Variant report

Variant	esv3693172
Chromosome Location	chr14:78130479-78152921
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	chr14:78137563-78137677	HepG2	liver:	n/a	n/a
2	BHLHE40	chr14:78135001-78135195	K562	blood:	n/a	n/a
3	BHLHE40	chr14:78136510-78136719	K562	blood:	n/a	chr14:78136592-78136601 chr14:78136592-78136601 chr14:78136591-78136600 chr14:78136586-78136607
4	CEBPB	chr14:78148180-78148232	HepG2	liver:	n/a	n/a
5	CEBPD	chr14:78131600-78131840	K562	blood:	n/a	n/a
6	CTCF	chr14:78152800-78152950	Caco-2	colon:	n/a	n/a
7	CTCF	chr14:78135124-78135265	GM10248	blood:	n/a	n/a
8	CTCF	chr14:78131085-78131146	LNCaP	prostate:	n/a	n/a
9	CTCF	chr14:78144828-78144855	Fibrobl	skin:	n/a	n/a
10	CUX1	chr14:78147832-78147884	GM12878	blood:	n/a	n/a
11	EP300	chr14:78148061-78148444	HepG2	liver:	n/a	n/a
12	EP300	chr14:78148513-78148932	HepG2	liver:	n/a	chr14:78148702-78148711 chr14:78148703-78148712
13	ESR1	chr14:78147615-78148129	T-47D	breast:	n/a	n/a
14	ESR1	chr14:78147709-78148341	T-47D	breast:	n/a	n/a
15	ESR1	chr14:78147670-78148086	T-47D	breast:	n/a	n/a
16	ESR1	chr14:78147628-78148055	T-47D	breast:	n/a	n/a
17	ESR1	chr14:78147608-78148447	T-47D	breast:	n/a	n/a
18	FOS	chr14:78148504-78148896	MCF10A-Er-Src	breast:	n/a	chr14:78148703-78148711 chr14:78148704-78148715 chr14:78148701-78148712 chr14:78148703-78148710 chr14:78148702-78148711
19	FOS	chr14:78148250-78148898	MCF10A-Er-Src	breast:	n/a	chr14:78148703-78148711 chr14:78148704-78148715 chr14:78148701-78148712 chr14:78148703-78148710 chr14:78148702-78148711
20	FOS	chr14:78148356-78148902	MCF10A-Er-Src	breast:	n/a	chr14:78148703-78148711 chr14:78148704-78148715 chr14:78148701-78148712 chr14:78148703-78148710 chr14:78148702-78148711
21	FOS	chr14:78148105-78148899	HUVEC	blood vessel:	n/a	chr14:78148703-78148711 chr14:78148704-78148715 chr14:78148701-78148712 chr14:78148703-78148710 chr14:78148702-78148711
22	FOS	chr14:78148517-78148899	MCF10A-Er-Src	breast:	n/a	chr14:78148703-78148711 chr14:78148704-78148715 chr14:78148701-78148712 chr14:78148703-78148710 chr14:78148702-78148711
23	FOSL2	chr14:78148474-78148935	MCF-7	breast:	n/a	chr14:78148703-78148711 chr14:78148704-78148715 chr14:78148700-78148711 chr14:78148703-78148710 chr14:78148702-78148711
24	FOSL2	chr14:78147976-78148497	HepG2	liver:	n/a	n/a
25	FOSL2	chr14:78148533-78148819	HepG2	liver:	n/a	chr14:78148703-78148711 chr14:78148704-78148715 chr14:78148700-78148711 chr14:78148703-78148710 chr14:78148702-78148711
26	FOSL2	chr14:78148437-78148871	A549	lung:	n/a	chr14:78148703-78148711 chr14:78148704-78148715 chr14:78148700-78148711 chr14:78148703-78148710 chr14:78148702-78148711
27	FOSL2	chr14:78137481-78137804	HepG2	liver:	n/a	n/a
28	FOSL2	chr14:78148568-78148902	HepG2	liver:	n/a	chr14:78148703-78148711 chr14:78148704-78148715 chr14:78148700-78148711 chr14:78148703-78148710 chr14:78148702-78148711
29	FOXA1	chr14:78147669-78148263	T-47D	breast:	n/a	n/a
30	FOXA1	chr14:78147989-78148805	A549	lung:	n/a	n/a
31	FOXA1	chr14:78148470-78148962	HepG2	liver:	n/a	n/a
32	FOXA1	chr14:78147954-78148454	HepG2	liver:	n/a	n/a
33	FOXA1	chr14:78148439-78148819	HepG2	liver:	n/a	n/a
34	FOXA1	chr14:78148337-78148865	A549	lung:	n/a	n/a
35	FOXA1	chr14:78147642-78148380	T-47D	breast:	n/a	n/a
36	FOXA1	chr14:78147943-78148388	HepG2	liver:	n/a	n/a
37	FOXA2	chr14:78148553-78148815	HepG2	liver:	n/a	n/a
38	FOXA2	chr14:78148493-78148921	A549	lung:	n/a	n/a
39	GATA3	chr14:78147908-78148108	SH-SY5Y	brain:	n/a	chr14:78147908-78147918 chr14:78147908-78147917
40	GATA3	chr14:78147594-78148884	MCF-7	breast:	n/a	chr14:78147642-78147649 chr14:78147908-78147918 chr14:78147908-78147917 chr14:78147624-78147635 chr14:78148701-78148710
41	GATA3	chr14:78134275-78134654	T-47D	breast:	n/a	n/a
42	GATA3	chr14:78147593-78148441	T-47D	breast:	n/a	chr14:78147642-78147649 chr14:78147908-78147918 chr14:78147908-78147917 chr14:78147624-78147635
43	GATA3	chr14:78147576-78148536	T-47D	breast:	n/a	chr14:78147642-78147649 chr14:78147908-78147918 chr14:78147908-78147917 chr14:78147624-78147635
44	GATA3	chr14:78143668-78144096	T-47D	breast:	n/a	chr14:78143890-78143911
45	GATA3	chr14:78134290-78134589	T-47D	breast:	n/a	n/a
46	HNF4A	chr14:78148054-78148402	HepG2	liver:	n/a	chr14:78148282-78148297
47	HNF4A	chr14:78148631-78148762	HepG2	liver:	n/a	chr14:78148712-78148720
