Variant report

Variant	esv3692941
Chromosome Location	chr7:112571420-112614215
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:670)
CpG islands
(count:795)
Chromatin interactive
region (count:39)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:670 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:112578133-112578400	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:112573670-112573961	K562	blood:	n/a	n/a
3	ARID3A	chr7:112579802-112580571	HepG2	liver:	n/a	n/a
4	ATF1	chr7:112579830-112580980	K562	blood:	n/a	n/a
5	ATF1	chr7:112591210-112591392	K562	blood:	n/a	n/a
6	ATF1	chr7:112599838-112599896	K562	blood:	n/a	n/a
7	ATF1	chr7:112610852-112610969	K562	blood:	n/a	n/a
8	ATF2	chr7:112579800-112580535	GM12878	blood:	n/a	n/a
9	ATF2	chr7:112580038-112580496	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr7:112573729-112573876	K562	blood:	n/a	n/a
11	ATF3	chr7:112580043-112580580	K562	blood:	n/a	chr7:112580257-112580270
12	BHLHE40	chr7:112579032-112579293	K562	blood:	n/a	n/a
13	BHLHE40	chr7:112579565-112580648	K562	blood:	n/a	n/a
14	BHLHE40	chr7:112579184-112579293	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:112579659-112580648	GM12878	blood:	n/a	n/a
16	CBX3	chr7:112579913-112580953	K562	blood:	n/a	n/a
17	CBX3	chr7:112579498-112580946	K562	blood:	n/a	n/a
18	CCNT2	chr7:112579172-112580391	K562	blood:	n/a	chr7:112579458-112579467 chr7:112579397-112579406
19	CEBPB	chr7:112598065-112598107	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:112607905-112608244	K562	blood:	n/a	n/a
21	CEBPB	chr7:112613905-112614205	IMR90	lung:	n/a	chr7:112614062-112614075 chr7:112614185-112614198 chr7:112614063-112614074
22	CEBPB	chr7:112607411-112607467	K562	blood:	n/a	n/a
23	CEBPB	chr7:112579977-112580010	A549	lung:	n/a	n/a
24	CEBPB	chr7:112581584-112581784	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:112613922-112614193	HepG2	liver:	n/a	chr7:112614062-112614075 chr7:112614063-112614074
26	CEBPB	chr7:112580045-112580514	K562	blood:	n/a	n/a
27	CEBPB	chr7:112613927-112614080	Hela-S3	cervix:	n/a	chr7:112614062-112614075 chr7:112614063-112614074
28	CEBPB	chr7:112607913-112608165	K562	blood:	n/a	n/a
29	CEBPB	chr7:112607909-112608293	K562	blood:	n/a	n/a
30	CEBPB	chr7:112579965-112580122	Hela-S3	cervix:	n/a	n/a
31	CEBPD	chr7:112579622-112579996	HepG2	liver:	n/a	n/a
32	CEBPD	chr7:112580088-112580457	HepG2	liver:	n/a	n/a
33	CHD1	chr7:112579462-112579597	GM12878	blood:	n/a	n/a
34	CHD1	chr7:112579250-112579700	H1-hESC	embryonic stem cell:	n/a	chr7:112579459-112579469
35	CHD1	chr7:112580191-112580486	GM12878	blood:	n/a	n/a
36	CHD2	chr7:112579811-112580620	K562	blood:	n/a	n/a
37	CHD2	chr7:112579799-112580440	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr7:112579214-112580775	GM12878	blood:	n/a	chr7:112579459-112579469
39	CHD2	chr7:112579621-112580347	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr7:112579591-112580402	HepG2	liver:	n/a	n/a
41	CREB1	chr7:112579684-112580483	A549	lung:	n/a	n/a
42	CREB1	chr7:112579759-112581102	K562	blood:	n/a	n/a
43	CREB1	chr7:112579385-112580823	K562	blood:	n/a	n/a
44	CREB1	chr7:112579538-112580681	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr7:112579519-112580715	HepG2	liver:	n/a	n/a
46	CREB1	chr7:112579684-112580648	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr7:112579464-112580650	GM12878	blood:	n/a	n/a
48	CTCF	chr7:112579600-112579750	GM12873	blood:	n/a	n/a
49	CTCF	chr7:112579640-112579790	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr7:112610994-112611058	HepG2	liver:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:112582716-112582766	ovcar-3	ovarian:	n/a
2	chr7:112579927-112579977	A549	lung:	n/a
3	chr7:112582716-112582766	ovcar-3	ovarian:	n/a
4	chr7:112579927-112579977	A549	lung:	n/a
5	chr7:112579992-112580042	GM12891	blood:	n/a
6	chr7:112580305-112580355	GM06990	blood:	n/a
7	chr7:112579998-112580048	NB4	blood:	n/a
8	chr7:112582716-112582766	HEEpiC	esophagus:	n/a
9	chr7:112580528-112580578	NH-A	brain:	n/a
10	chr7:112582716-112582766	HEK293	kidney:	embryo
11	chr7:112579927-112579977	NB4	blood:	n/a
12	chr7:112575866-112575916	HRCEpiC	kidney:	n/a
13	chr7:112582716-112582766	SKMC	muscle:	n/a
14	chr7:112580216-112580266	AG04449	skin:	fetal
15	chr7:112571476-112571526	HL-60	blood:	n/a
16	chr7:112579757-112579807	AG09319	gingival:	n/a
17	chr7:112579137-112579187	ECC-1	luminal epithelium:	n/a
18	chr7:112571476-112571526	AG04450	lung:	fetal
19	chr7:112575866-112575916	PFSK-1	brain:	n/a
20	chr7:112571476-112571526	HNPCEpiC	eye:	n/a
21	chr7:112580528-112580578	GM12878	blood:	n/a
22	chr7:112579998-112580048	AG04449	skin:	fetal
23	chr7:112579927-112579977	HEK293	kidney:	embryo
