Variant report

Variant	nsv540999
Chromosome Location	chr11:35021936-35185471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4844)
CpG islands
(count:1954)
Chromatin interactive
region (count:118)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4844 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:35061678-35062004	K562	blood:	n/a	n/a
2	ARID3A	chr11:35057639-35057839	K562	blood:	n/a	n/a
3	ARID3A	chr11:35060798-35061124	K562	blood:	n/a	n/a
4	ARID3A	chr11:35085029-35085388	K562	blood:	n/a	n/a
5	ARID3A	chr11:35062810-35063001	K562	blood:	n/a	n/a
6	ARID3A	chr11:35066842-35067235	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:35030945-35031794	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:35050350-35050388	K562	blood:	n/a	n/a
9	ARID3A	chr11:35052064-35052688	K562	blood:	n/a	n/a
10	ARID3A	chr11:35051547-35051772	K562	blood:	n/a	n/a
11	ATF1	chr11:35052215-35052684	K562	blood:	n/a	n/a
12	ATF1	chr11:35168376-35168687	K562	blood:	n/a	n/a
13	ATF1	chr11:35057558-35057855	K562	blood:	n/a	n/a
14	ATF1	chr11:35069966-35070150	K562	blood:	n/a	n/a
15	ATF1	chr11:35072155-35072504	K562	blood:	n/a	n/a
16	ATF1	chr11:35051470-35051839	K562	blood:	n/a	n/a
17	ATF1	chr11:35182060-35182303	K562	blood:	n/a	n/a
18	ATF1	chr11:35132632-35132924	K562	blood:	n/a	n/a
19	ATF1	chr11:35061743-35062041	K562	blood:	n/a	n/a
20	ATF1	chr11:35058226-35058583	K562	blood:	n/a	n/a
21	ATF1	chr11:35104027-35104396	K562	blood:	n/a	n/a
22	ATF1	chr11:35133237-35133513	K562	blood:	n/a	n/a
23	ATF1	chr11:35120645-35121044	K562	blood:	n/a	n/a
24	ATF1	chr11:35166888-35167161	K562	blood:	n/a	n/a
25	ATF1	chr11:35088676-35088928	K562	blood:	n/a	n/a
26	ATF1	chr11:35084885-35085469	K562	blood:	n/a	n/a
27	ATF1	chr11:35099273-35099414	K562	blood:	n/a	n/a
28	ATF1	chr11:35122859-35123088	K562	blood:	n/a	n/a
29	ATF1	chr11:35162652-35162835	K562	blood:	n/a	n/a
30	ATF1	chr11:35125408-35125579	K562	blood:	n/a	n/a
31	ATF1	chr11:35079662-35080134	K562	blood:	n/a	n/a
32	ATF1	chr11:35164287-35164318	K562	blood:	n/a	n/a
33	ATF2	chr11:35051400-35052011	GM12878	blood:	n/a	n/a
34	ATF2	chr11:35033822-35034746	GM12878	blood:	n/a	n/a
35	ATF2	chr11:35165624-35166332	GM12878	blood:	n/a	n/a
36	ATF2	chr11:35111179-35111661	GM12878	blood:	n/a	n/a
37	ATF2	chr11:35099013-35100141	GM12878	blood:	n/a	n/a
38	ATF2	chr11:35143863-35144425	GM12878	blood:	n/a	n/a
39	ATF2	chr11:35088511-35089104	GM12878	blood:	n/a	n/a
40	ATF2	chr11:35140337-35140923	GM12878	blood:	n/a	n/a
41	ATF2	chr11:35034838-35035662	GM12878	blood:	n/a	n/a
42	ATF2	chr11:35165372-35166426	GM12878	blood:	n/a	n/a
43	ATF2	chr11:35104602-35105713	GM12878	blood:	n/a	n/a
44	ATF2	chr11:35061618-35062666	GM12878	blood:	n/a	n/a
45	ATF2	chr11:35166448-35167418	GM12878	blood:	n/a	n/a
46	ATF2	chr11:35051409-35052182	GM12878	blood:	n/a	n/a
47	ATF2	chr11:35088556-35089100	GM12878	blood:	n/a	n/a
48	ATF2	chr11:35109062-35110065	GM12878	blood:	n/a	n/a
49	ATF2	chr11:35167580-35168640	GM12878	blood:	n/a	n/a
50	ATF2	chr11:35034814-35035772	GM12878	blood:	n/a	n/a

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:35159136-35159186	SAEC	small airway:	n/a
2	chr11:35032430-35032480	PANC-1	pancreas:	n/a
3	chr11:35159136-35159186	SAEC	small airway:	n/a
4	chr11:35032430-35032480	PANC-1	pancreas:	n/a
5	chr11:35099055-35099105	Caco-2	colon:	n/a
6	chr11:35086165-35086215	T-47D	breast:	n/a
7	chr11:35105199-35105249	GM12878	blood:	n/a
8	chr11:35160843-35160893	NHDF-neo	bronchial:	n/a
9	chr11:35133274-35133324	PANC-1	pancreas:	n/a
10	chr11:35160709-35160759	BJ	skin:	n/a
11	chr11:35039392-35039442	HNPCEpiC	eye:	n/a
12	chr11:35161900-35161950	NT2-D1	testis:	n/a
13	chr11:35167041-35167091	HPAEpiC	pulmonary alveolar:	n/a
14	chr11:35159136-35159186	HPAEpiC	pulmonary alveolar:	n/a
15	chr11:35160462-35160512	SKMC	muscle:	n/a
16	chr11:35160709-35160759	HEEpiC	esophagus:	n/a
17	chr11:35039392-35039442	GM06990	blood:	n/a
