Variant report

Variant	esv3434529
Chromosome Location	chr4:78388030-78470631
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:387)
CpG islands
(count:306)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:78459487-78459642	HepG2	liver:	n/a	n/a
2	BATF	chr4:78396627-78396929	GM12878	blood:	n/a	chr4:78396751-78396762
3	BATF	chr4:78414243-78414687	GM12878	blood:	n/a	n/a
4	BATF	chr4:78397250-78397558	GM12878	blood:	n/a	n/a
5	BATF	chr4:78415033-78415350	GM12878	blood:	n/a	chr4:78415230-78415241
6	BATF	chr4:78414250-78414612	GM12878	blood:	n/a	n/a
7	BATF	chr4:78426517-78427077	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:78414351-78414581	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:78414245-78414814	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:78415128-78415149	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:78414751-78414877	GM12878	blood:	n/a	n/a
12	BRCA1	chr4:78459389-78459628	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr4:78394805-78395005	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr4:78430250-78430382	HepG2	liver:	n/a	n/a
15	CEBPB	chr4:78390434-78390597	A549	lung:	n/a	n/a
16	CEBPB	chr4:78459319-78460204	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:78394705-78395034	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr4:78459408-78460075	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr4:78414570-78414662	GM12878	blood:	n/a	n/a
20	CTCF	chr4:78394780-78394930	A549	lung:	n/a	n/a
21	CTCF	chr4:78394811-78394953	GM10248	blood:	n/a	n/a
22	CTCF	chr4:78394800-78394950	Caco-2	colon:	n/a	n/a
23	CTCF	chr4:78394780-78394930	RPTEC	kidney:	n/a	n/a
24	CTCF	chr4:78394760-78394910	HVMF	connective:	n/a	n/a
25	CTCF	chr4:78394796-78394909	A549	lung:	n/a	n/a
26	CTCF	chr4:78394780-78394930	SAEC	small airway:	n/a	n/a
27	CTCF	chr4:78394772-78394974	GM13977	blood:	n/a	n/a
28	CTCF	chr4:78394800-78394950	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr4:78394746-78395004	K562	blood:	n/a	n/a
30	CTCF	chr4:78394800-78394950	GM12866	blood:	n/a	n/a
31	CTCF	chr4:78394836-78394958	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr4:78394760-78394910	GM12873	blood:	n/a	n/a
33	CTCF	chr4:78394780-78394930	NHEK	skin:	n/a	n/a
34	CTCF	chr4:78394792-78394852	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:78394761-78394993	ECC-1	luminal epithelium:	n/a	n/a
36	CTCF	chr4:78394800-78394950	AG04449	skin:	n/a	n/a
37	CTCF	chr4:78394778-78394874	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:78394563-78394630	GM19240	blood:	n/a	n/a
39	CTCF	chr4:78394820-78394970	GM12878	blood:	n/a	n/a
40	CTCF	chr4:78394720-78394870	NHLF	lung:	n/a	n/a
41	CTCF	chr4:78394780-78394930	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr4:78394780-78394930	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr4:78394785-78394968	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr4:78394764-78395003	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr4:78394760-78394910	AG09319	gingival:	n/a	n/a
46	CTCF	chr4:78394820-78394970	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr4:78394737-78394974	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr4:78389800-78390050	HepG2	liver:	n/a	n/a
49	CTCF	chr4:78394760-78394910	NHEK	skin:	n/a	n/a
50	CTCF	chr4:78394840-78394990	HBMEC	blood vessel:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:78432204-78432254	Hepatocyte	liver:	n/a
