Variant report

Variant	nsv1006342
Chromosome Location	chr4:9370690-9678661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1742)
CpG islands
(count:5801)
Chromatin interactive
region (count:4)
LncRNA
region (count:7)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1742 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9454189-9454353	HepG2	liver:	n/a	n/a
2	BACH1	chr4:9605857-9606056	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:9533750-9534097	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:9661377-9661663	GM12878	blood:	n/a	n/a
5	BATF	chr4:9609924-9610228	GM12878	blood:	n/a	n/a
6	BATF	chr4:9560693-9560899	GM12878	blood:	n/a	n/a
7	BATF	chr4:9582796-9583040	GM12878	blood:	n/a	n/a
8	BATF	chr4:9582818-9583030	GM12878	blood:	n/a	n/a
9	BATF	chr4:9661312-9661676	GM12878	blood:	n/a	n/a
10	BATF	chr4:9456872-9457051	GM12878	blood:	n/a	n/a
11	BATF	chr4:9496997-9497347	GM12878	blood:	n/a	n/a
12	BATF	chr4:9382976-9383219	GM12878	blood:	n/a	n/a
13	BATF	chr4:9605704-9606128	GM12878	blood:	n/a	n/a
14	BATF	chr4:9511928-9512224	GM12878	blood:	n/a	n/a
15	BATF	chr4:9481132-9481453	GM12878	blood:	n/a	n/a
16	BATF	chr4:9481131-9481403	GM12878	blood:	n/a	n/a
17	BATF	chr4:9431784-9432036	GM12878	blood:	n/a	n/a
18	BATF	chr4:9606281-9606749	GM12878	blood:	n/a	n/a
19	BATF	chr4:9383032-9383262	GM12878	blood:	n/a	n/a
20	BATF	chr4:9547853-9548038	GM12878	blood:	n/a	n/a
21	BATF	chr4:9606359-9606745	GM12878	blood:	n/a	n/a
22	BATF	chr4:9609959-9610276	GM12878	blood:	n/a	n/a
23	BATF	chr4:9560631-9560870	GM12878	blood:	n/a	n/a
24	BATF	chr4:9390689-9391024	GM12878	blood:	n/a	n/a
25	BATF	chr4:9637521-9637725	GM12878	blood:	n/a	n/a
26	BATF	chr4:9511904-9512243	GM12878	blood:	n/a	n/a
27	BCL11A	chr4:9605814-9606174	GM12878	blood:	n/a	n/a
28	BCL11A	chr4:9637557-9637806	GM12878	blood:	n/a	n/a
29	BCL11A	chr4:9606478-9606683	GM12878	blood:	n/a	n/a
30	BCL11A	chr4:9605779-9606088	GM12878	blood:	n/a	n/a
31	BCL11A	chr4:9382943-9383169	GM12878	blood:	n/a	n/a
32	BCL11A	chr4:9609991-9610319	GM12878	blood:	n/a	n/a
33	BCL11A	chr4:9547498-9547747	GM12878	blood:	n/a	n/a
34	BCL11A	chr4:9606348-9606693	GM12878	blood:	n/a	n/a
35	BCL11A	chr4:9497025-9497432	GM12878	blood:	n/a	chr4:9497121-9497129
36	BCL11A	chr4:9390633-9391020	GM12878	blood:	n/a	n/a
37	BCL11A	chr4:9661303-9661712	GM12878	blood:	n/a	n/a
38	BCL11A	chr4:9609970-9610277	GM12878	blood:	n/a	n/a
39	BCL11A	chr4:9390780-9390984	GM12878	blood:	n/a	n/a
40	BHLHE40	chr4:9533811-9533913	K562	blood:	n/a	n/a
41	BHLHE40	chr4:9661297-9661608	HepG2	liver:	n/a	n/a
42	BHLHE40	chr4:9390742-9390935	GM12878	blood:	n/a	n/a
43	CBX3	chr4:9597420-9597667	K562	blood:	n/a	n/a
44	CCNT2	chr4:9533734-9533999	K562	blood:	n/a	n/a
45	CEBPB	chr4:9430641-9430768	HepG2	liver:	n/a	chr4:9430673-9430686 chr4:9430674-9430685
46	CEBPB	chr4:9387057-9387237	HepG2	liver:	n/a	chr4:9387117-9387128
47	CEBPB	chr4:9639784-9639891	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr4:9585906-9586106	HepG2	liver:	n/a	chr4:9585991-9586002
49	CEBPB	chr4:9453481-9453664	HepG2	liver:	n/a	chr4:9453618-9453629
50	CEBPB	chr4:9596784-9597029	HepG2	liver:	n/a	chr4:9596883-9596894

