Variant report

Variant	esv1826605
Chromosome Location	chr6:57387021-57539592
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2113)
CpG islands
(count:122)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2113 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:57445471-57445872	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:57445284-57445884	K562	blood:	n/a	n/a
3	ARID3A	chr6:57392130-57392164	HepG2	liver:	n/a	n/a
4	ATF1	chr6:57529957-57530116	K562	blood:	n/a	n/a
5	ATF1	chr6:57388328-57388901	K562	blood:	n/a	n/a
6	ATF1	chr6:57414346-57414465	K562	blood:	n/a	n/a
7	ATF1	chr6:57433964-57434331	K562	blood:	n/a	n/a
8	ATF1	chr6:57422764-57422956	K562	blood:	n/a	n/a
9	ATF1	chr6:57487670-57487865	K562	blood:	n/a	n/a
10	ATF1	chr6:57432706-57432903	K562	blood:	n/a	n/a
11	ATF1	chr6:57483779-57483974	K562	blood:	n/a	n/a
12	ATF1	chr6:57483250-57483369	K562	blood:	n/a	n/a
13	BACH1	chr6:57501831-57501836	K562	blood:	n/a	n/a
14	BACH1	chr6:57486231-57486242	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:57408878-57409078	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:57526352-57526945	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:57419536-57419915	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:57488136-57488168	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr6:57388299-57388865	K562	blood:	n/a	n/a
20	BACH1	chr6:57439570-57440015	H1-hESC	embryonic stem cell:	n/a	n/a
21	BHLHE40	chr6:57450923-57451339	A549	lung:	n/a	n/a
22	BHLHE40	chr6:57469073-57469074	GM12878	blood:	n/a	n/a
23	BHLHE40	chr6:57395851-57396136	HepG2	liver:	n/a	n/a
24	BHLHE40	chr6:57474969-57474972	K562	blood:	n/a	n/a
25	BHLHE40	chr6:57473286-57473332	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:57519324-57519409	K562	blood:	n/a	n/a
27	BHLHE40	chr6:57440441-57440461	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:57396741-57396999	GM12878	blood:	n/a	n/a
29	BRCA1	chr6:57535844-57535916	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr6:57525275-57525333	GM12878	blood:	n/a	n/a
31	BRCA1	chr6:57512603-57512632	GM12878	blood:	n/a	n/a
32	BRCA1	chr6:57420502-57420568	GM12878	blood:	n/a	n/a
33	BRCA1	chr6:57420189-57420208	GM12878	blood:	n/a	n/a
34	BRCA1	chr6:57398324-57398744	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr6:57489991-57490136	GM12878	blood:	n/a	n/a
36	BRCA1	chr6:57459211-57459324	GM12878	blood:	n/a	n/a
37	BRCA1	chr6:57390670-57390900	GM12878	blood:	n/a	n/a
38	BRCA1	chr6:57488099-57488136	GM12878	blood:	n/a	n/a
39	BRCA1	chr6:57457747-57457841	GM12878	blood:	n/a	n/a
40	BRCA1	chr6:57412393-57412615	GM12878	blood:	n/a	n/a
41	BRCA1	chr6:57500697-57500736	GM12878	blood:	n/a	n/a
42	BRCA1	chr6:57518070-57518209	HepG2	liver:	n/a	n/a
43	BRCA1	chr6:57538781-57538788	GM12878	blood:	n/a	n/a
44	BRCA1	chr6:57463410-57463534	GM12878	blood:	n/a	n/a
45	BRF1	chr6:57432880-57433459	Hela-S3	cervix:	n/a	n/a
46	CCNT2	chr6:57467273-57467500	K562	blood:	n/a	n/a
47	CCNT2	chr6:57497968-57498977	K562	blood:	n/a	chr6:57498241-57498261 chr6:57498127-57498147
48	CEBPB	chr6:57538070-57538422	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr6:57419619-57419972	IMR90	lung:	n/a	chr6:57419794-57419805
50	CEBPB	chr6:57459166-57459470	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:57447898-57447948	A549	lung:	n/a
2	chr6:57447898-57447948	HRCEpiC	kidney:	n/a
3	chr6:57447898-57447948	SAEC	small airway:	n/a
4	chr6:57447898-57447948	AG10803	skin:	n/a
5	chr6:57391815-57391865	NT2-D1	testis:	n/a
6	chr6:57447898-57447948	HCT-116	colon:	n/a
7	chr6:57447898-57447948	GM12878	blood:	n/a
8	chr6:57447898-57447948	LNCaP	prostate:	n/a
9	chr6:57447898-57447948	AG04450	lung:	fetal
10	chr6:57447898-57447948	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:57391815-57391865	NHBE	bronchial:	n/a
12	chr6:57447898-57447948	SK-N-SH	brain:	n/a
13	chr6:57391815-57391865	HNPCEpiC	eye:	n/a
14	chr6:57391815-57391865	PFSK-1	brain:	n/a
15	chr6:57391815-57391865	Hepatocyte	liver:	n/a
16	chr6:57391815-57391865	NHDF-neo	bronchial:	n/a
