Variant report

Variant	nsv878640
Chromosome Location	chr4:9335853-9470222
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	BATF	chr4:9382976-9383219	GM12878	blood:	n/a	n/a
3	BATF	chr4:9456872-9457051	GM12878	blood:	n/a	n/a
4	BATF	chr4:9383032-9383262	GM12878	blood:	n/a	n/a
5	BATF	chr4:9431784-9432036	GM12878	blood:	n/a	n/a
6	BATF	chr4:9390689-9391024	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:9390633-9391020	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:9390780-9390984	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:9382943-9383169	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:9390742-9390935	GM12878	blood:	n/a	n/a
11	BRCA1	chr4:9352626-9352812	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:9387057-9387237	HepG2	liver:	n/a	chr4:9387117-9387128
13	CEBPB	chr4:9453481-9453664	HepG2	liver:	n/a	chr4:9453618-9453629
14	CEBPB	chr4:9430641-9430768	HepG2	liver:	n/a	chr4:9430673-9430686 chr4:9430674-9430685
15	CEBPB	chr4:9405866-9406215	HepG2	liver:	n/a	chr4:9406025-9406038 chr4:9406027-9406036 chr4:9406027-9406038 chr4:9406025-9406036 chr4:9406027-9406036 chr4:9406027-9406036 chr4:9406027-9406036
16	CEBPB	chr4:9405910-9406125	K562	blood:	n/a	chr4:9406025-9406038 chr4:9406027-9406036 chr4:9406027-9406038 chr4:9406025-9406036 chr4:9406027-9406036 chr4:9406027-9406036 chr4:9406027-9406036
17	CEBPB	chr4:9405864-9406123	A549	lung:	n/a	chr4:9406025-9406038 chr4:9406027-9406036 chr4:9406027-9406038 chr4:9406025-9406036 chr4:9406027-9406036 chr4:9406027-9406036 chr4:9406027-9406036
18	CTCF	chr4:9456833-9457043	K562	blood:	n/a	n/a
19	CTCF	chr4:9435188-9435315	Gliobla	brain:	n/a	n/a
20	CTCF	chr4:9373061-9373177	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr4:9383240-9383390	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr4:9382900-9383050	GM12865	blood:	n/a	n/a
23	CTCF	chr4:9383200-9383350	GM12865	blood:	n/a	n/a
24	CTCF	chr4:9435163-9435356	MCF-7	breast:	n/a	n/a
25	CTCF	chr4:9383096-9383259	HUVEC	blood vessel:	n/a	chr4:9383162-9383180 chr4:9383144-9383165 chr4:9383150-9383166 chr4:9383149-9383167 chr4:9383164-9383185
26	CTCF	chr4:9431855-9432080	A549	lung:	n/a	n/a
27	CTCF	chr4:9383220-9383370	HVMF	connective:	n/a	n/a
28	CTCF	chr4:9383047-9383276	ProgFib	skin:	n/a	chr4:9383162-9383180 chr4:9383144-9383165 chr4:9383150-9383166 chr4:9383149-9383167 chr4:9383164-9383185
29	CTCF	chr4:9383240-9383390	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr4:9435188-9435317	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:9382903-9383401	K562	blood:	n/a	chr4:9383162-9383180 chr4:9383144-9383165 chr4:9383150-9383166 chr4:9383149-9383167 chr4:9383164-9383185
32	CTCF	chr4:9431910-9432019	K562	blood:	n/a	n/a
33	CTCF	chr4:9383220-9383370	HL-60	blood:	n/a	n/a
34	CTCF	chr4:9383039-9383277	H1-hESC	embryonic stem cell:	n/a	chr4:9383162-9383180 chr4:9383144-9383165 chr4:9383150-9383166 chr4:9383149-9383167 chr4:9383164-9383185
35	CTCF	chr4:9382900-9383050	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr4:9435155-9435368	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:9431718-9432113	A549	lung:	n/a	n/a
38	CTCF	chr4:9382900-9383050	HFF	foreskin:	n/a	n/a
39	CTCF	chr4:9383024-9383319	GM10266	blood:	n/a	chr4:9383162-9383180 chr4:9383144-9383165 chr4:9383150-9383166 chr4:9383149-9383167 chr4:9383164-9383185
40	CTCF	chr4:9383023-9383294	NHEK	skin:	n/a	chr4:9383162-9383180 chr4:9383144-9383165 chr4:9383150-9383166 chr4:9383149-9383167 chr4:9383164-9383185
41	CTCF	chr4:9382900-9383050	HPF	lung:	n/a	n/a
42	CTCF	chr4:9382900-9383050	HRE	kidney:	n/a	n/a
43	CTCF	chr4:9417107-9417197	Lung_OC	lung:	n/a	n/a
44	CTCF	chr4:9445923-9445974	LNCaP	prostate:	n/a	n/a
45	CTCF	chr4:9431866-9432069	GM19238	blood:	n/a	n/a
46	CTCF	chr4:9382900-9383050	HepG2	liver:	n/a	n/a
47	CTCF	chr4:9383240-9383390	RPTEC	kidney:	n/a	n/a
