Variant report

Variant	nsv830843
Chromosome Location	chr6:150517411-150691173
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2176)
CpG islands
(count:855)
Chromatin interactive
region (count:171)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2176 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:150641709-150642002	K562	blood:	n/a	n/a
2	ARID3A	chr6:150648358-150648558	K562	blood:	n/a	n/a
3	ARID3A	chr6:150590022-150590355	K562	blood:	n/a	n/a
4	ARID3A	chr6:150644374-150644606	K562	blood:	n/a	n/a
5	ARID3A	chr6:150550926-150551098	K562	blood:	n/a	n/a
6	ARID3A	chr6:150574162-150574536	K562	blood:	n/a	n/a
7	ARID3A	chr6:150588787-150589697	K562	blood:	n/a	n/a
8	ARID3A	chr6:150614380-150615000	K562	blood:	n/a	n/a
9	ARID3A	chr6:150654386-150654755	K562	blood:	n/a	n/a
10	ARID3A	chr6:150597304-150598299	K562	blood:	n/a	n/a
11	ARID3A	chr6:150592169-150594225	K562	blood:	n/a	n/a
12	ARID3A	chr6:150656204-150656655	K562	blood:	n/a	n/a
13	ATF1	chr6:150533907-150534169	K562	blood:	n/a	n/a
14	ATF1	chr6:150690117-150690163	K562	blood:	n/a	n/a
15	ATF1	chr6:150597401-150597785	K562	blood:	n/a	n/a
16	ATF1	chr6:150633636-150633837	K562	blood:	n/a	n/a
17	ATF1	chr6:150574127-150574496	K562	blood:	n/a	n/a
18	ATF1	chr6:150532901-150533240	K562	blood:	n/a	n/a
19	ATF1	chr6:150551014-150551230	K562	blood:	n/a	n/a
20	ATF1	chr6:150623376-150623768	K562	blood:	n/a	n/a
21	ATF1	chr6:150531022-150531027	K562	blood:	n/a	n/a
22	ATF1	chr6:150618482-150618795	K562	blood:	n/a	n/a
23	ATF1	chr6:150638926-150639223	K562	blood:	n/a	n/a
24	ATF1	chr6:150588851-150589268	K562	blood:	n/a	n/a
25	ATF1	chr6:150593903-150594397	K562	blood:	n/a	n/a
26	ATF1	chr6:150592451-150593521	K562	blood:	n/a	n/a
27	ATF1	chr6:150614623-150615231	K562	blood:	n/a	n/a
28	ATF2	chr6:150562997-150563267	GM12878	blood:	n/a	n/a
29	ATF2	chr6:150562986-150563300	GM12878	blood:	n/a	n/a
30	ATF2	chr6:150657487-150657954	GM12878	blood:	n/a	n/a
31	ATF3	chr6:150623415-150623648	K562	blood:	n/a	n/a
32	ATF3	chr6:150614470-150615109	HCT-116	colon:	n/a	n/a
33	ATF3	chr6:150614600-150614969	K562	blood:	n/a	n/a
34	ATF3	chr6:150577691-150578166	HCT-116	colon:	n/a	n/a
35	ATF3	chr6:150638827-150639224	K562	blood:	n/a	n/a
36	ATF3	chr6:150592970-150593702	K562	blood:	n/a	n/a
37	ATF3	chr6:150598882-150599149	K562	blood:	n/a	n/a
38	ATF3	chr6:150610700-150610879	K562	blood:	n/a	chr6:150610772-150610781
39	BACH1	chr6:150597658-150597664	K562	blood:	n/a	n/a
40	BACH1	chr6:150594126-150594326	K562	blood:	n/a	chr6:150594262-150594276
41	BACH1	chr6:150664992-150665189	K562	blood:	n/a	n/a
42	BACH1	chr6:150574352-150574795	K562	blood:	n/a	n/a
43	BATF	chr6:150562985-150563211	GM12878	blood:	n/a	n/a
44	BATF	chr6:150574107-150574481	GM12878	blood:	n/a	chr6:150574310-150574320 chr6:150574309-150574320
45	BATF	chr6:150657444-150657852	GM12878	blood:	n/a	n/a
46	BATF	chr6:150657445-150657910	GM12878	blood:	n/a	n/a
47	BATF	chr6:150623375-150623659	GM12878	blood:	n/a	chr6:150623523-150623534 chr6:150623524-150623534 chr6:150623541-150623552
48	BATF	chr6:150595146-150595471	GM12878	blood:	n/a	n/a
49	BATF	chr6:150569468-150569707	GM12878	blood:	n/a	n/a
50	BATF	chr6:150625697-150625938	GM12878	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150690143-150690193	SKMC	muscle:	n/a
2	chr6:150690143-150690193	SKMC	muscle:	n/a
3	chr6:150690143-150690193	PFSK-1	brain:	n/a
4	chr6:150688748-150688798	NHBE	bronchial:	n/a
5	chr6:150547954-150548004	SK-N-MC	brain:	n/a
6	chr6:150530249-150530299	U87	brain:	n/a
7	chr6:150585229-150585279	HCM	heart:	n/a
8	chr6:150551646-150551696	HPAEpiC	pulmonary alveolar:	n/a
9	chr6:150688748-150688798	CMK	blood:	n/a
10	chr6:150589148-150589198	HCF	heart:	n/a
11	chr6:150690143-150690193	U87	brain:	n/a
12	chr6:150585229-150585279	AG09319	gingival:	n/a
