Variant report

Variant	nsv564874
Chromosome Location	chr14:55879685-56027815
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2520)
CpG islands
(count:1467)
Chromatin interactive
region (count:85)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2520 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:55912933-55913378	K562	blood:	n/a	n/a
2	ARID3A	chr14:55967006-55967310	K562	blood:	n/a	n/a
3	ARID3A	chr14:55912857-55913179	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:55886501-55886594	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:55884839-55884914	K562	blood:	n/a	n/a
6	ARID3A	chr14:55897005-55897180	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:55901366-55901865	HepG2	liver:	n/a	chr14:55901771-55901787
8	ARID3A	chr14:55896954-55897161	K562	blood:	n/a	n/a
9	ATF1	chr14:55936899-55937089	K562	blood:	n/a	n/a
10	ATF1	chr14:55966919-55967426	K562	blood:	n/a	n/a
11	ATF1	chr14:55921337-55921668	K562	blood:	n/a	n/a
12	ATF2	chr14:55917669-55918218	GM12878	blood:	n/a	n/a
13	ATF2	chr14:55925395-55925997	GM12878	blood:	n/a	n/a
14	ATF2	chr14:55896755-55897141	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr14:55925406-55926072	GM12878	blood:	n/a	n/a
16	ATF2	chr14:55917640-55918105	GM12878	blood:	n/a	n/a
17	BACH1	chr14:55896818-55897008	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr14:56014695-56015041	GM12878	blood:	n/a	chr14:56014882-56014893
19	BATF	chr14:55925499-55926006	GM12878	blood:	n/a	n/a
20	BATF	chr14:56012977-56013309	GM12878	blood:	n/a	chr14:56013151-56013162
21	BATF	chr14:55921257-55921589	GM12878	blood:	n/a	chr14:55921408-55921419
22	BATF	chr14:55917712-55918018	GM12878	blood:	n/a	n/a
23	BATF	chr14:55925457-55926073	GM12878	blood:	n/a	n/a
24	BCL11A	chr14:55917651-55918146	GM12878	blood:	n/a	n/a
25	BCL11A	chr14:55925473-55925886	GM12878	blood:	n/a	n/a
26	BCL11A	chr14:55921254-55921548	GM12878	blood:	n/a	n/a
27	BCL11A	chr14:55917714-55918012	GM12878	blood:	n/a	n/a
28	BCL11A	chr14:56012934-56013383	GM12878	blood:	n/a	n/a
29	BCL11A	chr14:55925432-55926028	GM12878	blood:	n/a	n/a
30	BCL3	chr14:55914719-55915425	A549	lung:	n/a	chr14:55915028-55915037 chr14:55914868-55914876
31	BCL3	chr14:55925453-55925988	GM12878	blood:	n/a	n/a
32	BCL3	chr14:55924201-55924609	GM12878	blood:	n/a	n/a
33	BHLHE40	chr14:55893630-55893941	K562	blood:	n/a	n/a
34	BHLHE40	chr14:55921036-55921563	K562	blood:	n/a	n/a
35	BHLHE40	chr14:55882151-55882265	GM12878	blood:	n/a	n/a
36	BHLHE40	chr14:55912882-55913119	GM12878	blood:	n/a	n/a
37	BHLHE40	chr14:55981695-55981883	K562	blood:	n/a	n/a
38	BHLHE40	chr14:55925584-55926069	GM12878	blood:	n/a	n/a
39	BHLHE40	chr14:56014705-56015289	GM12878	blood:	n/a	n/a
40	BHLHE40	chr14:55966942-55967818	K562	blood:	n/a	n/a
41	BHLHE40	chr14:56022774-56022826	A549	lung:	n/a	n/a
42	BHLHE40	chr14:55921470-55921605	HepG2	liver:	n/a	n/a
43	BRCA1	chr14:55921165-55921507	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr14:55894056-55894479	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr14:55914803-55915381	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr14:55896897-55897056	H1-hESC	embryonic stem cell:	n/a	n/a
47	CBX3	chr14:55914606-55915523	HCT-116	colon:	n/a	n/a
48	CBX3	chr14:55914460-55915611	HCT-116	colon:	n/a	n/a
49	CBX3	chr14:55894048-55894670	HCT-116	colon:	n/a	chr14:55894509-55894520
50	CBX3	chr14:55925453-55926145	HCT-116	colon:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:55907007-55907057	ovcar-3	ovarian:	n/a
2	chr14:55907460-55907510	HPAEpiC	pulmonary alveolar:	n/a
3	chr14:55907198-55907248	RPTEC	kidney:	n/a
4	chr14:55907007-55907057	ovcar-3	ovarian:	n/a
5	chr14:55907460-55907510	HPAEpiC	pulmonary alveolar:	n/a
6	chr14:55907198-55907248	RPTEC	kidney:	n/a
7	chr14:55907374-55907424	BE2_C	brain:	n/a
8	chr14:55910650-55910700	AG10803	skin:	n/a
