Variant report

Variant	esv3382633
Chromosome Location	chr22:29764347-29814462
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1298)
CpG islands
(count:1038)
Chromatin interactive
region (count:69)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1298 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:29778868-29779190	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	ARID3A	chr22:29784494-29784815	K562	blood:	n/a	n/a
5	ATF1	chr22:29797555-29797746	K562	blood:	n/a	n/a
6	ATF2	chr22:29765407-29765735	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr22:29784482-29784966	GM12878	blood:	n/a	n/a
8	BACH1	chr22:29765433-29765705	H1-hESC	embryonic stem cell:	n/a	chr22:29765575-29765589
9	BATF	chr22:29810856-29811337	GM12878	blood:	n/a	n/a
10	BATF	chr22:29808804-29809035	GM12878	blood:	n/a	n/a
11	BCL11A	chr22:29801979-29802220	GM12878	blood:	n/a	n/a
12	BCL3	chr22:29784461-29785020	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
13	BCLAF1	chr22:29781657-29782228	GM12878	blood:	n/a	chr22:29781963-29781972
14	BCLAF1	chr22:29784355-29784799	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
15	BCLAF1	chr22:29784167-29784915	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
16	BHLHE40	chr22:29784305-29784732	HepG2	liver:	n/a	n/a
17	BHLHE40	chr22:29783767-29784854	K562	blood:	n/a	chr22:29784290-29784306
18	BHLHE40	chr22:29810866-29811343	GM12878	blood:	n/a	n/a
19	BHLHE40	chr22:29779081-29779149	K562	blood:	n/a	n/a
20	BHLHE40	chr22:29783782-29784846	GM12878	blood:	n/a	chr22:29784290-29784306
21	BHLHE40	chr22:29765504-29765531	HepG2	liver:	n/a	n/a
22	BHLHE40	chr22:29807666-29807691	GM12878	blood:	n/a	n/a
23	BRCA1	chr22:29791082-29791132	HepG2	liver:	n/a	n/a
24	BRCA1	chr22:29784309-29784324	HepG2	liver:	n/a	n/a
25	BRCA1	chr22:29784487-29784668	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr22:29784370-29784766	K562	blood:	n/a	n/a
27	CCNT2	chr22:29784213-29784825	K562	blood:	n/a	n/a
28	CCNT2	chr22:29778935-29779230	K562	blood:	n/a	n/a
29	CEBPB	chr22:29765315-29765680	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr22:29771539-29771762	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr22:29765399-29765731	K562	blood:	n/a	n/a
32	CEBPB	chr22:29771588-29771690	A549	lung:	n/a	n/a
33	CEBPB	chr22:29804956-29805312	K562	blood:	n/a	chr22:29805152-29805163
34	CEBPB	chr22:29771478-29771805	K562	blood:	n/a	n/a
35	CEBPB	chr22:29804972-29805323	K562	blood:	n/a	chr22:29805152-29805163
36	CEBPB	chr22:29781370-29781510	HepG2	liver:	n/a	n/a
37	CEBPB	chr22:29784432-29784838	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr22:29771466-29771819	IMR90	lung:	n/a	n/a
39	CEBPB	chr22:29784560-29784804	K562	blood:	n/a	n/a
40	CEBPB	chr22:29805054-29805264	MCF-7	breast:	n/a	chr22:29805152-29805163
41	CEBPB	chr22:29771521-29771829	MCF-7	breast:	n/a	n/a
42	CEBPB	chr22:29765351-29765917	IMR90	lung:	n/a	n/a
43	CEBPB	chr22:29784634-29784925	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr22:29765357-29765938	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr22:29805051-29805224	K562	blood:	n/a	chr22:29805152-29805163
46	CEBPB	chr22:29765398-29765925	HepG2	liver:	n/a	n/a
47	CEBPB	chr22:29765292-29765790	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr22:29773811-29774403	MCF-7	breast:	n/a	n/a
49	CEBPB	chr22:29791176-29791249	K562	blood:	n/a	n/a
50	CEBPB	chr22:29773211-29773460	MCF-7	breast:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29785355-29785405	HPAEpiC	pulmonary alveolar:	n/a
2	chr22:29785355-29785405	HPAEpiC	pulmonary alveolar:	n/a
3	chr22:29784624-29784674	Hela-S3	cervix:	n/a
4	chr22:29784436-29784486	HCM	heart:	n/a
5	chr22:29784697-29784747	HEK293	kidney:	embryo
6	chr22:29784441-29784491	H1-hESC	embryonic stem cell:	embryo
7	chr22:29784697-29784747	NT2-D1	testis:	n/a
8	chr22:29785355-29785405	ProgFib	skin:	n/a
9	chr22:29778415-29778465	AG09309	skin:	n/a
10	chr22:29781841-29781891	AG09319	gingival:	n/a
11	chr22:29781841-29781891	NHDF-neo	bronchial:	n/a
12	chr22:29784441-29784491	CMK	blood:	n/a
13	chr22:29784813-29784863	HCT-116	colon:	n/a
14	chr22:29784813-29784863	K562	blood:	n/a
15	chr22:29784644-29784694	SAEC	small airway:	n/a
16	chr22:29784441-29784491	HRCEpiC	kidney:	n/a
17	chr22:29782753-29782803	U87	brain:	n/a
18	chr22:29778415-29778465	LNCaP	prostate:	n/a
19	chr22:29784436-29784486	Caco-2	colon:	n/a
20	chr22:29784237-29784287	HEEpiC	esophagus:	n/a
21	chr22:29784441-29784491	Hepatocyte	liver:	n/a