24	chr7:112580077-112580127	HCM	heart:	n/a
25	chr7:112575866-112575916	Caco-2	colon:	n/a
26	chr7:112580216-112580266	GM12891	blood:	n/a
27	chr7:112579992-112580042	CMK	blood:	n/a
28	chr7:112575866-112575916	NT2-D1	testis:	n/a
29	chr7:112575866-112575916	HAEpiC	amniotic membrane:	n/a
30	chr7:112580216-112580266	GM12892	blood:	n/a
31	chr7:112571476-112571526	GM06990	blood:	n/a
32	chr7:112579757-112579807	SK-N-SH	brain:	n/a
33	chr7:112579137-112579187	MCF10A-Er-Src	breast:	n/a
34	chr7:112579509-112579559	NHBE	bronchial:	n/a
35	chr7:112575866-112575916	GM12878	blood:	n/a
36	chr7:112575866-112575916	SAEC	small airway:	n/a
37	chr7:112575866-112575916	AG10803	skin:	n/a
38	chr7:112575866-112575916	AG04450	lung:	fetal
39	chr7:112580305-112580355	GM12878	blood:	n/a
40	chr7:112580528-112580578	HAEpiC	amniotic membrane:	n/a
41	chr7:112571476-112571526	K562	blood:	n/a
42	chr7:112579927-112579977	LNCaP	prostate:	n/a
43	chr7:112582716-112582766	PANC-1	pancreas:	n/a
44	chr7:112579992-112580042	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:112579927-112579977	HMEC	breast:	n/a
46	chr7:112579927-112579977	NHDF-neo	bronchial:	n/a
47	chr7:112580305-112580355	SK-N-SH	brain:	n/a
48	chr7:112579992-112580042	NB4	blood:	n/a
49	chr7:112579927-112579977	SK-N-MC	brain:	n/a
50	chr7:112579509-112579559	ProgFib	skin:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:112608892..112612012-chr7:112612504..112614943,3	MCF-7	breast:
2	chr7:112569158..112571513-chr7:112600317..112602732,2	MCF-7	breast:
3	chr7:112571595..112576462-chr7:112578042..112581629,5	K562	blood:
4	chr7:112428924..112430644-chr7:112579193..112581843,2	K562	blood:
5	chr6:129642024..129642655-chr7:112579975..112580488,2	MCF-7	breast:
6	chr7:112605934..112608716-chr7:112610889..112612705,2	K562	blood:
7	chr7:112601365..112604036-chr7:112606772..112610926,4	K562	blood:
8	chr7:112577667..112580375-chr7:112582881..112584475,2	MCF-7	breast:
9	chr7:112567908..112571735-chr7:112573454..112577571,5	K562	blood:
10	chr7:112572451..112576554-chr7:112577606..112581237,7	MCF-7	breast:
11	chr7:112570828..112572973-chr7:112579536..112581070,2	MCF-7	breast:
12	chr7:112569158..112571513-chr7:112600317..112602732,2	MCF-7	breast:
13	chr7:112601365..112604036-chr7:112606772..112610926,4	K562	blood:
14	chr7:112567908..112571735-chr7:112573454..112577571,5	K562	blood:
15	chr7:112570140..112571733-chr7:112574032..112575624,2	MCF-7	breast:
16	chr7:112580392..112582093-chr7:112599898..112601408,2	MCF-7	breast:
17	chr7:112583353..112585564-chr7:112597999..112600804,2	MCF-7	breast:
18	chr7:112570140..112571733-chr7:112574032..112575624,2	MCF-7	breast:
19	chr7:112602086..112604534-chr7:112611738..112613298,2	K562	blood:
20	chr7:112569955..112573095-chr7:112578523..112581204,3	K562	blood:
21	chr7:112574893..112577839-chr7:112578042..112580398,5	K562	blood:
22	chr7:112477234..112479370-chr7:112580510..112582070,2	K562	blood:
23	chr7:112609190..112612964-chr7:112622640..112627113,4	K562	blood:
24	chr7:112602086..112604534-chr7:112611738..112613298,2	K562	blood:
25	chr7:112430077..112432189-chr7:112593600..112595306,2	MCF-7	breast:
26	chr7:112579425..112581874-chr7:112585299..112587492,4	K562	blood:
27	chr7:112583353..112585564-chr7:112597999..112600804,2	MCF-7	breast:
28	chr7:112579376..112581874-chr7:112583714..112588388,6	K562	blood:
29	chr7:112605934..112608716-chr7:112610889..112612705,2	K562	blood:
30	chr7:112580392..112582093-chr7:112599898..112601408,2	MCF-7	breast:
31	chr7:112565275..112568159-chr7:112573101..112575582,2	MCF-7	breast:
32	chr7:112569568..112571455-chr7:112579198..112581204,2	K562	blood:
33	chr7:112608892..112612012-chr7:112612504..112614943,3	MCF-7	breast:
34	chr7:112568119..112570873-chr7:112572834..112576216,3	K562	blood:
35	chr7:112442436..112445188-chr7:112575668..112578638,2	K562	blood:
36	chr7:112578925..112581917-chr7:112594123..112596440,2	MCF-7	breast:
37	chr7:112573321..112577054-chr7:112577795..112579743,3	MCF-7	breast:
38	chr7:112578366..112581242-chr7:112590311..112591816,2	MCF-7	breast:
39	chr7:112578476..112580812-chr7:112583356..112586040,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf60-1	chr7:112593368-112593811	NONHSAT122803
2	lnc-C7orf60-1	chr7:112613674-112613727	ENSG00000234520
3	lnc-C7orf60-1	chr7:112594701-112594823	ENSG00000234520
4	lnc-C7orf60-1	chr7:112613660-112613727	NONHSAT122804
5	lnc-C7orf60-1	chr7:112596577-112596757	NONHSAT122803
6	lnc-C7orf60-1	chr7:112594658-112594823	NONHSAT122805
7	lnc-C7orf60-1	chr7:112596577-112596766	NONHSAT122806
8	lnc-C7orf60-1	chr7:112596577-112596766	NONHSAT122805
9	lnc-C7orf60-1	chr7:112596577-112596766	NONHSAT122804
