Variant report

Variant	nsv887373
Chromosome Location	chr7:4469845-4665570
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1378)
CpG islands
(count:611)
Chromatin interactive
region (count:39)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1378 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:4573177-4573308	K562	blood:	n/a	n/a
2	ARID3A	chr7:4660093-4660484	K562	blood:	n/a	n/a
3	ARID3A	chr7:4652803-4652829	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:4476207-4476541	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:4601500-4601710	K562	blood:	n/a	n/a
6	ARID3A	chr7:4650522-4650783	K562	blood:	n/a	n/a
7	ARID3A	chr7:4652371-4652682	K562	blood:	n/a	n/a
8	ATF1	chr7:4660080-4660484	K562	blood:	n/a	n/a
9	ATF2	chr7:4540407-4540709	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:4652660-4653213	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr7:4652472-4653166	K562	blood:	n/a	n/a
12	BHLHE40	chr7:4650500-4650772	HepG2	liver:	n/a	n/a
13	BHLHE40	chr7:4539804-4540066	HepG2	liver:	n/a	n/a
14	BHLHE40	chr7:4652444-4652618	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:4650487-4650840	K562	blood:	n/a	n/a
16	BHLHE40	chr7:4660028-4660440	K562	blood:	n/a	n/a
17	BRCA1	chr7:4665536-4665929	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr7:4519369-4519376	HepG2	liver:	n/a	n/a
19	CBX3	chr7:4523514-4523852	K562	blood:	n/a	n/a
20	CBX3	chr7:4539559-4539829	K562	blood:	n/a	n/a
21	CBX3	chr7:4662120-4662522	K562	blood:	n/a	n/a
22	CBX3	chr7:4652013-4652286	K562	blood:	n/a	n/a
23	CBX3	chr7:4659324-4659675	K562	blood:	n/a	n/a
24	CBX3	chr7:4592673-4592898	K562	blood:	n/a	n/a
25	CBX3	chr7:4659319-4659749	K562	blood:	n/a	n/a
26	CBX3	chr7:4539569-4539857	K562	blood:	n/a	n/a
27	CBX3	chr7:4659979-4660483	K562	blood:	n/a	n/a
28	CBX3	chr7:4523526-4523869	K562	blood:	n/a	n/a
29	CBX3	chr7:4652487-4653193	K562	blood:	n/a	n/a
30	CCNT2	chr7:4660139-4660356	K562	blood:	n/a	n/a
31	CCNT2	chr7:4665553-4665820	K562	blood:	n/a	n/a
32	CCNT2	chr7:4659360-4659678	K562	blood:	n/a	n/a
33	CEBPB	chr7:4653567-4653621	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:4661095-4661423	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:4650482-4650813	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr7:4606348-4606704	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:4606356-4606718	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:4653483-4653882	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:4606331-4606697	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr7:4606287-4606701	A549	lung:	n/a	n/a
41	CEBPB	chr7:4526863-4527183	MCF-7	breast:	n/a	chr7:4527026-4527037
42	CEBPB	chr7:4606357-4606697	A549	lung:	n/a	n/a
43	CEBPB	chr7:4526888-4527175	HepG2	liver:	n/a	chr7:4527026-4527037
44	CEBPB	chr7:4606335-4606705	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr7:4562197-4562343	HepG2	liver:	n/a	chr7:4562300-4562311
46	CEBPB	chr7:4510874-4511113	K562	blood:	n/a	chr7:4511007-4511018
47	CEBPB	chr7:4653460-4653851	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr7:4584957-4585000	HepG2	liver:	n/a	chr7:4584972-4584983
49	CEBPB	chr7:4606437-4606623	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:4526987-4527171	A549	lung:	n/a	chr7:4527026-4527037

