Variant report

Variant	nsv1019463
Chromosome Location	chr7:2848448-2881872
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:833)
CpG islands
(count:1285)
Chromatin interactive
region (count:64)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:833 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:2859980-2860564	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:2863083-2863193	K562	blood:	n/a	n/a
3	ARID3A	chr7:2859621-2859641	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:2848999-2849245	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:2857079-2857456	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:2878518-2878785	K562	blood:	n/a	n/a
7	ATF1	chr7:2878491-2878854	K562	blood:	n/a	n/a
8	ATF2	chr7:2864148-2864884	GM12878	blood:	n/a	n/a
9	ATF2	chr7:2864107-2864931	GM12878	blood:	n/a	n/a
10	ATF2	chr7:2860647-2861489	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:2863998-2865185	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:2864075-2865235	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr7:2860897-2861372	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr7:2860755-2861348	GM12878	blood:	n/a	n/a
15	BACH1	chr7:2864428-2865158	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr7:2860768-2861453	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:2854742-2855328	H1-hESC	embryonic stem cell:	n/a	chr7:2855072-2855086
18	BACH1	chr7:2859444-2859644	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr7:2858928-2859195	GM12878	blood:	n/a	chr7:2859128-2859138
20	BATF	chr7:2876969-2877377	GM12878	blood:	n/a	n/a
21	BATF	chr7:2864182-2864690	GM12878	blood:	n/a	n/a
22	BATF	chr7:2858902-2859218	GM12878	blood:	n/a	chr7:2859128-2859138
23	BCL11A	chr7:2864229-2864483	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:2858907-2859179	GM12878	blood:	n/a	chr7:2859127-2859136
25	BCL11A	chr7:2864247-2864685	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:2860821-2861154	GM12878	blood:	n/a	n/a
27	BCLAF1	chr7:2878410-2879002	GM12878	blood:	n/a	n/a
28	BCLAF1	chr7:2860793-2861293	GM12878	blood:	n/a	n/a
29	BCLAF1	chr7:2878539-2878905	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:2853832-2853954	K562	blood:	n/a	n/a
31	BHLHE40	chr7:2864295-2864717	GM12878	blood:	n/a	n/a
32	BRCA1	chr7:2850760-2850949	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:2878099-2878458	K562	blood:	n/a	chr7:2878277-2878288
34	CEBPB	chr7:2848991-2849260	IMR90	lung:	n/a	chr7:2849128-2849141 chr7:2849128-2849139
35	CEBPB	chr7:2860229-2860665	Hela-S3	cervix:	n/a	chr7:2860427-2860438
36	CEBPB	chr7:2874505-2875046	A549	lung:	n/a	chr7:2874902-2874913 chr7:2874900-2874911
37	CEBPB	chr7:2851118-2851462	Hela-S3	cervix:	n/a	chr7:2851274-2851285 chr7:2851272-2851283
38	CEBPB	chr7:2853085-2853102	K562	blood:	n/a	n/a
39	CEBPB	chr7:2878125-2878425	Hela-S3	cervix:	n/a	chr7:2878277-2878288
40	CEBPB	chr7:2861272-2861535	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:2852671-2852685	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr7:2861114-2861900	A549	lung:	n/a	n/a
43	CEBPB	chr7:2852583-2852652	K562	blood:	n/a	chr7:2852633-2852644
44	CEBPB	chr7:2870689-2871000	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:2878167-2878360	H1-hESC	embryonic stem cell:	n/a	chr7:2878277-2878288
46	CEBPB	chr7:2851120-2851403	A549	lung:	n/a	chr7:2851274-2851285 chr7:2851272-2851283
47	CEBPB	chr7:2853032-2853139	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:2870441-2870569	HepG2	liver:	n/a	chr7:2870525-2870536
49	CEBPB	chr7:2849008-2849223	A549	lung:	n/a	chr7:2849128-2849141 chr7:2849128-2849139
50	CEBPB	chr7:2852519-2852756	HepG2	liver:	n/a	chr7:2852633-2852644

(count:1285 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:2859672-2859722	ProgFib	skin:	n/a
2	chr7:2874568-2874618	GM19239	blood:	n/a
3	chr7:2854512-2854562	Caco-2	colon:	n/a
4	chr7:2872169-2872219	AG09309	skin:	n/a
5	chr7:2859672-2859722	ProgFib	skin:	n/a
6	chr7:2874568-2874618	GM19239	blood:	n/a
7	chr7:2854512-2854562	Caco-2	colon:	n/a
8	chr7:2872169-2872219	AG09309	skin:	n/a
9	chr7:2855625-2855675	H1-hESC	embryonic stem cell:	embryo
10	chr7:2872130-2872180	NB4	blood:	n/a
11	chr7:2880410-2880460	HEK293	kidney:	embryo
12	chr7:2874522-2874572	Hela-S3	cervix:	n/a
13	chr7:2870441-2870491	ovcar-3	ovarian:	n/a
