Variant report

Variant	nsv904143
Chromosome Location	chr15:43276345-43414673
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:912)
CpG islands
(count:793)
Chromatin interactive
region (count:87)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:912 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:43397648-43398773	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:43398251-43398659	K562	blood:	n/a	n/a
3	ARID3A	chr15:43388218-43388264	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:43397368-43397887	K562	blood:	n/a	n/a
5	ARID3A	chr15:43386853-43387247	K562	blood:	n/a	n/a
6	ARID3A	chr15:43414527-43414775	K562	blood:	n/a	n/a
7	ARID3A	chr15:43387449-43387830	K562	blood:	n/a	n/a
8	ATF1	chr15:43386875-43387161	K562	blood:	n/a	n/a
9	ATF1	chr15:43387460-43387755	K562	blood:	n/a	n/a
10	ATF1	chr15:43398151-43398528	K562	blood:	n/a	n/a
11	ATF2	chr15:43397682-43398573	GM12878	blood:	n/a	n/a
12	ATF2	chr15:43397991-43398451	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr15:43378722-43379113	GM12878	blood:	n/a	n/a
14	ATF3	chr15:43398117-43398486	HepG2	liver:	n/a	n/a
15	ATF3	chr15:43398097-43398441	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr15:43398126-43398472	K562	blood:	n/a	n/a
17	BACH1	chr15:43397593-43397889	K562	blood:	n/a	n/a
18	BACH1	chr15:43300070-43300234	K562	blood:	n/a	n/a
19	BATF	chr15:43317398-43317616	GM12878	blood:	n/a	chr15:43317546-43317557
20	BATF	chr15:43359977-43360156	GM12878	blood:	n/a	n/a
21	BATF	chr15:43388203-43388457	GM12878	blood:	n/a	n/a
22	BATF	chr15:43317425-43317631	GM12878	blood:	n/a	chr15:43317546-43317557
23	BATF	chr15:43359931-43360160	GM12878	blood:	n/a	n/a
24	BATF	chr15:43378759-43379062	GM12878	blood:	n/a	n/a
25	BATF	chr15:43378535-43379134	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:43368163-43368349	GM12878	blood:	n/a	n/a
27	BCLAF1	chr15:43397997-43398637	GM12878	blood:	n/a	n/a
28	BCLAF1	chr15:43397552-43398686	GM12878	blood:	n/a	n/a
29	BHLHE40	chr15:43382873-43382875	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:43397656-43398507	K562	blood:	n/a	n/a
31	BHLHE40	chr15:43397805-43398668	GM12878	blood:	n/a	n/a
32	BRCA1	chr15:43396304-43396666	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr15:43398031-43398634	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr15:43399955-43400320	K562	blood:	n/a	n/a
35	CBX3	chr15:43397993-43398585	K562	blood:	n/a	n/a
36	CCNT2	chr15:43398119-43398840	K562	blood:	n/a	n/a
37	CCNT2	chr15:43386885-43387085	K562	blood:	n/a	n/a
38	CEBPB	chr15:43276857-43276941	A549	lung:	n/a	n/a
39	CEBPB	chr15:43414590-43415017	IMR90	lung:	n/a	chr15:43414834-43414845 chr15:43414833-43414846
40	CEBPB	chr15:43286806-43287085	IMR90	lung:	n/a	n/a
41	CEBPB	chr15:43414659-43414977	Hela-S3	cervix:	n/a	chr15:43414834-43414845 chr15:43414833-43414846
42	CEBPB	chr15:43391438-43391791	K562	blood:	n/a	chr15:43391596-43391609 chr15:43391598-43391607 chr15:43391596-43391607 chr15:43391598-43391607 chr15:43391598-43391607
43	CEBPB	chr15:43391418-43391790	IMR90	lung:	n/a	chr15:43391596-43391609 chr15:43391598-43391607 chr15:43391596-43391607 chr15:43391598-43391607 chr15:43391598-43391607
44	CEBPB	chr15:43360346-43360517	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr15:43414614-43414973	K562	blood:	n/a	chr15:43414834-43414845 chr15:43414833-43414846
46	CEBPB	chr15:43374726-43375076	IMR90	lung:	n/a	chr15:43374901-43374912
47	CEBPB	chr15:43339371-43339585	HepG2	liver:	n/a	chr15:43339452-43339463
48	CEBPB	chr15:43391414-43391809	K562	blood:	n/a	chr15:43391596-43391609 chr15:43391598-43391607 chr15:43391596-43391607 chr15:43391598-43391607 chr15:43391598-43391607
49	CEBPB	chr15:43397293-43397795	K562	blood:	n/a	n/a
50	CEBPB	chr15:43391463-43391780	H1-hESC	embryonic stem cell:	n/a	chr15:43391596-43391609 chr15:43391598-43391607 chr15:43391596-43391607 chr15:43391598-43391607 chr15:43391598-43391607

