Variant report

Variant	nsv879874
Chromosome Location	chr4:124550693-124607201
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:685)
CpG islands
(count:306)
Chromatin interactive
region (count:22)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:685 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:124582329-124582671	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:124580402-124581271	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:124570740-124571648	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:124582321-124582641	K562	blood:	n/a	n/a
5	ATF2	chr4:124593104-124593606	GM12878	blood:	n/a	n/a
6	ATF2	chr4:124593144-124593558	GM12878	blood:	n/a	n/a
7	ATF3	chr4:124590284-124590714	K562	blood:	n/a	n/a
8	BATF	chr4:124593221-124593460	GM12878	blood:	n/a	n/a
9	BATF	chr4:124593166-124593441	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:124570413-124570743	GM12878	blood:	n/a	chr4:124570644-124570653
11	BCL11A	chr4:124570328-124570744	GM12878	blood:	n/a	chr4:124570644-124570653
12	BCLAF1	chr4:124593173-124593419	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:124570879-124571458	HepG2	liver:	n/a	n/a
14	BHLHE40	chr4:124593220-124593359	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:124570383-124570766	GM12878	blood:	n/a	n/a
16	BRCA1	chr4:124594295-124594637	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr4:124577670-124578150	K562	blood:	n/a	n/a
18	CEBPB	chr4:124570823-124571802	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:124588629-124589378	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:124561498-124561689	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:124578249-124578282	H1-hESC	embryonic stem cell:	n/a	chr4:124578263-124578274
22	CEBPB	chr4:124594193-124594432	K562	blood:	n/a	chr4:124594318-124594329
23	CEBPB	chr4:124570780-124571308	IMR90	lung:	n/a	chr4:124570798-124570815 chr4:124570799-124570812
24	CEBPB	chr4:124570802-124571231	A549	lung:	n/a	n/a
25	CEBPB	chr4:124561453-124561684	A549	lung:	n/a	n/a
26	CEBPB	chr4:124594097-124594463	MCF-7	breast:	n/a	chr4:124594318-124594329
27	CEBPB	chr4:124578197-124578381	HepG2	liver:	n/a	chr4:124578263-124578274
28	CEBPB	chr4:124593900-124594516	Hela-S3	cervix:	n/a	chr4:124594318-124594329
29	CEBPB	chr4:124594111-124594517	MCF-7	breast:	n/a	chr4:124594318-124594329
30	CEBPB	chr4:124574493-124574804	HepG2	liver:	n/a	chr4:124574662-124574671 chr4:124574660-124574673 chr4:124574660-124574671
31	CEBPB	chr4:124595197-124595455	MCF-7	breast:	n/a	chr4:124595334-124595347
32	CEBPB	chr4:124594049-124594561	ECC-1	luminal epithelium:	n/a	chr4:124594318-124594329
33	CEBPB	chr4:124594230-124594430	HepG2	liver:	n/a	chr4:124594318-124594329
34	CEBPB	chr4:124594143-124594482	A549	lung:	n/a	chr4:124594318-124594329
35	CEBPB	chr4:124594126-124594515	IMR90	lung:	n/a	chr4:124594318-124594329
36	CEBPB	chr4:124574481-124574659	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr4:124566378-124566585	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:124578193-124578433	A549	lung:	n/a	chr4:124578263-124578274
39	CEBPB	chr4:124561342-124561768	IMR90	lung:	n/a	n/a
40	CEBPB	chr4:124578158-124578435	IMR90	lung:	n/a	chr4:124578263-124578274
41	CEBPB	chr4:124594068-124594575	ECC-1	luminal epithelium:	n/a	chr4:124594318-124594329
42	CEBPB	chr4:124574508-124574726	A549	lung:	n/a	chr4:124574662-124574671 chr4:124574660-124574673 chr4:124574660-124574671
43	CEBPB	chr4:124566412-124566622	K562	blood:	n/a	n/a
44	CEBPB	chr4:124578212-124578289	K562	blood:	n/a	chr4:124578263-124578274
45	CEBPB	chr4:124570893-124571074	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:124594110-124594538	A549	lung:	n/a	chr4:124594318-124594329
47	CEBPD	chr4:124590388-124590618	K562	blood:	n/a	n/a
48	CEBPD	chr4:124590368-124590791	K562	blood:	n/a	n/a
49	CHD2	chr4:124604801-124605127	K562	blood:	n/a	n/a
50	CHD2	chr4:124570406-124570761	GM12878	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:124572578-124572628	HepG2	liver:	n/a
2	chr4:124572578-124572628	HepG2	liver:	n/a
3	chr4:124572578-124572628	AG09309	skin:	n/a
4	chr4:124594794-124594844	HRPEpiC	eye:	n/a
5	chr4:124606293-124606343	HRPEpiC	eye:	n/a
6	chr4:124572578-124572628	GM12892	blood:	n/a
7	chr4:124594794-124594844	ovcar-3	ovarian:	n/a
8	chr4:124572578-124572628	H1-hESC	embryonic stem cell:	embryo
9	chr4:124552897-124552947	HCPEpiC	choroid plexus:	n/a
10	chr4:124552897-124552947	GM12892	blood:	n/a
11	chr4:124594794-124594844	MCF-7	breast:	n/a
