Variant report

Variant	esv1844137
Chromosome Location	chr7:19862221-19970584
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:19967840-19968308	GM12878	blood:	n/a	n/a
2	ATF2	chr7:19967799-19968231	GM12878	blood:	n/a	n/a
3	ATF3	chr7:19939093-19939558	A549	lung:	n/a	n/a
4	BATF	chr7:19967879-19968267	GM12878	blood:	n/a	chr7:19968083-19968094 chr7:19968122-19968130
5	BATF	chr7:19967871-19968233	GM12878	blood:	n/a	chr7:19968083-19968094 chr7:19968122-19968130
6	BATF	chr7:19955619-19955990	GM12878	blood:	n/a	chr7:19955794-19955804
7	BATF	chr7:19955665-19955957	GM12878	blood:	n/a	chr7:19955794-19955804
8	BATF	chr7:19967522-19967794	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:19955612-19955973	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:19955737-19955878	GM12878	blood:	n/a	n/a
11	BCL3	chr7:19874216-19874751	A549	lung:	n/a	n/a
12	BCL3	chr7:19938976-19939578	A549	lung:	n/a	n/a
13	BCL3	chr7:19939130-19939601	A549	lung:	n/a	n/a
14	CBX3	chr7:19955600-19956120	HCT-116	colon:	n/a	n/a
15	CEBPB	chr7:19891158-19891210	A549	lung:	n/a	n/a
16	CEBPB	chr7:19939220-19939589	A549	lung:	n/a	n/a
17	CEBPB	chr7:19939022-19939616	A549	lung:	n/a	chr7:19939091-19939102 chr7:19939089-19939102
18	CEBPB	chr7:19938884-19939715	A549	lung:	n/a	chr7:19939091-19939102 chr7:19939089-19939102
19	CEBPB	chr7:19950721-19950944	IMR90	lung:	n/a	chr7:19950830-19950841
20	CEBPB	chr7:19891041-19891451	MCF-7	breast:	n/a	n/a
21	CEBPB	chr7:19880808-19880960	HepG2	liver:	n/a	chr7:19880896-19880907
22	CEBPB	chr7:19950695-19951007	A549	lung:	n/a	chr7:19950830-19950841
23	CEBPB	chr7:19950735-19950984	HepG2	liver:	n/a	chr7:19950830-19950841
24	CEBPB	chr7:19938870-19939659	MCF-7	breast:	n/a	chr7:19939091-19939102 chr7:19939089-19939102
25	CHD1	chr7:19968914-19968917	GM12878	blood:	n/a	n/a
26	CHD2	chr7:19967989-19968116	GM12878	blood:	n/a	n/a
27	CTCF	chr7:19960380-19960530	WERI-Rb-1	eye:	n/a	chr7:19960517-19960527 chr7:19960516-19960529 chr7:19960520-19960529
28	CTCF	chr7:19960415-19960628	H1-hESC	embryonic stem cell:	n/a	chr7:19960517-19960527 chr7:19960516-19960529 chr7:19960514-19960532 chr7:19960515-19960531 chr7:19960520-19960529
29	CTCF	chr7:19960560-19960710	HCM	heart:	n/a	n/a
30	CTCF	chr7:19897916-19897959	GM10266	blood:	n/a	n/a
31	CTCF	chr7:19960440-19960590	HBMEC	blood vessel:	n/a	chr7:19960517-19960527 chr7:19960516-19960529 chr7:19960514-19960532 chr7:19960515-19960531 chr7:19960520-19960529
32	CTCF	chr7:19960508-19960517	Gliobla	brain:	n/a	n/a
33	CTCF	chr7:19969940-19970090	A549	lung:	n/a	n/a
34	CTCF	chr7:19960380-19960530	HMF	breast:	n/a	chr7:19960517-19960527 chr7:19960516-19960529 chr7:19960520-19960529
35	CTCF	chr7:19960400-19960550	GM06990	blood:	n/a	chr7:19960517-19960527 chr7:19960516-19960529 chr7:19960514-19960532 chr7:19960515-19960531 chr7:19960520-19960529
36	CTCF	chr7:19904806-19904873	GM20000	blood:	n/a	n/a
37	CTCF	chr7:19960520-19960670	HCPEpiC	choroid plexus:	n/a	chr7:19960520-19960529
38	CTCF	chr7:19887620-19887770	HVMF	connective:	n/a	n/a
39	CTCF	chr7:19948700-19948850	Caco-2	colon:	n/a	n/a
40	CTCF	chr7:19965885-19965971	GM10248	blood:	n/a	n/a
41	CTCF	chr7:19960440-19960590	BE2_C	brain:	n/a	chr7:19960517-19960527 chr7:19960516-19960529 chr7:19960514-19960532 chr7:19960515-19960531 chr7:19960520-19960529
42	CTCF	chr7:19960423-19960623	K562	blood:	n/a	chr7:19960517-19960527 chr7:19960516-19960529 chr7:19960514-19960532 chr7:19960515-19960531 chr7:19960520-19960529
43	CTCF	chr7:19928916-19928983	GM20000	blood:	n/a	n/a
44	CTCF	chr7:19955380-19955530	HRE	kidney:	n/a	n/a
45	CTCF	chr7:19960360-19960510	GM12875	blood:	n/a	n/a
46	CTCF	chr7:19960466-19960588	K562	blood:	n/a	chr7:19960517-19960527 chr7:19960516-19960529 chr7:19960514-19960532 chr7:19960515-19960531 chr7:19960520-19960529
47	CTCF	chr7:19960510-19960514	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:19960460-19960610	BE2_C	brain:	n/a	chr7:19960517-19960527 chr7:19960516-19960529 chr7:19960514-19960532 chr7:19960515-19960531 chr7:19960520-19960529
