Variant report

Variant	nsv1033815
Chromosome Location	chr6:44845514-44938799
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:505)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:44918920-44919276	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:44888556-44889970	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:44934203-44935340	K562	blood:	n/a	n/a
4	ARID3A	chr6:44900932-44900942	K562	blood:	n/a	n/a
5	ARID3A	chr6:44928633-44929024	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:44907927-44908749	HepG2	liver:	n/a	n/a
7	ATF1	chr6:44934477-44934865	K562	blood:	n/a	n/a
8	ATF1	chr6:44888645-44888963	K562	blood:	n/a	n/a
9	ATF1	chr6:44893099-44893531	K562	blood:	n/a	n/a
10	ATF1	chr6:44876296-44876496	K562	blood:	n/a	n/a
11	ATF3	chr6:44934407-44934925	K562	blood:	n/a	n/a
12	BCL3	chr6:44934546-44934913	K562	blood:	n/a	n/a
13	BHLHE40	chr6:44934500-44934832	K562	blood:	n/a	n/a
14	BHLHE40	chr6:44928669-44928955	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:44891304-44891474	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:44888678-44889228	HepG2	liver:	n/a	n/a
17	CBX3	chr6:44934407-44934915	K562	blood:	n/a	n/a
18	CBX3	chr6:44934470-44934850	K562	blood:	n/a	n/a
19	CBX3	chr6:44934427-44934905	HCT-116	colon:	n/a	n/a
20	CBX3	chr6:44934371-44934913	HCT-116	colon:	n/a	n/a
21	CBX3	chr6:44889457-44889879	HCT-116	colon:	n/a	n/a
22	CBX3	chr6:44928552-44929041	HCT-116	colon:	n/a	n/a
23	CCNT2	chr6:44893177-44893452	K562	blood:	n/a	n/a
24	CCNT2	chr6:44888713-44888911	K562	blood:	n/a	chr6:44888832-44888852
25	CCNT2	chr6:44934499-44934885	K562	blood:	n/a	n/a
26	CEBPB	chr6:44888597-44889189	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:44888661-44888811	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:44934437-44934855	Hela-S3	cervix:	n/a	chr6:44934624-44934633
29	CEBPB	chr6:44908161-44908502	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:44934462-44934822	IMR90	lung:	n/a	chr6:44934624-44934633
31	CEBPB	chr6:44934459-44934809	A549	lung:	n/a	chr6:44934624-44934633
32	CEBPB	chr6:44934384-44934901	K562	blood:	n/a	chr6:44934624-44934633
33	CEBPB	chr6:44888558-44889173	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:44934324-44934972	HCT-116	colon:	n/a	chr6:44934911-44934923 chr6:44934624-44934633
35	CEBPB	chr6:44893092-44893440	K562	blood:	n/a	n/a
36	CEBPB	chr6:44934173-44934989	K562	blood:	n/a	chr6:44934911-44934923 chr6:44934624-44934633
37	CEBPB	chr6:44937623-44937821	IMR90	lung:	n/a	n/a
38	CEBPB	chr6:44934515-44934884	K562	blood:	n/a	chr6:44934624-44934633
39	CEBPB	chr6:44934438-44934906	HCT-116	colon:	n/a	chr6:44934624-44934633
40	CEBPB	chr6:44888607-44888936	K562	blood:	n/a	n/a
41	CEBPD	chr6:44934308-44934856	K562	blood:	n/a	n/a
42	CEBPD	chr6:44934366-44935016	K562	blood:	n/a	n/a
43	CREB1	chr6:44934380-44935056	K562	blood:	n/a	n/a
44	CTCF	chr6:44889737-44889793	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:44889633-44889846	HepG2	liver:	n/a	n/a
46	CTCF	chr6:44889540-44889690	Caco-2	colon:	n/a	n/a
47	CTCF	chr6:44889520-44889670	GM12872	blood:	n/a	n/a
48	CTCF	chr6:44889692-44889835	NHEK	skin:	n/a	n/a
49	CTCF	chr6:44883513-44883613	GM20000	blood:	n/a	n/a
50	CTCF	chr6:44889680-44889830	NHEK	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:44866054-44866104	ProgFib	skin:	n/a
2	chr6:44866054-44866104	RPTEC	kidney:	n/a
3	chr6:44866054-44866104	SKMC	muscle:	n/a
4	chr6:44866054-44866104	ECC-1	luminal epithelium:	n/a
5	chr6:44866054-44866104	HEK293	kidney:	embryo
6	chr6:44866054-44866104	HMEC	breast:	n/a
7	chr6:44866054-44866104	GM12891	blood:	n/a
8	chr6:44866054-44866104	HCM	heart:	n/a
9	chr6:44866054-44866104	H1-hESC	embryonic stem cell:	embryo
10	chr6:44866054-44866104	BE2_C	brain:	n/a
11	chr6:44866054-44866104	HPAEpiC	pulmonary alveolar:	n/a
12	chr6:44866054-44866104	NH-A	brain:	n/a
13	chr6:44866054-44866104	NB4	blood:	n/a
14	chr6:44866054-44866104	Caco-2	colon:	n/a
15	chr6:44866054-44866104	AG04450	lung:	fetal
16	chr6:44866054-44866104	GM19239	blood:	n/a
17	chr6:44866054-44866104	HCF	heart:	n/a
18	chr6:44866054-44866104	Hepatocyte	liver:	n/a
19	chr6:44866054-44866104	AG09309	skin:	n/a
20	chr6:44866054-44866104	HCT-116	colon:	n/a
21	chr6:44866054-44866104	MCF-7	breast:	n/a
22	chr6:44866054-44866104	AoSMC	blood vessel:	n/a
23	chr6:44866054-44866104	PFSK-1	brain:	n/a
24	chr6:44866054-44866104	SK-N-SH_RA	brain:	n/a
25	chr6:44866054-44866104	HRCEpiC	kidney:	n/a
26	chr6:44866054-44866104	HRE	kidney:	n/a
27	chr6:44866054-44866104	HEEpiC	esophagus:	n/a
28	chr6:44866054-44866104	GM06990	blood:	n/a
29	chr6:44866054-44866104	A549	lung:	n/a
30	chr6:44866054-44866104	HL-60	blood:	n/a
31	chr6:44866054-44866104	HepG2	liver:	n/a
32	chr6:44866054-44866104	HAEpiC	amniotic membrane:	n/a
33	chr6:44866054-44866104	AG10803	skin:	n/a
34	chr6:44866054-44866104	NHDF-neo	bronchial:	n/a
35	chr6:44866054-44866104	SK-N-MC	brain:	n/a
36	chr6:44866054-44866104	T-47D	breast:	n/a
37	chr6:44866054-44866104	Jurkat	blood:	n/a
