Variant report

Variant	nsv880242
Chromosome Location	chr4:148659137-148727355
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1005)
CpG islands
(count:366)
Chromatin interactive
region (count:55)
LncRNA
region (count:6)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1005 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:148698678-148698923	K562	blood:	n/a	n/a
2	ATF2	chr4:148670793-148671689	GM12878	blood:	n/a	n/a
3	ATF2	chr4:148715067-148715628	GM12878	blood:	n/a	n/a
4	ATF2	chr4:148676738-148677181	GM12878	blood:	n/a	n/a
5	ATF2	chr4:148720944-148721546	GM12878	blood:	n/a	n/a
6	ATF2	chr4:148699787-148702056	GM12878	blood:	n/a	n/a
7	ATF2	chr4:148715749-148716353	GM12878	blood:	n/a	n/a
8	ATF2	chr4:148720900-148721655	GM12878	blood:	n/a	n/a
9	ATF2	chr4:148699821-148702027	GM12878	blood:	n/a	n/a
10	ATF2	chr4:148715837-148716378	GM12878	blood:	n/a	n/a
11	BATF	chr4:148707206-148707498	GM12878	blood:	n/a	n/a
12	BATF	chr4:148699993-148700380	GM12878	blood:	n/a	n/a
13	BATF	chr4:148695019-148695248	GM12878	blood:	n/a	chr4:148695135-148695146
14	BATF	chr4:148715118-148715442	GM12878	blood:	n/a	n/a
15	BATF	chr4:148703385-148703766	GM12878	blood:	n/a	chr4:148703567-148703578 chr4:148703568-148703578 chr4:148703572-148703582
16	BATF	chr4:148701685-148702049	GM12878	blood:	n/a	n/a
17	BATF	chr4:148720994-148721450	GM12878	blood:	n/a	n/a
18	BATF	chr4:148699981-148700477	GM12878	blood:	n/a	n/a
19	BATF	chr4:148694992-148695217	GM12878	blood:	n/a	chr4:148695135-148695146
20	BATF	chr4:148701261-148701642	GM12878	blood:	n/a	n/a
21	BATF	chr4:148690607-148690856	GM12878	blood:	n/a	n/a
22	BATF	chr4:148676754-148677107	GM12878	blood:	n/a	n/a
23	BATF	chr4:148715935-148716441	GM12878	blood:	n/a	n/a
24	BATF	chr4:148693936-148694161	GM12878	blood:	n/a	chr4:148694046-148694057
25	BATF	chr4:148715146-148715470	GM12878	blood:	n/a	n/a
26	BATF	chr4:148671169-148671510	GM12878	blood:	n/a	n/a
27	BATF	chr4:148707131-148707513	GM12878	blood:	n/a	n/a
28	BATF	chr4:148670924-148671508	GM12878	blood:	n/a	n/a
29	BATF	chr4:148720975-148721510	GM12878	blood:	n/a	n/a
30	BATF	chr4:148676824-148677142	GM12878	blood:	n/a	n/a
31	BCL11A	chr4:148701247-148701622	GM12878	blood:	n/a	chr4:148701352-148701361
32	BCL11A	chr4:148720940-148721565	GM12878	blood:	n/a	n/a
33	BCL11A	chr4:148701217-148701594	GM12878	blood:	n/a	chr4:148701352-148701361
34	BCL11A	chr4:148700144-148700439	GM12878	blood:	n/a	n/a
35	BCL11A	chr4:148715958-148716320	GM12878	blood:	n/a	n/a
36	BCL11A	chr4:148721080-148721454	GM12878	blood:	n/a	n/a
37	BCL11A	chr4:148715960-148716296	GM12878	blood:	n/a	n/a
38	BCL11A	chr4:148699965-148700498	GM12878	blood:	n/a	n/a
39	BCL3	chr4:148701642-148702038	GM12878	blood:	n/a	chr4:148701763-148701772
40	BCL3	chr4:148699659-148700545	GM12878	blood:	n/a	n/a
41	BCL3	chr4:148676808-148677369	GM12878	blood:	n/a	n/a
42	BCL3	chr4:148699924-148700513	GM12878	blood:	n/a	n/a
43	BCL3	chr4:148720977-148721569	GM12878	blood:	n/a	n/a
44	BCL3	chr4:148721092-148721459	GM12878	blood:	n/a	n/a
45	BCL3	chr4:148701200-148701596	GM12878	blood:	n/a	chr4:148701352-148701361
46	BCLAF1	chr4:148699839-148700529	GM12878	blood:	n/a	n/a
47	BCLAF1	chr4:148720943-148721595	GM12878	blood:	n/a	n/a
48	BCLAF1	chr4:148670787-148671617	GM12878	blood:	n/a	chr4:148671394-148671403
49	BCLAF1	chr4:148720877-148721586	GM12878	blood:	n/a	n/a
50	BCLAF1	chr4:148699975-148700565	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:148715234-148715284	LNCaP	prostate:	n/a
2	chr4:148721238-148721288	HMEC	breast:	n/a
3	chr4:148721238-148721288	GM12878	blood:	n/a
4	chr4:148663146-148663196	GM12892	blood:	n/a
5	chr4:148663146-148663196	ProgFib	skin:	n/a
6	chr4:148721238-148721288	AG09319	gingival:	n/a
