Variant report

Variant	nsv931946
Chromosome Location	chr9:99895658-100005099
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1465)
CpG islands
(count:915)
Chromatin interactive
region (count:15)
LncRNA
region (count:42)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:100001930-100002027	K562	blood:	n/a	n/a
2	ARID3A	chr9:100000518-100000813	K562	blood:	n/a	n/a
3	ATF1	chr9:99898753-99898939	K562	blood:	n/a	n/a
4	ATF1	chr9:100000460-100001186	K562	blood:	n/a	n/a
5	ATF2	chr9:99976867-99977201	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:99981818-99984334	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:99982856-99984390	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr9:100000141-100001198	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr9:99981989-99982295	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr9:99977754-99978001	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr9:99984388-99985100	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr9:99995434-99995498	K562	blood:	n/a	n/a
13	BACH1	chr9:99955341-99955359	K562	blood:	n/a	n/a
14	BACH1	chr9:99983272-99983972	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:100000505-100000896	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr9:99995458-99995632	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr9:99928821-99929031	GM12878	blood:	n/a	n/a
18	BATF	chr9:99956088-99956460	GM12878	blood:	n/a	chr9:99956249-99956260 chr9:99956275-99956286
19	BATF	chr9:99987396-99987596	GM12878	blood:	n/a	n/a
20	BATF	chr9:99987054-99987282	GM12878	blood:	n/a	n/a
21	BATF	chr9:99984465-99984697	GM12878	blood:	n/a	n/a
22	BATF	chr9:99987390-99987620	GM12878	blood:	n/a	n/a
23	BCL11A	chr9:99984868-99985050	GM12878	blood:	n/a	chr9:99984918-99984927
24	BCL11A	chr9:99984436-99984715	GM12878	blood:	n/a	n/a
25	BCL11A	chr9:99987379-99987600	GM12878	blood:	n/a	n/a
26	BCL11A	chr9:99983942-99984126	GM12878	blood:	n/a	chr9:99983961-99983974
27	BCL11A	chr9:99984110-99984374	GM12878	blood:	n/a	chr9:99984153-99984166
28	BCL11A	chr9:99987376-99987628	GM12878	blood:	n/a	n/a
29	BCLAF1	chr9:100000332-100000976	K562	blood:	n/a	n/a
30	BHLHE40	chr9:99983908-99984108	K562	blood:	n/a	n/a
31	BHLHE40	chr9:100000372-100001175	K562	blood:	n/a	chr9:100000471-100000487
32	BHLHE40	chr9:99999689-99999889	K562	blood:	n/a	n/a
33	BHLHE40	chr9:99930605-99930636	K562	blood:	n/a	n/a
34	BHLHE40	chr9:99938665-99938753	K562	blood:	n/a	n/a
35	BRCA1	chr9:100000554-100001345	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr9:99983628-99983965	K562	blood:	n/a	n/a
37	CBX3	chr9:99994472-99995102	K562	blood:	n/a	n/a
38	CBX3	chr9:100000228-100001221	K562	blood:	n/a	n/a
39	CBX3	chr9:100000322-100000890	K562	blood:	n/a	n/a
40	CCNT2	chr9:100000409-100001029	K562	blood:	n/a	chr9:100000991-100001011
41	CCNT2	chr9:99983809-99984069	K562	blood:	n/a	n/a
42	CCNT2	chr9:99930594-99930784	K562	blood:	n/a	n/a
43	CEBPB	chr9:99941827-99942208	MCF-7	breast:	n/a	n/a
44	CEBPB	chr9:99994424-99994811	K562	blood:	n/a	chr9:99994608-99994619
45	CEBPB	chr9:100000626-100000727	K562	blood:	n/a	n/a
46	CEBPB	chr9:99993512-99993703	K562	blood:	n/a	n/a
47	CEBPB	chr9:99994400-99994971	K562	blood:	n/a	chr9:99994608-99994619
48	CEBPB	chr9:99997335-99997752	K562	blood:	n/a	n/a
49	CEBPB	chr9:99941985-99942301	MCF-7	breast:	n/a	n/a
50	CEBPB	chr9:100000573-100001274	Hela-S3	cervix:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:100000033-100000083	GM06990	blood:	n/a
2	chr9:99983211-99983261	HRPEpiC	eye:	n/a
3	chr9:100000415-100000465	Hela-S3	cervix:	n/a
4	chr9:99962350-99962400	IMR90	lung:	fetal
5	chr9:99915901-99915951	AG09309	skin:	n/a
6	chr9:99962039-99962089	PFSK-1	brain:	n/a
7	chr9:99983211-99983261	AG04449	skin:	fetal
8	chr9:100000464-100000514	H1-hESC	embryonic stem cell:	embryo
9	chr9:99963165-99963215	NH-A	brain:	n/a
10	chr9:99915901-99915951	BJ	skin:	n/a
11	chr9:99984136-99984186	NHDF-neo	bronchial:	n/a
12	chr9:99915901-99915951	HRPEpiC	eye:	n/a
13	chr9:99962350-99962400	AG09319	gingival:	n/a
14	chr9:99983211-99983261	HNPCEpiC	eye:	n/a
15	chr9:100000026-100000076	SKMC	muscle:	n/a
16	chr9:99963165-99963215	ECC-1	luminal epithelium:	n/a
17	chr9:99963165-99963215	GM12891	blood:	n/a
18	chr9:100000768-100000818	HMEC	breast:	n/a
19	chr9:99984521-99984571	SAEC	small airway:	n/a
20	chr9:100000415-100000465	SAEC	small airway:	n/a
21	chr9:99962350-99962400	BJ	skin:	n/a
22	chr9:99983156-99983206	HCM	heart:	n/a
23	chr9:100000768-100000818	K562	blood:	n/a
24	chr9:99962039-99962089	NH-A	brain:	n/a
25	chr9:99983211-99983261	GM06990	blood:	n/a
26	chr9:99984136-99984186	PFSK-1	brain:	n/a
