF-7	breast:
49	chr4:74052236..74053936-chr4:74063244..74066174,3	K562	blood:
50	chr4:74054562..74057067-chr4:74057401..74060235,2	K562	blood:

No data

Variant related genes	Relation type
ANKRD17	TF binding region
ANKRD17	CpG island
ENSG00000156140	chromatin interactions
ENSG00000250220	chromatin interactions
ENSG00000132466	chromatin interactions
ENSG00000169155	chromatin interactions

Extended variants
information (count: 2334 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2334 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2137445	chr4:74046221-74046222	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs3946807	chr4:74046258-74046259	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs528938677	chr4:74046328-74046329	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs148371534	chr4:74046403-74046404	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs565835447	chr4:74046406-74046407	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs532995818	chr4:74046438-74046439	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs551242060	chr4:74046441-74046442	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs190566524	chr4:74046499-74046500	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs569662609	chr4:74046522-74046523	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs369127281	chr4:74046560-74046561	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs556480443	chr4:74046582-74046583	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141597072	chr4:74046595-74046596	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs535915094	chr4:74046606-74046607	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553988848	chr4:74046722-74046723	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs112290027	chr4:74046723-74046724	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546445940	chr4:74046732-74046733	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182396260	chr4:74046746-74046747	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs564663409	chr4:74046754-74046755	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs138115405	chr4:74046979-74046980	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs565807328	chr4:74046983-74046984	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs561699813	chr4:74047026-74047027	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs185490142	chr4:74047030-74047031	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs541107146	chr4:74047057-74047058	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs373520819	chr4:74047072-74047073	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs531589991	chr4:74047080-74047081	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs190776550	chr4:74047093-74047094	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs75694348	chr4:74047133-74047134	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs377465425	chr4:74047195-74047196	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs183020435	chr4:74047215-74047216	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs78608102	chr4:74047297-74047298	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs561632366	chr4:74047302-74047303	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs76520446	chr4:74047329-74047330	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs529368594	chr4:74047356-74047357	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs568406443	chr4:74047358-74047359	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs375290318	chr4:74047370-74047371	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs368986086	chr4:74047371-74047372	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs10433670	chr4:74047516-74047517	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs549247377	chr4:74047535-74047536	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs188703534	chr4:74047536-74047537	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs10433671	chr4:74047545-74047546	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs534758319	chr4:74047585-74047586	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs566222168	chr4:74047615-74047616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371037972	chr4:74047690-74047691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10433672	chr4:74047711-74047712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142770131	chr4:74047743-74047744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576735398	chr4:74047760-74047761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs28587584	chr4:74047766-74047767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111431561	chr4:74047786-74047787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143812968	chr4:74047805-74047806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11728799	chr4:74047809-74047810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2041 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74008800-74059600	Weak transcription	Fetal Brain Male	brain
2	chr4:74014600-74046400	Weak transcription	Hela-S3	cervix
3	chr4:74018400-74055200	Weak transcription	Psoas Muscle	Psoas
4	chr4:74031600-74066800	Weak transcription	HMEC	breast
5	chr4:74031600-74077200	Weak transcription	Small Intestine	intestine
6	chr4:74036600-74046400	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr4:74036600-74046600	Weak transcription	Brain Angular Gyrus	brain
8	chr4:74036600-74046600	Weak transcription	Stomach Smooth Muscle	stomach
9	chr4:74036600-74088200	Weak transcription	Colonic Mucosa	Colon
10	chr4:74036800-74048600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr4:74036800-74049200	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr4:74036800-74055200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr4:74036800-74055200	Weak transcription	Pancreas	Pancrea
14	chr4:74036800-74059400	Weak transcription	Spleen	Spleen
15	chr4:74036800-74062800	Weak transcription	Aorta	Aorta
16	chr4:74036800-74064800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr4:74037000-74055200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:74037000-74064800	Weak transcription	Brain Anterior Caudate	brain
19	chr4:74037000-74072200	Weak transcription	Gastric	stomach
20	chr4:74037200-74048200	Weak transcription	HSMMtube	muscle
21	chr4:74037200-74058800	Weak transcription	NHEK	skin
22	chr4:74037200-74064400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr4:74037400-74050400	Weak transcription	Brain Substantia Nigra	brain
24	chr4:74037800-74052200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr4:74039400-74058000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr4:74039400-74062200	Weak transcription	HSMM	muscle
27	chr4:74039400-74064600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr4:74039400-74068800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr4:74039600-74051800	Weak transcription	HUVEC	blood vessel
30	chr4:74039600-74053000	Weak transcription	Rectal Smooth Muscle	rectum
31	chr4:74039600-74053800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr4:74039600-74055200	Weak transcription	Fetal Stomach	stomach
33	chr4:74039600-74062800	Weak transcription	Thymus	Thymus
34	chr4:74039600-74067600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr4:74039800-74055600	Weak transcription	Fetal Muscle Trunk	muscle
36	chr4:74039800-74066000	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr4:74039800-74074600	Weak transcription	Left Ventricle	heart
38	chr4:74040200-74064800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr4:74040200-74065800	Weak transcription	Fetal Muscle Leg	muscle
40	chr4:74040400-74053000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr4:74040400-74056400	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr4:74041200-74049200	Weak transcription	Fetal Intestine Small	intestine
43	chr4:74041200-74050000	Weak transcription	Ovary	ovary
44	chr4:74041200-74052600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr4:74041200-74052600	Weak transcription	Fetal Kidney	kidney
46	chr4:74041200-74053800	Weak transcription	Brain Germinal Matrix	brain
47	chr4:74041200-74059800	Weak transcription	NHLF	lung
48	chr4:74041600-74052800	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr4:74041600-74055200	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr4:74042000-74046400	Weak transcription	Primary B cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links