Variant report

Variant	nsv1035937
Chromosome Location	chr14:31447842-31579660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2662)
CpG islands
(count:2015)
Chromatin interactive
region (count:138)
LncRNA
region (count:1)
Mature miRNA
region (count: 2)
miRNA target
sites (count:1)

(count:2662 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:31522527-31522614	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:31559886-31561386	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:31499902-31500063	K562	blood:	n/a	n/a
4	ARID3A	chr14:31524101-31524173	K562	blood:	n/a	n/a
5	ARID3A	chr14:31549348-31549622	K562	blood:	n/a	n/a
6	ARID3A	chr14:31494572-31494997	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:31500666-31501248	K562	blood:	n/a	n/a
8	ARID3A	chr14:31449281-31449686	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:31449263-31449680	K562	blood:	n/a	n/a
10	ARID3A	chr14:31495906-31496401	K562	blood:	n/a	n/a
11	ARID3A	chr14:31573701-31573703	K562	blood:	n/a	n/a
12	ARID3A	chr14:31457859-31458088	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:31507099-31507550	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:31493234-31493623	HepG2	liver:	n/a	n/a
15	ARID3A	chr14:31507773-31508345	HepG2	liver:	n/a	n/a
16	ARID3A	chr14:31507685-31508382	K562	blood:	n/a	n/a
17	ARID3A	chr14:31495410-31496546	HepG2	liver:	n/a	n/a
18	ARID3A	chr14:31551219-31551628	HepG2	liver:	n/a	n/a
19	ARID3A	chr14:31502435-31503536	HepG2	liver:	n/a	n/a
20	ARID3A	chr14:31457293-31457333	HepG2	liver:	n/a	n/a
21	ARID3A	chr14:31528245-31529150	K562	blood:	n/a	n/a
22	ARID3A	chr14:31500874-31501088	HepG2	liver:	n/a	n/a
23	ARID3A	chr14:31501593-31501611	K562	blood:	n/a	n/a
24	ARID3A	chr14:31511604-31511770	K562	blood:	n/a	n/a
25	ARID3A	chr14:31561638-31561823	HepG2	liver:	n/a	n/a
26	ARID3A	chr14:31551258-31551518	K562	blood:	n/a	n/a
27	ATF1	chr14:31495558-31496394	K562	blood:	n/a	chr14:31496048-31496062
28	ATF1	chr14:31507743-31508407	K562	blood:	n/a	n/a
29	ATF1	chr14:31500491-31501137	K562	blood:	n/a	n/a
30	ATF1	chr14:31517729-31518127	K562	blood:	n/a	n/a
31	ATF1	chr14:31560047-31560326	K562	blood:	n/a	n/a
32	ATF1	chr14:31528770-31529181	K562	blood:	n/a	n/a
33	ATF2	chr14:31500675-31501137	GM12878	blood:	n/a	n/a
34	ATF2	chr14:31463771-31464461	GM12878	blood:	n/a	n/a
35	ATF2	chr14:31463711-31464507	GM12878	blood:	n/a	n/a
36	ATF2	chr14:31495923-31496436	GM12878	blood:	n/a	chr14:31496048-31496062
37	ATF2	chr14:31502127-31502530	GM12878	blood:	n/a	n/a
38	ATF2	chr14:31501963-31502660	GM12878	blood:	n/a	n/a
39	ATF2	chr14:31495869-31496347	H1-hESC	embryonic stem cell:	n/a	chr14:31496048-31496062
40	ATF3	chr14:31517760-31518091	K562	blood:	n/a	n/a
41	ATF3	chr14:31500739-31501068	K562	blood:	n/a	n/a
42	ATF3	chr14:31507734-31508127	K562	blood:	n/a	n/a
