Variant report

Variant	esv10194
Chromosome Location	chr22:29783647-29794087
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:705)
CpG islands
(count:856)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:705 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:29784494-29784815	K562	blood:	n/a	n/a
2	ARID3A	chr22:29790955-29791320	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:29784598-29784803	HepG2	liver:	n/a	n/a
4	ATF2	chr22:29784482-29784966	GM12878	blood:	n/a	n/a
5	BCL3	chr22:29784461-29785020	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
6	BCLAF1	chr22:29784355-29784799	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
7	BCLAF1	chr22:29784167-29784915	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
8	BHLHE40	chr22:29783767-29784854	K562	blood:	n/a	chr22:29784290-29784306
9	BHLHE40	chr22:29784305-29784732	HepG2	liver:	n/a	n/a
10	BHLHE40	chr22:29783782-29784846	GM12878	blood:	n/a	chr22:29784290-29784306
11	BRCA1	chr22:29784487-29784668	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr22:29784309-29784324	HepG2	liver:	n/a	n/a
13	BRCA1	chr22:29791082-29791132	HepG2	liver:	n/a	n/a
14	CBX3	chr22:29784370-29784766	K562	blood:	n/a	n/a
15	CCNT2	chr22:29784213-29784825	K562	blood:	n/a	n/a
16	CEBPB	chr22:29784560-29784804	K562	blood:	n/a	n/a
17	CEBPB	chr22:29784634-29784925	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr22:29784541-29784752	HepG2	liver:	n/a	n/a
19	CEBPB	chr22:29791176-29791249	K562	blood:	n/a	n/a
20	CEBPB	chr22:29784432-29784838	Hela-S3	cervix:	n/a	n/a
21	CEBPD	chr22:29784249-29784577	HepG2	liver:	n/a	n/a
22	CHD1	chr22:29784047-29784690	GM12878	blood:	n/a	chr22:29784363-29784373
23	CHD2	chr22:29784690-29784742	K562	blood:	n/a	n/a
24	CHD2	chr22:29783991-29784944	GM12878	blood:	n/a	chr22:29784363-29784373
25	CHD2	chr22:29791078-29791089	HepG2	liver:	n/a	n/a
26	CHD2	chr22:29784311-29784747	Hela-S3	cervix:	n/a	chr22:29784363-29784373
27	CHD2	chr22:29790975-29791296	GM12878	blood:	n/a	n/a
28	CHD2	chr22:29784280-29784804	H1-hESC	embryonic stem cell:	n/a	chr22:29784363-29784373
29	CHD2	chr22:29784755-29784887	HepG2	liver:	n/a	n/a
30	CREB1	chr22:29784199-29784929	HepG2	liver:	n/a	n/a
31	CREB1	chr22:29784307-29784902	GM12878	blood:	n/a	n/a
32	CREB1	chr22:29784315-29784717	ECC-1	luminal epithelium:	n/a	n/a
33	CREB1	chr22:29784344-29784793	A549	lung:	n/a	n/a
34	CTCF	chr22:29791100-29791250	GM12868	blood:	n/a	chr22:29791127-29791143
35	CTCF	chr22:29790760-29790910	GM12874	blood:	n/a	n/a
36	CTCF	chr22:29791080-29791230	K562	blood:	n/a	chr22:29791127-29791143
37	CTCF	chr22:29784600-29784750	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr22:29790980-29791291	HUVEC	blood vessel:	n/a	chr22:29791127-29791143
39	CTCF	chr22:29790960-29791271	ECC-1	luminal epithelium:	n/a	chr22:29791127-29791143
40	CTCF	chr22:29791080-29791230	AoAF	blood vessel:	n/a	chr22:29791127-29791143
41	CTCF	chr22:29790640-29790790	GM12868	blood:	n/a	n/a
42	CTCF	chr22:29791080-29791230	GM12870	blood:	n/a	chr22:29791127-29791143
43	CTCF	chr22:29784448-29784641	K562	blood:	n/a	n/a
44	CTCF	chr22:29784464-29784704	GM12878	blood:	n/a	n/a
45	CTCF	chr22:29791060-29791210	NHDF-neo	bronchial:	n/a	chr22:29791127-29791143
46	CTCF	chr22:29790999-29791274	Hela-S3	cervix:	n/a	chr22:29791127-29791143
47	CTCF	chr22:29784160-29784310	HCM	heart:	n/a	n/a
48	CTCF	chr22:29791080-29791230	GM12865	blood:	n/a	chr22:29791127-29791143
49	CTCF	chr22:29790990-29791284	MCF-7	breast:	n/a	chr22:29791127-29791143
50	CTCF	chr22:29784395-29784682	K562	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29787625-29787675	Hela-S3	cervix:	n/a
2	chr22:29784644-29784694	H1-hESC	embryonic stem cell:	embryo
3	chr22:29787625-29787675	Hela-S3	cervix:	n/a
4	chr22:29784644-29784694	H1-hESC	embryonic stem cell:	embryo
5	chr22:29784671-29784721	HPAEpiC	pulmonary alveolar:	n/a
6	chr22:29784692-29784742	HUVEC	blood vessel:	n/a
7	chr22:29783861-29783911	BE2_C	brain:	n/a
8	chr22:29784778-29784828	HL-60	blood:	n/a
9	chr22:29784813-29784863	HMEC	breast:	n/a
10	chr22:29783861-29783911	HepG2	liver:	n/a
11	chr22:29784644-29784694	GM12878	blood:	n/a
