Variant report

Variant	nsv427835
Chromosome Location	chr9:31994-235675
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2217)
CpG islands
(count:1770)
Chromatin interactive
region (count:33)
LncRNA
region (count:52)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2217 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:215966-216247	K562	blood:	n/a	n/a
2	ARID3A	chr9:95057-95158	K562	blood:	n/a	n/a
3	ARID3A	chr9:94438-94633	K562	blood:	n/a	chr9:94582-94598
4	ARID3A	chr9:229136-229466	K562	blood:	n/a	n/a
5	ARID3A	chr9:214214-215154	K562	blood:	n/a	n/a
6	ARID3A	chr9:210220-210873	K562	blood:	n/a	n/a
7	ATF1	chr9:94435-94576	K562	blood:	n/a	n/a
8	ATF1	chr9:222266-222777	K562	blood:	n/a	n/a
9	ATF1	chr9:211078-211816	K562	blood:	n/a	n/a
10	ATF1	chr9:44552-44676	K562	blood:	n/a	n/a
11	ATF3	chr9:44488-44733	K562	blood:	n/a	n/a
12	ATF3	chr9:210212-210461	K562	blood:	n/a	n/a
13	BACH1	chr9:63102-63125	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:214910-215270	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:114203-114262	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr9:113631-113796	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr9:214677-214706	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr9:207498-207603	K562	blood:	n/a	n/a
19	BATF	chr9:178082-178323	GM12878	blood:	n/a	n/a
20	BATF	chr9:31973-32255	GM12878	blood:	n/a	n/a
21	BATF	chr9:183522-184128	GM12878	blood:	n/a	n/a
22	BATF	chr9:120835-121041	GM12878	blood:	n/a	n/a
23	BATF	chr9:200387-200708	GM12878	blood:	n/a	chr9:200519-200530
24	BATF	chr9:167629-168111	GM12878	blood:	n/a	n/a
25	BATF	chr9:63198-63553	GM12878	blood:	n/a	chr9:63315-63325
26	BATF	chr9:74610-74907	GM12878	blood:	n/a	n/a
27	BATF	chr9:156608-156841	GM12878	blood:	n/a	n/a
28	BATF	chr9:178036-178376	GM12878	blood:	n/a	n/a
29	BATF	chr9:122820-123095	GM12878	blood:	n/a	n/a
30	BATF	chr9:152906-153110	GM12878	blood:	n/a	chr9:152982-152993
31	BATF	chr9:156926-157447	GM12878	blood:	n/a	n/a
32	BATF	chr9:32954-33132	GM12878	blood:	n/a	n/a
33	BATF	chr9:164778-164998	GM12878	blood:	n/a	n/a
34	BATF	chr9:194727-194900	GM12878	blood:	n/a	n/a
35	BATF	chr9:178645-179348	GM12878	blood:	n/a	chr9:179069-179082
36	BATF	chr9:160145-160379	GM12878	blood:	n/a	n/a
37	BATF	chr9:198874-199092	GM12878	blood:	n/a	chr9:198886-198895
38	BATF	chr9:184216-185020	GM12878	blood:	n/a	chr9:184501-184509
39	BATF	chr9:183636-184093	GM12878	blood:	n/a	n/a
40	BATF	chr9:156921-157465	GM12878	blood:	n/a	n/a
41	BATF	chr9:185826-186168	GM12878	blood:	n/a	n/a
42	BATF	chr9:184237-185449	GM12878	blood:	n/a	chr9:184501-184509
43	BATF	chr9:199639-200066	GM12878	blood:	n/a	n/a
44	BATF	chr9:63237-63452	GM12878	blood:	n/a	chr9:63315-63325
45	BATF	chr9:88649-88891	GM12878	blood:	n/a	chr9:88843-88853 chr9:88842-88853
46	BATF	chr9:198812-199262	GM12878	blood:	n/a	chr9:198886-198895
47	BATF	chr9:74615-74984	GM12878	blood:	n/a	n/a
48	BATF	chr9:156635-156839	GM12878	blood:	n/a	n/a
49	BATF	chr9:167541-168102	GM12878	blood:	n/a	n/a
50	BATF	chr9:88665-89067	GM12878	blood:	n/a	chr9:88843-88853 chr9:88842-88853

(count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:114140-114190	AG09319	gingival:	n/a
2	chr9:114140-114190	AG09319	gingival:	n/a
3	chr9:114434-114484	ECC-1	luminal epithelium:	n/a
4	chr9:215561-215611	BE2_C	brain:	n/a
5	chr9:118698-118748	SKMC	muscle:	n/a
6	chr9:73835-73885	HepG2	liver:	n/a
7	chr9:113530-113580	HEEpiC	esophagus:	n/a
8	chr9:112618-112668	AG04449	skin:	fetal
9	chr9:211689-211739	HCT-116	colon:	n/a
10	chr9:73568-73618	SKMC	muscle:	n/a
11	chr9:109039-109089	SKMC	muscle:	n/a
