Variant report

Variant	nsv832075
Chromosome Location	chr11:16391700-16490934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:331)
CpG islands
(count:427)
Chromatin interactive
region (count:70)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:16402660-16404886	K562	blood:	n/a	chr11:16403818-16403834 chr11:16402665-16402681 chr11:16403817-16403833
2	ARID3A	chr11:16407356-16407381	K562	blood:	n/a	n/a
3	ARID3A	chr11:16395516-16395658	K562	blood:	n/a	n/a
4	ARID3A	chr11:16430209-16430503	K562	blood:	n/a	n/a
5	ARID3A	chr11:16418976-16419247	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:16416874-16417492	K562	blood:	n/a	n/a
7	ARID3A	chr11:16396118-16396393	K562	blood:	n/a	n/a
8	ARID3A	chr11:16401295-16401408	K562	blood:	n/a	n/a
9	ARID3A	chr11:16399188-16399243	K562	blood:	n/a	n/a
10	ARID3A	chr11:16399521-16399937	K562	blood:	n/a	n/a
11	ARID3A	chr11:16406780-16406971	K562	blood:	n/a	n/a
12	ARID3A	chr11:16424180-16424827	HepG2	liver:	n/a	n/a
13	ARID3A	chr11:16394743-16394888	K562	blood:	n/a	n/a
14	ARID3A	chr11:16398111-16398614	K562	blood:	n/a	n/a
15	ATF1	chr11:16430309-16430617	K562	blood:	n/a	n/a
16	ATF2	chr11:16424453-16424972	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr11:16424326-16425117	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr11:16430210-16430629	K562	blood:	n/a	n/a
19	BACH1	chr11:16403929-16404129	K562	blood:	n/a	n/a
20	BCL11A	chr11:16424540-16424931	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr11:16424558-16424905	H1-hESC	embryonic stem cell:	n/a	n/a
22	BHLHE40	chr11:16414698-16415248	K562	blood:	n/a	n/a
23	CBX3	chr11:16397102-16397544	K562	blood:	n/a	n/a
24	CBX3	chr11:16392679-16393253	K562	blood:	n/a	n/a
25	CBX3	chr11:16392952-16393254	K562	blood:	n/a	n/a
26	CEBPB	chr11:16489641-16489872	K562	blood:	n/a	n/a
27	CEBPB	chr11:16446663-16446916	K562	blood:	n/a	chr11:16446790-16446803
28	CEBPB	chr11:16483729-16484007	HepG2	liver:	n/a	chr11:16483874-16483885
29	CEBPB	chr11:16428884-16429156	HepG2	liver:	n/a	chr11:16429014-16429025
30	CEBPB	chr11:16405810-16406156	K562	blood:	n/a	chr11:16405972-16405981 chr11:16405970-16405983 chr11:16405972-16405983 chr11:16405970-16405981
31	CEBPB	chr11:16433784-16434006	K562	blood:	n/a	chr11:16433958-16433975 chr11:16433938-16433951 chr11:16433939-16433950
32	CEBPB	chr11:16402755-16402988	K562	blood:	n/a	n/a
33	CEBPB	chr11:16430372-16430638	K562	blood:	n/a	n/a
34	CEBPB	chr11:16405843-16406078	HepG2	liver:	n/a	chr11:16405972-16405981 chr11:16405970-16405983 chr11:16405972-16405983 chr11:16405970-16405981
35	CEBPB	chr11:16483761-16483980	IMR90	lung:	n/a	chr11:16483874-16483885
36	CEBPB	chr11:16483752-16483988	A549	lung:	n/a	chr11:16483874-16483885
37	CEBPB	chr11:16433883-16434109	HepG2	liver:	n/a	chr11:16433958-16433975 chr11:16433938-16433951 chr11:16433939-16433950
38	CEBPB	chr11:16400525-16400721	K562	blood:	n/a	n/a
39	CEBPB	chr11:16454922-16455038	A549	lung:	n/a	n/a
40	CEBPB	chr11:16428840-16429189	K562	blood:	n/a	chr11:16429014-16429025
41	CEBPB	chr11:16414746-16415017	K562	blood:	n/a	n/a
42	CEBPB	chr11:16402204-16402414	IMR90	lung:	n/a	n/a
43	CEBPB	chr11:16475778-16476139	IMR90	lung:	n/a	chr11:16475838-16475851
44	CEBPB	chr11:16402255-16402392	A549	lung:	n/a	n/a
45	CEBPB	chr11:16428895-16429093	H1-hESC	embryonic stem cell:	n/a	chr11:16429014-16429025
46	CEBPB	chr11:16404712-16405222	K562	blood:	n/a	n/a
47	CEBPB	chr11:16405842-16406149	IMR90	lung:	n/a	chr11:16405972-16405981 chr11:16405970-16405983 chr11:16405972-16405983 chr11:16405970-16405981
48	CEBPB	chr11:16490512-16490884	K562	blood:	n/a	chr11:16490817-16490830 chr11:16490525-16490536 chr11:16490525-16490538
49	CEBPB	chr11:16404549-16405210	IMR90	lung:	n/a	chr11:16404615-16404626 chr11:16404616-16404628
50	CREB1	chr11:16424419-16425032	H1-hESC	embryonic stem cell:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:16424673-16424723	IMR90	lung:	fetal
2	chr11:16424708-16424758	HEEpiC	esophagus:	n/a
3	chr11:16430764-16430814	GM06990	blood:	n/a
4	chr11:16430764-16430814	SKMC	muscle:	n/a
5	chr11:16424935-16424985	HAEpiC	amniotic membrane:	n/a
6	chr11:16430764-16430814	PANC-1	pancreas:	n/a
7	chr11:16430764-16430814	H1-hESC	embryonic stem cell:	embryo
8	chr11:16424935-16424985	HIPEpiC	eye:	n/a
9	chr11:16431523-16431573	AoSMC	blood vessel:	n/a
10	chr11:16430247-16430297	NHDF-neo	bronchial:	n/a
11	chr11:16430247-16430297	NB4	blood:	n/a
12	chr11:16431523-16431573	H1-hESC	embryonic stem cell:	embryo
13	chr11:16431370-16431420	ECC-1	luminal epithelium:	n/a
