Variant report

Variant	esv2763375
Chromosome Location	chr4:90367678-90484894
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	chr4:90391150-90391650	GM12878	blood:	n/a	n/a
2	BATF	chr4:90391279-90391574	GM12878	blood:	n/a	chr4:90391457-90391468
3	BCLAF1	chr4:90391160-90391565	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:90430761-90431158	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:90391200-90391617	GM12878	blood:	n/a	n/a
6	BRCA1	chr4:90413826-90414201	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr4:90410621-90410643	GM12878	blood:	n/a	n/a
8	BRCA1	chr4:90419256-90419551	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr4:90460469-90460891	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr4:90471011-90471525	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:90413920-90414266	K562	blood:	n/a	chr4:90414088-90414099
12	CEBPB	chr4:90428298-90428542	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:90405751-90405898	H1-hESC	embryonic stem cell:	n/a	chr4:90405792-90405803
14	CEBPB	chr4:90431238-90431514	HepG2	liver:	n/a	chr4:90431369-90431382
15	CEBPB	chr4:90460613-90460971	A549	lung:	n/a	n/a
16	CEBPB	chr4:90382249-90382462	IMR90	lung:	n/a	chr4:90382375-90382392
17	CEBPB	chr4:90409379-90409397	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:90375324-90375621	MCF-7	breast:	n/a	chr4:90375399-90375410 chr4:90375401-90375410 chr4:90375401-90375410 chr4:90375401-90375412 chr4:90375399-90375412 chr4:90375401-90375410 chr4:90375401-90375410 chr4:90375399-90375412
19	CEBPB	chr4:90460668-90461006	A549	lung:	n/a	n/a
20	CEBPB	chr4:90460623-90461072	A549	lung:	n/a	n/a
21	CEBPB	chr4:90413543-90414473	Hela-S3	cervix:	n/a	chr4:90413773-90413784 chr4:90413617-90413630 chr4:90414088-90414099
22	CEBPB	chr4:90460561-90460979	IMR90	lung:	n/a	n/a
23	CEBPB	chr4:90431011-90431495	Hela-S3	cervix:	n/a	chr4:90431369-90431382
24	CEBPB	chr4:90405652-90405951	HepG2	liver:	n/a	chr4:90405792-90405803
25	CEBPB	chr4:90409345-90409618	HepG2	liver:	n/a	chr4:90409455-90409466
26	CEBPB	chr4:90375297-90375567	HepG2	liver:	n/a	chr4:90375399-90375410 chr4:90375401-90375410 chr4:90375401-90375410 chr4:90375401-90375412 chr4:90375399-90375412 chr4:90375401-90375410 chr4:90375401-90375410 chr4:90375399-90375412
27	CEBPB	chr4:90413875-90414288	A549	lung:	n/a	chr4:90414088-90414099
28	CEBPB	chr4:90477797-90478092	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:90477930-90478071	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr4:90472321-90472746	Hela-S3	cervix:	n/a	chr4:90472469-90472480
31	CEBPB	chr4:90408648-90408743	K562	blood:	n/a	chr4:90408693-90408704
32	CEBPB	chr4:90412831-90413117	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr4:90408636-90408740	HepG2	liver:	n/a	chr4:90408693-90408704
34	CEBPB	chr4:90413922-90414297	A549	lung:	n/a	chr4:90414088-90414099
35	CEBPB	chr4:90409295-90409626	IMR90	lung:	n/a	chr4:90409455-90409466 chr4:90409296-90409307
36	CEBPB	chr4:90419078-90419426	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr4:90431155-90431559	IMR90	lung:	n/a	chr4:90431369-90431382
38	CEBPB	chr4:90408543-90408843	HepG2	liver:	n/a	chr4:90408693-90408704
39	CEBPB	chr4:90409384-90409591	K562	blood:	n/a	chr4:90409455-90409466
40	CEBPB	chr4:90477744-90478138	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:90413854-90414272	HepG2	liver:	n/a	chr4:90414088-90414099
42	CEBPB	chr4:90460570-90461036	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr4:90414015-90414252	MCF-7	breast:	n/a	chr4:90414088-90414099
44	CEBPB	chr4:90431221-90431487	A549	lung:	n/a	chr4:90431369-90431382
45	CEBPB	chr4:90413977-90414189	H1-hESC	embryonic stem cell:	n/a	chr4:90414088-90414099
46	CEBPB	chr4:90375289-90375531	IMR90	lung:	n/a	chr4:90375399-90375410 chr4:90375401-90375410 chr4:90375401-90375410 chr4:90375401-90375412 chr4:90375399-90375412 chr4:90375401-90375410 chr4:90375401-90375410 chr4:90375399-90375412
47	CEBPB	chr4:90409320-90409557	A549	lung:	n/a	chr4:90409455-90409466
48	CEBPB	chr4:90471158-90471468	IMR90	lung:	n/a	n/a
49	CEBPB	chr4:90413815-90414366	A549	lung:	n/a	chr4:90414088-90414099
