Variant report

Variant	nsv538658
Chromosome Location	chr7:3141609-3311344
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1552)
CpG islands
(count:1525)
Chromatin interactive
region (count:80)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1552 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3284072-3284298	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:3234233-3234865	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:3186430-3186815	K562	blood:	n/a	n/a
4	ARID3A	chr7:3221006-3221355	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:3203948-3204296	HepG2	liver:	n/a	n/a
6	ATF1	chr7:3174282-3174626	K562	blood:	n/a	n/a
7	ATF2	chr7:3234272-3234806	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr7:3234177-3234810	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:3234182-3234735	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:3186439-3186846	K562	blood:	n/a	n/a
11	BACH1	chr7:3186456-3186829	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:3240149-3240409	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr7:3290428-3290814	GM12878	blood:	n/a	n/a
14	BATF	chr7:3146117-3146438	GM12878	blood:	n/a	n/a
15	BATF	chr7:3290378-3290743	GM12878	blood:	n/a	n/a
16	BATF	chr7:3192746-3193040	GM12878	blood:	n/a	chr7:3192912-3192923
17	BATF	chr7:3146112-3146482	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:3290486-3290751	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:3192760-3193070	GM12878	blood:	n/a	chr7:3192915-3192924 chr7:3192916-3192925
20	BCL11A	chr7:3192749-3193044	GM12878	blood:	n/a	chr7:3192915-3192924 chr7:3192916-3192925
21	BCL3	chr7:3220998-3221446	GM12878	blood:	n/a	n/a
22	BCL3	chr7:3221093-3221491	GM12878	blood:	n/a	n/a
23	BCL3	chr7:3234202-3234797	A549	lung:	n/a	n/a
24	BCL3	chr7:3146180-3146433	GM12878	blood:	n/a	n/a
25	BCLAF1	chr7:3194415-3194858	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:3216612-3216813	K562	blood:	n/a	n/a
27	BHLHE40	chr7:3186430-3186949	K562	blood:	n/a	n/a
28	BHLHE40	chr7:3168549-3168710	K562	blood:	n/a	chr7:3168685-3168694 chr7:3168679-3168700 chr7:3168683-3168696 chr7:3168686-3168695 chr7:3168685-3168694
29	BHLHE40	chr7:3307547-3307725	A549	lung:	n/a	n/a
30	BRCA1	chr7:3191484-3191701	GM12878	blood:	n/a	n/a
31	CCNT2	chr7:3186464-3186878	K562	blood:	n/a	chr7:3186464-3186473
32	CEBPB	chr7:3253678-3254005	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:3258481-3258795	HepG2	liver:	n/a	chr7:3258619-3258630
34	CEBPB	chr7:3255447-3256238	MCF-7	breast:	n/a	n/a
35	CEBPB	chr7:3153488-3153627	A549	lung:	n/a	chr7:3153567-3153578
36	CEBPB	chr7:3220965-3221379	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:3253634-3254152	A549	lung:	n/a	n/a
38	CEBPB	chr7:3186997-3187012	K562	blood:	n/a	n/a
39	CEBPB	chr7:3234322-3234665	A549	lung:	n/a	n/a
40	CEBPB	chr7:3253684-3254018	A549	lung:	n/a	n/a
41	CEBPB	chr7:3186407-3186786	K562	blood:	n/a	n/a
42	CEBPB	chr7:3298729-3298994	HepG2	liver:	n/a	chr7:3298896-3298907
43	CEBPB	chr7:3234293-3234711	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr7:3234300-3234711	A549	lung:	n/a	n/a
45	CEBPB	chr7:3253677-3254027	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr7:3234205-3234712	HepG2	liver:	n/a	n/a
47	CEBPB	chr7:3148437-3149086	MCF-7	breast:	n/a	n/a
48	CEBPB	chr7:3253683-3254028	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr7:3298853-3298916	IMR90	lung:	n/a	chr7:3298896-3298907
50	CEBPB	chr7:3253766-3254022	K562	blood:	n/a	n/a

