Variant report

Variant	nsv830066
Chromosome Location	chr4:132249894-132346541
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr4:132269393-132269798	GM12878	blood:	n/a	n/a
2	BATF	chr4:132269461-132269747	GM12878	blood:	n/a	n/a
3	CCNT2	chr4:132300478-132300751	K562	blood:	n/a	n/a
4	CEBPB	chr4:132299279-132299529	K562	blood:	n/a	n/a
5	CEBPB	chr4:132334395-132334652	IMR90	lung:	n/a	chr4:132334512-132334525 chr4:132334513-132334524 chr4:132334514-132334523 chr4:132334512-132334525 chr4:132334512-132334523
6	CEBPB	chr4:132334417-132334650	HepG2	liver:	n/a	chr4:132334512-132334525 chr4:132334513-132334524 chr4:132334514-132334523 chr4:132334512-132334525 chr4:132334512-132334523
7	CEBPB	chr4:132334422-132334633	K562	blood:	n/a	chr4:132334512-132334525 chr4:132334513-132334524 chr4:132334514-132334523 chr4:132334512-132334525 chr4:132334512-132334523
8	CEBPB	chr4:132300197-132300397	HepG2	liver:	n/a	chr4:132300269-132300282 chr4:132300270-132300281 chr4:132300256-132300267
9	CEBPB	chr4:132316111-132316328	HepG2	liver:	n/a	chr4:132316170-132316181 chr4:132316241-132316252 chr4:132316170-132316183 chr4:132316241-132316254 chr4:132316241-132316254
10	CTCF	chr4:132300500-132300750	GM12866	blood:	n/a	n/a
11	CTCF	chr4:132314586-132314638	GM10248	blood:	n/a	n/a
12	CTCF	chr4:132324785-132324802	GM20000	blood:	n/a	n/a
13	CTCF	chr4:132297223-132297230	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr4:132300627-132300750	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr4:132300624-132300790	LNCaP	prostate:	n/a	n/a
16	CTCF	chr4:132297734-132297808	K562	blood:	n/a	n/a
17	CTCF	chr4:132309520-132309670	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr4:132274246-132274320	Fibrobl	skin:	n/a	n/a
19	CTCF	chr4:132300602-132300797	K562	blood:	n/a	n/a
20	CTCF	chr4:132329407-132329475	GM12878	blood:	n/a	n/a
21	CTCF	chr4:132250711-132250756	GM20000	blood:	n/a	n/a
22	CUX1	chr4:132268574-132268624	GM12878	blood:	n/a	n/a
23	CUX1	chr4:132288323-132288355	GM12878	blood:	n/a	n/a
24	CUX1	chr4:132265015-132265133	GM12878	blood:	n/a	n/a
25	E2F4	chr4:132281532-132281727	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr4:132318447-132318622	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr4:132261138-132261402	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr4:132346504-132346744	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr4:132263288-132263448	MCF10A-Er-Src	breast:	n/a	n/a
30	EBF1	chr4:132269418-132269759	GM12878	blood:	n/a	n/a
31	EBF1	chr4:132272294-132272365	GM12878	blood:	n/a	n/a
32	EGR1	chr4:132279191-132279404	GM12878	blood:	n/a	n/a
33	EP300	chr4:132257466-132257469	K562	blood:	n/a	n/a
34	FAM48A	chr4:132255839-132255975	GM12878	blood:	n/a	n/a
35	FAM48A	chr4:132330359-132330513	GM12878	blood:	n/a	n/a
36	FOXA1	chr4:132324396-132324671	HepG2	liver:	n/a	n/a
37	FOXA1	chr4:132273881-132274128	HepG2	liver:	n/a	n/a
38	FOXA1	chr4:132273832-132274118	HepG2	liver:	n/a	n/a
39	FOXA1	chr4:132261790-132262117	HepG2	liver:	n/a	n/a
40	FOXA1	chr4:132273849-132274115	HepG2	liver:	n/a	n/a
41	FOXA2	chr4:132261809-132261997	HepG2	liver:	n/a	n/a
42	FOXA2	chr4:132273817-132274316	A549	lung:	n/a	n/a
43	FOXA2	chr4:132273845-132274179	A549	lung:	n/a	n/a
44	GATA3	chr4:132287593-132287948	MCF-7	breast:	n/a	n/a
