Variant report

Variant	nsv604516
Chromosome Location	chr6:110669514-110707820
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:186)
CpG islands
(count:854)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:186 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:110681939-110682233	HepG2	liver:	n/a	chr6:110682080-110682096
2	ARID3A	chr6:110676457-110676499	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:110706582-110707151	HepG2	liver:	n/a	n/a
4	BACH1	chr6:110676862-110677131	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr6:110706718-110706970	HepG2	liver:	n/a	n/a
6	CEBPB	chr6:110689322-110689356	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr6:110706660-110707028	HepG2	liver:	n/a	n/a
8	CEBPB	chr6:110706659-110707043	HepG2	liver:	n/a	n/a
9	CEBPB	chr6:110706761-110706964	HepG2	liver:	n/a	n/a
10	CHD2	chr6:110678259-110678293	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr6:110676315-110676665	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr6:110679140-110679290	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr6:110679460-110679610	SK-N-SH_RA	brain:	n/a	chr6:110679531-110679544
14	CTCF	chr6:110679120-110679270	AG09319	gingival:	n/a	n/a
15	CTCF	chr6:110691920-110692070	GM12872	blood:	n/a	n/a
16	CTCF	chr6:110679140-110679290	AG04449	skin:	n/a	n/a
17	CTCF	chr6:110679100-110679250	GM12864	blood:	n/a	n/a
18	CTCF	chr6:110684816-110684842	Fibrobl	skin:	n/a	n/a
19	CTCF	chr6:110679126-110679306	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr6:110671846-110671897	GM10248	blood:	n/a	n/a
21	CTCF	chr6:110699780-110699930	HVMF	connective:	n/a	n/a
22	CTCF	chr6:110699800-110699950	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr6:110679160-110679310	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr6:110699900-110700050	HEK293	kidney:	n/a	n/a
25	CTCF	chr6:110679000-110679150	GM12865	blood:	n/a	n/a
26	CTCF	chr6:110679120-110679270	HEK293	kidney:	n/a	n/a
27	CTCF	chr6:110699880-110700030	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr6:110679100-110679250	GM12874	blood:	n/a	n/a
29	CTCF	chr6:110699840-110699990	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr6:110699840-110699990	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr6:110679195-110679300	GM10266	blood:	n/a	n/a
32	CTCF	chr6:110679120-110679270	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr6:110679140-110679290	GM12865	blood:	n/a	n/a
34	CTCF	chr6:110679180-110679330	GM12868	blood:	n/a	n/a
35	CTCF	chr6:110679125-110679351	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr6:110679080-110679230	GM12873	blood:	n/a	n/a
37	CTCF	chr6:110679180-110679330	GM12870	blood:	n/a	n/a
38	CTCF	chr6:110699440-110699590	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr6:110679140-110679290	SAEC	small airway:	n/a	n/a
40	CTCF	chr6:110679208-110679316	GM12891	blood:	n/a	n/a
41	CTCF	chr6:110699867-110699991	HepG2	liver:	n/a	n/a
42	CTCF	chr6:110679120-110679270	Caco-2	colon:	n/a	n/a
43	CTCF	chr6:110679184-110679296	A549	lung:	n/a	n/a
44	CTCF	chr6:110679340-110679490	HEK293	kidney:	n/a	n/a
45	CTCF	chr6:110699763-110700080	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr6:110679180-110679275	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr6:110679120-110679270	GM12875	blood:	n/a	n/a
48	CTCF	chr6:110699880-110700030	HepG2	liver:	n/a	n/a
49	CTCF	chr6:110679113-110679335	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr6:110699840-110699990	Caco-2	colon:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:110707714-110707764	HRPEpiC	eye:	n/a
2	chr6:110678956-110679006	BJ	skin:	n/a
3	chr6:110680085-110680135	AG09319	gingival:	n/a
4	chr6:110678956-110679006	Hela-S3	cervix:	n/a
5	chr6:110676056-110676106	K562	blood:	n/a
6	chr6:110679107-110679157	HAEpiC	amniotic membrane:	n/a
7	chr6:110677913-110677963	HRPEpiC	eye:	n/a
8	chr6:110680085-110680135	SK-N-SH_RA	brain:	n/a
9	chr6:110678179-110678229	U87	brain:	n/a
10	chr6:110679400-110679450	MCF-7	breast:	n/a
11	chr6:110678179-110678229	HUVEC	blood vessel:	n/a
12	chr6:110707714-110707764	Hela-S3	cervix:	n/a
13	chr6:110678179-110678229	PFSK-1	brain:	n/a
14	chr6:110679400-110679450	K562	blood:	n/a
15	chr6:110678179-110678229	HAEpiC	amniotic membrane:	n/a
16	chr6:110678179-110678229	CMK	blood:	n/a
17	chr6:110679107-110679157	PFSK-1	brain:	n/a
18	chr6:110679400-110679450	CMK	blood:	n/a
19	chr6:110678956-110679006	HIPEpiC	eye:	n/a
20	chr6:110679832-110679882	A549	lung:	n/a
21	chr6:110677913-110677963	BE2_C	brain:	n/a
22	chr6:110678078-110678128	AG04450	lung:	fetal
23	chr6:110679107-110679157	NB4	blood:	n/a
24	chr6:110676056-110676106	CMK	blood:	n/a
25	chr6:110676056-110676106	SK-N-SH_RA	brain:	n/a
26	chr6:110680085-110680135	AG10803	skin:	n/a
27	chr6:110680085-110680135	HAEpiC	amniotic membrane:	n/a
28	chr6:110678179-110678229	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:110676056-110676106	AG09309	skin:	n/a
30	chr6:110679107-110679157	Hepatocyte	liver:	n/a
