Variant report

Variant	nsv1033968
Chromosome Location	chr6:57651564-58082939
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:501)
CpG islands
(count:488)
Chromatin interactive
region (count:2)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:501 , 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	BATF	chr6:57705851-57706122	GM12878	blood:	n/a	chr6:57706041-57706049
3	BATF	chr6:57705853-57706117	GM12878	blood:	n/a	chr6:57706041-57706049
4	BCL11A	chr6:57705843-57706108	GM12878	blood:	n/a	n/a
5	BCL11A	chr6:57705880-57706094	GM12878	blood:	n/a	n/a
6	CEBPB	chr6:57837290-57837331	A549	lung:	n/a	n/a
7	CEBPB	chr6:57813363-57813589	HepG2	liver:	n/a	chr6:57813503-57813514
8	CEBPB	chr6:57835893-57836113	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr6:57678653-57678665	HepG2	liver:	n/a	n/a
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	chr6:58030489-58030521	HepG2	liver:	n/a	chr6:58030490-58030499 chr6:58030490-58030501 chr6:58030490-58030499 chr6:58030490-58030499 chr6:58030490-58030501 chr6:58030490-58030499
12	CEBPB	chr6:57837128-57837338	HepG2	liver:	n/a	chr6:57837142-57837155
13	CEBPB	chr6:57813456-57813566	A549	lung:	n/a	chr6:57813503-57813514
14	CEBPB	chr6:57662657-57662806	HepG2	liver:	n/a	n/a
15	CEBPB	chr6:57813381-57813566	IMR90	lung:	n/a	chr6:57813503-57813514
16	CEBPD	chr6:57695715-57695998	K562	blood:	n/a	n/a
17	CHD2	chr6:57757439-57757666	K562	blood:	n/a	n/a
18	CTCF	chr6:57709964-57710007	GM13976	blood:	n/a	n/a
19	CTCF	chr6:57690081-57690125	GM12891	blood:	n/a	n/a
20	CTCF	chr6:57811475-57811602	Gliobla	brain:	n/a	n/a
21	CTCF	chr6:57766927-57767194	LNCaP	prostate:	n/a	n/a
22	CTCF	chr6:57726656-57726673	LNCaP	prostate:	n/a	n/a
23	CTCF	chr6:57689991-57690147	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr6:57799429-57799508	LNCaP	prostate:	n/a	n/a
25	CTCF	chr6:57811425-57811688	Medullo	brain:	n/a	chr6:57811427-57811440
26	CTCF	chr6:57768397-57768454	GM20000	blood:	n/a	n/a
27	CTCF	chr6:57811451-57811644	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr6:57811449-57811640	MCF-7	breast:	n/a	n/a
29	CTCF	chr6:57903892-57903974	GM20000	blood:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
30	CTCF	chr6:57767018-57767174	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:57811440-57811590	NB4	blood:	n/a	n/a
32	CTCF	chr6:57903833-57904036	Kidney_OC	kidney:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
33	CTCF	chr6:57692493-57692562	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:57692510-57692570	GM10266	blood:	n/a	n/a
35	CTCF	chr6:57754514-57754622	HepG2	liver:	n/a	n/a
36	CTCF	chr6:58077742-58077787	LNCaP	prostate:	n/a	n/a
37	CTCF	chr6:57722727-57722911	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr6:57811418-57811676	MCF-7	breast:	n/a	chr6:57811427-57811440
39	CTCF	chr6:57722769-57722898	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr6:57754509-57754609	GM12892	blood:	n/a	n/a
41	CTCF	chr6:57903700-57903850	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr6:57903680-57903830	BJ	skin:	n/a	n/a
43	CTCF	chr6:57869798-57869852	GM20000	blood:	n/a	n/a
44	CTCF	chr6:57690015-57690125	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr6:57708948-57709024	K562	blood:	n/a	chr6:57708990-57709006
46	CTCF	chr6:57811420-57811570	A549	lung:	n/a	chr6:57811427-57811440
47	CTCF	chr6:57811420-57811570	NHEK	skin:	n/a	chr6:57811427-57811440
48	CTCF	chr6:57766972-57767170	Gliobla	brain:	n/a	n/a
49	CTCF	chr6:57689960-57690110	HEK293	kidney:	n/a	n/a
50	CTCF	chr6:57722760-57722910	HMEC	breast:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:57972223-57972273	PANC-1	pancreas:	n/a
2	chr6:57970666-57970716	HCT-116	colon:	n/a
3	chr6:57972680-57972730	A549	lung:	n/a
4	chr6:57972349-57972399	GM19239	blood:	n/a
5	chr6:57972680-57972730	U87	brain:	n/a
6	chr6:57972223-57972273	GM06990	blood:	n/a
7	chr6:57972223-57972273	NH-A	brain:	n/a
8	chr6:58001971-58002021	SK-N-SH_RA	brain:	n/a
9	chr6:57972223-57972273	HEEpiC	esophagus:	n/a
10	chr6:57972721-57972771	Jurkat	blood:	n/a
11	chr6:57970592-57970642	SK-N-MC	brain:	n/a
12	chr6:58001971-58002021	ECC-1	luminal epithelium:	n/a
13	chr6:57972680-57972730	HPAEpiC	pulmonary alveolar:	n/a
14	chr6:57972349-57972399	A549	lung:	n/a
15	chr6:57972349-57972399	NHDF-neo	bronchial:	n/a
16	chr6:57972223-57972273	NB4	blood:	n/a
17	chr6:57972680-57972730	HEEpiC	esophagus:	n/a
18	chr6:57972721-57972771	U87	brain:	n/a
19	chr6:57972680-57972730	HCPEpiC	choroid plexus:	n/a
20	chr6:57972349-57972399	AoSMC	blood vessel:	n/a
21	chr6:57970666-57970716	HCPEpiC	choroid plexus:	n/a
22	chr6:57912662-57912712	Jurkat	blood:	n/a
23	chr6:57972223-57972273	AG09309	skin:	n/a
24	chr6:57970666-57970716	H1-hESC	embryonic stem cell:	embryo
25	chr6:57970666-57970716	CMK	blood:	n/a
26	chr6:57972721-57972771	AG04450	lung:	fetal
27	chr6:58001971-58002021	MCF10A-Er-Src	breast:	n/a
