Variant report

Variant	nsv1019356
Chromosome Location	chr6:86826097-86919420
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:415)
CpG islands
(count:62)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:86919119-86919208	K562	blood:	n/a	n/a
2	ATF3	chr6:86901866-86902226	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr6:86901939-86902219	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:86901914-86902069	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr6:86898846-86898863	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr6:86901978-86902056	GM12878	blood:	n/a	n/a
7	CEBPB	chr6:86889432-86889622	HepG2	liver:	n/a	chr6:86889487-86889498
8	CEBPB	chr6:86910122-86910322	HepG2	liver:	n/a	chr6:86910235-86910246
9	CEBPB	chr6:86906426-86906770	HepG2	liver:	n/a	chr6:86906591-86906602 chr6:86906590-86906603
10	CTCF	chr6:86884945-86885190	GM12878	blood:	n/a	n/a
11	CTCF	chr6:86901940-86902090	AG09309	skin:	n/a	n/a
12	CTCF	chr6:86857700-86857850	HEK293	kidney:	n/a	n/a
13	CTCF	chr6:86884944-86885178	MCF-7	breast:	n/a	n/a
14	CTCF	chr6:86884906-86885160	T-47D	breast:	n/a	n/a
15	CTCF	chr6:86901904-86902167	K562	blood:	n/a	n/a
16	CTCF	chr6:86901960-86902110	MCF-7	breast:	n/a	n/a
17	CTCF	chr6:86901920-86902070	GM12873	blood:	n/a	n/a
18	CTCF	chr6:86885400-86885550	GM12872	blood:	n/a	n/a
19	CTCF	chr6:86884924-86885191	MCF-7	breast:	n/a	n/a
20	CTCF	chr6:86901960-86902110	GM12868	blood:	n/a	n/a
21	CTCF	chr6:86901998-86902135	MCF-7	breast:	n/a	n/a
22	CTCF	chr6:86884954-86885180	LNCaP	prostate:	n/a	n/a
23	CTCF	chr6:86901960-86902110	GM12874	blood:	n/a	n/a
24	CTCF	chr6:86901982-86902139	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr6:86884975-86885130	Lung_OC	lung:	n/a	n/a
26	CTCF	chr6:86901980-86902130	HPF	lung:	n/a	n/a
27	CTCF	chr6:86902020-86902170	BJ	skin:	n/a	n/a
28	CTCF	chr6:86884971-86885169	Medullo	brain:	n/a	n/a
29	CTCF	chr6:86901880-86902030	GM12870	blood:	n/a	n/a
30	CTCF	chr6:86902020-86902170	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr6:86901960-86902110	HMEC	breast:	n/a	n/a
32	CTCF	chr6:86902000-86902150	GM12865	blood:	n/a	n/a
33	CTCF	chr6:86857740-86857890	GM12866	blood:	n/a	n/a
34	CTCF	chr6:86884983-86885155	GM19239	blood:	n/a	n/a
35	CTCF	chr6:86884940-86885090	GM12872	blood:	n/a	n/a
36	CTCF	chr6:86901962-86902145	GM12892	blood:	n/a	n/a
37	CTCF	chr6:86885048-86885072	NHEK	skin:	n/a	n/a
38	CTCF	chr6:86884960-86885110	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:86901880-86902030	HL-60	blood:	n/a	n/a
40	CTCF	chr6:86884940-86885090	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr6:86901920-86902070	HCT-116	colon:	n/a	n/a
42	CTCF	chr6:86884808-86885198	A549	lung:	n/a	n/a
43	CTCF	chr6:86902041-86902146	GM12891	blood:	n/a	n/a
44	CTCF	chr6:86901900-86902050	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr6:86901300-86901450	BE2_C	brain:	n/a	n/a
46	CTCF	chr6:86884980-86885130	GM12878	blood:	n/a	n/a
47	CTCF	chr6:86839772-86839834	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:86885000-86885150	GM12875	blood:	n/a	n/a
49	CTCF	chr6:86901960-86902110	AG04450	lung:	n/a	n/a
50	CTCF	chr6:86901960-86902110	SAEC	small airway:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:86862059-86862109	GM12891	blood:	n/a
2	chr6:86862059-86862109	GM12891	blood:	n/a
3	chr6:86862059-86862109	NH-A	brain:	n/a
4	chr6:86862059-86862109	AoSMC	blood vessel:	n/a
5	chr6:86862059-86862109	AG09309	skin:	n/a
6	chr6:86862059-86862109	Caco-2	colon:	n/a
7	chr6:86862059-86862109	SK-N-SH_RA	brain:	n/a
8	chr6:86862059-86862109	HCPEpiC	choroid plexus:	n/a
9	chr6:86862059-86862109	PrEC	prostate:	n/a
10	chr6:86862059-86862109	HL-60	blood:	n/a
11	chr6:86862059-86862109	ovcar-3	ovarian:	n/a
12	chr6:86862059-86862109	NHDF-neo	bronchial:	n/a
13	chr6:86862059-86862109	NT2-D1	testis:	n/a
14	chr6:86862059-86862109	PANC-1	pancreas:	n/a
15	chr6:86862059-86862109	SKMC	muscle:	n/a
16	chr6:86862059-86862109	AG04449	skin:	fetal
17	chr6:86862059-86862109	ProgFib	skin:	n/a
18	chr6:86862059-86862109	MCF-7	breast:	n/a
19	chr6:86862059-86862109	HMEC	breast:	n/a
20	chr6:86862059-86862109	T-47D	breast:	n/a
21	chr6:86862059-86862109	HCF	heart:	n/a
22	chr6:86862059-86862109	GM19239	blood:	n/a
23	chr6:86862059-86862109	GM06990	blood:	n/a
24	chr6:86862059-86862109	H1-hESC	embryonic stem cell:	embryo
25	chr6:86862059-86862109	HCM	heart:	n/a
26	chr6:86862059-86862109	SK-N-SH	brain:	n/a
27	chr6:86862059-86862109	BJ	skin:	n/a
28	chr6:86862059-86862109	A549	lung:	n/a
29	chr6:86862059-86862109	AG10803	skin:	n/a
30	chr6:86862059-86862109	GM12892	blood:	n/a
31	chr6:86862059-86862109	BE2_C	brain:	n/a
32	chr6:86862059-86862109	RPTEC	kidney:	n/a
33	chr6:86862059-86862109	NHBE	bronchial:	n/a
