Variant report

Variant	nsv880012
Chromosome Location	chr4:133165898-133397984
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	BACH1	chr4:133367293-133367347	K562	blood:	n/a	n/a
3	BHLHE40	chr4:133266102-133266846	K562	blood:	n/a	n/a
4	BHLHE40	chr4:133265695-133265813	K562	blood:	n/a	n/a
5	BHLHE40	chr4:133264871-133264883	K562	blood:	n/a	n/a
6	BRCA1	chr4:133266159-133266384	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr4:133265310-133265941	K562	blood:	n/a	n/a
8	CBX3	chr4:133266054-133266694	K562	blood:	n/a	n/a
9	CBX3	chr4:133338441-133338670	HCT-116	colon:	n/a	n/a
10	CCNT2	chr4:133266111-133266381	K562	blood:	n/a	n/a
11	CEBPB	chr4:133363932-133364193	H1-hESC	embryonic stem cell:	n/a	chr4:133364078-133364089 chr4:133364031-133364042
12	CEBPB	chr4:133246117-133246325	HepG2	liver:	n/a	chr4:133246262-133246273 chr4:133246273-133246286 chr4:133246273-133246284
13	CEBPB	chr4:133310833-133311100	HepG2	liver:	n/a	chr4:133310930-133310941
14	CEBPB	chr4:133240156-133240388	A549	lung:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
15	CEBPB	chr4:133234378-133234608	A549	lung:	n/a	n/a
16	CEBPB	chr4:133228262-133228577	IMR90	lung:	n/a	chr4:133228409-133228420
17	CEBPB	chr4:133240140-133240393	HepG2	liver:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
18	CEBPB	chr4:133294679-133295027	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:133294688-133295002	A549	lung:	n/a	n/a
20	CEBPB	chr4:133234404-133234637	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:133234391-133234624	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:133223604-133223874	HepG2	liver:	n/a	chr4:133223742-133223753 chr4:133223743-133223754 chr4:133223742-133223755
23	CEBPB	chr4:133363913-133364226	IMR90	lung:	n/a	chr4:133364078-133364089 chr4:133364031-133364042
24	CEBPB	chr4:133223702-133223847	H1-hESC	embryonic stem cell:	n/a	chr4:133223742-133223753 chr4:133223743-133223754 chr4:133223742-133223755
25	CEBPB	chr4:133278703-133278936	ECC-1	luminal epithelium:	n/a	chr4:133278842-133278859
26	CEBPB	chr4:133310830-133311107	IMR90	lung:	n/a	chr4:133310930-133310941
27	CEBPB	chr4:133318436-133318624	HepG2	liver:	n/a	chr4:133318505-133318516 chr4:133318505-133318518 chr4:133318507-133318518
28	CEBPB	chr4:133304647-133305173	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:133363956-133364215	HepG2	liver:	n/a	chr4:133364078-133364089 chr4:133364031-133364042
30	CEBPB	chr4:133330797-133331127	HepG2	liver:	n/a	chr4:133330971-133330982
31	CEBPB	chr4:133294679-133294861	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr4:133240074-133240372	K562	blood:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
33	CEBPB	chr4:133228257-133228566	HepG2	liver:	n/a	chr4:133228409-133228420
34	CEBPB	chr4:133254553-133255549	IMR90	lung:	n/a	chr4:133254713-133254724 chr4:133254713-133254726
35	CEBPB	chr4:133294673-133295022	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:133310826-133311039	H1-hESC	embryonic stem cell:	n/a	chr4:133310930-133310941
37	CEBPB	chr4:133266193-133266232	K562	blood:	n/a	n/a
38	CEBPB	chr4:133254850-133255208	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:133363937-133364232	K562	blood:	n/a	chr4:133364078-133364089 chr4:133364031-133364042
40	CHD2	chr4:133265720-133266696	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr4:133266055-133266671	K562	blood:	n/a	n/a
42	CTCF	chr4:133277795-133277877	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr4:133254340-133254490	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr4:133254196-133254392	Hela-S3	cervix:	n/a	chr4:133254290-133254299
45	CTCF	chr4:133254240-133254390	AG09319	gingival:	n/a	chr4:133254290-133254299
46	CTCF	chr4:133335380-133335530	GM12875	blood:	n/a	n/a
47	CTCF	chr4:133287320-133287470	GM12866	blood:	n/a	n/a
48	CTCF	chr4:133254260-133254376	Spleen_OC	spleen:	n/a	chr4:133254290-133254299
49	CTCF	chr4:133254180-133254330	GM12874	blood:	n/a	chr4:133254290-133254299
50	CTCF	chr4:133254180-133254330	HL-60	blood:	n/a	chr4:133254290-133254299

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:133266193-133266243	HL-60	blood:	n/a
2	chr4:133266322-133266372	RPTEC	kidney:	n/a
3	chr4:133266193-133266243	NT2-D1	testis:	n/a
4	chr4:133266322-133266372	Caco-2	colon:	n/a
5	chr4:133266193-133266243	RPTEC	kidney:	n/a
6	chr4:133266322-133266372	HCPEpiC	choroid plexus:	n/a
7	chr4:133266322-133266372	Jurkat	blood:	n/a
8	chr4:133266193-133266243	AoSMC	blood vessel:	n/a
9	chr4:133266322-133266372	NHDF-neo	bronchial:	n/a
10	chr4:133266193-133266243	AG10803	skin:	n/a
11	chr4:133266322-133266372	AoSMC	blood vessel:	n/a
12	chr4:133266193-133266243	PrEC	prostate:	n/a
13	chr4:133266193-133266243	NB4	blood:	n/a
14	chr4:133266322-133266372	MCF-7	breast:	n/a
15	chr4:133266193-133266243	HNPCEpiC	eye:	n/a
16	chr4:133266322-133266372	BJ	skin:	n/a
17	chr4:133266193-133266243	H1-hESC	embryonic stem cell:	embryo
18	chr4:133266322-133266372	GM06990	blood:	n/a
19	chr4:133266193-133266243	AG09319	gingival:	n/a
20	chr4:133266322-133266372	CMK	blood:	n/a
21	chr4:133266322-133266372	HCF	heart:	n/a
22	chr4:133266193-133266243	CMK	blood:	n/a
23	chr4:133266322-133266372	AG09309	skin:	n/a
24	chr4:133266322-133266372	GM12878	blood:	n/a
25	chr4:133266322-133266372	BE2_C	brain:	n/a