14	chr11:16424935-16424985	HEEpiC	esophagus:	n/a
15	chr11:16424708-16424758	GM06990	blood:	n/a
16	chr11:16431370-16431420	GM12878	blood:	n/a
17	chr11:16424673-16424723	Hela-S3	cervix:	n/a
18	chr11:16424673-16424723	HRCEpiC	kidney:	n/a
19	chr11:16424708-16424758	Jurkat	blood:	n/a
20	chr11:16424935-16424985	AG09319	gingival:	n/a
21	chr11:16431370-16431420	AG04449	skin:	fetal
22	chr11:16424935-16424985	HRCEpiC	kidney:	n/a
23	chr11:16424935-16424985	HL-60	blood:	n/a
24	chr11:16430247-16430297	Hepatocyte	liver:	n/a
25	chr11:16424708-16424758	SAEC	small airway:	n/a
26	chr11:16424708-16424758	HNPCEpiC	eye:	n/a
27	chr11:16431523-16431573	SK-N-SH	brain:	n/a
28	chr11:16430764-16430814	HUVEC	blood vessel:	n/a
29	chr11:16431370-16431420	HCT-116	colon:	n/a
30	chr11:16430247-16430297	LNCaP	prostate:	n/a
31	chr11:16431370-16431420	GM12892	blood:	n/a
32	chr11:16424708-16424758	HCPEpiC	choroid plexus:	n/a
33	chr11:16424708-16424758	BJ	skin:	n/a
34	chr11:16424708-16424758	LNCaP	prostate:	n/a
35	chr11:16430764-16430814	Hepatocyte	liver:	n/a
36	chr11:16424673-16424723	Hepatocyte	liver:	n/a
37	chr11:16431523-16431573	K562	blood:	n/a
38	chr11:16424673-16424723	MCF10A-Er-Src	breast:	n/a
39	chr11:16424935-16424985	ProgFib	skin:	n/a
40	chr11:16430247-16430297	T-47D	breast:	n/a
41	chr11:16424708-16424758	HMEC	breast:	n/a
42	chr11:16424708-16424758	HEK293	kidney:	embryo
43	chr11:16424673-16424723	U87	brain:	n/a
44	chr11:16431370-16431420	GM06990	blood:	n/a
45	chr11:16431523-16431573	RPTEC	kidney:	n/a
46	chr11:16430764-16430814	HAEpiC	amniotic membrane:	n/a
47	chr11:16424708-16424758	Hepatocyte	liver:	n/a
48	chr11:16431370-16431420	LNCaP	prostate:	n/a
49	chr11:16424935-16424985	BE2_C	brain:	n/a
50	chr11:16430247-16430297	SK-N-MC	brain:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:16415238..16417760-chr11:16419960..16422065,3	K562	blood:
2	chr11:16443168..16444876-chr11:16445251..16446841,2	K562	blood:
3	chr11:16402440..16405189-chr11:16626177..16627984,2	K562	blood:
4	chr11:16408487..16411265-chr11:16411284..16413231,2	K562	blood:
5	chr11:16391881..16394092-chr11:16627709..16630922,3	K562	blood:
6	chr11:16384106..16387046-chr11:16399381..16401065,2	K562	blood:
7	chr11:16428430..16430203-chr11:16538247..16541152,2	K562	blood:
8	chr11:16421221..16424057-chr11:16428605..16430186,2	K562	blood:
9	chr11:16421221..16424057-chr11:16428605..16430186,2	K562	blood:
10	chr11:16431065..16433163-chr11:16435913..16438616,2	K562	blood:
11	chr11:16411880..16414863-chr11:16415829..16421298,5	K562	blood:
12	chr11:16482295..16484749-chr11:16485134..16488693,3	K562	blood:
13	chr11:16389241..16392002-chr11:16405954..16407703,2	K562	blood:
14	chr11:16417809..16420055-chr11:16420290..16424235,6	K562	blood:
15	chr11:16408487..16411265-chr11:16411284..16413231,2	K562	blood:
16	chr11:16391881..16394012-chr11:16627949..16630922,2	K562	blood:
17	chr11:16460793..16462936-chr11:16464207..16467731,4	K562	blood:
18	chr11:16438021..16439726-chr11:16453871..16456445,2	K562	blood:
19	chr11:16457597..16459498-chr11:16627741..16630737,2	K562	blood:
20	chr10:14890585..14892105-chr11:16426390..16427972,2	MCF-7	breast:
21	chr11:16393645..16395882-chr11:16397951..16400592,2	K562	blood:
22	chr11:16399547..16401439-chr11:16628007..16630759,2	K562	blood:
23	chr11:16460793..16462936-chr11:16464207..16467731,4	K562	blood:
24	chr11:16393284..16394848-chr11:16402526..16404258,2	K562	blood:
25	chr11:16417840..16419695-chr11:16421289..16424235,2	K562	blood:
26	chr11:16419460..16421100-chr11:16436928..16438433,2	K562	blood:
27	chr11:16379429..16381172-chr11:16398247..16400946,3	K562	blood:
28	chr11:16399981..16401703-chr11:16417138..16418693,2	K562	blood:
29	chr11:16419460..16421100-chr11:16436928..16438433,2	K562	blood:
30	chr11:16445154..16447273-chr11:16624940..16627233,2	K562	blood:
31	chr11:16431065..16433163-chr11:16435913..16438616,2	K562	blood:
32	chr11:16378118..16380186-chr11:16404618..16407348,2	K562	blood:
33	chr11:16396650..16399546-chr11:16625547..16627427,2	K562	blood:
34	chr11:16475357..16477023-chr11:16487045..16488750,2	K562	blood:
35	chr11:16393645..16395882-chr11:16397951..16400592,2	K562	blood:
36	chr11:16415811..16418306-chr11:16427496..16429651,2	K562	blood:
37	chr11:16407671..16409392-chr11:16626901..16629555,2	K562	blood:
38	chr11:16357700..16360126-chr11:16394336..16397110,2	K562	blood:
39	chr11:16439945..16442891-chr11:16444169..16446797,2	K562	blood:
40	chr11:16482295..16484749-chr11:16485134..16488693,3	K562	blood:
