Variant report

Variant	nsv1024876
Chromosome Location	chr8:103512785-103576658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1674)
CpG islands
(count:1161)
Chromatin interactive
region (count:77)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1674 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:103553642-103554293	K562	blood:	n/a	n/a
2	ARID3A	chr8:103540422-103540495	K562	blood:	n/a	n/a
3	ARID3A	chr8:103540902-103541163	HepG2	liver:	n/a	n/a
4	ATF1	chr8:103513411-103513751	K562	blood:	n/a	n/a
5	ATF1	chr8:103540895-103541211	K562	blood:	n/a	n/a
6	ATF1	chr8:103553901-103554231	K562	blood:	n/a	n/a
7	ATF2	chr8:103546132-103547419	GM12878	blood:	n/a	n/a
8	ATF2	chr8:103567472-103568289	GM12878	blood:	n/a	n/a
9	ATF2	chr8:103542406-103542818	GM12878	blood:	n/a	n/a
10	ATF2	chr8:103568983-103569885	GM12878	blood:	n/a	n/a
11	ATF2	chr8:103542777-103543425	GM12878	blood:	n/a	n/a
12	ATF2	chr8:103546365-103547306	GM12878	blood:	n/a	n/a
13	ATF2	chr8:103547869-103548776	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr8:103542850-103543411	GM12878	blood:	n/a	n/a
15	ATF2	chr8:103567386-103568250	GM12878	blood:	n/a	n/a
16	ATF2	chr8:103540678-103541280	GM12878	blood:	n/a	n/a
17	ATF2	chr8:103569010-103570182	GM12878	blood:	n/a	n/a
18	ATF2	chr8:103547563-103548901	GM12878	blood:	n/a	n/a
19	ATF2	chr8:103547900-103548672	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr8:103547816-103548791	GM12878	blood:	n/a	n/a
21	ATF2	chr8:103540805-103541279	GM12878	blood:	n/a	n/a
22	BACH1	chr8:103522367-103522554	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr8:103556365-103556558	K562	blood:	n/a	n/a
24	BACH1	chr8:103517572-103517851	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr8:103567669-103567677	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr8:103548009-103548877	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr8:103553989-103554295	K562	blood:	n/a	n/a
28	BACH1	chr8:103549087-103549536	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr8:103544091-103544388	GM12878	blood:	n/a	n/a
30	BATF	chr8:103546533-103547273	GM12878	blood:	n/a	n/a
31	BATF	chr8:103547888-103548710	GM12878	blood:	n/a	chr8:103548046-103548056
32	BATF	chr8:103540852-103541211	GM12878	blood:	n/a	n/a
33	BATF	chr8:103546865-103547208	GM12878	blood:	n/a	n/a
34	BATF	chr8:103569172-103569766	GM12878	blood:	n/a	n/a
35	BATF	chr8:103542497-103542796	GM12878	blood:	n/a	n/a
36	BATF	chr8:103567478-103567932	GM12878	blood:	n/a	n/a
37	BATF	chr8:103569289-103569755	GM12878	blood:	n/a	n/a
38	BATF	chr8:103542519-103542832	GM12878	blood:	n/a	n/a
39	BATF	chr8:103543019-103543298	GM12878	blood:	n/a	n/a
40	BCL11A	chr8:103546539-103547304	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:103548111-103548617	H1-hESC	embryonic stem cell:	n/a	n/a
42	BCL11A	chr8:103569270-103569779	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:103569336-103569623	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:103567561-103567909	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:103546700-103547273	GM12878	blood:	n/a	n/a
46	BCL11A	chr8:103548037-103548629	GM12878	blood:	n/a	n/a
47	BCL11A	chr8:103567452-103567911	GM12878	blood:	n/a	n/a
48	BCL11A	chr8:103547879-103548475	GM12878	blood:	n/a	n/a
49	BCL3	chr8:103546717-103547311	GM12878	blood:	n/a	n/a
50	BCL3	chr8:103563509-103563875	GM12878	blood:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:103550807-103550857	IMR90	lung:	fetal
2	chr8:103541014-103541064	HPAEpiC	pulmonary alveolar:	n/a
3	chr8:103550807-103550857	IMR90	lung:	fetal
4	chr8:103541014-103541064	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:103563327-103563377	U87	brain:	n/a
6	chr8:103548145-103548195	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:103548145-103548195	T-47D	breast:	n/a
8	chr8:103563698-103563748	Caco-2	colon:	n/a
9	chr8:103549622-103549672	HAEpiC	amniotic membrane:	n/a
10	chr8:103568792-103568842	ECC-1	luminal epithelium:	n/a
11	chr8:103550807-103550857	BE2_C	brain:	n/a
12	chr8:103551067-103551117	U87	brain:	n/a
13	chr8:103572833-103572883	NHDF-neo	bronchial:	n/a
14	chr8:103563327-103563377	HRE	kidney:	n/a
15	chr8:103540839-103540889	Hela-S3	cervix:	n/a
16	chr8:103572833-103572883	MCF-7	breast:	n/a
17	chr8:103556749-103556799	LNCaP	prostate:	n/a
18	chr8:103564136-103564186	K562	blood:	n/a
19	chr8:103548145-103548195	HCF	heart:	n/a
20	chr8:103530461-103530511	SK-N-SH_RA	brain:	n/a
21	chr8:103550807-103550857	Hepatocyte	liver:	n/a
22	chr8:103564136-103564186	CMK	blood:	n/a
23	chr8:103541014-103541064	AG04450	lung:	fetal
24	chr8:103548145-103548195	HIPEpiC	eye:	n/a
25	chr8:103541014-103541064	Caco-2	colon:	n/a
26	chr8:103556749-103556799	GM12892	blood:	n/a