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4536864-4536914	SAEC	small airway:	n/a
2	chr7:4536864-4536914	SAEC	small airway:	n/a
3	chr7:4652765-4652815	ECC-1	luminal epithelium:	n/a
4	chr7:4573716-4573766	SKMC	muscle:	n/a
5	chr7:4646837-4646887	ECC-1	luminal epithelium:	n/a
6	chr7:4630518-4630568	HRE	kidney:	n/a
7	chr7:4630518-4630568	PFSK-1	brain:	n/a
8	chr7:4652671-4652721	HUVEC	blood vessel:	n/a
9	chr7:4536864-4536914	MCF-7	breast:	n/a
10	chr7:4652671-4652721	AG04450	lung:	fetal
11	chr7:4536838-4536888	PFSK-1	brain:	n/a
12	chr7:4652671-4652721	PANC-1	pancreas:	n/a
13	chr7:4573716-4573766	HRCEpiC	kidney:	n/a
14	chr7:4573535-4573585	SK-N-SH_RA	brain:	n/a
15	chr7:4630518-4630568	T-47D	breast:	n/a
16	chr7:4652842-4652892	HMEC	breast:	n/a
17	chr7:4652822-4652872	MCF10A-Er-Src	breast:	n/a
18	chr7:4573535-4573585	HRE	kidney:	n/a
19	chr7:4652765-4652815	AG10803	skin:	n/a
20	chr7:4536864-4536914	HCPEpiC	choroid plexus:	n/a
21	chr7:4652765-4652815	HNPCEpiC	eye:	n/a
22	chr7:4646837-4646887	NHBE	bronchial:	n/a
23	chr7:4536838-4536888	IMR90	lung:	fetal
24	chr7:4536864-4536914	Caco-2	colon:	n/a
25	chr7:4646837-4646887	U87	brain:	n/a
26	chr7:4652822-4652872	HIPEpiC	eye:	n/a
27	chr7:4652671-4652721	SK-N-SH_RA	brain:	n/a
28	chr7:4630518-4630568	PrEC	prostate:	n/a
29	chr7:4630518-4630568	HNPCEpiC	eye:	n/a
30	chr7:4573716-4573766	HEEpiC	esophagus:	n/a
31	chr7:4646837-4646887	HAEpiC	amniotic membrane:	n/a
32	chr7:4652842-4652892	NH-A	brain:	n/a
33	chr7:4536864-4536914	HRCEpiC	kidney:	n/a
34	chr7:4646837-4646887	T-47D	breast:	n/a
35	chr7:4652671-4652721	SK-N-SH	brain:	n/a
36	chr7:4652671-4652721	AG04449	skin:	fetal
37	chr7:4573716-4573766	LNCaP	prostate:	n/a
38	chr7:4652842-4652892	PFSK-1	brain:	n/a
39	chr7:4652842-4652892	A549	lung:	n/a
40	chr7:4652842-4652892	HEEpiC	esophagus:	n/a
41	chr7:4652842-4652892	AG04449	skin:	fetal
42	chr7:4573535-4573585	NH-A	brain:	n/a
43	chr7:4573535-4573585	HCF	heart:	n/a
44	chr7:4652671-4652721	HCF	heart:	n/a
45	chr7:4573535-4573585	GM06990	blood:	n/a
46	chr7:4652842-4652892	GM06990	blood:	n/a
47	chr7:4630518-4630568	GM06990	blood:	n/a
48	chr7:4652671-4652721	NH-A	brain:	n/a
49	chr7:4536838-4536888	HNPCEpiC	eye:	n/a
50	chr7:4630518-4630568	HUVEC	blood vessel:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4651116..4651675-chr7:4792877..4793723,2	MCF-7	breast:
2	chr7:4642981..4645443-chr7:4649025..4651972,2	K562	blood:
3	chr7:4658170..4661953-chr7:4663790..4665760,3	MCF-7	breast:
4	chr7:4074370..4074950-chr7:4518765..4519624,3	MCF-7	breast:
5	chr20:52556259..52556926-chr7:4599215..4599761,2	MCF-7	breast:
6	chr7:4649069..4651516-chr7:4792716..4794957,2	MCF-7	breast:
7	chr7:4613003..4615813-chr7:4681464..4683495,2	MCF-7	breast:
8	chr7:4650202..4651173-chr7:4793198..4794220,6	K562	blood:
9	chr7:4659487..4661247-chr7:4813243..4815825,2	MCF-7	breast:
10	chr7:4495018..4497948-chr7:4500566..4502684,3	K562	blood:
11	chr7:4195210..4197944-chr7:4502921..4505536,2	MCF-7	breast:
12	chr7:4646574..4649257-chr7:4668274..4670356,2	K562	blood:
13	chr7:4650192..4651154-chr7:5124831..5125751,2	K562	blood:
14	chr7:4660303..4661010-chr7:4722806..4723628,2	MCF-7	breast:
15	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
16	chr7:4601107..4601677-chr7:4670928..4671456,2	MCF-7	breast:
17	chr7:4401235..4402088-chr7:4518606..4519411,2	MCF-7	breast:
18	chr7:4659682..4660358-chr7:4671027..4671633,2	MCF-7	breast:
19	chr7:4652575..4653527-chr7:4793235..4794202,2	K562	blood:
20	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
21	chr7:4559356..4562288-chr7:4562408..4565136,2	MCF-7	breast:
22	chr7:4555170..4556862-chr7:4558765..4561124,2	K562	blood:
23	chr7:4541545..4543274-chr7:4543429..4546060,2	MCF-7	breast:
24	chr7:4495018..4497948-chr7:4500566..4502684,3	K562	blood:
25	chr7:4650266..4651114-chr7:4793024..4794119,8	MCF-7	breast:
26	chr7:4650149..4651186-chr7:4670931..4671949,8	K562	blood:
27	chr7:4559356..4562288-chr7:4562408..4565136,2	MCF-7	breast:
28	chr15:101629167..101629860-chr7:4485245..4486227,2	MCF-7	breast:
29	chr7:4642981..4645443-chr7:4649025..4651972,2	K562	blood:
30	chr7:4650215..4651217-chr7:4670962..4672255,11	MCF-7	breast:
31	chr7:4654217..4655804-chr7:4681235..4683651,2	MCF-7	breast:
32	chr7:4651340..4654171-chr7:4723682..4726491,2	K562	blood:
33	chr7:4650125..4650826-chr7:4837448..4838412,2	K562	blood:
34	chr7:4658170..4661953-chr7:4663790..4665760,3	MCF-7	breast:
35	chr7:4646417..4649112-chr7:4669955..4672673,2	MCF-7	breast:
36	chr7:4551212..4552814-chr7:4554906..4557306,2	K562	blood:
37	chr7:4650210..4650944-chr7:4922964..4923496,2	MCF-7	breast:
38	chr7:4665293..4667661-chr7:4670149..4671688,2	MCF-7	breast:
39	chr7:4143002..4143685-chr7:4518859..4519662,3	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RADIL-5	chr7:4472597-4475543	NONHSAT118861
2	lnc-RADIL-2	chr7:4645445-4645678	NONHSAT118868
3	lnc-RADIL-4	chr7:4513174-4513309	NONHSAT118863
4	lnc-SDK1-1	chr7:4482317-4482707	l_3355_chr7:4440443-4482707_testes
5	lnc-RADIL-2	chr7:4645445-4645678	FPKM1_group_29021_transcript_1
6	lnc-FOXK1-1	chr7:4515791-4518319	XLOC_005972
7	lnc-RADIL-2	chr7:4646510-4646515	FPKM1_group_29021_transcript_1
8	lnc-FOXK1-1	chr7:4473994-4474153	XLOC_005972
9	lnc-RADIL-2	chr7:4646511-4646569	XLOC_006345
10	lnc-RADIL-2	chr7:4646510-4646569	NONHSAT118868
11	lnc-RADIL-2	chr7:4645446-4645678	XLOC_006345
12	lnc-RADIL-4	chr7:4509330-4509430	NONHSAT118863