31	chr6:110680256-110680306	GM12891	blood:	n/a
32	chr6:110678179-110678229	Hepatocyte	liver:	n/a
33	chr6:110680256-110680306	HIPEpiC	eye:	n/a
34	chr6:110677913-110677963	ovcar-3	ovarian:	n/a
35	chr6:110676056-110676106	HMEC	breast:	n/a
36	chr6:110678179-110678229	NHBE	bronchial:	n/a
37	chr6:110678179-110678229	IMR90	lung:	fetal
38	chr6:110678920-110678970	Jurkat	blood:	n/a
39	chr6:110678078-110678128	HCF	heart:	n/a
40	chr6:110677913-110677963	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:110682827-110682877	T-47D	breast:	n/a
42	chr6:110680085-110680135	Caco-2	colon:	n/a
43	chr6:110678920-110678970	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:110679107-110679157	AoSMC	blood vessel:	n/a
45	chr6:110680256-110680306	SK-N-SH	brain:	n/a
46	chr6:110679400-110679450	GM12878	blood:	n/a
47	chr6:110678920-110678970	HepG2	liver:	n/a
48	chr6:110676056-110676106	AG04449	skin:	fetal
49	chr6:110679400-110679450	LNCaP	prostate:	n/a
50	chr6:110678078-110678128	HAEpiC	amniotic membrane:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:110674792..110677683-chr6:110688868..110690844,2	K562	blood:
2	chr6:110671256..110674188-chr6:110679968..110681627,2	K562	blood:
3	chr6:110674792..110677683-chr6:110688868..110690844,2	K562	blood:
4	chr6:110671256..110674188-chr6:110679968..110681627,2	K562	blood:
5	chr6:110705854..110707805-chr6:110709983..110712749,2	K562	blood:
6	chr6:110668811..110671157-chr6:110711492..110713993,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DDO-2	chr6:110678539-110679180	NONHSAT114418
2	lnc-CDC40-4	chr6:110673817-110673930	NONHSAT114419

No data

Variant related genes	Relation type
METTL24	TF binding region
METTL24	CpG island

Extended variants
information (count: 1298 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:1298 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17071490	chr6:110669514-110669515	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190149231	chr6:110669520-110669521	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs553597094	chr6:110669529-110669530	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs573469490	chr6:110669539-110669540	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs545572656	chr6:110669573-110669574	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs565476536	chr6:110669619-110669620	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs7770648	chr6:110669620-110669621	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs544701941	chr6:110669647-110669648	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs59351920	chr6:110669673-110669674	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs142498176	chr6:110669679-110669680	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs562207791	chr6:110669747-110669748	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs182742622	chr6:110669774-110669775	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs11759326	chr6:110669789-110669790	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs532273948	chr6:110669795-110669796	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs552096201	chr6:110669799-110669800	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs568698444	chr6:110669828-110669829	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs28681216	chr6:110669924-110669925	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs531432808	chr6:110669941-110669942	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs375584933	chr6:110669949-110669950	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs368229306	chr6:110670006-110670007	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs568079393	chr6:110670043-110670044	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs570772074	chr6:110670053-110670054	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs541622329	chr6:110670103-110670104	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs72935990	chr6:110670157-110670158	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs553492225	chr6:110670169-110670170	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs370558012	chr6:110670216-110670217	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs569376601	chr6:110670253-110670254	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs6937178	chr6:110670275-110670276	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs546059406	chr6:110670291-110670292	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs17569533	chr6:110670313-110670314	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs79925410	chr6:110670342-110670343	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs6937074	chr6:110670403-110670404	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs535306825	chr6:110670425-110670426	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs145994966	chr6:110670440-110670441	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs139932104	chr6:110670443-110670444	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs574843467	