12	chr9:112618-112668	Hepatocyte	liver:	n/a
13	chr9:214612-214662	AG09319	gingival:	n/a
14	chr9:118091-118141	NH-A	brain:	n/a
15	chr9:114140-114190	HepG2	liver:	n/a
16	chr9:113530-113580	SKMC	muscle:	n/a
17	chr9:114359-114409	GM06990	blood:	n/a
18	chr9:215368-215418	HRCEpiC	kidney:	n/a
19	chr9:112937-112987	Hela-S3	cervix:	n/a
20	chr9:73568-73618	AG09319	gingival:	n/a
21	chr9:215368-215418	Jurkat	blood:	n/a
22	chr9:117044-117094	HEK293	kidney:	embryo
23	chr9:73568-73618	MCF-7	breast:	n/a
24	chr9:117608-117658	MCF10A-Er-Src	breast:	n/a
25	chr9:118091-118141	HAEpiC	amniotic membrane:	n/a
26	chr9:114434-114484	HL-60	blood:	n/a
27	chr9:112937-112987	GM12878	blood:	n/a
28	chr9:72908-72958	HAEpiC	amniotic membrane:	n/a
29	chr9:213650-213700	SKMC	muscle:	n/a
30	chr9:214268-214318	HRE	kidney:	n/a
31	chr9:176893-176943	NHBE	bronchial:	n/a
32	chr9:113530-113580	Hela-S3	cervix:	n/a
33	chr9:112618-112668	HAEpiC	amniotic membrane:	n/a
34	chr9:104568-104618	Caco-2	colon:	n/a
35	chr9:214612-214662	BJ	skin:	n/a
36	chr9:117608-117658	HMEC	breast:	n/a
37	chr9:73704-73754	GM19239	blood:	n/a
38	chr9:214268-214318	Hela-S3	cervix:	n/a
39	chr9:114838-114888	HEK293	kidney:	embryo
40	chr9:114359-114409	GM12892	blood:	n/a
41	chr9:72908-72958	RPTEC	kidney:	n/a
42	chr9:73704-73754	K562	blood:	n/a
43	chr9:117608-117658	BE2_C	brain:	n/a
44	chr9:112618-112668	MCF-7	breast:	n/a
45	chr9:117608-117658	AoSMC	blood vessel:	n/a
46	chr9:112618-112668	HMEC	breast:	n/a
47	chr9:215368-215418	Hepatocyte	liver:	n/a
48	chr9:179409-179459	GM06990	blood:	n/a
49	chr9:113530-113580	NH-A	brain:	n/a
50	chr9:109039-109089	SK-N-SH_RA	brain:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:207871..210695-chr9:212521..216858,5	MCF-7	breast:
2	chr9:212545..218648-chr9:270340..281940,20	K562	blood:
3	chr9:213603..216956-chr9:218226..220394,3	K562	blood:
4	chr9:214285..216173-chr9:227690..229444,2	K562	blood:
5	chr9:214044..216353-chr9:222371..224502,2	MCF-7	breast:
6	chr9:218197..221460-chr9:224650..228237,4	K562	blood:
7	chr9:209849..211411-chr9:213516..215617,2	MCF-7	breast:
8	chr9:216842..219174-chr9:220888..224256,4	K562	blood:
9	chr9:217275..219531-chr9:301975..303827,2	MCF-7	breast:
10	chr9:214778..216543-chr9:219574..221163,2	MCF-7	breast:
11	chr9:224695..226653-chr9:227779..229816,2	K562	blood:
12	chr9:211063..213249-chr9:216572..219831,3	K562	blood:
13	chr9:216842..219174-chr9:220888..224256,4	K562	blood:
14	chr9:224695..226653-chr9:227779..229816,2	K562	blood:
15	chr9:224171..226015-chr9:253370..255238,2	MCF-7	breast:
16	chr9:207956..209819-chr9:211466..213662,2	MCF-7	breast:
17	chr9:207715..211592-chr9:270281..275557,5	K562	blood:
18	chr9:223210..226112-chr9:277917..282090,3	K562	blood:
19	chr9:218197..221460-chr9:224650..228237,4	K562	blood:
20	chr9:211912..213756-chr9:227781..229604,2	K562	blood:
21	chr9:213589..216422-chr9:270983..274599,7	K562	blood:
22	chr9:226722..229215-chr9:247840..250679,2	K562	blood:
23	chr9:211912..213756-chr9:227781..229604,2	K562	blood:
24	chr9:219964..222537-chr9:271277..273964,2	K562	blood:
25	chr20:61557637..61559255-chr9:214332..216174,2	MCF-7	breast:
26	chr9:210795..213326-chr9:213922..216378,4	MCF-7	breast:
27	chr9:211790..213319-chr9:241598..244495,2	K562	blood:
28	chr9:210056..211721-chr9:271493..274380,2	K562	blood:
29	chr9:227507..229537-chr9:238867..240547,2	K562	blood:
30	chr9:223853..225771-chr9:261619..263535,2	K562	blood:
31	chr9:211063..213249-chr9:216572..219831,3	K562	blood:
32	chr9:224153..226474-chr9:270248..273178,2	K562	blood:
33	chr9:207956..209819-chr9:211466..213662,2	MCF-7	breast:

(count:52 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXD4-2	chr9:102740-102850	NONHSAT129895
2	lnc-FOXD4-4	chr9:92740-92941	ucscGeneNc_uc003zfy_2
3	lnc-FOXD4-4	chr9:92740-92941	NONHSAT129893
4	lnc-FOXD4-2	chr9:103694-103754	NONHSAT129896
5	lnc-DOCK8-3	chr9:72716-72816	ENSG00000225655.1
6	lnc-FAM138C-2	chr9:34394-34957	NONHSAT129883
7	lnc-DOCK8-3	chr9:72706-72816	ENSG00000225655.1
8	lnc-FOXD4-5	chr9:161567-161647	NONHSAT129910
9	lnc-FAM138C-2	chr9:34394-34957	ENSG00000218839.3
10	lnc-FOXD4-4	chr9:91002-91304	NONHSAT129893
11	lnc-DOCK8-3	chr9:74882-75298	ENSG00000225655.1
12	lnc-FOXD4-1	chr9:112716-113067	ENSG00000231808
13	lnc-FAM138C-2	chr9:35060-35264	NONHSAT129883
14	lnc-FOXD4-2	chr9:108804-109469	NONHSAT129897
15	lnc-FOXD4-5	chr9:151745-152078	NONHSAT129910
16	lnc-FOXD4-4	chr9:92740-92850	NONHSAT129892
17	lnc-DOCK8-3	chr9:72701-72816	ENSG00000225655.1
18	lnc-FOXD4-1	chr9:113694-113754	ENSG00000231808
19	lnc-FOXD4-2	chr9:102716-103067	NONHSAT129896
20	lnc-FOXD4-4	chr9:90995-91304	ucscGeneNc_uc003zfy_2
21	lnc-DOCK8-6	chr9:62716-62816	NONHSAT129888
22	lnc-DOCK8-3	chr9:74882-75298	ENSG00000225655.1
23	lnc-FOXD4-4	chr9:92473-92541	NONHSAT129893
24	lnc-DOCK8-3	chr9:74149-74205	ENSG00000225655.1
25	lnc-FOXD4-5	chr9:156481-156527	NONHSAT129910
26	lnc-DOCK8-6	chr9:69345-69537	NONHSAT129886
27	lnc-FOXD4-5	chr9:154709-154795	NONHSAT129910
28	lnc-FOXD4-2	chr9:109316-109471	NONHSAT129895
29	lnc-FAM138C-2	chr9:35060-35264	ENSG00000218839.3
30	lnc-FOXD4-3	chr9:113606-113656	NONHSAT129899
31	lnc-FOXD4-2	chr9:101014-101304	NONHSAT129895
32	lnc-DOCK8-6	chr9:64882-65292	ucscGeneNc_uc003zfx_2
33	lnc-FOXD4-2	chr9:102473-102541	ENSG00000227917
34	lnc-DOCK8-6	chr9:62706-62816	NONHSAT129887
35	lnc-FAM138C-2	chr9:35028-35264	ENSG00000218839.3
36	lnc-FOXD4-3	chr9:114040-115772	NONHSAT129899
37	lnc-FOXD4-2	chr9:101002-101304	ENSG00000227917
38	lnc-FOXD4-2	chr9:102740-102941	ENSG00000227917
39	lnc-FAM138C-2	chr9:35504-35856	ENSG00000218839.3
40	lnc-DOCK8-3	chr9:79345-79537	ENSG00000225655.1
41	lnc-DOCK8-6	chr9:64882-65298	NONHSAT129888
42	lnc-DOCK8-6	chr9:64882-65298	NONHSAT129887
43	lnc-FOXD4-4	chr9:90804-91304	NONHSAT129892
44	lnc-FOXD4-2	chr9:109596-109842	NONHSAT129897
45	lnc-DOCK8-6	chr9:64149-64205	NONHSAT129888
46	lnc-DOCK8-6	chr9:62698-62816	ucscGeneNc_uc003zfx_2
47	lnc-DOCK8-3	chr9:88742-88826	ENSG00000225655.1
48	lnc-FOXD4-4	chr9:92473-92541	ucscGeneNc_uc003zfy_2
49	lnc-DOCK8-6	chr9:78742-78826	NONHSAT129886
50	lnc-FAM138C-2	chr9:35504-35841	ENSG00000218839.3

No data

Variant related genes	Relation type
DOCK8	TF binding region
ENSG00000231808	TF binding region
ENSG00000225655	TF binding region
FOXD4	TF binding region
ENSG00000144140	TF binding region
ENSG00000181404	TF binding region
ENSG00000227917	TF binding region
FAM138C	TF binding region
CBWD1	TF binding region
C9orf66	TF binding region
DOCK8	CpG island
ENSG00000231808	CpG island
ENSG00000225655	CpG island
FOXD4	CpG island
ENSG00000144140	CpG island
ENSG00000181404	CpG island
ENSG00000227917	CpG island
FAM138C	CpG island
CBWD1	CpG island
C9orf66	CpG island
ENSG00000183784	chromatin interactions
ENSG00000235880	chromatin interactions
ENSG00000101191	chromatin interactions
ENSG00000107099	chromatin interactions

Extended variants