27	chr9:100000026-100000076	HepG2	liver:	n/a
28	chr9:99998343-99998393	GM12891	blood:	n/a
29	chr9:100000026-100000076	HL-60	blood:	n/a
30	chr9:99962350-99962400	PANC-1	pancreas:	n/a
31	chr9:100000464-100000514	IMR90	lung:	fetal
32	chr9:99962039-99962089	MCF-7	breast:	n/a
33	chr9:99983211-99983261	NT2-D1	testis:	n/a
34	chr9:99998343-99998393	PANC-1	pancreas:	n/a
35	chr9:100000033-100000083	HepG2	liver:	n/a
36	chr9:100000464-100000514	A549	lung:	n/a
37	chr9:100000768-100000818	T-47D	breast:	n/a
38	chr9:99984521-99984571	GM06990	blood:	n/a
39	chr9:99895750-99895800	LNCaP	prostate:	n/a
40	chr9:99915901-99915951	HUVEC	blood vessel:	n/a
41	chr9:100000026-100000076	SK-N-SH_RA	brain:	n/a
42	chr9:99895750-99895800	AG09319	gingival:	n/a
43	chr9:100000464-100000514	GM12892	blood:	n/a
44	chr9:99984136-99984186	AG04449	skin:	fetal
45	chr9:99962039-99962089	U87	brain:	n/a
46	chr9:99984521-99984571	HCF	heart:	n/a
47	chr9:99962039-99962089	Hepatocyte	liver:	n/a
48	chr9:100000033-100000083	ovcar-3	ovarian:	n/a
49	chr9:100000415-100000465	GM12891	blood:	n/a
50	chr9:99983156-99983206	SAEC	small airway:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:41495372..41496932-chr9:99998502..100000578,3	K562	blood:
2	chr17:42083081..42083791-chr9:100000515..100001032,2	HCT-116	colon:
3	chr9:100003140..100004870-chr9:100029614..100032184,2	K562	blood:
4	chr9:99329436..99331023-chr9:99999393..100001023,2	K562	blood:
5	chr9:99995457..99997246-chr9:99998878..100000683,2	K562	blood:
6	chr9:99994043..99996478-chr9:99999503..100002032,3	K562	blood:
7	chr9:99999075..100002333-chr9:100004185..100008617,4	K562	blood:
8	chr9:99983881..99984841-chr9:100149024..100149576,2	MCF-7	breast:
9	chr13:41495372..41498388-chr9:99998502..100001030,4	K562	blood:
10	chr9:99994939..99996604-chr9:99997527..100000515,2	MCF-7	breast:
11	chr9:99985067..99987314-chr9:99998375..100001266,2	K562	blood:
12	chr6:26157894..26158726-chr9:100000252..100000813,2	HCT-116	colon:
13	chr9:99994043..99996478-chr9:99999503..100002032,3	K562	blood:
14	chr9:99999075..100001905-chr9:100002725..100008617,7	K562	blood:
15	chr9:99998207..100000626-chr9:100147568..100149189,2	K562	blood:

(count:42 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf174-1	chr9:99997167-99997296	XLOC_007483
2	lnc-CTSL2-4	chr9:99924847-99925128	ENSG00000159712.9
3	lnc-C9orf174-1	chr9:99995483-99995633	XLOC_007483
4	lnc-CTSL2-4	chr9:99949736-99949789	ENSG00000159712.9
5	lnc-CTSL2-4	chr9:99932889-99933018	ENSG00000159712.9
6	lnc-CTSL2-5	chr9:99915509-99916020	NONHSAT133483
7	lnc-CTSL2-4	chr9:99947724-99947797	ENSG00000159712.9
8	lnc-CTSL2-5	chr9:99916172-99916337	NONHSAT133483
9	lnc-CTSL2-4	chr9:99924037-99924248	ENSG00000159712.9
10	lnc-CTSL2-3	chr9:99958811-99958876	ENSG00000242375.1
11	lnc-CTSL2-6	chr9:99906742-99907022	NONHSAT133477
12	lnc-CTSL2-5	chr9:99962757-99962847	ENSG00000203279.3
13	lnc-CTSL2-4	chr9:99962741-99962847	ENSG00000159712.9
14	lnc-CTSL2-4	chr9:99942283-99943198	ENSG00000159712.9
15	lnc-CTSL2-4	chr9:99967143-99967316	ENSG00000159712.9
16	lnc-CTSL2-4	chr9:99973655-99973769	ENSG00000159712.9
17	lnc-CTSL2-5	chr9:100000705-100000960	ENSG00000203279
18	lnc-CTSL2-5	chr9:99973655-99973769	ENSG00000203279.3
19	lnc-CTSL2-3	chr9:99959802-99959969	ENSG00000242375.1
20	lnc-CTSL2-5	chr9:99918814-99918867	NONHSAT133483
21	lnc-CTSL2-6	chr9:99901930-99902236	NONHSAT133476
22	lnc-C9orf174-2	chr9:99974685-99974721	NONHSAT133490
23	lnc-CTSL2-5	chr9:99917886-99918005	NONHSAT133483
24	lnc-CTSL2-5	chr9:99924037-99924230	NONHSAT133483
25	lnc-CTSL2-4	chr9:99922464-99922684	ENSG00000159712.9
26	lnc-C9orf174-2	chr9:99973941-99974529	NONHSAT133490
27	lnc-CTSL2-4	chr9:99940546-99940695	ENSG00000159712.9
28	lnc-CTSL2-6	chr9:99906923-99907022	NONHSAT133476
29	lnc-CTSL2-5	chr9:99920066-99920111	NONHSAT133483
30	lnc-CTSL2-5	chr9:99922464-99922684	NONHSAT133483
31	lnc-CTSL2-5	chr9:100000705-100000982	ENSG00000203279.3
32	lnc-CTSL2-4	chr9:99935228-99935342	ENSG00000159712.9
33	lnc-CTSL2-4	chr9:99983312-99983538	ENSG00000159712.9
34	lnc-CTSL2-6	chr9:99906140-99906208	NONHSAT133476
35	lnc-CTSL2-5	chr9:100000046-100000367	ENSG00000203279
36	lnc-CTSL2-6	chr9:99910243-99911530	NONHSAT133477
37	lnc-CTSL2-4	chr9:99954013-99954080	ENSG00000159712.9
38	lnc-CTSL2-6	chr9:99910243-99911530	NONHSAT133476
39	lnc-CTSL2-3	chr9:99957620-99958989	NONHSAT133488
40	lnc-CTSL2-3	chr9:99957633-99957872	ENSG00000242375.1
41	lnc-CTSL2-4	chr9:99918175-99918867	ENSG00000159712.9
42	lnc-CTSL2-4	chr9:99956985-99957122	ENSG00000159712.9

No data

Variant related genes	Relation type
RNU6-798P	TF binding region
