Variant report

Variant	nsv830067
Chromosome Location	chr4:132299237-132396267
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	ATF2	chr4:132347383-132348003	GM12878	blood:	n/a	n/a
2	ATF2	chr4:132347459-132347932	GM12878	blood:	n/a	n/a
3	BACH1	chr4:132391570-132391880	K562	blood:	n/a	n/a
4	BACH1	chr4:132391549-132391886	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr4:132347469-132347900	GM12878	blood:	n/a	n/a
6	BATF	chr4:132347572-132347877	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:132347576-132347893	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:132347442-132347953	GM12878	blood:	n/a	n/a
9	BCL3	chr4:132347488-132347811	GM12878	blood:	n/a	n/a
10	BCLAF1	chr4:132347460-132347821	GM12878	blood:	n/a	n/a
11	BCLAF1	chr4:132347567-132347910	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:132369178-132369366	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:132347604-132347811	GM12878	blood:	n/a	n/a
14	CCNT2	chr4:132300478-132300751	K562	blood:	n/a	n/a
15	CEBPB	chr4:132388342-132388696	HepG2	liver:	n/a	chr4:132388526-132388535 chr4:132388524-132388537 chr4:132388526-132388535 chr4:132388526-132388535 chr4:132388526-132388535 chr4:132388524-132388535
16	CEBPB	chr4:132388438-132388648	A549	lung:	n/a	chr4:132388526-132388535 chr4:132388524-132388537 chr4:132388526-132388535 chr4:132388526-132388535 chr4:132388526-132388535 chr4:132388524-132388535
17	CEBPB	chr4:132300197-132300397	HepG2	liver:	n/a	chr4:132300269-132300282 chr4:132300270-132300281 chr4:132300256-132300267
18	CEBPB	chr4:132299279-132299529	K562	blood:	n/a	n/a
19	CEBPB	chr4:132388460-132388619	H1-hESC	embryonic stem cell:	n/a	chr4:132388526-132388535 chr4:132388524-132388537 chr4:132388526-132388535 chr4:132388526-132388535 chr4:132388526-132388535 chr4:132388524-132388535
20	CEBPB	chr4:132388354-132388710	K562	blood:	n/a	chr4:132388526-132388535 chr4:132388524-132388537 chr4:132388526-132388535 chr4:132388526-132388535 chr4:132388526-132388535 chr4:132388524-132388535
21	CEBPB	chr4:132334417-132334650	HepG2	liver:	n/a	chr4:132334512-132334525 chr4:132334513-132334524 chr4:132334514-132334523 chr4:132334512-132334525 chr4:132334512-132334523
22	CEBPB	chr4:132334395-132334652	IMR90	lung:	n/a	chr4:132334512-132334525 chr4:132334513-132334524 chr4:132334514-132334523 chr4:132334512-132334525 chr4:132334512-132334523
23	CEBPB	chr4:132334422-132334633	K562	blood:	n/a	chr4:132334512-132334525 chr4:132334513-132334524 chr4:132334514-132334523 chr4:132334512-132334525 chr4:132334512-132334523
24	CEBPB	chr4:132388167-132388715	IMR90	lung:	n/a	chr4:132388192-132388205 chr4:132388526-132388535 chr4:132388524-132388537 chr4:132388526-132388535 chr4:132388526-132388535 chr4:132388526-132388535 chr4:132388524-132388535
25	CEBPB	chr4:132316111-132316328	HepG2	liver:	n/a	chr4:132316170-132316181 chr4:132316241-132316252 chr4:132316170-132316183 chr4:132316241-132316254 chr4:132316241-132316254
26	CHD2	chr4:132347690-132347789	GM12878	blood:	n/a	n/a
27	CREB1	chr4:132380571-132380984	GM12878	blood:	n/a	n/a
28	CREB1	chr4:132347545-132347919	GM12878	blood:	n/a	n/a
29	CTCF	chr4:132351480-132351630	A549	lung:	n/a	n/a
30	CTCF	chr4:132351634-132351680	GM10248	blood:	n/a	chr4:132351638-132351659 chr4:132351643-132351661
31	CTCF	chr4:132351561-132351733	MCF-7	breast:	n/a	chr4:132351638-132351659 chr4:132351643-132351661
32	CTCF	chr4:132324785-132324802	GM20000	blood:	n/a	n/a
33	CTCF	chr4:132314586-132314638	GM10248	blood:	n/a	n/a
34	CTCF	chr4:132351440-132351590	BE2_C	brain:	n/a	n/a
35	CTCF	chr4:132351540-132351690	SK-N-SH_RA	brain:	n/a	chr4:132351638-132351659 chr4:132351643-132351661
36	CTCF	chr4:132380720-132380870	GM12865	blood:	n/a	n/a
37	CTCF	chr4:132351560-132351710	GM12865	blood:	n/a	chr4:132351638-132351659 chr4:132351643-132351661
38	CTCF	chr4:132351587-132351714	Medullo	brain:	n/a	chr4:132351638-132351659 chr4:132351643-132351661
39	CTCF	chr4:132380920-132381070	BE2_C	brain:	n/a	n/a
40	CTCF	chr4:132381047-132381098	GM12891	blood:	n/a	n/a
41	CTCF	chr4:132381040-132381190	GM12878	blood:	n/a	n/a
42	CTCF	chr4:132351620-132351770	GM12878	blood:	n/a	chr4:132351638-132351659 chr4:132351643-132351661
43	CTCF	chr4:132351575-132351728	GM13976	blood:	n/a	chr4:132351638-132351659 chr4:132351643-132351661
44	CTCF	chr4:132351575-132351688	GM19238	blood:	n/a	chr4:132351638-132351659 chr4:132351643-132351661
45	CTCF	chr4:132381000-132381150	GM12865	blood:	n/a	n/a
46	CTCF	chr4:132380999-132381125	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:132351600-132351750	GM12871	blood:	n/a	chr4:132351638-132351659 chr4:132351643-132351661
48	CTCF	chr4:132351520-132351670	GM12872	blood:	n/a	chr4:132351638-132351659 chr4:132351643-132351661
49	CTCF	chr4:132351575-132351697	MCF-7	breast:	n/a	chr4:132351638-132351659 chr4:132351643-132351661
50	CTCF	chr4:132351560-132351710	SK-N-SH_RA	brain:	n/a	chr4:132351638-132351659 chr4:132351643-132351661

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132300589-132300639	HRPEpiC	eye:	n/a
