Variant report

Variant	nsv1053657
Chromosome Location	chr13:90100510-90578568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1765)
CpG islands
(count:184)
Chromatin interactive
region (count:70)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1765 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:90512718-90512791	K562	blood:	n/a	n/a
2	ARID3A	chr13:90577420-90577637	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:90166877-90167409	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:90520785-90520820	K562	blood:	n/a	n/a
5	ARID3A	chr13:90551614-90552641	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:90497424-90497670	K562	blood:	n/a	n/a
7	ARID3A	chr13:90462884-90462897	HepG2	liver:	n/a	n/a
8	ATF1	chr13:90504797-90505152	K562	blood:	n/a	n/a
9	ATF1	chr13:90445517-90445688	K562	blood:	n/a	n/a
10	ATF1	chr13:90562006-90562368	K562	blood:	n/a	n/a
11	ATF1	chr13:90452879-90452924	K562	blood:	n/a	n/a
12	ATF1	chr13:90483482-90484025	K562	blood:	n/a	n/a
13	ATF1	chr13:90560976-90561171	K562	blood:	n/a	n/a
14	ATF1	chr13:90530348-90530819	K562	blood:	n/a	n/a
15	ATF1	chr13:90536949-90537223	K562	blood:	n/a	n/a
16	ATF1	chr13:90458876-90459006	K562	blood:	n/a	n/a
17	ATF1	chr13:90446074-90446297	K562	blood:	n/a	n/a
18	ATF1	chr13:90563357-90563940	K562	blood:	n/a	n/a
19	ATF1	chr13:90549520-90549719	K562	blood:	n/a	n/a
20	ATF1	chr13:90566492-90566927	K562	blood:	n/a	n/a
21	ATF1	chr13:90466783-90467103	K562	blood:	n/a	n/a
22	ATF1	chr13:90477390-90477952	K562	blood:	n/a	n/a
23	ATF1	chr13:90459939-90460250	K562	blood:	n/a	n/a
24	ATF1	chr13:90448578-90448855	K562	blood:	n/a	n/a
25	ATF1	chr13:90510751-90511105	K562	blood:	n/a	n/a
26	ATF1	chr13:90468064-90468577	K562	blood:	n/a	n/a
27	ATF1	chr13:90523739-90524152	K562	blood:	n/a	n/a
28	ATF1	chr13:90463731-90464784	K562	blood:	n/a	n/a
29	ATF3	chr13:90166748-90167411	A549	lung:	n/a	n/a
30	BACH1	chr13:90394961-90395002	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr13:90493756-90494221	K562	blood:	n/a	n/a
32	BACH1	chr13:90332823-90333002	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr13:90326568-90326595	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr13:90531046-90531430	K562	blood:	n/a	n/a
35	BACH1	chr13:90577633-90578315	K562	blood:	n/a	n/a
36	BACH1	chr13:90488380-90488753	K562	blood:	n/a	n/a
37	BACH1	chr13:90514969-90515132	K562	blood:	n/a	n/a
38	BACH1	chr13:90563752-90563952	K562	blood:	n/a	n/a
39	BATF	chr13:90117655-90117965	GM12878	blood:	n/a	chr13:90117764-90117775
40	BATF	chr13:90549997-90550299	GM12878	blood:	n/a	n/a
41	BATF	chr13:90549986-90550321	GM12878	blood:	n/a	n/a
42	BCL3	chr13:90166728-90167467	A549	lung:	n/a	n/a
43	BCL3	chr13:90166802-90167246	A549	lung:	n/a	n/a
44	BHLHE40	chr13:90514903-90515151	K562	blood:	n/a	n/a
45	BHLHE40	chr13:90511668-90511802	K562	blood:	n/a	n/a
46	BHLHE40	chr13:90551129-90551176	K562	blood:	n/a	n/a
47	BHLHE40	chr13:90472685-90473042	K562	blood:	n/a	n/a
48	BHLHE40	chr13:90563800-90563984	K562	blood:	n/a	n/a
49	BHLHE40	chr13:90569970-90570554	K562	blood:	n/a	n/a
50	BHLHE40	chr13:90556476-90556676	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:90557520-90557570	AoSMC	blood vessel:	n/a
2	chr13:90557520-90557570	AoSMC	blood vessel:	n/a
3	chr13:90557520-90557570	Jurkat	blood:	n/a
4	chr13:90557520-90557570	Hela-S3	cervix:	n/a
5	chr13:90419012-90419062	A549	lung:	n/a
6	chr13:90557520-90557570	NHDF-neo	bronchial:	n/a
7	chr13:90419012-90419062	HCT-116	colon:	n/a
8	chr13:90536270-90536320	MCF-7	breast:	n/a
9	chr13:90557520-90557570	BE2_C	brain:	n/a
10	chr13:90419012-90419062	HCF	heart:	n/a
11	chr13:90557520-90557570	PFSK-1	brain:	n/a
12	chr13:90419012-90419062	GM12892	blood:	n/a
13	chr13:90557520-90557570	AG04449	skin:	fetal
14	chr13:90419012-90419062	AG09319	gingival:	n/a