12	chr4:124572578-124572628	GM12891	blood:	n/a
13	chr4:124606293-124606343	HUVEC	blood vessel:	n/a
14	chr4:124571385-124571435	HEK293	kidney:	embryo
15	chr4:124572578-124572628	A549	lung:	n/a
16	chr4:124606293-124606343	LNCaP	prostate:	n/a
17	chr4:124606293-124606343	HRE	kidney:	n/a
18	chr4:124552897-124552947	K562	blood:	n/a
19	chr4:124594794-124594844	HCPEpiC	choroid plexus:	n/a
20	chr4:124606293-124606343	GM12892	blood:	n/a
21	chr4:124552897-124552947	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:124606293-124606343	CMK	blood:	n/a
23	chr4:124606293-124606343	HCM	heart:	n/a
24	chr4:124571385-124571435	AG09309	skin:	n/a
25	chr4:124594794-124594844	GM06990	blood:	n/a
26	chr4:124571385-124571435	AG10803	skin:	n/a
27	chr4:124606293-124606343	GM19239	blood:	n/a
28	chr4:124572578-124572628	HRE	kidney:	n/a
29	chr4:124594794-124594844	CMK	blood:	n/a
30	chr4:124606293-124606343	HL-60	blood:	n/a
31	chr4:124594794-124594844	HRCEpiC	kidney:	n/a
32	chr4:124571385-124571435	PANC-1	pancreas:	n/a
33	chr4:124552897-124552947	SK-N-SH_RA	brain:	n/a
34	chr4:124552897-124552947	HEK293	kidney:	embryo
35	chr4:124571385-124571435	HCF	heart:	n/a
36	chr4:124572578-124572628	HRCEpiC	kidney:	n/a
37	chr4:124606293-124606343	AoSMC	blood vessel:	n/a
38	chr4:124606293-124606343	Jurkat	blood:	n/a
39	chr4:124606293-124606343	SK-N-MC	brain:	n/a
40	chr4:124571385-124571435	Hepatocyte	liver:	n/a
41	chr4:124606293-124606343	NHDF-neo	bronchial:	n/a
42	chr4:124572578-124572628	PrEC	prostate:	n/a
43	chr4:124594794-124594844	NT2-D1	testis:	n/a
44	chr4:124571385-124571435	SAEC	small airway:	n/a
45	chr4:124606293-124606343	T-47D	breast:	n/a
46	chr4:124571385-124571435	PrEC	prostate:	n/a
47	chr4:124594794-124594844	SKMC	muscle:	n/a
48	chr4:124594794-124594844	HIPEpiC	eye:	n/a
49	chr4:124571385-124571435	HRCEpiC	kidney:	n/a
50	chr4:124606293-124606343	BE2_C	brain:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:124582206..124582930-chr4:125183080..125184000,2	MCF-7	breast:
2	chr4:124591127..124594016-chr4:124622193..124624753,2	K562	blood:
3	chr4:124485427..124486524-chr4:124580578..124581744,8	MCF-7	breast:
4	chr4:124485623..124486524-chr4:124581998..124582924,2	MCF-7	breast:
5	chr4:124485658..124486578-chr4:124582431..124582959,2	K562	blood:
6	chr4:124587417..124589691-chr4:124590873..124592860,2	K562	blood:
7	chr4:124591108..124593759-chr4:124596428..124598795,2	K562	blood:
8	chr4:124048317..124048943-chr4:124580795..124581655,2	MCF-7	breast:
9	chr4:124317878..124321716-chr4:124581134..124584700,4	MCF-7	breast:
10	chr4:124319981..124321573-chr4:124580466..124582446,2	MCF-7	breast:
11	chr4:124312099..124312874-chr4:124581927..124582437,2	MCF-7	breast:
12	chr4:124590521..124592638-chr4:124596281..124598290,3	K562	blood:
13	chr4:124591108..124593759-chr4:124596428..124598795,2	K562	blood:
14	chr4:124271082..124272019-chr4:124580612..124581573,2	MCF-7	breast:
15	chr4:124271449..124272025-chr4:124580652..124581509,3	MCF-7	breast:
16	chr4:124048111..124048748-chr4:124582168..124582901,2	MCF-7	breast:
17	chr4:124584154..124586562-chr4:124589727..124591476,2	K562	blood:
18	chr4:124311817..124312603-chr4:124581045..124581823,2	MCF-7	breast:
19	chr4:124587417..124589691-chr4:124590873..124592860,2	K562	blood:
20	chr4:124048090..124049080-chr4:124581973..124582933,2	K562	blood:
21	chr4:124590521..124592638-chr4:124596281..124598290,3	K562	blood:
22	chr4:124584154..124586562-chr4:124589727..124591476,2	K562	blood:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPRY1-2	chr4:124582908-124582988	ENSG00000249464
2	lnc-SPRY1-2	chr4:124573942-124574057	NONHSAT098194
3	lnc-SPRY1-2	chr4:124571422-124571487	ENSG00000249464
4	lnc-SPRY1-4	chr4:124561437-124561699	NONHSAT098193
5	lnc-SPRY1-2	chr4:124582908-124589223	NONHSAT098196
6	lnc-SPRY1-2	chr4:124571147-124571487	NONHSAT098194
7	lnc-SPRY1-2	chr4:124571390-124571503	NONHSAT098195
8	lnc-SPRY1-2	chr4:124591784-124592922	NONHSAT098194
9	lnc-SPRY1-2	chr4:124582908-124582988	NONHSAT098199
10	lnc-SPRY1-2	chr4:124573942-124574057	NONHSAT098196
11	lnc-SPRY1-2	chr4:124573942-124574057	ENSG00000249464
12	lnc-SPRY1-2	chr4:124571422-124571487	NONHSAT098196
13	lnc-SPRY1-2	chr4:124573942-124574057	NONHSAT098195
14	lnc-SPRY1-2	chr4:124580689-124580994	NONHSAT098194
15	lnc-SPRY1-2	chr4:124573942-124574057	ENSG00000249464
16	lnc-SPRY1-2	chr4:124573940-124574057	NONHSAT098199
17	lnc-SPRY1-2	chr4:124573942-124574057	ENSG00000249464
