Variant report

Variant	nsv1031888
Chromosome Location	chr4:132903485-133355824
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1271)
CpG islands
(count:490)
Chromatin interactive
region (count:27)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1271 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:133148599-133149231	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:133266134-133266306	K562	blood:	n/a	n/a
3	ARID3A	chr4:133149162-133149170	K562	blood:	n/a	n/a
4	ATF1	chr4:133045191-133045611	K562	blood:	n/a	n/a
5	ATF3	chr4:133148574-133148811	K562	blood:	n/a	n/a
6	BATF	chr4:133162320-133162585	GM12878	blood:	n/a	n/a
7	BATF	chr4:133045184-133045712	GM12878	blood:	n/a	n/a
8	BATF	chr4:133045220-133045708	GM12878	blood:	n/a	n/a
9	BATF	chr4:133162291-133162510	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:133045279-133045718	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:133045351-133045685	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:133266102-133266846	K562	blood:	n/a	n/a
13	BHLHE40	chr4:133265695-133265813	K562	blood:	n/a	n/a
14	BHLHE40	chr4:133090796-133091124	K562	blood:	n/a	n/a
15	BHLHE40	chr4:133148584-133148787	K562	blood:	n/a	n/a
16	BHLHE40	chr4:133264871-133264883	K562	blood:	n/a	n/a
17	BRCA1	chr4:133149007-133149207	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr4:133149025-133149135	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr4:133046730-133046899	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr4:133266159-133266384	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr4:133265310-133265941	K562	blood:	n/a	n/a
22	CBX3	chr4:133266054-133266694	K562	blood:	n/a	n/a
23	CBX3	chr4:133338441-133338670	HCT-116	colon:	n/a	n/a
24	CCNT2	chr4:133266111-133266381	K562	blood:	n/a	n/a
25	CEBPB	chr4:133153173-133153453	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:132933791-132934099	IMR90	lung:	n/a	chr4:132933900-132933911
27	CEBPB	chr4:133148995-133149201	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:133240074-133240372	K562	blood:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
29	CEBPB	chr4:133294673-133295022	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:133029986-133030260	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr4:133240140-133240393	HepG2	liver:	n/a	chr4:133240209-133240220 chr4:133240188-133240199 chr4:133240209-133240222
32	CEBPB	chr4:133110596-133110950	IMR90	lung:	n/a	n/a
33	CEBPB	chr4:133037868-133038106	HepG2	liver:	n/a	chr4:133037963-133037974 chr4:133037961-133037974 chr4:133037961-133037972
34	CEBPB	chr4:132911685-132911991	IMR90	lung:	n/a	chr4:132911802-132911813 chr4:132911802-132911815
35	CEBPB	chr4:132911717-132911917	A549	lung:	n/a	chr4:132911802-132911813 chr4:132911802-132911815
36	CEBPB	chr4:133310830-133311107	IMR90	lung:	n/a	chr4:133310930-133310941
37	CEBPB	chr4:132947841-132948176	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:133294679-133295027	HepG2	liver:	n/a	n/a
39	CEBPB	chr4:133294688-133295002	A549	lung:	n/a	n/a
40	CEBPB	chr4:132933770-132934069	HepG2	liver:	n/a	chr4:132933900-132933911
41	CEBPB	chr4:133130031-133130299	IMR90	lung:	n/a	chr4:133130148-133130161 chr4:133130148-133130161
42	CEBPB	chr4:133246117-133246325	HepG2	liver:	n/a	chr4:133246262-133246273 chr4:133246273-133246286 chr4:133246273-133246284
43	CEBPB	chr4:133228257-133228566	HepG2	liver:	n/a	chr4:133228409-133228420
44	CEBPB	chr4:133046379-133046732	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr4:133110608-133110932	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:133278703-133278936	ECC-1	luminal epithelium:	n/a	chr4:133278842-133278859
47	CEBPB	chr4:133266193-133266232	K562	blood:	n/a	n/a
48	CEBPB	chr4:133223702-133223847	H1-hESC	embryonic stem cell:	n/a	chr4:133223742-133223753 chr4:133223743-133223754 chr4:133223742-133223755
49	CEBPB	chr4:133294679-133294861	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr4:133130101-133130290	K562	blood:	n/a	chr4:133130148-133130161 chr4:133130148-133130161

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:133124741-133124791	AG04449	skin:	fetal
2	chr4:133124741-133124791	HRCEpiC	kidney:	n/a
3	chr4:133124741-133124791	AG04449	skin:	fetal
4	chr4:133124741-133124791	HRCEpiC	kidney:	n/a
5	chr4:133045114-133045164	Caco-2	colon:	n/a
6	chr4:133045158-133045208	HAEpiC	amniotic membrane:	n/a