28	chr6:57972223-57972273	K562	blood:	n/a
29	chr6:57972680-57972730	BE2_C	brain:	n/a
30	chr6:57972349-57972399	GM12892	blood:	n/a
31	chr6:57972349-57972399	HRPEpiC	eye:	n/a
32	chr6:57970666-57970716	SK-N-SH	brain:	n/a
33	chr6:57970592-57970642	HAEpiC	amniotic membrane:	n/a
34	chr6:57972721-57972771	SK-N-MC	brain:	n/a
35	chr6:58001971-58002021	HCT-116	colon:	n/a
36	chr6:57912662-57912712	AG09309	skin:	n/a
37	chr6:57972223-57972273	HCF	heart:	n/a
38	chr6:57970666-57970716	PANC-1	pancreas:	n/a
39	chr6:58001971-58002021	HRCEpiC	kidney:	n/a
40	chr6:57972721-57972771	AoSMC	blood vessel:	n/a
41	chr6:57972223-57972273	GM12878	blood:	n/a
42	chr6:57912662-57912712	HIPEpiC	eye:	n/a
43	chr6:57970666-57970716	A549	lung:	n/a
44	chr6:57972680-57972730	NHBE	bronchial:	n/a
45	chr6:57972223-57972273	HUVEC	blood vessel:	n/a
46	chr6:57972223-57972273	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:58001971-58002021	NHDF-neo	bronchial:	n/a
48	chr6:57912662-57912712	SK-N-MC	brain:	n/a
49	chr6:58001971-58002021	SK-N-MC	brain:	n/a
50	chr6:57970592-57970642	IMR90	lung:	fetal

(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-RAB23-13	chr6:57671339-57671489	NONHSAT113298
2	lnc-RAB23-15	chr6:57793932-57794280	NONHSAT113301
3	lnc-RAB23-14	chr6:57686969-57687949	NONHSAT113299
4	lnc-BAG2-11	chr6:57799352-57799604	NONHSAT113302
5	lnc-BAG2-3	chr6:57690895-57690956	XLOC_005331
6	lnc-BAG2-11	chr6:57798854-57798915	NONHSAT113302
7	lnc-BAG2-3	chr6:57691393-57691645	XLOC_005331
8	lnc-RAB23-13	chr6:57674277-57674350	NONHSAT113298

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: 2502 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2502 , 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	rs9476283	chr6:57651564-57651565	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561536877	chr6:57651566-57651567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573842949	chr6:57651620-57651621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567594090	chr6:57651703-57651704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544279004	chr6:57651758-57651759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562578604	chr6:57651791-57651792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533327399	chr6:57651792-57651793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9396408	chr6:57651803-57651804	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs560793957	chr6:57651830-57651831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527891279	chr6:57651839-57651840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549642025	chr6:57651865-57651866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs17752812	chr6:57651867-57651868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529031103	chr6:57651877-57651878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550658819	chr6:57651941-57651942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35896604	chr6:57651950-57651951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568781595	chr6:57651952-57651953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182363751	chr6:57652020-57652021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186642893	chr6:57652021-57652022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566798156	chr6:57652031-57652032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569596475	chr6:57652059-57652060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140854117	chr6:57652075-57652076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113667979	chr6:57652079-57652080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560240587	chr6:57652104-57652105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555171612	chr6:57652144-57652145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143280866	chr6:57652173-57652174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544315817	chr6:57652174-57652175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146596605	chr6:57652224-57652225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs55945673	chr6:57652227-57652228	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs141055692	chr6:57652233-57652234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554008410	chr6:57652276-57652277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560278962	chr6:57652281-57652282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528014521	chr6:57652285-57652286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543324874	chr6:57652295-57652296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114404259	chr6:57652296-57652297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531911159	chr6:57652308-57652309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550697632	chr6:57652334-57652335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568893515	