Variant report

Variant	nsv873374
Chromosome Location	chr1:241975147-242097624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1935)
CpG islands
(count:1345)
Chromatin interactive
region (count:171)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1935 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:241992816-241992894	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:242097404-242097718	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:242010326-242012219	K562	blood:	n/a	n/a
4	ARID3A	chr1:242059728-242060038	K562	blood:	n/a	n/a
5	ARID3A	chr1:242059677-242060049	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:242004667-242004671	K562	blood:	n/a	n/a
7	ARID3A	chr1:241998023-241998408	K562	blood:	n/a	n/a
8	ARID3A	chr1:241996568-241997431	K562	blood:	n/a	n/a
9	ARID3A	chr1:242010974-242011703	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:242079607-242079807	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:242087569-242087783	HepG2	liver:	n/a	n/a
12	ATF1	chr1:242010197-242012251	K562	blood:	n/a	n/a
13	ATF1	chr1:241998147-241998402	K562	blood:	n/a	n/a
14	ATF1	chr1:242058327-242058480	K562	blood:	n/a	n/a
15	ATF1	chr1:242059628-242059975	K562	blood:	n/a	n/a
16	ATF2	chr1:242097401-242097898	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr1:242010933-242011644	GM12878	blood:	n/a	chr1:242011450-242011461
18	ATF2	chr1:242010898-242011694	GM12878	blood:	n/a	chr1:242011450-242011461
19	ATF2	chr1:242011039-242011638	H1-hESC	embryonic stem cell:	n/a	chr1:242011450-242011461
20	ATF2	chr1:242097445-242097923	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr1:242010887-242011878	H1-hESC	embryonic stem cell:	n/a	chr1:242011450-242011461
22	ATF3	chr1:242010936-242011373	GM12878	blood:	n/a	n/a
23	ATF3	chr1:242010908-242011404	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr1:242010961-242011660	K562	blood:	n/a	chr1:242011449-242011462 chr1:242011449-242011460 chr1:242011448-242011463 chr1:242011452-242011459 chr1:242011449-242011462 chr1:242011452-242011460 chr1:242011450-242011461 chr1:242011449-242011459 chr1:242011450-242011463
25	ATF3	chr1:242010940-242011667	A549	lung:	n/a	chr1:242011449-242011462 chr1:242011449-242011460 chr1:242011448-242011463 chr1:242011452-242011459 chr1:242011449-242011462 chr1:242011452-242011460 chr1:242011450-242011461 chr1:242011449-242011459 chr1:242011450-242011463
26	ATF3	chr1:242011029-242011390	K562	blood:	n/a	n/a
27	ATF3	chr1:242010776-242011665	K562	blood:	n/a	chr1:242011449-242011462 chr1:242011449-242011460 chr1:242011448-242011463 chr1:242011452-242011459 chr1:242011449-242011462 chr1:242011452-242011460 chr1:242011450-242011461 chr1:242011449-242011459 chr1:242011450-242011463
28	BACH1	chr1:242010553-242011829	K562	blood:	n/a	n/a
29	BACH1	chr1:241997054-241997314	K562	blood:	n/a	n/a
30	BACH1	chr1:242009793-242010186	K562	blood:	n/a	n/a
31	BACH1	chr1:242011361-242011674	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr1:242044778-242045267	K562	blood:	n/a	n/a
33	BACH1	chr1:242003527-242003565	K562	blood:	n/a	n/a
34	BATF	chr1:242058396-242058614	GM12878	blood:	n/a	chr1:242058494-242058505
35	BATF	chr1:242002153-242002378	GM12878	blood:	n/a	chr1:242002248-242002259
36	BATF	chr1:242058355-242058646	GM12878	blood:	n/a	chr1:242058494-242058505
37	BCL3	chr1:241984714-241984948	GM12878	blood:	n/a	chr1:241984849-241984858
38	BCL3	chr1:242010896-242011832	A549	lung:	n/a	n/a
39	BCL3	chr1:242011006-242011704	A549	lung:	n/a	n/a
40	BCLAF1	chr1:242010932-242011704	K562	blood:	n/a	n/a
41	BCLAF1	chr1:242010948-242011805	GM12878	blood:	n/a	n/a
42	BHLHE40	chr1:242020408-242020638	GM12878	blood:	n/a	n/a
43	BHLHE40	chr1:242010326-242012591	K562	blood:	n/a	chr1:242011324-242011340
44	BHLHE40	chr1:242069373-242069700	K562	blood:	n/a	n/a
45	BHLHE40	chr1:241998213-241998241	HepG2	liver:	n/a	n/a
46	BHLHE40	chr1:241982978-241982979	K562	blood:	n/a	n/a
47	BHLHE40	chr1:242009738-242010104	K562	blood:	n/a	n/a
48	BHLHE40	chr1:241995475-241995775	K562	blood:	n/a	n/a
49	BHLHE40	chr1:241976056-241976164	K562	blood:	n/a	n/a
50	BRCA1	chr1:242011020-242011458	HepG2	liver:	n/a	n/a

