Variant report

Variant	nsv901634
Chromosome Location	chr14:36652690-36694219
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:36677815-36678352	HepG2	liver:	n/a	n/a
2	BACH1	chr14:36652686-36652942	K562	blood:	n/a	n/a
3	BHLHE40	chr14:36692826-36693409	K562	blood:	n/a	n/a
4	BHLHE40	chr14:36666611-36666626	GM12878	blood:	n/a	n/a
5	CEBPB	chr14:36680818-36681067	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:36677842-36678418	MCF-7	breast:	n/a	chr14:36678182-36678193
7	CEBPB	chr14:36677982-36678372	HepG2	liver:	n/a	chr14:36678182-36678193
8	CEBPB	chr14:36677917-36678321	HepG2	liver:	n/a	chr14:36678182-36678193
9	CEBPB	chr14:36686917-36687180	HepG2	liver:	n/a	n/a
10	CEBPB	chr14:36687741-36687945	HepG2	liver:	n/a	n/a
11	CEBPB	chr14:36678034-36678349	A549	lung:	n/a	chr14:36678182-36678193
12	CEBPB	chr14:36678023-36678290	HepG2	liver:	n/a	chr14:36678182-36678193
13	CEBPB	chr14:36677867-36678380	HepG2	liver:	n/a	chr14:36678182-36678193
14	CEBPB	chr14:36678045-36678328	Hela-S3	cervix:	n/a	chr14:36678182-36678193
15	CREB1	chr14:36677834-36678391	HepG2	liver:	n/a	n/a
16	CREB1	chr14:36677812-36678438	HepG2	liver:	n/a	n/a
17	CTCF	chr14:36676820-36676970	HRE	kidney:	n/a	n/a
18	CTCF	chr14:36676880-36677030	SAEC	small airway:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
19	CTCF	chr14:36676858-36676985	ProgFib	skin:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
20	CTCF	chr14:36676920-36677070	HPAF	blood vessel:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
21	CTCF	chr14:36676920-36677070	AoAF	blood vessel:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
22	CTCF	chr14:36676840-36676990	HEEpiC	esophagus:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
23	CTCF	chr14:36676840-36676990	HEK293	kidney:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
24	CTCF	chr14:36674034-36674100	HepG2	liver:	n/a	n/a
25	CTCF	chr14:36676907-36676927	GM13976	blood:	n/a	n/a
26	CTCF	chr14:36676859-36677065	Hela-S3	cervix:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
27	CTCF	chr14:36676900-36677050	HA-sp	spinal cord:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
28	CTCF	chr14:36673956-36674156	GM12878	blood:	n/a	n/a
29	CTCF	chr14:36676843-36677028	MCF-7	breast:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
30	CTCF	chr14:36676860-36677010	BE2_C	brain:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
31	CTCF	chr14:36676840-36676990	HRPEpiC	eye:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
32	CTCF	chr14:36676840-36676990	AG04449	skin:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
33	CTCF	chr14:36676880-36677030	AG10803	skin:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
34	CTCF	chr14:36676805-36677067	HepG2	liver:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
35	CTCF	chr14:36676840-36676990	HRE	kidney:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
36	CTCF	chr14:36676902-36677014	Kidney_OC	kidney:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
37	CTCF	chr14:36676880-36677030	HA-sp	spinal cord:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
38	CTCF	chr14:36676820-36676970	K562	blood:	n/a	n/a
39	CTCF	chr14:36676831-36677060	SK-N-SH_RA	brain:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
40	CTCF	chr14:36676880-36677030	RPTEC	kidney:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
41	CTCF	chr14:36676738-36677141	T-47D	breast:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
42	CTCF	chr14:36676960-36677110	WI-38	lung:	n/a	n/a
43	CTCF	chr14:36676900-36677050	SK-N-SH_RA	brain:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
44	CTCF	chr14:36676540-36676690	Caco-2	colon:	n/a	n/a
45	CTCF	chr14:36676916-36676991	GM12878	blood:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
46	CTCF	chr14:36676858-36677054	K562	blood:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
47	CTCF	chr14:36674040-36674190	HMF	breast:	n/a	n/a
48	CTCF	chr14:36676789-36677069	A549	lung:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
49	CTCF	chr14:36676900-36677050	HPF	lung:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974
50	CTCF	chr14:36676866-36677017	HepG2	liver:	n/a	chr14:36676959-36676980 chr14:36676957-36676975 chr14:36676958-36676974

