Variant report

Variant	esv3388243
Chromosome Location	chr22:30721827-30724050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:468)
CpG islands
(count:427)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:468 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr22:30722660-30722860	K562	blood:	n/a	n/a
5	BHLHE40	chr22:30722320-30723274	GM12878	blood:	n/a	chr22:30723102-30723118 chr22:30722920-30722936
6	BRCA1	chr22:30723121-30723307	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr22:30722666-30722767	GM12878	blood:	n/a	n/a
8	CCNT2	chr22:30722547-30723323	K562	blood:	n/a	chr22:30722972-30722981 chr22:30723083-30723092
9	CEBPB	chr22:30723951-30724319	H1-hESC	embryonic stem cell:	n/a	chr22:30724181-30724192
10	CEBPB	chr22:30724009-30724382	K562	blood:	n/a	chr22:30724181-30724192
11	CEBPB	chr22:30724027-30724343	HepG2	liver:	n/a	chr22:30724181-30724192
12	CEBPB	chr22:30724015-30724323	IMR90	lung:	n/a	chr22:30724181-30724192
13	CEBPB	chr22:30723929-30724341	K562	blood:	n/a	chr22:30724181-30724192
14	CEBPD	chr22:30722715-30723100	HepG2	liver:	n/a	n/a
15	CHD2	chr22:30723097-30723360	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr22:30722290-30722328	HepG2	liver:	n/a	n/a
17	CHD2	chr22:30722592-30723305	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr22:30722632-30722945	K562	blood:	n/a	n/a
19	CHD2	chr22:30721979-30723332	GM12878	blood:	n/a	n/a
20	CREB1	chr22:30722726-30723278	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chr22:30722672-30723282	A549	lung:	n/a	n/a
22	CREB1	chr22:30722661-30723417	HepG2	liver:	n/a	n/a
23	CTCF	chr22:30723800-30723950	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr22:30723840-30723990	BE2_C	brain:	n/a	n/a
25	CTCF	chr22:30723868-30724026	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr22:30723832-30724015	MCF-7	breast:	n/a	n/a
27	CTCF	chr22:30723884-30723987	GM19240	blood:	n/a	n/a
28	CTCF	chr22:30722700-30722850	AG04449	skin:	n/a	n/a
29	CTCF	chr22:30723828-30724061	MCF-7	breast:	n/a	n/a
30	CTCF	chr22:30723856-30724036	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr22:30723860-30724010	Caco-2	colon:	n/a	n/a
32	CTCF	chr22:30723880-30724030	GM12864	blood:	n/a	n/a
33	CTCF	chr22:30723860-30724010	GM06990	blood:	n/a	n/a
34	CTCF	chr22:30723880-30724030	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr22:30723786-30724056	HepG2	liver:	n/a	n/a
36	CTCF	chr22:30723781-30724121	HepG2	liver:	n/a	n/a
37	CTCF	chr22:30723880-30724030	HCT-116	colon:	n/a	n/a
38	CTCF	chr22:30723701-30724367	A549	lung:	n/a	n/a
39	CTCF	chr22:30723980-30724130	HCM	heart:	n/a	n/a
40	CTCF	chr22:30722390-30722416	GM12891	blood:	n/a	n/a
41	CTCF	chr22:30723880-30724030	SAEC	small airway:	n/a	n/a
42	CTCF	chr22:30723811-30724095	K562	blood:	n/a	n/a
43	CTCF	chr22:30722381-30722389	GM12891	blood:	n/a	n/a
