Variant report

Variant	nsv1008314
Chromosome Location	chr1:174080192-174311023
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3205)
CpG islands
(count:793)
Chromatin interactive
region (count:183)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3205 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:174085153-174085515	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:174208511-174209005	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:174227171-174227530	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:174199624-174199775	K562	blood:	n/a	n/a
5	ARID3A	chr1:174227162-174227507	K562	blood:	n/a	n/a
6	ARID3A	chr1:174135884-174136567	K562	blood:	n/a	n/a
7	ARID3A	chr1:174231871-174232199	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:174235526-174236877	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:174084054-174084445	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:174174954-174175051	K562	blood:	n/a	n/a
11	ARID3A	chr1:174131519-174131723	K562	blood:	n/a	n/a
12	ARID3A	chr1:174143355-174143434	K562	blood:	n/a	n/a
13	ARID3A	chr1:174186888-174187188	K562	blood:	n/a	n/a
14	ARID3A	chr1:174128281-174128688	HepG2	liver:	n/a	n/a
15	ARID3A	chr1:174143545-174143778	HepG2	liver:	n/a	n/a
16	ARID3A	chr1:174231891-174232149	K562	blood:	n/a	n/a
17	ARID3A	chr1:174129389-174129582	HepG2	liver:	n/a	n/a
18	ARID3A	chr1:174122862-174123098	HepG2	liver:	n/a	n/a
19	ARID3A	chr1:174239214-174239484	HepG2	liver:	n/a	n/a
20	ARID3A	chr1:174127629-174128583	K562	blood:	n/a	n/a
21	ARID3A	chr1:174125704-174126099	K562	blood:	n/a	n/a
22	ARID3A	chr1:174160161-174160263	K562	blood:	n/a	n/a
23	ARID3A	chr1:174122702-174123089	K562	blood:	n/a	n/a
24	ARID3A	chr1:174243609-174243996	HepG2	liver:	n/a	n/a
25	ARID3A	chr1:174174087-174174394	HepG2	liver:	n/a	n/a
26	ARID3A	chr1:174186896-174187175	HepG2	liver:	n/a	n/a
27	ARID3A	chr1:174133975-174134175	HepG2	liver:	n/a	n/a
28	ATF1	chr1:174263197-174263318	K562	blood:	n/a	n/a
29	ATF1	chr1:174135815-174136435	K562	blood:	n/a	n/a
30	ATF1	chr1:174277912-174277913	K562	blood:	n/a	n/a
31	ATF1	chr1:174122715-174123098	K562	blood:	n/a	n/a
32	ATF1	chr1:174127630-174128539	K562	blood:	n/a	n/a
33	ATF1	chr1:174104482-174105141	K562	blood:	n/a	n/a
34	ATF1	chr1:174235618-174235768	K562	blood:	n/a	n/a
35	ATF1	chr1:174083999-174084314	K562	blood:	n/a	n/a
36	ATF1	chr1:174201924-174202155	K562	blood:	n/a	n/a
37	ATF1	chr1:174199566-174199927	K562	blood:	n/a	n/a
38	ATF1	chr1:174169246-174169307	K562	blood:	n/a	n/a
39	ATF1	chr1:174173860-174174306	K562	blood:	n/a	n/a
40	ATF2	chr1:174126112-174126729	GM12878	blood:	n/a	n/a
41	ATF2	chr1:174143787-174144215	GM12878	blood:	n/a	n/a
42	ATF2	chr1:174102962-174103539	GM12878	blood:	n/a	n/a
43	ATF2	chr1:174127666-174128735	GM12878	blood:	n/a	n/a
44	ATF2	chr1:174245148-174245601	GM12878	blood:	n/a	n/a
45	ATF2	chr1:174173746-174174313	GM12878	blood:	n/a	n/a
46	ATF2	chr1:174122397-174123122	GM12878	blood:	n/a	n/a
47	ATF2	chr1:174126067-174126795	GM12878	blood:	n/a	n/a
48	ATF2	chr1:174135889-174137189	GM12878	blood:	n/a	n/a
49	ATF2	chr1:174135981-174137121	GM12878	blood:	n/a	n/a
50	ATF2	chr1:174175487-174176060	GM12878	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:174128297-174128347	AoSMC	blood vessel:	n/a
2	chr1:174129130-174129180	HL-60	blood:	n/a
3	chr1:174186816-174186866	AG04450	lung:	fetal
4	chr1:174208162-174208212	SK-N-SH_RA	brain:	n/a
5	chr1:174132239-174132289	AG09309	skin:	n/a
6	chr1:174128297-174128347	HCT-116	colon:	n/a
7	chr1:174128327-174128377	MCF10A-Er-Src	breast:	n/a
8	chr1:174208162-174208212	Caco-2	colon:	n/a
9	chr1:174129340-174129390	MCF-7	breast:	n/a
10	chr1:174128325-174128375	GM19239	blood:	n/a
11	chr1:174129275-174129325	SKMC	muscle:	n/a
12	chr1:174127462-174127512	SK-N-SH_RA	brain:	n/a
13	chr1:174186816-174186866	K562	blood:	n/a
14	chr1:174128327-174128377	GM12891	blood:	n/a
15	chr1:174127462-174127512	GM12891	blood:	n/a
