Variant report

Variant	nsv1032906
Chromosome Location	chr6:45069368-45212863
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:639)
CpG islands
(count:184)
Chromatin interactive
region (count:41)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:639 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:45166970-45168751	HepG2	liver:	n/a	chr6:45167947-45167963 chr6:45168678-45168694
2	ARID3A	chr6:45151435-45151460	K562	blood:	n/a	n/a
3	ARID3A	chr6:45152902-45153360	K562	blood:	n/a	n/a
4	ARID3A	chr6:45081891-45082077	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:45157824-45157850	K562	blood:	n/a	n/a
6	ARID3A	chr6:45090824-45091007	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:45159169-45159507	HepG2	liver:	n/a	n/a
8	ATF1	chr6:45123857-45124210	K562	blood:	n/a	n/a
9	ATF1	chr6:45123102-45123463	K562	blood:	n/a	n/a
10	ATF1	chr6:45190091-45190279	K562	blood:	n/a	n/a
11	ATF1	chr6:45153051-45153503	K562	blood:	n/a	n/a
12	ATF1	chr6:45177616-45177798	K562	blood:	n/a	n/a
13	BACH1	chr6:45153438-45153593	K562	blood:	n/a	n/a
14	BACH1	chr6:45180959-45180963	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr6:45132110-45132459	GM12878	blood:	n/a	n/a
16	BATF	chr6:45139190-45139394	GM12878	blood:	n/a	chr6:45139321-45139331
17	BATF	chr6:45139181-45139443	GM12878	blood:	n/a	chr6:45139321-45139331
18	BCL3	chr6:45132117-45132509	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:45086708-45086783	K562	blood:	n/a	n/a
20	BHLHE40	chr6:45131714-45131723	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:45123836-45124198	GM12878	blood:	n/a	n/a
22	CBX3	chr6:45199417-45199794	K562	blood:	n/a	n/a
23	CBX3	chr6:45109178-45109415	K562	blood:	n/a	n/a
24	CBX3	chr6:45208754-45209051	K562	blood:	n/a	n/a
25	CBX3	chr6:45210390-45210813	HCT-116	colon:	n/a	n/a
26	CBX3	chr6:45199449-45199702	K562	blood:	n/a	n/a
27	CBX3	chr6:45132012-45132577	HCT-116	colon:	n/a	n/a
28	CBX3	chr6:45208754-45209148	K562	blood:	n/a	n/a
29	CBX3	chr6:45207452-45207700	K562	blood:	n/a	n/a
30	CCNT2	chr6:45123918-45124143	K562	blood:	n/a	n/a
31	CCNT2	chr6:45166582-45166762	K562	blood:	n/a	n/a
32	CCNT2	chr6:45153145-45153493	K562	blood:	n/a	n/a
33	CEBPB	chr6:45155755-45155784	K562	blood:	n/a	n/a
34	CEBPB	chr6:45173401-45173601	K562	blood:	n/a	n/a
35	CEBPB	chr6:45122388-45122650	HepG2	liver:	n/a	n/a
36	CEBPB	chr6:45122501-45122512	K562	blood:	n/a	n/a
37	CEBPB	chr6:45153685-45153870	HepG2	liver:	n/a	n/a
38	CEBPB	chr6:45151791-45152121	K562	blood:	n/a	chr6:45151955-45151966
39	CEBPB	chr6:45151793-45152111	HepG2	liver:	n/a	chr6:45151955-45151966
40	CEBPB	chr6:45074584-45074778	IMR90	lung:	n/a	n/a
41	CEBPB	chr6:45200403-45200505	HepG2	liver:	n/a	n/a
42	CEBPB	chr6:45210528-45210647	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr6:45161799-45161980	HepG2	liver:	n/a	chr6:45161842-45161853
44	CEBPB	chr6:45155561-45155879	Hela-S3	cervix:	n/a	chr6:45155727-45155738
45	CEBPB	chr6:45155587-45155915	IMR90	lung:	n/a	chr6:45155727-45155738
46	CEBPB	chr6:45115571-45115701	IMR90	lung:	n/a	n/a
47	CEBPB	chr6:45153124-45153980	K562	blood:	n/a	n/a
48	CEBPB	chr6:45126932-45126979	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr6:45173462-45173620	K562	blood:	n/a	n/a
50	CEBPB	chr6:45184702-45184889	A549	lung:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:45079679-45079729	HMEC	breast:	n/a
2	chr6:45079679-45079729	HMEC	breast:	n/a
3	chr6:45079679-45079729	HIPEpiC	eye:	n/a
4	chr6:45152974-45153024	HUVEC	blood vessel:	n/a
5	chr6:45079679-45079729	HEK293	kidney:	embryo
6	chr6:45079679-45079729	HEEpiC	esophagus:	n/a
7	chr6:45079679-45079729	NB4	blood:	n/a
8	chr6:45143980-45144030	HRCEpiC	kidney:	n/a
9	chr6:45143980-45144030	HRPEpiC	eye:	n/a
10	chr6:45152974-45153024	U87	brain:	n/a
11	chr6:45079679-45079729	IMR90	lung:	fetal
12	chr6:45079679-45079729	HCF	heart:	n/a
13	chr6:45079679-45079729	CMK	blood:	n/a
14	chr6:45079679-45079729	HUVEC	blood vessel:	n/a
15	chr6:45079679-45079729	GM12892	blood:	n/a
16	chr6:45143980-45144030	HAEpiC	amniotic membrane:	n/a
17	chr6:45152974-45153024	MCF-7	breast:	n/a
18	chr6:45079679-45079729	HPAEpiC	pulmonary alveolar:	n/a
19	chr6:45079679-45079729	HNPCEpiC	eye:	n/a
20	chr6:45079679-45079729	NHDF-neo	bronchial:	n/a
