Variant report

Variant	nsv1024980
Chromosome Location	chr6:57656289-58145141
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:532)
CpG islands
(count:613)
Chromatin interactive
region (count:2)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	ATF3	chr6:58142472-58142715	K562	blood:	n/a	n/a
3	ATF3	chr6:58142478-58142721	A549	lung:	n/a	n/a
4	ATF3	chr6:58141691-58142004	K562	blood:	n/a	n/a
5	BATF	chr6:57705853-57706117	GM12878	blood:	n/a	chr6:57706041-57706049
6	BATF	chr6:57705851-57706122	GM12878	blood:	n/a	chr6:57706041-57706049
7	BCL11A	chr6:57705880-57706094	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:57705843-57706108	GM12878	blood:	n/a	n/a
9	CEBPB	chr6:57837128-57837338	HepG2	liver:	n/a	chr6:57837142-57837155
10	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
11	CEBPB	chr6:57835893-57836113	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr6:57837290-57837331	A549	lung:	n/a	n/a
13	CEBPB	chr6:57813456-57813566	A549	lung:	n/a	chr6:57813503-57813514
14	CEBPB	chr6:57813381-57813566	IMR90	lung:	n/a	chr6:57813503-57813514
15	CEBPB	chr6:57813363-57813589	HepG2	liver:	n/a	chr6:57813503-57813514
16	CEBPB	chr6:57662657-57662806	HepG2	liver:	n/a	n/a
17	CEBPB	chr6:57678653-57678665	HepG2	liver:	n/a	n/a
18	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
19	CEBPD	chr6:57695715-57695998	K562	blood:	n/a	n/a
20	CHD2	chr6:57757439-57757666	K562	blood:	n/a	n/a
21	CTCF	chr6:57690010-57690191	MCF-7	breast:	n/a	n/a
22	CTCF	chr6:57778614-57778670	MCF-7	breast:	n/a	n/a
23	CTCF	chr6:57766986-57767109	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr6:57903680-57903830	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr6:57767000-57767150	NHEK	skin:	n/a	n/a
26	CTCF	chr6:58060413-58060476	GM10248	blood:	n/a	n/a
27	CTCF	chr6:57725381-57725421	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr6:57862026-57862072	ProgFib	skin:	n/a	n/a
29	CTCF	chr6:58071598-58071641	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr6:58142480-58142630	HEK293	kidney:	n/a	n/a
31	CTCF	chr6:57689967-57690149	HepG2	liver:	n/a	n/a
32	CTCF	chr6:57767031-57767102	ProgFib	skin:	n/a	n/a
33	CTCF	chr6:57767018-57767081	GM12878	blood:	n/a	n/a
34	CTCF	chr6:57766987-57767126	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr6:57689939-57690168	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr6:57722720-57722870	SAEC	small airway:	n/a	n/a
37	CTCF	chr6:57903837-57903982	GM10266	blood:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
38	CTCF	chr6:57722760-57722910	HepG2	liver:	n/a	n/a
39	CTCF	chr6:57791167-57791299	Lung_OC	lung:	n/a	n/a
40	CTCF	chr6:57689984-57690148	ProgFib	skin:	n/a	n/a
41	CTCF	chr6:57811442-57811630	NHEK	skin:	n/a	n/a
42	CTCF	chr6:57903820-57904035	Hela-S3	cervix:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
43	CTCF	chr6:57722820-57722876	GM19239	blood:	n/a	n/a
44	CTCF	chr6:57791088-57791202	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr6:57903700-57903850	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr6:57754541-57754609	GM12878	blood:	n/a	n/a
47	CTCF	chr6:57800926-57800927	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:57903580-57903730	HMEC	breast:	n/a	n/a
49	CTCF	chr6:57704462-57704515	GM13976	blood:	n/a	n/a
50	CTCF	chr6:57903680-57903830	BJ	skin:	n/a	n/a