50	CEBPB	chr4:90391054-90391591	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:90418810-90418860	HCPEpiC	choroid plexus:	n/a
2	chr4:90418810-90418860	LNCaP	prostate:	n/a
3	chr4:90411303-90411353	Caco-2	colon:	n/a
4	chr4:90411303-90411353	SK-N-SH	brain:	n/a
5	chr4:90481402-90481452	Hepatocyte	liver:	n/a
6	chr4:90411303-90411353	AoSMC	blood vessel:	n/a
7	chr4:90411303-90411353	A549	lung:	n/a
8	chr4:90411303-90411353	SAEC	small airway:	n/a
9	chr4:90411303-90411353	HAEpiC	amniotic membrane:	n/a
10	chr4:90418810-90418860	Jurkat	blood:	n/a
11	chr4:90411303-90411353	Jurkat	blood:	n/a
12	chr4:90481402-90481452	NHDF-neo	bronchial:	n/a
13	chr4:90418810-90418860	HEEpiC	esophagus:	n/a
14	chr4:90481402-90481452	HRE	kidney:	n/a
15	chr4:90481402-90481452	MCF-7	breast:	n/a
16	chr4:90411303-90411353	ovcar-3	ovarian:	n/a
17	chr4:90411303-90411353	HMEC	breast:	n/a
18	chr4:90418810-90418860	BE2_C	brain:	n/a
19	chr4:90418810-90418860	ovcar-3	ovarian:	n/a
20	chr4:90481402-90481452	HCM	heart:	n/a
21	chr4:90411303-90411353	HCF	heart:	n/a
22	chr4:90418810-90418860	A549	lung:	n/a
23	chr4:90418810-90418860	SAEC	small airway:	n/a
24	chr4:90418810-90418860	AG09309	skin:	n/a
25	chr4:90481402-90481452	HepG2	liver:	n/a
26	chr4:90418810-90418860	NHBE	bronchial:	n/a
27	chr4:90481402-90481452	AG04450	lung:	fetal
28	chr4:90411303-90411353	HCM	heart:	n/a
29	chr4:90481402-90481452	HPAEpiC	pulmonary alveolar:	n/a
30	chr4:90418810-90418860	K562	blood:	n/a
31	chr4:90418810-90418860	HCM	heart:	n/a
32	chr4:90411303-90411353	BE2_C	brain:	n/a
33	chr4:90411303-90411353	BJ	skin:	n/a
34	chr4:90481402-90481452	LNCaP	prostate:	n/a
35	chr4:90418810-90418860	HCT-116	colon:	n/a
36	chr4:90481402-90481452	NT2-D1	testis:	n/a
37	chr4:90411303-90411353	PFSK-1	brain:	n/a
38	chr4:90418810-90418860	GM06990	blood:	n/a
39	chr4:90481402-90481452	ECC-1	luminal epithelium:	n/a
40	chr4:90481402-90481452	AG09319	gingival:	n/a
41	chr4:90418810-90418860	AG09319	gingival:	n/a
42	chr4:90411303-90411353	AG10803	skin:	n/a
43	chr4:90481402-90481452	HAEpiC	amniotic membrane:	n/a
44	chr4:90418810-90418860	GM12891	blood:	n/a
45	chr4:90481402-90481452	GM12878	blood:	n/a
46	chr4:90481402-90481452	NH-A	brain:	n/a
47	chr4:90411303-90411353	NT2-D1	testis:	n/a
48	chr4:90418810-90418860	MCF10A-Er-Src	breast:	n/a
49	chr4:90481402-90481452	AoSMC	blood vessel:	n/a
50	chr4:90418810-90418860	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:90429896..90432844-chr4:90433363..90434865,2	K562	blood:
2	chr4:90451896..90453776-chr4:90459193..90461296,2	K562	blood:
3	chr4:90432490..90434839-chr4:94741049..94742635,2	K562	blood:
4	chr4:90406838..90407643-chr4:90425886..90426561,2	MCF-7	breast:
5	chr4:90406838..90407643-chr4:90425886..90426561,2	MCF-7	breast:
6	chr4:90417759..90420073-chr4:90420806..90423347,2	K562	blood:
7	chr4:90417759..90420073-chr4:90420806..90423347,2	K562	blood:
8	chr4:90419228..90421468-chr4:90425184..90427670,2	K562	blood:
9	chr4:90451896..90453776-chr4:90459193..90461296,2	K562	blood:
10	chr4:90419228..90421468-chr4:90425184..90427670,2	K562	blood:
11	chr12:73050089..73050693-chr4:90478139..90478639,2	MCF-7	breast:
12	chr4:90429896..90432844-chr4:90433363..90434865,2	K562	blood:
13	chr4:90409604..90412521-chr4:90418396..90420706,2	K562	blood:
14	chr4:90409604..90412521-chr4:90418396..90420706,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNCA-2	chr4:90462023-90462178	XLOC_004016
2	lnc-GPRIN3-1	chr4:90381044-90381368	XLOC_004015
3	lnc-SNCA-2	chr4:90466475-90466738	XLOC_004016
4	lnc-TIGD2-1	chr4:90472606-90472721	NONHSAT097396
5	lnc-SNCA-2	chr4:90462023-90462178	NONHSAT097392
6	lnc-SNCA-2	chr4:90472211-90472707	XLOC_004016
7	lnc-MMRN1-2	chr4:90472507-90472721	ENSG00000251095.1
8	lnc-SNCA-2	chr4:90466477-90466585	NONHSAT097392
9	lnc-GPRIN3-3	chr4:90381444-90383659	ucscGeneNc_uc003hsl_1
10	lnc-SNCA-2	chr4:90472211-90472453	XLOC_004016
11	lnc-SNCA-2	chr4:90459430-90459537	NONHSAT097392
12	lnc-MMRN1-2	chr4:90472541-90472610	ENSG00000251095.1
13	lnc-GPRIN3-1	chr4:90388905-90388932	XLOC_004015
14	lnc-SNCA-2	chr4:90459367-90459537	XLOC_004016

Variant related genes	Relation type
