Variant report

Variant	nsv894724
Chromosome Location	chr10:1084942-1116294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1842)
CpG islands
(count:2321)
Chromatin interactive
region (count:64)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1842 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:1095998-1096413	K562	blood:	n/a	n/a
2	ARID3A	chr10:1103787-1104274	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:1095043-1095579	K562	blood:	n/a	n/a
4	ARID3A	chr10:1102391-1102956	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:1094678-1095649	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:1089053-1089112	HepG2	liver:	n/a	n/a
7	ATF1	chr10:1102088-1102899	K562	blood:	n/a	n/a
8	ATF1	chr10:1094740-1095525	K562	blood:	n/a	chr10:1094969-1094983
9	ATF2	chr10:1094938-1095655	GM12878	blood:	n/a	chr10:1094969-1094983
10	ATF2	chr10:1089557-1090172	GM12878	blood:	n/a	n/a
11	ATF2	chr10:1094934-1095367	H1-hESC	embryonic stem cell:	n/a	chr10:1094969-1094983
12	ATF2	chr10:1094297-1094676	GM12878	blood:	n/a	n/a
13	ATF2	chr10:1102460-1103019	GM12878	blood:	n/a	n/a
14	ATF2	chr10:1094706-1095632	GM12878	blood:	n/a	chr10:1094969-1094983
15	BACH1	chr10:1093937-1094012	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr10:1102460-1102639	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr10:1095490-1095589	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr10:1094282-1095268	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr10:1094179-1094576	K562	blood:	n/a	n/a
20	BACH1	chr10:1106651-1106781	K562	blood:	n/a	n/a
21	BACH1	chr10:1096647-1096826	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr10:1102914-1102926	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr10:1084512-1085225	GM12878	blood:	n/a	n/a
24	BCL11A	chr10:1084496-1085229	GM12878	blood:	n/a	n/a
25	BCL11A	chr10:1084497-1085246	GM12878	blood:	n/a	n/a
26	BCL11A	chr10:1094898-1095599	GM12878	blood:	n/a	n/a
27	BCL3	chr10:1102411-1103108	A549	lung:	n/a	chr10:1102459-1102472 chr10:1102742-1102751 chr10:1102455-1102468
28	BCL3	chr10:1102421-1103011	A549	lung:	n/a	chr10:1102459-1102472 chr10:1102742-1102751 chr10:1102455-1102468
29	BCL3	chr10:1094581-1095649	GM12878	blood:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
30	BCL3	chr10:1094143-1095663	A549	lung:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
31	BCL3	chr10:1114270-1114606	GM12878	blood:	n/a	n/a
32	BCL3	chr10:1094581-1096032	A549	lung:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
33	BCL3	chr10:1114853-1115151	GM12878	blood:	n/a	n/a
34	BCLAF1	chr10:1102103-1102936	GM12878	blood:	n/a	chr10:1102459-1102472 chr10:1102742-1102751 chr10:1102455-1102468
35	BCLAF1	chr10:1101969-1103085	GM12878	blood:	n/a	chr10:1102459-1102472 chr10:1102742-1102751 chr10:1102455-1102468
36	BCLAF1	chr10:1096469-1096975	GM12878	blood:	n/a	n/a
37	BCLAF1	chr10:1089332-1090130	GM12878	blood:	n/a	n/a
38	BCLAF1	chr10:1089365-1090103	GM12878	blood:	n/a	n/a
39	BCLAF1	chr10:1094215-1095692	GM12878	blood:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
40	BCLAF1	chr10:1094621-1095982	GM12878	blood:	n/a	chr10:1094686-1094695 chr10:1094626-1094635
41	BHLHE40	chr10:1102333-1103055	HepG2	liver:	n/a	chr10:1102886-1102902
42	BHLHE40	chr10:1094091-1095724	K562	blood:	n/a	n/a
43	BHLHE40	chr10:1096539-1096850	HepG2	liver:	n/a	n/a
44	BHLHE40	chr10:1100254-1100343	GM12878	blood:	n/a	n/a
45	BHLHE40	chr10:1096276-1096944	GM12878	blood:	n/a	n/a
46	BHLHE40	chr10:1094242-1095716	HepG2	liver:	n/a	n/a
47	BHLHE40	chr10:1094164-1095673	GM12878	blood:	n/a	n/a
48	BHLHE40	chr10:1102146-1102989	K562	blood:	n/a	chr10:1102886-1102902
49	BHLHE40	chr10:1096519-1096859	A549	lung:	n/a	n/a
50	BHLHE40	chr10:1101911-1102216	GM12878	blood:	n/a	n/a

(count:2321 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:1102456-1102506	GM12892	blood:	n/a
2	chr10:1103340-1103390	Hepatocyte	liver:	n/a
3	chr10:1095081-1095131	GM12878	blood:	n/a
4	chr10:1102456-1102506	GM12892	blood:	n/a
5	chr10:1103340-1103390	Hepatocyte	liver:	n/a
6	chr10:1095081-1095131	GM12878	blood:	n/a
7	chr10:1095228-1095278	NHBE	bronchial:	n/a
8	chr10:1102456-1102506	ProgFib	skin:	n/a
9	chr10:1102917-1102967	BE2_C	brain:	n/a
10	chr10:1102354-1102404	PrEC	prostate:	n/a
11	chr10:1103340-1103390	SKMC	muscle:	n/a
12	chr10:1102609-1102659	PFSK-1	brain:	n/a
13	chr10:1102112-1102162	PFSK-1	brain:	n/a
14	chr10:1102456-1102506	BJ	skin:	n/a
15	chr10:1094429-1094479	HRPEpiC	eye:	n/a
16	chr10:1095144-1095194	GM19239	blood:	n/a
17	chr10:1095554-1095604	MCF10A-Er-Src	breast:	n/a
