Variant report

Variant	nsv878802
Chromosome Location	chr4:29972531-30156463
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:258)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:30150521-30150828	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:30150568-30150857	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr4:30008870-30009070	K562	blood:	n/a	n/a
4	CEBPB	chr4:29990815-29990952	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr4:30075044-30075228	H1-hESC	embryonic stem cell:	n/a	chr4:30075114-30075127 chr4:30075116-30075127 chr4:30075114-30075125
6	CEBPB	chr4:30074742-30075297	HepG2	liver:	n/a	chr4:30075114-30075127 chr4:30075116-30075127 chr4:30075114-30075125
7	CEBPB	chr4:30074694-30075315	Hela-S3	cervix:	n/a	chr4:30075114-30075127 chr4:30075116-30075127 chr4:30075114-30075125
8	CEBPB	chr4:30003872-30004500	HCT-116	colon:	n/a	chr4:30003923-30003936
9	CEBPB	chr4:30074806-30075244	K562	blood:	n/a	chr4:30075114-30075127 chr4:30075116-30075127 chr4:30075114-30075125
10	CEBPB	chr4:30003974-30004354	HCT-116	colon:	n/a	n/a
11	CEBPB	chr4:30074756-30075302	IMR90	lung:	n/a	chr4:30075114-30075127 chr4:30075116-30075127 chr4:30075114-30075125
12	CEBPB	chr4:30074731-30075290	A549	lung:	n/a	chr4:30075114-30075127 chr4:30075116-30075127 chr4:30075114-30075125
13	CEBPB	chr4:30057751-30057980	H1-hESC	embryonic stem cell:	n/a	chr4:30057867-30057876
14	CEBPB	chr4:30096492-30096836	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:30031250-30031393	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:30003967-30004359	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr4:30030753-30030816	HepG2	liver:	n/a	n/a
18	CTCF	chr4:30155300-30155450	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr4:29972326-29972623	MCF-7	breast:	n/a	n/a
20	CTCF	chr4:29972420-29972570	RPTEC	kidney:	n/a	n/a
21	CTCF	chr4:29972317-29972608	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr4:29972278-29972597	MCF-7	breast:	n/a	n/a
23	CTCF	chr4:30097359-30097409	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr4:30155323-30155460	MCF-7	breast:	n/a	n/a
25	CTCF	chr4:30021922-30021937	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr4:30155366-30155440	MCF-7	breast:	n/a	n/a
27	CTCF	chr4:30016460-30016610	HCT-116	colon:	n/a	n/a
28	CTCF	chr4:29972292-29972551	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:30070141-30070281	GM12878	blood:	n/a	n/a
30	CTCF	chr4:30009079-30009131	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:29972270-29972617	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr4:30155344-30155437	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr4:30009040-30009190	HEK293	kidney:	n/a	n/a
34	CTCF	chr4:29972233-29972578	GM12878	blood:	n/a	n/a
35	CTCF	chr4:29972275-29972554	Gliobla	brain:	n/a	n/a
36	CTCF	chr4:30155331-30155455	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:29972306-29972534	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr4:29972440-29972590	NHEK	skin:	n/a	n/a
39	CTCF	chr4:30131880-30132030	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr4:29993859-29993911	GM20000	blood:	n/a	n/a
41	CTCF	chr4:29983372-29983467	Lung_OC	lung:	n/a	n/a
42	CTCF	chr4:29972312-29972532	LNCaP	prostate:	n/a	n/a
43	CTCF	chr4:30047703-30047721	GM13976	blood:	n/a	n/a
44	CTCF	chr4:30154740-30154890	GM12871	blood:	n/a	n/a
45	CTCF	chr4:30155385-30155425	Hela-S3	cervix:	n/a	n/a
