Variant report

Variant	nsv516203
Chromosome Location	chr4:88167878-88228228
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:478)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:5)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:88199339-88199978	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:88196507-88196704	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:88195615-88195678	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:88191313-88191649	HepG2	liver:	n/a	n/a
5	ATF1	chr4:88175943-88176099	K562	blood:	n/a	n/a
6	ATF2	chr4:88227219-88227557	GM12878	blood:	n/a	n/a
7	ATF2	chr4:88227105-88227643	GM12878	blood:	n/a	n/a
8	ATF3	chr4:88199549-88199769	HepG2	liver:	n/a	n/a
9	ATF3	chr4:88223744-88223892	K562	blood:	n/a	n/a
10	ATF3	chr4:88199339-88199930	HepG2	liver:	n/a	n/a
11	BACH1	chr4:88191402-88191656	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr4:88228029-88228308	GM12878	blood:	n/a	n/a
13	BATF	chr4:88227243-88227499	GM12878	blood:	n/a	chr4:88227386-88227397
14	BCL3	chr4:88225796-88226325	A549	lung:	n/a	n/a
15	BCL3	chr4:88227213-88227544	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:88199328-88199876	HepG2	liver:	n/a	n/a
17	BHLHE40	chr4:88199507-88199750	HepG2	liver:	n/a	n/a
18	BHLHE40	chr4:88199420-88199720	HepG2	liver:	n/a	n/a
19	BRCA1	chr4:88225715-88226363	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr4:88191281-88191673	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr4:88207920-88208188	K562	blood:	n/a	n/a
22	CBX3	chr4:88215016-88215405	K562	blood:	n/a	n/a
23	CEBPB	chr4:88195585-88195771	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:88171550-88171640	K562	blood:	n/a	n/a
25	CEBPB	chr4:88225791-88226474	MCF-7	breast:	n/a	n/a
26	CEBPB	chr4:88175187-88175378	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:88222879-88223179	HepG2	liver:	n/a	chr4:88223035-88223046
28	CEBPB	chr4:88222910-88223189	K562	blood:	n/a	chr4:88223035-88223046
29	CEBPB	chr4:88197413-88197511	HepG2	liver:	n/a	chr4:88197420-88197431
30	CEBPB	chr4:88222884-88223200	IMR90	lung:	n/a	chr4:88223035-88223046
31	CEBPB	chr4:88226731-88227502	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr4:88225700-88226496	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr4:88199523-88199974	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:88222901-88223173	A549	lung:	n/a	chr4:88223035-88223046
35	CREB1	chr4:88227197-88227666	GM12878	blood:	n/a	n/a
36	CTCF	chr4:88191400-88191550	GM12873	blood:	n/a	n/a
37	CTCF	chr4:88191378-88191659	K562	blood:	n/a	n/a
38	CTCF	chr4:88191480-88191630	GM12869	blood:	n/a	n/a
39	CTCF	chr4:88191400-88191550	AG04449	skin:	n/a	n/a
40	CTCF	chr4:88191440-88191590	HRE	kidney:	n/a	n/a
41	CTCF	chr4:88191425-88191533	GM10266	blood:	n/a	n/a
42	CTCF	chr4:88191312-88191584	A549	lung:	n/a	n/a
43	CTCF	chr4:88191380-88191530	K562	blood:	n/a	n/a
44	CTCF	chr4:88191360-88191510	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr4:88191380-88191530	BE2_C	brain:	n/a	n/a
46	CTCF	chr4:88191420-88191570	HepG2	liver:	n/a	n/a
47	CTCF	chr4:88191349-88191620	K562	blood:	n/a	n/a
48	CTCF	chr4:88191427-88191541	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:88191440-88191590	HAc	cerebellar:	n/a	n/a
50	CTCF	chr4:88191480-88191630	GM12864	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:88225834-88225884	RPTEC	kidney:	n/a
2	chr4:88225834-88225884	MCF10A-Er-Src	breast:	n/a