12	chr22:29784436-29784486	HPAEpiC	pulmonary alveolar:	n/a
13	chr22:29784441-29784491	RPTEC	kidney:	n/a
14	chr22:29784697-29784747	MCF10A-Er-Src	breast:	n/a
15	chr22:29784778-29784828	Jurkat	blood:	n/a
16	chr22:29787625-29787675	Caco-2	colon:	n/a
17	chr22:29783861-29783911	ovcar-3	ovarian:	n/a
18	chr22:29784237-29784287	SKMC	muscle:	n/a
19	chr22:29784436-29784486	HRE	kidney:	n/a
20	chr22:29784671-29784721	Hepatocyte	liver:	n/a
21	chr22:29784436-29784486	SK-N-MC	brain:	n/a
22	chr22:29784778-29784828	NHBE	bronchial:	n/a
23	chr22:29784237-29784287	HUVEC	blood vessel:	n/a
24	chr22:29784671-29784721	HIPEpiC	eye:	n/a
25	chr22:29784813-29784863	PrEC	prostate:	n/a
26	chr22:29784644-29784694	Hepatocyte	liver:	n/a
27	chr22:29784624-29784674	MCF-7	breast:	n/a
28	chr22:29784778-29784828	CMK	blood:	n/a
29	chr22:29787625-29787675	NHBE	bronchial:	n/a
30	chr22:29784813-29784863	LNCaP	prostate:	n/a
31	chr22:29784694-29784744	GM06990	blood:	n/a
32	chr22:29784644-29784694	HepG2	liver:	n/a
33	chr22:29784441-29784491	ECC-1	luminal epithelium:	n/a
34	chr22:29784436-29784486	HCM	heart:	n/a
35	chr22:29784813-29784863	HRCEpiC	kidney:	n/a
36	chr22:29784237-29784287	Hepatocyte	liver:	n/a
37	chr22:29784624-29784674	HUVEC	blood vessel:	n/a
38	chr22:29784813-29784863	H1-hESC	embryonic stem cell:	embryo
39	chr22:29784692-29784742	SAEC	small airway:	n/a
40	chr22:29784237-29784287	HEK293	kidney:	embryo
41	chr22:29784644-29784694	MCF10A-Er-Src	breast:	n/a
42	chr22:29784778-29784828	Caco-2	colon:	n/a
43	chr22:29784697-29784747	NHDF-neo	bronchial:	n/a
44	chr22:29785355-29785405	NHBE	bronchial:	n/a
45	chr22:29784692-29784742	HL-60	blood:	n/a
46	chr22:29784624-29784674	CMK	blood:	n/a
47	chr22:29784813-29784863	HCF	heart:	n/a
48	chr22:29784436-29784486	K562	blood:	n/a
49	chr22:29784237-29784287	SK-N-SH	brain:	n/a
50	chr22:29784436-29784486	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr22:29787252..29790791-chr22:29920718..29924086,3	MCF-7	breast:
2	chr22:29782601..29785697-chr22:29975164..29978533,5	MCF-7	breast:
3	chr22:29784194..29786218-chr22:29789472..29791131,2	K562	blood:
4	chr22:29781675..29783812-chr22:29788035..29790235,2	MCF-7	breast:
5	chr22:29783197..29785326-chr22:29874558..29877420,2	MCF-7	breast:
6	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
7	chr22:29790656..29791686-chr22:29920171..29921137,10	MCF-7	breast:
8	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
9	chr22:29771666..29773871-chr22:29789734..29792185,2	MCF-7	breast:
10	chr22:29792519..29794058-chr22:29864789..29867115,2	MCF-7	breast:
11	chr22:29784558..29786360-chr22:29786552..29791390,4	MCF-7	breast:
12	chr22:29771898..29775582-chr22:29781742..29783845,4	MCF-7	breast:
13	chr22:29708527..29710108-chr22:29782946..29784507,2	K562	blood:
14	chr22:29790720..29791562-chr22:29920209..29921282,4	MCF-7	breast:
15	chr22:29791047..29793663-chr22:29794223..29797120,2	MCF-7	breast:
16	chr22:29786384..29789088-chr22:29790926..29793690,2	K562	blood:
17	chr22:29780907..29784157-chr22:29912302..29916422,4	MCF-7	breast:
18	chr22:29781675..29783812-chr22:29788035..29790235,2	MCF-7	breast:
19	chr22:29792125..29793668-chr22:29802474..29805006,2	K562	blood:
20	chr22:29783150..29785946-chr22:29944649..29946343,2	MCF-7	breast:
21	chr22:29701804..29704290-chr22:29781998..29785634,5	MCF-7	breast:
22	chr22:29712026..29714411-chr22:29782149..29784555,3	K562	blood:
23	chr22:29786384..29789088-chr22:29790926..29793690,2	K562	blood:

No data

Variant related genes	Relation type
AP1B1	TF binding region
AP1B1	CpG island
ENSG00000273216	chromatin interactions
ENSG00000184117	chromatin interactions
ENSG00000185340	chromatin interactions
ENSG00000100285	chromatin interactions
ENSG00000100296	chromatin interactions
ENSG00000100280	chromatin interactions

Extended variants
