Variant report

Variant	nsv541001
Chromosome Location	chr11:35053717-35224624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4903)
CpG islands
(count:2015)
Chromatin interactive
region (count:119)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:4903 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

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	chr11:35062810-35063001	K562	blood:	n/a	n/a
3	ARID3A	chr11:35066842-35067235	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:35194753-35195096	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:35057639-35057839	K562	blood:	n/a	n/a
6	ARID3A	chr11:35085029-35085388	K562	blood:	n/a	n/a
7	ARID3A	chr11:35212245-35212521	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:35060798-35061124	K562	blood:	n/a	n/a
9	ATF1	chr11:35072155-35072504	K562	blood:	n/a	n/a
10	ATF1	chr11:35122859-35123088	K562	blood:	n/a	n/a
11	ATF1	chr11:35058226-35058583	K562	blood:	n/a	n/a
12	ATF1	chr11:35132632-35132924	K562	blood:	n/a	n/a
13	ATF1	chr11:35162652-35162835	K562	blood:	n/a	n/a
14	ATF1	chr11:35120645-35121044	K562	blood:	n/a	n/a
15	ATF1	chr11:35084885-35085469	K562	blood:	n/a	n/a
16	ATF1	chr11:35164287-35164318	K562	blood:	n/a	n/a
17	ATF1	chr11:35069966-35070150	K562	blood:	n/a	n/a
18	ATF1	chr11:35061743-35062041	K562	blood:	n/a	n/a
19	ATF1	chr11:35125408-35125579	K562	blood:	n/a	n/a
20	ATF1	chr11:35088676-35088928	K562	blood:	n/a	n/a
21	ATF1	chr11:35099273-35099414	K562	blood:	n/a	n/a
22	ATF1	chr11:35166888-35167161	K562	blood:	n/a	n/a
23	ATF1	chr11:35182060-35182303	K562	blood:	n/a	n/a
24	ATF1	chr11:35057558-35057855	K562	blood:	n/a	n/a
25	ATF1	chr11:35104027-35104396	K562	blood:	n/a	n/a
26	ATF1	chr11:35133237-35133513	K562	blood:	n/a	n/a
27	ATF1	chr11:35079662-35080134	K562	blood:	n/a	n/a
28	ATF1	chr11:35168376-35168687	K562	blood:	n/a	n/a
29	ATF2	chr11:35088511-35089104	GM12878	blood:	n/a	n/a
30	ATF2	chr11:35167420-35168628	GM12878	blood:	n/a	n/a
31	ATF2	chr11:35208765-35209181	GM12878	blood:	n/a	n/a
32	ATF2	chr11:35187310-35187972	GM12878	blood:	n/a	n/a
33	ATF2	chr11:35109087-35109714	GM12878	blood:	n/a	n/a
34	ATF2	chr11:35148675-35149703	GM12878	blood:	n/a	n/a
35	ATF2	chr11:35104016-35104542	GM12878	blood:	n/a	n/a
36	ATF2	chr11:35057252-35058734	GM12878	blood:	n/a	n/a
37	ATF2	chr11:35147513-35148569	GM12878	blood:	n/a	n/a
38	ATF2	chr11:35071638-35072445	GM12878	blood:	n/a	n/a
39	ATF2	chr11:35166629-35167313	GM12878	blood:	n/a	n/a
40	ATF2	chr11:35103848-35104479	GM12878	blood:	n/a	n/a
41	ATF2	chr11:35167580-35168640	GM12878	blood:	n/a	n/a
42	ATF2	chr11:35088556-35089100	GM12878	blood:	n/a	n/a
43	ATF2	chr11:35104602-35105713	GM12878	blood:	n/a	n/a
44	ATF2	chr11:35166448-35167418	GM12878	blood:	n/a	n/a
45	ATF2	chr11:35098997-35100135	GM12878	blood:	n/a	n/a
46	ATF2	chr11:35111179-35111661	GM12878	blood:	n/a	n/a
47	ATF2	chr11:35109062-35110065	GM12878	blood:	n/a	n/a
48	ATF2	chr11:35152590-35153181	GM12878	blood:	n/a	n/a
49	ATF2	chr11:35099013-35100141	GM12878	blood:	n/a	n/a
50	ATF2	chr11:35061566-35062695	GM12878	blood:	n/a	n/a

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:35086165-35086215	HL-60	blood:	n/a
2	chr11:35121378-35121428	MCF10A-Er-Src	breast:	n/a
3	chr11:35086165-35086215	HL-60	blood:	n/a
4	chr11:35121378-35121428	MCF10A-Er-Src	breast:	n/a
5	chr11:35138084-35138134	AG04449	skin:	fetal
6	chr11:35161900-35161950	MCF-7	breast:	n/a
7	chr11:35133274-35133324	HCT-116	colon:	n/a
8	chr11:35160843-35160893	ProgFib	skin:	n/a
9	chr11:35161183-35161233	RPTEC	kidney:	n/a
10	chr11:35159382-35159432	ProgFib	skin:	n/a
11	chr11:35188437-35188487	SK-N-SH_RA	brain:	n/a
12	chr11:35173592-35173642	Hepatocyte	liver:	n/a
13	chr11:35195513-35195563	HEEpiC	esophagus:	n/a
14	chr11:35201133-35201183	HRPEpiC	eye:	n/a
15	chr11:35160400-35160450	HIPEpiC	eye:	n/a
16	chr11:35138084-35138134	K562	blood:	n/a
17	chr11:35159382-35159432	HCF	heart:	n/a
18	chr11:35161900-35161950	SK-N-SH_RA	brain:	n/a
