Variant report

Variant	nsv515522
Chromosome Location	chr14:65746566-65771110
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1011)
CpG islands
(count:489)
Chromatin interactive
region (count:16)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1011 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:65768632-65768832	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:65768705-65769200	K562	blood:	n/a	n/a
3	ARID3A	chr14:65753359-65753508	K562	blood:	n/a	n/a
4	ATF1	chr14:65768621-65769228	K562	blood:	n/a	n/a
5	ATF2	chr14:65768475-65770569	GM12878	blood:	n/a	n/a
6	ATF2	chr14:65748696-65749114	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr14:65757607-65758179	GM12878	blood:	n/a	n/a
8	ATF2	chr14:65757578-65758080	GM12878	blood:	n/a	n/a
9	ATF2	chr14:65753772-65755054	GM12878	blood:	n/a	n/a
10	ATF2	chr14:65753855-65754948	GM12878	blood:	n/a	n/a
11	ATF2	chr14:65768211-65770878	GM12878	blood:	n/a	n/a
12	ATF2	chr14:65763499-65764113	GM12878	blood:	n/a	n/a
13	ATF2	chr14:65750848-65751422	GM12878	blood:	n/a	n/a
14	BATF	chr14:65763536-65763871	GM12878	blood:	n/a	n/a
15	BATF	chr14:65757577-65757994	GM12878	blood:	n/a	chr14:65757845-65757854 chr14:65757805-65757815 chr14:65757804-65757815
16	BATF	chr14:65768868-65769977	GM12878	blood:	n/a	n/a
17	BATF	chr14:65769438-65769968	GM12878	blood:	n/a	n/a
18	BATF	chr14:65757583-65757934	GM12878	blood:	n/a	chr14:65757845-65757854 chr14:65757805-65757815 chr14:65757804-65757815
19	BATF	chr14:65753870-65754875	GM12878	blood:	n/a	n/a
20	BCL11A	chr14:65769518-65769873	GM12878	blood:	n/a	n/a
21	BCL11A	chr14:65763555-65763876	GM12878	blood:	n/a	n/a
22	BCL11A	chr14:65753842-65754915	GM12878	blood:	n/a	chr14:65754374-65754387
23	BCL11A	chr14:65769122-65769997	GM12878	blood:	n/a	n/a
24	BCL11A	chr14:65757655-65757935	GM12878	blood:	n/a	chr14:65757804-65757813
25	BCL11A	chr14:65757589-65757991	GM12878	blood:	n/a	chr14:65757804-65757813
26	BCL3	chr14:65769450-65769963	GM12878	blood:	n/a	n/a
27	BCL3	chr14:65757542-65758002	GM12878	blood:	n/a	chr14:65757804-65757813
28	BCL3	chr14:65763508-65763953	GM12878	blood:	n/a	n/a
29	BCL3	chr14:65753859-65754757	GM12878	blood:	n/a	chr14:65754374-65754387
30	BCL3	chr14:65755730-65756095	GM12878	blood:	n/a	n/a
31	BCL3	chr14:65769453-65770701	GM12878	blood:	n/a	chr14:65770652-65770665 chr14:65770644-65770657
32	BCL3	chr14:65757586-65758016	GM12878	blood:	n/a	chr14:65757804-65757813
33	BCLAF1	chr14:65768275-65771420	GM12878	blood:	n/a	chr14:65770652-65770665 chr14:65770644-65770657
34	BCLAF1	chr14:65750816-65751375	GM12878	blood:	n/a	n/a
35	BCLAF1	chr14:65753713-65755013	GM12878	blood:	n/a	chr14:65754374-65754387
36	BCLAF1	chr14:65753069-65753596	GM12878	blood:	n/a	n/a
37	BCLAF1	chr14:65753808-65754859	GM12878	blood:	n/a	chr14:65754374-65754387
38	BCLAF1	chr14:65768393-65770585	GM12878	blood:	n/a	n/a
39	BCLAF1	chr14:65757588-65758069	GM12878	blood:	n/a	chr14:65757804-65757813
40	BCLAF1	chr14:65748730-65749160	GM12878	blood:	n/a	n/a
41	BCLAF1	chr14:65757571-65758013	GM12878	blood:	n/a	chr14:65757804-65757813
42	BHLHE40	chr14:65768549-65769962	GM12878	blood:	n/a	n/a
43	BHLHE40	chr14:65753875-65754888	GM12878	blood:	n/a	n/a
44	BHLHE40	chr14:65768854-65769149	K562	blood:	n/a	n/a
45	BHLHE40	chr14:65757692-65757969	GM12878	blood:	n/a	n/a
46	BHLHE40	chr14:65757761-65757789	K562	blood:	n/a	n/a
47	CBX3	chr14:65757420-65758246	HCT-116	colon:	n/a	n/a
48	CBX3	chr14:65768831-65769172	K562	blood:	n/a	n/a
49	CCNT2	chr14:65768772-65769188	K562	blood:	n/a	n/a
50	CEBPB	chr14:65754459-65754798	GM12878	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:65746603-65746653	HCF	heart:	n/a
2	chr14:65746603-65746653	HCF	heart:	n/a
3	chr14:65746603-65746653	BJ	skin:	n/a
4	chr14:65747802-65747852	NB4	blood:	n/a
5	chr14:65746971-65747021	GM12891	blood:	n/a
6	chr14:65746824-65746874	ProgFib	skin:	n/a
7	chr14:65770225-65770275	GM06990	blood:	n/a
8	chr14:65746603-65746653	AG04449	skin:	fetal
