Variant report

Variant	nsv879611
Chromosome Location	chr4:93707288-93987251
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	chr4:93890976-93891589	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:93915938-93916211	HepG2	liver:	n/a	n/a
3	ATF3	chr4:93891072-93891445	A549	lung:	n/a	n/a
4	ATF3	chr4:93891228-93891471	A549	lung:	n/a	n/a
5	BACH1	chr4:93728575-93728662	K562	blood:	n/a	n/a
6	BACH1	chr4:93967370-93967376	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr4:93951903-93952165	GM12878	blood:	n/a	n/a
8	BATF	chr4:93951951-93952159	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:93951916-93952178	GM12878	blood:	n/a	n/a
10	BCL3	chr4:93891030-93891647	A549	lung:	n/a	n/a
11	BHLHE40	chr4:93951978-93952126	GM12878	blood:	n/a	n/a
12	BRCA1	chr4:93890921-93891508	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr4:93891028-93891487	HCT-116	colon:	n/a	n/a
14	CEBPB	chr4:93965212-93965558	IMR90	lung:	n/a	chr4:93965391-93965400 chr4:93965389-93965402 chr4:93965389-93965400 chr4:93965391-93965400 chr4:93965391-93965400 chr4:93965444-93965457 chr4:93965391-93965400 chr4:93965391-93965402
15	CEBPB	chr4:93909470-93909870	A549	lung:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
16	CEBPB	chr4:93973333-93973620	HepG2	liver:	n/a	chr4:93973459-93973468 chr4:93973459-93973468 chr4:93973459-93973468
17	CEBPB	chr4:93730571-93730943	ECC-1	luminal epithelium:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
18	CEBPB	chr4:93891114-93891468	HepG2	liver:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
19	CEBPB	chr4:93866144-93866453	HepG2	liver:	n/a	chr4:93866274-93866283 chr4:93866272-93866283
20	CEBPB	chr4:93753510-93753717	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:93796324-93796523	HepG2	liver:	n/a	chr4:93796369-93796380
22	CEBPB	chr4:93909578-93909840	H1-hESC	embryonic stem cell:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
23	CEBPB	chr4:93873656-93873916	A549	lung:	n/a	chr4:93873803-93873814 chr4:93873761-93873772 chr4:93873801-93873812
24	CEBPB	chr4:93730571-93730930	Hela-S3	cervix:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
25	CEBPB	chr4:93965207-93965565	HepG2	liver:	n/a	chr4:93965391-93965400 chr4:93965389-93965402 chr4:93965389-93965400 chr4:93965391-93965400 chr4:93965391-93965400 chr4:93965444-93965457 chr4:93965391-93965400 chr4:93965391-93965402
26	CEBPB	chr4:93913075-93913264	A549	lung:	n/a	n/a
27	CEBPB	chr4:93847042-93847319	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:93940036-93940289	Hela-S3	cervix:	n/a	chr4:93940211-93940224 chr4:93940212-93940223 chr4:93940144-93940157
29	CEBPB	chr4:93909540-93909893	HepG2	liver:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
30	CEBPB	chr4:93891027-93891462	HCT-116	colon:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
31	CEBPB	chr4:93915947-93916152	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:93901011-93901535	MCF-7	breast:	n/a	chr4:93901280-93901291
33	CEBPB	chr4:93933499-93933739	A549	lung:	n/a	n/a
34	CEBPB	chr4:93730580-93730850	K562	blood:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
35	CEBPB	chr4:93901111-93901430	IMR90	lung:	n/a	chr4:93901280-93901291
36	CEBPB	chr4:93835580-93835776	HepG2	liver:	n/a	chr4:93835654-93835665
37	CEBPB	chr4:93940029-93940374	IMR90	lung:	n/a	chr4:93940211-93940224 chr4:93940212-93940223 chr4:93940144-93940157
38	CEBPB	chr4:93890904-93891675	A549	lung:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
39	CEBPB	chr4:93796260-93796522	H1-hESC	embryonic stem cell:	n/a	chr4:93796369-93796380
40	CEBPB	chr4:93901178-93901344	K562	blood:	n/a	chr4:93901280-93901291
41	CEBPB	chr4:93916625-93916817	IMR90	lung:	n/a	n/a
42	CEBPB	chr4:93890872-93891520	HepG2	liver:	n/a	chr4:93891255-93891266 chr4:93891253-93891264
43	CEBPB	chr4:93952911-93953173	HepG2	liver:	n/a	chr4:93953046-93953057
44	CEBPB	chr4:93730552-93730878	ECC-1	luminal epithelium:	n/a	chr4:93730724-93730735 chr4:93730738-93730749
45	CEBPB	chr4:93982600-93982828	A549	lung:	n/a	chr4:93982658-93982669
46	CEBPB	chr4:93933534-93933802	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:93965211-93965515	A549	lung:	n/a	chr4:93965391-93965400 chr4:93965389-93965402 chr4:93965389-93965400 chr4:93965391-93965400 chr4:93965391-93965400 chr4:93965444-93965457 chr4:93965391-93965400 chr4:93965391-93965402