13	chr6:150525304-150525354	MCF-7	breast:	n/a
14	chr6:150525359-150525409	HAEpiC	amniotic membrane:	n/a
15	chr6:150690143-150690193	ovcar-3	ovarian:	n/a
16	chr6:150572395-150572445	Jurkat	blood:	n/a
17	chr6:150551646-150551696	ovcar-3	ovarian:	n/a
18	chr6:150589148-150589198	BE2_C	brain:	n/a
19	chr6:150547954-150548004	Hela-S3	cervix:	n/a
20	chr6:150572395-150572445	HCM	heart:	n/a
21	chr6:150570246-150570296	GM12878	blood:	n/a
22	chr6:150530249-150530299	HepG2	liver:	n/a
23	chr6:150551646-150551696	BE2_C	brain:	n/a
24	chr6:150570246-150570296	PANC-1	pancreas:	n/a
25	chr6:150530249-150530299	MCF10A-Er-Src	breast:	n/a
26	chr6:150525359-150525409	AG09309	skin:	n/a
27	chr6:150551646-150551696	PrEC	prostate:	n/a
28	chr6:150690143-150690193	Jurkat	blood:	n/a
29	chr6:150525304-150525354	U87	brain:	n/a
30	chr6:150551646-150551696	HEK293	kidney:	embryo
31	chr6:150551646-150551696	ECC-1	luminal epithelium:	n/a
32	chr6:150690125-150690175	GM06990	blood:	n/a
33	chr6:150585229-150585279	HUVEC	blood vessel:	n/a
34	chr6:150570246-150570296	HRCEpiC	kidney:	n/a
35	chr6:150572395-150572445	BJ	skin:	n/a
36	chr6:150524628-150524678	GM12878	blood:	n/a
37	chr6:150690143-150690193	IMR90	lung:	fetal
38	chr6:150551646-150551696	MCF-7	breast:	n/a
39	chr6:150589148-150589198	SKMC	muscle:	n/a
40	chr6:150551646-150551696	SKMC	muscle:	n/a
41	chr6:150688748-150688798	HL-60	blood:	n/a
42	chr6:150525359-150525409	HEK293	kidney:	embryo
43	chr6:150690143-150690193	HepG2	liver:	n/a
44	chr6:150530249-150530299	CMK	blood:	n/a
45	chr6:150689918-150689968	HIPEpiC	eye:	n/a
46	chr6:150690143-150690193	HUVEC	blood vessel:	n/a
47	chr6:150547954-150548004	ECC-1	luminal epithelium:	n/a
48	chr6:150525304-150525354	GM06990	blood:	n/a
49	chr6:150690143-150690193	HAEpiC	amniotic membrane:	n/a
50	chr6:150525359-150525409	K562	blood:	n/a

(count:171 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:150633237..150635111-chr6:150636965..150639804,2	MCF-7	breast:
2	chr6:150543237..150546880-chr6:150548388..150552037,4	K562	blood:
3	chr6:150572452..150574254-chr6:150575448..150578031,3	K562	blood:
4	chr6:150523335..150526077-chr6:150588121..150590622,2	MCF-7	breast:
5	chr6:150401704..150402247-chr6:150654478..150655258,3	MCF-7	breast:
6	chr6:150549533..150552708-chr6:150557386..150559321,3	K562	blood:
7	chr6:150667580..150669709-chr6:150673147..150675127,2	MCF-7	breast:
8	chr6:150401082..150403253-chr6:150656281..150658165,2	MCF-7	breast:
9	chr6:150576665..150578563-chr6:150593687..150595296,2	MCF-7	breast:
10	chr6:150544515..150547384-chr6:150552847..150554983,2	K562	blood:
11	chr6:150576665..150578563-chr6:150593687..150595296,2	MCF-7	breast:
12	chr6:150521985..150525407-chr6:150525748..150528930,3	K562	blood:
13	chr6:150463574..150465134-chr6:150531593..150533755,2	K562	blood:
14	chr6:150664294..150666420-chr6:150694752..150697036,2	MCF-7	breast:
15	chr6:150512430..150514564-chr6:150515573..150518401,3	K562	blood:
16	chr6:150401003..150402693-chr6:150655609..150656984,12	MCF-7	breast:
17	chr6:150679855..150682122-chr6:150688615..150690541,2	K562	blood:
18	chr6:150564776..150567057-chr6:150571818..150574314,2	K562	blood:
19	chr6:150598333..150600619-chr6:150603264..150605565,3	K562	blood:
20	chr6:150607126..150608753-chr6:150627355..150629999,2	K562	blood:
21	chr6:150566857..150569459-chr6:150586928..150589779,2	K562	blood:
22	chr6:150627066..150629828-chr6:150636528..150638058,2	K562	blood:
23	chr6:150590870..150594725-chr6:150600682..150606277,5	K562	blood:
24	chr6:150668412..150670441-chr6:150671071..150673551,2	K562	blood:
25	chr6:150419610..150420185-chr6:150610668..150611430,2	K562	blood:
26	chr6:150624607..150626485-chr6:150639529..150642176,2	K562	blood:
27	chr6:150638163..150639671-chr6:150643884..150646332,2	MCF-7	breast:
28	chr6:150630670..150634449-chr6:150639443..150643580,5	K562	blood:
29	chr6:150489133..150490702-chr6:150526456..150528096,2	K562	blood:
30	chr6:150632599..150634459-chr6:150636479..150638879,2	K562	blood:
31	chr6:150664117..150665830-chr6:150669653..150671786,2	K562	blood:
32	chr6:150652538..150654492-chr6:150655790..150657493,2	K562	blood:
33	chr6:150515558..150517711-chr6:150540869..150542397,2	K562	blood:
34	chr6:150400447..150403376-chr6:150651283..150654200,2	K562	blood:
35	chr6:150601201..150603369-chr6:150639907..150641803,2	MCF-7	breast:
36	chr6:150572423..150575831-chr6:150576136..150578517,3	MCF-7	breast:
37	chr6:150586437..150588677-chr6:150642579..150644863,2	K562	blood:
38	chr6:150656170..150657781-chr6:150675338..150677174,2	K562	blood:
39	chr6:150542106..150544405-chr6:150549647..150551463,2	MCF-7	breast:
40	chr6:150463460..150465300-chr6:150528363..150530339,2	K562	blood:
41	chr6:150544515..150547384-chr6:150552847..150554983,2	K562	blood:
42	chr6:150531888..150534706-chr6:150587953..150589817,2	K562	blood:
43	chr6:150549697..150551669-chr6:150591233..150592989,2	K562	blood:
44	chr6:150518298..150521152-chr6:150523437..150526060,2	K562	blood:
45	chr6:150613086..150616937-chr6:150621463..150623679,3	MCF-7	breast:
46	chr6:150674133..150675776-chr6:150694464..150696455,2	K562	blood:
47	chr6:150582199..150585734-chr6:150587276..150589096,3	K562	blood:
48	chr6:150525124..150527770-chr6:150549822..150552808,2	K562	blood:
49	chr6:150555928..150559365-chr6:150559823..150562005,4	K562	blood:
50	chr6:150548351..150551820-chr6:150552592..150556737,3	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IYD-3	chr6:150635552-150635742	l_3297_chr6:150632564-150635742_testes
2	lnc-PPP1R14C-1	chr6:150590907-150591106	XLOC_005502
3	lnc-PPP1R14C-1	chr6:150590912-150591106	NONHSAT115534
4	lnc-PPP1R14C-1	chr6:150590872-150591106	XLOC_005502
5	lnc-IYD-3	chr6:150632565-150632799	l_3297_chr6:150632564-150635742_testes
6	lnc-PPP1R14C-1	chr6:150615916-150616896	XLOC_005502
7	lnc-PPP1R14C-1	chr6:150615916-150616004	XLOC_005502
8	lnc-PPP1R14C-1	chr6:150612026-150612202	XLOC_005502
9	lnc-PPP1R14C-1	chr6:150590912-150591106	NONHSAT115535
10	lnc-PPP1R14C-1	chr6:150593859-150594048	NONHSAT115534
11	lnc-IYD-3	chr6:150657609-150657837	l_3297_chr6:150632564-150635742_testes
12	lnc-IYD-3	chr6:150668413-150668936	l_3297_chr6:150632564-150635742_testes
13	lnc-PPP1R14C-1	chr6:150626922-150627165	NONHSAT115535
14	lnc-PPP1R14C-1	chr6:150593859-150593991	XLOC_005502
15	lnc-PPP1R14C-1	chr6:150615916-150616003	NONHSAT115535

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PPP1R14C	hsa-miR-29c-3p	chr6:150571331-150571351

Variant related genes	Relation type
IYD	TF binding region
RNU4-7P	TF binding region
IYD	CpG island
RNU4-7P	CpG island
ENSG00000198729	chromatin interactions
ENSG00000009765	chromatin interactions
ENSG00000201628	chromatin interactions
ENSG00000202538	chromatin interactions
CDC27	miRNA target sites
CDC25B	miRNA target sites

Extended variants
information (count: 7071 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:7071 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs67495600	chr6:150517452-150517453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563804365	chr6:150517455-150517456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs201050764	chr6:150517456-150517457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs199915027	chr6:150517457-150517458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs397750982	chr6:150517459-150517460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138778542	chr6:150517483-150517484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552559397	