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:242052841-242052891	HRPEpiC	eye:	n/a
2	chr1:242052841-242052891	BJ	skin:	n/a
3	chr1:241992272-241992322	HAEpiC	amniotic membrane:	n/a
4	chr1:242052841-242052891	HRPEpiC	eye:	n/a
5	chr1:242052841-242052891	BJ	skin:	n/a
6	chr1:241992272-241992322	HAEpiC	amniotic membrane:	n/a
7	chr1:242011057-242011107	T-47D	breast:	n/a
8	chr1:242030232-242030282	IMR90	lung:	fetal
9	chr1:242011587-242011637	HNPCEpiC	eye:	n/a
10	chr1:242044107-242044157	PFSK-1	brain:	n/a
11	chr1:242011587-242011637	GM12878	blood:	n/a
12	chr1:241981543-241981593	HRE	kidney:	n/a
13	chr1:242011162-242011212	SK-N-MC	brain:	n/a
14	chr1:241981543-241981593	AG09319	gingival:	n/a
15	chr1:242011898-242011948	PrEC	prostate:	n/a
16	chr1:242011587-242011637	HCT-116	colon:	n/a
17	chr1:242011382-242011432	BJ	skin:	n/a
18	chr1:242012049-242012099	AG09319	gingival:	n/a
19	chr1:242011396-242011446	HEEpiC	esophagus:	n/a
20	chr1:242011104-242011154	HepG2	liver:	n/a
21	chr1:242002464-242002514	PrEC	prostate:	n/a
22	chr1:242030232-242030282	HCM	heart:	n/a
23	chr1:242011587-242011637	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:242011743-242011793	PANC-1	pancreas:	n/a
25	chr1:242011396-242011446	HCPEpiC	choroid plexus:	n/a
26	chr1:242011587-242011637	GM12891	blood:	n/a
27	chr1:242012049-242012099	NH-A	brain:	n/a
28	chr1:242011057-242011107	Hepatocyte	liver:	n/a
29	chr1:242002464-242002514	AG10803	skin:	n/a
30	chr1:242010305-242010355	A549	lung:	n/a
31	chr1:241992272-241992322	HNPCEpiC	eye:	n/a
32	chr1:242011057-242011107	HCT-116	colon:	n/a
33	chr1:242052841-242052891	GM06990	blood:	n/a
34	chr1:242030232-242030282	Jurkat	blood:	n/a
35	chr1:242011162-242011212	HRE	kidney:	n/a
36	chr1:242011898-242011948	GM12892	blood:	n/a
37	chr1:242044107-242044157	SK-N-SH_RA	brain:	n/a
38	chr1:242011513-242011563	HEK293	kidney:	embryo
39	chr1:242011513-242011563	GM12892	blood:	n/a
40	chr1:242010305-242010355	HEEpiC	esophagus:	n/a
41	chr1:242052841-242052891	BE2_C	brain:	n/a
42	chr1:242012044-242012094	AoSMC	blood vessel:	n/a
43	chr1:242011382-242011432	SAEC	small airway:	n/a
44	chr1:241981543-241981593	HCM	heart:	n/a
45	chr1:242044107-242044157	HCT-116	colon:	n/a
46	chr1:242011898-242011948	SK-N-SH_RA	brain:	n/a
47	chr1:242002464-242002514	HEEpiC	esophagus:	n/a
48	chr1:242010305-242010355	AG10803	skin:	n/a
49	chr1:241992272-241992322	IMR90	lung:	fetal
50	chr1:242002464-242002514	HepG2	liver:	n/a

