Variant report

Variant	nsv880027
Chromosome Location	chr4:133223152-133449829
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	chr4:133266134-133266306	K562	blood:	n/a	n/a
2	ATF2	chr4:133416334-133416868	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:133416260-133417117	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:133367293-133367347	K562	blood:	n/a	n/a
5	BCL11A	chr4:133416681-133416977	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr4:133265695-133265813	K562	blood:	n/a	n/a
7	BHLHE40	chr4:133266102-133266846	K562	blood:	n/a	n/a
8	BHLHE40	chr4:133264871-133264883	K562	blood:	n/a	n/a
9	BRCA1	chr4:133266159-133266384	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr4:133338441-133338670	HCT-116	colon:	n/a	n/a
11	CBX3	chr4:133265310-133265941	K562	blood:	n/a	n/a
12	CBX3	chr4:133266054-133266694	K562	blood:	n/a	n/a
13	CCNT2	chr4:133266111-133266381	K562	blood:	n/a	n/a
14	CEBPB	chr4:133310826-133311039	H1-hESC	embryonic stem cell:	n/a	chr4:133310930-133310941
15	CEBPB	chr4:133246117-133246325	HepG2	liver:	n/a	chr4:133246262-133246273 chr4:133246273-133246286 chr4:133246273-133246284
16	CEBPB	chr4:133441707-133441832	K562	blood:	n/a	n/a
17	CEBPB	chr4:133408491-133408784	MCF-7	breast:	n/a	chr4:133408637-133408648
18	CEBPB	chr4:133310830-133311107	IMR90	lung:	n/a	chr4:133310930-133310941
19	CEBPB	chr4:133427760-133428011	HepG2	liver:	n/a	chr4:133427871-133427882 chr4:133427870-133427883 chr4:133427870-133427883 chr4:133427870-133427881 chr4:133427870-133427881
20	CEBPB	chr4:133223702-133223847	H1-hESC	embryonic stem cell:	n/a	chr4:133223742-133223753 chr4:133223743-133223754 chr4:133223742-133223755
21	CEBPB	chr4:133408509-133408832	K562	blood:	n/a	chr4:133408637-133408648
22	CEBPB	chr4:133363913-133364226	IMR90	lung:	n/a	chr4:133364078-133364089 chr4:133364031-133364042
23	CEBPB	chr4:133363937-133364232	K562	blood:	n/a	chr4:133364078-133364089 chr4:133364031-133364042
24	CEBPB	chr4:133408496-133408805	H1-hESC	embryonic stem cell:	n/a	chr4:133408637-133408648
25	CEBPB	chr4:133442333-133442655	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:133234391-133234624	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:133444564-133444877	HepG2	liver:	n/a	chr4:133444697-133444710 chr4:133444697-133444708 chr4:133444699-133444708
28	CEBPB	chr4:133408488-133408714	Hela-S3	cervix:	n/a	chr4:133408637-133408648
29	CEBPB	chr4:133278703-133278936	ECC-1	luminal epithelium:	n/a	chr4:133278842-133278859
30	CEBPB	chr4:133310833-133311100	HepG2	liver:	n/a	chr4:133310930-133310941
31	CEBPB	chr4:133294688-133295002	A549	lung:	n/a	n/a
32	CEBPB	chr4:133318436-133318624	HepG2	liver:	n/a	chr4:133318505-133318516 chr4:133318505-133318518 chr4:133318507-133318518
33	CEBPB	chr4:133228257-133228566	HepG2	liver:	n/a	chr4:133228409-133228420
34	CEBPB	chr4:133234378-133234608	A549	lung:	n/a	n/a
35	CEBPB	chr4:133441581-133441924	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:133294673-133295022	IMR90	lung:	n/a	n/a
37	CEBPB	chr4:133266193-133266232	K562	blood:	n/a	n/a
38	CEBPB	chr4:133223604-133223874	HepG2	liver:	n/a	chr4:133223742-133223753 chr4:133223743-133223754 chr4:133223742-133223755
39	CEBPB	chr4:133240074-133240372	K562	blood:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
40	CEBPB	chr4:133240140-133240393	HepG2	liver:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
41	CEBPB	chr4:133416429-133416947	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:133294679-133295027	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:133440969-133441202	HepG2	liver:	n/a	chr4:133441077-133441088
44	CEBPB	chr4:133304647-133305173	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr4:133363932-133364193	H1-hESC	embryonic stem cell:	n/a	chr4:133364078-133364089 chr4:133364031-133364042
46	CEBPB	chr4:133228262-133228577	IMR90	lung:	n/a	chr4:133228409-133228420
47	CEBPB	chr4:133254553-133255549	IMR90	lung:	n/a	chr4:133254713-133254724 chr4:133254713-133254726
48	CEBPB	chr4:133408492-133408827	HepG2	liver:	n/a	chr4:133408637-133408648
49	CEBPB	chr4:133441631-133441845	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr4:133441568-133441915	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:133266193-133266243	SAEC	small airway:	n/a
2	chr4:133266193-133266243	SK-N-SH	brain:	n/a
3	chr4:133266193-133266243	AG10803	skin:	n/a
4	chr4:133266193-133266243	HIPEpiC	eye:	n/a
5	chr4:133266322-133266372	BE2_C	brain:	n/a
6	chr4:133266322-133266372	AoSMC	blood vessel:	n/a
7	chr4:133266322-133266372	HMEC	breast:	n/a
8	chr4:133266193-133266243	AoSMC	blood vessel:	n/a
9	chr4:133266193-133266243	RPTEC	kidney:	n/a
10	chr4:133266322-133266372	HCT-116	colon:	n/a
11	chr4:133266322-133266372	MCF-7	breast:	n/a
12	chr4:133266193-133266243	LNCaP	prostate:	n/a
13	chr4:133266322-133266372	GM19239	blood:	n/a
14	chr4:133266193-133266243	U87	brain:	n/a
15	chr4:133266322-133266372	MCF10A-Er-Src	breast:	n/a
16	chr4:133266193-133266243	T-47D	breast:	n/a
17	chr4:133266322-133266372	HNPCEpiC	eye:	n/a
18	chr4:133266322-133266372	AG09319	gingival:	n/a
19	chr4:133266322-133266372	RPTEC	kidney:	n/a
20	chr4:133266193-133266243	HMEC	breast:	n/a
21	chr4:133266193-133266243	HNPCEpiC	eye:	n/a
22	chr4:133266193-133266243	GM06990	blood:	n/a
23	chr4:133266193-133266243	BE2_C	brain:	n/a
24	chr4:133266322-133266372	HCF	heart:	n/a
25	chr4:133266193-133266243	AG09319	gingival:	n/a
