Variant report

Variant	esv2759239
Chromosome Location	chr4:28543958-28839437
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	chr4:28823833-28823988	K562	blood:	n/a	n/a
2	BACH1	chr4:28572673-28572729	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr4:28684526-28684791	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:28789517-28789783	GM12878	blood:	n/a	n/a
5	CBX3	chr4:28688187-28688716	HCT-116	colon:	n/a	n/a
6	CEBPB	chr4:28629806-28630036	IMR90	lung:	n/a	chr4:28629918-28629929 chr4:28629918-28629931 chr4:28629918-28629931
7	CEBPB	chr4:28777649-28777964	Hela-S3	cervix:	n/a	chr4:28777661-28777672 chr4:28777821-28777830 chr4:28777784-28777795 chr4:28777821-28777830 chr4:28777819-28777832 chr4:28777784-28777793 chr4:28777821-28777830 chr4:28777820-28777831
8	CEBPB	chr4:28828214-28828396	K562	blood:	n/a	chr4:28828324-28828337 chr4:28828253-28828264
9	CEBPB	chr4:28825684-28826029	HepG2	liver:	n/a	chr4:28825857-28825866 chr4:28825855-28825868 chr4:28825855-28825868 chr4:28825855-28825866 chr4:28825856-28825867
10	CEBPB	chr4:28611081-28611306	HepG2	liver:	n/a	chr4:28611220-28611231
11	CEBPB	chr4:28611082-28611342	K562	blood:	n/a	chr4:28611220-28611231
12	CEBPB	chr4:28577778-28577973	A549	lung:	n/a	n/a
13	CEBPB	chr4:28655386-28655554	H1-hESC	embryonic stem cell:	n/a	chr4:28655487-28655498 chr4:28655485-28655496 chr4:28655487-28655496 chr4:28655485-28655498
14	CEBPB	chr4:28655370-28655599	K562	blood:	n/a	chr4:28655487-28655498 chr4:28655485-28655496 chr4:28655487-28655496 chr4:28655485-28655498
15	CEBPB	chr4:28666584-28666603	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:28663372-28663685	HepG2	liver:	n/a	chr4:28663629-28663640 chr4:28663629-28663640 chr4:28663426-28663439 chr4:28663482-28663494 chr4:28663629-28663642
17	CEBPB	chr4:28689104-28689305	IMR90	lung:	n/a	chr4:28689150-28689161
18	CEBPB	chr4:28777638-28778005	H1-hESC	embryonic stem cell:	n/a	chr4:28777661-28777672 chr4:28777821-28777830 chr4:28777784-28777795 chr4:28777821-28777830 chr4:28777819-28777832 chr4:28777784-28777793 chr4:28777821-28777830 chr4:28777820-28777831
19	CEBPB	chr4:28558833-28559087	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:28725878-28726242	H1-hESC	embryonic stem cell:	n/a	chr4:28726053-28726064 chr4:28725937-28725949
21	CEBPB	chr4:28725885-28726210	Hela-S3	cervix:	n/a	chr4:28726053-28726064 chr4:28725937-28725949
22	CEBPB	chr4:28689154-28689222	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:28598564-28598764	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:28663440-28663693	A549	lung:	n/a	chr4:28663629-28663640 chr4:28663629-28663640 chr4:28663482-28663494 chr4:28663629-28663642
25	CEBPB	chr4:28616211-28616411	A549	lung:	n/a	n/a
26	CEBPB	chr4:28777640-28777999	A549	lung:	n/a	chr4:28777661-28777672 chr4:28777821-28777830 chr4:28777784-28777795 chr4:28777821-28777830 chr4:28777819-28777832 chr4:28777784-28777793 chr4:28777821-28777830 chr4:28777820-28777831
27	CEBPB	chr4:28725875-28726235	A549	lung:	n/a	chr4:28726053-28726064 chr4:28725937-28725949
28	CEBPB	chr4:28585306-28585506	A549	lung:	n/a	n/a
29	CEBPB	chr4:28676408-28676634	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:28730328-28730676	MCF-7	breast:	n/a	n/a
31	CEBPB	chr4:28608808-28609008	IMR90	lung:	n/a	chr4:28608917-28608928 chr4:28608919-28608928
32	CEBPB	chr4:28730461-28730602	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:28707505-28707745	A549	lung:	n/a	n/a
34	CEBPB	chr4:28825718-28826010	IMR90	lung:	n/a	chr4:28825857-28825866 chr4:28825855-28825868 chr4:28825855-28825868 chr4:28825855-28825866 chr4:28825856-28825867
35	CEBPB	chr4:28825761-28825987	A549	lung:	n/a	chr4:28825857-28825866 chr4:28825855-28825868 chr4:28825855-28825868 chr4:28825855-28825866 chr4:28825856-28825867
36	CEBPB	chr4:28828136-28828421	IMR90	lung:	n/a	chr4:28828324-28828337 chr4:28828253-28828264
37	CEBPB	chr4:28666175-28666318	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:28629776-28630032	H1-hESC	embryonic stem cell:	n/a	chr4:28629918-28629929 chr4:28629918-28629931 chr4:28629918-28629931
39	CEBPB	chr4:28711314-28711622	IMR90	lung:	n/a	n/a
40	CEBPB	chr4:28725870-28726243	IMR90	lung:	n/a	chr4:28726053-28726064 chr4:28725937-28725949
41	CEBPB	chr4:28777642-28778300	HepG2	liver:	n/a	chr4:28777661-28777672 chr4:28777821-28777830 chr4:28777784-28777795 chr4:28777821-28777830 chr4:28777819-28777832 chr4:28777784-28777793 chr4:28777821-28777830 chr4:28777820-28777831
42	CEBPB	chr4:28711321-28711600	MCF-7	breast:	n/a	n/a
43	CEBPB	chr4:28721270-28721402	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:28655343-28655667	HepG2	liver:	n/a	chr4:28655487-28655498 chr4:28655485-28655496 chr4:28655487-28655496 chr4:28655485-28655498