(count:171 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:241789486..241791019-chr1:241984145..241986452,2	K562	blood:
2	chr1:242011208..242011713-chr5:40678933..40679886,2	Hela-S3	cervix:
3	chr1:241977423..241979473-chr1:242003229..242004895,2	K562	blood:
4	chr1:241910812..241913267-chr1:242003665..242006640,2	K562	blood:
5	chr1:241801875..241803572-chr1:242018952..242021381,2	K562	blood:
6	chr1:241773131..241776077-chr1:241996871..241998567,3	K562	blood:
7	chr1:242066650..242069303-chr1:242074434..242076420,2	K562	blood:
8	chr1:242024439..242027110-chr1:242027352..242028876,2	MCF-7	breast:
9	chr1:241774151..241775699-chr1:242004811..242007727,2	K562	blood:
10	chr1:241913661..241915313-chr1:242019528..242022307,2	K562	blood:
11	chr1:242041021..242042827-chr1:242044286..242047076,2	K562	blood:
12	chr1:242006223..242009236-chr1:242009443..242011752,4	MCF-7	breast:
13	chr1:242063761..242065381-chr1:242152078..242153652,2	MCF-7	breast:
14	chr1:242034800..242036646-chr1:242037118..242039497,2	MCF-7	breast:
15	chr1:241966386..241967889-chr1:241975945..241977942,2	MCF-7	breast:
16	chr1:241768247..241768861-chr1:241997787..241998355,2	K562	blood:
17	chr1:241793249..241795099-chr1:241983001..241985384,2	K562	blood:
18	chr1:241972003..241974042-chr1:241981060..241983771,2	K562	blood:
19	chr1:242010595..242011154-chr22:36781613..36782133,2	Hela-S3	cervix:
20	chr1:241680902..241684541-chr1:242009942..242012706,4	K562	blood:
21	chr1:242019796..242021724-chr1:242031300..242034090,2	K562	blood:
22	chr1:242022992..242027176-chr1:242044979..242047845,3	K562	blood:
23	chr1:242059480..242060334-chr1:242148747..242149804,4	K562	blood:
24	chr1:242059371..242060335-chr1:242161395..242162231,4	MCF-7	breast:
25	chr1:241788295..241791166-chr1:242001121..242003916,2	K562	blood:
26	chr1:241799658..241805161-chr1:242010004..242013743,14	K562	blood:
27	chr1:241980403..241982619-chr1:241984891..241986981,2	K562	blood:
28	chr1:242034731..242037217-chr1:242045770..242047901,2	K562	blood:
29	chr1:241694248..241695217-chr1:241997845..241998483,2	K562	blood:
30	chr1:241997002..241998699-chr1:242000011..242001897,2	K562	blood:
31	chr1:241994559..242000368-chr1:242001953..242006186,6	K562	blood:
32	chr1:242009986..242012755-chr1:245025033..245026742,2	K562	blood:
33	chr1:242034731..242037217-chr1:242045770..242047901,2	K562	blood:
34	chr1:242034639..242037217-chr1:242050358..242052283,2	K562	blood:
35	chr1:241773131..241774988-chr1:241996795..241998567,2	K562	blood:
36	chr1:241801647..241805071-chr1:241978967..241982321,4	MCF-7	breast:
37	chr1:242022063..242023665-chr1:242035192..242037679,2	K562	blood:
38	chr1:242024439..242027110-chr1:242027352..242028876,2	MCF-7	breast:
39	chr1:242060961..242063036-chr1:242175225..242177165,2	K562	blood:
40	chr1:241785761..241788632-chr1:241996400..241998922,2	MCF-7	breast:
41	chr1:242059953..242061763-chr1:242068532..242070106,2	K562	blood:
42	chr1:242026543..242030439-chr1:242041190..242044966,5	K562	blood:
43	chr1:241980697..241983127-chr1:241987544..241989477,2	K562	blood:
44	chr1:241787070..241789418-chr1:242025979..242027637,2	K562	blood:
45	chr1:241814475..241817056-chr1:242011284..242013767,3	K562	blood:
46	chr1:241871855..241872397-chr1:241980123..241980733,2	MCF-7	breast:
47	chr1:241964225..241965074-chr1:241980473..241981109,2	MCF-7	breast:
48	chr1:242037775..242040488-chr1:242043413..242045224,4	K562	blood:
49	chr1:241871925..241872739-chr1:241980132..241980807,2	MCF-7	breast:
50	chr1:241986331..241988478-chr1:241989134..241991324,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXO1-5	chr1:242079425-242079845	NONHSAT010558
2	lnc-EXO1-1	chr1:242072240-242072365	XLOC_000638
3	lnc-EXO1-1	chr1:242072153-242072836	NONHSAT010556
4	lnc-EXO1-1	chr1:242074676-242075035	XLOC_000638
5	lnc-EXO1-1	chr1:242061356-242061975	NONHSAT010556
6	lnc-EXO1-1	chr1:242071423-242071511	NONHSAT010556

No data

Variant related genes	Relation type
EXO1	TF binding region
ENSG00000229022	TF binding region
ENSG00000235990	TF binding region
EXO1	CpG island
ENSG00000229022	CpG island
ENSG00000235990	CpG island
ENSG00000054277	chromatin interactions
ENSG00000174371	chromatin interactions
ENSG00000157456	chromatin interactions
ENSG00000091483	chromatin interactions
ENSG00000140598	chromatin interactions
ENSG00000153187	chromatin interactions
ENSG00000140682	chromatin interactions
ENSG00000134884	chromatin interactions
ENSG00000117009	chromatin interactions
ENSG00000093000	chromatin interactions
ENSG00000162843	chromatin interactions
ENSG00000171522	chromatin interactions
ENSG00000229022	chromatin interactions
ENSG00000203668	chromatin interactions
CCNE1	miRNA target sites

