Variant report

Variant	nsv516606
Chromosome Location	chr4:122342575-122397006
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	chr4:122369407-122369765	HepG2	liver:	n/a	n/a
2	BATF	chr4:122394135-122394406	GM12878	blood:	n/a	n/a
3	BRCA1	chr4:122384011-122384012	GM12878	blood:	n/a	n/a
4	CBX3	chr4:122383685-122384304	HCT-116	colon:	n/a	n/a
5	CBX3	chr4:122369301-122369870	HCT-116	colon:	n/a	n/a
6	CEBPB	chr4:122394540-122394863	IMR90	lung:	n/a	chr4:122394694-122394705
7	CEBPB	chr4:122394598-122394735	H1-hESC	embryonic stem cell:	n/a	chr4:122394694-122394705
8	CEBPB	chr4:122375401-122375699	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr4:122351397-122351423	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:122369204-122369938	HCT-116	colon:	n/a	n/a
11	CEBPB	chr4:122394549-122394862	A549	lung:	n/a	chr4:122394694-122394705
12	CEBPB	chr4:122394531-122394871	HepG2	liver:	n/a	chr4:122394694-122394705
13	CTCF	chr4:122383960-122384110	HEEpiC	esophagus:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
14	CTCF	chr4:122383960-122384110	GM12801	blood:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
15	CTCF	chr4:122342840-122342990	NHEK	skin:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
16	CTCF	chr4:122383960-122384110	HPF	lung:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
17	CTCF	chr4:122342900-122343050	MCF-7	breast:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
18	CTCF	chr4:122386220-122386370	HCT-116	colon:	n/a	n/a
19	CTCF	chr4:122383860-122384010	WI-38	lung:	n/a	n/a
20	CTCF	chr4:122386140-122386290	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr4:122383833-122384294	MCF-7	breast:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
22	CTCF	chr4:122342880-122343030	HEEpiC	esophagus:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
23	CTCF	chr4:122383876-122384144	MCF-7	breast:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
24	CTCF	chr4:122383940-122384090	HCPEpiC	choroid plexus:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
25	CTCF	chr4:122342820-122342970	RPTEC	kidney:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
26	CTCF	chr4:122383909-122384065	GM12892	blood:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
27	CTCF	chr4:122383858-122384134	A549	lung:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
28	CTCF	chr4:122383646-122384369	HCT-116	colon:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
29	CTCF	chr4:122384000-122384150	HAc	cerebellar:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
30	CTCF	chr4:122342840-122342990	NHLF	lung:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
31	CTCF	chr4:122383908-122384069	GM19238	blood:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
32	CTCF	chr4:122383260-122383410	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr4:122383879-122384145	LNCaP	prostate:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
34	CTCF	chr4:122342870-122343062	Hela-S3	cervix:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
35	CTCF	chr4:122383940-122384090	GM12871	blood:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
36	CTCF	chr4:122383903-122384085	GM19239	blood:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
37	CTCF	chr4:122386160-122386310	GM12872	blood:	n/a	n/a
38	CTCF	chr4:122383853-122384148	ECC-1	luminal epithelium:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
39	CTCF	chr4:122383920-122384070	GM12869	blood:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
40	CTCF	chr4:122342860-122343010	GM12866	blood:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
41	CTCF	chr4:122383500-122383650	AG04450	lung:	n/a	n/a
42	CTCF	chr4:122383920-122384070	HMEC	breast:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
43	CTCF	chr4:122383940-122384090	BJ	skin:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
44	CTCF	chr4:122383960-122384110	RPTEC	kidney:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
45	CTCF	chr4:122383867-122384157	Gliobla	brain:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
46	CTCF	chr4:122383672-122383716	GM20000	blood:	n/a	n/a
47	CTCF	chr4:122383940-122384090	HBMEC	blood vessel:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
48	CTCF	chr4:122342940-122343090	GM12873	blood:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
49	CTCF	chr4:122384360-122384510	GM12872	blood:	n/a	n/a
50	CTCF	chr4:122342963-122343020	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:122376685-122376735	Hela-S3	cervix:	n/a
2	chr4:122376685-122376735	Hela-S3	cervix:	n/a
3	chr4:122376685-122376735	NT2-D1	testis:	n/a
4	chr4:122376685-122376735	Hepatocyte	liver:	n/a
5	chr4:122376685-122376735	SKMC	muscle:	n/a
6	chr4:122376685-122376735	GM12878	blood:	n/a
7	chr4:122376685-122376735	ovcar-3	ovarian:	n/a
8	chr4:122376685-122376735	NHBE	bronchial:	n/a
9	chr4:122376685-122376735	MCF-7	breast:	n/a
10	chr4:122376685-122376735	HCM	heart:	n/a
11	chr4:122376685-122376735	AG04449	skin:	fetal
12	chr4:122376685-122376735	HEK293	kidney:	embryo
13	chr4:122376685-122376735	GM12892	blood:	n/a
14	chr4:122376685-122376735	HRE	kidney:	n/a
15	chr4:122376685-122376735	ECC-1	luminal epithelium:	n/a
16	chr4:122376685-122376735	H1-hESC	embryonic stem cell:	embryo
17	chr4:122376685-122376735	SK-N-MC	brain:	n/a
18	chr4:122376685-122376735	AG10803	skin:	n/a
