Variant report

Variant	nsv607428
Chromosome Location	chr7:67526074-67788551
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1014)
CpG islands
(count:366)
Chromatin interactive
region (count:8)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1014 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:67574482-67574651	K562	blood:	n/a	n/a
2	ATF2	chr7:67710768-67711549	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:67596288-67596309	K562	blood:	n/a	n/a
4	BACH1	chr7:67594628-67594813	K562	blood:	n/a	n/a
5	BACH1	chr7:67711132-67711708	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:67657959-67658129	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:67554081-67554133	K562	blood:	n/a	n/a
8	BACH1	chr7:67574324-67574634	K562	blood:	n/a	n/a
9	BACH1	chr7:67718928-67718937	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr7:67574444-67574521	K562	blood:	n/a	n/a
11	BHLHE40	chr7:67745207-67745467	HepG2	liver:	n/a	n/a
12	BHLHE40	chr7:67734594-67734639	A549	lung:	n/a	n/a
13	BRCA1	chr7:67703401-67703667	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr7:67714721-67714908	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chr7:67584456-67584660	K562	blood:	n/a	n/a
16	CBX3	chr7:67730984-67731405	K562	blood:	n/a	n/a
17	CBX3	chr7:67731057-67731386	K562	blood:	n/a	n/a
18	CEBPB	chr7:67785930-67786474	MCF-7	breast:	n/a	n/a
19	CEBPB	chr7:67536045-67536325	A549	lung:	n/a	chr7:67536196-67536207
20	CEBPB	chr7:67641838-67642094	HepG2	liver:	n/a	chr7:67641929-67641940
21	CEBPB	chr7:67536064-67536302	K562	blood:	n/a	chr7:67536196-67536207
22	CEBPB	chr7:67595665-67595865	HepG2	liver:	n/a	chr7:67595833-67595844
23	CEBPB	chr7:67695457-67695708	K562	blood:	n/a	n/a
24	CEBPB	chr7:67711906-67712223	A549	lung:	n/a	chr7:67712197-67712208 chr7:67712054-67712067 chr7:67712054-67712065
25	CEBPB	chr7:67627266-67627501	K562	blood:	n/a	chr7:67627358-67627369
26	CEBPB	chr7:67532681-67532931	A549	lung:	n/a	chr7:67532798-67532811 chr7:67532798-67532809 chr7:67532798-67532811
27	CEBPB	chr7:67711962-67712165	K562	blood:	n/a	chr7:67712054-67712067 chr7:67712054-67712065
28	CEBPB	chr7:67532667-67532979	HepG2	liver:	n/a	chr7:67532798-67532811 chr7:67532798-67532809 chr7:67532798-67532811
29	CEBPB	chr7:67536022-67536356	K562	blood:	n/a	chr7:67536196-67536207
30	CEBPB	chr7:67595716-67596026	H1-hESC	embryonic stem cell:	n/a	chr7:67595833-67595844
31	CEBPB	chr7:67542875-67543062	HepG2	liver:	n/a	chr7:67542989-67543000 chr7:67542988-67543001
32	CEBPB	chr7:67535118-67535207	A549	lung:	n/a	n/a
33	CEBPB	chr7:67595719-67595969	K562	blood:	n/a	chr7:67595833-67595844
34	CEBPB	chr7:67727542-67727594	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:67635294-67635342	HepG2	liver:	n/a	chr7:67635312-67635323
36	CEBPB	chr7:67627321-67627436	H1-hESC	embryonic stem cell:	n/a	chr7:67627358-67627369
37	CEBPB	chr7:67785980-67786546	MCF-7	breast:	n/a	n/a
38	CEBPB	chr7:67567941-67568001	HepG2	liver:	n/a	chr7:67567983-67567994
39	CEBPB	chr7:67536090-67536324	H1-hESC	embryonic stem cell:	n/a	chr7:67536196-67536207
40	CEBPB	chr7:67703451-67703660	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr7:67532732-67532945	IMR90	lung:	n/a	chr7:67532798-67532811 chr7:67532798-67532809 chr7:67532798-67532811
42	CEBPB	chr7:67595758-67596000	MCF-7	breast:	n/a	chr7:67595833-67595844
43	CEBPB	chr7:67753886-67754099	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr7:67620646-67621120	MCF-7	breast:	n/a	n/a
45	CEBPB	chr7:67753912-67754096	K562	blood:	n/a	n/a
46	CEBPB	chr7:67527670-67527834	HepG2	liver:	n/a	n/a
47	CEBPB	chr7:67575320-67575365	A549	lung:	n/a	n/a
48	CEBPB	chr7:67536054-67536289	IMR90	lung:	n/a	chr7:67536196-67536207
49	CEBPB	chr7:67695518-67695744	HepG2	liver:	n/a	n/a
50	CEBPB	chr7:67635234-67635424	A549	lung:	n/a	chr7:67635312-67635323