38	chr6:44866054-44866104	U87	brain:	n/a
39	chr6:44866054-44866104	AG09319	gingival:	n/a
40	chr6:44866054-44866104	IMR90	lung:	fetal
41	chr6:44866054-44866104	K562	blood:	n/a
42	chr6:44866054-44866104	HNPCEpiC	eye:	n/a
43	chr6:44866054-44866104	SAEC	small airway:	n/a
44	chr6:44866054-44866104	PANC-1	pancreas:	n/a
45	chr6:44866054-44866104	HUVEC	blood vessel:	n/a
46	chr6:44866054-44866104	MCF10A-Er-Src	breast:	n/a
47	chr6:44866054-44866104	NT2-D1	testis:	n/a
48	chr6:44866054-44866104	CMK	blood:	n/a
49	chr6:44866054-44866104	HCPEpiC	choroid plexus:	n/a
50	chr6:44866054-44866104	GM12878	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:44935484..44938452-chr6:44939240..44940813,2	K562	blood:
2	chr6:44878819..44880569-chr6:44884458..44887437,2	MCF-7	breast:
3	chr6:44863793..44865900-chr6:44866802..44868640,2	K562	blood:
4	chr6:44863539..44865317-chr6:44876149..44878495,2	K562	blood:
5	chr6:44874731..44877061-chr6:44885216..44887016,2	K562	blood:
6	chr6:44924333..44926933-chr6:44928218..44930920,2	K562	blood:
7	chr6:44863793..44865900-chr6:44866802..44868640,2	K562	blood:
8	chr6:44917876..44920561-chr6:44920562..44922585,2	MCF-7	breast:
9	chr6:44928658..44930221-chr6:45326668..45328264,2	K562	blood:
10	chr6:44917876..44920561-chr6:44920562..44922585,2	MCF-7	breast:
11	chr6:44878819..44880569-chr6:44884458..44887437,2	MCF-7	breast:
12	chr6:44879682..44885595-chr6:44885746..44891635,7	K562	blood:
13	chr6:44879682..44885595-chr6:44885746..44891635,7	K562	blood:
14	chr6:44917939..44922059-chr6:44925666..44928514,3	K562	blood:
15	chr6:44874731..44877061-chr6:44885216..44887016,2	K562	blood:
16	chr6:44888776..44891351-chr6:45344894..45347692,2	K562	blood:
17	chr6:44924333..44926933-chr6:44928218..44930920,2	K562	blood:
18	chr6:44917939..44922059-chr6:44925666..44928514,3	K562	blood:
19	chr6:44863539..44865317-chr6:44876149..44878495,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUNX2-5	chr6:44866448-44867032	NONHSAT112969

No data

Variant related genes	Relation type
SUPT3H	TF binding region
NUDT19P4	TF binding region
SUPT3H	CpG island
NUDT19P4	CpG island
ENSG00000196284	chromatin interactions

Extended variants
information (count: 3872 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3872 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3799979	chr6:44845514-44845515	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559873083	chr6:44845524-44845525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533215059	chr6:44845532-44845533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112912924	chr6:44845545-44845546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551750392	chr6:44845574-44845575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544836629	chr6:44845582-44845583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570258922	chr6:44845646-44845647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73438898	chr6:44845680-44845681	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs192150729	chr6:44845720-44845721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567545267	chr6:44845734-44845735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184043554	chr6:44845739-44845740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553491207	chr6:44845810-44845811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs137960351	chr6:44845828-44845829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539065369	chr6:44845831-44845832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557696991	chr6:44845907-44845908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373446016	chr6:44845920-44845921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576275158	chr6:44845932-44845933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185236953	chr6:44845949-44845950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375520010	chr6:44845962-44845963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4714828	chr6:44846008-44846009	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs541220973	chr6:44846052-44846053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374171981	chr6:44846059-44846060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs578012491	chr6:44846067-44846068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545087116	chr6:44846082-44846083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563669451	chr6:44846106-44846107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs80226990	chr6:44846112-44846113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs202107031	chr6:44846114-44846115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549298024	chr6:44846129-44846130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541550183	chr6:44846137-44846138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6921903	chr6:44846150-44846151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560537090	chr6:44846166-44846167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370847114	