Variant report

Variant	esv1808132
Chromosome Location	chr4:68790619-68842841
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	ATF1	chr4:68799641-68799825	K562	blood:	n/a	n/a
2	ATF1	chr4:68794343-68794570	K562	blood:	n/a	n/a
3	BACH1	chr4:68794347-68794496	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr4:68795302-68795527	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr4:68794230-68794706	MCF-7	breast:	n/a	n/a
6	CEBPB	chr4:68795056-68795621	HCT-116	colon:	n/a	n/a
7	CEBPB	chr4:68794296-68794614	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr4:68795096-68795523	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr4:68794274-68794457	K562	blood:	n/a	n/a
10	CEBPB	chr4:68813237-68813501	HepG2	liver:	n/a	chr4:68813348-68813359
11	CTCF	chr4:68793176-68793248	MCF-7	breast:	n/a	n/a
12	CTCF	chr4:68802980-68803130	GM06990	blood:	n/a	n/a
13	CTCF	chr4:68794585-68794605	K562	blood:	n/a	n/a
14	CTCF	chr4:68819804-68819825	LNCaP	prostate:	n/a	n/a
15	CTCF	chr4:68823280-68823333	GM10266	blood:	n/a	n/a
16	CTCF	chr4:68793106-68793192	Fibrobl	skin:	n/a	n/a
17	E2F4	chr4:68809655-68809657	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr4:68795165-68795377	MCF10A-Er-Src	breast:	n/a	n/a
19	EP300	chr4:68795138-68795510	Hela-S3	cervix:	n/a	n/a
20	EP300	chr4:68795219-68795500	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr4:68794220-68794884	MCF-7	breast:	n/a	n/a
22	EP300	chr4:68794245-68794728	MCF-7	breast:	n/a	n/a
23	EP300	chr4:68795229-68795494	SK-N-SH_RA	brain:	n/a	n/a
24	ESR1	chr4:68794370-68794707	T-47D	breast:	n/a	chr4:68794515-68794532 chr4:68794516-68794531 chr4:68794496-68794511
25	ESR1	chr4:68794389-68794607	T-47D	breast:	n/a	chr4:68794515-68794532 chr4:68794516-68794531 chr4:68794496-68794511
26	ESR1	chr4:68794354-68794677	T-47D	breast:	n/a	chr4:68794515-68794532 chr4:68794516-68794531 chr4:68794496-68794511
27	FOS	chr4:68796964-68797173	MCF10A-Er-Src	breast:	n/a	chr4:68797085-68797092 chr4:68797084-68797093 chr4:68797084-68797092 chr4:68797083-68797092
28	FOS	chr4:68796859-68797351	MCF10A-Er-Src	breast:	n/a	chr4:68797085-68797092 chr4:68797084-68797093 chr4:68797084-68797092 chr4:68797083-68797092
29	FOS	chr4:68794176-68794607	MCF10A-Er-Src	breast:	n/a	chr4:68794319-68794328
30	FOS	chr4:68795114-68795590	MCF10A-Er-Src	breast:	n/a	chr4:68795296-68795305 chr4:68795410-68795420
31	FOS	chr4:68799523-68799825	MCF10A-Er-Src	breast:	n/a	chr4:68799670-68799679
32	FOS	chr4:68796933-68797350	MCF10A-Er-Src	breast:	n/a	chr4:68797085-68797092 chr4:68797084-68797093 chr4:68797084-68797092 chr4:68797083-68797092
33	FOS	chr4:68795014-68795873	MCF10A-Er-Src	breast:	n/a	chr4:68795296-68795305 chr4:68795410-68795420
34	FOS	chr4:68795064-68795826	MCF10A-Er-Src	breast:	n/a	chr4:68795296-68795305 chr4:68795410-68795420
35	FOS	chr4:68796937-68797293	MCF10A-Er-Src	breast:	n/a	chr4:68797085-68797092 chr4:68797084-68797093 chr4:68797084-68797092 chr4:68797083-68797092
36	FOS	chr4:68794141-68794602	MCF10A-Er-Src	breast:	n/a	chr4:68794319-68794328
37	FOS	chr4:68799563-68799759	MCF10A-Er-Src	breast:	n/a	chr4:68799670-68799679
38	FOS	chr4:68799523-68799790	MCF10A-Er-Src	breast:	n/a	chr4:68799670-68799679
39	FOS	chr4:68794333-68794503	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:68795144-68795590	MCF10A-Er-Src	breast:	n/a	chr4:68795296-68795305 chr4:68795410-68795420
41	FOSL1	chr4:68794198-68794644	HCT-116	colon:	n/a	chr4:68794319-68794328
42	FOSL1	chr4:68795061-68795651	HCT-116	colon:	n/a	chr4:68795296-68795305 chr4:68795410-68795420
43	FOXA1	chr4:68794489-68794740	HepG2	liver:	n/a	chr4:68794641-68794656 chr4:68794663-68794678
44	FOXA1	chr4:68838589-68838865	HepG2	liver:	n/a	n/a
45	FOXA1	chr4:68794560-68794794	T-47D	breast:	n/a	chr4:68794641-68794656 chr4:68794663-68794678
46	FOXA2	chr4:68838389-68839047	A549	lung:	n/a	n/a
47	FOXA2	chr4:68794555-68794727	HepG2	liver:	n/a	n/a
48	FOXA2	chr4:68838563-68838938	A549	lung:	n/a	n/a
49	FOXM1	chr4:68794210-68794723	MCF-7	breast:	n/a	n/a
50	FOXM1	chr4:68794212-68794781	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68829101-68829151	HAEpiC	amniotic membrane:	n/a
2	chr4:68830227-68830277	GM12878	blood:	n/a
3	chr4:68829101-68829151	Caco-2	colon:	n/a
4	chr4:68830227-68830277	HIPEpiC	eye:	n/a
5	chr4:68830227-68830277	AG04449	skin:	fetal
6	chr4:68830227-68830277	AG10803	skin:	n/a
7	chr4:68801145-68801195	A549	lung:	n/a
8	chr4:68829101-68829151	MCF-7	breast:	n/a
9	chr4:68801145-68801195	HRCEpiC	kidney:	n/a
10	chr4:68830227-68830277	GM06990	blood:	n/a
11	chr4:68829101-68829151	Hepatocyte	liver:	n/a
12	chr4:68829101-68829151	AG04449	skin:	fetal
13	chr4:68830227-68830277	HUVEC	blood vessel:	n/a
14	chr4:68801145-68801195	HAEpiC	amniotic membrane:	n/a
15	chr4:68830227-68830277	ECC-1	luminal epithelium:	n/a
16	chr4:68830227-68830277	BJ	skin:	n/a
17	chr4:68801145-68801195	SAEC	small airway:	n/a
18	chr4:68829101-68829151	NT2-D1	testis:	n/a
19	chr4:68829101-68829151	Jurkat	blood:	n/a
20	chr4:68829101-68829151	SK-N-SH_RA	brain:	n/a
21	chr4:68829101-68829151	LNCaP	prostate:	n/a
22	chr4:68829101-68829151	Hela-S3	cervix:	n/a
23	chr4:68801145-68801195	HEEpiC	esophagus:	n/a
24	chr4:68801145-68801195	Caco-2	colon:	n/a
25	chr4:68801145-68801195	GM12891	blood:	n/a
26	chr4:68801145-68801195	PFSK-1	brain:	n/a