19	chr11:35158283-35158333	PrEC	prostate:	n/a
20	chr11:35179802-35179852	IMR90	lung:	fetal
21	chr11:35173592-35173642	GM19239	blood:	n/a
22	chr11:35160709-35160759	AG09309	skin:	n/a
23	chr11:35160892-35160942	GM19239	blood:	n/a
24	chr11:35160462-35160512	HEEpiC	esophagus:	n/a
25	chr11:35173592-35173642	HCF	heart:	n/a
26	chr11:35161900-35161950	RPTEC	kidney:	n/a
27	chr11:35173592-35173642	HEEpiC	esophagus:	n/a
28	chr11:35186440-35186490	AG09309	skin:	n/a
29	chr11:35160709-35160759	HCPEpiC	choroid plexus:	n/a
30	chr11:35161183-35161233	Hela-S3	cervix:	n/a
31	chr11:35158283-35158333	MCF10A-Er-Src	breast:	n/a
32	chr11:35161229-35161279	GM12891	blood:	n/a
33	chr11:35173592-35173642	BJ	skin:	n/a
34	chr11:35159136-35159186	AG10803	skin:	n/a
35	chr11:35188437-35188487	AG04450	lung:	fetal
36	chr11:35195513-35195563	ProgFib	skin:	n/a
37	chr11:35198201-35198251	HL-60	blood:	n/a
38	chr11:35201133-35201183	SK-N-SH_RA	brain:	n/a
39	chr11:35198201-35198251	NH-A	brain:	n/a
40	chr11:35158283-35158333	AG04450	lung:	fetal
41	chr11:35160571-35160621	GM19239	blood:	n/a
42	chr11:35164485-35164535	K562	blood:	n/a
43	chr11:35121378-35121428	NHBE	bronchial:	n/a
44	chr11:35160892-35160942	HAEpiC	amniotic membrane:	n/a
45	chr11:35110045-35110095	BJ	skin:	n/a
46	chr11:35195513-35195563	A549	lung:	n/a
47	chr11:35160571-35160621	MCF10A-Er-Src	breast:	n/a
48	chr11:35161183-35161233	SKMC	muscle:	n/a
49	chr11:35160892-35160942	GM12891	blood:	n/a
50	chr11:35179802-35179852	HCPEpiC	choroid plexus:	n/a

(count:119 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:35086278..35088027-chr11:35090428..35092324,3	K562	blood:
2	chr11:35160506..35161348-chr5:172198026..172198579,2	Hela-S3	cervix:
3	chr11:35172301..35174738-chr11:35189496..35192114,2	MCF-7	breast:
4	chr11:35050517..35052677-chr11:35065091..35067302,2	K562	blood:
5	chr11:35059235..35060888-chr11:35161011..35163300,2	MCF-7	breast:
6	chr1:207503349..207504173-chr11:35160887..35161695,2	Hela-S3	cervix:
7	chr11:35163163..35167316-chr11:35171190..35174236,4	K562	blood:
8	chr11:35172301..35174738-chr11:35189496..35192114,2	MCF-7	breast:
9	chr11:35166380..35169022-chr11:35170596..35172915,2	MCF-7	breast:
10	chr11:35055142..35056681-chr11:35058687..35060261,2	MCF-7	breast:
11	chr11:35054850..35057258-chr11:35063545..35065206,3	MCF-7	breast:
12	chr11:35160366..35160877-chr15:44069390..44069929,2	Hela-S3	cervix:
13	chr11:35193443..35196303-chr11:35198924..35201669,2	MCF-7	breast:
14	chr11:35121498..35123460-chr11:35254836..35257289,2	K562	blood:
15	chr11:35143665..35146006-chr11:35146722..35148953,2	MCF-7	breast:
16	chr11:35122584..35124925-chr11:35126765..35129371,2	MCF-7	breast:
17	chr11:35059235..35060888-chr11:35161011..35163300,2	MCF-7	breast:
18	chr11:34947703..34949304-chr11:35057040..35059668,2	K562	blood:
19	chr11:35188706..35190323-chr11:35204261..35206876,2	K562	blood:
20	chr11:35058493..35060030-chr11:35060277..35061819,2	K562	blood:
21	chr11:35184295..35186190-chr11:35191742..35193747,2	MCF-7	breast:
22	chr11:35050379..35055023-chr11:35058548..35063780,5	MCF-7	breast:
23	chr11:35199491..35202638-chr11:35207456..35210593,3	MCF-7	breast:
24	chr11:35121360..35123846-chr11:35132606..35135309,2	K562	blood:
25	chr11:35110163..35112423-chr11:35159701..35161676,2	MCF-7	breast:
26	chr11:35052336..35054064-chr11:35054789..35057693,2	K562	blood:
27	chr11:35122584..35124925-chr11:35126765..35129371,2	MCF-7	breast:
28	chr11:35101233..35103768-chr11:35185557..35187275,2	MCF-7	breast:
29	chr11:35058680..35060384-chr11:35065548..35067389,2	MCF-7	breast:
30	chr11:35097231..35099674-chr11:35101240..35103980,3	K562	blood:
31	chr11:35208907..35210567-chr11:35212909..35215234,2	MCF-7	breast:
32	chr11:35060552..35062107-chr11:35062837..35064622,2	MCF-7	breast:
33	chr11:35186608..35189447-chr11:35199235..35201624,2	MCF-7	breast:
34	chr11:35123473..35125204-chr11:35129634..35132229,2	MCF-7	breast:
35	chr11:35054850..35057258-chr11:35063545..35065206,3	MCF-7	breast:
36	chr1:153606580..153607386-chr11:35159581..35160522,2	Hela-S3	cervix:
37	chr11:35161963..35164830-chr11:35383993..35385550,2	MCF-7	breast:
38	chr1:153930650..153931150-chr11:35161047..35161739,2	Hela-S3	cervix:
39	chr11:35160324..35161311-chr3:14444116..14444878,2	Hela-S3	cervix:
40	chr11:35052321..35054037-chr11:35088777..35091263,2	K562	blood:
41	chr11:35193443..35196303-chr11:35198924..35201669,2	MCF-7	breast:
42	chr11:35056767..35059035-chr11:35065294..35067500,2	K562	blood:
43	chr11:34947697..34948269-chr11:35163627..35164578,3	K562	blood:
44	chr11:35118109..35120819-chr11:35160068..35162189,2	MCF-7	breast:
45	chr11:35198118..35199850-chr11:35204330..35207060,2	K562	blood:
46	chr11:35135735..35137455-chr11:35149991..35152217,2	K562	blood:
47	chr1:11968192..11969146-chr11:35160267..35160843,2	Hela-S3	cervix:
48	chr11:35184295..35186190-chr11:35191742..35193747,2	MCF-7	breast:
49	chr11:35132300..35135003-chr11:35146023..35147940,2	MCF-7	breast:
50	chr11:35058680..35060384-chr11:35065548..35067389,2	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC1A2-2	chr11:35157893-35158173	ENSG00000255521.1
2	lnc-CD44-4	chr11:35124735-35124991	NONHSAT018773
3	lnc-APIP-1	chr11:35088226-35088723	NONHSAT018769
4	lnc-PDHX-3	chr11:35109985-35110151	NONHSAT018768
5	lnc-CD44-5	chr11:35103203-35103622	NONHSAT018771
6	lnc-CD44-3	chr11:35132621-35132927	NONHSAT018774
7	lnc-PDHX-3	chr11:35071626-35071672	NONHSAT018768
8	lnc-SLC1A2-2	chr11:35154202-35154687	ENSG00000255521.1
9	lnc-PDHX-5	chr11:35223215-35223334	NONHSAT018781
10	lnc-PDHX-4	chr11:35218709-35219340	NONHSAT018780
11	lnc-PDHX-5	chr11:35211473-35211612	NONHSAT018779
12	lnc-PDHX-5	chr11:35222691-35222742	NONHSAT018781
13	lnc-SLC1A2-2	chr11:35157781-35158173	ENSG00000255521.1
14	lnc-PDHX-3	chr11:35107760-35107870	NONHSAT018772
15	lnc-APIP-1	chr11:35095464-35095505	XLOC_009415
16	lnc-APIP-1	chr11:35086667-35086860	NONHSAT018769
17	lnc-SLC1A2-2	chr11:35159245-35159273	ENSG00000255521.1
18	lnc-PDHX-3	chr11:35112276-35112331	NONHSAT018772
19	lnc-APIP-1	chr11:35086673-35086860	XLOC_009415
20	lnc-PDHX-3	chr11:35108965-35110133	NONHSAT018772
21	lnc-PDHX-4	chr11:35219416-35220102	NONHSAT018780
22	lnc-PDHX-3	chr11:35119168-35119365	NONHSAT018768
23	lnc-SLC1A2-2	chr11:35150431-35150467	XLOC_009416
24	lnc-SLC1A2-2	chr11:35159245-35159579	ENSG00000255521.1
25	lnc-PDHX-3	chr11:35119065-35120242	NONHSAT018772
26	lnc-SLC1A2-2	chr11:35157893-35158084	XLOC_009416
27	lnc-APIP-1	chr11:35080723-35081531	NONHSAT018769
28	lnc-PDHX-3	chr11:35140600-35142723	NONHSAT018772
29	lnc-PDHX-5	chr11:35223168-35223334	NONHSAT018782

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CD44	hsa-miR-520c-3p	chr11:35211491-35211514
2	CD44	hsa-miR-373-3p	chr11:35211492-35211514

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
ENSG00000160741	chromatin interactions
ENSG00000269766	chromatin interactions
ENSG00000109089	chromatin interactions
ENSG00000120129	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000026508	chromatin interactions
ENSG00000177971	chromatin interactions
ENSG00000065243	chromatin interactions
ENSG00000149089	chromatin interactions
ENSG00000143549	chromatin interactions
ENSG00000232519	chromatin interactions
ENSG00000197837	chromatin interactions
ENSG00000131389	chromatin interactions
ENSG00000128886	chromatin interactions
ENSG00000160813	chromatin interactions
ENSG00000272030	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000269946	chromatin interactions
ENSG00000255521	chromatin interactions
ENSG00000125459	chromatin interactions
ENSG00000271853	chromatin interactions
ENSG00000110435	chromatin interactions
GANAB	miRNA target sites
CUEDC2	miRNA target sites
POU2F1	miRNA target sites

Extended variants