26	chr4:133266322-133266372	K562	blood:	n/a
27	chr4:133266193-133266243	PrEC	prostate:	n/a
28	chr4:133266322-133266372	ovcar-3	ovarian:	n/a
29	chr4:133266322-133266372	HRCEpiC	kidney:	n/a
30	chr4:133266193-133266243	Jurkat	blood:	n/a
31	chr4:133266193-133266243	HEK293	kidney:	embryo
32	chr4:133266322-133266372	HUVEC	blood vessel:	n/a
33	chr4:133266193-133266243	HCT-116	colon:	n/a
34	chr4:133266322-133266372	Hela-S3	cervix:	n/a
35	chr4:133266322-133266372	NH-A	brain:	n/a
36	chr4:133266193-133266243	HepG2	liver:	n/a
37	chr4:133266322-133266372	HAEpiC	amniotic membrane:	n/a
38	chr4:133266322-133266372	SK-N-SH_RA	brain:	n/a
39	chr4:133266322-133266372	HRE	kidney:	n/a
40	chr4:133266193-133266243	HEEpiC	esophagus:	n/a
41	chr4:133266193-133266243	GM19239	blood:	n/a
42	chr4:133266193-133266243	SK-N-SH_RA	brain:	n/a
43	chr4:133266193-133266243	H1-hESC	embryonic stem cell:	embryo
44	chr4:133266322-133266372	SKMC	muscle:	n/a
45	chr4:133266322-133266372	HL-60	blood:	n/a
46	chr4:133266193-133266243	GM12892	blood:	n/a
47	chr4:133266322-133266372	GM12891	blood:	n/a
48	chr4:133266322-133266372	T-47D	breast:	n/a
49	chr4:133266322-133266372	ProgFib	skin:	n/a
50	chr4:133266193-133266243	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:133294490..133296244-chr4:133317464..133320179,2	K562	blood:
2	chr4:133116257..133118225-chr4:133445549..133447464,2	MCF-7	breast:
3	chr4:133294490..133296244-chr4:133317464..133320179,2	K562	blood:
4	chr4:133254539..133258188-chr4:133265340..133266888,3	K562	blood:
5	chr4:133352255..133354798-chr4:133356746..133359488,2	K562	blood:
6	chr4:133246638..133249812-chr4:133265864..133268563,3	K562	blood:
7	chr4:133263144..133265552-chr4:133295032..133296835,2	K562	blood:
8	chr4:133265507..133268108-chr4:133268991..133271558,3	K562	blood:
9	chr4:133263144..133265552-chr4:133295032..133296835,2	K562	blood:
10	chr4:133337477..133339790-chr4:133339994..133342745,2	K562	blood:
11	chr4:133346218..133346845-chr6:148869148..148869834,2	MCF-7	breast:
12	chr4:133264521..133268108-chr4:133268991..133272057,6	K562	blood:
13	chr4:133254539..133258188-chr4:133265340..133266888,3	K562	blood:
14	chr4:133264521..133268108-chr4:133268991..133272057,6	K562	blood:
15	chr4:133246638..133249812-chr4:133265864..133268563,3	K562	blood:
16	chr4:133352255..133354798-chr4:133356746..133359488,2	K562	blood:
17	chr4:133265507..133268108-chr4:133268991..133271558,3	K562	blood:
18	chr4:133337477..133339790-chr4:133339994..133342745,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-62N21.1.1-11	chr4:133288941-133289634	NONHSAT098333

Variant related genes	Relation type
ELL2P2	TF binding region
ENSG00000248369	TF binding region
ELL2P2	CpG island
ENSG00000248369	CpG island

Extended variants
information (count: 3148 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:3148 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13103069	chr4:133223152-133223153	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546064883	chr4:133223181-133223182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556345230	chr4:133223216-133223217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149792259	chr4:133223270-133223271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576617252	chr4:133223276-133223277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568905310	chr4:133223300-133223301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375169841	chr4:133223301-133223302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542307159	chr4:133223304-133223305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147617098	chr4:133223318-133223319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527711733	chr4:133223418-133223419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555371589	chr4:133223459-133223460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185550855	chr4:133223470-133223471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142159713	chr4:133223484-133223485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190249891	chr4:133223489-133223490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182180698	chr4:133223494-133223495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371933541	chr4:133223501-133223502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185268184	chr4:133223554-133223555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114312967	chr4:133223580-133223581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569554996	chr4:133223615-133223616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568132989	chr4:133223636-133223637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533594812	chr4:133223637-133223638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547363432	chr4:133223652-133223653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570656692	chr4:133223660-133223661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543044534	chr4:133223763-133223764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556405988	chr4:133223807-133223808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs17049225	chr4:133223830-133223831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535623487	chr4:133223865-133223866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149757699	chr4:133223936-133223937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115649193	chr4:133223943-133223944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191808808	