No data

Variant related genes	Relation type
CYP3A54P	TF binding region
CYP3A54P	CpG island
ENSG00000164916	chromatin interactions
ENSG00000242802	chromatin interactions
ENSG00000157927	chromatin interactions
ENSG00000261809	chromatin interactions
ENSG00000236352	chromatin interactions
VEGFA	miRNA target sites
TTC30A	miRNA target sites
TXNRD1	miRNA target sites

Extended variants
information (count: 4420 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4420 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541886015	chr7:4471643-4471644	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs371693231	chr7:4471713-4471714	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs571384756	chr7:4471722-4471723	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs575546550	chr7:4471774-4471775	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs376248320	chr7:4471775-4471776	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs564454426	chr7:4471814-4471815	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs11760266	chr7:4471874-4471875	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs540468218	chr7:4471875-4471876	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs139349978	chr7:4471902-4471903	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs529022507	chr7:4471903-4471904	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs10224151	chr7:4471919-4471920	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs562355139	chr7:4472041-4472042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190387870	chr7:4472052-4472053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549834305	chr7:4472059-4472060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6462833	chr7:4472073-4472074	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs546958671	chr7:4472147-4472148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182567754	chr7:4472154-4472155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539726299	chr7:4472170-4472171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186850255	chr7:4472190-4472191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191262661	chr7:4472204-4472205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535556981	chr7:4472205-4472206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555790014	chr7:4472206-4472207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575639282	chr7:4472230-4472231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538268220	chr7:4472260-4472261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557852395	chr7:4472266-4472267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs578010582	chr7:4472267-4472268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184062223	chr7:4472293-4472294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560394765	chr7:4472309-4472310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35263916	chr7:4472336-4472337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs74780265	chr7:4472349-4472350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs398003475	chr7:4472350-4472351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188950976	chr7:4472371-4472372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542449971	chr7:4472402-4472403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193241709	chr7:4472436-4472437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565019481	chr7:4472483-4472484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531282898	chr7:4472484-4472485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs36046293	chr7:4472505-4472506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185298015	chr7:4472515-4472516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111425512	chr7:4472539-4472540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533467498	chr7:4472617-4472618	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs75365288	chr7:4472618-4472619	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs200006163	chr7:4472619-4472620	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs188846392	chr7:4472628-4472629	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs532367330	chr7:4472648-4472649	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs566731228	chr7:4472663-4472664	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs191780938	chr7:4472669-4472670	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs183864502	chr7:4472677-4472678	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs569369371	chr7:4472705-4472706	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs188203102	chr7:4472710-4472711	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs558155306	chr7:4472760-4472761	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
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
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD

Chromatin state (count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4471600-4472000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
2	chr7:4472000-4473600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:4473200-4474000	Enhancers	Fetal Muscle Trunk	muscle
4	chr7:4473600-4473800	Enhancers	Fetal Stomach	stomach
5	chr7:4473600-4474000	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr7:4473600-4474200	Enhancers	Fetal Kidney	kidney
7	chr7:4473800-4474000	Flanking Active TSS	Fetal Stomach	stomach
8	chr7:4473800-4475200	Active TSS	Skeletal Muscle Male	skeletal muscle
9	chr7:4474000-4474200	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
10	chr7:4474000-4476600	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr7:4474200-4474400	Active TSS	Fetal Stomach	stomach
12	chr7:4474200-4475200	Enhancers	Fetal Intestine Large	intestine
13	chr7:4474600-4478200	Enhancers	Fetal Intestine Small	intestine
14	chr7:4475000-4475200	Enhancers	Pancreas	Pancrea
15	chr7:4475000-4477400	Enhancers	Stomach Mucosa	stomach
16	chr7:4475200-4475400	Enhancers	A549	lung
17	chr7:4475200-4475600	Flanking Active TSS	Fetal Intestine Large	intestine
18	chr7:4475400-4476600	Weak transcription	Pancreas	Pancrea
19	chr7:4475400-4476600	Weak transcription	A549	lung
20	chr7:4475600-4478200	Enhancers	Fetal Intestine Large	intestine
21	chr7:4475800-4477200	Bivalent Enhancer	HepG2	liver
22	chr7:4476600-4477200	Enhancers	Pancreas	Pancrea
23	chr7:4476600-4477400	Enhancers	A549	lung
24	chr7:4476800-4477200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:4476800-4477200	Enhancers	Gastric	stomach
26	chr7:4477000-4477400	Enhancers	Fetal Muscle Trunk	muscle
27	chr7:4477000-4478200	Enhancers	Fetal Muscle Leg	muscle
28	chr7:4478000-4479400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:4478200-4483400	Weak transcription	Fetal Intestine Small	intestine
30	chr7:4482200-4486000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
31	chr7:4483000-4483200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:4483400-4485000	Enhancers	Fetal Intestine Large	intestine
33	chr7:4483400-4485000	Enhancers	Fetal Intestine Small	intestine
34	chr7:4483600-4483800	Enhancers	Fetal Kidney	kidney
35	chr7:4483800-4485400	Weak transcription	Fetal Kidney	kidney
36	chr7:4485000-4488600	Weak transcription	Fetal Intestine Large	intestine
37	chr7:4485000-4488600	Weak transcription	Fetal Intestine Small	intestine
38	chr7:4485400-4485800	ZNF genes & repeats	Fetal Kidney	kidney
39	chr7:4485600-4485800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr7:4485800-4491400	Weak transcription	Fetal Kidney	kidney
41	chr7:4488600-4489400	Enhancers	HepG2	liver
42	chr7:4488600-4489600	Enhancers	Fetal Intestine Large	intestine
43	chr7:4488600-4489600	Enhancers	Fetal Intestine Small	intestine
44	chr7:4489000-4489600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:4497200-4498000	Enhancers	Fetal Muscle Trunk	muscle
46	chr7:4497400-4498200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr7:4497400-4498200	Enhancers	Adipose Nuclei	Adipose
48	chr7:4497400-4498600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr7:4497400-4498600	Enhancers	Fetal Muscle Leg	muscle
50	chr7:4497400-4498600	Enhancers	Skeletal Muscle Female	skeletal muscle

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