Variant report

Variant	nsv603197
Chromosome Location	chr6:57535593-58075480
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1165)
CpG islands
(count:550)
Chromatin interactive
region (count:10)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1165 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:57996881-57996935	K562	blood:	n/a	n/a
2	ATF1	chr6:57573821-57574021	K562	blood:	n/a	n/a
3	ATF1	chr6:57618389-57618391	K562	blood:	n/a	n/a
4	BACH1	chr6:57541125-57541357	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:57545381-57545540	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr6:57705853-57706117	GM12878	blood:	n/a	chr6:57706041-57706049
7	BATF	chr6:57705851-57706122	GM12878	blood:	n/a	chr6:57706041-57706049
8	BCL11A	chr6:57705880-57706094	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:57705843-57706108	GM12878	blood:	n/a	n/a
10	BRCA1	chr6:57554228-57554351	GM12878	blood:	n/a	n/a
11	BRCA1	chr6:57574332-57574500	GM12878	blood:	n/a	n/a
12	BRCA1	chr6:57540464-57540783	HepG2	liver:	n/a	n/a
13	BRCA1	chr6:57535844-57535916	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr6:57540290-57540327	GM12878	blood:	n/a	n/a
15	BRCA1	chr6:57538781-57538788	GM12878	blood:	n/a	n/a
16	CBX3	chr6:57553568-57553847	HCT-116	colon:	n/a	n/a
17	CEBPB	chr6:57538070-57538422	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr6:57837290-57837331	A549	lung:	n/a	n/a
19	CEBPB	chr6:57611670-57611837	IMR90	lung:	n/a	chr6:57611723-57611734
20	CEBPB	chr6:57813363-57813589	HepG2	liver:	n/a	chr6:57813503-57813514
21	CEBPB	chr6:57837128-57837338	HepG2	liver:	n/a	chr6:57837142-57837155
22	CEBPB	chr6:57594574-57594773	HepG2	liver:	n/a	chr6:57594706-57594717
23	CEBPB	chr6:58030489-58030521	HepG2	liver:	n/a	chr6:58030490-58030499 chr6:58030490-58030501 chr6:58030490-58030499 chr6:58030490-58030499 chr6:58030490-58030501 chr6:58030490-58030499
24	CEBPB	chr6:57813456-57813566	A549	lung:	n/a	chr6:57813503-57813514
25	CEBPB	chr6:57662657-57662806	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:57835893-57836113	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr6:57813381-57813566	IMR90	lung:	n/a	chr6:57813503-57813514
28	CEBPB	chr6:57678653-57678665	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:57611571-57611877	HepG2	liver:	n/a	chr6:57611723-57611734
30	CEBPB	chr6:57678625-57678743	K562	blood:	n/a	chr6:57678645-57678662 chr6:57678650-57678661 chr6:57678648-57678661 chr6:57678648-57678659 chr6:57678648-57678661 chr6:57678650-57678661
31	CEBPD	chr6:57695715-57695998	K562	blood:	n/a	n/a
32	CEBPZ	chr6:57537160-57537269	HepG2	liver:	n/a	n/a
33	CEBPZ	chr6:57562587-57562688	HepG2	liver:	n/a	n/a
34	CEBPZ	chr6:57566746-57566820	HepG2	liver:	n/a	n/a
35	CHD1	chr6:57566626-57566680	GM12878	blood:	n/a	n/a
36	CHD2	chr6:57574789-57574824	GM12878	blood:	n/a	n/a
37	CHD2	chr6:57757439-57757666	K562	blood:	n/a	n/a
38	CTCF	chr6:57689980-57690130	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:57766956-57767184	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:57539323-57539879	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:57539460-57539610	BJ	skin:	n/a	n/a
42	CTCF	chr6:57574500-57574650	HCT-116	colon:	n/a	n/a
43	CTCF	chr6:57539500-57539650	GM12878	blood:	n/a	n/a
44	CTCF	chr6:57540460-57540610	Hela-S3	cervix:	n/a	chr6:57540553-57540566
45	CTCF	chr6:57574820-57574970	HPF	lung:	n/a	n/a
46	CTCF	chr6:57540480-57540630	AG10803	skin:	n/a	chr6:57540553-57540566
47	CTCF	chr6:57540421-57540765	H1-hESC	embryonic stem cell:	n/a	chr6:57540553-57540566
48	CTCF	chr6:57539520-57539670	HMF	breast:	n/a	n/a
49	CTCF	chr6:57539520-57539670	AG10803	skin:	n/a	n/a