information (count: 5919 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:5919 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201346916	chr9:32129-32130	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs199663182	chr9:32167-32168	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs376972705	chr9:32363-32364	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs533093000	chr9:32376-32377	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs200942212	chr9:32416-32417	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs551734841	chr9:32424-32425	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs566750729	chr9:32465-32466	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs201297388	chr9:32518-32519	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs199650447	chr9:32538-32539	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs113861604	chr9:32566-32567	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs201601403	chr9:32616-32617	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs549191316	chr9:32829-32830	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs370315977	chr9:32918-32919	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs199916539	chr9:32932-32933	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs567379825	chr9:32949-32950	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs377070882	chr9:33043-33044	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs370378093	chr9:33114-33115	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs374124029	chr9:33139-33140	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs368308360	chr9:33162-33163	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs370768223	chr9:33183-33184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs184525769	chr9:33204-33205	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs201325758	chr9:33302-33303	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs200166559	chr9:33312-33313	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs368717168	chr9:33316-33317	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs537917198	chr9:33324-33325	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs375386825	chr9:33338-33339	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs62531165	chr9:33382-33383	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs201110820	chr9:33439-33440	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs368732264	chr9:33489-33490	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs371692642	chr9:33530-33531	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs62531166	chr9:34493-34494	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs62531167	chr9:34553-34554	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs200002845	chr9:34568-34569	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs145629991	chr9:34737-34738	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs424484	chr9:35070-35071	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs374850	chr9:35099-35100	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs9408059	chr9:35199-35200	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs201982037	chr9:35541-35542	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs200029577	chr9:36269-36270	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs201108047	chr9:36307-36308	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs202117845	chr9:36313-36314	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs79012958	chr9:36508-36509	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs201244578	chr9:37221-37222	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs202182986	chr9:37345-37346	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs200492591	chr9:37371-37372	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs201767999	chr9:37499-37500	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs199544297	chr9:37619-37620	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs200271684	chr9:37822-37823	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs201113295	chr9:37925-37926	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs199728703	chr9:38185-38186	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