information (count: 6887 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:6887 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536198926	chr11:35053743-35053744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs141883067	chr11:35053750-35053751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576191781	chr11:35053772-35053773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2553795	chr11:35053783-35053784	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs564943928	chr11:35053784-35053785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572184033	chr11:35053785-35053786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2553794	chr11:35053817-35053818	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs555246724	chr11:35053838-35053839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146265126	chr11:35053980-35053981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530413475	chr11:35054007-35054008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543797806	chr11:35054017-35054018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563887846	chr11:35054039-35054040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550397212	chr11:35054058-35054059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs117527968	chr11:35054173-35054174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552369963	chr11:35054174-35054175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565795160	chr11:35054182-35054183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2732521	chr11:35054185-35054186	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs548174089	chr11:35054212-35054213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140033906	chr11:35054243-35054244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs80340693	chr11:35054251-35054252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185680659	chr11:35054254-35054255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569953056	chr11:35054272-35054273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142250173	chr11:35054313-35054314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558794091	chr11:35054321-35054322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79111620	chr11:35054350-35054351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541170043	chr11:35054383-35054384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2553793	chr11:35054400-35054401	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs544550066	chr11:35054411-35054412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150851379	chr11:35054421-35054422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562852962	chr11:35054430-35054431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563796283	chr11:35054432-35054433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532851116	chr11:35054471-35054472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545947513	chr11:35054516-35054517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530255361	chr11:35054522-35054523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76045940	chr11:35054580-35054581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528554820	chr11:35054612-35054613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548309429	chr11:35054615-35054616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189621676	chr11:35054620-35054621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530782541	chr11:35054643-35054644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2553792	chr11:35054654-35054655	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs569807311	chr11:35054680-35054681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538925975	chr11:35054682-35054683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558779565	chr11:35054718-35054719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs386752404	chr11:35054727-35054728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2553791	chr11:35054729-35054730	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs554680189	chr11:35054730-35054731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150006722	chr11:35054738-35054739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147727993	chr11:35054739-35054740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142514817	chr11:35054788-35054789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554244093	chr11:35054792-35054793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:5806 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35039800-35059200	Weak transcription	Pancreas	Pancrea
