Variant report

Variant	esv10795
Chromosome Location	chr4:9508396-9745703
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1857)
CpG islands
(count:2811)
Chromatin interactive
region (count:7)
LncRNA
region (count:10)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1857 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9705188-9705304	HepG2	liver:	n/a	n/a
2	ATF1	chr4:9693437-9693703	K562	blood:	n/a	n/a
3	BACH1	chr4:9689846-9689882	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:9533750-9534097	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:9605857-9606056	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr4:9560693-9560899	GM12878	blood:	n/a	n/a
7	BATF	chr4:9661377-9661663	GM12878	blood:	n/a	n/a
8	BATF	chr4:9606281-9606749	GM12878	blood:	n/a	n/a
9	BATF	chr4:9606359-9606745	GM12878	blood:	n/a	n/a
10	BATF	chr4:9582818-9583030	GM12878	blood:	n/a	n/a
11	BATF	chr4:9697635-9697868	GM12878	blood:	n/a	n/a
12	BATF	chr4:9709608-9710002	GM12878	blood:	n/a	n/a
13	BATF	chr4:9582796-9583040	GM12878	blood:	n/a	n/a
14	BATF	chr4:9715614-9715953	GM12878	blood:	n/a	n/a
15	BATF	chr4:9637521-9637725	GM12878	blood:	n/a	n/a
16	BATF	chr4:9661312-9661676	GM12878	blood:	n/a	n/a
17	BATF	chr4:9560631-9560870	GM12878	blood:	n/a	n/a
18	BATF	chr4:9605704-9606128	GM12878	blood:	n/a	n/a
19	BATF	chr4:9609959-9610276	GM12878	blood:	n/a	n/a
20	BATF	chr4:9547853-9548038	GM12878	blood:	n/a	n/a
21	BATF	chr4:9609924-9610228	GM12878	blood:	n/a	n/a
22	BATF	chr4:9511928-9512224	GM12878	blood:	n/a	n/a
23	BATF	chr4:9709684-9709950	GM12878	blood:	n/a	n/a
24	BATF	chr4:9511904-9512243	GM12878	blood:	n/a	n/a
25	BCL11A	chr4:9606478-9606683	GM12878	blood:	n/a	n/a
26	BCL11A	chr4:9637557-9637806	GM12878	blood:	n/a	n/a
27	BCL11A	chr4:9709714-9709970	GM12878	blood:	n/a	n/a
28	BCL11A	chr4:9547498-9547747	GM12878	blood:	n/a	n/a
29	BCL11A	chr4:9605814-9606174	GM12878	blood:	n/a	n/a
30	BCL11A	chr4:9606348-9606693	GM12878	blood:	n/a	n/a
31	BCL11A	chr4:9609970-9610277	GM12878	blood:	n/a	n/a
32	BCL11A	chr4:9609991-9610319	GM12878	blood:	n/a	n/a
33	BCL11A	chr4:9605779-9606088	GM12878	blood:	n/a	n/a
34	BCL11A	chr4:9693955-9694191	GM12878	blood:	n/a	n/a
35	BCL11A	chr4:9661303-9661712	GM12878	blood:	n/a	n/a
36	BCL11A	chr4:9709736-9710003	GM12878	blood:	n/a	n/a
37	BHLHE40	chr4:9693347-9693648	GM12878	blood:	n/a	n/a
38	BHLHE40	chr4:9705121-9705321	K562	blood:	n/a	n/a
39	BHLHE40	chr4:9733756-9733953	K562	blood:	n/a	n/a
40	BHLHE40	chr4:9533811-9533913	K562	blood:	n/a	n/a
41	BHLHE40	chr4:9693184-9693740	K562	blood:	n/a	n/a
42	BHLHE40	chr4:9693135-9693538	HepG2	liver:	n/a	chr4:9693155-9693171
43	BHLHE40	chr4:9661297-9661608	HepG2	liver:	n/a	n/a
44	BHLHE40	chr4:9697620-9697865	HepG2	liver:	n/a	n/a
45	BHLHE40	chr4:9705080-9705313	GM12878	blood:	n/a	n/a
46	CBX3	chr4:9597420-9597667	K562	blood:	n/a	n/a
47	CBX3	chr4:9709655-9709945	K562	blood:	n/a	n/a
48	CCNT2	chr4:9693190-9693570	K562	blood:	n/a	n/a
49	CCNT2	chr4:9533734-9533999	K562	blood:	n/a	n/a
50	CEBPB	chr4:9530664-9530884	K562	blood:	n/a	n/a