chr6:110670471-110670472	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs112537321	chr6:110670493-110670494	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs141767345	chr6:110670530-110670531	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs73763041	chr6:110670546-110670547	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs548466228	chr6:110670561-110670562	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs573309556	chr6:110670637-110670638	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs545674130	chr6:110670638-110670639	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs555141109	chr6:110670669-110670670	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs187473016	chr6:110670697-110670698	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs146261641	chr6:110670698-110670699	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs148483782	chr6:110670709-110670710	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs565491987	chr6:110670727-110670728	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs192722316	chr6:110670786-110670787	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs547511701	chr6:110670885-110670886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142749375	chr6:110670901-110670902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:763 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:110651600-110670200	Weak transcription	Pancreas	Pancrea
2	chr6:110662000-110674400	Enhancers	Colon Smooth Muscle	Colon
3	chr6:110663400-110670400	Weak transcription	Brain Anterior Caudate	brain
4	chr6:110663800-110672400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:110665000-110670200	Weak transcription	Fetal Brain Male	brain
6	chr6:110665200-110670000	Weak transcription	Fetal Brain Female	brain
7	chr6:110665200-110672600	Weak transcription	Fetal Kidney	kidney
8	chr6:110665200-110673200	Weak transcription	Aorta	Aorta
9	chr6:110665600-110670200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:110669000-110670200	Enhancers	Rectal Smooth Muscle	rectum
11	chr6:110669200-110669600	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr6:110669200-110671600	Enhancers	Fetal Stomach	stomach
13	chr6:110669400-110670200	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr6:110669400-110670800	Flanking Active TSS	Stomach Smooth Muscle	stomach
15	chr6:110669600-110670800	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr6:110669600-110671200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr6:110670000-110670600	Enhancers	Fetal Brain Female	brain
18	chr6:110670200-110670400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:110670200-110670400	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr6:110670200-110670600	Flanking Active TSS	Rectal Smooth Muscle	rectum
21	chr6:110670200-110670800	Enhancers	Brain Substantia Nigra	brain
22	chr6:110670200-110671000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:110670200-110671000	Enhancers	Fetal Brain Male	brain
24	chr6:110670200-110671200	Enhancers	Pancreas	Pancrea
25	chr6:110670200-110671400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:110670200-110673800	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr6:110670400-110670600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr6:110670400-110670600	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr6:110670400-110670800	Enhancers	Brain Hippocampus Middle	brain
30	chr6:110670400-110670800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr6:110670400-110670800	Enhancers	Lung	lung
32	chr6:110670400-110671000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr6:110670400-110671200	Enhancers	Brain Anterior Caudate	brain
34	chr6:110670600-110672000	Enhancers	Rectal Smooth Muscle	rectum
35	chr6:110670600-110672800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:110670600-110674200	Weak transcription	Fetal Brain Female	brain
37	chr6:110670600-110678200	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr6:110670800-110671400	Enhancers	Stomach Smooth Muscle	stomach
39	chr6:110670800-110672600	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr6:110670800-110676400	Weak transcription	Brain Hippocampus Middle	brain
41	chr6:110670800-110676400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr6:110670800-110678000	Weak transcription	Lung	lung
43	chr6:110670800-110678600	Weak transcription	Brain Substantia Nigra	brain
44	chr6:110671000-110671400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:110671000-110673400	Weak transcription	Fetal Brain Male	brain
46	chr6:110671200-110673200	Weak transcription	Brain Anterior Caudate	brain
47	chr6:110671200-110674000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr6:110671200-110676400	Weak transcription	Pancreas	Pancrea
49	chr6:110671400-110671600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:110671400-110672200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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