48	CEBPB	chr4:93973306-93973627	IMR90	lung:	n/a	chr4:93973459-93973468 chr4:93973459-93973468 chr4:93973459-93973468
49	CEBPB	chr4:93909536-93909890	IMR90	lung:	n/a	chr4:93909702-93909713 chr4:93909783-93909794
50	CEBPB	chr4:93901112-93901404	HepG2	liver:	n/a	chr4:93901280-93901291

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:93930622-93930672	HL-60	blood:	n/a
2	chr4:93930622-93930672	HL-60	blood:	n/a
3	chr4:93930622-93930672	LNCaP	prostate:	n/a
4	chr4:93930622-93930672	HIPEpiC	eye:	n/a
5	chr4:93930622-93930672	HCF	heart:	n/a
6	chr4:93930622-93930672	MCF-7	breast:	n/a
7	chr4:93930622-93930672	HepG2	liver:	n/a
8	chr4:93930622-93930672	GM06990	blood:	n/a
9	chr4:93930622-93930672	PFSK-1	brain:	n/a
10	chr4:93930622-93930672	Hepatocyte	liver:	n/a
11	chr4:93930622-93930672	IMR90	lung:	fetal
12	chr4:93930622-93930672	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:93930622-93930672	AG10803	skin:	n/a
14	chr4:93930622-93930672	GM19239	blood:	n/a
15	chr4:93930622-93930672	ECC-1	luminal epithelium:	n/a
16	chr4:93930622-93930672	SAEC	small airway:	n/a
17	chr4:93930622-93930672	CMK	blood:	n/a
18	chr4:93930622-93930672	GM12878	blood:	n/a
19	chr4:93930622-93930672	BE2_C	brain:	n/a
20	chr4:93930622-93930672	ovcar-3	ovarian:	n/a
21	chr4:93930622-93930672	HRCEpiC	kidney:	n/a
22	chr4:93930622-93930672	BJ	skin:	n/a
23	chr4:93930622-93930672	PANC-1	pancreas:	n/a
24	chr4:93930622-93930672	Hela-S3	cervix:	n/a
25	chr4:93930622-93930672	NHDF-neo	bronchial:	n/a
26	chr4:93930622-93930672	NHBE	bronchial:	n/a
27	chr4:93930622-93930672	NB4	blood:	n/a
28	chr4:93930622-93930672	HMEC	breast:	n/a
29	chr4:93930622-93930672	Caco-2	colon:	n/a
30	chr4:93930622-93930672	SK-N-MC	brain:	n/a
31	chr4:93930622-93930672	RPTEC	kidney:	n/a
32	chr4:93930622-93930672	SKMC	muscle:	n/a
33	chr4:93930622-93930672	GM12891	blood:	n/a
34	chr4:93930622-93930672	NH-A	brain:	n/a
35	chr4:93930622-93930672	SK-N-SH_RA	brain:	n/a
36	chr4:93930622-93930672	AoSMC	blood vessel:	n/a
37	chr4:93930622-93930672	Jurkat	blood:	n/a
38	chr4:93930622-93930672	SK-N-SH	brain:	n/a
39	chr4:93930622-93930672	HEEpiC	esophagus:	n/a
40	chr4:93930622-93930672	K562	blood:	n/a
41	chr4:93930622-93930672	AG09319	gingival:	n/a
42	chr4:93930622-93930672	H1-hESC	embryonic stem cell:	embryo
43	chr4:93930622-93930672	HAEpiC	amniotic membrane:	n/a
44	chr4:93930622-93930672	NT2-D1	testis:	n/a
45	chr4:93930622-93930672	U87	brain:	n/a
46	chr4:93930622-93930672	ProgFib	skin:	n/a
47	chr4:93930622-93930672	GM12892	blood:	n/a
48	chr4:93930622-93930672	AG09309	skin:	n/a
49	chr4:93930622-93930672	MCF10A-Er-Src	breast:	n/a
50	chr4:93930622-93930672	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:93970682..93973329-chr4:93973340..93974971,2	MCF-7	breast:
2	chr4:93968750..93971596-chr4:93971794..93974511,2	MCF-7	breast:
3	chr4:93920911..93923301-chr4:93923626..93925669,2	MCF-7	breast:
4	chr4:93886231..93887821-chr4:93901908..93903959,2	K562	blood:
5	chr4:93846312..93847841-chr4:93851226..93853929,2	K562	blood:
6	chr4:93825096..93827296-chr4:93828128..93830318,2	K562	blood:
7	chr4:93908293..93911044-chr4:93911588..93914279,2	MCF-7	breast:
8	chr4:93886231..93887821-chr4:93901908..93903959,2	K562	blood:
9	chr4:93970682..93973329-chr4:93973340..93974971,2	MCF-7	breast:
10	chr4:93825096..93827296-chr4:93828128..93830318,2	K562	blood:
11	chr4:93846312..93847841-chr4:93851226..93853929,2	K562	blood:
12	chr4:93968750..93971596-chr4:93971794..93974511,2	MCF-7	breast:
13	chr4:93757984..93759775-chr4:93817140..93819795,2	MCF-7	breast:
14	chr4:93757984..93759775-chr4:93817140..93819795,2	MCF-7	breast:
15	chr4:93922270..93924469-chr4:93926058..93927823,2	MCF-7	breast:
16	chr4:93773449..93776266-chr4:93779103..93780772,2	MCF-7	breast:
17	chr4:93773449..93776266-chr4:93779103..93780772,2	MCF-7	breast:
18	chr4:93908293..93911044-chr4:93911588..93914279,2	MCF-7	breast:
19	chr4:93827426..93829042-chr4:93829198..93830745,2	K562	blood:
20	chr4:93827426..93829042-chr4:93829198..93830745,2	K562	blood:
21	chr4:93922270..93924469-chr4:93926058..93927823,2	MCF-7	breast:
22	chr4:93920911..93923301-chr4:93923626..93925669,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-9B6.1.1-2	chr4:93754836-93755124	ENSG00000248627.1
2	lnc-ATOH1-1	chr4:93805814-93806258	NONHSAT097436