43	ATF3	chr14:31517648-31518167	HCT-116	colon:	n/a	n/a
44	ATF3	chr14:31528688-31529112	K562	blood:	n/a	n/a
45	ATF3	chr14:31495599-31495819	K562	blood:	n/a	n/a
46	ATF3	chr14:31494662-31495480	HepG2	liver:	n/a	n/a
47	BACH1	chr14:31528791-31529048	K562	blood:	n/a	n/a
48	BACH1	chr14:31551367-31551442	K562	blood:	n/a	n/a
49	BACH1	chr14:31449306-31449453	K562	blood:	n/a	n/a
50	BACH1	chr14:31551362-31551542	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31458174-31458224	ECC-1	luminal epithelium:	n/a
2	chr14:31495002-31495052	IMR90	lung:	fetal
3	chr14:31458174-31458224	ECC-1	luminal epithelium:	n/a
4	chr14:31495002-31495052	IMR90	lung:	fetal
5	chr14:31494210-31494260	GM12878	blood:	n/a
6	chr14:31494594-31494644	HCF	heart:	n/a
7	chr14:31458174-31458224	HCM	heart:	n/a
8	chr14:31495561-31495611	SAEC	small airway:	n/a
9	chr14:31495704-31495754	HIPEpiC	eye:	n/a
10	chr14:31494616-31494666	AG09309	skin:	n/a
11	chr14:31549691-31549741	HepG2	liver:	n/a
12	chr14:31495561-31495611	SKMC	muscle:	n/a
13	chr14:31495899-31495949	IMR90	lung:	fetal
14	chr14:31560529-31560579	K562	blood:	n/a
15	chr14:31495427-31495477	PrEC	prostate:	n/a
16	chr14:31484468-31484518	NHDF-neo	bronchial:	n/a
17	chr14:31562255-31562305	HAEpiC	amniotic membrane:	n/a
18	chr14:31494210-31494260	CMK	blood:	n/a
19	chr14:31495531-31495581	LNCaP	prostate:	n/a
20	chr14:31494210-31494260	ovcar-3	ovarian:	n/a
21	chr14:31495002-31495052	NH-A	brain:	n/a
22	chr14:31495946-31495996	Caco-2	colon:	n/a
23	chr14:31494237-31494287	MCF-7	breast:	n/a
24	chr14:31494527-31494577	AG10803	skin:	n/a
25	chr14:31529383-31529433	HUVEC	blood vessel:	n/a
26	chr14:31464361-31464411	HAEpiC	amniotic membrane:	n/a
27	chr14:31495002-31495052	SK-N-SH	brain:	n/a
28	chr14:31495531-31495581	HCM	heart:	n/a
29	chr14:31496854-31496904	SK-N-SH	brain:	n/a
30	chr14:31562255-31562305	SKMC	muscle:	n/a
31	chr14:31485052-31485102	HRE	kidney:	n/a
32	chr14:31495946-31495996	IMR90	lung:	fetal
33	chr14:31549691-31549741	HAEpiC	amniotic membrane:	n/a
34	chr14:31496258-31496308	Jurkat	blood:	n/a
35	chr14:31529383-31529433	SAEC	small airway:	n/a
36	chr14:31494237-31494287	U87	brain:	n/a
37	chr14:31495791-31495841	NT2-D1	testis:	n/a
38	chr14:31496028-31496078	Jurkat	blood:	n/a
39	chr14:31494616-31494666	PFSK-1	brain:	n/a
40	chr14:31496258-31496308	GM06990	blood:	n/a
41	chr14:31562255-31562305	NHDF-neo	bronchial:	n/a
42	chr14:31495704-31495754	HCF	heart:	n/a
43	chr14:31495704-31495754	GM12891	blood:	n/a
44	chr14:31495681-31495731	HIPEpiC	eye:	n/a
45	chr14:31554343-31554393	HRCEpiC	kidney:	n/a
46	chr14:31500033-31500083	HCF	heart:	n/a
47	chr14:31496028-31496078	K562	blood:	n/a
48	chr14:31495704-31495754	K562	blood:	n/a
49	chr14:31496854-31496904	HCT-116	colon:	n/a
50	chr14:31495561-31495611	PANC-1	pancreas:	n/a

