Variant report

Variant	esv3401331
Chromosome Location	chr14:85332747-85716351
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	chr14:85589256-85589486	HepG2	liver:	n/a	n/a
2	BCL11A	chr14:85621151-85621340	GM12878	blood:	n/a	n/a
3	BHLHE40	chr14:85504871-85505190	GM12878	blood:	n/a	n/a
4	BHLHE40	chr14:85530250-85530337	GM12878	blood:	n/a	n/a
5	BRCA1	chr14:85597979-85598064	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr14:85468850-85468851	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr14:85688313-85688514	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr14:85520754-85521010	IMR90	lung:	n/a	chr14:85520874-85520885
9	CEBPB	chr14:85554658-85554927	MCF-7	breast:	n/a	chr14:85554757-85554768 chr14:85554757-85554768 chr14:85554795-85554806 chr14:85554755-85554766 chr14:85554755-85554768 chr14:85554755-85554768
10	CEBPB	chr14:85662929-85663167	HepG2	liver:	n/a	n/a
11	CEBPB	chr14:85715601-85715842	K562	blood:	n/a	chr14:85715715-85715724 chr14:85715713-85715726 chr14:85715714-85715725
12	CEBPB	chr14:85457461-85457820	IMR90	lung:	n/a	chr14:85457637-85457650 chr14:85457638-85457649 chr14:85457637-85457650 chr14:85457637-85457650
13	CEBPB	chr14:85715482-85715898	ECC-1	luminal epithelium:	n/a	chr14:85715715-85715724 chr14:85715713-85715726 chr14:85715714-85715725
14	CEBPB	chr14:85715461-85715947	ECC-1	luminal epithelium:	n/a	chr14:85715715-85715724 chr14:85715713-85715726 chr14:85715714-85715725
15	CEBPB	chr14:85598896-85599024	HepG2	liver:	n/a	n/a
16	CEBPB	chr14:85385542-85385850	A549	lung:	n/a	chr14:85385677-85385688
17	CEBPB	chr14:85705032-85705053	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr14:85593945-85593963	IMR90	lung:	n/a	n/a
19	CEBPB	chr14:85592950-85593190	A549	lung:	n/a	n/a
20	CEBPB	chr14:85345568-85345819	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr14:85385539-85385851	HepG2	liver:	n/a	chr14:85385677-85385688
22	CEBPB	chr14:85557095-85557301	IMR90	lung:	n/a	n/a
23	CEBPB	chr14:85476561-85476863	Hela-S3	cervix:	n/a	chr14:85476660-85476671 chr14:85476623-85476636
24	CEBPB	chr14:85584537-85584917	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr14:85707452-85707711	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr14:85679844-85680186	IMR90	lung:	n/a	chr14:85679995-85680006
27	CEBPB	chr14:85554611-85554896	HepG2	liver:	n/a	chr14:85554757-85554768 chr14:85554757-85554768 chr14:85554795-85554806 chr14:85554755-85554766 chr14:85554755-85554768 chr14:85554755-85554768
28	CEBPB	chr14:85662899-85663214	A549	lung:	n/a	n/a
29	CEBPB	chr14:85641898-85642252	IMR90	lung:	n/a	n/a
30	CEBPB	chr14:85349237-85349529	K562	blood:	n/a	chr14:85349378-85349389
31	CEBPB	chr14:85349197-85349570	HepG2	liver:	n/a	chr14:85349378-85349389
32	CEBPB	chr14:85594061-85594147	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr14:85385558-85385830	H1-hESC	embryonic stem cell:	n/a	chr14:85385677-85385688
34	CEBPB	chr14:85550687-85551014	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr14:85679835-85680135	HepG2	liver:	n/a	chr14:85679995-85680006
36	CEBPB	chr14:85554610-85554904	A549	lung:	n/a	chr14:85554757-85554768 chr14:85554757-85554768 chr14:85554795-85554806 chr14:85554755-85554766 chr14:85554755-85554768 chr14:85554755-85554768
37	CEBPB	chr14:85667797-85668014	HepG2	liver:	n/a	chr14:85667920-85667931 chr14:85667920-85667933 chr14:85667921-85667932
38	CEBPB	chr14:85715553-85715868	A549	lung:	n/a	chr14:85715715-85715724 chr14:85715713-85715726 chr14:85715714-85715725
39	CEBPB	chr14:85349235-85349589	Hela-S3	cervix:	n/a	chr14:85349378-85349389
40	CEBPB	chr14:85715486-85715879	MCF-7	breast:	n/a	chr14:85715715-85715724 chr14:85715713-85715726 chr14:85715714-85715725
41	CEBPB	chr14:85354164-85354397	IMR90	lung:	n/a	n/a
42	CEBPB	chr14:85385519-85385863	IMR90	lung:	n/a	chr14:85385677-85385688
43	CEBPB	chr14:85576221-85576509	A549	lung:	n/a	n/a
44	CEBPB	chr14:85679835-85680112	A549	lung:	n/a	chr14:85679995-85680006
45	CEBPB	chr14:85506788-85506891	HepG2	liver:	n/a	n/a
46	CEBPB	chr14:85349285-85349541	H1-hESC	embryonic stem cell:	n/a	chr14:85349378-85349389
