Variant report

Variant	esv3374115
Chromosome Location	chr22:31030477-31033325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:31030411-31030713	K562	blood:	n/a	n/a
2	ATF2	chr22:31030369-31030793	GM12878	blood:	n/a	n/a
3	ATF2	chr22:31030439-31030785	GM12878	blood:	n/a	n/a
4	ATF2	chr22:31030345-31030798	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr22:31030313-31030776	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr22:31030321-31030701	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr22:31030831-31031102	GM12878	blood:	n/a	chr22:31031013-31031023
8	BATF	chr22:31030413-31031139	GM12878	blood:	n/a	chr22:31031013-31031023
9	BCLAF1	chr22:31030331-31030892	GM12878	blood:	n/a	chr22:31030358-31030371
10	BHLHE40	chr22:31030330-31030932	GM12878	blood:	n/a	n/a
11	BHLHE40	chr22:31030421-31030752	HepG2	liver:	n/a	n/a
12	BHLHE40	chr22:31031376-31031921	GM12878	blood:	n/a	n/a
13	BHLHE40	chr22:31031664-31031883	K562	blood:	n/a	n/a
14	BHLHE40	chr22:31030382-31030783	K562	blood:	n/a	n/a
15	BRCA1	chr22:31030427-31030750	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr22:31031636-31031891	K562	blood:	n/a	n/a
17	CCNT2	chr22:31031513-31032077	K562	blood:	n/a	chr22:31031558-31031567
18	CEBPB	chr22:31030475-31030749	K562	blood:	n/a	n/a
19	CEBPB	chr22:31030449-31030796	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr22:31030368-31030845	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr22:31031398-31031553	GM12878	blood:	n/a	n/a
22	CHD1	chr22:31032567-31032598	GM12878	blood:	n/a	n/a
23	CHD1	chr22:31030212-31033049	IMR90	lung:	n/a	n/a
24	CHD2	chr22:31030480-31030608	K562	blood:	n/a	n/a
25	CHD2	chr22:31032860-31033049	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr22:31031407-31031899	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr22:31030454-31030785	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr22:31031386-31031590	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr22:31030474-31030702	HepG2	liver:	n/a	n/a
30	CHD2	chr22:31030466-31031753	GM12878	blood:	n/a	n/a
31	CREB1	chr22:31030348-31030648	A549	lung:	n/a	n/a
32	CREB1	chr22:31031350-31031650	A549	lung:	n/a	n/a
33	CTBP2	chr22:31030359-31031574	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr22:31031360-31031510	GM12878	blood:	n/a	chr22:31031444-31031462 chr22:31031446-31031459 chr22:31031450-31031459
35	CTCF	chr22:31031380-31031530	AG09309	skin:	n/a	chr22:31031444-31031462 chr22:31031446-31031459 chr22:31031450-31031459
36	CTCF	chr22:31031440-31031590	HAc	cerebellar:	n/a	chr22:31031444-31031462 chr22:31031446-31031459 chr22:31031450-31031459
37	CTCF	chr22:31031066-31031235	HepG2	liver:	n/a	chr22:31031144-31031154 chr22:31031139-31031157
38	CTCF	chr22:31030980-31031130	GM12871	blood:	n/a	n/a
39	CTCF	chr22:31032940-31033090	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr22:31031380-31031530	HEK293	kidney:	n/a	chr22:31031444-31031462 chr22:31031446-31031459 chr22:31031450-31031459
41	CTCF	chr22:31031100-31031250	AG04450	lung:	n/a	chr22:31031144-31031154 chr22:31031139-31031157
42	CTCF	chr22:31031060-31031210	K562	blood:	n/a	chr22:31031144-31031154 chr22:31031139-31031157
43	CTCF	chr22:31030435-31030716	K562	blood:	n/a	chr22:31030569-31030582 chr22:31030566-31030584 chr22:31030568-31030589 chr22:31030569-31030582 chr22:31030571-31030581 chr22:31030567-31030583 chr22:31030569-31030578
44	CTCF	chr22:31032957-31033064	ProgFib	skin:	n/a	n/a
45	CTCF	chr22:31030500-31030650	GM12866	blood:	n/a	chr22:31030569-31030582 chr22:31030566-31030584 chr22:31030568-31030589 chr22:31030569-31030582 chr22:31030571-31030581 chr22:31030567-31030583 chr22:31030569-31030578
46	CTCF	chr22:31030295-31030828	MCF-7	breast:	n/a	chr22:31030569-31030582 chr22:31030566-31030584 chr22:31030568-31030589 chr22:31030569-31030582 chr22:31030571-31030581 chr22:31030567-31030583 chr22:31030569-31030578
47	CTCF	chr22:31031380-31031530	HPF	lung:	n/a	chr22:31031444-31031462 chr22:31031446-31031459 chr22:31031450-31031459
48	CTCF	chr22:31031040-31031190	AG04449	skin:	n/a	chr22:31031144-31031154 chr22:31031139-31031157
49	CTCF	chr22:31030402-31030740	GM19240	blood:	n/a	chr22:31030569-31030582 chr22:31030566-31030584 chr22:31030568-31030589 chr22:31030569-31030582 chr22:31030571-31030581 chr22:31030567-31030583 chr22:31030569-31030578
50	CTCF	chr22:31031380-31031530	AG04450	lung:	n/a	chr22:31031444-31031462 chr22:31031446-31031459 chr22:31031450-31031459

