Variant report

Variant	nsv1005240
Chromosome Location	chr4:121093285-121420997
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	ARID3A	chr4:121297907-121297919	HepG2	liver:	n/a	n/a
2	ATF2	chr4:121252954-121253319	GM12878	blood:	n/a	n/a
3	ATF2	chr4:121387529-121388007	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:121387504-121388036	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:121252922-121253430	GM12878	blood:	n/a	n/a
6	ATF2	chr4:121248398-121248789	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:121158096-121158364	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr4:121252898-121253394	GM12878	blood:	n/a	n/a
9	BCL3	chr4:121344997-121345240	GM12878	blood:	n/a	n/a
10	BRCA1	chr4:121252523-121252606	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr4:121402998-121403202	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr4:121236020-121236194	H1-hESC	embryonic stem cell:	n/a	n/a
13	CCNT2	chr4:121310347-121310670	K562	blood:	n/a	n/a
14	CEBPB	chr4:121149201-121149515	Hela-S3	cervix:	n/a	chr4:121149393-121149404
15	CEBPB	chr4:121301462-121301727	A549	lung:	n/a	chr4:121301622-121301633
16	CEBPB	chr4:121159540-121159761	HepG2	liver:	n/a	chr4:121159674-121159687
17	CEBPB	chr4:121182334-121182551	K562	blood:	n/a	chr4:121182442-121182453
18	CEBPB	chr4:121239008-121239259	Hela-S3	cervix:	n/a	chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239125-121239136 chr4:121239126-121239135 chr4:121239124-121239137
19	CEBPB	chr4:121238961-121239287	A549	lung:	n/a	chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239125-121239136 chr4:121239126-121239135 chr4:121239124-121239137
20	CEBPB	chr4:121239034-121239218	K562	blood:	n/a	chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239125-121239136 chr4:121239126-121239135 chr4:121239124-121239137
21	CEBPB	chr4:121182336-121182588	Hela-S3	cervix:	n/a	chr4:121182442-121182453
22	CEBPB	chr4:121097525-121097707	HepG2	liver:	n/a	chr4:121097565-121097576
23	CEBPB	chr4:121403118-121403430	IMR90	lung:	n/a	chr4:121403253-121403266 chr4:121403240-121403251 chr4:121403241-121403252 chr4:121403240-121403253
24	CEBPB	chr4:121301474-121301774	IMR90	lung:	n/a	chr4:121301622-121301633
25	CEBPB	chr4:121146760-121147063	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:121351274-121351565	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr4:121119561-121119883	HepG2	liver:	n/a	chr4:121119710-121119721
28	CEBPB	chr4:121403127-121403384	A549	lung:	n/a	chr4:121403253-121403266 chr4:121403240-121403251 chr4:121403241-121403252 chr4:121403240-121403253
29	CEBPB	chr4:121259008-121259162	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:121238898-121239307	ECC-1	luminal epithelium:	n/a	chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239125-121239136 chr4:121239126-121239135 chr4:121239124-121239137
31	CEBPB	chr4:121211615-121211681	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:121149208-121149525	HepG2	liver:	n/a	chr4:121149393-121149404
33	CEBPB	chr4:121199908-121200095	K562	blood:	n/a	n/a
34	CEBPB	chr4:121420255-121420416	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:121250569-121250896	HepG2	liver:	n/a	chr4:121250732-121250743
36	CEBPB	chr4:121403103-121403414	HepG2	liver:	n/a	chr4:121403253-121403266 chr4:121403240-121403251 chr4:121403241-121403252 chr4:121403240-121403253
37	CEBPB	chr4:121250604-121250879	H1-hESC	embryonic stem cell:	n/a	chr4:121250732-121250743
38	CEBPB	chr4:121239010-121239220	MCF-7	breast:	n/a	chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239125-121239136 chr4:121239126-121239135 chr4:121239124-121239137
39	CEBPB	chr4:121238920-121239347	ECC-1	luminal epithelium:	n/a	chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239125-121239136 chr4:121239126-121239135 chr4:121239124-121239137
40	CEBPB	chr4:121238964-121239306	H1-hESC	embryonic stem cell:	n/a	chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239126-121239135 chr4:121239125-121239136 chr4:121239126-121239135 chr4:121239124-121239137
41	CEBPB	chr4:121387574-121388036	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:121182270-121182601	HepG2	liver:	n/a	chr4:121182442-121182453
43	CEBPB	chr4:121237991-121238191	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:121301451-121301770	HepG2	liver:	n/a	chr4:121301622-121301633
45	CEBPB	chr4:121250585-121250915	A549	lung:	n/a	chr4:121250732-121250743
46	CEBPB	chr4:121250566-121250911	IMR90	lung:	n/a	chr4:121250732-121250743
47	CEBPB	chr4:121182369-121182486	HepG2	liver:	n/a	chr4:121182442-121182453
48	CEBPB	chr4:121182264-121182609	K562	blood:	n/a	chr4:121182442-121182453
