Variant report

Variant	nsv588894
Chromosome Location	chr22:31833759-31977594
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2959)
CpG islands
(count:1651)
Chromatin interactive
region (count:172)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2959 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:31885756-31886129	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:31976705-31977060	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:31952687-31952977	K562	blood:	n/a	n/a
4	ARID3A	chr22:31926449-31927040	HepG2	liver:	n/a	n/a
5	ARID3A	chr22:31940907-31941077	HepG2	liver:	n/a	n/a
6	ARID3A	chr22:31885903-31886096	K562	blood:	n/a	n/a
7	ARID3A	chr22:31957357-31957557	HepG2	liver:	n/a	n/a
8	ARID3A	chr22:31975747-31976264	HepG2	liver:	n/a	n/a
9	ARID3A	chr22:31891935-31892132	K562	blood:	n/a	n/a
10	ARID3A	chr22:31957277-31957608	K562	blood:	n/a	n/a
11	ATF1	chr22:31886331-31887022	K562	blood:	n/a	n/a
12	ATF2	chr22:31942847-31943380	GM12878	blood:	n/a	n/a
13	ATF2	chr22:31891884-31892640	GM12878	blood:	n/a	n/a
14	ATF2	chr22:31932852-31933662	GM12878	blood:	n/a	n/a
15	ATF2	chr22:31885674-31887011	GM12878	blood:	n/a	n/a
16	ATF2	chr22:31890028-31890425	GM12878	blood:	n/a	n/a
17	ATF2	chr22:31892058-31892446	GM12878	blood:	n/a	n/a
18	ATF2	chr22:31942840-31943481	GM12878	blood:	n/a	n/a
19	ATF2	chr22:31932812-31933569	GM12878	blood:	n/a	n/a
20	ATF2	chr22:31934659-31935425	GM12878	blood:	n/a	n/a
21	ATF2	chr22:31948663-31949396	GM12878	blood:	n/a	n/a
22	ATF2	chr22:31885885-31886967	GM12878	blood:	n/a	n/a
23	ATF2	chr22:31934714-31935235	GM12878	blood:	n/a	n/a
24	BACH1	chr22:31885925-31886679	K562	blood:	n/a	n/a
25	BACH1	chr22:31887242-31887555	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr22:31891900-31893464	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr22:31891840-31892521	K562	blood:	n/a	n/a
28	BACH1	chr22:31885818-31886837	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr22:31841657-31841961	GM12878	blood:	n/a	chr22:31841853-31841863
30	BATF	chr22:31940080-31940317	GM12878	blood:	n/a	chr22:31940238-31940249
31	BATF	chr22:31932926-31933388	GM12878	blood:	n/a	n/a
32	BATF	chr22:31943024-31943467	GM12878	blood:	n/a	n/a
33	BATF	chr22:31916079-31916329	GM12878	blood:	n/a	n/a
34	BATF	chr22:31893442-31893799	GM12878	blood:	n/a	n/a
35	BATF	chr22:31932933-31933569	GM12878	blood:	n/a	n/a
36	BATF	chr22:31946678-31946964	GM12878	blood:	n/a	n/a
37	BATF	chr22:31916048-31916368	GM12878	blood:	n/a	n/a
38	BATF	chr22:31886386-31886943	GM12878	blood:	n/a	n/a
39	BATF	chr22:31884307-31884694	GM12878	blood:	n/a	chr22:31884501-31884511 chr22:31884504-31884515
40	BATF	chr22:31934780-31935139	GM12878	blood:	n/a	n/a
41	BATF	chr22:31942842-31943493	GM12878	blood:	n/a	n/a
42	BATF	chr22:31940880-31941085	GM12878	blood:	n/a	n/a
43	BCL11A	chr22:31934808-31935153	GM12878	blood:	n/a	n/a
44	BCL11A	chr22:31890124-31890662	GM12878	blood:	n/a	n/a
45	BCL11A	chr22:31932986-31933351	GM12878	blood:	n/a	n/a
46	BCL11A	chr22:31886348-31886970	GM12878	blood:	n/a	chr22:31886609-31886618
47	BCL11A	chr22:31942936-31943481	GM12878	blood:	n/a	chr22:31943225-31943234
48	BCL3	chr22:31932953-31933350	GM12878	blood:	n/a	n/a
49	BCL3	chr22:31885736-31886877	GM12878	blood:	n/a	chr22:31886110-31886123 chr22:31885839-31885848 chr22:31885911-31885924 chr22:31886109-31886118 chr22:31886609-31886618
50	BCL3	chr22:31928591-31928965	GM12878	blood:	n/a	n/a

(count:1651 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:31889592-31889642	NB4	blood:	n/a
2	chr22:31885298-31885348	AG10803	skin:	n/a
3	chr22:31886454-31886504	PANC-1	pancreas:	n/a
4	chr22:31897078-31897128	HMEC	breast:	n/a
5	chr22:31889592-31889642	NB4	blood:	n/a
6	chr22:31885298-31885348	AG10803	skin:	n/a
7	chr22:31886454-31886504	PANC-1	pancreas:	n/a
8	chr22:31897078-31897128	HMEC	breast:	n/a
9	chr22:31892045-31892095	MCF10A-Er-Src	breast:	n/a
10	chr22:31884264-31884314	AG04450	lung:	fetal
11	chr22:31892067-31892117	AG10803	skin:	n/a
12	chr22:31885763-31885813	A549	lung:	n/a
13	chr22:31892114-31892164	HUVEC	blood vessel:	n/a
14	chr22:31884264-31884314	HL-60	blood:	n/a
15	chr22:31892067-31892117	SK-N-MC	brain:	n/a
16	chr22:31897078-31897128	HepG2	liver:	n/a
17	chr22:31891804-31891854	K562	blood:	n/a
18	chr22:31885763-31885813	U87	brain:	n/a
