Variant report

Variant	esv2757955
Chromosome Location	chr4:133153860-133298149
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	BATF	chr4:133162291-133162510	GM12878	blood:	n/a	n/a
3	BATF	chr4:133162320-133162585	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:133264871-133264883	K562	blood:	n/a	n/a
5	BHLHE40	chr4:133266102-133266846	K562	blood:	n/a	n/a
6	BHLHE40	chr4:133265695-133265813	K562	blood:	n/a	n/a
7	BRCA1	chr4:133266159-133266384	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr4:133265310-133265941	K562	blood:	n/a	n/a
9	CBX3	chr4:133266054-133266694	K562	blood:	n/a	n/a
10	CCNT2	chr4:133266111-133266381	K562	blood:	n/a	n/a
11	CEBPB	chr4:133246117-133246325	HepG2	liver:	n/a	chr4:133246262-133246273 chr4:133246273-133246286 chr4:133246273-133246284
12	CEBPB	chr4:133228257-133228566	HepG2	liver:	n/a	chr4:133228409-133228420
13	CEBPB	chr4:133254850-133255208	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr4:133266193-133266232	K562	blood:	n/a	n/a
15	CEBPB	chr4:133240156-133240388	A549	lung:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
16	CEBPB	chr4:133234391-133234624	IMR90	lung:	n/a	n/a
17	CEBPB	chr4:133278703-133278936	ECC-1	luminal epithelium:	n/a	chr4:133278842-133278859
18	CEBPB	chr4:133240140-133240393	HepG2	liver:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
19	CEBPB	chr4:133240074-133240372	K562	blood:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
20	CEBPB	chr4:133234378-133234608	A549	lung:	n/a	n/a
21	CEBPB	chr4:133223604-133223874	HepG2	liver:	n/a	chr4:133223742-133223753 chr4:133223743-133223754 chr4:133223742-133223755
22	CEBPB	chr4:133294679-133295027	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:133234404-133234637	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:133294679-133294861	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:133294688-133295002	A549	lung:	n/a	n/a
26	CEBPB	chr4:133228262-133228577	IMR90	lung:	n/a	chr4:133228409-133228420
27	CEBPB	chr4:133294673-133295022	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:133254553-133255549	IMR90	lung:	n/a	chr4:133254713-133254724 chr4:133254713-133254726
29	CEBPB	chr4:133223702-133223847	H1-hESC	embryonic stem cell:	n/a	chr4:133223742-133223753 chr4:133223743-133223754 chr4:133223742-133223755
30	CHD2	chr4:133266055-133266671	K562	blood:	n/a	n/a
31	CHD2	chr4:133265720-133266696	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr4:133254220-133254370	MCF-7	breast:	n/a	chr4:133254290-133254299
33	CTCF	chr4:133254160-133254310	GM12870	blood:	n/a	chr4:133254290-133254299
34	CTCF	chr4:133254188-133254397	GM12878	blood:	n/a	chr4:133254290-133254299
35	CTCF	chr4:133254220-133254370	HEEpiC	esophagus:	n/a	chr4:133254290-133254299
36	CTCF	chr4:133254420-133254570	BJ	skin:	n/a	n/a
37	CTCF	chr4:133254260-133254410	BJ	skin:	n/a	chr4:133254290-133254299
38	CTCF	chr4:133254146-133254399	H1-hESC	embryonic stem cell:	n/a	chr4:133254290-133254299
39	CTCF	chr4:133254183-133254355	HepG2	liver:	n/a	chr4:133254290-133254299
40	CTCF	chr4:133254220-133254370	HCPEpiC	choroid plexus:	n/a	chr4:133254290-133254299
41	CTCF	chr4:133254200-133254350	HVMF	connective:	n/a	chr4:133254290-133254299
42	CTCF	chr4:133254220-133254370	HPAF	blood vessel:	n/a	chr4:133254290-133254299
43	CTCF	chr4:133254180-133254330	HUVEC	blood vessel:	n/a	chr4:133254290-133254299
44	CTCF	chr4:133254200-133254350	HCPEpiC	choroid plexus:	n/a	chr4:133254290-133254299
45	CTCF	chr4:133254240-133254390	HCT-116	colon:	n/a	chr4:133254290-133254299
46	CTCF	chr4:133254260-133254410	HBMEC	blood vessel:	n/a	chr4:133254290-133254299
47	CTCF	chr4:133254220-133254370	HMEC	breast:	n/a	chr4:133254290-133254299
48	CTCF	chr4:133254240-133254390	Caco-2	colon:	n/a	chr4:133254290-133254299
49	CTCF	chr4:133254200-133254350	Caco-2	colon:	n/a	chr4:133254290-133254299
50	CTCF	chr4:133254151-133254415	IMR90	lung:	n/a	chr4:133254290-133254299

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:133266322-133266372	SKMC	muscle:	n/a
2	chr4:133266322-133266372	T-47D	breast:	n/a
3	chr4:133266322-133266372	Hela-S3	cervix:	n/a
4	chr4:133266322-133266372	AG09309	skin:	n/a
5	chr4:133266193-133266243	GM12878	blood:	n/a
6	chr4:133266322-133266372	RPTEC	kidney:	n/a
7	chr4:133266322-133266372	HMEC	breast:	n/a
8	chr4:133266322-133266372	CMK	blood:	n/a
9	chr4:133266193-133266243	A549	lung:	n/a
10	chr4:133266193-133266243	RPTEC	kidney:	n/a
11	chr4:133266322-133266372	SK-N-SH_RA	brain:	n/a
12	chr4:133266193-133266243	SAEC	small airway:	n/a
13	chr4:133266193-133266243	SK-N-SH_RA	brain:	n/a
14	chr4:133266322-133266372	HUVEC	blood vessel:	n/a
15	chr4:133266322-133266372	NHDF-neo	bronchial:	n/a
16	chr4:133266193-133266243	GM06990	blood:	n/a
17	chr4:133266193-133266243	BE2_C	brain:	n/a
18	chr4:133266193-133266243	ECC-1	luminal epithelium:	n/a
19	chr4:133266193-133266243	HIPEpiC	eye:	n/a
20	chr4:133266322-133266372	MCF10A-Er-Src	breast:	n/a
21	chr4:133266193-133266243	HepG2	liver:	n/a
22	chr4:133266193-133266243	NHDF-neo	bronchial:	n/a
23	chr4:133266193-133266243	AG09309	skin:	n/a