18	chr11:35158283-35158333	HRPEpiC	eye:	n/a
19	chr11:35105199-35105249	Jurkat	blood:	n/a
20	chr11:35167041-35167091	ProgFib	skin:	n/a
21	chr11:35133274-35133324	HEEpiC	esophagus:	n/a
22	chr11:35160892-35160942	HUVEC	blood vessel:	n/a
23	chr11:35159136-35159186	GM12878	blood:	n/a
24	chr11:35161345-35161395	GM06990	blood:	n/a
25	chr11:35160843-35160893	BJ	skin:	n/a
26	chr11:35159087-35159137	K562	blood:	n/a
27	chr11:35164485-35164535	SK-N-SH	brain:	n/a
28	chr11:35105199-35105249	A549	lung:	n/a
29	chr11:35160330-35160380	NH-A	brain:	n/a
30	chr11:35105199-35105249	NHBE	bronchial:	n/a
31	chr11:35160330-35160380	Caco-2	colon:	n/a
32	chr11:35160709-35160759	NH-A	brain:	n/a
33	chr11:35159382-35159432	NHDF-neo	bronchial:	n/a
34	chr11:35032430-35032480	HRPEpiC	eye:	n/a
35	chr11:35160462-35160512	SAEC	small airway:	n/a
36	chr11:35160498-35160548	GM12878	blood:	n/a
37	chr11:35159136-35159186	AG04449	skin:	fetal
38	chr11:35105199-35105249	BJ	skin:	n/a
39	chr11:35158283-35158333	AG04450	lung:	fetal
40	chr11:35032430-35032480	IMR90	lung:	fetal
41	chr11:35121378-35121428	PFSK-1	brain:	n/a
42	chr11:35164485-35164535	MCF-7	breast:	n/a
43	chr11:35086165-35086215	SK-N-MC	brain:	n/a
44	chr11:35173592-35173642	HMEC	breast:	n/a
45	chr11:35086165-35086215	NH-A	brain:	n/a
46	chr11:35159136-35159186	Hela-S3	cervix:	n/a
47	chr11:35052388-35052438	HNPCEpiC	eye:	n/a
48	chr11:35159382-35159432	Hela-S3	cervix:	n/a
49	chr11:35159382-35159432	Jurkat	blood:	n/a
50	chr11:35072710-35072760	HCT-116	colon:	n/a

(count:118 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:35021693..35023212-chr11:35050497..35053250,2	MCF-7	breast:
2	chr11:35087035..35089860-chr11:35091064..35093898,2	MCF-7	breast:
3	chr11:35039461..35041795-chr11:35050641..35052600,2	K562	blood:
4	chr11:35104262..35106718-chr11:35159601..35161198,2	MCF-7	breast:
5	chr11:35050517..35052677-chr11:35065091..35067302,2	K562	blood:
6	chr11:35028741..35031427-chr11:35032787..35035913,3	K562	blood:
7	chr11:35026967..35028548-chr11:35162664..35165084,2	MCF-7	breast:
8	chr11:35160364..35160882-chr15:75932271..75932998,2	Hela-S3	cervix:
9	chr11:35163163..35167316-chr11:35171190..35174236,4	K562	blood:
10	chr11:35160366..35160877-chr15:44069390..44069929,2	Hela-S3	cervix:
11	chr11:35183121..35185456-chr11:35188061..35190243,2	MCF-7	breast:
12	chr11:34947703..34949304-chr11:35057040..35059668,2	K562	blood:
13	chr11:35060552..35062107-chr11:35062837..35064622,2	MCF-7	breast:
14	chr11:35027303..35029685-chr11:35029694..35032602,2	MCF-7	breast:
15	chr11:35160535..35161197-chr7:100033923..100034574,2	Hela-S3	cervix:
16	chr11:35052321..35054037-chr11:35088777..35091263,2	K562	blood:
17	chr11:34938093..34939698-chr11:35166380..35168722,2	MCF-7	breast:
18	chr11:35059235..35060888-chr11:35161011..35163300,2	MCF-7	breast:
19	chr11:35123473..35125204-chr11:35129634..35132229,2	MCF-7	breast:
20	chr11:35020698..35022815-chr11:35039638..35042046,2	K562	blood:
21	chr11:35160374..35163354-chr11:35164253..35168964,4	K562	blood:
22	chr11:35143665..35146006-chr11:35146722..35148953,2	MCF-7	breast:
23	chr11:35054364..35057868-chr11:35058147..35061755,3	K562	blood:
24	chr11:35129946..35132170-chr11:35133262..35135380,2	K562	blood:
25	chr11:35119495..35120096-chr11:35412276..35412995,2	MCF-7	breast:
26	chr11:35052336..35054064-chr11:35054789..35057693,2	K562	blood:
27	chr11:35121360..35123846-chr11:35132606..35135309,2	K562	blood:
28	chr1:207503349..207504173-chr11:35160887..35161695,2	Hela-S3	cervix:
29	chr11:35172301..35174738-chr11:35189496..35192114,2	MCF-7	breast:
30	chr11:35118109..35120819-chr11:35160068..35162189,2	MCF-7	breast:
31	chr11:35163163..35167316-chr11:35171190..35174236,4	K562	blood:
32	chr11:35020698..35022815-chr11:35039638..35042046,2	K562	blood:
33	chr11:35137747..35140053-chr11:35157394..35160229,2	MCF-7	breast:
34	chr11:35028741..35031427-chr11:35032787..35035913,3	K562	blood:
35	chr11:35026581..35028709-chr11:35030070..35032050,2	K562	blood:
36	chr11:35160872..35161372-chr12:14923610..14924453,2	Hela-S3	cervix:
37	chr11:35135735..35137455-chr11:35149991..35152217,2	K562	blood:
38	chr11:35184295..35186190-chr11:35191742..35193747,2	MCF-7	breast:
39	chr11:35026967..35028548-chr11:35162664..35165084,2	MCF-7	breast:
40	chr11:35054850..35057258-chr11:35063545..35065206,3	MCF-7	breast:
41	chr11:35161963..35164830-chr11:35383993..35385550,2	MCF-7	breast:
42	chr11:35155392..35158105-chr11:35159031..35160697,2	MCF-7	breast:
43	chr11:35160028..35162902-chr11:35183937..35186481,3	MCF-7	breast:
44	chr1:153930650..153931150-chr11:35161047..35161739,2	Hela-S3	cervix:
45	chr11:35122584..35124925-chr11:35126765..35129371,2	MCF-7	breast:
46	chr11:35160584..35161366-chr17:72983348..72984211,2	Hela-S3	cervix:
47	chr11:35097231..35099674-chr11:35101240..35103980,3	K562	blood:
48	chr11:35023109..35024756-chr11:35037668..35039573,2	K562	blood:
49	chr1:155579443..155580336-chr11:35160348..35160978,2	NB4	blood:
50	chr11:35050379..35055023-chr11:35058548..35063780,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-APIP-1	chr11:35086673-35086860	XLOC_009415
2	lnc-SLC1A2-2	chr11:35157893-35158084	XLOC_009416
3	lnc-PDHX-3	chr11:35140600-35142723	NONHSAT018772
4	lnc-SLC1A2-2	chr11:35157893-35158173	ENSG00000255521.1
5	lnc-APIP-1	chr11:35080723-35081531	NONHSAT018769
6	lnc-APIP-1	chr11:35088226-35088723	NONHSAT018769
7	lnc-PDHX-3	chr11:35112276-35112331	NONHSAT018772
8	lnc-SLC1A2-2	chr11:35159245-35159579	ENSG00000255521.1
9	lnc-CD44-3	chr11:35132621-35132927	NONHSAT018774
10	lnc-APIP-1	chr11:35086667-35086860	NONHSAT018769
11	lnc-SLC1A2-2	chr11:35154202-35154687	ENSG00000255521.1
12	lnc-PDHX-3	chr11:35119065-35120242	NONHSAT018772
13	lnc-CD44-4	chr11:35124735-35124991	NONHSAT018773
14	lnc-SLC1A2-2	chr11:35150431-35150467	XLOC_009416
15	lnc-CD44-5	chr11:35103203-35103622	NONHSAT018771
16	lnc-PDHX-3	chr11:35119168-35119365	NONHSAT018768
17	lnc-SLC1A2-2	chr11:35159245-35159273	ENSG00000255521.1
18	lnc-PDHX-3	chr11:35071626-35071672	NONHSAT018768
19	lnc-PDHX-3	chr11:35107760-35107870	NONHSAT018772
20	lnc-PDHX-3	chr11:35108965-35110133	NONHSAT018772
21	lnc-PDHX-3	chr11:35109985-35110151	NONHSAT018768
22	lnc-APIP-1	chr11:35095464-35095505	XLOC_009415
23	lnc-SLC1A2-2	chr11:35157781-35158173	ENSG00000255521.1

No data

Variant related genes	Relation type
ENSG00000269766	TF binding region
CD44	TF binding region
ENSG00000255521	TF binding region
ENSG00000269766	CpG island
CD44	CpG island
ENSG00000255521	CpG island
ENSG00000269946	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000149089	chromatin interactions
ENSG00000160813	chromatin interactions
ENSG00000197837	chromatin interactions
ENSG00000232519	chromatin interactions
ENSG00000026508	chromatin interactions
ENSG00000160741	chromatin interactions
ENSG00000271853	chromatin interactions
ENSG00000120129	chromatin interactions
ENSG00000109089	chromatin interactions
ENSG00000272030	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000128886	chromatin interactions
ENSG00000110435	chromatin interactions
ENSG00000269766	chromatin interactions
ENSG00000125459	chromatin interactions
ENSG00000131389	chromatin interactions
ENSG00000177971	chromatin interactions
ENSG00000255521	chromatin interactions
ENSG00000143549	chromatin interactions
ENSG00000065243	chromatin interactions
POU2F1	miRNA target sites
GANAB	miRNA target sites
CUEDC2	miRNA target sites

Extended variants
