Variant report

Variant	nsv522306
Chromosome Location	chr22:28378472-28402624
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	BHLHE40	chr22:28386502-28387249	K562	blood:	n/a	chr22:28386634-28386650
2	CEBPB	chr22:28399005-28399086	K562	blood:	n/a	chr22:28399033-28399046 chr22:28399034-28399045 chr22:28399035-28399044
3	CEBPB	chr22:28386729-28386998	K562	blood:	n/a	chr22:28386869-28386882 chr22:28386870-28386881
4	CEBPB	chr22:28398846-28399226	Hela-S3	cervix:	n/a	chr22:28399033-28399046 chr22:28399034-28399045 chr22:28399035-28399044
5	CEBPB	chr22:28386788-28387035	IMR90	lung:	n/a	chr22:28386869-28386882 chr22:28386870-28386881
6	CEBPB	chr22:28398994-28399126	HepG2	liver:	n/a	chr22:28399033-28399046 chr22:28399034-28399045 chr22:28399035-28399044
7	CEBPB	chr22:28386729-28387385	HepG2	liver:	n/a	chr22:28386869-28386882 chr22:28386870-28386881
8	CEBPB	chr22:28386759-28387316	H1-hESC	embryonic stem cell:	n/a	chr22:28386869-28386882 chr22:28386870-28386881
9	CEBPB	chr22:28383493-28383851	IMR90	lung:	n/a	n/a
10	CEBPB	chr22:28386713-28387364	MCF-7	breast:	n/a	chr22:28386869-28386882 chr22:28386870-28386881
11	CEBPB	chr22:28386715-28387391	K562	blood:	n/a	chr22:28386869-28386882 chr22:28386870-28386881
12	CEBPB	chr22:28398876-28399208	MCF-7	breast:	n/a	chr22:28399033-28399046 chr22:28399034-28399045 chr22:28399035-28399044
13	CEBPB	chr22:28398910-28399168	IMR90	lung:	n/a	chr22:28399033-28399046 chr22:28399034-28399045 chr22:28399035-28399044
14	CHD1	chr22:28393692-28393774	GM12878	blood:	n/a	n/a
15	CHD2	chr22:28386949-28387418	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr22:28386881-28387438	MCF-7	breast:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
17	CTCF	chr22:28398460-28398610	NHLF	lung:	n/a	n/a
18	CTCF	chr22:28387040-28387190	HFF	foreskin:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
19	CTCF	chr22:28387002-28387285	MCF-7	breast:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
20	CTCF	chr22:28387080-28387230	BE2_C	brain:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
21	CTCF	chr22:28387080-28387230	HCPEpiC	choroid plexus:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
22	CTCF	chr22:28386980-28387130	HAc	cerebellar:	n/a	n/a
23	CTCF	chr22:28387420-28387570	AG04450	lung:	n/a	n/a
24	CTCF	chr22:28387120-28387270	HEEpiC	esophagus:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
25	CTCF	chr22:28398560-28398710	AG04449	skin:	n/a	n/a
26	CTCF	chr22:28387092-28387231	Pancreas_OC	pancreas:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
27	CTCF	chr22:28387080-28387230	AG10803	skin:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
28	CTCF	chr22:28387032-28387337	IMR90	lung:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
29	CTCF	chr22:28398680-28398722	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr22:28387100-28387250	GM12864	blood:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
31	CTCF	chr22:28387068-28387270	Hela-S3	cervix:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
32	CTCF	chr22:28387100-28387250	MCF-7	breast:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
33	CTCF	chr22:28387150-28387194	Medullo	brain:	n/a	chr22:28387158-28387171
34	CTCF	chr22:28387056-28387262	Fibrobl	skin:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
35	CTCF	chr22:28387100-28387250	HRPEpiC	eye:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
36	CTCF	chr22:28387049-28387297	HUVEC	blood vessel:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
37	CTCF	chr22:28386900-28387262	H1-hESC	embryonic stem cell:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
38	CTCF	chr22:28400205-28400233	GM12892	blood:	n/a	n/a
39	CTCF	chr22:28398473-28398801	GM12878	blood:	n/a	n/a
40	CTCF	chr22:28387105-28387232	GM13976	blood:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
41	CTCF	chr22:28387040-28387190	GM12866	blood:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
42	CTCF	chr22:28398540-28398690	AG10803	skin:	n/a	n/a
43	CTCF	chr22:28387060-28387210	HBMEC	blood vessel:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
44	CTCF	chr22:28387030-28387273	GM19240	blood:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
45	CTCF	chr22:28387140-28387290	AG09309	skin:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
46	CTCF	chr22:28387080-28387230	HMF	breast:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
47	CTCF	chr22:28387038-28387276	GM12878	blood:	n/a	chr22:28387145-28387158 chr22:28387158-28387171
48	CTCF	chr22:28387000-28387150	GM12870	blood:	n/a	n/a
49	CTCF	chr22:28398500-28398650	HCM	heart:	n/a	n/a
50	CTCF	chr22:28387100-28387250	HMF	breast:	n/a	chr22:28387145-28387158 chr22:28387158-28387171

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:28402098-28402148	NT2-D1	testis:	n/a