ZNF322P1	TF binding region
ENSG00000242375	TF binding region
ENSG00000254876	TF binding region
ANKRD18CP	TF binding region
ENSG00000254483	TF binding region
ENSG00000255036	TF binding region
CCDC180	TF binding region
ENSG00000235494	TF binding region
ENSG00000203279	TF binding region
RNU6-798P	CpG island
ZNF322P1	CpG island
ENSG00000242375	CpG island
ENSG00000254876	CpG island
ANKRD18CP	CpG island
ENSG00000254483	CpG island
ENSG00000255036	CpG island
CCDC180	CpG island
ENSG00000235494	CpG island
ENSG00000203279	CpG island
ENSG00000161653	chromatin interactions
ENSG00000235494	chromatin interactions
ENSG00000168852	chromatin interactions
ENSG00000239827	chromatin interactions
ENSG00000197816	chromatin interactions
ENSG00000254483	chromatin interactions
ENSG00000081377	chromatin interactions
ENSG00000203279	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000254876	chromatin interactions
KLHL28	miRNA target sites
CHIC2	miRNA target sites

Extended variants
information (count: 3938 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:3938 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2001382	chr9:99895662-99895663	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531000390	chr9:99895718-99895719	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552773465	chr9:99895750-99895751	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147982587	chr9:99895788-99895789	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535143181	chr9:99895802-99895803	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111647494	chr9:99895822-99895823	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568478007	chr9:99895876-99895877	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372961386	chr9:99895877-99895878	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535703788	chr9:99895884-99895885	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113726278	chr9:99895909-99895910	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575641152	chr9:99895999-99896000	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs60971320	chr9:99896011-99896012	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs557952592	chr9:99896059-99896060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572815186	chr9:99896068-99896069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534290318	chr9:99896091-99896092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116965369	chr9:99896135-99896136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376889571	chr9:99896174-99896175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12685813	chr9:99896238-99896239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561478887	chr9:99896241-99896242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532036938	chr9:99896268-99896269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113656864	chr9:99896302-99896303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375131172	chr9:99896307-99896308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535285799	chr9:99896360-99896361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563626099	chr9:99896405-99896406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531138153	chr9:99896418-99896419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552468360	chr9:99896449-99896450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564720823	chr9:99896496-99896497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565731219	chr9:99896497-99896498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547140867	chr9:99896534-99896535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547076779	chr9:99896553-99896554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192319420	chr9:99896661-99896662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368085656	chr9:99896679-99896680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535831854	chr9:99896703-99896704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551021309	chr9:99896712-99896713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569143580	chr9:99896716-99896717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539734935	chr9:99896719-99896720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557626987	chr9:99896756-99896757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183215227	chr9:99896772-99896773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533793281	chr9:99896785-99896786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555035738	chr9:99896791-99896792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573437326	