7	chr4:148715234-148715284	HL-60	blood:	n/a
8	chr4:148663146-148663196	PANC-1	pancreas:	n/a
9	chr4:148663146-148663196	MCF-7	breast:	n/a
10	chr4:148709144-148709194	AoSMC	blood vessel:	n/a
11	chr4:148721238-148721288	MCF10A-Er-Src	breast:	n/a
12	chr4:148697111-148697161	HAEpiC	amniotic membrane:	n/a
13	chr4:148697111-148697161	H1-hESC	embryonic stem cell:	embryo
14	chr4:148709144-148709194	NHBE	bronchial:	n/a
15	chr4:148709144-148709194	AG09309	skin:	n/a
16	chr4:148701131-148701181	GM12878	blood:	n/a
17	chr4:148709144-148709194	HCPEpiC	choroid plexus:	n/a
18	chr4:148709144-148709194	HEK293	kidney:	embryo
19	chr4:148721238-148721288	GM12892	blood:	n/a
20	chr4:148715234-148715284	ProgFib	skin:	n/a
21	chr4:148721238-148721288	AG10803	skin:	n/a
22	chr4:148697111-148697161	NHBE	bronchial:	n/a
23	chr4:148709144-148709194	A549	lung:	n/a
24	chr4:148697111-148697161	AG04449	skin:	fetal
25	chr4:148663146-148663196	SK-N-SH_RA	brain:	n/a
26	chr4:148715234-148715284	HCM	heart:	n/a
27	chr4:148663146-148663196	HMEC	breast:	n/a
28	chr4:148721238-148721288	AG09309	skin:	n/a
29	chr4:148697111-148697161	Hepatocyte	liver:	n/a
30	chr4:148721238-148721288	ovcar-3	ovarian:	n/a
31	chr4:148715234-148715284	NB4	blood:	n/a
32	chr4:148663146-148663196	AoSMC	blood vessel:	n/a
33	chr4:148701131-148701181	ECC-1	luminal epithelium:	n/a
34	chr4:148697111-148697161	RPTEC	kidney:	n/a
35	chr4:148663146-148663196	AG09309	skin:	n/a
36	chr4:148715234-148715284	Jurkat	blood:	n/a
37	chr4:148721238-148721288	NHDF-neo	bronchial:	n/a
38	chr4:148709144-148709194	AG04450	lung:	fetal
39	chr4:148701131-148701181	HCPEpiC	choroid plexus:	n/a
40	chr4:148709144-148709194	PFSK-1	brain:	n/a
41	chr4:148715234-148715284	GM12891	blood:	n/a
42	chr4:148663146-148663196	HEK293	kidney:	embryo
43	chr4:148697111-148697161	K562	blood:	n/a
44	chr4:148721238-148721288	HCT-116	colon:	n/a
45	chr4:148663146-148663196	Hela-S3	cervix:	n/a
46	chr4:148709144-148709194	BJ	skin:	n/a
47	chr4:148715234-148715284	BJ	skin:	n/a
48	chr4:148709144-148709194	HCM	heart:	n/a
49	chr4:148709144-148709194	HRCEpiC	kidney:	n/a
50	chr4:148697111-148697161	HRE	kidney:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:148681678..148684071-chr4:148684909..148686495,2	MCF-7	breast:
2	chr4:148652006..148653543-chr4:148675428..148676957,2	MCF-7	breast:
3	chr4:148651510..148654715-chr4:148697202..148699343,3	MCF-7	breast:
4	chr4:140373742..140376231-chr4:148662153..148664287,2	MCF-7	breast:
5	chr4:148660544..148662110-chr4:148679159..148680950,2	MCF-7	breast:
6	chr4:148652230..148654234-chr4:148679966..148681868,2	MCF-7	breast:
7	chr4:148713641..148716368-chr4:148719518..148721494,2	MCF-7	breast:
8	chr4:148681067..148682789-chr4:148764324..148765969,2	MCF-7	breast:
9	chr4:148706652..148708945-chr4:148723113..148725039,2	MCF-7	breast:
10	chr4:148698864..148701739-chr4:148701803..148703521,2	MCF-7	breast:
11	chr4:148681549..148683602-chr4:148686887..148689104,2	MCF-7	breast:
12	chr4:148655205..148657346-chr4:148658350..148660032,2	MCF-7	breast:
13	chr4:148691338..148693292-chr4:148693665..148695844,2	MCF-7	breast:
14	chr4:148662885..148664901-chr4:148710340..148713204,2	MCF-7	breast:
15	chr4:148679061..148682709-chr4:148682971..148685662,3	MCF-7	breast:
16	chr4:148691338..148693292-chr4:148693665..148695844,2	MCF-7	breast:
17	chr4:148702279..148704768-chr4:148706718..148708415,3	MCF-7	breast:
18	chr4:148682484..148684278-chr4:148691381..148693216,2	MCF-7	breast:
19	chr4:148682718..148685526-chr4:148687157..148689131,2	K562	blood:
20	chr4:148655598..148657433-chr4:148661220..148663896,2	MCF-7	breast:
21	chr4:148706652..148708945-chr4:148723113..148725039,2	MCF-7	breast:
22	chr4:148682484..148684278-chr4:148691381..148693216,2	MCF-7	breast:
