Variant report

Variant	esv1791934
Chromosome Location	chr22:31846234-31874194
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	BCLAF1	chr22:31873324-31873809	GM12878	blood:	n/a	chr22:31873513-31873522
2	CEBPB	chr22:31868067-31868236	A549	lung:	n/a	n/a
3	CEBPB	chr22:31868091-31868292	HepG2	liver:	n/a	n/a
4	CEBPB	chr22:31848162-31848408	HepG2	liver:	n/a	chr22:31848262-31848275 chr22:31848262-31848275 chr22:31848262-31848275 chr22:31848262-31848273 chr22:31848263-31848274
5	CEBPB	chr22:31870726-31871133	IMR90	lung:	n/a	chr22:31870864-31870875
6	CTCF	chr22:31847820-31847970	AoAF	blood vessel:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
7	CTCF	chr22:31847760-31847994	K562	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
8	CTCF	chr22:31847800-31847950	HMEC	breast:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
9	CTCF	chr22:31847780-31847930	GM12871	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
10	CTCF	chr22:31847773-31847930	MCF-7	breast:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
11	CTCF	chr22:31847820-31847970	HCM	heart:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
12	CTCF	chr22:31847780-31847930	HCM	heart:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
13	CTCF	chr22:31847760-31847910	NHEK	skin:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
14	CTCF	chr22:31847800-31847950	WI-38	lung:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
15	CTCF	chr22:31847820-31847970	BJ	skin:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
16	CTCF	chr22:31847852-31847958	Kidney_OC	kidney:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
17	CTCF	chr22:31847820-31847970	GM12870	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
18	CTCF	chr22:31847860-31848010	K562	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
19	CTCF	chr22:31847756-31847957	NHEK	skin:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
20	CTCF	chr22:31847631-31848119	MCF-7	breast:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
21	CTCF	chr22:31847780-31847930	GM12872	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
22	CTCF	chr22:31847687-31847977	A549	lung:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
23	CTCF	chr22:31847777-31847975	Hela-S3	cervix:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
24	CTCF	chr22:31847689-31847985	SK-N-SH_RA	brain:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
25	CTCF	chr22:31847802-31847971	GM10248	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
26	CTCF	chr22:31847751-31847974	ProgFib	skin:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
27	CTCF	chr22:31847800-31847950	HPF	lung:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
28	CTCF	chr22:31847820-31847970	AG09319	gingival:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
29	CTCF	chr22:31847707-31848076	IMR90	lung:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
30	CTCF	chr22:31847800-31847950	HVMF	connective:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
31	CTCF	chr22:31847820-31847970	HCPEpiC	choroid plexus:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
32	CTCF	chr22:31847820-31847970	HRPEpiC	eye:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
33	CTCF	chr22:31847820-31847970	NB4	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
34	CTCF	chr22:31847795-31847966	GM13976	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
35	CTCF	chr22:31847749-31847950	A549	lung:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
36	CTCF	chr22:31847672-31848189	HCT-116	colon:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
37	CTCF	chr22:31847774-31847975	SK-N-SH_RA	brain:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
38	CTCF	chr22:31847800-31847950	GM06990	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
39	CTCF	chr22:31847800-31847950	GM12864	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
40	CTCF	chr22:31847820-31847970	HCT-116	colon:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
41	CTCF	chr22:31847744-31847950	HepG2	liver:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
42	CTCF	chr22:31847860-31848010	GM06990	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
43	CTCF	chr22:31847600-31847750	WI-38	lung:	n/a	n/a
44	CTCF	chr22:31847840-31847990	HFF-Myc	foreskin:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
45	CTCF	chr22:31847725-31847989	Gliobla	brain:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
46	CTCF	chr22:31847820-31847970	Caco-2	colon:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
47	CTCF	chr22:31847780-31847930	HMEC	breast:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
48	CTCF	chr22:31847800-31847950	HEEpiC	esophagus:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
49	CTCF	chr22:31847780-31847930	GM12874	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899
50	CTCF	chr22:31847843-31847910	GM20000	blood:	n/a	chr22:31847884-31847905 chr22:31847882-31847900 chr22:31847885-31847898 chr22:31847887-31847895 chr22:31847883-31847899

