Variant report

Variant	nsv885916
Chromosome Location	chr6:57308960-57381883
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	chr6:57364923-57365929	HepG2	liver:	n/a	n/a
2	ATF1	chr6:57329848-57330048	K562	blood:	n/a	n/a
3	BACH1	chr6:57363671-57363854	K562	blood:	n/a	n/a
4	BACH1	chr6:57350106-57350125	K562	blood:	n/a	n/a
5	BACH1	chr6:57334050-57334159	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:57337567-57337643	K562	blood:	n/a	n/a
7	BACH1	chr6:57364094-57364109	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:57365814-57365865	K562	blood:	n/a	n/a
9	BHLHE40	chr6:57375272-57375472	GM12878	blood:	n/a	n/a
10	BRCA1	chr6:57381413-57381830	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr6:57370484-57370781	GM12878	blood:	n/a	n/a
12	CCNT2	chr6:57376252-57377005	K562	blood:	n/a	n/a
13	CCNT2	chr6:57337935-57338250	K562	blood:	n/a	n/a
14	CCNT2	chr6:57354598-57355019	K562	blood:	n/a	n/a
15	CEBPB	chr6:57342573-57342758	K562	blood:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
16	CEBPB	chr6:57342545-57342922	K562	blood:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
17	CEBPB	chr6:57380150-57380500	Hela-S3	cervix:	n/a	chr6:57380307-57380318
18	CEBPB	chr6:57380175-57380499	A549	lung:	n/a	chr6:57380307-57380318
19	CEBPB	chr6:57339218-57339525	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:57339921-57340252	Hela-S3	cervix:	n/a	chr6:57340072-57340083
21	CEBPB	chr6:57380194-57380517	H1-hESC	embryonic stem cell:	n/a	chr6:57380307-57380318
22	CEBPB	chr6:57339741-57340235	A549	lung:	n/a	chr6:57340072-57340083
23	CEBPB	chr6:57309469-57309669	IMR90	lung:	n/a	chr6:57309567-57309578 chr6:57309569-57309580 chr6:57309567-57309580
24	CEBPB	chr6:57370190-57370638	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr6:57339225-57340861	IMR90	lung:	n/a	chr6:57340669-57340680 chr6:57340072-57340083
26	CEBPB	chr6:57345012-57345358	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:57380157-57380496	IMR90	lung:	n/a	chr6:57380307-57380318
28	CEBPB	chr6:57365064-57365775	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:57351453-57351791	A549	lung:	n/a	n/a
30	CEBPB	chr6:57340499-57340835	HepG2	liver:	n/a	chr6:57340669-57340680
31	CEBPB	chr6:57309423-57309721	HepG2	liver:	n/a	chr6:57309567-57309578 chr6:57309569-57309580 chr6:57309567-57309580
32	CEBPB	chr6:57351508-57351781	K562	blood:	n/a	n/a
33	CEBPB	chr6:57342505-57343002	A549	lung:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
34	CEBPB	chr6:57363427-57363693	K562	blood:	n/a	chr6:57363543-57363556 chr6:57363543-57363556 chr6:57363543-57363556 chr6:57363543-57363554
35	CEBPB	chr6:57342549-57342911	A549	lung:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
36	CEBPB	chr6:57342547-57342915	HepG2	liver:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
37	CEBPB	chr6:57340502-57340798	A549	lung:	n/a	chr6:57340669-57340680
38	CEBPB	chr6:57380136-57380500	HepG2	liver:	n/a	chr6:57380307-57380318
39	CEBPB	chr6:57380170-57380548	MCF-7	breast:	n/a	chr6:57380307-57380318
40	CEBPB	chr6:57345045-57345323	A549	lung:	n/a	n/a
41	CEBPB	chr6:57380149-57380488	K562	blood:	n/a	chr6:57380307-57380318
42	CEBPB	chr6:57351451-57351812	HepG2	liver:	n/a	n/a
43	CEBPB	chr6:57345014-57345344	IMR90	lung:	n/a	n/a
44	CEBPB	chr6:57342549-57342911	H1-hESC	embryonic stem cell:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
45	CEBPB	chr6:57339745-57340267	HepG2	liver:	n/a	chr6:57340072-57340083
46	CEBPB	chr6:57380130-57380666	MCF-7	breast:	n/a	chr6:57380307-57380318
47	CEBPB	chr6:57342547-57342921	IMR90	lung:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
48	CEBPB	chr6:57342559-57342815	K562	blood:	n/a	chr6:57342732-57342743 chr6:57342730-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741 chr6:57342730-57342743 chr6:57342732-57342741
49	CEBPB	chr6:57351364-57351927	IMR90	lung:	n/a	n/a
50	CEBPB	chr6:57372189-57372470	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:57339858-57339908	HEK293	kidney:	embryo
2	chr6:57339858-57339908	HEK293	kidney:	embryo
3	chr6:57339858-57339908	HCPEpiC	choroid plexus:	n/a
4	chr6:57339858-57339908	GM19239	blood:	n/a
5	chr6:57359134-57359184	NT2-D1	testis:	n/a
6	chr6:57359134-57359184	HCM	heart:	n/a
7	chr6:57339858-57339908	H1-hESC	embryonic stem cell:	embryo
8	chr6:57335405-57335455	HAEpiC	amniotic membrane:	n/a
9	chr6:57359134-57359184	HIPEpiC	eye:	n/a
10	chr6:57339858-57339908	SAEC	small airway:	n/a
11	chr6:57359134-57359184	Caco-2	colon:	n/a
12	chr6:57339858-57339908	SKMC	muscle:	n/a
13	chr6:57339858-57339908	K562	blood:	n/a
14	chr6:57339858-57339908	Jurkat	blood:	n/a
15	chr6:57350270-57350320	HCM	heart:	n/a
16	chr6:57339858-57339908	HCF	heart:	n/a
17	chr6:57339858-57339908	AG10803	skin:	n/a
18	chr6:57359134-57359184	HCT-116	colon:	n/a
19	chr6:57335405-57335455	AG04450	lung:	fetal
20	chr6:57359134-57359184	HNPCEpiC	eye:	n/a
21	chr6:57350270-57350320	AG04450	lung:	fetal
22	chr6:57335405-57335455	NB4	blood:	n/a
23	chr6:57335405-57335455	HNPCEpiC	eye:	n/a
24	chr6:57339858-57339908	HL-60	blood:	n/a
25	chr6:57359134-57359184	MCF10A-Er-Src	breast:	n/a
26	chr6:57335405-57335455	T-47D	breast:	n/a
27	chr6:57335405-57335455	LNCaP	prostate:	n/a
28	chr6:57359134-57359184	NHDF-neo	bronchial:	n/a
29	chr6:57359134-57359184	ProgFib	skin:	n/a
30	chr6:57335405-57335455	AG10803	skin:	n/a
31	chr6:57350270-57350320	MCF-7	breast:	n/a
