Variant report

Variant	nsv563812
Chromosome Location	chr14:20404091-20694968
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:819)
CpG islands
(count:977)
Chromatin interactive
region (count:33)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:819 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20645562-20646086	K562	blood:	n/a	n/a
2	ARID3A	chr14:20584982-20585271	K562	blood:	n/a	n/a
3	ARID3A	chr14:20644582-20645133	K562	blood:	n/a	n/a
4	ARID3A	chr14:20512405-20512844	K562	blood:	n/a	n/a
5	ATF1	chr14:20561670-20561913	K562	blood:	n/a	n/a
6	ATF1	chr14:20584956-20585164	K562	blood:	n/a	n/a
7	ATF1	chr14:20608626-20608778	K562	blood:	n/a	n/a
8	ATF1	chr14:20645594-20645932	K562	blood:	n/a	n/a
9	ATF3	chr14:20645584-20645910	K562	blood:	n/a	n/a
10	ATF3	chr14:20512489-20512787	K562	blood:	n/a	n/a
11	ATF3	chr14:20584968-20585229	K562	blood:	n/a	n/a
12	ATF3	chr14:20638032-20638356	K562	blood:	n/a	n/a
13	BACH1	chr14:20687322-20687431	H1-hESC	embryonic stem cell:	n/a	chr14:20687387-20687401
14	BACH1	chr14:20584638-20585505	K562	blood:	n/a	n/a
15	BACH1	chr14:20687217-20687569	K562	blood:	n/a	chr14:20687387-20687401
16	BHLHE40	chr14:20653018-20653080	K562	blood:	n/a	n/a
17	BHLHE40	chr14:20645542-20646303	K562	blood:	n/a	n/a
18	CBX3	chr14:20645492-20645863	K562	blood:	n/a	n/a
19	CBX3	chr14:20450329-20450560	K562	blood:	n/a	n/a
20	CBX3	chr14:20632656-20632932	K562	blood:	n/a	n/a
21	CBX3	chr14:20512416-20512761	K562	blood:	n/a	n/a
22	CBX3	chr14:20632642-20632904	K562	blood:	n/a	n/a
23	CBX3	chr14:20586982-20587337	K562	blood:	n/a	n/a
24	CBX3	chr14:20586942-20587293	K562	blood:	n/a	n/a
25	CBX3	chr14:20645515-20645980	K562	blood:	n/a	n/a
26	CBX3	chr14:20584916-20585201	K562	blood:	n/a	n/a
27	CCNT2	chr14:20645714-20646195	K562	blood:	n/a	n/a
28	CCNT2	chr14:20516381-20516636	K562	blood:	n/a	n/a
29	CCNT2	chr14:20677752-20678071	K562	blood:	n/a	n/a
30	CEBPB	chr14:20668546-20668738	A549	lung:	n/a	n/a
31	CEBPB	chr14:20638926-20639276	K562	blood:	n/a	chr14:20639103-20639114
32	CEBPB	chr14:20631110-20631224	HepG2	liver:	n/a	chr14:20631171-20631182
33	CEBPB	chr14:20659063-20659394	HepG2	liver:	n/a	chr14:20659228-20659241 chr14:20659229-20659240 chr14:20659227-20659244
34	CEBPB	chr14:20434386-20434443	K562	blood:	n/a	n/a
35	CEBPB	chr14:20578626-20578939	A549	lung:	n/a	n/a
36	CEBPB	chr14:20470476-20470862	A549	lung:	n/a	chr14:20470615-20470626
37	CEBPB	chr14:20578686-20578922	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr14:20667315-20667616	A549	lung:	n/a	chr14:20667443-20667454
39	CEBPB	chr14:20439827-20439886	Hela-S3	cervix:	n/a	chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
40	CEBPB	chr14:20439826-20440010	IMR90	lung:	n/a	chr14:20439990-20440001 chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
41	CEBPB	chr14:20439816-20439966	A549	lung:	n/a	chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879
42	CEBPB	chr14:20683466-20683657	K562	blood:	n/a	chr14:20683523-20683534
43	CEBPB	chr14:20578635-20578967	HepG2	liver:	n/a	n/a
44	CEBPB	chr14:20643233-20643506	K562	blood:	n/a	chr14:20643311-20643324
45	CEBPB	chr14:20652454-20652480	HepG2	liver:	n/a	n/a
46	CEBPB	chr14:20683376-20683687	A549	lung:	n/a	chr14:20683523-20683534
47	CEBPB	chr14:20639049-20639270	IMR90	lung:	n/a	chr14:20639103-20639114
48	CEBPB	chr14:20667283-20667629	HepG2	liver:	n/a	chr14:20667443-20667454
49	CEBPB	chr14:20683384-20683692	Hela-S3	cervix:	n/a	chr14:20683523-20683534
50	CEBPB	chr14:20439841-20439948	K562	blood:	n/a	chr14:20439867-20439880 chr14:20439867-20439878 chr14:20439867-20439880 chr14:20439868-20439879

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20584239-20584289	HEK293	kidney:	embryo
2	chr14:20584239-20584289	HEK293	kidney:	embryo
3	chr14:20444164-20444214	PANC-1	pancreas:	n/a
4	chr14:20404281-20404331	Caco-2	colon:	n/a
5	chr14:20611779-20611829	NB4	blood:	n/a
6	chr14:20404281-20404331	GM12892	blood:	n/a
7	chr14:20528812-20528862	AoSMC	blood vessel:	n/a
8	chr14:20444164-20444214	GM12878	blood:	n/a
9	chr14:20612220-20612270	ovcar-3	ovarian:	n/a
10	chr14:20586367-20586417	NB4	blood:	n/a
11	chr14:20482899-20482949	HNPCEpiC	eye:	n/a
12	chr14:20664580-20664630	MCF-7	breast:	n/a
13	chr14:20585753-20585803	Hela-S3	cervix:	n/a
14	chr14:20585753-20585803	AG09309	skin:	n/a
15	chr14:20692622-20692672	A549	lung:	n/a
16	chr14:20586367-20586417	PrEC	prostate:	n/a
17	chr14:20612220-20612270	NB4	blood:	n/a
18	chr14:20404281-20404331	SAEC	small airway:	n/a