chr4:133223993-133223994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564466692	chr4:133224153-133224154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7667347	chr4:133224190-133224191	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs184092239	chr4:133224215-133224216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145606509	chr4:133224224-133224225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188239648	chr4:133224275-133224276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs193177284	chr4:133224309-133224310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551748084	chr4:133224319-133224320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34530687	chr4:133224322-133224323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561680658	chr4:133224354-133224355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7667592	chr4:133224362-133224363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs547086060	chr4:133224435-133224436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115940868	chr4:133224463-133224464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117846732	chr4:133224509-133224510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74640788	chr4:133224513-133224514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183131103	chr4:133224517-133224518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535686398	chr4:133224521-133224522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555493091	chr4:133224523-133224524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs17049245	chr4:133224547-133224548	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs553871876	chr4:133224570-133224571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187099645	chr4:133224594-133224595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:133222600-133224800	Weak transcription	Fetal Lung	lung
2	chr4:133224800-133225000	Enhancers	Fetal Lung	lung
3	chr4:133234400-133235400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr4:133235000-133235400	Enhancers	Brain Anterior Caudate	brain
5	chr4:133236800-133237000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:133237000-133237200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:133242200-133242400	Enhancers	H9 Cell Line	embryonic stem cell
8	chr4:133254000-133255200	Enhancers	NHLF	lung
9	chr4:133254400-133255600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:133254800-133255600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr4:133254800-133255600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:133265000-133265200	Enhancers	Hela-S3	cervix
13	chr4:133265200-133265400	Enhancers	Placenta	Placenta
14	chr4:133265200-133265600	Flanking Active TSS	Hela-S3	cervix
15	chr4:133265200-133267200	Active TSS	K562	blood
16	chr4:133265400-133265600	Flanking Active TSS	Placenta	Placenta
17	chr4:133265600-133267000	Active TSS	Placenta	Placenta
18	chr4:133265600-133267000	Active TSS	Hela-S3	cervix
19	chr4:133266200-133266600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
20	chr4:133266400-133266600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr4:133269200-133270400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:133276000-133276600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:133276400-133276600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr4:133276600-133282200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr4:133282200-133282400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr4:133285200-133285800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:133287000-133287400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
28	chr4:133287200-133288000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
29	chr4:133287200-133288000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
30	chr4:133287200-133288000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr4:133287400-133287800	ZNF genes & repeats	Dnd41	blood
32	chr4:133288000-133289000	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr4:133290200-133290800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr4:133311000-133311200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:133316800-133317200	Enhancers	Fetal Kidney	kidney
36	chr4:133317200-133318200	Weak transcription	Fetal Kidney	kidney
37	chr4:133317600-133318400	Enhancers	NH-A	brain
38	chr4:133318200-133318400	Enhancers	Fetal Kidney	kidney
39	chr4:133324600-133325400	ZNF genes & repeats	Dnd41	blood
40	chr4:133324600-133325600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:133335400-133336200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:133335400-133336800	ZNF genes & repeats	Dnd41	blood
43	chr4:133336800-133340400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
44	chr4:133338000-133339400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
45	chr4:133338200-133338800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
46	chr4:133338800-133341000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
47	chr4:133340000-133340800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr4:133340000-133340800	ZNF genes & repeats	Dnd41	blood
49	chr4:133340200-133340600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
50	chr4:133340200-133341400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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