Variant report

Variant	esv3417521
Chromosome Location	chr19:45149062-45152260
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:61)
CpG islands
(count:184)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:61 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:45150122-45150322	K562	blood:	n/a	n/a
2	BCL3	chr19:45151741-45152588	A549	lung:	n/a	n/a
3	CEBPB	chr19:45150056-45150190	HepG2	liver:	n/a	n/a
4	CEBPB	chr19:45150010-45150195	IMR90	lung:	n/a	n/a
5	CEBPB	chr19:45149995-45150209	A549	lung:	n/a	n/a
6	CEBPB	chr19:45151899-45152104	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr19:45150055-45150165	K562	blood:	n/a	n/a
8	CREB1	chr19:45150637-45150966	A549	lung:	n/a	n/a
9	FOS	chr19:45152016-45152342	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr19:45151898-45152422	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr19:45152093-45152182	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr19:45151892-45152465	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr19:45152037-45152533	HUVEC	blood vessel:	n/a	n/a
14	MAFK	chr19:45151924-45152056	Hela-S3	cervix:	n/a	n/a
15	MAFK	chr19:45150151-45150251	K562	blood:	n/a	n/a
16	MAFK	chr19:45150069-45150358	H1-hESC	embryonic stem cell:	n/a	n/a
17	MXI1	chr19:45151572-45152309	IMR90	lung:	n/a	n/a
18	MYC	chr19:45151898-45152149	MCF10A-Er-Src	breast:	n/a	n/a
19	MYC	chr19:45150734-45150840	MCF-7	breast:	n/a	n/a
20	POLR2A	chr19:45150195-45150327	ProgFib	skin:	n/a	n/a
21	POLR2A	chr19:45151797-45151816	HUVEC	blood vessel:	n/a	n/a
22	POLR2A	chr19:45150434-45150848	A549	lung:	n/a	n/a
23	POLR2A	chr19:45151538-45152701	HUVEC	blood vessel:	n/a	n/a
24	POLR2A	chr19:45151038-45152171	HUVEC	blood vessel:	n/a	n/a
25	POLR2A	chr19:45152091-45152107	HepG2	liver:	n/a	n/a
26	POLR2A	chr19:45151179-45151369	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr19:45151083-45151595	HepG2	liver:	n/a	n/a
28	POLR2A	chr19:45150410-45150717	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr19:45150448-45150649	A549	lung:	n/a	n/a
30	POLR2A	chr19:45150171-45150964	HUVEC	blood vessel:	n/a	n/a
31	POLR2A	chr19:45151603-45151639	HepG2	liver:	n/a	n/a
32	POLR2A	chr19:45148928-45149781	HUVEC	blood vessel:	n/a	n/a
33	POLR2A	chr19:45150403-45150843	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr19:45150448-45150687	A549	lung:	n/a	n/a
35	POLR2A	chr19:45150610-45150850	A549	lung:	n/a	n/a
36	POLR2A	chr19:45148677-45149830	HUVEC	blood vessel:	n/a	n/a
37	POLR2A	chr19:45149195-45149425	HUVEC	blood vessel:	n/a	n/a
38	POLR2A	chr19:45150419-45150875	A549	lung:	n/a	n/a
39	POLR2A	chr19:45152121-45152494	HepG2	liver:	n/a	n/a
40	POLR2A	chr19:45150688-45150835	A549	lung:	n/a	n/a
41	POLR2A	chr19:45151581-45151612	HUVEC	blood vessel:	n/a	n/a
42	POLR2A	chr19:45151915-45152071	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr19:45152097-45152643	HUVEC	blood vessel:	n/a	n/a
44	POLR2A	chr19:45150315-45150986	HUVEC	blood vessel:	n/a	n/a
45	POLR2A	chr19:45151057-45151531	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr19:45151659-45151764	HUVEC	blood vessel:	n/a	n/a
