Variant report

Variant	esv3325406
Chromosome Location	chr22:30721477-30724325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:506)
CpG islands
(count:549)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:506 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:30723854-30724440	K562	blood:	n/a	n/a
2	BACH1	chr22:30722688-30722752	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr22:30723031-30723383	A549	lung:	n/a	n/a
4	BHLHE40	chr22:30722320-30723274	GM12878	blood:	n/a	chr22:30723102-30723118 chr22:30722920-30722936
5	BHLHE40	chr22:30722660-30722860	K562	blood:	n/a	n/a
6	BHLHE40	chr22:30721356-30721649	K562	blood:	n/a	chr22:30721537-30721550 chr22:30721540-30721549 chr22:30721539-30721548 chr22:30721539-30721548
7	BRCA1	chr22:30722666-30722767	GM12878	blood:	n/a	n/a
8	BRCA1	chr22:30723121-30723307	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr22:30722547-30723323	K562	blood:	n/a	chr22:30722972-30722981 chr22:30723083-30723092
10	CCNT2	chr22:30724080-30724254	K562	blood:	n/a	n/a
11	CEBPB	chr22:30724015-30724323	IMR90	lung:	n/a	chr22:30724181-30724192
12	CEBPB	chr22:30724099-30724328	Hela-S3	cervix:	n/a	chr22:30724181-30724192
13	CEBPB	chr22:30724009-30724382	K562	blood:	n/a	chr22:30724181-30724192
14	CEBPB	chr22:30723951-30724319	H1-hESC	embryonic stem cell:	n/a	chr22:30724181-30724192
15	CEBPB	chr22:30724054-30724331	K562	blood:	n/a	chr22:30724181-30724192
16	CEBPB	chr22:30723929-30724341	K562	blood:	n/a	chr22:30724181-30724192
17	CEBPB	chr22:30724027-30724343	HepG2	liver:	n/a	chr22:30724181-30724192
18	CEBPD	chr22:30722715-30723100	HepG2	liver:	n/a	n/a
19	CHD1	chr22:30721516-30721550	GM12878	blood:	n/a	n/a
20	CHD2	chr22:30722632-30722945	K562	blood:	n/a	n/a
21	CHD2	chr22:30721979-30723332	GM12878	blood:	n/a	n/a
22	CHD2	chr22:30723097-30723360	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr22:30722290-30722328	HepG2	liver:	n/a	n/a
24	CHD2	chr22:30722592-30723305	Hela-S3	cervix:	n/a	n/a
25	CREB1	chr22:30722661-30723417	HepG2	liver:	n/a	n/a
26	CREB1	chr22:30722672-30723282	A549	lung:	n/a	n/a
27	CREB1	chr22:30722726-30723278	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr22:30723860-30724010	MCF-7	breast:	n/a	n/a
29	CTCF	chr22:30723860-30724010	GM06990	blood:	n/a	n/a
30	CTCF	chr22:30723860-30724010	Caco-2	colon:	n/a	n/a
31	CTCF	chr22:30723884-30723987	GM19240	blood:	n/a	n/a
32	CTCF	chr22:30723900-30724050	SAEC	small airway:	n/a	n/a
33	CTCF	chr22:30723840-30723990	NHEK	skin:	n/a	n/a
34	CTCF	chr22:30723800-30723950	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr22:30723920-30724070	GM12874	blood:	n/a	n/a
36	CTCF	chr22:30723817-30724024	IMR90	lung:	n/a	n/a
37	CTCF	chr22:30722700-30722850	AG04449	skin:	n/a	n/a
38	CTCF	chr22:30723840-30723990	HMEC	breast:	n/a	n/a
39	CTCF	chr22:30723832-30724015	MCF-7	breast:	n/a	n/a
40	CTCF	chr22:30721360-30721510	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr22:30723781-30724121	HepG2	liver:	n/a	n/a
42	CTCF	chr22:30723849-30724005	MCF-7	breast:	n/a	n/a
43	CTCF	chr22:30723960-30724110	GM12873	blood:	n/a	n/a
44	CTCF	chr22:30723912-30723955	GM10266	blood:	n/a	n/a
45	CTCF	chr22:30723780-30723930	HPF	lung:	n/a	n/a
46	CTCF	chr22:30723960-30724110	HAc	cerebellar:	n/a	n/a
47	CTCF	chr22:30723940-30724090	HCT-116	colon:	n/a	n/a
48	CTCF	chr22:30723860-30724010	HMF	breast:	n/a	n/a
49	CTCF	chr22:30723840-30723990	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr22:30723813-30724038	NHEK	skin:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30722865-30722915	CMK	blood:	n/a
2	chr22:30723363-30723413	IMR90	lung:	fetal
3	chr22:30722865-30722915	AG10803	skin:	n/a
4	chr22:30722865-30722915	SK-N-MC	brain:	n/a
5	chr22:30723217-30723267	HNPCEpiC	eye:	n/a
6	chr22:30723217-30723267	GM12891	blood:	n/a
7	chr22:30723217-30723267	NH-A	brain:	n/a
8	chr22:30723217-30723267	SK-N-SH	brain:	n/a
9	chr22:30723212-30723262	IMR90	lung:	fetal
10	chr22:30722865-30722915	HAEpiC	amniotic membrane:	n/a
11	chr22:30723212-30723262	HCT-116	colon:	n/a
12	chr22:30721543-30721593	PANC-1	pancreas:	n/a
13	chr22:30722865-30722915	HIPEpiC	eye:	n/a
14	chr22:30721543-30721593	HMEC	breast:	n/a
15	chr22:30723125-30723175	HIPEpiC	eye:	n/a
