Variant report

Variant	nsv828473
Chromosome Location	chr19:18975130-18994875
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:737)
CpG islands
(count:732)
Chromatin interactive
region (count:65)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:737 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:18977308-18977516	K562	blood:	n/a	n/a
2	ATF2	chr19:18978833-18979057	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr19:18977382-18977631	K562	blood:	n/a	n/a
4	BACH1	chr19:18977358-18977412	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr19:18979866-18980234	GM12878	blood:	n/a	n/a
6	BCLAF1	chr19:18977263-18977782	GM12878	blood:	n/a	n/a
7	BCLAF1	chr19:18977278-18977659	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:18977341-18977678	GM12878	blood:	n/a	n/a
9	BHLHE40	chr19:18977359-18977636	K562	blood:	n/a	n/a
10	BRCA1	chr19:18977410-18977502	HepG2	liver:	n/a	n/a
11	BRCA1	chr19:18977422-18977638	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr19:18977259-18977719	K562	blood:	n/a	n/a
13	CBX3	chr19:18987609-18988117	K562	blood:	n/a	n/a
14	CBX3	chr19:18987701-18988011	K562	blood:	n/a	n/a
15	CCNT2	chr19:18977359-18977812	K562	blood:	n/a	n/a
16	CEBPB	chr19:18985426-18985441	HepG2	liver:	n/a	n/a
17	CEBPD	chr19:18982392-18982826	K562	blood:	n/a	n/a
18	CHD2	chr19:18977398-18977669	GM12878	blood:	n/a	n/a
19	CHD2	chr19:18990474-18990549	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr19:18977389-18977639	HepG2	liver:	n/a	n/a
21	CHD2	chr19:18977359-18977672	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr19:18977388-18977668	K562	blood:	n/a	n/a
23	CHD2	chr19:18977345-18977589	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr19:18990897-18991061	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr19:18977720-18977807	GM19238	blood:	n/a	n/a
26	CTCF	chr19:18977400-18977550	GM12868	blood:	n/a	n/a
27	CTCF	chr19:18977355-18977665	GM13977	blood:	n/a	n/a
28	CTCF	chr19:18977272-18977659	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr19:18977420-18977570	HCM	heart:	n/a	n/a
30	CTCF	chr19:18977420-18977570	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr19:18977217-18977261	GM12892	blood:	n/a	n/a
32	CTCF	chr19:18977420-18977570	RPTEC	kidney:	n/a	n/a
33	CTCF	chr19:18977389-18977648	MCF-7	breast:	n/a	n/a
34	CTCF	chr19:18977440-18977590	GM12878	blood:	n/a	n/a
35	CTCF	chr19:18977260-18977410	NHEK	skin:	n/a	n/a
36	CTCF	chr19:18977280-18977430	A549	lung:	n/a	n/a
37	CTCF	chr19:18977420-18977570	HCT-116	colon:	n/a	n/a
38	CTCF	chr19:18977353-18977653	Lung_OC	lung:	n/a	n/a
39	CTCF	chr19:18977400-18977550	BJ	skin:	n/a	n/a
40	CTCF	chr19:18977460-18977610	RPTEC	kidney:	n/a	n/a
41	CTCF	chr19:18977480-18977630	WI-38	lung:	n/a	n/a
42	CTCF	chr19:18979340-18979490	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr19:18977356-18977684	K562	blood:	n/a	n/a
44	CTCF	chr19:18977360-18977672	GM10248	blood:	n/a	n/a
45	CTCF	chr19:18977374-18977660	GM10266	blood:	n/a	n/a
46	CTCF	chr19:18977362-18977658	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr19:18977380-18977530	GM12872	blood:	n/a	n/a
48	CTCF	chr19:18977420-18977570	MCF-7	breast:	n/a	n/a
49	CTCF	chr19:18977420-18977570	AG04450	lung:	n/a	n/a
50	CTCF	chr19:18977420-18977570	AG09319	gingival:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18980744-18980794	HCM	heart:	n/a
2	chr19:18977405-18977455	GM12892	blood:	n/a
3	chr19:18979397-18979447	Caco-2	colon:	n/a
4	chr19:18979397-18979447	GM12891	blood:	n/a
5	chr19:18980103-18980153	NH-A	brain:	n/a
6	chr19:18977240-18977290	NHDF-neo	bronchial:	n/a
7	chr19:18980103-18980153	GM12891	blood:	n/a
8	chr19:18979364-18979414	T-47D	breast:	n/a
9	chr19:18977240-18977290	Hela-S3	cervix:	n/a
10	chr19:18977240-18977290	BJ	skin:	n/a
11	chr19:18988945-18988995	SAEC	small airway:	n/a
12	chr19:18980110-18980160	A549	lung:	n/a
13	chr19:18977814-18977864	GM12891	blood:	n/a
14	chr19:18983753-18983803	CMK	blood:	n/a
15	chr19:18983753-18983803	NB4	blood:	n/a
16	chr19:18979397-18979447	NH-A	brain:	n/a
17	chr19:18983753-18983803	RPTEC	kidney:	n/a
18	chr19:18983753-18983803	HepG2	liver:	n/a
19	chr19:18988945-18988995	HMEC	breast:	n/a
20	chr19:18979397-18979447	GM19239	blood:	n/a
21	chr19:18988945-18988995	HCT-116	colon:	n/a
22	chr19:18988945-18988995	HCPEpiC	choroid plexus:	n/a
23	chr19:18980443-18980493	H1-hESC	embryonic stem cell:	embryo
24	chr19:18977405-18977455	NHDF-neo	bronchial:	n/a
25	chr19:18980110-18980160	NB4	blood:	n/a
26	chr19:18977814-18977864	PFSK-1	brain:	n/a
27	chr19:18980103-18980153	NHDF-neo	bronchial:	n/a
28	chr19:18979397-18979447	ECC-1	luminal epithelium:	n/a