ENSG00000251095	TF binding region
ENSG00000251095	CpG island
ENSG00000252342	chromatin interactions

Extended variants
information (count: 3055 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3055 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541580049	chr4:90367690-90367691	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs540800259	chr4:90367714-90367715	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs144976645	chr4:90367715-90367716	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs535199636	chr4:90367733-90367734	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs113576431	chr4:90367761-90367762	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs79347028	chr4:90367791-90367792	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs112955831	chr4:90367795-90367796	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs189486763	chr4:90367798-90367799	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs372718665	chr4:90367850-90367851	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs146018356	chr4:90367851-90367852	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs373730343	chr4:90367888-90367889	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs533121590	chr4:90367909-90367910	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs376443714	chr4:90367951-90367952	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs138738484	chr4:90367957-90367958	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs375958487	chr4:90367958-90367959	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs140574078	chr4:90368001-90368002	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs559993910	chr4:90368016-90368017	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs527633383	chr4:90368039-90368040	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs549149699	chr4:90368078-90368079	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs370952535	chr4:90368091-90368092	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs373738050	chr4:90368093-90368094	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs567306793	chr4:90368116-90368117	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs138400710	chr4:90368141-90368142	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs76103934	chr4:90368150-90368151	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs538046207	chr4:90368155-90368156	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs549875849	chr4:90368157-90368158	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs528507842	chr4:90378010-90378011	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs148744030	chr4:90378014-90378015	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs142257345	chr4:90378022-90378023	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs535250853	chr4:90378028-90378029	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs550409182	chr4:90378031-90378032	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs192381445	chr4:90378032-90378033	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs182472567	chr4:90378041-90378042	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs151251866	chr4:90378046-90378047	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs557839752	chr4:90378069-90378070	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs572724734	chr4:90378118-90378119	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs368423667	chr4:90378146-90378147	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs11292868	chr4:90378155-90378156	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs549700690	chr4:90378174-90378175	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs566265088	chr4:90378224-90378225	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs112197346	chr4:90378246-90378247	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs542430181	chr4:90378260-90378261	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs80098442	chr4:90378300-90378301	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs76343853	chr4:90378334-90378335	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs369140221	chr4:90378339-90378340	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs150490255	chr4:90378341-90378342	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs564619768	chr4:90378343-90378344	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs373684895	chr4:90378368-90378369	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs147718569	chr4:90378378-90378379	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs560921657	chr4:90379696-90379697	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Autism	22495311	CNVD