23	chr4:148652741..148654893-chr4:148705162..148708132,2	MCF-7	breast:
24	chr4:148706733..148708272-chr4:148709553..148712261,2	MCF-7	breast:
25	chr4:148692827..148694690-chr4:148699168..148701568,2	K562	blood:
26	chr4:148702969..148703554-chr4:148758460..148759449,2	MCF-7	breast:
27	chr4:148651355..148654142-chr4:148663991..148665938,2	MCF-7	breast:
28	chr4:148662885..148664901-chr4:148710340..148713204,2	MCF-7	breast:
29	chr4:148698864..148701739-chr4:148701803..148703521,2	MCF-7	breast:
30	chr4:148681678..148684071-chr4:148684909..148686495,2	MCF-7	breast:
31	chr4:148697444..148700218-chr4:148710161..148711929,2	MCF-7	breast:
32	chr4:148661332..148664177-chr4:148751893..148754827,2	MCF-7	breast:
33	chr4:148671335..148673992-chr4:148761092..148763924,2	MCF-7	breast:
34	chr4:148716400..148719081-chr4:148721482..148723868,2	MCF-7	breast:
35	chr4:148665114..148667939-chr4:148668217..148671015,2	MCF-7	breast:
36	chr4:148713641..148716368-chr4:148719518..148721494,2	MCF-7	breast:
37	chr4:148693468..148695247-chr4:148729923..148731609,2	K562	blood:
38	chr4:148660544..148662110-chr4:148679159..148680950,2	MCF-7	breast:
39	chr4:148682718..148685526-chr4:148687157..148689131,2	K562	blood:
40	chr4:148652319..148654744-chr4:148676605..148679799,3	MCF-7	breast:
41	chr4:148722956..148724829-chr4:148728693..148731642,2	MCF-7	breast:
42	chr4:148692638..148695831-chr4:148697652..148700222,4	MCF-7	breast:
43	chr4:148681549..148683602-chr4:148686887..148689104,2	MCF-7	breast:
44	chr4:148652539..148655321-chr4:148686401..148688051,2	MCF-7	breast:
45	chr4:148655373..148657177-chr4:148661205..148664133,2	K562	blood:
46	chr4:148652497..148654668-chr4:148658383..148660519,2	MCF-7	breast:
47	chr4:148706733..148708272-chr4:148709553..148712261,2	MCF-7	breast:
48	chr4:148697444..148700218-chr4:148710161..148711929,2	MCF-7	breast:
49	chr4:148655157..148657016-chr4:148664536..148666375,2	MCF-7	breast:
50	chr4:148679061..148682709-chr4:148682971..148685662,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM184C-4	chr4:148713818-148713908	ucscGeneNc_uc003ikz_1
2	lnc-TMEM184C-4	chr4:148716045-148716167	ucscGeneNc_uc003ikz_1
3	lnc-TMEM184C-4	chr4:148719333-148719457	ucscGeneNc_uc003ikz_1
4	lnc-TMEM184C-4	chr4:148713283-148713402	ucscGeneNc_uc003ikz_1
5	lnc-TMEM184C-4	chr4:148711390-148711532	ucscGeneNc_uc003ikz_1
6	lnc-TMEM184C-4	chr4:148708208-148708310	ucscGeneNc_uc003ikz_1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4799-5p	chr4:148703755-148703776	MIMAT0019976
hsa-miR-4799-3p	chr4:148703790-148703811	MIMAT0019977

No data

Variant related genes	Relation type
RNA5SP165	TF binding region
MIR4799	TF binding region
RN7SL254P	TF binding region
RNA5SP165	CpG island
MIR4799	CpG island
RN7SL254P	CpG island
ENSG00000071205	chromatin interactions
ENSG00000264274	chromatin interactions
ENSG00000240014	chromatin interactions
ENSG00000172007	chromatin interactions
ENSG00000252951	chromatin interactions
ENSG00000273247	chromatin interactions

Extended variants
information (count: 2666 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:2666 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17023732	chr4:148659137-148659138	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186595192	chr4:148659173-148659174	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143690540	chr4:148659202-148659203	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563946183	chr4:148659343-148659344	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs538038053	chr4:148659376-148659377	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs554469329	chr4:148659390-148659391	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189816412	