22	chr22:29784436-29784486	HIPEpiC	eye:	n/a
23	chr22:29783861-29783911	PFSK-1	brain:	n/a
24	chr22:29782753-29782803	HRE	kidney:	n/a
25	chr22:29784671-29784721	NH-A	brain:	n/a
26	chr22:29785355-29785405	HRE	kidney:	n/a
27	chr22:29781841-29781891	T-47D	breast:	n/a
28	chr22:29784436-29784486	T-47D	breast:	n/a
29	chr22:29784441-29784491	HRE	kidney:	n/a
30	chr22:29784697-29784747	SK-N-MC	brain:	n/a
31	chr22:29778415-29778465	SK-N-SH	brain:	n/a
32	chr22:29784697-29784747	Hela-S3	cervix:	n/a
33	chr22:29784237-29784287	AG04449	skin:	fetal
34	chr22:29784671-29784721	HEK293	kidney:	embryo
35	chr22:29784441-29784491	K562	blood:	n/a
36	chr22:29784778-29784828	NHBE	bronchial:	n/a
37	chr22:29784813-29784863	SAEC	small airway:	n/a
38	chr22:29784694-29784744	HIPEpiC	eye:	n/a
39	chr22:29784624-29784674	U87	brain:	n/a
40	chr22:29784436-29784486	Hepatocyte	liver:	n/a
41	chr22:29778415-29778465	CMK	blood:	n/a
42	chr22:29784692-29784742	A549	lung:	n/a
43	chr22:29783861-29783911	HCPEpiC	choroid plexus:	n/a
44	chr22:29784778-29784828	Caco-2	colon:	n/a
45	chr22:29782753-29782803	HNPCEpiC	eye:	n/a
46	chr22:29787625-29787675	Hela-S3	cervix:	n/a
47	chr22:29784624-29784674	SK-N-SH_RA	brain:	n/a
48	chr22:29784441-29784491	HMEC	breast:	n/a
49	chr22:29784237-29784287	HCF	heart:	n/a
50	chr22:29784441-29784491	NHBE	bronchial:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr22:29771898..29775582-chr22:29781742..29783845,4	MCF-7	breast:
2	chr22:29792125..29793668-chr22:29802474..29805006,2	K562	blood:
3	chr22:29704102..29706466-chr22:29771552..29773376,2	MCF-7	breast:
4	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
5	chr22:29790656..29791686-chr22:29920171..29921137,10	MCF-7	breast:
6	chr22:29780492..29782846-chr22:29865528..29867159,2	MCF-7	breast:
7	chr22:29771733..29774744-chr22:29774993..29776760,3	MCF-7	breast:
8	chr22:29764682..29767147-chr22:29767285..29770224,2	MCF-7	breast:
9	chr22:29704896..29707829-chr22:29780262..29782390,2	MCF-7	breast:
10	chr22:29781329..29782720-chr22:29913118..29914020,4	MCF-7	breast:
11	chr22:29701804..29704290-chr22:29781998..29785634,5	MCF-7	breast:
12	chr22:29777011..29779930-chr22:29821335..29822984,2	K562	blood:
13	chr22:29781675..29783812-chr22:29788035..29790235,2	MCF-7	breast:
14	chr22:29794482..29794991-chr22:29913162..29914018,2	MCF-7	breast:
15	chr22:29737136..29739598-chr22:29772687..29775574,2	MCF-7	breast:
16	chr22:29770398..29771976-chr22:29778753..29780431,2	K562	blood:
17	chr22:29783197..29785326-chr22:29874558..29877420,2	MCF-7	breast:
18	chr22:29774109..29774727-chr22:29781778..29782854,8	MCF-7	breast:
19	chr22:29771666..29773871-chr22:29789734..29792185,2	MCF-7	breast:
20	chr22:29770398..29771976-chr22:29778753..29780431,2	K562	blood:
21	chr22:29702455..29704377-chr22:29769522..29771265,2	MCF-7	breast:
22	chr22:29774091..29774727-chr22:29781651..29782814,5	MCF-7	breast:
23	chr22:29792519..29794058-chr22:29864789..29867115,2	MCF-7	breast:
24	chr22:29760830..29763484-chr22:29765100..29766942,2	K562	blood:
25	chr22:29708527..29710108-chr22:29782946..29784507,2	K562	blood:
26	chr22:29712026..29714411-chr22:29782149..29784555,3	K562	blood:
27	chr22:29771666..29773871-chr22:29789734..29792185,2	MCF-7	breast:
28	chr22:29771898..29775582-chr22:29781742..29783845,4	MCF-7	breast:
29	chr22:29771983..29774340-chr22:29774881..29776429,2	K562	blood:
30	chr22:29784558..29786360-chr22:29786552..29791390,4	MCF-7	breast:
31	chr22:29774109..29774727-chr22:29781778..29782854,8	MCF-7	breast:
32	chr22:29792125..29793668-chr22:29802474..29805006,2	K562	blood:
33	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
34	chr22:29771983..29774340-chr22:29774881..29776429,2	K562	blood:
35	chr22:29787252..29790791-chr22:29920718..29924086,3	MCF-7	breast:
36	chr22:29783150..29785946-chr22:29944649..29946343,2	MCF-7	breast:
37	chr22:29770782..29772689-chr22:29780811..29782872,2	K562	blood:
38	chr22:29771733..29774744-chr22:29774993..29776760,3	MCF-7	breast:
39	chr22:29762328..29763973-chr22:29771513..29774228,2	MCF-7	breast:
40	chr22:29791047..29793663-chr22:29794223..29797120,2	MCF-7	breast:
41	chr22:29739232..29740930-chr22:29780922..29783404,2	MCF-7	breast:
42	chr22:29771731..29774347-chr22:29784237..29785863,2	MCF-7	breast:
43	chr22:29791047..29793663-chr22:29794223..29797120,2	MCF-7	breast:
44	chr22:29781864..29782673-chr22:29877575..29878342,2	MCF-7	breast:
45	chr22:29790720..29791562-chr22:29920209..29921282,4	MCF-7	breast:
46	chr22:29774954..29777707-chr22:29779123..29781815,2	K562	blood:
47	chr22:29209443..29210342-chr22:29781715..29782736,4	MCF-7	breast:
48	chr22:29774954..29777707-chr22:29779123..29781815,2	K562	blood:
49	chr22:29776140..29778611-chr22:29995991..29998407,2	K562	blood:
50	chr22:29775197..29780621-chr22:29782246..29785885,8	K562	blood:

No data

Variant related genes	Relation type
AP1B1	TF binding region
AP1B1	CpG island
ENSG00000100296	chromatin interactions
ENSG00000184117	chromatin interactions
ENSG00000100285	chromatin interactions
ENSG00000182944	chromatin interactions
ENSG00000273216	chromatin interactions
ENSG00000100280	chromatin interactions
ENSG00000185340	chromatin interactions
ENSG00000100263	chromatin interactions

Extended variants
information (count: 1575 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1575 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560861101	chr22:29764428-29764429	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141319385	chr22:29764468-29764469	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552659047	chr22:29764504-29764505	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148401875	chr22:29764583-29764584	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532338307	chr22:29764596-29764597	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554894246	chr22:29764618-29764619	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542817282	chr22:29764687-29764688	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181237687	chr22:29764697-29764698	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs3044030	chr22:29764702-29764703	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs397836413	chr22:29764706-29764707	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543802139	chr22:29764730-29764731	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376102714	chr22:29764745-29764746	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561549462	chr22:29764746-29764747	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559203010	chr22:29764813-29764814	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs577316478	chr22:29764823-29764824	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs738903	chr22:29764836-29764837	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs531480803	chr22:29764896-29764897	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs530243747	chr22:29764922-29764923	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs148054188	chr22:29764930-29764931	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs542292028	chr22:29764969-29764970	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs145704136	chr22:29764975-29764976	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs530726928	chr22:29765042-29765043	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs147747312	chr22:29765075-29765076	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs542003116	chr22:29765101-29765102	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs142588278	chr22:29765102-29765103	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs528089838	chr22:29765114-29765115	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs144842227	chr22:29765120-29765121	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567697073	chr22:29765130-29765131	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs574212554	chr22:29765165-29765166	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs201835374	chr22:29765183-29765184	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs6006110	chr22:29765199-29765200	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs570203821	chr22:29765342-29765343	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs537608202	chr22:29765346-29765347	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs549896567	chr22:29765382-29765383	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs200775402	chr22:29765389-29765390	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs577581611	chr22:29765412-29765413	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs77513763	chr22:29765458-29765459	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs150429047	chr22:29765476-29765477	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs186478896	chr22:29765489-29765490	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs574873578	chr22:29765506-29765507	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs75756579	chr22:29765524-29765525	