Variant report

Variant	nsv464161
Chromosome Location	chr1:160747615-160852046
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2051)
CpG islands
(count:1650)
Chromatin interactive
region (count:74)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2051 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:160750006-160750086	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:160804805-160805113	K562	blood:	n/a	n/a
3	ATF1	chr1:160788878-160789017	K562	blood:	n/a	n/a
4	ATF1	chr1:160759551-160759815	K562	blood:	n/a	n/a
5	ATF1	chr1:160783083-160783328	K562	blood:	n/a	n/a
6	ATF2	chr1:160759317-160760285	GM12878	blood:	n/a	n/a
7	ATF2	chr1:160765624-160766184	GM12878	blood:	n/a	n/a
8	ATF2	chr1:160807191-160808166	GM12878	blood:	n/a	n/a
9	ATF2	chr1:160766887-160767734	GM12878	blood:	n/a	n/a
10	ATF2	chr1:160751696-160752491	GM12878	blood:	n/a	n/a
11	ATF2	chr1:160751780-160752499	GM12878	blood:	n/a	n/a
12	ATF2	chr1:160766987-160767620	GM12878	blood:	n/a	n/a
13	ATF2	chr1:160807646-160808148	GM12878	blood:	n/a	n/a
14	ATF2	chr1:160832358-160832826	GM12878	blood:	n/a	n/a
15	ATF2	chr1:160759300-160760405	GM12878	blood:	n/a	n/a
16	ATF2	chr1:160765576-160766188	GM12878	blood:	n/a	n/a
17	ATF2	chr1:160825222-160825712	GM12878	blood:	n/a	n/a
18	ATF3	chr1:160783018-160783305	K562	blood:	n/a	n/a
19	BACH1	chr1:160783042-160783344	K562	blood:	n/a	n/a
20	BACH1	chr1:160783101-160783353	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr1:160776288-160776310	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr1:160807287-160807613	GM12878	blood:	n/a	n/a
23	BATF	chr1:160807671-160808077	GM12878	blood:	n/a	chr1:160807896-160807907
24	BATF	chr1:160759492-160760019	GM12878	blood:	n/a	n/a
25	BATF	chr1:160767045-160767572	GM12878	blood:	n/a	n/a
26	BATF	chr1:160766995-160767658	GM12878	blood:	n/a	n/a
27	BATF	chr1:160765691-160766140	GM12878	blood:	n/a	n/a
28	BATF	chr1:160807683-160808087	GM12878	blood:	n/a	chr1:160807896-160807907
29	BATF	chr1:160752023-160752431	GM12878	blood:	n/a	n/a
30	BATF	chr1:160751941-160752498	GM12878	blood:	n/a	n/a
31	BATF	chr1:160783095-160783391	GM12878	blood:	n/a	n/a
32	BATF	chr1:160832529-160832890	GM12878	blood:	n/a	n/a
33	BATF	chr1:160760126-160760469	GM12878	blood:	n/a	n/a
34	BATF	chr1:160759556-160760463	GM12878	blood:	n/a	n/a
35	BCL11A	chr1:160832394-160832781	GM12878	blood:	n/a	n/a
36	BCL11A	chr1:160807711-160808086	GM12878	blood:	n/a	chr1:160807896-160807905
37	BCL11A	chr1:160765741-160766090	GM12878	blood:	n/a	n/a
38	BCL11A	chr1:160759465-160760315	GM12878	blood:	n/a	n/a
39	BCL11A	chr1:160759529-160760376	GM12878	blood:	n/a	n/a
40	BCL11A	chr1:160807751-160808042	GM12878	blood:	n/a	chr1:160807896-160807905
41	BCL11A	chr1:160752081-160752398	GM12878	blood:	n/a	chr1:160752214-160752223 chr1:160752303-160752312
42	BCL11A	chr1:160751980-160752430	GM12878	blood:	n/a	chr1:160752214-160752223 chr1:160752303-160752312
43	BCL11A	chr1:160765688-160766135	GM12878	blood:	n/a	n/a
44	BCL3	chr1:160751937-160752390	GM12878	blood:	n/a	chr1:160752214-160752223 chr1:160752303-160752312
45	BCL3	chr1:160848890-160849098	GM12878	blood:	n/a	n/a
46	BCL3	chr1:160796157-160796667	A549	lung:	n/a	n/a
47	BCL3	chr1:160759201-160759702	GM12878	blood:	n/a	n/a
48	BCL3	chr1:160765683-160766115	GM12878	blood:	n/a	n/a
49	BCL3	chr1:160765654-160766085	GM12878	blood:	n/a	n/a
50	BCL3	chr1:160759191-160759665	GM12878	blood:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:160833560-160833610	Caco-2	colon:	n/a
2	chr1:160824025-160824075	GM19239	blood:	n/a
3	chr1:160771900-160771950	BJ	skin:	n/a
4	chr1:160833560-160833610	Caco-2	colon:	n/a
5	chr1:160824025-160824075	GM19239	blood:	n/a
6	chr1:160771900-160771950	BJ	skin:	n/a
7	chr1:160771696-160771746	SK-N-SH_RA	brain:	n/a
8	chr1:160765349-160765399	NHBE	bronchial:	n/a
9	chr1:160797850-160797900	NHBE	bronchial:	n/a
