Variant report

Variant	nsv1046326
Chromosome Location	chr14:47629646-47845903
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	BACH1	chr14:47804741-47804747	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr14:47840011-47840068	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr14:47827183-47827600	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr14:47657519-47657543	GM12878	blood:	n/a	n/a
5	CEBPB	chr14:47743081-47743545	MCF-7	breast:	n/a	n/a
6	CEBPB	chr14:47743152-47743532	IMR90	lung:	n/a	n/a
7	CEBPB	chr14:47649136-47649487	HepG2	liver:	n/a	chr14:47649288-47649299 chr14:47649318-47649329
8	CEBPB	chr14:47738957-47739196	A549	lung:	n/a	n/a
9	CEBPB	chr14:47834961-47835168	HepG2	liver:	n/a	n/a
10	CEBPB	chr14:47649201-47649458	K562	blood:	n/a	chr14:47649288-47649299 chr14:47649318-47649329
11	CEBPB	chr14:47649150-47649476	H1-hESC	embryonic stem cell:	n/a	chr14:47649288-47649299 chr14:47649318-47649329
12	CEBPB	chr14:47758514-47758816	IMR90	lung:	n/a	chr14:47758676-47758687 chr14:47758675-47758688
13	CEBPB	chr14:47743164-47743546	MCF-7	breast:	n/a	n/a
14	CEBPB	chr14:47773674-47773940	HepG2	liver:	n/a	chr14:47773834-47773847 chr14:47773812-47773823
15	CEBPB	chr14:47804079-47804205	HepG2	liver:	n/a	chr14:47804143-47804160 chr14:47804146-47804157
16	CEBPB	chr14:47743168-47743530	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr14:47649134-47649469	A549	lung:	n/a	chr14:47649288-47649299 chr14:47649318-47649329
18	CEBPB	chr14:47652631-47652824	HepG2	liver:	n/a	chr14:47652761-47652772
19	CEBPB	chr14:47670575-47670926	HepG2	liver:	n/a	chr14:47670750-47670761
20	CEBPB	chr14:47649198-47649493	ECC-1	luminal epithelium:	n/a	chr14:47649288-47649299 chr14:47649318-47649329
21	CEBPB	chr14:47758740-47758766	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr14:47769492-47769763	IMR90	lung:	n/a	n/a
23	CEBPB	chr14:47647084-47647297	A549	lung:	n/a	n/a
24	CEBPB	chr14:47738926-47739455	HCT-116	colon:	n/a	chr14:47739390-47739403
25	CEBPB	chr14:47649157-47649470	Hela-S3	cervix:	n/a	chr14:47649288-47649299 chr14:47649318-47649329
26	CEBPB	chr14:47743156-47743521	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr14:47649141-47649487	IMR90	lung:	n/a	chr14:47649288-47649299 chr14:47649318-47649329
28	CEBPB	chr14:47743126-47743498	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr14:47743152-47743531	K562	blood:	n/a	n/a
30	CEBPB	chr14:47702336-47702586	HepG2	liver:	n/a	chr14:47702442-47702455 chr14:47702442-47702453
31	CEBPB	chr14:47743099-47743552	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr14:47743201-47743510	A549	lung:	n/a	n/a
33	CEBPB	chr14:47815725-47815829	H1-hESC	embryonic stem cell:	n/a	chr14:47815797-47815808
34	CEBPB	chr14:47738946-47739612	Hela-S3	cervix:	n/a	chr14:47739390-47739403
35	CEBPB	chr14:47670622-47670894	IMR90	lung:	n/a	chr14:47670750-47670761
36	CEBPB	chr14:47815640-47815914	HepG2	liver:	n/a	chr14:47815797-47815808
37	CEBPB	chr14:47758518-47758817	HepG2	liver:	n/a	chr14:47758676-47758687 chr14:47758675-47758688
38	CEBPB	chr14:47743181-47743550	HCT-116	colon:	n/a	n/a
39	CEBPB	chr14:47758513-47758743	A549	lung:	n/a	chr14:47758676-47758687 chr14:47758675-47758688
40	CEBPB	chr14:47738831-47739429	HCT-116	colon:	n/a	chr14:47739390-47739403 chr14:47738862-47738879 chr14:47738864-47738876
41	CTCF	chr14:47802302-47802392	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr14:47747540-47747690	GM12872	blood:	n/a	chr14:47747629-47747647 chr14:47747630-47747646 chr14:47747624-47747645 chr14:47747631-47747644
43	CTCF	chr14:47747560-47747710	GM12871	blood:	n/a	chr14:47747629-47747647 chr14:47747630-47747646 chr14:47747624-47747645 chr14:47747631-47747644
44	CTCF	chr14:47747560-47747710	GM12870	blood:	n/a	chr14:47747629-47747647 chr14:47747630-47747646 chr14:47747624-47747645 chr14:47747631-47747644
45	CTCF	chr14:47747411-47747819	A549	lung:	n/a	chr14:47747629-47747647 chr14:47747630-47747646 chr14:47747624-47747645 chr14:47747631-47747644
46	CTCF	chr14:47747580-47747730	GM12875	blood:	n/a	chr14:47747629-47747647 chr14:47747630-47747646 chr14:47747624-47747645 chr14:47747631-47747644
47	CTCF	chr14:47747540-47747690	GM12870	blood:	n/a	chr14:47747629-47747647 chr14:47747630-47747646 chr14:47747624-47747645 chr14:47747631-47747644