Breast cancer	21858162	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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:90366400-90368200	ZNF genes & repeats	Adipose Nuclei	Adipose
2	chr4:90378000-90378400	ZNF genes & repeats	Aorta	Aorta
3	chr4:90379600-90380000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr4:90380600-90382000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:90389400-90390600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr4:90389400-90391400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr4:90389600-90391200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:90389600-90391400	Enhancers	Primary B cells from cord blood	blood
9	chr4:90389600-90391600	Enhancers	Primary hematopoietic stem cells	blood
10	chr4:90389800-90390000	Enhancers	Primary B cells from peripheral blood	blood
11	chr4:90389800-90390200	Enhancers	Ovary	ovary
12	chr4:90389800-90390400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:90389800-90390800	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr4:90389800-90390800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr4:90389800-90390800	Enhancers	NHLF	lung
16	chr4:90389800-90391000	Enhancers	A549	lung
17	chr4:90389800-90391000	Enhancers	NHDF-Ad	bronchial
18	chr4:90389800-90391600	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr4:90389800-90391600	Enhancers	Colon Smooth Muscle	Colon
20	chr4:90389800-90391800	Enhancers	NHEK	skin
21	chr4:90389800-90392000	Enhancers	Hela-S3	cervix
22	chr4:90389800-90392200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr4:90390000-90390800	Weak transcription	Primary B cells from peripheral blood	blood
24	chr4:90390000-90390800	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr4:90390000-90391000	Enhancers	Primary T cells from cord blood	blood
26	chr4:90390000-90391000	Enhancers	GM12878-XiMat	blood
27	chr4:90390000-90391200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:90390000-90392000	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr4:90390000-90392200	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr4:90390000-90392200	Enhancers	HSMM	muscle
31	chr4:90390200-90390600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:90390200-90391000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr4:90390400-90390800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr4:90390400-90391000	Enhancers	Osteobl	bone
35	chr4:90390400-90391600	Enhancers	HUVEC	blood vessel
36	chr4:90390600-90390800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr4:90390600-90390800	Enhancers	HMEC	breast
38	chr4:90390600-90391000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr4:90390600-90391000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr4:90390600-90391000	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr4:90390600-90391200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr4:90390600-90391200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
43	chr4:90390600-90391400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr4:90390600-90391800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr4:90390600-90392000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr4:90390600-90392000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr4:90390800-90391000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr4:90390800-90391000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr4:90390800-90391200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
50	chr4:90390800-90391200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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