Variant report

Variant	nsv1038396
Chromosome Location	chr14:35714499-35788189
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1148)
CpG islands
(count:735)
Chromatin interactive
region (count:116)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1148 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35759977-35760372	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35761081-35761818	HepG2	liver:	n/a	n/a
3	ATF1	chr14:35727736-35727930	K562	blood:	n/a	n/a
4	ATF2	chr14:35723934-35724302	GM12878	blood:	n/a	n/a
5	ATF2	chr14:35761368-35761827	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr14:35754239-35755796	GM12878	blood:	n/a	n/a
7	ATF2	chr14:35761033-35761707	GM12878	blood:	n/a	n/a
8	ATF2	chr14:35754385-35755598	GM12878	blood:	n/a	n/a
9	ATF2	chr14:35761056-35761846	GM12878	blood:	n/a	n/a
10	ATF2	chr14:35756617-35757269	GM12878	blood:	n/a	n/a
11	ATF3	chr14:35761088-35761778	A549	lung:	n/a	chr14:35761499-35761508
12	BACH1	chr14:35761667-35761945	K562	blood:	n/a	n/a
13	BACH1	chr14:35761241-35761956	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr14:35762278-35762558	GM12878	blood:	n/a	chr14:35762381-35762392
15	BATF	chr14:35754462-35755192	GM12878	blood:	n/a	n/a
16	BATF	chr14:35762243-35762537	GM12878	blood:	n/a	chr14:35762381-35762392
17	BATF	chr14:35763507-35763814	GM12878	blood:	n/a	n/a
18	BATF	chr14:35723939-35724282	GM12878	blood:	n/a	n/a
19	BATF	chr14:35754332-35755553	GM12878	blood:	n/a	n/a
20	BATF	chr14:35761159-35761679	GM12878	blood:	n/a	chr14:35761412-35761420
21	BATF	chr14:35784063-35784375	GM12878	blood:	n/a	n/a
22	BATF	chr14:35761733-35762035	GM12878	blood:	n/a	n/a
23	BCL11A	chr14:35723969-35724182	GM12878	blood:	n/a	n/a
24	BCL11A	chr14:35754449-35755253	GM12878	blood:	n/a	chr14:35755115-35755124
25	BCL11A	chr14:35723979-35724282	GM12878	blood:	n/a	n/a
26	BCL11A	chr14:35754512-35755241	GM12878	blood:	n/a	chr14:35755115-35755124
27	BCL3	chr14:35770568-35770946	GM12878	blood:	n/a	n/a
28	BCL3	chr14:35761106-35762076	A549	lung:	n/a	n/a
29	BCL3	chr14:35761121-35762015	GM12878	blood:	n/a	n/a
30	BCL3	chr14:35754485-35754975	GM12878	blood:	n/a	n/a
31	BCL3	chr14:35761055-35762324	A549	lung:	n/a	n/a
32	BCLAF1	chr14:35761125-35761849	GM12878	blood:	n/a	n/a
33	BCLAF1	chr14:35723999-35724323	GM12878	blood:	n/a	n/a
34	BCLAF1	chr14:35754318-35755358	GM12878	blood:	n/a	chr14:35755115-35755124
35	BCLAF1	chr14:35754245-35755679	GM12878	blood:	n/a	chr14:35755115-35755124
36	BCLAF1	chr14:35760949-35761900	GM12878	blood:	n/a	n/a
37	BHLHE40	chr14:35723918-35724258	GM12878	blood:	n/a	n/a
38	BHLHE40	chr14:35761252-35761995	K562	blood:	n/a	n/a
39	BHLHE40	chr14:35761227-35761981	HepG2	liver:	n/a	n/a
40	BHLHE40	chr14:35727666-35727984	K562	blood:	n/a	n/a
41	BHLHE40	chr14:35754435-35755560	GM12878	blood:	n/a	n/a
42	BHLHE40	chr14:35761085-35761833	GM12878	blood:	n/a	n/a
43	BHLHE40	chr14:35756719-35757058	GM12878	blood:	n/a	n/a
44	BRCA1	chr14:35761557-35761849	GM12878	blood:	n/a	n/a
45	BRCA1	chr14:35761264-35761915	HepG2	liver:	n/a	n/a
46	BRCA1	chr14:35761203-35761723	Hela-S3	cervix:	n/a	n/a
47	CBX3	chr14:35761126-35761734	K562	blood:	n/a	n/a
48	CCNT2	chr14:35761345-35762173	K562	blood:	n/a	chr14:35761499-35761508
49	CEBPB	chr14:35766428-35766621	K562	blood:	n/a	n/a
50	CEBPB	chr14:35780228-35780708	HepG2	liver:	n/a	chr14:35780258-35780269

