Variant report

Variant	nsv1032012
Chromosome Location	chr6:58376124-58774716
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:639)
CpG islands
(count:244)
Chromatin interactive
region (count:7)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:639 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:58774342-58780018	K562	blood:	n/a	n/a
2	ATF1	chr6:58773485-58774093	K562	blood:	n/a	n/a
3	BACH1	chr6:58773467-58774102	K562	blood:	n/a	n/a
4	BATF	chr6:58764416-58764615	GM12878	blood:	n/a	n/a
5	BATF	chr6:58737236-58737386	GM12878	blood:	n/a	n/a
6	BATF	chr6:58773550-58780199	GM12878	blood:	n/a	n/a
7	BATF	chr6:58773483-58774907	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:58773535-58780209	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:58773554-58780191	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:58737244-58737378	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:58737228-58737405	HepG2	liver:	n/a	n/a
12	BHLHE40	chr6:58773547-58780210	HepG2	liver:	n/a	n/a
13	BRCA1	chr6:58773464-58774101	GM12878	blood:	n/a	n/a
14	BRCA1	chr6:58774347-58780025	HepG2	liver:	n/a	n/a
15	BRCA1	chr6:58773462-58774102	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr6:58774347-58780021	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr6:58774350-58780022	GM12878	blood:	n/a	n/a
18	CEBPB	chr6:58524581-58524685	IMR90	lung:	n/a	n/a
19	CEBPB	chr6:58385936-58386118	IMR90	lung:	n/a	n/a
20	CEBPB	chr6:58506303-58506382	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:58773594-58774222	GM12878	blood:	n/a	n/a
22	CEBPB	chr6:58774302-58774846	GM12878	blood:	n/a	n/a
23	CEBPB	chr6:58576509-58576728	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:58441968-58442111	HepG2	liver:	n/a	chr6:58442072-58442083 chr6:58442073-58442084
25	CEBPB	chr6:58524736-58524936	Hela-S3	cervix:	n/a	n/a
26	CHD1	chr6:58774350-58780020	GM12878	blood:	n/a	n/a
27	CHD1	chr6:58773464-58774101	GM12878	blood:	n/a	n/a
28	CHD2	chr6:58774351-58780021	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr6:58773462-58774101	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr6:58689626-58689700	LNCaP	prostate:	n/a	n/a
31	CTCF	chr6:58508063-58508279	Lung_OC	lung:	n/a	chr6:58508122-58508143 chr6:58508127-58508145
32	CTCF	chr6:58512598-58512652	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr6:58710713-58710741	Fibrobl	skin:	n/a	n/a
34	CTCF	chr6:58507900-58508050	A549	lung:	n/a	n/a
35	CTCF	chr6:58648217-58648254	LNCaP	prostate:	n/a	n/a
36	CTCF	chr6:58508048-58508243	Spleen_OC	spleen:	n/a	chr6:58508122-58508143 chr6:58508127-58508145
37	CTCF	chr6:58693345-58693373	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr6:58642123-58642176	GM10266	blood:	n/a	n/a
39	CTCF	chr6:58481989-58482053	GM10248	blood:	n/a	n/a
40	CTCF	chr6:58507900-58508050	BJ	skin:	n/a	n/a
41	CTCF	chr6:58507900-58508050	HRE	kidney:	n/a	n/a
42	CTCF	chr6:58440347-58440485	MCF-7	breast:	n/a	n/a
43	CTCF	chr6:58384696-58384752	LNCaP	prostate:	n/a	n/a
44	CTCF	chr6:58451233-58451313	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr6:58418346-58418400	GM12878	blood:	n/a	n/a
46	CTCF	chr6:58504116-58504128	GM10248	blood:	n/a	n/a
47	CTCF	chr6:58537538-58537622	GM13977	blood:	n/a	n/a
