Variant report

Variant	nsv829938
Chromosome Location	chr4:55836964-55857893
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	BHLHE40	chr4:55837752-55837763	GM12878	blood:	n/a	n/a
2	BRCA1	chr4:55837596-55838229	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr4:55852340-55852662	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr4:55852204-55852788	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTBP2	chr4:55852301-55853046	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr4:55837549-55838189	H1-hESC	embryonic stem cell:	n/a	chr4:55837720-55837741 chr4:55837967-55837975 chr4:55837719-55837735
7	CTCF	chr4:55843000-55843150	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr4:55837904-55838078	GM12878	blood:	n/a	chr4:55837967-55837975
9	CTCF	chr4:55842954-55843122	HepG2	liver:	n/a	n/a
10	CTCF	chr4:55837280-55837430	HCM	heart:	n/a	n/a
11	CTCF	chr4:55837860-55838010	Caco-2	colon:	n/a	chr4:55837967-55837975
12	CTCF	chr4:55837760-55837910	GM12867	blood:	n/a	n/a
13	CTCF	chr4:55842980-55843130	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr4:55837500-55838131	ECC-1	luminal epithelium:	n/a	chr4:55837720-55837741 chr4:55837967-55837975 chr4:55837719-55837735
15	CTCF	chr4:55837540-55838085	ECC-1	luminal epithelium:	n/a	chr4:55837720-55837741 chr4:55837967-55837975 chr4:55837719-55837735
16	CTCF	chr4:55837904-55838078	HepG2	liver:	n/a	chr4:55837967-55837975
17	CTCF	chr4:55837680-55837830	NHDF-neo	bronchial:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
18	CTCF	chr4:55837680-55837830	AoAF	blood vessel:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
19	CTCF	chr4:55837612-55837827	GM10248	blood:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
20	CTCF	chr4:55837940-55838090	HEK293	kidney:	n/a	chr4:55837967-55837975
21	CTCF	chr4:55837568-55838103	K562	blood:	n/a	chr4:55837720-55837741 chr4:55837967-55837975 chr4:55837719-55837735
22	CTCF	chr4:55837800-55837950	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr4:55837920-55838070	AG04449	skin:	n/a	chr4:55837967-55837975
24	CTCF	chr4:55837926-55838079	NHEK	skin:	n/a	chr4:55837967-55837975
25	CTCF	chr4:55837592-55838078	LNCaP	prostate:	n/a	chr4:55837720-55837741 chr4:55837967-55837975 chr4:55837719-55837735
26	CTCF	chr4:55842920-55843132	A549	lung:	n/a	n/a
27	CTCF	chr4:55842940-55843090	HMEC	breast:	n/a	n/a
28	CTCF	chr4:55837660-55837810	AG10803	skin:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
29	CTCF	chr4:55842878-55843243	K562	blood:	n/a	n/a
30	CTCF	chr4:55842960-55843110	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr4:55837640-55837790	HPAF	blood vessel:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
32	CTCF	chr4:55842900-55843050	HCT-116	colon:	n/a	n/a
33	CTCF	chr4:55837660-55837810	GM12871	blood:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
34	CTCF	chr4:55842752-55843349	K562	blood:	n/a	n/a
35	CTCF	chr4:55837600-55837750	NB4	blood:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
36	CTCF	chr4:55837940-55838090	GM12866	blood:	n/a	chr4:55837967-55837975
37	CTCF	chr4:55837680-55837830	HBMEC	blood vessel:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
38	CTCF	chr4:55837921-55838107	Fibrobl	skin:	n/a	chr4:55837967-55837975
39	CTCF	chr4:55837660-55837810	GM12873	blood:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
40	CTCF	chr4:55837660-55837810	SAEC	small airway:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
41	CTCF	chr4:55837660-55837810	A549	lung:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
42	CTCF	chr4:55837860-55838010	AG09319	gingival:	n/a	chr4:55837967-55837975
43	CTCF	chr4:55837680-55837830	HUVEC	blood vessel:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
44	CTCF	chr4:55837800-55837950	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr4:55837660-55837810	AG04450	lung:	n/a	chr4:55837720-55837741 chr4:55837719-55837735
46	CTCF	chr4:55837597-55838052	Spleen_OC	spleen:	n/a	chr4:55837720-55837741 chr4:55837967-55837975 chr4:55837719-55837735
47	CTCF	chr4:55837484-55838210	T-47D	breast:	n/a	chr4:55837720-55837741 chr4:55837967-55837975 chr4:55837719-55837735
48	CTCF	chr4:55837575-55838119	K562	blood:	n/a	chr4:55837720-55837741 chr4:55837967-55837975 chr4:55837719-55837735
49	CTCF	chr4:55837300-55837450	GM12878	blood:	n/a	n/a
50	CTCF	chr4:55837620-55837770	GM12873	blood:	n/a	chr4:55837720-55837741 chr4:55837719-55837735