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35757441-35757491	HIPEpiC	eye:	n/a
2	chr14:35761197-35761247	SKMC	muscle:	n/a
3	chr14:35761689-35761739	K562	blood:	n/a
4	chr14:35757441-35757491	HIPEpiC	eye:	n/a
5	chr14:35761197-35761247	SKMC	muscle:	n/a
6	chr14:35761689-35761739	K562	blood:	n/a
7	chr14:35761689-35761739	PANC-1	pancreas:	n/a
8	chr14:35761327-35761377	AG09319	gingival:	n/a
9	chr14:35761327-35761377	HRPEpiC	eye:	n/a
10	chr14:35761197-35761247	HUVEC	blood vessel:	n/a
11	chr14:35761831-35761881	HL-60	blood:	n/a
12	chr14:35761633-35761683	Hela-S3	cervix:	n/a
13	chr14:35761165-35761215	MCF10A-Er-Src	breast:	n/a
14	chr14:35761922-35761972	Caco-2	colon:	n/a
15	chr14:35761401-35761451	HNPCEpiC	eye:	n/a
16	chr14:35786537-35786587	AG04450	lung:	fetal
17	chr14:35761551-35761601	NB4	blood:	n/a
18	chr14:35761327-35761377	GM12878	blood:	n/a
19	chr14:35761165-35761215	AG09319	gingival:	n/a
20	chr14:35761197-35761247	Hepatocyte	liver:	n/a
21	chr14:35757441-35757491	HUVEC	blood vessel:	n/a
22	chr14:35761401-35761451	SK-N-SH_RA	brain:	n/a
23	chr14:35761420-35761470	HAEpiC	amniotic membrane:	n/a
24	chr14:35761831-35761881	RPTEC	kidney:	n/a
25	chr14:35761327-35761377	HL-60	blood:	n/a
26	chr14:35761922-35761972	MCF10A-Er-Src	breast:	n/a
27	chr14:35786537-35786587	HCPEpiC	choroid plexus:	n/a
28	chr14:35761165-35761215	HEK293	kidney:	embryo
29	chr14:35761327-35761377	GM19239	blood:	n/a
30	chr14:35761689-35761739	NHDF-neo	bronchial:	n/a
31	chr14:35761689-35761739	HIPEpiC	eye:	n/a
32	chr14:35761633-35761683	NHBE	bronchial:	n/a
33	chr14:35761689-35761739	HPAEpiC	pulmonary alveolar:	n/a
34	chr14:35761551-35761601	LNCaP	prostate:	n/a
35	chr14:35786537-35786587	U87	brain:	n/a
36	chr14:35786537-35786587	HMEC	breast:	n/a
37	chr14:35761551-35761601	NHBE	bronchial:	n/a
38	chr14:35761633-35761683	MCF10A-Er-Src	breast:	n/a
39	chr14:35761633-35761683	HRPEpiC	eye:	n/a
40	chr14:35761197-35761247	ECC-1	luminal epithelium:	n/a
41	chr14:35761327-35761377	HIPEpiC	eye:	n/a
42	chr14:35761197-35761247	HRPEpiC	eye:	n/a
43	chr14:35761922-35761972	PFSK-1	brain:	n/a
44	chr14:35757441-35757491	HRCEpiC	kidney:	n/a
45	chr14:35761327-35761377	ProgFib	skin:	n/a
46	chr14:35761831-35761881	SK-N-SH_RA	brain:	n/a
47	chr14:35761689-35761739	GM19239	blood:	n/a
48	chr14:35761165-35761215	ovcar-3	ovarian:	n/a
49	chr14:35761401-35761451	GM12891	blood:	n/a
50	chr14:35761922-35761972	HEEpiC	esophagus:	n/a