49	CEBPB	chr4:121182349-121182600	A549	lung:	n/a	chr4:121182442-121182453
50	CEBPB	chr4:121119601-121119788	H1-hESC	embryonic stem cell:	n/a	chr4:121119710-121119721

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:121387400-121387450	HEK293	kidney:	embryo
2	chr4:121387400-121387450	Caco-2	colon:	n/a
3	chr4:121185048-121185098	SAEC	small airway:	n/a
4	chr4:121185048-121185098	ovcar-3	ovarian:	n/a
5	chr4:121387400-121387450	IMR90	lung:	fetal
6	chr4:121387400-121387450	HCM	heart:	n/a
7	chr4:121387400-121387450	H1-hESC	embryonic stem cell:	embryo
8	chr4:121387400-121387450	HPAEpiC	pulmonary alveolar:	n/a
9	chr4:121387400-121387450	BJ	skin:	n/a
10	chr4:121185048-121185098	SK-N-SH_RA	brain:	n/a
11	chr4:121387400-121387450	SK-N-SH_RA	brain:	n/a
12	chr4:121387400-121387450	AG09309	skin:	n/a
13	chr4:121387400-121387450	HRE	kidney:	n/a
14	chr4:121185048-121185098	HEEpiC	esophagus:	n/a
15	chr4:121387400-121387450	AoSMC	blood vessel:	n/a
16	chr4:121387400-121387450	SK-N-SH	brain:	n/a
17	chr4:121185048-121185098	BE2_C	brain:	n/a
18	chr4:121387400-121387450	PANC-1	pancreas:	n/a
19	chr4:121387400-121387450	NT2-D1	testis:	n/a
20	chr4:121387400-121387450	SKMC	muscle:	n/a
21	chr4:121387400-121387450	ECC-1	luminal epithelium:	n/a
22	chr4:121185048-121185098	Hepatocyte	liver:	n/a
23	chr4:121185048-121185098	CMK	blood:	n/a
24	chr4:121185048-121185098	GM19239	blood:	n/a
25	chr4:121387400-121387450	MCF-7	breast:	n/a
26	chr4:121387400-121387450	GM12878	blood:	n/a
27	chr4:121387400-121387450	AG04450	lung:	fetal
28	chr4:121185048-121185098	HL-60	blood:	n/a
29	chr4:121387400-121387450	GM06990	blood:	n/a
30	chr4:121185048-121185098	PrEC	prostate:	n/a
31	chr4:121387400-121387450	HEEpiC	esophagus:	n/a
32	chr4:121185048-121185098	MCF-7	breast:	n/a
33	chr4:121387400-121387450	ovcar-3	ovarian:	n/a
34	chr4:121185048-121185098	HRPEpiC	eye:	n/a
35	chr4:121185048-121185098	HepG2	liver:	n/a
36	chr4:121387400-121387450	CMK	blood:	n/a
37	chr4:121185048-121185098	T-47D	breast:	n/a
38	chr4:121185048-121185098	HEK293	kidney:	embryo
39	chr4:121185048-121185098	AG04450	lung:	fetal
40	chr4:121185048-121185098	U87	brain:	n/a
41	chr4:121387400-121387450	HMEC	breast:	n/a
42	chr4:121185048-121185098	ProgFib	skin:	n/a
43	chr4:121185048-121185098	RPTEC	kidney:	n/a
44	chr4:121387400-121387450	NB4	blood:	n/a
45	chr4:121185048-121185098	GM12878	blood:	n/a
46	chr4:121387400-121387450	Jurkat	blood:	n/a
47	chr4:121387400-121387450	T-47D	breast:	n/a
48	chr4:121185048-121185098	HMEC	breast:	n/a
49	chr4:121185048-121185098	SK-N-MC	brain:	n/a
50	chr4:121185048-121185098	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:120985495..120988183-chr4:121111194..121113222,2	K562	blood:
2	chr4:23802609..23803478-chr4:121273037..121273864,2	MCF-7	breast:
3	chr4:121185242..121187871-chr4:121188856..121190633,2	K562	blood:
4	chr4:121341832..121344209-chr4:121346289..121348125,2	K562	blood:
5	chr4:121303352..121305526-chr4:121306861..121309621,3	K562	blood:
6	chr4:121303352..121305526-chr4:121306861..121309621,3	K562	blood:
7	chr4:121130697..121133786-chr4:121135139..121137341,3	K562	blood:
8	chr4:121077293..121077941-chr4:121207746..121208633,3	MCF-7	breast:
9	chr17:58501463..58503848-chr4:121259806..121262242,2	MCF-7	breast:
10	chr2:162678536..162680855-chr4:121354549..121356105,2	MCF-7	breast:
11	chr4:121228431..121230743-chr4:121233140..121235922,2	K562	blood:
12	chr4:121257279..121258865-chr4:121260585..121262446,2	K562	blood:
13	chr4:121185242..121187871-chr4:121188856..121190633,2	K562	blood:
14	chr4:121228431..121230743-chr4:121233140..121235922,2	K562	blood:
15	chr4:121130697..121133786-chr4:121135139..121137341,3	K562	blood:
16	chr4:121257279..121258865-chr4:121260585..121262446,2	K562	blood:
17	chr4:121309932..121311519-chr4:121313046..121315204,2	K562	blood:
18	chr4:121361067..121362763-chr4:121362852..121365271,2	MCF-7	breast:
19	chr4:121309932..121311519-chr4:121313046..121315204,2	K562	blood:
20	chr4:121167566..121169623-chr4:121176920..121179543,2	MCF-7	breast:
21	chr4:121189633..121192348-chr4:121208319..121209845,2	K562	blood:
22	chr4:121341832..121344209-chr4:121346289..121348125,2	K562	blood:
23	chr4:121189633..121192348-chr4:121208319..121209845,2	K562	blood:
24	chr4:121167566..121169623-chr4:121176920..121179543,2	MCF-7	breast:
25	chr4:121361067..121362763-chr4:121362852..121365271,2	MCF-7	breast:
26	chr4:121396849..121398573-chr4:121700140..121702182,2	K562	blood:
27	chr4:121078843..121079513-chr4:121208025..121208601,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC110373.1-13	chr4:121263211-121263802	NONHSAT098122
2	lnc-AC110373.1-6	chr4:121256793-121256886	ENSG00000250938.1
