Variant report

Variant	nsv1008501
Chromosome Location	chr4:122326054-122395119
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	BCL3	chr4:122334423-122334652	GM12878	blood:	n/a	n/a
4	BRCA1	chr4:122384011-122384012	GM12878	blood:	n/a	n/a
5	CBX3	chr4:122369301-122369870	HCT-116	colon:	n/a	n/a
6	CBX3	chr4:122383685-122384304	HCT-116	colon:	n/a	n/a
7	CEBPB	chr4:122394540-122394863	IMR90	lung:	n/a	chr4:122394694-122394705
8	CEBPB	chr4:122369204-122369938	HCT-116	colon:	n/a	n/a
9	CEBPB	chr4:122375401-122375699	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr4:122394531-122394871	HepG2	liver:	n/a	chr4:122394694-122394705
11	CEBPB	chr4:122351397-122351423	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:122394549-122394862	A549	lung:	n/a	chr4:122394694-122394705
13	CEBPB	chr4:122394598-122394735	H1-hESC	embryonic stem cell:	n/a	chr4:122394694-122394705
14	CTCF	chr4:122342860-122343010	WERI-Rb-1	eye:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
15	CTCF	chr4:122383940-122384090	HMF	breast:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
16	CTCF	chr4:122383940-122384090	GM12871	blood:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
17	CTCF	chr4:122386200-122386350	HPAF	blood vessel:	n/a	n/a
18	CTCF	chr4:122383980-122384130	AG10803	skin:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
19	CTCF	chr4:122383940-122384090	AG04449	skin:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
20	CTCF	chr4:122342840-122342990	HFF	foreskin:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
21	CTCF	chr4:122342940-122343090	RPTEC	kidney:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
22	CTCF	chr4:122383880-122384158	LNCaP	prostate:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
23	CTCF	chr4:122386240-122386390	RPTEC	kidney:	n/a	n/a
24	CTCF	chr4:122342940-122343090	GM12868	blood:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
25	CTCF	chr4:122386160-122386310	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr4:122386060-122386210	NB4	blood:	n/a	n/a
27	CTCF	chr4:122383920-122384070	AG09309	skin:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
28	CTCF	chr4:122342840-122342990	Hela-S3	cervix:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
29	CTCF	chr4:122383910-122384147	A549	lung:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
30	CTCF	chr4:122383875-122384172	Medullo	brain:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
31	CTCF	chr4:122342842-122343072	HUVEC	blood vessel:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
32	CTCF	chr4:122342860-122343010	HCM	heart:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
33	CTCF	chr4:122386200-122386350	GM12864	blood:	n/a	n/a
34	CTCF	chr4:122386220-122386370	HepG2	liver:	n/a	n/a
35	CTCF	chr4:122383960-122384110	BE2_C	brain:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
36	CTCF	chr4:122383940-122384090	GM12874	blood:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
37	CTCF	chr4:122342840-122342990	GM12872	blood:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
38	CTCF	chr4:122386180-122386330	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr4:122383940-122384090	GM12873	blood:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
40	CTCF	chr4:122384280-122384430	GM06990	blood:	n/a	n/a
41	CTCF	chr4:122383857-122384171	HUVEC	blood vessel:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
42	CTCF	chr4:122386180-122386330	RPTEC	kidney:	n/a	n/a
43	CTCF	chr4:122342900-122343050	HMEC	breast:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
44	CTCF	chr4:122342900-122343050	MCF-7	breast:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
45	CTCF	chr4:122383620-122384383	SK-N-SH	brain:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
46	CTCF	chr4:122383908-122384069	GM19238	blood:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
47	CTCF	chr4:122383960-122384110	MCF-7	breast:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
48	CTCF	chr4:122386180-122386330	SAEC	small airway:	n/a	n/a
49	CTCF	chr4:122384000-122384150	HAc	cerebellar:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
50	CTCF	chr4:122342834-122343078	Medullo	brain:	n/a	chr4:122342943-122342964 chr4:122342949-122342965

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:122376685-122376735	AG10803	skin:	n/a
2	chr4:122376685-122376735	IMR90	lung:	fetal
3	chr4:122376685-122376735	HCPEpiC	choroid plexus:	n/a
4	chr4:122376685-122376735	HCF	heart:	n/a
5	chr4:122376685-122376735	HNPCEpiC	eye:	n/a
6	chr4:122376685-122376735	HRE	kidney:	n/a
7	chr4:122376685-122376735	GM19239	blood:	n/a
8	chr4:122376685-122376735	SK-N-SH_RA	brain:	n/a
9	chr4:122376685-122376735	LNCaP	prostate:	n/a
10	chr4:122376685-122376735	HMEC	breast:	n/a
11	chr4:122376685-122376735	NB4	blood:	n/a
12	chr4:122376685-122376735	Hela-S3	cervix:	n/a
13	chr4:122376685-122376735	HCM	heart:	n/a
14	chr4:122376685-122376735	PFSK-1	brain:	n/a
15	chr4:122376685-122376735	SK-N-MC	brain:	n/a
16	chr4:122376685-122376735	AoSMC	blood vessel:	n/a
17	chr4:122376685-122376735	GM06990	blood:	n/a
18	chr4:122376685-122376735	PANC-1	pancreas:	n/a
19	chr4:122376685-122376735	SAEC	small airway:	n/a
20	chr4:122376685-122376735	ovcar-3	ovarian:	n/a
