Variant report

Variant	nsv1050174
Chromosome Location	chr14:37556357-37664143
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1819)
CpG islands
(count:976)
Chromatin interactive
region (count:91)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1819 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:37643767-37644084	K562	blood:	n/a	n/a
2	ARID3A	chr14:37612843-37612931	K562	blood:	n/a	n/a
3	ARID3A	chr14:37636859-37637271	K562	blood:	n/a	n/a
4	ARID3A	chr14:37618944-37619276	K562	blood:	n/a	n/a
5	ARID3A	chr14:37636253-37636339	K562	blood:	n/a	n/a
6	ARID3A	chr14:37556845-37557096	K562	blood:	n/a	n/a
7	ARID3A	chr14:37618939-37620096	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:37619710-37620155	K562	blood:	n/a	n/a
9	ARID3A	chr14:37640896-37641730	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:37637980-37638323	K562	blood:	n/a	n/a
11	ARID3A	chr14:37638798-37638998	K562	blood:	n/a	chr14:37638878-37638894 chr14:37638877-37638893
12	ARID3A	chr14:37563047-37563431	K562	blood:	n/a	n/a
13	ARID3A	chr14:37558841-37558905	K562	blood:	n/a	n/a
14	ARID3A	chr14:37641543-37641674	K562	blood:	n/a	n/a
15	ARID3A	chr14:37591599-37591821	HepG2	liver:	n/a	n/a
16	ARID3A	chr14:37642484-37642976	K562	blood:	n/a	n/a
17	ARID3A	chr14:37640439-37641338	K562	blood:	n/a	n/a
18	ATF1	chr14:37637957-37638275	K562	blood:	n/a	n/a
19	ATF1	chr14:37558607-37559216	K562	blood:	n/a	n/a
20	ATF1	chr14:37636855-37637252	K562	blood:	n/a	n/a
21	ATF2	chr14:37641089-37641818	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr14:37636749-37637333	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr14:37636807-37637410	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr14:37641468-37642010	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr14:37650651-37650943	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr14:37639465-37639767	K562	blood:	n/a	n/a
27	ATF3	chr14:37641048-37641567	A549	lung:	n/a	n/a
28	BACH1	chr14:37636967-37637160	K562	blood:	n/a	n/a
29	BACH1	chr14:37636808-37637367	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr14:37641174-37642006	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL3	chr14:37641013-37641625	A549	lung:	n/a	n/a
32	BCL3	chr14:37640978-37641543	A549	lung:	n/a	n/a
33	BCL3	chr14:37586083-37586621	A549	lung:	n/a	chr14:37586327-37586336
34	BCLAF1	chr14:37640954-37641540	K562	blood:	n/a	n/a
35	BHLHE40	chr14:37563542-37564042	K562	blood:	n/a	n/a
36	BHLHE40	chr14:37562651-37562925	K562	blood:	n/a	n/a
37	BHLHE40	chr14:37641028-37642076	K562	blood:	n/a	n/a
38	BHLHE40	chr14:37637932-37638567	K562	blood:	n/a	n/a
39	BHLHE40	chr14:37591614-37591878	HepG2	liver:	n/a	n/a
40	BRCA1	chr14:37586806-37587108	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr14:37641134-37641473	HepG2	liver:	n/a	n/a