47	POLR2A	chr19:45149300-45149548	HepG2	liver:	n/a	n/a
48	POLR2A	chr19:45150651-45150681	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr19:45151914-45152075	HepG2	liver:	n/a	n/a
50	POLR2A	chr19:45150701-45150739	MCF-7	breast:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:45150725-45150775	T-47D	breast:	n/a
2	chr19:45150725-45150775	T-47D	breast:	n/a
3	chr19:45150725-45150775	HIPEpiC	eye:	n/a
4	chr19:45150513-45150563	Caco-2	colon:	n/a
5	chr19:45150513-45150563	SK-N-MC	brain:	n/a
6	chr19:45150725-45150775	HCF	heart:	n/a
7	chr19:45150513-45150563	AoSMC	blood vessel:	n/a
8	chr19:45150513-45150563	NHDF-neo	bronchial:	n/a
9	chr19:45150552-45150602	RPTEC	kidney:	n/a
10	chr19:45150725-45150775	GM12891	blood:	n/a
11	chr19:45150725-45150775	PANC-1	pancreas:	n/a
12	chr19:45150552-45150602	NHBE	bronchial:	n/a
13	chr19:45150552-45150602	NHDF-neo	bronchial:	n/a
14	chr19:45150725-45150775	NB4	blood:	n/a
15	chr19:45150513-45150563	IMR90	lung:	fetal
16	chr19:45150513-45150563	Hela-S3	cervix:	n/a
17	chr19:45150552-45150602	HNPCEpiC	eye:	n/a
18	chr19:45150725-45150775	HCT-116	colon:	n/a
19	chr19:45150552-45150602	ECC-1	luminal epithelium:	n/a
20	chr19:45150725-45150775	HCM	heart:	n/a
21	chr19:45150725-45150775	BJ	skin:	n/a
22	chr19:45150552-45150602	SK-N-MC	brain:	n/a
23	chr19:45150552-45150602	U87	brain:	n/a
24	chr19:45150725-45150775	AG09309	skin:	n/a
25	chr19:45150552-45150602	A549	lung:	n/a
26	chr19:45150725-45150775	NH-A	brain:	n/a
27	chr19:45150725-45150775	Jurkat	blood:	n/a
28	chr19:45150513-45150563	NB4	blood:	n/a
29	chr19:45150513-45150563	HCT-116	colon:	n/a
30	chr19:45150513-45150563	HRE	kidney:	n/a
31	chr19:45150552-45150602	AG04449	skin:	fetal
32	chr19:45150552-45150602	GM19239	blood:	n/a
33	chr19:45150513-45150563	HepG2	liver:	n/a
34	chr19:45150552-45150602	AG09309	skin:	n/a
35	chr19:45150725-45150775	U87	brain:	n/a
36	chr19:45150513-45150563	HAEpiC	amniotic membrane:	n/a
37	chr19:45150725-45150775	PrEC	prostate:	n/a
38	chr19:45150552-45150602	H1-hESC	embryonic stem cell:	embryo
39	chr19:45150513-45150563	CMK	blood:	n/a
40	chr19:45150513-45150563	HCPEpiC	choroid plexus:	n/a
41	chr19:45150513-45150563	HEEpiC	esophagus:	n/a
42	chr19:45150513-45150563	GM12891	blood:	n/a
43	chr19:45150725-45150775	SK-N-MC	brain:	n/a
44	chr19:45150513-45150563	HUVEC	blood vessel:	n/a
45	chr19:45150725-45150775	A549	lung:	n/a
46	chr19:45150552-45150602	NT2-D1	testis:	n/a
47	chr19:45150513-45150563	HCF	heart:	n/a
48	chr19:45150725-45150775	ovcar-3	ovarian:	n/a
49	chr19:45150552-45150602	MCF10A-Er-Src	breast:	n/a
50	chr19:45150725-45150775	MCF10A-Er-Src	breast:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:45147094..45148808-chr19:45149467..45152344,2	MCF-7	breast:
2	chr19:45150946..45153817-chr19:45251773..45254167,2	MCF-7	breast:
3	chr19:45149403..45152148-chr19:45154474..45156366,2	K562	blood:
4	chr19:45149710..45152694-chr19:45240654..45242344,2	MCF-7	breast:
5	chr19:45148126..45150959-chr19:45153045..45156023,2	K562	blood:

No data

Variant related genes	Relation type
PVR	TF binding region
PVR	CpG island
ENSG00000069399	chromatin interactions
ENSG00000073008	chromatin interactions

Extended variants
information (count: 134 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:134 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62119283	chr19:45149113-45149114	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557935621	chr19:45149122-45149123	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs528181151	chr19:45149143-45149144	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs28483039	chr19:45149235-45149236	Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs540346847	chr19:45149238-45149239	Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs564854942	chr19:45149267-45149268	Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs573930109	chr19:45149320-45149321	Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs185083472	chr19:45149409-45149410	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs561826276	chr19:45149415-45149416	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs567960630	chr19:45149478-45149479	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs148971121	chr19:45149489-45149490	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs186790448	chr19:45149491-45149492	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs56261258	chr19:45149613-45149614	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs114228201	chr19:45149648-45149649	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs113508538	chr19:45149657-45149658	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs138350865	chr19:45149716-45149717	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs116443653	chr19:45149727-45149728	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs143920016	chr19:45149738-45149739	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs528865414	chr19:45149739-45149740	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs36106668	chr19:45149750-45149751	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs28718535	chr19:45149768-45149769	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs569163387	chr19:45149829-45149830	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs148363175	chr19:45149840-45149841	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs57616673	chr19:45149886-45149887	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs148460573	chr19:45149887-45149888	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs144668770	chr19:45149888-45149889	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs141564432	chr19:45149905-45149906	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563957641	chr19:45149935-45149936	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs150914051	chr19:45149936-45149937	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs28559829	chr19:45149958-45149959	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs141499364	chr19:45149970-45149971	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs574121022	chr19:45149984-45149985	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs203703	chr19:45149993-45149994	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs139154918	chr19:45150002-45150003	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs536454797	chr19:45150058-45150059	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs575569189	chr19:45150084-45150085	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs648195	chr19:45150092-45150093	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs77038858	chr19:45150094-45150095	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs74172482	chr19:45150098-45150099	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs648203	chr19:45150100-45150101	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs10717624	chr19:45150118-45150119	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs648256	chr19:45150139-45150140	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs67538065	chr19:45150140-45150141	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs113976564	chr19:45150149-45150150	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs372869046	chr19:45150161-45150162	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs35644025	chr19:45150208-45150209	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs5828214	chr19:45150218-45150219	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs398101236	chr19:45150220-45150221	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562162407	chr19:45150234-45150235	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs536901972	chr19:45150311-45150312	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	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
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Adrenocortical carcinoma	18281524	CNVD

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:45146600-45149200	Active TSS	Osteobl	bone
2	chr19:45146800-45149200	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr19:45146800-45149200	Active TSS	A549	lung
4	chr19:45146800-45149200	Active TSS	Hela-S3	cervix
5	chr19:45147000-45149200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr19:45147000-45149200	Active TSS	Fetal Intestine Large	intestine
7	chr19:45147200-45149200	Active TSS	NHLF	lung
8	chr19:45148000-45149800	Weak transcription	Fetal Heart	heart
9	chr19:45148000-45150600	Weak transcription	Esophagus	oesophagus
10	chr19:45148000-45150600	Weak transcription	Gastric	stomach
11	chr19:45148000-45150600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr19:45148000-45151400	Weak transcription	GM12878-XiMat	blood
13	chr19:45148000-45151600	Weak transcription	Aorta	Aorta
14	chr19:45148000-45152800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr19:45148000-45153200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr19:45148000-45153200	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr19:45148000-45153200	Weak transcription	Small Intestine	intestine
18	chr19:45148000-45165000	Weak transcription	K562	blood
19	chr19:45148200-45149200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr19:45148200-45149200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr19:45148200-45149200	Enhancers	Fetal Muscle Leg	muscle
22	chr19:45148200-45149200	Weak transcription	HepG2	liver
23	chr19:45148200-45149400	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr19:45148200-45149400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr19:45148200-45150200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr19:45148200-45150400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr19:45148200-45150400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr19:45148200-45150400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr19:45148200-45150400	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr19:45148200-45150400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr19:45148200-45150400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr19:45148200-45150400	Weak transcription	Fetal Muscle Trunk	muscle
33	chr19:45148200-45150400	Weak transcription	Lung	lung
34	chr19:45148200-45150400	Weak transcription	Ovary	ovary
35	chr19:45148200-45150400	Weak transcription	HSMM	muscle
36	chr19:45148200-45150600	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr19:45148200-45150600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr19:45148200-45150600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr19:45148200-45150600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr19:45148200-45150600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr19:45148200-45150600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr19:45148200-45150600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr19:45148200-45150600	Weak transcription	Brain Angular Gyrus	brain
44	chr19:45148200-45150600	Weak transcription	Brain Germinal Matrix	brain
45	chr19:45148200-45150600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr19:45148200-45150600	Weak transcription	Colonic Mucosa	Colon
47	chr19:45148200-45150600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr19:45148200-45150600	Weak transcription	Stomach Smooth Muscle	stomach
49	chr19:45148200-45150600	Weak transcription	Spleen	Spleen
50	chr19:45148200-45150600	Weak transcription	Monocytes-CD14+_RO01746	blood

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