Variant report

Variant	nsv538852
Chromosome Location	chr7:53758613-53860523
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:181)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:181 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:53799543-53799740	K562	blood:	n/a	chr7:53799691-53799702
2	CEBPB	chr7:53795752-53795945	HepG2	liver:	n/a	n/a
3	CEBPB	chr7:53769885-53770064	HepG2	liver:	n/a	n/a
4	CEBPB	chr7:53812152-53812345	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr7:53769952-53770117	A549	lung:	n/a	n/a
6	CEBPB	chr7:53799530-53799792	HepG2	liver:	n/a	chr7:53799691-53799702
7	CHD2	chr7:53827893-53827955	HepG2	liver:	n/a	n/a
8	CTCF	chr7:53812320-53812470	NHEK	skin:	n/a	n/a
9	CTCF	chr7:53788000-53788150	GM12865	blood:	n/a	n/a
10	CTCF	chr7:53798469-53798519	GM10248	blood:	n/a	n/a
11	CTCF	chr7:53786280-53786430	AoAF	blood vessel:	n/a	n/a
12	CTCF	chr7:53812360-53812510	SAEC	small airway:	n/a	n/a
13	CTCF	chr7:53839560-53839710	Caco-2	colon:	n/a	n/a
14	CTCF	chr7:53812205-53812512	NHEK	skin:	n/a	n/a
15	CTCF	chr7:53812300-53812450	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr7:53812310-53812447	MCF-7	breast:	n/a	n/a
17	CTCF	chr7:53812420-53812570	HMEC	breast:	n/a	n/a
18	CTCF	chr7:53812300-53812450	HEEpiC	esophagus:	n/a	n/a
19	CTCF	chr7:53812342-53812438	MCF-7	breast:	n/a	n/a
20	CTCF	chr7:53831287-53831358	Medullo	brain:	n/a	n/a
21	CTCF	chr7:53812266-53812487	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr7:53812200-53812350	HMEC	breast:	n/a	n/a
23	CTCF	chr7:53812280-53812430	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr7:53812320-53812470	MCF-7	breast:	n/a	n/a
25	CTCF	chr7:53812240-53812390	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr7:53812280-53812430	NHEK	skin:	n/a	n/a
27	CTCF	chr7:53812240-53812390	SAEC	small airway:	n/a	n/a
28	CTCF	chr7:53832160-53832258	GM20000	blood:	n/a	n/a
29	CTCF	chr7:53763774-53763842	LNCaP	prostate:	n/a	n/a
30	CTCF	chr7:53812342-53812432	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:53770168-53770236	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr7:53812274-53812443	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr7:53812300-53812450	HMEC	breast:	n/a	n/a
34	CUX1	chr7:53852087-53852157	K562	blood:	n/a	n/a
35	E2F4	chr7:53774256-53774532	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr7:53841238-53841365	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr7:53814719-53815107	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F6	chr7:53858746-53858895	K562	blood:	n/a	n/a
39	EBF1	chr7:53811553-53811682	GM12878	blood:	n/a	chr7:53811597-53811608
40	EP300	chr7:53821327-53821343	K562	blood:	n/a	n/a
41	EP300	chr7:53794137-53794157	K562	blood:	n/a	n/a
42	FOS	chr7:53807883-53808172	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr7:53849932-53850040	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr7:53849911-53850086	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr7:53786893-53787202	MCF10A-Er-Src	breast:	n/a	chr7:53787079-53787091 chr7:53787033-53787041 chr7:53787031-53787043 chr7:53787029-53787040 chr7:53787032-53787043 chr7:53787031-53787038
46	FOS	chr7:53786893-53787190	MCF10A-Er-Src	breast:	n/a	chr7:53787079-53787091 chr7:53787033-53787041 chr7:53787031-53787043 chr7:53787029-53787040 chr7:53787032-53787043 chr7:53787031-53787038
47	FOS	chr7:53849847-53850102	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr7:53785714-53785797	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr7:53807962-53808171	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr7:53807963-53808165	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:53811402-53811452	H1-hESC	embryonic stem cell:	embryo
2	chr7:53811402-53811452	Hela-S3	cervix:	n/a
3	chr7:53811402-53811452	HCT-116	colon:	n/a
4	chr7:53811402-53811452	GM12891	blood:	n/a
5	chr7:53811402-53811452	SAEC	small airway:	n/a
