Variant report

Variant	esv1807842
Chromosome Location	chr4:68795815-68877576
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	CEBPB	chr4:68854296-68854552	K562	blood:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
3	CEBPB	chr4:68867136-68867337	Hela-S3	cervix:	n/a	chr4:68867240-68867257
4	CEBPB	chr4:68855153-68855430	MCF-7	breast:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
5	CEBPB	chr4:68813237-68813501	HepG2	liver:	n/a	chr4:68813348-68813359
6	CEBPB	chr4:68855215-68855252	K562	blood:	n/a	n/a
7	CEBPB	chr4:68867081-68867455	MCF-7	breast:	n/a	chr4:68867240-68867257
8	CEBPB	chr4:68867084-68867396	A549	lung:	n/a	chr4:68867240-68867257
9	CEBPB	chr4:68867138-68867338	H1-hESC	embryonic stem cell:	n/a	chr4:68867240-68867257
10	CEBPB	chr4:68854270-68854590	HepG2	liver:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
11	CEBPB	chr4:68853094-68853163	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:68867062-68867417	IMR90	lung:	n/a	chr4:68867240-68867257
13	CEBPB	chr4:68856229-68856393	HepG2	liver:	n/a	chr4:68856321-68856332 chr4:68856323-68856334 chr4:68856323-68856332
14	CEBPB	chr4:68854260-68854618	IMR90	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
15	CEBPB	chr4:68856283-68856483	K562	blood:	n/a	chr4:68856321-68856332 chr4:68856323-68856334 chr4:68856323-68856332
16	CEBPB	chr4:68861899-68862052	HepG2	liver:	n/a	chr4:68861967-68861980 chr4:68861968-68861979
17	CEBPB	chr4:68854271-68854605	Hela-S3	cervix:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
18	CEBPB	chr4:68855216-68855371	HepG2	liver:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
19	CEBPB	chr4:68867077-68867408	HepG2	liver:	n/a	chr4:68867240-68867257
20	CEBPB	chr4:68857875-68858075	H1-hESC	embryonic stem cell:	n/a	chr4:68857997-68858014
21	CEBPB	chr4:68854301-68854524	A549	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
22	CTCF	chr4:68854269-68854391	GM13976	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
23	CTCF	chr4:68823280-68823333	GM10266	blood:	n/a	n/a
24	CTCF	chr4:68854260-68854410	MCF-7	breast:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
25	CTCF	chr4:68854265-68854271	Fibrobl	skin:	n/a	n/a
26	CTCF	chr4:68854124-68854522	K562	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
27	CTCF	chr4:68854300-68854450	HA-sp	spinal cord:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
28	CTCF	chr4:68857900-68858050	NHEK	skin:	n/a	n/a
29	CTCF	chr4:68854240-68854390	GM12871	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
30	CTCF	chr4:68854220-68854370	GM12878	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
31	CTCF	chr4:68854160-68854310	GM12867	blood:	n/a	n/a
32	CTCF	chr4:68854207-68854395	A549	lung:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
33	CTCF	chr4:68854200-68854350	HCT-116	colon:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
34	CTCF	chr4:68854280-68854430	HMEC	breast:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
35	CTCF	chr4:68854260-68854410	GM12873	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
36	CTCF	chr4:68854220-68854370	GM12874	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
37	CTCF	chr4:68854300-68854450	HFF	foreskin:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
38	CTCF	chr4:68854131-68854526	GM12878	blood:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
39	CTCF	chr4:68861685-68861779	GM10248	blood:	n/a	n/a
40	CTCF	chr4:68854260-68854410	HEEpiC	esophagus:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
41	CTCF	chr4:68854260-68854410	HRPEpiC	eye:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
42	CTCF	chr4:68854187-68854322	MCF-7	breast:	n/a	chr4:68854303-68854316 chr4:68854300-68854318
43	CTCF	chr4:68854460-68854610	GM12870	blood:	n/a	n/a
44	CTCF	chr4:68854220-68854370	MCF-7	breast:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
45	CTCF	chr4:68854300-68854450	Caco-2	colon:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
46	CTCF	chr4:68854249-68854409	LNCaP	prostate:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
47	CTCF	chr4:68854279-68854392	Fibrobl	skin:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
48	CTCF	chr4:68854240-68854390	Caco-2	colon:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
49	CTCF	chr4:68854260-68854410	HepG2	liver:	n/a	chr4:68854303-68854316 chr4:68854300-68854318 chr4:68854302-68854323
50	CTCF	chr4:68819804-68819825	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68829101-68829151	RPTEC	kidney:	n/a
2	chr4:68830227-68830277	U87	brain:	n/a
3	chr4:68830227-68830277	HEK293	kidney:	embryo
4	chr4:68801145-68801195	CMK	blood:	n/a
5	chr4:68829101-68829151	HCM	heart:	n/a
6	chr4:68801145-68801195	PANC-1	pancreas:	n/a
7	chr4:68830227-68830277	SK-N-MC	brain:	n/a
8	chr4:68801145-68801195	SK-N-SH_RA	brain:	n/a
9	chr4:68801145-68801195	GM12892	blood:	n/a
10	chr4:68829101-68829151	A549	lung:	n/a
11	chr4:68801145-68801195	ECC-1	luminal epithelium:	n/a
12	chr4:68829101-68829151	PrEC	prostate:	n/a
13	chr4:68830227-68830277	HCM	heart:	n/a
14	chr4:68830227-68830277	SKMC	muscle:	n/a
15	chr4:68801145-68801195	GM12891	blood:	n/a
16	chr4:68829101-68829151	HAEpiC	amniotic membrane:	n/a
17	chr4:68829101-68829151	HepG2	liver:	n/a
18	chr4:68830227-68830277	Caco-2	colon:	n/a
19	chr4:68829101-68829151	ovcar-3	ovarian:	n/a