Extended variants
information (count: 5500 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:5500 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4658798	chr1:241975147-241975148	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs367841025	chr1:241975166-241975167	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563438296	chr1:241975223-241975224	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs529123517	chr1:241975308-241975309	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs185930455	chr1:241975344-241975345	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs566174789	chr1:241975353-241975354	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534847458	chr1:241975401-241975402	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs78470071	chr1:241975428-241975429	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs547732220	chr1:241975449-241975450	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs571581720	chr1:241975451-241975452	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs564886577	chr1:241975470-241975471	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs537335773	chr1:241975520-241975521	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs148395197	chr1:241975548-241975549	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547519880	chr1:241975588-241975589	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs35068715	chr1:241975638-241975639	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs34090405	chr1:241975654-241975655	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs370674533	chr1:241975655-241975656	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs10665235	chr1:241975656-241975657	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536454493	chr1:241975669-241975670	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs190791274	chr1:241975672-241975673	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs183303802	chr1:241975739-241975740	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540796648	chr1:241975746-241975747	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs564093291	chr1:241975759-241975760	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs142568549	chr1:241975790-241975791	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs188917282	chr1:241975795-241975796	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs563579117	chr1:241975803-241975804	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529060070	chr1:241975807-241975808	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575570149	chr1:241975817-241975818	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549153601	chr1:241975818-241975819	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs368361928	chr1:241975828-241975829	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs559333698	chr1:241975884-241975885	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs1137508	chr1:241975900-241975901	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs528566128	chr1:241975910-241975911	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs551619548	chr1:241975921-241975922	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs35207344	chr1:241975925-241975926	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs571276042	chr1:241975939-241975940	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs537048508	chr1:241975947-241975948	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs193269430	chr1:241975956-241975957	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs567607178	chr1:241976006-241976007	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs116207147	chr1:241976053-241976054	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs553508893	chr1:241976102-241976103	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561407595	chr1:241976162-241976163	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs114536806	chr1:241976205-241976206	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs534680234	chr1:241976206-241976207	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs150968359	chr1:241976220-241976221	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577664753	chr1:241976223-241976224	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs118043249	chr1:241976242-241976243	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs368233869	chr1:241976270-241976271	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573981875	chr1:241976297-241976298	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs368971547	chr1:241976320-241976321	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Glioblastoma	18772890	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Brain overgrowth syndrome	24179207	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1429 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:241973400-241978600	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr1:241974000-241975200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr1:241974800-241975800	Weak transcription	K562	blood
4	chr1:241975200-241976600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr1:241975800-241976600	Enhancers	K562	blood
6	chr1:241976600-241977200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr1:241976600-241977400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr1:241976600-241981000	Weak transcription	Aorta	Aorta
9	chr1:241976600-241981400	Weak transcription	K562	blood
10	chr1:241976800-241977000	Enhancers	Hela-S3	cervix
11	chr1:241977000-241977200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr1:241977000-241977200	Enhancers	Muscle Satellite Cultured Cells	--
13	chr1:241977000-241977400	Flanking Active TSS	Hela-S3	cervix
14	chr1:241977000-241978200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:241977200-241979200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr1:241977200-241980200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr1:241977400-241977800	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr1:241977400-241981800	Enhancers	Hela-S3	cervix
19	chr1:241977600-241980200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr1:241977800-241978200	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr1:241978200-241978400	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr1:241978200-241980200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:241978400-241980000	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr1:241978600-241980000	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr1:241979200-241979400	Enhancers	Muscle Satellite Cultured Cells	--
26	chr1:241979400-241980200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr1:241979400-241982000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:241980000-241981800	Enhancers	NHLF	lung
29	chr1:241980000-241982000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:241980000-241982200	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr1:241980000-241982200	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr1:241980200-241980600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:241980200-241980800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:241980200-241981200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr1:241980200-241981200	Enhancers	Osteobl	bone
36	chr1:241980200-241981800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr1:241980200-241981800	Enhancers	Muscle Satellite Cultured Cells	--
38	chr1:241980200-241981800	Enhancers	NHDF-Ad	bronchial
39	chr1:241980400-241981000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:241980400-241981200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr1:241980400-241981200	Enhancers	A549	lung
42	chr1:241980400-241981200	Enhancers	GM12878-XiMat	blood
43	chr1:241980400-241981200	Enhancers	NH-A	brain
44	chr1:241980800-241982000	Enhancers	Primary B cells from cord blood	blood
45	chr1:241981000-241981800	Enhancers	Aorta	Aorta
46	chr1:241981000-241982000	Enhancers	Primary B cells from peripheral blood	blood
47	chr1:241981200-241984800	Weak transcription	A549	lung
48	chr1:241981200-241992000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:241981400-241982200	Enhancers	K562	blood
50	chr1:241981800-241984200	Weak transcription	Hela-S3	cervix

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