15	chr13:90419012-90419062	AG04450	lung:	fetal
16	chr13:90536270-90536320	HL-60	blood:	n/a
17	chr13:90536270-90536320	HNPCEpiC	eye:	n/a
18	chr13:90419012-90419062	BJ	skin:	n/a
19	chr13:90536270-90536320	AG04450	lung:	fetal
20	chr13:90419012-90419062	HRCEpiC	kidney:	n/a
21	chr13:90419012-90419062	LNCaP	prostate:	n/a
22	chr13:90557520-90557570	HCM	heart:	n/a
23	chr13:90557520-90557570	CMK	blood:	n/a
24	chr13:90557520-90557570	SKMC	muscle:	n/a
25	chr13:90557520-90557570	GM19239	blood:	n/a
26	chr13:90536270-90536320	Jurkat	blood:	n/a
27	chr13:90536270-90536320	ECC-1	luminal epithelium:	n/a
28	chr13:90557520-90557570	GM12891	blood:	n/a
29	chr13:90536270-90536320	AG10803	skin:	n/a
30	chr13:90557520-90557570	HNPCEpiC	eye:	n/a
31	chr13:90419012-90419062	HIPEpiC	eye:	n/a
32	chr13:90557520-90557570	NT2-D1	testis:	n/a
33	chr13:90557520-90557570	AG09319	gingival:	n/a
34	chr13:90557520-90557570	HRPEpiC	eye:	n/a
35	chr13:90536270-90536320	ProgFib	skin:	n/a
36	chr13:90557520-90557570	ovcar-3	ovarian:	n/a
37	chr13:90419012-90419062	NH-A	brain:	n/a
38	chr13:90557520-90557570	HUVEC	blood vessel:	n/a
39	chr13:90536270-90536320	CMK	blood:	n/a
40	chr13:90536270-90536320	GM19239	blood:	n/a
41	chr13:90419012-90419062	HNPCEpiC	eye:	n/a
42	chr13:90536270-90536320	ovcar-3	ovarian:	n/a
43	chr13:90536270-90536320	NH-A	brain:	n/a
44	chr13:90557520-90557570	HMEC	breast:	n/a
45	chr13:90419012-90419062	HUVEC	blood vessel:	n/a
46	chr13:90419012-90419062	AG04449	skin:	fetal
47	chr13:90536270-90536320	PANC-1	pancreas:	n/a
48	chr13:90557520-90557570	ECC-1	luminal epithelium:	n/a
49	chr13:90419012-90419062	T-47D	breast:	n/a
50	chr13:90419012-90419062	SK-N-SH	brain:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:90418481..90420847-chr13:90437525..90440214,2	MCF-7	breast:
2	chr13:90471832..90475214-chr13:90475498..90478937,3	K562	blood:
3	chr13:90476201..90479176-chr13:90479802..90482619,4	K562	blood:
4	chr13:90511605..90514028-chr13:90549100..90551730,2	K562	blood:
5	chr13:90497518..90499702-chr13:90509556..90511719,2	K562	blood:
6	chr13:90512365..90514845-chr13:90515836..90518602,3	K562	blood:
7	chr13:90442816..90446344-chr13:90446714..90450498,3	K562	blood:
8	chr13:90544412..90546341-chr13:90551514..90554190,2	K562	blood:
9	chr13:90438180..90442021-chr13:90442191..90444686,4	K562	blood:
10	chr13:90497383..90499732-chr13:90531093..90533343,2	K562	blood:
11	chr13:81107224..81110748-chr13:90439942..90442170,3	K562	blood:
12	chr13:90544412..90546341-chr13:90551514..90554190,2	K562	blood:
13	chr13:90494528..90497292-chr13:90501979..90504191,2	K562	blood:
14	chr13:81104877..81107145-chr13:90439895..90442181,2	K562	blood:
15	chr13:90458920..90462227-chr13:90462309..90464800,3	K562	blood:
16	chr13:90485791..90488603-chr13:90572909..90574724,2	K562	blood:
17	chr13:90546450..90548296-chr13:90550837..90552817,2	K562	blood:
18	chr13:90559611..90562842-chr13:90563397..90566907,4	K562	blood:
19	chr13:90458920..90462227-chr13:90462309..90464800,3	K562	blood:
20	chr13:90449351..90452223-chr13:90453733..90455503,2	K562	blood:
21	chr13:90567117..90569538-chr13:90570624..90572320,2	K562	blood:
22	chr13:90520551..90523101-chr13:90523541..90526179,2	K562	blood:
23	chr13:90559611..90562586-chr13:90563397..90565407,2	K562	blood:
24	chr13:90535683..90539242-chr13:90544865..90546775,3	K562	blood:
25	chr13:90418481..90420847-chr13:90437525..90440214,2	MCF-7	breast:
26	chr13:90503021..90505248-chr13:90522528..90525027,2	K562	blood:
27	chr13:90517201..90517899-chr4:180957059..180957638,2	MCF-7	breast:
28	chr13:90559611..90562842-chr13:90563397..90566907,4	K562	blood:
29	chr13:90461092..90463944-chr13:90499339..90502245,2	K562	blood:
30	chr13:90462886..90465501-chr13:90466757..90468821,2	K562	blood:
31	chr13:90172699..90174465-chr13:90182640..90184619,2	MCF-7	breast:
32	chr13:90436471..90441172-chr13:90442955..90446450,4	K562	blood:
33	chr13:90535683..90539242-chr13:90544865..90546775,3	K562	blood:
34	chr13:90451472..90453159-chr13:90467765..90470147,2	K562	blood:
35	chr13:90497383..90499732-chr13:90531093..90533343,2	K562	blood:
36	chr13:90494528..90497292-chr13:90501979..90504191,2	K562	blood:
37	chr13:90573050..90575053-chr13:90601953..90604544,2	K562	blood:
38	chr13:90471832..90475214-chr13:90475498..90478937,3	K562	blood:
39	chr13:90546450..90548296-chr13:90550837..90552817,2	K562	blood:
40	chr13:90576825..90578329-chr13:90580661..90582682,2	K562	blood:
41	chr13:81107870..81110072-chr13:90437576..90439628,3	K562	blood:
42	chr13:90576287..90578487-chr13:90579534..90581109,2	K562	blood:
43	chr13:90520551..90523101-chr13:90523541..90526179,2	K562	blood:
44	chr13:90347808..90348492-chr13:90905964..90906495,2	MCF-7	breast:
45	chr13:90512365..90514845-chr13:90515836..90519409,3	K562	blood:
46	chr13:90451578..90453716-chr13:90460021..90462776,2	K562	blood:
47	chr13:90505837..90509625-chr13:90510722..90514871,5	K562	blood:
48	chr13:90503021..90505248-chr13:90522528..90525027,2	K562	blood:
49	chr13:90172699..90174465-chr13:90182640..90184619,2	MCF-7	breast:
50	chr13:90539319..90541574-chr13:91998332..92001318,2	K562	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-26	chr13:90353649-90353765	NONHSAT034635
2	lnc-GPC5-4	chr13:90204359-90204643	ENSG00000271395.1
3	lnc-SLITRK6-12	chr13:90204359-90204643	XLOC_010686
4	lnc-SLITRK6-12	chr13:90203455-90203544	NONHSAT034632
5	lnc-SLITRK5-28	chr13:90186815-90187120	NONHSAT034630
6	lnc-GPC5-4	chr13:90203039-90203531	XLOC_010468
7	lnc-SLITRK6-12	chr13:90205985-90206058	XLOC_010686
8	lnc-GPC5-4	chr13:90204359-90204606	XLOC_010468
9	lnc-GPC5-4	chr13:90203487-90203531	ENSG00000271395.1
10	lnc-SLITRK6-28	chr13:90577868-90578113	NONHSAT034638
11	lnc-SLITRK6-12	chr13:90216586-90216667	NONHSAT034632
12	lnc-SLITRK6-28	chr13:90577907-90578113	NONHSAT034639
13	lnc-SLITRK6-26	chr13:90376736-90376852	NONHSAT034635
14	lnc-SLITRK6-27	chr13:90537509-90537789	NONHSAT034637
15	lnc-SLITRK5-28	chr13:90186444-90186646	NONHSAT034630
16	lnc-SLITRK6-26	chr13:90361586-90361709	NONHSAT034635
17	lnc-SLITRK6-27	chr13:90539777-90539848	NONHSAT034637
18	lnc-SLITRK6-11	chr13:90129862-90130391	XLOC_010685
19	lnc-SLITRK6-12	chr13:90203455-90203544	XLOC_010686
20	lnc-SLITRK6-12	chr13:90201048-90201465	NONHSAT034632
21	lnc-SLITRK6-12	chr13:90203487-90203531	XLOC_010686
22	lnc-SLITRK6-26	chr13:90343642-90343795	NONHSAT034635
23	lnc-SLITRK6-26	chr13:90341209-90342696	NONHSAT034635
24	lnc-SLITRK6-26	chr13:90351476-90351493	NONHSAT034635
25	lnc-SLITRK6-11	chr13:90152628-90152763	XLOC_010685
26	lnc-SLITRK6-28	chr13:90577876-90578113	l_900_chr13:90577875-90581583_kidney
27	lnc-SLITRK6-12	chr13:90200945-90201465	XLOC_010686
28	lnc-SLITRK6-12	chr13:90205985-90206049	NONHSAT034632

No data

Variant related genes	Relation type
RPL7L1P1	TF binding region
ENSG00000200733	TF binding region
LINC01040	TF binding region
LINC00353	TF binding region
ENSG00000271395	TF binding region
RPL7L1P1	CpG island
ENSG00000200733	CpG island
LINC01040	CpG island
LINC00353	CpG island
ENSG00000271395	CpG island
ENSG00000215417	chromatin interactions
ENSG00000234227	chromatin interactions
ENSG00000200733	chromatin interactions
MBNL1	miRNA target sites
HSP90B1	miRNA target sites

Extended variants
information (count: 8102 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:8102 , 50 per page) page: 1 2 3 4 5 6 7 ... 163