(count:2811 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9537404-9537454	T-47D	breast:	n/a
2	chr4:9510286-9510336	HNPCEpiC	eye:	n/a
3	chr4:9693312-9693362	GM12892	blood:	n/a
4	chr4:9604780-9604830	AG10803	skin:	n/a
5	chr4:9534062-9534112	HEK293	kidney:	embryo
6	chr4:9537404-9537454	T-47D	breast:	n/a
7	chr4:9510286-9510336	HNPCEpiC	eye:	n/a
8	chr4:9693312-9693362	GM12892	blood:	n/a
9	chr4:9604780-9604830	AG10803	skin:	n/a
10	chr4:9534062-9534112	HEK293	kidney:	embryo
11	chr4:9534062-9534112	HepG2	liver:	n/a
12	chr4:9709042-9709092	HL-60	blood:	n/a
13	chr4:9692836-9692886	HIPEpiC	eye:	n/a
14	chr4:9510572-9510622	HRPEpiC	eye:	n/a
15	chr4:9514864-9514914	AG10803	skin:	n/a
16	chr4:9653008-9653058	NT2-D1	testis:	n/a
17	chr4:9510572-9510622	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:9653008-9653058	SK-N-MC	brain:	n/a
19	chr4:9514840-9514890	Caco-2	colon:	n/a
20	chr4:9534366-9534416	AG04449	skin:	fetal
21	chr4:9509830-9509880	HL-60	blood:	n/a
22	chr4:9604187-9604237	ECC-1	luminal epithelium:	n/a
23	chr4:9692836-9692886	GM06990	blood:	n/a
24	chr4:9509787-9509837	AoSMC	blood vessel:	n/a
25	chr4:9692836-9692886	HUVEC	blood vessel:	n/a
26	chr4:9689364-9689414	ProgFib	skin:	n/a
27	chr4:9661405-9661455	PFSK-1	brain:	n/a
28	chr4:9514810-9514860	HEEpiC	esophagus:	n/a
29	chr4:9523635-9523685	PFSK-1	brain:	n/a
30	chr4:9534313-9534363	SKMC	muscle:	n/a
31	chr4:9533426-9533476	IMR90	lung:	fetal
32	chr4:9696916-9696966	HRCEpiC	kidney:	n/a
33	chr4:9558077-9558127	HEK293	kidney:	embryo
34	chr4:9509830-9509880	NHBE	bronchial:	n/a
35	chr4:9604877-9604927	HRCEpiC	kidney:	n/a
36	chr4:9604187-9604237	BJ	skin:	n/a
37	chr4:9557805-9557855	IMR90	lung:	fetal
38	chr4:9509787-9509837	GM12892	blood:	n/a
39	chr4:9510572-9510622	HEEpiC	esophagus:	n/a
40	chr4:9534313-9534363	HMEC	breast:	n/a
41	chr4:9557805-9557855	GM12892	blood:	n/a
42	chr4:9693764-9693814	NHBE	bronchial:	n/a
43	chr4:9534313-9534363	HL-60	blood:	n/a
44	chr4:9558077-9558127	BE2_C	brain:	n/a
45	chr4:9523635-9523685	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:9510286-9510336	LNCaP	prostate:	n/a
47	chr4:9693516-9693566	PrEC	prostate:	n/a
48	chr4:9653008-9653058	SK-N-SH	brain:	n/a
49	chr4:9533426-9533476	HRCEpiC	kidney:	n/a
50	chr4:9523653-9523703	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:9699934..9701585-chr4:10019007..10021805,2	K562	blood:
2	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:
3	chr4:9705013..9706114-chr4:10020117..10020881,3	MCF-7	breast:
4	chr4:9704873..9705750-chr4:10016280..10017221,3	K562	blood:
5	chr4:9705037..9705657-chr4:9778184..9778690,2	K562	blood:
6	chr4:9704779..9705714-chr4:10015117..10016069,5	MCF-7	breast:
7	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1396O13.13.1-3	chr4:9555234-9555605	NONHSAT095137
2	lnc-SLC2A9-1	chr4:9691882-9692319	XLOC_003881
3	lnc-DRD5-15	chr4:9680112-9680551	l_2602_chr4:9680111-9682135_thyroid
4	lnc-DRD5-15	chr4:9681973-9682135	l_2602_chr4:9680111-9682135_thyroid
5	lnc-SLC2A9-6	chr4:9681968-9682164	l_2603_chr4:9680179-9682164_kidney
6	lnc-SLC2A9-1	chr4:9686325-9686330	XLOC_003881
7	lnc-DRD5-16	chr4:9678932-9679558	NONHSAT095141
8	lnc-SLC2A9-2	chr4:9693361-9693365	XLOC_003880
9	lnc-SLC2A9-6	chr4:9680180-9680546	l_2603_chr4:9680179-9682164_kidney
10	lnc-SLC2A9-2	chr4:9682416-9682671	XLOC_003880

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548i	chr4:9557878-9557899	MIMAT0005935_1

No data

Variant related genes	Relation type
ENSG00000249799	TF binding region
ENPP7P11	TF binding region
MIR548I2	TF binding region
FAM86MP	TF binding region
ENSG00000249443	TF binding region
ENSG00000249563	TF binding region
OR7E83P	TF binding region
ALG1L3P	TF binding region
ENSG00000265901	TF binding region
ENSG00000242034	TF binding region
ENSG00000244004	TF binding region
ENSG00000249799	CpG island
ENPP7P11	CpG island
MIR548I2	CpG island
FAM86MP	CpG island
ENSG00000249443	CpG island
ENSG00000249563	CpG island
OR7E83P	CpG island
ALG1L3P	CpG island
ENSG00000265901	CpG island
ENSG00000242034	CpG island
ENSG00000244004	CpG island
ENSG00000109667	chromatin interactions
FBXW7	miRNA target sites