9	chr14:55908301-55908351	U87	brain:	n/a
10	chr14:55982148-55982198	MCF10A-Er-Src	breast:	n/a
11	chr14:55885957-55886007	MCF10A-Er-Src	breast:	n/a
12	chr14:55966172-55966222	AG04449	skin:	fetal
13	chr14:55885957-55886007	ECC-1	luminal epithelium:	n/a
14	chr14:55907007-55907057	Jurkat	blood:	n/a
15	chr14:55908365-55908415	CMK	blood:	n/a
16	chr14:55982148-55982198	PrEC	prostate:	n/a
17	chr14:55907122-55907172	HPAEpiC	pulmonary alveolar:	n/a
18	chr14:55966172-55966222	HEEpiC	esophagus:	n/a
19	chr14:55907385-55907435	RPTEC	kidney:	n/a
20	chr14:55907007-55907057	ECC-1	luminal epithelium:	n/a
21	chr14:55895678-55895728	K562	blood:	n/a
22	chr14:56023591-56023641	AG09319	gingival:	n/a
23	chr14:55914753-55914803	NHBE	bronchial:	n/a
24	chr14:55907299-55907349	RPTEC	kidney:	n/a
25	chr14:55907198-55907248	Jurkat	blood:	n/a
26	chr14:55966172-55966222	GM12878	blood:	n/a
27	chr14:55907299-55907349	AG09319	gingival:	n/a
28	chr14:55907501-55907551	AoSMC	blood vessel:	n/a
29	chr14:55908301-55908351	HCPEpiC	choroid plexus:	n/a
30	chr14:55982148-55982198	HEK293	kidney:	embryo
31	chr14:55910650-55910700	NHDF-neo	bronchial:	n/a
32	chr14:55907417-55907467	NH-A	brain:	n/a
33	chr14:55908301-55908351	HCT-116	colon:	n/a
34	chr14:55920683-55920733	HRPEpiC	eye:	n/a
35	chr14:56023591-56023641	MCF-7	breast:	n/a
36	chr14:55907501-55907551	GM12892	blood:	n/a
37	chr14:56007778-56007828	GM12892	blood:	n/a
38	chr14:55907460-55907510	PFSK-1	brain:	n/a
39	chr14:55914753-55914803	NT2-D1	testis:	n/a
40	chr14:55999890-55999940	IMR90	lung:	fetal
41	chr14:55907007-55907057	HUVEC	blood vessel:	n/a
42	chr14:55907501-55907551	H1-hESC	embryonic stem cell:	embryo
43	chr14:55907299-55907349	GM12878	blood:	n/a
44	chr14:55907374-55907424	NT2-D1	testis:	n/a
45	chr14:55895678-55895728	H1-hESC	embryonic stem cell:	embryo
46	chr14:55905105-55905155	SKMC	muscle:	n/a
47	chr14:55907198-55907248	AG04450	lung:	fetal
48	chr14:55907122-55907172	HRCEpiC	kidney:	n/a
49	chr14:55907417-55907467	HCT-116	colon:	n/a
50	chr14:55907427-55907477	GM12878	blood:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:55934279..55936415-chr14:55944398..55946379,2	K562	blood:
2	chr14:56000693..56002605-chr14:56044189..56046854,2	MCF-7	breast:
3	chr14:55832090..55833883-chr14:55878712..55880700,2	MCF-7	breast:
4	chr14:55930242..55933239-chr14:55934431..55937260,2	MCF-7	breast:
5	chr14:56010848..56011450-chr15:45879305..45879811,2	Hela-S3	cervix:
6	chr14:55967592..55969824-chr14:55972621..55974139,2	K562	blood:
7	chr14:55917476..55919752-chr14:55927927..55929751,2	MCF-7	breast:
8	chr14:55920824..55921477-chr8:146175730..146176235,2	HCT-116	colon:
9	chr14:55930242..55933239-chr14:55934431..55937260,2	MCF-7	breast:
10	chr14:55882209..55883793-chr14:55889649..55891588,2	K562	blood:
11	chr14:55934279..55936415-chr14:55944398..55946379,2	K562	blood:
12	chr14:55736296..55738259-chr14:55878149..55880015,2	MCF-7	breast:
13	chr14:55679463..55680489-chr14:55896488..55897538,5	K562	blood:
14	chr14:55935385..55938314-chr14:55948231..55949890,2	MCF-7	breast:
15	chr14:56008500..56010380-chr14:56023755..56025494,2	MCF-7	breast:
16	chr14:55737969..55739630-chr14:55884088..55886762,2	K562	blood:
17	chr14:55736801..55739686-chr14:55896880..55899657,2	K562	blood:
18	chr14:55894393..55896757-chr14:55902007..55905006,2	MCF-7	breast:
19	chr14:55737206..55739469-chr14:55885262..55887168,2	K562	blood:
20	chr14:55935385..55938314-chr14:55948231..55949890,2	MCF-7	breast:
21	chr14:55737659..55738319-chr14:55883486..55884142,2	MCF-7	breast:
22	chr14:55930308..55932383-chr14:55934152..55936312,2	K562	blood:
23	chr14:55995958..55999191-chr14:56000283..56002949,4	MCF-7	breast:
24	chr14:56007987..56009584-chr14:56010088..56012589,2	MCF-7	breast:
25	chr14:55924018..55926617-chr14:55931310..55932885,2	K562	blood:
26	chr14:55995958..55999191-chr14:56000283..56002949,4	MCF-7	breast:
27	chr14:55936925..55938790-chr14:55938821..55940391,2	K562	blood:
28	chr14:55924018..55926617-chr14:55931310..55932885,2	K562	blood:
29	chr14:55904613..55905202-chr14:56806452..56807250,2	MCF-7	breast:
30	chr14:55913503..55916476-chr14:55916660..55918746,2	K562	blood:
31	chr14:55913599..55916759-chr14:56004997..56009666,4	MCF-7	breast:
32	chr14:55964950..55967727-chr14:56010356..56012905,2	K562	blood:
33	chr14:55946573..55948131-chr14:56047906..56049458,2	K562	blood:
34	chr14:55912628..55913132-chr14:56940932..56941697,2	MCF-7	breast:
35	chr14:55873181..55876141-chr14:55896106..55898564,2	K562	blood:
36	chr14:55889778..55893394-chr14:55894134..55896526,3	K562	blood:
37	chr14:55947632..55950014-chr14:55951455..55953042,2	K562	blood:
38	chr14:55936925..55938790-chr14:55938821..55940391,2	K562	blood:
39	chr14:55932703..55935495-chr14:55937792..55940291,2	MCF-7	breast:
40	chr14:55737932..55740165-chr14:55894081..55895808,2	MCF-7	breast:
41	chr14:55679464..55680429-chr14:55912644..55913465,2	K562	blood:
42	chr14:55905450..55907568-chr14:56045550..56047292,2	MCF-7	breast:
43	chr14:55888467..55890762-chr14:55899523..55901753,2	K562	blood:
44	chr14:55877783..55881962-chr14:55882620..55887567,10	MCF-7	breast:
45	chr14:55910738..55912957-chr14:56045973..56048447,2	MCF-7	breast:
46	chr14:55883538..55884193-chr14:55896578..55897445,2	MCF-7	breast:
47	chr14:55878684..55880292-chr14:55881926..55883661,2	K562	blood:
48	chr14:55882209..55883793-chr14:55889649..55891588,2	K562	blood:
49	chr14:55877415..55882128-chr14:55883755..55887346,6	K562	blood:
50	chr14:56017947..56022061-chr14:56043828..56047582,3	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KTN1-3	chr14:55964856-55966219	NONHSAT037010
2	lnc-TBPL2-1	chr14:56024690-56026492	XLOC_011036
3	lnc-ATG14-2	chr14:55880274-55880777	NONHSAT037009
4	lnc-TBPL2-1	chr14:55965996-55966211	ENSG00000186615.6
5	lnc-TBPL2-1	chr14:56027807-56027881	ENSG00000186615
6	lnc-TBPL2-3	chr14:56016058-56016636	NONHSAT037012
7	lnc-TBPL2-1	chr14:56027807-56027881	ENSG00000186615.6
8	lnc-TBPL2-1	chr14:56024690-56026492	ENSG00000186615
9	lnc-TBPL2-1	chr14:56027807-56027881	XLOC_011036

No data

Variant related genes	Relation type
ATG14	TF binding region
ENSG00000271484	TF binding region
TBPL2	TF binding region
RPL21P6	TF binding region
KTN1	TF binding region
RPL7AP4	TF binding region
ATG14	CpG island
ENSG00000271484	CpG island
TBPL2	CpG island
RPL21P6	CpG island
KTN1	CpG island
RPL7AP4	CpG island
ENSG00000186615	chromatin interactions
ENSG00000104164	chromatin interactions
ENSG00000126775	chromatin interactions
ENSG00000271484	chromatin interactions
ENSG00000170631	chromatin interactions
ENSG00000260170	chromatin interactions
ENSG00000126777	chromatin interactions
ENSG00000213641	chromatin interactions
ENSG00000258413	chromatin interactions
ENSG00000239199	chromatin interactions
ENSG00000178974	chromatin interactions
NLK	miRNA target sites

Extended variants
information (count: 5419 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:5419 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10138446	chr14:55879685-55879686	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377028211	chr14:55879743-55879744	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs80073159	chr14:55879749-55879750	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs567362674	chr14:55879753-55879754	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs538005978	chr14:55879782-55879783	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs184391194	chr14:55879793-55879794	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs149878026	chr14:55879815-55879816	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs11624331	