19	chr14:20584239-20584289	LNCaP	prostate:	n/a
20	chr14:20444164-20444214	MCF10A-Er-Src	breast:	n/a
21	chr14:20611779-20611829	SKMC	muscle:	n/a
22	chr14:20611696-20611746	GM06990	blood:	n/a
23	chr14:20585753-20585803	PrEC	prostate:	n/a
24	chr14:20528812-20528862	NHDF-neo	bronchial:	n/a
25	chr14:20612220-20612270	AG04450	lung:	fetal
26	chr14:20586367-20586417	Jurkat	blood:	n/a
27	chr14:20585753-20585803	BJ	skin:	n/a
28	chr14:20692622-20692672	GM12878	blood:	n/a
29	chr14:20502658-20502708	K562	blood:	n/a
30	chr14:20611779-20611829	HCM	heart:	n/a
31	chr14:20664021-20664071	CMK	blood:	n/a
32	chr14:20611779-20611829	MCF-7	breast:	n/a
33	chr14:20586367-20586417	HL-60	blood:	n/a
34	chr14:20482899-20482949	HCM	heart:	n/a
35	chr14:20404281-20404331	PANC-1	pancreas:	n/a
36	chr14:20612220-20612270	GM12892	blood:	n/a
37	chr14:20664021-20664071	PrEC	prostate:	n/a
38	chr14:20611696-20611746	SK-N-SH_RA	brain:	n/a
39	chr14:20612220-20612270	PFSK-1	brain:	n/a
40	chr14:20611779-20611829	HEK293	kidney:	embryo
41	chr14:20664580-20664630	SK-N-SH_RA	brain:	n/a
42	chr14:20691777-20691827	ovcar-3	ovarian:	n/a
43	chr14:20692622-20692672	HAEpiC	amniotic membrane:	n/a
44	chr14:20611779-20611829	H1-hESC	embryonic stem cell:	embryo
45	chr14:20444164-20444214	NB4	blood:	n/a
46	chr14:20528812-20528862	HCPEpiC	choroid plexus:	n/a
47	chr14:20585753-20585803	Hepatocyte	liver:	n/a
48	chr14:20612220-20612270	GM19239	blood:	n/a
49	chr14:20611696-20611746	SAEC	small airway:	n/a
50	chr14:20482899-20482949	HUVEC	blood vessel:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:20583619..20586533-chr14:20649310..20650931,2	K562	blood:
2	chr14:20479309..20481272-chr14:20484820..20486760,2	K562	blood:
3	chr14:20530040..20532845-chr14:20547946..20550280,2	K562	blood:
4	chr14:20674085..20677001-chr14:20687478..20690164,2	MCF-7	breast:
5	chr14:20518924..20521802-chr14:20525808..20527615,2	K562	blood:
6	chr14:20645666..20648683-chr14:20649468..20653312,5	K562	blood:
7	chr14:20623957..20624479-chr3:64655642..64656615,2	MCF-7	breast:
8	chr14:20578711..20580377-chr14:20580738..20583327,2	K562	blood:
9	chr14:20691139..20693631-chr14:20695657..20698105,2	K562	blood:
10	chr14:20645875..20648132-chr14:20651152..20653312,3	K562	blood:
11	chr14:20653449..20656373-chr14:20661305..20663533,2	MCF-7	breast:
12	chr14:20518924..20521802-chr14:20525808..20527615,2	K562	blood:
13	chr14:20615947..20618319-chr14:20622650..20625486,3	K562	blood:
14	chr14:20453392..20455779-chr14:20560575..20562246,2	K562	blood:
15	chr14:20582658..20584245-chr14:20584576..20586426,2	K562	blood:
16	chr14:20421291..20423829-chr14:20424473..20427279,2	MCF-7	breast:
17	chr14:20611730..20613442-chr14:20616450..20619196,2	K562	blood:
18	chr14:20615947..20618319-chr14:20622650..20625017,2	K562	blood:
19	chr14:20657790..20659854-chr14:20660139..20662743,2	K562	blood:
20	chr14:20674085..20677001-chr14:20687478..20690164,2	MCF-7	breast:
21	chr14:20611730..20613442-chr14:20616450..20619196,2	K562	blood:
22	chr14:20642540..20645135-chr14:20796578..20798741,2	K562	blood:
23	chr14:20653650..20655621-chr14:20656798..20658985,2	K562	blood:
24	chr14:20530040..20532845-chr14:20547946..20550280,2	K562	blood:
25	chr14:20649377..20653239-chr14:20653513..20656414,3	K562	blood:
26	chr14:20578711..20580377-chr14:20580738..20583327,2	K562	blood:
27	chr14:20623640..20625607-chr14:20644962..20647182,2	K562	blood:
28	chr14:20653650..20655621-chr14:20656798..20658985,2	K562	blood:
29	chr14:20479309..20481272-chr14:20484820..20486760,2	K562	blood:
30	chr14:20657790..20659854-chr14:20660139..20662743,2	K562	blood:
31	chr14:20653449..20656373-chr14:20661305..20663533,2	MCF-7	breast:
32	chr14:20623640..20625607-chr14:20644962..20647182,2	K562	blood:
33	chr14:20649377..20653239-chr14:20653513..20656414,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4N5-1	chr14:20617391-20617904	NONHSAT035552

No data

Variant related genes	Relation type
RNA5SP380	TF binding region
OR4K13	TF binding region
OR4N5	TF binding region
OR4K17	TF binding region
OR4K16P	TF binding region
OR11H5P	TF binding region
OR4K14	TF binding region
RNA5SP381	TF binding region
ENSG00000266336	TF binding region
OR11G1P	TF binding region
ENSG00000265199	TF binding region
OR4T1P	TF binding region
OR4K15	TF binding region
OR11G2	TF binding region
OR4L1	TF binding region
OR4Q2	TF binding region
OR11H6	TF binding region
OR4U1P	TF binding region
ENSG00000259095	TF binding region
OR11H7	TF binding region
PSMB7P1	TF binding region