information (count: 6600 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:6600 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563741897	chr11:35022053-35022054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs187747500	chr11:35022115-35022116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552422880	chr11:35022164-35022165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559689371	chr11:35022194-35022195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371803861	chr11:35022205-35022206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572808653	chr11:35022239-35022240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528523579	chr11:35022401-35022402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547623655	chr11:35022407-35022408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567238692	chr11:35022415-35022416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543304545	chr11:35022424-35022425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536011072	chr11:35022508-35022509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549544528	chr11:35022542-35022543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569551236	chr11:35022620-35022621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538718889	chr11:35022669-35022670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558416744	chr11:35022687-35022688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571962495	chr11:35022734-35022735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534328230	chr11:35022752-35022753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs16926673	chr11:35022765-35022766	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs575235600	chr11:35022803-35022804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140699241	chr11:35022907-35022908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2767033	chr11:35022908-35022909	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs144752021	chr11:35022954-35022955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192460244	chr11:35023082-35023083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546590337	chr11:35023094-35023095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546275541	chr11:35023107-35023108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532038674	chr11:35023114-35023115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559595658	chr11:35023134-35023135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528451882	chr11:35023214-35023215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372338485	chr11:35023230-35023231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561773967	chr11:35023237-35023238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184829654	chr11:35023242-35023243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549703918	chr11:35023249-35023250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189643131	chr11:35023262-35023263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs118036918	chr11:35023353-35023354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542332960	chr11:35023368-35023369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181574922	chr11:35023440-35023441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565656179	chr11:35023489-35023490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377126180	chr11:35023509-35023510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113005659	chr11:35023520-35023521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369905271	chr11:35023533-35023534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10650273	chr11:35023628-35023629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568098980	chr11:35023634-35023635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374623540	chr11:35023681-35023682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537732007	chr11:35023697-35023698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147476144	chr11:35023719-35023720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184353951	chr11:35023735-35023736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs80198534	chr11:35023736-35023737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553402924	chr11:35023779-35023780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573233755	chr11:35023786-35023787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11032972	chr11:35023802-35023803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4864 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34985200-35026600	Weak transcription	Colonic Mucosa	Colon
