Variant report

Variant	esv3396933
Chromosome Location	chr14:69906914-70001258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1253)
CpG islands
(count:1342)
Chromatin interactive
region (count:68)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1253 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:69941910-69942131	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:69941879-69942182	K562	blood:	n/a	n/a
3	ARID3A	chr14:69926824-69927161	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:69970593-69970792	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:69926831-69927180	K562	blood:	n/a	n/a
6	ATF1	chr14:69926858-69927169	K562	blood:	n/a	n/a
7	ATF2	chr14:69908600-69909033	GM12878	blood:	n/a	n/a
8	ATF2	chr14:69908532-69909151	GM12878	blood:	n/a	n/a
9	BACH1	chr14:69950648-69951056	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:69948935-69949141	K562	blood:	n/a	n/a
11	BACH1	chr14:69968018-69968246	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr14:69948920-69949253	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr14:69938610-69938873	GM12878	blood:	n/a	chr14:69938787-69938797 chr14:69938790-69938801
14	BATF	chr14:69908732-69909008	GM12878	blood:	n/a	n/a
15	BATF	chr14:69938611-69938940	GM12878	blood:	n/a	chr14:69938787-69938797 chr14:69938790-69938801
16	BCL3	chr14:69973295-69973474	GM12878	blood:	n/a	n/a
17	BCLAF1	chr14:69908687-69909114	GM12878	blood:	n/a	n/a
18	BCLAF1	chr14:69908614-69909193	GM12878	blood:	n/a	n/a
19	BHLHE40	chr14:69926882-69927125	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:69926849-69927149	K562	blood:	n/a	n/a
21	BHLHE40	chr14:69938666-69938985	GM12878	blood:	n/a	n/a
22	BHLHE40	chr14:69908751-69908998	GM12878	blood:	n/a	n/a
23	BHLHE40	chr14:69925845-69926040	K562	blood:	n/a	n/a
24	BRCA1	chr14:69926810-69927151	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr14:69957851-69957951	K562	blood:	n/a	chr14:69957884-69957895
26	CEBPB	chr14:69950226-69950924	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr14:69926851-69927177	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr14:69926814-69927165	IMR90	lung:	n/a	n/a
29	CEBPB	chr14:69959034-69959265	HepG2	liver:	n/a	chr14:69959128-69959139 chr14:69959127-69959140
30	CEBPB	chr14:69957726-69958039	HepG2	liver:	n/a	chr14:69957884-69957895
31	CEBPB	chr14:69908733-69908954	HepG2	liver:	n/a	chr14:69908819-69908830
32	CEBPB	chr14:69959052-69959243	A549	lung:	n/a	chr14:69959128-69959139 chr14:69959127-69959140
33	CEBPB	chr14:69996257-69996629	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:69997339-69997516	IMR90	lung:	n/a	n/a
35	CEBPB	chr14:69908758-69908848	H1-hESC	embryonic stem cell:	n/a	chr14:69908819-69908830
36	CEBPB	chr14:69935812-69935918	IMR90	lung:	n/a	n/a
37	CEBPB	chr14:69996347-69996513	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:69908498-69909192	GM12878	blood:	n/a	chr14:69908819-69908830 chr14:69908644-69908652
39	CEBPB	chr14:69923739-69924095	MCF-7	breast:	n/a	n/a
40	CEBPB	chr14:69940288-69940504	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr14:69908709-69908954	IMR90	lung:	n/a	chr14:69908819-69908830
42	CEBPB	chr14:69997428-69997514	A549	lung:	n/a	n/a
43	CEBPB	chr14:69925222-69925301	HepG2	liver:	n/a	n/a
44	CEBPB	chr14:69926890-69927205	A549	lung:	n/a	n/a
45	CHD1	chr14:69908595-69908794	GM12878	blood:	n/a	n/a
46	CHD2	chr14:69950982-69951100	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr14:69926903-69927066	GM12878	blood:	n/a	n/a
48	CREB1	chr14:69926775-69927172	GM12878	blood:	n/a	n/a
49	CREB1	chr14:69926663-69927279	K562	blood:	n/a	n/a
50	CREB1	chr14:69926650-69927291	GM12878	blood:	n/a	n/a

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:69951211-69951261	NH-A	brain:	n/a
2	chr14:69951422-69951472	T-47D	breast:	n/a
3	chr14:69951781-69951831	BJ	skin:	n/a
4	chr14:69951495-69951545	AG04449	skin:	fetal
5	chr14:69951322-69951372	U87	brain:	n/a
6	chr14:69951311-69951361	NHDF-neo	bronchial:	n/a
7	chr14:69986021-69986071	SAEC	small airway:	n/a
8	chr14:69968273-69968323	IMR90	lung:	fetal
9	chr14:69952104-69952154	RPTEC	kidney:	n/a
10	chr14:69951720-69951770	Hela-S3	cervix:	n/a
11	chr14:69947271-69947321	RPTEC	kidney:	n/a
12	chr14:69968273-69968323	AG09309	skin:	n/a
13	chr14:69995178-69995228	HL-60	blood:	n/a
14	chr14:69951372-69951422	AG10803	skin:	n/a
15	chr14:69951781-69951831	ovcar-3	ovarian:	n/a
16	chr14:69954135-69954185	HPAEpiC	pulmonary alveolar:	n/a
17	chr14:69950116-69950166	T-47D	breast:	n/a
18	chr14:69951372-69951422	ovcar-3	ovarian:	n/a
19	chr14:69952003-69952053	Jurkat	blood:	n/a
20	chr14:69951305-69951355	HRCEpiC	kidney:	n/a