Extended variants
information (count: 15107 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:15107 , 50 per page) page: 1 2 3 4 5 6 7 ... 303

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561829658	chr4:9509402-9509403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149759845	chr4:9509420-9509421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188317177	chr4:9509423-9509424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs193030503	chr4:9509424-9509425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145877814	chr4:9509429-9509430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562978678	chr4:9509432-9509433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533584776	chr4:9509435-9509436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185772775	chr4:9509447-9509448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148577161	chr4:9509457-9509458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189899453	chr4:9509465-9509466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549035539	chr4:9509470-9509471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145592249	chr4:9509476-9509477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531353137	chr4:9509477-9509478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549856959	chr4:9509481-9509482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112784902	chr4:9509486-9509487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538847557	chr4:9509487-9509488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553748436	chr4:9509488-9509489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565670287	chr4:9509496-9509497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142113009	chr4:9509498-9509499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182108820	chr4:9509524-9509525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185422595	chr4:9509529-9509530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116568019	chr4:9509538-9509539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs544342975	chr4:9509553-9509554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188722791	chr4:9509570-9509571	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs181205385	chr4:9509571-9509572	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs528685379	chr4:9509595-9509596	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs184926346	chr4:9509629-9509630	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs528020507	chr4:9509634-9509635	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs191099508	chr4:9509639-9509640	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs145860165	chr4:9509648-9509649	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs531340629	chr4:9509658-9509659	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs549582097	chr4:9509682-9509683	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs542396382	chr4:9509683-9509684	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs183755569	chr4:9509692-9509693	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs11724460	chr4:9509698-9509699	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs530636980	chr4:9509712-9509713	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs565632940	chr4:9509747-9509748	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs536179003	chr4:9509788-9509789	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs2086431	chr4:9509791-9509792	Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs187596537	chr4:9509797-9509798	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs72488982	chr4:9509822-9509823	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs386671490	chr4:9509831-9509832	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs370959128	chr4:9509837-9509838	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs545251541	chr4:9509841-9509842	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs373149416	chr4:9509848-9509849	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs191518148	chr4:9509851-9509852	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs543304108	chr4:9509862-9509863	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs80273983	chr4:9509865-9509866	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs183180129	chr4:9509868-9509869	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs543439172	chr4:9509869-9509870	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9509400-9509800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
2	chr4:9515400-9515800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:9521400-9522000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr4:9521400-9522200	Enhancers	Muscle Satellite Cultured Cells	--
5	chr4:9522000-9522200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:9522000-9522600	Enhancers	Fetal Muscle Trunk	muscle
7	chr4:9522600-9523600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr4:9523600-9523800	Enhancers	Fetal Muscle Trunk	muscle
9	chr4:9530000-9532400	Enhancers	Fetal Thymus	thymus
10	chr4:9530800-9532000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr4:9531000-9531400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:9531000-9531400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:9531000-9531400	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr4:9531000-9531800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr4:9531000-9531800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr4:9531000-9531800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:9531000-9531800	Enhancers	Primary hematopoietic stem cells	blood
18	chr4:9531000-9531800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr4:9531000-9531800	Enhancers	Fetal Muscle Trunk	muscle
20	chr4:9531000-9532000	Enhancers	H1 Cell Line	embryonic stem cell
21	chr4:9531000-9532000	Enhancers	Fetal Muscle Leg	muscle
22	chr4:9531000-9532200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:9531000-9532200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr4:9531200-9531400	Enhancers	Thymus	Thymus
25	chr4:9531200-9531600	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr4:9531200-9532000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr4:9531200-9532400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr4:9531400-9531600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
29	chr4:9531400-9531800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:9531600-9531800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr4:9531600-9533600	Weak transcription	Thymus	Thymus
32	chr4:9531800-9533600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr4:9531800-9533800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr4:9531800-9534000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr4:9531800-9534000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:9531800-9534000	Weak transcription	Primary hematopoietic stem cells	blood
37	chr4:9532000-9532400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
38	chr4:9532000-9533200	Weak transcription	Fetal Muscle Leg	muscle
39	chr4:9532000-9533600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr4:9532400-9533600	Weak transcription	Fetal Thymus	thymus
41	chr4:9533200-9533400	Enhancers	Fetal Muscle Leg	muscle
42	chr4:9533200-9533600	Enhancers	Spleen	Spleen
43	chr4:9533400-9533800	Weak transcription	Fetal Muscle Leg	muscle
44	chr4:9533400-9534000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
45	chr4:9533400-9534000	Enhancers	Lung	lung
46	chr4:9533600-9533800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
47	chr4:9533600-9533800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr4:9533600-9533800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
49	chr4:9533600-9533800	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr4:9533600-9533800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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