Variant report

Variant	nsv888936
Chromosome Location	chr7:105119308-105193051
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1902)
CpG islands
(count:1836)
Chromatin interactive
region (count:131)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1902 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:105173865-105174045	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:105162675-105163137	K562	blood:	n/a	n/a
3	ARID3A	chr7:105128201-105128752	K562	blood:	n/a	n/a
4	ARID3A	chr7:105141763-105141769	K562	blood:	n/a	n/a
5	ARID3A	chr7:105162532-105162842	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:105172276-105172771	K562	blood:	n/a	n/a
7	ARID3A	chr7:105172230-105172894	HepG2	liver:	n/a	n/a
8	ATF1	chr7:105128345-105128752	K562	blood:	n/a	n/a
9	ATF2	chr7:105172329-105172807	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:105171988-105172822	GM12878	blood:	n/a	n/a
11	ATF2	chr7:105172257-105172894	GM12878	blood:	n/a	n/a
12	ATF2	chr7:105162441-105162701	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr7:105172202-105172799	K562	blood:	n/a	n/a
14	ATF3	chr7:105162419-105162922	K562	blood:	n/a	chr7:105162516-105162525
15	ATF3	chr7:105162479-105162756	A549	lung:	n/a	chr7:105162516-105162525
16	BACH1	chr7:105161884-105162223	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:105172426-105172817	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:105162629-105162935	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:105172328-105172846	K562	blood:	n/a	n/a
20	BATF	chr7:105172440-105172791	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:105172537-105172868	GM12878	blood:	n/a	n/a
22	BCL3	chr7:105172316-105172982	A549	lung:	n/a	n/a
23	BCL3	chr7:105172270-105172911	A549	lung:	n/a	n/a
24	BCL3	chr7:105162453-105163079	A549	lung:	n/a	chr7:105162468-105162481 chr7:105162470-105162483
25	BCLAF1	chr7:105172218-105172996	K562	blood:	n/a	n/a
26	BCLAF1	chr7:105172328-105172981	K562	blood:	n/a	n/a
27	BCLAF1	chr7:105172346-105172920	GM12878	blood:	n/a	n/a
28	BCLAF1	chr7:105162157-105163019	K562	blood:	n/a	chr7:105162468-105162481 chr7:105162470-105162483
29	BCLAF1	chr7:105172265-105172905	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:105172018-105173029	K562	blood:	n/a	n/a
31	BHLHE40	chr7:105161610-105163105	K562	blood:	n/a	n/a
32	BHLHE40	chr7:105172056-105172791	HepG2	liver:	n/a	n/a
33	BHLHE40	chr7:105161948-105162953	HepG2	liver:	n/a	n/a
34	BHLHE40	chr7:105162517-105162823	A549	lung:	n/a	n/a
35	BHLHE40	chr7:105171963-105172867	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:105162519-105162872	HepG2	liver:	n/a	n/a
37	BHLHE40	chr7:105128299-105128701	K562	blood:	n/a	n/a
38	BHLHE40	chr7:105174117-105174180	K562	blood:	n/a	n/a
39	BHLHE40	chr7:105161582-105163259	GM12878	blood:	n/a	n/a
40	BRCA1	chr7:105172446-105172663	GM12878	blood:	n/a	n/a
41	BRCA1	chr7:105172361-105172945	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr7:105161980-105162068	HepG2	liver:	n/a	n/a
43	BRCA1	chr7:105162680-105163061	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr7:105172354-105173016	K562	blood:	n/a	n/a
45	CBX3	chr7:105161716-105162247	K562	blood:	n/a	n/a
46	CBX3	chr7:105161068-105162276	K562	blood:	n/a	n/a
47	CBX3	chr7:105162379-105163324	K562	blood:	n/a	n/a
48	CBX3	chr7:105171840-105173469	K562	blood:	n/a	n/a
49	CCNT2	chr7:105172155-105172950	K562	blood:	n/a	n/a
50	CCNT2	chr7:105161929-105162925	K562	blood:	n/a	n/a

(count:1836 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105162888-105162938	SKMC	muscle:	n/a
2	chr7:105162600-105162650	Jurkat	blood:	n/a
3	chr7:105170241-105170291	LNCaP	prostate:	n/a
4	chr7:105176805-105176855	HCPEpiC	choroid plexus:	n/a
5	chr7:105162577-105162627	BJ	skin:	n/a
6	chr7:105160482-105160532	Jurkat	blood:	n/a
7	chr7:105162888-105162938	SKMC	muscle:	n/a
8	chr7:105162600-105162650	Jurkat	blood:	n/a
9	chr7:105170241-105170291	LNCaP	prostate:	n/a
10	chr7:105176805-105176855	HCPEpiC	choroid plexus:	n/a
11	chr7:105162577-105162627	BJ	skin:	n/a
12	chr7:105160482-105160532	Jurkat	blood:	n/a
13	chr7:105172520-105172570	NB4	blood:	n/a
14	chr7:105162735-105162785	GM19239	blood:	n/a
15	chr7:105173132-105173182	SK-N-SH	brain:	n/a
16	chr7:105165592-105165642	MCF10A-Er-Src	breast:	n/a
17	chr7:105162600-105162650	K562	blood:	n/a
18	chr7:105173132-105173182	PANC-1	pancreas:	n/a
19	chr7:105171843-105171893	A549	lung:	n/a
20	chr7:105162470-105162520	GM19239	blood:	n/a
21	chr7:105172974-105173024	SK-N-MC	brain:	n/a
22	chr7:105162878-105162928	SK-N-SH_RA	brain:	n/a
23	chr7:105137683-105137733	HMEC	breast:	n/a
24	chr7:105172168-105172218	U87	brain:	n/a
25	chr7:105162888-105162938	SAEC	small airway:	n/a
26	chr7:105172403-105172453	K562	blood:	n/a
27	chr7:105137683-105137733	HEK293	kidney:	embryo