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:67555703-67555753	SKMC	muscle:	n/a
2	chr7:67554611-67554661	NB4	blood:	n/a
3	chr7:67555703-67555753	ECC-1	luminal epithelium:	n/a
4	chr7:67555703-67555753	PFSK-1	brain:	n/a
5	chr7:67741356-67741406	HMEC	breast:	n/a
6	chr7:67722023-67722073	U87	brain:	n/a
7	chr7:67711231-67711281	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:67554611-67554661	HRE	kidney:	n/a
9	chr7:67554611-67554661	HIPEpiC	eye:	n/a
10	chr7:67555703-67555753	MCF10A-Er-Src	breast:	n/a
11	chr7:67741356-67741406	H1-hESC	embryonic stem cell:	embryo
12	chr7:67711231-67711281	IMR90	lung:	fetal
13	chr7:67711231-67711281	HAEpiC	amniotic membrane:	n/a
14	chr7:67722023-67722073	HMEC	breast:	n/a
15	chr7:67554611-67554661	HCT-116	colon:	n/a
16	chr7:67741356-67741406	ECC-1	luminal epithelium:	n/a
17	chr7:67554611-67554661	HCPEpiC	choroid plexus:	n/a
18	chr7:67741356-67741406	SK-N-SH	brain:	n/a
19	chr7:67741356-67741406	HRE	kidney:	n/a
20	chr7:67555703-67555753	HMEC	breast:	n/a
21	chr7:67711231-67711281	AG10803	skin:	n/a
22	chr7:67555703-67555753	GM12891	blood:	n/a
23	chr7:67711231-67711281	BJ	skin:	n/a
24	chr7:67555703-67555753	NHDF-neo	bronchial:	n/a
25	chr7:67711231-67711281	Jurkat	blood:	n/a
26	chr7:67554611-67554661	HEEpiC	esophagus:	n/a
27	chr7:67554611-67554661	SAEC	small airway:	n/a
28	chr7:67711231-67711281	HCM	heart:	n/a
29	chr7:67741356-67741406	PANC-1	pancreas:	n/a
30	chr7:67554611-67554661	GM12891	blood:	n/a
31	chr7:67741356-67741406	K562	blood:	n/a
32	chr7:67711231-67711281	HL-60	blood:	n/a
33	chr7:67741356-67741406	LNCaP	prostate:	n/a
34	chr7:67554611-67554661	HRCEpiC	kidney:	n/a
35	chr7:67548326-67548376	BJ	skin:	n/a
36	chr7:67554611-67554661	AG04449	skin:	fetal
37	chr7:67722023-67722073	HEK293	kidney:	embryo
38	chr7:67741356-67741406	HL-60	blood:	n/a
39	chr7:67548326-67548376	HCT-116	colon:	n/a
40	chr7:67548326-67548376	PFSK-1	brain:	n/a
41	chr7:67711231-67711281	K562	blood:	n/a
42	chr7:67555703-67555753	HL-60	blood:	n/a
43	chr7:67741356-67741406	HAEpiC	amniotic membrane:	n/a
44	chr7:67555703-67555753	RPTEC	kidney:	n/a
45	chr7:67548326-67548376	Hela-S3	cervix:	n/a
46	chr7:67548326-67548376	HMEC	breast:	n/a
47	chr7:67722023-67722073	SK-N-SH_RA	brain:	n/a
48	chr7:67711231-67711281	HepG2	liver:	n/a
49	chr7:67741356-67741406	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:67711231-67711281	RPTEC	kidney:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:67717767..67720334-chr7:67720415..67723355,2	K562	blood:
2	chr7:67715289..67716804-chr7:67731193..67733479,2	MCF-7	breast:
3	chr7:67642068..67642613-chr7:68532024..68532784,2	MCF-7	breast:
4	chr7:67717767..67720334-chr7:67720415..67723355,2	K562	blood:
5	chr7:67715692..67717667-chr7:67720871..67723372,2	K562	blood:
6	chr7:67715692..67717667-chr7:67720871..67723372,2	K562	blood:
7	chr7:67642131..67642666-chr7:69626249..69626967,2	K562	blood:
8	chr7:67641923..67642579-chr7:68532274..68532877,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STAG3L4-9	chr7:67706624-67707254	NONHSAT121299
2	lnc-SBDS-7	chr7:67615270-67615310	ENSG00000226829.1
3	lnc-SBDS-7	chr7:67620016-67620171	ENSG00000226829.1
4	lnc-SBDS-7	chr7:67753042-67753220	ENSG00000226829.1
5	lnc-SBDS-7	chr7:67649777-67649903	ENSG00000226829.1
6	lnc-SBDS-7	chr7:67701286-67701423	ENSG00000226829.1
7	lnc-STAG3L4-3	chr7:67556210-67556312	ENSG00000236531.2
8	lnc-STAG3L4-3	chr7:67583542-67584196	ENSG00000236531.2
9	lnc-STAG3L4-3	chr7:67583542-67584196	XLOC_006140
10	lnc-STAG3L4-3	chr7:67582818-67582867	XLOC_006140