chr6:150517553-150517554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs367962823	chr6:150517590-150517591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs59863369	chr6:150517602-150517603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149358825	chr6:150517617-150517618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535358865	chr6:150517631-150517632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548374401	chr6:150517640-150517641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11965489	chr6:150517647-150517648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148072070	chr6:150517675-150517676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116841317	chr6:150517693-150517694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114441336	chr6:150517701-150517702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539045387	chr6:150517746-150517747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189167850	chr6:150517753-150517754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76290012	chr6:150517810-150517811	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs116671467	chr6:150517828-150517829	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs372954911	chr6:150517837-150517838	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs561969949	chr6:150517839-150517840	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs567532519	chr6:150517846-150517847	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs575461974	chr6:150517854-150517855	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs544438365	chr6:150517870-150517871	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs191867584	chr6:150517886-150517887	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs532676074	chr6:150517943-150517944	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs182251744	chr6:150517966-150517967	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs116543761	chr6:150517987-150517988	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs528751943	chr6:150518111-150518112	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs548433887	chr6:150518223-150518224	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs568418137	chr6:150518234-150518235	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs576360379	chr6:150518236-150518237	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs537221115	chr6:150518246-150518247	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs146017365	chr6:150518271-150518272	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs570430821	chr6:150518279-150518280	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs34244559	chr6:150518322-150518323	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs527816890	chr6:150518325-150518326	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs552684359	chr6:150518370-150518371	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs566420358	chr6:150518376-150518377	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs186489592	chr6:150518385-150518386	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs572861343	chr6:150518393-150518394	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs555669750	chr6:150518395-150518396	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs148780781	chr6:150518399-150518400	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs370697016	chr6:150518439-150518440	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs375774139	chr6:150518451-150518452	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs139925957	chr6:150518453-150518454	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs574613721	chr6:150518504-150518505	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs141713275	chr6:150518505-150518506	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs546322199	chr6:150518533-150518534	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Developmental delay	21147756	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1881 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150499600-150519600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:150510600-150518000	Weak transcription	Psoas Muscle	Psoas
