Variant report

Variant	nsv886009
Chromosome Location	chr6:65698500-65918809
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:354)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:65866932-65867276	HepG2	liver:	n/a	n/a
2	CEBPB	chr6:65866943-65867264	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr6:65716700-65717039	HepG2	liver:	n/a	chr6:65716874-65716885
4	CEBPB	chr6:65716699-65717038	H1-hESC	embryonic stem cell:	n/a	chr6:65716874-65716885
5	CEBPB	chr6:65755702-65756077	Hela-S3	cervix:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
6	CEBPB	chr6:65757460-65757715	HepG2	liver:	n/a	chr6:65757602-65757613
7	CEBPB	chr6:65867884-65868178	IMR90	lung:	n/a	chr6:65867989-65868002 chr6:65867991-65868000 chr6:65867991-65868002
8	CEBPB	chr6:65755724-65756051	K562	blood:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
9	CEBPB	chr6:65909779-65909892	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr6:65755738-65756070	IMR90	lung:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
11	CEBPB	chr6:65866950-65867272	IMR90	lung:	n/a	n/a
12	CEBPB	chr6:65714814-65714999	A549	lung:	n/a	chr6:65714880-65714891
13	CEBPB	chr6:65877133-65877402	HepG2	liver:	n/a	chr6:65877288-65877299
14	CEBPB	chr6:65909589-65909973	MCF-7	breast:	n/a	n/a
15	CEBPB	chr6:65840033-65840285	HepG2	liver:	n/a	chr6:65840147-65840158
16	CEBPB	chr6:65769840-65770057	HepG2	liver:	n/a	chr6:65769968-65769979
17	CEBPB	chr6:65895166-65895539	HepG2	liver:	n/a	chr6:65895346-65895357
18	CEBPB	chr6:65866986-65867268	A549	lung:	n/a	n/a
19	CEBPB	chr6:65852457-65852466	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:65755716-65756078	HepG2	liver:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
21	CEBPB	chr6:65755777-65756072	A549	lung:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
22	CEBPB	chr6:65867011-65867264	K562	blood:	n/a	n/a
23	CEBPB	chr6:65895196-65895497	A549	lung:	n/a	chr6:65895346-65895357
24	CEBPB	chr6:65714828-65715032	HepG2	liver:	n/a	chr6:65714880-65714891
25	CHD2	chr6:65740417-65740502	HepG2	liver:	n/a	n/a
26	CTCF	chr6:65723547-65723666	Gliobla	brain:	n/a	n/a
27	CTCF	chr6:65783645-65783977	MCF-7	breast:	n/a	n/a
28	CTCF	chr6:65723582-65723667	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr6:65723520-65723670	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr6:65783716-65783806	LNCaP	prostate:	n/a	n/a
31	CTCF	chr6:65783788-65783862	MCF-7	breast:	n/a	n/a
32	CTCF	chr6:65912320-65912470	K562	blood:	n/a	n/a
33	CTCF	chr6:65714320-65714470	HEK293	kidney:	n/a	n/a
34	CTCF	chr6:65723547-65723695	MCF-7	breast:	n/a	n/a
35	CTCF	chr6:65723520-65723670	GM12873	blood:	n/a	n/a
36	CTCF	chr6:65723460-65723610	GM12871	blood:	n/a	n/a
37	CTCF	chr6:65783714-65783870	LNCaP	prostate:	n/a	n/a
38	CTCF	chr6:65912441-65912442	HepG2	liver:	n/a	n/a
39	CTCF	chr6:65723560-65723710	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:65723540-65723690	HepG2	liver:	n/a	n/a
41	CTCF	chr6:65723580-65723730	K562	blood:	n/a	n/a
42	CTCF	chr6:65723500-65723650	GM12867	blood:	n/a	n/a
43	CTCF	chr6:65723560-65723710	GM12872	blood:	n/a	n/a
44	CTCF	chr6:65912360-65912510	HepG2	liver:	n/a	n/a
45	CTCF	chr6:65723540-65723690	NB4	blood:	n/a	n/a
46	CTCF	chr6:65723500-65723650	GM12872	blood:	n/a	n/a
47	CTCF	chr6:65723520-65723670	GM12878	blood:	n/a	n/a
48	CTCF	chr6:65836720-65836870	GM12871	blood:	n/a	n/a
49	CTCF	chr6:65723440-65723590	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr6:65723540-65723690	GM12872	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:65779514-65779564	HIPEpiC	eye:	n/a
2	chr6:65779514-65779564	NB4	blood:	n/a
3	chr6:65779514-65779564	Hepatocyte	liver:	n/a
4	chr6:65779514-65779564	MCF10A-Er-Src	breast:	n/a
5	chr6:65779514-65779564	BJ	skin:	n/a
6	chr6:65779514-65779564	LNCaP	prostate:	n/a
7	chr6:65779514-65779564	PFSK-1	brain:	n/a
8	chr6:65779514-65779564	HEEpiC	esophagus:	n/a
9	chr6:65779514-65779564	Jurkat	blood:	n/a
10	chr6:65779514-65779564	NHBE	bronchial:	n/a
11	chr6:65779514-65779564	NT2-D1	testis:	n/a
12	chr6:65779514-65779564	MCF-7	breast:	n/a
13	chr6:65779514-65779564	HRE	kidney:	n/a
14	chr6:65779514-65779564	HCT-116	colon:	n/a
15	chr6:65779514-65779564	NHDF-neo	bronchial:	n/a
16	chr6:65779514-65779564	PANC-1	pancreas:	n/a
17	chr6:65779514-65779564	AG10803	skin:	n/a
18	chr6:65779514-65779564	GM12892	blood:	n/a
19	chr6:65779514-65779564	HRCEpiC	kidney:	n/a
20	chr6:65779514-65779564	BE2_C	brain:	n/a
21	chr6:65779514-65779564	Caco-2	colon:	n/a
22	chr6:65779514-65779564	K562	blood:	n/a
23	chr6:65779514-65779564	HPAEpiC	pulmonary alveolar:	n/a
24	chr6:65779514-65779564	HMEC	breast:	n/a
25	chr6:65779514-65779564	HUVEC	blood vessel:	n/a
26	chr6:65779514-65779564	AG04450	lung:	fetal
27	chr6:65779514-65779564	PrEC	prostate:	n/a
28	chr6:65779514-65779564	NH-A	brain:	n/a
29	chr6:65779514-65779564	RPTEC	kidney:	n/a
30	chr6:65779514-65779564	HepG2	liver:	n/a
31	chr6:65779514-65779564	AG09309	skin:	n/a
32	chr6:65779514-65779564	Hela-S3	cervix:	n/a
33	chr6:65779514-65779564	ProgFib	skin:	n/a