48	CTCF	chr14:47747560-47747710	Hela-S3	cervix:	n/a	chr14:47747629-47747647 chr14:47747630-47747646 chr14:47747624-47747645 chr14:47747631-47747644
49	CTCF	chr14:47676920-47677070	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr14:47747580-47747730	GM12865	blood:	n/a	chr14:47747629-47747647 chr14:47747630-47747646 chr14:47747624-47747645 chr14:47747631-47747644

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:47769981-47770031	CMK	blood:	n/a
2	chr14:47812515-47812565	AG10803	skin:	n/a
3	chr14:47769981-47770031	HIPEpiC	eye:	n/a
4	chr14:47769981-47770031	HMEC	breast:	n/a
5	chr14:47769981-47770031	NH-A	brain:	n/a
6	chr14:47812515-47812565	HMEC	breast:	n/a
7	chr14:47812515-47812565	AG09319	gingival:	n/a
8	chr14:47769981-47770031	AoSMC	blood vessel:	n/a
9	chr14:47812515-47812565	NHDF-neo	bronchial:	n/a
10	chr14:47812515-47812565	PFSK-1	brain:	n/a
11	chr14:47769981-47770031	HAEpiC	amniotic membrane:	n/a
12	chr14:47670060-47670110	H1-hESC	embryonic stem cell:	embryo
13	chr14:47834520-47834570	ECC-1	luminal epithelium:	n/a
14	chr14:47769981-47770031	H1-hESC	embryonic stem cell:	embryo
15	chr14:47670060-47670110	NHBE	bronchial:	n/a
16	chr14:47769981-47770031	BE2_C	brain:	n/a
17	chr14:47812515-47812565	HCT-116	colon:	n/a
18	chr14:47834520-47834570	T-47D	breast:	n/a
19	chr14:47670060-47670110	IMR90	lung:	fetal
20	chr14:47670060-47670110	HRPEpiC	eye:	n/a
21	chr14:47812515-47812565	SKMC	muscle:	n/a
22	chr14:47670060-47670110	LNCaP	prostate:	n/a
23	chr14:47670060-47670110	GM06990	blood:	n/a
24	chr14:47834520-47834570	SKMC	muscle:	n/a
25	chr14:47812515-47812565	ECC-1	luminal epithelium:	n/a
26	chr14:47812515-47812565	LNCaP	prostate:	n/a
27	chr14:47834520-47834570	AG09309	skin:	n/a
28	chr14:47834520-47834570	K562	blood:	n/a
29	chr14:47834520-47834570	NB4	blood:	n/a
30	chr14:47812515-47812565	HepG2	liver:	n/a
31	chr14:47834520-47834570	Hela-S3	cervix:	n/a
32	chr14:47812515-47812565	SAEC	small airway:	n/a
33	chr14:47670060-47670110	GM12891	blood:	n/a
34	chr14:47670060-47670110	HUVEC	blood vessel:	n/a
35	chr14:47834520-47834570	HRE	kidney:	n/a
36	chr14:47834520-47834570	HAEpiC	amniotic membrane:	n/a
37	chr14:47834520-47834570	NH-A	brain:	n/a
38	chr14:47670060-47670110	HPAEpiC	pulmonary alveolar:	n/a
39	chr14:47670060-47670110	RPTEC	kidney:	n/a
40	chr14:47812515-47812565	HL-60	blood:	n/a
41	chr14:47670060-47670110	GM19239	blood:	n/a
42	chr14:47769981-47770031	LNCaP	prostate:	n/a
43	chr14:47670060-47670110	SK-N-MC	brain:	n/a
44	chr14:47812515-47812565	HEK293	kidney:	embryo
45	chr14:47670060-47670110	AG10803	skin:	n/a
46	chr14:47834520-47834570	HIPEpiC	eye:	n/a
47	chr14:47812515-47812565	AoSMC	blood vessel:	n/a
48	chr14:47812515-47812565	Hela-S3	cervix:	n/a
49	chr14:47769981-47770031	HCM	heart:	n/a
50	chr14:47812515-47812565	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:47749473..47749973-chr5:68319722..68320581,2	MCF-7	breast:
2	chr14:47811604..47813341-chr14:47823132..47825953,2	K562	blood:
3	chr14:47706399..47708616-chr14:47715847..47717651,2	MCF-7	breast:
4	chr14:47729955..47732269-chr14:47732563..47734465,2	MCF-7	breast:
5	chr14:47825822..47827429-chr14:47839476..47841080,2	K562	blood:
6	chr14:47699505..47700030-chr20:46283707..46284523,2	MCF-7	breast:
7	chr14:47729955..47732269-chr14:47732563..47734465,2	MCF-7	breast:
8	chr14:47525262..47526210-chr14:47747163..47747902,2	MCF-7	breast:
9	chr14:47825822..47827429-chr14:47839476..47841080,2	K562	blood:
10	chr14:47706399..47708616-chr14:47715847..47717651,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-12	chr14:47766804-47767153	l_979_chr14:47733075-47748994_testes
2	lnc-FANCM-12	chr14:47751190-47751359	l_979_chr14:47733075-47748994_testes
3	lnc-RPL10L-3	chr14:47812301-47812319	NONHSAT036687
4	lnc-RPL10L-3	chr14:47768550-47768742	NONHSAT036687
5	lnc-RPL10L-3	chr14:47775280-47775345	NONHSAT036687
6	lnc-RPL10L-3	chr14:47772661-47773179	l_980_chr14:47772660-47799743_76bGuttman_hES
7	lnc-RPL10L-2	chr14:47669778-47670307	NONHSAT036686
8	lnc-FANCM-12	chr14:47765169-47765272	l_979_chr14:47733075-47748994_testes
9	lnc-FANCM-12	chr14:47747104-47747220	l_979_chr14:47733075-47748994_testes
10	lnc-FANCM-12	chr14:47748394-47748994	l_979_chr14:47733075-47748994_testes
11	lnc-RPL10L-3	chr14:47798814-47799743	l_980_chr14:47772660-47799743_76bGuttman_hES
12	lnc-RPL10L-3	chr14:47770614-47770753	NONHSAT036687
13	lnc-RPL10L-3	chr14:47774434-47774526	NONHSAT036687