3	chr6:150514800-150524000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:150515000-150517800	Weak transcription	Fetal Brain Female	brain
5	chr6:150515200-150518200	Weak transcription	Right Atrium	heart
6	chr6:150515400-150519600	Weak transcription	Fetal Brain Male	brain
7	chr6:150516000-150517800	Enhancers	Fetal Heart	heart
8	chr6:150516400-150517600	Enhancers	Left Ventricle	heart
9	chr6:150516400-150518400	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr6:150516400-150519000	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr6:150516600-150518200	Enhancers	Fetal Kidney	kidney
12	chr6:150516800-150518000	Enhancers	Primary B cells from cord blood	blood
13	chr6:150516800-150518800	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr6:150516800-150518800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:150516800-150518800	Enhancers	Fetal Intestine Large	intestine
16	chr6:150516800-150518800	Enhancers	Fetal Intestine Small	intestine
17	chr6:150516800-150518800	Enhancers	Fetal Muscle Leg	muscle
18	chr6:150517000-150517600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:150517000-150517600	Enhancers	Right Ventricle	heart
20	chr6:150517000-150518000	Enhancers	Duodenum Mucosa	Duodenum
21	chr6:150517000-150518200	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr6:150517000-150518200	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr6:150517000-150518400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr6:150517000-150518600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:150517000-150518600	Enhancers	HMEC	breast
26	chr6:150517000-150518600	Enhancers	NHEK	skin
27	chr6:150517000-150519000	Enhancers	Colonic Mucosa	Colon
28	chr6:150517200-150517600	Enhancers	Primary B cells from peripheral blood	blood
29	chr6:150517200-150518200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:150517200-150518200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr6:150517200-150518200	Enhancers	Fetal Lung	lung
32	chr6:150517200-150518200	Weak transcription	Fetal Muscle Trunk	muscle
33	chr6:150517200-150518200	Weak transcription	Lung	lung
34	chr6:150517200-150518200	Weak transcription	Pancreas	Pancrea
35	chr6:150517200-150518200	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr6:150517200-150518200	Enhancers	Stomach Mucosa	stomach
37	chr6:150517200-150518400	Enhancers	Esophagus	oesophagus
38	chr6:150517200-150518400	Enhancers	Rectal Smooth Muscle	rectum
39	chr6:150517400-150518400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr6:150517400-150518400	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr6:150517400-150519000	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr6:150517400-150519800	Weak transcription	K562	blood
43	chr6:150517600-150517800	Enhancers	Osteobl	bone
44	chr6:150517600-150518000	Weak transcription	Left Ventricle	heart
45	chr6:150517600-150518000	Weak transcription	Right Ventricle	heart
46	chr6:150517600-150529200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:150517800-150518200	Flanking Active TSS	Fetal Heart	heart
48	chr6:150517800-150518600	Enhancers	Fetal Brain Female	brain
49	chr6:150518000-150518200	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr6:150518000-150518400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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