27	chr8:103563653-103563703	HCPEpiC	choroid plexus:	n/a
28	chr8:103541014-103541064	HRCEpiC	kidney:	n/a
29	chr8:103551067-103551117	SK-N-SH	brain:	n/a
30	chr8:103563327-103563377	AoSMC	blood vessel:	n/a
31	chr8:103572833-103572883	MCF10A-Er-Src	breast:	n/a
32	chr8:103530461-103530511	GM12892	blood:	n/a
33	chr8:103548145-103548195	AG04449	skin:	fetal
34	chr8:103563327-103563377	IMR90	lung:	fetal
35	chr8:103563327-103563377	ECC-1	luminal epithelium:	n/a
36	chr8:103551067-103551117	PFSK-1	brain:	n/a
37	chr8:103540783-103540833	HRPEpiC	eye:	n/a
38	chr8:103556749-103556799	CMK	blood:	n/a
39	chr8:103562972-103563022	CMK	blood:	n/a
40	chr8:103548145-103548195	MCF-7	breast:	n/a
41	chr8:103563653-103563703	NT2-D1	testis:	n/a
42	chr8:103564136-103564186	HRCEpiC	kidney:	n/a
43	chr8:103548145-103548195	GM06990	blood:	n/a
44	chr8:103564136-103564186	AG10803	skin:	n/a
45	chr8:103572833-103572883	U87	brain:	n/a
46	chr8:103540839-103540889	HAEpiC	amniotic membrane:	n/a
47	chr8:103549622-103549672	K562	blood:	n/a
48	chr8:103551067-103551117	ProgFib	skin:	n/a
49	chr8:103556749-103556799	HCT-116	colon:	n/a
50	chr8:103540839-103540889	PFSK-1	brain:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:103567304..103569694-chr8:103578366..103580055,2	MCF-7	breast:
2	chr8:103422537..103425322-chr8:103540234..103542841,3	K562	blood:
3	chr8:103423499..103426368-chr8:103552580..103554247,2	K562	blood:
4	chr8:103541502..103544412-chr8:103664265..103666950,2	MCF-7	breast:
5	chr8:103540102..103543996-chr8:103574718..103578411,4	MCF-7	breast:
6	chr8:103513875..103516395-chr8:103517961..103519634,2	K562	blood:
7	chr8:103561720..103564415-chr8:103565108..103567782,4	K562	blood:
8	chr8:103561576..103563655-chr8:103568323..103570576,2	MCF-7	breast:
9	chr8:103540947..103542816-chr8:103666262..103668771,2	K562	blood:
10	chr8:103423160..103425899-chr8:103539167..103542509,5	MCF-7	breast:
11	chr8:103547915..103550298-chr8:103554370..103557167,3	K562	blood:
12	chr8:103547915..103550298-chr8:103554370..103557167,3	K562	blood:
13	chr8:103554141..103557178-chr8:103560582..103564192,4	K562	blood:
14	chr8:103575313..103581780-chr8:103582663..103591933,12	MCF-7	breast:
15	chr8:103566130..103569047-chr8:103588313..103590545,3	MCF-7	breast:
16	chr8:103422090..103425844-chr8:103540841..103544782,4	MCF-7	breast:
17	chr8:103424626..103426785-chr8:103521695..103523265,2	MCF-7	breast:
18	chr8:103502255..103505125-chr8:103511782..103514239,2	MCF-7	breast:
19	chr8:103422537..103426688-chr8:103540100..103542473,3	K562	blood:
20	chr8:103540698..103544207-chr8:103546696..103550142,4	MCF-7	breast:
21	chr8:103423608..103426588-chr8:103558212..103561124,2	K562	blood:
22	chr8:103523075..103527068-chr8:103533179..103535230,3	MCF-7	breast:
23	chr8:103531973..103534873-chr8:103588952..103591472,2	K562	blood:
24	chr8:103525311..103527226-chr8:103533440..103535357,2	K562	blood:
25	chr8:103553403..103555856-chr8:103556123..103559694,3	MCF-7	breast:
26	chr8:103561236..103562878-chr8:103564860..103566759,2	MCF-7	breast:
27	chr8:103422775..103425553-chr8:103523894..103525443,2	MCF-7	breast:
28	chr8:103548290..103549858-chr8:103666660..103669466,2	K562	blood:
29	chr8:103552849..103555582-chr8:103602690..103604723,2	K562	blood:
30	chr8:103568483..103570807-chr8:103581196..103582779,2	MCF-7	breast:
31	chr8:103545032..103547830-chr8:103548926..103551199,2	MCF-7	breast:
32	chr8:103437958..103439977-chr8:103547146..103549346,2	MCF-7	breast:
33	chr8:103423156..103426710-chr8:103547734..103551186,4	MCF-7	breast:
34	chr8:103537823..103539914-chr8:103541615..103544140,2	K562	blood:
35	chr8:103523075..103527068-chr8:103533179..103535230,3	MCF-7	breast:
36	chr8:103520610..103522494-chr8:103820924..103823364,2	MCF-7	breast:
37	chr8:103537823..103539914-chr8:103541615..103544140,2	K562	blood:
38	chr8:103528321..103530383-chr8:103533029..103535139,2	K562	blood:
39	chr8:103561837..103564044-chr8:103571936..103573800,2	MCF-7	breast:
40	chr8:103561236..103562878-chr8:103564860..103566759,2	MCF-7	breast:
41	chr8:103525311..103527226-chr8:103533440..103535357,2	K562	blood:
42	chr8:103523909..103525501-chr8:103526582..103528205,2	MCF-7	breast:
43	chr8:103539619..103542009-chr8:103547137..103548824,2	MCF-7	breast:
44	chr8:103571721..103574356-chr8:103574864..103576859,2	MCF-7	breast:
45	chr20:45990214..45992945-chr8:103550491..103553250,2	MCF-7	breast:
46	chr8:103570250..103572915-chr8:103665541..103668437,2	MCF-7	breast:
47	chr8:103541696..103544133-chr8:103825198..103827958,2	MCF-7	breast:
48	chr8:103552930..103556301-chr8:103557588..103560805,4	K562	blood:
49	chr8:103528321..103530383-chr8:103533029..103535139,2	K562	blood:
50	chr8:103540168..103543141-chr8:103550290..103553115,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ODF1-2	chr8:103562735-103563312	NONHSAT128101
2	lnc-ODF1-1	chr8:103540968-103541083	NONHSAT128098
3	lnc-ODF1-2	chr8:103561889-103562037	NONHSAT128101
4	lnc-ODF1-1	chr8:103541539-103541931	XLOC_006892
5	lnc-KB-1980E6.3.1-2	chr8:103515981-103516365	NONHSAT128097
6	lnc-ODF1-1	chr8:103545983-103546093	NONHSAT128098
7	lnc-KLF10-5	chr8:103562771-103563312	NONHSAT128100
8	lnc-ODF1-1	chr8:103547961-103548188	NONHSAT128098
9	lnc-ODF1-1	chr8:103550612-103550896	NONHSAT128098
10	lnc-KLF10-5	chr8:103553392-103553821	NONHSAT128100
11	lnc-ODF1-1	chr8:103541045-103541083	XLOC_006892

No data

Variant related genes	Relation type
ENSG00000253633	TF binding region
RPS12P15	TF binding region
ODF1	TF binding region
RNU6-1224P	TF binding region
ENSG00000253633	CpG island
RPS12P15	CpG island
ODF1	CpG island
RNU6-1224P	CpG island
ENSG00000104517	chromatin interactions
ENSG00000246263	chromatin interactions
ENSG00000252593	chromatin interactions
ENSG00000155090	chromatin interactions
ENSG00000155087	chromatin interactions
ENSG00000240724	chromatin interactions
ENSG00000253633	chromatin interactions

Extended variants
information (count: 2545 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:2545 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6983758	chr8:103512785-103512786	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536676106	chr8:103512820-103512821	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs369680386	chr8:103512837-103512838	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs872901	chr8:103512870-103512871	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs77153939	chr8:103512881-103512882	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs7005430	chr8:103512906-103512907	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs141141876	chr8:103512983-103512984	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs12056666	chr8:103512984-103512985	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs2002177	chr8:103513013-103513014	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs530403597	chr8:103513136-103513137	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs149494583	chr8:103513184-103513185	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs143340576	chr8:103513206-103513207	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528218753	chr8:103513207-103513208	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs7006028	chr8:103513235-103513236	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs375663851	chr8:103513246-103513247	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs4734628	chr8:103513280-103513281	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs189280952	chr8:103513300-103513301	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs571593720	chr8:103513308-103513309	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs551277266	chr8:103513325-103513326	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs569608181	chr8:103513328-103513329	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs79542357	chr8:103513468-103513469	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs75756734	chr8:103513472-103513473	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs549944228	chr8:103513491-103513492	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs566863832	chr8:103513507-103513508	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs12114624	chr8:103513523-103513524	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs181013797	chr8:103513532-103513533	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs577734563	chr8:103513581-103513582	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs538473941	chr8:103513609-103513610	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs375563301	chr8:103513640-103513641	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs556819206	chr8:103513670-103513671	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs186094465	chr8:103513690-103513691	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs542210379	chr8:103513706-103513707	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs12114928	chr8:103513715-103513716	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs11313727	chr8:103513738-103513739	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs398086862	chr8:103513743-103513744	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs370507044	chr8:103513821-103513822	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs12114692	chr8:103513858-103513859	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs114387610	chr8:103513865-103513866	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs138635086	