2	chr4:132300589-132300639	HCT-116	colon:	n/a
3	chr4:132300589-132300639	U87	brain:	n/a
4	chr4:132300589-132300639	IMR90	lung:	fetal
5	chr4:132300589-132300639	SAEC	small airway:	n/a
6	chr4:132300589-132300639	H1-hESC	embryonic stem cell:	embryo
7	chr4:132300589-132300639	Caco-2	colon:	n/a
8	chr4:132300589-132300639	HPAEpiC	pulmonary alveolar:	n/a
9	chr4:132300589-132300639	ProgFib	skin:	n/a
10	chr4:132300589-132300639	HIPEpiC	eye:	n/a
11	chr4:132300589-132300639	BE2_C	brain:	n/a
12	chr4:132300589-132300639	CMK	blood:	n/a
13	chr4:132300589-132300639	ECC-1	luminal epithelium:	n/a
14	chr4:132300589-132300639	HRE	kidney:	n/a
15	chr4:132300589-132300639	ovcar-3	ovarian:	n/a
16	chr4:132300589-132300639	HEEpiC	esophagus:	n/a
17	chr4:132300589-132300639	K562	blood:	n/a
18	chr4:132300589-132300639	SK-N-SH_RA	brain:	n/a
19	chr4:132300589-132300639	AoSMC	blood vessel:	n/a
20	chr4:132300589-132300639	PANC-1	pancreas:	n/a
21	chr4:132300589-132300639	RPTEC	kidney:	n/a
22	chr4:132300589-132300639	PrEC	prostate:	n/a
23	chr4:132300589-132300639	AG04450	lung:	fetal
24	chr4:132300589-132300639	NH-A	brain:	n/a
25	chr4:132300589-132300639	SK-N-MC	brain:	n/a
26	chr4:132300589-132300639	HAEpiC	amniotic membrane:	n/a
27	chr4:132300589-132300639	HCM	heart:	n/a
28	chr4:132300589-132300639	BJ	skin:	n/a
29	chr4:132300589-132300639	SKMC	muscle:	n/a
30	chr4:132300589-132300639	Hepatocyte	liver:	n/a
31	chr4:132300589-132300639	Hela-S3	cervix:	n/a
32	chr4:132300589-132300639	HRCEpiC	kidney:	n/a
33	chr4:132300589-132300639	HNPCEpiC	eye:	n/a
34	chr4:132300589-132300639	GM19239	blood:	n/a
35	chr4:132300589-132300639	GM12892	blood:	n/a
36	chr4:132300589-132300639	NB4	blood:	n/a
37	chr4:132300589-132300639	MCF10A-Er-Src	breast:	n/a
38	chr4:132300589-132300639	AG09309	skin:	n/a
39	chr4:132300589-132300639	MCF-7	breast:	n/a
40	chr4:132300589-132300639	GM12891	blood:	n/a
41	chr4:132300589-132300639	A549	lung:	n/a
42	chr4:132300589-132300639	NHBE	bronchial:	n/a
43	chr4:132300589-132300639	AG09319	gingival:	n/a
44	chr4:132300589-132300639	T-47D	breast:	n/a
45	chr4:132300589-132300639	AG10803	skin:	n/a
46	chr4:132300589-132300639	GM06990	blood:	n/a
47	chr4:132300589-132300639	Jurkat	blood:	n/a
48	chr4:132300589-132300639	GM12878	blood:	n/a
49	chr4:132300589-132300639	HEK293	kidney:	embryo
50	chr4:132300589-132300639	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:
2	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:
3	chr4:132387674..132388400-chr4:132565905..132566424,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH10-7	chr4:132300925-132301522	NONHSAT098311
2	lnc-PCDH10-7	chr4:132301168-132301496	ENSG00000250102.1

Variant related genes	Relation type
ENSG00000250102	TF binding region
ENSG00000250102	CpG island

Extended variants
information (count: 550 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116563146	chr4:132299367-132299368	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs201800843	chr4:132299411-132299412	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs199941883	chr4:132299412-132299413	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs200332889	chr4:132299422-132299423	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs562834891	chr4:132299425-132299426	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201809430	chr4:132299428-132299429	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs201327685	chr4:132299432-132299433	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs201962383	chr4:132299433-132299434	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs200191501	chr4:132299436-132299437	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs76912234	chr4:132299439-132299440	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs75414943	chr4:132299440-132299441	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs28499075	chr4:132299461-132299462	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs12647445	chr4:132299683-132299684	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs566434230	chr4:132299738-132299739	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs186360131	chr4:132299906-132299907	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs552295469	chr4:132299928-132299929	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs73851326	chr4:132299936-132299937	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs530780763	chr4:132299946-132299947	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs140292581	chr4:132299948-132299949	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs149932091	chr4:132299978-132299979	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs201523892	chr4:132299987-132299988	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs553761373	chr4:132300198-132300199	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs576869895	chr4:132300224-132300225	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs28575404	chr4:132300246-132300247	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs118083256	chr4:132300257-132300258	