Intracranial ependymoma	16609018	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Primary immunodeficiency	22942019	CNVD
Melanoma	20877625	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	21215367	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:1662 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:39400-40200	Enhancers	K562	blood
2	chr9:40200-41200	Weak transcription	K562	blood
3	chr9:40800-41200	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr9:41000-42000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr9:41000-42000	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr9:41200-41600	Enhancers	K562	blood
7	chr9:41200-41600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr9:41600-42400	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr9:41600-43800	Weak transcription	K562	blood
10	chr9:42400-43800	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr9:43800-44000	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr9:43800-44800	Enhancers	K562	blood
13	chr9:44000-44200	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr9:44800-46200	Weak transcription	K562	blood
15	chr9:46200-47600	Enhancers	K562	blood
16	chr9:46400-46600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr9:48400-52400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr9:52400-53400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr9:52600-53000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr9:62000-62200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr9:62200-63000	Enhancers	Fetal Thymus	thymus
22	chr9:62800-63000	Enhancers	Dnd41	blood
23	chr9:63000-63200	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr9:63000-63200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr9:63000-63200	Flanking Active TSS	Fetal Thymus	thymus
26	chr9:63000-63200	Flanking Active TSS	Dnd41	blood
27	chr9:63000-63400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr9:63000-63400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr9:63000-63400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr9:63000-63600	Enhancers	Primary T cells fromperipheralblood	blood
31	chr9:63000-63600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr9:63000-63600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr9:63000-63600	Enhancers	Fetal Lung	lung
34	chr9:63000-64000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr9:63000-64200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr9:63200-63400	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr9:63200-63400	Active TSS	Fetal Thymus	thymus
38	chr9:63200-64000	Active TSS	Dnd41	blood
39	chr9:63600-65800	Weak transcription	Fetal Lung	lung
40	chr9:64000-64200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr9:64000-64200	Flanking Active TSS	Dnd41	blood
42	chr9:64200-64800	Enhancers	Dnd41	blood
43	chr9:65800-66000	Enhancers	Fetal Lung	lung
44	chr9:72200-74000	Active TSS	NHLF	lung
45	chr9:72600-73000	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
46	chr9:72800-73000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr9:72800-73000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
48	chr9:72800-73000	Enhancers	Primary hematopoietic stem cells	blood
49	chr9:72800-73000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr9:72800-73000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin

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