18	lnc-SPRY1-2	chr4:124582908-124587987	ENSG00000249464
19	lnc-SPRY1-2	chr4:124582908-124582988	ENSG00000249464
20	lnc-SPRY1-2	chr4:124571446-124571484	ENSG00000249464
21	lnc-SPRY1-2	chr4:124582908-124582988	NONHSAT098195
22	lnc-SPRY1-2	chr4:124597135-124597951	NONHSAT098194
23	lnc-SPRY1-2	chr4:124595989-124596918	NONHSAT098194
24	lnc-SPRY1-2	chr4:124571446-124571487	ENSG00000249464
25	lnc-SPRY1-2	chr4:124582908-124582990	NONHSAT098194
26	lnc-SPRY1-2	chr4:124560706-124560877	NONHSAT098194
27	lnc-SPRY1-2	chr4:124597995-124598491	NONHSAT098194

No data

Variant related genes	Relation type
LINC01091	TF binding region
LINC01091	CpG island
ENSG00000164056	chromatin interactions
FRAT2	miRNA target sites
SCD	miRNA target sites
GLB1L3	miRNA target sites
C5orf24	miRNA target sites
ARL2BP	miRNA target sites
E2F7	miRNA target sites
DAND5	miRNA target sites
DUSP3	miRNA target sites
EGR1	miRNA target sites

Extended variants
information (count: 1963 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1963 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2589864	chr4:124550693-124550694	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190766056	chr4:124550697-124550698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73844826	chr4:124550706-124550707	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs535853692	chr4:124550713-124550714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537132681	chr4:124550724-124550725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557050546	chr4:124550729-124550730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576875737	chr4:124550738-124550739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182442037	chr4:124550764-124550765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552716968	chr4:124550855-124550856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572680131	chr4:124550892-124550893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541363370	chr4:124550910-124550911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561139170	chr4:124550934-124550935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74693018	chr4:124550948-124550949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs62322889	chr4:124550950-124550951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554614020	chr4:124550977-124550978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543610111	chr4:124551020-124551021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563145057	chr4:124551086-124551087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186824797	chr4:124551139-124551140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563398004	chr4:124551145-124551146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532512300	chr4:124551148-124551149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552515989	chr4:124551183-124551184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576079753	chr4:124551260-124551261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143549658	chr4:124551270-124551271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144239622	chr4:124551286-124551287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs13107493	chr4:124551287-124551288	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs548542711	chr4:124551304-124551305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10518419	chr4:124551325-124551326	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs115647001	chr4:124551401-124551402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371068364	chr4:124551413-124551414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78508121	chr4:124551425-124551426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs55744961	chr4:124551432-124551433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557208373	chr4:124551489-124551490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140438374	chr4:124551563-124551564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190845205	chr4:124551564-124551565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368387573	chr4:124551629-124551630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145574948	chr4:124551630-124551631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550205467	chr4:124551666-124551667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62322890	chr4:124551705-124551706	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs183472464	chr4:124551722-124551723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541876997	