20	chr4:68829101-68829151	HRE	kidney:	n/a
21	chr4:68830227-68830277	PANC-1	pancreas:	n/a
22	chr4:68801145-68801195	NHDF-neo	bronchial:	n/a
23	chr4:68801145-68801195	HRE	kidney:	n/a
24	chr4:68830227-68830277	BE2_C	brain:	n/a
25	chr4:68830227-68830277	HMEC	breast:	n/a
26	chr4:68829101-68829151	BJ	skin:	n/a
27	chr4:68830227-68830277	AG10803	skin:	n/a
28	chr4:68801145-68801195	IMR90	lung:	fetal
29	chr4:68829101-68829151	HL-60	blood:	n/a
30	chr4:68830227-68830277	GM12891	blood:	n/a
31	chr4:68830227-68830277	HRE	kidney:	n/a
32	chr4:68829101-68829151	GM19239	blood:	n/a
33	chr4:68801145-68801195	PrEC	prostate:	n/a
34	chr4:68829101-68829151	SKMC	muscle:	n/a
35	chr4:68829101-68829151	SK-N-SH_RA	brain:	n/a
36	chr4:68830227-68830277	H1-hESC	embryonic stem cell:	embryo
37	chr4:68830227-68830277	HCT-116	colon:	n/a
38	chr4:68830227-68830277	AG04450	lung:	fetal
39	chr4:68829101-68829151	NHDF-neo	bronchial:	n/a
40	chr4:68801145-68801195	AG09309	skin:	n/a
41	chr4:68830227-68830277	LNCaP	prostate:	n/a
42	chr4:68830227-68830277	IMR90	lung:	fetal
43	chr4:68801145-68801195	HMEC	breast:	n/a
44	chr4:68801145-68801195	AG04449	skin:	fetal
45	chr4:68830227-68830277	HIPEpiC	eye:	n/a
46	chr4:68801145-68801195	AG09319	gingival:	n/a
47	chr4:68801145-68801195	NB4	blood:	n/a
48	chr4:68830227-68830277	GM06990	blood:	n/a
49	chr4:68801145-68801195	RPTEC	kidney:	n/a
50	chr4:68829101-68829151	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
2	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
3	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
4	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
5	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
6	chr4:68793797..68796085-chr4:69232793..69234726,2	MCF-7	breast:
7	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
8	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
9	chr4:68782641..68784982-chr4:68793433..68796175,2	MCF-7	breast:
10	chr4:68784089..68784796-chr4:68853790..68854411,2	MCF-7	breast:
11	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
12	chr4:68853837..68854799-chr4:69040919..69041918,3	MCF-7	breast:
13	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:
14	chr4:68854785..68855326-chr4:69041026..69041997,2	MCF-7	breast:
15	chr4:68853962..68854562-chr4:69041076..69041834,2	K562	blood:
16	chr4:68565498..68567091-chr4:68824885..68827731,2	K562	blood:
17	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
18	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
19	chr4:68787068..68789277-chr4:68795494..68798392,2	MCF-7	breast:

Variant related genes	Relation type
TMPRSS11A	TF binding region
RNU6-95P	TF binding region
TMPRSS11GP	TF binding region
TMPRSS11A	CpG island
RNU6-95P	CpG island
TMPRSS11GP	CpG island
ENSG00000248049	chromatin interactions
ENSG00000033178	chromatin interactions

Extended variants
information (count: 1554 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1554 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17578509	chr4:68795815-68795816	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs11929790	chr4:68795859-68795860	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs547631931	chr4:68795883-68795884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs61641677	chr4:68795900-68795901	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs529960604	chr4:68795909-68795910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549989707	chr4:68795910-68795911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569406642	chr4:68795916-68795917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77213435	chr4:68795950-68795951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557889122	chr4:68795959-68795960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569883483	chr4:68795969-68795970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79043085	chr4:68795981-68795982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554397136	chr4:68795996-68795997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369596233	chr4:68796001-68796002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574243722	chr4:68796054-68796055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536483948	chr4:68796057-68796058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140224184	chr4:68796073-68796074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145292160	chr4:68796098-68796099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544671963	chr4:68796103-68796104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79153150	chr4:68796126-68796127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs36032989	chr4:68796147-68796148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571962309	chr4:68796174-68796175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373047996	chr4:68796178-68796179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540665130	chr4:68796191-68796192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114026474	chr4:68796199-68796200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184276739	chr4:68796203-68796204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550026415	chr4:68796222-68796223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563444546	chr4:68796267-68796268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369511105	