Variant report

Variant	nsv1026951
Chromosome Location	chr7:39429036-39642261
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2655)
CpG islands
(count:2016)
Chromatin interactive
region (count:87)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2655 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:39528586-39528662	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:39559568-39560308	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:39629196-39629849	K562	blood:	n/a	n/a
4	ARID3A	chr7:39559554-39559774	K562	blood:	n/a	n/a
5	ARID3A	chr7:39619920-39620322	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:39504617-39504923	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:39605696-39606077	HepG2	liver:	n/a	n/a
8	ATF1	chr7:39620042-39620358	K562	blood:	n/a	n/a
9	ATF1	chr7:39544575-39544759	K562	blood:	n/a	n/a
10	ATF1	chr7:39629296-39629800	K562	blood:	n/a	n/a
11	ATF2	chr7:39605695-39606255	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:39629214-39629775	GM12878	blood:	n/a	n/a
13	ATF2	chr7:39629257-39629794	GM12878	blood:	n/a	n/a
14	ATF2	chr7:39620059-39620415	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr7:39629296-39629758	K562	blood:	n/a	n/a
16	ATF3	chr7:39629324-39629589	K562	blood:	n/a	n/a
17	BACH1	chr7:39431848-39432018	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:39623626-39623709	K562	blood:	n/a	n/a
19	BACH1	chr7:39460082-39460104	K562	blood:	n/a	n/a
20	BACH1	chr7:39504575-39505029	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:39504641-39505056	K562	blood:	n/a	n/a
22	BACH1	chr7:39453441-39454296	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:39605695-39606256	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:39605642-39605702	K562	blood:	n/a	n/a
25	BATF	chr7:39629280-39629727	GM12878	blood:	n/a	chr7:39629520-39629531
26	BATF	chr7:39629347-39629718	GM12878	blood:	n/a	chr7:39629520-39629531
27	BATF	chr7:39504633-39504960	GM12878	blood:	n/a	n/a
28	BATF	chr7:39504666-39504886	GM12878	blood:	n/a	n/a
29	BATF	chr7:39431880-39432090	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:39629238-39629667	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:39629312-39629663	GM12878	blood:	n/a	n/a
32	BCL3	chr7:39605532-39606336	A549	lung:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
33	BCL3	chr7:39629295-39629695	GM12878	blood:	n/a	n/a
34	BCL3	chr7:39556282-39556573	GM12878	blood:	n/a	n/a
35	BCLAF1	chr7:39605736-39606198	K562	blood:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
36	BCLAF1	chr7:39605624-39606257	GM12878	blood:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
37	BCLAF1	chr7:39605565-39606356	GM12878	blood:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
38	BHLHE40	chr7:39555294-39555818	K562	blood:	n/a	n/a
39	BHLHE40	chr7:39605270-39606262	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:39620025-39620413	HepG2	liver:	n/a	n/a
41	BHLHE40	chr7:39446015-39446266	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:39556351-39556520	K562	blood:	n/a	n/a
43	BHLHE40	chr7:39605211-39606254	K562	blood:	n/a	n/a
44	BHLHE40	chr7:39629275-39629703	K562	blood:	n/a	n/a
45	BHLHE40	chr7:39559598-39559764	GM12878	blood:	n/a	n/a
46	BHLHE40	chr7:39620025-39620654	GM12878	blood:	n/a	n/a
47	BHLHE40	chr7:39629250-39629748	GM12878	blood:	n/a	n/a
48	BHLHE40	chr7:39619986-39620611	K562	blood:	n/a	n/a
49	BHLHE40	chr7:39453754-39454208	GM12878	blood:	n/a	chr7:39454190-39454206
50	BHLHE40	chr7:39559617-39559759	K562	blood:	n/a	n/a

(count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:39503619-39503669	U87	brain:	n/a
2	chr7:39606965-39607015	GM12891	blood:	n/a
3	chr7:39454310-39454360	GM06990	blood:	n/a
4	chr7:39503619-39503669	U87	brain:	n/a
5	chr7:39606965-39607015	GM12891	blood:	n/a
6	chr7:39454310-39454360	GM06990	blood:	n/a
7	chr7:39453784-39453834	NB4	blood:	n/a
8	chr7:39606002-39606052	AoSMC	blood vessel:	n/a
9	chr7:39605777-39605827	HCPEpiC	choroid plexus:	n/a
10	chr7:39605805-39605855	SK-N-SH_RA	brain:	n/a
11	chr7:39612363-39612413	AG04449	skin:	fetal
12	chr7:39450193-39450243	A549	lung:	n/a
13	chr7:39606013-39606063	HCM	heart:	n/a
14	chr7:39454310-39454360	BJ	skin:	n/a
15	chr7:39454310-39454360	AG09319	gingival:	n/a
16	chr7:39453532-39453582	MCF10A-Er-Src	breast:	n/a
17	chr7:39605536-39605586	ProgFib	skin:	n/a
18	chr7:39453784-39453834	SK-N-MC	brain:	n/a
19	chr7:39446909-39446959	HNPCEpiC	eye:	n/a
20	chr7:39629290-39629340	AG04449	skin:	fetal
21	chr7:39606002-39606052	NB4	blood:	n/a
22	chr7:39605790-39605840	AG09319	gingival:	n/a
23	chr7:39453625-39453675	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:39629290-39629340	AG10803	skin:	n/a
25	chr7:39606071-39606121	NT2-D1	testis:	n/a
26	chr7:39609343-39609393	GM19239	blood:	n/a
27	chr7:39453784-39453834	NHDF-neo	bronchial:	n/a
