Variant report

Variant	nsv997478
Chromosome Location	chr4:80578536-80669871
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:235)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:235 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:80599630-80600187	K562	blood:	n/a	n/a
2	ATF1	chr4:80599574-80600070	K562	blood:	n/a	n/a
3	ATF1	chr4:80621566-80621751	K562	blood:	n/a	n/a
4	ATF3	chr4:80599406-80600004	K562	blood:	n/a	n/a
5	BACH1	chr4:80599834-80600042	K562	blood:	n/a	n/a
6	BHLHE40	chr4:80599720-80600214	K562	blood:	n/a	n/a
7	BRCA1	chr4:80606631-80606641	HepG2	liver:	n/a	n/a
8	CBX3	chr4:80599555-80600094	K562	blood:	n/a	n/a
9	CCNT2	chr4:80599582-80600184	K562	blood:	n/a	n/a
10	CEBPB	chr4:80599685-80600123	K562	blood:	n/a	chr4:80599946-80599957
11	CEBPB	chr4:80621616-80621838	K562	blood:	n/a	n/a
12	CEBPB	chr4:80599604-80600033	K562	blood:	n/a	chr4:80599946-80599957
13	CEBPB	chr4:80618621-80618857	HepG2	liver:	n/a	chr4:80618717-80618728
14	CEBPB	chr4:80599550-80600162	K562	blood:	n/a	chr4:80599946-80599957
15	CEBPB	chr4:80621582-80621882	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr4:80593568-80593779	HepG2	liver:	n/a	chr4:80593711-80593722
17	CEBPD	chr4:80599581-80600155	K562	blood:	n/a	n/a
18	CEBPD	chr4:80599473-80600111	K562	blood:	n/a	n/a
19	CHD2	chr4:80655647-80655866	K562	blood:	n/a	n/a
20	CREB1	chr4:80599524-80600128	K562	blood:	n/a	n/a
21	CTCF	chr4:80612060-80612210	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr4:80644800-80644950	GM12867	blood:	n/a	n/a
23	CTCF	chr4:80640863-80640895	GM20000	blood:	n/a	n/a
24	CTCF	chr4:80596159-80596208	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr4:80661160-80661310	GM06990	blood:	n/a	n/a
26	CTCF	chr4:80617744-80617786	Medullo	brain:	n/a	n/a
27	CTCF	chr4:80589144-80589211	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr4:80659600-80659750	Caco-2	colon:	n/a	n/a
29	CTCF	chr4:80606480-80606630	HPF	lung:	n/a	n/a
30	CTCF	chr4:80601211-80601376	K562	blood:	n/a	n/a
31	CTCF	chr4:80602200-80602350	BE2_C	brain:	n/a	n/a
32	CTCF	chr4:80589200-80589350	GM12870	blood:	n/a	n/a
33	CTCF	chr4:80585127-80585131	K562	blood:	n/a	n/a
34	CUX1	chr4:80599672-80600555	K562	blood:	n/a	n/a
35	E2F4	chr4:80654520-80654523	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr4:80667915-80667992	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr4:80653191-80653519	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr4:80585849-80586007	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F6	chr4:80599827-80600098	K562	blood:	n/a	n/a
40	E2F6	chr4:80599815-80600050	K562	blood:	n/a	n/a
41	EBF1	chr4:80601124-80601292	GM12878	blood:	n/a	chr4:80601204-80601215
42	EGR1	chr4:80599731-80600127	K562	blood:	n/a	n/a
43	EGR1	chr4:80598507-80598744	K562	blood:	n/a	n/a
44	EP300	chr4:80598370-80598447	K562	blood:	n/a	n/a
45	EP300	chr4:80599626-80600025	K562	blood:	n/a	chr4:80599825-80599839 chr4:80599634-80599643
46	EP300	chr4:80599489-80600145	K562	blood:	n/a	chr4:80599825-80599839 chr4:80599634-80599643
47	ESR1	chr4:80583829-80584306	ECC-1	luminal epithelium:	n/a	n/a
48	ESR1	chr4:80583887-80584662	ECC-1	luminal epithelium:	n/a	n/a
49	ESR1	chr4:80658711-80658993	ECC-1	luminal epithelium:	n/a	n/a
50	FOS	chr4:80597866-80598260	MCF10A-Er-Src	breast:	n/a	chr4:80598033-80598045 chr4:80598036-80598043