49	CTCF	chr7:19960440-19960590	AG09319	gingival:	n/a	chr7:19960517-19960527 chr7:19960516-19960529 chr7:19960514-19960532 chr7:19960515-19960531 chr7:19960520-19960529
50	CTCF	chr7:19961313-19961366	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:19961027-19961077	NH-A	brain:	n/a
2	chr7:19961027-19961077	BJ	skin:	n/a
3	chr7:19961027-19961077	Caco-2	colon:	n/a
4	chr7:19961027-19961077	ovcar-3	ovarian:	n/a
5	chr7:19961027-19961077	SKMC	muscle:	n/a
6	chr7:19961027-19961077	SAEC	small airway:	n/a
7	chr7:19961027-19961077	HCF	heart:	n/a
8	chr7:19961027-19961077	HCPEpiC	choroid plexus:	n/a
9	chr7:19961027-19961077	NHBE	bronchial:	n/a
10	chr7:19961027-19961077	BE2_C	brain:	n/a
11	chr7:19961027-19961077	HNPCEpiC	eye:	n/a
12	chr7:19961027-19961077	HMEC	breast:	n/a
13	chr7:19961027-19961077	SK-N-SH_RA	brain:	n/a
14	chr7:19961027-19961077	HL-60	blood:	n/a
15	chr7:19961027-19961077	PFSK-1	brain:	n/a
16	chr7:19961027-19961077	GM06990	blood:	n/a
17	chr7:19961027-19961077	HepG2	liver:	n/a
18	chr7:19961027-19961077	HCT-116	colon:	n/a
19	chr7:19961027-19961077	MCF-7	breast:	n/a
20	chr7:19961027-19961077	HRCEpiC	kidney:	n/a
21	chr7:19961027-19961077	LNCaP	prostate:	n/a
22	chr7:19961027-19961077	SK-N-MC	brain:	n/a
23	chr7:19961027-19961077	ECC-1	luminal epithelium:	n/a
24	chr7:19961027-19961077	AG04449	skin:	fetal
25	chr7:19961027-19961077	GM12891	blood:	n/a
26	chr7:19961027-19961077	Jurkat	blood:	n/a
27	chr7:19961027-19961077	A549	lung:	n/a
28	chr7:19961027-19961077	AG04450	lung:	fetal
29	chr7:19961027-19961077	Hepatocyte	liver:	n/a
30	chr7:19961027-19961077	T-47D	breast:	n/a
31	chr7:19961027-19961077	GM12878	blood:	n/a
32	chr7:19961027-19961077	AoSMC	blood vessel:	n/a
33	chr7:19961027-19961077	IMR90	lung:	fetal
34	chr7:19961027-19961077	K562	blood:	n/a
35	chr7:19961027-19961077	HIPEpiC	eye:	n/a
36	chr7:19961027-19961077	NHDF-neo	bronchial:	n/a
37	chr7:19961027-19961077	AG10803	skin:	n/a
38	chr7:19961027-19961077	HAEpiC	amniotic membrane:	n/a
39	chr7:19961027-19961077	AG09319	gingival:	n/a
40	chr7:19961027-19961077	GM12892	blood:	n/a
41	chr7:19961027-19961077	SK-N-SH	brain:	n/a
42	chr7:19961027-19961077	PANC-1	pancreas:	n/a
43	chr7:19961027-19961077	CMK	blood:	n/a
44	chr7:19961027-19961077	Hela-S3	cervix:	n/a
45	chr7:19961027-19961077	ProgFib	skin:	n/a
46	chr7:19961027-19961077	RPTEC	kidney:	n/a
47	chr7:19961027-19961077	MCF10A-Er-Src	breast:	n/a
48	chr7:19961027-19961077	NT2-D1	testis:	n/a
49	chr7:19961027-19961077	HRE	kidney:	n/a
50	chr7:19961027-19961077	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:19899612..19901422-chr7:19904101..19906352,2	MCF-7	breast:
2	chr7:19953806..19956698-chr7:19965814..19968012,2	K562	blood:
3	chr7:19880470..19882183-chr7:19884471..19887080,2	K562	blood:
4	chr7:19899734..19901908-chr7:19902300..19904189,2	K562	blood:
5	chr7:19900301..19903128-chr7:19903366..19905836,3	MCF-7	breast:
6	chr7:19953806..19956698-chr7:19965814..19968012,2	K562	blood:
7	chr7:19880470..19882183-chr7:19884471..19887080,2	K562	blood:
8	chr7:19899734..19901908-chr7:19902300..19904189,2	K562	blood:
9	chr7:19873630..19875873-chr7:19878314..19880296,2	K562	blood:
10	chr7:19873630..19875873-chr7:19878314..19880296,2	K562	blood:
11	chr7:19899612..19901422-chr7:19904101..19906352,2	MCF-7	breast:
12	chr7:19900301..19903128-chr7:19903366..19905836,3	MCF-7	breast:
13	chr3:63777404..63778151-chr7:19886673..19887328,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM196-1	chr7:19867978-19868096	XLOC_006365
2	lnc-MACC1-1	chr7:19958615-19958883	ENSG00000243004.1
3	lnc-MACC1-1	chr7:19958604-19958883	ENSG00000243004.1
4	lnc-MACC1-1	chr7:19959489-19959600	ENSG00000243004.1
5	lnc-MACC1-1	chr7:19959489-19960253	NONHSAT119395
6	lnc-MACC1-1	chr7:19938142-19938370	NONHSAT119395
7	lnc-TMEM196-1	chr7:19867710-19867838	XLOC_006365
8	lnc-MACC1-1	chr7:19958823-19958883	ENSG00000243004.1
9	lnc-MACC1-1	chr7:19958602-19958883	NONHSAT119395
10	lnc-MACC1-1	chr7:19958604-19958883	NR_110114
11	lnc-TMEM196-1	chr7:19871002-19871039	XLOC_006365