47	CEBPB	chr14:85715533-85715884	HepG2	liver:	n/a	chr14:85715715-85715724 chr14:85715713-85715726 chr14:85715714-85715725
48	CEBPB	chr14:85383125-85383348	HepG2	liver:	n/a	chr14:85383210-85383221
49	CEBPB	chr14:85715532-85715941	Hela-S3	cervix:	n/a	chr14:85715715-85715724 chr14:85715713-85715726 chr14:85715714-85715725
50	CEBPB	chr14:85520728-85520988	A549	lung:	n/a	chr14:85520874-85520885

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:85667733-85667783	HCPEpiC	choroid plexus:	n/a
2	chr14:85667733-85667783	HRPEpiC	eye:	n/a
3	chr14:85689636-85689686	MCF10A-Er-Src	breast:	n/a
4	chr14:85667733-85667783	H1-hESC	embryonic stem cell:	embryo
5	chr14:85715831-85715881	T-47D	breast:	n/a
6	chr14:85715831-85715881	PrEC	prostate:	n/a
7	chr14:85667733-85667783	HL-60	blood:	n/a
8	chr14:85715831-85715881	H1-hESC	embryonic stem cell:	embryo
9	chr14:85667733-85667783	HIPEpiC	eye:	n/a
10	chr14:85715831-85715881	HEK293	kidney:	embryo
11	chr14:85715831-85715881	GM19239	blood:	n/a
12	chr14:85689636-85689686	GM06990	blood:	n/a
13	chr14:85715831-85715881	HCF	heart:	n/a
14	chr14:85667733-85667783	SK-N-SH	brain:	n/a
15	chr14:85715831-85715881	HRE	kidney:	n/a
16	chr14:85715831-85715881	Caco-2	colon:	n/a
17	chr14:85667733-85667783	NHDF-neo	bronchial:	n/a
18	chr14:85715831-85715881	HRPEpiC	eye:	n/a
19	chr14:85689636-85689686	ProgFib	skin:	n/a
20	chr14:85715831-85715881	AoSMC	blood vessel:	n/a
21	chr14:85715831-85715881	A549	lung:	n/a
22	chr14:85667733-85667783	PrEC	prostate:	n/a
23	chr14:85715831-85715881	HCT-116	colon:	n/a
24	chr14:85689636-85689686	GM19239	blood:	n/a
25	chr14:85715831-85715881	AG04449	skin:	fetal
26	chr14:85689636-85689686	Jurkat	blood:	n/a
27	chr14:85689636-85689686	AG09319	gingival:	n/a
28	chr14:85667733-85667783	Jurkat	blood:	n/a
29	chr14:85689636-85689686	PFSK-1	brain:	n/a
30	chr14:85667733-85667783	HEEpiC	esophagus:	n/a
31	chr14:85689636-85689686	Hela-S3	cervix:	n/a
32	chr14:85715831-85715881	NH-A	brain:	n/a
33	chr14:85715831-85715881	LNCaP	prostate:	n/a
34	chr14:85689636-85689686	GM12892	blood:	n/a
35	chr14:85689636-85689686	AoSMC	blood vessel:	n/a
36	chr14:85715831-85715881	RPTEC	kidney:	n/a
37	chr14:85667733-85667783	PFSK-1	brain:	n/a
38	chr14:85689636-85689686	Caco-2	colon:	n/a
39	chr14:85715831-85715881	AG04450	lung:	fetal
40	chr14:85667733-85667783	T-47D	breast:	n/a
41	chr14:85667733-85667783	AG04449	skin:	fetal
42	chr14:85689636-85689686	GM12891	blood:	n/a
43	chr14:85715831-85715881	HRCEpiC	kidney:	n/a
44	chr14:85715831-85715881	MCF10A-Er-Src	breast:	n/a
45	chr14:85667733-85667783	U87	brain:	n/a
46	chr14:85715831-85715881	NB4	blood:	n/a
47	chr14:85667733-85667783	K562	blood:	n/a
48	chr14:85715831-85715881	NT2-D1	testis:	n/a
49	chr14:85715831-85715881	PANC-1	pancreas:	n/a
50	chr14:85715831-85715881	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:62607627..62609150-chr14:85611227..85612747,2	K562	blood:
2	chr14:85716141..85718309-chr14:85719086..85721853,2	MCF-7	breast:
3	chr14:85490593..85492977-chr14:85499997..85502268,2	K562	blood:
4	chr14:85563318..85564867-chr14:85565112..85566756,2	MCF-7	breast:
5	chr14:85504367..85505311-chr9:111430924..111431510,2	MCF-7	breast:
6	chr14:85611226..85611727-chr17:41463821..41464360,2	HCT-116	colon:
7	chr14:83766559..83767404-chr14:85597812..85598521,2	MCF-7	breast:
8	chr14:85490593..85492977-chr14:85499997..85502268,2	K562	blood:
9	chr14:85611227..85612747-chr17:41464225..41466390,2	K562	blood:
10	chr14:85563318..85564867-chr14:85565112..85566756,2	MCF-7	breast:
11	chr14:85609727..85612747-chr17:41464783..41468587,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GALC-10	chr14:85705748-85705818	ENSG00000259044
2	lnc-GALC-10	chr14:85669193-85669576	ENSG00000259044
3	lnc-RP11-497E19.2.1-6	chr14:85606972-85607064	l_1023_chr14:85606971-85664205_whiteBloodCell
4	lnc-GALC-10	chr14:85701133-85701270	ENSG00000259044
5	lnc-GALC-15	chr14:85464622-85465640	NONHSAT038108
6	lnc-RP11-497E19.2.1-6	chr14:85664047-85664205	l_1023_chr14:85606971-85664205_whiteBloodCell

Variant related genes	Relation type
ENSG00000259044	TF binding region
ENSG00000258506	TF binding region
ENSG00000271712	TF binding region
ENSG00000259044	CpG island