9	chr14:65746603-65746653	BE2_C	brain:	n/a
10	chr14:65749247-65749297	HEK293	kidney:	embryo
11	chr14:65747552-65747602	HRPEpiC	eye:	n/a
12	chr14:65770225-65770275	HepG2	liver:	n/a
13	chr14:65747802-65747852	K562	blood:	n/a
14	chr14:65746971-65747021	HCT-116	colon:	n/a
15	chr14:65746824-65746874	SK-N-SH	brain:	n/a
16	chr14:65749247-65749297	LNCaP	prostate:	n/a
17	chr14:65770225-65770275	GM12891	blood:	n/a
18	chr14:65747552-65747602	GM12892	blood:	n/a
19	chr14:65746971-65747021	HCF	heart:	n/a
20	chr14:65770225-65770275	A549	lung:	n/a
21	chr14:65747480-65747530	HepG2	liver:	n/a
22	chr14:65747802-65747852	LNCaP	prostate:	n/a
23	chr14:65770225-65770275	HAEpiC	amniotic membrane:	n/a
24	chr14:65747552-65747602	T-47D	breast:	n/a
25	chr14:65746971-65747021	ECC-1	luminal epithelium:	n/a
26	chr14:65747480-65747530	HCF	heart:	n/a
27	chr14:65747552-65747602	NHDF-neo	bronchial:	n/a
28	chr14:65770225-65770275	AG10803	skin:	n/a
29	chr14:65747480-65747530	RPTEC	kidney:	n/a
30	chr14:65770225-65770275	Jurkat	blood:	n/a
31	chr14:65747802-65747852	NT2-D1	testis:	n/a
32	chr14:65749247-65749297	MCF10A-Er-Src	breast:	n/a
33	chr14:65746824-65746874	HPAEpiC	pulmonary alveolar:	n/a
34	chr14:65746971-65747021	SK-N-SH	brain:	n/a
35	chr14:65746603-65746653	HL-60	blood:	n/a
36	chr14:65747480-65747530	HEK293	kidney:	embryo
37	chr14:65747480-65747530	A549	lung:	n/a
38	chr14:65749247-65749297	Caco-2	colon:	n/a
39	chr14:65770225-65770275	AG04449	skin:	fetal
40	chr14:65749247-65749297	CMK	blood:	n/a
41	chr14:65770225-65770275	Hepatocyte	liver:	n/a
42	chr14:65770225-65770275	BE2_C	brain:	n/a
43	chr14:65746603-65746653	HRCEpiC	kidney:	n/a
44	chr14:65749247-65749297	NHBE	bronchial:	n/a
45	chr14:65746971-65747021	AG04449	skin:	fetal
46	chr14:65770225-65770275	Caco-2	colon:	n/a
47	chr14:65747480-65747530	HRE	kidney:	n/a
48	chr14:65747552-65747602	A549	lung:	n/a
49	chr14:65770225-65770275	HCPEpiC	choroid plexus:	n/a
50	chr14:65746824-65746874	A549	lung:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:65689030..65689582-chr14:65752932..65753476,2	MCF-7	breast:
2	chr14:65770511..65773505-chr14:65781617..65783190,2	MCF-7	breast:
3	chr14:65763015..65765090-chr14:65776527..65778731,2	MCF-7	breast:
4	chr14:65751346..65755635-chr14:65876089..65881787,7	MCF-7	breast:
5	chr14:65769045..65770910-chr14:65878599..65880667,2	MCF-7	breast:
6	chr14:65753408..65755484-chr14:65877640..65880155,2	MCF-7	breast:
7	chr14:65696039..65697546-chr14:65753255..65754853,2	MCF-7	breast:
8	chr14:65748171..65751140-chr14:65753934..65755557,2	MCF-7	breast:
9	chr14:65758925..65761020-chr14:65877259..65880093,2	MCF-7	breast:
10	chr14:65763315..65764947-chr14:65767837..65770740,2	MCF-7	breast:
11	chr14:65742677..65744892-chr14:65746374..65749095,2	MCF-7	breast:
12	chr14:65745595..65748280-chr14:65878483..65880878,2	MCF-7	breast:
13	chr14:65748171..65751140-chr14:65753934..65755557,2	MCF-7	breast:
14	chr14:65721766..65724259-chr14:65752829..65756528,3	MCF-7	breast:
15	chr14:65753112..65753905-chr14:65878434..65879178,4	MCF-7	breast:
16	chr14:65751559..65753214-chr14:65820526..65823180,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAX-7	chr14:65746949-65747035	NONHSAT037382
2	lnc-MAX-7	chr14:65747340-65747503	NONHSAT037382
3	lnc-MAX-8	chr14:65759383-65759816	NONHSAT037383
4	lnc-FUT8-4	chr14:65763797-65763905	NONHSAT037384

No data

Variant related genes	Relation type
ENSG00000258760	TF binding region
ENSG00000258760	CpG island
ENSG00000033170	chromatin interactions
ENSG00000258760	chromatin interactions
ENSG00000255002	chromatin interactions

Extended variants