34	chr6:86862059-86862109	HRCEpiC	kidney:	n/a
35	chr6:86862059-86862109	HAEpiC	amniotic membrane:	n/a
36	chr6:86862059-86862109	HEK293	kidney:	embryo
37	chr6:86862059-86862109	ECC-1	luminal epithelium:	n/a
38	chr6:86862059-86862109	SK-N-MC	brain:	n/a
39	chr6:86862059-86862109	GM12878	blood:	n/a
40	chr6:86862059-86862109	CMK	blood:	n/a
41	chr6:86862059-86862109	AG04450	lung:	fetal
42	chr6:86862059-86862109	HepG2	liver:	n/a
43	chr6:86862059-86862109	U87	brain:	n/a
44	chr6:86862059-86862109	HUVEC	blood vessel:	n/a
45	chr6:86862059-86862109	SAEC	small airway:	n/a
46	chr6:86862059-86862109	HRE	kidney:	n/a
47	chr6:86862059-86862109	K562	blood:	n/a
48	chr6:86862059-86862109	NB4	blood:	n/a
49	chr6:86862059-86862109	IMR90	lung:	fetal
50	chr6:86862059-86862109	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:86632367..86633291-chr6:86884579..86885474,2	MCF-7	breast:
2	chr6:86897792..86900051-chr6:86901438..86903650,2	K562	blood:
3	chr6:86897792..86900051-chr6:86901438..86903650,2	K562	blood:
4	chr6:86632071..86633265-chr6:86884594..86886454,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM165A-3	chr6:86880165-86880736	NONHSAT113876

No data

Variant related genes	Relation type
ENSG00000217272	TF binding region
ENSG00000217272	CpG island

Extended variants
information (count: 2434 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2434 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs220397	chr6:86826442-86826443	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143734435	chr6:86826465-86826466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183035395	chr6:86826496-86826497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76110757	chr6:86826503-86826504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188705050	chr6:86826510-86826511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138383562	chr6:86826527-86826528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564568738	chr6:86826532-86826533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6929564	chr6:86826552-86826553	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs560192724	chr6:86826556-86826557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567747465	chr6:86826581-86826582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559257011	chr6:86826599-86826600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529927692	chr6:86826618-86826619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149887064	chr6:86826642-86826643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547826815	chr6:86826655-86826656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191792211	chr6:86826692-86826693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532101746	chr6:86826721-86826722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184123306	chr6:86826733-86826734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552011613	chr6:86826734-86826735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570509288	chr6:86826759-86826760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187475902	chr6:86826787-86826788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73497244	chr6:86826813-86826814	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs568819402	chr6:86826819-86826820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143866261	chr6:86826830-86826831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs220398	chr6:86826836-86826837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs575724471	chr6:86826842-86826843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75222268	chr6:86826858-86826859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192778395	chr6:86826872-86826873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184081650	chr6:86826873-86826874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576487909	chr6:86826897-86826898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376014227	chr6:86826901-86826902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540468004	chr6:86826936-86826937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201802450	chr6:86826937-86826938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377356054	chr6:86826959-86826960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545981433	chr6:86826971-86826972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556131399	chr6:86826981-86826982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540907121	chr6:86827020-86827021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559117209	chr6:86827033-86827034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147238946	chr6:86827036-86827037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79012055	