16	chr22:30721636-30721686	GM12891	blood:	n/a
17	chr22:30723125-30723175	NHBE	bronchial:	n/a
18	chr22:30721543-30721593	HEK293	kidney:	embryo
19	chr22:30721543-30721593	ProgFib	skin:	n/a
20	chr22:30721543-30721593	GM12892	blood:	n/a
21	chr22:30722331-30722381	H1-hESC	embryonic stem cell:	embryo
22	chr22:30723125-30723175	SK-N-SH_RA	brain:	n/a
23	chr22:30723212-30723262	PFSK-1	brain:	n/a
24	chr22:30723217-30723267	HCPEpiC	choroid plexus:	n/a
25	chr22:30722331-30722381	Hela-S3	cervix:	n/a
26	chr22:30723212-30723262	HCM	heart:	n/a
27	chr22:30722594-30722644	ProgFib	skin:	n/a
28	chr22:30723217-30723267	AG10803	skin:	n/a
29	chr22:30723125-30723175	HMEC	breast:	n/a
30	chr22:30722594-30722644	HCT-116	colon:	n/a
31	chr22:30721636-30721686	U87	brain:	n/a
32	chr22:30721543-30721593	NHDF-neo	bronchial:	n/a
33	chr22:30722865-30722915	AoSMC	blood vessel:	n/a
34	chr22:30721636-30721686	MCF10A-Er-Src	breast:	n/a
35	chr22:30723217-30723267	GM06990	blood:	n/a
36	chr22:30723125-30723175	HEEpiC	esophagus:	n/a
37	chr22:30721543-30721593	MCF10A-Er-Src	breast:	n/a
38	chr22:30721543-30721593	H1-hESC	embryonic stem cell:	embryo
39	chr22:30721543-30721593	K562	blood:	n/a
40	chr22:30722331-30722381	HRCEpiC	kidney:	n/a
41	chr22:30723217-30723267	H1-hESC	embryonic stem cell:	embryo
42	chr22:30722865-30722915	NHBE	bronchial:	n/a
43	chr22:30723217-30723267	GM12878	blood:	n/a
44	chr22:30723217-30723267	Caco-2	colon:	n/a
45	chr22:30723212-30723262	AG10803	skin:	n/a
46	chr22:30722331-30722381	HCT-116	colon:	n/a
47	chr22:30722594-30722644	HRCEpiC	kidney:	n/a
48	chr22:30722331-30722381	AG09309	skin:	n/a
49	chr22:30721636-30721686	PANC-1	pancreas:	n/a
50	chr22:30723363-30723413	Jurkat	blood:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:30722006..30724246-chr22:30752442..30754508,2	K562	blood:
2	chr22:30720496..30722809-chr22:30723809..30726893,3	MCF-7	breast:
3	chr22:30723090..30724854-chr22:30725952..30728416,2	K562	blood:
4	chr22:30715065..30719307-chr22:30719404..30722412,5	K562	blood:
5	chr22:30681692..30688141-chr22:30720232..30725114,19	MCF-7	breast:
6	chr22:30678847..30680505-chr22:30720237..30722502,2	MCF-7	breast:
7	chr22:30716894..30719257-chr22:30719729..30722601,2	MCF-7	breast:
8	chr22:30715065..30718690-chr22:30719404..30722127,4	K562	blood:
9	chr22:30656777..30659153-chr22:30723216..30725905,2	MCF-7	breast:
10	chr22:30710430..30716803-chr22:30717996..30724228,10	MCF-7	breast:
11	chr22:30721494..30724747-chr22:30781448..30784941,5	MCF-7	breast:
12	chr22:30720496..30722809-chr22:30723809..30726893,3	MCF-7	breast:
13	chr22:30692849..30696422-chr22:30721996..30724187,4	MCF-7	breast:
14	chr22:30722860..30724693-chr22:30742029..30744821,2	K562	blood:
15	chr22:30701046..30703997-chr22:30721368..30724437,4	K562	blood:
16	chr22:30683778..30684535-chr22:30723476..30724412,5	MCF-7	breast:
17	chr22:30722006..30725049-chr22:30749886..30754508,5	K562	blood:
18	chr22:30722829..30724775-chr22:30819297..30822266,2	MCF-7	breast:
19	chr22:30719392..30722349-chr22:30722422..30724349,2	K562	blood:
20	chr22:30721434..30723843-chr22:30737479..30740425,2	K562	blood:
21	chr22:30683311..30684720-chr22:30723282..30724915,12	MCF-7	breast:
22	chr22:30683831..30686273-chr22:30722432..30724567,2	K562	blood:
23	chr22:30723840..30727994-chr22:30728827..30733130,4	K562	blood:
24	chr22:30679226..30682000-chr22:30723679..30728534,4	K562	blood:
25	chr22:30641352..30643505-chr22:30721621..30724253,3	MCF-7	breast:
26	chr22:30692473..30695111-chr22:30722676..30724964,2	K562	blood:
27	chr22:30719395..30724233-chr22:30750032..30754717,7	MCF-7	breast:
28	chr22:30720936..30724991-chr22:30750350..30754449,10	MCF-7	breast:

No data

Variant related genes	Relation type
TBC1D10A	TF binding region
TBC1D10A	CpG island
ENSG00000187860	chromatin interactions
ENSG00000099999	chromatin interactions
ENSG00000268812	chromatin interactions
ENSG00000248751	chromatin interactions
ENSG00000128342	chromatin interactions
ENSG00000099995	chromatin interactions
ENSG00000099992	chromatin interactions
ENSG00000239282	chromatin interactions
ENSG00000242114	chromatin interactions

Extended variants