(count:138 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:31461833..31464355-chr14:31467976..31470646,2	MCF-7	breast:
2	chr14:31492694..31496105-chr14:31530771..31532724,3	K562	blood:
3	chr14:31458647..31460710-chr14:31463564..31465601,2	K562	blood:
4	chr14:31450203..31451782-chr14:31545197..31546790,2	K562	blood:
5	chr14:31548388..31550747-chr14:31553010..31555958,3	K562	blood:
6	chr12:125398908..125399620-chr14:31495071..31496049,2	Hela-S3	cervix:
7	chr14:31444951..31447153-chr14:31557312..31559493,2	MCF-7	breast:
8	chr14:31500766..31503051-chr14:31511227..31514419,3	MCF-7	breast:
9	chr14:31465612..31467146-chr14:31491620..31494583,2	K562	blood:
10	chr14:31474762..31478016-chr14:31494036..31497480,5	MCF-7	breast:
11	chr14:31499033..31500685-chr14:31501316..31504225,4	MCF-7	breast:
12	chr14:31454546..31456657-chr14:31675532..31677690,2	K562	blood:
13	chr14:31457071..31460059-chr14:31491796..31493863,2	MCF-7	breast:
14	chr14:31476012..31477905-chr14:31492310..31494262,2	MCF-7	breast:
15	chr14:31493895..31497563-chr14:31505325..31509450,6	K562	blood:
16	chr14:31495964..31498060-chr14:31518106..31520616,2	MCF-7	breast:
17	chr14:31545887..31548153-chr14:31549801..31551382,2	K562	blood:
18	chr14:31494285..31496570-chr14:31503012..31504525,2	K562	blood:
19	chr14:31506901..31509349-chr14:31549757..31552004,2	K562	blood:
20	chr10:72393706..72394219-chr14:31466138..31467112,2	HCT-116	colon:
21	chr14:31449675..31451460-chr14:31453567..31455215,2	K562	blood:
22	chr14:31506672..31509497-chr14:31888212..31890928,2	K562	blood:
23	chr14:31500047..31501717-chr14:31510659..31513368,2	K562	blood:
24	chr14:31520948..31523210-chr14:31526631..31529023,2	K562	blood:
25	chr14:31566343..31568008-chr14:31570057..31571588,2	K562	blood:
26	chr14:31465641..31468716-chr14:31477772..31480895,4	K562	blood:
27	chr14:31529023..31531109-chr14:31534744..31536932,2	K562	blood:
28	chr14:31077974..31078580-chr14:31550888..31551785,2	K562	blood:
29	chr14:31504745..31506428-chr14:31545787..31548074,2	K562	blood:
30	chr14:31449482..31451358-chr14:31494020..31496170,2	MCF-7	breast:
31	chr14:31454381..31456866-chr14:31494760..31497508,2	MCF-7	breast:
32	chr14:31494908..31497563-chr14:31507813..31509450,3	K562	blood:
33	chr14:31462254..31468952-chr14:31492285..31496312,7	MCF-7	breast:
34	chr14:31471843..31474502-chr14:31478571..31481121,2	K562	blood:
35	chr14:31469435..31474245-chr14:31493637..31497268,6	MCF-7	breast:
36	chr14:31458519..31461343-chr14:31465487..31467458,2	K562	blood:
37	chr14:31373196..31374094-chr14:31550924..31551881,2	MCF-7	breast:
38	chr14:31343274..31345144-chr14:31492852..31495272,2	K562	blood:
39	chr14:31491737..31493873-chr14:31520369..31522639,2	K562	blood:
40	chr14:31449089..31449999-chr14:31550935..31551485,3	K562	blood:
41	chr14:31461174..31464156-chr14:31494227..31496386,3	MCF-7	breast:
42	chr14:31495967..31497568-chr14:31552055..31553964,3	K562	blood:
43	chr14:31492305..31494786-chr14:31552941..31555332,2	K562	blood:
44	chr14:31495967..31497568-chr14:31552055..31553964,2	K562	blood:
45	chr14:31495841..31497461-chr21:46493757..46496010,2	K562	blood:
46	chr14:31494105..31496790-chr14:31544703..31548574,4	MCF-7	breast:
47	chr14:31499033..31500685-chr14:31501316..31504225,4	MCF-7	breast:
48	chr14:31498429..31503635-chr14:31504922..31508361,9	K562	blood:
49	chr14:31406134..31408433-chr14:31516211..31518078,2	K562	blood:
50	chr14:31570609..31573539-chr14:31583523..31586049,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP4S1-3	chr14:31468245-31469103	ncRnaDb_ncrna_FR171143_1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-624-3p	chr14:31483875-31483895	MIMAT0004807
hsa-miR-624-5p	chr14:31483912-31483933	MIMAT0003293