45	CEBPB	chr4:28746053-28746244	HepG2	liver:	n/a	chr4:28746141-28746152
46	CEBPB	chr4:28629823-28630109	HepG2	liver:	n/a	chr4:28629918-28629929 chr4:28629918-28629931 chr4:28629918-28629931
47	CEBPB	chr4:28828127-28828387	A549	lung:	n/a	chr4:28828324-28828337 chr4:28828253-28828264
48	CEBPB	chr4:28725882-28726242	HepG2	liver:	n/a	chr4:28726053-28726064 chr4:28725937-28725949
49	CEBPB	chr4:28641171-28641469	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:28559366-28559708	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:28829667-28829717	AG09309	skin:	n/a
2	chr4:28725306-28725356	CMK	blood:	n/a
3	chr4:28829667-28829717	GM19239	blood:	n/a
4	chr4:28725306-28725356	HRCEpiC	kidney:	n/a
5	chr4:28829667-28829717	NB4	blood:	n/a
6	chr4:28725306-28725356	HRPEpiC	eye:	n/a
7	chr4:28829667-28829717	HCF	heart:	n/a
8	chr4:28829667-28829717	AoSMC	blood vessel:	n/a
9	chr4:28829667-28829717	HMEC	breast:	n/a
10	chr4:28829667-28829717	HIPEpiC	eye:	n/a
11	chr4:28829667-28829717	U87	brain:	n/a
12	chr4:28829667-28829717	ECC-1	luminal epithelium:	n/a
13	chr4:28725306-28725356	ovcar-3	ovarian:	n/a
14	chr4:28725306-28725356	NB4	blood:	n/a
15	chr4:28829667-28829717	H1-hESC	embryonic stem cell:	embryo
16	chr4:28829667-28829717	HUVEC	blood vessel:	n/a
17	chr4:28725306-28725356	SK-N-MC	brain:	n/a
18	chr4:28829667-28829717	CMK	blood:	n/a
19	chr4:28725306-28725356	HCF	heart:	n/a
20	chr4:28725306-28725356	GM12878	blood:	n/a
21	chr4:28725306-28725356	HNPCEpiC	eye:	n/a
22	chr4:28829667-28829717	AG10803	skin:	n/a
23	chr4:28829667-28829717	HCM	heart:	n/a
24	chr4:28829667-28829717	BE2_C	brain:	n/a
25	chr4:28829667-28829717	HRPEpiC	eye:	n/a
26	chr4:28725306-28725356	A549	lung:	n/a
27	chr4:28725306-28725356	PANC-1	pancreas:	n/a
28	chr4:28725306-28725356	MCF-7	breast:	n/a
29	chr4:28829667-28829717	HRE	kidney:	n/a
30	chr4:28725306-28725356	H1-hESC	embryonic stem cell:	embryo
31	chr4:28725306-28725356	SK-N-SH_RA	brain:	n/a
32	chr4:28829667-28829717	IMR90	lung:	fetal
33	chr4:28829667-28829717	SK-N-MC	brain:	n/a
34	chr4:28725306-28725356	SK-N-SH	brain:	n/a
35	chr4:28829667-28829717	AG04450	lung:	fetal
36	chr4:28725306-28725356	K562	blood:	n/a
37	chr4:28725306-28725356	NHBE	bronchial:	n/a
38	chr4:28725306-28725356	ProgFib	skin:	n/a
39	chr4:28725306-28725356	SKMC	muscle:	n/a
40	chr4:28829667-28829717	BJ	skin:	n/a
41	chr4:28725306-28725356	AoSMC	blood vessel:	n/a
42	chr4:28829667-28829717	AG09319	gingival:	n/a
43	chr4:28725306-28725356	AG04449	skin:	fetal
44	chr4:28829667-28829717	A549	lung:	n/a
45	chr4:28829667-28829717	PrEC	prostate:	n/a
46	chr4:28829667-28829717	PFSK-1	brain:	n/a
47	chr4:28725306-28725356	Hepatocyte	liver:	n/a
48	chr4:28829667-28829717	Jurkat	blood:	n/a
49	chr4:28725306-28725356	HEK293	kidney:	embryo
50	chr4:28725306-28725356	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:28823073..28825418-chr4:28842573..28844204,2	MCF-7	breast:
2	chr17:45078439..45078999-chr4:28740495..28741046,2	MCF-7	breast:
3	chr4:28787492..28790119-chr4:28809128..28811907,2	K562	blood:
4	chr4:28654800..28656998-chr4:28661413..28663386,2	MCF-7	breast:
5	chr4:28760216..28762213-chr4:28762423..28765367,2	K562	blood:
6	chr4:28642172..28644284-chr4:28671364..28674142,2	MCF-7	breast:
7	chr4:28642172..28644284-chr4:28671364..28674142,2	MCF-7	breast:
8	chr4:28797752..28800390-chr4:28800946..28802986,2	K562	blood:
9	chr4:28619270..28620926-chr4:28622787..28624765,2	MCF-7	breast:
10	chr4:28756009..28757657-chr4:28759258..28762060,2	MCF-7	breast:
11	chr4:28690061..28692565-chr4:28693804..28695877,2	K562	blood:
12	chr4:28699826..28702524-chr4:28704115..28706351,2	MCF-7	breast:
13	chr4:28797752..28800390-chr4:28800946..28802986,2	K562	blood:
14	chr4:28599052..28601001-chr4:28607450..28609596,2	MCF-7	breast:
15	chr4:28712094..28713787-chr4:28714088..28715942,2	MCF-7	breast:
16	chr4:28699826..28702524-chr4:28704115..28706351,2	MCF-7	breast:
17	chr4:28464145..28465046-chr4:28688173..28688894,2	MCF-7	breast:
18	chr4:28778617..28781313-chr4:28801513..28803129,2	K562	blood:
19	chr4:28787492..28790119-chr4:28809128..28811907,2	K562	blood:
20	chr4:28690061..28692565-chr4:28693804..28695877,2	K562	blood:
21	chr4:28778617..28781313-chr4:28801513..28803129,2	K562	blood:
22	chr4:28535821..28537946-chr4:28547892..28550438,2	MCF-7	breast:
23	chr2:19310340..19311108-chr4:28646906..28647846,2	MCF-7	breast:
24	chr4:28683044..28685145-chr4:28691951..28693893,2	K562	blood:
25	chr4:28599052..28601001-chr4:28607450..28609596,2	MCF-7	breast:
26	chr4:28666962..28669631-chr4:28671140..28674094,2	K562	blood:
27	chr4:28619270..28620926-chr4:28622787..28624765,2	MCF-7	breast:
28	chr4:28666962..28669631-chr4:28671140..28674094,2	K562	blood:
29	chr4:28654800..28656998-chr4:28661413..28663386,2	MCF-7	breast:
30	chr14:46737193..46737995-chr4:28770057..28770960,2	MCF-7	breast:
31	chr4:28805670..28808284-chr4:28808958..28811325,2	K562	blood:
32	chr4:28805670..28808284-chr4:28808958..28811325,2	K562	blood:
33	chr4:28756009..28757657-chr4:28759258..28762060,2	MCF-7	breast:
34	chr4:28683044..28685145-chr4:28691951..28693893,2	K562	blood:
35	chr4:28760216..28762213-chr4:28762423..28765367,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STIM2-4	chr4:28601669-28601897	ENSG00000250064
2	lnc-STIM2-5	chr4:28754781-28754905	XLOC_003488
3	lnc-RP11-180C1.1.1-3	chr4:28586520-28586645	NONHSAT095913
4	lnc-STIM2-4	chr4:28579538-28579618	ENSG00000250064
5	lnc-RP11-180C1.1.1-3	chr4:28586781-28586911	NONHSAT095913
6	lnc-STIM2-8	chr4:28712820-28713094	NONHSAT095914
7	lnc-STIM2-5	chr4:28754425-28754728	XLOC_003488

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4275	chr4:28821214-28821230	MIMAT0016905

Variant related genes	Relation type
RN7SL101P	TF binding region
MESTP3	TF binding region
RN7SL101P	CpG island
MESTP3	CpG island
ENSG00000243548	chromatin interactions
MTMR9	miRNA target sites

Extended variants
information (count: 6078 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:6078 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545238268	chr4:28543958-28543959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs292015	chr4:28543970-28543971	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs114223929	chr4:28543973-28543974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190720013	chr4:28544026-28544027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560957125	chr4:28544027-28544028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368671426	chr4:28544074-28544075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113958975	chr4:28544093-28544094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529616232	chr4:28544152-28544153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540533891	chr4:28544171-28544172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147969122	chr4:28544184-28544185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376769091	chr4:28544186-28544187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539055074	chr4:28544218-28544219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374917289	chr4:28544245-28544246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532436260	chr4:28544256-28544257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557737786	chr4:28544258-28544259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577537901	chr4:28544268-28544269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs292016	chr4:28544298-28544299	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs568936521	chr4:28544355-28544356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149292421	chr4:28544359-28544360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535685199	chr4:28544363-28544364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550761101	chr4:28544365-28544366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567655245	chr4:28544398-28544399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs292017	chr4:28544405-28544406	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs193030731	chr4:28544435-28544436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573382188	chr4:28544453-28544454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566858514	chr4:28544497-28544498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376081573	chr4:28544502-28544503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538927159	chr4:28544518-28544519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs67828300	chr4:28544551-28544552	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs575716972	chr4:28544578-28544579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544306571	chr4:28544583-28544584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554318623	chr4:28544599-28544600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371325343	chr4:28544621-28544622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574469465	chr4:28544651-28544652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144534431	chr4:28544661-28544662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185316111	chr4:28544673-28544674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532476227	chr4:28544681-28544682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201710012	chr4:28544714-28544715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574646096	