2	chr22:28402098-28402148	H1-hESC	embryonic stem cell:	embryo
3	chr22:28402098-28402148	K562	blood:	n/a
4	chr22:28402098-28402148	SK-N-SH_RA	brain:	n/a
5	chr22:28402098-28402148	HRPEpiC	eye:	n/a
6	chr22:28402098-28402148	IMR90	lung:	fetal
7	chr22:28402098-28402148	Hepatocyte	liver:	n/a
8	chr22:28402098-28402148	ovcar-3	ovarian:	n/a
9	chr22:28402098-28402148	HCPEpiC	choroid plexus:	n/a
10	chr22:28402098-28402148	HPAEpiC	pulmonary alveolar:	n/a
11	chr22:28402098-28402148	ECC-1	luminal epithelium:	n/a
12	chr22:28402098-28402148	Caco-2	colon:	n/a
13	chr22:28402098-28402148	A549	lung:	n/a
14	chr22:28402098-28402148	AG09319	gingival:	n/a
15	chr22:28402098-28402148	PrEC	prostate:	n/a
16	chr22:28402098-28402148	AG04449	skin:	fetal
17	chr22:28402098-28402148	AG04450	lung:	fetal
18	chr22:28402098-28402148	NHBE	bronchial:	n/a
19	chr22:28402098-28402148	HUVEC	blood vessel:	n/a
20	chr22:28402098-28402148	HNPCEpiC	eye:	n/a
21	chr22:28402098-28402148	NH-A	brain:	n/a
22	chr22:28402098-28402148	U87	brain:	n/a
23	chr22:28402098-28402148	GM06990	blood:	n/a
24	chr22:28402098-28402148	HMEC	breast:	n/a
25	chr22:28402098-28402148	GM12891	blood:	n/a
26	chr22:28402098-28402148	GM12878	blood:	n/a
27	chr22:28402098-28402148	NB4	blood:	n/a
28	chr22:28402098-28402148	PFSK-1	brain:	n/a
29	chr22:28402098-28402148	HL-60	blood:	n/a
30	chr22:28402098-28402148	HRE	kidney:	n/a
31	chr22:28402098-28402148	Hela-S3	cervix:	n/a
32	chr22:28402098-28402148	MCF-7	breast:	n/a
33	chr22:28402098-28402148	SAEC	small airway:	n/a
34	chr22:28402098-28402148	HCT-116	colon:	n/a
35	chr22:28402098-28402148	PANC-1	pancreas:	n/a
36	chr22:28402098-28402148	GM19239	blood:	n/a
37	chr22:28402098-28402148	BE2_C	brain:	n/a
38	chr22:28402098-28402148	GM12892	blood:	n/a
39	chr22:28402098-28402148	T-47D	breast:	n/a
40	chr22:28402098-28402148	AG10803	skin:	n/a
41	chr22:28402098-28402148	HEK293	kidney:	embryo
42	chr22:28402098-28402148	AG09309	skin:	n/a
43	chr22:28402098-28402148	RPTEC	kidney:	n/a
44	chr22:28402098-28402148	AoSMC	blood vessel:	n/a
45	chr22:28402098-28402148	HRCEpiC	kidney:	n/a
46	chr22:28402098-28402148	HEEpiC	esophagus:	n/a
47	chr22:28402098-28402148	ProgFib	skin:	n/a
48	chr22:28402098-28402148	SK-N-SH	brain:	n/a
49	chr22:28402098-28402148	Jurkat	blood:	n/a
50	chr22:28402098-28402148	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:28386424..28391096-chr22:28391178..28396307,7	MCF-7	breast:
2	chr22:28386424..28391096-chr22:28391178..28396307,7	MCF-7	breast:
3	chr22:28378900..28382846-chr22:28384194..28387433,3	K562	blood:
4	chr22:28361846..28364536-chr22:28378435..28381037,2	K562	blood:
5	chr22:28396428..28399039-chr22:28886798..28889695,2	MCF-7	breast:
6	chr22:28373482..28376187-chr22:28381012..28382815,2	MCF-7	breast:
7	chr22:28314687..28317374-chr22:28386537..28389209,3	MCF-7	breast:
8	chr22:28386554..28387584-chr22:28405047..28405963,3	MCF-7	breast:
9	chr22:28401393..28403661-chr22:28406646..28408733,2	MCF-7	breast:
10	chr22:28386557..28389416-chr22:28392270..28394268,2	MCF-7	breast:
11	chr22:28315453..28316982-chr22:28398952..28401333,2	MCF-7	breast:
12	chr22:28315267..28317072-chr22:28379506..28381389,2	MCF-7	breast:
13	chr22:28401032..28403259-chr22:28403789..28405576,2	K562	blood:
14	chr22:28387405..28389960-chr22:28390673..28392531,2	K562	blood:
15	chr22:28387405..28389960-chr22:28390673..28392531,2	K562	blood:
16	chr22:28276614..28277411-chr22:28398597..28399104,2	MCF-7	breast:
17	chr22:28282285..28283174-chr22:28386700..28387606,3	K562	blood:
18	chr22:28400747..28403073-chr22:28409689..28411221,2	K562	blood:
19	chr22:28386557..28389416-chr22:28392270..28394268,2	MCF-7	breast:
20	chr22:28373494..28375523-chr22:28377881..28379772,3	MCF-7	breast:
21	chr22:28383984..28385856-chr22:29195199..29196840,2	MCF-7	breast:
22	chr22:28382655..28384335-chr22:28385888..28387881,2	MCF-7	breast:
23	chr22:28371840..28377290-chr22:28378156..28383171,5	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSCB-1	chr22:28393399-28393411	ENSG00000235954
2	lnc-HSCB-1	chr22:28395418-28395991	NONHSAT084643
3	lnc-HSCB-1	chr22:28381680-28382380	ENSG00000235954
4	lnc-HSCB-1	chr22:28388916-28389523	ENSG00000235954
5	lnc-HSCB-1	chr22:28381680-28382217	ENSG00000235954
6	lnc-HSCB-1	chr22:28390461-28390641	ENSG00000235954
7	lnc-HSCB-1	chr22:28393399-28393688	ENSG00000235954
8	lnc-HSCB-1	chr22:28390461-28390641	ENSG00000235954
9	lnc-HSCB-1	chr22:28395418-28395645	ENSG00000235954
10	lnc-HSCB-1	chr22:28381680-28382349	NONHSAT084631
11	lnc-HSCB-1	chr22:28388457-28389523	ENSG00000235954
12	lnc-HSCB-1	chr22:28390461-28390641	ENSG00000235954
13	lnc-HSCB-1	chr22:28390461-28390641	ENSG00000235954
14	lnc-HSCB-1	chr22:28385879-28386014	NONHSAT084636
15	lnc-HSCB-1	chr22:28385870-28386014	ENSG00000235954
16	lnc-HSCB-1	chr22:28393399-28393763	ENSG00000235954