7	chr4:132984188-132984238	NH-A	brain:	n/a
8	chr4:133124741-133124791	HAEpiC	amniotic membrane:	n/a
9	chr4:133045158-133045208	PrEC	prostate:	n/a
10	chr4:132984152-132984202	PFSK-1	brain:	n/a
11	chr4:133124741-133124791	Caco-2	colon:	n/a
12	chr4:132984188-132984238	SK-N-MC	brain:	n/a
13	chr4:133045114-133045164	SK-N-SH	brain:	n/a
14	chr4:132984152-132984202	SK-N-SH_RA	brain:	n/a
15	chr4:133045158-133045208	HEEpiC	esophagus:	n/a
16	chr4:133266322-133266372	ProgFib	skin:	n/a
17	chr4:132984152-132984202	HEEpiC	esophagus:	n/a
18	chr4:133045114-133045164	A549	lung:	n/a
19	chr4:133124741-133124791	Hepatocyte	liver:	n/a
20	chr4:133045158-133045208	ovcar-3	ovarian:	n/a
21	chr4:133266193-133266243	HRE	kidney:	n/a
22	chr4:133124741-133124791	NB4	blood:	n/a
23	chr4:133266322-133266372	CMK	blood:	n/a
24	chr4:133045178-133045228	GM12892	blood:	n/a
25	chr4:133045114-133045164	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:133266193-133266243	HCPEpiC	choroid plexus:	n/a
27	chr4:132984152-132984202	GM19239	blood:	n/a
28	chr4:133266193-133266243	A549	lung:	n/a
29	chr4:133045114-133045164	HMEC	breast:	n/a
30	chr4:132984152-132984202	GM12878	blood:	n/a
31	chr4:132984188-132984238	HUVEC	blood vessel:	n/a
32	chr4:132984152-132984202	HCT-116	colon:	n/a
33	chr4:133266322-133266372	HEK293	kidney:	embryo
34	chr4:133045114-133045164	HCPEpiC	choroid plexus:	n/a
35	chr4:133045178-133045228	SK-N-MC	brain:	n/a
36	chr4:132984152-132984202	ECC-1	luminal epithelium:	n/a
37	chr4:133266193-133266243	Hepatocyte	liver:	n/a
38	chr4:133266322-133266372	HCPEpiC	choroid plexus:	n/a
39	chr4:133045114-133045164	MCF10A-Er-Src	breast:	n/a
40	chr4:132984152-132984202	HCM	heart:	n/a
41	chr4:133045158-133045208	HRE	kidney:	n/a
42	chr4:133045158-133045208	NB4	blood:	n/a
43	chr4:133124741-133124791	HCM	heart:	n/a
44	chr4:132984152-132984202	HRPEpiC	eye:	n/a
45	chr4:133045158-133045208	AG09309	skin:	n/a
46	chr4:133045178-133045228	AG04450	lung:	fetal
47	chr4:132984188-132984238	T-47D	breast:	n/a
48	chr4:132984152-132984202	AG09319	gingival:	n/a
49	chr4:132984188-132984238	Hela-S3	cervix:	n/a
50	chr4:132984152-132984202	NHDF-neo	bronchial:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:133062137..133063772-chr4:133065440..133067202,2	K562	blood:
2	chr4:133246638..133249812-chr4:133265864..133268563,3	K562	blood:
3	chr4:133016619..133019412-chr4:133020673..133022375,2	K562	blood:
4	chr4:133246638..133249812-chr4:133265864..133268563,3	K562	blood:
5	chr4:133016619..133019412-chr4:133020673..133022375,2	K562	blood:
6	chr4:133264521..133268108-chr4:133268991..133272057,6	K562	blood:
7	chr4:133116257..133118225-chr4:133445549..133447464,2	MCF-7	breast:
8	chr4:133294490..133296244-chr4:133317464..133320179,2	K562	blood:
9	chr4:133294490..133296244-chr4:133317464..133320179,2	K562	blood:
10	chr4:133264521..133268108-chr4:133268991..133272057,6	K562	blood:
11	chr4:133265507..133268108-chr4:133268991..133271558,3	K562	blood:
12	chr1:249200230..249200936-chr4:132915036..132915536,2	Hela-S3	cervix:
13	chr1:163041256..163042238-chr4:133048166..133048870,2	MCF-7	breast:
14	chr4:133346218..133346845-chr6:148869148..148869834,2	MCF-7	breast:
15	chr4:133337477..133339790-chr4:133339994..133342745,2	K562	blood:
16	chr10:16933616..16934139-chr4:132930526..132931027,2	HCT-116	colon:
17	chr4:133352255..133354798-chr4:133356746..133359488,2	K562	blood:
18	chr4:133265507..133268108-chr4:133268991..133271558,3	K562	blood:
19	chr4:133062137..133063772-chr4:133065440..133067202,2	K562	blood:
20	chr4:133254539..133258188-chr4:133265340..133266888,3	K562	blood:
21	chr4:133254539..133258188-chr4:133265340..133266888,3	K562	blood:
22	chr4:132949068..132951871-chr4:133002686..133005668,2	K562	blood:
23	chr4:133263144..133265552-chr4:133295032..133296835,2	K562	blood:
24	chr4:133263144..133265552-chr4:133295032..133296835,2	K562	blood:
25	chr21:46369779..46370335-chr4:133015624..133016125,2	MCF-7	breast:
26	chr11:46257959..46258806-chr4:132939267..132939767,2	NB4	blood:
27	chr4:133337477..133339790-chr4:133339994..133342745,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH10-12	chr4:132931815-132932069	l_2731_chr4:132914718-132932069_testes
2	lnc-RP11-62N21.1.1-1	chr4:133045006-133045186	XLOC_004078
3	lnc-RP11-62N21.1.1-1	chr4:132949501-132949636	XLOC_004078
4	lnc-PCDH10-12	chr4:132914719-132914974	l_2731_chr4:132914718-132932069_testes