chr14:55879827-55879828	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs578213386	chr14:55879865-55879866	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs76108186	chr14:55879910-55879911	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs553728686	chr14:55879914-55879915	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs115752844	chr14:55879916-55879917	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs536741748	chr14:55879935-55879936	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs144189566	chr14:55879936-55879937	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs369018552	chr14:55879939-55879940	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs540555613	chr14:55879972-55879973	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs1009647	chr14:55880047-55880048	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs556411899	chr14:55880098-55880099	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs187246853	chr14:55880130-55880131	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs375609904	chr14:55880138-55880139	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs1009648	chr14:55880169-55880170	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs565438169	chr14:55880213-55880214	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs373369131	chr14:55880215-55880216	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs543413753	chr14:55880257-55880258	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs376979599	chr14:55880258-55880259	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs143171564	chr14:55880276-55880277	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs527249297	chr14:55880318-55880319	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs1572610	chr14:55880341-55880342	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs560792302	chr14:55880360-55880361	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs191864973	chr14:55880361-55880362	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs111274844	chr14:55880374-55880375	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs368131303	chr14:55880377-55880378	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs184718162	chr14:55880379-55880380	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs371849060	chr14:55880386-55880387	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs17128452	chr14:55880440-55880441	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs374389071	chr14:55880557-55880558	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs148687359	chr14:55880588-55880589	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs547725941	chr14:55880618-55880619	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs566043342	chr14:55880632-55880633	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs142181616	chr14:55880676-55880677	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs554971985	chr14:55880688-55880689	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs570021871	chr14:55880700-55880701	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs946056	chr14:55880730-55880731	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs556387490	chr14:55880738-55880739	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs560899496	chr14:55880785-55880786	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs577950956	chr14:55880795-55880796	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs545231041	chr14:55880802-55880803	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs554060380	chr14:55880807-55880808	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs572326390	chr14:55880827-55880828	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs542223214	chr14:55880832-55880833	Weak transcription	Chromatin interactive region	2 gene(s)	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