48	CTCF	chr4:9431835-9432103	Gliobla	brain:	n/a	n/a
49	CTCF	chr4:9376999-9377235	K562	blood:	n/a	chr4:9377043-9377064
50	CTCF	chr4:9383240-9383390	HPF	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9445586-9445636	SKMC	muscle:	n/a
2	chr4:9382961-9383011	IMR90	lung:	fetal
3	chr4:9355351-9355401	RPTEC	kidney:	n/a
4	chr4:9352827-9352877	SAEC	small airway:	n/a
5	chr4:9352827-9352877	HEK293	kidney:	embryo
6	chr4:9445586-9445636	SKMC	muscle:	n/a
7	chr4:9382961-9383011	IMR90	lung:	fetal
8	chr4:9355351-9355401	RPTEC	kidney:	n/a
9	chr4:9352827-9352877	SAEC	small airway:	n/a
10	chr4:9352827-9352877	HEK293	kidney:	embryo
11	chr4:9383942-9383992	HRE	kidney:	n/a
12	chr4:9457681-9457731	AG04449	skin:	fetal
13	chr4:9445586-9445636	HRPEpiC	eye:	n/a
14	chr4:9445586-9445636	NH-A	brain:	n/a
15	chr4:9383942-9383992	HL-60	blood:	n/a
16	chr4:9457681-9457731	HRE	kidney:	n/a
17	chr4:9355351-9355401	HCT-116	colon:	n/a
18	chr4:9355372-9355422	HRCEpiC	kidney:	n/a
19	chr4:9453650-9453700	HCF	heart:	n/a
20	chr4:9355351-9355401	BJ	skin:	n/a
21	chr4:9457537-9457587	HEK293	kidney:	embryo
22	chr4:9383942-9383992	HCM	heart:	n/a
23	chr4:9371043-9371093	MCF10A-Er-Src	breast:	n/a
24	chr4:9385754-9385804	HepG2	liver:	n/a
25	chr4:9352827-9352877	HCPEpiC	choroid plexus:	n/a
26	chr4:9352827-9352877	HEEpiC	esophagus:	n/a
27	chr4:9382953-9383003	T-47D	breast:	n/a
28	chr4:9352827-9352877	GM12878	blood:	n/a
29	chr4:9382066-9382116	NHDF-neo	bronchial:	n/a
30	chr4:9445158-9445208	HRPEpiC	eye:	n/a
31	chr4:9352827-9352877	HL-60	blood:	n/a
32	chr4:9379166-9379216	SK-N-SH	brain:	n/a
33	chr4:9457537-9457587	ovcar-3	ovarian:	n/a
34	chr4:9352827-9352877	T-47D	breast:	n/a
35	chr4:9379166-9379216	H1-hESC	embryonic stem cell:	embryo
36	chr4:9355351-9355401	HRPEpiC	eye:	n/a
37	chr4:9457681-9457731	BE2_C	brain:	n/a
38	chr4:9355372-9355422	PFSK-1	brain:	n/a
39	chr4:9453084-9453134	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:9385754-9385804	HRCEpiC	kidney:	n/a
41	chr4:9453650-9453700	NB4	blood:	n/a
42	chr4:9379166-9379216	HepG2	liver:	n/a
43	chr4:9382961-9383011	T-47D	breast:	n/a
44	chr4:9382961-9383011	HIPEpiC	eye:	n/a
45	chr4:9355372-9355422	Hepatocyte	liver:	n/a
46	chr4:9385754-9385804	T-47D	breast:	n/a
47	chr4:9457537-9457587	HepG2	liver:	n/a
48	chr4:9371392-9371442	HCF	heart:	n/a
49	chr4:9445586-9445636	RPTEC	kidney:	n/a
50	chr4:9457537-9457587	BJ	skin:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1396O13.13.1-1	chr4:9388003-9388085	XLOC_003878
2	lnc-RP11-1396O13.13.1-2	chr4:9390589-9390785	l_2601_chr4:9381878-9390785_kidney
3	lnc-RP11-1396O13.13.1-1	chr4:9387384-9387466	XLOC_003878
4	lnc-RP11-1396O13.13.1-1	chr4:9376809-9376876	XLOC_003878
5	lnc-RP11-1396O13.13.1-2	chr4:9381879-9382091	l_2601_chr4:9381878-9390785_kidney

Variant related genes	Relation type
RNA5SP153	TF binding region
ENSG00000266246	TF binding region
ENSG00000232773	TF binding region
OR7E84P	TF binding region
USP17L29	TF binding region
OR7E86P	TF binding region
ENSG00000219492	TF binding region
DEFB131	TF binding region
USP17L9P	TF binding region
USP17L5	TF binding region
USP17L30	TF binding region
ENSG00000188438	TF binding region
USP17L26	TF binding region
USP17L6P	TF binding region
USP17L27	TF binding region
USP17L28	TF binding region
RNA5SP153	CpG island
ENSG00000266246	CpG island
ENSG00000232773	CpG island
OR7E84P	CpG island
USP17L29	CpG island
OR7E86P	CpG island
ENSG00000219492	CpG island
DEFB131	CpG island
USP17L9P	CpG island
USP17L5	CpG island
USP17L30	CpG island
ENSG00000188438	CpG island
USP17L26	CpG island
USP17L6P	CpG island
USP17L27	CpG island
USP17L28	CpG island

Extended variants
