Variant report

Variant	nsv603352
Chromosome Location	chr6:63286366-63596112
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:701)
CpG islands
(count:184)
Chromatin interactive
region (count:15)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:63485401-63485684	HepG2	liver:	n/a	n/a
2	BACH1	chr6:63343076-63343099	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr6:63476348-63476567	GM12878	blood:	n/a	n/a
4	BRCA1	chr6:63297856-63298053	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr6:63362575-63362854	K562	blood:	n/a	n/a
6	CBX3	chr6:63362679-63362919	K562	blood:	n/a	n/a
7	CBX3	chr6:63362595-63362988	HCT-116	colon:	n/a	n/a
8	CEBPB	chr6:63326560-63326798	MCF-7	breast:	n/a	chr6:63326660-63326671
9	CEBPB	chr6:63326483-63326806	MCF-7	breast:	n/a	chr6:63326660-63326671
10	CEBPB	chr6:63517862-63517964	K562	blood:	n/a	chr6:63517900-63517913 chr6:63517900-63517911
11	CEBPB	chr6:63517820-63517987	HepG2	liver:	n/a	chr6:63517900-63517913 chr6:63517900-63517911
12	CEBPB	chr6:63311181-63311407	MCF-7	breast:	n/a	n/a
13	CEBPB	chr6:63350334-63350675	HepG2	liver:	n/a	chr6:63350634-63350645 chr6:63350477-63350488 chr6:63350476-63350489
14	CEBPB	chr6:63571959-63572191	HepG2	liver:	n/a	chr6:63572068-63572079
15	CEBPB	chr6:63512982-63513172	H1-hESC	embryonic stem cell:	n/a	chr6:63513016-63513027
16	CEBPB	chr6:63350553-63351067	A549	lung:	n/a	chr6:63350634-63350645
17	CEBPB	chr6:63512841-63513198	HepG2	liver:	n/a	chr6:63513016-63513027
18	CEBPB	chr6:63377486-63377807	HepG2	liver:	n/a	chr6:63377653-63377664
19	CEBPB	chr6:63316649-63316921	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:63479626-63479944	HepG2	liver:	n/a	chr6:63479783-63479794
21	CEBPB	chr6:63512795-63513283	MCF-7	breast:	n/a	chr6:63513016-63513027
22	CEBPB	chr6:63512957-63513198	IMR90	lung:	n/a	chr6:63513016-63513027
23	CEBPB	chr6:63476559-63476780	HepG2	liver:	n/a	chr6:63476688-63476699
24	CEBPB	chr6:63486528-63486800	HepG2	liver:	n/a	n/a
25	CEBPB	chr6:63311156-63311399	A549	lung:	n/a	n/a
26	CEBPB	chr6:63326531-63326747	HepG2	liver:	n/a	chr6:63326660-63326671
27	CEBPB	chr6:63541693-63541860	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:63525042-63525285	HepG2	liver:	n/a	chr6:63525158-63525169
29	CEBPB	chr6:63520524-63520675	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr6:63554061-63554290	A549	lung:	n/a	n/a
31	CEBPZ	chr6:63362626-63362905	HepG2	liver:	n/a	n/a
32	CHD1	chr6:63347777-63347984	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr6:63297860-63298054	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr6:63457023-63457040	GM12878	blood:	n/a	n/a
35	CHD2	chr6:63576492-63576565	GM12878	blood:	n/a	n/a
36	CTCF	chr6:63367889-63367926	LNCaP	prostate:	n/a	n/a
37	CTCF	chr6:63484880-63485030	RPTEC	kidney:	n/a	n/a
38	CTCF	chr6:63485440-63485590	SK-N-SH_RA	brain:	n/a	chr6:63485525-63485541 chr6:63485526-63485539 chr6:63485524-63485542 chr6:63485519-63485540 chr6:63485530-63485539
39	CTCF	chr6:63417160-63417310	HEK293	kidney:	n/a	n/a
40	CTCF	chr6:63573237-63573279	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr6:63324481-63324637	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr6:63485446-63485653	GM10266	blood:	n/a	chr6:63485525-63485541 chr6:63485526-63485539 chr6:63485524-63485542 chr6:63485519-63485540 chr6:63485530-63485539
43	CTCF	chr6:63325720-63325870	GM12874	blood:	n/a	n/a
44	CTCF	chr6:63485460-63485610	GM12867	blood:	n/a	chr6:63485525-63485541 chr6:63485526-63485539 chr6:63485524-63485542 chr6:63485519-63485540 chr6:63485530-63485539
45	CTCF	chr6:63433780-63433930	HEK293	kidney:	n/a	n/a
46	CTCF	chr6:63485700-63485850	HEK293	kidney:	n/a	n/a
47	CTCF	chr6:63485785-63485807	GM12892	blood:	n/a	n/a