34	chr6:65779514-65779564	HCF	heart:	n/a
35	chr6:65779514-65779564	IMR90	lung:	fetal
36	chr6:65779514-65779564	SK-N-SH_RA	brain:	n/a
37	chr6:65779514-65779564	CMK	blood:	n/a
38	chr6:65779514-65779564	HEK293	kidney:	embryo
39	chr6:65779514-65779564	HNPCEpiC	eye:	n/a
40	chr6:65779514-65779564	AG09319	gingival:	n/a
41	chr6:65779514-65779564	GM06990	blood:	n/a
42	chr6:65779514-65779564	HL-60	blood:	n/a
43	chr6:65779514-65779564	U87	brain:	n/a
44	chr6:65779514-65779564	GM12878	blood:	n/a
45	chr6:65779514-65779564	SK-N-MC	brain:	n/a
46	chr6:65779514-65779564	ovcar-3	ovarian:	n/a
47	chr6:65779514-65779564	HCPEpiC	choroid plexus:	n/a
48	chr6:65779514-65779564	HAEpiC	amniotic membrane:	n/a
49	chr6:65779514-65779564	SAEC	small airway:	n/a
50	chr6:65779514-65779564	SK-N-SH	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:65821770..65824951-chr6:65826871..65829970,3	K562	blood:
2	chr6:65781439..65783033-chr6:65783370..65784893,2	MCF-7	breast:
3	chr11:62312608..62314638-chr6:65744579..65746564,2	MCF-7	breast:
4	chr6:65761200..65763394-chr6:65766854..65768992,2	K562	blood:
5	chr6:65695796..65698770-chr6:65700016..65702026,2	K562	blood:
6	chr6:65778187..65780499-chr6:65782117..65784614,2	K562	blood:
7	chr6:65695796..65698770-chr6:65700016..65702026,2	K562	blood:
8	chr6:65821770..65824951-chr6:65826871..65829970,3	K562	blood:
9	chr6:65879743..65881792-chr6:65884642..65887053,2	MCF-7	breast:
10	chr6:65879743..65881792-chr6:65884642..65887053,2	MCF-7	breast:
11	chr6:65781439..65783033-chr6:65783370..65784893,2	MCF-7	breast:
12	chr6:65821523..65823761-chr6:65825584..65828218,2	MCF-7	breast:
13	chr6:65778187..65780499-chr6:65782117..65784614,2	K562	blood:
14	chr6:65821523..65823761-chr6:65825584..65828218,2	MCF-7	breast:
15	chr6:65761200..65763394-chr6:65766854..65768992,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000256352	TF binding region
ENSG00000256352	CpG island
ENSG00000257058	chromatin interactions
ENSG00000124942	chromatin interactions

Extended variants
information (count: 3179 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3179 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9345577	chr6:65698500-65698501	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs151311807	chr6:65698571-65698572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140557012	chr6:65698583-65698584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551235370	chr6:65698622-65698623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191041048	chr6:65698633-65698634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs9363306	chr6:65698750-65698751	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs182063715	chr6:65698753-65698754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565357987	chr6:65698765-65698766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs9363307	chr6:65698830-65698831	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs554278210	chr6:65698837-65698838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568221663	chr6:65698841-65698842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186037255	chr6:65698927-65698928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs72875947	chr6:65698962-65698963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548258816	chr6:65698976-65698977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546123663	chr6:65699015-65699016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376933650	chr6:65699039-65699040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566493111	chr6:65699072-65699073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553375372	chr6:65699082-65699083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149998174	chr6:65699101-65699102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9345578	chr6:65699119-65699120	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs373148243	chr6:65699196-65699197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146584388	chr6:65699199-65699200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190925969	chr6:65699204-65699205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs71553508	chr6:65699286-65699287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs67811515	chr6:65699288-65699289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72077653	chr6:65699299-65699300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183192300	chr6:65699309-65699310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs13205619	chr6:65699310-65699311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2349997	chr6:65699311-65699312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141186637	chr6:65699312-65699313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372288581	chr6:65699356-65699357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549850886	chr6:65699375-65699376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188073748	chr6:65699466-65699467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145020013	chr6:65699490-65699491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552728149	