Variant report

Variant	nsv438344
Chromosome Location	chr22:29856079-29886043
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:880)
CpG islands
(count:1103)
Chromatin interactive
region (count:52)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:880 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:29874677-29874753	K562	blood:	n/a	n/a
2	ATF1	chr22:29876859-29877274	K562	blood:	n/a	chr22:29877047-29877061
3	ATF1	chr22:29866399-29866713	K562	blood:	n/a	n/a
4	ATF2	chr22:29876824-29877313	H1-hESC	embryonic stem cell:	n/a	chr22:29877047-29877061
5	ATF2	chr22:29866249-29866840	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr22:29866348-29866798	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr22:29876895-29877255	K562	blood:	n/a	n/a
8	BACH1	chr22:29873953-29874359	K562	blood:	n/a	n/a
9	BACH1	chr22:29865736-29866729	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr22:29873931-29874298	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr22:29876282-29878043	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr22:29874505-29875008	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr22:29877630-29877960	K562	blood:	n/a	n/a
14	BATF	chr22:29872228-29872571	GM12878	blood:	n/a	n/a
15	BATF	chr22:29872240-29872536	GM12878	blood:	n/a	n/a
16	BHLHE40	chr22:29866494-29866668	GM12878	blood:	n/a	chr22:29866564-29866580
17	BHLHE40	chr22:29871734-29871824	GM12878	blood:	n/a	n/a
18	BHLHE40	chr22:29876615-29877342	K562	blood:	n/a	n/a
19	BHLHE40	chr22:29866439-29866628	K562	blood:	n/a	chr22:29866564-29866580
20	BHLHE40	chr22:29874650-29874757	K562	blood:	n/a	n/a
21	BRCA1	chr22:29876551-29877266	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr22:29866416-29866674	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr22:29866030-29866149	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr22:29866362-29866663	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr22:29876900-29877127	K562	blood:	n/a	n/a
26	CBX3	chr22:29876659-29877329	K562	blood:	n/a	n/a
27	CCNT2	chr22:29876392-29876480	K562	blood:	n/a	n/a
28	CCNT2	chr22:29877774-29877862	K562	blood:	n/a	chr22:29877810-29877819
29	CCNT2	chr22:29876839-29877354	K562	blood:	n/a	chr22:29877154-29877163
30	CCNT2	chr22:29866404-29866693	K562	blood:	n/a	n/a
31	CEBPB	chr22:29860381-29860566	HepG2	liver:	n/a	n/a
32	CEBPB	chr22:29860981-29861232	IMR90	lung:	n/a	chr22:29861062-29861073
33	CEBPB	chr22:29860377-29860518	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr22:29860994-29861400	HepG2	liver:	n/a	chr22:29861062-29861073
35	CEBPB	chr22:29861007-29861085	A549	lung:	n/a	chr22:29861062-29861073
36	CEBPB	chr22:29866422-29866622	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr22:29860955-29861197	K562	blood:	n/a	chr22:29861062-29861073
38	CEBPD	chr22:29868525-29868860	K562	blood:	n/a	n/a
39	CHD1	chr22:29866394-29866710	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr22:29877654-29877842	K562	blood:	n/a	n/a
41	CHD2	chr22:29866397-29866653	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr22:29876225-29876306	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr22:29876574-29877980	H1-hESC	embryonic stem cell:	n/a	chr22:29877153-29877163
44	CHD2	chr22:29866422-29866737	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr22:29876627-29877354	K562	blood:	n/a	chr22:29877153-29877163
46	CHD2	chr22:29876939-29877217	GM12878	blood:	n/a	chr22:29877153-29877163
47	CREB1	chr22:29876556-29877462	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr22:29876930-29877300	GM12878	blood:	n/a	n/a
49	CREB1	chr22:29866137-29866847	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr22:29866418-29866796	ECC-1	luminal epithelium:	n/a	n/a

(count:1103 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29876945-29876995	RPTEC	kidney:	n/a
2	chr22:29863270-29863320	HRCEpiC	kidney:	n/a
3	chr22:29866414-29866464	GM12878	blood:	n/a
4	chr22:29876363-29876413	SAEC	small airway:	n/a
5	chr22:29867475-29867525	BE2_C	brain:	n/a
6	chr22:29876945-29876995	RPTEC	kidney:	n/a
7	chr22:29863270-29863320	HRCEpiC	kidney:	n/a
8	chr22:29866414-29866464	GM12878	blood:	n/a
9	chr22:29876363-29876413	SAEC	small airway:	n/a
10	chr22:29867475-29867525	BE2_C	brain:	n/a
11	chr22:29876206-29876256	AG10803	skin:	n/a
12	chr22:29876942-29876992	SK-N-SH_RA	brain:	n/a
13	chr22:29876945-29876995	NH-A	brain:	n/a
14	chr22:29876945-29876995	MCF10A-Er-Src	breast:	n/a
15	chr22:29876206-29876256	CMK	blood:	n/a
16	chr22:29876363-29876413	AG09309	skin:	n/a
17	chr22:29876942-29876992	HCPEpiC	choroid plexus:	n/a
18	chr22:29876206-29876256	HRCEpiC	kidney:	n/a
19	chr22:29866414-29866464	HL-60	blood:	n/a
20	chr22:29866624-29866674	BJ	skin:	n/a