21	chr14:69951495-69951545	HMEC	breast:	n/a
22	chr14:69995178-69995228	HEK293	kidney:	embryo
23	chr14:69968273-69968323	PrEC	prostate:	n/a
24	chr14:69950043-69950093	A549	lung:	n/a
25	chr14:69951311-69951361	MCF10A-Er-Src	breast:	n/a
26	chr14:69951720-69951770	SK-N-MC	brain:	n/a
27	chr14:69951311-69951361	BE2_C	brain:	n/a
28	chr14:69950043-69950093	RPTEC	kidney:	n/a
29	chr14:69951305-69951355	AG04449	skin:	fetal
30	chr14:69951322-69951372	GM12878	blood:	n/a
31	chr14:69950043-69950093	MCF-7	breast:	n/a
32	chr14:69951305-69951355	H1-hESC	embryonic stem cell:	embryo
33	chr14:69952003-69952053	HUVEC	blood vessel:	n/a
34	chr14:69951311-69951361	Hela-S3	cervix:	n/a
35	chr14:69951781-69951831	A549	lung:	n/a
36	chr14:69951322-69951372	CMK	blood:	n/a
37	chr14:69950116-69950166	GM06990	blood:	n/a
38	chr14:69951372-69951422	AG04450	lung:	fetal
39	chr14:69968273-69968323	Jurkat	blood:	n/a
40	chr14:69951305-69951355	HEK293	kidney:	embryo
41	chr14:69952003-69952053	AG10803	skin:	n/a
42	chr14:69952104-69952154	Caco-2	colon:	n/a
43	chr14:69986021-69986071	GM12892	blood:	n/a
44	chr14:69995178-69995228	SK-N-SH_RA	brain:	n/a
45	chr14:69951839-69951889	NHBE	bronchial:	n/a
46	chr14:69951495-69951545	ovcar-3	ovarian:	n/a
47	chr14:69954135-69954185	T-47D	breast:	n/a
48	chr14:69951781-69951831	SK-N-SH	brain:	n/a
49	chr14:69950043-69950093	Jurkat	blood:	n/a
50	chr14:69947271-69947321	GM19239	blood:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:69970211..69971130-chr14:70193442..70194320,2	MCF-7	breast:
2	chr14:69932792..69935168-chr14:70232400..70234408,2	K562	blood:
3	chr14:69891176..69893252-chr14:69916771..69918608,2	MCF-7	breast:
4	chr14:69914267..69916921-chr17:41462308..41463864,2	MCF-7	breast:
5	chr14:69949476..69951469-chr14:70232962..70234565,2	MCF-7	breast:
6	chr14:69864699..69866812-chr14:69943113..69945643,2	MCF-7	breast:
7	chr14:69708308..69710896-chr14:69926995..69929013,2	MCF-7	breast:
8	chr14:69947992..69950774-chr14:69962839..69965276,2	K562	blood:
9	chr14:69958713..69961679-chr14:69965168..69967666,2	MCF-7	breast:
10	chr14:69989183..69991893-chr14:70006349..70008257,2	MCF-7	breast:
11	chr14:69970253..69971296-chr14:70001641..70002581,3	MCF-7	breast:
12	chr14:69865072..69867138-chr14:69919938..69922880,2	MCF-7	breast:
13	chr14:69863307..69865409-chr14:69940498..69943105,2	MCF-7	breast:
14	chr14:69946123..69947705-chr14:69948349..69951147,2	MCF-7	breast:
15	chr14:69877530..69878097-chr14:69941616..69942179,2	MCF-7	breast:
16	chr14:69725416..69728127-chr14:69925008..69927270,2	MCF-7	breast:
17	chr14:69829365..69831341-chr14:69925811..69928602,2	MCF-7	breast:
18	chr14:69959710..69961607-chr14:69966720..69969108,2	MCF-7	breast:
19	chr14:69941960..69942511-chr14:69967141..69968031,2	MCF-7	breast:
20	chr14:70000714..70002427-chr14:70038896..70041033,2	MCF-7	breast:
21	chr14:69714947..69715448-chr14:69926707..69927678,2	MCF-7	breast:
22	chr14:69987420..69989705-chr14:69990371..69993160,2	MCF-7	breast:
23	chr14:69959710..69961607-chr14:69966720..69969108,2	MCF-7	breast:
24	chr14:69950456..69952040-chr14:70233397..70235258,2	MCF-7	breast:
25	chr14:69993102..69995388-chr14:70040159..70042492,2	K562	blood:
26	chr14:69862767..69865090-chr14:69948473..69950881,2	MCF-7	breast:
27	chr14:69865252..69866906-chr14:69922886..69924769,3	MCF-7	breast:
28	chr14:69951736..69954477-chr14:69954891..69957562,2	MCF-7	breast:
29	chr14:69969961..69971754-chr14:70233921..70235579,2	K562	blood:
30	chr14:69947992..69950774-chr14:69962839..69965833,3	K562	blood:
31	chr14:69906509..69908579-chr14:69909822..69912590,2	K562	blood:
32	chr14:69946123..69947705-chr14:69948349..69951147,2	MCF-7	breast:
33	chr14:69979995..69982443-chr14:69986701..69988588,2	MCF-7	breast:
34	chr14:69819465..69821642-chr14:69923369..69926196,2	MCF-7	breast:
35	chr14:69941960..69942511-chr14:69967141..69968031,2	MCF-7	breast:
36	chr14:69708990..69709961-chr14:69926423..69927285,4	MCF-7	breast:
37	chr14:69951736..69954477-chr14:69954891..69957562,2	MCF-7	breast:
38	chr14:69979995..69982443-chr14:69986701..69988588,2	MCF-7	breast:
39	chr14:69833381..69834049-chr14:69926658..69927452,2	MCF-7	breast:
40	chr14:69947861..69950985-chr14:69958572..69961159,3	MCF-7	breast:
41	chr14:69951860..69952360-chr7:104652907..104653592,2	Hela-S3	cervix:
42	chr14:69958713..69961679-chr14:69965168..69967666,2	MCF-7	breast:
43	chr14:69947992..69950774-chr14:69962839..69965276,2	K562	blood:
44	chr14:69905430..69909394-chr14:69909607..69912590,4	K562	blood:
45	chr14:69947992..69950774-chr14:69962839..69965833,3	K562	blood:
46	chr14:69920954..69922535-chr14:69924046..69926530,2	MCF-7	breast:
47	chr14:69815842..69819268-chr14:69923313..69926949,3	MCF-7	breast:
48	chr14:69970362..69971107-chr14:70041144..70041646,2	K562	blood:
49	chr14:69863801..69866366-chr14:69909938..69912439,2	MCF-7	breast:
50	chr14:69952428..69953410-chr5:19316375..19317263,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERH-1	chr14:69925417-69926228	ENSG00000249775

No data

Variant related genes	Relation type
SLC39A9	TF binding region
PLEKHD1	TF binding region
SLC39A9	CpG island
PLEKHD1	CpG island
ENSG00000258520	chromatin interactions
ENSG00000100632	chromatin interactions
ENSG00000100626	chromatin interactions
ENSG00000175985	chromatin interactions
ENSG00000267909	chromatin interactions
ENSG00000029364	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000100650	chromatin interactions
ENSG00000139990	chromatin interactions
DDX17	miRNA target sites

Extended variants
information (count: 2953 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2953 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537833342	chr14:69906994-69906995	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs556027019	chr14:69907008-69907009	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs574473238	chr14:69907015-69907016	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs547431461	chr14:69907025-69907026	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs140105147	chr14:69907051-69907052	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs557290237	chr14:69907053-69907054	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs572273790	chr14:69907115-69907116	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs546112951	chr14:69907121-69907122	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs137983251	chr14:69907145-69907146	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs374391299	chr14:69907177-69907178	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs73275019	chr14:69907189-69907190	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs574556609	chr14:69907222-69907223	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372673299	chr14:69907257-69907258	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113061422	chr14:69907260-69907261	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547538669	chr14:69907284-69907285	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566694686	chr14:69907331-69907332	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527460782	chr14:69907356-69907357	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552534812	chr14:69907364-69907365	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570381662	chr14:69907367-69907368	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537491720	chr14:69907407-69907408	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149084442	chr14:69907445-69907446	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567924926	chr14:69907450-69907451	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535555323	chr14:69907524-69907525	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537605161	chr14:69907526-69907527	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs55708330	chr14:69907528-69907529	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs138914958	chr14:69907537-69907538	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545975754	chr14:69907538-69907539	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184931419	chr14:69907539-69907540	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188277740	chr14:69907567-69907568	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543715249	chr14:69907587-69907588	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191587287	chr14:69907598-69907599	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184838033	chr14:69907627-69907628	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189715938	chr14:69907628-69907629	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559870356	chr14:69907650-69907651	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11624756	chr14:69907677-69907678	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs535582133	chr14:69907680-69907681	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553477969	chr14:69907691-69907692	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs8021143	chr14:69907734-69907735	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs370498618	chr14:69907757-69907758	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181488046	chr14:69907769-69907770	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549774706	chr14:69907831-69907832	