Variant report

Variant	nsv548343
Chromosome Location	chr1:179958809-180071987
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:180023732-180023861	K562	blood:	n/a	n/a
2	ARID3A	chr1:180027943-180027952	K562	blood:	n/a	n/a
3	ARID3A	chr1:180026837-180027685	K562	blood:	n/a	n/a
4	ARID3A	chr1:180022917-180023445	K562	blood:	n/a	n/a
5	ATF1	chr1:180068146-180068158	K562	blood:	n/a	n/a
6	ATF1	chr1:180022859-180023490	K562	blood:	n/a	n/a
7	ATF1	chr1:179986755-179986766	K562	blood:	n/a	n/a
8	ATF2	chr1:179972174-179972960	GM12878	blood:	n/a	n/a
9	ATF3	chr1:180023152-180023468	K562	blood:	n/a	n/a
10	ATF3	chr1:179960014-179960325	K562	blood:	n/a	n/a
11	BACH1	chr1:180027050-180027297	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:180026917-180027441	K562	blood:	n/a	n/a
13	BATF	chr1:179972484-179972723	GM12878	blood:	n/a	n/a
14	BATF	chr1:179965258-179965498	GM12878	blood:	n/a	n/a
15	BCLAF1	chr1:179972185-179972836	GM12878	blood:	n/a	n/a
16	BRCA1	chr1:180067388-180068197	Hela-S3	cervix:	n/a	chr1:180067957-180067964
17	CCNT2	chr1:180023071-180023396	K562	blood:	n/a	n/a
18	CCNT2	chr1:180039551-180039603	K562	blood:	n/a	n/a
19	CEBPB	chr1:180023086-180023473	K562	blood:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
20	CEBPB	chr1:179992386-179992548	HepG2	liver:	n/a	chr1:179992470-179992483 chr1:179992471-179992482
21	CEBPB	chr1:180012982-180013252	K562	blood:	n/a	n/a
22	CEBPB	chr1:179959474-179959672	H1-hESC	embryonic stem cell:	n/a	chr1:179959546-179959557 chr1:179959544-179959561 chr1:179959545-179959556 chr1:179959545-179959558
23	CEBPB	chr1:179958971-179959019	Hela-S3	cervix:	n/a	chr1:179959002-179959015 chr1:179959002-179959015 chr1:179959002-179959013
24	CEBPB	chr1:180025022-180025218	K562	blood:	n/a	n/a
25	CEBPB	chr1:179960000-179960373	K562	blood:	n/a	chr1:179960185-179960198 chr1:179960185-179960196
26	CEBPB	chr1:180023121-180023491	IMR90	lung:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
27	CEBPB	chr1:180027022-180027346	K562	blood:	n/a	n/a
28	CEBPB	chr1:179960021-179960349	H1-hESC	embryonic stem cell:	n/a	chr1:179960185-179960198 chr1:179960185-179960196
29	CEBPB	chr1:180056279-180056563	HepG2	liver:	n/a	chr1:180056431-180056442
30	CEBPB	chr1:179958955-179959052	HepG2	liver:	n/a	chr1:179959002-179959015 chr1:179959002-179959015 chr1:179959002-179959013
31	CEBPB	chr1:179959433-179959643	IMR90	lung:	n/a	chr1:179959546-179959557 chr1:179959544-179959561 chr1:179959545-179959556 chr1:179959545-179959558
32	CEBPB	chr1:180067636-180067924	MCF-7	breast:	n/a	chr1:180067796-180067805 chr1:180067794-180067807 chr1:180067794-180067807 chr1:180067796-180067805 chr1:180067796-180067805
33	CEBPB	chr1:180028937-180029135	K562	blood:	n/a	chr1:180029030-180029041
34	CEBPB	chr1:180067539-180068240	A549	lung:	n/a	chr1:180067796-180067805 chr1:180067794-180067807 chr1:180067794-180067807 chr1:180067796-180067805 chr1:180067796-180067805
35	CEBPB	chr1:180023128-180023461	HepG2	liver:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
36	CEBPB	chr1:180023156-180023475	A549	lung:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
37	CEBPB	chr1:180067549-180068008	A549	lung:	n/a	chr1:180067796-180067805 chr1:180067794-180067807 chr1:180067794-180067807 chr1:180067796-180067805 chr1:180067796-180067805
38	CEBPB	chr1:179960081-179960203	HepG2	liver:	n/a	chr1:179960185-179960198 chr1:179960185-179960196
39	CEBPB	chr1:179997206-179997674	Hela-S3	cervix:	n/a	chr1:179997478-179997491 chr1:179997493-179997504 chr1:179997492-179997503 chr1:179997478-179997489 chr1:179997492-179997503
40	CEBPB	chr1:180023140-180023488	Hela-S3	cervix:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
41	CEBPB	chr1:179958843-179959023	K562	blood:	n/a	chr1:179959002-179959015 chr1:179959002-179959015 chr1:179959002-179959013
42	CEBPB	chr1:180012065-180012825	IMR90	lung:	n/a	n/a
43	CEBPB	chr1:179961390-179961503	HepG2	liver:	n/a	chr1:179961453-179961464
