Variant report

Variant	nsv600870
Chromosome Location	chr6:4391872-4429310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:340)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:4420426-4420740	K562	blood:	n/a	n/a
2	ATF1	chr6:4420436-4420836	K562	blood:	n/a	n/a
3	ATF2	chr6:4407962-4408329	GM12878	blood:	n/a	n/a
4	BACH1	chr6:4402639-4403061	H1-hESC	embryonic stem cell:	n/a	chr6:4402848-4402862
5	BACH1	chr6:4402693-4402960	K562	blood:	n/a	chr6:4402848-4402862
6	BATF	chr6:4402678-4402929	GM12878	blood:	n/a	chr6:4402851-4402862 chr6:4402852-4402862
7	BATF	chr6:4407963-4408218	GM12878	blood:	n/a	chr6:4408088-4408099
8	BATF	chr6:4402702-4403013	GM12878	blood:	n/a	chr6:4402851-4402862 chr6:4402852-4402862
9	BATF	chr6:4407908-4408272	GM12878	blood:	n/a	chr6:4408088-4408099
10	BCL11A	chr6:4407993-4408322	GM12878	blood:	n/a	n/a
11	BCLAF1	chr6:4407905-4408328	GM12878	blood:	n/a	n/a
12	BCLAF1	chr6:4408007-4408284	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:4402531-4402707	K562	blood:	n/a	n/a
14	BHLHE40	chr6:4402992-4403270	K562	blood:	n/a	n/a
15	BHLHE40	chr6:4404118-4404418	K562	blood:	n/a	chr6:4404288-4404297 chr6:4404287-4404296 chr6:4404285-4404298 chr6:4404281-4404302 chr6:4404287-4404296
16	BHLHE40	chr6:4420487-4420718	K562	blood:	n/a	n/a
17	BHLHE40	chr6:4408013-4408375	GM12878	blood:	n/a	n/a
18	CEBPB	chr6:4401697-4401931	A549	lung:	n/a	n/a
19	CEBPB	chr6:4399911-4400259	K562	blood:	n/a	n/a
20	CEBPB	chr6:4395195-4395274	K562	blood:	n/a	n/a
21	CEBPB	chr6:4399954-4400281	K562	blood:	n/a	n/a
22	CEBPB	chr6:4399774-4400004	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:4428089-4428101	A549	lung:	n/a	n/a
24	CEBPB	chr6:4402701-4402913	IMR90	lung:	n/a	n/a
25	CEBPB	chr6:4395019-4395453	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr6:4428063-4428111	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr6:4428066-4428179	K562	blood:	n/a	chr6:4428101-4428112
28	CEBPB	chr6:4399774-4399975	IMR90	lung:	n/a	n/a
29	CEBPB	chr6:4427950-4428239	HepG2	liver:	n/a	chr6:4428101-4428112
30	CEBPB	chr6:4394855-4395504	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr6:4428230-4428338	GM12878	blood:	n/a	n/a
32	CEBPB	chr6:4401561-4401944	MCF-7	breast:	n/a	n/a
33	CEBPB	chr6:4402784-4402965	A549	lung:	n/a	n/a
34	CEBPB	chr6:4401655-4402129	A549	lung:	n/a	n/a
35	CHD2	chr6:4403033-4403039	HepG2	liver:	n/a	n/a
36	CHD2	chr6:4408036-4408350	GM12878	blood:	n/a	n/a
37	CTCF	chr6:4396320-4396470	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr6:4396400-4396550	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr6:4402780-4402930	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr6:4396340-4396490	WI-38	lung:	n/a	n/a
41	CTCF	chr6:4396520-4396670	HVMF	connective:	n/a	n/a
42	CTCF	chr6:4396420-4396570	AG04450	lung:	n/a	n/a
43	CTCF	chr6:4406215-4406357	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr6:4403389-4403453	Lung_OC	lung:	n/a	n/a
45	CTCF	chr6:4396380-4396530	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr6:4413360-4413510	AG04449	skin:	n/a	n/a
47	CTCF	chr6:4413440-4413590	HPF	lung:	n/a	n/a
48	CTCF	chr6:4396480-4396630	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:4413360-4413510	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr6:4396420-4396570	HCFaa	heart:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:4427110-4427160	AG04450	lung:	fetal
2	chr6:4427110-4427160	HRPEpiC	eye:	n/a
3	chr6:4428712-4428762	GM12891	blood:	n/a
4	chr6:4427110-4427160	Hela-S3	cervix:	n/a
5	chr6:4428712-4428762	BJ	skin:	n/a
6	chr6:4428712-4428762	HCM	heart:	n/a
7	chr6:4428712-4428762	HCF	heart:	n/a
8	chr6:4428712-4428762	SK-N-MC	brain:	n/a
9	chr6:4403020-4403070	AoSMC	blood vessel:	n/a
10	chr6:4428712-4428762	HRPEpiC	eye:	n/a
11	chr6:4427110-4427160	AG04449	skin:	fetal
12	chr6:4403020-4403070	T-47D	breast:	n/a
13	chr6:4428712-4428762	NT2-D1	testis:	n/a
14	chr6:4403020-4403070	CMK	blood:	n/a
15	chr6:4428712-4428762	PANC-1	pancreas:	n/a
16	chr6:4428712-4428762	HMEC	breast:	n/a
17	chr6:4427110-4427160	SK-N-SH_RA	brain:	n/a
