Variant report

Variant	esv2759500
Chromosome Location	chr7:3286625-3560229
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2209)
CpG islands
(count:1832)
Chromatin interactive
region (count:108)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2209 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3340556-3340788	K562	blood:	n/a	n/a
2	ARID3A	chr7:3340510-3340769	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:3419747-3420059	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:3418058-3418349	HepG2	liver:	n/a	n/a
5	ATF1	chr7:3385311-3385328	K562	blood:	n/a	n/a
6	ATF2	chr7:3439424-3439867	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:3356180-3356380	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:3336841-3337035	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:3420718-3420741	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:3370227-3370294	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:3339959-3340991	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:3341623-3341680	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:3515387-3515402	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr7:3290428-3290814	GM12878	blood:	n/a	n/a
15	BATF	chr7:3290378-3290743	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:3439465-3439755	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr7:3290486-3290751	GM12878	blood:	n/a	n/a
18	BCLAF1	chr7:3340395-3340873	GM12878	blood:	n/a	chr7:3340634-3340647 chr7:3340524-3340537 chr7:3340744-3340757
19	BCLAF1	chr7:3340441-3340719	GM12878	blood:	n/a	chr7:3340634-3340647 chr7:3340524-3340537
20	BHLHE40	chr7:3519977-3520319	K562	blood:	n/a	n/a
21	BHLHE40	chr7:3340387-3340937	GM12878	blood:	n/a	chr7:3340519-3340535 chr7:3340527-3340543
22	BHLHE40	chr7:3307547-3307725	A549	lung:	n/a	n/a
23	BHLHE40	chr7:3418024-3418475	HepG2	liver:	n/a	n/a
24	BHLHE40	chr7:3340409-3341002	HepG2	liver:	n/a	chr7:3340932-3340948 chr7:3340519-3340535 chr7:3340527-3340543
25	BHLHE40	chr7:3340404-3341008	K562	blood:	n/a	chr7:3340932-3340948 chr7:3340519-3340535 chr7:3340527-3340543
26	BRCA1	chr7:3340563-3340738	HepG2	liver:	n/a	n/a
27	BRCA1	chr7:3522141-3522202	GM12878	blood:	n/a	n/a
28	CBX3	chr7:3340439-3340719	K562	blood:	n/a	n/a
29	CBX3	chr7:3340323-3340885	HCT-116	colon:	n/a	n/a
30	CBX3	chr7:3340484-3340710	K562	blood:	n/a	n/a
31	CCNT2	chr7:3340411-3341005	K562	blood:	n/a	n/a
32	CEBPB	chr7:3522089-3522651	Hela-S3	cervix:	n/a	chr7:3522481-3522492
33	CEBPB	chr7:3522292-3522669	IMR90	lung:	n/a	chr7:3522481-3522492
34	CEBPB	chr7:3478751-3479563	A549	lung:	n/a	chr7:3479156-3479167
35	CEBPB	chr7:3522164-3522619	HCT-116	colon:	n/a	chr7:3522481-3522492
36	CEBPB	chr7:3475773-3476125	HepG2	liver:	n/a	chr7:3475940-3475949 chr7:3475939-3475950 chr7:3475940-3475949
37	CEBPB	chr7:3551499-3551703	HepG2	liver:	n/a	chr7:3551564-3551575
38	CEBPB	chr7:3345730-3345964	A549	lung:	n/a	chr7:3345834-3345845 chr7:3345783-3345796 chr7:3345848-3345859 chr7:3345832-3345845 chr7:3345834-3345845
39	CEBPB	chr7:3478893-3479425	A549	lung:	n/a	chr7:3479156-3479167
40	CEBPB	chr7:3369047-3369093	K562	blood:	n/a	n/a
41	CEBPB	chr7:3479036-3479317	K562	blood:	n/a	chr7:3479156-3479167
42	CEBPB	chr7:3307646-3307946	IMR90	lung:	n/a	n/a
43	CEBPB	chr7:3475761-3476128	IMR90	lung:	n/a	chr7:3475940-3475949 chr7:3475939-3475950 chr7:3475940-3475949
44	CEBPB	chr7:3417979-3418421	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:3457543-3457997	H1-hESC	embryonic stem cell:	n/a	chr7:3457585-3457598 chr7:3457585-3457598
46	CEBPB	chr7:3515364-3515642	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:3419990-3420315	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:3515394-3515623	A549	lung:	n/a	n/a
49	CEBPB	chr7:3478943-3479301	ECC-1	luminal epithelium:	n/a	chr7:3479156-3479167
50	CEBPB	chr7:3515281-3515612	MCF-7	breast:	n/a	n/a

(count:1832 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3470434-3470484	Jurkat	blood:	n/a
2	chr7:3411503-3411553	HAEpiC	amniotic membrane:	n/a
3	chr7:3470434-3470484	Jurkat	blood:	n/a
4	chr7:3411503-3411553	HAEpiC	amniotic membrane:	n/a
5	chr7:3419305-3419355	NHBE	bronchial:	n/a
6	chr7:3340459-3340509	RPTEC	kidney:	n/a
7	chr7:3313269-3313319	ProgFib	skin:	n/a
8	chr7:3411503-3411553	HepG2	liver:	n/a
9	chr7:3304614-3304664	SKMC	muscle:	n/a
10	chr7:3341694-3341744	ECC-1	luminal epithelium:	n/a
11	chr7:3337443-3337493	K562	blood:	n/a
12	chr7:3343830-3343880	HCM	heart:	n/a