44	CEBPB	chr1:180054895-180055030	K562	blood:	n/a	n/a
45	CEBPB	chr1:179997168-179997603	HepG2	liver:	n/a	chr1:179997478-179997491 chr1:179997493-179997504 chr1:179997492-179997503 chr1:179997478-179997489 chr1:179997492-179997503
46	CEBPB	chr1:180067533-180067970	K562	blood:	n/a	chr1:180067796-180067805 chr1:180067794-180067807 chr1:180067794-180067807 chr1:180067796-180067805 chr1:180067796-180067805
47	CEBPB	chr1:179997108-179997690	IMR90	lung:	n/a	chr1:179997478-179997491 chr1:179997493-179997504 chr1:179997492-179997503 chr1:179997478-179997489 chr1:179997492-179997503
48	CEBPB	chr1:180056300-180056560	A549	lung:	n/a	chr1:180056431-180056442
49	CEBPB	chr1:180023114-180023449	K562	blood:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
50	CEBPB	chr1:179960111-179960258	K562	blood:	n/a	chr1:179960185-179960198 chr1:179960185-179960196

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:180012272-180012322	Caco-2	colon:	n/a
2	chr1:180069210-180069260	Hela-S3	cervix:	n/a
3	chr1:180069210-180069260	ECC-1	luminal epithelium:	n/a
4	chr1:180012272-180012322	SK-N-SH_RA	brain:	n/a
5	chr1:180012272-180012322	NB4	blood:	n/a
6	chr1:179997704-179997754	NH-A	brain:	n/a
7	chr1:180012272-180012322	GM06990	blood:	n/a
8	chr1:179997704-179997754	ProgFib	skin:	n/a
9	chr1:180012272-180012322	LNCaP	prostate:	n/a
10	chr1:179997704-179997754	Hela-S3	cervix:	n/a
11	chr1:180012272-180012322	T-47D	breast:	n/a
12	chr1:179997704-179997754	PANC-1	pancreas:	n/a
13	chr1:180069210-180069260	NT2-D1	testis:	n/a
14	chr1:180069210-180069260	GM12891	blood:	n/a
15	chr1:180069210-180069260	AG09319	gingival:	n/a
16	chr1:180012272-180012322	MCF10A-Er-Src	breast:	n/a
17	chr1:180069210-180069260	H1-hESC	embryonic stem cell:	embryo
18	chr1:179997704-179997754	AG09309	skin:	n/a
19	chr1:180069210-180069260	SK-N-SH	brain:	n/a
20	chr1:180069210-180069260	HIPEpiC	eye:	n/a
21	chr1:179997704-179997754	SAEC	small airway:	n/a
22	chr1:180012272-180012322	HIPEpiC	eye:	n/a
23	chr1:180012272-180012322	IMR90	lung:	fetal
24	chr1:179997704-179997754	GM19239	blood:	n/a
25	chr1:179997704-179997754	GM12892	blood:	n/a
26	chr1:180069210-180069260	HL-60	blood:	n/a
27	chr1:179997704-179997754	HEK293	kidney:	embryo
28	chr1:179997704-179997754	NHDF-neo	bronchial:	n/a
29	chr1:179997704-179997754	Jurkat	blood:	n/a
30	chr1:180069210-180069260	AoSMC	blood vessel:	n/a
31	chr1:180069210-180069260	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:179997704-179997754	GM12891	blood:	n/a
33	chr1:180069210-180069260	LNCaP	prostate:	n/a
34	chr1:180069210-180069260	HMEC	breast:	n/a
35	chr1:180012272-180012322	Jurkat	blood:	n/a
36	chr1:180069210-180069260	Caco-2	colon:	n/a
37	chr1:180069210-180069260	MCF-7	breast:	n/a
38	chr1:179997704-179997754	AG09319	gingival:	n/a
39	chr1:180012272-180012322	SK-N-MC	brain:	n/a
40	chr1:180069210-180069260	GM19239	blood:	n/a
41	chr1:180012272-180012322	ECC-1	luminal epithelium:	n/a
42	chr1:180069210-180069260	AG04449	skin:	fetal
43	chr1:180069210-180069260	GM12878	blood:	n/a
44	chr1:179997704-179997754	U87	brain:	n/a
45	chr1:179997704-179997754	PrEC	prostate:	n/a
46	chr1:179997704-179997754	BE2_C	brain:	n/a
47	chr1:179997704-179997754	SK-N-MC	brain:	n/a
48	chr1:180069210-180069260	T-47D	breast:	n/a
49	chr1:180069210-180069260	SK-N-SH_RA	brain:	n/a
50	chr1:180069210-180069260	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:179994934..179997849-chr1:180033158..180035390,2	MCF-7	breast:
2	chr1:179999019..180000801-chr1:180002803..180004316,2	K562	blood:
3	chr1:179833882..179836832-chr1:180042170..180044941,2	K562	blood:
4	chr1:179999019..180000801-chr1:180002803..180004316,2	K562	blood:
5	chr1:180064498..180066210-chr1:180067083..180069817,2	K562	blood:
6	chr1:179845496..179847681-chr1:180038078..180039850,2	MCF-7	breast:
7	chr1:180002453..180005081-chr1:180006068..180008636,2	K562	blood:
8	chr1:179965716..179968520-chr1:179975367..179977989,2	MCF-7	breast:
9	chr1:179988661..179990796-chr1:179997546..179999054,2	K562	blood:
10	chr1:180049598..180051873-chr1:180198863..180200788,2	MCF-7	breast:
11	chr1:179850618..179853198-chr1:180070366..180073320,2	K562	blood:
12	chr1:180012630..180014181-chr1:180020336..180022043,2	K562	blood:
13	chr1:179972601..179974993-chr1:179975734..179978646,3	K562	blood:
14	chr1:179923781..179925306-chr1:179959371..179960994,2	K562	blood:
15	chr1:180060328..180062536-chr1:180064967..180067433,2	MCF-7	breast:
16	chr1:179980682..179985119-chr1:179997024..179999746,4	MCF-7	breast:
17	chr1:180029884..180031484-chr1:180035395..180037562,2	MCF-7	breast:
18	chr1:180012692..180014319-chr1:180015730..180017884,2	MCF-7	breast:
19	chr1:180060871..180062560-chr1:180065238..180067423,2	K562	blood:
20	chr1:180067070..180070022-chr1:180093157..180094949,2	K562	blood:
21	chr1:180061211..180064450-chr1:180123630..180126274,3	MCF-7	breast:
22	chr1:179972601..179974993-chr1:179975734..179978646,3	K562	blood:
23	chr1:180060321..180062626-chr1:180121553..180123534,4	MCF-7	breast:
24	chr1:179850786..179852448-chr1:180017093..180019020,2	MCF-7	breast:
25	chr1:179845220..179846816-chr1:179967799..179969791,2	MCF-7	breast:
26	chr1:179923652..179925688-chr1:180038496..180041388,2	MCF-7	breast:
27	chr1:179924257..179926025-chr1:179973260..179975368,2	K562	blood:
28	chr1:179921867..179924634-chr1:180042656..180044466,2	MCF-7	breast:
29	chr1:179965716..179968520-chr1:179975367..179977989,2	MCF-7	breast:
30	chr1:179992324..179995143-chr1:180001757..180004164,2	K562	blood:
31	chr1:180055883..180058867-chr1:180060209..180061948,2	MCF-7	breast:
32	chr1:180048120..180049622-chr1:180134453..180137364,2	MCF-7	breast:
33	chr1:179947029..179952263-chr1:179955680..179959791,6	MCF-7	breast:
34	chr1:179959937..179962261-chr1:179974244..179975764,2	K562	blood:
35	chr1:180007479..180009332-chr1:180027865..180030769,2	K562	blood:
36	chr1:180067842..180070098-chr1:180124230..180125960,2	MCF-7	breast:
37	chr1:179852071..179854287-chr1:179987673..179989356,2	MCF-7	breast:
38	chr1:180009163..180012089-chr1:180014307..180016921,2	K562	blood:
39	chr1:179998356..180000949-chr1:180019994..180021642,2	K562	blood:
40	chr1:180051158..180053588-chr1:180124507..180126558,2	K562	blood:
41	chr1:180009514..180012969-chr1:180025548..180028168,4	MCF-7	breast:
42	chr1:179965148..179965648-chr8:43093862..43094700,2	MCF-7	breast:
43	chr1:179849763..179851404-chr1:180027993..180029985,2	K562	blood:
44	chr1:179851196..179853828-chr1:180057356..180059281,2	K562	blood:
45	chr1:180055883..180058867-chr1:180060209..180061948,2	MCF-7	breast:
46	chr1:179988661..179990796-chr1:179997546..179999054,2	K562	blood:
47	chr1:179973630..179975308-chr1:179977263..179979537,2	MCF-7	breast:
48	chr1:180012692..180014319-chr1:180015730..180017884,2	MCF-7	breast:
49	chr1:180010544..180012138-chr1:180019393..180021137,2	K562	blood:
50	chr1:179969658..179972086-chr1:179982002..179983576,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOR1AIP2-6	chr1:179969573-179969943	NONHSAT008237

Variant related genes	Relation type
ENSG00000223450	TF binding region
CEP350	TF binding region
ENSG00000223450	CpG island
CEP350	CpG island
ENSG00000169905	chromatin interactions
ENSG00000223450	chromatin interactions
ENSG00000135837	chromatin interactions
ENSG00000121454	chromatin interactions
ENSG00000116260	chromatin interactions
ENSG00000143337	chromatin interactions
ENSG00000260360	chromatin interactions
ENSG00000272906	chromatin interactions
ENSG00000258664	chromatin interactions

Extended variants