3	chr4:88225834-88225884	GM12892	blood:	n/a
4	chr4:88225834-88225884	LNCaP	prostate:	n/a
5	chr4:88225834-88225884	PFSK-1	brain:	n/a
6	chr4:88225834-88225884	SK-N-SH	brain:	n/a
7	chr4:88225834-88225884	AG09319	gingival:	n/a
8	chr4:88225834-88225884	BE2_C	brain:	n/a
9	chr4:88225834-88225884	SK-N-SH_RA	brain:	n/a
10	chr4:88225834-88225884	NH-A	brain:	n/a
11	chr4:88225834-88225884	AG04449	skin:	fetal
12	chr4:88225834-88225884	PrEC	prostate:	n/a
13	chr4:88225834-88225884	Hela-S3	cervix:	n/a
14	chr4:88225834-88225884	HepG2	liver:	n/a
15	chr4:88225834-88225884	AoSMC	blood vessel:	n/a
16	chr4:88225834-88225884	U87	brain:	n/a
17	chr4:88225834-88225884	Hepatocyte	liver:	n/a
18	chr4:88225834-88225884	ovcar-3	ovarian:	n/a
19	chr4:88225834-88225884	SK-N-MC	brain:	n/a
20	chr4:88225834-88225884	A549	lung:	n/a
21	chr4:88225834-88225884	MCF-7	breast:	n/a
22	chr4:88225834-88225884	Caco-2	colon:	n/a
23	chr4:88225834-88225884	HUVEC	blood vessel:	n/a
24	chr4:88225834-88225884	GM12878	blood:	n/a
25	chr4:88225834-88225884	HCPEpiC	choroid plexus:	n/a
26	chr4:88225834-88225884	HRE	kidney:	n/a
27	chr4:88225834-88225884	HIPEpiC	eye:	n/a
28	chr4:88225834-88225884	HAEpiC	amniotic membrane:	n/a
29	chr4:88225834-88225884	K562	blood:	n/a
30	chr4:88225834-88225884	T-47D	breast:	n/a
31	chr4:88225834-88225884	NHBE	bronchial:	n/a
32	chr4:88225834-88225884	GM12891	blood:	n/a
33	chr4:88225834-88225884	BJ	skin:	n/a
34	chr4:88225834-88225884	HPAEpiC	pulmonary alveolar:	n/a
35	chr4:88225834-88225884	HRPEpiC	eye:	n/a
36	chr4:88225834-88225884	HEK293	kidney:	embryo
37	chr4:88225834-88225884	CMK	blood:	n/a
38	chr4:88225834-88225884	HCM	heart:	n/a
39	chr4:88225834-88225884	AG09309	skin:	n/a
40	chr4:88225834-88225884	SKMC	muscle:	n/a
41	chr4:88225834-88225884	ProgFib	skin:	n/a
42	chr4:88225834-88225884	GM06990	blood:	n/a
43	chr4:88225834-88225884	SAEC	small airway:	n/a
44	chr4:88225834-88225884	NB4	blood:	n/a
45	chr4:88225834-88225884	AG04450	lung:	fetal
46	chr4:88225834-88225884	HL-60	blood:	n/a
47	chr4:88225834-88225884	HEEpiC	esophagus:	n/a
48	chr4:88225834-88225884	GM19239	blood:	n/a
49	chr4:88225834-88225884	HNPCEpiC	eye:	n/a
50	chr4:88225834-88225884	HCT-116	colon:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:88226132..88228278-chr4:88229243..88230944,2	MCF-7	breast:
2	chr4:88132419..88135036-chr4:88191101..88193543,2	K562	blood:
3	chr4:88190901..88191577-chr4:88769909..88770797,2	MCF-7	breast:
4	chr4:88224415..88227242-chr4:88231505..88233396,2	K562	blood:
5	chr4:88225790..88227669-chr4:88236912..88239118,2	MCF-7	breast:
6	chr4:88225793..88228433-chr4:88233021..88235909,2	MCF-7	breast:
7	chr4:88216757..88219177-chr4:88220101..88221682,2	MCF-7	breast:
8	chr10:46970031..46970993-chr4:88194361..88194882,2	MCF-7	breast:
9	chr4:88141337..88143545-chr4:88209433..88211061,2	MCF-7	breast:
10	chr4:88140123..88141719-chr4:88189481..88191440,2	MCF-7	breast:
11	chr4:88177898..88180525-chr4:88185534..88188362,3	K562	blood:
12	chr4:88161337..88162947-chr4:88190418..88192890,2	K562	blood:
13	chr4:88183411..88186658-chr4:88187924..88190841,3	K562	blood:
14	chr4:88216757..88219177-chr4:88220101..88221682,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSD17B13-1	chr4:88183083-88183251	XLOC_004009
2	lnc-HSD17B13-1	chr4:88187887-88187974	XLOC_004009
3	lnc-AFF1-1	chr4:88198781-88198895	XLOC_003601
4	lnc-AFF1-1	chr4:88192262-88192330	XLOC_003601
5	lnc-AFF1-1	chr4:88199776-88199855	XLOC_003601