2	chr11:35049600-35054800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:35050600-35054400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:35051000-35053800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr11:35051000-35055400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr11:35051200-35054200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr11:35051200-35055400	Enhancers	Primary T cells from cord blood	blood
8	chr11:35051200-35056000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr11:35051400-35053800	Enhancers	Primary T cells fromperipheralblood	blood
10	chr11:35051400-35053800	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr11:35051400-35054000	Enhancers	NHLF	lung
12	chr11:35051600-35053800	Enhancers	HSMM	muscle
13	chr11:35051600-35053800	Enhancers	HUVEC	blood vessel
14	chr11:35051600-35054000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr11:35051600-35054200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr11:35051600-35054200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr11:35051600-35054600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr11:35051600-35054600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr11:35051600-35055400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr11:35051600-35055400	Enhancers	Placenta	Placenta
21	chr11:35051800-35055600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr11:35052000-35054400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr11:35052200-35055000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr11:35052200-35055400	Enhancers	HMEC	breast
25	chr11:35052200-35056400	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr11:35052200-35056600	Weak transcription	Primary hematopoietic stem cells	blood
27	chr11:35052400-35053800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr11:35052400-35061800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr11:35052600-35054000	Enhancers	NH-A	brain
30	chr11:35052600-35055000	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr11:35052600-35055400	Enhancers	GM12878-XiMat	blood
32	chr11:35052800-35054000	Enhancers	Placenta Amnion	Placenta Amnion
33	chr11:35052800-35054000	Enhancers	Osteobl	bone
34	chr11:35052800-35054400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr11:35052800-35054400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:35052800-35054600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr11:35052800-35054600	Enhancers	NHDF-Ad	bronchial
38	chr11:35052800-35055200	Enhancers	NHEK	skin
39	chr11:35052800-35057000	Weak transcription	Aorta	Aorta
40	chr11:35052800-35061800	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr11:35052800-35066800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:35053000-35054000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr11:35053000-35054000	Enhancers	Muscle Satellite Cultured Cells	--
44	chr11:35053000-35054000	Enhancers	A549	lung
45	chr11:35053000-35055800	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr11:35053000-35056000	Enhancers	K562	blood
47	chr11:35053000-35056200	Enhancers	Hela-S3	cervix
48	chr11:35053000-35056400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr11:35053000-35057000	Weak transcription	Primary B cells from peripheral blood	blood
50	chr11:35053000-35057800	Weak transcription	Psoas Muscle	Psoas

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