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:80604140-80604190	NB4	blood:	n/a
2	chr4:80604140-80604190	HCT-116	colon:	n/a
3	chr4:80644890-80644940	K562	blood:	n/a
4	chr4:80604140-80604190	PFSK-1	brain:	n/a
5	chr4:80604140-80604190	HAEpiC	amniotic membrane:	n/a
6	chr4:80604140-80604190	HUVEC	blood vessel:	n/a
7	chr4:80644890-80644940	ECC-1	luminal epithelium:	n/a
8	chr4:80644890-80644940	SK-N-SH	brain:	n/a
9	chr4:80644890-80644940	RPTEC	kidney:	n/a
10	chr4:80604140-80604190	BJ	skin:	n/a
11	chr4:80644890-80644940	GM19239	blood:	n/a
12	chr4:80604140-80604190	HEEpiC	esophagus:	n/a
13	chr4:80604140-80604190	HIPEpiC	eye:	n/a
14	chr4:80604140-80604190	NH-A	brain:	n/a
15	chr4:80644890-80644940	Hela-S3	cervix:	n/a
16	chr4:80644890-80644940	GM12878	blood:	n/a
17	chr4:80604140-80604190	GM12892	blood:	n/a
18	chr4:80604140-80604190	HL-60	blood:	n/a
19	chr4:80644890-80644940	HRE	kidney:	n/a
20	chr4:80644890-80644940	SKMC	muscle:	n/a
21	chr4:80604140-80604190	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:80604140-80604190	MCF-7	breast:	n/a
23	chr4:80644890-80644940	PANC-1	pancreas:	n/a
24	chr4:80644890-80644940	HRPEpiC	eye:	n/a
25	chr4:80604140-80604190	MCF10A-Er-Src	breast:	n/a
26	chr4:80644890-80644940	AG10803	skin:	n/a
27	chr4:80644890-80644940	H1-hESC	embryonic stem cell:	embryo
28	chr4:80644890-80644940	BE2_C	brain:	n/a
29	chr4:80604140-80604190	SK-N-MC	brain:	n/a
30	chr4:80644890-80644940	HCF	heart:	n/a
31	chr4:80644890-80644940	HCPEpiC	choroid plexus:	n/a
32	chr4:80604140-80604190	AG04450	lung:	fetal
33	chr4:80644890-80644940	CMK	blood:	n/a
34	chr4:80604140-80604190	GM19239	blood:	n/a
35	chr4:80604140-80604190	ovcar-3	ovarian:	n/a
36	chr4:80604140-80604190	PrEC	prostate:	n/a
37	chr4:80644890-80644940	AG09309	skin:	n/a
38	chr4:80604140-80604190	RPTEC	kidney:	n/a
39	chr4:80604140-80604190	Caco-2	colon:	n/a
40	chr4:80604140-80604190	HRCEpiC	kidney:	n/a
41	chr4:80604140-80604190	AoSMC	blood vessel:	n/a
42	chr4:80644890-80644940	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:80604140-80604190	HepG2	liver:	n/a
44	chr4:80604140-80604190	NHBE	bronchial:	n/a
45	chr4:80604140-80604190	Hepatocyte	liver:	n/a
46	chr4:80604140-80604190	T-47D	breast:	n/a
47	chr4:80604140-80604190	U87	brain:	n/a
48	chr4:80604140-80604190	K562	blood:	n/a
49	chr4:80604140-80604190	SKMC	muscle:	n/a
50	chr4:80644890-80644940	HRCEpiC	kidney:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:80648491..80650120-chr4:80667527..80670366,2	K562	blood:
2	chr4:80623187..80625432-chr4:80633610..80635287,2	MCF-7	breast:
3	chr4:80619168..80620918-chr4:80690936..80692886,2	K562	blood:
4	chr4:80604769..80607470-chr4:80609950..80612780,2	K562	blood:
5	chr4:80604769..80607470-chr4:80609950..80612780,2	K562	blood:
6	chr4:80623187..80625432-chr4:80633610..80635287,2	MCF-7	breast:
7	chr4:80648491..80650120-chr4:80667527..80670366,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRDM8-2	chr4:80589143-80589281	XLOC_003588
2	lnc-PRDM8-8	chr4:80653963-80654080	ucscGeneNc_uc003hlv_2
3	lnc-PRDM8-2	chr4:80584859-80585002	NONHSAT097119
4	lnc-PRDM8-2	chr4:80589005-80589731	NONHSAT097119
5	lnc-PRDM8-2	chr4:80617567-80617991	XLOC_003588
6	lnc-PRDM8-2	chr4:80588084-80588280	NONHSAT097119
7	lnc-PRDM8-8	chr4:80632771-80632952	ucscGeneNc_uc003hlv_2
8	lnc-PRDM8-2	chr4:80584915-80585002	XLOC_003588
9	lnc-PRDM8-8	chr4:80633330-80633763	ucscGeneNc_uc003hlv_2
10	lnc-PRDM8-2	chr4:80611142-80611230	XLOC_003588

No data

Variant related genes	Relation type
ENSG00000248408	TF binding region
ENSG00000248408	CpG island