3	lnc-RP11-9B6.1.1-2	chr4:93759934-93759993	ENSG00000248627.1
4	lnc-RP11-9B6.1.1-6	chr4:93743137-93744069	NONHSAT097434

Variant related genes	Relation type
ENSG00000248750	TF binding region
ENSG00000249239	TF binding region
ENSG00000248627	TF binding region
GRID2	TF binding region
ENSG00000248750	CpG island
ENSG00000249239	CpG island
ENSG00000248627	CpG island
GRID2	CpG island

Extended variants
information (count: 7831 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:7831 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7671095	chr4:93707288-93707289	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560552327	chr4:93707309-93707310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144430076	chr4:93707335-93707336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541726470	chr4:93707350-93707351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12647836	chr4:93707374-93707375	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs555890057	chr4:93707403-93707404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181272085	chr4:93707462-93707463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550397019	chr4:93707509-93707510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564104328	chr4:93707515-93707516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372235043	chr4:93707518-93707519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533070126	chr4:93707550-93707551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185585921	chr4:93707568-93707569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373555966	chr4:93707570-93707571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs80241603	chr4:93707607-93707608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538730914	chr4:93707616-93707617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114847779	chr4:93707632-93707633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569603780	chr4:93707672-93707673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372696517	chr4:93707679-93707680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77548316	chr4:93707748-93707749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561835042	chr4:93707769-93707770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572245856	chr4:93707789-93707790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556742894	chr4:93707796-93707797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs578083586	chr4:93707801-93707802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189655915	chr4:93707812-93707813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182342093	chr4:93707846-93707847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187384961	chr4:93708004-93708005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542655684	chr4:93708010-93708011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs118072552	chr4:93708122-93708123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564603452	chr4:93708172-93708173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191981108	chr4:93708189-93708190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544151037	chr4:93708246-93708247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564322298	chr4:93708265-93708266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532936668	chr4:93708302-93708303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544236323	chr4:93708408-93708409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562738616	chr4:93708419-93708420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533271768	chr4:93708483-93708484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546770842	chr4:93708538-93708539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373213310	chr4:93708541-93708542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560029065	chr4:93708603-93708604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1079758	chr4:93708605-93708606	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs549025552	chr4:93708632-93708633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563551499	chr4:93708651-93708652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568839520	chr4:93708745-93708746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183505386	chr4:93708749-93708750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373903275	chr4:93708766-93708767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34273002	chr4:93708802-93708803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529517458	chr4:93708877-93708878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76253952	chr4:93708889-93708890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571817615	chr4:93708939-93708940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534175969	chr4:93708971-93708972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