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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	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	21633010	CNVD
Breast cancer	22032731	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Medulloblastoma	21163964	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1415 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:55878800-55879800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
2	chr14:55878800-55879800	Flanking Active TSS	Hela-S3	cervix
3	chr14:55878800-55880200	Flanking Active TSS	NHEK	skin
4	chr14:55879000-55879800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr14:55879000-55880200	Enhancers	Stomach Mucosa	stomach
6	chr14:55879200-55879800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr14:55879200-55880000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr14:55879200-55885200	Weak transcription	Right Ventricle	heart
9	chr14:55879400-55879800	Active TSS	Primary B cells from cord blood	blood
10	chr14:55879400-55879800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr14:55879400-55879800	Active TSS	Brain Anterior Caudate	brain
12	chr14:55879400-55879800	Enhancers	K562	blood
13	chr14:55879400-55880200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr14:55879400-55880400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr14:55879400-55880400	Weak transcription	Liver	Liver
16	chr14:55879400-55880600	Weak transcription	Psoas Muscle	Psoas
17	chr14:55879400-55883200	Weak transcription	Fetal Intestine Large	intestine
18	chr14:55879400-55883400	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr14:55879400-55883400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr14:55879400-55883400	Weak transcription	GM12878-XiMat	blood
21	chr14:55879600-55879800	Enhancers	Duodenum Mucosa	Duodenum
22	chr14:55879600-55879800	Enhancers	HMEC	breast
23	chr14:55879600-55880400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr14:55879600-55881400	Weak transcription	Fetal Heart	heart
25	chr14:55879600-55884000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr14:55879800-55880000	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr14:55879800-55880800	Enhancers	Hela-S3	cervix
28	chr14:55879800-55883800	Weak transcription	K562	blood
29	chr14:55879800-55885200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr14:55880000-55880600	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr14:55880200-55880600	Enhancers	NHEK	skin
32	chr14:55880400-55880600	Enhancers	Liver	Liver
33	chr14:55880600-55880800	Enhancers	Psoas Muscle	Psoas
34	chr14:55880600-55880800	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr14:55881400-55882000	Enhancers	Fetal Heart	heart
36	chr14:55882000-55883800	Weak transcription	Fetal Heart	heart
37	chr14:55883200-55884800	Enhancers	Fetal Intestine Large	intestine
38	chr14:55883200-55886800	Enhancers	Fetal Intestine Small	intestine
39	chr14:55883400-55883600	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr14:55883400-55883600	Enhancers	GM12878-XiMat	blood
41	chr14:55883400-55884000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr14:55883400-55885000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr14:55883600-55884200	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr14:55883600-55884600	Enhancers	Small Intestine	intestine
45	chr14:55883600-55885400	Enhancers	Stomach Mucosa	stomach
46	chr14:55883800-55886000	Enhancers	HUVEC	blood vessel
47	chr14:55883800-55886000	Enhancers	K562	blood
48	chr14:55883800-55886400	Enhancers	Fetal Heart	heart
49	chr14:55884200-55884400	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr14:55884400-55884800	Enhancers	Duodenum Mucosa	Duodenum

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