17	lnc-HSCB-1	chr22:28402517-28404569	ENSG00000235954
18	lnc-HSCB-1	chr22:28381680-28382349	NONHSAT084634
19	lnc-HSCB-1	chr22:28389112-28389523	ENSG00000235954
20	lnc-HSCB-1	chr22:28393399-28393619	ENSG00000235954
21	lnc-HSCB-1	chr22:28389112-28389280	ENSG00000235954
22	lnc-HSCB-1	chr22:28389112-28389493	ENSG00000235954
23	lnc-HSCB-1	chr22:28393399-28393655	ENSG00000235954
24	lnc-HSCB-1	chr22:28393399-28393727	ENSG00000235954
25	lnc-HSCB-1	chr22:28389112-28389514	NONHSAT084636
26	lnc-HSCB-1	chr22:28393399-28393727	ENSG00000235954
27	lnc-HSCB-1	chr22:28394953-28395002	NONHSAT084643
28	lnc-HSCB-1	chr22:28395418-28397646	ENSG00000235954
29	lnc-HSCB-1	chr22:28381680-28382330	ENSG00000235954

Variant related genes	Relation type
TTC28	TF binding region
TTC28-AS1	TF binding region
TTC28	CpG island
TTC28-AS1	CpG island
ENSG00000100219	chromatin interactions
ENSG00000180957	chromatin interactions
ENSG00000100154	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000235954	chromatin interactions
ENSG00000264073	chromatin interactions

Extended variants
information (count: 929 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:929 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5762430	chr22:28378472-28378473	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
2	rs573932994	chr22:28378520-28378521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374503154	chr22:28378549-28378550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111364834	chr22:28378613-28378614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376363546	chr22:28378614-28378615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201481979	chr22:28378630-28378631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369054200	chr22:28378643-28378644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373252711	chr22:28378658-28378659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs9613558	chr22:28378688-28378689	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs555889472	chr22:28378724-28378725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577173665	chr22:28378725-28378726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192610058	chr22:28378732-28378733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371102203	chr22:28378780-28378781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs202068761	chr22:28378810-28378811	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572223686	chr22:28378811-28378812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542940557	chr22:28378816-28378817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373286553	chr22:28378833-28378834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144350540	chr22:28378838-28378839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370917225	chr22:28378839-28378840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184835480	chr22:28378866-28378867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374544992	chr22:28378867-28378868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533331940	chr22:28378869-28378870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551506894	chr22:28378899-28378900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566886681	chr22:28378914-28378915	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs527964221	chr22:28378936-28378937	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs549693274	chr22:28378994-28378995	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs17482652	chr22:28378998-28378999	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs189781469	chr22:28379016-28379017	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs147787655	chr22:28379040-28379041	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs5762431	chr22:28379058-28379059	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs538752652	chr22:28379066-28379067	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs143483336	chr22:28379070-28379071	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs553471572	chr22:28379102-28379103	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs148825394	chr22:28379103-28379104	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373188785	chr22:28379106-28379107	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143432636	chr22:28379120-28379121	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs372409227	chr22:28379127-28379128	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs549696928	chr22:28379175-28379176	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs576263878	chr22:28379208-28379209	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs77293143	chr22:28379262-28379263	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs200880887	chr22:28379270-28379271	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562943069	chr22:28379284-28379285	