28	chr7:105171843-105171893	T-47D	breast:	n/a
29	chr7:105134734-105134784	HepG2	liver:	n/a
30	chr7:105162888-105162938	PrEC	prostate:	n/a
31	chr7:105162735-105162785	AG04450	lung:	fetal
32	chr7:105172974-105173024	BJ	skin:	n/a
33	chr7:105173132-105173182	NT2-D1	testis:	n/a
34	chr7:105162735-105162785	SK-N-SH	brain:	n/a
35	chr7:105171843-105171893	PrEC	prostate:	n/a
36	chr7:105162814-105162864	NB4	blood:	n/a
37	chr7:105172403-105172453	NB4	blood:	n/a
38	chr7:105161983-105162033	NT2-D1	testis:	n/a
39	chr7:105162470-105162520	BJ	skin:	n/a
40	chr7:105176805-105176855	HL-60	blood:	n/a
41	chr7:105162814-105162864	ECC-1	luminal epithelium:	n/a
42	chr7:105172520-105172570	GM12892	blood:	n/a
43	chr7:105161983-105162033	HEEpiC	esophagus:	n/a
44	chr7:105162735-105162785	NB4	blood:	n/a
45	chr7:105173132-105173182	PrEC	prostate:	n/a
46	chr7:105172664-105172714	AG09319	gingival:	n/a
47	chr7:105172403-105172453	HCT-116	colon:	n/a
48	chr7:105162735-105162785	U87	brain:	n/a
49	chr7:105162941-105162991	ovcar-3	ovarian:	n/a
50	chr7:105170241-105170291	SK-N-MC	brain:	n/a

(count:131 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:105171193..105173393-chr7:105516904..105519168,2	K562	blood:
2	chr17:19551197..19552117-chr7:105161941..105162797,2	Hela-S3	cervix:
3	chr7:105148472..105150405-chr7:105160556..105162918,2	MCF-7	breast:
4	chr7:105139662..105141341-chr7:105152826..105155555,3	K562	blood:
5	chr7:105135383..105138778-chr7:105145127..105148143,3	MCF-7	breast:
6	chr7:105148185..105149870-chr7:105160014..105161672,2	K562	blood:
7	chr7:105161098..105164204-chr7:105164483..105168107,5	MCF-7	breast:
8	chr7:104653151..104655503-chr7:105160083..105164345,7	K562	blood:
9	chr7:105171405..105173628-chr7:105221272..105223628,2	MCF-7	breast:
10	chr7:105143860..105147794-chr7:105158802..105162576,5	K562	blood:
11	chr7:105111430..105113380-chr7:105117315..105120062,2	K562	blood:
12	chr7:105139311..105141593-chr7:105161601..105163492,2	K562	blood:
13	chr7:105141175..105142796-chr7:105145360..105147513,2	MCF-7	breast:
14	chr7:104653438..104655052-chr7:105156845..105159544,2	K562	blood:
15	chr7:105162231..105163027-chr7:105172004..105172750,2	K562	blood:
16	chr17:56708735..56709467-chr7:105162240..105162879,2	MCF-7	breast:
17	chr7:105160261..105165362-chr7:105168599..105174293,22	MCF-7	breast:
18	chr7:104772977..104775390-chr7:105160456..105162601,2	K562	blood:
19	chr7:105174872..105176393-chr7:105185290..105187742,2	MCF-7	breast:
20	chr7:105174875..105178422-chr7:105279003..105282206,4	MCF-7	breast:
21	chr7:104652163..104655972-chr7:105160292..105163807,4	MCF-7	breast:
22	chr7:105083591..105086006-chr7:105160365..105162043,2	K562	blood:
23	chr7:105125271..105127106-chr7:105136833..105138910,2	K562	blood:
24	chr7:105139662..105141341-chr7:105152826..105155555,3	K562	blood:
25	chr7:105143860..105147794-chr7:105158802..105162576,5	K562	blood:
26	chr7:105136272..105139151-chr7:105160934..105162836,3	MCF-7	breast:
27	chr7:105143576..105146396-chr7:105147042..105149947,3	K562	blood:
28	chr7:105129866..105132116-chr7:105135974..105138549,2	K562	blood:
29	chr7:105126837..105131294-chr7:105131811..105135446,3	K562	blood:
30	chr7:105171534..105175507-chr7:105231963..105234533,3	K562	blood:
31	chr7:105178950..105184769-chr7:105189536..105192769,5	K562	blood:
32	chr7:105123891..105126807-chr7:105127065..105130619,3	K562	blood:
33	chr7:105159598..105163989-chr7:105219696..105223115,7	MCF-7	breast:
34	chr19:1261170..1262083-chr7:105162048..105162685,2	Hela-S3	cervix:
35	chr7:105128652..105130431-chr7:105155897..105157484,2	MCF-7	breast:
36	chr7:105027746..105030082-chr7:105160759..105163665,5	MCF-7	breast:
37	chr7:105069861..105070836-chr7:105128119..105128880,2	MCF-7	breast:
38	chr7:105160846..105164326-chr7:105166102..105168555,5	MCF-7	breast:
39	chr7:105039517..105040114-chr7:105128184..105128801,2	MCF-7	breast:
40	chr7:105121563..105123153-chr7:105161155..105163117,2	MCF-7	breast:
41	chr7:105158727..105165017-chr7:105166972..105176993,56	K562	blood:
42	chr7:105152955..105155476-chr7:105155749..105158829,5	K562	blood:
43	chr7:104652025..104655487-chr7:105171171..105176319,6	K562	blood:
44	chr7:105126837..105131294-chr7:105131811..105135446,3	K562	blood:
45	chr7:105171071..105173381-chr7:105188092..105190983,2	MCF-7	breast:
46	chr7:105148994..105150495-chr7:105172517..105174104,2	MCF-7	breast:
47	chr7:104653151..104655346-chr7:105160083..105164134,5	K562	blood:
48	chr7:105116272..105117859-chr7:105118414..105120932,2	K562	blood:
49	chr1:209957159..209957989-chr7:105162027..105162579,2	Hela-S3	cervix:
50	chr17:41465807..41466363-chr7:105162224..105162878,2	NB4	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDHR3-5	chr7:105182048-105182302	NONHSAT122624