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43398365-43398415	HCF	heart:	n/a
2	chr15:43398101-43398151	HAEpiC	amniotic membrane:	n/a
3	chr15:43398365-43398415	AG09319	gingival:	n/a
4	chr15:43398302-43398352	T-47D	breast:	n/a
5	chr15:43297145-43297195	HAEpiC	amniotic membrane:	n/a
6	chr15:43399625-43399675	HIPEpiC	eye:	n/a
7	chr15:43399625-43399675	HPAEpiC	pulmonary alveolar:	n/a
8	chr15:43387679-43387729	HepG2	liver:	n/a
9	chr15:43398435-43398485	U87	brain:	n/a
10	chr15:43398581-43398631	Caco-2	colon:	n/a
11	chr15:43398346-43398396	MCF-7	breast:	n/a
12	chr15:43387679-43387729	AG04450	lung:	fetal
13	chr15:43398365-43398415	ovcar-3	ovarian:	n/a
14	chr15:43398270-43398320	Hepatocyte	liver:	n/a
15	chr15:43399625-43399675	HMEC	breast:	n/a
16	chr15:43398173-43398223	K562	blood:	n/a
17	chr15:43297145-43297195	SKMC	muscle:	n/a
18	chr15:43399625-43399675	AG09309	skin:	n/a
19	chr15:43398101-43398151	ovcar-3	ovarian:	n/a
20	chr15:43398365-43398415	SAEC	small airway:	n/a
21	chr15:43398338-43398388	Hela-S3	cervix:	n/a
22	chr15:43398365-43398415	PFSK-1	brain:	n/a
23	chr15:43398435-43398485	SK-N-SH	brain:	n/a
24	chr15:43297145-43297195	HCF	heart:	n/a
25	chr15:43398338-43398388	NHDF-neo	bronchial:	n/a
26	chr15:43399625-43399675	BE2_C	brain:	n/a
27	chr15:43399625-43399675	K562	blood:	n/a
28	chr15:43297145-43297195	AG04450	lung:	fetal
29	chr15:43398173-43398223	MCF10A-Er-Src	breast:	n/a
30	chr15:43398173-43398223	HepG2	liver:	n/a
31	chr15:43398270-43398320	GM12892	blood:	n/a
32	chr15:43398270-43398320	HCT-116	colon:	n/a
33	chr15:43398435-43398485	NT2-D1	testis:	n/a
34	chr15:43398826-43398876	PFSK-1	brain:	n/a
35	chr15:43398365-43398415	NH-A	brain:	n/a
36	chr15:43398435-43398485	AG04450	lung:	fetal
37	chr15:43398435-43398485	HEEpiC	esophagus:	n/a
38	chr15:43398101-43398151	PFSK-1	brain:	n/a
39	chr15:43387679-43387729	GM06990	blood:	n/a
40	chr15:43297145-43297195	Hepatocyte	liver:	n/a
41	chr15:43398338-43398388	GM12891	blood:	n/a
42	chr15:43398270-43398320	HEK293	kidney:	embryo
43	chr15:43398581-43398631	T-47D	breast:	n/a
44	chr15:43297145-43297195	HEK293	kidney:	embryo
45	chr15:43398270-43398320	HPAEpiC	pulmonary alveolar:	n/a
46	chr15:43398826-43398876	HNPCEpiC	eye:	n/a
47	chr15:43399625-43399675	Caco-2	colon:	n/a
48	chr15:43398365-43398415	BE2_C	brain:	n/a
49	chr15:43398173-43398223	ProgFib	skin:	n/a
50	chr15:43398101-43398151	SK-N-SH	brain:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:43388815..43390634-chr15:43391926..43394516,2	K562	blood:
2	chr15:43397983..43399514-chr15:43421683..43423629,2	K562	blood:
3	chr15:43325373..43328292-chr15:43334536..43336063,2	K562	blood:
4	chr15:43346995..43348533-chr15:43350036..43351977,2	K562	blood:
5	chr15:43414412..43417295-chr15:43437126..43440064,2	K562	blood:
6	chr15:43380004..43382980-chr15:43386018..43388996,5	K562	blood:
7	chr15:43398288..43398793-chr19:2050787..2051312,2	NB4	blood:
8	chr15:43383221..43388610-chr15:43389653..43393489,4	K562	blood:
9	chr15:43380437..43382771-chr15:43396547..43398200,2	K562	blood:
10	chr15:43368519..43371458-chr15:43478469..43480102,2	K562	blood:
11	chr15:43326792..43329076-chr15:43333977..43336036,2	K562	blood:
12	chr15:43337776..43340565-chr15:43396734..43398497,2	K562	blood:
13	chr15:43396979..43399675-chr15:43425245..43427228,2	MCF-7	breast:
14	chr15:43397628..43400398-chr15:43414771..43418048,4	MCF-7	breast:
15	chr1:145382743..145383443-chr15:43397728..43398383,2	Hela-S3	cervix:
16	chr15:43411630..43413526-chr15:43413981..43416399,3	K562	blood:
17	chr15:43283254..43285115-chr15:43286974..43289576,2	K562	blood:
18	chr15:43277125..43279751-chr15:43281410..43283345,2	K562	blood:
19	chr15:43392059..43394941-chr15:43396768..43399559,3	K562	blood:
20	chr15:43278687..43281856-chr15:43291013..43293652,3	K562	blood:
21	chr15:43398177..43400764-chr15:43410402..43412286,2	MCF-7	breast:
22	chr15:43395932..43399418-chr15:43425897..43428585,4	K562	blood:
23	chr15:43356222..43358202-chr15:43362263..43364733,2	MCF-7	breast:
24	chr15:43390055..43391666-chr15:43396242..43397765,2	MCF-7	breast:
25	chr15:43397447..43400554-chr15:43409058..43413462,5	K562	blood:
26	chr15:43278687..43281856-chr15:43291013..43293652,3	K562	blood:
27	chr15:43414543..43416437-chr15:43476770..43479731,2	K562	blood:
28	chr15:43402075..43404958-chr15:43407508..43410226,3	K562	blood:
29	chr15:43389228..43394941-chr15:43395904..43400327,7	K562	blood:
30	chr15:43356222..43358202-chr15:43362263..43364733,2	MCF-7	breast:
31	chr15:43385287..43387946-chr15:43396303..43398701,2	K562	blood:
32	chr15:43397688..43398582-chr8:41909391..41910087,2	Hela-S3	cervix:
33	chr15:43394707..43396213-chr15:43401061..43403612,2	K562	blood:
34	chr15:43383221..43385892-chr15:43389653..43392510,3	K562	blood:
35	chr15:43327543..43330321-chr15:43334414..43337253,2	MCF-7	breast:
36	chr15:43282136..43285343-chr15:43291276..43293438,3	K562	blood:
37	chr15:43397638..43400095-chr15:43409049..43412270,4	K562	blood:
38	chr15:43380437..43382771-chr15:43396547..43398200,2	K562	blood:
39	chr15:43282136..43285343-chr15:43291276..43293438,3	K562	blood:
40	chr15:43388815..43390634-chr15:43391926..43394516,2	K562	blood:
41	chr15:43392028..43394734-chr15:43397894..43400122,2	MCF-7	breast:
42	chr15:43398098..43400146-chr15:43707936..43709689,2	K562	blood:
43	chr15:43283018..43285343-chr15:43291276..43293330,3	K562	blood:
44	chr15:43354633..43356543-chr15:43359222..43361458,2	K562	blood:
45	chr15:43326792..43329076-chr15:43333977..43336036,2	K562	blood:
46	chr15:43383221..43388610-chr15:43389653..43393489,4	K562	blood:
47	chr15:43360121..43362777-chr15:43399326..43401275,2	MCF-7	breast:
48	chr15:43285221..43287358-chr15:43299885..43302016,2	K562	blood:
49	chr15:43397794..43398667-chr16:1755602..1756312,2	Hela-S3	cervix:
50	chr15:43318855..43320896-chr15:43323404..43325415,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPB42-2	chr15:43398666-43398735	NONHSAT042053
2	lnc-EPB42-2	chr15:43398423-43398493	NONHSAT042053
3	lnc-EPB42-2	chr15:43401117-43401168	NONHSAT042053