48	CTCF	chr6:63485540-63485690	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr6:63485700-63485850	HVMF	connective:	n/a	n/a
50	CTCF	chr6:63417080-63417230	GM12873	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:63572411-63572461	HEEpiC	esophagus:	n/a
2	chr6:63572411-63572461	HEEpiC	esophagus:	n/a
3	chr6:63553575-63553625	GM12878	blood:	n/a
4	chr6:63572411-63572461	HCPEpiC	choroid plexus:	n/a
5	chr6:63553575-63553625	Jurkat	blood:	n/a
6	chr6:63572411-63572461	PFSK-1	brain:	n/a
7	chr6:63553575-63553625	NH-A	brain:	n/a
8	chr6:63553575-63553625	HCPEpiC	choroid plexus:	n/a
9	chr6:63553575-63553625	AG04449	skin:	fetal
10	chr6:63553575-63553625	AG09309	skin:	n/a
11	chr6:63572411-63572461	ovcar-3	ovarian:	n/a
12	chr6:63553575-63553625	MCF-7	breast:	n/a
13	chr6:63572411-63572461	NT2-D1	testis:	n/a
14	chr6:63553575-63553625	GM06990	blood:	n/a
15	chr6:63572411-63572461	SK-N-MC	brain:	n/a
16	chr6:63572411-63572461	Hepatocyte	liver:	n/a
17	chr6:63553696-63553746	HUVEC	blood vessel:	n/a
18	chr6:63553696-63553746	Hela-S3	cervix:	n/a
19	chr6:63553696-63553746	AG09319	gingival:	n/a
20	chr6:63553575-63553625	HNPCEpiC	eye:	n/a
21	chr6:63553575-63553625	NHBE	bronchial:	n/a
22	chr6:63553696-63553746	HCPEpiC	choroid plexus:	n/a
23	chr6:63572411-63572461	AG04450	lung:	fetal
24	chr6:63553696-63553746	BE2_C	brain:	n/a
25	chr6:63553575-63553625	SKMC	muscle:	n/a
26	chr6:63553696-63553746	AG04450	lung:	fetal
27	chr6:63553575-63553625	K562	blood:	n/a
28	chr6:63572411-63572461	H1-hESC	embryonic stem cell:	embryo
29	chr6:63572411-63572461	A549	lung:	n/a
30	chr6:63553575-63553625	CMK	blood:	n/a
31	chr6:63553575-63553625	HCF	heart:	n/a
32	chr6:63553696-63553746	GM12892	blood:	n/a
33	chr6:63553575-63553625	SK-N-SH_RA	brain:	n/a
34	chr6:63553575-63553625	RPTEC	kidney:	n/a
35	chr6:63572411-63572461	NHDF-neo	bronchial:	n/a
36	chr6:63572411-63572461	NB4	blood:	n/a
37	chr6:63553575-63553625	HRE	kidney:	n/a
38	chr6:63553575-63553625	PFSK-1	brain:	n/a
39	chr6:63553696-63553746	NB4	blood:	n/a
40	chr6:63572411-63572461	Hela-S3	cervix:	n/a
41	chr6:63553575-63553625	A549	lung:	n/a
42	chr6:63553696-63553746	ovcar-3	ovarian:	n/a
43	chr6:63553575-63553625	ECC-1	luminal epithelium:	n/a
44	chr6:63553696-63553746	SK-N-MC	brain:	n/a
45	chr6:63553696-63553746	GM12878	blood:	n/a
46	chr6:63553696-63553746	CMK	blood:	n/a
47	chr6:63572411-63572461	HCT-116	colon:	n/a
48	chr6:63572411-63572461	LNCaP	prostate:	n/a
49	chr6:63553696-63553746	HCT-116	colon:	n/a
50	chr6:63572411-63572461	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr17:41399298..41401661-chr6:63530253..63531773,2	K562	blood:
2	chr17:41400811..41402656-chr6:63530253..63531773,2	MCF-7	breast:
3	chr22:19006105..19008372-chr6:63457723..63459244,2	K562	blood:
4	chr17:41466567..41467237-chr6:63529754..63530273,2	NB4	blood:
5	chr6:63514284..63517012-chr6:63519494..63521413,2	MCF-7	breast:
6	chr17:41400213..41402082-chr6:63530273..63531773,2	MCF-7	breast:
7	chr6:63381016..63382588-chr6:63383396..63385763,2	K562	blood:
8	chr6:63514284..63517012-chr6:63519494..63521413,2	MCF-7	breast:
9	chr1:17229945..17231648-chr6:63349079..63350580,2	MCF-7	breast:
10	chr17:41400161..41402651-chr6:63528753..63531753,3	K562	blood:
11	chr6:63381016..63382588-chr6:63383396..63385763,2	K562	blood:
12	chr17:41465690..41468054-chr6:63528753..63530254,3	MCF-7	breast:
13	chr6:63441335..63443879-chr6:63445998..63448155,2	K562	blood:
14	chr6:63441335..63443879-chr6:63445998..63448155,2	K562	blood:
15	chr17:41466229..41468054-chr6:63528754..63531753,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KHDRBS2-3	chr6:63298023-63298059	NONHSAT113335
2	lnc-KHDRBS2-3	chr6:63297418-63297607	NONHSAT113335