24	chr4:133266322-133266372	K562	blood:	n/a
25	chr4:133266193-133266243	MCF10A-Er-Src	breast:	n/a
26	chr4:133266322-133266372	GM19239	blood:	n/a
27	chr4:133266193-133266243	HL-60	blood:	n/a
28	chr4:133266193-133266243	LNCaP	prostate:	n/a
29	chr4:133266322-133266372	MCF-7	breast:	n/a
30	chr4:133266322-133266372	NHBE	bronchial:	n/a
31	chr4:133266193-133266243	NB4	blood:	n/a
32	chr4:133266322-133266372	PFSK-1	brain:	n/a
33	chr4:133266193-133266243	CMK	blood:	n/a
34	chr4:133266193-133266243	HUVEC	blood vessel:	n/a
35	chr4:133266322-133266372	HCF	heart:	n/a
36	chr4:133266322-133266372	NB4	blood:	n/a
37	chr4:133266322-133266372	GM12878	blood:	n/a
38	chr4:133266322-133266372	BJ	skin:	n/a
39	chr4:133266322-133266372	HAEpiC	amniotic membrane:	n/a
40	chr4:133266322-133266372	NT2-D1	testis:	n/a
41	chr4:133266193-133266243	SKMC	muscle:	n/a
42	chr4:133266322-133266372	SK-N-MC	brain:	n/a
43	chr4:133266193-133266243	NT2-D1	testis:	n/a
44	chr4:133266193-133266243	MCF-7	breast:	n/a
45	chr4:133266193-133266243	Hepatocyte	liver:	n/a
46	chr4:133266193-133266243	HRCEpiC	kidney:	n/a
47	chr4:133266193-133266243	U87	brain:	n/a
48	chr4:133266322-133266372	GM12891	blood:	n/a
49	chr4:133266322-133266372	Jurkat	blood:	n/a
50	chr4:133266193-133266243	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:133264521..133268108-chr4:133268991..133272057,6	K562	blood:
2	chr4:133246638..133249812-chr4:133265864..133268563,3	K562	blood:
3	chr4:133246638..133249812-chr4:133265864..133268563,3	K562	blood:
4	chr4:133254539..133258188-chr4:133265340..133266888,3	K562	blood:
5	chr4:133263144..133265552-chr4:133295032..133296835,2	K562	blood:
6	chr4:133265507..133268108-chr4:133268991..133271558,3	K562	blood:
7	chr4:133294490..133296244-chr4:133317464..133320179,2	K562	blood:
8	chr4:133263144..133265552-chr4:133295032..133296835,2	K562	blood:
9	chr4:133265507..133268108-chr4:133268991..133271558,3	K562	blood:
10	chr4:133254539..133258188-chr4:133265340..133266888,3	K562	blood:
11	chr4:133264521..133268108-chr4:133268991..133272057,6	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
ELL2P2	CpG island

Extended variants
information (count: 1923 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1923 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564910206	chr4:133153872-133153873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs11727344	chr4:133153894-133153895	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs369378470	chr4:133153932-133153933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567352385	chr4:133153949-133153950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs9995181	chr4:133153959-133153960	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs546534766	chr4:133153984-133153985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540893510	chr4:133153997-133153998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2657414	chr4:133154003-133154004	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs573822265	chr4:133154026-133154027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558800221	chr4:133154038-133154039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529597847	chr4:133154061-133154062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569104785	chr4:133154096-133154097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549522797	chr4:133154131-133154132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554808631	chr4:133154144-133154145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574838117	chr4:133154215-133154216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540273551	chr4:133154276-133154277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs74324544	chr4:133154284-133154285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577136322	chr4:133154296-133154297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546123145	chr4:133154297-133154298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532108641	chr4:133154347-133154348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576276540	chr4:133154351-133154352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542400200	chr4:133154372-133154373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2657413	chr4:133154382-133154383	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs529746501	chr4:133154400-133154401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575316551	chr4:133154469-133154470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571832939	chr4:133154515-133154516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2657412	chr4:133154530-133154531	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs564265569	chr4:133154533-133154534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147794271	chr4:133154553-133154554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567967474	chr4:133154593-133154594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560153648	chr4:133154611-133154612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536992976	