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	AP4S1	hsa-miR-15b-5p	chr14:31554320-31554342

Variant related genes	Relation type
MIR624	TF binding region
STRN3	TF binding region
AP4S1	TF binding region
HECTD1	TF binding region
ENSG00000258968	TF binding region
MIR624	CpG island
STRN3	CpG island
AP4S1	CpG island
HECTD1	CpG island
ENSG00000258968	CpG island
ENSG00000141499	chromatin interactions
ENSG00000258968	chromatin interactions
ENSG00000197381	chromatin interactions
ENSG00000129493	chromatin interactions
ENSG00000150991	chromatin interactions
ENSG00000258640	chromatin interactions
ENSG00000152700	chromatin interactions
ENSG00000207952	chromatin interactions
ENSG00000141510	chromatin interactions
ENSG00000250365	chromatin interactions
ENSG00000235374	chromatin interactions
ENSG00000059758	chromatin interactions
ENSG00000129480	chromatin interactions
ENSG00000092148	chromatin interactions
ENSG00000203546	chromatin interactions
ENSG00000100473	chromatin interactions
ENSG00000196792	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000100478	chromatin interactions
ENSG00000189143	chromatin interactions
FXN	Mature miRNA region
PTPRG	Mature miRNA region

Extended variants
information (count: 5126 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:5126 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs67898509	chr14:31447863-31447864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529584907	chr14:31447875-31447876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148306227	chr14:31447966-31447967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574903025	chr14:31447981-31447982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557362215	chr14:31447990-31447991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7158106	chr14:31448055-31448056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7158412	chr14:31448065-31448066	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs564660629	chr14:31448074-31448075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150862196	chr14:31448230-31448231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10585744	chr14:31448262-31448263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532707883	chr14:31448264-31448265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs578187555	chr14:31448296-31448297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540825149	chr14:31448325-31448326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368665191	chr14:31448331-31448332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562208537	chr14:31448335-31448336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572570466	chr14:31448427-31448428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115192726	chr14:31448478-31448479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543840049	chr14:31448597-31448598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139989598	chr14:31448604-31448605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540447596	chr14:31448605-31448606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555268332	chr14:31448632-31448633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143944747	chr14:31448638-31448639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79567890	chr14:31448659-31448660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566230964	chr14:31448674-31448675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147305397	chr14:31448705-31448706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549178389	chr14:31448806-31448807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547226105	chr14:31448828-31448829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567435822	chr14:31448851-31448852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538171671	chr14:31448874-31448875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192663257	chr14:31448891-31448892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552000111	chr14:31448917-31448918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543702932	chr14:31448923-31448924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184928747	chr14:31448935-31448936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558237933	chr14:31448956-31448957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs71417938	chr14:31448990-31448991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573389028	chr14:31449007-31449008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540453562	chr14:31449025-31449026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555955969	chr14:31449029-31449030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574247956	chr14:31449056-31449057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573919171	chr14:31449063-31449064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140989364	chr14:31449104-31449105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562849965	chr14:31449147-31449148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532718356	chr14:31449158-31449159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7143388	chr14:31449162-31449163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs61976799	chr14:31449190-31449191	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs187137107	chr14:31449192-31449193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527418660	chr14:31449193-31449194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs5807609	chr14:31449205-31449206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548885987	chr14:31449226-31449227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201573660	chr14:31449239-31449240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
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
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
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
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3527 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31420200-31464400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr14:31436000-31457400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr14:31436200-31449200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr14:31436200-31457200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr14:31436400-31455200	Weak transcription	Rectal Smooth Muscle	rectum
6	chr14:31436400-31457200	Weak transcription	HSMM	muscle
7	chr14:31436400-31457800	Weak transcription	NHEK	skin
8	chr14:31437000-31451600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr14:31440000-31457200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr14:31440400-31455200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr14:31440400-31462000	Weak transcription	Right Atrium	heart
12	chr14:31441000-31464800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr14:31441200-31457000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr14:31441200-31457400	Weak transcription	NH-A	brain
15	chr14:31441600-31449800	Weak transcription	K562	blood
16	chr14:31441600-31464200	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr14:31442400-31449800	Weak transcription	Fetal Intestine Small	intestine
18	chr14:31442400-31461400	Weak transcription	Left Ventricle	heart
19	chr14:31442400-31494400	Weak transcription	Gastric	stomach
20	chr14:31442600-31457800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr14:31443000-31459800	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr14:31443200-31450600	Weak transcription	Primary T cells from cord blood	blood
23	chr14:31443200-31460200	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr14:31443400-31451400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr14:31443400-31460000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr14:31443400-31493800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr14:31443600-31462200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr14:31444000-31450400	Weak transcription	GM12878-XiMat	blood
29	chr14:31444000-31472800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr14:31444200-31449200	Weak transcription	NHDF-Ad	bronchial
31	chr14:31444200-31457000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr14:31444200-31459800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr14:31444200-31464000	Weak transcription	Brain Anterior Caudate	brain
34	chr14:31444400-31449200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr14:31444400-31460600	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr14:31444600-31449200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr14:31444800-31455800	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr14:31445000-31449200	Weak transcription	Primary B cells from peripheral blood	blood
39	chr14:31445000-31458200	Weak transcription	Psoas Muscle	Psoas
40	chr14:31445000-31460600	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr14:31445800-31449200	Weak transcription	A549	lung
42	chr14:31445800-31455000	Weak transcription	Colon Smooth Muscle	Colon
43	chr14:31445800-31459600	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr14:31446400-31449200	Weak transcription	Liver	Liver
45	chr14:31446400-31457000	Weak transcription	Fetal Stomach	stomach
46	chr14:31446600-31459800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:31446600-31461600	Weak transcription	Fetal Muscle Leg	muscle
48	chr14:31447400-31449200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr14:31447400-31450000	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr14:31447600-31449600	Weak transcription	HepG2	liver

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