chr4:148659398-148659399	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559797681	chr4:148659418-148659419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs386680611	chr4:148659424-148659425	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541437391	chr4:148659430-148659431	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs561414902	chr4:148659440-148659441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs7687208	chr4:148659442-148659443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550294769	chr4:148659474-148659475	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574454409	chr4:148659477-148659478	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs570614459	chr4:148659490-148659491	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs180675896	chr4:148659493-148659494	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs546828114	chr4:148659511-148659512	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs369141320	chr4:148659518-148659519	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs1969102	chr4:148659633-148659634	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs534982948	chr4:148659703-148659704	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555025947	chr4:148659707-148659708	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs9994150	chr4:148659709-148659710	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537529944	chr4:148659710-148659711	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs1969103	chr4:148659711-148659712	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577366780	chr4:148659712-148659713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs546089113	chr4:148659724-148659725	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs116751768	chr4:148659788-148659789	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs185389610	chr4:148659810-148659811	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542142684	chr4:148659863-148659864	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144981612	chr4:148659881-148659882	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs530463357	chr4:148659891-148659892	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543899951	chr4:148659928-148659929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs191277524	chr4:148659989-148659990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs183128693	chr4:148660015-148660016	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs138780126	chr4:148660018-148660019	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs188573731	chr4:148660019-148660020	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529184199	chr4:148660071-148660072	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs191772356	chr4:148660072-148660073	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78619931	chr4:148660133-148660134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs150772434	chr4:148660194-148660195	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs139132168	chr4:148660230-148660231	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs570870180	chr4:148660256-148660257	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs539992993	chr4:148660274-148660275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs553266673	chr4:148660294-148660295	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs564766893	chr4:148660298-148660299	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs149506195	chr4:148660321-148660322	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs80148116	chr4:148660340-148660341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs535737417	chr4:148660350-148660351	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs59965552	