No data

Variant related genes	Relation type
ENSG00000264410	TF binding region
ENSG00000262566	TF binding region
ENSG00000216072	TF binding region
ENSG00000264410	CpG island
ENSG00000262566	CpG island
ENSG00000216072	CpG island
ENSG00000272426	chromatin interactions
ENSG00000270393	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 10059 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:10059 , 50 per page) page: 1 2 3 4 5 6 7 ... 202

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532825487	chr6:63293224-63293225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548088618	chr6:63293252-63293253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185701904	chr6:63293291-63293292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371354874	chr6:63293292-63293293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548809613	chr6:63293310-63293311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569601568	chr6:63293312-63293313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs61350037	chr6:63293338-63293339	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs1475765	chr6:63293368-63293369	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs576455410	chr6:63293381-63293382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190573715	chr6:63293435-63293436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552832638	chr6:63293447-63293448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574433030	chr6:63293488-63293489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541657342	chr6:63293528-63293529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148500973	chr6:63293538-63293539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576423335	chr6:63293542-63293543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543917103	chr6:63293585-63293586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558659240	chr6:63293600-63293601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554591097	chr6:63293609-63293610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182369980	chr6:63293624-63293625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144312593	chr6:63293639-63293640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546510042	chr6:63293663-63293664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186925452	chr6:63293666-63293667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572490566	chr6:63293667-63293668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568470818	chr6:63293680-63293681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527963228	chr6:63293681-63293682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570248423	chr6:63293698-63293699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548127341	chr6:63293704-63293705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10943041	chr6:63293725-63293726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368486791	chr6:63293726-63293727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372285619	chr6:63293743-63293744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570249528	chr6:63293763-63293764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs9351928	chr6:63293783-63293784	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs564610408	chr6:63293788-63293789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190420603	chr6:63293794-63293795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73498799	chr6:63293809-63293810	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs535755045	chr6:63293860-63293861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181272142	chr6:63293861-63293862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575373284	chr6:63293901-63293902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545714501	chr6:63293917-63293918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74811815	chr6:63293919-63293920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535614791	chr6:63293927-63293928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577458512	chr6:63293940-63293941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541387753	chr6:63293952-63293953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559792165	chr6:63293973-63293974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530297444	chr6:63293999-63294000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116290153	chr6:63294023-63294024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555699896	chr6:63294033-63294034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531121415	chr6:63294067-63294068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs80058637	chr6:63294082-63294083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377519819	chr6:63294087-63294088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
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
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	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
Acute lymphoblastic leukemia	18458336	CNVD
Schizophrenia	23813976	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD

Chromatin state (count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:63293200-63294200	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr6:63293400-63293800	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr6:63293400-63294400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr6:63293800-63294000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr6:63293800-63294400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr6:63293800-63297800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr6:63294400-63297800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr6:63295200-63297800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr6:63297800-63298000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:63297800-63298000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:63297800-63298000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
12	chr6:63297800-63298000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
13	chr6:63297800-63298000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
14	chr6:63297800-63298000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr6:63297800-63298000	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
16	chr6:63297800-63298000	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
17	chr6:63297800-63298000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
18	chr6:63297800-63298000	Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr6:63297800-63298000	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
20	chr6:63297800-63298000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
21	chr6:63297800-63298000	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
22	chr6:63297800-63298000	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr6:63297800-63298000	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
24	chr6:63297800-63298000	ZNF genes & repeats	Colon Smooth Muscle	Colon
25	chr6:63297800-63298000	ZNF genes & repeats	Gastric	stomach
26	chr6:63297800-63298000	ZNF genes & repeats	Stomach Mucosa	stomach
27	chr6:63297800-63298200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
28	chr6:63297800-63298200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
29	chr6:63298000-63304800	Weak transcription	Gastric	stomach
30	chr6:63298200-63298800	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr6:63298200-63301000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr6:63301000-63301200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr6:63318600-63319600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr6:63318800-63319600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr6:63318800-63320000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr6:63319000-63319400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:63319000-63319800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:63319200-63319400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr6:63319400-63319600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
40	chr6:63319400-63319800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr6:63319400-63320000	Enhancers	H1 Cell Line	embryonic stem cell
42	chr6:63319400-63320000	Enhancers	H9 Cell Line	embryonic stem cell
43	chr6:63319400-63323800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr6:63321800-63323000	Enhancers	Fetal Intestine Small	intestine
45	chr6:63322000-63322400	Enhancers	Stomach Mucosa	stomach
46	chr6:63322000-63322600	Enhancers	Fetal Intestine Large	intestine
47	chr6:63322400-63325400	Weak transcription	Stomach Mucosa	stomach
48	chr6:63322600-63324000	Weak transcription	Fetal Intestine Large	intestine
49	chr6:63323000-63323200	Weak transcription	Fetal Intestine Small	intestine
50	chr6:63323200-63324800	ZNF genes & repeats	Fetal Intestine Small	intestine

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