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540332033	chr14:69907919-69907920	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186608262	chr14:69907922-69907923	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535085506	chr14:69907931-69907932	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142925255	chr14:69908014-69908015	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374494973	chr14:69908025-69908026	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188969020	chr14:69908047-69908048	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs367657959	chr14:69908068-69908069	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181724547	chr14:69908139-69908140	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576525423	chr14:69908264-69908265	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hematopoietic stem cell	20738155	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1332 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69868000-69923200	Weak transcription	Esophagus	oesophagus
2	chr14:69886400-69908200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr14:69887400-69913000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr14:69889200-69922400	Weak transcription	Brain Substantia Nigra	brain
5	chr14:69889200-69923400	Weak transcription	Colon Smooth Muscle	Colon
6	chr14:69889400-69923200	Weak transcription	Pancreas	Pancrea
7	chr14:69890000-69922400	Weak transcription	Fetal Brain Male	brain
8	chr14:69890800-69922400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr14:69891200-69922800	Weak transcription	Colonic Mucosa	Colon
10	chr14:69891200-69923000	Weak transcription	NHLF	lung
11	chr14:69892000-69920600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr14:69892200-69931400	Weak transcription	K562	blood
13	chr14:69893000-69908600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr14:69893000-69919800	Weak transcription	Spleen	Spleen
15	chr14:69893000-69922800	Weak transcription	Aorta	Aorta
16	chr14:69893200-69926800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr14:69893400-69910800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr14:69893400-69922200	Weak transcription	Left Ventricle	heart
19	chr14:69893400-69922400	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr14:69893400-69922600	Weak transcription	Brain Germinal Matrix	brain
21	chr14:69893400-69922800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr14:69893400-69923000	Weak transcription	Lung	lung
23	chr14:69893600-69908400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr14:69893600-69908600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr14:69893600-69908800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr14:69893600-69908800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr14:69893600-69920200	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr14:69893600-69920400	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr14:69893600-69922000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr14:69893600-69922400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr14:69893600-69922400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr14:69893600-69922800	Weak transcription	Brain Hippocampus Middle	brain
33	chr14:69893600-69923200	Weak transcription	Gastric	stomach
34	chr14:69893600-69925000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr14:69893800-69908600	Weak transcription	Hela-S3	cervix
36	chr14:69893800-69908800	Weak transcription	HSMM	muscle
37	chr14:69894000-69908600	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr14:69894000-69916000	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr14:69894000-69922200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr14:69894000-69922800	Weak transcription	Brain Cingulate Gyrus	brain
41	chr14:69894000-69924400	Weak transcription	Brain Angular Gyrus	brain
42	chr14:69894200-69907600	Weak transcription	Fetal Intestine Small	intestine
43	chr14:69894400-69908800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr14:69894400-69908800	Weak transcription	Fetal Intestine Large	intestine
45	chr14:69894400-69919800	Weak transcription	Ovary	ovary
46	chr14:69894600-69907600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr14:69894600-69908800	Weak transcription	Osteobl	bone
48	chr14:69894600-69909800	Weak transcription	HUVEC	blood vessel
49	chr14:69894600-69910800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr14:69894600-69919200	Weak transcription	Primary T helper cells fromperipheralblood	blood

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