32	chr6:57339858-57339908	HNPCEpiC	eye:	n/a
33	chr6:57335405-57335455	HCPEpiC	choroid plexus:	n/a
34	chr6:57335405-57335455	Hela-S3	cervix:	n/a
35	chr6:57359134-57359184	HEK293	kidney:	embryo
36	chr6:57335405-57335455	HUVEC	blood vessel:	n/a
37	chr6:57339858-57339908	HRE	kidney:	n/a
38	chr6:57359134-57359184	AG04450	lung:	fetal
39	chr6:57359134-57359184	SK-N-SH_RA	brain:	n/a
40	chr6:57350270-57350320	K562	blood:	n/a
41	chr6:57350270-57350320	AG10803	skin:	n/a
42	chr6:57359134-57359184	HL-60	blood:	n/a
43	chr6:57339858-57339908	ECC-1	luminal epithelium:	n/a
44	chr6:57359134-57359184	H1-hESC	embryonic stem cell:	embryo
45	chr6:57350270-57350320	Jurkat	blood:	n/a
46	chr6:57359134-57359184	AG09309	skin:	n/a
47	chr6:57339858-57339908	SK-N-SH_RA	brain:	n/a
48	chr6:57335405-57335455	CMK	blood:	n/a
49	chr6:57335405-57335455	ovcar-3	ovarian:	n/a
50	chr6:57350270-57350320	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:57370604..57372865-chr6:57373848..57376238,2	K562	blood:
2	chr6:57358740..57361214-chr6:57362213..57364300,2	K562	blood:
3	chr6:57344628..57347602-chr6:57348060..57349813,2	K562	blood:
4	chr6:57337415..57340116-chr6:57349926..57352459,2	K562	blood:
5	chr6:57346719..57348670-chr6:57349128..57351994,2	MCF-7	breast:
6	chr6:57344628..57347602-chr6:57348060..57349813,2	K562	blood:
7	chr6:57370604..57372865-chr6:57373848..57376238,2	K562	blood:
8	chr6:57232895..57235001-chr6:57373838..57375777,2	K562	blood:
9	chr6:57371365..57373576-chr6:57373848..57375922,2	K562	blood:
10	chr6:57349293..57351634-chr6:57356907..57359151,3	MCF-7	breast:
11	chr6:57371365..57373576-chr6:57373848..57375922,2	K562	blood:
12	chr6:57368098..57370585-chr6:57379961..57384432,3	K562	blood:
13	chr6:57346719..57348670-chr6:57349128..57351994,2	MCF-7	breast:
14	chr6:57358740..57361214-chr6:57362213..57364300,2	K562	blood:
15	chr6:57361390..57363831-chr6:57368584..57370615,2	MCF-7	breast:
16	chr6:57380965..57383908-chr6:57390419..57392004,2	K562	blood:
17	chr6:57337415..57340116-chr6:57349926..57352459,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAG2-1	chr6:57358736-57358845	ENSG00000266579.1
2	lnc-BAG2-1	chr6:57362331-57362565	ENSG00000266579.1

Variant related genes	Relation type
PRIM2	TF binding region
ENSG00000266579	TF binding region
PRIM2	CpG island
ENSG00000266579	CpG island
ENSG00000266579	chromatin interactions
ENSG00000146143	chromatin interactions

Extended variants
information (count: 4515 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4515 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7738530	chr6:57308960-57308961	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs62399073	chr6:57308974-57308975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533012468	chr6:57309093-57309094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145974315	chr6:57309094-57309095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374064587	chr6:57309095-57309096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138391603	chr6:57309132-57309133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74584198	chr6:57309137-57309138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113713942	chr6:57309138-57309139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370714674	chr6:57309142-57309143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs62399074	chr6:57309148-57309149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550236997	chr6:57309162-57309163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62399075	chr6:57309177-57309178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9475966	chr6:57309223-57309224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs386701532	chr6:57309232-57309233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112314560	chr6:57309234-57309235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113618226	chr6:57309238-57309239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538877524	chr6:57309255-57309256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111336989	chr6:57309290-57309291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182544691	chr6:57309300-57309301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9475967	chr6:57309313-57309314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs151207245	chr6:57309320-57309321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533678114	chr6:57309337-57309338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554938129	chr6:57309351-57309352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377038495	chr6:57309352-57309353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9475968	chr6:57309356-57309357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142115128	chr6:57309364-57309365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111769633	chr6:57309365-57309366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200028615	chr6:57309369-57309370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs66824143	chr6:57309381-57309382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573582144	chr6:57309382-57309383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574180838	chr6:57309400-57309401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370822569	chr6:57309417-57309418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9475969	