Variant report

Variant	esv1828210
Chromosome Location	chr2:74005068-74038451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1240)
CpG islands
(count:977)
Chromatin interactive
region (count:13)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1240 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:74007137-74007484	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:74007134-74007461	K562	blood:	n/a	n/a
3	ATF1	chr2:74007156-74007480	K562	blood:	n/a	n/a
4	ATF2	chr2:74007108-74007486	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:74006879-74007503	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr2:74006835-74007549	GM12878	blood:	n/a	n/a
7	BACH1	chr2:74007174-74007501	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr2:74022114-74022314	GM12878	blood:	n/a	n/a
9	BATF	chr2:74021832-74022127	GM12878	blood:	n/a	n/a
10	BATF	chr2:74011334-74011570	GM12878	blood:	n/a	n/a
11	BATF	chr2:74011141-74011519	GM12878	blood:	n/a	n/a
12	BATF	chr2:74035636-74036014	GM12878	blood:	n/a	n/a
13	BATF	chr2:74017217-74017417	GM12878	blood:	n/a	n/a
14	BATF	chr2:74012316-74012516	GM12878	blood:	n/a	n/a
15	BATF	chr2:74036598-74036799	GM12878	blood:	n/a	n/a
16	BATF	chr2:74025837-74026193	GM12878	blood:	n/a	n/a
17	BATF	chr2:74031912-74032112	GM12878	blood:	n/a	n/a
18	BATF	chr2:74016042-74016398	GM12878	blood:	n/a	n/a
19	BATF	chr2:74020939-74021295	GM12878	blood:	n/a	n/a
20	BATF	chr2:74012103-74012308	GM12878	blood:	n/a	n/a
21	BATF	chr2:74031630-74031925	GM12878	blood:	n/a	n/a
22	BATF	chr2:74016935-74017230	GM12878	blood:	n/a	n/a
23	BATF	chr2:74027012-74027212	GM12878	blood:	n/a	n/a
24	BATF	chr2:74030737-74031093	GM12878	blood:	n/a	n/a
25	BATF	chr2:74026730-74027025	GM12878	blood:	n/a	n/a
26	BCL11A	chr2:74025981-74026328	GM12878	blood:	n/a	n/a
27	BCL11A	chr2:74030881-74031228	GM12878	blood:	n/a	n/a
28	BCL11A	chr2:74035780-74036074	GM12878	blood:	n/a	n/a
29	BCL11A	chr2:74030798-74030991	GM12878	blood:	n/a	n/a
30	BCL11A	chr2:74019834-74020077	GM12878	blood:	n/a	n/a
31	BCL11A	chr2:74025898-74026091	GM12878	blood:	n/a	n/a
32	BCL11A	chr2:74012160-74012430	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:74016103-74016296	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:74021083-74021430	GM12878	blood:	n/a	n/a
35	BCL11A	chr2:74021000-74021193	GM12878	blood:	n/a	n/a
36	BCL11A	chr2:74011201-74011579	GM12878	blood:	n/a	n/a
37	BCL11A	chr2:74024732-74024975	GM12878	blood:	n/a	n/a
38	BCL11A	chr2:74016186-74016533	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:74014937-74015180	GM12878	blood:	n/a	n/a
40	BCL3	chr2:74006599-74007543	A549	lung:	n/a	chr2:74007320-74007328
41	BCLAF1	chr2:74006649-74007528	GM12878	blood:	n/a	chr2:74007320-74007328
42	BHLHE40	chr2:74024538-74024760	HepG2	liver:	n/a	n/a
43	BHLHE40	chr2:74019640-74019862	HepG2	liver:	n/a	n/a
44	BHLHE40	chr2:74006743-74007489	K562	blood:	n/a	n/a
45	BHLHE40	chr2:74014743-74014965	HepG2	liver:	n/a	n/a
46	BHLHE40	chr2:74007076-74007512	GM12878	blood:	n/a	n/a
47	BHLHE40	chr2:74029434-74029671	HepG2	liver:	n/a	n/a
48	BHLHE40	chr2:74034334-74034571	HepG2	liver:	n/a	n/a
49	BRCA1	chr2:74007079-74007455	HepG2	liver:	n/a	n/a
50	BRCA1	chr2:74007201-74007451	H1-hESC	embryonic stem cell:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:74010621-74010671	HIPEpiC	eye:	n/a
2	chr2:74010621-74010671	HIPEpiC	eye:	n/a
3	chr2:74007273-74007323	A549	lung:	n/a
4	chr2:74010621-74010671	NH-A	brain:	n/a
5	chr2:74008401-74008451	ovcar-3	ovarian:	n/a
6	chr2:74007273-74007323	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:74007064-74007114	PANC-1	pancreas:	n/a
8	chr2:74007273-74007323	GM12892	blood:	n/a
9	chr2:74008401-74008451	HL-60	blood:	n/a
10	chr2:74010621-74010671	SKMC	muscle:	n/a
11	chr2:74007273-74007323	HEK293	kidney:	embryo
12	chr2:74006961-74007011	BE2_C	brain:	n/a
13	chr2:74007420-74007470	AG04449	skin:	fetal
14	chr2:74006665-74006715	AoSMC	blood vessel:	n/a
15	chr2:74006665-74006715	NH-A	brain:	n/a
16	chr2:74007064-74007114	NH-A	brain:	n/a
17	chr2:74007265-74007315	HepG2	liver:	n/a
18	chr2:74007366-74007416	CMK	blood:	n/a
19	chr2:74007366-74007416	HCPEpiC	choroid plexus:	n/a
20	chr2:74006961-74007011	H1-hESC	embryonic stem cell:	embryo
21	chr2:74007147-74007197	A549	lung:	n/a
22	chr2:74008058-74008108	H1-hESC	embryonic stem cell:	embryo
23	chr2:74006665-74006715	HRE	kidney:	n/a
24	chr2:74007064-74007114	SAEC	small airway:	n/a
25	chr2:74010290-74010340	GM12891	blood:	n/a
26	chr2:74007273-74007323	K562	blood:	n/a
27	chr2:74007324-74007374	CMK	blood:	n/a
28	chr2:74008401-74008451	GM12878	blood:	n/a
29	chr2:74007425-74007475	AG04450	lung:	fetal
30	chr2:74010554-74010604	NH-A	brain:	n/a
31	chr2:74010396-74010446	MCF10A-Er-Src	breast:	n/a
32	chr2:74007324-74007374	NH-A	brain:	n/a
33	chr2:74007064-74007114	Hela-S3	cervix:	n/a
34	chr2:74007425-74007475	Caco-2	colon:	n/a
35	chr2:74007064-74007114	HMEC	breast:	n/a
36	chr2:74007064-74007114	A549	lung:	n/a
37	chr2:74007366-74007416	HCM	heart:	n/a
38	chr2:74008058-74008108	AG09309	skin:	n/a
39	chr2:74010621-74010671	Caco-2	colon:	n/a