21	chr22:29876534-29876584	MCF10A-Er-Src	breast:	n/a
22	chr22:29876206-29876256	HMEC	breast:	n/a
23	chr22:29875592-29875642	HCT-116	colon:	n/a
24	chr22:29876206-29876256	HL-60	blood:	n/a
25	chr22:29867475-29867525	HCF	heart:	n/a
26	chr22:29875592-29875642	HRE	kidney:	n/a
27	chr22:29876206-29876256	PANC-1	pancreas:	n/a
28	chr22:29875784-29875834	HEEpiC	esophagus:	n/a
29	chr22:29876942-29876992	Hepatocyte	liver:	n/a
30	chr22:29875947-29875997	SK-N-MC	brain:	n/a
31	chr22:29876945-29876995	SK-N-SH_RA	brain:	n/a
32	chr22:29875947-29875997	HEK293	kidney:	embryo
33	chr22:29876942-29876992	ECC-1	luminal epithelium:	n/a
34	chr22:29875578-29875628	GM06990	blood:	n/a
35	chr22:29877285-29877335	GM19239	blood:	n/a
36	chr22:29875578-29875628	HEEpiC	esophagus:	n/a
37	chr22:29875592-29875642	AG04449	skin:	fetal
38	chr22:29875784-29875834	AG09309	skin:	n/a
39	chr22:29866414-29866464	SK-N-SH_RA	brain:	n/a
40	chr22:29875991-29876041	AoSMC	blood vessel:	n/a
41	chr22:29876942-29876992	AoSMC	blood vessel:	n/a
42	chr22:29875784-29875834	NHBE	bronchial:	n/a
43	chr22:29876534-29876584	LNCaP	prostate:	n/a
44	chr22:29876534-29876584	PFSK-1	brain:	n/a
45	chr22:29875991-29876041	MCF-7	breast:	n/a
46	chr22:29873338-29873388	HCF	heart:	n/a
47	chr22:29876534-29876584	HL-60	blood:	n/a
48	chr22:29875784-29875834	HEK293	kidney:	embryo
49	chr22:29875592-29875642	GM12892	blood:	n/a
50	chr22:29873338-29873388	NB4	blood:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr22:29880175..29882219-chr22:29882325..29884408,2	MCF-7	breast:
2	chr22:29866353..29868086-chr22:29877604..29879531,2	K562	blood:
3	chr22:29877857..29880129-chr22:29887823..29890747,2	MCF-7	breast:
4	chr22:29877412..29878391-chr22:29912701..29914203,38	MCF-7	breast:
5	chr22:29880175..29882219-chr22:29882325..29884408,2	MCF-7	breast:
6	chr22:29782475..29785188-chr22:29878200..29879873,2	MCF-7	breast:
7	chr22:29873982..29876378-chr22:29880807..29882421,2	MCF-7	breast:
8	chr22:29877386..29878406-chr22:29912849..29914254,52	MCF-7	breast:
9	chr22:29878444..29879004-chr22:29913024..29913767,2	MCF-7	breast:
10	chr22:29857796..29860960-chr22:29861526..29863568,3	K562	blood:
11	chr22:29856440..29859200-chr22:29892109..29894504,2	MCF-7	breast:
12	chr22:29865857..29867643-chr22:29876448..29878393,2	MCF-7	breast:
13	chr22:29877422..29878326-chr22:29912754..29914005,18	MCF-7	breast:
14	chr22:29781864..29782673-chr22:29877575..29878342,2	MCF-7	breast:
15	chr22:29783197..29785326-chr22:29874558..29877420,2	MCF-7	breast:
16	chr22:29858710..29861591-chr22:29861924..29864616,2	K562	blood:
17	chr22:29702481..29704174-chr22:29874105..29876353,2	K562	blood:
18	chr22:29877072..29879814-chr22:29891846..29894236,2	MCF-7	breast:
19	chr22:29858816..29860851-chr22:29864972..29867318,2	MCF-7	breast:
20	chr22:29873715..29877046-chr22:29940798..29944268,3	K562	blood:
21	chr22:29865857..29867643-chr22:29876448..29878393,2	MCF-7	breast:
22	chr22:29861087..29864747-chr22:29865747..29867984,3	K562	blood:
23	chr22:29858710..29861591-chr22:29861924..29864616,2	K562	blood:
24	chr22:29863203..29869053-chr22:29871800..29876725,7	K562	blood:
25	chr22:29858816..29860851-chr22:29864972..29867318,2	MCF-7	breast:
26	chr22:29877043..29879359-chr22:29911623..29914922,6	MCF-7	breast:
27	chr22:29865572..29868086-chr22:29877991..29879531,2	K562	blood:
28	chr22:29861087..29864747-chr22:29865747..29867984,3	K562	blood:
29	chr22:29877350..29878233-chr22:29913108..29913740,2	MCF-7	breast:
30	chr22:29866353..29868086-chr22:29877604..29879531,2	K562	blood:
31	chr22:29878566..29879231-chr22:29913094..29913812,2	MCF-7	breast:
32	chr22:29855896..29858129-chr22:29860085..29862045,2	K562	blood:
33	chr22:29865160..29867687-chr22:29913906..29916895,2	MCF-7	breast:
34	chr22:29783147..29785605-chr22:29854207..29856370,2	MCF-7	breast:
35	chr22:29857259..29859794-chr22:29863672..29866457,2	K562	blood:
36	chr22:29866152..29869730-chr22:29872379..29875672,4	MCF-7	breast:
37	chr22:29857796..29860960-chr22:29861526..29863568,3	K562	blood:
38	chr22:29877541..29878058-chr22:29914348..29915105,2	MCF-7	breast:
39	chr22:29865572..29868086-chr22:29877991..29879531,2	K562	blood:
40	chr22:29857259..29859794-chr22:29863672..29866457,2	K562	blood:
41	chr22:29876809..29879806-chr22:29881526..29883122,2	K562	blood:
42	chr22:29792519..29794058-chr22:29864789..29867115,2	MCF-7	breast:
43	chr22:29866168..29866984-chr22:29877594..29878224,2	K562	blood:
44	chr22:29663630..29665723-chr22:29877193..29880137,2	K562	blood:
45	chr22:29855896..29858129-chr22:29860085..29862045,2	K562	blood:
46	chr22:29866168..29866984-chr22:29877594..29878224,2	K562	blood:
47	chr22:29781578..29782726-chr22:29877337..29878344,7	MCF-7	breast:
48	chr22:29780492..29782846-chr22:29865528..29867159,2	MCF-7	breast:
49	chr22:29859668..29861171-chr22:29911922..29914850,2	MCF-7	breast:
50	chr22:29852290..29855034-chr22:29863929..29866105,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THOC5-1	chr22:29873999-29874059	ENSG00000224381.1
2	lnc-AP1B1-1	chr22:29868295-29868435	ENSG00000225465.6
3	lnc-AP1B1-1	chr22:29873999-29874164	ENSG00000225465.6
4	lnc-THOC5-1	chr22:29867930-29868438	ENSG00000224381.1
5	lnc-AP1B1-1	chr22:29864108-29864312	NONHSAT084707
6	lnc-AP1B1-1	chr22:29876241-29876321	NONHSAT084703
7	lnc-AP1B1-1	chr22:29873999-29874133	NONHSAT084704
8	lnc-AP1B1-1	chr22:29868295-29868435	NONHSAT084700
9	lnc-AP1B1-1	chr22:29873999-29874115	NONHSAT084700
10	lnc-AP1B1-1	chr22:29864122-29864148	NONHSAT084706

No data

Variant related genes	Relation type
RFPL1S	TF binding region
NEFH	TF binding region
RFPL1S	CpG island
NEFH	CpG island
ENSG00000185340	chromatin interactions
ENSG00000225465	chromatin interactions
ENSG00000100285	chromatin interactions
ENSG00000100280	chromatin interactions
ENSG00000100263	chromatin interactions
ENSG00000100296	chromatin interactions
ENSG00000182944	chromatin interactions

Extended variants
information (count: 1293 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9613919	chr22:29856079-29856080	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114752104	chr22:29856153-29856154	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs78013650	chr22:29856220-29856221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs529380486	chr22:29856226-29856227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375421341	chr22:29856235-29856236	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs556072480	chr22:29856265-29856266	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185380569	chr22:29856287-29856288	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs114120458	chr22:29856304-29856305	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs374533640	chr22:29856309-29856310	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs549359648	chr22:29856324-29856325	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs76515071	chr22:29856382-29856383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553489954	chr22:29856383-29856384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571964257	chr22:29856397-29856398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs149370579	chr22:29856462-29856463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189146632	chr22:29856493-29856494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113526596	chr22:29856526-29856527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529541527	chr22:29856535-29856536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144702996	chr22:29856541-29856542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563064434	chr22:29856546-29856547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139861064	chr22:29856551-29856552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552004323	chr22:29856568-29856569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566792571	chr22:29856599-29856600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527682080	chr22:29856612-29856613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541541646	chr22:29856616-29856617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549093256	chr22:29856617-29856618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143793800	chr22:29856620-29856621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367999606	chr22:29856690-29856691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191949453	chr22:29856719-29856720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372147690	chr22:29856731-29856732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184285287	chr22:29856824-29856825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs13055259	chr22:29856892-29856893	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs74746258	chr22:29856915-29856916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35633008	chr22:29856917-29856918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75684531	chr22:29856919-29856920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77043295	chr22:29856920-29856921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78040826	chr22:29856921-29856922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538562985	chr22:29856942-29856943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147431594	chr22:29856957-29856958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189054562	chr22:29856990-29856991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139736141	