Variant report

Variant	nsv542025
Chromosome Location	chr14:34834260-34992049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2590)
CpG islands
(count:978)
Chromatin interactive
region (count:169)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2590 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:34905586-34905976	HepG2	liver:	n/a	chr14:34905782-34905798
2	ARID3A	chr14:34929903-34932054	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:34906447-34906805	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:34919326-34920261	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:34837371-34838296	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:34969548-34969921	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:34938206-34938421	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:34975027-34975388	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:34934231-34934837	K562	blood:	n/a	n/a
10	ARID3A	chr14:34976759-34976917	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:34966063-34967571	HepG2	liver:	n/a	n/a
12	ARID3A	chr14:34967988-34968420	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:34966093-34966592	K562	blood:	n/a	n/a
14	ATF1	chr14:34965963-34966707	K562	blood:	n/a	n/a
15	ATF1	chr14:34934357-34934890	K562	blood:	n/a	n/a
16	ATF3	chr14:34966038-34966443	K562	blood:	n/a	n/a
17	ATF3	chr14:34894748-34894948	K562	blood:	n/a	n/a
18	ATF3	chr14:34934313-34934807	K562	blood:	n/a	n/a
19	ATF3	chr14:34966016-34966535	HepG2	liver:	n/a	n/a
20	BACH1	chr14:34966388-34966391	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr14:34931844-34931959	K562	blood:	n/a	n/a
22	BACH1	chr14:34858099-34858362	H1-hESC	embryonic stem cell:	n/a	chr14:34858182-34858196
23	BACH1	chr14:34934068-34935041	K562	blood:	n/a	n/a
24	BACH1	chr14:34934415-34934834	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr14:34930764-34932380	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL3	chr14:34965672-34966667	A549	lung:	n/a	chr14:34966277-34966286 chr14:34966278-34966287
27	BCL3	chr14:34837383-34838250	A549	lung:	n/a	n/a
28	BCL3	chr14:34965668-34967101	A549	lung:	n/a	chr14:34966277-34966286 chr14:34966278-34966287
29	BCLAF1	chr14:34931197-34931534	GM12878	blood:	n/a	chr14:34931198-34931211
30	BCLAF1	chr14:34930480-34931128	GM12878	blood:	n/a	n/a
31	BHLHE40	chr14:34960561-34960835	HepG2	liver:	n/a	n/a
32	BHLHE40	chr14:34965905-34966483	K562	blood:	n/a	n/a
33	BHLHE40	chr14:34966072-34966515	HepG2	liver:	n/a	n/a
34	BHLHE40	chr14:34894689-34894952	K562	blood:	n/a	n/a
35	BHLHE40	chr14:34934120-34934252	K562	blood:	n/a	n/a
36	BHLHE40	chr14:34968137-34968262	GM12878	blood:	n/a	n/a
37	BHLHE40	chr14:34894697-34895041	HepG2	liver:	n/a	n/a
38	BHLHE40	chr14:34931902-34932178	K562	blood:	n/a	n/a
39	BHLHE40	chr14:34931257-34931717	GM12878	blood:	n/a	n/a
40	BHLHE40	chr14:34934480-34934801	K562	blood:	n/a	n/a
41	BHLHE40	chr14:34931266-34931663	K562	blood:	n/a	n/a
42	BHLHE40	chr14:34969615-34969812	HepG2	liver:	n/a	n/a
43	BHLHE40	chr14:34930806-34932350	HepG2	liver:	n/a	n/a
44	BHLHE40	chr14:34841818-34841921	A549	lung:	n/a	n/a
45	BHLHE40	chr14:34837569-34838034	HepG2	liver:	n/a	n/a
46	BHLHE40	chr14:34966762-34967159	HepG2	liver:	n/a	n/a
47	BRCA1	chr14:34931545-34931879	GM12878	blood:	n/a	n/a
48	BRCA1	chr14:34965923-34966768	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr14:34837316-34838520	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr14:34930066-34931920	Hela-S3	cervix:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:34931577-34931627	Hepatocyte	liver:	n/a
2	chr14:34906118-34906168	AoSMC	blood vessel:	n/a
3	chr14:34931577-34931627	Hepatocyte	liver:	n/a
4	chr14:34906118-34906168	AoSMC	blood vessel:	n/a
5	chr14:34931798-34931848	HUVEC	blood vessel:	n/a
6	chr14:34931803-34931853	BJ	skin:	n/a
7	chr14:34931577-34931627	NT2-D1	testis:	n/a
8	chr14:34906118-34906168	RPTEC	kidney:	n/a
9	chr14:34931458-34931508	HRCEpiC	kidney:	n/a
10	chr14:34931798-34931848	SK-N-MC	brain:	n/a
11	chr14:34931822-34931872	ProgFib	skin:	n/a
12	chr14:34944819-34944869	ECC-1	luminal epithelium:	n/a
13	chr14:34971569-34971619	HL-60	blood:	n/a
14	chr14:34931967-34932017	ECC-1	luminal epithelium:	n/a
15	chr14:34931026-34931076	MCF10A-Er-Src	breast:	n/a
16	chr14:34966313-34966363	AG04450	lung:	fetal
17	chr14:34931391-34931441	HRCEpiC	kidney:	n/a
18	chr14:34944819-34944869	Jurkat	blood:	n/a
19	chr14:34838703-34838753	HAEpiC	amniotic membrane:	n/a
20	chr14:34931026-34931076	HCPEpiC	choroid plexus:	n/a
21	chr14:34931803-34931853	AG09319	gingival:	n/a
22	chr14:34945225-34945275	HRPEpiC	eye:	n/a