18	chr6:4428712-4428762	ovcar-3	ovarian:	n/a
19	chr6:4428712-4428762	AG10803	skin:	n/a
20	chr6:4427110-4427160	NT2-D1	testis:	n/a
21	chr6:4428712-4428762	HAEpiC	amniotic membrane:	n/a
22	chr6:4428712-4428762	Jurkat	blood:	n/a
23	chr6:4427110-4427160	LNCaP	prostate:	n/a
24	chr6:4428712-4428762	HPAEpiC	pulmonary alveolar:	n/a
25	chr6:4403020-4403070	ovcar-3	ovarian:	n/a
26	chr6:4428712-4428762	ProgFib	skin:	n/a
27	chr6:4403020-4403070	AG09309	skin:	n/a
28	chr6:4428712-4428762	NHBE	bronchial:	n/a
29	chr6:4428712-4428762	CMK	blood:	n/a
30	chr6:4428712-4428762	BE2_C	brain:	n/a
31	chr6:4427110-4427160	HRCEpiC	kidney:	n/a
32	chr6:4403020-4403070	PFSK-1	brain:	n/a
33	chr6:4403020-4403070	HAEpiC	amniotic membrane:	n/a
34	chr6:4403020-4403070	HNPCEpiC	eye:	n/a
35	chr6:4427110-4427160	U87	brain:	n/a
36	chr6:4427110-4427160	NB4	blood:	n/a
37	chr6:4403020-4403070	HRE	kidney:	n/a
38	chr6:4427110-4427160	Hepatocyte	liver:	n/a
39	chr6:4428712-4428762	K562	blood:	n/a
40	chr6:4427110-4427160	NH-A	brain:	n/a
41	chr6:4403020-4403070	HCT-116	colon:	n/a
42	chr6:4427110-4427160	SKMC	muscle:	n/a
43	chr6:4427110-4427160	CMK	blood:	n/a
44	chr6:4403020-4403070	MCF10A-Er-Src	breast:	n/a
45	chr6:4427110-4427160	GM12892	blood:	n/a
46	chr6:4403020-4403070	HEEpiC	esophagus:	n/a
47	chr6:4427110-4427160	HUVEC	blood vessel:	n/a
48	chr6:4427110-4427160	T-47D	breast:	n/a
49	chr6:4428712-4428762	ECC-1	luminal epithelium:	n/a
50	chr6:4403020-4403070	NH-A	brain:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:4401864..4404753-chr6:4405538..4407059,2	MCF-7	breast:
2	chr6:4398942..4400523-chr6:4402964..4405624,2	K562	blood:
3	chr6:4423287..4425558-chr6:4426635..4429033,2	K562	blood:
4	chr6:4324445..4326506-chr6:4412431..4414561,2	MCF-7	breast:
5	chr6:4401864..4404753-chr6:4405538..4407059,2	MCF-7	breast:
6	chr6:4401718..4402258-chr6:4475763..4476371,2	MCF-7	breast:
7	chr6:4401256..4404324-chr6:4774451..4776953,3	MCF-7	breast:
8	chr6:4398942..4400523-chr6:4402964..4405624,2	K562	blood:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf201-21	chr6:4402442-4402570	NONHSAT107419
2	lnc-C6orf201-20	chr6:4392903-4393826	NONHSAT107417
3	lnc-C6orf201-21	chr6:4401562-4401936	NONHSAT107419
4	lnc-C6orf201-22	chr6:4426308-4426556	NONHSAT107410
5	lnc-C6orf201-21	chr6:4400025-4400116	NONHSAT107419
6	lnc-C6orf201-21	chr6:4404826-4405130	NONHSAT107419
7	lnc-C6orf201-20	chr6:4392149-4392453	NONHSAT107417
8	lnc-C6orf201-20	chr6:4392663-4392785	NONHSAT107417
9	lnc-C6orf201-21	chr6:4402757-4403005	NONHSAT107419
10	lnc-C6orf201-21	chr6:4403126-4403388	NONHSAT107419
11	lnc-C6orf201-21	chr6:4396599-4397931	NONHSAT107419
12	lnc-C6orf201-22	chr6:4428897-4429019	NONHSAT107410
13	lnc-CDYL-21	chr6:4421551-4421814	NONHSAT107425
14	lnc-C6orf201-21	chr6:4405340-4405462	NONHSAT107419
15	lnc-C6orf201-21	chr6:4395892-4396201	NONHSAT107419
16	lnc-ECI2-3	chr6:4401444-4401474	XLOC_005590
17	lnc-C6orf201-22	chr6:4424582-4424720	NONHSAT107410
18	lnc-C6orf201-22	chr6:4424801-4425015	NONHSAT107410
19	lnc-C6orf201-21	chr6:4405580-4406503	NONHSAT107419
20	lnc-CDYL-21	chr6:4417111-4417210	NONHSAT107425
21	lnc-C6orf201-22	chr6:4428383-4428687	NONHSAT107410
22	lnc-C6orf201-22	chr6:4429137-4430060	NONHSAT107410
23	lnc-C6orf201-22	chr6:4425113-4425487	NONHSAT107410
24	lnc-C6orf201-21	chr6:4401030-4401168	NONHSAT107419
25	lnc-C6orf201-22	chr6:4423011-4423314	NONHSAT107410
26	lnc-ECI2-3	chr6:4399913-4400113	XLOC_005590
27	lnc-C6orf201-22	chr6:4425993-4426121	NONHSAT107410
28	lnc-C6orf201-22	chr6:4420566-4421476	NONHSAT107410
29	lnc-C6orf201-21	chr6:4400384-4400521	NONHSAT107419
30	lnc-C6orf201-22	chr6:4423935-4424072	NONHSAT107410
31	lnc-C6orf201-21	chr6:4399466-4399769	NONHSAT107419
32	lnc-C6orf201-22	chr6:4423570-4423661	NONHSAT107410
33	lnc-C6orf201-22	chr6:4426677-4426939	NONHSAT107410
34	lnc-C6orf201-21	chr6:4401250-4401464	NONHSAT107419

No data

Variant related genes	Relation type
RNA5SP202	TF binding region
RNA5SP202	CpG island
ENSG00000201185	chromatin interactions