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:31031786-31031836	A549	lung:	n/a
2	chr22:31030599-31030649	AoSMC	blood vessel:	n/a
3	chr22:31031786-31031836	A549	lung:	n/a
4	chr22:31030599-31030649	AoSMC	blood vessel:	n/a
5	chr22:31030599-31030649	Caco-2	colon:	n/a
6	chr22:31030599-31030649	AG09309	skin:	n/a
7	chr22:31030599-31030649	CMK	blood:	n/a
8	chr22:31031670-31031720	HCF	heart:	n/a
9	chr22:31031786-31031836	RPTEC	kidney:	n/a
10	chr22:31031685-31031735	PANC-1	pancreas:	n/a
11	chr22:31031688-31031738	HRCEpiC	kidney:	n/a
12	chr22:31031670-31031720	NH-A	brain:	n/a
13	chr22:31030599-31030649	BJ	skin:	n/a
14	chr22:31031670-31031720	AG04449	skin:	fetal
15	chr22:31031670-31031720	AG04450	lung:	fetal
16	chr22:31031786-31031836	HEK293	kidney:	embryo
17	chr22:31031670-31031720	HPAEpiC	pulmonary alveolar:	n/a
18	chr22:31031044-31031094	Hepatocyte	liver:	n/a
19	chr22:31031786-31031836	SKMC	muscle:	n/a
20	chr22:31031786-31031836	IMR90	lung:	fetal
21	chr22:31031688-31031738	AG09309	skin:	n/a
22	chr22:31031786-31031836	PrEC	prostate:	n/a
23	chr22:31031867-31031917	NB4	blood:	n/a
24	chr22:31031688-31031738	A549	lung:	n/a
25	chr22:31031867-31031917	HRPEpiC	eye:	n/a
26	chr22:31032613-31032663	T-47D	breast:	n/a
27	chr22:31031867-31031917	AG09319	gingival:	n/a
28	chr22:31030853-31030903	HEEpiC	esophagus:	n/a
29	chr22:31031685-31031735	PFSK-1	brain:	n/a
30	chr22:31031688-31031738	U87	brain:	n/a
31	chr22:31031786-31031836	HUVEC	blood vessel:	n/a
32	chr22:31031867-31031917	HAEpiC	amniotic membrane:	n/a
33	chr22:31031867-31031917	ECC-1	luminal epithelium:	n/a
34	chr22:31032613-31032663	PANC-1	pancreas:	n/a
35	chr22:31032613-31032663	HUVEC	blood vessel:	n/a
36	chr22:31032613-31032663	ProgFib	skin:	n/a
37	chr22:31030853-31030903	AoSMC	blood vessel:	n/a
38	chr22:31030853-31030903	SK-N-SH	brain:	n/a
39	chr22:31031685-31031735	H1-hESC	embryonic stem cell:	embryo
40	chr22:31030853-31030903	BE2_C	brain:	n/a
41	chr22:31031670-31031720	HL-60	blood:	n/a
42	chr22:31031786-31031836	AG09319	gingival:	n/a
43	chr22:31032613-31032663	GM12878	blood:	n/a
44	chr22:31030853-31030903	AG09309	skin:	n/a
45	chr22:31031867-31031917	MCF-7	breast:	n/a
46	chr22:31031685-31031735	A549	lung:	n/a
47	chr22:31031670-31031720	HMEC	breast:	n/a
48	chr22:31031044-31031094	U87	brain:	n/a
49	chr22:31031688-31031738	SK-N-SH	brain:	n/a
50	chr22:31031670-31031720	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:31030229..31031056-chr22:31150888..31151995,5	MCF-7	breast:
2	chr22:31030338..31033016-chr22:31062140..31065480,4	MCF-7	breast:
3	chr22:31030552..31033273-chr22:31061698..31065017,4	MCF-7	breast:
4	chr22:31030117..31031164-chr22:31286279..31286856,3	MCF-7	breast:
5	chr22:31031588..31032094-chr22:31090123..31090949,2	MCF-7	breast:

Variant related genes	Relation type
SLC35E4	TF binding region
SLC35E4	CpG island
ENSG00000184792	chromatin interactions
ENSG00000167065	chromatin interactions