6	chr7:53811402-53811452	K562	blood:	n/a
7	chr7:53811402-53811452	HIPEpiC	eye:	n/a
8	chr7:53811402-53811452	RPTEC	kidney:	n/a
9	chr7:53811402-53811452	A549	lung:	n/a
10	chr7:53811402-53811452	CMK	blood:	n/a
11	chr7:53811402-53811452	HRE	kidney:	n/a
12	chr7:53811402-53811452	GM06990	blood:	n/a
13	chr7:53811402-53811452	SK-N-MC	brain:	n/a
14	chr7:53811402-53811452	MCF10A-Er-Src	breast:	n/a
15	chr7:53811402-53811452	SK-N-SH	brain:	n/a
16	chr7:53811402-53811452	AG04449	skin:	fetal
17	chr7:53811402-53811452	HCPEpiC	choroid plexus:	n/a
18	chr7:53811402-53811452	HMEC	breast:	n/a
19	chr7:53811402-53811452	GM12878	blood:	n/a
20	chr7:53811402-53811452	GM19239	blood:	n/a
21	chr7:53811402-53811452	ECC-1	luminal epithelium:	n/a
22	chr7:53811402-53811452	PrEC	prostate:	n/a
23	chr7:53811402-53811452	NHDF-neo	bronchial:	n/a
24	chr7:53811402-53811452	Caco-2	colon:	n/a
25	chr7:53811402-53811452	MCF-7	breast:	n/a
26	chr7:53811402-53811452	PFSK-1	brain:	n/a
27	chr7:53811402-53811452	SKMC	muscle:	n/a
28	chr7:53811402-53811452	HRCEpiC	kidney:	n/a
29	chr7:53811402-53811452	U87	brain:	n/a
30	chr7:53811402-53811452	LNCaP	prostate:	n/a
31	chr7:53811402-53811452	NH-A	brain:	n/a
32	chr7:53811402-53811452	PANC-1	pancreas:	n/a
33	chr7:53811402-53811452	NHBE	bronchial:	n/a
34	chr7:53811402-53811452	T-47D	breast:	n/a
35	chr7:53811402-53811452	HCM	heart:	n/a
36	chr7:53811402-53811452	ProgFib	skin:	n/a
37	chr7:53811402-53811452	AG10803	skin:	n/a
38	chr7:53811402-53811452	NT2-D1	testis:	n/a
39	chr7:53811402-53811452	HNPCEpiC	eye:	n/a
40	chr7:53811402-53811452	IMR90	lung:	fetal
41	chr7:53811402-53811452	HL-60	blood:	n/a
42	chr7:53811402-53811452	AoSMC	blood vessel:	n/a
43	chr7:53811402-53811452	AG09309	skin:	n/a
44	chr7:53811402-53811452	GM12892	blood:	n/a
45	chr7:53811402-53811452	HEEpiC	esophagus:	n/a
46	chr7:53811402-53811452	HCF	heart:	n/a
47	chr7:53811402-53811452	Hepatocyte	liver:	n/a
48	chr7:53811402-53811452	HepG2	liver:	n/a
49	chr7:53811402-53811452	BJ	skin:	n/a
50	chr7:53811402-53811452	BE2_C	brain:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:53827998..53830937-chr7:53834103..53836205,2	K562	blood:
2	chr7:53857172..53859056-chr7:53860252..53862922,2	K562	blood:
3	chr7:53827998..53830937-chr7:53834103..53836205,2	K562	blood:
4	chr7:53776017..53777686-chr7:53778643..53780568,2	MCF-7	breast:
5	chr7:53841058..53842718-chr7:53850373..53853368,2	K562	blood:
6	chr7:53817997..53820497-chr7:53821045..53822573,2	K562	blood:
7	chr7:53779269..53780799-chr7:53781860..53784209,2	MCF-7	breast:
8	chr3:73159725..73160594-chr7:53843395..53843920,2	HCT-116	colon:
9	chr7:53849409..53852274-chr7:53856069..53858017,2	K562	blood:
10	chr7:53779269..53780799-chr7:53781860..53784209,2	MCF-7	breast:
11	chr7:53818690..53823967-chr7:53825430..53828073,4	K562	blood:
12	chr7:53841458..53843486-chr7:53862183..53865020,2	K562	blood:
13	chr7:53820582..53822348-chr7:53824215..53825903,2	K562	blood:
14	chr7:53849409..53852274-chr7:53856069..53858017,2	K562	blood:
15	chr7:53776017..53777686-chr7:53778643..53780568,2	MCF-7	breast:
16	chr7:53857172..53859056-chr7:53860252..53862922,2	K562	blood:
17	chr7:53761755..53764043-chr7:53877913..53879807,2	K562	blood:
18	chr7:53817997..53820497-chr7:53821045..53822573,2	K562	blood:
19	chr7:53841058..53842718-chr7:53850373..53853368,2	K562	blood:
20	chr7:53818690..53823967-chr7:53825430..53828073,4	K562	blood:
21	chr7:53820582..53822348-chr7:53824215..53825903,2	K562	blood:
22	chr5:135485656..135486185-chr7:53838517..53839265,2	MCF-7	breast:
23	chr7:53848619..53849339-chr7:53918094..53918709,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POM121L12-10	chr7:53847707-53847956	NONHSAT120643
2	lnc-POM121L12-9	chr7:53832905-53833852	NONHSAT120640
3	lnc-POM121L12-10	chr7:53847476-53847617	NONHSAT120643
4	lnc-POM121L12-9	chr7:53832374-53832647	NONHSAT120640

