Variant report

Variant	nsv5532
Chromosome Location	chr10:1079499-1101700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1378)
CpG islands
(count:1344)
Chromatin interactive
region (count:59)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1378 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:1094678-1095649	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:1089053-1089112	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:1084284-1084467	K562	blood:	n/a	n/a
4	ARID3A	chr10:1095998-1096413	K562	blood:	n/a	n/a
5	ARID3A	chr10:1095043-1095579	K562	blood:	n/a	n/a
6	ATF1	chr10:1094740-1095525	K562	blood:	n/a	chr10:1094969-1094983
7	ATF2	chr10:1082069-1082686	GM12878	blood:	n/a	n/a
8	ATF2	chr10:1094297-1094676	GM12878	blood:	n/a	n/a
9	ATF2	chr10:1094938-1095655	GM12878	blood:	n/a	chr10:1094969-1094983
10	ATF2	chr10:1094706-1095632	GM12878	blood:	n/a	chr10:1094969-1094983
11	ATF2	chr10:1094934-1095367	H1-hESC	embryonic stem cell:	n/a	chr10:1094969-1094983
12	ATF2	chr10:1089557-1090172	GM12878	blood:	n/a	n/a
13	ATF2	chr10:1082149-1082622	GM12878	blood:	n/a	n/a
14	ATF3	chr10:1082274-1082739	GM12878	blood:	n/a	n/a
15	BACH1	chr10:1093937-1094012	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr10:1096647-1096826	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr10:1080949-1081008	K562	blood:	n/a	n/a
18	BACH1	chr10:1095490-1095589	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr10:1094282-1095268	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr10:1094179-1094576	K562	blood:	n/a	n/a
21	BATF	chr10:1084512-1085225	GM12878	blood:	n/a	n/a
22	BATF	chr10:1082165-1082531	GM12878	blood:	n/a	chr10:1082362-1082373
23	BATF	chr10:1082166-1082527	GM12878	blood:	n/a	chr10:1082362-1082373
24	BCL11A	chr10:1094898-1095599	GM12878	blood:	n/a	n/a
25	BCL11A	chr10:1084497-1085246	GM12878	blood:	n/a	n/a
26	BCL11A	chr10:1084496-1085229	GM12878	blood:	n/a	n/a
27	BCL3	chr10:1094581-1095649	GM12878	blood:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
28	BCL3	chr10:1084491-1084703	GM12878	blood:	n/a	n/a
29	BCL3	chr10:1082151-1082620	GM12878	blood:	n/a	n/a
30	BCL3	chr10:1094581-1096032	A549	lung:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
31	BCL3	chr10:1094143-1095663	A549	lung:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
32	BCLAF1	chr10:1094215-1095692	GM12878	blood:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
33	BCLAF1	chr10:1089332-1090130	GM12878	blood:	n/a	n/a
34	BCLAF1	chr10:1089365-1090103	GM12878	blood:	n/a	n/a
35	BCLAF1	chr10:1094621-1095982	GM12878	blood:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
36	BCLAF1	chr10:1082229-1082665	GM12878	blood:	n/a	n/a
37	BCLAF1	chr10:1096469-1096975	GM12878	blood:	n/a	n/a
38	BHLHE40	chr10:1094164-1095673	GM12878	blood:	n/a	n/a
39	BHLHE40	chr10:1100254-1100343	GM12878	blood:	n/a	n/a
40	BHLHE40	chr10:1096438-1096929	HepG2	liver:	n/a	n/a
41	BHLHE40	chr10:1094091-1095724	K562	blood:	n/a	n/a
42	BHLHE40	chr10:1082257-1082631	K562	blood:	n/a	n/a
43	BHLHE40	chr10:1094242-1095716	HepG2	liver:	n/a	n/a
44	BHLHE40	chr10:1096519-1096859	A549	lung:	n/a	n/a
45	BHLHE40	chr10:1096043-1096938	K562	blood:	n/a	n/a
46	BHLHE40	chr10:1082356-1082728	GM12878	blood:	n/a	n/a
47	BHLHE40	chr10:1096539-1096850	HepG2	liver:	n/a	n/a
48	BHLHE40	chr10:1096276-1096944	GM12878	blood:	n/a	n/a
49	BRCA1	chr10:1094521-1094634	GM12878	blood:	n/a	n/a
50	BRCA1	chr10:1095799-1096042	Hela-S3	cervix:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:1084935-1084985	BJ	skin:	n/a
2	chr10:1095446-1095496	HCF	heart:	n/a
3	chr10:1084935-1084985	BJ	skin:	n/a
4	chr10:1095446-1095496	HCF	heart:	n/a
5	chr10:1094976-1095026	HEK293	kidney:	embryo