48	HNF4A	chr14:78148093-78148460	HepG2	liver:	n/a	chr14:78148282-78148297
49	HNF4A	chr14:78137591-78137774	HepG2	liver:	n/a	n/a
50	HNF4A	chr14:78137606-78137763	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:78147567-78147617	AG04449	skin:	fetal
2	chr14:78147567-78147617	GM06990	blood:	n/a
3	chr14:78147567-78147617	HRE	kidney:	n/a
4	chr14:78147567-78147617	A549	lung:	n/a
5	chr14:78147567-78147617	HEEpiC	esophagus:	n/a
6	chr14:78147567-78147617	AG09319	gingival:	n/a
7	chr14:78147567-78147617	SK-N-SH	brain:	n/a
8	chr14:78147567-78147617	IMR90	lung:	fetal
9	chr14:78147567-78147617	HPAEpiC	pulmonary alveolar:	n/a
10	chr14:78147567-78147617	H1-hESC	embryonic stem cell:	embryo
11	chr14:78147567-78147617	SKMC	muscle:	n/a
12	chr14:78147567-78147617	PANC-1	pancreas:	n/a
13	chr14:78147567-78147617	CMK	blood:	n/a
14	chr14:78147567-78147617	HCT-116	colon:	n/a
15	chr14:78147567-78147617	HCF	heart:	n/a
16	chr14:78147567-78147617	AoSMC	blood vessel:	n/a
17	chr14:78147567-78147617	GM19239	blood:	n/a
18	chr14:78147567-78147617	NT2-D1	testis:	n/a
19	chr14:78147567-78147617	BJ	skin:	n/a
20	chr14:78147567-78147617	NHDF-neo	bronchial:	n/a
21	chr14:78147567-78147617	AG10803	skin:	n/a
22	chr14:78147567-78147617	LNCaP	prostate:	n/a
23	chr14:78147567-78147617	GM12892	blood:	n/a
24	chr14:78147567-78147617	Caco-2	colon:	n/a
25	chr14:78147567-78147617	HIPEpiC	eye:	n/a
26	chr14:78147567-78147617	Hela-S3	cervix:	n/a
27	chr14:78147567-78147617	HepG2	liver:	n/a
28	chr14:78147567-78147617	HCPEpiC	choroid plexus:	n/a
29	chr14:78147567-78147617	HL-60	blood:	n/a
30	chr14:78147567-78147617	AG09309	skin:	n/a
31	chr14:78147567-78147617	ECC-1	luminal epithelium:	n/a
32	chr14:78147567-78147617	ovcar-3	ovarian:	n/a
33	chr14:78147567-78147617	AG04450	lung:	fetal
34	chr14:78147567-78147617	T-47D	breast:	n/a
35	chr14:78147567-78147617	HUVEC	blood vessel:	n/a
36	chr14:78147567-78147617	NHBE	bronchial:	n/a
37	chr14:78147567-78147617	Jurkat	blood:	n/a
38	chr14:78147567-78147617	SK-N-SH_RA	brain:	n/a
39	chr14:78147567-78147617	SK-N-MC	brain:	n/a
40	chr14:78147567-78147617	ProgFib	skin:	n/a
41	chr14:78147567-78147617	K562	blood:	n/a
42	chr14:78147567-78147617	HRPEpiC	eye:	n/a
43	chr14:78147567-78147617	HRCEpiC	kidney:	n/a
44	chr14:78147567-78147617	NH-A	brain:	n/a
45	chr14:78147567-78147617	SAEC	small airway:	n/a
46	chr14:78147567-78147617	PFSK-1	brain:	n/a
47	chr14:78147567-78147617	HAEpiC	amniotic membrane:	n/a
48	chr14:78147567-78147617	HNPCEpiC	eye:	n/a
49	chr14:78147567-78147617	GM12878	blood:	n/a
50	chr14:78147567-78147617	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:78143127..78144900-chr14:78173251..78175527,2	MCF-7	breast:
2	chr14:78133661..78136302-chr14:78138970..78141654,2	K562	blood:
3	chr14:78145812..78147839-chr14:78160539..78163248,2	MCF-7	breast:
4	chr14:78137716..78140274-chr14:78142246..78143787,2	MCF-7	breast:
5	chr14:78132831..78134732-chr14:78142365..78145336,2	MCF-7	breast:
6	chr14:78129873..78132369-chr14:78135143..78137756,2	MCF-7	breast:
7	chr14:78138709..78140424-chr14:78170369..78172653,2	MCF-7	breast:
8	chr14:78145857..78148967-chr14:78171085..78175520,5	MCF-7	breast:
9	chr14:78132831..78134732-chr14:78142365..78145336,2	MCF-7	breast:
10	chr14:78137716..78140274-chr14:78142246..78143787,2	MCF-7	breast:
11	chr14:78133661..78136302-chr14:78138970..78141654,2	K562	blood:
12	chr11:63103438..63104964-chr14:78144218..78145718,2	MCF-7	breast:
13	chr14:78136536..78139253-chr14:78155471..78158284,2	MCF-7	breast:
14	chr14:78124444..78126288-chr14:78139672..78142055,2	K562	blood:
15	chr14:78139849..78142125-chr14:78173577..78176178,2	K562	blood:
16	chr14:78144032..78145859-chr14:78266366..78267961,2	K562	blood:
17	chr14:78129873..78132369-chr14:78135143..78137756,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNW1-6	chr14:78150215-78150332	NONHSAT037999
2	lnc-SLIRP-2	chr14:78137913-78138440	NONHSAT037998
3	lnc-SNW1-6	chr14:78149545-78149916	NONHSAT037999

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ALKBH1	hsa-miR-98-5p	chr14:78139813-78139807
2	ALKBH1	hsa-miR-98-5p	chr14:78139033-78139055

Variant related genes	Relation type
RPL21P10	TF binding region
RPL21P10	CpG island
ENSG00000119705	chromatin interactions
ENSG00000063761	chromatin interactions