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs189433405	chr22:29765547-29765548	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs530627427	chr22:29765550-29765551	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs545947461	chr22:29765551-29765552	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs564061471	chr22:29765566-29765567	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs564541845	chr22:29765599-29765600	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs528398178	chr22:29765611-29765612	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs73403058	chr22:29765624-29765625	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs149141330	chr22:29765626-29765627	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs371605420	chr22:29765673-29765674	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	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:1971 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29723000-29765000	Strong transcription	Primary T helper cells fromperipheralblood	blood
2	chr22:29741000-29782800	Weak transcription	Hela-S3	cervix
3	chr22:29745000-29765200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr22:29750600-29765200	Weak transcription	NHDF-Ad	bronchial
5	chr22:29750600-29766800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr22:29750800-29764400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr22:29753000-29777600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr22:29754600-29770400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr22:29754800-29765200	Weak transcription	HSMM	muscle
10	chr22:29755000-29765200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr22:29755000-29772200	Weak transcription	Aorta	Aorta
12	chr22:29755000-29783800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr22:29755200-29765000	Weak transcription	NH-A	brain
14	chr22:29755200-29773800	Weak transcription	Stomach Mucosa	stomach
15	chr22:29755200-29781000	Weak transcription	Fetal Brain Male	brain
16	chr22:29755200-29782800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr22:29755400-29764600	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr22:29755400-29765400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr22:29755400-29783600	Weak transcription	Fetal Kidney	kidney
20	chr22:29755600-29771400	Weak transcription	Psoas Muscle	Psoas
21	chr22:29755600-29778600	Weak transcription	Fetal Lung	lung
22	chr22:29755800-29776600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr22:29756000-29764400	Weak transcription	Brain Angular Gyrus	brain
24	chr22:29756000-29764400	Weak transcription	NHEK	skin
25	chr22:29756000-29764600	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr22:29756000-29764600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr22:29756000-29764600	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr22:29756000-29765200	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr22:29756000-29765200	Weak transcription	HepG2	liver
30	chr22:29756000-29765200	Weak transcription	Osteobl	bone
31	chr22:29756000-29765400	Weak transcription	A549	lung
32	chr22:29756000-29766400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr22:29756000-29766400	Weak transcription	Stomach Smooth Muscle	stomach
34	chr22:29756000-29766600	Weak transcription	Pancreas	Pancrea
35	chr22:29756000-29769000	Weak transcription	Gastric	stomach
36	chr22:29756000-29771400	Weak transcription	Esophagus	oesophagus
37	chr22:29756000-29771400	Weak transcription	HMEC	breast
38	chr22:29756000-29771800	Weak transcription	NHLF	lung
39	chr22:29756000-29772200	Weak transcription	Right Atrium	heart
40	chr22:29756000-29776200	Weak transcription	Small Intestine	intestine
41	chr22:29756000-29779800	Weak transcription	Brain Germinal Matrix	brain
42	chr22:29756000-29783600	Weak transcription	Right Ventricle	heart
43	chr22:29756000-29783800	Weak transcription	Ovary	ovary
44	chr22:29756200-29764600	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr22:29756200-29764600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr22:29756200-29764800	Weak transcription	Rectal Smooth Muscle	rectum
47	chr22:29756200-29765000	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr22:29756200-29765000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr22:29756200-29765000	Weak transcription	HSMMtube	muscle
50	chr22:29756200-29779200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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