16	chr1:174129340-174129390	PrEC	prostate:	n/a
17	chr1:174129340-174129390	SK-N-SH	brain:	n/a
18	chr1:174129130-174129180	AG04450	lung:	fetal
19	chr1:174132239-174132289	AG09319	gingival:	n/a
20	chr1:174129335-174129385	SAEC	small airway:	n/a
21	chr1:174129275-174129325	BJ	skin:	n/a
22	chr1:174208162-174208212	LNCaP	prostate:	n/a
23	chr1:174129335-174129385	HIPEpiC	eye:	n/a
24	chr1:174128942-174128992	BE2_C	brain:	n/a
25	chr1:174208162-174208212	HUVEC	blood vessel:	n/a
26	chr1:174208162-174208212	MCF10A-Er-Src	breast:	n/a
27	chr1:174128942-174128992	IMR90	lung:	fetal
28	chr1:174208162-174208212	SAEC	small airway:	n/a
29	chr1:174128325-174128375	AoSMC	blood vessel:	n/a
30	chr1:174129335-174129385	Caco-2	colon:	n/a
31	chr1:174128942-174128992	HCM	heart:	n/a
32	chr1:174128297-174128347	AG09309	skin:	n/a
33	chr1:174128325-174128375	CMK	blood:	n/a
34	chr1:174128942-174128992	K562	blood:	n/a
35	chr1:174128327-174128377	NB4	blood:	n/a
36	chr1:174128327-174128377	HCM	heart:	n/a
37	chr1:174186816-174186866	HNPCEpiC	eye:	n/a
38	chr1:174132239-174132289	SK-N-MC	brain:	n/a
39	chr1:174186816-174186866	ProgFib	skin:	n/a
40	chr1:174128942-174128992	AG04449	skin:	fetal
41	chr1:174127462-174127512	HIPEpiC	eye:	n/a
42	chr1:174128327-174128377	HepG2	liver:	n/a
43	chr1:174125205-174125255	A549	lung:	n/a
44	chr1:174129340-174129390	GM12892	blood:	n/a
45	chr1:174125205-174125255	NHBE	bronchial:	n/a
46	chr1:174127462-174127512	HRPEpiC	eye:	n/a
47	chr1:174208162-174208212	Hela-S3	cervix:	n/a
48	chr1:174129275-174129325	GM12878	blood:	n/a
49	chr1:174129335-174129385	SK-N-MC	brain:	n/a
50	chr1:174129340-174129390	HRCEpiC	kidney:	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr1:173836588..173838443-chr1:174165895..174168713,2	MCF-7	breast:
2	chr1:174134604..174137057-chr1:174160693..174163339,2	K562	blood:
3	chr1:174231547..174232813-chr1:174695220..174696649,6	MCF-7	breast:
4	chr1:174193716..174196579-chr1:174196717..174200011,3	MCF-7	breast:
5	chr1:174158960..174161694-chr1:174164662..174167169,2	K562	blood:
6	chr1:174294663..174296200-chr1:174300746..174303006,2	MCF-7	breast:
7	chr1:174190274..174193024-chr1:174230012..174232463,2	K562	blood:
8	chr1:174136409..174138753-chr1:174139089..174145165,6	K562	blood:
9	chr1:174186060..174188372-chr1:174193893..174195942,2	K562	blood:
10	chr1:174186060..174188372-chr1:174193893..174195942,2	K562	blood:
11	chr1:174127362..174130761-chr1:174131482..174135069,5	MCF-7	breast:
12	chr1:173837020..173839325-chr1:174127377..174129524,4	K562	blood:
13	chr1:174127315..174129542-chr1:174157922..174159805,2	K562	blood:
14	chr1:174082792..174085808-chr1:174127455..174130130,3	MCF-7	breast:
15	chr1:174217947..174220664-chr1:174222845..174224894,3	K562	blood:
16	chr1:174136409..174138753-chr1:174139089..174145165,6	K562	blood:
17	chr1:174128038..174128892-chr9:139440176..139441167,2	Hela-S3	cervix:
18	chr1:174127641..174129187-chr1:174162745..174164653,2	MCF-7	breast:
19	chr1:174126773..174130158-chr1:174148620..174150674,4	K562	blood:
20	chr1:174138379..174140424-chr1:174154123..174156234,2	K562	blood:
21	chr1:174217947..174220664-chr1:174222845..174224894,3	K562	blood:
22	chr1:174227366..174227954-chr1:174695618..174696250,2	K562	blood:
23	chr1:149859137..149859656-chr1:174128361..174129122,2	Hela-S3	cervix:
24	chr1:174257821..174260787-chr1:174268762..174270773,2	MCF-7	breast:
25	chr1:174225306..174226872-chr1:174233081..174234854,2	K562	blood:
26	chr1:174156183..174157757-chr1:174183127..174185978,2	K562	blood:
27	chr1:174127383..174130207-chr1:174164914..174166564,2	K562	blood:
28	chr1:174156183..174157757-chr1:174183127..174185978,2	K562	blood:
29	chr1:173791511..173794568-chr1:174127376..174130126,4	K562	blood:
30	chr1:174134591..174137742-chr1:174149123..174151486,3	K562	blood:
31	chr1:174208904..174211373-chr1:174212924..174214774,3	MCF-7	breast:
32	chr1:174152071..174154187-chr1:174154617..174157580,2	K562	blood:
33	chr1:174128812..174129312-chr19:47291339..47292302,2	NB4	blood:
34	chr1:174209547..174211969-chr1:174214945..174217167,2	MCF-7	breast:
35	chr1:174287001..174289924-chr1:174290747..174293393,2	K562	blood:
36	chr1:174207103..174211366-chr1:174211395..174216784,8	MCF-7	breast:
37	chr1:174169989..174171765-chr1:174171980..174175775,3	K562	blood:
38	chr1:174119010..174121477-chr1:174128126..174130744,2	MCF-7	breast:
39	chr1:174152447..174154110-chr1:174154958..174156995,2	K562	blood:
40	chr1:174182240..174184495-chr1:174184755..174187025,3	K562	blood:
41	chr1:174287001..174289924-chr1:174290747..174293393,2	K562	blood:
42	chr1:174215485..174217028-chr1:174218870..174220698,2	MCF-7	breast:
43	chr1:174109106..174110896-chr1:174126371..174129198,3	K562	blood:
44	chr1:174178345..174180252-chr1:174182223..174184373,2	K562	blood:
45	chr1:174134604..174137311-chr1:174161839..174164526,2	K562	blood:
46	chr1:173792385..173795057-chr1:174174691..174177146,2	K562	blood:
47	chr1:174159869..174162419-chr1:174173364..174176167,2	K562	blood:
48	chr1:174040693..174043497-chr1:174175491..174177375,2	K562	blood:
49	chr1:173991432..173994922-chr1:174124746..174129302,4	K562	blood:
50	chr1:174127794..174129583-chr1:174152496..174155394,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RC3H1-1	chr1:174124765-174124835	ENSG00000227373
2	lnc-RC3H1-1	chr1:174083005-174084584	NONHSAT007721
3	lnc-RC3H1-1	chr1:174128025-174128291	ENSG00000227373
4	lnc-RC3H1-1	chr1:174124765-174124835	ENSG00000227373
5	lnc-RC3H1-1	chr1:174084438-174084787	ENSG00000227373
6	lnc-RC3H1-3	chr1:174144306-174144529	NONHSAT007727
7	lnc-RC3H1-1	chr1:174128302-174128425	ENSG00000227373
8	lnc-RC3H1-1	chr1:174124765-174124835	ENSG00000227373
9	lnc-RC3H1-1	chr1:174124765-174124835	ENSG00000227373
10	lnc-RC3H1-1	chr1:174084521-174084787	ENSG00000227373
11	lnc-RC3H1-1	chr1:174083921-174084787	NONHSAT007722
12	lnc-RC3H1-3	chr1:174140521-174140895	NONHSAT007727
13	lnc-RC3H1-1	chr1:174091222-174091330	ENSG00000227373
14	lnc-RC3H1-1	chr1:174128025-174128271	ENSG00000227373
15	lnc-RC3H1-1	chr1:174128025-174128128	ENSG00000227373
16	lnc-RC3H1-1	chr1:174090776-174090924	ENSG00000227373
17	lnc-RC3H1-1	chr1:174128302-174128799	NONHSAT007722
18	lnc-RC3H1-1	chr1:174128025-174128128	NONHSAT007722
19	lnc-RC3H1-1	chr1:174084739-174084781	ENSG00000227373
20	lnc-RC3H1-1	chr1:174129055-174129142	ENSG00000227373
21	lnc-RC3H1-1	chr1:174124765-174124835	NONHSAT007722
22	lnc-RC3H1-3	chr1:174156215-174156272	NONHSAT007727

No data

Variant related genes	Relation type
ENSG00000227373	TF binding region
RABGAP1L	TF binding region
ENSG00000238872	TF binding region
ENSG00000227373	CpG island
RABGAP1L	CpG island
ENSG00000238872	CpG island
ENSG00000227373	chromatin interactions
ENSG00000116161	chromatin interactions
ENSG00000070756	chromatin interactions
ENSG00000117593	chromatin interactions
ENSG00000135870	chromatin interactions
ENSG00000136068	chromatin interactions
ENSG00000238872	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000105281	chromatin interactions
ENSG00000224977	chromatin interactions
ENSG00000162664	chromatin interactions
ENSG00000255198	chromatin interactions
ENSG00000237886	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000179580	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000117592	chromatin interactions
ENSG00000265181	chromatin interactions
ENSG00000140988	chromatin interactions
ENSG00000152061	chromatin interactions
ENSG00000120334	chromatin interactions
ENSG00000148400	chromatin interactions
ENSG00000115129	chromatin interactions
ENSG00000208317	chromatin interactions
ENSG00000184270	chromatin interactions

Extended variants