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs566588643	chr4:132300292-132300293	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs116789613	chr4:132300337-132300338	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs369534760	chr4:132300349-132300350	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs542425155	chr4:132300409-132300410	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs562238919	chr4:132300412-132300413	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs527998955	chr4:132300418-132300419	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs541784768	chr4:132300456-132300457	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs564766756	chr4:132300473-132300474	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs190817149	chr4:132300524-132300525	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs373037954	chr4:132300532-132300533	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs551870007	chr4:132300556-132300557	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs4864038	chr4:132300566-132300567	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs116657489	chr4:132300586-132300587	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs547982929	chr4:132300630-132300631	ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs567876260	chr4:132300651-132300652	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs533731622	chr4:132300655-132300656	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs72936591	chr4:132300699-132300700	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs200031482	chr4:132300728-132300729	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs570636388	chr4:132300743-132300744	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs77010604	chr4:132300756-132300757	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs556250079	chr4:132300780-132300781	ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs576505328	chr4:132300850-132300851	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs76051695	chr4:132300879-132300880	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs72936593	chr4:132300886-132300887	Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs146492436	chr4:132300921-132300922	Active TSS	TF binding region	1 gene(s)	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
small cell lung cancer	20016488	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132300400-132300600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:132300600-132300800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:132300600-132302200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr4:132300800-132302400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr4:132301000-132301200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:132301000-132301600	Active TSS	K562	blood
7	chr4:132301000-132302000	Active TSS	Osteobl	bone
8	chr4:132301200-132301400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:132331200-132332200	ZNF genes & repeats	Dnd41	blood
10	chr4:132331600-132332200	Active TSS	Fetal Heart	heart
11	chr4:132347200-132348200	Enhancers	GM12878-XiMat	blood
12	chr4:132348000-132348600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr4:132348000-132348800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:132348200-132348600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr4:132348400-132348800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr4:132350000-132350600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr4:132351600-132352400	Enhancers	Dnd41	blood
18	chr4:132351800-132352200	Enhancers	Hela-S3	cervix
19	chr4:132361800-132362600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:132369000-132369400	Enhancers	Fetal Brain Male	brain
21	chr4:132369200-132369600	Active TSS	Fetal Heart	heart
22	chr4:132371200-132371600	Enhancers	Dnd41	blood
23	chr4:132371600-132372200	Flanking Active TSS	Dnd41	blood
24	chr4:132371600-132372400	Active TSS	GM12878-XiMat	blood
25	chr4:132372200-132372600	Enhancers	Dnd41	blood
26	chr4:132378600-132379000	Enhancers	Dnd41	blood
27	chr4:132378800-132379000	Weak transcription	GM12878-XiMat	blood
28	chr4:132379000-132379200	Enhancers	GM12878-XiMat	blood
29	chr4:132379000-132379400	Flanking Active TSS	Dnd41	blood
30	chr4:132379000-132381800	Enhancers	Primary T cells from cord blood	blood
31	chr4:132379200-132380600	Weak transcription	GM12878-XiMat	blood
32	chr4:132379400-132380400	Enhancers	Dnd41	blood
33	chr4:132379800-132381600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:132380400-132381600	Flanking Active TSS	Dnd41	blood
35	chr4:132380600-132381200	Enhancers	Fetal Thymus	thymus
36	chr4:132380600-132381400	Flanking Active TSS	GM12878-XiMat	blood
37	chr4:132381600-132382000	Enhancers	Dnd41	blood
38	chr4:132381600-132382200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:132382200-132382400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:132391600-132392200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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