26	chr4:133266322-133266372	GM19239	blood:	n/a
27	chr4:133266193-133266243	HEK293	kidney:	embryo
28	chr4:133266322-133266372	HEK293	kidney:	embryo
29	chr4:133266193-133266243	K562	blood:	n/a
30	chr4:133266193-133266243	HUVEC	blood vessel:	n/a
31	chr4:133266322-133266372	SK-N-MC	brain:	n/a
32	chr4:133266322-133266372	MCF10A-Er-Src	breast:	n/a
33	chr4:133266193-133266243	ProgFib	skin:	n/a
34	chr4:133266193-133266243	HMEC	breast:	n/a
35	chr4:133266193-133266243	LNCaP	prostate:	n/a
36	chr4:133266322-133266372	NT2-D1	testis:	n/a
37	chr4:133266193-133266243	BJ	skin:	n/a
38	chr4:133266193-133266243	HAEpiC	amniotic membrane:	n/a
39	chr4:133266193-133266243	HRCEpiC	kidney:	n/a
40	chr4:133266322-133266372	ovcar-3	ovarian:	n/a
41	chr4:133266193-133266243	IMR90	lung:	fetal
42	chr4:133266322-133266372	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:133266322-133266372	HRE	kidney:	n/a
44	chr4:133266193-133266243	MCF10A-Er-Src	breast:	n/a
45	chr4:133266193-133266243	T-47D	breast:	n/a
46	chr4:133266193-133266243	HRPEpiC	eye:	n/a
47	chr4:133266193-133266243	NHDF-neo	bronchial:	n/a
48	chr4:133266193-133266243	GM19239	blood:	n/a
49	chr4:133266322-133266372	PANC-1	pancreas:	n/a
50	chr4:133266322-133266372	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:133263144..133265552-chr4:133295032..133296835,2	K562	blood:
2	chr4:133263144..133265552-chr4:133295032..133296835,2	K562	blood:
3	chr4:133294490..133296244-chr4:133317464..133320179,2	K562	blood:
4	chr4:133346218..133346845-chr6:148869148..148869834,2	MCF-7	breast:
5	chr4:133264521..133268108-chr4:133268991..133272057,6	K562	blood:
6	chr4:133265507..133268108-chr4:133268991..133271558,3	K562	blood:
7	chr4:133337477..133339790-chr4:133339994..133342745,2	K562	blood:
8	chr4:133265507..133268108-chr4:133268991..133271558,3	K562	blood:
9	chr4:133294490..133296244-chr4:133317464..133320179,2	K562	blood:
10	chr4:133246638..133249812-chr4:133265864..133268563,3	K562	blood:
11	chr4:133246638..133249812-chr4:133265864..133268563,3	K562	blood:
12	chr4:133352255..133354798-chr4:133356746..133359488,2	K562	blood:
13	chr4:133264521..133268108-chr4:133268991..133272057,6	K562	blood:
14	chr4:133337477..133339790-chr4:133339994..133342745,2	K562	blood:
15	chr4:133254539..133258188-chr4:133265340..133266888,3	K562	blood:
16	chr4:133254539..133258188-chr4:133265340..133266888,3	K562	blood:
17	chr4:133352255..133354798-chr4:133356746..133359488,2	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: 2473 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2473 , 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	rs1499328	chr4:133165898-133165899	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549327922	chr4:133166022-133166023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371793436	chr4:133166027-133166028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558758037	chr4:133166029-133166030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138612442	chr4:133166032-133166033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144493736	chr4:133166066-133166067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34566834	chr4:133166067-133166068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs34159314	chr4:133166068-133166069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542469714	chr4:133166069-133166070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35004707	chr4:133166070-133166071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs377166522	chr4:133166120-133166121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569281825	chr4:133166125-133166126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537840939	chr4:133166180-133166181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139652101	chr4:133166195-133166196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183536032	chr4:133166219-133166220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540443930	chr4:133166285-133166286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144520199	chr4:133166353-133166354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577345178	chr4:133166357-133166358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545135806	chr4:133166359-133166360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564823902	chr4:133166374-133166375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562247519	chr4:133166509-133166510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186574677	chr4:133166536-133166537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561191252	chr4:133166570-133166571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575566717	chr4:133166588-133166589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529980131	chr4:133166593-133166594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544295642	chr4:133166603-133166604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114159160	chr4:133166617-133166618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570537000	chr4:133166622-133166623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564505901	chr4:133166691-133166692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552679413	chr4:133166692-133166693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543771673	