2	lnc-RINT1-2	chr7:105170656-105171118	NONHSAT122622
3	lnc-PUS7-1	chr7:105170677-105170904	NONHSAT122623
4	lnc-CDHR3-5	chr7:105182855-105183003	NONHSAT122624
5	lnc-PUS7-1	chr7:105171944-105171973	NONHSAT122623

No data

Variant related genes	Relation type
RINT1	TF binding region
ENSG00000223886	TF binding region
PUS7	TF binding region
RINT1	CpG island
ENSG00000223886	CpG island
PUS7	CpG island
ENSG00000188825	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000223886	chromatin interactions
ENSG00000231167	chromatin interactions
ENSG00000125503	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000128536	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000014123	chromatin interactions
ENSG00000272604	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000223473	chromatin interactions
ENSG00000099622	chromatin interactions
ENSG00000185055	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000237310	chromatin interactions
ENSG00000162757	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000230508	chromatin interactions
ENSG00000072210	chromatin interactions
ENSG00000146776	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000233797	chromatin interactions
ENSG00000135250	chromatin interactions

Extended variants
information (count: 3009 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3009 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6466069	chr7:105119308-105119309	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs77189770	chr7:105119309-105119310	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577001791	chr7:105119321-105119322	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs191003133	chr7:105119391-105119392	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs77519777	chr7:105119406-105119407	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs201638886	chr7:105119421-105119422	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs117994971	chr7:105119446-105119447	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528394595	chr7:105119478-105119479	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs376179434	chr7:105119497-105119498	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373871574	chr7:105119540-105119541	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs183318967	chr7:105119591-105119592	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs530791228	chr7:105119605-105119606	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550703990	chr7:105119616-105119617	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs73415587	chr7:105119642-105119643	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs556139076	chr7:105119664-105119665	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547182737	chr7:105119668-105119669	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs187543289	chr7:105119692-105119693	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs139587257	chr7:105119802-105119803	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs574396183	chr7:105119803-105119804	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs6976702	chr7:105119856-105119857	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs192766155	chr7:105119879-105119880	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574517518	chr7:105119959-105119960	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs541698846	chr7:105119961-105119962	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs370234800	chr7:105120013-105120014	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs17148749	chr7:105120038-105120039	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557138535	chr7:105120072-105120073	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145786444	chr7:105120096-105120097	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545538939	chr7:105120162-105120163	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545121594	chr7:105120192-105120193	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148955943	chr7:105120216-105120217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541749000	chr7:105120221-105120222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561639956	chr7:105120231-105120232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562242040	chr7:105120273-105120274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183217203	chr7:105120314-105120315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187915816	chr7:105120375-105120376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533484513	chr7:105120393-105120394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560479283	chr7:105120409-105120410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs818467	chr7:105120430-105120431	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs117864030	