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5705	chr4:88221657-88221679	MIMAT0022499

No data

Variant related genes	Relation type
ENSG00000250572	TF binding region
MIR5705	TF binding region
ENSG00000250572	CpG island
MIR5705	CpG island
ENSG00000204176	chromatin interactions
ENSG00000250572	chromatin interactions
ENSG00000145332	chromatin interactions
CREG1	miRNA target sites
CREBZF	miRNA target sites

Extended variants
information (count: 1552 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1552 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141890455	chr4:88171205-88171206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs113666584	chr4:88171252-88171253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557148749	chr4:88171259-88171260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575616604	chr4:88171268-88171269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539341507	chr4:88171281-88171282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187930312	chr4:88171283-88171284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189657448	chr4:88171302-88171303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116806860	chr4:88171310-88171311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113028125	chr4:88171333-88171334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147867430	chr4:88171384-88171385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs375531776	chr4:88171407-88171408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186951929	chr4:88171415-88171416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533133848	chr4:88171496-88171497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563531844	chr4:88171649-88171650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141553614	chr4:88171675-88171676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192657917	chr4:88171687-88171688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79528304	chr4:88171699-88171700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572222924	chr4:88171746-88171747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6822384	chr4:88171749-88171750	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs72670111	chr4:88171752-88171753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560893191	chr4:88171760-88171761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs71660128	chr4:88171761-88171762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568166220	chr4:88171762-88171763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556225098	chr4:88171775-88171776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs58370856	chr4:88171776-88171777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs199843893	chr4:88171780-88171781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs199677422	chr4:88171781-88171782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116179654	chr4:88171835-88171836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150049179	chr4:88171846-88171847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374305334	chr4:88171847-88171848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs72670112	chr4:88171966-88171967	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs557752195	chr4:88171990-88171991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs368725481	chr4:88172021-88172022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566725342	chr4:88172023-88172024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534728463	chr4:88172030-88172031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552902238	chr4:88172060-88172061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574633821	chr4:88172129-88172130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541918563	chr4:88172135-88172136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557160664	chr4:88172136-88172137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs79112029	chr4:88172181-88172182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546346805	chr4:88172189-88172190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35530475	chr4:88172211-88172212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564650396	chr4:88172224-88172225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528738317	chr4:88172231-88172232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75831434	chr4:88172248-88172249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs367646850	chr4:88172309-88172310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149227831	chr4:88172364-88172365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs143330444	chr4:88172401-88172402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550670966	chr4:88172436-88172437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560919552	chr4:88172445-88172446	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	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
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	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
Breast cancer	22522925	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:88171200-88171600	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr4:88171200-88172200	Enhancers	Rectal Mucosa Donor 29	rectum
3	chr4:88171400-88171600	Enhancers	Brain Cingulate Gyrus	brain
4	chr4:88171400-88172800	Enhancers	Liver	Liver
5	chr4:88171400-88173400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr4:88171400-88174000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:88172000-88173000	Enhancers	Brain Hippocampus Middle	brain
8	chr4:88172200-88173000	Enhancers	Brain Angular Gyrus	brain
9	chr4:88172200-88173000	Enhancers	Fetal Brain Male	brain
10	chr4:88172400-88172800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr4:88172600-88173000	Enhancers	Brain Anterior Caudate	brain
12	chr4:88172600-88173000	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr4:88172600-88173000	Enhancers	Brain Substantia Nigra	brain
14	chr4:88173000-88178000	Weak transcription	Brain Hippocampus Middle	brain
15	chr4:88173000-88178000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr4:88173000-88178200	Weak transcription	Brain Anterior Caudate	brain
17	chr4:88173000-88178200	Weak transcription	Brain Substantia Nigra	brain
18	chr4:88177000-88177200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
19	chr4:88177000-88177600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
20	chr4:88177200-88179600	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr4:88177600-88178200	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr4:88178000-88179000	Enhancers	Brain Hippocampus Middle	brain
23	chr4:88178000-88179800	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr4:88178200-88178800	Enhancers	Brain Cingulate Gyrus	brain
25	chr4:88178200-88178800	Enhancers	Brain Substantia Nigra	brain
26	chr4:88178200-88179600	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr4:88178200-88180000	Enhancers	Brain Anterior Caudate	brain
28	chr4:88178400-88178600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr4:88178600-88179400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr4:88178800-88179200	Flanking Active TSS	Brain Substantia Nigra	brain
31	chr4:88178800-88179400	Weak transcription	Brain Cingulate Gyrus	brain
32	chr4:88179000-88179400	Flanking Active TSS	Brain Hippocampus Middle	brain
33	chr4:88179200-88179600	Enhancers	Brain Substantia Nigra	brain
34	chr4:88179400-88179600	Enhancers	Brain Cingulate Gyrus	brain
35	chr4:88179400-88179600	Enhancers	Brain Hippocampus Middle	brain
36	chr4:88179400-88179800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr4:88184600-88191400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:88185000-88186000	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr4:88185200-88185800	Enhancers	Primary B cells from peripheral blood	blood
40	chr4:88185200-88185800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr4:88185400-88185800	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr4:88185600-88186200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:88185800-88186400	Enhancers	Primary hematopoietic stem cells	blood
44	chr4:88186200-88187600	Weak transcription	Aorta	Aorta
45	chr4:88187600-88188400	Enhancers	Aorta	Aorta
46	chr4:88187800-88189200	Enhancers	Adipose Nuclei	Adipose
47	chr4:88188000-88188200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:88188000-88188400	Enhancers	Fetal Kidney	kidney
49	chr4:88188200-88188600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr4:88188400-88188800	Weak transcription	Fetal Kidney	kidney

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