50	CTCF	chr6:57767011-57767114	K562	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:57970666-57970716	NHBE	bronchial:	n/a
2	chr6:57970666-57970716	NHBE	bronchial:	n/a
3	chr6:57970592-57970642	LNCaP	prostate:	n/a
4	chr6:57972223-57972273	GM12878	blood:	n/a
5	chr6:57972349-57972399	HL-60	blood:	n/a
6	chr6:57912662-57912712	HNPCEpiC	eye:	n/a
7	chr6:57972721-57972771	MCF-7	breast:	n/a
8	chr6:57972680-57972730	AG09319	gingival:	n/a
9	chr6:57972223-57972273	Hela-S3	cervix:	n/a
10	chr6:57970592-57970642	AG04450	lung:	fetal
11	chr6:57614321-57614371	SK-N-MC	brain:	n/a
12	chr6:57614321-57614371	PFSK-1	brain:	n/a
13	chr6:57970666-57970716	ProgFib	skin:	n/a
14	chr6:57972223-57972273	AG04449	skin:	fetal
15	chr6:57614321-57614371	BE2_C	brain:	n/a
16	chr6:57972680-57972730	BJ	skin:	n/a
17	chr6:57970666-57970716	K562	blood:	n/a
18	chr6:57970666-57970716	PANC-1	pancreas:	n/a
19	chr6:57972680-57972730	AG04449	skin:	fetal
20	chr6:57972349-57972399	GM12891	blood:	n/a
21	chr6:57972721-57972771	SKMC	muscle:	n/a
22	chr6:57912662-57912712	HRCEpiC	kidney:	n/a
23	chr6:57614321-57614371	NHBE	bronchial:	n/a
24	chr6:57614321-57614371	AG09309	skin:	n/a
25	chr6:57972721-57972771	ovcar-3	ovarian:	n/a
26	chr6:58001971-58002021	SK-N-SH	brain:	n/a
27	chr6:57912662-57912712	BJ	skin:	n/a
28	chr6:57972680-57972730	GM12892	blood:	n/a
29	chr6:57972349-57972399	MCF10A-Er-Src	breast:	n/a
30	chr6:57972349-57972399	BJ	skin:	n/a
31	chr6:57614321-57614371	HEK293	kidney:	embryo
32	chr6:57972223-57972273	CMK	blood:	n/a
33	chr6:58001971-58002021	NT2-D1	testis:	n/a
34	chr6:57912662-57912712	SK-N-SH	brain:	n/a
35	chr6:57970592-57970642	HUVEC	blood vessel:	n/a
36	chr6:57972223-57972273	SK-N-SH_RA	brain:	n/a
37	chr6:57972223-57972273	GM12892	blood:	n/a
38	chr6:58001971-58002021	HCF	heart:	n/a
39	chr6:57972223-57972273	HepG2	liver:	n/a
40	chr6:57614321-57614371	GM19239	blood:	n/a
41	chr6:57970592-57970642	ECC-1	luminal epithelium:	n/a
42	chr6:57912662-57912712	AG09309	skin:	n/a
43	chr6:58001971-58002021	AG04449	skin:	fetal
44	chr6:57972349-57972399	Hepatocyte	liver:	n/a
45	chr6:57972349-57972399	NB4	blood:	n/a
46	chr6:58001971-58002021	HUVEC	blood vessel:	n/a
47	chr6:57970592-57970642	HepG2	liver:	n/a
48	chr6:57972349-57972399	ECC-1	luminal epithelium:	n/a
49	chr6:57912662-57912712	HAEpiC	amniotic membrane:	n/a
50	chr6:57972223-57972273	HMEC	breast:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:17753668..17754453-chr6:57615850..57616702,2	MCF-7	breast:
2	chr6:57444969..57446432-chr6:57539130..57540030,7	MCF-7	breast:
3	chr6:57541185..57543919-chr8:104728155..104729992,2	MCF-7	breast:
4	chr6:57766644..57767228-chr6:62859661..62860581,2	MCF-7	breast:
5	chr6:57445326..57445995-chr6:57539539..57540106,2	MCF-7	breast:
6	chr5:21570110..21571992-chr6:57575867..57577390,2	K562	blood:
7	chr6:57445356..57445958-chr6:57689666..57690275,2	MCF-7	breast:
8	chr6:57445250..57446013-chr6:57537509..57538705,3	MCF-7	breast:
9	chr18:1906473..1906973-chr6:57539499..57540003,2	MCF-7	breast:
10	chr6:57217129..57218039-chr6:57539079..57539990,3	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAG2-11	chr6:57798854-57798915	NONHSAT113302
2	lnc-RAB23-12	chr6:57551484-57551584	NONHSAT113297
3	lnc-BAG2-3	chr6:57690895-57690956	XLOC_005331
4	lnc-BAG2-11	chr6:57799352-57799604	NONHSAT113302
5	lnc-RAB23-15	chr6:57793932-57794280	NONHSAT113301
6	lnc-RAB23-14	chr6:57686969-57687949	NONHSAT113299
7	lnc-RAB23-13	chr6:57674277-57674350	NONHSAT113298
8	lnc-RAB23-13	chr6:57671339-57671489	NONHSAT113298
9	lnc-BAG2-3	chr6:57691393-57691645	XLOC_005331
10	lnc-RAB23-12	chr6:57543887-57544127	NONHSAT113297