2	chr4:78432204-78432254	Hepatocyte	liver:	n/a
3	chr4:78431407-78431457	MCF10A-Er-Src	breast:	n/a
4	chr4:78432011-78432061	AG04450	lung:	fetal
5	chr4:78432204-78432254	BE2_C	brain:	n/a
6	chr4:78432204-78432254	K562	blood:	n/a
7	chr4:78431407-78431457	NB4	blood:	n/a
8	chr4:78432204-78432254	HRE	kidney:	n/a
9	chr4:78432901-78432951	HCF	heart:	n/a
10	chr4:78432204-78432254	Caco-2	colon:	n/a
11	chr4:78432403-78432453	CMK	blood:	n/a
12	chr4:78432403-78432453	GM12878	blood:	n/a
13	chr4:78432403-78432453	A549	lung:	n/a
14	chr4:78432204-78432254	AG09309	skin:	n/a
15	chr4:78432901-78432951	NHDF-neo	bronchial:	n/a
16	chr4:78432204-78432254	PFSK-1	brain:	n/a
17	chr4:78432403-78432453	Jurkat	blood:	n/a
18	chr4:78432011-78432061	HRCEpiC	kidney:	n/a
19	chr4:78431407-78431457	Hepatocyte	liver:	n/a
20	chr4:78432011-78432061	LNCaP	prostate:	n/a
21	chr4:78431407-78431457	AG04450	lung:	fetal
22	chr4:78431407-78431457	AG09319	gingival:	n/a
23	chr4:78432011-78432061	NT2-D1	testis:	n/a
24	chr4:78432901-78432951	HEEpiC	esophagus:	n/a
25	chr4:78431407-78431457	HepG2	liver:	n/a
26	chr4:78432403-78432453	HRPEpiC	eye:	n/a
27	chr4:78432403-78432453	SK-N-SH_RA	brain:	n/a
28	chr4:78432901-78432951	HRCEpiC	kidney:	n/a
29	chr4:78432403-78432453	HIPEpiC	eye:	n/a
30	chr4:78432204-78432254	SK-N-SH	brain:	n/a
31	chr4:78432403-78432453	RPTEC	kidney:	n/a
32	chr4:78432901-78432951	SK-N-SH	brain:	n/a
33	chr4:78432901-78432951	RPTEC	kidney:	n/a
34	chr4:78432403-78432453	ECC-1	luminal epithelium:	n/a
35	chr4:78432204-78432254	HEEpiC	esophagus:	n/a
36	chr4:78432011-78432061	PFSK-1	brain:	n/a
37	chr4:78432204-78432254	NH-A	brain:	n/a
38	chr4:78432403-78432453	ProgFib	skin:	n/a
39	chr4:78432901-78432951	U87	brain:	n/a
40	chr4:78432901-78432951	BE2_C	brain:	n/a
41	chr4:78432901-78432951	PFSK-1	brain:	n/a
42	chr4:78432204-78432254	MCF-7	breast:	n/a
43	chr4:78432204-78432254	NB4	blood:	n/a
44	chr4:78432403-78432453	Hela-S3	cervix:	n/a
45	chr4:78432403-78432453	HMEC	breast:	n/a
46	chr4:78432901-78432951	SAEC	small airway:	n/a
47	chr4:78432011-78432061	NH-A	brain:	n/a
48	chr4:78432011-78432061	Hepatocyte	liver:	n/a
49	chr4:78432204-78432254	GM19239	blood:	n/a
50	chr4:78432403-78432453	NT2-D1	testis:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:78415447..78417883-chr4:78418165..78419847,2	K562	blood:
2	chr4:78386121..78388787-chr4:78517468..78520191,2	MCF-7	breast:
3	chr4:78306597..78307214-chr4:78394387..78394937,2	K562	blood:
4	chr4:78430923..78433836-chr4:78456770..78459197,2	K562	blood:
5	chr4:78161473..78162127-chr4:78394685..78395318,2	K562	blood:
6	chr4:78413961..78416702-chr4:78422045..78423560,2	MCF-7	breast:
7	chr1:245028107..245028813-chr4:78427168..78428011,2	MCF-7	breast:
8	chr4:78394658..78395254-chr4:78520671..78521209,2	MCF-7	breast:
9	chr4:78415252..78417531-chr4:78420466..78422240,2	K562	blood:
10	chr4:78415447..78417883-chr4:78418165..78419847,2	K562	blood:
11	chr4:78446246..78448492-chr4:78458851..78460486,2	MCF-7	breast:
12	chr4:78394433..78394946-chr4:78521807..78522340,2	MCF-7	breast:
13	chr4:78446246..78448492-chr4:78458851..78460486,2	MCF-7	breast:
14	chr4:78394741..78395310-chr4:78522044..78522649,2	MCF-7	breast:
15	chr4:78394417..78395263-chr4:78619202..78620108,2	MCF-7	breast:
16	chr4:78428052..78429618-chr4:78431660..78434411,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNOT6L-1	chr4:78415319-78415440	XLOC_003994