chr6:65699505-65699506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546902805	chr6:65699516-65699517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565319078	chr6:65699664-65699665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138879468	chr6:65699693-65699694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs3033931	chr6:65699694-65699695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9345579	chr6:65699696-65699697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540972262	chr6:65699717-65699718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs70999183	chr6:65699719-65699720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9345580	chr6:65699723-65699724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369984295	chr6:65699725-65699726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9354198	chr6:65699727-65699728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs66591902	chr6:65699781-65699782	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs548263297	chr6:65699834-65699835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138747548	chr6:65699852-65699853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537158452	chr6:65699868-65699869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538108612	chr6:65699876-65699877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Epilepsy	20502679	CNVD
Dyslexia	22102821	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:65697000-65698600	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr6:65697600-65699000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:65697600-65700000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:65698200-65698800	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr6:65698200-65699200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr6:65698200-65705000	Weak transcription	Pancreas	Pancrea
7	chr6:65698800-65699000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr6:65699000-65699200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr6:65699000-65700400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr6:65700000-65700400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:65700400-65700600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:65700400-65700800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:65700800-65701800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:65705000-65705200	Enhancers	Pancreas	Pancrea
15	chr6:65705200-65706200	Weak transcription	Pancreas	Pancrea
16	chr6:65706200-65707000	Enhancers	Pancreas	Pancrea
17	chr6:65706400-65707000	Enhancers	Fetal Heart	heart
18	chr6:65707000-65716000	Weak transcription	Pancreas	Pancrea
19	chr6:65707400-65707600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr6:65707600-65709400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr6:65708400-65712000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr6:65709200-65709800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr6:65709400-65709600	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr6:65709400-65709800	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr6:65709600-65709800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr6:65712000-65715000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr6:65716000-65716200	Enhancers	Pancreas	Pancrea
28	chr6:65716400-65716800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr6:65716400-65717000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr6:65716600-65717000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr6:65716600-65717000	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr6:65730400-65731000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:65731000-65740200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:65738800-65743200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr6:65739800-65740200	Enhancers	Pancreas	Pancrea
36	chr6:65740200-65740400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr6:65740200-65740600	ZNF genes & repeats	Pancreas	Pancrea
38	chr6:65743200-65743400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr6:65767200-65767800	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr6:65767800-65768600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr6:65774800-65775000	Enhancers	Spleen	Spleen
42	chr6:65784800-65786400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr6:65785400-65786600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr6:65785800-65786200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr6:65786600-65788400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr6:65788400-65788600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr6:65788600-65789000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr6:65789800-65791400	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr6:65807800-65808200	Enhancers	Fetal Brain Female	brain
50	chr6:65808000-65808400	Enhancers	Fetal Brain Male	brain

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