46	E2F4	chr4:30105207-30105419	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr4:30072851-30073194	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr4:30133264-30133489	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr4:30034731-30034799	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr4:29988120-29988317	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:30095297-30095347	Hela-S3	cervix:	n/a
2	chr4:30095297-30095347	U87	brain:	n/a
3	chr4:30095297-30095347	AoSMC	blood vessel:	n/a
4	chr4:30095297-30095347	GM12891	blood:	n/a
5	chr4:30095297-30095347	HIPEpiC	eye:	n/a
6	chr4:30095297-30095347	NT2-D1	testis:	n/a
7	chr4:30095297-30095347	IMR90	lung:	fetal
8	chr4:30095297-30095347	HEK293	kidney:	embryo
9	chr4:30095297-30095347	HCT-116	colon:	n/a
10	chr4:30095297-30095347	AG09309	skin:	n/a
11	chr4:30095297-30095347	NHDF-neo	bronchial:	n/a
12	chr4:30095297-30095347	SK-N-SH	brain:	n/a
13	chr4:30095297-30095347	MCF-7	breast:	n/a
14	chr4:30095297-30095347	HUVEC	blood vessel:	n/a
15	chr4:30095297-30095347	BJ	skin:	n/a
16	chr4:30095297-30095347	ProgFib	skin:	n/a
17	chr4:30095297-30095347	AG04449	skin:	fetal
18	chr4:30095297-30095347	SK-N-SH_RA	brain:	n/a
19	chr4:30095297-30095347	HEEpiC	esophagus:	n/a
20	chr4:30095297-30095347	HRPEpiC	eye:	n/a
21	chr4:30095297-30095347	PANC-1	pancreas:	n/a
22	chr4:30095297-30095347	HCF	heart:	n/a
23	chr4:30095297-30095347	SKMC	muscle:	n/a
24	chr4:30095297-30095347	SK-N-MC	brain:	n/a
25	chr4:30095297-30095347	PFSK-1	brain:	n/a
26	chr4:30095297-30095347	AG04450	lung:	fetal
27	chr4:30095297-30095347	CMK	blood:	n/a
28	chr4:30095297-30095347	Hepatocyte	liver:	n/a
29	chr4:30095297-30095347	NHBE	bronchial:	n/a
30	chr4:30095297-30095347	HCM	heart:	n/a
31	chr4:30095297-30095347	Caco-2	colon:	n/a
32	chr4:30095297-30095347	GM12892	blood:	n/a
33	chr4:30095297-30095347	AG09319	gingival:	n/a
34	chr4:30095297-30095347	BE2_C	brain:	n/a
35	chr4:30095297-30095347	K562	blood:	n/a
36	chr4:30095297-30095347	GM12878	blood:	n/a
37	chr4:30095297-30095347	HepG2	liver:	n/a
38	chr4:30095297-30095347	HRE	kidney:	n/a
39	chr4:30095297-30095347	RPTEC	kidney:	n/a
40	chr4:30095297-30095347	HMEC	breast:	n/a
41	chr4:30095297-30095347	HCPEpiC	choroid plexus:	n/a
42	chr4:30095297-30095347	PrEC	prostate:	n/a
43	chr4:30095297-30095347	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:30095297-30095347	H1-hESC	embryonic stem cell:	embryo
45	chr4:30095297-30095347	GM19239	blood:	n/a
46	chr4:30095297-30095347	T-47D	breast:	n/a
47	chr4:30095297-30095347	GM06990	blood:	n/a
48	chr4:30095297-30095347	MCF10A-Er-Src	breast:	n/a
49	chr4:30095297-30095347	HRCEpiC	kidney:	n/a
50	chr4:30095297-30095347	NH-A	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:30128238..30130674-chr4:30130839..30133717,2	MCF-7	breast:
2	chr13:46714477..46715323-chr4:30113851..30114490,2	MCF-7	breast:
3	chr4:30055206..30057309-chr4:30063037..30065592,2	MCF-7	breast:
4	chr4:30108481..30110842-chr4:30143021..30145744,2	K562	blood:
5	chr4:30108481..30110842-chr4:30143021..30145744,2	K562	blood:
6	chr4:30128238..30130674-chr4:30130839..30133717,2	MCF-7	breast:
7	chr1:67965802..67966741-chr4:29984559..29985348,2	MCF-7	breast:
8	chr4:29972062..29972801-chr4:30382123..30382658,2	MCF-7	breast:
9	chr4:30055206..30057309-chr4:30063037..30065592,2	MCF-7	breast:
10	chr4:30009302..30010813-chr4:30012975..30015571,2	MCF-7	breast:
11	chr2:63558377..63559158-chr4:30081687..30082401,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-180C1.1.1-8	chr4:30009047-30009938	NONHSAT095932
2	lnc-RP11-180C1.1.1-8	chr4:30008573-30008672	NONHSAT095932