No.	Distal block	Cell Line	Cell type
1	22:31864703-31891033..22:31936958-31958600	GM12878	blood:
2	chr22:31847213..31849082-chr22:31849317..31851160,2	K562	blood:
3	22:31836635-31847259..22:31861680-31864703	K562	blood:
4	chr22:31862991..31864545-chr22:31885430..31887272,2	MCF-7	breast:
5	22:31861680-31864703..22:33339333-33353583	K562	blood:
6	22:31864703-31891033..22:32347255-32351014	K562	blood:
7	chr22:31850201..31852811-chr22:31884349..31886700,2	MCF-7	breast:
8	chr22:31847213..31849082-chr22:31849317..31851160,2	K562	blood:
9	22:31861680-31864703..22:32012966-32043914	GM12878	blood:
10	chr22:31855754..31858470-chr22:31860369..31863363,2	K562	blood:
11	22:31836635-31847259..22:31936958-31958600	GM12878	blood:
12	22:31803954-31807204..22:31861680-31864703	GM12878	blood:
13	chr22:31838625..31840945-chr22:31858613..31860728,2	MCF-7	breast:
14	chr22:31844458..31846488-chr22:31846838..31850631,3	K562	blood:
15	22:31836635-31847259..22:32529813-32538538	K562	blood:
16	chr22:31847385..31848306-chr22:32029522..32030382,2	MCF-7	breast:
17	chr22:31853776..31856046-chr22:31858521..31860568,2	MCF-7	breast:
18	22:31861680-31864703..22:31978142-31983723	GM12878	blood:
19	chr22:31853776..31856046-chr22:31858521..31860568,2	MCF-7	breast:
20	chr22:31849740..31852347-chr22:31891078..31892965,2	K562	blood:
21	chr22:31742672..31744282-chr22:31844664..31847017,2	MCF-7	breast:
22	22:31864703-31891033..22:31930706-31935473	GM12878	blood:
23	22:31861680-31864703..22:31961151-31976153	K562	blood:
24	chr22:31853100..31854749-chr22:31856675..31859325,2	K562	blood:
25	22:31861680-31864703..22:32750950-32761732	K562	blood:
26	chr22:31373202..31375614-chr22:31847172..31848695,2	K562	blood:
27	chr22:31867263..31868960-chr22:31885475..31887155,2	K562	blood:
28	22:31836635-31847259..22:32284948-32287956	Hela-S3	cervix:
29	chr22:31848344..31851110-chr22:31853744..31855617,2	K562	blood:
30	chr22:31847674..31848482-chr22:31892087..31892811,2	MCF-7	breast:
31	chr22:31850678..31853429-chr22:31854151..31856041,2	MCF-7	breast:
32	chr22:31844458..31846488-chr22:31846838..31850631,3	K562	blood:

Variant related genes	Relation type
ENSG00000224623	TF binding region
EIF4ENIF1	TF binding region
ENSG00000240591	TF binding region
ENSG00000214093	chromatin interactions
ENSG00000224623	chromatin interactions
ENSG00000229169	chromatin interactions
ENSG00000238910	chromatin interactions
ENSG00000232707	chromatin interactions
ENSG00000269987	chromatin interactions
ENSG00000271093	chromatin interactions
ENSG00000184708	chromatin interactions
ENSG00000198089	chromatin interactions
ENSG00000240591	chromatin interactions
ENSG00000241878	chromatin interactions
ENSG00000185666	chromatin interactions
ENSG00000205853	chromatin interactions
ENSG00000269972	chromatin interactions
ENSG00000213888	chromatin interactions
ENSG00000239674	chromatin interactions
ENSG00000227813	chromatin interactions
ENSG00000128276	chromatin interactions