chr22:29857070-29857071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554741575	chr22:29857080-29857081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181198178	chr22:29857088-29857089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554787833	chr22:29857111-29857112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185056943	chr22:29857112-29857113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571583320	chr22:29857132-29857133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536650010	chr22:29857145-29857146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560816459	chr22:29857155-29857156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527712305	chr22:29857178-29857179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548979260	chr22:29857212-29857213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542743780	chr22:29857221-29857222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:924 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29836000-29859400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr22:29836200-29863200	Weak transcription	Fetal Brain Female	brain
3	chr22:29836600-29866000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr22:29847400-29864800	Weak transcription	Brain Germinal Matrix	brain
5	chr22:29850600-29856200	Weak transcription	Fetal Intestine Small	intestine
6	chr22:29850600-29867200	Weak transcription	Ovary	ovary
7	chr22:29852600-29859600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr22:29852600-29859800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr22:29852800-29860000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr22:29853200-29866200	Weak transcription	Right Atrium	heart
11	chr22:29853400-29860000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr22:29853400-29860000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr22:29855400-29856200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr22:29855600-29856400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr22:29855800-29856200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr22:29855800-29856200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr22:29855800-29856400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr22:29856000-29856200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr22:29856000-29856200	Enhancers	H9 Cell Line	embryonic stem cell
20	chr22:29856000-29856200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr22:29856000-29856200	Enhancers	Brain Angular Gyrus	brain
22	chr22:29856200-29857400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr22:29856200-29865600	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr22:29857400-29857600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr22:29857600-29859400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr22:29857800-29858000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr22:29859400-29859600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr22:29859400-29859800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr22:29859400-29860000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr22:29859400-29860600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr22:29859600-29860200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr22:29859600-29860600	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr22:29859600-29860600	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr22:29859600-29865600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr22:29859800-29860000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr22:29859800-29860600	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr22:29859800-29860600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr22:29860000-29860200	Enhancers	H1 Cell Line	embryonic stem cell
39	chr22:29860000-29860200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr22:29860000-29860400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr22:29860000-29862600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr22:29860000-29865400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr22:29860600-29863400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr22:29860600-29865800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr22:29861600-29873200	Weak transcription	Brain Anterior Caudate	brain
46	chr22:29862600-29862800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr22:29863000-29863200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr22:29863200-29863400	Enhancers	Gastric	stomach
49	chr22:29863200-29863400	Enhancers	Spleen	Spleen
50	chr22:29863200-29863800	Strong transcription	Fetal Brain Female	brain

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