RNA5SP380	CpG island
OR4K13	CpG island
OR4N5	CpG island
OR4K17	CpG island
OR4K16P	CpG island
OR11H5P	CpG island
OR4K14	CpG island
RNA5SP381	CpG island
ENSG00000266336	CpG island
OR11G1P	CpG island
ENSG00000265199	CpG island
OR4T1P	CpG island
OR4K15	CpG island
OR11G2	CpG island
OR4L1	CpG island
OR4Q2	CpG island
OR11H6	CpG island
OR4U1P	CpG island
ENSG00000259095	CpG island
OR11H7	CpG island
PSMB7P1	CpG island
ENSG00000258822	chromatin interactions
ENSG00000100814	chromatin interactions
ENSG00000176230	chromatin interactions
ENSG00000258641	chromatin interactions
ENSG00000184394	chromatin interactions
ENSG00000259074	chromatin interactions
ENSG00000258806	chromatin interactions
ENSG00000258468	chromatin interactions

Extended variants
information (count: 4073 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:4073 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190776502	chr14:20404401-20404402	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs149331048	chr14:20404411-20404412	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs373364499	chr14:20404416-20404417	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs200761942	chr14:20404427-20404428	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs149331677	chr14:20404428-20404429	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs201955766	chr14:20404432-20404433	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs373472554	chr14:20404437-20404438	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs376119424	chr14:20404459-20404460	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs141997601	chr14:20404494-20404495	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs199618384	chr14:20404495-20404496	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs145757525	chr14:20404501-20404502	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs370432667	chr14:20404533-20404534	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs137893475	chr14:20404571-20404572	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs142429554	chr14:20404578-20404579	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs145971130	chr14:20404582-20404583	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs139885856	chr14:20404601-20404602	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs34608158	chr14:20404614-20404615	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs147347995	chr14:20404621-20404622	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs543752160	chr14:20404636-20404637	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs199701811	chr14:20404654-20404655	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs377096800	chr14:20404656-20404657	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs141721875	chr14:20404671-20404672	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs2792147	chr14:20404690-20404691	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs144917067	chr14:20404721-20404722	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs370557685	chr14:20404725-20404726	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs34394400	chr14:20404735-20404736	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs2792146	chr14:20404736-20404737	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs138753104	chr14:20404758-20404759	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs2792145	chr14:20404767-20404768	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs544780291	chr14:20404778-20404779	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs373594766	chr14:20404784-20404785	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs540194760	chr14:20406269-20406270	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs545054622	chr14:20406288-20406289	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs564988049	chr14:20406328-20406329	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs532204663	chr14:20406344-20406345	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs142484813	chr14:20406355-20406356	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs563938981	chr14:20406373-20406374	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs531000138	chr14:20406406-20406407	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs549695518	chr14:20406412-20406413	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs567574991	chr14:20406416-20406417	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs188731539	chr14:20406437-20406438	