42	BRCA1	chr14:37641083-37642134	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr14:37641014-37641539	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr14:37641193-37641780	K562	blood:	n/a	n/a
45	CBX3	chr14:37575419-37575791	K562	blood:	n/a	n/a
46	CBX3	chr14:37637860-37638321	K562	blood:	n/a	n/a
47	CBX3	chr14:37640981-37641764	HCT-116	colon:	n/a	n/a
48	CCNT2	chr14:37641112-37641994	K562	blood:	n/a	n/a
49	CCNT2	chr14:37637920-37638412	K562	blood:	n/a	n/a
50	CCNT2	chr14:37577934-37578134	K562	blood:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:37640455-37640505	ECC-1	luminal epithelium:	n/a
2	chr14:37644675-37644725	HRPEpiC	eye:	n/a
3	chr14:37641600-37641650	ovcar-3	ovarian:	n/a
4	chr14:37664088-37664138	HRE	kidney:	n/a
5	chr14:37641134-37641184	Hepatocyte	liver:	n/a
6	chr14:37641964-37642014	AG04450	lung:	fetal
7	chr14:37641660-37641710	PANC-1	pancreas:	n/a
8	chr14:37641600-37641650	HCT-116	colon:	n/a
9	chr14:37664088-37664138	HRPEpiC	eye:	n/a
10	chr14:37644675-37644725	AG10803	skin:	n/a
11	chr14:37641660-37641710	PFSK-1	brain:	n/a
12	chr14:37639757-37639807	SK-N-MC	brain:	n/a
13	chr14:37641436-37641486	SKMC	muscle:	n/a
14	chr14:37641261-37641311	HCPEpiC	choroid plexus:	n/a
15	chr14:37641660-37641710	H1-hESC	embryonic stem cell:	embryo
16	chr14:37638478-37638528	HUVEC	blood vessel:	n/a
17	chr14:37640455-37640505	HCF	heart:	n/a
18	chr14:37641660-37641710	MCF10A-Er-Src	breast:	n/a
19	chr14:37641261-37641311	K562	blood:	n/a
20	chr14:37664088-37664138	T-47D	breast:	n/a
21	chr14:37640247-37640297	PFSK-1	brain:	n/a
22	chr14:37641964-37642014	HCF	heart:	n/a
23	chr14:37641726-37641776	CMK	blood:	n/a
24	chr14:37640455-37640505	NB4	blood:	n/a
25	chr14:37641964-37642014	HepG2	liver:	n/a
26	chr14:37641660-37641710	AoSMC	blood vessel:	n/a
27	chr14:37641462-37641512	HL-60	blood:	n/a
28	chr14:37640247-37640297	BE2_C	brain:	n/a
29	chr14:37641964-37642014	HCM	heart:	n/a
30	chr14:37558604-37558654	HMEC	breast:	n/a
31	chr14:37640455-37640505	AG09319	gingival:	n/a
32	chr14:37641261-37641311	HRPEpiC	eye:	n/a
33	chr14:37664088-37664138	PANC-1	pancreas:	n/a
34	chr14:37640247-37640297	SK-N-SH_RA	brain:	n/a
35	chr14:37641726-37641776	HIPEpiC	eye:	n/a
36	chr14:37644675-37644725	Hepatocyte	liver:	n/a
37	chr14:37641600-37641650	HCM	heart:	n/a
38	chr14:37644675-37644725	K562	blood:	n/a
39	chr14:37638478-37638528	Jurkat	blood:	n/a
40	chr14:37644675-37644725	GM19239	blood:	n/a
41	chr14:37644675-37644725	Caco-2	colon:	n/a
42	chr14:37641462-37641512	SKMC	muscle:	n/a
43	chr14:37641660-37641710	BE2_C	brain:	n/a
44	chr14:37641462-37641512	HEEpiC	esophagus:	n/a
45	chr14:37641600-37641650	HepG2	liver:	n/a
46	chr14:37638478-37638528	BE2_C	brain:	n/a
47	chr14:37664088-37664138	SAEC	small airway:	n/a
48	chr14:37641191-37641241	HEK293	kidney:	embryo
49	chr14:37641134-37641184	MCF-7	breast:	n/a
50	chr14:37638478-37638528	AG04449	skin:	fetal