14	chr7:2855704-2855754	LNCaP	prostate:	n/a
15	chr7:2859672-2859722	AG04449	skin:	fetal
16	chr7:2859695-2859745	SK-N-MC	brain:	n/a
17	chr7:2855759-2855809	ovcar-3	ovarian:	n/a
18	chr7:2851991-2852041	A549	lung:	n/a
19	chr7:2855759-2855809	HAEpiC	amniotic membrane:	n/a
20	chr7:2855704-2855754	AG09319	gingival:	n/a
21	chr7:2854958-2855008	GM12891	blood:	n/a
22	chr7:2872169-2872219	AG10803	skin:	n/a
23	chr7:2855704-2855754	Hela-S3	cervix:	n/a
24	chr7:2855759-2855809	GM06990	blood:	n/a
25	chr7:2855759-2855809	U87	brain:	n/a
26	chr7:2851991-2852041	AoSMC	blood vessel:	n/a
27	chr7:2859672-2859722	A549	lung:	n/a
28	chr7:2880410-2880460	IMR90	lung:	fetal
29	chr7:2855759-2855809	HCT-116	colon:	n/a
30	chr7:2854512-2854562	HNPCEpiC	eye:	n/a
31	chr7:2859695-2859745	HL-60	blood:	n/a
32	chr7:2874522-2874572	HRE	kidney:	n/a
33	chr7:2874595-2874645	RPTEC	kidney:	n/a
34	chr7:2872954-2873004	AoSMC	blood vessel:	n/a
35	chr7:2864192-2864242	HCM	heart:	n/a
36	chr7:2859695-2859745	HCT-116	colon:	n/a
37	chr7:2854705-2854755	MCF-7	breast:	n/a
38	chr7:2855625-2855675	NB4	blood:	n/a
39	chr7:2872169-2872219	NH-A	brain:	n/a
40	chr7:2874568-2874618	AG04450	lung:	fetal
41	chr7:2872954-2873004	HCF	heart:	n/a
42	chr7:2864192-2864242	HL-60	blood:	n/a
43	chr7:2854705-2854755	RPTEC	kidney:	n/a
44	chr7:2855625-2855675	HEEpiC	esophagus:	n/a
45	chr7:2851991-2852041	AG09319	gingival:	n/a
46	chr7:2874568-2874618	MCF-7	breast:	n/a
47	chr7:2861855-2861905	RPTEC	kidney:	n/a
48	chr7:2874568-2874618	ovcar-3	ovarian:	n/a
49	chr7:2874595-2874645	NHBE	bronchial:	n/a
50	chr7:2855625-2855675	SK-N-SH	brain:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:2851198..2852997-chr7:2868294..2871241,3	MCF-7	breast:
2	chr7:2861030..2862759-chr7:2864211..2866084,2	MCF-7	breast:
3	chr7:2865761..2868470-chr7:2869606..2871660,2	K562	blood:
4	chr7:2852817..2855372-chr7:2857055..2858634,2	MCF-7	breast:
5	chr7:2871109..2874393-chr7:2876005..2877937,3	K562	blood:
6	chr7:2857161..2858928-chr7:2879727..2881596,2	MCF-7	breast:
7	chr7:2869377..2877481-chr7:2880306..2885399,15	MCF-7	breast:
8	chr7:2852392..2854635-chr7:2859767..2862192,2	K562	blood:
9	chr7:2728674..2730877-chr7:2866251..2868525,3	MCF-7	breast:
10	chr7:2848223..2850269-chr7:2862070..2864443,2	MCF-7	breast:
11	chr7:2865761..2868437-chr7:2870160..2873131,2	K562	blood:
12	chr7:2861030..2862759-chr7:2864211..2866084,2	MCF-7	breast:
13	chr7:2793932..2796644-chr7:2849190..2850814,2	MCF-7	breast:
14	chr7:2841478..2843040-chr7:2849710..2851515,2	MCF-7	breast:
15	chr7:2863813..2865647-chr7:2882548..2884596,2	MCF-7	breast:
16	chr17:57922933..57924665-chr7:2875857..2878835,2	MCF-7	breast:
17	chr7:2861025..2862941-chr7:2863044..2865953,2	K562	blood:
18	chr7:2796001..2798506-chr7:2858838..2860975,2	MCF-7	breast:
19	chr7:2871109..2874393-chr7:2876005..2877937,3	K562	blood:
20	chr7:2725790..2728515-chr7:2861035..2863274,2	MCF-7	breast:
21	chr7:2846127..2848012-chr7:2869367..2871756,2	K562	blood:
22	chr7:2857088..2858665-chr7:2859530..2861799,2	K562	blood:
23	chr7:2861472..2864463-chr7:2865444..2867684,3	MCF-7	breast:
24	chr7:2846081..2849160-chr7:2882142..2884295,3	MCF-7	breast:
25	chr7:2869377..2877481-chr7:2880306..2885399,15	MCF-7	breast:
26	chr7:2811026..2812536-chr7:2872365..2874848,2	MCF-7	breast:
27	chr7:2726641..2729918-chr7:2858663..2861748,4	MCF-7	breast:
28	chr7:2865761..2868437-chr7:2870160..2873131,2	K562	blood:
29	chr7:2861472..2864463-chr7:2865444..2867684,3	MCF-7	breast:
30	chr7:2857314..2858833-chr7:2861762..2864042,2	MCF-7	breast:
31	chr7:2861786..2864969-chr7:2867313..2871458,3	MCF-7	breast:
32	chr7:2857161..2858928-chr7:2879727..2881596,2	MCF-7	breast:
33	chr7:2850439..2853182-chr7:2881989..2885398,4	MCF-7	breast:
34	chr7:2878232..2880029-chr7:2884178..2886023,2	MCF-7	breast:
35	chr7:2843836..2848178-chr7:2849131..2851589,3	MCF-7	breast:
36	chr7:2870014..2872603-chr7:2880108..2883747,4	K562	blood:
37	chr7:2855867..2858678-chr7:2858785..2861343,3	MCF-7	breast:
38	chr7:2726267..2731021-chr7:2868792..2873151,4	MCF-7	breast:
39	chr7:2865761..2868470-chr7:2869606..2871660,2	K562	blood:
40	chr7:2726313..2732670-chr7:2878755..2886203,10	MCF-7	breast:
41	chr7:2861786..2864969-chr7:2867313..2871458,3	MCF-7	breast:
42	chr7:2760607..2761112-chr7:2860852..2861356,2	MCF-7	breast:
43	chr7:2861025..2862941-chr7:2863044..2865953,2	K562	blood:
44	chr7:2857088..2858665-chr7:2859530..2861799,2	K562	blood:
45	chr7:2850088..2852383-chr7:2882234..2885067,2	MCF-7	breast:
46	chr7:2727601..2730936-chr7:2847456..2852448,6	MCF-7	breast:
47	chr7:2861792..2865677-chr7:2882259..2884341,3	K562	blood:
48	chr7:2865169..2866732-chr7:2874192..2876662,2	K562	blood:
49	chr7:2852392..2854635-chr7:2859767..2862192,2	K562	blood:
50	chr7:2837950..2839626-chr7:2864748..2866453,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000231357	TF binding region
GNA12	TF binding region
ENSG00000231357	CpG island
GNA12	CpG island
ENSG00000146535	chromatin interactions
ENSG00000231357	chromatin interactions
ENSG00000174945	chromatin interactions

Extended variants
information (count: 1707 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1707 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371536415	chr7:2848458-2848459	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs140525108	chr7:2848467-2848468	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs187635682	chr7:2848490-2848491	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs373630803	chr7:2848557-2848558	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs112555166	chr7:2848578-2848579	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs117867554	chr7:2848598-2848599	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs544411825	chr7:2848601-2848602	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs74919938	chr7:2848609-2848610	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs371598648	chr7:2848610-2848611	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs546626525	chr7:2848616-2848617	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs757789	chr7:2848649-2848650	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs540105966	chr7:2848670-2848671	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs528504578	chr7:2848716-2848717	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs548146814	chr7:2848741-2848742	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs77706734	chr7:2848751-2848752	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs112934008	chr7:2848785-2848786	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs560056580	chr7:2848787-2848788	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs191667557	chr7:2848808-2848809	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs757790	chr7:2848827-2848828	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs137974815	chr7:2848866-2848867	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs59179165	chr7:2848909-2848910	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs368135946	chr7:2848927-2848928	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs558597700	chr7:2848980-2848981	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs115794276	chr7:2849012-2849013	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs184258542	chr7:2849035-2849036	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs143545604	chr7:2849062-2849063	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs187692476	chr7:2849076-2849077	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs78633868	chr7:2849084-2849085	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs577805104	chr7:2849085-2849086	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs80127198	chr7:2849093-2849094	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs147134209	chr7:2849121-2849122	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs79457534	chr7:2849134-2849135	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs554292966	chr7:2849149-2849150	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs372290751	chr7:2849150-2849151	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs58695207	chr7:2849158-2849159	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs138407899	chr7:2849168-2849169	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs561708457	chr7:2849194-2849195	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs192357608	chr7:2849208-2849209	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs551052291	chr7:2849225-2849226	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576864641	chr7:2849255-2849256	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs533396376	