Variant report

Variant	nsv1036105
Chromosome Location	chr9:100131266-100171816
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1135)
CpG islands
(count:244)
Chromatin interactive
region (count:56)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1135 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:100150037-100150163	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:100166871-100167523	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:100168891-100169509	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:100144516-100145302	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:100157383-100157429	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:100149238-100149598	HepG2	liver:	n/a	n/a
7	ATF2	chr9:100159452-100159921	GM12878	blood:	n/a	n/a
8	ATF2	chr9:100149164-100149647	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr9:100149264-100149618	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr9:100159366-100159963	GM12878	blood:	n/a	n/a
11	ATF2	chr9:100150995-100151417	GM12878	blood:	n/a	n/a
12	BACH1	chr9:100168835-100169211	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr9:100161450-100161726	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr9:100152181-100152548	GM12878	blood:	n/a	n/a
15	BATF	chr9:100159456-100159960	GM12878	blood:	n/a	n/a
16	BATF	chr9:100167903-100168147	GM12878	blood:	n/a	n/a
17	BATF	chr9:100159459-100159895	GM12878	blood:	n/a	n/a
18	BATF	chr9:100151007-100151436	GM12878	blood:	n/a	n/a
19	BCL11A	chr9:100159538-100159872	GM12878	blood:	n/a	n/a
20	BCL11A	chr9:100159468-100159859	GM12878	blood:	n/a	n/a
21	BCL11A	chr9:100151084-100151386	GM12878	blood:	n/a	chr9:100151207-100151216
22	BCL3	chr9:100151001-100151489	GM12878	blood:	n/a	chr9:100151207-100151216
23	BHLHE40	chr9:100161427-100161775	GM12878	blood:	n/a	n/a
24	BHLHE40	chr9:100149291-100149617	GM12878	blood:	n/a	chr9:100149481-100149497
25	BHLHE40	chr9:100157290-100157586	HepG2	liver:	n/a	n/a
26	BHLHE40	chr9:100149327-100149717	K562	blood:	n/a	chr9:100149481-100149497
27	BHLHE40	chr9:100161386-100161734	HepG2	liver:	n/a	n/a
28	BHLHE40	chr9:100167024-100167434	HepG2	liver:	n/a	n/a
29	BHLHE40	chr9:100134980-100135180	K562	blood:	n/a	n/a
30	BHLHE40	chr9:100161437-100161778	K562	blood:	n/a	n/a
31	BHLHE40	chr9:100151127-100151455	GM12878	blood:	n/a	n/a
32	BRCA1	chr9:100149457-100149581	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr9:100150996-100151161	GM12878	blood:	n/a	n/a
34	BRCA1	chr9:100148708-100148736	HepG2	liver:	n/a	n/a
35	BRCA1	chr9:100161372-100161717	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr9:100152514-100152537	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr9:100165891-100166560	K562	blood:	n/a	n/a
38	CBX3	chr9:100161372-100161732	K562	blood:	n/a	n/a
39	CBX3	chr9:100165998-100166296	K562	blood:	n/a	n/a
40	CBX3	chr9:100131252-100131573	K562	blood:	n/a	n/a
41	CBX3	chr9:100149215-100149703	K562	blood:	n/a	n/a
42	CBX3	chr9:100165938-100166465	HCT-116	colon:	n/a	n/a
43	CCNT2	chr9:100149438-100149637	K562	blood:	n/a	n/a
44	CEBPB	chr9:100134983-100135166	K562	blood:	n/a	n/a
45	CEBPB	chr9:100166981-100167354	HepG2	liver:	n/a	n/a
46	CEBPB	chr9:100168572-100168673	HepG2	liver:	n/a	n/a
47	CEBPB	chr9:100169047-100169335	HepG2	liver:	n/a	chr9:100169180-100169191
48	CEBPB	chr9:100134896-100135249	K562	blood:	n/a	n/a
49	CEBPB	chr9:100167006-100167402	HepG2	liver:	n/a	n/a
50	CEBPB	chr9:100147037-100147553	HepG2	liver:	n/a	chr9:100147161-100147172 chr9:100147159-100147172 chr9:100147161-100147172 chr9:100147121-100147134

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:100158232-100158282	HEEpiC	esophagus:	n/a
2	chr9:100159057-100159107	SK-N-SH_RA	brain:	n/a
3	chr9:100149720-100149770	ProgFib	skin:	n/a
4	chr9:100159780-100159830	GM12891	blood:	n/a
5	chr9:100159780-100159830	HPAEpiC	pulmonary alveolar:	n/a
6	chr9:100159057-100159107	CMK	blood:	n/a
7	chr9:100159057-100159107	NT2-D1	testis:	n/a
8	chr9:100159780-100159830	Jurkat	blood:	n/a