information (count: 1382 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1382 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201282879	chr4:9352692-9352693	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs199777440	chr4:9352801-9352802	Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs538004740	chr4:9355388-9355389	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs528711746	chr4:9361104-9361105	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs148542026	chr4:9361112-9361113	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs546949225	chr4:9361123-9361124	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs562382092	chr4:9361166-9361167	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs200909464	chr4:9361177-9361178	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs62411732	chr4:9361199-9361200	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs151101082	chr4:9361227-9361228	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs371122734	chr4:9361305-9361306	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs141044478	chr4:9361342-9361343	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs143768469	chr4:9361351-9361352	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs146882260	chr4:9361362-9361363	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs140706735	chr4:9361370-9361371	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs375893498	chr4:9361371-9361372	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs145274487	chr4:9361398-9361399	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs112333937	chr4:9362201-9362202	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs112907537	chr4:9362341-9362342	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs138313496	chr4:9366832-9366833	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs149564237	chr4:9366834-9366835	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs140840527	chr4:9366840-9366841	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs150130936	chr4:9366853-9366854	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs138665907	chr4:9366866-9366867	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs149317389	chr4:9366875-9366876	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs143261933	chr4:9366885-9366886	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs138807362	chr4:9366887-9366888	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs562307825	chr4:9376820-9376821	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs532979579	chr4:9376855-9376856	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs544853678	chr4:9376869-9376870	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs7440028	chr4:9381891-9381892	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs536363150	chr4:9381895-9381896	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs6449098	chr4:9381935-9381936	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs192928279	chr4:9381951-9381952	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs574280001	chr4:9381953-9381954	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs544056016	chr4:9381986-9381987	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs558979955	chr4:9381997-9381998	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs577514796	chr4:9382002-9382003	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs541008304	chr4:9382009-9382010	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs11727028	chr4:9382025-9382026	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs6414762	chr4:9382029-9382030	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs184099936	chr4:9382034-9382035	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs188361290	chr4:9382038-9382039	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs530627305	chr4:9382045-9382046	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs368484663	chr4:9382062-9382063	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs181818679	chr4:9382080-9382081	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs372388208	chr4:9382081-9382082	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs533530199	chr4:9382430-9382431	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545657344	chr4:9382435-9382436	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs62411755	chr4:9382510-9382511	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21858162	CNVD