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:36684553-36684603	PANC-1	pancreas:	n/a
2	chr14:36691116-36691166	HIPEpiC	eye:	n/a
3	chr14:36684553-36684603	MCF-7	breast:	n/a
4	chr14:36691116-36691166	U87	brain:	n/a
5	chr14:36691116-36691166	Jurkat	blood:	n/a
6	chr14:36693238-36693288	NHBE	bronchial:	n/a
7	chr14:36693238-36693288	PrEC	prostate:	n/a
8	chr14:36691116-36691166	AG04450	lung:	fetal
9	chr14:36691116-36691166	H1-hESC	embryonic stem cell:	embryo
10	chr14:36693238-36693288	NB4	blood:	n/a
11	chr14:36684553-36684603	NHDF-neo	bronchial:	n/a
12	chr14:36684553-36684603	Hepatocyte	liver:	n/a
13	chr14:36693238-36693288	HCF	heart:	n/a
14	chr14:36691116-36691166	T-47D	breast:	n/a
15	chr14:36693238-36693288	ovcar-3	ovarian:	n/a
16	chr14:36684553-36684603	NT2-D1	testis:	n/a
17	chr14:36684553-36684603	GM12878	blood:	n/a
18	chr14:36691116-36691166	SKMC	muscle:	n/a
19	chr14:36691116-36691166	HEEpiC	esophagus:	n/a
20	chr14:36693238-36693288	Caco-2	colon:	n/a
21	chr14:36684553-36684603	GM06990	blood:	n/a
22	chr14:36684553-36684603	NB4	blood:	n/a
23	chr14:36684553-36684603	BJ	skin:	n/a
24	chr14:36693238-36693288	HL-60	blood:	n/a
25	chr14:36684553-36684603	PrEC	prostate:	n/a
26	chr14:36684553-36684603	AoSMC	blood vessel:	n/a
27	chr14:36691116-36691166	HepG2	liver:	n/a
28	chr14:36684553-36684603	SAEC	small airway:	n/a
29	chr14:36684553-36684603	HPAEpiC	pulmonary alveolar:	n/a
30	chr14:36693238-36693288	NH-A	brain:	n/a
31	chr14:36693238-36693288	HNPCEpiC	eye:	n/a
32	chr14:36691116-36691166	HMEC	breast:	n/a
33	chr14:36691116-36691166	HCT-116	colon:	n/a
34	chr14:36691116-36691166	K562	blood:	n/a
35	chr14:36693238-36693288	GM19239	blood:	n/a
36	chr14:36691116-36691166	Hepatocyte	liver:	n/a
37	chr14:36684553-36684603	HUVEC	blood vessel:	n/a
38	chr14:36693238-36693288	AG04450	lung:	fetal
39	chr14:36684553-36684603	SKMC	muscle:	n/a
40	chr14:36691116-36691166	ovcar-3	ovarian:	n/a
41	chr14:36693238-36693288	HAEpiC	amniotic membrane:	n/a
42	chr14:36693238-36693288	SKMC	muscle:	n/a
43	chr14:36691116-36691166	SK-N-SH	brain:	n/a
44	chr14:36693238-36693288	GM12891	blood:	n/a
45	chr14:36693238-36693288	A549	lung:	n/a
46	chr14:36684553-36684603	K562	blood:	n/a
47	chr14:36684553-36684603	AG04449	skin:	fetal
48	chr14:36684553-36684603	Caco-2	colon:	n/a
49	chr14:36693238-36693288	SAEC	small airway:	n/a
50	chr14:36684553-36684603	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:36692567..36694676-chr14:36694678..36697500,2	MCF-7	breast:
2	chr14:36676468..36677430-chr14:36842915..36843825,2	MCF-7	breast:
3	chr14:36674915..36676965-chr14:36682336..36684243,2	K562	blood:
4	chr14:36672609..36674507-chr14:36674625..36676988,2	MCF-7	breast:
5	chr14:36539400..36540077-chr14:36676431..36676939,2	MCF-7	breast:
6	chr14:36676984..36677491-chr14:36843145..36844040,2	MCF-7	breast:
7	chr14:36676675..36678036-chr14:36919496..36920913,3	MCF-7	breast:
8	chr14:36672609..36674507-chr14:36674625..36676988,2	MCF-7	breast:
9	chr14:36676641..36677323-chr14:36994485..36995249,2	MCF-7	breast:
10	chr14:36683929..36686660-chr14:36694552..36697045,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BRMS1L-3	chr14:36690500-36690685	XLOC_010798
2	lnc-BRMS1L-2	chr14:36691502-36691569	NONHSAT036421
3	lnc-BRMS1L-3	chr14:36683813-36684264	ENSG00000258844
4	lnc-BRMS1L-2	chr14:36684165-36684264	NONHSAT036417
5	lnc-BRMS1L-3	chr14:36684580-36684721	ENSG00000258844
6	lnc-BRMS1L-3	chr14:36684580-36685567	XLOC_010797
7	lnc-BRMS1L-2	chr14:36684580-36684697	NONHSAT036417
8	lnc-BRMS1L-3	chr14:36690500-36690689	XLOC_010798
9	lnc-BRMS1L-2	chr14:36690499-36690689	NONHSAT036421
10	lnc-BRMS1L-3	chr14:36683885-36684264	XLOC_010797
11	lnc-BRMS1L-3	chr14:36691503-36691569	XLOC_010798