information (count: 369 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146150435	chr22:29783658-29783659	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs567308623	chr22:29783669-29783670	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs535860554	chr22:29783677-29783678	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs182028339	chr22:29783678-29783679	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs556169651	chr22:29783707-29783708	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs556311101	chr22:29783740-29783741	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs138994153	chr22:29783761-29783762	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs142144694	chr22:29783766-29783767	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs576367813	chr22:29783789-29783790	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs77131175	chr22:29783973-29783974	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs695416	chr22:29783978-29783979	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs695506	chr22:29783981-29783982	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs695556	chr22:29783982-29783983	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs695585	chr22:29783983-29783984	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs376699948	chr22:29784003-29784004	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs573381527	chr22:29784020-29784021	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs369387676	chr22:29784031-29784032	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs200965446	chr22:29784042-29784043	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs202102342	chr22:29784043-29784044	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs540612310	chr22:29784060-29784061	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs375909120	chr22:29784079-29784080	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs577562377	chr22:29784118-29784119	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs529275946	chr22:29784149-29784150	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs544221089	chr22:29784150-29784151	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs76890695	chr22:29784170-29784171	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs558431209	chr22:29784197-29784198	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs533273821	chr22:29784198-29784199	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs551803184	chr22:29784235-29784236	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs566594407	chr22:29784263-29784264	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs5997470	chr22:29784289-29784290	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs695429	chr22:29784292-29784293	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs549328126	chr22:29784297-29784298	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs6006118	chr22:29784329-29784330	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs139631882	chr22:29784363-29784364	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs538106505	chr22:29784365-29784366	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs552926265	chr22:29784375-29784376	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs184797861	chr22:29784437-29784438	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs571177275	chr22:29784467-29784468	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs371803296	chr22:29784472-29784473	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs538403212	chr22:29784512-29784513	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs573392267	chr22:29784528-29784529	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs376343234	chr22:29784556-29784557	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs540404809	chr22:29784633-29784634	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs555510339	chr22:29784642-29784643	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs376481520	chr22:29784645-29784646	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs574009835	chr22:29784656-29784657	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs544461482	chr22:29784658-29784659	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs562740262	chr22:29784702-29784703	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs5752906	chr22:29784786-29784787	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs543788372	chr22:29784791-29784792	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