No data

Variant related genes	Relation type
RNU2-29P	TF binding region
ENSG00000271306	TF binding region
ENSG00000232418	TF binding region
RNU2-29P	CpG island
ENSG00000271306	CpG island
ENSG00000232418	CpG island
ENSG00000223247	chromatin interactions
ENSG00000205628	chromatin interactions

Extended variants
information (count: 1417 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:1417 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561233295	chr7:53758645-53758646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532353647	chr7:53758649-53758650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531542963	chr7:53758650-53758651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79769754	chr7:53758670-53758671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549675322	chr7:53758678-53758679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571062267	chr7:53758689-53758690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141745274	chr7:53758726-53758727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548663838	chr7:53758731-53758732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187335940	chr7:53758732-53758733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147098189	chr7:53758739-53758740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79315676	chr7:53758745-53758746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571189771	chr7:53758755-53758756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551436591	chr7:53758857-53758858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138317742	chr7:53758940-53758941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575294238	chr7:53758954-53758955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190673749	chr7:53759023-53759024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547434792	chr7:53759055-53759056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565671726	chr7:53759116-53759117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73373811	chr7:53759119-53759120	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs572923140	chr7:53759170-53759171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540065800	chr7:53759173-53759174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564825619	chr7:53759184-53759185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183640633	chr7:53759194-53759195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189086376	chr7:53759202-53759203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547920709	chr7:53759210-53759211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs77162400	chr7:53759212-53759213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201638357	chr7:53759241-53759242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562691283	chr7:53759247-53759248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28429378	chr7:53759285-53759286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs541922029	chr7:53759338-53759339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560655153	chr7:53759357-53759358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73373812	chr7:53759390-53759391	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs578193232	chr7:53759408-53759409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372663682	chr7:53759412-53759413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192184936	chr7:53759415-53759416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571150027	chr7:53759431-53759432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79043816	chr7:53759447-53759448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550506709	chr7:53759453-53759454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79181801	chr7:53759462-53759463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554219457	chr7:53759463-53759464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373242590	chr7:53759472-53759473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377095552	chr7:53759487-53759488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143404914	chr7:53759540-53759541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554346936	chr7:53759588-53759589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572495122	chr7:53759619-53759620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542093035	chr7:53759620-53759621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74865512	chr7:53759648-53759649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370526434	chr7:53759679-53759680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561087541	chr7:53759692-53759693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76853204	chr7:53759762-53759763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	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
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Cognitive impairment	21505072	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioblastoma multiforme	21525872	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:53751800-53761400	Weak transcription	Aorta	Aorta
2	chr7:53781800-53782200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr7:53782200-53783400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr7:53783400-53783800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr7:53783600-53783800	Enhancers	H9 Cell Line	embryonic stem cell
6	chr7:53783800-53789000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr7:53785400-53785800	Enhancers	Ovary	ovary
8	chr7:53789000-53789200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr7:53807000-53811400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:53811400-53811600	Enhancers	NHEK	skin
11	chr7:53811400-53812000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr7:53811400-53812000	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr7:53811400-53812400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr7:53811400-53812400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:53811400-53812400	Enhancers	HMEC	breast
16	chr7:53811400-53812600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr7:53811400-53812600	Enhancers	Esophagus	oesophagus
18	chr7:53811600-53812200	Flanking Active TSS	NHEK	skin
19	chr7:53811600-53812400	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr7:53811800-53812200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:53811800-53812200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr7:53811800-53812400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr7:53812200-53812600	Active TSS	Spleen	Spleen
24	chr7:53812200-53812600	Enhancers	NHEK	skin
25	chr7:53827800-53828200	Enhancers	Brain Hippocampus Middle	brain
26	chr7:53832000-53837800	Weak transcription	K562	blood
27	chr7:53836200-53836600	Enhancers	Fetal Stomach	stomach
28	chr7:53837800-53839200	Strong transcription	K562	blood
29	chr7:53838200-53838800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:53839000-53839400	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr7:53839200-53847000	Weak transcription	K562	blood
32	chr7:53839400-53844200	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr7:53840400-53840800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:53840800-53843200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr7:53841200-53842000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:53843200-53843400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:53843400-53843600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:53844000-53844200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:53844200-53844600	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr7:53844600-53844800	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr7:53844800-53845200	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr7:53847000-53847200	Strong transcription	K562	blood
43	chr7:53847200-53848400	Weak transcription	K562	blood

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