41	chr11:16439945..16442891-chr11:16444169..16446797,2	K562	blood:
42	chr11:16389058..16392285-chr11:16392287..16396695,4	K562	blood:
43	chr11:16474204..16476721-chr11:16494126..16495783,2	K562	blood:
44	chr11:16490554..16493241-chr11:16624494..16627232,2	K562	blood:
45	chr11:16419446..16421077-chr11:16594061..16596211,2	K562	blood:
46	chr11:16438435..16440114-chr11:16441772..16443288,2	K562	blood:
47	chr11:16398988..16400507-chr11:16625140..16626803,2	K562	blood:
48	chr11:16428545..16430895-chr11:16628105..16630228,2	K562	blood:
49	chr11:16443168..16444876-chr11:16445251..16446841,2	K562	blood:
50	chr11:16402054..16403718-chr11:16411141..16413467,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHA7-4	chr11:16470335-16470824	NONHSAT018174
2	lnc-PLEKHA7-4	chr11:16470836-16472422	NONHSAT018174
3	lnc-PLEKHA7-3	chr11:16487328-16487363	NONHSAT018175
4	lnc-PLEKHA7-3	chr11:16487338-16487363	NONHSAT018176

No data

Variant related genes	Relation type
SOX6	TF binding region
SOX6	CpG island
ENSG00000110693	chromatin interactions

Extended variants
information (count: 3262 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3262 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78215797	chr11:16391729-16391730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs568165877	chr11:16391768-16391769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373241063	chr11:16391814-16391815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547611660	chr11:16391840-16391841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568747377	chr11:16391911-16391912	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs565820310	chr11:16391912-16391913	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539747471	chr11:16391951-16391952	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs138801778	chr11:16392024-16392025	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570478320	chr11:16392098-16392099	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs189890404	chr11:16392099-16392100	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs556189313	chr11:16392174-16392175	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs149387750	chr11:16392207-16392208	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs297328	chr11:16392216-16392217	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs144655998	chr11:16392284-16392285	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs546488759	chr11:16392368-16392369	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs564782996	chr11:16392383-16392384	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs538327884	chr11:16392389-16392390	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs543490915	chr11:16392423-16392424	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs561620555	chr11:16392459-16392460	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs556417497	chr11:16392460-16392461	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs76649594	chr11:16392545-16392546	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs571213344	chr11:16392549-16392550	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529017678	chr11:16392561-16392562	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547252374	chr11:16392705-16392706	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201200642	chr11:16392711-16392712	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs138216683	chr11:16392740-16392741	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs536029681	chr11:16392765-16392766	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs554420383	chr11:16392771-16392772	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs75305309	chr11:16392885-16392886	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs143031589	chr11:16392911-16392912	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs569617319	chr11:16392944-16392945	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs537844527	chr11:16392950-16392951	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs146157077	chr11:16392967-16392968	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs145034253	chr11:16393013-16393014	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs568441129	chr11:16393017-16393018	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs368112673	chr11:16393019-16393020	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs212445	chr11:16393020-16393021	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572559799	chr11:16393089-16393090	