ENSG00000258506	CpG island
ENSG00000271712	CpG island
ENSG00000188825	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 7285 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:7285 , 50 per page) page: 1 2 3 4 5 6 7 ... 146

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115450003	chr14:85337806-85337807	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs188009315	chr14:85337848-85337849	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs375747637	chr14:85337861-85337862	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs709854	chr14:85337905-85337906	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs180985662	chr14:85337913-85337914	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs552154115	chr14:85337944-85337945	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs186990437	chr14:85337945-85337946	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs33938397	chr14:85339802-85339803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565909407	chr14:85339817-85339818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs56728736	chr14:85339818-85339819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs397839120	chr14:85339840-85339841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs3081785	chr14:85339844-85339845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs142368355	chr14:85339883-85339884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531359440	chr14:85339946-85339947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs28457811	chr14:85339968-85339969	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs534843913	chr14:85340016-85340017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115028057	chr14:85340065-85340066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs193244399	chr14:85340075-85340076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548543496	chr14:85340093-85340094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs17120355	chr14:85340262-85340263	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs557710134	chr14:85340318-85340319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146148444	chr14:85340327-85340328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540036078	chr14:85340340-85340341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188858615	chr14:85340346-85340347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573383092	chr14:85340385-85340386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192153336	chr14:85340413-85340414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576122709	chr14:85340419-85340420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555029840	chr14:85340480-85340481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535365414	chr14:85340499-85340500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567153602	chr14:85340516-85340517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543775705	chr14:85340563-85340564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562445688	chr14:85340572-85340573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75152987	chr14:85340627-85340628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs117245619	chr14:85340628-85340629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534250568	chr14:85340640-85340641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs367808659	chr14:85340649-85340650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552139181	chr14:85340709-85340710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs17120357	chr14:85340775-85340776	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs547148460	chr14:85340795-85340796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555560539	chr14:85340803-85340804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568529544	chr14:85340826-85340827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529310443	chr14:85340827-85340828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550955956	chr14:85340835-85340836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550167783	chr14:85340889-85340890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183876669	