5	lnc-RP11-62N21.1.1-1	chr4:132948330-132948587	XLOC_004078
6	lnc-RP11-62N21.1.1-1	chr4:132949501-132949589	XLOC_004078
7	lnc-RP11-62N21.1.1-11	chr4:133288941-133289634	NONHSAT098333
8	lnc-RP11-62N21.1.1-1	chr4:132925965-132926229	XLOC_004078

No data

Variant related genes	Relation type
ENSG00000249463	TF binding region
ELL2P2	TF binding region
ENSG00000251598	TF binding region
ENSG00000249463	CpG island
ELL2P2	CpG island
ENSG00000251598	CpG island
ENSG00000185220	chromatin interactions
ENSG00000249463	chromatin interactions
ENSG00000117152	chromatin interactions
ADCY9	miRNA target sites

Extended variants
information (count: 6547 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:6547 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75062796	chr4:132909016-132909017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368462692	chr4:132909100-132909101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535481466	chr4:132909101-132909102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568595834	chr4:132909123-132909124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs58746400	chr4:132909131-132909132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189626397	chr4:132909159-132909160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539984216	chr4:132909240-132909241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181480014	chr4:132909273-132909274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540051666	chr4:132909280-132909281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555776041	chr4:132909283-132909284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576803517	chr4:132909287-132909288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545494220	chr4:132909297-132909298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562757339	chr4:132909322-132909323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531650963	chr4:132909329-132909330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186989554	chr4:132909332-132909333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191073142	chr4:132909338-132909339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145754146	chr4:132909364-132909365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs193240	chr4:132909387-132909388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534858607	chr4:132910613-132910614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182718261	chr4:132910614-132910615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570521038	chr4:132910704-132910705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539207458	chr4:132910723-132910724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556104078	chr4:132910767-132910768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576142159	chr4:132910781-132910782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541864102	chr4:132910794-132910795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376650083	chr4:132910833-132910834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188739861	chr4:132910843-132910844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368695055	chr4:132910852-132910853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564167246	chr4:132910913-132910914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113218926	chr4:132910938-132910939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564083344	chr4:132910958-132910959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531283145	chr4:132911001-132911002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs578046015	chr4:132911028-132911029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539694262	chr4:132911037-132911038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528386431	chr4:132911047-132911048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563325605	chr4:132911075-132911076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529213633	chr4:132911114-132911115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548985110	chr4:132911116-132911117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559580305	chr4:132911123-132911124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192572721	chr4:132911125-132911126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551474954	chr4:132911169-132911170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551949152	