40	chr2:74010554-74010604	K562	blood:	n/a
41	chr2:74007273-74007323	BE2_C	brain:	n/a
42	chr2:74008401-74008451	HCPEpiC	choroid plexus:	n/a
43	chr2:74007265-74007315	H1-hESC	embryonic stem cell:	embryo
44	chr2:74007273-74007323	AG10803	skin:	n/a
45	chr2:74007273-74007323	SK-N-SH	brain:	n/a
46	chr2:74010621-74010671	HEK293	kidney:	embryo
47	chr2:74007273-74007323	SK-N-SH_RA	brain:	n/a
48	chr2:74008058-74008108	AoSMC	blood vessel:	n/a
49	chr2:74008401-74008451	GM12891	blood:	n/a
50	chr2:74007425-74007475	NT2-D1	testis:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:74005698..74008068-chr2:74153454..74156032,2	K562	blood:
2	chr15:65588082..65588674-chr2:74006742..74007364,2	NB4	blood:
3	chr15:91259827..91260516-chr2:74006481..74007325,2	Hela-S3	cervix:
4	chr11:61128877..61129641-chr2:74006964..74007920,2	HCT-116	colon:
5	chr2:74006723..74007498-chr2:86668036..86668909,2	Hela-S3	cervix:
6	chr2:73991479..73993446-chr2:74004055..74006417,2	MCF-7	breast:
7	chr2:73983484..73986212-chr2:74007345..74009528,2	K562	blood:
8	chr2:73964502..73966089-chr2:74005861..74007990,2	MCF-7	breast:
9	chr2:74003041..74008140-chr2:74055591..74058388,4	MCF-7	breast:
10	chr2:74004444..74007409-chr2:74053786..74057952,3	K562	blood:
11	chr2:74004444..74006020-chr2:74053313..74055286,2	K562	blood:
12	chr2:74004281..74006417-chr2:74210868..74213227,2	MCF-7	breast:
13	chr2:73963771..73965386-chr2:74005336..74008448,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TPRKB-2	chr2:74007001-74007005	NONHSAT071634
2	lnc-TPRKB-2	chr2:74005428-74005503	NONHSAT071634
3	lnc-STAMBP-3	chr2:74028839-74029096	expReg_chr2_5950_+

No data

Variant related genes	Relation type
DUSP11	TF binding region
C2orf78	TF binding region
DUSP11	CpG island
C2orf78	CpG island
ENSG00000149483	chromatin interactions
ENSG00000162144	chromatin interactions
ENSG00000144034	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000115548	chromatin interactions
ENSG00000259736	chromatin interactions
ENSG00000124356	chromatin interactions
ENSG00000235499	chromatin interactions
ENSG00000114956	chromatin interactions

Extended variants
information (count: 371 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557296939	chr2:74005090-74005091	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs569186814	chr2:74005119-74005120	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146297318	chr2:74005120-74005121	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs558619375	chr2:74005145-74005146	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537812638	chr2:74005208-74005209	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs567555052	chr2:74005310-74005311	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs567302039	chr2:74005311-74005312	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs566467982	chr2:74005318-74005319	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs533914328	chr2:74005334-74005335	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs375284952	chr2:74005368-74005369	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs139537978	chr2:74005403-74005404	Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs61758449	chr2:74005423-74005424	Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs61757364	chr2:74005426-74005427	Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs540779010	chr2:74005499-74005500	Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs372146613	chr2:74005511-74005512	Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs201327566	chr2:74005514-74005515	Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs3738850	chr2:74005516-74005517	Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs200053499	chr2:74005522-74005523	Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs376099907	chr2:74005566-74005567	Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs552263243	chr2:74005594-74005595	Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs541579338	chr2:74005691-74005692	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs570842693	chr2:74005744-74005745	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs563269283	chr2:74005754-74005755	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs144471020	chr2:74005755-74005756	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs376766892	chr2:74005875-74005876	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs183909545	chr2:74005887-74005888	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs564725838	chr2:74005992-74005993	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs188346210	chr2:74006025-74006026	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs368858012	chr2:74006049-74006050	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs547183262	chr2:74006072-74006073	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs568693466	chr2:74006086-74006087	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs529368107	chr2:74006107-74006108	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs550830272	chr2:74006121-74006122	