48	CTCF	chr6:58418308-58418469	LNCaP	prostate:	n/a	n/a
49	CTCF	chr6:58542031-58542072	GM10248	blood:	n/a	n/a
50	CTCF	chr6:58507900-58508050	RPTEC	kidney:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:58399793-58399843	HCM	heart:	n/a
2	chr6:58584053-58584103	CMK	blood:	n/a
3	chr6:58399599-58399649	NH-A	brain:	n/a
4	chr6:58584053-58584103	PFSK-1	brain:	n/a
5	chr6:58399793-58399843	IMR90	lung:	fetal
6	chr6:58584053-58584103	HRCEpiC	kidney:	n/a
7	chr6:58399599-58399649	HEEpiC	esophagus:	n/a
8	chr6:58399664-58399714	ProgFib	skin:	n/a
9	chr6:58399664-58399714	U87	brain:	n/a
10	chr6:58584053-58584103	HCF	heart:	n/a
11	chr6:58399793-58399843	HL-60	blood:	n/a
12	chr6:58399664-58399714	HCT-116	colon:	n/a
13	chr6:58584053-58584103	SK-N-SH_RA	brain:	n/a
14	chr6:58399664-58399714	NT2-D1	testis:	n/a
15	chr6:58399793-58399843	AG04449	skin:	fetal
16	chr6:58399664-58399714	GM12891	blood:	n/a
17	chr6:58399793-58399843	HepG2	liver:	n/a
18	chr6:58399664-58399714	HMEC	breast:	n/a
19	chr6:58399793-58399843	AG09319	gingival:	n/a
20	chr6:58399793-58399843	HIPEpiC	eye:	n/a
21	chr6:58399793-58399843	PANC-1	pancreas:	n/a
22	chr6:58399664-58399714	HAEpiC	amniotic membrane:	n/a
23	chr6:58399599-58399649	PrEC	prostate:	n/a
24	chr6:58584053-58584103	HEK293	kidney:	embryo
25	chr6:58399664-58399714	HL-60	blood:	n/a
26	chr6:58399599-58399649	SK-N-MC	brain:	n/a
27	chr6:58584053-58584103	NB4	blood:	n/a
28	chr6:58584053-58584103	PrEC	prostate:	n/a
29	chr6:58399793-58399843	NB4	blood:	n/a
30	chr6:58399793-58399843	HEK293	kidney:	embryo
31	chr6:58399664-58399714	Hela-S3	cervix:	n/a
32	chr6:58584053-58584103	MCF-7	breast:	n/a
33	chr6:58584053-58584103	Hela-S3	cervix:	n/a
34	chr6:58584053-58584103	MCF10A-Er-Src	breast:	n/a
35	chr6:58399793-58399843	ProgFib	skin:	n/a
36	chr6:58399664-58399714	GM19239	blood:	n/a
37	chr6:58399599-58399649	LNCaP	prostate:	n/a
38	chr6:58584053-58584103	HepG2	liver:	n/a
39	chr6:58399793-58399843	AoSMC	blood vessel:	n/a
40	chr6:58399793-58399843	NT2-D1	testis:	n/a
41	chr6:58399664-58399714	AG04449	skin:	fetal
42	chr6:58584053-58584103	IMR90	lung:	fetal
43	chr6:58584053-58584103	Hepatocyte	liver:	n/a
44	chr6:58399599-58399649	HCF	heart:	n/a
45	chr6:58584053-58584103	Jurkat	blood:	n/a
46	chr6:58399793-58399843	MCF10A-Er-Src	breast:	n/a
47	chr6:58399599-58399649	AG09309	skin:	n/a
48	chr6:58399664-58399714	NH-A	brain:	n/a
49	chr6:58399664-58399714	NHDF-neo	bronchial:	n/a
50	chr6:58399664-58399714	HCF	heart:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:38032912..38033432-chr6:58774035..58775015,2	MCF-7	breast:
2	chr6:58772143..58775007-chr6:58776713..58778919,5	K562	blood:
3	chr20:36661511..36663112-chr6:58773928..58776889,2	K562	blood:
4	chr20:56089136..56089874-chr6:58774030..58774536,2	MCF-7	breast:
5	chr6:58772384..58775379-chr6:58777406..58779060,3	K562	blood:
6	chr6:58773141..58775009-chr6:58776566..58778429,2	MCF-7	breast:
7	chr19:27738271..27739820-chr6:58772163..58774918,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAG2-7	chr6:58488888-58489027	ENSG00000223633.1
2	lnc-BAG2-7	chr6:58513504-58513860	ENSG00000223633.2
3	lnc-BAG2-7	chr6:58488888-58489027	ENSG00000223633.2
4	lnc-RAB23-19	chr6:58397998-58399412	NONHSAT113321