29	chr19:18979364-18979414	HRE	kidney:	n/a
30	chr19:18977405-18977455	HRE	kidney:	n/a
31	chr19:18979397-18979447	H1-hESC	embryonic stem cell:	embryo
32	chr19:18980443-18980493	HMEC	breast:	n/a
33	chr19:18977814-18977864	AG04450	lung:	fetal
34	chr19:18980744-18980794	GM19239	blood:	n/a
35	chr19:18980443-18980493	ovcar-3	ovarian:	n/a
36	chr19:18981378-18981428	HepG2	liver:	n/a
37	chr19:18979397-18979447	AG04449	skin:	fetal
38	chr19:18979397-18979447	SAEC	small airway:	n/a
39	chr19:18980103-18980153	HCPEpiC	choroid plexus:	n/a
40	chr19:18983753-18983803	GM12891	blood:	n/a
41	chr19:18988945-18988995	ProgFib	skin:	n/a
42	chr19:18988945-18988995	AG04450	lung:	fetal
43	chr19:18980110-18980160	LNCaP	prostate:	n/a
44	chr19:18980443-18980493	RPTEC	kidney:	n/a
45	chr19:18980443-18980493	SKMC	muscle:	n/a
46	chr19:18977240-18977290	RPTEC	kidney:	n/a
47	chr19:18979397-18979447	Jurkat	blood:	n/a
48	chr19:18977240-18977290	MCF10A-Er-Src	breast:	n/a
49	chr19:18981378-18981428	HMEC	breast:	n/a
50	chr19:18979364-18979414	GM12878	blood:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:18974657..18976730-chr19:18979703..18982678,3	MCF-7	breast:
2	chr19:18981107..18982659-chr19:18985530..18987661,2	MCF-7	breast:
3	chr19:18991039..18992593-chr19:18993016..18994928,3	K562	blood:
4	chr19:18959200..18960777-chr19:18978860..18981735,2	K562	blood:
5	chr19:18976801..18979191-chr19:18979322..18983754,5	MCF-7	breast:
6	chr19:18981741..18983441-chr19:18990489..18991991,2	K562	blood:
7	chr19:18705056..18705581-chr19:18976858..18977563,2	MCF-7	breast:
8	chr19:18976763..18977741-chr19:19007184..19008142,2	MCF-7	breast:
9	chr19:18973585..18975733-chr19:18989912..18992220,3	K562	blood:
10	chr19:18979537..18984476-chr19:19027015..19031327,4	K562	blood:
11	chr19:18941192..18944158-chr19:18989151..18991227,3	K562	blood:
12	chr19:18994287..18995894-chr19:19028412..19030492,2	MCF-7	breast:
13	chr19:18992536..18993055-chr19:19005219..19006075,2	MCF-7	breast:
14	chr19:18976234..18978409-chr19:19004531..19006846,2	MCF-7	breast:
15	chr19:18989338..18991884-chr19:19005552..19007379,3	MCF-7	breast:
16	chr19:18976765..18981353-chr19:18988726..18992565,5	K562	blood:
17	chr19:18984024..18987729-chr19:18988322..18991283,4	K562	blood:
18	chr19:18960784..18962475-chr19:18978438..18980131,2	K562	blood:
19	chr19:18986436..18988009-chr19:18990126..18992850,2	K562	blood:
20	chr19:18990686..18992268-chr19:19005562..19008438,2	K562	blood:
21	chr19:18975867..18978694-chr19:18984023..18986004,2	MCF-7	breast:
22	chr19:18985117..18986798-chr19:19004374..19006931,2	MCF-7	breast:
23	chr19:18989707..18992076-chr19:19050980..19053421,2	K562	blood:
24	chr19:18977071..18977951-chr19:19051666..19052520,2	K562	blood:
25	chr19:18970329..18972979-chr19:18987867..18989860,2	MCF-7	breast:
26	chr19:18990993..18992539-chr19:18993328..18994928,2	K562	blood:
27	chr19:18965125..18967769-chr19:18981345..18983154,2	K562	blood:
28	chr19:18977856..18980338-chr19:18985315..18988284,3	K562	blood:
29	chr19:18993425..18995899-chr19:19009767..19011976,2	K562	blood:
30	chr19:18965705..18968424-chr19:18988642..18991060,2	K562	blood:
31	chr19:18992522..18994119-chr19:18996300..18998941,2	K562	blood:
32	chr19:18990660..18992183-chr19:19041463..19043164,2	K562	blood:
33	chr19:18985509..18988367-chr19:18988371..18990146,2	MCF-7	breast:
34	chr19:18975867..18978694-chr19:18984023..18986004,2	MCF-7	breast:
35	chr19:18979325..18981152-chr19:19008928..19011883,2	K562	blood:
36	chr19:18984024..18987729-chr19:18988322..18991283,4	K562	blood:
37	chr19:18977096..18978227-chr19:19097259..19098244,6	K562	blood:
38	chr19:18941414..18944401-chr19:18975795..18980469,5	MCF-7	breast:
39	chr19:18963646..18965570-chr19:18977086..18979214,2	K562	blood:
40	chr19:18990686..18992579-chr19:19006938..19009413,2	K562	blood:
41	chr19:18977453..18979163-chr19:18981290..18984197,2	K562	blood:
42	chr19:18974657..18976730-chr19:18979703..18982678,3	MCF-7	breast:
43	chr19:18977079..18977984-chr19:19097300..19098157,3	MCF-7	breast:
44	chr19:18977248..18977957-chr19:19026218..19027076,2	MCF-7	breast:
45	chr19:18882176..18882866-chr19:18977411..18977945,2	MCF-7	breast:
46	chr19:18986591..18988341-chr19:19043846..19046489,2	K562	blood:
47	chr19:18977344..18982900-chr19:19025214..19031477,5	MCF-7	breast:
48	chr19:18985509..18988367-chr19:18988371..18990146,2	MCF-7	breast:
49	chr19:18977856..18980338-chr19:18985315..18988284,3	K562	blood:
50	chr19:18977453..18979163-chr19:18981290..18984197,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UPF1-2	chr19:18993896-18994185	ENSG00000269694.1