chr4:124551741-124551742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554793171	chr4:124551744-124551745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532545854	chr4:124551769-124551770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552629627	chr4:124551774-124551775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116572558	chr4:124551789-124551790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543573290	chr4:124551863-124551864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374900036	chr4:124551885-124551886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534047314	chr4:124551916-124551917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188239637	chr4:124551924-124551925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532614923	chr4:124551928-124551929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs116074955	chr4:124551949-124551950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	18765545	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:574 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124543200-124552800	Weak transcription	Adipose Nuclei	Adipose
2	chr4:124552600-124553800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:124552600-124553800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr4:124552600-124554000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr4:124552600-124554200	Enhancers	Fetal Lung	lung
6	chr4:124552800-124553000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:124552800-124553000	Enhancers	NH-A	brain
8	chr4:124552800-124553200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:124552800-124553200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr4:124552800-124553400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr4:124552800-124553400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:124552800-124553400	Enhancers	NHEK	skin
13	chr4:124552800-124553600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:124552800-124553600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:124552800-124553600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:124552800-124553600	Enhancers	Fetal Muscle Leg	muscle
17	chr4:124552800-124553600	Enhancers	HMEC	breast
18	chr4:124552800-124553600	Enhancers	NHDF-Ad	bronchial
19	chr4:124552800-124553800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr4:124552800-124553800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr4:124552800-124553800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr4:124552800-124553800	Enhancers	Adipose Nuclei	Adipose
23	chr4:124552800-124554000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:124552800-124554000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr4:124552800-124554000	Enhancers	Fetal Kidney	kidney
26	chr4:124552800-124554000	Enhancers	Osteobl	bone
27	chr4:124552800-124554400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:124553000-124553200	Enhancers	HSMMtube	muscle
29	chr4:124553000-124553400	Enhancers	HSMM	muscle
30	chr4:124553000-124553800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr4:124553000-124553800	Enhancers	Colon Smooth Muscle	Colon
32	chr4:124553000-124559000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr4:124553200-124553600	Enhancers	Fetal Stomach	stomach
34	chr4:124553200-124554400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr4:124553400-124554000	Enhancers	Primary hematopoietic stem cells	blood
36	chr4:124553600-124553800	Enhancers	NH-A	brain
37	chr4:124553800-124554000	Enhancers	HSMMtube	muscle
38	chr4:124553800-124564400	Weak transcription	Colon Smooth Muscle	Colon
39	chr4:124558400-124569800	Weak transcription	Psoas Muscle	Psoas
40	chr4:124559000-124559800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr4:124559400-124560600	Enhancers	HepG2	liver
42	chr4:124559800-124560000	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:124560000-124562400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:124560200-124560400	Enhancers	Fetal Muscle Leg	muscle
45	chr4:124560200-124560600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:124560200-124560600	Enhancers	Fetal Stomach	stomach
47	chr4:124560400-124569000	Weak transcription	Fetal Muscle Leg	muscle
48	chr4:124560600-124568600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:124561600-124561800	Enhancers	NHDF-Ad	bronchial
50	chr4:124561600-124562000	Weak transcription	Fetal Kidney	kidney

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