chr6:44846186-44846187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534997505	chr6:44846188-44846189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561236059	chr6:44846208-44846209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528707193	chr6:44846231-44846232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529685912	chr6:44846234-44846235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546742159	chr6:44846290-44846291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34973168	chr6:44846318-44846319	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs118096352	chr6:44846327-44846328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558421978	chr6:44846355-44846356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149457794	chr6:44846357-44846358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190041864	chr6:44846375-44846376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530567055	chr6:44846430-44846431	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182658268	chr6:44846441-44846442	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs199867793	chr6:44846451-44846452	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563597063	chr6:44846469-44846470	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187027740	chr6:44846496-44846497	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192707052	chr6:44846517-44846518	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550202184	chr6:44846529-44846530	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573983771	chr6:44846570-44846571	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
lymphocytic leukemia	21291569	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44833600-44849400	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr6:44838200-44848800	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr6:44838400-44854200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:44844200-44847800	Weak transcription	Dnd41	blood
5	chr6:44845200-44847800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr6:44845800-44846400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:44846400-44847600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr6:44846400-44848000	Enhancers	HepG2	liver
9	chr6:44846600-44846800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:44846800-44847200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr6:44854600-44866200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr6:44859200-44889400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr6:44860000-44860600	Enhancers	Right Ventricle	heart
14	chr6:44860000-44860800	Enhancers	Fetal Brain Male	brain
15	chr6:44860000-44860800	Enhancers	Fetal Heart	heart
16	chr6:44860800-44862800	Weak transcription	Fetal Heart	heart
17	chr6:44862600-44889400	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr6:44862800-44863600	Enhancers	Fetal Heart	heart
19	chr6:44863000-44865600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr6:44863200-44866600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr6:44863600-44870400	Weak transcription	Aorta	Aorta
22	chr6:44864000-44866600	Enhancers	Fetal Lung	lung
23	chr6:44864200-44866600	Enhancers	Fetal Stomach	stomach
24	chr6:44864800-44888400	Weak transcription	Primary T cells from cord blood	blood
25	chr6:44865000-44865800	Weak transcription	HSMM	muscle
26	chr6:44865800-44866200	Genic enhancers	HSMM	muscle
27	chr6:44866000-44866200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr6:44866000-44866600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr6:44866000-44866600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:44866000-44866600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr6:44866000-44866600	Enhancers	Gastric	stomach
32	chr6:44866000-44866600	Enhancers	HSMMtube	muscle
33	chr6:44866000-44866600	Enhancers	NHDF-Ad	bronchial
34	chr6:44866000-44866600	Enhancers	NHLF	lung
35	chr6:44866200-44866400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr6:44866200-44866600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr6:44866200-44866600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:44866200-44866600	Enhancers	Placenta	Placenta
39	chr6:44866200-44866600	Enhancers	NH-A	brain
40	chr6:44866200-44866800	Enhancers	HSMM	muscle
41	chr6:44866400-44866600	Enhancers	Pancreas	Pancrea
42	chr6:44866400-44868600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr6:44866600-44869600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr6:44866600-44879600	Weak transcription	Pancreas	Pancrea
45	chr6:44867400-44868000	Enhancers	K562	blood
46	chr6:44867600-44868000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr6:44867800-44868800	ZNF genes & repeats	Fetal Intestine Small	intestine
48	chr6:44868000-44874600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr6:44868600-44868800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr6:44868800-44869000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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