18	chr10:1095081-1095131	NHDF-neo	bronchial:	n/a
19	chr10:1102917-1102967	HCPEpiC	choroid plexus:	n/a
20	chr10:1102456-1102506	SKMC	muscle:	n/a
21	chr10:1095228-1095278	PFSK-1	brain:	n/a
22	chr10:1102942-1102992	Hela-S3	cervix:	n/a
23	chr10:1095554-1095604	HRE	kidney:	n/a
24	chr10:1102351-1102401	PANC-1	pancreas:	n/a
25	chr10:1102313-1102363	ovcar-3	ovarian:	n/a
26	chr10:1084935-1084985	GM12892	blood:	n/a
27	chr10:1103535-1103585	NH-A	brain:	n/a
28	chr10:1099945-1099995	AG04450	lung:	fetal
29	chr10:1095144-1095194	HCT-116	colon:	n/a
30	chr10:1103535-1103585	ovcar-3	ovarian:	n/a
31	chr10:1102609-1102659	HRE	kidney:	n/a
32	chr10:1102917-1102967	HepG2	liver:	n/a
33	chr10:1102313-1102363	Jurkat	blood:	n/a
34	chr10:1102351-1102401	RPTEC	kidney:	n/a
35	chr10:1102351-1102401	HUVEC	blood vessel:	n/a
36	chr10:1094306-1094356	Jurkat	blood:	n/a
37	chr10:1095235-1095285	T-47D	breast:	n/a
38	chr10:1102667-1102717	AG10803	skin:	n/a
39	chr10:1102351-1102401	Caco-2	colon:	n/a
40	chr10:1095554-1095604	GM19239	blood:	n/a
41	chr10:1102713-1102763	HL-60	blood:	n/a
42	chr10:1098826-1098876	MCF-7	breast:	n/a
43	chr10:1094976-1095026	HPAEpiC	pulmonary alveolar:	n/a
44	chr10:1094306-1094356	CMK	blood:	n/a
45	chr10:1102715-1102765	AG09309	skin:	n/a
46	chr10:1102461-1102511	HRCEpiC	kidney:	n/a
47	chr10:1102726-1102776	ECC-1	luminal epithelium:	n/a
48	chr10:1086904-1086954	NHDF-neo	bronchial:	n/a
49	chr10:1102942-1102992	NB4	blood:	n/a
50	chr10:1102835-1102885	Jurkat	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:1103349..1104850-chr10:1118792..1120558,2	K562	blood:
2	chr10:1031887..1035944-chr10:1099515..1103666,8	MCF-7	breast:
3	chr10:1034471..1036574-chr10:1093266..1095946,3	K562	blood:
4	chr10:974670..978531-chr10:1101117..1104171,5	K562	blood:
5	chr10:1093530..1095103-chr10:3109700..3112335,2	K562	blood:
6	chr10:1038435..1041115-chr10:1083089..1086536,3	K562	blood:
7	chr10:1115932..1118235-chr10:1118338..1121067,2	MCF-7	breast:
8	chr10:1033990..1039615-chr10:1093691..1098446,7	MCF-7	breast:
9	chr10:1094378..1094891-chr14:74353245..74354003,2	Hela-S3	cervix:
10	chr10:975330..979545-chr10:1093428..1097529,6	K562	blood:
11	chr10:1100725..1104850-chr10:1118585..1122154,6	K562	blood:
12	chr10:1082418..1085956-chr10:1093172..1097957,6	MCF-7	breast:
13	chr10:975799..978442-chr10:1098842..1102725,4	MCF-7	breast:
14	chr10:1041791..1044346-chr10:1102809..1104842,2	MCF-7	breast:
15	chr10:1032470..1034485-chr10:1092422..1096343,5	MCF-7	breast:
16	chr10:1086551..1092852-chr10:1093358..1097808,14	MCF-7	breast:
17	chr1:91966057..91966769-chr10:1094298..1095218,2	Hela-S3	cervix:
18	chr10:1082960..1085323-chr10:1085566..1087572,2	MCF-7	breast:
19	chr10:1094316..1094876-chr5:40835238..40835957,2	Hela-S3	cervix:
20	chr10:1032122..1034803-chr10:1098980..1100497,2	MCF-7	breast:
21	chr10:1090197..1098635-chr10:1098667..1108160,39	K562	blood:
22	chr10:989792..992480-chr10:1084980..1087131,2	MCF-7	breast:
23	chr10:1033680..1035425-chr10:1096903..1098612,2	MCF-7	breast:
24	chr10:833990..835898-chr10:1099433..1102164,2	K562	blood:
25	chr10:1082336..1085683-chr10:1088908..1090721,3	MCF-7	breast:
26	chr10:1093376..1095260-chr10:1119342..1122305,3	MCF-7	breast:
27	chr10:1113860..1116650-chr10:1118248..1120322,2	K562	blood:
28	chr10:977031..978658-chr10:1101205..1103073,2	K562	blood:
29	chr10:862621..864941-chr10:1093601..1095368,2	K562	blood:
30	chr10:1095340..1097626-chr10:1118637..1120510,2	MCF-7	breast:
31	chr10:1071929..1076596-chr10:1081976..1085253,4	K562	blood:
32	chr10:1115087..1117560-chr10:1123514..1126172,2	MCF-7	breast:
33	chr10:1094730..1096731-chr10:1096992..1098586,2	MCF-7	breast:
34	chr10:1083077..1085466-chr10:1096305..1099633,3	MCF-7	breast:
35	chr10:976647..980794-chr10:1093154..1097319,8	MCF-7	breast:
36	chr10:1094364..1094918-chr11:131779867..131780867,3	Hela-S3	cervix:
37	chr10:1083077..1085466-chr10:1096305..1099633,3	MCF-7	breast:
38	chr10:1086551..1092852-chr10:1093358..1097808,14	MCF-7	breast:
39	chr10:1031711..1035740-chr10:1100728..1103796,4	K562	blood:
40	chr10:975330..979257-chr10:1093215..1097529,5	K562	blood:
41	chr10:1082336..1085683-chr10:1088908..1090721,3	MCF-7	breast:
42	chr10:1103509..1105162-chr10:1115825..1118791,2	MCF-7	breast:
43	chr10:1093873..1095888-chr10:1114642..1117199,3	MCF-7	breast:
44	chr10:976152..979108-chr10:1085303..1088696,4	MCF-7	breast:
45	chr10:1094228..1094918-chr5:56205474..56206086,2	Hela-S3	cervix:
46	chr10:1101227..1103442-chr17:57918099..57920735,2	MCF-7	breast:
47	chr10:976791..979037-chr10:1103503..1105214,2	K562	blood:
48	chr10:1103509..1105162-chr10:1115825..1118791,2	MCF-7	breast:
49	chr10:1024931..1026734-chr10:1099565..1101968,2	MCF-7	breast:
50	chr10:1115150..1117674-chr10:1118822..1121037,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTPBP4-1	chr10:1089469-1089623	ENSG00000232656.3
2	lnc-IDI1-2	chr10:1102249-1102613	NONHSAT010897
3	lnc-IDI1-2	chr10:1099888-1100616	NONHSAT010896
4	lnc-IDI1-2	chr10:1099766-1100185	NONHSAT010897
5	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
ENSG00000107929	chromatin interactions
ENSG00000155542	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000067057	chromatin interactions
ENSG00000182667	chromatin interactions
ENSG00000107937	chromatin interactions
ENSG00000265451	chromatin interactions
ENSG00000229869	chromatin interactions
ENSG00000249673	chromatin interactions
ENSG00000097046	chromatin interactions
ENSG00000067064	chromatin interactions
ENSG00000119725	chromatin interactions
ENSG00000074054	chromatin interactions
ENSG00000205740	chromatin interactions
ENSG00000047056	chromatin interactions
ENSG00000238924	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000109736	chromatin interactions
ENSG00000264229	chromatin interactions

Extended variants
information (count: 1330 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1330 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55924373	chr10:1084942-1084943	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs34010314	chr10:1084945-1084946	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs113644510	chr10:1084953-1084954	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs376502582	chr10:1084954-1084955	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs35371391	chr10:1084973-1084974	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs112682041	chr10:1084985-1084986	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs548850799	chr10:1085002-1085003	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs112191493	chr10:1085008-1085009	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs113670915	chr10:1085016-1085017	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374044012	chr10:1085017-1085018	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs58504590	chr10:1085036-1085037	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs368255705	chr10:1085049-1085050	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs60492320	chr10:1085071-1085072	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs111245711	chr10:1085111-1085112	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs534402369	chr10:1085133-1085134	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs56153104	chr10:1085134-1085135	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs61487661	chr10:1085143-1085144	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs56995948	chr10:1085174-1085175	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs539513849	chr10:1085181-1085182	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs573044919	chr10:1085231-1085232	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs556160774	chr10:1085237-1085238	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs576006487	chr10:1085283-1085284	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs544133936	chr10:1085292-1085293	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs185939452	chr10:1085302-1085303	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs190410433	chr10:1085338-1085339	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs376386304	chr10:1085353-1085354	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs560047367	chr10:1085368-1085369	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs61830995	chr10:1085429-1085430	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs149826603	chr10:1085458-1085459	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs565035609	chr10:1085534-1085535	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs4880758	chr10:1085572-1085573	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs566391313	chr10:1085595-1085596	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs562493709	chr10:1085677-1085678	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs368942435	chr10:1085774-1085775	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs371385081	chr10:1085776-1085777	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs386739790	chr10:1085783-1085784	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs182593111	chr10:1085787-1085788	