No data

Variant related genes	Relation type
ENSG00000248281	TF binding region
ENSG00000248281	CpG island
ENSG00000248281	chromatin interactions

Extended variants
information (count: 2493 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2493 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6848673	chr4:29972531-29972532	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565701101	chr4:29972560-29972561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534729925	chr4:29972586-29972587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144719822	chr4:29972595-29972596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577905041	chr4:29972608-29972609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537239093	chr4:29972625-29972626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183153403	chr4:29972634-29972635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556835207	chr4:29972636-29972637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573786316	chr4:29972649-29972650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542718953	chr4:29972653-29972654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148542981	chr4:29972718-29972719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559617989	chr4:29972800-29972801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150482385	chr4:29985640-29985641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373654701	chr4:29985646-29985647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558066624	chr4:29985673-29985674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs367641510	chr4:29985698-29985699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543646392	chr4:29985699-29985700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563548065	chr4:29985768-29985769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs80091402	chr4:30008599-30008600	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs112790287	chr4:30008629-30008630	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs140277732	chr4:30008672-30008673	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs533469859	chr4:30009068-30009069	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs145716406	chr4:30009078-30009079	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs183610109	chr4:30009138-30009139	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs535566736	chr4:30009140-30009141	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs555874538	chr4:30009141-30009142	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs188293353	chr4:30009145-30009146	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs13101782	chr4:30009146-30009147	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs558198896	chr4:30009163-30009164	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs577978647	chr4:30009217-30009218	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs543766799	chr4:30009244-30009245	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs573827513	chr4:30009256-30009257	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs542460289	chr4:30009330-30009331	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs559359472	chr4:30009343-30009344	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs528192525	chr4:30009361-30009362	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs79628547	chr4:30009363-30009364	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs138667916	chr4:30009364-30009365	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs533432930	chr4:30009367-30009368	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs372802391	chr4:30009376-30009377	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs191546790	chr4:30009417-30009418	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs62617131	chr4:30009422-30009423	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs114813159	chr4:30009459-30009460	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs79689368	chr4:30009497-30009498	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs148834658	chr4:30009504-30009505	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs535144092	chr4:30009528-30009529	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs531523063	chr4:30009533-30009534	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs571703027	chr4:30009541-30009542	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs537340431	chr4:30009559-30009560	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs143495731	chr4:30009560-30009561	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs148015119	chr4:30009586-30009587	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	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
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Tetralogy of Fallot	22912587	CNVD
Renal cell carcinoma	18194544	CNVD
Colorectal cancer	16774939	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:29972200-29972800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr4:29985600-29985800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:30013800-30014600	ZNF genes & repeats	Adipose Nuclei	Adipose
4	chr4:30026400-30026600	Enhancers	Fetal Lung	lung
5	chr4:30029800-30030600	Enhancers	Brain Germinal Matrix	brain
6	chr4:30045800-30046600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr4:30046000-30046400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr4:30057000-30058000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr4:30057200-30058000	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr4:30057400-30058000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr4:30057400-30058200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr4:30057600-30057800	Active TSS	Brain Hippocampus Middle	brain
13	chr4:30057600-30058000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:30057600-30058000	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr4:30057600-30058200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr4:30057600-30058200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr4:30057800-30058000	Flanking Active TSS	Brain Hippocampus Middle	brain
18	chr4:30058000-30058600	Enhancers	Brain Hippocampus Middle	brain
19	chr4:30058000-30062800	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr4:30062800-30063600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr4:30069200-30069400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:30069600-30074400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr4:30074200-30074800	Enhancers	Fetal Lung	lung
24	chr4:30074400-30075200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr4:30074400-30075200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:30082800-30083600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:30085600-30086800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr4:30086000-30086600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr4:30086200-30086600	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr4:30086200-30086600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:30093800-30094200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:30094200-30094400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr4:30094200-30094800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:30094600-30095400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:30104000-30106000	Enhancers	HUVEC	blood vessel
36	chr4:30104400-30106000	Enhancers	Muscle Satellite Cultured Cells	--
37	chr4:30104800-30106000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr4:30105200-30105600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr4:30105600-30117200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:30107000-30107400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
41	chr4:30107400-30107600	Enhancers	H9 Cell Line	embryonic stem cell
42	chr4:30107600-30108000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr4:30117200-30118800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr4:30117400-30117800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:30117400-30118400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:30117600-30117800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr4:30118000-30118400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr4:30122800-30123000	Enhancers	Fetal Lung	lung
49	chr4:30123200-30124200	Weak transcription	Fetal Lung	lung
50	chr4:30124200-30125600	Enhancers	Fetal Lung	lung

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