19	chr22:31892067-31892117	A549	lung:	n/a
20	chr22:31892152-31892202	PrEC	prostate:	n/a
21	chr22:31897078-31897128	MCF-7	breast:	n/a
22	chr22:31892114-31892164	GM12891	blood:	n/a
23	chr22:31885739-31885789	HRE	kidney:	n/a
24	chr22:31892045-31892095	U87	brain:	n/a
25	chr22:31892053-31892103	AG10803	skin:	n/a
26	chr22:31885141-31885191	PrEC	prostate:	n/a
27	chr22:31885298-31885348	PANC-1	pancreas:	n/a
28	chr22:31892152-31892202	GM19239	blood:	n/a
29	chr22:31889592-31889642	A549	lung:	n/a
30	chr22:31885640-31885690	Jurkat	blood:	n/a
31	chr22:31892074-31892124	HRE	kidney:	n/a
32	chr22:31885141-31885191	ECC-1	luminal epithelium:	n/a
33	chr22:31885739-31885789	GM12878	blood:	n/a
34	chr22:31886454-31886504	LNCaP	prostate:	n/a
35	chr22:31885141-31885191	GM19239	blood:	n/a
36	chr22:31885763-31885813	NHBE	bronchial:	n/a
37	chr22:31885763-31885813	AG10803	skin:	n/a
38	chr22:31884264-31884314	ProgFib	skin:	n/a
39	chr22:31892045-31892095	NHDF-neo	bronchial:	n/a
40	chr22:31885573-31885623	T-47D	breast:	n/a
41	chr22:31885573-31885623	HL-60	blood:	n/a
42	chr22:31885763-31885813	AG04449	skin:	fetal
43	chr22:31892067-31892117	NH-A	brain:	n/a
44	chr22:31892045-31892095	HEK293	kidney:	embryo
45	chr22:31892053-31892103	BJ	skin:	n/a
46	chr22:31885780-31885830	NB4	blood:	n/a
47	chr22:31886228-31886278	A549	lung:	n/a
48	chr22:31892148-31892198	NH-A	brain:	n/a
49	chr22:31892343-31892393	GM06990	blood:	n/a
50	chr22:31893096-31893146	Jurkat	blood:	n/a

(count:172 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr22:31793990..31796986-chr22:31884678..31887767,3	K562	blood:
2	chr22:31838625..31840945-chr22:31858613..31860728,2	MCF-7	breast:
3	chr22:31956388..31959069-chr22:32024748..32027076,2	MCF-7	breast:
4	22:31861680-31864703..22:32750950-32761732	K562	blood:
5	22:31976153-31978142..22:32162110-32166713	Hela-S3	cervix:
6	chr22:31884998..31887254-chr22:32026687..32028800,2	K562	blood:
7	chr22:31867263..31868960-chr22:31885475..31887155,2	K562	blood:
8	chr22:31840904..31842503-chr22:31846475..31848717,2	MCF-7	breast:
9	chr22:31957051..31957599-chr22:32025028..32025686,2	MCF-7	breast:
10	chr22:31884421..31887375-chr22:32024434..32026202,2	MCF-7	breast:
11	chr22:31952329..31953130-chr22:32056984..32057496,2	K562	blood:
12	chr22:31956959..31958076-chr22:32029583..32030405,5	MCF-7	breast:
13	chr22:31892881..31894794-chr22:31897314..31900016,2	K562	blood:
14	chr22:31831980..31833973-chr22:31840875..31843201,2	MCF-7	breast:
15	22:31936958-31958600..22:32338420-32342898	K562	blood:
16	22:31930706-31935473..22:32012966-32043914	GM12878	blood:
17	chr22:31362414..31364814-chr22:31884704..31886596,2	K562	blood:
18	chr22:31895925..31897585-chr22:31899327..31902230,2	K562	blood:
19	chr22:31847674..31848482-chr22:31892087..31892811,2	MCF-7	breast:
20	chr22:31892433..31894421-chr22:31898516..31901632,3	K562	blood:
21	22:31936958-31958600..22:32868055-32872511	K562	blood:
22	22:31961151-31976153..22:33253287-33262063	K562	blood:
23	chr22:31880474..31882997-chr22:31883937..31886891,2	K562	blood:
24	chr22:31974704..31977587-chr22:32057867..32059822,2	MCF-7	breast:
25	chr22:31895925..31897585-chr22:31899327..31902230,2	K562	blood:
26	chr22:31847213..31849082-chr22:31849317..31851160,2	K562	blood:
27	chr22:31839629..31841921-chr22:31886106..31888362,2	K562	blood:
28	chr22:31955506..31958197-chr22:32020735..32022732,2	MCF-7	breast:
29	chr22:31880006..31882997-chr22:31884265..31886891,3	K562	blood:
30	chr22:31793990..31795602-chr22:31885862..31887767,2	K562	blood:
31	chr22:31895644..31897585-chr22:31899488..31902230,2	K562	blood:
32	chr22:31841016..31842621-chr22:31845708..31848427,2	MCF-7	breast:
33	22:31936958-31958600..22:32860159-32865649	K562	blood:
34	22:31936958-31958600..22:32264718-32278135	Hela-S3	cervix:
35	22:31864703-31891033..22:31930706-31935473	GM12878	blood:
36	chr22:31915170..31916943-chr22:31918334..31921689,3	K562	blood:
37	chr22:31793416..31795998-chr22:31841397..31844290,2	MCF-7	breast:
38	chr22:31742672..31744282-chr22:31844664..31847017,2	MCF-7	breast:
39	chr22:31974878..31977685-chr22:31979541..31981630,2	K562	blood:
40	chr22:31862991..31864545-chr22:31885430..31887272,2	MCF-7	breast:
41	22:31836635-31847259..22:31861680-31864703	K562	blood:
42	chr22:31739363..31741917-chr22:31884740..31886779,4	MCF-7	breast:
43	chr22:31849740..31852347-chr22:31891078..31892965,2	K562	blood:
44	chr22:31950555..31952408-chr22:31956023..31958715,2	K562	blood:
45	chr22:31946590..31949361-chr22:32340204..32341908,2	K562	blood:
46	chr22:31884599..31887538-chr22:32147471..32150641,3	K562	blood:
47	22:31936958-31958600..22:32012966-32043914	GM12878	blood:
48	22:31829733-31836635..22:32162110-32166713	GM12878	blood:
49	chr22:31958875..31961811-chr22:32027409..32029066,2	MCF-7	breast:
50	chr22:31850201..31852811-chr22:31884349..31886700,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SFI1-2	chr22:31904241-31904362	NONHSAT084896
2	lnc-SFI1-2	chr22:31884674-31884769	NONHSAT084895
3	lnc-SFI1-2	chr22:31924676-31924852	NONHSAT084896
4	lnc-SFI1-3	chr22:31831223-31834552	NONHSAT084887
5	lnc-EIF4ENIF1-1	chr22:31833672-31833804	ENSG00000240529.1
6	lnc-DRG1-1	chr22:31976074-31976350	NONHSAT084901
7	lnc-DRG1-1	chr22:31973934-31974438	NONHSAT084900
8	lnc-SFI1-2	chr22:31924676-31925053	NONHSAT084895
9	lnc-SFI1-2	chr22:31904241-31904362	NONHSAT084895
10	lnc-EIF4ENIF1-4	chr22:31917185-31917578	NONHSAT084897
11	lnc-EIF4ENIF1-5	chr22:31934338-31934575	NONHSAT084898
12	lnc-EIF4ENIF1-1	chr22:31835796-31835893	ENSG00000240529.1
13	lnc-SFI1-2	chr22:31892450-31892623	NONHSAT084896
14	lnc-SFI1-2	chr22:31917221-31917306	NONHSAT084896

No data

Variant related genes	Relation type
ENSG00000229169	TF binding region
ENSG00000224623	TF binding region
EIF4ENIF1	TF binding region
H2AFZP6	TF binding region
SFI1	TF binding region
RNU6-28P	TF binding region
ENSG00000214093	TF binding region
ENSG00000240591	TF binding region
ENSG00000229169	CpG island
ENSG00000224623	CpG island
EIF4ENIF1	CpG island
H2AFZP6	CpG island
SFI1	CpG island
RNU6-28P	CpG island
ENSG00000214093	CpG island
ENSG00000240591	CpG island
ENSG00000128253	chromatin interactions
ENSG00000128245	chromatin interactions
ENSG00000229169	chromatin interactions
ENSG00000242082	chromatin interactions
ENSG00000100150	chromatin interactions
ENSG00000100105	chromatin interactions
ENSG00000128276	chromatin interactions
ENSG00000101639	chromatin interactions
ENSG00000198089	chromatin interactions
ENSG00000213888	chromatin interactions
ENSG00000198327	chromatin interactions
ENSG00000224623	chromatin interactions
ENSG00000183530	chromatin interactions
ENSG00000183531	chromatin interactions
ENSG00000232707	chromatin interactions
ENSG00000254718	chromatin interactions
ENSG00000240591	chromatin interactions
ENSG00000100225	chromatin interactions
ENSG00000128254	chromatin interactions
ENSG00000205853	chromatin interactions
ENSG00000232218	chromatin interactions
ENSG00000185721	chromatin interactions
ENSG00000241878	chromatin interactions
ENSG00000241954	chromatin interactions
ENSG00000271093	chromatin interactions
ENSG00000251890	chromatin interactions
ENSG00000269987	chromatin interactions
ENSG00000214093	chromatin interactions
ENSG00000243519	chromatin interactions
ENSG00000134333	chromatin interactions
ENSG00000227813	chromatin interactions
ENSG00000254127	chromatin interactions
ENSG00000199248	chromatin interactions
ENSG00000100614	chromatin interactions
ENSG00000238910	chromatin interactions
ENSG00000185666	chromatin interactions
ENSG00000133422	chromatin interactions
ENSG00000184459	chromatin interactions
ENSG00000266969	chromatin interactions
ENSG00000234479	chromatin interactions
ENSG00000184708	chromatin interactions
ENSG00000239674	chromatin interactions
ENSG00000269972	chromatin interactions
ENSG00000230736	chromatin interactions
ENSG00000100170	chromatin interactions
ENSG00000252909	chromatin interactions

Extended variants
information (count: 5747 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5747 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs695455	chr22:31833759-31833760	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140804910	chr22:31833797-31833798	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
3	rs549231412	chr22:31833852-31833853	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
4	rs569060617	chr22:31833942-31833943	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
5	rs538001285	chr22:31833948-31833949	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