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs374218831	chr10:1085816-1085817	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs548651310	chr10:1085891-1085892	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs375704654	chr10:1085917-1085918	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs568740654	chr10:1085931-1085932	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs527940277	chr10:1085946-1085947	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs547986774	chr10:1086004-1086005	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570685149	chr10:1086010-1086011	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs55879610	chr10:1086064-1086065	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs1285	chr10:1086116-1086117	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs529765180	chr10:1086126-1086127	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs370330064	chr10:1086155-1086156	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs556223851	chr10:1086177-1086178	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs569754855	chr10:1086204-1086205	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD

Chromatin state (count:2738 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

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	chr10:1064000-1088400	Weak transcription	Rectal Smooth Muscle	rectum
6	chr10:1065600-1086000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr10:1065600-1086200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr10:1065800-1086200	Weak transcription	Colon Smooth Muscle	Colon
9	chr10:1065800-1087800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr10:1066000-1086000	Weak transcription	HSMMtube	muscle
11	chr10:1066200-1085200	Weak transcription	HUVEC	blood vessel
12	chr10:1066200-1086000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr10:1066200-1086200	Weak transcription	Fetal Kidney	kidney
14	chr10:1066600-1088200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr10:1066800-1085000	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr10:1066800-1085200	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr10:1066800-1085600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr10:1066800-1085800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr10:1067000-1085200	Weak transcription	HSMM	muscle
20	chr10:1067200-1086200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr10:1067400-1089400	Weak transcription	Pancreas	Pancrea
22	chr10:1070800-1085800	Weak transcription	Osteobl	bone
23	chr10:1073400-1091800	Weak transcription	Fetal Heart	heart
24	chr10:1076600-1086800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr10:1079800-1087800	Weak transcription	Ovary	ovary
26	chr10:1080200-1086200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr10:1081600-1085000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr10:1081600-1089600	Weak transcription	Psoas Muscle	Psoas
29	chr10:1081800-1085200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr10:1081800-1086200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr10:1081800-1086200	Weak transcription	HepG2	liver
32	chr10:1081800-1089200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr10:1082000-1089800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr10:1082200-1086800	Strong transcription	Primary T cells from cord blood	blood
35	chr10:1082200-1086800	Strong transcription	Fetal Brain Female	brain
36	chr10:1082400-1085000	Strong transcription	Lung	lung
37	chr10:1082400-1085200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr10:1082400-1085200	Strong transcription	Fetal Stomach	stomach
39	chr10:1082400-1086800	Strong transcription	Fetal Muscle Leg	muscle
40	chr10:1082400-1088800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr10:1082400-1089000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr10:1082400-1089800	Strong transcription	Brain Germinal Matrix	brain
43	chr10:1082400-1090200	Strong transcription	Fetal Intestine Large	intestine
44	chr10:1082600-1085200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr10:1082600-1085200	Strong transcription	Spleen	Spleen
46	chr10:1082600-1086200	Weak transcription	K562	blood
47	chr10:1082600-1087400	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr10:1082600-1089400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr10:1082600-1089400	Strong transcription	Rectal Mucosa Donor 31	rectum
50	chr10:1082600-1089600	Strong transcription	Duodenum Mucosa	Duodenum

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