10	lnc-C7orf60-1	chr7:112594718-112594823	NONHSAT122808
11	lnc-C7orf60-1	chr7:112596577-112596768	NONHSAT122808
12	lnc-C7orf60-1	chr7:112593368-112593811	NONHSAT122806
13	lnc-C7orf60-1	chr7:112593368-112593811	NONHSAT122804
14	lnc-C7orf60-1	chr7:112594658-112594823	NONHSAT122806
15	lnc-C7orf60-1	chr7:112596577-112596757	NR_110162
16	lnc-C7orf60-1	chr7:112594690-112594823	NR_110162
17	lnc-C7orf60-1	chr7:112613660-112613727	NR_110162
18	lnc-C7orf60-1	chr7:112596577-112596757	ENSG00000234520
19	lnc-C7orf60-1	chr7:112593368-112593811	NONHSAT122805
20	lnc-C7orf60-1	chr7:112594658-112594823	NONHSAT122803
21	lnc-C7orf60-1	chr7:112594658-112594823	NONHSAT122804
22	lnc-C7orf60-1	chr7:112613660-112613727	ENSG00000234520

No data

Variant related genes	Relation type
C7orf60	TF binding region
C7orf60	CpG island
ENSG00000164603	chromatin interactions
ENSG00000146802	chromatin interactions

Extended variants
information (count: 1398 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1398 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2197953	chr7:112571420-112571421	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370167187	chr7:112571428-112571429	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs191832146	chr7:112571442-112571443	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144861059	chr7:112571519-112571520	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs13242574	chr7:112571565-112571566	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs534323638	chr7:112571576-112571577	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs552525942	chr7:112571605-112571606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs373381006	chr7:112571661-112571662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs148587877	chr7:112571664-112571665	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs73195098	chr7:112571685-112571686	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs142898206	chr7:112571744-112571745	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs559874098	chr7:112571750-112571751	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs544764278	chr7:112571769-112571770	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs542764895	chr7:112571770-112571771	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs563063784	chr7:112571809-112571810	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs377358278	chr7:112571817-112571818	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs573345735	chr7:112571845-112571846	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs183234302	chr7:112571854-112571855	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs150672188	chr7:112571859-112571860	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs532870241	chr7:112571865-112571866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs544576229	chr7:112571871-112571872	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs563140692	chr7:112571935-112571936	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532189300	chr7:112571969-112571970	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs551443143	chr7:112572011-112572012	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs530242287	chr7:112572082-112572083	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs55796683	chr7:112572108-112572109	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs567047307	chr7:112572123-112572124	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs528156196	chr7:112572142-112572143	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs546213997	chr7:112572201-112572202	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs568960068	chr7:112572227-112572228	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs538962789	chr7:112572250-112572251	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs537155172	chr7:112572261-112572262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556984205	chr7:112572269-112572270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs117314425	chr7:112572283-112572284	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs536079716	chr7:112572320-112572321	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143729526	chr7:112572328-112572329	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs188559875	chr7:112572357-112572358	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs537425001	chr7:112572409-112572410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs112333678	chr7:112572430-112572431	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs35813811	chr7:112572505-112572506	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs540708722	chr7:112572537-112572538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs193157306	