Variant report

Variant	nsv833793
Chromosome Location	chr19:24269209-24424795
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:962)
CpG islands
(count:488)
Chromatin interactive
region (count:24)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:962 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:24324328-24324741	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:24322919-24323218	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:24269634-24269992	K562	blood:	n/a	n/a
4	ARID3A	chr19:24277965-24278090	HepG2	liver:	n/a	n/a
5	ATF1	chr19:24269666-24270047	K562	blood:	n/a	n/a
6	ATF2	chr19:24269632-24269953	GM12878	blood:	n/a	n/a
7	BACH1	chr19:24310904-24310905	K562	blood:	n/a	n/a
8	BACH1	chr19:24390853-24391219	K562	blood:	n/a	n/a
9	BACH1	chr19:24270502-24270514	K562	blood:	n/a	n/a
10	BACH1	chr19:24400119-24400496	K562	blood:	n/a	n/a
11	BCL3	chr19:24269688-24270514	A549	lung:	n/a	n/a
12	BCL3	chr19:24269800-24270463	A549	lung:	n/a	n/a
13	BCL3	chr19:24269789-24270455	GM12878	blood:	n/a	n/a
14	BCLAF1	chr19:24269773-24270344	GM12878	blood:	n/a	n/a
15	BHLHE40	chr19:24400205-24400377	HepG2	liver:	n/a	n/a
16	BHLHE40	chr19:24390853-24391220	K562	blood:	n/a	n/a
17	BHLHE40	chr19:24397872-24397882	K562	blood:	n/a	n/a
18	BHLHE40	chr19:24269821-24270044	K562	blood:	n/a	n/a
19	BHLHE40	chr19:24322904-24323240	HepG2	liver:	n/a	n/a
20	BHLHE40	chr19:24400119-24400495	K562	blood:	n/a	n/a
21	BRCA1	chr19:24390859-24391172	GM12878	blood:	n/a	n/a
22	BRCA1	chr19:24397698-24397890	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr19:24397746-24398044	GM12878	blood:	n/a	n/a
24	CBX3	chr19:24269975-24270349	K562	blood:	n/a	n/a
25	CEBPB	chr19:24375530-24375933	MCF-7	breast:	n/a	chr19:24375690-24375701
26	CEBPB	chr19:24375584-24376150	HepG2	liver:	n/a	chr19:24375690-24375701
27	CEBPB	chr19:24365606-24365797	HepG2	liver:	n/a	chr19:24365638-24365649
28	CEBPB	chr19:24367671-24368348	A549	lung:	n/a	n/a
29	CEBPB	chr19:24367145-24367873	HepG2	liver:	n/a	n/a
30	CEBPB	chr19:24322977-24323148	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:24269746-24270087	K562	blood:	n/a	n/a
32	CEBPB	chr19:24400120-24400495	K562	blood:	n/a	n/a
33	CEBPB	chr19:24322260-24322436	A549	lung:	n/a	chr19:24322338-24322349
34	CEBPB	chr19:24269736-24270125	K562	blood:	n/a	n/a
35	CEBPB	chr19:24371886-24371892	A549	lung:	n/a	n/a
36	CEBPB	chr19:24368573-24368768	A549	lung:	n/a	n/a
37	CEBPB	chr19:24375510-24376151	A549	lung:	n/a	chr19:24375690-24375701
38	CEBPB	chr19:24322923-24323248	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr19:24378203-24378471	HepG2	liver:	n/a	chr19:24378316-24378327 chr19:24378318-24378329
40	CEBPB	chr19:24269699-24270116	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr19:24364763-24364998	HepG2	liver:	n/a	n/a
42	CEBPB	chr19:24378188-24378497	A549	lung:	n/a	chr19:24378316-24378327 chr19:24378318-24378329
43	CEBPB	chr19:24322853-24323265	MCF-7	breast:	n/a	n/a
44	CEBPB	chr19:24365491-24365804	A549	lung:	n/a	chr19:24365638-24365649
45	CEBPB	chr19:24322902-24323255	HepG2	liver:	n/a	n/a
46	CEBPB	chr19:24372590-24372792	K562	blood:	n/a	n/a
47	CEBPB	chr19:24322212-24322412	HepG2	liver:	n/a	chr19:24322338-24322349
48	CEBPB	chr19:24322970-24323229	K562	blood:	n/a	n/a
49	CEBPB	chr19:24372510-24373055	A549	lung:	n/a	n/a
50	CEBPB	chr19:24367168-24367446	IMR90	lung:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:24345179-24345229	AG09319	gingival:	n/a
2	chr19:24269890-24269940	HAEpiC	amniotic membrane:	n/a
3	chr19:24269968-24270018	SK-N-MC	brain:	n/a
4	chr19:24345179-24345229	MCF-7	breast:	n/a
5	chr19:24311037-24311087	HUVEC	blood vessel:	n/a
6	chr19:24270073-24270123	ECC-1	luminal epithelium:	n/a
7	chr19:24270468-24270518	HCM	heart:	n/a
8	chr19:24270073-24270123	SAEC	small airway:	n/a
9	chr19:24270007-24270057	BE2_C	brain:	n/a
10	chr19:24345179-24345229	SKMC	muscle:	n/a
11	chr19:24269968-24270018	HMEC	breast:	n/a
12	chr19:24269975-24270025	SK-N-SH	brain:	n/a
13	chr19:24270007-24270057	Hela-S3	cervix:	n/a
14	chr19:24269890-24269940	HRCEpiC	kidney:	n/a
15	chr19:24270007-24270057	ovcar-3	ovarian:	n/a
16	chr19:24269890-24269940	ECC-1	luminal epithelium:	n/a
17	chr19:24270073-24270123	AG09319	gingival:	n/a