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:37619466..37622016-chr14:37640735..37643299,2	K562	blood:
2	chr14:37641825..37643910-chr14:37649630..37653751,3	K562	blood:
3	chr14:37535319..37537304-chr14:37555545..37557530,2	K562	blood:
4	chr14:37591458..37594181-chr14:37641204..37642829,2	MCF-7	breast:
5	chr14:37632758..37634640-chr14:37640795..37642566,2	MCF-7	breast:
6	chr14:37561103..37563065-chr14:37576715..37579105,2	MCF-7	breast:
7	chr14:37558524..37560785-chr14:37561161..37564362,3	K562	blood:
8	chr14:37610927..37613306-chr14:37640197..37642903,2	MCF-7	breast:
9	chr14:37640543..37642943-chr20:48598351..48600093,2	MCF-7	breast:
10	chr14:37636501..37638947-chr14:37664211..37667966,4	K562	blood:
11	chr14:37638241..37643981-chr14:37665773..37670423,8	MCF-7	breast:
12	chr14:37528200..37530680-chr14:37600178..37602513,2	K562	blood:
13	chr14:37595811..37599038-chr14:37602068..37604327,3	MCF-7	breast:
14	chr14:37131202..37132825-chr14:37638068..37640984,2	K562	blood:
15	chr14:37642507..37644578-chr14:38042317..38044678,2	MCF-7	breast:
16	chr14:37639617..37644848-chr14:37662875..37669924,15	K562	blood:
17	chr14:37115310..37117842-chr14:37618181..37620146,4	MCF-7	breast:
18	chr14:37116948..37117690-chr14:37591347..37592244,2	MCF-7	breast:
19	chr14:37641087..37642667-chr14:38063502..38066629,3	MCF-7	breast:
20	chr14:37587663..37589305-chr14:37591557..37593848,2	MCF-7	breast:
21	chr14:37563198..37565090-chr14:38061386..38063484,2	MCF-7	breast:
22	chr14:37578874..37583867-chr14:37583944..37587801,9	MCF-7	breast:
23	chr14:37411236..37411778-chr14:37586529..37587352,2	MCF-7	breast:
24	chr14:37620516..37622748-chr14:37640146..37642235,2	K562	blood:
25	chr14:37639061..37645694-chr14:37661777..37669317,18	MCF-7	breast:
26	chr14:37619842..37620362-chr14:37699681..37700515,2	K562	blood:
27	chr14:37639617..37644848-chr14:37662875..37669924,15	K562	blood:
28	chr14:37548599..37550986-chr14:37557970..37560958,2	K562	blood:
29	chr14:37662314..37664941-chr14:37664960..37666969,2	K562	blood:
30	chr14:37623137..37627783-chr14:37639890..37642738,4	MCF-7	breast:
31	chr14:37577414..37579393-chr14:37583140..37584879,2	K562	blood:
32	chr14:37560763..37563483-chr14:37564350..37566033,2	MCF-7	breast:
33	chr14:37129932..37131787-chr14:37640970..37642806,2	MCF-7	breast:
34	chr14:37595328..37597132-chr14:37600634..37602952,2	K562	blood:
35	chr14:37640829..37643687-chr14:37650994..37653256,2	K562	blood:
36	chr14:37561103..37563065-chr14:37576715..37579105,2	MCF-7	breast:
37	chr14:37638513..37640081-chr14:37646893..37648669,2	MCF-7	breast:
38	chr14:37652408..37654436-chr14:37665348..37666994,2	MCF-7	breast:
39	chr14:37073041..37076852-chr14:37619126..37621412,3	MCF-7	breast:
40	chr14:37493069..37493723-chr14:37618601..37619945,3	MCF-7	breast:
41	chr14:37578874..37583867-chr14:37583944..37587801,9	MCF-7	breast:
42	chr14:37580174..37584845-chr14:37588606..37592760,5	MCF-7	breast:
43	chr14:37593584..37594175-chr14:37619119..37620412,3	MCF-7	breast:
44	chr14:37527584..37529968-chr14:37590390..37592949,2	MCF-7	breast:
45	chr14:37593584..37594175-chr14:37619119..37620412,3	MCF-7	breast:
46	chr14:37640646..37642882-chr14:37648236..37650097,2	MCF-7	breast:
47	chr14:37577414..37579393-chr14:37583140..37584879,2	K562	blood:
48	chr14:36918851..36919626-chr14:37586517..37587298,2	MCF-7	breast:
49	chr14:37639697..37645467-chr14:37664720..37672395,14	K562	blood:
50	chr14:37619316..37621404-chr14:37664460..37668196,4	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXA1-3	chr14:37566267-37566380	ENSG00000258827.1
2	lnc-FOXA1-3	chr14:37567056-37567768	ENSG00000258827.1
3	lnc-FOXA1-3	chr14:37567062-37567768	ENSG00000258827.2
4	lnc-FOXA1-3	chr14:37566267-37566387	ENSG00000258827.2
5	lnc-MIPOL1-5	chr14:37641231-37642998	NR_033240