21	chr6:45143980-45144030	HCPEpiC	choroid plexus:	n/a
22	chr6:45143980-45144030	ECC-1	luminal epithelium:	n/a
23	chr6:45079679-45079729	HRE	kidney:	n/a
24	chr6:45152974-45153024	Hela-S3	cervix:	n/a
25	chr6:45079679-45079729	H1-hESC	embryonic stem cell:	embryo
26	chr6:45143980-45144030	HCF	heart:	n/a
27	chr6:45143980-45144030	A549	lung:	n/a
28	chr6:45079679-45079729	AG04449	skin:	fetal
29	chr6:45143980-45144030	HNPCEpiC	eye:	n/a
30	chr6:45143980-45144030	PFSK-1	brain:	n/a
31	chr6:45143980-45144030	Hela-S3	cervix:	n/a
32	chr6:45143980-45144030	SAEC	small airway:	n/a
33	chr6:45143980-45144030	AG09319	gingival:	n/a
34	chr6:45152974-45153024	GM19239	blood:	n/a
35	chr6:45143980-45144030	H1-hESC	embryonic stem cell:	embryo
36	chr6:45079679-45079729	GM12891	blood:	n/a
37	chr6:45152974-45153024	LNCaP	prostate:	n/a
38	chr6:45152974-45153024	NHDF-neo	bronchial:	n/a
39	chr6:45079679-45079729	Jurkat	blood:	n/a
40	chr6:45079679-45079729	LNCaP	prostate:	n/a
41	chr6:45152974-45153024	NB4	blood:	n/a
42	chr6:45079679-45079729	PANC-1	pancreas:	n/a
43	chr6:45152974-45153024	NT2-D1	testis:	n/a
44	chr6:45079679-45079729	K562	blood:	n/a
45	chr6:45079679-45079729	SKMC	muscle:	n/a
46	chr6:45143980-45144030	ProgFib	skin:	n/a
47	chr6:45152974-45153024	SK-N-MC	brain:	n/a
48	chr6:45143980-45144030	MCF10A-Er-Src	breast:	n/a
49	chr6:45079679-45079729	HRPEpiC	eye:	n/a
50	chr6:45143980-45144030	GM19239	blood:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:45172898..45174663-chr6:45183138..45184691,2	K562	blood:
2	chr6:45083331..45086142-chr6:45155794..45158780,2	K562	blood:
3	chr6:45117043..45119503-chr6:45122120..45124121,2	K562	blood:
4	chr6:45120420..45122464-chr6:45122631..45125594,2	K562	blood:
5	chr6:45163170..45165177-chr6:45169368..45170904,2	K562	blood:
6	chr6:45163170..45165177-chr6:45169368..45170904,2	K562	blood:
7	chr6:45124236..45126557-chr6:45137066..45139205,2	MCF-7	breast:
8	chr6:45171517..45174411-chr6:45178235..45180217,2	K562	blood:
9	chr6:45170143..45173003-chr6:45173758..45175670,2	MCF-7	breast:
10	chr6:45083331..45086142-chr6:45155794..45158780,2	K562	blood:
11	chr6:45124236..45126557-chr6:45137066..45139205,2	MCF-7	breast:
12	chr6:45128101..45130973-chr6:45345066..45347922,2	K562	blood:
13	chr6:44996729..44999425-chr6:45119837..45121459,2	K562	blood:
14	chr6:45138020..45139823-chr6:45139972..45141878,2	MCF-7	breast:
15	chr6:45092014..45095175-chr6:45095501..45098870,4	K562	blood:
16	chr6:45155462..45157708-chr6:45161468..45163917,2	MCF-7	breast:
17	chr6:45093713..45096382-chr6:45127644..45129447,2	K562	blood:
18	chr6:45119653..45122627-chr6:45134013..45136661,2	MCF-7	breast:
19	chr6:45071425..45074350-chr6:45080859..45082948,2	MCF-7	breast:
20	chr19:27731523..27732363-chr6:45117749..45118249,2	MCF-7	breast:
21	chr6:45151957..45156034-chr6:45156930..45160308,3	K562	blood:
22	chr6:45120420..45122464-chr6:45122631..45125594,2	K562	blood:
23	chr6:45169238..45172047-chr6:45343941..45345557,2	MCF-7	breast:
24	chr6:45160972..45165246-chr6:45178939..45182549,3	K562	blood:
25	chr15:98568515..98569332-chr6:45179144..45180022,2	MCF-7	breast:
26	chr6:45151957..45156034-chr6:45156930..45160308,3	K562	blood:
27	chr6:45071425..45074350-chr6:45080859..45082948,2	MCF-7	breast:
28	chr6:45092014..45095175-chr6:45095501..45098870,4	K562	blood:
29	chr6:45200553..45203015-chr6:45211837..45214861,3	K562	blood:
30	chr6:45138020..45139823-chr6:45139972..45141878,2	MCF-7	breast:
31	chr6:45171517..45174411-chr6:45178235..45180217,2	K562	blood:
32	chr6:45093713..45096382-chr6:45127644..45129447,2	K562	blood:
33	chr6:45160972..45165246-chr6:45178939..45182549,3	K562	blood:
34	chr6:45170143..45173003-chr6:45173758..45175670,2	MCF-7	breast:
35	chr6:45200553..45203015-chr6:45211837..45214861,3	K562	blood:
36	chr6:45172898..45174663-chr6:45183138..45184691,2	K562	blood:
37	chr6:45155462..45157708-chr6:45161468..45163917,2	MCF-7	breast:
38	chr6:45117043..45119503-chr6:45122120..45124121,2	K562	blood:
39	chr6:45126389..45128813-chr6:45129445..45131831,2	K562	blood:
40	chr6:45119653..45122627-chr6:45134013..45136661,2	MCF-7	breast:
41	chr6:45091825..45094517-chr6:45344694..45347186,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUNX2-4	chr6:45126607-45127248	NONHSAT112972

