Variant report

Variant	esv1850196
Chromosome Location	chr5:74890618-75138443
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2356)
CpG islands
(count:2136)
Chromatin interactive
region (count:132)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2356 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74906446-74906556	K562	blood:	n/a	n/a
2	ARID3A	chr5:74913152-74913154	K562	blood:	n/a	n/a
3	ARID3A	chr5:74912064-74912380	K562	blood:	n/a	n/a
4	ARID3A	chr5:75016714-75017107	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:74976935-74977330	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:75012722-75013708	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:74974294-74974363	K562	blood:	n/a	n/a
8	ARID3A	chr5:75017531-75017690	K562	blood:	n/a	n/a
9	ARID3A	chr5:74916424-74916742	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:74977101-74977345	K562	blood:	n/a	n/a
11	ARID3A	chr5:75002735-75003318	K562	blood:	n/a	n/a
12	ARID3A	chr5:74964985-74965304	K562	blood:	n/a	n/a
13	ARID3A	chr5:74915925-74916471	K562	blood:	n/a	n/a
14	ARID3A	chr5:74904794-74905021	K562	blood:	n/a	n/a
15	ARID3A	chr5:75003873-75004464	K562	blood:	n/a	n/a
16	ARID3A	chr5:74903955-74904149	K562	blood:	n/a	n/a
17	ARID3A	chr5:75012873-75013653	K562	blood:	n/a	n/a
18	ATF1	chr5:75017575-75017756	K562	blood:	n/a	n/a
19	ATF1	chr5:75012865-75013638	K562	blood:	n/a	n/a
20	ATF1	chr5:74912163-74912344	K562	blood:	n/a	n/a
21	ATF1	chr5:75002668-75002999	K562	blood:	n/a	n/a
22	ATF1	chr5:75114533-75114536	K562	blood:	n/a	n/a
23	ATF1	chr5:74964828-74965541	K562	blood:	n/a	n/a
24	ATF2	chr5:75012610-75013409	GM12878	blood:	n/a	n/a
25	ATF2	chr5:74964607-74965672	GM12878	blood:	n/a	n/a
26	ATF2	chr5:74944406-74945026	GM12878	blood:	n/a	n/a
27	ATF2	chr5:74955853-74956931	GM12878	blood:	n/a	n/a
28	ATF2	chr5:75012659-75013437	GM12878	blood:	n/a	n/a
29	ATF2	chr5:74964701-74965511	GM12878	blood:	n/a	n/a
30	ATF2	chr5:75133129-75133647	GM12878	blood:	n/a	n/a
31	ATF3	chr5:75012887-75013324	K562	blood:	n/a	n/a
32	ATF3	chr5:74964960-74965310	K562	blood:	n/a	n/a
33	ATF3	chr5:75012817-75013399	A549	lung:	n/a	chr5:75013389-75013398 chr5:75013337-75013346
34	ATF3	chr5:75017407-75017825	K562	blood:	n/a	n/a
35	ATF3	chr5:74944630-74944858	K562	blood:	n/a	n/a
36	BACH1	chr5:75012979-75013333	K562	blood:	n/a	n/a
37	BACH1	chr5:74907812-74907884	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr5:75031171-75031207	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr5:75012859-75013622	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr5:74965141-74965322	K562	blood:	n/a	n/a
41	BACH1	chr5:75032146-75032464	H1-hESC	embryonic stem cell:	n/a	n/a
42	BATF	chr5:75012773-75013177	GM12878	blood:	n/a	n/a
43	BATF	chr5:74964664-74965323	GM12878	blood:	n/a	n/a
44	BATF	chr5:75062447-75062640	GM12878	blood:	n/a	n/a
45	BATF	chr5:74944597-74944931	GM12878	blood:	n/a	chr5:74944774-74944785 chr5:74944775-74944785
46	BATF	chr5:75062439-75062727	GM12878	blood:	n/a	n/a
47	BATF	chr5:74964753-74965201	GM12878	blood:	n/a	n/a
48	BATF	chr5:74956551-74956791	GM12878	blood:	n/a	n/a
49	BATF	chr5:74956488-74956876	GM12878	blood:	n/a	n/a
50	BATF	chr5:74944508-74945014	GM12878	blood:	n/a	chr5:74944774-74944785 chr5:74944775-74944785

(count:2136 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74965039-74965089	PFSK-1	brain:	n/a
2	chr5:74965039-74965089	PFSK-1	brain:	n/a
3	chr5:74910129-74910179	GM19239	blood:	n/a
4	chr5:75013490-75013540	HepG2	liver:	n/a
5	chr5:75013131-75013181	A549	lung:	n/a
6	chr5:74907694-74907744	T-47D	breast:	n/a
7	chr5:74991826-74991876	HEK293	kidney:	embryo
8	chr5:74908125-74908175	AG09319	gingival:	n/a
9	chr5:75012313-75012363	Hela-S3	cervix:	n/a
10	chr5:74907287-74907337	AG10803	skin:	n/a
11	chr5:75013682-75013732	SK-N-SH_RA	brain:	n/a
12	chr5:75013329-75013379	NHBE	bronchial:	n/a
13	chr5:75127862-75127912	SAEC	small airway:	n/a