No data

Variant related genes	Relation type
ENSG00000226829	TF binding region
ENSG00000232975	TF binding region
ENSG00000237754	TF binding region
MTND4P3	TF binding region
ENSG00000236531	TF binding region
ENSG00000226829	CpG island
ENSG00000232975	CpG island
ENSG00000237754	CpG island
MTND4P3	CpG island
ENSG00000236531	CpG island
ENSG00000225959	chromatin interactions

Extended variants
information (count: 6981 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:6981 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2533479	chr7:67526074-67526075	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560302472	chr7:67526096-67526097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556651392	chr7:67526132-67526133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557953459	chr7:67526138-67526139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376264128	chr7:67526141-67526142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138132284	chr7:67526149-67526150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537046018	chr7:67526169-67526170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187720250	chr7:67526187-67526188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574003496	chr7:67526199-67526200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542876877	chr7:67526257-67526258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553172325	chr7:67526260-67526261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143485067	chr7:67526271-67526272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545129630	chr7:67526272-67526273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564828064	chr7:67526311-67526312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs115368100	chr7:67526340-67526341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543876566	chr7:67526345-67526346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373153377	chr7:67526371-67526372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112010789	chr7:67526372-67526373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370638653	chr7:67526373-67526374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546897265	chr7:67526380-67526381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35446850	chr7:67526388-67526389	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs532333740	chr7:67526389-67526390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551895874	chr7:67526405-67526406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs887421	chr7:67526411-67526412	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs192649365	chr7:67526422-67526423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550713701	chr7:67526426-67526427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs887420	chr7:67526452-67526453	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs536575205	chr7:67526491-67526492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553243604	chr7:67526510-67526511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370406307	chr7:67526562-67526563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75387881	chr7:67526605-67526606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4330582	chr7:67526606-67526607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559069501	chr7:67526623-67526624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575261323	chr7:67526635-67526636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544269500	chr7:67526659-67526660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141149377	chr7:67526660-67526661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574472664	chr7:67526669-67526670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374295797	chr7:67526718-67526719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183563304	chr7:67526728-67526729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs199960739	chr7:67526756-67526757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74891060	chr7:67526762-67526763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs887419	chr7:67526824-67526825	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs367555113	chr7:67526829-67526830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562667776	chr7:67526846-67526847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536962691	chr7:67526855-67526856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530929086	chr7:67526914-67526915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2533477	chr7:67527012-67527013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs567355785	chr7:67527020-67527021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150729458	chr7:67527032-67527033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111290337	chr7:67527099-67527100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:67525600-67526200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:67525600-67526600	Enhancers	Dnd41	blood
3	chr7:67525800-67531400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:67530200-67530400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr7:67530400-67531000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr7:67530400-67531200	Enhancers	Adipose Nuclei	Adipose
7	chr7:67530400-67531600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr7:67530400-67531800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr7:67530600-67530800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr7:67530600-67531000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr7:67530600-67531800	Enhancers	H9 Cell Line	embryonic stem cell
12	chr7:67531400-67531600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr7:67531400-67531800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:67532800-67533000	Enhancers	Fetal Brain Male	brain
15	chr7:67532800-67533200	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr7:67532800-67533400	Enhancers	Brain Germinal Matrix	brain
17	chr7:67533000-67533400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:67533000-67533800	Weak transcription	Fetal Brain Male	brain
19	chr7:67533400-67543000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr7:67533800-67535000	Enhancers	Fetal Brain Male	brain
21	chr7:67538800-67539600	Active TSS	A549	lung
22	chr7:67539200-67539600	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:67539600-67543000	Weak transcription	A549	lung
24	chr7:67540000-67540400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:67540800-67541400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr7:67543000-67543400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:67543000-67543800	Enhancers	Brain Germinal Matrix	brain
28	chr7:67543000-67543800	Flanking Active TSS	A549	lung
29	chr7:67543000-67544000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr7:67543000-67544400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr7:67543200-67543600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr7:67543800-67544000	Enhancers	A549	lung
33	chr7:67545200-67545800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr7:67545800-67546000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr7:67547600-67548600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr7:67549400-67549800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:67561200-67561400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:67566600-67567800	Enhancers	Primary hematopoietic stem cells	blood
39	chr7:67566800-67568200	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr7:67570400-67570800	Enhancers	H9 Cell Line	embryonic stem cell
41	chr7:67571800-67572600	Bivalent Enhancer	Fetal Heart	heart
42	chr7:67572000-67572200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:67572000-67572400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr7:67572000-67572400	Enhancers	Fetal Muscle Leg	muscle
45	chr7:67572000-67572400	Enhancers	Left Ventricle	heart
46	chr7:67572000-67572400	Enhancers	Right Ventricle	heart
47	chr7:67572000-67572600	Enhancers	Fetal Muscle Trunk	muscle
48	chr7:67572000-67572600	Enhancers	Ovary	ovary
49	chr7:67572000-67572600	Enhancers	Right Atrium	heart
50	chr7:67572000-67572800	Enhancers	Fetal Stomach	stomach

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