9	chr9:100159057-100159107	GM12891	blood:	n/a
10	chr9:100149720-100149770	K562	blood:	n/a
11	chr9:100159780-100159830	SKMC	muscle:	n/a
12	chr9:100149720-100149770	HRE	kidney:	n/a
13	chr9:100159780-100159830	H1-hESC	embryonic stem cell:	embryo
14	chr9:100159780-100159830	Caco-2	colon:	n/a
15	chr9:100158232-100158282	SAEC	small airway:	n/a
16	chr9:100149720-100149770	AG10803	skin:	n/a
17	chr9:100149720-100149770	SK-N-MC	brain:	n/a
18	chr9:100159057-100159107	ovcar-3	ovarian:	n/a
19	chr9:100158232-100158282	HUVEC	blood vessel:	n/a
20	chr9:100149720-100149770	AG09319	gingival:	n/a
21	chr9:100158232-100158282	SK-N-SH_RA	brain:	n/a
22	chr9:100159780-100159830	GM06990	blood:	n/a
23	chr9:100159780-100159830	ECC-1	luminal epithelium:	n/a
24	chr9:100159057-100159107	RPTEC	kidney:	n/a
25	chr9:100158232-100158282	HIPEpiC	eye:	n/a
26	chr9:100149720-100149770	AoSMC	blood vessel:	n/a
27	chr9:100159780-100159830	MCF-7	breast:	n/a
28	chr9:100158232-100158282	MCF10A-Er-Src	breast:	n/a
29	chr9:100159780-100159830	AG10803	skin:	n/a
30	chr9:100159780-100159830	AG04450	lung:	fetal
31	chr9:100158232-100158282	HCM	heart:	n/a
32	chr9:100149720-100149770	HCT-116	colon:	n/a
33	chr9:100158232-100158282	SK-N-SH	brain:	n/a
34	chr9:100159057-100159107	HUVEC	blood vessel:	n/a
35	chr9:100158232-100158282	HPAEpiC	pulmonary alveolar:	n/a
36	chr9:100149720-100149770	HPAEpiC	pulmonary alveolar:	n/a
37	chr9:100158232-100158282	NH-A	brain:	n/a
38	chr9:100159057-100159107	AoSMC	blood vessel:	n/a
39	chr9:100159780-100159830	HRE	kidney:	n/a
40	chr9:100158232-100158282	HAEpiC	amniotic membrane:	n/a
41	chr9:100159780-100159830	T-47D	breast:	n/a
42	chr9:100149720-100149770	HCM	heart:	n/a
43	chr9:100158232-100158282	BJ	skin:	n/a
44	chr9:100158232-100158282	HepG2	liver:	n/a
45	chr9:100149720-100149770	HEK293	kidney:	embryo
46	chr9:100149720-100149770	BJ	skin:	n/a
47	chr9:100158232-100158282	MCF-7	breast:	n/a
48	chr9:100159780-100159830	HCPEpiC	choroid plexus:	n/a
49	chr9:100158232-100158282	HEK293	kidney:	embryo
50	chr9:100158232-100158282	AG04449	skin:	fetal

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:100125915..100128768-chr9:100134081..100137040,2	MCF-7	breast:
2	chr9:100148987..100149894-chr9:100173635..100174632,7	MCF-7	breast:
3	chr9:100159957..100161541-chr9:100168022..100169977,2	MCF-7	breast:
4	chr9:100149625..100153516-chr9:100159731..100163036,3	MCF-7	breast:
5	chr9:100149070..100149799-chr9:100162402..100162985,2	MCF-7	breast:
6	chr9:100149070..100149799-chr9:100162402..100162985,2	MCF-7	breast:
7	chr9:99619931..99620679-chr9:100161154..100161699,2	K562	blood:
8	chr9:100156242..100157797-chr9:100387232..100389420,2	K562	blood:
9	chr9:100136304..100137136-chr9:100161582..100162137,2	MCF-7	breast:
10	chr9:100158999..100160647-chr9:100162275..100163910,2	MCF-7	breast:
11	chr9:100148981..100149950-chr9:100161161..100161940,4	MCF-7	breast:
12	chr9:100148966..100149836-chr9:100377517..100378454,2	K562	blood:
13	chr9:100148879..100149573-chr9:100377949..100378512,2	MCF-7	breast:
14	chr9:100139724..100142040-chr9:100160057..100161608,2	MCF-7	breast:
15	chr9:100166117..100171813-chr9:100172266..100175744,7	MCF-7	breast:
16	chr9:100153969..100155704-chr9:100162657..100165252,2	K562	blood:
17	chr9:100127178..100130349-chr9:100134319..100136599,3	K562	blood:
18	chr9:100149125..100151047-chr9:100151218..100153967,3	K562	blood:
19	chr9:100161183..100163141-chr9:100166715..100169432,2	K562	blood:
20	chr9:100149689..100151422-chr9:100157235..100158759,2	MCF-7	breast:
21	chr9:100126892..100129618-chr9:100133900..100135494,2	MCF-7	breast:
22	chr9:100150440..100152091-chr9:100159690..100161456,2	MCF-7	breast:
23	chr9:100149345..100149902-chr9:100161061..100161631,4	K562	blood:
24	chr9:100136304..100137136-chr9:100161582..100162137,2	MCF-7	breast:
25	chr9:100135703..100138230-chr9:100150823..100152336,2	K562	blood:
26	chr9:100146001..100148830-chr9:100172962..100175244,2	MCF-7	breast:
27	chr9:99983391..99984311-chr9:100161330..100162132,2	MCF-7	breast:
28	chr9:100161183..100163141-chr9:100166715..100169432,2	K562	blood:
29	chr9:100123731..100126487-chr9:100154413..100156921,2	K562	blood:
30	chr9:100135703..100138230-chr9:100150823..100152336,2	K562	blood:
31	chr9:99983881..99984841-chr9:100149024..100149576,2	MCF-7	breast:
32	chr9:100149345..100149902-chr9:100161061..100161631,4	K562	blood:
33	chr9:100159957..100161541-chr9:100168022..100169977,2	MCF-7	breast:
34	chr9:100148981..100149950-chr9:100161161..100161940,4	MCF-7	breast:
35	chr9:100135058..100137231-chr9:100142276..100144723,2	MCF-7	breast:
36	chr9:100161147..100162387-chr9:100173743..100174617,6	MCF-7	breast:
37	chr9:99998207..100000626-chr9:100147568..100149189,2	K562	blood:
38	chr9:100149125..100152015-chr9:100152467..100154475,2	K562	blood:
39	chr9:100139724..100142040-chr9:100160057..100161608,2	MCF-7	breast:
40	chr9:100158859..100160754-chr9:100392262..100394128,2	K562	blood:
41	chr9:100149241..100149908-chr9:100249138..100249846,2	MCF-7	breast:
42	chr9:100159820..100162414-chr9:100401342..100403835,2	MCF-7	breast:
43	chr9:100150282..100151155-chr9:100159898..100160560,2	MCF-7	breast:
44	chr9:99617834..99619865-chr9:100161774..100163833,2	MCF-7	breast:
45	chr9:100149625..100153516-chr9:100159731..100163036,3	MCF-7	breast:
46	chr9:100160143..100162987-chr9:100172478..100174284,2	MCF-7	breast:
47	chr9:100148865..100149895-chr9:100161070..100162054,16	MCF-7	breast:
48	chr9:100149125..100152015-chr9:100152467..100154475,2	K562	blood:
49	chr9:100150282..100151155-chr9:100159898..100160560,2	MCF-7	breast:
50	chr9:100149125..100151047-chr9:100151218..100153967,3	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSTD2-7	chr9:100161824-100161923	NONHSAT133506
2	lnc-TSTD2-3	chr9:100164458-100167072	XLOC_007796
3	lnc-TSTD2-4	chr9:100155511-100155646	NONHSAT133504
4	lnc-TSTD2-4	chr9:100158332-100158458	XLOC_007795
5	lnc-TSTD2-4	chr9:100158332-100158458	NONHSAT133504
6	lnc-TSTD2-4	chr9:100154937-100154996	NONHSAT133504
7	lnc-TSTD2-4	chr9:100153118-100154996	NONHSAT133503
8	lnc-TSTD2-4	chr9:100153121-100154560	XLOC_007795
9	lnc-TSTD2-4	chr9:100158779-100158973	NONHSAT133504
10	lnc-TSTD2-4	chr9:100155508-100156790	NONHSAT133503
11	lnc-TSTD2-4	chr9:100154937-100154996	XLOC_007795
12	lnc-TSTD2-4	chr9:100153119-100154560	NONHSAT133504
13	lnc-TDRD7-1	chr9:100137736-100140806	NONHSAT133501
14	lnc-TDRD7-1	chr9:100132923-100136930	NONHSAT133501
15	lnc-TSTD2-4	chr9:100158779-100158973	XLOC_007795
16	lnc-TDRD7-1	chr9:100131560-100132364	NONHSAT133501
17	lnc-TSTD2-7	chr9:100163508-100163651	NONHSAT133506
18	lnc-TSTD2-4	chr9:100154852-100155460	NONHSAT133505
19	lnc-TSTD2-4	chr9:100158779-100158947	NONHSAT133503
20	lnc-TSTD2-4	chr9:100155511-100155646	XLOC_007795
21	lnc-TSTD2-4	chr9:100155760-100155816	XLOC_007795
22	lnc-TSTD2-4	chr9:100158332-100158458	NONHSAT133503
23	lnc-TSTD2-4	chr9:100155760-100155816	NONHSAT133504

No data

Variant related genes	Relation type
ENSG00000228957	TF binding region
TDRD7	TF binding region
CCDC180	TF binding region
ENSG00000228957	CpG island
TDRD7	CpG island
CCDC180	CpG island
ENSG00000228957	chromatin interactions
ENSG00000196116	chromatin interactions
ENSG00000221269	chromatin interactions
ENSG00000197816	chromatin interactions
ENSG00000136925	chromatin interactions
ENSG00000159712	chromatin interactions

Extended variants
information (count: 1440 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1440 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551770402	chr9:100131294-100131295	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs566629249	chr9:100131295-100131296	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs534099634	chr9:100131328-100131329	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs374666373	chr9:100131369-100131370	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs184069625	chr9:100131374-100131375	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs529349188	chr9:100131387-100131388	