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs142155108	chr14:20406481-20406482	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs542216281	chr14:20406501-20406502	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs74033425	chr14:20406541-20406542	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs181154138	chr14:20406571-20406572	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs557159826	chr14:20406572-20406573	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs369460502	chr14:20406580-20406581	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs148191374	chr14:20406587-20406588	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs575438403	chr14:20406602-20406603	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs536011478	chr14:20406608-20406609	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20404400-20404800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
2	chr14:20406200-20406800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
3	chr14:20410000-20410400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:20411600-20412200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:20412800-20413000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr14:20415600-20416000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr14:20415600-20416000	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr14:20415600-20416000	Active TSS	HepG2	liver
9	chr14:20415600-20416200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr14:20415600-20416200	Active TSS	A549	lung
11	chr14:20416200-20417200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr14:20416400-20417000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr14:20417200-20417800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr14:20420200-20420600	Enhancers	Adipose Nuclei	Adipose
15	chr14:20437800-20438200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr14:20437800-20438200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr14:20438000-20438800	Enhancers	Dnd41	blood
18	chr14:20438200-20438600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr14:20438200-20441400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr14:20438600-20438800	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr14:20438600-20438800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr14:20438800-20441400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr14:20438800-20441400	Weak transcription	Dnd41	blood
24	chr14:20440000-20440800	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr14:20440200-20440400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr14:20440200-20440400	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr14:20440200-20444000	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr14:20440400-20441400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr14:20440600-20441600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr14:20440800-20441200	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr14:20441200-20444200	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr14:20441400-20441600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr14:20441400-20442200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr14:20441400-20443800	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr14:20441400-20444200	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr14:20441400-20444400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr14:20441400-20444400	Enhancers	Dnd41	blood
38	chr14:20441400-20444600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr14:20441600-20443800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr14:20441800-20443000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr14:20442200-20443800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr14:20443000-20443200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr14:20443200-20443800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr14:20443800-20444000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr14:20444600-20445800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr14:20445800-20446000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr14:20448800-20449000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:20461200-20461600	Enhancers	Dnd41	blood
49	chr14:20461600-20462400	ZNF genes & repeats	Dnd41	blood
50	chr14:20470000-20471200	Enhancers	Primary monocytes fromperipheralblood	blood

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