10	chr1:160765919-160765969	A549	lung:	n/a
11	chr1:160850377-160850427	MCF-7	breast:	n/a
12	chr1:160764791-160764841	MCF-7	breast:	n/a
13	chr1:160764664-160764714	ECC-1	luminal epithelium:	n/a
14	chr1:160765225-160765275	HIPEpiC	eye:	n/a
15	chr1:160768549-160768599	HIPEpiC	eye:	n/a
16	chr1:160765919-160765969	HCT-116	colon:	n/a
17	chr1:160765805-160765855	GM12892	blood:	n/a
18	chr1:160832662-160832712	ProgFib	skin:	n/a
19	chr1:160774690-160774740	BJ	skin:	n/a
20	chr1:160768549-160768599	MCF10A-Er-Src	breast:	n/a
21	chr1:160771696-160771746	NT2-D1	testis:	n/a
22	chr1:160765349-160765399	AoSMC	blood vessel:	n/a
23	chr1:160764664-160764714	AG09319	gingival:	n/a
24	chr1:160771763-160771813	HUVEC	blood vessel:	n/a
25	chr1:160833560-160833610	HPAEpiC	pulmonary alveolar:	n/a
26	chr1:160774690-160774740	GM12878	blood:	n/a
27	chr1:160833560-160833610	HNPCEpiC	eye:	n/a
28	chr1:160770752-160770802	AG10803	skin:	n/a
29	chr1:160771696-160771746	GM12878	blood:	n/a
30	chr1:160797850-160797900	HAEpiC	amniotic membrane:	n/a
31	chr1:160765225-160765275	NH-A	brain:	n/a
32	chr1:160800192-160800242	HAEpiC	amniotic membrane:	n/a
33	chr1:160765225-160765275	HUVEC	blood vessel:	n/a
34	chr1:160832662-160832712	GM06990	blood:	n/a
35	chr1:160766535-160766585	AG09309	skin:	n/a
36	chr1:160771763-160771813	Caco-2	colon:	n/a
37	chr1:160769081-160769131	HRPEpiC	eye:	n/a
38	chr1:160771850-160771900	SK-N-MC	brain:	n/a
39	chr1:160765919-160765969	GM19239	blood:	n/a
40	chr1:160833560-160833610	HUVEC	blood vessel:	n/a
41	chr1:160768549-160768599	AG04449	skin:	fetal
42	chr1:160771763-160771813	Hepatocyte	liver:	n/a
43	chr1:160769081-160769131	NB4	blood:	n/a
44	chr1:160833560-160833610	NH-A	brain:	n/a
45	chr1:160770752-160770802	GM12891	blood:	n/a
46	chr1:160824025-160824075	A549	lung:	n/a
47	chr1:160765225-160765275	NHDF-neo	bronchial:	n/a
48	chr1:160800192-160800242	MCF10A-Er-Src	breast:	n/a
49	chr1:160832662-160832712	Hepatocyte	liver:	n/a
50	chr1:160824025-160824075	CMK	blood:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:160802328..160804621-chr1:160806389..160808035,2	K562	blood:
2	chr1:160791268..160793471-chr1:160795431..160798157,2	MCF-7	breast:
3	chr1:160746903..160747909-chr1:160800008..160800911,3	MCF-7	breast:
4	chr1:160749538..160750510-chr1:160799614..160800626,3	K562	blood:
5	chr1:160850691..160852389-chr1:160852476..160855044,2	MCF-7	breast:
6	chr1:160748693..160751200-chr1:160804767..160806895,2	MCF-7	breast:
7	chr1:160696061..160696740-chr1:160749784..160750511,2	K562	blood:
8	chr1:160750574..160752770-chr1:160766750..160768788,2	K562	blood:
9	chr1:160806018..160807839-chr1:160809156..160811151,2	K562	blood:
10	chr1:160697110..160698910-chr1:160790378..160792048,2	K562	blood:
11	chr1:160749538..160750510-chr1:160799614..160800626,3	K562	blood:
12	chr1:160748693..160751200-chr1:160804767..160806895,2	MCF-7	breast:
13	chr1:160829381..160830881-chr5:89705288..89707065,2	MCF-7	breast:
14	chr1:160791393..160792131-chr1:160959742..160960435,2	K562	blood:
15	chr1:160805876..160808335-chr1:160811999..160814822,2	K562	blood:
16	chr1:160779866..160781807-chr1:160913798..160915545,2	MCF-7	breast:
17	chr1:160791238..160791974-chr1:160800115..160801037,2	MCF-7	breast:
18	chr1:160804559..160806292-chr1:161014093..161016199,2	K562	blood:
19	chr1:160651216..160652600-chr1:160800013..160800990,10	K562	blood:
20	chr1:160808897..160810604-chr1:160813448..160815134,2	MCF-7	breast:
21	chr1:160802328..160804621-chr1:160806389..160808035,2	K562	blood:
22	chr1:160804453..160805506-chr1:160920895..160922480,10	MCF-7	breast:
23	chr1:160750002..160750637-chr1:160923747..160924410,3	K562	blood:
24	chr1:160805876..160809429-chr1:160811999..160815816,3	K562	blood:
25	chr1:160746990..160747846-chr1:160800020..160801002,2	K562	blood:
26	chr1:160776649..160779858-chr1:160780478..160783432,4	K562	blood:
27	chr1:160787480..160789463-chr1:161085547..161088382,2	K562	blood:
28	chr1:160811365..160813058-chr1:160817059..160818706,2	K562	blood:
29	chr1:160779738..160781417-chr1:160790589..160793548,2	K562	blood:
30	chr1:160791238..160791974-chr1:160800115..160801037,2	MCF-7	breast:
31	chr1:160746479..160747897-chr1:160799771..160800945,11	MCF-7	breast:
32	chr1:160786153..160788877-chr1:160788974..160791369,2	K562	blood:
33	chr1:160696291..160697336-chr1:160800205..160801082,4	MCF-7	breast:
34	chr1:160750241..160751876-chr1:160779481..160781374,2	MCF-7	breast:
35	chr1:160815023..160816835-chr1:160823211..160824951,2	K562	blood:
36	chr1:160696717..160697289-chr1:160775794..160776301,2	MCF-7	breast:
37	chr1:160750574..160752770-chr1:160766750..160768788,2	K562	blood:
38	chr1:160696267..160696909-chr1:160747036..160748093,3	MCF-7	breast:
39	chr1:160769451..160770985-chr1:160774299..160776734,2	K562	blood:
40	chr1:160769451..160770985-chr1:160774299..160776734,2	K562	blood:
41	chr1:160749523..160750339-chr1:160920946..160921479,2	MCF-7	breast:
42	chr1:160750735..160751494-chr1:160800341..160800905,2	MCF-7	breast:
43	chr1:160749583..160750608-chr1:160800056..160801037,9	MCF-7	breast:
44	chr1:160830058..160833659-chr1:160834744..160837496,3	K562	blood:
45	chr1:160815023..160816835-chr1:160823211..160824951,2	K562	blood:
46	chr1:160696348..160697194-chr1:160749478..160750155,4	MCF-7	breast:
47	chr1:160806018..160807839-chr1:160809156..160811151,2	K562	blood:
48	chr1:160791268..160793471-chr1:160795431..160798157,2	MCF-7	breast:
49	chr1:160749553..160750469-chr1:160800278..160801014,5	MCF-7	breast:
50	chr1:160822600..160825606-chr1:160827669..160829423,3	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLAMF7-9	chr1:160789093-160789164	NONHSAT007077
2	lnc-ITLN1-1	chr1:160802309-160802365	NONHSAT007080
3	lnc-SLAMF7-9	chr1:160793298-160793586	NONHSAT007077
4	lnc-SLAMF7-9	chr1:160793256-160793586	NONHSAT007078
5	lnc-ITLN1-1	chr1:160803841-160803906	NONHSAT007080
6	lnc-CD244-1	chr1:160796887-160797066	l_141_chr1:160788935-160797689_testes
7	lnc-ITLN1-1	chr1:160808241-160808308	NONHSAT007080
8	lnc-CD244-1	chr1:160797652-160797689	l_141_chr1:160788935-160797689_testes
9	lnc-LY9-2	chr1:160830898-160831203	expReg_chr1_18595_+
10	lnc-SLAMF7-9	chr1:160797539-160797606	NONHSAT007077
11	lnc-SLAMF7-9	chr1:160797539-160797606	NONHSAT007078
12	lnc-SLAMF7-9	chr1:160789093-160789164	NONHSAT007078
13	lnc-SLAMF7-9	chr1:160793972-160794039	NONHSAT007078
14	lnc-ITLN1-1	chr1:160808610-160808955	NONHSAT007080
15	lnc-SLAMF7-7	chr1:160768616-160769454	NONHSAT007076
16	lnc-CD244-1	chr1:160788936-160789060	l_141_chr1:160788935-160797689_testes
17	lnc-SLAMF7-7	chr1:160766001-160766101	NONHSAT007076

No data

Variant related genes	Relation type
ENSG00000226003	TF binding region
LY9	TF binding region
ITLN1	TF binding region
CD244	TF binding region
ENSG00000226003	CpG island
LY9	CpG island
ITLN1	CpG island
CD244	CpG island
ENSG00000158764	chromatin interactions
ENSG00000122223	chromatin interactions
ENSG00000255647	chromatin interactions
ENSG00000122224	chromatin interactions
ENSG00000153140	chromatin interactions
ENSG00000179914	chromatin interactions
ENSG00000158793	chromatin interactions
ENSG00000158773	chromatin interactions
ENSG00000143256	chromatin interactions
ENSG00000226003	chromatin interactions

Extended variants