14	lnc-RPL10L-3	chr14:47774384-47774574	l_980_chr14:47772660-47799743_76bGuttman_hES
15	lnc-FANCM-12	chr14:47743855-47743971	l_979_chr14:47733075-47748994_testes
16	lnc-FANCM-12	chr14:47733076-47733185	l_979_chr14:47733075-47748994_testes
17	lnc-FANCM-12	chr14:47752540-47752618	l_979_chr14:47733075-47748994_testes

Variant related genes	Relation type
RPL13AP2	TF binding region
MDGA2	TF binding region
RPL13AP2	CpG island
MDGA2	CpG island
ENSG00000139915	chromatin interactions

Extended variants
information (count: 5634 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:5634 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182870520	chr14:47629661-47629662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114425413	chr14:47629717-47629718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148892600	chr14:47635823-47635824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542552502	chr14:47635826-47635827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533446362	chr14:47635842-47635843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76199375	chr14:47635847-47635848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572342808	chr14:47635857-47635858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534317332	chr14:47635904-47635905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545399051	chr14:47635916-47635917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377370516	chr14:47635932-47635933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183202790	chr14:47635977-47635978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111694549	chr14:47635992-47635993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs376069437	chr14:47635993-47635994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186442634	chr14:47636015-47636016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs41534646	chr14:47636016-47636017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561137162	chr14:47636052-47636053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189655683	chr14:47636073-47636074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546931159	chr14:47636102-47636103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535856315	chr14:47636211-47636212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150983837	chr14:47636262-47636263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142110728	chr14:47636286-47636287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116390517	chr14:47636340-47636341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543041803	chr14:47636373-47636374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs367729991	chr14:47636374-47636375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117663423	chr14:47636386-47636387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145857891	chr14:47636399-47636400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557138405	chr14:47636416-47636417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138685121	chr14:47636457-47636458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536455217	chr14:47636523-47636524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142709508	chr14:47636540-47636541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543121887	chr14:47636586-47636587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182255318	chr14:47636587-47636588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555741791	chr14:47636668-47636669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569211351	chr14:47636669-47636670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188156884	chr14:47636715-47636716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146921443	chr14:47636786-47636787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538193884	chr14:47636787-47636788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575275762	chr14:47636789-47636790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs192715987	chr14:47636807-47636808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373001317	chr14:47636832-47636833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77626777	chr14:47636853-47636854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547188978	chr14:47636870-47636871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183501964	