chr9:99896792-99896793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543783896	chr9:99896797-99896798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555762730	chr9:99896799-99896800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116358621	chr9:99896806-99896807	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546487788	chr9:99896807-99896808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187926171	chr9:99896821-99896822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528685056	chr9:99896854-99896855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540502419	chr9:99896892-99896893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562140168	chr9:99896896-99896897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145185016	chr9:99896903-99896904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1238 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:99875800-99895800	Strong transcription	HUES48 Cell Line	embryonic stem cell
2	chr9:99882000-99896600	Weak transcription	Right Atrium	heart
3	chr9:99882000-99897400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:99884000-99897000	Weak transcription	Dnd41	blood
5	chr9:99889200-99895800	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr9:99889400-99908200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr9:99892800-99895800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:99893800-99896400	Strong transcription	H1 Cell Line	embryonic stem cell
9	chr9:99893800-99896400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
10	chr9:99894000-99898800	Weak transcription	Spleen	Spleen
11	chr9:99894200-99896000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr9:99894400-99898800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr9:99894400-99900400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr9:99894600-99901400	Weak transcription	Pancreas	Pancrea
15	chr9:99895400-99895800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr9:99895600-99896000	Enhancers	Fetal Intestine Large	intestine
17	chr9:99895600-99896600	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr9:99895600-99898000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr9:99895600-99901000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr9:99895800-99897800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr9:99895800-99898800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr9:99895800-99900800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr9:99895800-99902000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr9:99896000-99897800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr9:99896000-99898400	Weak transcription	Fetal Intestine Large	intestine
26	chr9:99896400-99897200	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr9:99896400-99898600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr9:99896600-99898400	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr9:99897200-99899800	Strong transcription	H1 Cell Line	embryonic stem cell
30	chr9:99897800-99902600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr9:99897800-99907600	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr9:99898000-99902200	Strong transcription	H9 Cell Line	embryonic stem cell
33	chr9:99898400-99899200	Enhancers	Fetal Intestine Large	intestine
34	chr9:99898400-99908600	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr9:99898600-99898800	Genic enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr9:99898600-99899200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr9:99898800-99899000	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr9:99898800-99899000	Enhancers	Spleen	Spleen
39	chr9:99898800-99899200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr9:99898800-99899400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
41	chr9:99898800-99908000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr9:99899000-99900200	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr9:99899400-99899600	Genic enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr9:99899600-99900400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr9:99899800-99900600	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr9:99900200-99902400	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr9:99900400-99901000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr9:99900400-99901600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
49	chr9:99900400-99902800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
50	chr9:99900600-99908800	Strong transcription	H1 Cell Line	embryonic stem cell

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