Extended variants
information (count: 1183 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1183 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199968604	chr22:31846250-31846251	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs529241777	chr22:31846264-31846265	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs35464866	chr22:31846275-31846276	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs34991412	chr22:31846281-31846282	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs144858676	chr22:31846315-31846316	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs200910304	chr22:31846341-31846342	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs549193244	chr22:31846345-31846346	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs368246559	chr22:31846362-31846363	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs569098662	chr22:31846401-31846402	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs531695733	chr22:31846405-31846406	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs148925197	chr22:31846432-31846433	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs143672540	chr22:31846449-31846450	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs113996880	chr22:31846455-31846456	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs534200508	chr22:31846471-31846472	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs554130243	chr22:31846480-31846481	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs567611376	chr22:31846487-31846488	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs148093114	chr22:31846617-31846618	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs556318030	chr22:31846700-31846701	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs10550760	chr22:31846706-31846707	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs549537621	chr22:31846708-31846709	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs371509660	chr22:31846709-31846710	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs72364290	chr22:31846715-31846716	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs371258614	chr22:31846722-31846723	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs112393033	chr22:31846726-31846727	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs35468789	chr22:31846727-31846728	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs67884467	chr22:31846728-31846729	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs13058217	chr22:31846729-31846730	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs576264484	chr22:31846731-31846732	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs13054059	chr22:31846735-31846736	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs141281737	chr22:31846749-31846750	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs557858309	chr22:31846755-31846756	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs10568332	chr22:31846763-31846764	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs546874610	chr22:31846764-31846765	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs577522155	chr22:31846769-31846770	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs13058360	chr22:31846771-31846772	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs145060853	chr22:31846775-31846776	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs539744824	chr22:31846781-31846782	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs191105161	chr22:31846783-31846784	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs200615107	chr22:31846784-31846785	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs182243772	chr22:31846785-31846786	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs369820618	chr22:31846787-31846788	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs575070240	chr22:31846798-31846799	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs562636694	chr22:31846800-31846801	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs375457860	chr22:31846811-31846812	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs139052348	chr22:31846818-31846819	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs201156381	chr22:31846827-31846828	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs372740127	chr22:31846830-31846831	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs531554905	chr22:31846844-31846845	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs66798925	chr22:31846871-31846872	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs551537496	chr22:31846879-31846880	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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

Chromatin state (count:957 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31797000-31884400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr22:31797000-31884400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr22:31797200-31846400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr22:31797200-31860600	Strong transcription	Fetal Stomach	stomach
5	chr22:31797400-31846800	Strong transcription	Duodenum Mucosa	Duodenum
6	chr22:31797800-31846800	Strong transcription	Primary T cells fromperipheralblood	blood
7	chr22:31799200-31846600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr22:31804600-31847000	Strong transcription	Sigmoid Colon	Sigmoid Colon
9	chr22:31814000-31846400	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr22:31814200-31846800	Strong transcription	Cortex derived primary cultured neurospheres	brain
11	chr22:31814400-31846800	Strong transcription	Fetal Intestine Large	intestine
12	chr22:31814800-31846600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr22:31815000-31846600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr22:31815000-31846800	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr22:31815000-31868200	Strong transcription	Dnd41	blood
16	chr22:31815000-31883400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr22:31815400-31846600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr22:31815400-31846600	Strong transcription	Duodenum Smooth Muscle	Duodenum
19	chr22:31822200-31846600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr22:31822400-31859800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr22:31823600-31884600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr22:31826600-31846400	Strong transcription	Brain Germinal Matrix	brain
23	chr22:31827200-31846600	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr22:31827600-31846600	Strong transcription	Osteobl	bone
25	chr22:31829600-31846400	Strong transcription	Brain Substantia Nigra	brain
26	chr22:31829600-31852000	Strong transcription	Stomach Smooth Muscle	stomach
27	chr22:31829800-31846600	Strong transcription	HSMM	muscle
28	chr22:31831200-31850000	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr22:31832600-31846400	Strong transcription	Brain Inferior Temporal Lobe	brain
30	chr22:31832600-31867800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr22:31832800-31846800	Strong transcription	Brain Anterior Caudate	brain
32	chr22:31833000-31846600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr22:31833000-31846800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr22:31833200-31847200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr22:31833600-31846800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr22:31836200-31846800	Strong transcription	Adipose Nuclei	Adipose
37	chr22:31836200-31873600	Weak transcription	Stomach Mucosa	stomach
38	chr22:31836800-31853000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr22:31837000-31846800	Strong transcription	Placenta	Placenta
40	chr22:31838200-31859000	Weak transcription	Hela-S3	cervix
41	chr22:31838400-31849800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr22:31838600-31854400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr22:31838800-31846400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr22:31839200-31850000	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr22:31840800-31857200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr22:31841200-31849800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr22:31841400-31848200	Weak transcription	NH-A	brain
48	chr22:31841400-31850200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr22:31842200-31848400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr22:31842600-31848000	Weak transcription	NHDF-Ad	bronchial

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