2	chr11:35000600-35035000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:35000800-35031000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr11:35007000-35026600	Weak transcription	Fetal Intestine Small	intestine
5	chr11:35007000-35028000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:35007000-35029800	Weak transcription	Esophagus	oesophagus
7	chr11:35007200-35035200	Weak transcription	Fetal Stomach	stomach
8	chr11:35007400-35026600	Weak transcription	Fetal Intestine Large	intestine
9	chr11:35007400-35026800	Weak transcription	Fetal Brain Female	brain
10	chr11:35007400-35027800	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr11:35008600-35025200	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr11:35008600-35026600	Weak transcription	Fetal Muscle Leg	muscle
13	chr11:35008600-35026600	Weak transcription	Pancreas	Pancrea
14	chr11:35008600-35030800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr11:35009000-35025200	Weak transcription	Aorta	Aorta
16	chr11:35009000-35028000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr11:35009200-35024600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr11:35009400-35026600	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr11:35009400-35026800	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr11:35011000-35024600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr11:35011200-35025000	Weak transcription	NH-A	brain
22	chr11:35011400-35028200	Weak transcription	HSMMtube	muscle
23	chr11:35011600-35026800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr11:35015000-35024600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr11:35016000-35024600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr11:35016600-35025000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr11:35016800-35026600	Weak transcription	Liver	Liver
28	chr11:35016800-35026800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr11:35017200-35030800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr11:35019600-35022000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr11:35019600-35022000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr11:35019600-35022000	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr11:35019800-35035400	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr11:35020000-35022000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr11:35020000-35025000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr11:35020000-35028000	Weak transcription	Small Intestine	intestine
37	chr11:35020000-35030400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:35020200-35024600	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr11:35020200-35024600	Weak transcription	HSMM	muscle
40	chr11:35020200-35026600	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr11:35020200-35028200	Weak transcription	Fetal Lung	lung
42	chr11:35020200-35028400	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr11:35020200-35029800	Weak transcription	NHDF-Ad	bronchial
44	chr11:35020400-35024600	Weak transcription	HMEC	breast
45	chr11:35020400-35024800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr11:35020400-35024800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr11:35020400-35024800	Weak transcription	A549	lung
48	chr11:35020400-35025000	Weak transcription	Osteobl	bone
49	chr11:35020600-35025200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr11:35021000-35024400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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