3	lnc-AC110373.1-6	chr4:121256793-121256886	ENSG00000250938.1
4	lnc-AC110373.1-6	chr4:121249688-121249741	ENSG00000250938.1
5	lnc-AC110373.1-13	chr4:121263212-121263784	NONHSAT098123
6	lnc-AC110373.1-6	chr4:121314655-121314709	ENSG00000250938.1
7	lnc-AC110373.1-6	chr4:121314655-121314877	ENSG00000250938.1
8	lnc-AC110373.1-12	chr4:121102663-121102842	NONHSAT098121
9	lnc-AC110373.1-6	chr4:121249688-121249741	ENSG00000250938.1
10	lnc-AC110373.1-12	chr4:121103326-121103369	NONHSAT098121
11	lnc-AC110373.1-6	chr4:121337705-121337921	ENSG00000250938.1

Variant related genes	Relation type
ENSG00000225665	TF binding region
ENSG00000225665	CpG island
ENSG00000250938	chromatin interactions
ENSG00000164109	chromatin interactions

Extended variants
information (count: 6682 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:6682 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138890292	chr4:121096648-121096649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552868328	chr4:121096698-121096699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191237587	chr4:121096710-121096711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs80177145	chr4:121096784-121096785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568563814	chr4:121096919-121096920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548400242	chr4:121096924-121096925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527245125	chr4:121096974-121096975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547110587	chr4:121097039-121097040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567925726	chr4:121097057-121097058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368122105	chr4:121097105-121097106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530372829	chr4:121097108-121097109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550339326	chr4:121097120-121097121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181901121	chr4:121097135-121097136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141459749	chr4:121097154-121097155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537556671	chr4:121097160-121097161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558598308	chr4:121097211-121097212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565853241	chr4:121097268-121097269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535003556	chr4:121097305-121097306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186916819	chr4:121097310-121097311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs17011279	chr4:121097313-121097314	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs542599510	chr4:121097327-121097328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556509960	chr4:121097386-121097387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191161679	chr4:121097393-121097394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79981610	chr4:121097394-121097395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570171750	chr4:121097417-121097418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200658412	chr4:121097468-121097469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564956429	chr4:121097555-121097556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565815997	chr4:121097566-121097567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35739693	chr4:121097586-121097587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527422355	chr4:121097621-121097622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541017219	chr4:121097631-121097632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558296513	chr4:121097637-121097638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183295771	chr4:121097684-121097685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529702409	chr4:121097790-121097791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13133646	chr4:121097803-121097804	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs16997625	chr4:121097886-121097887	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs16997627	chr4:121097913-121097914	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs56822808	chr4:121097929-121097930	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs565815574	chr4:121097939-121097940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150573513	chr4:121097973-121097974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187765353	chr4:121097995-121097996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78733768	chr4:121098015-121098016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537471941	chr4:121098057-121098058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556460866	chr4:121098100-121098101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372677117	chr4:121098191-121098192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189893219	chr4:121098192-121098193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538813143	chr4:121098228-121098229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558832686	chr4:121098250-121098251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182630618	chr4:121098251-121098252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540727608	chr4:121098261-121098262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Autism	22495311	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