chr7:2849266-2849267	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs547181275	chr7:2849298-2849299	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs567192245	chr7:2849309-2849310	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs563607104	chr7:2849334-2849335	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs555410397	chr7:2849363-2849364	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs568798297	chr7:2849393-2849394	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs200057520	chr7:2849401-2849402	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs537843613	chr7:2849422-2849423	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs572657594	chr7:2849426-2849427	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs184645203	chr7:2849647-2849648	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1797 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:2837000-2850600	Weak transcription	Stomach Smooth Muscle	stomach
2	chr7:2839400-2848600	Enhancers	Fetal Heart	heart
3	chr7:2839400-2850800	Weak transcription	Primary B cells from cord blood	blood
4	chr7:2841000-2850200	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr7:2842400-2850800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr7:2842600-2850600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:2842600-2869400	Weak transcription	Primary T cells from cord blood	blood
8	chr7:2842800-2850800	Weak transcription	HMEC	breast
9	chr7:2842800-2851800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr7:2843000-2848600	Weak transcription	Stomach Mucosa	stomach
11	chr7:2843000-2860800	Weak transcription	Esophagus	oesophagus
12	chr7:2843200-2849800	Weak transcription	Osteobl	bone
13	chr7:2843200-2850200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:2843200-2850600	Weak transcription	Brain Anterior Caudate	brain
15	chr7:2843200-2850800	Weak transcription	Aorta	Aorta
16	chr7:2843200-2855200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:2843200-2857400	Weak transcription	Brain Germinal Matrix	brain
18	chr7:2843200-2860800	Weak transcription	HSMMtube	muscle
19	chr7:2843200-2864400	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr7:2843400-2850000	Weak transcription	Brain Hippocampus Middle	brain
21	chr7:2843400-2854400	Weak transcription	Colonic Mucosa	Colon
22	chr7:2843600-2852800	Weak transcription	Dnd41	blood
23	chr7:2843600-2857200	Weak transcription	Colon Smooth Muscle	Colon
24	chr7:2843600-2860600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr7:2843600-2864400	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr7:2843800-2849200	Weak transcription	HUVEC	blood vessel
27	chr7:2843800-2850000	Weak transcription	NH-A	brain
28	chr7:2843800-2850600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr7:2843800-2854800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr7:2844000-2858800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:2844200-2850600	Weak transcription	Psoas Muscle	Psoas
32	chr7:2844200-2853400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr7:2845000-2853000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr7:2845800-2862200	Weak transcription	K562	blood
35	chr7:2846600-2849000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:2847000-2848800	Enhancers	Primary hematopoietic stem cells	blood
37	chr7:2847200-2848600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr7:2847200-2848600	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr7:2847200-2848800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr7:2847400-2848800	Enhancers	Fetal Muscle Trunk	muscle
41	chr7:2847400-2848800	Enhancers	Right Atrium	heart
42	chr7:2847400-2848800	Enhancers	GM12878-XiMat	blood
43	chr7:2847400-2849000	Enhancers	H1 Cell Line	embryonic stem cell
44	chr7:2847400-2849000	Enhancers	Primary B cells from peripheral blood	blood
45	chr7:2847400-2849200	Enhancers	Placenta	Placenta
46	chr7:2847400-2849200	Enhancers	Left Ventricle	heart
47	chr7:2847400-2853200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr7:2847600-2848600	Enhancers	H9 Cell Line	embryonic stem cell
49	chr7:2847600-2848600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr7:2847600-2848600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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