information (count: 931 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:931 , 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	rs4902379	chr14:65746566-65746567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576318487	chr14:65746577-65746578	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs538580480	chr14:65746673-65746674	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs78329993	chr14:65746735-65746736	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368458127	chr14:65746772-65746773	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs117543192	chr14:65746808-65746809	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs188339764	chr14:65746811-65746812	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs571489035	chr14:65746824-65746825	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs542848210	chr14:65746830-65746831	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs559368503	chr14:65746846-65746847	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145367874	chr14:65746851-65746852	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs4902380	chr14:65746869-65746870	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs551801934	chr14:65746892-65746893	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs565242583	chr14:65746905-65746906	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs527685642	chr14:65746913-65746914	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs531298800	chr14:65746914-65746915	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs547905588	chr14:65746955-65746956	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs567798720	chr14:65746957-65746958	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs4902381	chr14:65746962-65746963	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs549975852	chr14:65747021-65747022	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs569769059	chr14:65747126-65747127	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs538888619	chr14:65747183-65747184	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs547899742	chr14:65747232-65747233	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs558582100	chr14:65747322-65747323	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs148314199	chr14:65747329-65747330	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs534356979	chr14:65747342-65747343	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs567425876	chr14:65747357-65747358	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs1256530	chr14:65747360-65747361	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs574222412	chr14:65747363-65747364	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs116745061	chr14:65747370-65747371	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs111951602	chr14:65747376-65747377	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs55911819	chr14:65747445-65747446	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs545636472	chr14:65747469-65747470	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs565483518	chr14:65747498-65747499	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs527674428	chr14:65747552-65747553	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs191886889	chr14:65747575-65747576	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs73278008	chr14:65747591-65747592	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs530184997	chr14:65747597-65747598	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs550309640	chr14:65747601-65747602	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs55766901	chr14:65747611-65747612	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs569788063	chr14:65747629-65747630	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs182592994	chr14:65747725-65747726	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs578209518	chr14:65747728-65747729	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs55759426	chr14:65747729-65747730	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs77960450	chr14:65747754-65747755	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs1256531	chr14:65747759-65747760	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