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:57970666-57970716	HIPEpiC	eye:	n/a
2	chr6:57972680-57972730	K562	blood:	n/a
3	chr6:57912662-57912712	HEK293	kidney:	embryo
4	chr6:57970666-57970716	HIPEpiC	eye:	n/a
5	chr6:57972680-57972730	K562	blood:	n/a
6	chr6:57912662-57912712	HEK293	kidney:	embryo
7	chr6:57972680-57972730	SK-N-MC	brain:	n/a
8	chr6:58141890-58141940	A549	lung:	n/a
9	chr6:58141890-58141940	BE2_C	brain:	n/a
10	chr6:57972721-57972771	LNCaP	prostate:	n/a
11	chr6:57970666-57970716	AoSMC	blood vessel:	n/a
12	chr6:57970666-57970716	HEEpiC	esophagus:	n/a
13	chr6:57970592-57970642	HEK293	kidney:	embryo
14	chr6:57972721-57972771	ECC-1	luminal epithelium:	n/a
15	chr6:57912662-57912712	ovcar-3	ovarian:	n/a
16	chr6:57972680-57972730	HRPEpiC	eye:	n/a
17	chr6:57972223-57972273	SK-N-SH_RA	brain:	n/a
18	chr6:58001971-58002021	HRCEpiC	kidney:	n/a
19	chr6:57972349-57972399	LNCaP	prostate:	n/a
20	chr6:57970666-57970716	HCF	heart:	n/a
21	chr6:58001971-58002021	PrEC	prostate:	n/a
22	chr6:58141890-58141940	PFSK-1	brain:	n/a
23	chr6:57912662-57912712	K562	blood:	n/a
24	chr6:58141890-58141940	T-47D	breast:	n/a
25	chr6:57972721-57972771	HCT-116	colon:	n/a
26	chr6:58142044-58142094	NT2-D1	testis:	n/a
27	chr6:57972349-57972399	PrEC	prostate:	n/a
28	chr6:57972349-57972399	GM06990	blood:	n/a
29	chr6:57972680-57972730	HCPEpiC	choroid plexus:	n/a
30	chr6:57972223-57972273	SKMC	muscle:	n/a
31	chr6:57972721-57972771	ProgFib	skin:	n/a
32	chr6:58141890-58141940	GM06990	blood:	n/a
33	chr6:58142044-58142094	U87	brain:	n/a
34	chr6:57912662-57912712	Jurkat	blood:	n/a
35	chr6:58141890-58141940	GM19239	blood:	n/a
36	chr6:58141890-58141940	MCF-7	breast:	n/a
37	chr6:57970666-57970716	H1-hESC	embryonic stem cell:	embryo
38	chr6:57970666-57970716	PANC-1	pancreas:	n/a
39	chr6:57972680-57972730	SK-N-SH_RA	brain:	n/a
40	chr6:57972349-57972399	A549	lung:	n/a
41	chr6:57970592-57970642	AG09309	skin:	n/a
42	chr6:58001971-58002021	AG04450	lung:	fetal
43	chr6:58142044-58142094	ovcar-3	ovarian:	n/a
44	chr6:57972721-57972771	BJ	skin:	n/a
45	chr6:57970592-57970642	NT2-D1	testis:	n/a
46	chr6:57972721-57972771	A549	lung:	n/a
47	chr6:57970592-57970642	NHBE	bronchial:	n/a
48	chr6:58141890-58141940	NB4	blood:	n/a
49	chr6:57972680-57972730	Jurkat	blood:	n/a
50	chr6:57972349-57972399	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:57445356..57445958-chr6:57689666..57690275,2	MCF-7	breast:
2	chr6:57766644..57767228-chr6:62859661..62860581,2	MCF-7	breast:

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

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

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
NR3C1	miRNA target sites
PNN	miRNA target sites