chr6:57309433-57309434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs5023908	chr6:57309445-57309446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs5023907	chr6:57309475-57309476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs5023906	chr6:57309537-57309538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544486969	chr6:57309609-57309610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113581850	chr6:57309635-57309636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs137868454	chr6:57309639-57309640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs5003054	chr6:57309681-57309682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556194904	chr6:57309789-57309790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200057294	chr6:57309790-57309791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs5003055	chr6:57309813-57309814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs5003056	chr6:57309839-57309840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs371471388	chr6:57309841-57309842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs560536811	chr6:57309845-57309846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572554684	chr6:57309872-57309873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191682085	chr6:57309912-57309913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs5003057	chr6:57309914-57309915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs5003058	chr6:57309915-57309916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
small cell lung cancer	20016488	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
Lung cancer	18438408	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
Acute lymphoblastic leukemia	18458336	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
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:824 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57286600-57310200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:57289000-57310000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr6:57298000-57309800	Weak transcription	Dnd41	blood
4	chr6:57298600-57310800	Weak transcription	Colon Smooth Muscle	Colon
5	chr6:57302800-57310600	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr6:57303800-57311400	Weak transcription	Pancreas	Pancrea
7	chr6:57306000-57310600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr6:57306000-57310600	Weak transcription	HSMMtube	muscle
9	chr6:57306200-57310000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr6:57306200-57310600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:57306400-57310400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:57306800-57310000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:57306800-57310200	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr6:57307200-57310400	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr6:57307200-57310400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr6:57307200-57311400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr6:57307400-57310400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr6:57307400-57311600	Weak transcription	Left Ventricle	heart
19	chr6:57307600-57310200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr6:57307800-57310600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr6:57307800-57310600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr6:57307800-57313400	Weak transcription	Fetal Heart	heart
23	chr6:57308000-57310200	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr6:57308000-57310200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr6:57308000-57310200	Weak transcription	HSMM	muscle
26	chr6:57308200-57310200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr6:57308200-57311200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr6:57308400-57310000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr6:57308400-57310000	Weak transcription	Osteobl	bone
30	chr6:57308400-57310600	Weak transcription	NHDF-Ad	bronchial
31	chr6:57308600-57310600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:57309600-57311800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr6:57309800-57310200	Enhancers	HUVEC	blood vessel
34	chr6:57309800-57311800	Enhancers	Dnd41	blood
35	chr6:57309800-57313000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr6:57310000-57310200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr6:57310000-57310600	Enhancers	H1 Cell Line	embryonic stem cell
38	chr6:57310000-57310800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:57310000-57310800	Enhancers	Primary T cells from cord blood	blood
40	chr6:57310000-57310800	ZNF genes & repeats	HepG2	liver
41	chr6:57310000-57311000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:57310000-57311000	Enhancers	GM12878-XiMat	blood
43	chr6:57310000-57311000	Enhancers	Osteobl	bone
44	chr6:57310200-57310400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr6:57310200-57310600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:57310200-57310600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr6:57310200-57310600	Enhancers	HSMM	muscle
48	chr6:57310200-57310600	Weak transcription	NHLF	lung
49	chr6:57310200-57310800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr6:57310200-57311000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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