chr8:103513887-103513888	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs532739592	chr8:103513891-103513892	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs75355974	chr8:103513892-103513893	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs77229990	chr8:103513893-103513894	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs12114119	chr8:103513909-103513910	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs570311003	chr8:103513917-103513918	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs34949613	chr8:103514012-103514013	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs62524798	chr8:103514072-103514073	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs186266154	chr8:103514085-103514086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563742856	chr8:103514096-103514097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542747668	chr8:103514123-103514124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs62524800	chr8:103514169-103514170	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1095 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103502800-103529800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:103503000-103517400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:103508800-103513400	Weak transcription	Osteobl	bone
4	chr8:103508800-103514600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:103508800-103517400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr8:103509000-103517400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr8:103510000-103516000	Weak transcription	Pancreas	Pancrea
8	chr8:103511200-103513200	Weak transcription	HepG2	liver
9	chr8:103513200-103513800	Enhancers	HepG2	liver
10	chr8:103513200-103513800	Enhancers	K562	blood
11	chr8:103513800-103515600	Weak transcription	HepG2	liver
12	chr8:103514600-103514800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr8:103514600-103514800	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr8:103514600-103515400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr8:103514800-103515400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr8:103514800-103517200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:103515000-103515400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr8:103515000-103515400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr8:103515200-103515400	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr8:103515400-103517400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr8:103515400-103517400	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr8:103515400-103517400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr8:103515400-103517400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr8:103515400-103517400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr8:103515600-103517800	Enhancers	HepG2	liver
26	chr8:103515800-103516200	Enhancers	Lung	lung
27	chr8:103516000-103516200	Enhancers	Pancreas	Pancrea
28	chr8:103516000-103517400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr8:103516200-103518000	Enhancers	A549	lung
30	chr8:103517200-103518000	Enhancers	H1 Cell Line	embryonic stem cell
31	chr8:103517400-103517800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr8:103517400-103518000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr8:103517400-103518000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr8:103517400-103518000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr8:103517400-103518000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr8:103517400-103518000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr8:103517400-103518000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr8:103517400-103518000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr8:103517400-103518000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr8:103517400-103518200	Enhancers	H9 Cell Line	embryonic stem cell
41	chr8:103517400-103518200	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr8:103517400-103518400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr8:103517600-103518000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr8:103517600-103518000	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr8:103517800-103519200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr8:103517800-103520600	Weak transcription	HepG2	liver
47	chr8:103518000-103520600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr8:103518000-103520600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr8:103518200-103529600	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr8:103518200-103529600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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