44	CTCF	chr22:30723753-30724188	MCF-7	breast:	n/a	n/a
45	CTCF	chr22:30723876-30724044	LNCaP	prostate:	n/a	n/a
46	CTCF	chr22:30723912-30723955	GM10266	blood:	n/a	n/a
47	CTCF	chr22:30723765-30724102	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr22:30723834-30723990	MCF-7	breast:	n/a	n/a
49	CTCF	chr22:30723900-30724050	GM12875	blood:	n/a	n/a
50	CTCF	chr22:30723849-30724005	MCF-7	breast:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30723217-30723267	HCF	heart:	n/a
2	chr22:30723125-30723175	ECC-1	luminal epithelium:	n/a
3	chr22:30723212-30723262	MCF-7	breast:	n/a
4	chr22:30722331-30722381	Hepatocyte	liver:	n/a
5	chr22:30722865-30722915	ProgFib	skin:	n/a
6	chr22:30722331-30722381	U87	brain:	n/a
7	chr22:30723363-30723413	MCF-7	breast:	n/a
8	chr22:30722865-30722915	HCT-116	colon:	n/a
9	chr22:30723212-30723262	H1-hESC	embryonic stem cell:	embryo
10	chr22:30722865-30722915	HNPCEpiC	eye:	n/a
11	chr22:30723212-30723262	HCT-116	colon:	n/a
12	chr22:30722331-30722381	SK-N-SH	brain:	n/a
13	chr22:30722331-30722381	HCF	heart:	n/a
14	chr22:30722865-30722915	Hela-S3	cervix:	n/a
15	chr22:30723363-30723413	HMEC	breast:	n/a
16	chr22:30722594-30722644	GM06990	blood:	n/a
17	chr22:30723125-30723175	AG09319	gingival:	n/a
18	chr22:30723212-30723262	K562	blood:	n/a
19	chr22:30723125-30723175	A549	lung:	n/a
20	chr22:30723363-30723413	HepG2	liver:	n/a
21	chr22:30723212-30723262	IMR90	lung:	fetal
22	chr22:30723125-30723175	MCF-7	breast:	n/a
23	chr22:30723212-30723262	HAEpiC	amniotic membrane:	n/a
24	chr22:30723212-30723262	NB4	blood:	n/a
25	chr22:30723217-30723267	AG09309	skin:	n/a
26	chr22:30723217-30723267	NHBE	bronchial:	n/a
27	chr22:30722331-30722381	PFSK-1	brain:	n/a
28	chr22:30723125-30723175	Jurkat	blood:	n/a
29	chr22:30723363-30723413	NHDF-neo	bronchial:	n/a
30	chr22:30723125-30723175	MCF10A-Er-Src	breast:	n/a
31	chr22:30723212-30723262	RPTEC	kidney:	n/a
32	chr22:30723217-30723267	ProgFib	skin:	n/a
33	chr22:30722331-30722381	GM12891	blood:	n/a
34	chr22:30723125-30723175	ProgFib	skin:	n/a
35	chr22:30723363-30723413	AG04450	lung:	fetal
36	chr22:30722594-30722644	HRCEpiC	kidney:	n/a
37	chr22:30722331-30722381	HCPEpiC	choroid plexus:	n/a
38	chr22:30723212-30723262	LNCaP	prostate:	n/a
39	chr22:30722865-30722915	SK-N-SH_RA	brain:	n/a
40	chr22:30722594-30722644	BE2_C	brain:	n/a
41	chr22:30722331-30722381	BE2_C	brain:	n/a
42	chr22:30722331-30722381	ProgFib	skin:	n/a
43	chr22:30723125-30723175	BE2_C	brain:	n/a
44	chr22:30722594-30722644	HPAEpiC	pulmonary alveolar:	n/a
45	chr22:30722331-30722381	Caco-2	colon:	n/a
46	chr22:30722865-30722915	HIPEpiC	eye:	n/a
47	chr22:30723217-30723267	MCF-7	breast:	n/a
48	chr22:30722594-30722644	Hepatocyte	liver:	n/a
49	chr22:30723125-30723175	HRPEpiC	eye:	n/a
50	chr22:30723212-30723262	GM12892	blood:	n/a