chr14:47636896-47636897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560597236	chr14:47637073-47637074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76284261	chr14:47637128-47637129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552632951	chr14:47637156-47637157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571257879	chr14:47637161-47637162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs537045046	chr14:47637176-47637177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114708455	chr14:47637199-47637200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555396115	chr14:47640010-47640011	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Schizophrenia	20967226	CNVD
Gastric cancer	18160780	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19214233	CNVD

Chromatin state (count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:47629600-47629800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:47635800-47637200	Enhancers	Fetal Kidney	kidney
3	chr14:47640000-47641600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
4	chr14:47640800-47641400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr14:47640800-47641600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr14:47641000-47641400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
7	chr14:47641000-47641600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr14:47651600-47652000	Enhancers	HUVEC	blood vessel
9	chr14:47652000-47655200	Weak transcription	HUVEC	blood vessel
10	chr14:47655200-47656800	Enhancers	HUVEC	blood vessel
11	chr14:47655600-47655800	Enhancers	Brain Germinal Matrix	brain
12	chr14:47655600-47655800	Enhancers	Fetal Kidney	kidney
13	chr14:47655600-47656200	Enhancers	NH-A	brain
14	chr14:47655800-47656200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr14:47655800-47658400	Weak transcription	Brain Germinal Matrix	brain
16	chr14:47656200-47661000	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr14:47656200-47661000	Weak transcription	NH-A	brain
18	chr14:47656600-47657400	Weak transcription	Fetal Kidney	kidney
19	chr14:47657400-47658600	Enhancers	Fetal Kidney	kidney
20	chr14:47658400-47658600	Enhancers	Brain Germinal Matrix	brain
21	chr14:47658600-47659000	Weak transcription	Brain Germinal Matrix	brain
22	chr14:47659000-47659400	Enhancers	Brain Germinal Matrix	brain
23	chr14:47659400-47659600	Enhancers	Pancreas	Pancrea
24	chr14:47661000-47661400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr14:47661000-47661400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr14:47661000-47661400	Enhancers	NH-A	brain
27	chr14:47661000-47661600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr14:47661400-47662200	Weak transcription	NH-A	brain
29	chr14:47661400-47662400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr14:47662200-47663000	Enhancers	NH-A	brain
31	chr14:47662400-47664200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr14:47662400-47664200	Enhancers	HUVEC	blood vessel
33	chr14:47662600-47664200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr14:47663000-47664000	Weak transcription	NH-A	brain
35	chr14:47663000-47664200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr14:47664000-47664200	Enhancers	NH-A	brain
37	chr14:47664200-47664800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:47664800-47665000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr14:47669000-47671200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr14:47669600-47671600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr14:47671200-47672200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr14:47671400-47672000	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr14:47671600-47672000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr14:47671600-47672000	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr14:47671600-47672200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr14:47671600-47672200	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr14:47671800-47672200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr14:47671800-47672400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr14:47671800-47672400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr14:47672000-47680400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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