14	chr5:74907694-74907744	PANC-1	pancreas:	n/a
15	chr5:74910129-74910179	SKMC	muscle:	n/a
16	chr5:74907287-74907337	PFSK-1	brain:	n/a
17	chr5:75013392-75013442	SK-N-SH_RA	brain:	n/a
18	chr5:74952444-74952494	HCM	heart:	n/a
19	chr5:75013392-75013442	AG09309	skin:	n/a
20	chr5:75013592-75013642	HRCEpiC	kidney:	n/a
21	chr5:74908170-74908220	HCPEpiC	choroid plexus:	n/a
22	chr5:74913041-74913091	HIPEpiC	eye:	n/a
23	chr5:74906150-74906200	ovcar-3	ovarian:	n/a
24	chr5:74991826-74991876	HNPCEpiC	eye:	n/a
25	chr5:75013392-75013442	Hepatocyte	liver:	n/a
26	chr5:75013227-75013277	HRE	kidney:	n/a
27	chr5:75012816-75012866	HEK293	kidney:	embryo
28	chr5:75013227-75013277	ProgFib	skin:	n/a
29	chr5:75013592-75013642	GM12878	blood:	n/a
30	chr5:75013227-75013277	GM12892	blood:	n/a
31	chr5:75009428-75009478	GM19239	blood:	n/a
32	chr5:75013227-75013277	Jurkat	blood:	n/a
33	chr5:74907287-74907337	HAEpiC	amniotic membrane:	n/a
34	chr5:75013490-75013540	HCM	heart:	n/a
35	chr5:74904484-74904534	ovcar-3	ovarian:	n/a
36	chr5:75013592-75013642	IMR90	lung:	fetal
37	chr5:74906150-74906200	HCF	heart:	n/a
38	chr5:74991826-74991876	IMR90	lung:	fetal
39	chr5:74907592-74907642	HUVEC	blood vessel:	n/a
40	chr5:74908125-74908175	BJ	skin:	n/a
41	chr5:74908125-74908175	U87	brain:	n/a
42	chr5:75013392-75013442	HCF	heart:	n/a
43	chr5:75014259-75014309	BE2_C	brain:	n/a
44	chr5:75013342-75013392	K562	blood:	n/a
45	chr5:74906150-74906200	K562	blood:	n/a
46	chr5:74898460-74898510	BJ	skin:	n/a
47	chr5:74907287-74907337	HRE	kidney:	n/a
48	chr5:74910129-74910179	Hela-S3	cervix:	n/a
49	chr5:74907694-74907744	A549	lung:	n/a
50	chr5:74898460-74898510	HCPEpiC	choroid plexus:	n/a

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:75032759..75033454-chr5:151772671..151773601,2	HCT-116	colon:
2	chr5:74804574..74807080-chr5:74963425..74964973,2	K562	blood:
3	chr5:74907136..74909579-chr5:74911861..74913808,3	K562	blood:
4	chr5:75012994..75014594-chr5:75126997..75129169,2	K562	blood:
5	chr5:74915137..74918881-chr5:74947780..74950531,3	K562	blood:
6	chr5:74980503..74982901-chr5:74987691..74991437,3	K562	blood:
7	chr5:74952495..74955459-chr5:74961686..74963716,2	K562	blood:
8	chr5:74786766..74788653-chr5:74965428..74967574,2	K562	blood:
9	chr5:74889934..74892388-chr5:74899059..74901805,2	K562	blood:
10	chr20:49341351..49342130-chr5:75119338..75119859,2	MCF-7	breast:
11	chr5:74953873..74956590-chr5:75014538..75016068,2	K562	blood:
12	chr5:74950997..74952941-chr5:74954987..74957253,2	K562	blood:
13	chr5:74972829..74974939-chr5:74988828..74991642,2	K562	blood:
14	chr5:74956949..74958847-chr5:74961293..74964249,2	K562	blood:
15	chr5:74959210..74961845-chr5:74965195..74967227,2	K562	blood:
16	chr5:74959210..74961845-chr5:74965195..74967227,2	K562	blood:
17	chr5:74987714..74990328-chr5:75012640..75014673,2	MCF-7	breast:
18	chr5:74913060..74915078-chr5:74915803..74919443,3	K562	blood:
19	chr5:74997231..74999217-chr5:75000460..75002166,2	K562	blood:
20	chr5:74986312..74988640-chr5:74991101..74992756,2	K562	blood:
21	chr5:74980613..74983267-chr5:74984574..74986964,2	K562	blood:
22	chr5:75006833..75009692-chr5:75010741..75014580,11	K562	blood:
23	chr5:74889934..74892388-chr5:74899059..74901805,2	K562	blood:
24	chr5:75012127..75015075-chr5:75015855..75021206,8	K562	blood:
25	chr5:74981038..74984120-chr5:75011699..75013859,3	K562	blood:
26	chr5:74532263..74533179-chr5:74962383..74963086,2	K562	blood:
27	chr5:74986971..74989471-chr5:74989787..74992402,2	MCF-7	breast:
28	chr5:75020599..75023096-chr5:75030019..75031562,2	K562	blood:
29	chr5:74952495..74954524-chr5:74962216..74966504,3	K562	blood:
30	chr17:3571470..3572129-chr5:75012688..75013610,2	Hela-S3	cervix:
31	chr5:74806025..74808781-chr5:74906137..74908952,2	MCF-7	breast:
32	chr5:74880080..74881244-chr5:74962362..74964218,14	MCF-7	breast:
33	chr5:75010275..75012442-chr5:75036890..75039813,2	K562	blood:
34	chr5:74735308..74738290-chr5:74961776..74964047,2	K562	blood:
35	chr5:74912024..74914449-chr5:74921744..74924749,4	K562	blood:
36	chr5:75008837..75011583-chr5:75016834..75018987,2	K562	blood:
37	chr5:74905446..74908420-chr5:74909324..74911813,2	MCF-7	breast:
38	chr5:75001250..75005615-chr5:75010572..75014500,9	K562	blood:
39	chr5:74532317..74532921-chr5:74976842..74977712,2	K562	blood:
40	chr5:74951852..74953716-chr5:74968580..74970630,2	K562	blood:
41	chr5:74965127..74967340-chr5:75010605..75013451,3	K562	blood:
42	chr5:75050757..75053657-chr5:75055621..75057191,2	K562	blood:
43	chr5:74912858..74914560-chr5:74917246..74919606,2	K562	blood:
44	chr5:74933475..74935667-chr5:74961312..74963106,2	K562	blood:
45	chr5:75030734..75031635-chr5:75551827..75552781,3	MCF-7	breast:
46	chr5:75018075..75020883-chr5:75022591..75024693,2	K562	blood:
47	chr5:74910178..74911723-chr5:74917267..74920194,2	K562	blood:
48	chr5:74953873..74956590-chr5:75014538..75016068,2	K562	blood:
49	chr5:74889870..74892388-chr5:74899059..74901805,3	K562	blood:
50	chr5:74952495..74955459-chr5:74961686..74963716,2	K562	blood:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKDD1B-4	chr5:75002560-75002734	ucscGeneNc_uc010izt_1
2	lnc-POLK-2	chr5:74966804-74967175	NONHSAT102216
3	lnc-POLK-1	chr5:74955108-74955129	NONHSAT102215
4	lnc-POC5-3	chr5:75048395-75049304	NONHSAT102224
5	lnc-ANKDD1B-3	chr5:74892939-74893003	NONHSAT102209
6	lnc-ANKDD1B-4	chr5:74998373-74998574	ucscGeneNc_uc010izt_1
7	lnc-ANKDD1B-3	chr5:74893759-74893813	NONHSAT102210
8	lnc-ANKDD1B-4	chr5:74984723-74984821	ucscGeneNc_uc010izt_1
9	lnc-POC5-1	chr5:74894952-74895205	ENSG00000248881.1
10	lnc-ANKDD1B-5	chr5:75018947-75019386	NONHSAT102223
11	lnc-ANKDD1B-2	chr5:74904642-74905808	ENSG00000272040.1
12	lnc-POC5-4	chr5:74907076-74907508	NONHSAT102214
13	lnc-ANKDD1B-4	chr5:74987610-74987708	ucscGeneNc_uc010izt_1
14	lnc-ANKDD1B-4	chr5:74990864-74990962	ucscGeneNc_uc010izt_1
15	lnc-ANKDD1B-3	chr5:74893572-74893865	NONHSAT102209
16	lnc-ANKDD1B-4	chr5:74994975-74995070	ucscGeneNc_uc010izt_1
17	lnc-POLK-1	chr5:74948967-74949065	NONHSAT102215
18	lnc-ANKDD1B-3	chr5:74893242-74893614	NONHSAT102210
19	lnc-ANKDD1B-4	chr5:74943057-74943408	ucscGeneNc_uc010izt_1
20	lnc-ANKDD1B-1	chr5:74906143-74906582	XLOC_004431
21	lnc-POLK-1	chr5:74951854-74951952	NONHSAT102215
22	lnc-POLK-2	chr5:74965019-74965208	NONHSAT102216
23	lnc-POLK-1	chr5:74931137-74931707	NONHSAT102215
24	lnc-POC5-1	chr5:74894307-74894806	ENSG00000248881.1
25	lnc-POC5-4	chr5:74907701-74908056	NONHSAT102214
26	lnc-ANKDD1B-1	chr5:74902446-74902775	XLOC_004431

No data

Variant related genes	Relation type
POLK	TF binding region
ENSG00000272040	TF binding region
ENSG00000251419	TF binding region
SLC25A5P9	TF binding region
RNU6-680P	TF binding region
POC5	TF binding region
ANKDD1B	TF binding region
ENSG00000248881	TF binding region
POLK	CpG island
ENSG00000272040	CpG island
ENSG00000251419	CpG island
SLC25A5P9	CpG island
RNU6-680P	CpG island
POC5	CpG island
ANKDD1B	CpG island
ENSG00000248881	CpG island
ENSG00000251078	chromatin interactions
ENSG00000148468	chromatin interactions
ENSG00000247372	chromatin interactions
ENSG00000207333	chromatin interactions
ENSG00000113163	chromatin interactions
ENSG00000127774	chromatin interactions
ENSG00000163608	chromatin interactions
ENSG00000240057	chromatin interactions
ENSG00000113161	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000248881	chromatin interactions
ENSG00000152359	chromatin interactions
ENSG00000145700	chromatin interactions
ENSG00000122008	chromatin interactions
ENSG00000251419	chromatin interactions
ENSG00000213977	chromatin interactions
ENSG00000189045	chromatin interactions

Extended variants