ENSG00000100601	chromatin interactions
ENSG00000258917	chromatin interactions

Extended variants
information (count: 916 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4903626	chr14:78130479-78130480	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187412712	chr14:78130516-78130517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561594144	chr14:78130523-78130524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4903627	chr14:78130569-78130570	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs7151836	chr14:78130579-78130580	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs576746814	chr14:78130649-78130650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564422367	chr14:78130657-78130658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190232270	chr14:78130673-78130674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552545517	chr14:78130687-78130688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115247923	chr14:78130706-78130707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531884110	chr14:78130729-78130730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182052852	chr14:78130734-78130735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72685230	chr14:78130817-78130818	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs534417581	chr14:78130830-78130831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554042128	chr14:78130854-78130855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571125681	chr14:78130904-78130905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548384654	chr14:78130947-78130948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539702856	chr14:78130967-78130968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556163245	chr14:78131004-78131005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575627910	chr14:78131005-78131006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143087031	chr14:78131061-78131062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186647023	chr14:78131106-78131107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11624103	chr14:78131117-78131118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs571774243	chr14:78131125-78131126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs117131659	chr14:78131126-78131127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117424242	chr14:78131127-78131128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11624213	chr14:78131155-78131156	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs199878103	chr14:78131193-78131194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376525076	chr14:78131194-78131195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371487933	chr14:78131196-78131197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201791717	chr14:78131198-78131199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35254593	chr14:78131201-78131202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201728313	chr14:78131202-78131203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142161167	chr14:78131224-78131225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117224357	chr14:78131231-78131232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs397802258	chr14:78131234-78131235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529508602	chr14:78131237-78131238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531731727	chr14:78131240-78131241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548564748	chr14:78131241-78131242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11628838	chr14:78131262-78131263	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs527758205	chr14:78131265-78131266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190563559	chr14:78131308-78131309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566371181	chr14:78131342-78131343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138819985	chr14:78131381-78131382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182809889	chr14:78131500-78131501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575188468	chr14:78131563-78131564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs61992861	chr14:78131585-78131586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141445277	chr14:78131587-78131588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76542974	chr14:78131588-78131589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200488015	chr14:78131593-78131594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Hepatocellular carcinoma	16750200	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Biliary cancer	19435499	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Intracranial aneurysm	16715129	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	22209245	CNVD