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

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

No data

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

Extended variants
information (count: 71 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:71 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	rs373772052	chr22:30722827-30722828	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs543791449	chr22:30722834-30722835	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs565185429	chr22:30722840-30722841	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs532425732	chr22:30722843-30722844	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs547318495	chr22:30722846-30722847	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs376248925	chr22:30722855-30722856	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs370634113	chr22:30722873-30722874	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs529818297	chr22:30722883-30722884	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	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
34	rs569367743	chr22:30722921-30722922	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs1297766	chr22:30722990-30722991	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs536658730	chr22:30722994-30722995	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs551747680	chr22:30723010-30723011	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs113445389	chr22:30723041-30723042	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs374023974	chr22:30723057-30723058	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs539298150	chr22:30723077-30723078	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs554105682	chr22:30723166-30723167	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs572616681	chr22:30723187-30723188	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs553102632	chr22:30723221-30723222	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs536416096	chr22:30723233-30723234	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs180948893	chr22:30723241-30723242	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs4820833	chr22:30723272-30723273	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs138777147	chr22:30723274-30723275	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs77108806	chr22:30723275-30723276	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs577088725	chr22:30723276-30723277	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs142724751	chr22:30723315-30723316	Flanking Active TSS Active TSS Enhancers 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:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30719400-30722200	Transcr. at gene 5' and 3'	Dnd41	blood
2	chr22:30720000-30722000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
3	chr22:30720000-30722000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
4	chr22:30720000-30722200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr22:30720000-30722200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
6	chr22:30720000-30722200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
7	chr22:30720000-30722200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr22:30720000-30722200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr22:30720000-30722200	Flanking Active TSS	Adipose Nuclei	Adipose
10	chr22:30720000-30722200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr22:30720000-30722200	Flanking Active TSS	Osteobl	bone
12	chr22:30720000-30722400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
13	chr22:30720000-30722400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
14	chr22:30720000-30722400	Flanking Active TSS	Stomach Smooth Muscle	stomach
15	chr22:30720200-30722000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr22:30720200-30722000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
17	chr22:30720200-30722000	Flanking Active TSS	GM12878-XiMat	blood
18	chr22:30720200-30722200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
19	chr22:30720200-30722200	Flanking Active TSS	Duodenum Mucosa	Duodenum
20	chr22:30720200-30722200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
21	chr22:30720200-30722200	Flanking Active TSS	Thymus	Thymus
22	chr22:30720200-30722400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
23	chr22:30720200-30722400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr22:30720200-30722400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
25	chr22:30720200-30722400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr22:30720400-30722000	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr22:30720400-30722000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr22:30720400-30722000	Flanking Active TSS	NHLF	lung
29	chr22:30720400-30722200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
30	chr22:30720400-30722200	Flanking Active TSS	Colon Smooth Muscle	Colon
31	chr22:30720400-30722400	Flanking Active TSS	Brain Hippocampus Middle	brain
32	chr22:30720400-30722600	Flanking Active TSS	Primary B cells from cord blood	blood
33	chr22:30720600-30722000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
34	chr22:30720600-30722000	Flanking Active TSS	HSMM	muscle
35	chr22:30720600-30722000	Flanking Active TSS	NHDF-Ad	bronchial
36	chr22:30720600-30722200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr22:30720600-30722200	Enhancers	Fetal Heart	heart
38	chr22:30720600-30722200	Flanking Active TSS	Rectal Smooth Muscle	rectum
39	chr22:30720600-30722200	Flanking Active TSS	NH-A	brain
40	chr22:30720800-30722000	Flanking Active TSS	Brain Anterior Caudate	brain
41	chr22:30720800-30722000	Flanking Active TSS	Brain Cingulate Gyrus	brain
42	chr22:30720800-30722000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
43	chr22:30720800-30722000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
44	chr22:30720800-30722200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr22:30720800-30722200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr22:30720800-30722200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr22:30720800-30722200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr22:30720800-30722200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr22:30720800-30722200	Flanking Active TSS	Placenta	Placenta
50	chr22:30720800-30722400	Flanking Active TSS	Primary hematopoietic stem cells	blood

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