lymphocytic leukemia	21291569	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
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
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
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Autism	20841430	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:93688400-93720400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:93702000-93727400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr4:93709200-93752000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr4:93711000-93711200	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr4:93711000-93711200	Enhancers	Fetal Brain Male	brain
6	chr4:93711000-93711200	Enhancers	HUVEC	blood vessel
7	chr4:93711400-93713000	Weak transcription	Fetal Brain Male	brain
8	chr4:93711600-93712800	Weak transcription	HUVEC	blood vessel
9	chr4:93711600-93713800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr4:93712800-93713400	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr4:93712800-93713400	Enhancers	Small Intestine	intestine
12	chr4:93712800-93713600	Enhancers	HUVEC	blood vessel
13	chr4:93713000-93713800	Enhancers	Fetal Brain Male	brain
14	chr4:93713000-93713800	Enhancers	Fetal Heart	heart
15	chr4:93713200-93713400	Enhancers	Fetal Kidney	kidney
16	chr4:93713400-93713600	Enhancers	Right Atrium	heart
17	chr4:93715000-93727200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr4:93718200-93718400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:93720400-93720600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr4:93723600-93724000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:93738600-93753600	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr4:93743800-93744200	ZNF genes & repeats	Pancreas	Pancrea
23	chr4:93745000-93745200	Enhancers	Fetal Intestine Large	intestine
24	chr4:93745000-93745200	Enhancers	Fetal Intestine Small	intestine
25	chr4:93745200-93746200	Weak transcription	Fetal Intestine Large	intestine
26	chr4:93745200-93746200	Weak transcription	Fetal Intestine Small	intestine
27	chr4:93745400-93758200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr4:93746200-93747200	Enhancers	Fetal Heart	heart
29	chr4:93746200-93747200	Enhancers	Fetal Intestine Large	intestine
30	chr4:93746200-93747200	Enhancers	Fetal Intestine Small	intestine
31	chr4:93746400-93747000	Enhancers	Fetal Lung	lung
32	chr4:93746600-93746800	Enhancers	Fetal Brain Male	brain
33	chr4:93746800-93747200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:93747200-93747400	Flanking Active TSS	Fetal Heart	heart
35	chr4:93747400-93747600	Enhancers	Fetal Brain Male	brain
36	chr4:93752000-93752400	Strong transcription	H1 Cell Line	embryonic stem cell
37	chr4:93752400-93757800	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr4:93757800-93758200	Enhancers	H1 Cell Line	embryonic stem cell
39	chr4:93757800-93758600	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr4:93757800-93759200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr4:93758200-93758400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr4:93758200-93802200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr4:93758400-93764200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr4:93758600-93760000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr4:93759200-93759600	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr4:93759600-93759800	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:93759800-93767400	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr4:93760000-93760200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr4:93760000-93760400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr4:93760000-93760400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood

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