Variant related genes	Relation type
ENSG00000212071	TF binding region
ENSG00000258844	TF binding region
ENSG00000212071	CpG island
ENSG00000258844	CpG island
ENSG00000257585	chromatin interactions
ENSG00000258844	chromatin interactions
AKT3	miRNA target sites
SHPK	miRNA target sites
TNFRSF11B	miRNA target sites

Extended variants
information (count: 874 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1766118	chr14:36652690-36652691	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573907031	chr14:36652716-36652717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs61996595	chr14:36652717-36652718	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs562840268	chr14:36652720-36652721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576212457	chr14:36652722-36652723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544999963	chr14:36652773-36652774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564695633	chr14:36652809-36652810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527409629	chr14:36652834-36652835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573127457	chr14:36652867-36652868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540756371	chr14:36652894-36652895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553422866	chr14:36652916-36652917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530273144	chr14:36652933-36652934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550104473	chr14:36652956-36652957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1766119	chr14:36653021-36653022	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs144344840	chr14:36653022-36653023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75500993	chr14:36653087-36653088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181320178	chr14:36653101-36653102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183869413	chr14:36653102-36653103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76648508	chr14:36653125-36653126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188210517	chr14:36653188-36653189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs180773208	chr14:36653204-36653205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568556378	chr14:36653287-36653288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs59387931	chr14:36653290-36653291	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs186372812	chr14:36653298-36653299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148759468	chr14:36653305-36653306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191954145	chr14:36653333-36653334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558793905	chr14:36653357-36653358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571743403	chr14:36653384-36653385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141683677	chr14:36653428-36653429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147178469	chr14:36653435-36653436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529693722	chr14:36653474-36653475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182144585	chr14:36653476-36653477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186789843	chr14:36653488-36653489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532861473	chr14:36653497-36653498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544594975	chr14:36653523-36653524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562829465	chr14:36653551-36653552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191646364	chr14:36653561-36653562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566358546	chr14:36653582-36653583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182757000	chr14:36653607-36653608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548597287	chr14:36653622-36653623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187041633	chr14:36653623-36653624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566822650	chr14:36653634-36653635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533352300	chr14:36653662-36653663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189986313	chr14:36653679-36653680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569781362	chr14:36653683-36653684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs58444823	chr14:36653702-36653703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115688411	chr14:36653751-36653752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140389855	chr14:36653759-36653760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144238696	chr14:36653776-36653777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540628830	chr14:36653786-36653787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	21569311	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:36638200-36654200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr14:36663800-36664000	Enhancers	HSMM	muscle
3	chr14:36665400-36665600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:36665800-36667000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr14:36667000-36667400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:36677200-36677600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr14:36677600-36681400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr14:36678000-36678400	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr14:36681400-36684200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr14:36682800-36683200	Enhancers	Gastric	stomach
11	chr14:36682800-36683400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr14:36682800-36683400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr14:36682800-36683400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr14:36682800-36683400	Enhancers	Brain Cingulate Gyrus	brain
15	chr14:36682800-36684400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr14:36682800-36684400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr14:36682800-36684800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr14:36682800-36685200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr14:36682800-36685200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr14:36683000-36683200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr14:36683000-36683600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr14:36683000-36684000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr14:36683000-36684200	Enhancers	HMEC	breast
24	chr14:36683000-36685000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr14:36683200-36685400	Weak transcription	Gastric	stomach
26	chr14:36683400-36683800	Enhancers	H1 Cell Line	embryonic stem cell
27	chr14:36683400-36683800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr14:36683400-36684400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr14:36683400-36690200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr14:36683600-36684000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr14:36683800-36684000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr14:36683800-36684400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr14:36684000-36684400	Enhancers	H1 Cell Line	embryonic stem cell
34	chr14:36684000-36684600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr14:36684000-36684800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr14:36684000-36692200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr14:36684200-36685000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr14:36684200-36686400	Weak transcription	HMEC	breast
39	chr14:36684400-36686600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:36684400-36692200	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr14:36684600-36685000	Bivalent Enhancer	Stomach Mucosa	stomach
42	chr14:36684800-36690200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr14:36685000-36686600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr14:36685000-36690200	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr14:36685200-36686600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr14:36685200-36690400	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr14:36685400-36685600	Enhancers	Gastric	stomach
48	chr14:36685400-36686400	Active TSS	Lung	lung
49	chr14:36686000-36686400	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr14:36686000-36686600	Bivalent Enhancer	Stomach Mucosa	stomach

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