chr4:68796286-68796287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs78929359	chr4:68796300-68796301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189178228	chr4:68796342-68796343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534240332	chr4:68796344-68796345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181065769	chr4:68796361-68796362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567647411	chr4:68796438-68796439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185658090	chr4:68796459-68796460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs202166943	chr4:68796469-68796470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs202134401	chr4:68796472-68796473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556356970	chr4:68796500-68796501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs544678862	chr4:68796523-68796524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs67302217	chr4:68796527-68796528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs199853339	chr4:68796549-68796550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs57391851	chr4:68796579-68796580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538351424	chr4:68796586-68796587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188820513	chr4:68796593-68796594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572034521	chr4:68796624-68796625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74855579	chr4:68796627-68796628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138118752	chr4:68796672-68796673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs574878824	chr4:68796703-68796704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574803087	chr4:68796767-68796768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs62302862	chr4:68796802-68796803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531029121	chr4:68796808-68796809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68793400-68806600	Weak transcription	Esophagus	oesophagus
2	chr4:68793600-68799800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:68794200-68796400	Enhancers	Hela-S3	cervix
4	chr4:68794200-68799000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:68794400-68796000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:68794400-68796000	Enhancers	HMEC	breast
7	chr4:68794400-68796200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:68794400-68797800	Enhancers	NHEK	skin
9	chr4:68794800-68799200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr4:68794800-68799800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr4:68795200-68800000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr4:68796000-68799400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:68796200-68797400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:68797400-68797800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr4:68797800-68800200	Weak transcription	NHEK	skin
18	chr4:68797800-68800400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:68798600-68802000	Enhancers	Dnd41	blood
20	chr4:68798800-68799000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr4:68799000-68799400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:68799000-68800000	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr4:68799200-68802200	Enhancers	Primary hematopoietic stem cells	blood
24	chr4:68799400-68799600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:68799400-68800000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:68799400-68800200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr4:68799400-68801000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr4:68799400-68801000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr4:68799600-68800000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:68799800-68801000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:68799800-68801000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr4:68799800-68801000	Enhancers	Fetal Heart	heart
33	chr4:68799800-68801200	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr4:68800000-68800600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr4:68800000-68800800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr4:68800000-68801000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr4:68800000-68801200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr4:68800000-68801200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr4:68800200-68800400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr4:68800200-68800800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr4:68800200-68800800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr4:68800200-68800800	Enhancers	NHEK	skin
43	chr4:68800200-68801200	Enhancers	Fetal Intestine Small	intestine
44	chr4:68800400-68800600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr4:68800400-68800800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:68800400-68800800	Enhancers	Brain Germinal Matrix	brain
47	chr4:68800400-68800800	Enhancers	Thymus	Thymus
48	chr4:68800400-68801000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr4:68800600-68800800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr4:68800600-68801000	Enhancers	H1 Cell Line	embryonic stem cell

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