27	chr4:68830227-68830277	PANC-1	pancreas:	n/a
28	chr4:68801145-68801195	HCPEpiC	choroid plexus:	n/a
29	chr4:68829101-68829151	AG09319	gingival:	n/a
30	chr4:68830227-68830277	HRCEpiC	kidney:	n/a
31	chr4:68801145-68801195	Hela-S3	cervix:	n/a
32	chr4:68830227-68830277	U87	brain:	n/a
33	chr4:68830227-68830277	MCF10A-Er-Src	breast:	n/a
34	chr4:68801145-68801195	NB4	blood:	n/a
35	chr4:68801145-68801195	AG09319	gingival:	n/a
36	chr4:68829101-68829151	PrEC	prostate:	n/a
37	chr4:68801145-68801195	HMEC	breast:	n/a
38	chr4:68830227-68830277	LNCaP	prostate:	n/a
39	chr4:68830227-68830277	NH-A	brain:	n/a
40	chr4:68801145-68801195	HEK293	kidney:	embryo
41	chr4:68829101-68829151	NB4	blood:	n/a
42	chr4:68801145-68801195	MCF-7	breast:	n/a
43	chr4:68829101-68829151	HCT-116	colon:	n/a
44	chr4:68829101-68829151	HIPEpiC	eye:	n/a
45	chr4:68801145-68801195	HIPEpiC	eye:	n/a
46	chr4:68830227-68830277	GM19239	blood:	n/a
47	chr4:68829101-68829151	ECC-1	luminal epithelium:	n/a
48	chr4:68830227-68830277	SK-N-MC	brain:	n/a
49	chr4:68829101-68829151	PFSK-1	brain:	n/a
50	chr4:68830227-68830277	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:68788622..68791120-chr4:68792670..68794501,2	MCF-7	breast:
2	chr4:68788622..68791120-chr4:68792670..68794501,2	MCF-7	breast:
3	chr4:68794157..68794866-chr4:69050816..69051359,2	MCF-7	breast:
4	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
5	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
6	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
7	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
8	chr4:68785311..68788293-chr4:68790779..68793140,2	MCF-7	breast:
9	chr4:68788496..68791205-chr4:68791799..68795295,5	MCF-7	breast:
10	chr4:68787068..68789277-chr4:68795494..68798392,2	MCF-7	breast:
11	chr4:68788496..68791205-chr4:68791799..68795295,5	MCF-7	breast:
12	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:
13	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
14	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
15	chr4:68793797..68796085-chr4:69232793..69234726,2	MCF-7	breast:
16	chr4:68794355..68794979-chr4:68995102..68995843,2	MCF-7	breast:
17	chr4:68577504..68578308-chr4:68794030..68794919,2	MCF-7	breast:
18	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:
19	chr4:68794060..68794853-chr4:68904568..68905079,2	MCF-7	breast:
20	chr4:68794052..68794960-chr4:69050850..69051709,2	MCF-7	breast:
21	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
22	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
23	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
24	chr4:68782641..68784982-chr4:68793433..68796175,2	MCF-7	breast:
25	chr4:68565498..68567091-chr4:68824885..68827731,2	K562	blood:
26	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:

Variant related genes	Relation type
TMPRSS11A	TF binding region
TMPRSS11A	CpG island
ENSG00000033178	chromatin interactions
ENSG00000248049	chromatin interactions
ENSG00000198092	chromatin interactions

Extended variants
information (count: 1312 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1312 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185898235	chr4:68790629-68790630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546086920	chr4:68790633-68790634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559600198	chr4:68790650-68790651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148005544	chr4:68790675-68790676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200893655	chr4:68790692-68790693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551079954	chr4:68790693-68790694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200833086	chr4:68790710-68790711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372192004	chr4:68790822-68790823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs17088772	chr4:68790864-68790865	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs561474287	chr4:68790901-68790902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530123522	chr4:68790981-68790982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76014260	chr4:68790992-68790993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140756111	chr4:68791017-68791018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538960542	chr4:68791093-68791094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552412924	chr4:68791250-68791251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566145356	chr4:68791270-68791271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535265448	chr4:68791280-68791281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537055030	chr4:68791310-68791311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs17088773	chr4:68791313-68791314	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs574508074	chr4:68791382-68791383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150115286	chr4:68791389-68791390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs353158	chr4:68791400-68791401	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs76385564	chr4:68791500-68791501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375123968	chr4:68791518-68791519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546125487	chr4:68791529-68791530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368862624	