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540318289	chr13:90100522-90100523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372965087	chr13:90100523-90100524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187756029	chr13:90100543-90100544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544127519	chr13:90100600-90100601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545087375	chr13:90100601-90100602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs9555893	chr13:90100619-90100620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375577157	chr13:90100684-90100685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545460720	chr13:90100686-90100687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529903564	chr13:90100687-90100688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548094269	chr13:90100689-90100690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560248876	chr13:90100704-90100705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192713437	chr13:90100713-90100714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185013640	chr13:90100720-90100721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189393201	chr13:90100723-90100724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368364213	chr13:90100784-90100785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564906801	chr13:90100810-90100811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145305773	chr13:90100817-90100818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532531048	chr13:90100841-90100842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550957975	chr13:90100845-90100846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569577556	chr13:90100848-90100849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536897999	chr13:90100852-90100853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554908832	chr13:90100864-90100865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562906023	chr13:90100892-90100893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533683689	chr13:90100893-90100894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558598665	chr13:90100895-90100896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576501870	chr13:90100928-90100929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531814598	chr13:90100937-90100938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111379231	chr13:90100972-90100973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543821873	chr13:90101065-90101066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555699398	chr13:90101068-90101069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs36113720	chr13:90101071-90101072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200986835	chr13:90101098-90101099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574395850	chr13:90101114-90101115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77119422	chr13:90101124-90101125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs199652046	chr13:90101161-90101162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141063069	chr13:90101210-90101211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs80078778	chr13:90101216-90101217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540402427	chr13:90101220-90101221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1199476	chr13:90101260-90101261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542358616	chr13:90101379-90101380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181815028	chr13:90101380-90101381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532607564	chr13:90101384-90101385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550995072	chr13:90101390-90101391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569268987	chr13:90101414-90101415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530366708	chr13:90101434-90101435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs58367484	chr13:90101449-90101450	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs9522565	chr13:90101479-90101480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116460407	chr13:90101501-90101502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548106940	chr13:90101508-90101509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184609614	chr13:90101515-90101516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Burkitt''s lymphoma	20823134	CNVD