chr14:85340935-85340936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs17120360	chr14:85340952-85340953	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs188555644	chr14:85340955-85340956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566987830	chr14:85341053-85341054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570531123	chr14:85341082-85341083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs180716892	chr14:85341094-85341095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21569311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:697 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85337800-85338000	ZNF genes & repeats	Psoas Muscle	Psoas
2	chr14:85339800-85340600	Enhancers	Ovary	ovary
3	chr14:85340000-85340800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr14:85340000-85341000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr14:85340200-85340800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr14:85340400-85341600	Enhancers	Fetal Brain Male	brain
7	chr14:85340800-85343400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr14:85340800-85343400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr14:85341000-85341400	Enhancers	Fetal Brain Female	brain
10	chr14:85343400-85343600	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr14:85343400-85343800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr14:85351200-85351600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr14:85351200-85351600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr14:85351200-85351600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr14:85351200-85352000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr14:85351200-85352200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr14:85351200-85352200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr14:85351200-85352400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr14:85351400-85351800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr14:85351400-85352200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr14:85351600-85352000	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr14:85351600-85352600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr14:85352000-85352200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr14:85352600-85352800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr14:85353800-85354600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr14:85382600-85382800	Enhancers	Colon Smooth Muscle	Colon
27	chr14:85383600-85384400	Enhancers	Brain Germinal Matrix	brain
28	chr14:85384400-85384800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr14:85388600-85389000	Enhancers	Fetal Brain Female	brain
30	chr14:85393200-85394800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr14:85393400-85394600	Enhancers	Fetal Heart	heart
32	chr14:85393600-85394200	Enhancers	Adipose Nuclei	Adipose
33	chr14:85393600-85394400	Enhancers	Fetal Lung	lung
34	chr14:85393600-85394600	Enhancers	Brain Germinal Matrix	brain
35	chr14:85393600-85394800	Enhancers	Fetal Brain Male	brain
36	chr14:85393800-85394000	Enhancers	Right Atrium	heart
37	chr14:85393800-85394200	Enhancers	Brain Hippocampus Middle	brain
38	chr14:85393800-85394600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr14:85394600-85396200	Weak transcription	Fetal Heart	heart
40	chr14:85396200-85396800	Enhancers	Fetal Heart	heart
41	chr14:85398600-85399800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr14:85403800-85404200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr14:85413800-85414000	Enhancers	Pancreas	Pancrea
44	chr14:85414000-85421600	Weak transcription	Pancreas	Pancrea
45	chr14:85414800-85415200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr14:85425400-85426000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
47	chr14:85426000-85426200	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr14:85426000-85427000	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr14:85426000-85427000	Enhancers	HUVEC	blood vessel
50	chr14:85426200-85426400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell

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