Extended variants
information (count: 2535 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2535 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530952799	chr6:57656307-57656308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs375675257	chr6:57656308-57656309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564329114	chr6:57656325-57656326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528442124	chr6:57656365-57656366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546906965	chr6:57656368-57656369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568450776	chr6:57656386-57656387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535727675	chr6:57656468-57656469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115853223	chr6:57656537-57656538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4131418	chr6:57656540-57656541	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs536756527	chr6:57656541-57656542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558575177	chr6:57656547-57656548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190780656	chr6:57656561-57656562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183434677	chr6:57656572-57656573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4587175	chr6:57656579-57656580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs77124095	chr6:57656599-57656600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542140213	chr6:57656615-57656616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532370980	chr6:57656720-57656721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142400449	chr6:57656725-57656726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375463224	chr6:57656733-57656734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368706715	chr6:57656742-57656743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188027545	chr6:57656758-57656759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145978731	chr6:57656782-57656783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34573953	chr6:57656784-57656785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376441124	chr6:57656785-57656786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs55666501	chr6:57656801-57656802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564572668	chr6:57656825-57656826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13215397	chr6:57656853-57656854	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs9476284	chr6:57656869-57656870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561745273	chr6:57656876-57656877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529585340	chr6:57656880-57656881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368388702	chr6:57657059-57657060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191494880	chr6:57657119-57657120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569354254	chr6:57657149-57657150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539995125	chr6:57657180-57657181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552001503	chr6:57657214-57657215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114482521	chr6:57657224-57657225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528293041	chr6:57657284-57657285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114297079	chr6:57657292-57657293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553048661	chr6:57657368-57657369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs76782963	chr6:57657433-57657434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182964700	chr6:57657465-57657466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187257267	chr6:57657466-57657467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375885470	chr6:57657476-57657477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546016064	chr6:57657525-57657526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557647769	chr6:57657564-57657565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573049998	chr6:57657588-57657589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192642878	chr6:57657646-57657647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9349914	chr6:57657654-57657655	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs56805961	chr6:57657711-57657712	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs544600714	chr6:57657777-57657778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57655600-57659000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:57655600-57659000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr6:57659000-57659400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr6:57659000-57659400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr6:57659000-57659400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr6:57660800-57663000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:57663000-57663400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:57663000-57663400	ZNF genes & repeats	Pancreas	Pancrea
9	chr6:57663200-57663400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr6:57670200-57671200	Active TSS	Fetal Heart	heart
11	chr6:57704800-57706000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:57705000-57706600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:57718000-57718400	Active TSS	Fetal Heart	heart
14	chr6:57718200-57718800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:57726400-57726600	Enhancers	Fetal Intestine Small	intestine
16	chr6:57726600-57727200	Weak transcription	Fetal Intestine Small	intestine
17	chr6:57726600-57727800	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr6:57727200-57727800	Enhancers	Fetal Intestine Small	intestine
19	chr6:57727400-57727800	Enhancers	Fetal Intestine Large	intestine
20	chr6:57727400-57728000	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr6:57727600-57729600	Enhancers	Dnd41	blood
22	chr6:57734800-57736800	Enhancers	Fetal Intestine Large	intestine
23	chr6:57735000-57736800	Enhancers	Fetal Intestine Small	intestine
24	chr6:57746800-57747800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr6:57747400-57748000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr6:57748000-57748400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr6:57748400-57748800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr6:57749800-57750000	Enhancers	Fetal Intestine Large	intestine
29	chr6:57750000-57751200	Weak transcription	Fetal Intestine Large	intestine
30	chr6:57750200-57751800	Enhancers	Fetal Intestine Small	intestine
31	chr6:57751200-57751800	Enhancers	Fetal Intestine Large	intestine
32	chr6:57760200-57760600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr6:57766400-57766800	Enhancers	Brain Cingulate Gyrus	brain
34	chr6:57766400-57766800	Enhancers	Brain Hippocampus Middle	brain
35	chr6:57766600-57767000	Enhancers	Fetal Brain Male	brain
36	chr6:57766800-57767000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:57766800-57767200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr6:57767400-57768400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr6:57768400-57768800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr6:57768400-57769200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr6:57768400-57769200	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr6:57789800-57790400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:57790000-57790600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr6:57808400-57808800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr6:57808800-57810400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr6:57810400-57812000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr6:57810400-57812000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr6:57810600-57811400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr6:57810600-57812000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr6:57810600-57812000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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