chr4:148660354-148660355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs74665904	chr4:148660389-148660390	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2177 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148655400-148662600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr4:148655400-148662600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr4:148655600-148662600	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr4:148655600-148662800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:148655600-148681600	Weak transcription	Fetal Muscle Trunk	muscle
6	chr4:148655800-148660200	Weak transcription	Placenta	Placenta
7	chr4:148655800-148663400	Enhancers	Fetal Heart	heart
8	chr4:148655800-148665600	Weak transcription	Lung	lung
9	chr4:148656000-148659200	Enhancers	Adipose Nuclei	Adipose
10	chr4:148656000-148659400	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr4:148656000-148660000	Enhancers	Colon Smooth Muscle	Colon
12	chr4:148656000-148662400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr4:148656600-148661800	Weak transcription	Fetal Lung	lung
14	chr4:148656600-148676800	Weak transcription	Duodenum Mucosa	Duodenum
15	chr4:148656800-148659200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr4:148656800-148659200	Enhancers	Psoas Muscle	Psoas
17	chr4:148656800-148660200	Enhancers	Left Ventricle	heart
18	chr4:148656800-148662800	Weak transcription	Small Intestine	intestine
19	chr4:148656800-148675200	Weak transcription	Fetal Stomach	stomach
20	chr4:148657000-148663000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr4:148657000-148668600	Weak transcription	Gastric	stomach
22	chr4:148657400-148659200	Enhancers	Right Ventricle	heart
23	chr4:148657400-148662800	Weak transcription	Esophagus	oesophagus
24	chr4:148657400-148668600	Weak transcription	Fetal Intestine Small	intestine
25	chr4:148657600-148659200	Enhancers	HSMMtube	muscle
26	chr4:148657600-148659200	Enhancers	NH-A	brain
27	chr4:148657600-148659200	Enhancers	NHLF	lung
28	chr4:148657800-148659600	Enhancers	Ovary	ovary
29	chr4:148657800-148662600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr4:148658000-148659200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr4:148658000-148659400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:148658000-148659800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr4:148658000-148660000	Weak transcription	Fetal Intestine Large	intestine
34	chr4:148658000-148662200	Weak transcription	A549	lung
35	chr4:148658200-148659200	Enhancers	GM12878-XiMat	blood
36	chr4:148658200-148659400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr4:148658200-148660400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr4:148658200-148660400	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr4:148658200-148660400	Weak transcription	HSMM	muscle
40	chr4:148658200-148660600	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr4:148658200-148660600	Weak transcription	Rectal Smooth Muscle	rectum
42	chr4:148658200-148660600	Weak transcription	NHDF-Ad	bronchial
43	chr4:148658200-148660600	Weak transcription	Osteobl	bone
44	chr4:148658200-148660800	Enhancers	H1 Cell Line	embryonic stem cell
45	chr4:148658200-148661200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr4:148658200-148661400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:148658200-148661400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:148658200-148661600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr4:148658200-148661800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr4:148658200-148662400	Weak transcription	HMEC	breast

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