Variant related genes	Relation type
ENSG00000237921	TF binding region
ENSG00000237921	CpG island
PGAM4	miRNA target sites
C13orf34	miRNA target sites
CD46	miRNA target sites

Extended variants
information (count: 2073 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2073 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546794421	chr7:19867712-19867713	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs11375636	chr7:19867713-19867714	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs34744873	chr7:19867714-19867715	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs568379310	chr7:19867759-19867760	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs535780669	chr7:19867769-19867770	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs187451690	chr7:19867772-19867773	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs192299360	chr7:19867777-19867778	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs539910499	chr7:19867805-19867806	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs138761127	chr7:19867813-19867814	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs188568468	chr7:19868006-19868007	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs557871860	chr7:19868080-19868081	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs576683769	chr7:19871032-19871033	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs141178147	chr7:19873202-19873203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190187057	chr7:19873210-19873211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544752044	chr7:19873234-19873235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564331965	chr7:19873286-19873287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181223595	chr7:19873313-19873314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546810875	chr7:19873324-19873325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568379226	chr7:19873370-19873371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4721830	chr7:19873383-19873384	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs528424570	chr7:19873420-19873421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs147377374	chr7:19873432-19873433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571764722	chr7:19873460-19873461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539538996	chr7:19873463-19873464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139497096	chr7:19873467-19873468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145010738	chr7:19873483-19873484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147648082	chr7:19873529-19873530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139606397	chr7:19873540-19873541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573840400	chr7:19873560-19873561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs78229956	chr7:19873606-19873607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555886180	chr7:19873661-19873662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577610632	chr7:19873662-19873663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544616412	chr7:19873671-19873672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534520196	chr7:19873683-19873684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186501700	chr7:19873704-19873705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78221371	chr7:19873708-19873709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540409085	chr7:19873730-19873731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562332096	chr7:19873829-19873830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35232581	chr7:19873833-19873834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs80209090	chr7:19873844-19873845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs80142101	chr7:19873885-19873886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191487981	chr7:19873894-19873895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34634884	chr7:19873895-19873896	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs551822666	