6	chr10:1083304-1083354	BJ	skin:	n/a
7	chr10:1084866-1084916	ProgFib	skin:	n/a
8	chr10:1094976-1095026	ProgFib	skin:	n/a
9	chr10:1084866-1084916	HCF	heart:	n/a
10	chr10:1084866-1084916	HCPEpiC	choroid plexus:	n/a
11	chr10:1098826-1098876	RPTEC	kidney:	n/a
12	chr10:1083259-1083309	HEK293	kidney:	embryo
13	chr10:1095038-1095088	SK-N-SH	brain:	n/a
14	chr10:1095578-1095628	NB4	blood:	n/a
15	chr10:1082432-1082482	HRCEpiC	kidney:	n/a
16	chr10:1082432-1082482	PFSK-1	brain:	n/a
17	chr10:1099945-1099995	AG10803	skin:	n/a
18	chr10:1095578-1095628	HEK293	kidney:	embryo
19	chr10:1099945-1099995	Hela-S3	cervix:	n/a
20	chr10:1086904-1086954	HRE	kidney:	n/a
21	chr10:1095482-1095532	PANC-1	pancreas:	n/a
22	chr10:1095038-1095088	AG04450	lung:	fetal
23	chr10:1083259-1083309	HUVEC	blood vessel:	n/a
24	chr10:1083192-1083242	MCF-7	breast:	n/a
25	chr10:1095144-1095194	AoSMC	blood vessel:	n/a
26	chr10:1094429-1094479	BE2_C	brain:	n/a
27	chr10:1083259-1083309	AG04449	skin:	fetal
28	chr10:1095069-1095119	AoSMC	blood vessel:	n/a
29	chr10:1083259-1083309	SK-N-SH_RA	brain:	n/a
30	chr10:1084935-1084985	ECC-1	luminal epithelium:	n/a
31	chr10:1095038-1095088	HL-60	blood:	n/a
32	chr10:1082432-1082482	HRPEpiC	eye:	n/a
33	chr10:1095069-1095119	HAEpiC	amniotic membrane:	n/a
34	chr10:1094306-1094356	GM19239	blood:	n/a
35	chr10:1084866-1084916	NHBE	bronchial:	n/a
36	chr10:1082432-1082482	HepG2	liver:	n/a
37	chr10:1095081-1095131	SAEC	small airway:	n/a
38	chr10:1095554-1095604	SK-N-SH_RA	brain:	n/a
39	chr10:1099945-1099995	HUVEC	blood vessel:	n/a
40	chr10:1094429-1094479	PANC-1	pancreas:	n/a
41	chr10:1094976-1095026	IMR90	lung:	fetal
42	chr10:1083192-1083242	NB4	blood:	n/a
43	chr10:1095482-1095532	ECC-1	luminal epithelium:	n/a
44	chr10:1086904-1086954	HL-60	blood:	n/a
45	chr10:1094306-1094356	AG09319	gingival:	n/a
46	chr10:1095235-1095285	HCT-116	colon:	n/a
47	chr10:1083192-1083242	AG09319	gingival:	n/a
48	chr10:1083259-1083309	AG10803	skin:	n/a
49	chr10:1095482-1095532	SKMC	muscle:	n/a
50	chr10:1095081-1095131	HepG2	liver:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:1094654..1095194-chr4:2936214..2937126,2	HCT-116	colon:
2	chr10:1093530..1095103-chr10:3109700..3112335,2	K562	blood:
3	chr10:1034471..1036574-chr10:1093266..1095946,3	K562	blood:
4	chr10:977031..978658-chr10:1101205..1103073,2	K562	blood:
5	chr10:1073124..1075286-chr10:1080099..1081711,2	MCF-7	breast:
6	chr10:974670..978531-chr10:1101117..1104171,5	K562	blood:
7	chr10:1002935..1005856-chr10:1082299..1084442,2	MCF-7	breast:
8	chr10:1033326..1035673-chr10:1079332..1082355,3	K562	blood:
9	chr10:1033196..1035740-chr10:1100283..1103390,4	K562	blood:
10	chr10:1086551..1092852-chr10:1093358..1097808,14	MCF-7	breast:
11	chr10:1033990..1039615-chr10:1093691..1098446,7	MCF-7	breast:
12	chr10:1094378..1094891-chr14:74353245..74354003,2	Hela-S3	cervix:
13	chr10:1090197..1098635-chr10:1098667..1108160,39	K562	blood:
14	chr10:1082336..1085683-chr10:1088908..1090721,3	MCF-7	breast:
15	chr10:1024931..1026734-chr10:1099565..1101968,2	MCF-7	breast:
16	chr10:1038435..1041115-chr10:1083089..1086536,3	K562	blood:
17	chr10:1077434..1080726-chr10:1080852..1083466,3	MCF-7	breast:
18	chr10:1033680..1035425-chr10:1096903..1098612,2	MCF-7	breast:
19	chr10:1074940..1077735-chr10:1077967..1081308,3	K562	blood:
20	chr10:976200..979208-chr10:1093606..1097726,5	MCF-7	breast:
21	chr10:1101227..1103442-chr17:57918099..57920735,2	MCF-7	breast:
22	chr10:1090197..1098635-chr10:1098667..1108160,39	K562	blood:
23	chr10:1078267..1081381-chr10:1081878..1091698,9	MCF-7	breast:
24	chr10:1031711..1035740-chr10:1100728..1103796,4	K562	blood:
25	chr10:1083077..1085466-chr10:1096305..1099633,3	MCF-7	breast:
26	chr10:1094129..1095350-chr2:122287877..122288767,3	Hela-S3	cervix:
27	chr10:1082960..1085323-chr10:1085566..1087572,2	MCF-7	breast:
28	chr1:91966057..91966769-chr10:1094298..1095218,2	Hela-S3	cervix:
29	chr10:1094364..1094918-chr11:131779867..131780867,3	Hela-S3	cervix:
30	chr10:1071929..1076596-chr10:1081976..1085253,4	K562	blood:
31	chr10:1094730..1096731-chr10:1096992..1098586,2	MCF-7	breast:
32	chr10:976647..980794-chr10:1093154..1097319,8	MCF-7	breast:
33	chr10:862621..864941-chr10:1093601..1095368,2	K562	blood:
34	chr10:1034367..1036220-chr10:1101305..1103834,2	MCF-7	breast:
35	chr10:1032122..1034803-chr10:1098980..1100497,2	MCF-7	breast:
36	chr10:1100725..1104850-chr10:1118585..1122154,6	K562	blood:
37	chr10:1080311..1084643-chr10:1093225..1095856,7	MCF-7	breast:
38	chr10:1075654..1077725-chr10:1080611..1082815,2	MCF-7	breast:
39	chr10:975330..979257-chr10:1093215..1097529,5	K562	blood:
40	chr10:1086551..1092852-chr10:1093358..1097808,14	MCF-7	breast:
41	chr10:1032470..1034485-chr10:1092422..1096343,5	MCF-7	breast:
42	chr10:1082912..1084464-chr10:1086801..1088755,2	MCF-7	breast:
43	chr10:976152..979108-chr10:1085303..1088696,4	MCF-7	breast:
44	chr10:1094228..1094918-chr5:56205474..56206086,2	Hela-S3	cervix:
45	chr10:975330..979545-chr10:1093428..1097529,6	K562	blood:
46	chr10:975799..978442-chr10:1098842..1102725,4	MCF-7	breast:
47	chr10:1095340..1097626-chr10:1118637..1120510,2	MCF-7	breast:
48	chr10:989792..992480-chr10:1084980..1087131,2	MCF-7	breast:
49	chr10:1031887..1035944-chr10:1099515..1103666,8	MCF-7	breast:
50	chr10:1101511..1104003-chr10:3108866..3111744,3	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IDI1-2	chr10:1099766-1100185	NONHSAT010897
2	lnc-GTPBP4-1	chr10:1081754-1081916	ENSG00000232656.3
3	lnc-GTPBP4-1	chr10:1081754-1081861	ENSG00000232656.3
4	lnc-GTPBP4-1	chr10:1082729-1082833	ENSG00000232656.3
5	lnc-GTPBP4-1	chr10:1081230-1081446	ENSG00000232656.3
6	lnc-IDI1-2	chr10:1099888-1100616	NONHSAT010896
7	lnc-GTPBP4-1	chr10:1081230-1081362	ENSG00000232656.3
8	lnc-GTPBP4-1	chr10:1089469-1089623	ENSG00000232656.3
9	lnc-IDI1-2	chr10:1095956-1096415	NONHSAT010896

No data

Variant related genes	Relation type
WDR37	TF binding region
IDI1	TF binding region
RNU7-163P	TF binding region
WDR37	CpG island
IDI1	CpG island
RNU7-163P	CpG island
ENSG00000145592	chromatin interactions
ENSG00000182667	chromatin interactions
ENSG00000229869	chromatin interactions
ENSG00000097046	chromatin interactions
ENSG00000107937	chromatin interactions
ENSG00000155542	chromatin interactions
ENSG00000107929	chromatin interactions
ENSG00000119725	chromatin interactions
ENSG00000067057	chromatin interactions
ENSG00000238924	chromatin interactions
ENSG00000265451	chromatin interactions
ENSG00000249673	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000264229	chromatin interactions
ENSG00000047056	chromatin interactions
ENSG00000074054	chromatin interactions
ENSG00000067064	chromatin interactions
ENSG00000109736	chromatin interactions
ENSG00000205740	chromatin interactions

Extended variants
information (count: 998 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:998 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192801396	chr10:1079512-1079513	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs142587218	chr10:1079537-1079538	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs575054950	chr10:1079542-1079543	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs3793779	chr10:1079579-1079580	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs184091233	chr10:1079587-1079588	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs117384950	chr10:1079598-1079599	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs543914227	