18	chr19:24311037-24311087	HCT-116	colon:	n/a
19	chr19:24345179-24345229	AG09309	skin:	n/a
20	chr19:24345179-24345229	Jurkat	blood:	n/a
21	chr19:24270007-24270057	PANC-1	pancreas:	n/a
22	chr19:24270468-24270518	HL-60	blood:	n/a
23	chr19:24270468-24270518	HCPEpiC	choroid plexus:	n/a
24	chr19:24270073-24270123	SK-N-SH_RA	brain:	n/a
25	chr19:24311037-24311087	AG10803	skin:	n/a
26	chr19:24270007-24270057	Caco-2	colon:	n/a
27	chr19:24269975-24270025	AoSMC	blood vessel:	n/a
28	chr19:24311037-24311087	NHDF-neo	bronchial:	n/a
29	chr19:24270007-24270057	HAEpiC	amniotic membrane:	n/a
30	chr19:24270073-24270123	NH-A	brain:	n/a
31	chr19:24269890-24269940	HEK293	kidney:	embryo
32	chr19:24270468-24270518	SK-N-SH	brain:	n/a
33	chr19:24270468-24270518	HEK293	kidney:	embryo
34	chr19:24311037-24311087	AG04450	lung:	fetal
35	chr19:24270007-24270057	AG09319	gingival:	n/a
36	chr19:24270468-24270518	CMK	blood:	n/a
37	chr19:24270073-24270123	NHDF-neo	bronchial:	n/a
38	chr19:24270073-24270123	NB4	blood:	n/a
39	chr19:24270468-24270518	NHBE	bronchial:	n/a
40	chr19:24270468-24270518	HCF	heart:	n/a
41	chr19:24270073-24270123	PrEC	prostate:	n/a
42	chr19:24269890-24269940	SAEC	small airway:	n/a
43	chr19:24269890-24269940	Hepatocyte	liver:	n/a
44	chr19:24269890-24269940	HMEC	breast:	n/a
45	chr19:24311037-24311087	Hela-S3	cervix:	n/a
46	chr19:24269975-24270025	SKMC	muscle:	n/a
47	chr19:24311037-24311087	AG04449	skin:	fetal
48	chr19:24269975-24270025	ECC-1	luminal epithelium:	n/a
49	chr19:24270007-24270057	NB4	blood:	n/a
50	chr19:24270007-24270057	NHBE	bronchial:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:24278737..24281409-chr19:24289986..24291875,2	K562	blood:
2	chr19:24269869..24271737-chr19:24281128..24282836,2	MCF-7	breast:
3	chr19:24273653..24275947-chr19:24283763..24286065,2	K562	blood:
4	chr19:23299713..23300295-chr19:24269911..24270643,3	Hela-S3	cervix:
5	chr19:24309408..24311273-chr19:24321594..24323328,2	MCF-7	breast:
6	chr19:24273653..24275947-chr19:24283763..24286065,2	K562	blood:
7	chr19:24269481..24270366-chr8:29940201..29940789,2	NB4	blood:
8	chr19:24266915..24268889-chr19:24271542..24273329,2	MCF-7	breast:
9	chr19:24269905..24270406-chr19:47616316..47616816,2	Hela-S3	cervix:
10	chr19:24269855..24272221-chr19:24274367..24277034,2	K562	blood:
11	chr19:24269735..24271787-chr19:24289462..24293668,3	MCF-7	breast:
12	chr19:24216051..24217841-chr19:24269020..24271219,2	MCF-7	breast:
13	chr19:24269801..24271346-chr19:24277835..24280239,2	K562	blood:
14	chr19:24269806..24272597-chr19:24274053..24277432,4	K562	blood:
15	chr19:24269191..24271795-chr19:24273714..24276847,3	MCF-7	breast:
16	chr19:24214690..24216513-chr19:24269521..24272423,2	K562	blood:
17	chr19:24269939..24272519-chr19:24310930..24313655,2	K562	blood:
18	chr19:24269211..24271747-chr19:24290443..24293090,2	K562	blood:
19	chr19:24278737..24281409-chr19:24289986..24291875,2	K562	blood:
20	chr19:24216492..24217018-chr19:24270056..24270717,2	Hela-S3	cervix:
21	chr19:24269869..24271737-chr19:24281128..24282836,2	MCF-7	breast:
22	chr19:24309408..24311273-chr19:24321594..24323328,2	MCF-7	breast:
23	chr19:24214637..24216513-chr19:24268176..24271021,2	K562	blood:
24	chr19:24097706..24100500-chr19:24267529..24270344,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF681-6	chr19:24344995-24346249	NONHSAT063959
2	lnc-ZNF681-5	chr19:24281227-24281782	NONHSAT063956
3	lnc-ZNF726-3	chr19:24286988-24290154	NONHSAT063958

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF254	hsa-miR-155-5p	chr19:24312469-24312491
2	ZNF254	hsa-miR-155-5p	chr19:24311154-24311177

Variant related genes	Relation type
HAVCR1P1	TF binding region
ENSG00000268058	TF binding region
ZNF254	TF binding region
HAVCR1P1	CpG island
ENSG00000268058	CpG island
ZNF254	CpG island
ENSG00000268058	chromatin interactions
ENSG00000268362	chromatin interactions
ENSG00000142230	chromatin interactions
ENSG00000213967	chromatin interactions
ENSG00000272256	chromatin interactions
ENSG00000183850	chromatin interactions
ENSG00000133872	chromatin interactions
ENSG00000213096	chromatin interactions

Extended variants