chr7:19873924-19873925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs149722887	chr7:19874002-19874003	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545446931	chr7:19874010-19874011	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34642757	chr7:19874013-19874014	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534324032	chr7:19874017-19874018	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555579581	chr7:19874047-19874048	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569813129	chr7:19874094-19874095	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19873200-19873800	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr7:19873800-19874000	Enhancers	A549	lung
3	chr7:19873800-19874400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr7:19873800-19874800	Enhancers	NHEK	skin
5	chr7:19874000-19874400	Flanking Active TSS	A549	lung
6	chr7:19874200-19875000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:19874400-19874600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr7:19874400-19875200	Enhancers	A549	lung
9	chr7:19874800-19875200	Enhancers	HMEC	breast
10	chr7:19880600-19881200	ZNF genes & repeats	Small Intestine	intestine
11	chr7:19881000-19881200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:19887600-19888000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr7:19889800-19890000	Enhancers	Pancreas	Pancrea
14	chr7:19890000-19891200	Weak transcription	Pancreas	Pancrea
15	chr7:19890800-19891000	Enhancers	A549	lung
16	chr7:19891000-19891400	Flanking Active TSS	A549	lung
17	chr7:19891200-19891400	ZNF genes & repeats	Pancreas	Pancrea
18	chr7:19891400-19891600	Weak transcription	Pancreas	Pancrea
19	chr7:19891600-19892000	Enhancers	Pancreas	Pancrea
20	chr7:19896000-19896400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:19904000-19904600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr7:19914000-19914200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr7:19915400-19916000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:19916600-19917000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:19916600-19917000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
26	chr7:19929000-19929600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:19938200-19938400	Enhancers	Colon Smooth Muscle	Colon
28	chr7:19938200-19938600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
29	chr7:19938400-19939200	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr7:19938600-19939600	Enhancers	A549	lung
31	chr7:19939000-19939200	Enhancers	Colon Smooth Muscle	Colon
32	chr7:19939000-19939400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr7:19939000-19939800	Enhancers	NHDF-Ad	bronchial
34	chr7:19939000-19940000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr7:19939000-19940000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:19939000-19940000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:19939200-19939400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr7:19939200-19939600	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr7:19939400-19955400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr7:19939600-19940000	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr7:19939600-19940000	Flanking Active TSS	A549	lung
42	chr7:19945200-19947000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
43	chr7:19945400-19946400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:19945400-19947800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
45	chr7:19945600-19946200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:19946800-19947200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
47	chr7:19951000-19952200	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr7:19951200-19959800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr7:19952000-19960000	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr7:19952200-19954600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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