13	chr7:3343830-3343880	HRCEpiC	kidney:	n/a
14	chr7:3342048-3342098	NHBE	bronchial:	n/a
15	chr7:3304614-3304664	HCM	heart:	n/a
16	chr7:3341524-3341574	HCM	heart:	n/a
17	chr7:3341524-3341574	PFSK-1	brain:	n/a
18	chr7:3337443-3337493	HRE	kidney:	n/a
19	chr7:3478077-3478127	SK-N-SH	brain:	n/a
20	chr7:3341934-3341984	HEEpiC	esophagus:	n/a
21	chr7:3304614-3304664	HAEpiC	amniotic membrane:	n/a
22	chr7:3533958-3534008	GM06990	blood:	n/a
23	chr7:3304614-3304664	AoSMC	blood vessel:	n/a
24	chr7:3343830-3343880	U87	brain:	n/a
25	chr7:3340860-3340910	GM19239	blood:	n/a
26	chr7:3337443-3337493	GM12878	blood:	n/a
27	chr7:3339766-3339816	Hela-S3	cervix:	n/a
28	chr7:3313269-3313319	HCM	heart:	n/a
29	chr7:3488816-3488866	K562	blood:	n/a
30	chr7:3340866-3340916	K562	blood:	n/a
31	chr7:3340866-3340916	LNCaP	prostate:	n/a
32	chr7:3385318-3385368	GM19239	blood:	n/a
33	chr7:3341524-3341574	T-47D	breast:	n/a
34	chr7:3341934-3341984	HAEpiC	amniotic membrane:	n/a
35	chr7:3340860-3340910	SK-N-SH	brain:	n/a
36	chr7:3549961-3550011	GM06990	blood:	n/a
37	chr7:3338723-3338773	HCPEpiC	choroid plexus:	n/a
38	chr7:3375859-3375909	A549	lung:	n/a
39	chr7:3341694-3341744	HRPEpiC	eye:	n/a
40	chr7:3419305-3419355	GM19239	blood:	n/a
41	chr7:3341694-3341744	U87	brain:	n/a
42	chr7:3419305-3419355	T-47D	breast:	n/a
43	chr7:3419305-3419355	Caco-2	colon:	n/a
44	chr7:3341630-3341680	HEEpiC	esophagus:	n/a
45	chr7:3304614-3304664	HRPEpiC	eye:	n/a
46	chr7:3339766-3339816	NHBE	bronchial:	n/a
47	chr7:3358214-3358264	H1-hESC	embryonic stem cell:	embryo
48	chr7:3338723-3338773	HMEC	breast:	n/a
49	chr7:3304614-3304664	GM12892	blood:	n/a
50	chr7:3341694-3341744	SK-N-MC	brain:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:3351745..3355702-chr7:3356161..3359964,4	K562	blood:
2	chr7:3425641..3430182-chr7:3430225..3435357,4	MCF-7	breast:
3	chr7:3424678..3427459-chr7:3437708..3440654,2	MCF-7	breast:
4	chr7:3436200..3439462-chr7:3442138..3445077,3	K562	blood:
5	chr7:3537080..3539372-chr7:3543955..3546696,2	MCF-7	breast:
6	chr7:3250247..3250807-chr7:3340190..3341077,3	MCF-7	breast:
7	chr7:3438230..3440428-chr7:3448766..3450871,2	MCF-7	breast:
8	chr7:3318661..3320574-chr7:3339181..3342087,2	MCF-7	breast:
9	chr7:3398782..3400855-chr7:3415548..3417886,2	MCF-7	breast:
10	chr7:3340838..3343187-chr7:3343470..3345833,2	MCF-7	breast:
11	chr7:3441889..3444490-chr7:3452543..3454242,2	MCF-7	breast:
12	chr7:3339718..3341766-chr7:3458306..3459954,2	K562	blood:
13	chr7:3463184..3466150-chr7:3469039..3471328,2	MCF-7	breast:
14	chr7:3521696..3522495-chr7:3631928..3632648,2	MCF-7	breast:
15	chr7:3427962..3429690-chr7:3438000..3440152,2	K562	blood:
16	chr7:3555349..3557729-chr7:3560043..3561605,2	K562	blood:
17	chr7:3348530..3349530-chr7:3439336..3440173,5	MCF-7	breast:
18	chr7:3553060..3555067-chr7:3563741..3566106,2	MCF-7	breast:
19	chr7:3443032..3445719-chr7:3938528..3940389,2	MCF-7	breast:
20	chr7:3424678..3427459-chr7:3437708..3440654,2	MCF-7	breast:
21	chr7:3351745..3355702-chr7:3356161..3359964,4	K562	blood:
22	chr7:3427962..3429690-chr7:3438000..3440152,2	K562	blood:
23	chr7:3379742..3382229-chr7:3382243..3386040,3	K562	blood:
24	chr7:3404631..3406335-chr7:3408611..3410804,2	MCF-7	breast:
25	chr7:3254030..3256348-chr7:3338235..3340171,2	MCF-7	breast:
26	chr7:3339718..3341766-chr7:3458306..3459954,2	K562	blood:
27	chr7:3439202..3440208-chr7:3521793..3522518,3	MCF-7	breast:
28	chr7:3546340..3548906-chr7:3559233..3561540,2	MCF-7	breast:
29	chr7:3381518..3384288-chr7:3389563..3392329,2	MCF-7	breast:
30	chr7:3452987..3455737-chr7:3457417..3460056,3	MCF-7	breast:
31	chr7:3436200..3438648-chr7:3443337..3445077,2	K562	blood:
32	chr7:3388931..3391698-chr7:3393863..3395884,2	K562	blood:
33	chr7:3421160..3422732-chr7:3429225..3430935,2	MCF-7	breast:
34	chr7:3354663..3356940-chr7:3364964..3367662,2	K562	blood:
35	chr7:3463184..3466150-chr7:3469039..3471328,2	MCF-7	breast:
36	chr7:3444047..3446365-chr7:3452049..3455174,3	MCF-7	breast:
37	chr7:3521340..3522302-chr7:4671144..4671918,2	MCF-7	breast:
38	chr7:3284325..3287180-chr7:3291361..3294316,3	MCF-7	breast:
39	chr7:3388931..3391698-chr7:3393863..3395884,2	K562	blood:
40	chr7:3421160..3422732-chr7:3429225..3430935,2	MCF-7	breast:
41	chr7:3444122..3444632-chr7:3471439..3472016,2	MCF-7	breast:
42	chr7:3349154..3351811-chr7:3384855..3387148,2	MCF-7	breast:
43	chr7:3439202..3440208-chr7:3521793..3522518,3	MCF-7	breast:
44	chr7:3194262..3194922-chr7:3439333..3439841,2	MCF-7	breast:
45	chr7:3349072..3350762-chr7:3354639..3356462,2	K562	blood:
46	chr7:3466489..3468571-chr7:3470496..3474286,3	MCF-7	breast:
47	chr7:3438230..3440428-chr7:3448766..3450871,2	MCF-7	breast:
48	chr7:3194510..3195232-chr7:3340158..3340723,2	MCF-7	breast:
49	chr7:3385347..3387562-chr7:3388126..3390584,2	K562	blood:
50	chr7:3521823..3522640-chr7:3807742..3808264,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMZ1-7	chr7:3377758-3378233	NONHSAT118851
2	lnc-AC091801.1.1-6	chr7:3303664-3304421	ENSG00000236708.1
3	lnc-AMZ1-7	chr7:3377521-3378121	NONHSAT118850
4	lnc-AC091801.1.1-6	chr7:3341861-3342084	ENSG00000236708.1

No data

Variant related genes	Relation type
ENSG00000236708	TF binding region
ENSG00000224593	TF binding region
ENSG00000211544	TF binding region
SDK1	TF binding region
ENSG00000236708	CpG island
ENSG00000224593	CpG island
ENSG00000211544	CpG island
SDK1	CpG island
ENSG00000236708	chromatin interactions
ENSG00000211544	chromatin interactions
ENSG00000146555	chromatin interactions

Extended variants
information (count: 14986 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:14986 , 50 per page) page: 1 2 3 4 5 6 7 ... 300

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546297942	chr7:3286640-3286641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559449868	chr7:3286641-3286642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs6461944	chr7:3286650-3286651	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs573266602	chr7:3286730-3286731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548472262	chr7:3286734-3286735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375310187	chr7:3286745-3286746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115853804	chr7:3286774-3286775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540514706	chr7:3286795-3286796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565464415	chr7:3286818-3286819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190528973	chr7:3286821-3286822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112797438	chr7:3286871-3286872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539116537	chr7:3286879-3286880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185362995	chr7:3286880-3286881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199705518	chr7:3286988-3286989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200967562	chr7:3287001-3287002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17374220	chr7:3287017-3287018	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs535480451	chr7:3287028-3287029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138314385	chr7:3287037-3287038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575641140	chr7:3287075-3287076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368178212	chr7:3287094-3287095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188516596	chr7:3287127-3287128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577769220	chr7:3287134-3287135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6461946	chr7:3287141-3287142	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs376102891	chr7:3287142-3287143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201131355	chr7:3287183-3287184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6461947	chr7:3287200-3287201	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs112114349	chr7:3287204-3287205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560039331	chr7:3287214-3287215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541858999	chr7:3287215-3287216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184903525	chr7:3287250-3287251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531082221	chr7:3287254-3287255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189763788	chr7:3287261-3287262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145089489	chr7:3287268-3287269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374853384	chr7:3287364-3287365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200132946	chr7:3287387-3287388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10565310	chr7:3287389-3287390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527373150	chr7:3287414-3287415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533613940	chr7:3287436-3287437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371753665	