chr7:112572548-112572549	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs559040696	chr7:112572550-112572551	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs556847152	chr7:112572602-112572603	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs577160230	chr7:112572620-112572621	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs544556355	chr7:112572626-112572627	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs139449582	chr7:112572672-112572673	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs563044905	chr7:112572694-112572695	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs17160069	chr7:112572786-112572787	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs118056586	chr7:112572787-112572788	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
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
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21248843	CNVD

Chromatin state (count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112530400-112576600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr7:112541400-112578800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:112549400-112574200	Weak transcription	Fetal Brain Female	brain
4	chr7:112551600-112575600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr7:112551600-112575800	Weak transcription	GM12878-XiMat	blood
6	chr7:112551600-112576200	Weak transcription	Ovary	ovary
7	chr7:112551600-112577400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr7:112551600-112578600	Weak transcription	Fetal Muscle Trunk	muscle
9	chr7:112551600-112579400	Weak transcription	Spleen	Spleen
10	chr7:112553800-112578800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr7:112554000-112577200	Weak transcription	Primary B cells from cord blood	blood
12	chr7:112555400-112578000	Weak transcription	Adipose Nuclei	Adipose
13	chr7:112555600-112572600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr7:112556000-112573600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr7:112556200-112575800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr7:112556800-112573000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:112556800-112576200	Weak transcription	Left Ventricle	heart
18	chr7:112556800-112577600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:112557000-112578600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr7:112562200-112572600	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr7:112562800-112576400	Weak transcription	Fetal Intestine Small	intestine
22	chr7:112563200-112578200	Weak transcription	HUVEC	blood vessel
23	chr7:112565200-112578600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr7:112566800-112572600	Weak transcription	Fetal Heart	heart
25	chr7:112568400-112576200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr7:112568400-112578200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr7:112569200-112571800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr7:112569200-112571800	Enhancers	Osteobl	bone
29	chr7:112569400-112571800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:112569400-112571800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr7:112569800-112571800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr7:112569800-112575600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr7:112569800-112576200	Weak transcription	Fetal Intestine Large	intestine
34	chr7:112570000-112571800	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr7:112570200-112571600	Enhancers	NHDF-Ad	bronchial
36	chr7:112570200-112571800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr7:112570200-112571800	Enhancers	HepG2	liver
38	chr7:112570200-112571800	Enhancers	HSMMtube	muscle
39	chr7:112570200-112572000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr7:112570200-112572800	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr7:112570400-112572000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr7:112570400-112578400	Weak transcription	NH-A	brain
43	chr7:112570600-112571600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:112570600-112571600	Enhancers	Brain Germinal Matrix	brain
45	chr7:112570600-112571800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:112570600-112571800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr7:112570600-112571800	Enhancers	Brain Angular Gyrus	brain
48	chr7:112570600-112572000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr7:112570600-112572600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr7:112570800-112571600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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