28	chr7:39454090-39454140	PFSK-1	brain:	n/a
29	chr7:39453784-39453834	HNPCEpiC	eye:	n/a
30	chr7:39453532-39453582	Caco-2	colon:	n/a
31	chr7:39450193-39450243	HEK293	kidney:	embryo
32	chr7:39605683-39605733	Hepatocyte	liver:	n/a
33	chr7:39472716-39472766	PFSK-1	brain:	n/a
34	chr7:39453784-39453834	HRCEpiC	kidney:	n/a
35	chr7:39605805-39605855	IMR90	lung:	fetal
36	chr7:39605790-39605840	SK-N-MC	brain:	n/a
37	chr7:39612363-39612413	SKMC	muscle:	n/a
38	chr7:39457814-39457864	HEK293	kidney:	embryo
39	chr7:39500223-39500273	NH-A	brain:	n/a
40	chr7:39472716-39472766	U87	brain:	n/a
41	chr7:39605996-39606046	HUVEC	blood vessel:	n/a
42	chr7:39605536-39605586	PANC-1	pancreas:	n/a
43	chr7:39609343-39609393	U87	brain:	n/a
44	chr7:39446909-39446959	NB4	blood:	n/a
45	chr7:39454090-39454140	A549	lung:	n/a
46	chr7:39605683-39605733	HNPCEpiC	eye:	n/a
47	chr7:39454310-39454360	NT2-D1	testis:	n/a
48	chr7:39606013-39606063	GM12878	blood:	n/a
49	chr7:39450193-39450243	HRPEpiC	eye:	n/a
50	chr7:39612363-39612413	PrEC	prostate:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:39638996..39641307-chr7:39643111..39644755,2	K562	blood:
2	chr7:39581559..39584136-chr7:39585096..39587437,2	K562	blood:
3	chr7:39620205..39622227-chr7:39661483..39663721,3	K562	blood:
4	chr7:38836355..38837155-chr7:39503792..39504917,3	MCF-7	breast:
5	chr7:39440359..39443090-chr7:39454354..39455934,2	K562	blood:
6	chr7:39612446..39614989-chr7:39616627..39618783,2	MCF-7	breast:
7	chr7:39493099..39494043-chr7:39559206..39560190,4	MCF-7	breast:
8	chr7:39538705..39540633-chr7:39541459..39543564,2	K562	blood:
9	chr7:39619664..39620687-chr7:39782996..39783915,3	K562	blood:
10	chr7:39619675..39620675-chr7:39785462..39786424,9	MCF-7	breast:
11	chr7:39635799..39637643-chr7:39637768..39639590,2	MCF-7	breast:
12	chr7:39620191..39622665-chr7:39628141..39629776,2	K562	blood:
13	chr7:39573042..39574543-chr7:39580412..39582259,2	K562	blood:
14	chr7:39493116..39494045-chr7:39504502..39505143,2	K562	blood:
15	chr7:39597542..39600192-chr7:39605435..39607184,2	MCF-7	breast:
16	chr7:39612446..39614989-chr7:39616627..39618783,2	MCF-7	breast:
17	chr7:39559251..39560178-chr7:39581010..39581845,2	K562	blood:
18	chr7:39632294..39634662-chr7:39653376..39655988,2	K562	blood:
19	chr7:39620146..39620721-chr7:39781543..39782233,2	MCF-7	breast:
20	chr7:39609139..39613691-chr7:39613860..39617111,6	K562	blood:
21	chr7:39432032..39434536-chr7:39435628..39438240,2	K562	blood:
22	chr7:39635799..39637643-chr7:39637768..39639590,2	MCF-7	breast:
23	chr7:39581559..39584136-chr7:39585096..39587437,2	K562	blood:
24	chr7:39573042..39574543-chr7:39580412..39582259,2	K562	blood:
25	chr7:39619647..39620204-chr7:40092201..40092766,2	K562	blood:
26	chr7:38836202..38837177-chr7:39504337..39505154,4	K562	blood:
27	chr7:39606078..39608053-chr7:39609216..39613025,4	MCF-7	breast:
28	chr7:39595139..39597686-chr7:39605135..39607425,2	K562	blood:
29	chr7:38944229..38945857-chr7:39522828..39525500,2	K562	blood:
30	chr7:39617765..39620727-chr7:39709688..39712417,2	K562	blood:
31	chr7:39640592..39642673-chr7:39644409..39647009,2	K562	blood:
32	chr7:39604590..39607851-chr7:39609967..39614867,7	K562	blood:
33	chr7:39498982..39501819-chr7:39501974..39504808,2	K562	blood:
34	chr7:39597430..39600567-chr7:39603197..39606224,3	MCF-7	breast:
35	chr7:39619917..39620450-chr7:39831240..39831746,2	K562	blood:
36	chr7:39621618..39625232-chr7:39625771..39627613,3	K562	blood:
37	chr7:39575609..39577326-chr7:39580919..39582737,2	MCF-7	breast:
38	chr7:39630501..39633434-chr7:39759020..39762831,5	K562	blood:
39	chr7:39634741..39636459-chr7:39661820..39664615,2	K562	blood:
40	chr7:39623431..39626186-chr7:39627006..39629338,2	MCF-7	breast:
41	chr7:39638958..39641769-chr7:39651985..39654836,2	K562	blood:
42	chr7:39424668..39427286-chr7:39432218..39433755,2	MCF-7	breast:
43	chr7:39492607..39495001-chr7:39495505..39498185,2	K562	blood:
44	chr7:39619733..39620697-chr7:39781534..39782496,5	K562	blood:
45	chr7:39440359..39443090-chr7:39454354..39455934,2	K562	blood:
46	chr7:39493099..39494043-chr7:39559206..39560190,4	MCF-7	breast:
47	chr7:39619358..39620673-chr7:39785487..39786442,10	K562	blood:
48	chr7:39604710..39608797-chr7:39663149..39665225,4	K562	blood:
49	chr7:39605969..39608430-chr7:39663149..39665540,3	K562	blood:
50	chr7:39492607..39495001-chr7:39495505..39498185,2	K562	blood:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VPS41-2	chr7:39444526-39444604	ENSG00000224122.1
2	lnc-C7orf11-7	chr7:39585249-39585492	XLOC_006414
3	lnc-VPS41-2	chr7:39445933-39445945	NR_046711
4	lnc-POU6F2-1	chr7:39504691-39504775	NONHSAT120203
5	lnc-RALA-3	chr7:39622404-39622930	NONHSAT120209
6	lnc-VPS41-2	chr7:39445616-39445728	NONHSAT120202
7	lnc-VPS41-2	chr7:39444198-39444382	NR_046711
8	lnc-VPS41-2	chr7:39444526-39444604	NONHSAT120202