(count:116 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:35753303..35755635-chr14:35756425..35758168,2	MCF-7	breast:
2	chr14:35786509..35789581-chr14:35793946..35797059,3	K562	blood:
3	chr14:35734999..35737663-chr14:35744257..35745770,2	MCF-7	breast:
4	chr14:35779341..35783565-chr14:35868727..35873122,4	K562	blood:
5	chr14:35787677..35790283-chr14:35804787..35806837,2	MCF-7	breast:
6	chr14:35780877..35783983-chr14:35784818..35787644,3	K562	blood:
7	chr14:35724152..35726170-chr14:35727566..35729303,2	K562	blood:
8	chr14:35769773..35772812-chr14:35867526..35872347,5	MCF-7	breast:
9	chr14:35769727..35774156-chr14:35872374..35875665,4	K562	blood:
10	chr14:35760099..35762622-chr14:35771893..35774075,2	K562	blood:
11	chr14:35767335..35771562-chr14:35774308..35778069,5	MCF-7	breast:
12	chr14:35745539..35747078-chr14:35765050..35766913,2	K562	blood:
13	chr14:35714388..35715903-chr14:35719645..35721798,2	MCF-7	breast:
14	chr14:35778204..35779930-chr14:35870130..35871675,2	MCF-7	breast:
15	chr14:35767852..35773242-chr14:35799435..35804534,8	MCF-7	breast:
16	chr14:35753303..35755635-chr14:35756425..35758168,2	MCF-7	breast:
17	chr14:35767249..35769056-chr14:35785281..35787174,2	MCF-7	breast:
18	chr14:35745755..35748037-chr14:35772284..35774064,2	MCF-7	breast:
19	chr14:35745539..35747078-chr14:35765050..35766913,2	K562	blood:
20	chr14:35713971..35716399-chr14:35872514..35875136,2	MCF-7	breast:
21	chr14:35711268..35715087-chr14:35870152..35873955,3	MCF-7	breast:
22	chr14:35761352..35763158-chr14:35768733..35771516,3	K562	blood:
23	chr14:35774042..35776362-chr14:35810358..35812429,2	MCF-7	breast:
24	chr14:35737913..35739770-chr14:35744109..35746101,2	K562	blood:
25	chr14:35744140..35746636-chr14:35750906..35752624,2	K562	blood:
26	chr14:35752690..35754734-chr14:35759585..35761550,2	MCF-7	breast:
27	chr12:69885101..69887587-chr14:35765375..35767747,2	MCF-7	breast:
28	chr14:35763080..35765371-chr14:35856574..35858405,2	MCF-7	breast:
29	chr14:35723222..35726200-chr14:35728941..35731510,2	MCF-7	breast:
30	chr14:35745478..35748219-chr14:35761998..35763705,2	MCF-7	breast:
31	chr14:35740819..35741319-chr8:98791814..98792317,2	MCF-7	breast:
32	chr14:35514228..35515878-chr14:35780242..35782321,2	MCF-7	breast:
33	chr14:35777000..35779255-chr14:35781790..35784953,3	K562	blood:
34	chr14:35762611..35765182-chr14:35880296..35882619,2	K562	blood:
35	chr14:35718039..35721234-chr14:35721513..35723379,3	MCF-7	breast:
36	chr14:35730609..35736672-chr14:35871862..35876542,13	MCF-7	breast:
37	chr14:35774532..35776059-chr14:35873613..35875501,2	K562	blood:
38	chr14:35726193..35729165-chr14:35868329..35870557,3	MCF-7	breast:
39	chr14:35760689..35762512-chr8:131454589..131456596,2	MCF-7	breast:
40	chr14:35757780..35767592-chr14:35866063..35878024,53	MCF-7	breast:
41	chr14:35756501..35758878-chr14:35872345..35875637,3	K562	blood:
42	chr14:35763961..35764722-chr17:56709176..56710000,2	MCF-7	breast:
43	chr14:35774559..35776882-chr14:35872342..35875113,2	K562	blood:
44	chr14:35698917..35700420-chr14:35714304..35715826,2	MCF-7	breast:
45	chr14:35753115..35758805-chr14:35759547..35762790,7	MCF-7	breast:
46	chr14:35718039..35721234-chr14:35721513..35723379,3	MCF-7	breast:
47	chr14:35722200..35727003-chr14:35872302..35875908,5	MCF-7	breast:
48	chr14:35727211..35729177-chr14:35871536..35873485,2	MCF-7	breast:
49	chr14:35022063..35024959-chr14:35748089..35750712,2	MCF-7	breast:
50	chr14:35755052..35758727-chr14:35759764..35761284,4	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-173D9.3.1-3	chr14:35760251-35760436	l_963_chr14:35700899-35775195_brain
2	lnc-RP11-173D9.3.1-3	chr14:35750644-35751518	l_963_chr14:35700899-35775195_brain
3	lnc-RP11-173D9.3.1-3	chr14:35774111-35775195	l_963_chr14:35700899-35775195_brain
4	lnc-RP11-173D9.3.1-3	chr14:35754331-35754755	l_963_chr14:35700899-35775195_brain
5	lnc-RP11-173D9.3.1-3	chr14:35751529-35754015	l_963_chr14:35700899-35775195_brain
6	lnc-PPP2R3C-4	chr14:35715251-35715712	l_962_chr14:35668508-35676460_thyroid

No data

Variant related genes	Relation type
ENSG00000265530	TF binding region
RPL9P3	TF binding region
PSMA6	TF binding region
ENSG00000265530	CpG island
RPL9P3	CpG island
PSMA6	CpG island
ENSG00000212195	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000240023	chromatin interactions
ENSG00000265530	chromatin interactions
ENSG00000151327	chromatin interactions
ENSG00000256243	chromatin interactions
ENSG00000153317	chromatin interactions
ENSG00000100902	chromatin interactions