No data

Variant related genes	Relation type
ENSG00000258827	TF binding region
SLC25A21-AS1	TF binding region
SLC25A21	TF binding region
RNU6-273P	TF binding region
MIPOL1	TF binding region
ENSG00000258827	CpG island
SLC25A21-AS1	CpG island
SLC25A21	CpG island
RNU6-273P	CpG island
MIPOL1	CpG island
ENSG00000129514	chromatin interactions
ENSG00000124216	chromatin interactions
ENSG00000258708	chromatin interactions
ENSG00000183032	chromatin interactions
ENSG00000198807	chromatin interactions
ENSG00000151338	chromatin interactions
ENSG00000136327	chromatin interactions
ENSG00000139865	chromatin interactions

Extended variants
information (count: 3587 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3587 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4363773	chr14:37556357-37556358	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377099213	chr14:37556389-37556390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs193011959	chr14:37556407-37556408	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs556059542	chr14:37556409-37556410	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs574101875	chr14:37556412-37556413	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs147521533	chr14:37556469-37556470	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs140083059	chr14:37556470-37556471	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs544568834	chr14:37556482-37556483	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs2057171	chr14:37556511-37556512	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs183061584	chr14:37556547-37556548	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs557503469	chr14:37556598-37556599	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs571036906	chr14:37556605-37556606	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs372930132	chr14:37556625-37556626	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs374562643	chr14:37556634-37556635	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs549821970	chr14:37556732-37556733	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs142752044	chr14:37556741-37556742	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs553495621	chr14:37556752-37556753	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs573324551	chr14:37556765-37556766	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs187652742	chr14:37556810-37556811	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs192505298	chr14:37556824-37556825	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs574643019	chr14:37556847-37556848	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs543327491	chr14:37556883-37556884	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs147367194	chr14:37556935-37556936	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs377442552	chr14:37556947-37556948	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs563174803	chr14:37557005-37557006	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs532162642	chr14:37557006-37557007	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs545537631	chr14:37557080-37557081	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs185023849	chr14:37557081-37557082	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs545237826	chr14:37557097-37557098	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs17106275	chr14:37557124-37557125	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs548133649	chr14:37557223-37557224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562265857	chr14:37557241-37557242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375477877	chr14:37557284-37557285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560069392	chr14:37557310-37557311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550977596	chr14:37557352-37557353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs527617849	chr14:37557443-37557444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548882375	chr14:37557452-37557453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2415384	chr14:37557468-37557469	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs7140183	chr14:37557476-37557477	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549355280	chr14:37557478-37557479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189391541	chr14:37557485-37557486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192407737	chr14:37557517-37557518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535499645	chr14:37557531-37557532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10220281	chr14:37557598-37557599	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs551983944	chr14:37557619-37557620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1950376	chr14:37557700-37557701	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs34099085	chr14:37557722-37557723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534360113	chr14:37557723-37557724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537389858	chr14:37557760-37557761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139046887	chr14:37557894-37557895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
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
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
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
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Cancer	20164919	CNVD

Chromatin state (count:642 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37553400-37562600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:37553600-37556400	Weak transcription	K562	blood
3	chr14:37553600-37557800	Weak transcription	Pancreas	Pancrea
4	chr14:37556400-37556600	Active TSS	K562	blood
5	chr14:37556600-37557200	Flanking Active TSS	K562	blood
6	chr14:37557200-37558000	Enhancers	K562	blood
7	chr14:37557600-37559400	Enhancers	Brain Germinal Matrix	brain
8	chr14:37557800-37558000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr14:37557800-37558200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr14:37557800-37559600	Enhancers	Fetal Stomach	stomach
11	chr14:37558000-37558800	Active TSS	K562	blood
12	chr14:37558000-37559000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr14:37558800-37559400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr14:37558800-37559600	Flanking Active TSS	K562	blood
15	chr14:37559000-37559200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr14:37559000-37559600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr14:37559200-37559400	Enhancers	NHDF-Ad	bronchial
18	chr14:37559200-37559600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr14:37559400-37559600	Enhancers	Lung	lung
20	chr14:37559400-37559600	Enhancers	Pancreas	Pancrea
21	chr14:37559400-37559800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr14:37559400-37559800	Enhancers	Esophagus	oesophagus
23	chr14:37559400-37559800	Flanking Active TSS	NHDF-Ad	bronchial
24	chr14:37559600-37559800	Enhancers	K562	blood
25	chr14:37559800-37562800	Weak transcription	K562	blood
26	chr14:37560600-37561000	Enhancers	NH-A	brain
27	chr14:37561000-37561400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr14:37561400-37568000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr14:37562600-37562800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:37562800-37564800	Enhancers	K562	blood
31	chr14:37578000-37584400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr14:37582400-37585400	Enhancers	Muscle Satellite Cultured Cells	--
33	chr14:37582400-37587600	Enhancers	Hela-S3	cervix
34	chr14:37582400-37602800	Weak transcription	K562	blood
35	chr14:37582600-37582800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr14:37582800-37583600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr14:37583200-37583400	Enhancers	HSMMtube	muscle
38	chr14:37583200-37583800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr14:37583200-37584400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr14:37583200-37585400	Weak transcription	Aorta	Aorta
41	chr14:37583400-37584200	Enhancers	A549	lung
42	chr14:37583400-37586200	Weak transcription	HSMMtube	muscle
43	chr14:37583600-37583800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr14:37583600-37584000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr14:37583800-37584000	Enhancers	HSMM	muscle
46	chr14:37583800-37585600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr14:37583800-37586400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr14:37584000-37585400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr14:37584200-37585000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr14:37584200-37585400	Weak transcription	A549	lung

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