chr4:68791563-68791564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141550752	chr4:68791584-68791585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369224888	chr4:68791590-68791591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146268658	chr4:68791632-68791633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542043591	chr4:68791803-68791804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190614346	chr4:68791890-68791891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71669186	chr4:68791946-68791947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs386400382	chr4:68791949-68791950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs72599781	chr4:68791954-68791955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376551691	chr4:68791955-68791956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530232628	chr4:68791967-68791968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552355496	chr4:68792040-68792041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553664638	chr4:68792059-68792060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549827290	chr4:68792109-68792110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183186343	chr4:68792148-68792149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186399106	chr4:68792154-68792155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138153586	chr4:68792190-68792191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566400210	chr4:68792204-68792205	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs192057537	chr4:68792206-68792207	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs570969738	chr4:68792212-68792213	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs548789601	chr4:68792245-68792246	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs568528476	chr4:68792266-68792267	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs374999319	chr4:68792290-68792291	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs537154914	chr4:68792304-68792305	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs353157	chr4:68792305-68792306	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68779800-68792200	Weak transcription	Esophagus	oesophagus
2	chr4:68792200-68792400	ZNF genes & repeats	Esophagus	oesophagus
3	chr4:68792200-68793400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:68792400-68793200	Genic enhancers	Esophagus	oesophagus
5	chr4:68792600-68793400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:68792600-68793600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:68793000-68793200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:68793000-68793400	Enhancers	Spleen	Spleen
9	chr4:68793200-68793400	ZNF genes & repeats	Esophagus	oesophagus
10	chr4:68793200-68794400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:68793400-68806600	Weak transcription	Esophagus	oesophagus
12	chr4:68793600-68794800	Enhancers	Primary hematopoietic stem cells	blood
13	chr4:68793600-68799800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:68794200-68796400	Enhancers	Hela-S3	cervix
18	chr4:68794200-68799000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:68794400-68796000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:68794400-68796000	Enhancers	HMEC	breast
21	chr4:68794400-68796200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr4:68794400-68797800	Enhancers	NHEK	skin
23	chr4:68794600-68795200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr4:68794800-68799200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:68794800-68799800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr4:68795200-68800000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr4:68796000-68799400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:68796200-68797400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:68797400-68797800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:68797800-68800200	Weak transcription	NHEK	skin
33	chr4:68797800-68800400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:68798600-68802000	Enhancers	Dnd41	blood
35	chr4:68798800-68799000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr4:68799000-68799400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:68799000-68800000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr4:68799200-68802200	Enhancers	Primary hematopoietic stem cells	blood
39	chr4:68799400-68799600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr4:68799400-68800000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr4:68799400-68800200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr4:68799400-68801000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr4:68799400-68801000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr4:68799600-68800000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:68799800-68801000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:68799800-68801000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr4:68799800-68801000	Enhancers	Fetal Heart	heart
48	chr4:68799800-68801200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr4:68800000-68800600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr4:68800000-68800800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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