19	chr4:122376685-122376735	IMR90	lung:	fetal
20	chr4:122376685-122376735	U87	brain:	n/a
21	chr4:122376685-122376735	HEEpiC	esophagus:	n/a
22	chr4:122376685-122376735	HAEpiC	amniotic membrane:	n/a
23	chr4:122376685-122376735	LNCaP	prostate:	n/a
24	chr4:122376685-122376735	SK-N-SH	brain:	n/a
25	chr4:122376685-122376735	HIPEpiC	eye:	n/a
26	chr4:122376685-122376735	HNPCEpiC	eye:	n/a
27	chr4:122376685-122376735	GM06990	blood:	n/a
28	chr4:122376685-122376735	PANC-1	pancreas:	n/a
29	chr4:122376685-122376735	GM12891	blood:	n/a
30	chr4:122376685-122376735	MCF10A-Er-Src	breast:	n/a
31	chr4:122376685-122376735	HepG2	liver:	n/a
32	chr4:122376685-122376735	BE2_C	brain:	n/a
33	chr4:122376685-122376735	HPAEpiC	pulmonary alveolar:	n/a
34	chr4:122376685-122376735	NHDF-neo	bronchial:	n/a
35	chr4:122376685-122376735	RPTEC	kidney:	n/a
36	chr4:122376685-122376735	HMEC	breast:	n/a
37	chr4:122376685-122376735	HUVEC	blood vessel:	n/a
38	chr4:122376685-122376735	HRCEpiC	kidney:	n/a
39	chr4:122376685-122376735	A549	lung:	n/a
40	chr4:122376685-122376735	PFSK-1	brain:	n/a
41	chr4:122376685-122376735	NH-A	brain:	n/a
42	chr4:122376685-122376735	AoSMC	blood vessel:	n/a
43	chr4:122376685-122376735	NB4	blood:	n/a
44	chr4:122376685-122376735	T-47D	breast:	n/a
45	chr4:122376685-122376735	SAEC	small airway:	n/a
46	chr4:122376685-122376735	HCT-116	colon:	n/a
47	chr4:122376685-122376735	K562	blood:	n/a
48	chr4:122376685-122376735	HCF	heart:	n/a
49	chr4:122376685-122376735	CMK	blood:	n/a
50	chr4:122376685-122376735	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:122379568..122382631-chr4:122383920..122387075,3	K562	blood:
2	chr4:122383988..122384720-chr4:122555173..122555707,2	K562	blood:
3	chr4:122379568..122382631-chr4:122383920..122387075,3	K562	blood:
4	chr4:122291624..122292430-chr4:122342879..122343479,3	MCF-7	breast:
5	chr4:122390684..122392219-chr4:122410927..122413477,2	K562	blood:
6	chr4:122383962..122386021-chr4:122397166..122399393,2	K562	blood:
7	chr4:122383570..122384412-chr6:100888804..100889304,2	MCF-7	breast:
8	chr4:122198494..122199456-chr4:122342475..122343364,3	MCF-7	breast:
9	chr4:122383589..122384125-chr4:122456174..122457010,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC079341.1-7	chr4:122372696-122373122	NONHSAT098142

Variant related genes	Relation type
TUBB4BP5	TF binding region
TUBB4BP5	CpG island

Extended variants
information (count: 1186 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1186 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28513945	chr4:122349876-122349877	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78987177	chr4:122349879-122349880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs13132003	chr4:122349897-122349898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559829959	chr4:122350015-122350016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs28461852	chr4:122350016-122350017	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs59363516	chr4:122350031-122350032	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs28600811	chr4:122350043-122350044	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs568007800	chr4:122350044-122350045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530536855	chr4:122350053-122350054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530776429	chr4:122350063-122350064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192853387	chr4:122350088-122350089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550868765	chr4:122350092-122350093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116624729	chr4:122350095-122350096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146075008	chr4:122350108-122350109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570341887	chr4:122350135-122350136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs691198	chr4:122350140-122350141	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs377616883	chr4:122350146-122350147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552892186	chr4:122350180-122350181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566429093	chr4:122350183-122350184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34368000	chr4:122350235-122350236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535697122	chr4:122350250-122350251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554673361	chr4:122350263-122350264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs62320828	chr4:122350300-122350301	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs543572082	chr4:122350395-122350396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557467217	chr4:122350415-122350416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs691442	chr4:122350430-122350431	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs566612918	chr4:122350436-122350437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546409160	chr4:122350439-122350440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560135991	chr4:122350469-122350470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573581014	chr4:122350518-122350519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs6842836	chr4:122350537-122350538	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs578056011	