information (count: 94 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:94 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554537973	chr22:30721483-30721484	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs149919905	chr22:30721529-30721530	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs5753068	chr22:30721534-30721535	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs544491705	chr22:30721595-30721596	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs149026605	chr22:30721597-30721598	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs141716031	chr22:30721598-30721599	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs181403550	chr22:30721612-30721613	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs185255535	chr22:30721620-30721621	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs545538368	chr22:30721627-30721628	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs374184735	chr22:30721679-30721680	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs189964983	chr22:30721694-30721695	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs13053595	chr22:30721701-30721702	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs531626912	chr22:30721728-30721729	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs115820915	chr22:30721731-30721732	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs561244490	chr22:30721812-30721813	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs531671367	chr22:30721833-30721834	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs565139497	chr22:30721860-30721861	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs146485957	chr22:30721912-30721913	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs532207962	chr22:30721926-30721927	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs547526985	chr22:30721956-30721957	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs565675834	chr22:30722004-30722005	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs536340810	chr22:30722016-30722017	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs13053508	chr22:30722135-30722136	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs551265680	chr22:30722154-30722155	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs569328293	chr22:30722181-30722182	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs536623959	chr22:30722208-30722209	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs144872683	chr22:30722263-30722264	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs577877039	chr22:30722272-30722273	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs545319599	chr22:30722275-30722276	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs554340145	chr22:30722366-30722367	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs572477119	chr22:30722443-30722444	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs367932486	chr22:30722559-30722560	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs370747585	chr22:30722650-30722651	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs375400780	chr22:30722679-30722680	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs138242222	chr22:30722713-30722714	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs149588287	chr22:30722718-30722719	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs368710092	chr22:30722766-30722767	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs370312386	chr22:30722771-30722772	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs144236899	chr22:30722797-30722798	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs373772052	chr22:30722827-30722828	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs543791449	chr22:30722834-30722835	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs565185429	chr22:30722840-30722841	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs532425732	chr22:30722843-30722844	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs547318495	chr22:30722846-30722847	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs376248925	chr22:30722855-30722856	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs370634113	chr22:30722873-30722874	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs529818297	chr22:30722883-30722884	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs547905778	chr22:30722900-30722901	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs569367743	chr22:30722921-30722922	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs1297766	chr22:30722990-30722991	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD

Chromatin state (count:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30719400-30721800	Enhancers	Sigmoid Colon	Sigmoid Colon
2	chr22:30719400-30722200	Transcr. at gene 5' and 3'	Dnd41	blood
3	chr22:30719600-30721600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr22:30720000-30721600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr22:30720000-30721600	Enhancers	Brain Substantia Nigra	brain
6	chr22:30720000-30721800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr22:30720000-30721800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
8	chr22:30720000-30721800	Enhancers	Fetal Brain Male	brain
9	chr22:30720000-30722000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
10	chr22:30720000-30722000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
11	chr22:30720000-30722200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr22:30720000-30722200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
13	chr22:30720000-30722200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr22:30720000-30722200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr22:30720000-30722200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr22:30720000-30722200	Flanking Active TSS	Adipose Nuclei	Adipose
17	chr22:30720000-30722200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr22:30720000-30722200	Flanking Active TSS	Osteobl	bone
19	chr22:30720000-30722400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
20	chr22:30720000-30722400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
21	chr22:30720000-30722400	Flanking Active TSS	Stomach Smooth Muscle	stomach
22	chr22:30720200-30721600	Flanking Active TSS	HSMMtube	muscle
23	chr22:30720200-30721800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr22:30720200-30721800	Enhancers	Small Intestine	intestine
25	chr22:30720200-30722000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr22:30720200-30722000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
27	chr22:30720200-30722000	Flanking Active TSS	GM12878-XiMat	blood
28	chr22:30720200-30722200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr22:30720200-30722200	Flanking Active TSS	Duodenum Mucosa	Duodenum
30	chr22:30720200-30722200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
31	chr22:30720200-30722200	Flanking Active TSS	Thymus	Thymus
32	chr22:30720200-30722400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
33	chr22:30720200-30722400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr22:30720200-30722400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr22:30720200-30722400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr22:30720400-30721600	Enhancers	Primary B cells from peripheral blood	blood
37	chr22:30720400-30722000	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr22:30720400-30722000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr22:30720400-30722000	Flanking Active TSS	NHLF	lung
40	chr22:30720400-30722200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
41	chr22:30720400-30722200	Flanking Active TSS	Colon Smooth Muscle	Colon
42	chr22:30720400-30722400	Flanking Active TSS	Brain Hippocampus Middle	brain
43	chr22:30720400-30722600	Flanking Active TSS	Primary B cells from cord blood	blood
44	chr22:30720600-30722000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
45	chr22:30720600-30722000	Flanking Active TSS	HSMM	muscle
46	chr22:30720600-30722000	Flanking Active TSS	NHDF-Ad	bronchial
47	chr22:30720600-30722200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr22:30720600-30722200	Enhancers	Fetal Heart	heart
49	chr22:30720600-30722200	Flanking Active TSS	Rectal Smooth Muscle	rectum
50	chr22:30720600-30722200	Flanking Active TSS	NH-A	brain

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