17	chr6:57447898-57447948	HIPEpiC	eye:	n/a
18	chr6:57447898-57447948	Hepatocyte	liver:	n/a
19	chr6:57447898-57447948	H1-hESC	embryonic stem cell:	embryo
20	chr6:57391815-57391865	HCF	heart:	n/a
21	chr6:57391815-57391865	HCM	heart:	n/a
22	chr6:57391815-57391865	GM12878	blood:	n/a
23	chr6:57391815-57391865	MCF-7	breast:	n/a
24	chr6:57447898-57447948	AG04449	skin:	fetal
25	chr6:57391815-57391865	GM06990	blood:	n/a
26	chr6:57391815-57391865	GM12891	blood:	n/a
27	chr6:57447898-57447948	PrEC	prostate:	n/a
28	chr6:57447898-57447948	HL-60	blood:	n/a
29	chr6:57447898-57447948	GM19239	blood:	n/a
30	chr6:57391815-57391865	RPTEC	kidney:	n/a
31	chr6:57447898-57447948	MCF-7	breast:	n/a
32	chr6:57447898-57447948	ProgFib	skin:	n/a
33	chr6:57447898-57447948	SKMC	muscle:	n/a
34	chr6:57447898-57447948	AoSMC	blood vessel:	n/a
35	chr6:57447898-57447948	GM06990	blood:	n/a
36	chr6:57391815-57391865	GM12892	blood:	n/a
37	chr6:57447898-57447948	Hela-S3	cervix:	n/a
38	chr6:57391815-57391865	ovcar-3	ovarian:	n/a
39	chr6:57447898-57447948	HRPEpiC	eye:	n/a
40	chr6:57447898-57447948	PANC-1	pancreas:	n/a
41	chr6:57447898-57447948	MCF10A-Er-Src	breast:	n/a
42	chr6:57447898-57447948	Jurkat	blood:	n/a
43	chr6:57391815-57391865	SK-N-SH_RA	brain:	n/a
44	chr6:57391815-57391865	U87	brain:	n/a
45	chr6:57391815-57391865	BJ	skin:	n/a
46	chr6:57447898-57447948	NH-A	brain:	n/a
47	chr6:57447898-57447948	HepG2	liver:	n/a
48	chr6:57391815-57391865	AG09319	gingival:	n/a
49	chr6:57391815-57391865	HCPEpiC	choroid plexus:	n/a
50	chr6:57391815-57391865	Caco-2	colon:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:57437551..57439992-chr6:57443844..57446833,2	K562	blood:
2	chr6:57445250..57446013-chr6:57537509..57538705,3	MCF-7	breast:
3	chr6:57445326..57445995-chr6:57539539..57540106,2	MCF-7	breast:
4	chr6:57460058..57461813-chr6:57464595..57467531,2	MCF-7	breast:
5	chr6:57489928..57493477-chr6:57494690..57497411,3	K562	blood:
6	chr6:57386101..57388103-chr6:57389445..57391300,2	K562	blood:
7	chr6:57472415..57474751-chr6:57478817..57480386,2	K562	blood:
8	chr6:57394320..57396660-chr6:58286293..58287831,2	MCF-7	breast:
9	chr6:57413449..57416181-chr6:57416496..57418603,2	K562	blood:
10	chr6:57429189..57431102-chr6:57440501..57442862,2	MCF-7	breast:
11	chr6:57489928..57492575-chr6:57494690..57497411,2	K562	blood:
12	chr6:57489928..57493477-chr6:57494690..57497411,3	K562	blood:
13	chr6:57421846..57424167-chr6:57427801..57430462,3	MCF-7	breast:
14	chr6:57393591..57395977-chr6:57407320..57409957,2	MCF-7	breast:
15	chr4:92702026..92702759-chr6:57445422..57446224,2	MCF-7	breast:
16	chr6:57444969..57446432-chr6:57539130..57540030,7	MCF-7	breast:
17	chr6:57405693..57407850-chr6:57408076..57409919,2	K562	blood:
18	chr3:81978758..81979420-chr6:57518103..57518962,2	MCF-7	breast:
19	chr6:57413449..57416181-chr6:57416496..57418603,2	K562	blood:
20	chr6:57445356..57445958-chr6:57689666..57690275,2	MCF-7	breast:
21	chr6:57445326..57445995-chr6:57539539..57540106,2	MCF-7	breast:
22	chr6:57429189..57431102-chr6:57440501..57442862,2	MCF-7	breast:
23	chr6:57393591..57395977-chr6:57407320..57409957,2	MCF-7	breast:
24	chr6:57380965..57383908-chr6:57390419..57392004,2	K562	blood:
25	chr6:57217129..57218039-chr6:57539079..57539990,3	MCF-7	breast:
26	chr6:57437551..57439992-chr6:57443844..57446833,2	K562	blood:
27	chr6:57489928..57492575-chr6:57494690..57497411,2	K562	blood:
28	chr6:57460058..57461813-chr6:57464595..57467531,2	MCF-7	breast:
29	chr18:1906473..1906973-chr6:57539499..57540003,2	MCF-7	breast:
30	chr6:57396857..57397774-chr9:95368803..95369303,2	MCF-7	breast:
31	chr6:57386101..57388103-chr6:57389445..57391300,2	K562	blood:
32	chr6:57472415..57474751-chr6:57478817..57480386,2	K562	blood:
33	chr6:57421846..57424167-chr6:57427801..57430462,3	MCF-7	breast:
34	chr6:57445250..57446013-chr6:57537509..57538705,3	MCF-7	breast:
35	chr6:57444969..57446432-chr6:57539130..57540030,7	MCF-7	breast:
36	chr6:57405693..57407850-chr6:57408076..57409919,2	K562	blood:
37	chr6:57445367..57446031-chr6:62860058..62860574,2	MCF-7	breast:

No data

Variant related genes	Relation type
PRIM2	TF binding region
PRIM2	CpG island
ENSG00000263745	chromatin interactions
ENSG00000215190	chromatin interactions

Extended variants
information (count: 9911 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:9911 , 50 per page) page: 1 2 3 4 5 6 7 ... 199

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9370618	chr6:57387021-57387022	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs62399792	chr6:57387024-57387025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571001235	chr6:57387030-57387031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565270588	chr6:57387055-57387056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs62399793	chr6:57387059-57387060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147883922	chr6:57387114-57387115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs5741637	chr6:57387128-57387129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs33919308	chr6:57387129-57387130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201789049	chr6:57387130-57387131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200305860	chr6:57387131-57387132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4587172	chr6:57387138-57387139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4590272	chr6:57387155-57387156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs5876589	chr6:57387177-57387178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs397977132	chr6:57387178-57387179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs5018505	chr6:57387189-57387190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4587173	chr6:57387199-57387200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532553941	chr6:57387229-57387230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548068981	chr6:57387236-57387237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566391241	chr6:57387237-57387238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111782761	chr6:57387247-57387248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs5018504	chr6:57387248-57387249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs5018503	chr6:57387259-57387260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570262634	chr6:57387263-57387264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537532371	chr6:57387274-57387275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555889497	chr6:57387294-57387295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs5014210	chr6:57387331-57387332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570865701	chr6:57387341-57387342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2397488	chr6:57387352-57387353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538259126	chr6:57387354-57387355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs5014209	chr6:57387372-57387373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553617771	chr6:57387378-57387379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572273179	chr6:57387385-57387386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2397489	chr6:57387420-57387421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75005259	chr6:57387430-57387431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs199751175	chr6:57387433-57387434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs72483573	chr6:57387444-57387445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188193781	chr6:57387465-57387466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2894905	chr6:57387466-57387467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2894906	chr6:57387467-57387468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542938243	chr6:57387525-57387526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554453106	chr6:57387532-57387533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576228522	chr6:57387541-57387542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2397490	chr6:57387542-57387543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs55971712	chr6:57387571-57387572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2894907	chr6:57387634-57387635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11961385	chr6:57387640-57387641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532513603	chr6:57387697-57387698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2894908	chr6:57387741-57387742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs375362917	chr6:57387759-57387760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2397491	chr6:57387811-57387812	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57383400-57390400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:57384400-57387200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:57385200-57387400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr6:57385400-57387200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr6:57385400-57387200	Enhancers	H1 Cell Line	embryonic stem cell
6	chr6:57385400-57387200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr6:57385400-57387200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr6:57385400-57387200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr6:57385400-57387400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr6:57385400-57387600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr6:57385400-57395600	Weak transcription	Osteobl	bone
12	chr6:57385600-57387600	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr6:57385600-57389000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr6:57386000-57387200	Enhancers	Primary T cells from cord blood	blood
15	chr6:57386200-57387200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr6:57386600-57387400	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr6:57386800-57387200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr6:57386800-57387200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr6:57386800-57393600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr6:57387000-57401200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:57387200-57388000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr6:57387200-57388200	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr6:57387200-57388200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr6:57387200-57388200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:57387200-57388200	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr6:57387200-57388200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr6:57387200-57388400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr6:57387200-57388400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:57387200-57389000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr6:57387400-57387800	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr6:57387400-57387800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr6:57387600-57388000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr6:57387600-57388400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr6:57387600-57388400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr6:57387800-57388400	Weak transcription	A549	lung
36	chr6:57387800-57388600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:57387800-57388800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr6:57387800-57389000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr6:57387800-57391400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
40	chr6:57388000-57388800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr6:57388000-57389000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr6:57388200-57388400	Enhancers	H9 Cell Line	embryonic stem cell
43	chr6:57388200-57388600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr6:57388200-57388600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:57388200-57388600	Enhancers	Hela-S3	cervix
46	chr6:57388200-57388600	ZNF genes & repeats	HepG2	liver
47	chr6:57388200-57388600	Enhancers	NHEK	skin
48	chr6:57388200-57388800	Enhancers	NHDF-Ad	bronchial
49	chr6:57388200-57389000	Enhancers	H1 Cell Line	embryonic stem cell
50	chr6:57388200-57389000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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