Prostate cancer	22553170	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:729 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78120600-78138200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr14:78121400-78139800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr14:78121800-78139800	Weak transcription	Gastric	stomach
4	chr14:78122000-78139600	Weak transcription	Fetal Intestine Large	intestine
5	chr14:78122000-78139800	Weak transcription	Pancreas	Pancrea
6	chr14:78123000-78137400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr14:78123400-78138800	Weak transcription	Liver	Liver
8	chr14:78123800-78136600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr14:78123800-78139000	Weak transcription	Left Ventricle	heart
10	chr14:78125400-78139800	Weak transcription	Right Ventricle	heart
11	chr14:78126600-78138000	Weak transcription	Primary B cells from cord blood	blood
12	chr14:78126800-78138800	Weak transcription	Duodenum Mucosa	Duodenum
13	chr14:78126800-78139000	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr14:78126800-78139800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr14:78126800-78139800	Weak transcription	Spleen	Spleen
16	chr14:78127400-78138800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr14:78127400-78139800	Weak transcription	Lung	lung
18	chr14:78127400-78173200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr14:78127600-78137400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr14:78127600-78138600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr14:78127600-78138800	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr14:78127600-78138800	Weak transcription	Brain Anterior Caudate	brain
23	chr14:78127600-78139000	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr14:78127600-78139200	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr14:78127600-78139200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr14:78127600-78139800	Weak transcription	Brain Cingulate Gyrus	brain
27	chr14:78127600-78140000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr14:78127600-78140000	Weak transcription	Esophagus	oesophagus
29	chr14:78127800-78138000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr14:78127800-78138600	Weak transcription	Brain Hippocampus Middle	brain
31	chr14:78127800-78139600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr14:78127800-78139800	Weak transcription	Brain Germinal Matrix	brain
33	chr14:78128000-78132400	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr14:78128000-78138000	Weak transcription	Fetal Brain Female	brain
35	chr14:78128000-78138600	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr14:78128000-78138800	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr14:78128000-78139000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr14:78128000-78157800	Weak transcription	Fetal Brain Male	brain
39	chr14:78128200-78139600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr14:78128600-78130600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr14:78128800-78130600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr14:78128800-78138800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr14:78129000-78138800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:78129000-78138800	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr14:78129000-78139800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr14:78129200-78132600	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr14:78129200-78139600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr14:78129400-78130800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr14:78129800-78147600	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr14:78130000-78130600	Enhancers	Adipose Nuclei	Adipose

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