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs533444178	chr22:28379335-28379336	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs61746677	chr22:28379367-28379368	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs377260379	chr22:28379374-28379375	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs369095042	chr22:28379385-28379386	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs527733267	chr22:28379480-28379481	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549367773	chr22:28379508-28379509	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs567631583	chr22:28379531-28379532	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs112515614	chr22:28379571-28379572	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Breast cancer	21509527	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
Ovine squamous-cell carcinoma	17599052	CNVD
Cat eye syndrome	16708226	CNVD
Olfactory neuroblastoma	18408657	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
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
NF2	0	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:754 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:28318800-28382000	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr22:28319600-28383000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr22:28321400-28379000	Weak transcription	Primary B cells from cord blood	blood
4	chr22:28355400-28387800	Weak transcription	Fetal Brain Male	brain
5	chr22:28358600-28379400	Weak transcription	Rectal Smooth Muscle	rectum
6	chr22:28360000-28379400	Weak transcription	Colonic Mucosa	Colon
7	chr22:28360200-28382800	Weak transcription	HSMM	muscle
8	chr22:28360800-28392400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr22:28368400-28383400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr22:28368800-28385800	Weak transcription	Brain Angular Gyrus	brain
11	chr22:28369000-28381200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr22:28369200-28398400	Weak transcription	Hela-S3	cervix
13	chr22:28369400-28394000	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr22:28370400-28382400	Weak transcription	Stomach Mucosa	stomach
15	chr22:28370400-28387200	Weak transcription	Fetal Kidney	kidney
16	chr22:28371800-28386800	Weak transcription	NHDF-Ad	bronchial
17	chr22:28371800-28395000	Weak transcription	Small Intestine	intestine
18	chr22:28372000-28382600	Weak transcription	NH-A	brain
19	chr22:28372000-28382800	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr22:28372000-28386400	Weak transcription	HUVEC	blood vessel
21	chr22:28372200-28378600	Weak transcription	Osteobl	bone
22	chr22:28372800-28380600	Weak transcription	Brain Substantia Nigra	brain
23	chr22:28372800-28382000	Weak transcription	K562	blood
24	chr22:28373600-28404000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr22:28373800-28383000	Strong transcription	Dnd41	blood
26	chr22:28373800-28386400	Strong transcription	Fetal Muscle Leg	muscle
27	chr22:28373800-28398200	Strong transcription	Fetal Brain Female	brain
28	chr22:28373800-28404200	Strong transcription	Fetal Stomach	stomach
29	chr22:28373800-28405200	Strong transcription	Fetal Intestine Small	intestine
30	chr22:28374600-28386400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr22:28376000-28379600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr22:28376200-28378600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr22:28376200-28382600	Strong transcription	Brain Germinal Matrix	brain
34	chr22:28376400-28383800	Strong transcription	Ovary	ovary
35	chr22:28376600-28382600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr22:28376800-28383600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr22:28377000-28378600	Weak transcription	Fetal Thymus	thymus
38	chr22:28377000-28381800	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr22:28377000-28383400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr22:28377000-28383400	Strong transcription	Placenta	Placenta
41	chr22:28377200-28379600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr22:28377200-28383400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr22:28377200-28385800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr22:28377200-28386400	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr22:28377200-28386800	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr22:28377200-28386800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr22:28377200-28387200	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr22:28377200-28388600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr22:28377600-28379800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr22:28377600-28382800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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