2	lnc-UPF1-1	chr19:18980844-18981428	NONHSAT062999
3	lnc-UPF1-1	chr19:18989740-18989858	NONHSAT062999
4	lnc-UPF1-2	chr19:18992489-18992881	ENSG00000269694.1

No data

Variant related genes	Relation type
ENSG00000269694	TF binding region
ENSG00000269694	CpG island
ENSG00000130283	chromatin interactions
ENSG00000223802	chromatin interactions
ENSG00000268193	chromatin interactions
ENSG00000269694	chromatin interactions
ENSG00000006016	chromatin interactions
ENSG00000105671	chromatin interactions
ENSG00000005007	chromatin interactions
ENSG00000051128	chromatin interactions
ENSG00000105669	chromatin interactions
ENSG00000268199	chromatin interactions
ENSG00000269019	chromatin interactions

Extended variants
information (count: 735 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112648440	chr19:18975136-18975137	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
2	rs560689381	chr19:18975144-18975145	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs529735638	chr19:18975170-18975171	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs551759089	chr19:18975195-18975196	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs118134406	chr19:18975201-18975202	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373341315	chr19:18975205-18975206	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532297206	chr19:18975218-18975219	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552212344	chr19:18975227-18975228	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139890559	chr19:18975238-18975239	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534197063	chr19:18975264-18975265	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184430675	chr19:18975357-18975358	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567808646	chr19:18975387-18975388	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200366136	chr19:18975403-18975404	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11666657	chr19:18975477-18975478	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10682791	chr19:18975564-18975565	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536722793	chr19:18975582-18975583	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374500506	chr19:18975625-18975626	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556750542	chr19:18975700-18975701	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs28650812	chr19:18975732-18975733	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187355815	chr19:18975749-18975750	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545536442	chr19:18975835-18975836	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs558995593	chr19:18975877-18975878	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs576499462	chr19:18975900-18975901	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572395878	chr19:18975904-18975905	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs143272545	chr19:18975962-18975963	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs538807946	chr19:18975970-18975971	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559543116	chr19:18975979-18975980	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560523571	chr19:18975981-18975982	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs529771347	chr19:18976012-18976013	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs372261124	chr19:18976057-18976058	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs144600297	chr19:18976153-18976154	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs375690310	chr19:18976154-18976155	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs371146514	chr19:18976204-18976205	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs374505878	chr19:18976251-18976252	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369028382	chr19:18976267-18976268	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs201930024	chr19:18976288-18976289	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs191847010	chr19:18976295-18976296	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs200672817	chr19:18976296-18976297	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs146682701	chr19:18976303-18976304	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs528392980	chr19:18976313-18976314	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs76650420	chr19:18976323-18976324	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs567649928	chr19:18976327-18976328	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs374827956	chr19:18976342-18976343	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs200015046	chr19:18976343-18976344	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs376681085	chr19:18976404-18976405	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs550009751	chr19:18976408-18976409	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs139317612	chr19:18976409-18976410	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570091602	chr19:18976415-18976416	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs144073786	chr19:18976433-18976434	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs146339873	chr19:18976449-18976450	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	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