6	rs185228322	chr22:31833954-31833955	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
7	rs554422869	chr22:31833975-31833976	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
8	rs368305951	chr22:31833996-31833997	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
9	rs571512357	chr22:31834013-31834014	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
10	rs534261848	chr22:31834021-31834022	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
11	rs554342704	chr22:31834039-31834040	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
12	rs573946095	chr22:31834052-31834053	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
13	rs185374349	chr22:31834057-31834058	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
14	rs556772729	chr22:31834060-31834061	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
15	rs190669273	chr22:31834103-31834104	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
16	rs370863550	chr22:31834120-31834121	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
17	rs545335068	chr22:31834124-31834125	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
18	rs565136076	chr22:31834125-31834126	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
19	rs527909140	chr22:31834151-31834152	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
20	rs114253798	chr22:31834176-31834177	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
21	rs560011217	chr22:31834195-31834196	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
22	rs12628465	chr22:31834200-31834201	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs542738490	chr22:31834223-31834224	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
24	rs548711848	chr22:31834229-31834230	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
25	rs568873122	chr22:31834259-31834260	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
26	rs531631690	chr22:31834267-31834268	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
27	rs146708123	chr22:31834276-31834277	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
28	rs140283203	chr22:31834287-31834288	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
29	rs533995003	chr22:31834340-31834341	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
30	rs554213189	chr22:31834341-31834342	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
31	rs567660587	chr22:31834371-31834372	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
32	rs536610473	chr22:31834405-31834406	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
33	rs556274562	chr22:31834406-31834407	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
34	rs150358190	chr22:31834442-31834443	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
35	rs538925259	chr22:31834472-31834473	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
36	rs558858303	chr22:31834518-31834519	Strong transcription Weak transcription	Chromatin interactive region lncRNA	13 gene(s)	Overlapped CNVs	n/a
37	rs549932973	chr22:31834591-31834592	Strong transcription Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
38	rs541227887	chr22:31834617-31834618	Strong transcription Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
39	rs181423026	chr22:31834619-31834620	Strong transcription Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
40	rs78048764	chr22:31834643-31834644	Strong transcription Weak transcription	Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
41	rs542752286	chr22:31834668-31834669	Strong transcription Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs138047413	chr22:31834752-31834753	Strong transcription Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs185951142	chr22:31834770-31834771	Strong transcription Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs5753617	chr22:31834779-31834780	Strong transcription Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs551668887	chr22:31834786-31834787	Strong transcription Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs372339932	chr22:31834795-31834796	Strong transcription Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs62236215	chr22:31834823-31834824	Strong transcription Weak transcription	Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs8140830	chr22:31834843-31834844	Strong transcription Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