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs192975456	chr11:16393112-16393113	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs140197660	chr11:16393131-16393132	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576851108	chr11:16393149-16393150	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543428519	chr11:16393152-16393153	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs561750747	chr11:16393154-16393155	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs573575871	chr11:16393156-16393157	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs78193621	chr11:16393179-16393180	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs559189800	chr11:16393197-16393198	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs558518991	chr11:16393200-16393201	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532915230	chr11:16393236-16393237	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141508913	chr11:16393297-16393298	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs150889943	chr11:16393387-16393388	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD

Chromatin state (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16387800-16392000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr11:16388200-16397000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr11:16388200-16414200	Weak transcription	Fetal Intestine Small	intestine
4	chr11:16389200-16397800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:16391400-16391800	Enhancers	Aorta	Aorta
6	chr11:16391400-16391800	Enhancers	K562	blood
7	chr11:16391800-16392600	Weak transcription	K562	blood
8	chr11:16392000-16393000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr11:16392600-16393400	ZNF genes & repeats	K562	blood
10	chr11:16393400-16394000	Weak transcription	K562	blood
11	chr11:16394000-16395200	Enhancers	K562	blood
12	chr11:16395200-16395600	Weak transcription	K562	blood
13	chr11:16395600-16395800	Enhancers	K562	blood
14	chr11:16395600-16397200	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr11:16395800-16398000	Weak transcription	K562	blood
16	chr11:16396600-16396800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr11:16396800-16397800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr11:16397200-16402000	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr11:16397800-16398200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr11:16397800-16399400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr11:16398000-16398200	Enhancers	K562	blood
22	chr11:16398200-16398400	Flanking Active TSS	K562	blood
23	chr11:16398200-16403000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr11:16398400-16399800	Active TSS	K562	blood
25	chr11:16399400-16404000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr11:16399800-16400600	Weak transcription	K562	blood
27	chr11:16400600-16401000	Enhancers	Psoas Muscle	Psoas
28	chr11:16400600-16401400	Enhancers	K562	blood
29	chr11:16401400-16401800	Weak transcription	K562	blood
30	chr11:16401800-16403600	Active TSS	K562	blood
31	chr11:16402000-16403000	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr11:16402200-16403000	Enhancers	NHDF-Ad	bronchial
33	chr11:16402400-16403200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr11:16402400-16405600	Enhancers	NHLF	lung
35	chr11:16403000-16403800	Weak transcription	NHDF-Ad	bronchial
36	chr11:16403000-16404000	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr11:16403200-16403800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:16403600-16404400	Flanking Active TSS	K562	blood
39	chr11:16403800-16405200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr11:16403800-16405400	Enhancers	NHDF-Ad	bronchial
41	chr11:16404000-16404600	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr11:16404000-16405400	Enhancers	Muscle Satellite Cultured Cells	--
43	chr11:16404000-16405600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr11:16404400-16405400	Enhancers	K562	blood
45	chr11:16404600-16405000	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr11:16404600-16405200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr11:16405000-16406600	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr11:16405600-16407400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr11:16406600-16408000	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr11:16406800-16415200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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