ENSG00000153046	chromatin interactions
ENSG00000236336	chromatin interactions

Extended variants
information (count: 1863 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1863 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1023017	chr6:4391872-4391873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1023016	chr6:4391900-4391901	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs555973917	chr6:4391926-4391927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576094591	chr6:4391932-4391933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535034584	chr6:4391953-4391954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554962867	chr6:4391979-4391980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145513159	chr6:4391984-4391985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370548445	chr6:4391993-4391994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560441153	chr6:4392015-4392016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111648760	chr6:4392032-4392033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577363015	chr6:4392060-4392061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546387711	chr6:4392109-4392110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562795848	chr6:4392146-4392147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546613228	chr6:4392158-4392159	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs112372542	chr6:4392163-4392164	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs531855100	chr6:4392208-4392209	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs548570514	chr6:4392210-4392211	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs191851320	chr6:4392235-4392236	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs527717368	chr6:4392240-4392241	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs371476988	chr6:4392258-4392259	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs56395845	chr6:4392272-4392273	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs374267128	chr6:4392285-4392286	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs183899997	chr6:4392323-4392324	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs541612073	chr6:4392364-4392365	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs549949019	chr6:4392372-4392373	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs569621645	chr6:4392373-4392374	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs142317837	chr6:4392383-4392384	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs555075935	chr6:4392384-4392385	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs145977225	chr6:4392408-4392409	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs535704466	chr6:4392409-4392410	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs188434276	chr6:4392469-4392470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539218503	chr6:4392497-4392498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554130285	chr6:4392551-4392552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs202034097	chr6:4392600-4392601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs5873929	chr6:4392601-4392602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs3030355	chr6:4392602-4392603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs397760313	chr6:4392606-4392607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201064318	chr6:4392607-4392608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139856236	chr6:4392674-4392675	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs538553343	chr6:4392686-4392687	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs138922391	chr6:4392688-4392689	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs200954639	chr6:4392689-4392690	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs576256542	chr6:4392722-4392723	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs549709512	chr6:4392744-4392745	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs546053819	chr6:4392759-4392760	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs199521931	chr6:4392822-4392823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563114244	chr6:4392893-4392894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576745844	chr6:4392899-4392900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs72846184	chr6:4392902-4392903	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs562213812	chr6:4392909-4392910	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