chr7:105120480-105120481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146552407	chr7:105120499-105120500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73421611	chr7:105120506-105120507	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs141193048	chr7:105120509-105120510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192535459	chr7:105120524-105120525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560505117	chr7:105120576-105120577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114445861	chr7:105120583-105120584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570316437	chr7:105120634-105120635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145178425	chr7:105120644-105120645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571433323	chr7:105120667-105120668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184173395	chr7:105120673-105120674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552770248	chr7:105120675-105120676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:2671 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:105080000-105161200	Weak transcription	Pancreas	Pancrea
2	chr7:105080200-105126800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr7:105088200-105142600	Weak transcription	Esophagus	oesophagus
4	chr7:105088200-105152800	Weak transcription	Gastric	stomach
5	chr7:105088400-105140400	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr7:105089200-105127000	Weak transcription	Primary hematopoietic stem cells	blood
7	chr7:105089200-105142600	Weak transcription	Fetal Thymus	thymus
8	chr7:105089600-105145200	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr7:105089600-105145800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr7:105090000-105126800	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr7:105090000-105128200	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr7:105090800-105120200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr7:105093600-105153000	Weak transcription	Small Intestine	intestine
14	chr7:105094400-105120200	Weak transcription	Lung	lung
15	chr7:105094800-105137200	Weak transcription	Fetal Kidney	kidney
16	chr7:105095000-105128200	Weak transcription	Primary B cells from cord blood	blood
17	chr7:105095200-105140600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr7:105095200-105142600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:105095600-105128400	Weak transcription	Brain Angular Gyrus	brain
20	chr7:105095600-105128400	Weak transcription	Brain Cingulate Gyrus	brain
21	chr7:105096000-105126400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:105096000-105127600	Weak transcription	NHLF	lung
23	chr7:105096000-105141000	Weak transcription	Colonic Mucosa	Colon
24	chr7:105096200-105128200	Weak transcription	Brain Hippocampus Middle	brain
25	chr7:105096400-105128000	Weak transcription	Brain Substantia Nigra	brain
26	chr7:105096400-105145600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr7:105098200-105151200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr7:105098600-105121000	Weak transcription	Brain Germinal Matrix	brain
29	chr7:105098600-105128400	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr7:105099400-105130800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr7:105099800-105127600	Weak transcription	NHDF-Ad	bronchial
32	chr7:105099800-105153000	Weak transcription	Psoas Muscle	Psoas
33	chr7:105100000-105141800	Weak transcription	Placenta	Placenta
34	chr7:105102000-105121000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr7:105102400-105119600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr7:105102400-105120600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:105102400-105128000	Weak transcription	Fetal Lung	lung
38	chr7:105102400-105134000	Weak transcription	Aorta	Aorta
39	chr7:105102400-105134000	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr7:105102400-105140800	Weak transcription	Right Ventricle	heart
41	chr7:105102800-105126800	Weak transcription	Ovary	ovary
42	chr7:105103000-105126400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr7:105103200-105126200	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr7:105105200-105119600	Weak transcription	Fetal Intestine Large	intestine
45	chr7:105105200-105126200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr7:105105200-105126200	Weak transcription	Stomach Smooth Muscle	stomach
47	chr7:105105200-105126400	Weak transcription	Fetal Brain Female	brain
48	chr7:105105200-105128200	Weak transcription	Fetal Brain Male	brain
49	chr7:105106000-105121400	Weak transcription	NH-A	brain
50	chr7:105107400-105121200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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