23	chr14:34931458-34931508	HAEpiC	amniotic membrane:	n/a
24	chr14:34931577-34931627	AG04449	skin:	fetal
25	chr14:34931391-34931441	BJ	skin:	n/a
26	chr14:34966313-34966363	PANC-1	pancreas:	n/a
27	chr14:34931026-34931076	HNPCEpiC	eye:	n/a
28	chr14:34931798-34931848	SAEC	small airway:	n/a
29	chr14:34971569-34971619	NB4	blood:	n/a
30	chr14:34902862-34902912	NHDF-neo	bronchial:	n/a
31	chr14:34944819-34944869	HEK293	kidney:	embryo
32	chr14:34931822-34931872	BJ	skin:	n/a
33	chr14:34931026-34931076	GM06990	blood:	n/a
34	chr14:34966313-34966363	HCT-116	colon:	n/a
35	chr14:34931798-34931848	CMK	blood:	n/a
36	chr14:34931967-34932017	HepG2	liver:	n/a
37	chr14:34931026-34931076	AG10803	skin:	n/a
38	chr14:34906118-34906168	HAEpiC	amniotic membrane:	n/a
39	chr14:34945475-34945525	HCF	heart:	n/a
40	chr14:34945225-34945275	A549	lung:	n/a
41	chr14:34931026-34931076	Caco-2	colon:	n/a
42	chr14:34971569-34971619	HPAEpiC	pulmonary alveolar:	n/a
43	chr14:34902862-34902912	GM12892	blood:	n/a
44	chr14:34931822-34931872	CMK	blood:	n/a
45	chr14:34931967-34932017	NHBE	bronchial:	n/a
46	chr14:34931967-34932017	AG09319	gingival:	n/a
47	chr14:34971569-34971619	SAEC	small airway:	n/a
48	chr14:34931026-34931076	NH-A	brain:	n/a
49	chr14:34945225-34945275	SK-N-SH	brain:	n/a
50	chr14:34971569-34971619	AG04449	skin:	fetal

(count:169 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr14:34851488..34853508-chr14:35021790..35024186,2	MCF-7	breast:
2	chr14:34906840..34909474-chr14:34911416..34913752,2	K562	blood:
3	chr14:34635250..34638092-chr14:34922730..34924638,2	MCF-7	breast:
4	chr14:34838344..34842091-chr14:34845007..34847766,4	MCF-7	breast:
5	chr14:34853536..34855341-chr14:34855493..34858071,3	K562	blood:
6	chr14:34836773..34839966-chr14:34841911..34844333,3	MCF-7	breast:
7	chr14:34945242..34947731-chr14:34948944..34951768,2	MCF-7	breast:
8	chr14:34889752..34892468-chr14:34930579..34933211,2	MCF-7	breast:
9	chr14:34822809..34824821-chr14:34835490..34838130,2	K562	blood:
10	chr14:34836739..34838554-chr14:35017235..35019391,2	MCF-7	breast:
11	chr14:34964955..34967907-chr14:34973617..34975342,2	MCF-7	breast:
12	chr14:34930899..34931823-chr2:97425912..97426737,2	Hela-S3	cervix:
13	chr14:34917560..34921859-chr14:34930023..34933382,10	MCF-7	breast:
14	chr14:34841266..34842852-chr14:34928524..34930795,2	MCF-7	breast:
15	chr14:34985976..34987931-chr14:35007272..35009359,2	MCF-7	breast:
16	chr14:34800581..34801486-chr14:34967721..34968650,2	K562	blood:
17	chr14:34933203..34935041-chr14:34939513..34941719,2	K562	blood:
18	chr14:34914176..34917088-chr14:34919017..34921361,2	K562	blood:
19	chr14:34845403..34847934-chr14:34917916..34920495,2	K562	blood:
20	chr14:34827197..34829438-chr14:34832825..34835803,3	MCF-7	breast:
21	chr14:34801106..34802609-chr14:34842166..34844322,2	MCF-7	breast:
22	chr14:34823851..34826767-chr14:34832124..34834268,2	MCF-7	breast:
23	chr14:34930222..34933359-chr14:34947773..34950795,3	MCF-7	breast:
24	chr14:34929806..34931757-chr14:34938226..34940059,2	K562	blood:
25	chr14:34825095..34827811-chr14:34836037..34838598,2	K562	blood:
26	chr14:34800085..34801493-chr14:34967404..34968713,17	MCF-7	breast:
27	chr14:34920582..34922864-chr14:35018787..35021782,2	K562	blood:
28	chr14:34932436..34934680-chr14:34965867..34967830,2	K562	blood:
29	chr14:34957508..34960404-chr14:34964346..34966873,2	K562	blood:
30	chr14:34934706..34936748-chr14:34939832..34941960,2	MCF-7	breast:
31	chr14:34843016..34844833-chr14:34930028..34932374,3	MCF-7	breast:
32	chr14:34923565..34925509-chr14:34925743..34927516,2	MCF-7	breast:
33	chr14:34930543..34933153-chr14:35015586..35017251,2	MCF-7	breast:
34	chr14:34966374..34968147-chr14:35008912..35011090,2	MCF-7	breast:
35	chr14:34916477..34918370-chr14:34929972..34931910,2	K562	blood:
36	chr14:34844480..34846950-chr14:34854084..34856726,2	K562	blood:
37	chr14:34930482..34933296-chr14:34952569..34954350,2	MCF-7	breast:
38	chr14:34947380..34950273-chr14:34964851..34967790,4	MCF-7	breast:
39	chr14:34926801..34930347-chr14:34965269..34966847,3	K562	blood:
40	chr14:34846670..34848998-chr14:35021037..35023983,2	MCF-7	breast:
41	chr14:34922503..34924704-chr14:35007891..35010342,2	MCF-7	breast:
42	chr14:34845081..34846863-chr14:35021889..35024894,3	MCF-7	breast:
43	chr14:34831090..34836007-chr14:34929679..34932517,6	MCF-7	breast:
44	chr14:34835401..34839083-chr14:34893653..34895439,3	MCF-7	breast:
45	chr14:34844429..34846266-chr14:34846306..34850742,6	MCF-7	breast:
46	chr14:34894353..34897341-chr14:34909649..34911382,2	K562	blood:
47	chr14:34832361..34834926-chr14:35022070..35024104,2	K562	blood:
48	chr14:34883972..34886715-chr14:34889275..34892253,2	K562	blood:
49	chr14:34928753..34932995-chr14:34963537..34968945,14	MCF-7	breast:
50	chr14:34882267..34884337-chr14:35018117..35021042,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPTSSA-2	chr14:34885893-34886808	NONHSAT036328
2	lnc-SPTSSA-1	chr14:34931922-34931980	NONHSAT036319

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C14orf147	hsa-miR-221-3p	chr14:34903362-34903355
2	C14orf147	hsa-miR-221-3p	chr14:34903356-34903378

Variant related genes	Relation type
ENSG00000223593	TF binding region
SPTSSA	TF binding region
EGLN3	TF binding region
ENSG00000237450	TF binding region
ENSG00000223593	CpG island
SPTSSA	CpG island
EGLN3	CpG island
ENSG00000237450	CpG island
ENSG00000158158	chromatin interactions
ENSG00000199071	chromatin interactions
ENSG00000129518	chromatin interactions
ENSG00000206596	chromatin interactions
ENSG00000240463	chromatin interactions
ENSG00000129521	chromatin interactions
ENSG00000143368	chromatin interactions
ENSG00000126653	chromatin interactions
ENSG00000206588	chromatin interactions
ENSG00000165389	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000223593	chromatin interactions

Extended variants
information (count: 5684 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:5684 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545473425	chr14:34834300-34834301	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs77656142	chr14:34834332-34834333	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs139116977	chr14:34834341-34834342	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs141769724	chr14:34834384-34834385	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs561534233	chr14:34834392-34834393	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs568981808	chr14:34834434-34834435	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs528905766	chr14:34834435-34834436	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs35881258	chr14:34834461-34834462	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs181633966	chr14:34834464-34834465	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs76075802	chr14:34834470-34834471	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs552486660	chr14:34834567-34834568	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs376256257	chr14:34834639-34834640	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs150585230	chr14:34834664-34834665	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs186597274	chr14:34834680-34834681	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs527449447	chr14:34834681-34834682	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs75179519	chr14:34834708-34834709	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs74543157	chr14:34834752-34834753	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs58564811	chr14:34834784-34834785	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs191503568	chr14:34834799-34834800	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs570027671	chr14:34834823-34834824	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs539166149	chr14:34834837-34834838	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs373779374	chr14:34834854-34834855	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs559080877	chr14:34834871-34834872	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs77072414	chr14:34834873-34834874	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs541610430	chr14:34834918-34834919	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs555248227	chr14:34834982-34834983	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs574992723	chr14:34835035-34835036	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs544086560	chr14:34835036-34835037	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs531396593	chr14:34835069-34835070	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs139663920	chr14:34835129-34835130	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs531319495	chr14:34835168-34835169	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs149716540	chr14:34835173-34835174	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs199543672	chr14:34835232-34835233	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs114222814	chr14:34835240-34835241	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs147407157	chr14:34835281-34835282	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs76069632	chr14:34835351-34835352	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs567442605	chr14:34835413-34835414	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs529989106	