miRNA name	Chromosome Location	mirBase accession
hsa-miR-586	chr6:45165471-45165492	MIMAT0003252

No data

Variant related genes	Relation type
MIR586	TF binding region
ENSG00000219384	TF binding region
MIR586	CpG island
ENSG00000219384	CpG island
ENSG00000219384	chromatin interactions
ENSG00000196284	chromatin interactions
ENSG00000252477	chromatin interactions

Extended variants
information (count: 4929 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:4929 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553809790	chr6:45069384-45069385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs188035029	chr6:45069425-45069426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs193050266	chr6:45069441-45069442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116410102	chr6:45069450-45069451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534346223	chr6:45069471-45069472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564166300	chr6:45069480-45069481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576206967	chr6:45069516-45069517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs71566519	chr6:45069542-45069543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116191913	chr6:45069561-45069562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562254051	chr6:45069614-45069615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529543442	chr6:45069646-45069647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9381364	chr6:45069673-45069674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs557764313	chr6:45069686-45069687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141657704	chr6:45069687-45069688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34955247	chr6:45069693-45069694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533319171	chr6:45069699-45069700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185313916	chr6:45069799-45069800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551488607	chr6:45069808-45069809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569762968	chr6:45069845-45069846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532048490	chr6:45069880-45069881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73737885	chr6:45069894-45069895	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs563933139	chr6:45069904-45069905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577337549	chr6:45069938-45069939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545907950	chr6:45069946-45069947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139182677	chr6:45070016-45070017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7750380	chr6:45070034-45070035	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs112249042	chr6:45070045-45070046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150508322	chr6:45070132-45070133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113130475	chr6:45070137-45070138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571789470	chr6:45070140-45070141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35548001	chr6:45070142-45070143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548221434	chr6:45070144-45070145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189023795	chr6:45070243-45070244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539107956	chr6:45070244-45070245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557460292	chr6:45070280-45070281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192709940	chr6:45070336-45070337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543524176	chr6:45070370-45070371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9472439	chr6:45070400-45070401	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs547606525	chr6:45070401-45070402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149841125	chr6:45070427-45070428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184937472	chr6:45070462-45070463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549786934	chr6:45070463-45070464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145815825	