(count:5801 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9514810-9514860	SK-N-MC	brain:	n/a
2	chr4:9383942-9383992	GM12892	blood:	n/a
3	chr4:9482233-9482283	HMEC	breast:	n/a
4	chr4:9379166-9379216	PANC-1	pancreas:	n/a
5	chr4:9533948-9533998	IMR90	lung:	fetal
6	chr4:9383942-9383992	AG10803	skin:	n/a
7	chr4:9514810-9514860	SK-N-MC	brain:	n/a
8	chr4:9383942-9383992	GM12892	blood:	n/a
9	chr4:9482233-9482283	HMEC	breast:	n/a
10	chr4:9379166-9379216	PANC-1	pancreas:	n/a
11	chr4:9533948-9533998	IMR90	lung:	fetal
12	chr4:9383942-9383992	AG10803	skin:	n/a
13	chr4:9494211-9494261	HL-60	blood:	n/a
14	chr4:9493536-9493586	SAEC	small airway:	n/a
15	chr4:9514810-9514860	HRCEpiC	kidney:	n/a
16	chr4:9558893-9558943	ECC-1	luminal epithelium:	n/a
17	chr4:9493231-9493281	HNPCEpiC	eye:	n/a
18	chr4:9523653-9523703	AG04449	skin:	fetal
19	chr4:9493231-9493281	NHBE	bronchial:	n/a
20	chr4:9514810-9514860	PrEC	prostate:	n/a
21	chr4:9494211-9494261	LNCaP	prostate:	n/a
22	chr4:9604340-9604390	RPTEC	kidney:	n/a
23	chr4:9385754-9385804	AG09319	gingival:	n/a
24	chr4:9509787-9509837	SKMC	muscle:	n/a
25	chr4:9558077-9558127	HCF	heart:	n/a
26	chr4:9537404-9537454	GM12878	blood:	n/a
27	chr4:9537404-9537454	HCPEpiC	choroid plexus:	n/a
28	chr4:9661422-9661472	HRPEpiC	eye:	n/a
29	chr4:9558077-9558127	Jurkat	blood:	n/a
30	chr4:9534041-9534091	RPTEC	kidney:	n/a
31	chr4:9479947-9479997	NT2-D1	testis:	n/a
32	chr4:9509787-9509837	Hela-S3	cervix:	n/a
33	chr4:9484735-9484785	T-47D	breast:	n/a
34	chr4:9495205-9495255	GM12892	blood:	n/a
35	chr4:9494487-9494537	CMK	blood:	n/a
36	chr4:9371392-9371442	HRPEpiC	eye:	n/a
37	chr4:9508177-9508227	IMR90	lung:	fetal
38	chr4:9510572-9510622	PANC-1	pancreas:	n/a
39	chr4:9371392-9371442	HCPEpiC	choroid plexus:	n/a
40	chr4:9453010-9453060	NHBE	bronchial:	n/a
41	chr4:9557805-9557855	AG09309	skin:	n/a
42	chr4:9661422-9661472	NT2-D1	testis:	n/a
43	chr4:9482233-9482283	T-47D	breast:	n/a
44	chr4:9497357-9497407	HCM	heart:	n/a
45	chr4:9478126-9478176	MCF-7	breast:	n/a
46	chr4:9604877-9604927	PFSK-1	brain:	n/a
47	chr4:9510572-9510622	HCM	heart:	n/a
48	chr4:9371392-9371442	PANC-1	pancreas:	n/a
49	chr4:9379166-9379216	BJ	skin:	n/a
50	chr4:9534366-9534416	HIPEpiC	eye:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:
2	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:
3	chr4:4147469..4148009-chr4:9497278..9497791,2	MCF-7	breast:
4	chr4:4147498..4148004-chr4:9497288..9497793,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1396O13.13.1-2	chr4:9381879-9382091	l_2601_chr4:9381878-9390785_kidney
2	lnc-RP11-1396O13.13.1-1	chr4:9376809-9376876	XLOC_003878
3	lnc-RP11-1396O13.13.1-3	chr4:9555234-9555605	NONHSAT095137
4	lnc-DEFB131-1	chr4:9470746-9471694	NONHSAT095133
5	lnc-RP11-1396O13.13.1-1	chr4:9388003-9388085	XLOC_003878
6	lnc-RP11-1396O13.13.1-1	chr4:9387384-9387466	XLOC_003878
7	lnc-RP11-1396O13.13.1-2	chr4:9390589-9390785	l_2601_chr4:9381878-9390785_kidney