abnormal development	18461090	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
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	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
Breast cancer	22522925	CNVD

Chromatin state (count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29755000-29783800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr22:29756000-29783800	Weak transcription	Ovary	ovary
3	chr22:29768000-29783800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr22:29774200-29784000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr22:29779000-29783800	Weak transcription	Aorta	Aorta
6	chr22:29779200-29783800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr22:29780000-29783800	Weak transcription	Lung	lung
8	chr22:29780800-29785200	Flanking Active TSS	Primary B cells from cord blood	blood
9	chr22:29781000-29783800	Enhancers	Fetal Brain Male	brain
10	chr22:29781000-29784200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr22:29781400-29783800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr22:29781800-29783800	Enhancers	Spleen	Spleen
13	chr22:29782000-29783800	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr22:29782200-29783800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
15	chr22:29782200-29784000	Flanking Active TSS	Primary B cells from peripheral blood	blood
16	chr22:29782400-29783800	Enhancers	Primary T cells fromperipheralblood	blood
17	chr22:29782600-29783800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr22:29782600-29783800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr22:29782800-29783800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr22:29782800-29783800	Enhancers	Placenta Amnion	Placenta Amnion
21	chr22:29782800-29784000	Flanking Active TSS	Duodenum Mucosa	Duodenum
22	chr22:29782800-29784200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr22:29783000-29783800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr22:29783000-29783800	Enhancers	Small Intestine	intestine
25	chr22:29783000-29784200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr22:29783000-29785000	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr22:29783200-29784200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr22:29783200-29784800	Active TSS	Fetal Intestine Large	intestine
29	chr22:29783200-29784800	Active TSS	GM12878-XiMat	blood
30	chr22:29783200-29785400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr22:29783400-29783800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr22:29783400-29783800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr22:29783400-29784000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr22:29783400-29784000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr22:29783400-29784000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
36	chr22:29783400-29784000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr22:29783400-29784000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
38	chr22:29783400-29784200	Flanking Active TSS	Primary T cells from cord blood	blood
39	chr22:29783400-29784200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr22:29783400-29784200	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr22:29783400-29784200	Flanking Active TSS	Stomach Smooth Muscle	stomach
42	chr22:29783400-29784200	Flanking Active TSS	Dnd41	blood
43	chr22:29783400-29784800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr22:29783400-29784800	Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr22:29783400-29784800	Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr22:29783400-29784800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr22:29783400-29785000	Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr22:29783400-29785200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr22:29783400-29785200	Active TSS	Right Atrium	heart
50	chr22:29783600-29783800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell

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