45	HEY1	chr4:132301153-132301352	HepG2	liver:	n/a	n/a
46	HEY1	chr4:132300303-132300523	K562	blood:	n/a	n/a
47	HEY1	chr4:132301130-132301317	HepG2	liver:	n/a	n/a
48	JUN	chr4:132264948-132265148	K562	blood:	n/a	n/a
49	JUN	chr4:132288661-132288958	HepG2	liver:	n/a	chr4:132288785-132288798
50	JUND	chr4:132304191-132304395	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132273830-132273880	AG04449	skin:	fetal
2	chr4:132300589-132300639	HCPEpiC	choroid plexus:	n/a
3	chr4:132300589-132300639	HPAEpiC	pulmonary alveolar:	n/a
4	chr4:132300589-132300639	GM19239	blood:	n/a
5	chr4:132273830-132273880	AoSMC	blood vessel:	n/a
6	chr4:132300589-132300639	AG04449	skin:	fetal
7	chr4:132300589-132300639	NH-A	brain:	n/a
8	chr4:132273830-132273880	HL-60	blood:	n/a
9	chr4:132300589-132300639	ProgFib	skin:	n/a
10	chr4:132273830-132273880	LNCaP	prostate:	n/a
11	chr4:132300589-132300639	IMR90	lung:	fetal
12	chr4:132300589-132300639	AoSMC	blood vessel:	n/a
13	chr4:132300589-132300639	MCF10A-Er-Src	breast:	n/a
14	chr4:132273830-132273880	SK-N-SH_RA	brain:	n/a
15	chr4:132300589-132300639	HIPEpiC	eye:	n/a
16	chr4:132273830-132273880	GM19239	blood:	n/a
17	chr4:132300589-132300639	Jurkat	blood:	n/a
18	chr4:132300589-132300639	RPTEC	kidney:	n/a
19	chr4:132273830-132273880	HNPCEpiC	eye:	n/a
20	chr4:132273830-132273880	HRPEpiC	eye:	n/a
21	chr4:132273830-132273880	NH-A	brain:	n/a
22	chr4:132273830-132273880	HCM	heart:	n/a
23	chr4:132273830-132273880	GM12892	blood:	n/a
24	chr4:132300589-132300639	T-47D	breast:	n/a
25	chr4:132273830-132273880	T-47D	breast:	n/a
26	chr4:132300589-132300639	CMK	blood:	n/a
27	chr4:132300589-132300639	NHBE	bronchial:	n/a
28	chr4:132273830-132273880	HCPEpiC	choroid plexus:	n/a
29	chr4:132273830-132273880	K562	blood:	n/a
30	chr4:132273830-132273880	GM12891	blood:	n/a
31	chr4:132273830-132273880	NHDF-neo	bronchial:	n/a
32	chr4:132273830-132273880	GM06990	blood:	n/a
33	chr4:132300589-132300639	HepG2	liver:	n/a
34	chr4:132273830-132273880	ProgFib	skin:	n/a
35	chr4:132300589-132300639	GM12891	blood:	n/a
36	chr4:132300589-132300639	Caco-2	colon:	n/a
37	chr4:132273830-132273880	PrEC	prostate:	n/a
38	chr4:132273830-132273880	HUVEC	blood vessel:	n/a
39	chr4:132273830-132273880	PANC-1	pancreas:	n/a
40	chr4:132300589-132300639	HAEpiC	amniotic membrane:	n/a
41	chr4:132300589-132300639	PrEC	prostate:	n/a
42	chr4:132300589-132300639	HL-60	blood:	n/a
43	chr4:132300589-132300639	NHDF-neo	bronchial:	n/a
44	chr4:132273830-132273880	BE2_C	brain:	n/a
45	chr4:132300589-132300639	MCF-7	breast:	n/a
46	chr4:132273830-132273880	SK-N-SH	brain:	n/a
47	chr4:132300589-132300639	HEEpiC	esophagus:	n/a
48	chr4:132273830-132273880	MCF-7	breast:	n/a
49	chr4:132273830-132273880	BJ	skin:	n/a
50	chr4:132273830-132273880	HAEpiC	amniotic membrane:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:
2	chr4:132287444..132289970-chr4:132292320..132294677,2	K562	blood:
3	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:
4	chr4:132287444..132289970-chr4:132292320..132294677,2	K562	blood:
5	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:
6	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH10-7	chr4:132300925-132301522	NONHSAT098311
2	lnc-PCDH10-7	chr4:132301168-132301496	ENSG00000250102.1