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
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Schizophrenia	20967226	CNVD
Basal cell lymphoma	21115979	CNVD

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4389400-4399200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:4389600-4394000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:4389600-4394600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:4389600-4395000	Weak transcription	A549	lung
5	chr6:4390000-4395000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr6:4394000-4395400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:4394200-4395000	Weak transcription	K562	blood
8	chr6:4394400-4394800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr6:4394600-4395200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:4395000-4395200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr6:4395000-4395200	Enhancers	HSMMtube	muscle
12	chr6:4395000-4395200	Enhancers	K562	blood
13	chr6:4395000-4395400	Enhancers	H9 Cell Line	embryonic stem cell
14	chr6:4395000-4395400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:4395000-4395400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr6:4395000-4395400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr6:4395000-4395400	Enhancers	Placenta	Placenta
18	chr6:4395000-4395400	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr6:4395000-4395400	Enhancers	A549	lung
20	chr6:4395000-4395600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr6:4395000-4395600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr6:4395000-4395600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr6:4395000-4395600	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr6:4395000-4396000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr6:4395200-4395400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr6:4395200-4395400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr6:4395200-4395400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:4395200-4395400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:4395200-4395400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr6:4395200-4395400	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr6:4395200-4395400	Bivalent Enhancer	K562	blood
32	chr6:4395200-4395600	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr6:4395400-4397200	Weak transcription	HSMMtube	muscle
34	chr6:4395400-4397600	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr6:4395400-4400200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr6:4395400-4400600	Weak transcription	A549	lung
37	chr6:4395400-4402000	Weak transcription	Placenta	Placenta
38	chr6:4395400-4402600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:4395600-4397600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr6:4395600-4405800	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr6:4396000-4402400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr6:4397000-4398600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr6:4397200-4399800	Enhancers	HSMM	muscle
44	chr6:4397200-4400400	Enhancers	HSMMtube	muscle
45	chr6:4397200-4406800	Enhancers	Fetal Muscle Leg	muscle
46	chr6:4397400-4399600	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr6:4397600-4397800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:4397600-4397800	Enhancers	Fetal Lung	lung
49	chr6:4397600-4398000	Enhancers	Brain Anterior Caudate	brain
50	chr6:4397600-4398000	Enhancers	Brain Hippocampus Middle	brain

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