Melanoma	18172304	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
Adenoid cystic carcinoma	18698036	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
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Myelodysplastic syndrome	18508791	CNVD
small cell lung cancer	20016488	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121096600-121097000	Weak transcription	Psoas Muscle	Psoas
2	chr4:121097000-121097200	Enhancers	Psoas Muscle	Psoas
3	chr4:121097200-121103000	Weak transcription	Psoas Muscle	Psoas
4	chr4:121103000-121103800	ZNF genes & repeats	Psoas Muscle	Psoas
5	chr4:121105200-121108000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:121112800-121113200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr4:121116000-121118400	Weak transcription	Aorta	Aorta
8	chr4:121118400-121118800	ZNF genes & repeats	Aorta	Aorta
9	chr4:121118800-121119800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr4:121118800-121120200	Enhancers	HMEC	breast
11	chr4:121119200-121119600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr4:121121600-121121800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr4:121121800-121122800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr4:121122600-121123000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr4:121122600-121123000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:121122600-121124000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr4:121122800-121124000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:121122800-121124000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr4:121123000-121123400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr4:121123000-121123400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:121123000-121124000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:121123000-121124000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr4:121123400-121124000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:121123400-121124200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr4:121123600-121124000	Enhancers	H1 Cell Line	embryonic stem cell
26	chr4:121123600-121124000	Enhancers	H9 Cell Line	embryonic stem cell
27	chr4:121123600-121124000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr4:121126400-121137400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr4:121133000-121133400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr4:121133000-121133600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr4:121133400-121136200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:121136200-121136400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:121139600-121140800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:121140600-121141000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr4:121146600-121147400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr4:121146800-121147200	Enhancers	HepG2	liver
37	chr4:121147400-121148800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:121148800-121150000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr4:121148800-121151400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:121149200-121149600	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr4:121149200-121151600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr4:121149400-121150000	Enhancers	Adipose Nuclei	Adipose
43	chr4:121149600-121150000	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr4:121149600-121150000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr4:121150000-121151000	Weak transcription	Adipose Nuclei	Adipose
46	chr4:121150200-121151200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr4:121151200-121151400	Enhancers	Adipose Nuclei	Adipose
48	chr4:121151200-121152200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr4:121153000-121153600	Enhancers	Osteobl	bone
50	chr4:121153400-121153600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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