chr4:28544779-28544780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546091030	chr4:28544877-28544878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537244858	chr4:28545001-28545002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373007788	chr4:28545005-28545006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs167104	chr4:28545048-28545049	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs292018	chr4:28545090-28545091	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs564525996	chr4:28545102-28545103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71185583	chr4:28545105-28545106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201837774	chr4:28545108-28545109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545019603	chr4:28545118-28545119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374973657	chr4:28545125-28545126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567695365	chr4:28545127-28545128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	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
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:28539600-28555200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:28547400-28547800	Enhancers	Fetal Brain Male	brain
3	chr4:28549600-28550800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:28549800-28550600	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr4:28549800-28551000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr4:28550000-28551000	Active TSS	Right Atrium	heart
7	chr4:28550200-28550400	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr4:28550200-28550600	Enhancers	Fetal Muscle Leg	muscle
9	chr4:28550200-28550800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:28550400-28550600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr4:28550400-28551000	Active TSS	Fetal Heart	heart
12	chr4:28555200-28556000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:28556000-28560600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:28557000-28557800	Enhancers	HUVEC	blood vessel
15	chr4:28557400-28558200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:28557600-28557800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:28557800-28558200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr4:28557800-28559200	Weak transcription	HUVEC	blood vessel
19	chr4:28558200-28559200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:28559200-28559600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr4:28559200-28559800	Enhancers	HUVEC	blood vessel
22	chr4:28559200-28561000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:28559400-28561000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:28559600-28566600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr4:28560600-28561200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr4:28561200-28564000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:28564000-28564200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:28564200-28564800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:28564800-28565400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:28565400-28568000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr4:28566600-28567200	Enhancers	Fetal Stomach	stomach
32	chr4:28566600-28567600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr4:28568000-28570600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:28570600-28587400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:28583600-28583800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr4:28587400-28588200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:28588200-28623400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:28590400-28591000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr4:28590600-28591200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:28602000-28602600	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr4:28602200-28602600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr4:28602400-28602800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr4:28602600-28603600	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr4:28602800-28603800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr4:28603800-28604000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr4:28603800-28604000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr4:28611400-28611800	Enhancers	Fetal Heart	heart
48	chr4:28622800-28623800	Enhancers	Muscle Satellite Cultured Cells	--
49	chr4:28623000-28623600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:28623400-28623800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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