Osteosarcoma	21215367	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:90078800-90107200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr13:90100200-90103000	Weak transcription	Fetal Heart	heart
3	chr13:90103000-90103400	Enhancers	Fetal Heart	heart
4	chr13:90103600-90107200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr13:90104200-90107600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr13:90106600-90111600	Enhancers	NHEK	skin
7	chr13:90107000-90111600	Enhancers	HMEC	breast
8	chr13:90107200-90110600	Enhancers	HUVEC	blood vessel
9	chr13:90107200-90111400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr13:90107200-90111400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr13:90107600-90107800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr13:90107800-90108200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr13:90108000-90108200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr13:90108000-90108200	Enhancers	Hela-S3	cervix
15	chr13:90108000-90108400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr13:90108200-90109600	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr13:90108200-90111600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr13:90108400-90108800	Enhancers	Placenta Amnion	Placenta Amnion
19	chr13:90108600-90109800	Weak transcription	Hela-S3	cervix
20	chr13:90108800-90109800	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr13:90109600-90111200	Enhancers	Muscle Satellite Cultured Cells	--
22	chr13:90109800-90110000	Enhancers	Placenta Amnion	Placenta Amnion
23	chr13:90109800-90110200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr13:90109800-90110200	Enhancers	A549	lung
25	chr13:90109800-90110600	Enhancers	Hela-S3	cervix
26	chr13:90109800-90110800	Enhancers	Adipose Nuclei	Adipose
27	chr13:90109800-90111000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr13:90109800-90111200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr13:90110200-90110600	Flanking Active TSS	A549	lung
30	chr13:90111600-90112600	Weak transcription	HMEC	breast
31	chr13:90114600-90115600	Enhancers	Fetal Heart	heart
32	chr13:90116200-90117200	Weak transcription	HMEC	breast
33	chr13:90117200-90118000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr13:90117200-90118200	Enhancers	HMEC	breast
35	chr13:90117800-90118000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr13:90118000-90119000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr13:90119000-90119600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr13:90138200-90138600	Enhancers	Fetal Heart	heart
39	chr13:90138600-90139400	Weak transcription	Fetal Heart	heart
40	chr13:90139400-90139600	Enhancers	Fetal Heart	heart
41	chr13:90148600-90149000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:90148600-90149000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr13:90148600-90149000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr13:90148600-90149000	Enhancers	Fetal Heart	heart
45	chr13:90149000-90149800	Weak transcription	Fetal Heart	heart
46	chr13:90149800-90150000	Enhancers	Fetal Heart	heart
47	chr13:90150000-90151000	Weak transcription	Fetal Heart	heart
48	chr13:90151000-90151200	Enhancers	Fetal Heart	heart
49	chr13:90160000-90160400	Enhancers	A549	lung
50	chr13:90162600-90164800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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