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

No data

Variant related genes	Relation type
RNA5SP153	TF binding region
OR7E85P	TF binding region
ENSG00000266246	TF binding region
ENSG00000249799	TF binding region
ENPP7P11	TF binding region
ENSG00000232773	TF binding region
OR7E84P	TF binding region
OR7E86P	TF binding region
ENSG00000219492	TF binding region
MIR548I2	TF binding region
DEFB131	TF binding region
ENSG00000249443	TF binding region
UNC93B7	TF binding region
ENSG00000188438	TF binding region
OR7E83P	TF binding region
ENSG00000265901	TF binding region
ENSG00000242034	TF binding region
ENSG00000244004	TF binding region
RNA5SP153	CpG island
OR7E85P	CpG island
ENSG00000266246	CpG island
ENSG00000249799	CpG island
ENPP7P11	CpG island
ENSG00000232773	CpG island
OR7E84P	CpG island
OR7E86P	CpG island
ENSG00000219492	CpG island
MIR548I2	CpG island
DEFB131	CpG island
ENSG00000249443	CpG island
UNC93B7	CpG island
ENSG00000188438	CpG island
OR7E83P	CpG island
ENSG00000265901	CpG island
ENSG00000242034	CpG island
ENSG00000244004	CpG island

Extended variants
information (count: 14086 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:14086 , 50 per page) page: 1 2 3 4 5 6 7 ... 282