chr4:122350577-122350578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561551883	chr4:122350579-122350580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558640412	chr4:122350593-122350594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185357677	chr4:122350618-122350619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550439099	chr4:122350648-122350649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs575327471	chr4:122350650-122350651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77072218	chr4:122350690-122350691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573551510	chr4:122350721-122350722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76312205	chr4:122350764-122350765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200934727	chr4:122350783-122350784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201295864	chr4:122350787-122350788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10685690	chr4:122350788-122350789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs691474	chr4:122350802-122350803	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs9992786	chr4:122350803-122350804	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs568388459	chr4:122350817-122350818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537436964	chr4:122350827-122350828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557530470	chr4:122350885-122350886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577412958	chr4:122350897-122350898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539895358	chr4:122350916-122350917	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
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
Myelofibrosis	22110671	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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:122349800-122350600	Enhancers	Muscle Satellite Cultured Cells	--
2	chr4:122349800-122350800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:122349800-122351000	Enhancers	Hela-S3	cervix
4	chr4:122350000-122350400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr4:122350000-122350400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr4:122350000-122350400	Enhancers	NH-A	brain
7	chr4:122350000-122350600	Enhancers	HMEC	breast
8	chr4:122350000-122350800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:122350200-122350800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:122360400-122361200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:122360600-122361000	ZNF genes & repeats	Pancreas	Pancrea
12	chr4:122360600-122361200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr4:122360600-122361200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:122360600-122361200	ZNF genes & repeats	Gastric	stomach
15	chr4:122360600-122361200	Enhancers	Right Ventricle	heart
16	chr4:122360600-122361400	ZNF genes & repeats	Spleen	Spleen
17	chr4:122360800-122361200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:122361000-122361200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr4:122361200-122372600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:122368400-122369600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:122369000-122370000	Enhancers	Fetal Intestine Small	intestine
22	chr4:122369000-122370000	Enhancers	Stomach Mucosa	stomach
23	chr4:122369200-122369800	Enhancers	HepG2	liver
24	chr4:122370000-122375600	Weak transcription	Stomach Mucosa	stomach
25	chr4:122370400-122371200	Enhancers	Fetal Kidney	kidney
26	chr4:122372600-122373000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:122372600-122373000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr4:122373000-122375800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:122374000-122374200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr4:122374200-122374400	Enhancers	Fetal Lung	lung
31	chr4:122374200-122375400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr4:122374600-122375600	Weak transcription	Fetal Lung	lung
33	chr4:122375000-122376800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr4:122375400-122376600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr4:122375400-122376600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr4:122375400-122376600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr4:122375600-122376000	Enhancers	Left Ventricle	heart
38	chr4:122375600-122376000	Enhancers	Stomach Mucosa	stomach
39	chr4:122375600-122376000	Enhancers	Hela-S3	cervix
40	chr4:122375600-122376200	Enhancers	H9 Cell Line	embryonic stem cell
41	chr4:122375600-122376200	Enhancers	Fetal Lung	lung
42	chr4:122375600-122376600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr4:122375600-122376600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr4:122375600-122376600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr4:122375600-122376600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr4:122375600-122376800	Enhancers	H1 Cell Line	embryonic stem cell
47	chr4:122375800-122376000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr4:122375800-122376000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:122375800-122376200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr4:122375800-122376600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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