chr6:45070470-45070471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140054667	chr6:45070493-45070494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145465096	chr6:45070497-45070498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188129439	chr6:45070540-45070541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565860921	chr6:45070554-45070555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191489830	chr6:45070575-45070576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76619528	chr6:45070590-45070591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142411502	chr6:45070654-45070655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	16608533	CNVD

Chromatin state (count:588 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45064200-45076000	Weak transcription	Dnd41	blood
2	chr6:45064600-45071000	Weak transcription	Lung	lung
3	chr6:45071000-45077800	Weak transcription	HSMM	muscle
4	chr6:45072600-45073800	Enhancers	Osteobl	bone
5	chr6:45072600-45074000	Enhancers	Muscle Satellite Cultured Cells	--
6	chr6:45073000-45073200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:45073000-45073800	Enhancers	NHDF-Ad	bronchial
8	chr6:45073200-45073600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:45073200-45076400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:45073400-45083600	Weak transcription	Pancreas	Pancrea
11	chr6:45074000-45074200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr6:45076000-45076600	Enhancers	Dnd41	blood
13	chr6:45076000-45077000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr6:45076200-45076400	Enhancers	Primary T cells from cord blood	blood
15	chr6:45076400-45076600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:45076400-45077400	Weak transcription	Primary T cells from cord blood	blood
17	chr6:45076600-45077000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:45076600-45082800	Weak transcription	Dnd41	blood
19	chr6:45077000-45077400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr6:45077000-45077800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr6:45077400-45077800	Enhancers	Primary T cells from cord blood	blood
22	chr6:45077400-45078000	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr6:45077400-45078000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr6:45077600-45078400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr6:45077800-45078400	Enhancers	HSMM	muscle
26	chr6:45077800-45078800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr6:45077800-45083400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr6:45078400-45079600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr6:45078400-45083400	Weak transcription	HSMM	muscle
30	chr6:45078600-45080000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr6:45078800-45079400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr6:45079400-45079600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr6:45079400-45079800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr6:45079600-45079800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr6:45079800-45080200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr6:45080200-45080600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr6:45080200-45081200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr6:45081000-45081200	Enhancers	Fetal Heart	heart
39	chr6:45081200-45083200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr6:45081600-45084200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr6:45082400-45083000	Enhancers	HepG2	liver
42	chr6:45082400-45085600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr6:45082800-45085200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr6:45082800-45085800	Enhancers	Dnd41	blood
45	chr6:45083200-45085400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:45083200-45086200	Enhancers	Fetal Heart	heart
47	chr6:45083400-45084200	Enhancers	Muscle Satellite Cultured Cells	--
48	chr6:45083400-45084400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr6:45083400-45084600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr6:45083400-45084600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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