chr14:34835435-34835436	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs28658463	chr14:34835448-34835449	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs569986405	chr14:34835469-34835470	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs181100550	chr14:34835482-34835483	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs4396443	chr14:34835564-34835565	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs575643551	chr14:34835623-34835624	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs566134519	chr14:34835624-34835625	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs2383589	chr14:34835638-34835639	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs554906805	chr14:34835668-34835669	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs574974808	chr14:34835675-34835676	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs147657923	chr14:34835684-34835685	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs78311966	chr14:34835714-34835715	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs575651980	chr14:34835718-34835719	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2498 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:34826000-34837200	Weak transcription	Pancreas	Pancrea
2	chr14:34829400-34834800	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr14:34829400-34837200	Weak transcription	HMEC	breast
4	chr14:34829400-34838600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr14:34830000-34835400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr14:34831000-34837200	Weak transcription	Adipose Nuclei	Adipose
7	chr14:34831400-34834800	Weak transcription	Brain Anterior Caudate	brain
8	chr14:34831400-34834800	Weak transcription	Brain Substantia Nigra	brain
9	chr14:34831400-34837200	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr14:34831400-34838000	Weak transcription	Esophagus	oesophagus
11	chr14:34831400-34839400	Weak transcription	Lung	lung
12	chr14:34831600-34834600	Weak transcription	Brain Hippocampus Middle	brain
13	chr14:34831600-34834800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr14:34831600-34838200	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr14:34831600-34840000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr14:34832600-34837000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr14:34832800-34834800	Weak transcription	Osteobl	bone
18	chr14:34833400-34834600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr14:34833400-34835400	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr14:34833400-34837000	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr14:34833400-34838000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr14:34833400-34838000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr14:34833600-34834800	Weak transcription	Hela-S3	cervix
24	chr14:34833600-34834800	Weak transcription	NH-A	brain
25	chr14:34833600-34837200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr14:34833800-34834400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr14:34833800-34834400	Enhancers	NHEK	skin
28	chr14:34833800-34837200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr14:34834200-34834400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr14:34834400-34834600	Enhancers	HepG2	liver
31	chr14:34834400-34837000	Weak transcription	NHEK	skin
32	chr14:34834400-34837400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr14:34834400-34837800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr14:34834600-34834800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr14:34834600-34834800	Enhancers	A549	lung
36	chr14:34834600-34835200	Enhancers	Liver	Liver
37	chr14:34834600-34835200	Flanking Active TSS	HepG2	liver
38	chr14:34834600-34835400	Enhancers	Brain Hippocampus Middle	brain
39	chr14:34834800-34835000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr14:34834800-34835000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr14:34834800-34835000	Enhancers	Fetal Intestine Large	intestine
42	chr14:34834800-34835000	Enhancers	Placenta	Placenta
43	chr14:34834800-34835000	Enhancers	Stomach Mucosa	stomach
44	chr14:34834800-34835000	Enhancers	NH-A	brain
45	chr14:34834800-34835000	Enhancers	Osteobl	bone
46	chr14:34834800-34835200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr14:34834800-34835200	Enhancers	Brain Anterior Caudate	brain
48	chr14:34834800-34835200	Enhancers	Brain Substantia Nigra	brain
49	chr14:34834800-34835200	Flanking Active TSS	A549	lung
50	chr14:34834800-34835400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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