information (count: 4461 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:4461 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7556098	chr1:160747615-160747616	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114921533	chr1:160747616-160747617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372062817	chr1:160747640-160747641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12077897	chr1:160747685-160747686	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs529608	chr1:160747718-160747719	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs540253797	chr1:160747778-160747779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560155441	chr1:160747785-160747786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142728137	chr1:160747807-160747808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs117965691	chr1:160747820-160747821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562600974	chr1:160747826-160747827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs531446260	chr1:160747829-160747830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182157414	chr1:160747841-160747842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368842597	chr1:160747871-160747872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187378233	chr1:160747883-160747884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78283574	chr1:160747894-160747895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189340919	chr1:160747915-160747916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575991878	chr1:160747931-160747932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146960433	chr1:160747986-160747987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570089583	chr1:160748019-160748020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547915020	chr1:160748028-160748029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532466	chr1:160748041-160748042	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs572545006	chr1:160748045-160748046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs137898407	chr1:160748054-160748055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540040300	chr1:160748097-160748098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113178103	chr1:160748145-160748146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541780325	chr1:160748175-160748176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs80161759	chr1:160748186-160748187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149470526	chr1:160748256-160748257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545775362	chr1:160748286-160748287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185812600	chr1:160748294-160748295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11265476	chr1:160748342-160748343	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs560324944	chr1:160748368-160748369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541683044	chr1:160748424-160748425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561888884	chr1:160748465-160748466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73015971	chr1:160748475-160748476	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs552467569	chr1:160748477-160748478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542258391	chr1:160748513-160748514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570402663	chr1:160748581-160748582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533161579	chr1:160748596-160748597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144124284	chr1:160748620-160748621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377199600	chr1:160748683-160748684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190342348	chr1:160748700-160748701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555562239	chr1:160748717-160748718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566303561	chr1:160748779-160748780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs115330979	chr1:160748900-160748901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558529744	chr1:160748919-160748920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552307691	chr1:160748936-160748937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539065750	chr1:160748948-160748949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182561614	chr1:160748997-160748998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576075587	chr1:160749038-160749039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1332 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160744800-160747800	Enhancers	Fetal Thymus	thymus