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562307825	chr4:9376820-9376821	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs532979579	chr4:9376855-9376856	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs544853678	chr4:9376869-9376870	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs7440028	chr4:9381891-9381892	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs536363150	chr4:9381895-9381896	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs6449098	chr4:9381935-9381936	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs192928279	chr4:9381951-9381952	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs574280001	chr4:9381953-9381954	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs544056016	chr4:9381986-9381987	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs558979955	chr4:9381997-9381998	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs577514796	chr4:9382002-9382003	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs541008304	chr4:9382009-9382010	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs11727028	chr4:9382025-9382026	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs6414762	chr4:9382029-9382030	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs184099936	chr4:9382034-9382035	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs188361290	chr4:9382038-9382039	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs530627305	chr4:9382045-9382046	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs368484663	chr4:9382062-9382063	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs181818679	chr4:9382080-9382081	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs372388208	chr4:9382081-9382082	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs533530199	chr4:9382430-9382431	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545657344	chr4:9382435-9382436	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs62411755	chr4:9382510-9382511	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs528342851	chr4:9382547-9382548	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187011672	chr4:9382548-9382549	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565696989	chr4:9382571-9382572	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530030539	chr4:9382607-9382608	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369686640	chr4:9382612-9382613	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10008799	chr4:9382654-9382655	Active TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs570031296	chr4:9382661-9382662	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs527374621	chr4:9382685-9382686	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190999033	chr4:9382706-9382707	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs4246700	chr4:9382730-9382731	Active TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs535286238	chr4:9382732-9382733	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115999260	chr4:9382743-9382744	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575247746	chr4:9382770-9382771	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567263375	chr4:9382775-9382776	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535440175	chr4:9382782-9382783	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556944253	chr4:9382784-9382785	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575232366	chr4:9382788-9382789	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143915901	chr4:9382793-9382794	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs28422470	chr4:9382804-9382805	Active TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs550059103	chr4:9382817-9382818	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374284468	chr4:9382841-9382842	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572711259	chr4:9382847-9382848	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540080728	chr4:9382852-9382853	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571367529	chr4:9382863-9382864	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs34796356	chr4:9382871-9382872	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527524346	chr4:9382878-9382879	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139713415	chr4:9382891-9382892	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Melanoma	20688739	CNVD
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
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	21858162	CNVD
Breast cancer	22522925	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1065 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9382400-9382600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr4:9382400-9382600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr4:9382400-9382600	Enhancers	Colonic Mucosa	Colon
4	chr4:9382400-9382600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr4:9382400-9382600	Enhancers	Pancreas	Pancrea
6	chr4:9382400-9382600	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr4:9382400-9382800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr4:9382400-9383000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr4:9382400-9383200	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr4:9382400-9383200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:9382400-9383200	Active TSS	Duodenum Mucosa	Duodenum
12	chr4:9382600-9382800	Enhancers	Primary T cells fromperipheralblood	blood
13	chr4:9382600-9382800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr4:9382600-9382800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:9382600-9382800	Enhancers	Fetal Muscle Leg	muscle
16	chr4:9382600-9382800	Enhancers	Lung	lung
17	chr4:9382600-9382800	Enhancers	Psoas Muscle	Psoas
18	chr4:9382600-9383000	Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chr4:9382600-9383000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
20	chr4:9382600-9383000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:9382600-9383000	Enhancers	Adipose Nuclei	Adipose
22	chr4:9382600-9383000	Active TSS	Brain Angular Gyrus	brain
23	chr4:9382600-9383000	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr4:9382600-9383000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr4:9382600-9383000	Flanking Active TSS	Colonic Mucosa	Colon
26	chr4:9382600-9383000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
27	chr4:9382600-9383000	Flanking Active TSS	Pancreas	Pancrea
28	chr4:9382600-9383000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr4:9382600-9383000	Active TSS	NH-A	brain
30	chr4:9382600-9383200	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr4:9382600-9383200	Enhancers	Primary hematopoietic stem cells	blood
32	chr4:9382600-9383200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
33	chr4:9382600-9383200	Active TSS	Primary T helper cells fromperipheralblood	blood
34	chr4:9382600-9383200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr4:9382600-9383200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr4:9382600-9383200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr4:9382600-9383200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr4:9382600-9383200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:9382600-9383200	Active TSS	Colon Smooth Muscle	Colon
40	chr4:9382600-9383200	Active TSS	Fetal Brain Female	brain
41	chr4:9382600-9383200	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr4:9382600-9383200	Active TSS	Rectal Smooth Muscle	rectum
43	chr4:9382600-9383200	Active TSS	Skeletal Muscle Male	skeletal muscle
44	chr4:9382600-9383200	Active TSS	Stomach Smooth Muscle	stomach
45	chr4:9382800-9383000	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr4:9382800-9383000	Enhancers	Primary B cells from peripheral blood	blood
47	chr4:9382800-9383000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
48	chr4:9382800-9383000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr4:9382800-9383000	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr4:9382800-9383000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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