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs569225923	chr2:74006173-74006174	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs539495065	chr2:74006174-74006175	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs201818726	chr2:74006182-74006183	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs558135138	chr2:74006231-74006232	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs146638151	chr2:74006252-74006253	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs180814049	chr2:74006301-74006302	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs186305449	chr2:74006345-74006346	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs190450512	chr2:74006367-74006368	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs139832237	chr2:74006376-74006377	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs149823642	chr2:74006448-74006449	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs575302908	chr2:74006452-74006453	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs545443439	chr2:74006470-74006471	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs145834078	chr2:74006483-74006484	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs528769258	chr2:74006543-74006544	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs556623421	chr2:74006566-74006567	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs115421275	chr2:74006625-74006626	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs562252206	chr2:74006639-74006640	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73964600-74005400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:73982000-74005200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:73982200-74005200	Strong transcription	Primary T cells fromperipheralblood	blood
4	chr2:73983600-74005400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr2:73983600-74006400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr2:73983800-74006000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr2:73986200-74005200	Strong transcription	Fetal Thymus	thymus
8	chr2:73987000-74005200	Strong transcription	Fetal Muscle Leg	muscle
9	chr2:73987200-74005400	Weak transcription	Psoas Muscle	Psoas
10	chr2:73988200-74005400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr2:73988200-74005600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr2:73992600-74006000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:73992800-74005600	Weak transcription	Stomach Mucosa	stomach
14	chr2:73993400-74006200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:73993800-74005400	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr2:73994000-74005600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr2:73995600-74006000	Weak transcription	Right Ventricle	heart
18	chr2:73995600-74006200	Weak transcription	Aorta	Aorta
19	chr2:73995600-74006600	Weak transcription	Spleen	Spleen
20	chr2:73996000-74006600	Weak transcription	Gastric	stomach
21	chr2:73997000-74005600	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr2:73998600-74005600	Weak transcription	Lung	lung
23	chr2:73999400-74005400	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr2:74000400-74005400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr2:74000600-74005400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr2:74000800-74005400	Strong transcription	K562	blood
27	chr2:74002200-74005800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr2:74002400-74005400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr2:74002400-74005400	Weak transcription	Colonic Mucosa	Colon
30	chr2:74002400-74005400	Weak transcription	Colon Smooth Muscle	Colon
31	chr2:74002400-74005400	Weak transcription	Fetal Heart	heart
32	chr2:74002400-74006200	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr2:74003000-74005400	Strong transcription	Ovary	ovary
34	chr2:74003400-74005200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr2:74003400-74005400	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr2:74003400-74005400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr2:74003400-74005400	Strong transcription	Primary B cells from cord blood	blood
38	chr2:74003400-74005600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:74003800-74005400	Strong transcription	A549	lung
40	chr2:74004000-74005200	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr2:74004000-74005400	Genic enhancers	Muscle Satellite Cultured Cells	--
42	chr2:74004000-74005400	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr2:74004000-74005400	Genic enhancers	Dnd41	blood
44	chr2:74004000-74005600	Transcr. at gene 5' and 3'	NHEK	skin
45	chr2:74004200-74005400	Weak transcription	Fetal Brain Male	brain
46	chr2:74004200-74005400	Genic enhancers	HSMM	muscle
47	chr2:74004200-74005400	Genic enhancers	NHDF-Ad	bronchial
48	chr2:74004200-74005600	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr2:74004400-74005200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr2:74004400-74005200	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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