information (count: 4076 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:4076 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2501618	chr1:179958809-179958810	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527356222	chr1:179958833-179958834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541125496	chr1:179958857-179958858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544849899	chr1:179958863-179958864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78737770	chr1:179958878-179958879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs151133686	chr1:179958894-179958895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12130673	chr1:179958907-179958908	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs140217958	chr1:179958917-179958918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569234547	chr1:179958925-179958926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12130675	chr1:179958931-179958932	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs371384978	chr1:179958942-179958943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551646026	chr1:179958999-179959000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571819524	chr1:179959003-179959004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534034051	chr1:179959009-179959010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149898978	chr1:179959026-179959027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145022534	chr1:179959039-179959040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536676094	chr1:179959047-179959048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556617160	chr1:179959085-179959086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576371154	chr1:179959100-179959101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538945368	chr1:179959193-179959194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191038232	chr1:179959207-179959208	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10913921	chr1:179959297-179959298	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs540758230	chr1:179959307-179959308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377109217	chr1:179959308-179959309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564803650	chr1:179959318-179959319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561072001	chr1:179959336-179959337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574073480	chr1:179959440-179959441	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs542983057	chr1:179959491-179959492	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs562957952	chr1:179959504-179959505	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs531842650	chr1:179959545-179959546	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs567975866	chr1:179959552-179959553	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs369434488	chr1:179959615-179959616	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs552053057	chr1:179959707-179959708	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs115186595	chr1:179959724-179959725	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs140306241	chr1:179959750-179959751	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs547554278	chr1:179959816-179959817	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs567738179	chr1:179959824-179959825	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536759077	chr1:179959881-179959882	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs550159034	chr1:179959921-179959922	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs570069992	chr1:179959935-179959936	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs184884786	chr1:179959943-179959944	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs558851624	chr1:179960023-179960024	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2477109	chr1:179960034-179960035	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs534846605	chr1:179960090-179960091	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs73032376	chr1:179960104-179960105	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs189790218	chr1:179960142-179960143	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs141423145	chr1:179960143-179960144	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs367654758	chr1:179960148-179960149	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs370223764	chr1:179960179-179960180	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs529095108	chr1:179960252-179960253	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3309 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179924800-179963600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:179926800-179961400	Weak transcription	A549	lung