Breast cancer	22522925	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:137 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9352600-9352800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:9352600-9353000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:9352600-9353000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:9352600-9353000	ZNF genes & repeats	Gastric	stomach
5	chr4:9352600-9353000	ZNF genes & repeats	Pancreas	Pancrea
6	chr4:9352600-9353000	ZNF genes & repeats	Spleen	Spleen
7	chr4:9352800-9353000	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:9382400-9382600	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr4:9382400-9382600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr4:9382400-9382600	Enhancers	Colonic Mucosa	Colon
11	chr4:9382400-9382600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr4:9382400-9382600	Enhancers	Pancreas	Pancrea
13	chr4:9382400-9382600	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr4:9382400-9382800	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr4:9382400-9383000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr4:9382400-9383200	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr4:9382400-9383200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr4:9382400-9383200	Active TSS	Duodenum Mucosa	Duodenum
19	chr4:9382600-9382800	Enhancers	Primary T cells fromperipheralblood	blood
20	chr4:9382600-9382800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:9382600-9382800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:9382600-9382800	Enhancers	Fetal Muscle Leg	muscle
23	chr4:9382600-9382800	Enhancers	Lung	lung
24	chr4:9382600-9382800	Enhancers	Psoas Muscle	Psoas
25	chr4:9382600-9383000	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr4:9382600-9383000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr4:9382600-9383000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr4:9382600-9383000	Enhancers	Adipose Nuclei	Adipose
29	chr4:9382600-9383000	Active TSS	Brain Angular Gyrus	brain
30	chr4:9382600-9383000	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr4:9382600-9383000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
32	chr4:9382600-9383000	Flanking Active TSS	Colonic Mucosa	Colon
33	chr4:9382600-9383000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
34	chr4:9382600-9383000	Flanking Active TSS	Pancreas	Pancrea
35	chr4:9382600-9383000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr4:9382600-9383000	Active TSS	NH-A	brain
37	chr4:9382600-9383200	Active TSS	ES-I3 Cell Line	embryonic stem cell
38	chr4:9382600-9383200	Enhancers	Primary hematopoietic stem cells	blood
39	chr4:9382600-9383200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
40	chr4:9382600-9383200	Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr4:9382600-9383200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:9382600-9383200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr4:9382600-9383200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr4:9382600-9383200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:9382600-9383200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:9382600-9383200	Active TSS	Colon Smooth Muscle	Colon
47	chr4:9382600-9383200	Active TSS	Fetal Brain Female	brain
48	chr4:9382600-9383200	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr4:9382600-9383200	Active TSS	Rectal Smooth Muscle	rectum
50	chr4:9382600-9383200	Active TSS	Skeletal Muscle Male	skeletal muscle

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