9	lnc-VPS41-2	chr7:39444197-39444382	ENSG00000224122.1
10	lnc-C7orf11-14	chr7:39608975-39609797	NONHSAT120207
11	lnc-C7orf11-7	chr7:39605742-39605943	XLOC_006414
12	lnc-C7orf11-7	chr7:39585245-39585492	ENSG00000227172.2
13	lnc-POU6F2-1	chr7:39510687-39510841	NONHSAT120203
14	lnc-VPS41-2	chr7:39445933-39445945	ENSG00000224122.1
15	lnc-VPS41-2	chr7:39446035-39446111	NONHSAT120202
16	lnc-C7orf11-7	chr7:39605742-39605838	XLOC_006414
17	lnc-VPS41-2	chr7:39445616-39445718	ENSG00000224122.1
18	lnc-VPS41-2	chr7:39444526-39444604	NR_046711
19	lnc-C7orf11-7	chr7:39605742-39605838	ENSG00000227172.2
20	lnc-POU6F2-1	chr7:39532643-39532694	NONHSAT120203
21	lnc-C7orf11-7	chr7:39593494-39593543	XLOC_006414
22	lnc-C7orf11-7	chr7:39593475-39593543	XLOC_006414
23	lnc-C7orf11-7	chr7:39593475-39593543	ENSG00000227172.2
24	lnc-VPS41-2	chr7:39445616-39445718	NR_046711
25	lnc-POU6F2-1	chr7:39529969-39530208	NONHSAT120203
26	lnc-VPS41-2	chr7:39444343-39444382	NONHSAT120202

No data

Variant related genes	Relation type
YAE1D1	TF binding region
POU6F2-AS1	TF binding region
POU6F2	TF binding region
ENSG00000236015	TF binding region
ENSG00000227172	TF binding region
YAE1D1	CpG island
POU6F2-AS1	CpG island
POU6F2	CpG island
ENSG00000236015	CpG island
ENSG00000227172	CpG island
ENSG00000106536	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000236015	chromatin interactions
ENSG00000227172	chromatin interactions
ENSG00000006715	chromatin interactions
ENSG00000188185	chromatin interactions
ENSG00000241127	chromatin interactions
ENSG00000006451	chromatin interactions
ENSG00000202538	chromatin interactions

Extended variants
information (count: 6859 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:6859 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17686887	chr7:39429036-39429037	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534562310	chr7:39429110-39429111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553446791	chr7:39429116-39429117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557620290	chr7:39429121-39429122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564175585	chr7:39429127-39429128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536618465	chr7:39429129-39429130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528380213	chr7:39429160-39429161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574885670	chr7:39429220-39429221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150781101	chr7:39429257-39429258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555949173	chr7:39429269-39429270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs28538843	chr7:39429337-39429338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572667563	chr7:39429351-39429352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369200497	chr7:39429352-39429353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs77215424	chr7:39429379-39429380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542341145	chr7:39429389-39429390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191410812	chr7:39429433-39429434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs41402647	chr7:39429482-39429483	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs543419512	chr7:39429518-39429519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563829033	chr7:39429537-39429538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371344933	chr7:39429625-39429626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375780764	chr7:39429639-39429640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs77418101	chr7:39429644-39429645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183179600	chr7:39429647-39429648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559160621	chr7:39429657-39429658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139751200	chr7:39429666-39429667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374543038	chr7:39429671-39429672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551289108	chr7:39429680-39429681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571433789	chr7:39429697-39429698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537064207	chr7:39429768-39429769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576206412	chr7:39429833-39429834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115631230	chr7:39429910-39429911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370117078	chr7:39429919-39429920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567358411	chr7:39429931-39429932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187777759	chr7:39429973-39429974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191315018	chr7:39430074-39430075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572707682	