information (count: 6077 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6077 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5744707	chr5:74890618-74890619	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562627344	chr5:74890638-74890639	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs183992975	chr5:74890639-74890640	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs531815554	chr5:74890749-74890750	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs117958865	chr5:74890781-74890782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568456736	chr5:74890801-74890802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372494796	chr5:74890802-74890803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527980590	chr5:74890804-74890805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143199956	chr5:74890814-74890815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375152421	chr5:74890824-74890825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570471512	chr5:74890830-74890831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs5744708	chr5:74890889-74890890	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs551188076	chr5:74890920-74890921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539379990	chr5:74890922-74890923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552011912	chr5:74890927-74890928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189882186	chr5:74890945-74890946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538075999	chr5:74890946-74890947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554815230	chr5:74890975-74890976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs5744709	chr5:74891002-74891003	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs533867832	chr5:74891027-74891028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs193171729	chr5:74891028-74891029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141403558	chr5:74891043-74891044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146989781	chr5:74891050-74891051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs60032269	chr5:74891094-74891095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs58783164	chr5:74891098-74891099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562690164	chr5:74891114-74891115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185307430	chr5:74891169-74891170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190551669	chr5:74891198-74891199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs5744710	chr5:74891298-74891299	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs541873485	chr5:74891372-74891373	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs200196211	chr5:74891374-74891375	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs5744711	chr5:74891380-74891381	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs561965541	chr5:74891431-74891432	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs138064836	chr5:74891448-74891449	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs141473008	chr5:74891461-74891462	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs567695467	chr5:74891475-74891476	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs547810609	chr5:74891480-74891481	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs538333992	chr5:74891481-74891482	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs150426523	chr5:74891504-74891505	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs182089487	chr5:74891568-74891569	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs368674681	chr5:74891574-74891575	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs552191047	chr5:74891578-74891579	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs568828004	chr5:74891597-74891598	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs537945321	chr5:74891626-74891627	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs548281800	chr5:74891642-74891643	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs568280008	chr5:74891646-74891647	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs533976235	chr5:74891722-74891723	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149556097	chr5:74891760-74891761	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76416852	chr5:74891833-74891834	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539490728	chr5:74891898-74891899	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3569 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74818200-74897400	Weak transcription	Thymus	Thymus