Extended variants
information (count: 2727 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2727 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8015175	chr14:35714499-35714500	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549855945	chr14:35714536-35714537	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs570041535	chr14:35714573-35714574	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs532356188	chr14:35714597-35714598	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs552857467	chr14:35714614-35714615	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs554703444	chr14:35714637-35714638	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566206974	chr14:35714646-35714647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs535319371	chr14:35714658-35714659	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs555230374	chr14:35714668-35714669	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs568666847	chr14:35714715-35714716	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs569710014	chr14:35714731-35714732	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs4982249	chr14:35714759-35714760	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs4981281	chr14:35714820-35714821	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs148156831	chr14:35714843-35714844	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs372763930	chr14:35714847-35714848	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs377377050	chr14:35714944-35714945	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs112407490	chr14:35714956-35714957	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370704613	chr14:35715015-35715016	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs142031407	chr14:35715016-35715017	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs558512503	chr14:35715030-35715031	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs150666720	chr14:35715036-35715037	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540926344	chr14:35715062-35715063	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs560791397	chr14:35715082-35715083	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs182380422	chr14:35715148-35715149	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375558507	chr14:35715218-35715219	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75326973	chr14:35715237-35715238	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs186661327	chr14:35715258-35715259	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs563604855	chr14:35715260-35715261	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs192549214	chr14:35715301-35715302	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs140950412	chr14:35715362-35715363	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs566041792	chr14:35715369-35715370	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs553351517	chr14:35715370-35715371	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs143226954	chr14:35715393-35715394	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs7159390	chr14:35715411-35715412	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs183871369	chr14:35715445-35715446	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs565794422	chr14:35715498-35715499	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs371251614	chr14:35715571-35715572	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs556243537	chr14:35715576-35715577	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs188567856	chr14:35715586-35715587	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs375002850	chr14:35715589-35715590	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs118191550	chr14:35715605-35715606	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs558316761	chr14:35715657-35715658	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs147158460	chr14:35715692-35715693	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs35322359	chr14:35715695-35715696	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs200975165	chr14:35715704-35715705	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs540938575	chr14:35715715-35715716	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs193088762	chr14:35715720-35715721	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs28510695	chr14:35715809-35715810	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs543219214	chr14:35715870-35715871	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs563484111	chr14:35716023-35716024	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Lung adenocarcinoma	17982442	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2177 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35643400-35724000	Weak transcription	Left Ventricle	heart
2	chr14:35661000-35736400	Weak transcription	Fetal Intestine Small	intestine
3	chr14:35672000-35742200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr14:35674800-35737000	Weak transcription	Lung	lung
5	chr14:35678000-35719600	Weak transcription	Primary B cells from peripheral blood	blood
6	chr14:35680800-35729800	Weak transcription	Primary B cells from cord blood	blood
7	chr14:35681000-35729800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr14:35684600-35737000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr14:35684600-35760800	Weak transcription	HSMM	muscle
10	chr14:35686800-35735800	Weak transcription	Fetal Intestine Large	intestine
11	chr14:35687400-35716400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr14:35690200-35730000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr14:35690600-35735800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr14:35691200-35735800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr14:35693800-35717000	Weak transcription	HSMMtube	muscle
16	chr14:35694600-35726800	Weak transcription	K562	blood
17	chr14:35699200-35717200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr14:35699800-35735800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr14:35700200-35729600	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr14:35700200-35738000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr14:35700400-35716600	Weak transcription	Fetal Thymus	thymus
22	chr14:35700400-35717400	Weak transcription	Thymus	Thymus
23	chr14:35700400-35729600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr14:35700400-35735800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr14:35700600-35729200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr14:35700800-35717400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr14:35703400-35729800	Weak transcription	Liver	Liver
28	chr14:35703800-35716600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr14:35703800-35717200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr14:35703800-35729800	Weak transcription	Dnd41	blood
31	chr14:35704200-35716000	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr14:35704200-35716400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr14:35705400-35749800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:35705600-35726800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr14:35705600-35729800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr14:35705800-35735800	Weak transcription	HMEC	breast
37	chr14:35706800-35760800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr14:35708000-35729200	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr14:35708200-35720400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr14:35708600-35723800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr14:35709800-35753600	Weak transcription	Small Intestine	intestine
42	chr14:35710000-35717800	Weak transcription	HepG2	liver
43	chr14:35710200-35736000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr14:35710400-35723800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr14:35711000-35717000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr14:35711000-35737000	Weak transcription	Aorta	Aorta
47	chr14:35712400-35718000	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr14:35712400-35735800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr14:35713200-35716600	Weak transcription	GM12878-XiMat	blood
50	chr14:35713800-35714600	Strong transcription	Primary T cells from cord blood	blood

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