chr4:133154618-133154619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2648815	chr4:133154625-133154626	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs13140752	chr4:133154663-133154664	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs545157589	chr4:133154667-133154668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188162253	chr4:133154674-133154675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537656802	chr4:133154700-133154701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548320975	chr4:133154711-133154712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559026739	chr4:133154726-133154727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568485850	chr4:133154742-133154743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs180912923	chr4:133154792-133154793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184609187	chr4:133154797-133154798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs553835093	chr4:133154840-133154841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76275569	chr4:133154865-133154866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs67935670	chr4:133154882-133154883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550670898	chr4:133154909-133154910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576288745	chr4:133154935-133154936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560811204	chr4:133154949-133154950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190293688	chr4:133154961-133154962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562279511	chr4:133154965-133154966	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:133153400-133155400	Enhancers	Dnd41	blood
2	chr4:133159400-133160400	Enhancers	Stomach Mucosa	stomach
3	chr4:133159800-133160400	Enhancers	Fetal Intestine Large	intestine
4	chr4:133159800-133161600	Enhancers	Fetal Intestine Small	intestine
5	chr4:133160000-133160600	Enhancers	Duodenum Mucosa	Duodenum
6	chr4:133160000-133160600	Enhancers	Gastric	stomach
7	chr4:133160400-133161400	Weak transcription	Fetal Intestine Large	intestine
8	chr4:133160400-133165600	Weak transcription	Stomach Mucosa	stomach
9	chr4:133160600-133165000	Weak transcription	Duodenum Mucosa	Duodenum
10	chr4:133160800-133161600	Enhancers	HUVEC	blood vessel
11	chr4:133161200-133161600	Enhancers	Dnd41	blood
12	chr4:133161400-133161600	Enhancers	Fetal Intestine Large	intestine
13	chr4:133161600-133165600	Weak transcription	Fetal Intestine Small	intestine
14	chr4:133165400-133167000	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr4:133165600-133166200	Enhancers	Stomach Mucosa	stomach
16	chr4:133165600-133167000	Enhancers	Fetal Intestine Small	intestine
17	chr4:133165800-133167000	Enhancers	Fetal Lung	lung
18	chr4:133166600-133166800	Enhancers	Duodenum Mucosa	Duodenum
19	chr4:133167000-133169600	Weak transcription	Fetal Intestine Small	intestine
20	chr4:133183000-133184800	Weak transcription	Fetal Thymus	thymus
21	chr4:133184000-133190000	Enhancers	Dnd41	blood
22	chr4:133184800-133185600	Enhancers	Fetal Lung	lung
23	chr4:133184800-133185600	Enhancers	Fetal Thymus	thymus
24	chr4:133185000-133185600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr4:133185600-133187600	Weak transcription	Fetal Lung	lung
26	chr4:133185600-133187800	Weak transcription	Fetal Thymus	thymus
27	chr4:133187400-133188600	Enhancers	Primary T cells from cord blood	blood
28	chr4:133187600-133188000	Enhancers	Fetal Lung	lung
29	chr4:133187600-133188400	Enhancers	Primary B cells from cord blood	blood
30	chr4:133187800-133188600	Enhancers	Fetal Thymus	thymus
31	chr4:133188200-133188800	Enhancers	Thymus	Thymus
32	chr4:133188600-133190000	Weak transcription	Fetal Thymus	thymus
33	chr4:133190000-133190400	Weak transcription	Dnd41	blood
34	chr4:133190000-133190800	ZNF genes & repeats	Fetal Thymus	thymus
35	chr4:133190400-133191000	ZNF genes & repeats	Dnd41	blood
36	chr4:133190600-133190800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:133190600-133191000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr4:133200000-133200400	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr4:133201200-133201600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:133201600-133205600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:133204200-133204600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr4:133204200-133204600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr4:133204600-133205800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr4:133205600-133206400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:133205600-133207400	ZNF genes & repeats	Dnd41	blood
46	chr4:133205800-133206000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
47	chr4:133205800-133206200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
48	chr4:133217600-133218200	Active TSS	Primary B cells from cord blood	blood
49	chr4:133217600-133219200	Enhancers	Fetal Lung	lung
50	chr4:133217800-133218200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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