3	chr1:179927000-179965600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr1:179938000-179983200	Weak transcription	Brain Germinal Matrix	brain
5	chr1:179938600-179959000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr1:179938600-179965800	Weak transcription	Esophagus	oesophagus
7	chr1:179938600-179975800	Weak transcription	Thymus	Thymus
8	chr1:179938600-179983200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr1:179938600-179984600	Weak transcription	Lung	lung
10	chr1:179938800-179959800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:179939000-179989000	Weak transcription	Gastric	stomach
12	chr1:179939800-179959400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:179939800-179974800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr1:179940000-179961200	Weak transcription	HSMM	muscle
15	chr1:179941000-179959000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr1:179941400-180031800	Weak transcription	Spleen	Spleen
17	chr1:179946400-179959000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr1:179946400-179959000	Weak transcription	Right Ventricle	heart
19	chr1:179946400-179959200	Weak transcription	Osteobl	bone
20	chr1:179946400-179963200	Weak transcription	HUVEC	blood vessel
21	chr1:179946400-179965600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr1:179946400-179972800	Weak transcription	Brain Cingulate Gyrus	brain
23	chr1:179946400-179983000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:179946400-179989200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:179946600-179961200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr1:179946600-179961400	Weak transcription	HepG2	liver
27	chr1:179946600-179965800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr1:179946600-179965800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr1:179946600-179983200	Weak transcription	Brain Angular Gyrus	brain
30	chr1:179946800-179959200	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr1:179946800-179959200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:179946800-179963800	Weak transcription	Adipose Nuclei	Adipose
33	chr1:179947800-179989400	Weak transcription	Small Intestine	intestine
34	chr1:179948000-179961200	Weak transcription	Colon Smooth Muscle	Colon
35	chr1:179948400-179965800	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr1:179948400-179971800	Weak transcription	Fetal Heart	heart
37	chr1:179948600-179983200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr1:179949200-179961200	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr1:179949200-179963800	Weak transcription	Fetal Muscle Trunk	muscle
40	chr1:179949400-179980600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr1:179950000-179980600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr1:179950200-179966000	Weak transcription	Fetal Brain Female	brain
43	chr1:179951400-179972200	Weak transcription	Psoas Muscle	Psoas
44	chr1:179951400-179974600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr1:179951800-179974800	Weak transcription	Hela-S3	cervix
46	chr1:179952400-179965600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:179953200-179960000	Weak transcription	Right Atrium	heart
48	chr1:179953400-179965400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr1:179953600-179959800	Weak transcription	Placenta	Placenta
50	chr1:179953600-179964800	Weak transcription	Muscle Satellite Cultured Cells	--

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