information (count: 7025 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:7025 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571859547	chr19:24269233-24269234	Weak transcription Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs559002859	chr19:24269257-24269258	Weak transcription Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs75203133	chr19:24269303-24269304	Weak transcription Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs544593805	chr19:24269341-24269342	Weak transcription Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs563607829	chr19:24269346-24269347	Weak transcription Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs139816717	chr19:24269349-24269350	Weak transcription Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs542503118	chr19:24269389-24269390	Weak transcription Strong transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs181876827	chr19:24269416-24269417	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs374276650	chr19:24269459-24269460	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs561087399	chr19:24269468-24269469	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs528180311	chr19:24269478-24269479	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs142992112	chr19:24269482-24269483	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs534343526	chr19:24269498-24269499	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs7257370	chr19:24269499-24269500	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs185011904	chr19:24269623-24269624	Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs550147504	chr19:24269655-24269656	Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs569492812	chr19:24269706-24269707	Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs78310782	chr19:24269710-24269711	Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs548500876	chr19:24269733-24269734	Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs573647563	chr19:24269735-24269736	Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs373954567	chr19:24269743-24269744	Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs567013444	chr19:24269809-24269810	Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs139931205	chr19:24270040-24270041	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs559067247	chr19:24270065-24270066	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs369338295	chr19:24270067-24270068	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs570940837	chr19:24270076-24270077	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs376526337	chr19:24270087-24270088	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs372542320	chr19:24270091-24270092	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs375542329	chr19:24270102-24270103	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs117766010	chr19:24270119-24270120	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs145474972	chr19:24270129-24270130	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs187884426	chr19:24270165-24270166	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs373535067	chr19:24270177-24270178	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs542264497	chr19:24270184-24270185	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs542863053	chr19:24270197-24270198	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs368210871	chr19:24270210-24270211	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs554481854	chr19:24270228-24270229	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs370123802	chr19:24270240-24270241	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs151071668	chr19:24270242-24270243	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs564674463	chr19:24270304-24270305	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs532071149	chr19:24270347-24270348	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs372224098	chr19:24270350-24270351	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs542280443	chr19:24270359-24270360	Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs530336816	chr19:24270419-24270420	Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs548830347	chr19:24270426-24270427	Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs566974056	chr19:24270432-24270433	Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs113731529	chr19:24270468-24270469	Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs527920883	chr19:24270484-24270485	Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs552793266	chr19:24270486-24270487	Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs571004267	chr19:24270523-24270524	Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:43)