2	chr5:74822800-74896000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr5:74833400-74906800	Weak transcription	Brain Substantia Nigra	brain
4	chr5:74839400-74897400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr5:74841200-74899400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr5:74850200-74896200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr5:74862200-74897800	Weak transcription	Brain Germinal Matrix	brain
8	chr5:74862600-74897200	Weak transcription	Lung	lung
9	chr5:74862800-74897400	Weak transcription	Pancreas	Pancrea
10	chr5:74862800-74897400	Weak transcription	Spleen	Spleen
11	chr5:74862800-74897600	Weak transcription	Gastric	stomach
12	chr5:74862800-74907200	Weak transcription	Esophagus	oesophagus
13	chr5:74863000-74896200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr5:74863600-74905800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr5:74863800-74906800	Weak transcription	Rectal Smooth Muscle	rectum
16	chr5:74864000-74897400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr5:74864000-74897400	Weak transcription	NHEK	skin
18	chr5:74864000-74899600	Weak transcription	Hela-S3	cervix
19	chr5:74864000-74907000	Weak transcription	Psoas Muscle	Psoas
20	chr5:74865800-74906800	Weak transcription	Colonic Mucosa	Colon
21	chr5:74867600-74907200	Weak transcription	Small Intestine	intestine
22	chr5:74869400-74893400	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr5:74871400-74897400	Weak transcription	Aorta	Aorta
24	chr5:74871400-74897400	Weak transcription	Brain Angular Gyrus	brain
25	chr5:74871400-74897400	Weak transcription	Brain Hippocampus Middle	brain
26	chr5:74871400-74897400	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr5:74871800-74900600	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr5:74872200-74893000	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr5:74872400-74898400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:74873600-74907000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr5:74873800-74899200	Weak transcription	K562	blood
32	chr5:74873800-74901000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr5:74874600-74897400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr5:74875200-74892200	Weak transcription	Brain Anterior Caudate	brain
35	chr5:74875200-74907000	Weak transcription	Right Ventricle	heart
36	chr5:74875800-74903400	Weak transcription	Fetal Thymus	thymus
37	chr5:74877000-74898400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:74877400-74896200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr5:74877400-74899200	Weak transcription	HUVEC	blood vessel
40	chr5:74878200-74892000	Weak transcription	Fetal Kidney	kidney
41	chr5:74878200-74892400	Weak transcription	Fetal Brain Female	brain
42	chr5:74878200-74899000	Weak transcription	HMEC	breast
43	chr5:74878400-74898200	Weak transcription	Fetal Brain Male	brain
44	chr5:74878600-74901200	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr5:74879000-74907000	Weak transcription	HepG2	liver
46	chr5:74879600-74897800	Weak transcription	NHLF	lung
47	chr5:74881400-74895800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr5:74881800-74896800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr5:74882400-74897000	Weak transcription	Fetal Lung	lung
50	chr5:74884200-74893600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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