(count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3215287-3215337	GM06990	blood:	n/a
2	chr7:3157722-3157772	HCPEpiC	choroid plexus:	n/a
3	chr7:3227332-3227382	AG04450	lung:	fetal
4	chr7:3234697-3234747	HIPEpiC	eye:	n/a
5	chr7:3214400-3214450	SK-N-SH_RA	brain:	n/a
6	chr7:3280545-3280595	AG04450	lung:	fetal
7	chr7:3221150-3221200	H1-hESC	embryonic stem cell:	embryo
8	chr7:3258347-3258397	AoSMC	blood vessel:	n/a
9	chr7:3221228-3221278	HEEpiC	esophagus:	n/a
10	chr7:3221150-3221200	A549	lung:	n/a
11	chr7:3186788-3186838	H1-hESC	embryonic stem cell:	embryo
12	chr7:3280668-3280718	ovcar-3	ovarian:	n/a
13	chr7:3284394-3284444	NH-A	brain:	n/a
14	chr7:3280545-3280595	ProgFib	skin:	n/a
15	chr7:3227277-3227327	GM19239	blood:	n/a
16	chr7:3258347-3258397	SAEC	small airway:	n/a
17	chr7:3157722-3157772	T-47D	breast:	n/a
18	chr7:3214289-3214339	IMR90	lung:	fetal
19	chr7:3221228-3221278	HCPEpiC	choroid plexus:	n/a
20	chr7:3284394-3284444	SAEC	small airway:	n/a
21	chr7:3186788-3186838	PFSK-1	brain:	n/a
22	chr7:3186766-3186816	AoSMC	blood vessel:	n/a
23	chr7:3207719-3207769	BJ	skin:	n/a
24	chr7:3186788-3186838	SKMC	muscle:	n/a
25	chr7:3221150-3221200	AG04450	lung:	fetal
26	chr7:3208793-3208843	ECC-1	luminal epithelium:	n/a
27	chr7:3175091-3175141	NB4	blood:	n/a
28	chr7:3208493-3208543	GM12878	blood:	n/a
29	chr7:3227332-3227382	PFSK-1	brain:	n/a
30	chr7:3186788-3186838	BE2_C	brain:	n/a
31	chr7:3227277-3227327	A549	lung:	n/a
32	chr7:3186788-3186838	HAEpiC	amniotic membrane:	n/a
33	chr7:3280545-3280595	HMEC	breast:	n/a
34	chr7:3214289-3214339	HRCEpiC	kidney:	n/a
35	chr7:3214289-3214339	SAEC	small airway:	n/a
36	chr7:3215287-3215337	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:3227277-3227327	HRCEpiC	kidney:	n/a
38	chr7:3227277-3227327	CMK	blood:	n/a
39	chr7:3256369-3256419	HCF	heart:	n/a
40	chr7:3280668-3280718	HEEpiC	esophagus:	n/a
41	chr7:3227262-3227312	GM19239	blood:	n/a
42	chr7:3284394-3284444	Caco-2	colon:	n/a
43	chr7:3280668-3280718	AG09309	skin:	n/a
44	chr7:3221373-3221423	Hepatocyte	liver:	n/a
45	chr7:3215543-3215593	SK-N-MC	brain:	n/a
46	chr7:3280646-3280696	HEK293	kidney:	embryo
47	chr7:3258347-3258397	HUVEC	blood vessel:	n/a
48	chr7:3280646-3280696	HAEpiC	amniotic membrane:	n/a
49	chr7:3221228-3221278	K562	blood:	n/a
50	chr7:3280646-3280696	HCM	heart:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:3272491..3276076-chr7:3339000..3342579,3	MCF-7	breast:
2	chr7:3254337..3257238-chr7:3340637..3342323,2	MCF-7	breast:
3	chr7:3205607..3207977-chr7:3220687..3223407,2	K562	blood:
4	chr7:3255528..3257837-chr7:3259945..3262892,2	MCF-7	breast:
5	chr7:3254376..3256017-chr7:3281440..3283827,2	MCF-7	breast:
6	chr7:2913057..2915172-chr7:3198284..3201204,2	MCF-7	breast:
7	chr7:3184853..3186673-chr7:3189363..3191376,2	K562	blood:
8	chr7:2710484..2711053-chr7:3194317..3194955,2	K562	blood:
9	chr7:3148059..3150534-chr7:3151006..3152602,2	K562	blood:
10	chr7:3105046..3105933-chr7:3194248..3194999,3	K562	blood:
11	chr7:2921568..2923869-chr7:3228214..3231115,2	MCF-7	breast:
12	chr7:3149067..3151848-chr7:3153141..3155558,2	K562	blood:
13	chr7:3154011..3155575-chr7:3158921..3161053,2	K562	blood:
14	chr7:3249846..3250536-chr7:3341685..3342449,3	MCF-7	breast:
15	chr7:3104998..3105685-chr7:3239854..3240733,2	MCF-7	breast:
16	chr7:2926533..2927268-chr7:3239915..3240463,3	MCF-7	breast:
17	chr7:3284325..3287180-chr7:3291361..3294316,3	MCF-7	breast:
18	chr7:3250247..3250807-chr7:3340190..3341077,3	MCF-7	breast:
19	chr7:3240198..3242825-chr7:3445733..3447901,2	K562	blood:
20	chr7:3140254..3142201-chr7:3143047..3144954,2	MCF-7	breast:
21	chr7:3227729..3230209-chr7:3232264..3234725,2	MCF-7	breast:
22	chr7:3278324..3280048-chr7:3280557..3282668,2	K562	blood:
23	chr7:3253620..3255788-chr7:3339992..3342861,2	MCF-7	breast:
24	chr7:3148059..3150534-chr7:3151006..3152602,2	K562	blood:
25	chr7:3283973..3284780-chr7:3307461..3308331,2	MCF-7	breast:
26	chr7:3196705..3199377-chr7:3282005..3284080,2	MCF-7	breast:
27	chr7:3254030..3256348-chr7:3338235..3340171,2	MCF-7	breast:
28	chr7:3276084..3280543-chr7:3282350..3285635,4	MCF-7	breast:
29	chr7:3255932..3258041-chr7:3261586..3263750,2	MCF-7	breast:
30	chr7:3256947..3259532-chr7:3270807..3273199,2	MCF-7	breast:
31	chr7:2912750..2915143-chr7:3228683..3231010,3	MCF-7	breast:
32	chr7:2914055..2915867-chr7:3204506..3206043,2	MCF-7	breast:
33	chr7:3278981..3281763-chr7:3282187..3285186,3	K562	blood:
34	chr7:3278324..3280048-chr7:3280557..3282668,2	K562	blood:
35	chr7:3251471..3253553-chr7:3281258..3284246,2	MCF-7	breast:
36	chr7:2915975..2917721-chr7:3231286..3232804,2	MCF-7	breast:
37	chr7:3278981..3281763-chr7:3282187..3285186,3	K562	blood:
38	chr7:3256947..3259532-chr7:3270807..3273199,2	MCF-7	breast:
39	chr7:3149067..3151848-chr7:3153141..3155558,2	K562	blood:
40	chr11:108535309..108536048-chr7:3168253..3168776,2	HCT-116	colon:
41	chr7:3153512..3155575-chr7:3157437..3160421,2	K562	blood:
42	chr7:3201417..3202351-chr7:3240242..3240878,3	MCF-7	breast:
43	chr7:2926249..2926927-chr7:3240062..3240775,2	MCF-7	breast:
44	chr7:3153512..3155575-chr7:3157437..3160421,2	K562	blood:
45	chr7:3201417..3202351-chr7:3240242..3240878,3	MCF-7	breast:
46	chr7:3172781..3176010-chr7:3179517..3182340,3	K562	blood:
47	chr7:3255775..3258559-chr7:3276222..3279313,3	MCF-7	breast:
48	chr7:3140254..3142201-chr7:3143047..3144954,2	MCF-7	breast:
49	chr7:3254376..3256017-chr7:3281440..3283827,2	MCF-7	breast:
50	chr7:3194262..3194922-chr7:3439333..3439841,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC091801.1.1-1	chr7:3214230-3214287	XLOC_006339
2	lnc-AC091801.1.1-2	chr7:3233737-3234256	XLOC_006340
3	lnc-AC091801.1.1-1	chr7:3205664-3205764	NONHSAT118844
4	lnc-AC091801.1.1-8	chr7:3172190-3172290	ucscGeneNc_uc003smw_1
5	lnc-AC091801.1.1-1	chr7:3186629-3186905	NONHSAT118844
6	lnc-AC091801.1.1-1	chr7:3214230-3214287	NONHSAT118844
7	lnc-AC091801.1.1-4	chr7:3242576-3242787	XLOC_006342
8	lnc-AC091801.1.1-1	chr7:3179828-3179930	XLOC_006339
9	lnc-AC091801.1.1-8	chr7:3180756-3180813	ucscGeneNc_uc003smw_1
10	lnc-AC091801.1.1-8	chr7:3153155-3153431	ucscGeneNc_uc003smw_1
11	lnc-AC091801.1.1-1	chr7:3197771-3197975	XLOC_006339
12	lnc-AC091801.1.1-2	chr7:3234354-3234428	XLOC_006340
13	lnc-AC091801.1.1-4	chr7:3243575-3243666	XLOC_006342
14	lnc-CARD11-4	chr7:3204171-3204221	NONHSAT118845
15	lnc-AC091801.1.1-8	chr7:3164297-3164414	ucscGeneNc_uc003smw_1
16	lnc-AC091801.1.1-6	chr7:3303664-3304421	ENSG00000236708.1
17	lnc-AC091801.1.1-1	chr7:3197771-3197888	XLOC_006339
18	lnc-CARD11-4	chr7:3204353-3204414	NONHSAT118845
19	lnc-AC091801.1.1-1	chr7:3205664-3205764	XLOC_006339
20	lnc-AC091801.1.1-5	chr7:3157609-3157650	XLOC_006338
21	lnc-CARD11-4	chr7:3202784-3203088	NONHSAT118845
22	lnc-AC091801.1.1-1	chr7:3186629-3186905	XLOC_006339