chr7:3287510-3287511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551948245	chr7:3287514-3287515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546373094	chr7:3287527-3287528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs180994353	chr7:3287538-3287539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73301070	chr7:3287559-3287560	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs548962123	chr7:3287561-3287562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187274669	chr7:3287570-3287571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371962794	chr7:3287623-3287624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558127277	chr7:3287736-3287737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138605221	chr7:3287750-3287751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192113723	chr7:3287779-3287780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553178895	chr7:3287854-3287855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2013 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3280600-3302000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:3285800-3287600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:3286200-3288200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:3286400-3288200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr7:3287600-3288600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:3287800-3289400	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr7:3288000-3288800	Enhancers	Brain Hippocampus Middle	brain
8	chr7:3288200-3288600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr7:3288200-3288800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:3288200-3288800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr7:3288600-3289000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:3288800-3299400	Weak transcription	Brain Hippocampus Middle	brain
13	chr7:3289000-3293600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr7:3293600-3295400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr7:3294600-3295200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:3295400-3296400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr7:3296400-3296800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr7:3296400-3296800	Active TSS	Spleen	Spleen
19	chr7:3296800-3298600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:3298600-3299800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:3298600-3301000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:3299000-3299200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:3299000-3299200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr7:3299000-3299600	Enhancers	Fetal Stomach	stomach
25	chr7:3299000-3299800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:3299000-3300200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr7:3299200-3299400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr7:3299200-3299400	Enhancers	Brain Cingulate Gyrus	brain
29	chr7:3299200-3299400	Enhancers	Colon Smooth Muscle	Colon
30	chr7:3299200-3299400	Bivalent Enhancer	HepG2	liver
31	chr7:3299200-3299600	Enhancers	Ovary	ovary
32	chr7:3299200-3299600	Enhancers	HSMMtube	muscle
33	chr7:3299200-3299800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:3299200-3299800	Enhancers	NH-A	brain
35	chr7:3299200-3300200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr7:3299200-3300600	Active TSS	Rectal Smooth Muscle	rectum
37	chr7:3299200-3303600	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr7:3299400-3299600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr7:3299400-3299600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:3299400-3299600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr7:3299400-3299600	Enhancers	Fetal Intestine Large	intestine
42	chr7:3299400-3299600	Enhancers	Fetal Intestine Small	intestine
43	chr7:3299400-3299600	Active TSS	Fetal Muscle Trunk	muscle
44	chr7:3299400-3299600	Bivalent Enhancer	Fetal Muscle Leg	muscle
45	chr7:3299400-3299600	Flanking Bivalent TSS/Enh	HepG2	liver
46	chr7:3299400-3299600	Enhancers	NHLF	lung
47	chr7:3299400-3299800	Flanking Active TSS	Brain Cingulate Gyrus	brain
48	chr7:3299400-3299800	Enhancers	Placenta	Placenta
49	chr7:3299400-3300200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:3299400-3300200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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