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:740 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18951800-18977000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:18953200-18977600	Weak transcription	Fetal Heart	heart
3	chr19:18954800-18979800	Strong transcription	Dnd41	blood
4	chr19:18956200-18978400	Strong transcription	Thymus	Thymus
5	chr19:18956800-18975200	Strong transcription	HepG2	liver
6	chr19:18958200-18977000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr19:18958400-18977600	Strong transcription	Fetal Intestine Large	intestine
8	chr19:18958400-18979000	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr19:18958400-18979200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
10	chr19:18958400-18979400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr19:18958400-18979400	Strong transcription	Primary T cells from cord blood	blood
12	chr19:18958400-18979400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr19:18958400-18980200	Strong transcription	Sigmoid Colon	Sigmoid Colon
14	chr19:18958600-18976200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr19:18958600-18979000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
16	chr19:18958600-18979200	Strong transcription	HUES48 Cell Line	embryonic stem cell
17	chr19:18958600-18979400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr19:18958600-18979600	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr19:18958800-18979200	Strong transcription	H1 Cell Line	embryonic stem cell
20	chr19:18958800-18979200	Strong transcription	Brain Germinal Matrix	brain
21	chr19:18959000-18979000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr19:18959000-18979000	Strong transcription	Gastric	stomach
23	chr19:18959200-18979200	Strong transcription	Primary T helper cells PMA-I stimulated	--
24	chr19:18959800-18978800	Strong transcription	Fetal Brain Female	brain
25	chr19:18960000-18979400	Strong transcription	Placenta Amnion	Placenta Amnion
26	chr19:18960400-18977600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr19:18960400-18978600	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr19:18960400-18978800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr19:18960400-18979200	Strong transcription	Fetal Intestine Small	intestine
30	chr19:18960600-18977000	Strong transcription	Primary hematopoietic stem cells	blood
31	chr19:18960600-18979000	Strong transcription	H9 Cell Line	embryonic stem cell
32	chr19:18960600-18979200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr19:18960600-18979400	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr19:18960600-18979600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr19:18960600-18982600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr19:18960800-18975400	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr19:18960800-18979200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr19:18960800-18979400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr19:18960800-18979400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr19:18961000-18979200	Strong transcription	Osteobl	bone
41	chr19:18961000-18979400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr19:18961000-18979600	Strong transcription	Muscle Satellite Cultured Cells	--
43	chr19:18961000-18979600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr19:18961200-18979400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr19:18961200-18979400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr19:18961400-18979600	Strong transcription	Aorta	Aorta
47	chr19:18961600-18979400	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr19:18961600-18979800	Strong transcription	Primary neutrophils fromperipheralblood	blood
49	chr19:18961600-18979800	Strong transcription	NHLF	lung
50	chr19:18961600-18980800	Strong transcription	Pancreas	Pancrea

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