21	chr4:122376685-122376735	HepG2	liver:	n/a
22	chr4:122376685-122376735	Caco-2	colon:	n/a
23	chr4:122376685-122376735	HRPEpiC	eye:	n/a
24	chr4:122376685-122376735	SKMC	muscle:	n/a
25	chr4:122376685-122376735	HL-60	blood:	n/a
26	chr4:122376685-122376735	HUVEC	blood vessel:	n/a
27	chr4:122376685-122376735	RPTEC	kidney:	n/a
28	chr4:122376685-122376735	MCF10A-Er-Src	breast:	n/a
29	chr4:122376685-122376735	NHDF-neo	bronchial:	n/a
30	chr4:122376685-122376735	U87	brain:	n/a
31	chr4:122376685-122376735	GM12878	blood:	n/a
32	chr4:122376685-122376735	NT2-D1	testis:	n/a
33	chr4:122376685-122376735	ECC-1	luminal epithelium:	n/a
34	chr4:122376685-122376735	K562	blood:	n/a
35	chr4:122376685-122376735	Hepatocyte	liver:	n/a
36	chr4:122376685-122376735	A549	lung:	n/a
37	chr4:122376685-122376735	SK-N-SH	brain:	n/a
38	chr4:122376685-122376735	AG04449	skin:	fetal
39	chr4:122376685-122376735	AG09309	skin:	n/a
40	chr4:122376685-122376735	AG04450	lung:	fetal
41	chr4:122376685-122376735	HEEpiC	esophagus:	n/a
42	chr4:122376685-122376735	MCF-7	breast:	n/a
43	chr4:122376685-122376735	NH-A	brain:	n/a
44	chr4:122376685-122376735	NHBE	bronchial:	n/a
45	chr4:122376685-122376735	PrEC	prostate:	n/a
46	chr4:122376685-122376735	HAEpiC	amniotic membrane:	n/a
47	chr4:122376685-122376735	H1-hESC	embryonic stem cell:	embryo
48	chr4:122376685-122376735	ProgFib	skin:	n/a
49	chr4:122376685-122376735	HIPEpiC	eye:	n/a
50	chr4:122376685-122376735	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:122383570..122384412-chr6:100888804..100889304,2	MCF-7	breast:
2	chr4:122379568..122382631-chr4:122383920..122387075,3	K562	blood:
3	chr4:122383988..122384720-chr4:122555173..122555707,2	K562	blood:
4	chr4:122379568..122382631-chr4:122383920..122387075,3	K562	blood:
5	chr4:122383962..122386021-chr4:122397166..122399393,2	K562	blood:
6	chr4:122383589..122384125-chr4:122456174..122457010,2	MCF-7	breast:
7	chr4:122390684..122392219-chr4:122410927..122413477,2	K562	blood:
8	chr4:122291624..122292430-chr4:122342879..122343479,3	MCF-7	breast:
9	chr4:122198494..122199456-chr4:122342475..122343364,3	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
ENSG00000264927	TF binding region
TUBB4BP5	CpG island
ENSG00000264927	CpG island

Extended variants
information (count: 1294 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1294 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548203979	chr4:122328608-122328609	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs573213630	chr4:122331224-122331225	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs13146901	chr4:122331293-122331294	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs541838149	chr4:122331313-122331314	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs143859704	chr4:122331357-122331358	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs191454559	chr4:122331388-122331389	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs183193204	chr4:122331394-122331395	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs188904442	chr4:122331411-122331412	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs7675991	chr4:122331416-122331417	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs533324400	chr4:122331490-122331491	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs547286135	chr4:122331641-122331642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs114190155	chr4:122331647-122331648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528909771	chr4:122331661-122331662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548684674	chr4:122331759-122331760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1813400	chr4:122331860-122331861	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs193062253	chr4:122331890-122331891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550975883	chr4:122331901-122331902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373954771	chr4:122331921-122331922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534484774	chr4:122331927-122331928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551024835	chr4:122332015-122332016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185238680	chr4:122332027-122332028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142111188	chr4:122332031-122332032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568032253	chr4:122332037-122332038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368433810	chr4:122332069-122332070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533815540	chr4:122332091-122332092	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs151313093	chr4:122332093-122332094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139361642	chr4:122332116-122332117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188109106	chr4:122332151-122332152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535884063	chr4:122332189-122332190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191802266	chr4:122332242-122332243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs76102164	chr4:122332364-122332365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116299370	