Disease	PMID	Source
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2384 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:24236200-24269400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr19:24239800-24269600	Weak transcription	Small Intestine	intestine
3	chr19:24242000-24269800	Weak transcription	Stomach Mucosa	stomach
4	chr19:24242400-24269400	Weak transcription	Fetal Thymus	thymus
5	chr19:24243600-24269600	Weak transcription	NHLF	lung
6	chr19:24244200-24269400	Weak transcription	HUVEC	blood vessel
7	chr19:24245200-24270000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr19:24251000-24269400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr19:24251200-24269600	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr19:24251200-24269800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr19:24251400-24269600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr19:24251600-24269600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr19:24251600-24269600	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr19:24251800-24269400	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr19:24255800-24269600	Weak transcription	Osteobl	bone
16	chr19:24256200-24269600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr19:24256200-24269600	Weak transcription	HSMM	muscle
18	chr19:24256600-24269600	Weak transcription	NHDF-Ad	bronchial
19	chr19:24256600-24269800	Weak transcription	Colon Smooth Muscle	Colon
20	chr19:24256800-24269600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr19:24256800-24270000	Weak transcription	Fetal Brain Male	brain
22	chr19:24257000-24269400	Weak transcription	Brain Hippocampus Middle	brain
23	chr19:24257000-24269400	Weak transcription	Pancreas	Pancrea
24	chr19:24257000-24269600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr19:24257000-24269800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr19:24257000-24270000	Weak transcription	Aorta	Aorta
27	chr19:24257200-24269400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr19:24257200-24269800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr19:24257400-24269400	Weak transcription	Thymus	Thymus
30	chr19:24257400-24269600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr19:24257400-24269800	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr19:24257400-24269800	Weak transcription	Ovary	ovary
33	chr19:24257400-24270000	Weak transcription	Gastric	stomach
34	chr19:24257600-24269400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr19:24257600-24269400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr19:24257600-24269400	Weak transcription	Adipose Nuclei	Adipose
37	chr19:24257600-24269400	Weak transcription	Duodenum Mucosa	Duodenum
38	chr19:24257600-24269400	Weak transcription	Lung	lung
39	chr19:24257600-24269400	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr19:24257600-24269400	Weak transcription	Hela-S3	cervix
41	chr19:24257600-24269600	Weak transcription	HMEC	breast
42	chr19:24257800-24269600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr19:24257800-24269800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr19:24258000-24269600	Weak transcription	Fetal Intestine Large	intestine
45	chr19:24258000-24269800	Weak transcription	Brain Anterior Caudate	brain
46	chr19:24258000-24269800	Weak transcription	Fetal Kidney	kidney
47	chr19:24258200-24269400	Weak transcription	Primary T cells from cord blood	blood
48	chr19:24258200-24269600	Weak transcription	Fetal Brain Female	brain
49	chr19:24258200-24269600	Weak transcription	Stomach Smooth Muscle	stomach
50	chr19:24258200-24269600	Weak transcription	Monocytes-CD14+_RO01746	blood

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