information (count: 7405 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:7405 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576974537	chr1:174080217-174080218	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs539553102	chr1:174080249-174080250	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs553173491	chr1:174080262-174080263	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs148794828	chr1:174080269-174080270	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs182216891	chr1:174080295-174080296	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs577439109	chr1:174080305-174080306	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs560297827	chr1:174080613-174080614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs28566138	chr1:174080631-174080632	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs140153328	chr1:174080673-174080674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34214670	chr1:174080698-174080699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35070530	chr1:174080701-174080702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569491395	chr1:174080823-174080824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531923738	chr1:174080860-174080861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10912733	chr1:174080897-174080898	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs570481610	chr1:174080930-174080931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539516868	chr1:174081007-174081008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553136276	chr1:174081026-174081027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs61827891	chr1:174081048-174081049	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs535685873	chr1:174081059-174081060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545469539	chr1:174081104-174081105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555274377	chr1:174081113-174081114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533093755	chr1:174081131-174081132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575454919	chr1:174081222-174081223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544194032	chr1:174081271-174081272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115468099	chr1:174081272-174081273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190246121	chr1:174081284-174081285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538947630	chr1:174081287-174081288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs374749557	chr1:174081355-174081356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368137156	chr1:174081400-174081401	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs142480835	chr1:174081401-174081402	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs540320847	chr1:174081441-174081442	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs182583280	chr1:174081471-174081472	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs529373549	chr1:174081483-174081484	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs543169036	chr1:174081489-174081490	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs542652874	chr1:174081490-174081491	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs562958510	chr1:174081498-174081499	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs532001630	chr1:174081499-174081500	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs57424674	chr1:174081505-174081506	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs548734167	chr1:174081606-174081607	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186563728	chr1:174081636-174081637	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376271741	chr1:174081643-174081644	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373860457	chr1:174081681-174081682	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546713844	chr1:174081700-174081701	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566513170	chr1:174081719-174081720	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375319018	chr1:174081740-174081741	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535206607	chr1:174081747-174081748	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs367700410	chr1:174081777-174081778	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73031288	chr1:174081815-174081816	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs191291843	chr1:174081877-174081878	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs370351409	chr1:174082019-174082020	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD

Chromatin state (count:3113 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174080600-174080800	Enhancers	Stomach Smooth Muscle	stomach
2	chr1:174080600-174081600	Enhancers	Pancreas	Pancrea
3	chr1:174081200-174081400	Enhancers	Ovary	ovary
4	chr1:174081400-174081600	Flanking Active TSS	Ovary	ovary
5	chr1:174081400-174082400	Enhancers	Rectal Smooth Muscle	rectum
6	chr1:174081400-174082800	Enhancers	Fetal Heart	heart
7	chr1:174081600-174081800	Enhancers	Osteobl	bone
8	chr1:174081600-174082000	Active TSS	Aorta	Aorta
9	chr1:174081600-174082000	Active TSS	Duodenum Smooth Muscle	Duodenum
10	chr1:174081600-174082200	Active TSS	Ovary	ovary
11	chr1:174081600-174082200	Active TSS	Stomach Smooth Muscle	stomach
12	chr1:174081800-174082000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:174081800-174083200	Enhancers	Colon Smooth Muscle	Colon
14	chr1:174081800-174086200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:174082000-174082200	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr1:174082000-174083400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:174082200-174082400	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr1:174082200-174082600	Weak transcription	Stomach Smooth Muscle	stomach
19	chr1:174082200-174084000	Weak transcription	Ovary	ovary
20	chr1:174082600-174082800	Enhancers	Stomach Smooth Muscle	stomach
21	chr1:174082800-174084000	Weak transcription	Fetal Heart	heart
22	chr1:174082800-174084000	Weak transcription	Stomach Smooth Muscle	stomach
23	chr1:174083400-174083600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:174083600-174084800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:174083800-174084000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:174083800-174084400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:174084000-174084200	Enhancers	Duodenum Smooth Muscle	Duodenum
28	chr1:174084000-174084200	Enhancers	Psoas Muscle	Psoas
29	chr1:174084000-174084200	Enhancers	HepG2	liver
30	chr1:174084000-174084400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:174084000-174084400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr1:174084000-174084400	Enhancers	Adipose Nuclei	Adipose
33	chr1:174084000-174084400	Enhancers	Ovary	ovary
34	chr1:174084000-174084600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr1:174084000-174084600	Enhancers	Fetal Heart	heart
36	chr1:174084000-174084600	Enhancers	NHDF-Ad	bronchial
37	chr1:174084000-174085000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:174084000-174085200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:174084000-174085200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr1:174084200-174084600	Enhancers	Fetal Intestine Large	intestine
41	chr1:174084200-174084600	Flanking Active TSS	HepG2	liver
42	chr1:174084200-174084800	Enhancers	Fetal Intestine Small	intestine
43	chr1:174084200-174085400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:174084200-174085600	Enhancers	Hela-S3	cervix
45	chr1:174084600-174085600	Enhancers	HepG2	liver
46	chr1:174084600-174088000	Weak transcription	Fetal Heart	heart
47	chr1:174084800-174085800	Enhancers	HMEC	breast
48	chr1:174085000-174085400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr1:174085400-174085600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:174086600-174087200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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