Extended variants
information (count: 125 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:125 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575204082	chr22:31030524-31030525	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs5753259	chr22:31030528-31030529	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs564148251	chr22:31030533-31030534	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs533094011	chr22:31030549-31030550	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs5753260	chr22:31030592-31030593	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs140579217	chr22:31030597-31030598	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs191736224	chr22:31030600-31030601	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs549266342	chr22:31030632-31030633	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs569120104	chr22:31030646-31030647	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs12159171	chr22:31030681-31030682	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs550364239	chr22:31030716-31030717	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs570011916	chr22:31030750-31030751	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs534070329	chr22:31030754-31030755	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs4820023	chr22:31030781-31030782	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs573900061	chr22:31030803-31030804	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs7284161	chr22:31030839-31030840	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs114083076	chr22:31030872-31030873	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs146593116	chr22:31030935-31030936	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs544179252	chr22:31030952-31030953	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs564109434	chr22:31030960-31030961	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs564325390	chr22:31030992-31030993	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs183568387	chr22:31030997-31030998	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs566041564	chr22:31031020-31031021	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs535051595	chr22:31031046-31031047	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs558477805	chr22:31031053-31031054	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs560347511	chr22:31031079-31031080	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529099424	chr22:31031085-31031086	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs548975836	chr22:31031095-31031096	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs9621053	chr22:31031133-31031134	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs141354673	chr22:31031139-31031140	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs150255944	chr22:31031153-31031154	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs374864576	chr22:31031161-31031162	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs543995120	chr22:31031212-31031213	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs112424164	chr22:31031223-31031224	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs573628668	chr22:31031260-31031261	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs149014720	chr22:31031290-31031291	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs73881499	chr22:31031313-31031314	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs536872869	chr22:31031321-31031322	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs13054505	chr22:31031418-31031419	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs570319398	chr22:31031422-31031423	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs539008631	chr22:31031448-31031449	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs557738408	chr22:31031452-31031453	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs200419549	chr22:31031488-31031489	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs187023950	chr22:31031510-31031511	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs117562471	chr22:31031522-31031523	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs533024289	chr22:31031559-31031560	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs573685447	chr22:31031565-31031566	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs143437977	chr22:31031566-31031567	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562584092	chr22:31031572-31031573	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs376729873	chr22:31031582-31031583	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	2 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
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
Autism	22495309	CNVD

Chromatin state (count:564 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31003200-31031200	Weak transcription	Aorta	Aorta
2	chr22:31003800-31030600	Weak transcription	Thymus	Thymus
3	chr22:31006000-31030600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr22:31006000-31030600	Weak transcription	Colonic Mucosa	Colon
5	chr22:31006200-31030600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr22:31007000-31030600	Weak transcription	Fetal Brain Male	brain
7	chr22:31011800-31030600	Weak transcription	Right Ventricle	heart
8	chr22:31012000-31030600	Weak transcription	Brain Angular Gyrus	brain
9	chr22:31013600-31030600	Weak transcription	Pancreas	Pancrea
10	chr22:31013800-31030600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr22:31014000-31030800	Weak transcription	Gastric	stomach
12	chr22:31014000-31030800	Weak transcription	Ovary	ovary
13	chr22:31015800-31030600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr22:31015800-31030600	Weak transcription	Fetal Lung	lung
15	chr22:31017000-31030600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr22:31017200-31030600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr22:31019200-31030600	Weak transcription	Colon Smooth Muscle	Colon
18	chr22:31019200-31030600	Weak transcription	Left Ventricle	heart
19	chr22:31019200-31030800	Weak transcription	Lung	lung
20	chr22:31023000-31030600	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr22:31023000-31030600	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr22:31023000-31030600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr22:31023000-31030600	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr22:31023200-31030600	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr22:31023200-31030600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr22:31023200-31030600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr22:31023200-31030600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr22:31023200-31030600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr22:31023200-31030600	Weak transcription	Adipose Nuclei	Adipose
30	chr22:31023200-31030600	Weak transcription	Fetal Brain Female	brain
31	chr22:31024000-31030600	Weak transcription	Spleen	Spleen
32	chr22:31025000-31030600	Weak transcription	Brain Germinal Matrix	brain
33	chr22:31025200-31031200	Weak transcription	Right Atrium	heart
34	chr22:31026200-31030600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr22:31026400-31031000	Weak transcription	Fetal Heart	heart
36	chr22:31030200-31030600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr22:31030200-31030600	Enhancers	Primary B cells from peripheral blood	blood
38	chr22:31030200-31030600	Enhancers	Primary T cells fromperipheralblood	blood
39	chr22:31030200-31030600	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr22:31030200-31030600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr22:31030200-31030600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr22:31030200-31030600	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr22:31030200-31030600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr22:31030200-31030600	Enhancers	Brain Cingulate Gyrus	brain
45	chr22:31030200-31030600	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr22:31030200-31030600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr22:31030200-31030600	Enhancers	Brain Substantia Nigra	brain
48	chr22:31030200-31030600	Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr22:31030200-31030600	Enhancers	GM12878-XiMat	blood
50	chr22:31030200-31030600	Enhancers	HUVEC	blood vessel

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