47	rs114799801	chr14:65747769-65747770	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567733051	chr14:65747811-65747812	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs55865853	chr14:65747837-65747838	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs556783834	chr14:65747859-65747860	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:786 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65697200-65746800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr14:65727400-65749600	Weak transcription	Gastric	stomach
3	chr14:65735800-65748600	Weak transcription	GM12878-XiMat	blood
4	chr14:65736200-65748400	Weak transcription	Primary B cells from peripheral blood	blood
5	chr14:65741600-65746800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr14:65742400-65747000	Enhancers	Brain Hippocampus Middle	brain
7	chr14:65743400-65746800	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr14:65744000-65748600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr14:65744000-65748600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr14:65744000-65748600	Weak transcription	Duodenum Mucosa	Duodenum
11	chr14:65744000-65748800	Weak transcription	HSMMtube	muscle
12	chr14:65744200-65748400	Weak transcription	NHDF-Ad	bronchial
13	chr14:65744200-65748600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr14:65744200-65748600	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr14:65744200-65748600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr14:65744200-65748600	Weak transcription	Brain Angular Gyrus	brain
17	chr14:65744200-65748600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr14:65744200-65748600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr14:65744200-65748600	Weak transcription	A549	lung
20	chr14:65744200-65748800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr14:65744200-65748800	Weak transcription	NHEK	skin
22	chr14:65744200-65749000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr14:65744600-65748400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr14:65744600-65748600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr14:65744600-65748600	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr14:65744600-65748800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr14:65744600-65748800	Weak transcription	HMEC	breast
28	chr14:65744800-65748600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr14:65744800-65748600	Weak transcription	Small Intestine	intestine
30	chr14:65745000-65746600	Weak transcription	Fetal Intestine Small	intestine
31	chr14:65745000-65748800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr14:65745400-65748600	Weak transcription	Brain Anterior Caudate	brain
33	chr14:65745400-65748600	Weak transcription	Brain Substantia Nigra	brain
34	chr14:65745600-65748400	Weak transcription	Stomach Mucosa	stomach
35	chr14:65745600-65748800	Weak transcription	HepG2	liver
36	chr14:65746600-65746800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr14:65746600-65748000	ZNF genes & repeats	Fetal Intestine Small	intestine
38	chr14:65746800-65747000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr14:65746800-65747600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr14:65746800-65747600	Enhancers	Pancreas	Pancrea
41	chr14:65746800-65748000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr14:65746800-65748400	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr14:65747000-65747800	Weak transcription	Brain Hippocampus Middle	brain
44	chr14:65747000-65749000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr14:65747400-65747600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr14:65747600-65748800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr14:65747600-65749400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr14:65747600-65758400	Weak transcription	Pancreas	Pancrea
49	chr14:65747800-65748600	Enhancers	Brain Hippocampus Middle	brain
50	chr14:65748000-65748600	Weak transcription	Fetal Intestine Small	intestine

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