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs140242996	chr9:100131415-100131416	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs187806265	chr9:100131488-100131489	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs555868919	chr9:100131510-100131511	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs577551668	chr9:100131522-100131523	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs370982973	chr9:100131534-100131535	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs10981800	chr9:100131550-100131551	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs577772457	chr9:100131594-100131595	Weak transcription ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs568607994	chr9:100131597-100131598	Weak transcription ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs10981801	chr9:100131654-100131655	Weak transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs149875348	chr9:100131655-100131656	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
17	rs36162116	chr9:100131659-100131660	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
18	rs67349968	chr9:100131696-100131697	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
19	rs200829059	chr9:100131697-100131698	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
20	rs377747441	chr9:100131701-100131702	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
21	rs368812940	chr9:100131702-100131703	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
22	rs200924232	chr9:100131711-100131712	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
23	rs540927389	chr9:100131748-100131749	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
24	rs3052478	chr9:100131751-100131752	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
25	rs368571176	chr9:100131752-100131753	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
26	rs1564050	chr9:100131843-100131844	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs149033812	chr9:100131884-100131885	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs544693884	chr9:100131970-100131971	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs562937205	chr9:100132010-100132011	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs533490812	chr9:100132020-100132021	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs559072046	chr9:100132079-100132080	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs551441770	chr9:100132082-100132083	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs113638156	chr9:100132085-100132086	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs527582038	chr9:100132135-100132136	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs374581126	chr9:100132142-100132143	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs201788156	chr9:100132176-100132177	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs2169456	chr9:100132194-100132195	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs567102377	chr9:100132210-100132211	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs138542626	chr9:100132214-100132215	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs141508161	chr9:100132220-100132221	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs61741729	chr9:100132241-100132242	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs540538354	chr9:100132242-100132243	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs375265202	chr9:100132252-100132253	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs200929163	chr9:100132281-100132282	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs571225137	chr9:100132303-100132304	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs145469075	chr9:100132308-100132309	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs202226425	chr9:100132320-100132321	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs147680830	chr9:100132331-100132332	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs373880004	chr9:100132338-100132339	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs141047389	chr9:100132347-100132348	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD
Neurodevelopmental disorder	22521361	CNVD
Nicotine dependence	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:688 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100070000-100131400	Weak transcription	Fetal Kidney	kidney
2	chr9:100077000-100140800	Weak transcription	Fetal Brain Male	brain
3	chr9:100086600-100132000	Weak transcription	Thymus	Thymus
4	chr9:100088600-100132800	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr9:100090600-100133800	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr9:100091600-100149200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr9:100099000-100132200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr9:100104400-100142000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr9:100106800-100143200	Weak transcription	Liver	Liver
10	chr9:100107000-100131400	Weak transcription	Primary hematopoietic stem cells	blood
11	chr9:100107200-100138400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr9:100108000-100148200	Weak transcription	Esophagus	oesophagus
13	chr9:100110200-100132200	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr9:100115400-100144600	Weak transcription	Hela-S3	cervix
15	chr9:100115600-100139200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr9:100117400-100132400	Weak transcription	Fetal Intestine Large	intestine
17	chr9:100117400-100145000	Weak transcription	Colon Smooth Muscle	Colon
18	chr9:100117600-100146400	Weak transcription	Small Intestine	intestine
19	chr9:100118200-100132400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr9:100118200-100141600	Weak transcription	Primary T cells from cord blood	blood
21	chr9:100120000-100137800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr9:100121800-100137800	Weak transcription	Gastric	stomach
23	chr9:100125400-100132200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr9:100126400-100131400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr9:100126400-100137800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr9:100126600-100141600	Weak transcription	Primary B cells from peripheral blood	blood
27	chr9:100126600-100148400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr9:100127000-100148600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr9:100128800-100132600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr9:100129000-100131400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr9:100129000-100131400	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr9:100129000-100131800	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr9:100129000-100132000	Weak transcription	Ovary	ovary
34	chr9:100129000-100132000	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr9:100129000-100132200	Weak transcription	Lung	lung
36	chr9:100129000-100132400	Weak transcription	Brain Angular Gyrus	brain
37	chr9:100129000-100132400	Weak transcription	Brain Cingulate Gyrus	brain
38	chr9:100129000-100134800	Weak transcription	Spleen	Spleen
39	chr9:100129000-100137200	Weak transcription	Aorta	Aorta
40	chr9:100129000-100137800	Weak transcription	Pancreas	Pancrea
41	chr9:100129000-100138200	Weak transcription	Brain Substantia Nigra	brain
42	chr9:100129000-100144400	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr9:100129200-100131400	Weak transcription	Brain Anterior Caudate	brain
44	chr9:100129200-100131400	Weak transcription	Duodenum Mucosa	Duodenum
45	chr9:100129200-100131600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr9:100129200-100131800	Weak transcription	Fetal Intestine Small	intestine
47	chr9:100129200-100132000	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr9:100129200-100132200	Weak transcription	Stomach Smooth Muscle	stomach
49	chr9:100129200-100132400	Weak transcription	Right Ventricle	heart
50	chr9:100129200-100132400	Weak transcription	Skeletal Muscle Male	skeletal muscle

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