2	chr1:160745200-160750200	Weak transcription	NHEK	skin
3	chr1:160745200-160750400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:160745200-160751200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr1:160745400-160750200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:160745400-160750800	Weak transcription	HMEC	breast
7	chr1:160745400-160764800	Weak transcription	Primary T cells from cord blood	blood
8	chr1:160746000-160747800	Enhancers	Primary B cells from peripheral blood	blood
9	chr1:160746400-160751000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr1:160747000-160747800	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr1:160747000-160751400	Weak transcription	Primary B cells from cord blood	blood
12	chr1:160747400-160747800	Enhancers	Primary T cells fromperipheralblood	blood
13	chr1:160747400-160747800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr1:160747400-160748600	Weak transcription	GM12878-XiMat	blood
15	chr1:160747600-160747800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:160747600-160747800	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr1:160747600-160748400	Enhancers	Esophagus	oesophagus
18	chr1:160747600-160748600	Weak transcription	Lung	lung
19	chr1:160747800-160748800	Weak transcription	Primary B cells from peripheral blood	blood
20	chr1:160747800-160750200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:160747800-160750800	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr1:160747800-160750800	Weak transcription	Fetal Thymus	thymus
23	chr1:160747800-160751000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr1:160747800-160751400	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr1:160748000-160750200	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr1:160748400-160750800	Weak transcription	Esophagus	oesophagus
27	chr1:160748600-160748800	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr1:160748600-160748800	Enhancers	Lung	lung
29	chr1:160748600-160749600	Enhancers	Brain Cingulate Gyrus	brain
30	chr1:160748600-160751600	Enhancers	GM12878-XiMat	blood
31	chr1:160748800-160750800	Weak transcription	Lung	lung
32	chr1:160748800-160753400	Enhancers	Primary B cells from peripheral blood	blood
33	chr1:160749600-160749800	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr1:160749600-160753400	Enhancers	Placenta	Placenta
35	chr1:160750200-160750400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr1:160750200-160750800	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr1:160750200-160751200	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr1:160750200-160751400	Enhancers	Duodenum Mucosa	Duodenum
39	chr1:160750200-160751600	Enhancers	Stomach Mucosa	stomach
40	chr1:160750200-160752400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr1:160750200-160752400	Enhancers	NHEK	skin
42	chr1:160750200-160752800	Enhancers	Fetal Intestine Large	intestine
43	chr1:160750200-160752800	Enhancers	Fetal Intestine Small	intestine
44	chr1:160750200-160753000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr1:160750400-160752200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:160750400-160752400	Enhancers	Placenta Amnion	Placenta Amnion
47	chr1:160750400-160762000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:160750600-160751000	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr1:160750800-160751200	Enhancers	Small Intestine	intestine
50	chr1:160750800-160751400	Enhancers	Esophagus	oesophagus

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