No data

Variant related genes	Relation type
ENSG00000217455	TF binding region
ENSG00000231892	TF binding region
ENSG00000217455	CpG island
ENSG00000231892	CpG island
ENSG00000178105	chromatin interactions
ENSG00000236708	chromatin interactions
ENSG00000146555	chromatin interactions
ENSG00000217455	chromatin interactions
HIPK3	miRNA target sites

Extended variants
information (count: 9072 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:9072 , 50 per page) page: 1 2 3 4 5 6 7 ... 182

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571075955	chr7:3141656-3141657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577922000	chr7:3141666-3141667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548631471	chr7:3141667-3141668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540263490	chr7:3141688-3141689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs117933630	chr7:3141704-3141705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527842743	chr7:3141740-3141741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6461836	chr7:3141756-3141757	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs543373102	chr7:3141866-3141867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150483288	chr7:3141885-3141886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192182196	chr7:3141906-3141907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545087560	chr7:3141907-3141908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138352202	chr7:3141920-3141921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6945364	chr7:3141983-3141984	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs569912300	chr7:3141985-3141986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs118172470	chr7:3141987-3141988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529917152	chr7:3142010-3142011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149216379	chr7:3142021-3142022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146846782	chr7:3142051-3142052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566763215	chr7:3142054-3142055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538449309	chr7:3142055-3142056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552000433	chr7:3142062-3142063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs56763759	chr7:3142095-3142096	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs183977626	chr7:3142100-3142101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6461838	chr7:3142104-3142105	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs574001051	chr7:3142109-3142110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536912358	chr7:3142111-3142112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537390974	chr7:3142122-3142123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78659352	chr7:3142126-3142127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545615824	chr7:3142145-3142146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4719791	chr7:3142158-3142159	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs572022153	chr7:3142178-3142179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541141557	chr7:3142194-3142195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560684867	chr7:3142199-3142200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4719792	chr7:3142211-3142212	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs549618077	chr7:3142217-3142218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563239355	chr7:3142218-3142219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13238433	chr7:3142220-3142221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552070922	chr7:3142225-3142226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558810522	chr7:3142236-3142237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112056242	chr7:3142268-3142269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534009629	chr7:3142274-3142275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547886561	chr7:3142295-3142296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35704239	chr7:3142307-3142308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577596250	chr7:3142314-3142315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536652934	chr7:3142315-3142316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556642680	chr7:3142324-3142325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181389768	chr7:3142334-3142335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539377352	chr7:3142347-3142348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370719101	chr7:3142354-3142355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs57248180	chr7:3142415-3142416	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD

Chromatin state (count:1205 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3136400-3141800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:3136400-3145600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr7:3136800-3142000	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr7:3136800-3142000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr7:3137000-3146000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr7:3140200-3141800	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr7:3140800-3142200	Enhancers	Primary hematopoietic stem cells	blood
8	chr7:3140800-3143800	Weak transcription	Fetal Thymus	thymus
9	chr7:3141000-3142000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr7:3141000-3142200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:3141400-3142000	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr7:3141400-3142200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr7:3141400-3143800	Enhancers	Primary T cells from cord blood	blood
14	chr7:3141400-3148000	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr7:3141600-3143000	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr7:3141800-3142200	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr7:3141800-3142200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:3142000-3142800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr7:3142000-3143000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr7:3142000-3143800	Enhancers	Primary T cells fromperipheralblood	blood
21	chr7:3142000-3156200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:3142200-3144000	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr7:3142200-3146000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr7:3142200-3146000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:3142800-3143600	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr7:3143000-3144000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr7:3143000-3145800	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr7:3143400-3143600	Enhancers	Aorta	Aorta
29	chr7:3143400-3143600	Enhancers	Brain Substantia Nigra	brain
30	chr7:3143400-3143600	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr7:3143400-3144800	Enhancers	Adipose Nuclei	Adipose
32	chr7:3143600-3144800	Weak transcription	Aorta	Aorta
33	chr7:3143600-3145600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr7:3143800-3144200	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr7:3143800-3144200	Enhancers	Fetal Thymus	thymus
36	chr7:3143800-3144400	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr7:3143800-3146200	Weak transcription	Primary T cells from cord blood	blood
38	chr7:3144000-3144200	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr7:3144000-3144200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr7:3144000-3145400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr7:3144200-3144400	Enhancers	Spleen	Spleen
42	chr7:3144200-3144800	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr7:3144200-3145600	Weak transcription	Fetal Thymus	thymus
44	chr7:3144200-3148000	Enhancers	Primary T cells fromperipheralblood	blood
45	chr7:3144200-3152200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr7:3144400-3144600	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr7:3144600-3145200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr7:3144800-3145000	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr7:3144800-3146800	Enhancers	Aorta	Aorta
50	chr7:3145000-3145800	Weak transcription	Primary T helper cells fromperipheralblood	blood

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