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:55852467-55852517	AG04449	skin:	fetal
2	chr4:55852467-55852517	HRCEpiC	kidney:	n/a
3	chr4:55852467-55852517	HCT-116	colon:	n/a
4	chr4:55852467-55852517	U87	brain:	n/a
5	chr4:55852467-55852517	SK-N-SH_RA	brain:	n/a
6	chr4:55852467-55852517	HEK293	kidney:	embryo
7	chr4:55852467-55852517	HRE	kidney:	n/a
8	chr4:55852467-55852517	HNPCEpiC	eye:	n/a
9	chr4:55852467-55852517	NH-A	brain:	n/a
10	chr4:55852467-55852517	T-47D	breast:	n/a
11	chr4:55852467-55852517	SAEC	small airway:	n/a
12	chr4:55852467-55852517	AG09309	skin:	n/a
13	chr4:55852467-55852517	HCF	heart:	n/a
14	chr4:55852467-55852517	GM06990	blood:	n/a
15	chr4:55852467-55852517	Caco-2	colon:	n/a
16	chr4:55852467-55852517	H1-hESC	embryonic stem cell:	embryo
17	chr4:55852467-55852517	GM12892	blood:	n/a
18	chr4:55852467-55852517	GM12891	blood:	n/a
19	chr4:55852467-55852517	ovcar-3	ovarian:	n/a
20	chr4:55852467-55852517	LNCaP	prostate:	n/a
21	chr4:55852467-55852517	K562	blood:	n/a
22	chr4:55852467-55852517	AG10803	skin:	n/a
23	chr4:55852467-55852517	PFSK-1	brain:	n/a
24	chr4:55852467-55852517	HUVEC	blood vessel:	n/a
25	chr4:55852467-55852517	SK-N-SH	brain:	n/a
26	chr4:55852467-55852517	NHDF-neo	bronchial:	n/a
27	chr4:55852467-55852517	ECC-1	luminal epithelium:	n/a
28	chr4:55852467-55852517	NHBE	bronchial:	n/a
29	chr4:55852467-55852517	HPAEpiC	pulmonary alveolar:	n/a
30	chr4:55852467-55852517	HIPEpiC	eye:	n/a
31	chr4:55852467-55852517	HL-60	blood:	n/a
32	chr4:55852467-55852517	PANC-1	pancreas:	n/a
33	chr4:55852467-55852517	MCF10A-Er-Src	breast:	n/a
34	chr4:55852467-55852517	NT2-D1	testis:	n/a
35	chr4:55852467-55852517	GM12878	blood:	n/a
36	chr4:55852467-55852517	Jurkat	blood:	n/a
37	chr4:55852467-55852517	AG09319	gingival:	n/a
38	chr4:55852467-55852517	HMEC	breast:	n/a
39	chr4:55852467-55852517	BE2_C	brain:	n/a
40	chr4:55852467-55852517	IMR90	lung:	fetal
41	chr4:55852467-55852517	BJ	skin:	n/a
42	chr4:55852467-55852517	HepG2	liver:	n/a
43	chr4:55852467-55852517	HRPEpiC	eye:	n/a
44	chr4:55852467-55852517	NB4	blood:	n/a
45	chr4:55852467-55852517	SKMC	muscle:	n/a
46	chr4:55852467-55852517	ProgFib	skin:	n/a
47	chr4:55852467-55852517	RPTEC	kidney:	n/a
48	chr4:55852467-55852517	SK-N-MC	brain:	n/a
49	chr4:55852467-55852517	A549	lung:	n/a
50	chr4:55852467-55852517	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:55842594..55843356-chr4:56187739..56188757,3	MCF-7	breast:
2	chr4:55835539..55837213-chr4:56212289..56215225,2	K562	blood:
3	chr4:55837377..55838442-chr4:56187562..56188922,11	MCF-7	breast:
4	chr4:55837666..55838201-chr4:56602502..56603198,2	K562	blood:
5	chr4:55837333..55838455-chr4:56187448..56188491,5	MCF-7	breast:
6	chr4:55837282..55838240-chr4:56052038..56052925,2	MCF-7	breast:
7	chr4:55839440..55840292-chr4:56187965..56188568,2	MCF-7	breast:
8	chr4:55837401..55838448-chr4:56187626..56188482,4	K562	blood:
9	chr4:55841032..55843418-chr4:55929631..55932494,2	K562	blood:
10	chr4:55189198..55189880-chr4:55837437..55838307,2	MCF-7	breast:

Variant related genes	Relation type
RPL38P3	TF binding region
RPL38P3	CpG island
ENSG00000244034	chromatin interactions
ENSG00000128039	chromatin interactions

Extended variants
information (count: 678 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111697396	chr4:55837002-55837003	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs530444985	chr4:55837036-55837037	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs546584824	chr4:55837111-55837112	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs560173230	chr4:55837165-55837166	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532171559	chr4:55837195-55837196	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs552295140	chr4:55837211-55837212	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs374423817	chr4:55837404-55837405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552387534	chr4:55837411-55837412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573307394	chr4:55837441-55837442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188995606	chr4:55837480-55837481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112436622	chr4:55837495-55837496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560810951	chr4:55837510-55837511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532132990	chr4:55837532-55837533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181240517	chr4:55837550-55837551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368490456	chr4:55837557-55837558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371057567	chr4:55837558-55837559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540585348	chr4:55837566-55837567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs13114647	chr4:55837578-55837579	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs531453412	chr4:55837654-55837655	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs138784978	chr4:55837682-55837683	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs367574756	chr4:55837692-55837693	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs61397712	chr4:55837744-55837745	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs141827411	chr4:55837761-55837762	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs570423729	chr4:55837865-55837866	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs538601572	chr4:55837891-55837892	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs376514889	chr4:55837898-55837899	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs397775996	chr4:55837906-55837907	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs397791381	chr4:55837907-55837908	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs183862823	chr4:55837944-55837945	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs569218962	chr4:55837949-55837950	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs538321381	chr4:55837958-55837959	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs145282482	chr4:55837962-55837963	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs35712806	chr4:55837991-55837992	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs376005540	chr4:55838041-55838042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs137891511	chr4:55838112-55838113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554462894	chr4:55838117-55838118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs9631802	chr4:55838161-55838162	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs34003687	chr4:55838210-55838211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530722559	chr4:55838234-55838235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368330716	chr4:55838273-55838274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189030005	chr4:55838277-55838278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201743473	chr4:55838405-55838406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531238412	chr4:55838406-55838407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112160818	chr4:55838426-55838427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372390134	chr4:55838450-55838451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561674122	chr4:55838457-55838458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576541348	chr4:55838485-55838486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561125940	chr4:55838491-55838492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527443530	chr4:55838507-55838508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547192245	chr4:55838536-55838537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Hodgkin''s lymphoma	17606441	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
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164920	CNVD
Cancer	22183965	CNVD
Autism	22543975	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55837400-55838200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:55837400-55838400	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr4:55837600-55838000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:55837800-55838200	Enhancers	HUVEC	blood vessel
5	chr4:55837800-55838400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr4:55837800-55838400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr4:55838000-55838400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:55838000-55838800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr4:55838400-55842800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr4:55838400-55842800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr4:55838400-55843000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr4:55838400-55843200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr4:55839400-55839600	Enhancers	Esophagus	oesophagus
14	chr4:55839400-55840000	Enhancers	Fetal Brain Male	brain
15	chr4:55842800-55843400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr4:55842800-55843400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:55842800-55843800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr4:55842800-55843800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr4:55842800-55844400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:55843000-55843400	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr4:55843000-55843400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr4:55843200-55843400	Enhancers	H9 Cell Line	embryonic stem cell
23	chr4:55843200-55843400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr4:55843200-55843600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr4:55843200-55843600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr4:55843200-55843800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:55843400-55852600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr4:55851200-55853200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr4:55851400-55853400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr4:55851400-55853400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr4:55851800-55853600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr4:55852000-55852200	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr4:55852000-55852400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:55852000-55853200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr4:55852000-55853600	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr4:55852200-55852400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr4:55852200-55853400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr4:55852200-55853400	Enhancers	H1 Cell Line	embryonic stem cell
39	chr4:55852400-55852600	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr4:55852600-55853000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr4:55852600-55853000	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr4:55852600-55853200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr4:55852600-55853200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr4:55852600-55853400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:55853000-55853200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr4:55853000-55853400	Enhancers	HUES6 Cell Line	embryonic stem cell

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