No data

Variant related genes	Relation type
ENSG00000250102	TF binding region
ENSG00000250102	CpG island

Extended variants
information (count: 587 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146733827	chr4:132265618-132265619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374141271	chr4:132265688-132265689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191050105	chr4:132265696-132265697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555804334	chr4:132265769-132265770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183228513	chr4:132265827-132265828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558520851	chr4:132265873-132265874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530186363	chr4:132265960-132265961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186079204	chr4:132265980-132265981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs28393912	chr4:132266007-132266008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148884811	chr4:132266025-132266026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578262743	chr4:132266052-132266053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544121001	chr4:132266072-132266073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562493797	chr4:132266136-132266137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143543136	chr4:132266205-132266206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541960408	chr4:132266213-132266214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs10684564	chr4:132266214-132266215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370805404	chr4:132266215-132266216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397756248	chr4:132266216-132266217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs202219982	chr4:132266217-132266218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75825231	chr4:132266251-132266252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527496245	chr4:132266253-132266254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547615637	chr4:132266309-132266310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564116542	chr4:132266371-132266372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111793073	chr4:132266410-132266411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141786192	chr4:132266437-132266438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569736577	chr4:132266447-132266448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs17051176	chr4:132266511-132266512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs373925556	chr4:132266526-132266527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs59402364	chr4:132266527-132266528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549220550	chr4:132266534-132266535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558653539	chr4:132266541-132266542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs201030889	chr4:132266542-132266543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566121325	chr4:132266563-132266564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147037278	chr4:132266564-132266565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558374527	chr4:132266582-132266583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189767833	chr4:132266637-132266638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs386679579	chr4:132266670-132266671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78706920	chr4:132266671-132266672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201217961	chr4:132266679-132266680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576113746	chr4:132266735-132266736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541798763	chr4:132266736-132266737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555064069	chr4:132266783-132266784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113521258	chr4:132266797-132266798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540753878	chr4:132266813-132266814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531217043	chr4:132266829-132266830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564334517	chr4:132266875-132266876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182451382	chr4:132266897-132266898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs80008185	chr4:132266908-132266909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563202785	chr4:132266950-132266951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188373521	chr4:132266957-132266958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
Olfactory neuroblastoma	18408657	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132265600-132266600	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr4:132265800-132269800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:132265800-132269800	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr4:132266000-132266200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr4:132266000-132266400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr4:132266000-132266600	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr4:132266000-132266800	Enhancers	H1 Cell Line	embryonic stem cell
8	chr4:132266000-132266800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr4:132266000-132268800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr4:132266600-132267600	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr4:132266600-132267600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr4:132266800-132267800	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr4:132266800-132267800	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr4:132267600-132268600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:132267600-132269800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr4:132267800-132268200	Enhancers	H9 Cell Line	embryonic stem cell
17	chr4:132267800-132268400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr4:132267800-132268400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr4:132267800-132268400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr4:132268400-132270800	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr4:132268600-132269000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr4:132268800-132270800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr4:132269000-132269200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr4:132269000-132269800	Active TSS	GM12878-XiMat	blood
25	chr4:132269200-132270800	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr4:132269800-132270800	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr4:132269800-132270800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr4:132270800-132271000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr4:132270800-132271000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr4:132270800-132271000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr4:132270800-132271000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr4:132270800-132271200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:132274000-132274400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:132284400-132285200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr4:132285200-132287600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr4:132287600-132288200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr4:132287800-132288200	Active TSS	A549	lung
38	chr4:132298000-132298400	Active TSS	A549	lung
39	chr4:132300400-132300600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:132300600-132300800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:132300600-132302200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:132300800-132302400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr4:132301000-132301200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr4:132301000-132301600	Active TSS	K562	blood
45	chr4:132301000-132302000	Active TSS	Osteobl	bone
46	chr4:132301200-132301400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr4:132331200-132332200	ZNF genes & repeats	Dnd41	blood
48	chr4:132331600-132332200	Active TSS	Fetal Heart	heart

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