No data

Variant related genes	Relation type
ENSG00000223633	TF binding region
ENSG00000216687	TF binding region
RBBP4P4	TF binding region
ENSG00000223633	CpG island
ENSG00000216687	CpG island
RBBP4P4	CpG island
ENSG00000101407	chromatin interactions
ENSG00000101413	chromatin interactions

Extended variants
information (count: 2731 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2731 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2926966	chr6:58382809-58382810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373585282	chr6:58382859-58382860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540543776	chr6:58382890-58382891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2936325	chr6:58382936-58382937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529187894	chr6:58382961-58382962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1224768	chr6:58383014-58383015	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs192880818	chr6:58383021-58383022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532883548	chr6:58383023-58383024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371018950	chr6:58383037-58383038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2926967	chr6:58383047-58383048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147871607	chr6:58383065-58383066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184706578	chr6:58383069-58383070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2926968	chr6:58383078-58383079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs9404726	chr6:58383139-58383140	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs147059943	chr6:58383142-58383143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567905185	chr6:58383228-58383229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35680854	chr6:58383277-58383278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs386407266	chr6:58383282-58383283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368796786	chr6:58383317-58383318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148102965	chr6:58383328-58383329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs578051281	chr6:58383355-58383356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2996212	chr6:58383417-58383418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539152017	chr6:58383421-58383422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1224769	chr6:58383440-58383441	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs2926969	chr6:58383524-58383525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2926970	chr6:58383550-58383551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377156721	chr6:58383574-58383575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573078246	chr6:58383577-58383578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1224770	chr6:58383592-58383593	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs561913075	chr6:58383606-58383607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532164448	chr6:58383612-58383613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188580695	chr6:58383653-58383654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181377160	chr6:58383671-58383672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562357214	chr6:58383724-58383725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1381230	chr6:58383725-58383726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1381231	chr6:58383758-58383759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532724418	chr6:58383768-58383769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138608707	chr6:58383774-58383775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551061788	chr6:58383787-58383788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559861829	chr6:58383797-58383798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1381232	chr6:58383809-58383810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545527061	chr6:58383835-58383836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559000033	chr6:58383859-58383860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183691873	chr6:58383917-58383918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1381233	chr6:58383940-58383941	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs537836735	chr6:58383988-58383989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189196143	chr6:58384260-58384261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2996211	chr6:58384295-58384296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372686647	chr6:58384339-58384340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375989686	chr6:58384348-58384349	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
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58382800-58383000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:58383000-58385200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:58385200-58385600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:58385400-58386000	Enhancers	Osteobl	bone
5	chr6:58385600-58386000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:58385600-58386000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:58385600-58386000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr6:58385600-58386000	Enhancers	Brain Anterior Caudate	brain
9	chr6:58385600-58386000	Enhancers	HSMM	muscle
10	chr6:58385800-58386200	Enhancers	Adipose Nuclei	Adipose
11	chr6:58394000-58394800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr6:58399600-58399800	ZNF genes & repeats	Gastric	stomach
13	chr6:58399600-58400000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:58417400-58419000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr6:58417800-58418800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr6:58417800-58419000	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:58439600-58440400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:58440000-58440400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr6:58440000-58440600	Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr6:58440000-58440600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
21	chr6:58440000-58441000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:58440200-58441000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:58440400-58440800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:58440800-58441000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:58441000-58443600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:58441000-58443600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr6:58441000-58443600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:58443600-58444000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:58443600-58444400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:58443600-58444400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:58450800-58453400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:58451000-58452000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:58452000-58452600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:58452600-58452800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:58452800-58454200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:58453400-58454200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr6:58454200-58454800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:58454200-58455600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr6:58454400-58454800	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr6:58454800-58455400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:58455400-58455600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:58518400-58519600	Enhancers	NHEK	skin
43	chr6:58519200-58520000	Enhancers	Muscle Satellite Cultured Cells	--
44	chr6:58519600-58520200	Active TSS	NHEK	skin
45	chr6:58519800-58520200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr6:58520200-58524000	Weak transcription	NHEK	skin
47	chr6:58522000-58522200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr6:58524000-58525800	Enhancers	NHEK	skin
49	chr6:58591000-58591400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr6:58607000-58607400	Active TSS	Stomach Mucosa	stomach

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