chr4:133166725-133166726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371812385	chr4:133166746-133166747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs6811946	chr4:133166779-133166780	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376273258	chr4:133166787-133166788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568100045	chr4:133166808-133166809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534250407	chr4:133166875-133166876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191882810	chr4:133166877-133166878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs34921057	chr4:133166895-133166896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs146633916	chr4:133167036-133167037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532693619	chr4:133167042-133167043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140850339	chr4:133167146-133167147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182855646	chr4:133167163-133167164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74287583	chr4:133167176-133167177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377365073	chr4:133167180-133167181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544243907	chr4:133167185-133167186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560899797	chr4:133167223-133167224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529690681	chr4:133167248-133167249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149661431	chr4:133167257-133167258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560175555	chr4:133167267-133167268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532344054	chr4:133167295-133167296	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:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:133165400-133167000	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr4:133165600-133166200	Enhancers	Stomach Mucosa	stomach
3	chr4:133165600-133167000	Enhancers	Fetal Intestine Small	intestine
4	chr4:133165800-133167000	Enhancers	Fetal Lung	lung
5	chr4:133166600-133166800	Enhancers	Duodenum Mucosa	Duodenum
6	chr4:133167000-133169600	Weak transcription	Fetal Intestine Small	intestine
7	chr4:133183000-133184800	Weak transcription	Fetal Thymus	thymus
8	chr4:133184000-133190000	Enhancers	Dnd41	blood
9	chr4:133184800-133185600	Enhancers	Fetal Lung	lung
10	chr4:133184800-133185600	Enhancers	Fetal Thymus	thymus
11	chr4:133185000-133185600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr4:133185600-133187600	Weak transcription	Fetal Lung	lung
13	chr4:133185600-133187800	Weak transcription	Fetal Thymus	thymus
14	chr4:133187400-133188600	Enhancers	Primary T cells from cord blood	blood
15	chr4:133187600-133188000	Enhancers	Fetal Lung	lung
16	chr4:133187600-133188400	Enhancers	Primary B cells from cord blood	blood
17	chr4:133187800-133188600	Enhancers	Fetal Thymus	thymus
18	chr4:133188200-133188800	Enhancers	Thymus	Thymus
19	chr4:133188600-133190000	Weak transcription	Fetal Thymus	thymus
20	chr4:133190000-133190400	Weak transcription	Dnd41	blood
21	chr4:133190000-133190800	ZNF genes & repeats	Fetal Thymus	thymus
22	chr4:133190400-133191000	ZNF genes & repeats	Dnd41	blood
23	chr4:133190600-133190800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:133190600-133191000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr4:133200000-133200400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr4:133201200-133201600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:133201600-133205600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr4:133204200-133204600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr4:133204200-133204600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr4:133204600-133205800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr4:133205600-133206400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:133205600-133207400	ZNF genes & repeats	Dnd41	blood
33	chr4:133205800-133206000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
34	chr4:133205800-133206200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
35	chr4:133217600-133218200	Active TSS	Primary B cells from cord blood	blood
36	chr4:133217600-133219200	Enhancers	Fetal Lung	lung
37	chr4:133217800-133218200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:133218200-133218800	Weak transcription	Primary B cells from cord blood	blood
39	chr4:133218200-133221000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:133218400-133218800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:133218400-133219000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:133218800-133219600	Enhancers	Primary B cells from cord blood	blood
43	chr4:133219200-133220600	Weak transcription	Fetal Lung	lung
44	chr4:133220600-133221600	Enhancers	Fetal Lung	lung
45	chr4:133221000-133221400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr4:133221600-133222400	Weak transcription	Fetal Lung	lung
47	chr4:133222400-133222600	Enhancers	Fetal Lung	lung
48	chr4:133222600-133224800	Weak transcription	Fetal Lung	lung
49	chr4:133224800-133225000	Enhancers	Fetal Lung	lung
50	chr4:133234400-133235400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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