No data

Variant related genes	Relation type
UBR1	TF binding region
RPS3AP47	TF binding region
TMEM62	TF binding region
UBR1	CpG island
RPS3AP47	CpG island
TMEM62	CpG island
ENSG00000201558	chromatin interactions
ENSG00000168803	chromatin interactions
ENSG00000168806	chromatin interactions
ENSG00000205871	chromatin interactions
ENSG00000159459	chromatin interactions
ENSG00000166946	chromatin interactions
ENSG00000261687	chromatin interactions
ENSG00000099875	chromatin interactions
ENSG00000137842	chromatin interactions
ENSG00000083168	chromatin interactions
ENSG00000138834	chromatin interactions
ENSG00000260928	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000067369	chromatin interactions

Extended variants
information (count: 4773 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:4773 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28715873	chr15:43276345-43276346	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78008459	chr15:43276376-43276377	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182809813	chr15:43276431-43276432	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563835257	chr15:43276440-43276441	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142867747	chr15:43276486-43276487	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186783980	chr15:43276525-43276526	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566228355	chr15:43276550-43276551	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs377117380	chr15:43276601-43276602	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528801995	chr15:43276641-43276642	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552141974	chr15:43276694-43276695	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567190001	chr15:43276696-43276697	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368244963	chr15:43276736-43276737	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527816052	chr15:43276826-43276827	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111232789	chr15:43276897-43276898	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574081520	chr15:43276909-43276910	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372847741	chr15:43276935-43276936	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs74570754	chr15:43276936-43276937	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73413054	chr15:43276971-43276972	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs544759203	chr15:43276996-43276997	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556667262	chr15:43277001-43277002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371516734	chr15:43277004-43277005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567370762	chr15:43277030-43277031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535938292	chr15:43277033-43277034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537704321	chr15:43277037-43277038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375269406	chr15:43277038-43277039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201614880	chr15:43277039-43277040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369507336	chr15:43277040-43277041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200918479	chr15:43277042-43277043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112219112	chr15:43277055-43277056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370655651	chr15:43277068-43277069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141869423	chr15:43277094-43277095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372661227	chr15:43277125-43277126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374903655	chr15:43277156-43277157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558470901	chr15:43277161-43277162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369047276	chr15:43277166-43277167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575429784	chr15:43277179-43277180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201091488	chr15:43277183-43277184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563503122	chr15:43277265-43277266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529413819	chr15:43277304-43277305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543101062	chr15:43277330-43277331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191535749	chr15:43277420-43277421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534469250	chr15:43277421-43277422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140983589	chr15:43277423-43277424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138077192	chr15:43277438-43277439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201128611	chr15:43277531-43277532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141472166	chr15:43277578-43277579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531075768	chr15:43277581-43277582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185622823	chr15:43277610-43277611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545591012	chr15:43277619-43277620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs199566110	chr15:43277620-43277621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Cancer	20164919	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Intellectual disability	21811512	CNVD

Chromatin state (count:4246 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43232000-43362800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:43244000-43276400	Weak transcription	Psoas Muscle	Psoas
3	chr15:43248000-43320600	Weak transcription	Stomach Mucosa	stomach
4	chr15:43249600-43283200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr15:43252400-43298400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr15:43252800-43295800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr15:43255200-43278800	Weak transcription	Esophagus	oesophagus
8	chr15:43258800-43277600	Weak transcription	Colonic Mucosa	Colon
9	chr15:43261000-43277000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr15:43262400-43276800	Strong transcription	Primary B cells from peripheral blood	blood
11	chr15:43262600-43292000	Strong transcription	Fetal Muscle Trunk	muscle
12	chr15:43263400-43284000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr15:43264000-43283000	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr15:43265800-43277200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr15:43265800-43278800	Weak transcription	NHLF	lung
16	chr15:43265800-43283600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr15:43265800-43296800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr15:43266000-43292200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr15:43266400-43294800	Weak transcription	Pancreas	Pancrea
20	chr15:43266800-43286800	Weak transcription	A549	lung
21	chr15:43267000-43276400	Weak transcription	Brain Substantia Nigra	brain
22	chr15:43267200-43278600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr15:43267200-43278800	Weak transcription	Gastric	stomach
24	chr15:43267200-43278800	Weak transcription	Spleen	Spleen
25	chr15:43267200-43323000	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr15:43268200-43278800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr15:43269000-43277600	Weak transcription	Right Ventricle	heart
28	chr15:43269000-43296800	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr15:43269000-43298400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr15:43269000-43312800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr15:43269200-43397200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr15:43269400-43278800	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr15:43269600-43278400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr15:43269600-43278600	Weak transcription	Brain Germinal Matrix	brain
35	chr15:43269600-43279000	Weak transcription	Aorta	Aorta
36	chr15:43269600-43300200	Weak transcription	Rectal Smooth Muscle	rectum
37	chr15:43269800-43276400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr15:43269800-43279000	Weak transcription	Lung	lung
39	chr15:43269800-43314800	Weak transcription	Fetal Brain Male	brain
40	chr15:43269800-43335200	Weak transcription	Small Intestine	intestine
41	chr15:43270400-43278200	Weak transcription	Fetal Heart	heart
42	chr15:43270400-43300600	Weak transcription	K562	blood
43	chr15:43270800-43281400	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr15:43271400-43286200	Strong transcription	Fetal Muscle Leg	muscle
45	chr15:43271800-43277600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr15:43271800-43283800	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr15:43272000-43282200	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr15:43272000-43286600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr15:43272200-43277200	Strong transcription	Adipose Nuclei	Adipose
50	chr15:43272200-43282800	Strong transcription	Placenta	Placenta

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