chr10:1079631-1079632	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs545886186	chr10:1079639-1079640	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs373328707	chr10:1079705-1079706	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs150577305	chr10:1079726-1079727	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs530735130	chr10:1079773-1079774	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs368890026	chr10:1079804-1079805	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs139628223	chr10:1079825-1079826	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs116334037	chr10:1079830-1079831	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs529816692	chr10:1079852-1079853	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs35431428	chr10:1079853-1079854	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs546722760	chr10:1079863-1079864	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs56293499	chr10:1079869-1079870	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs117813061	chr10:1079962-1079963	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs144231065	chr10:1079969-1079970	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs140740035	chr10:1079980-1079981	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs536186306	chr10:1080012-1080013	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs538555341	chr10:1080016-1080017	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs376781633	chr10:1080027-1080028	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs56289911	chr10:1080038-1080039	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs111525636	chr10:1080151-1080152	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs540818160	chr10:1080181-1080182	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs554299274	chr10:1080184-1080185	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs532981237	chr10:1080186-1080187	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs186934344	chr10:1080187-1080188	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs546250555	chr10:1080191-1080192	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs562755435	chr10:1080198-1080199	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs11814057	chr10:1080206-1080207	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs544127586	chr10:1080211-1080212	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs549185086	chr10:1080212-1080213	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs529879053	chr10:1080219-1080220	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs111635470	chr10:1080240-1080241	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs560248934	chr10:1080243-1080244	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs183683402	chr10:1080277-1080278	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs11250229	chr10:1080289-1080290	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs568908249	chr10:1080290-1080291	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs373594209	chr10:1080298-1080299	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs537821830	chr10:1080329-1080330	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs548937654	chr10:1080332-1080333	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs568776722	chr10:1080344-1080345	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs11250230	chr10:1080347-1080348	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs201178498	chr10:1080370-1080371	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs151105191	chr10:1080391-1080392	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs35405102	chr10:1080393-1080394	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs571328764	chr10:1080402-1080403	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD

Chromatin state (count:2195 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:1035000-1094000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr10:1060000-1091600	Weak transcription	Hela-S3	cervix
3	chr10:1063200-1092000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr10:1063600-1088200	Weak transcription	Fetal Brain Male	brain
5	chr10:1064000-1083000	Weak transcription	NHDF-Ad	bronchial
6	chr10:1064000-1084400	Weak transcription	Colonic Mucosa	Colon
7	chr10:1064000-1088400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr10:1064400-1082600	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr10:1065200-1084800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr10:1065400-1082800	Weak transcription	Primary hematopoietic stem cells	blood
11	chr10:1065600-1083800	Weak transcription	Fetal Lung	lung
12	chr10:1065600-1086000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr10:1065600-1086200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr10:1065800-1082600	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr10:1065800-1086200	Weak transcription	Colon Smooth Muscle	Colon
16	chr10:1065800-1087800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr10:1066000-1080800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr10:1066000-1081000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr10:1066000-1081200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr10:1066000-1082000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr10:1066000-1082400	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr10:1066000-1082600	Weak transcription	Aorta	Aorta
23	chr10:1066000-1083000	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr10:1066000-1086000	Weak transcription	HSMMtube	muscle
25	chr10:1066200-1079600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr10:1066200-1082200	Weak transcription	Duodenum Mucosa	Duodenum
27	chr10:1066200-1082200	Weak transcription	NH-A	brain
28	chr10:1066200-1082400	Weak transcription	Stomach Smooth Muscle	stomach
29	chr10:1066200-1083200	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr10:1066200-1083400	Weak transcription	Liver	Liver
31	chr10:1066200-1085200	Weak transcription	HUVEC	blood vessel
32	chr10:1066200-1086000	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr10:1066200-1086200	Weak transcription	Fetal Kidney	kidney
34	chr10:1066600-1081200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:1066600-1082400	Weak transcription	Primary B cells from cord blood	blood
36	chr10:1066600-1082800	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr10:1066600-1084000	Weak transcription	Placenta	Placenta
38	chr10:1066600-1088200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr10:1066800-1079600	Weak transcription	Ovary	ovary
40	chr10:1066800-1079600	Weak transcription	HMEC	breast
41	chr10:1066800-1080400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr10:1066800-1081400	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr10:1066800-1081600	Weak transcription	Fetal Thymus	thymus
44	chr10:1066800-1081800	Weak transcription	Esophagus	oesophagus
45	chr10:1066800-1082200	Weak transcription	Primary T cells from cord blood	blood
46	chr10:1066800-1082400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr10:1066800-1082400	Weak transcription	Fetal Muscle Leg	muscle
48	chr10:1066800-1082400	Weak transcription	Lung	lung
49	chr10:1066800-1082600	Weak transcription	Spleen	Spleen
50	chr10:1066800-1083000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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