No data

Variant related genes	Relation type
ENSG00000249036	TF binding region
CXCL13	TF binding region
ENSG00000249036	CpG island
CXCL13	CpG island
ENSG00000249036	chromatin interactions
ENSG00000156234	chromatin interactions

Extended variants
information (count: 1809 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1809 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189522789	chr4:78388044-78388045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs62302445	chr4:78388084-78388085	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs371283452	chr4:78388090-78388091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs62302446	chr4:78388105-78388106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555699561	chr4:78388107-78388108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7667156	chr4:78388108-78388109	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs201500810	chr4:78388126-78388127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142919969	chr4:78388127-78388128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62304068	chr4:78388128-78388129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543429886	chr4:78388157-78388158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563379248	chr4:78388160-78388161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529229729	chr4:78388256-78388257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139734844	chr4:78388257-78388258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559609076	chr4:78388263-78388264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181398318	chr4:78388295-78388296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs60135956	chr4:78388332-78388333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532852411	chr4:78388333-78388334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549884237	chr4:78388343-78388344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569694913	chr4:78388395-78388396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535437993	chr4:78388414-78388415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4859850	chr4:78388443-78388444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111856832	chr4:78388444-78388445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565792011	chr4:78388484-78388485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150664983	chr4:78388524-78388525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116204264	chr4:78388574-78388575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577753662	chr4:78388575-78388576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12508391	chr4:78388592-78388593	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs184352410	chr4:78388594-78388595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374618854	chr4:78388613-78388614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189154255	chr4:78388614-78388615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12508421	chr4:78388668-78388669	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs147896077	chr4:78388669-78388670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545597818	chr4:78388671-78388672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370000699	chr4:78388672-78388673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531109535	chr4:78388673-78388674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141656519	chr4:78388677-78388678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373793899	chr4:78388678-78388679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563360141	chr4:78388680-78388681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528902458	chr4:78388707-78388708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548974289	chr4:78388712-78388713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs367896212	chr4:78388780-78388781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534647787	chr4:78388794-78388795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10581543	chr4:78388835-78388836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551632320	chr4:78388837-78388838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571399736	chr4:78388842-78388843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs398063713	chr4:78388845-78388846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536839593	chr4:78388872-78388873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557045949	chr4:78388874-78388875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573751086	chr4:78388893-78388894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536268761	chr4:78388966-78388967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Glioblastoma multiforme	21922591	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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
primary effusion lymphomas	17116491	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78388000-78394400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:78392600-78394800	Enhancers	Esophagus	oesophagus
3	chr4:78393000-78393400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr4:78393000-78394000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:78393000-78394000	Enhancers	NHEK	skin
6	chr4:78393000-78394200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:78393000-78394200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:78393000-78394600	Enhancers	HMEC	breast
9	chr4:78394400-78394600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:78398600-78402400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:78400200-78400800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:78400400-78400800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr4:78400800-78401800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr4:78400800-78402200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr4:78401800-78404400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:78402200-78403600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr4:78402400-78402600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr4:78402400-78403400	Enhancers	HSMMtube	muscle
19	chr4:78402600-78403000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:78402800-78403600	Enhancers	HMEC	breast
21	chr4:78402800-78403600	Enhancers	HSMM	muscle
22	chr4:78402800-78403800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:78403000-78403600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:78403000-78403600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:78403200-78403400	Weak transcription	Pancreas	Pancrea
26	chr4:78404400-78409600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:78405800-78406200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:78406000-78406200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr4:78407000-78407200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr4:78409600-78410400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr4:78409800-78410200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr4:78409800-78410400	Enhancers	Adipose Nuclei	Adipose
33	chr4:78409800-78410400	Enhancers	HSMM	muscle
34	chr4:78410000-78410400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr4:78410200-78410400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr4:78410200-78410400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr4:78410400-78414400	Weak transcription	HSMM	muscle
38	chr4:78410400-78415000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr4:78414000-78414200	Enhancers	GM12878-XiMat	blood
40	chr4:78414000-78415000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr4:78414000-78415200	Enhancers	Primary B cells from peripheral blood	blood
42	chr4:78414000-78415400	Active TSS	Liver	Liver
43	chr4:78414000-78419000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr4:78414200-78415000	Flanking Active TSS	GM12878-XiMat	blood
45	chr4:78414200-78415600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr4:78414400-78415400	Enhancers	Primary hematopoietic stem cells	blood
47	chr4:78414400-78415600	Enhancers	HMEC	breast
48	chr4:78414400-78415600	Enhancers	HSMM	muscle
49	chr4:78414600-78415400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr4:78414600-78415600	Enhancers	HSMMtube	muscle

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