Extended variants
information (count: 1401 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1401 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56190714	chr4:80578570-80578571	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs151160469	chr4:80578595-80578596	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs188702625	chr4:80582425-80582426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542941087	chr4:80582433-80582434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191914785	chr4:80582456-80582457	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs184155492	chr4:80582457-80582458	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs563715454	chr4:80582474-80582475	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs190345222	chr4:80582480-80582481	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs4572901	chr4:80582492-80582493	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs58795949	chr4:80582494-80582495	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs528694553	chr4:80582505-80582506	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs150048565	chr4:80582531-80582532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115427641	chr4:80582582-80582583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537796580	chr4:80582587-80582588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556528258	chr4:80582597-80582598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566933333	chr4:80582615-80582616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145343218	chr4:80582651-80582652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4535357	chr4:80582672-80582673	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs181672856	chr4:80582731-80582732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4975101	chr4:80582793-80582794	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs568926440	chr4:80583833-80583834	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs116762121	chr4:80583922-80583923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs554833288	chr4:80583947-80583948	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs182640143	chr4:80583982-80583983	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs534124024	chr4:80584026-80584027	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs531185295	chr4:80584101-80584102	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs149489412	chr4:80584122-80584123	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs6846624	chr4:80584132-80584133	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs113238249	chr4:80584136-80584137	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs6823216	chr4:80584211-80584212	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs185414666	chr4:80584223-80584224	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs67659266	chr4:80584279-80584280	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs147156869	chr4:80584287-80584288	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs57395415	chr4:80584300-80584301	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs561192278	chr4:80584308-80584309	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs546592915	chr4:80584319-80584320	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs530317781	chr4:80584321-80584322	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs546894713	chr4:80584337-80584338	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs140383034	chr4:80584386-80584387	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs566490506	chr4:80584408-80584409	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs199687532	chr4:80584440-80584441	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs191947360	chr4:80584491-80584492	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs551923680	chr4:80584492-80584493	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs6833807	chr4:80584512-80584513	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs147350941	chr4:80584552-80584553	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs114487530	chr4:80584619-80584620	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs148596956	chr4:80584623-80584624	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs111679345	chr4:80584648-80584649	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs534031808	chr4:80584670-80584671	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs554055709	chr4:80584698-80584699	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelodysplastic syndrome	18508791	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80578400-80578600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
2	chr4:80582400-80582800	Enhancers	NHEK	skin
3	chr4:80584000-80584600	Enhancers	Aorta	Aorta
4	chr4:80584000-80584600	Enhancers	Placenta	Placenta
5	chr4:80584400-80585200	Enhancers	Fetal Kidney	kidney
6	chr4:80584800-80585200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr4:80585200-80589400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr4:80594400-80596000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr4:80594600-80595800	Enhancers	Dnd41	blood
10	chr4:80594600-80596000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr4:80594600-80596000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr4:80594800-80595000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:80594800-80596000	Enhancers	Primary B cells from peripheral blood	blood
14	chr4:80594800-80596200	Enhancers	Primary hematopoietic stem cells	blood
15	chr4:80595400-80596000	Enhancers	Primary B cells from cord blood	blood
16	chr4:80595800-80597600	Weak transcription	Dnd41	blood
17	chr4:80596000-80597200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:80596000-80597800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr4:80596000-80598400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr4:80596200-80596600	Weak transcription	Primary hematopoietic stem cells	blood
21	chr4:80596600-80598400	Enhancers	Primary hematopoietic stem cells	blood
22	chr4:80597200-80597400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr4:80597400-80597800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr4:80597600-80599800	Enhancers	Dnd41	blood
25	chr4:80597800-80599800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:80597800-80601200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr4:80598000-80599800	Enhancers	K562	blood
28	chr4:80598400-80598800	Weak transcription	Primary hematopoietic stem cells	blood
29	chr4:80598400-80601000	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr4:80598600-80598800	Enhancers	Fetal Thymus	thymus
31	chr4:80598800-80599000	Enhancers	Primary hematopoietic stem cells	blood
32	chr4:80598800-80599800	Weak transcription	Fetal Thymus	thymus
33	chr4:80598800-80600800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr4:80599000-80599800	Weak transcription	Primary hematopoietic stem cells	blood
35	chr4:80599800-80600000	Enhancers	Aorta	Aorta
36	chr4:80599800-80600200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:80599800-80600200	Flanking Active TSS	K562	blood
38	chr4:80599800-80600200	Enhancers	NH-A	brain
39	chr4:80599800-80600600	Flanking Active TSS	Dnd41	blood
40	chr4:80599800-80601200	Enhancers	Primary hematopoietic stem cells	blood
41	chr4:80599800-80601600	Enhancers	Fetal Thymus	thymus
42	chr4:80600000-80604000	Weak transcription	Aorta	Aorta
43	chr4:80600200-80601200	Enhancers	K562	blood
44	chr4:80600200-80601400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr4:80600200-80603200	Weak transcription	NH-A	brain
46	chr4:80600600-80601600	Enhancers	Dnd41	blood
47	chr4:80601200-80606000	Weak transcription	Primary hematopoietic stem cells	blood
48	chr4:80601600-80605800	Weak transcription	Dnd41	blood
49	chr4:80602800-80604600	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr4:80603200-80604400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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