No data

Variant related genes	Relation type
ENSG00000270213	TF binding region
ENSG00000231273	TF binding region
GAPDHP41	TF binding region
RBBP4P3	TF binding region
ENSG00000262828	TF binding region
ENSG00000270213	CpG island
ENSG00000231273	CpG island
GAPDHP41	CpG island
RBBP4P3	CpG island
ENSG00000262828	CpG island
ENSG00000263745	chromatin interactions
NR3C1	miRNA target sites
PNN	miRNA target sites

Extended variants
information (count: 6398 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:6398 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9476225	chr6:57535593-57535594	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577391312	chr6:57535601-57535602	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs73753377	chr6:57535607-57535608	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs73753378	chr6:57535612-57535613	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs544745588	chr6:57535620-57535621	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs560230608	chr6:57535626-57535627	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs572049249	chr6:57535635-57535636	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs79700250	chr6:57535645-57535646	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs75943453	chr6:57535680-57535681	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs77173749	chr6:57535682-57535683	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs74424879	chr6:57535714-57535715	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs76108031	chr6:57535775-57535776	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs62405807	chr6:57535782-57535783	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs62405808	chr6:57535794-57535795	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs561158676	chr6:57535807-57535808	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs62405809	chr6:57535811-57535812	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs531597204	chr6:57535815-57535816	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs9476226	chr6:57535820-57535821	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs73753379	chr6:57535832-57535833	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs564896261	chr6:57535849-57535850	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs532371287	chr6:57535855-57535856	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs74348524	chr6:57535862-57535863	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs146674236	chr6:57535875-57535876	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs67014056	chr6:57535876-57535877	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs79711043	chr6:57535877-57535878	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs79151697	chr6:57535889-57535890	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs78226910	chr6:57535891-57535892	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs376489389	chr6:57535893-57535894	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs547550023	chr6:57535908-57535909	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs62405810	chr6:57535931-57535932	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs77712256	chr6:57535951-57535952	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs565879039	chr6:57535956-57535957	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs536235114	chr6:57535965-57535966	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs548136274	chr6:57535974-57535975	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs79377372	chr6:57535977-57535978	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs537318876	chr6:57536005-57536006	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs74649841	chr6:57536006-57536007	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs79171137	chr6:57536055-57536056	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs74628765	chr6:57536071-57536072	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs147244314	chr6:57536086-57536087	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs77762742	chr6:57536087-57536088	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs77828016	chr6:57536105-57536106	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs577353431	chr6:57536135-57536136	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs9464545	chr6:57536142-57536143	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs553901696	chr6:57536148-57536149	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs572212757	chr6:57536161-57536162	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs55693315	chr6:57536181-57536182	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs560838396	chr6:57536193-57536194	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs74294547	chr6:57536204-57536205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576121662	chr6:57536210-57536211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
Ovarian cancer	21720365	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57533000-57538200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:57534200-57535600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:57534400-57536000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr6:57534400-57536200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:57534400-57537000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:57534600-57536200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr6:57534600-57536200	Enhancers	Osteobl	bone
8	chr6:57534600-57538000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:57534600-57538000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr6:57534800-57538000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr6:57535000-57535800	ZNF genes & repeats	HUVEC	blood vessel
12	chr6:57535000-57536200	Enhancers	NHDF-Ad	bronchial
13	chr6:57535200-57535800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:57535600-57536200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:57535600-57536200	Bivalent Enhancer	Aorta	Aorta
16	chr6:57535800-57538400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr6:57536200-57537000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr6:57536200-57537800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr6:57536200-57538000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr6:57536200-57538000	Weak transcription	Osteobl	bone
21	chr6:57536800-57537000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr6:57536800-57537000	Bivalent Enhancer	Aorta	Aorta
23	chr6:57537000-57537200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr6:57537000-57537200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr6:57537000-57538000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr6:57537000-57538000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr6:57537200-57538000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:57537200-57538000	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr6:57537800-57538600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
30	chr6:57537800-57540800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr6:57538000-57538200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:57538000-57538800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:57538000-57539000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:57538000-57539000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:57538000-57539400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:57538000-57539400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr6:57538000-57539400	Enhancers	H9 Cell Line	embryonic stem cell
38	chr6:57538000-57539400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:57538000-57539400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr6:57538000-57539600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr6:57538000-57539600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr6:57538000-57539600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr6:57538000-57539600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:57538000-57540800	Enhancers	Osteobl	bone
45	chr6:57538000-57541200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
46	chr6:57538200-57538400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr6:57538200-57538600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr6:57538200-57539000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:57538200-57539400	Enhancers	H1 Cell Line	embryonic stem cell
50	chr6:57538200-57540400	Enhancers	NHDF-Ad	bronchial

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