chr6:57652365-57652366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192975408	chr6:57652387-57652388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374642548	chr6:57652411-57652412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184670827	chr6:57652412-57652413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566322797	chr6:57652442-57652443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533870646	chr6:57652482-57652483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577139362	chr6:57652618-57652619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555208681	chr6:57652627-57652628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs5876692	chr6:57652631-57652632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567148904	chr6:57652644-57652645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200854176	chr6:57652645-57652646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537604566	chr6:57652654-57652655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556394957	chr6:57652671-57652672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188855458	chr6:57652706-57652707	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:141 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57649000-57652400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:57650200-57653800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:57653200-57655600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr6:57653600-57655600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr6:57653800-57654600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:57654200-57655600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr6:57655000-57655600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr6:57655200-57655600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr6:57655600-57659000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr6:57655600-57659000	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr6:57659000-57659400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr6:57659000-57659400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr6:57659000-57659400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr6:57660800-57663000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:57663000-57663400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:57663000-57663400	ZNF genes & repeats	Pancreas	Pancrea
17	chr6:57663200-57663400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr6:57670200-57671200	Active TSS	Fetal Heart	heart
19	chr6:57704800-57706000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:57705000-57706600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:57718000-57718400	Active TSS	Fetal Heart	heart
22	chr6:57718200-57718800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:57726400-57726600	Enhancers	Fetal Intestine Small	intestine
24	chr6:57726600-57727200	Weak transcription	Fetal Intestine Small	intestine
25	chr6:57726600-57727800	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr6:57727200-57727800	Enhancers	Fetal Intestine Small	intestine
27	chr6:57727400-57727800	Enhancers	Fetal Intestine Large	intestine
28	chr6:57727400-57728000	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr6:57727600-57729600	Enhancers	Dnd41	blood
30	chr6:57734800-57736800	Enhancers	Fetal Intestine Large	intestine
31	chr6:57735000-57736800	Enhancers	Fetal Intestine Small	intestine
32	chr6:57746800-57747800	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr6:57747400-57748000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr6:57748000-57748400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr6:57748400-57748800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr6:57749800-57750000	Enhancers	Fetal Intestine Large	intestine
37	chr6:57750000-57751200	Weak transcription	Fetal Intestine Large	intestine
38	chr6:57750200-57751800	Enhancers	Fetal Intestine Small	intestine
39	chr6:57751200-57751800	Enhancers	Fetal Intestine Large	intestine
40	chr6:57760200-57760600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:57766400-57766800	Enhancers	Brain Cingulate Gyrus	brain
42	chr6:57766400-57766800	Enhancers	Brain Hippocampus Middle	brain
43	chr6:57766600-57767000	Enhancers	Fetal Brain Male	brain
44	chr6:57766800-57767000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr6:57766800-57767200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr6:57767400-57768400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr6:57768400-57768800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr6:57768400-57769200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr6:57768400-57769200	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr6:57789800-57790400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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