chr4:122332542-122332543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558247946	chr4:122332545-122332546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184345599	chr4:122332611-122332612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10014084	chr4:122332612-122332613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540447609	chr4:122332624-122332625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538946029	chr4:122332641-122332642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145513815	chr4:122332658-122332659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188250652	chr4:122332677-122332678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542258998	chr4:122332700-122332701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562156280	chr4:122332706-122332707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575443389	chr4:122332722-122332723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531175976	chr4:122332736-122332737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551084495	chr4:122332750-122332751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536354646	chr4:122332776-122332777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570990324	chr4:122332794-122332795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78007981	chr4:122332799-122332800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115642618	chr4:122332837-122332838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567597471	chr4:122332845-122332846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35366158	chr4:122332850-122332851	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:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:122331200-122331600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
2	chr4:122331600-122333400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr4:122331800-122333000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:122331800-122333200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr4:122332000-122332400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr4:122332000-122332600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr4:122332000-122332800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr4:122332000-122332800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr4:122332000-122332800	Enhancers	Left Ventricle	heart
10	chr4:122332600-122332800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:122333000-122333200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:122333200-122333400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr4:122339400-122340400	Enhancers	Left Ventricle	heart
14	chr4:122349800-122350600	Enhancers	Muscle Satellite Cultured Cells	--
15	chr4:122349800-122350800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:122349800-122351000	Enhancers	Hela-S3	cervix
17	chr4:122350000-122350400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr4:122350000-122350400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr4:122350000-122350400	Enhancers	NH-A	brain
20	chr4:122350000-122350600	Enhancers	HMEC	breast
21	chr4:122350000-122350800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:122350200-122350800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:122360400-122361200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:122360600-122361000	ZNF genes & repeats	Pancreas	Pancrea
25	chr4:122360600-122361200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:122360600-122361200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:122360600-122361200	ZNF genes & repeats	Gastric	stomach
28	chr4:122360600-122361200	Enhancers	Right Ventricle	heart
29	chr4:122360600-122361400	ZNF genes & repeats	Spleen	Spleen
30	chr4:122360800-122361200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:122361000-122361200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr4:122361200-122372600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:122368400-122369600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr4:122369000-122370000	Enhancers	Fetal Intestine Small	intestine
35	chr4:122369000-122370000	Enhancers	Stomach Mucosa	stomach
36	chr4:122369200-122369800	Enhancers	HepG2	liver
37	chr4:122370000-122375600	Weak transcription	Stomach Mucosa	stomach
38	chr4:122370400-122371200	Enhancers	Fetal Kidney	kidney
39	chr4:122372600-122373000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:122372600-122373000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:122373000-122375800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr4:122374000-122374200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr4:122374200-122374400	Enhancers	Fetal Lung	lung
44	chr4:122374200-122375400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr4:122374600-122375600	Weak transcription	Fetal Lung	lung
46	chr4:122375000-122376800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr4:122375400-122376600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:122375400-122376600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:122375400-122376600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr4:122375600-122376000	Enhancers	Left Ventricle	heart

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