chr6:86827082-86827083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563216875	chr6:86827084-86827085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541791074	chr6:86827086-86827087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552137306	chr6:86827137-86827138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561940366	chr6:86827153-86827154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535410667	chr6:86827181-86827182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139002695	chr6:86827182-86827183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546672873	chr6:86827199-86827200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187337055	chr6:86827213-86827214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527704818	chr6:86827222-86827223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141793504	chr6:86827245-86827246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565801024	chr6:86827257-86827258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	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
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
craniofacial dysmorphism	21918468	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
abnormal development	18461090	CNVD
Myelodysplastic syndrome	18508791	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:86826400-86826600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:86826600-86839600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:86839600-86839800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:86852200-86852800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:86852800-86856800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:86854600-86854800	Enhancers	Ovary	ovary
7	chr6:86854800-86865800	Weak transcription	Ovary	ovary
8	chr6:86856800-86857000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:86856800-86857000	Enhancers	Pancreas	Pancrea
10	chr6:86857000-86858200	Weak transcription	Pancreas	Pancrea
11	chr6:86857200-86857400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
12	chr6:86858200-86858800	Enhancers	Pancreas	Pancrea
13	chr6:86858800-86862200	Weak transcription	Pancreas	Pancrea
14	chr6:86860800-86862600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:86861000-86861200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr6:86861200-86862600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:86861400-86861600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
18	chr6:86861400-86862400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:86861400-86862800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr6:86861400-86862800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr6:86861600-86862600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr6:86861800-86862600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:86861800-86862800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr6:86862000-86863000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr6:86862200-86862600	Enhancers	Pancreas	Pancrea
26	chr6:86862400-86862800	Enhancers	H9 Cell Line	embryonic stem cell
27	chr6:86862400-86863400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:86862600-86863400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr6:86862600-86863800	Weak transcription	Pancreas	Pancrea
30	chr6:86863000-86863200	Enhancers	Aorta	Aorta
31	chr6:86863200-86865400	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr6:86863400-86863600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr6:86863400-86864400	Weak transcription	Aorta	Aorta
34	chr6:86863800-86864200	Enhancers	Pancreas	Pancrea
35	chr6:86864200-86865800	Weak transcription	Pancreas	Pancrea
36	chr6:86865400-86866400	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr6:86865800-86866200	Enhancers	Pancreas	Pancrea
38	chr6:86865800-86866200	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr6:86865800-86866200	Enhancers	Stomach Mucosa	stomach
40	chr6:86865800-86866400	Enhancers	Ovary	ovary
41	chr6:86866200-86868400	Weak transcription	Pancreas	Pancrea
42	chr6:86866400-86866600	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr6:86866400-86869400	Weak transcription	Ovary	ovary
44	chr6:86868600-86868800	Enhancers	Pancreas	Pancrea
45	chr6:86869400-86869600	Enhancers	Ovary	ovary
46	chr6:86869600-86870200	Weak transcription	Ovary	ovary
47	chr6:86870200-86870600	Enhancers	Ovary	ovary
48	chr6:86870600-86870800	Weak transcription	Ovary	ovary
49	chr6:86870800-86871200	Enhancers	Ovary	ovary
50	chr6:86882800-86883200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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