chr4:132911178-132911179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571779079	chr4:132911186-132911187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139513597	chr4:132911191-132911192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12640926	chr4:132911206-132911207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs569788688	chr4:132911227-132911228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183193802	chr4:132911235-132911236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs207465075	chr4:132911246-132911247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2863923	chr4:132911261-132911262	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs572360874	chr4:132911304-132911305	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Anaplastic thyroid cancer	18753363	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132909000-132909400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:132910600-132912600	Enhancers	Fetal Intestine Large	intestine
3	chr4:132911000-132911800	Enhancers	Fetal Intestine Small	intestine
4	chr4:132911800-132912400	Weak transcription	Fetal Intestine Small	intestine
5	chr4:132912400-132912600	Enhancers	Fetal Intestine Small	intestine
6	chr4:132918800-132919200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:132919200-132919400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:132919400-132919800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:132919800-132925000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:132922600-132923200	Enhancers	Muscle Satellite Cultured Cells	--
11	chr4:132922600-132923200	Enhancers	HMEC	breast
12	chr4:132922600-132923400	Enhancers	NHEK	skin
13	chr4:132923600-132924800	Enhancers	Fetal Intestine Small	intestine
14	chr4:132924600-132924800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
15	chr4:132924800-132925200	Enhancers	H9 Cell Line	embryonic stem cell
16	chr4:132924800-132925400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:132925000-132925600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:132925200-132925400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:132935400-132937200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr4:132937800-132938000	Enhancers	Fetal Intestine Large	intestine
21	chr4:132938200-132938800	Enhancers	Fetal Intestine Small	intestine
22	chr4:132938600-132938800	Enhancers	Fetal Intestine Large	intestine
23	chr4:132946600-132948000	Enhancers	Fetal Brain Male	brain
24	chr4:132946600-132948600	Enhancers	Fetal Intestine Large	intestine
25	chr4:132946600-132948600	Enhancers	Fetal Intestine Small	intestine
26	chr4:132947200-132947600	Enhancers	Dnd41	blood
27	chr4:132947200-132947800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr4:132947400-132947800	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr4:132947400-132947800	Enhancers	Brain Germinal Matrix	brain
30	chr4:132947400-132948000	Enhancers	Fetal Brain Female	brain
31	chr4:132947400-132948200	Enhancers	Fetal Lung	lung
32	chr4:132947400-132948600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:132947600-132948000	Enhancers	NHEK	skin
34	chr4:132947600-132948200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr4:132977600-132977800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:132977800-132979200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr4:132978200-132978600	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr4:132979000-132980400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:132979200-132979600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:132979200-132979800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:132979200-132980400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
42	chr4:132979600-132980000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:132979800-132980200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:132979800-132983000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:132980000-132980200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:132980200-132980600	Enhancers	NHEK	skin
47	chr4:132980200-132980800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr4:132980400-132983200	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr4:132980400-132983200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:132980600-132980800	Enhancers	HMEC	breast

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