chr7:39430079-39430080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372993658	chr7:39430088-39430089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183848291	chr7:39430107-39430108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187719640	chr7:39430148-39430149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540192579	chr7:39430198-39430199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149810394	chr7:39430205-39430206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563497356	chr7:39430243-39430244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573685992	chr7:39430252-39430253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192521765	chr7:39430282-39430283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62455938	chr7:39430342-39430343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559398154	chr7:39430344-39430345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73125530	chr7:39430360-39430361	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs77526124	chr7:39430390-39430391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565206185	chr7:39430411-39430412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185264800	chr7:39430412-39430413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2247 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39426000-39432800	Weak transcription	Fetal Muscle Leg	muscle
2	chr7:39431400-39431600	Enhancers	Fetal Muscle Trunk	muscle
3	chr7:39431800-39432200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr7:39431800-39432200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr7:39431800-39432400	Enhancers	Fetal Stomach	stomach
6	chr7:39431800-39432600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr7:39431800-39432800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr7:39432000-39432200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr7:39432000-39432400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr7:39432000-39432400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr7:39432000-39432400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:39432000-39432400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:39432000-39432400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:39432000-39433200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:39432400-39434000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:39432400-39434000	Weak transcription	Fetal Stomach	stomach
17	chr7:39432400-39439600	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr7:39432400-39439800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr7:39432800-39433200	Enhancers	Fetal Muscle Leg	muscle
20	chr7:39432800-39433200	Enhancers	HSMMtube	muscle
21	chr7:39433200-39434400	Weak transcription	HSMMtube	muscle
22	chr7:39433200-39439400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr7:39434000-39434200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:39434000-39434200	Enhancers	Fetal Stomach	stomach
25	chr7:39434000-39438800	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr7:39434200-39434400	Enhancers	Fetal Kidney	kidney
27	chr7:39434400-39434600	Enhancers	HSMMtube	muscle
28	chr7:39436200-39436400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr7:39436200-39436800	Enhancers	HSMMtube	muscle
30	chr7:39436400-39445400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:39437600-39446000	Weak transcription	Pancreas	Pancrea
32	chr7:39438800-39441000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr7:39439400-39441200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr7:39439600-39440200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr7:39439600-39440600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:39439600-39440800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr7:39439600-39440800	Enhancers	H1 Cell Line	embryonic stem cell
38	chr7:39439600-39440800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr7:39439600-39441600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr7:39439800-39440000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:39439800-39441000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr7:39439800-39441000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr7:39439800-39441400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:39440000-39440800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr7:39440200-39446000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr7:39440400-39440800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr7:39440600-39440800	Enhancers	Right Atrium	heart
48	chr7:39440600-39441800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr7:39440800-39446000	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr7:39441000-39446000	Weak transcription	H9 Cell Line	embryonic stem cell

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