49	rs190024155	chr22:31834890-31834891	Strong transcription Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
50	rs368090726	chr22:31834934-31834935	Strong transcription Weak transcription	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
Breast cancer	17142309	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:4495 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31796800-31835600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr22:31797000-31836600	Strong transcription	Placenta	Placenta
3	chr22:31797000-31884400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr22:31797000-31884400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr22:31797200-31845400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr22:31797200-31846200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr22:31797200-31846400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr22:31797200-31860600	Strong transcription	Fetal Stomach	stomach
9	chr22:31797400-31846800	Strong transcription	Duodenum Mucosa	Duodenum
10	chr22:31797600-31835800	Strong transcription	Fetal Muscle Trunk	muscle
11	chr22:31797800-31844800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr22:31797800-31846800	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr22:31799000-31845400	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr22:31799200-31846600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr22:31803600-31844600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr22:31804600-31847000	Strong transcription	Sigmoid Colon	Sigmoid Colon
17	chr22:31805000-31844800	Strong transcription	Primary B cells from peripheral blood	blood
18	chr22:31805600-31844800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr22:31806800-31842400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr22:31812000-31842000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr22:31813600-31845000	Strong transcription	Fetal Thymus	thymus
22	chr22:31814000-31838000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr22:31814000-31841200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr22:31814000-31846400	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr22:31814200-31846800	Strong transcription	Cortex derived primary cultured neurospheres	brain
26	chr22:31814400-31845600	Strong transcription	Primary T helper cells PMA-I stimulated	--
27	chr22:31814400-31845800	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr22:31814400-31846800	Strong transcription	Fetal Intestine Large	intestine
29	chr22:31814600-31841400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr22:31814600-31841600	Strong transcription	Lung	lung
31	chr22:31814800-31844600	Strong transcription	Thymus	Thymus
32	chr22:31814800-31846600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr22:31815000-31841400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr22:31815000-31844600	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr22:31815000-31846600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr22:31815000-31846800	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr22:31815000-31868200	Strong transcription	Dnd41	blood
38	chr22:31815000-31883400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr22:31815400-31844400	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr22:31815400-31844400	Strong transcription	Rectal Mucosa Donor 31	rectum
41	chr22:31815400-31846200	Strong transcription	Primary neutrophils fromperipheralblood	blood
42	chr22:31815400-31846600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr22:31815400-31846600	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr22:31815600-31839200	Strong transcription	H1 Cell Line	embryonic stem cell
45	chr22:31815600-31844200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
46	chr22:31815800-31841600	Strong transcription	Muscle Satellite Cultured Cells	--
47	chr22:31816000-31839000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr22:31816200-31842200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr22:31821000-31844600	Strong transcription	Primary B cells from cord blood	blood
50	chr22:31821000-31845000	Strong transcription	Primary T cells from cord blood	blood

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