Variant report

Variant	esv1829662
Chromosome Location	chr22:30171725-30304390
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2667)
CpG islands
(count:1528)
Chromatin interactive
region (count:153)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:2667 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:30236540-30236830	K562	blood:	n/a	n/a
2	ARID3A	chr22:30234310-30234611	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:30217223-30217734	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:30174552-30174561	HepG2	liver:	n/a	n/a
5	ARID3A	chr22:30176852-30177186	K562	blood:	n/a	n/a
6	ARID3A	chr22:30195198-30195651	HepG2	liver:	n/a	n/a
7	ARID3A	chr22:30223319-30223468	K562	blood:	n/a	n/a
8	ARID3A	chr22:30238777-30239114	HepG2	liver:	n/a	n/a
9	ARID3A	chr22:30195264-30195441	K562	blood:	n/a	n/a
10	ARID3A	chr22:30217230-30217886	K562	blood:	n/a	n/a
11	ARID3A	chr22:30303627-30304585	K562	blood:	n/a	n/a
12	ARID3A	chr22:30174808-30175310	HepG2	liver:	n/a	n/a
13	ATF1	chr22:30303730-30304206	K562	blood:	n/a	n/a
14	ATF1	chr22:30236566-30236895	K562	blood:	n/a	n/a
15	ATF1	chr22:30238700-30238944	K562	blood:	n/a	n/a
16	ATF1	chr22:30217232-30217860	K562	blood:	n/a	n/a
17	ATF2	chr22:30193251-30193741	GM12878	blood:	n/a	n/a
18	ATF2	chr22:30217125-30217773	GM12878	blood:	n/a	n/a
19	ATF2	chr22:30234033-30234573	GM12878	blood:	n/a	n/a
20	ATF2	chr22:30193350-30193707	GM12878	blood:	n/a	n/a
21	ATF3	chr22:30303685-30304113	K562	blood:	n/a	n/a
22	ATF3	chr22:30209520-30209905	K562	blood:	n/a	n/a
23	ATF3	chr22:30217182-30217864	K562	blood:	n/a	n/a
24	ATF3	chr22:30195219-30195441	K562	blood:	n/a	n/a
25	BACH1	chr22:30195202-30195718	K562	blood:	n/a	n/a
26	BACH1	chr22:30279479-30279812	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr22:30267819-30267923	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr22:30217234-30217659	GM12878	blood:	n/a	chr22:30217429-30217440
29	BATF	chr22:30193388-30193664	GM12878	blood:	n/a	n/a
30	BATF	chr22:30217238-30217685	GM12878	blood:	n/a	chr22:30217429-30217440
31	BCL11A	chr22:30193366-30193692	GM12878	blood:	n/a	n/a
32	BCL11A	chr22:30193406-30193675	GM12878	blood:	n/a	n/a
33	BCL3	chr22:30223588-30224061	GM12878	blood:	n/a	n/a
34	BCLAF1	chr22:30279600-30279919	GM12878	blood:	n/a	n/a
35	BCLAF1	chr22:30217248-30217784	GM12878	blood:	n/a	n/a
36	BCLAF1	chr22:30217132-30217694	GM12878	blood:	n/a	n/a
37	BCLAF1	chr22:30193259-30193741	GM12878	blood:	n/a	n/a
38	BHLHE40	chr22:30183559-30183919	HepG2	liver:	n/a	n/a
39	BHLHE40	chr22:30209626-30210228	K562	blood:	n/a	n/a
40	BHLHE40	chr22:30195108-30195777	K562	blood:	n/a	n/a
41	BHLHE40	chr22:30217275-30217758	K562	blood:	n/a	n/a
42	BHLHE40	chr22:30195275-30195771	HepG2	liver:	n/a	n/a
43	BHLHE40	chr22:30278918-30279151	GM12878	blood:	n/a	chr22:30279006-30279022 chr22:30279105-30279121
44	BHLHE40	chr22:30279106-30279791	K562	blood:	n/a	chr22:30279511-30279527
45	BHLHE40	chr22:30178686-30178708	GM12878	blood:	n/a	n/a
46	BHLHE40	chr22:30234227-30234672	K562	blood:	n/a	n/a
47	BHLHE40	chr22:30176737-30177220	K562	blood:	n/a	n/a
48	BRCA1	chr22:30279281-30279298	HepG2	liver:	n/a	n/a
49	BRCA1	chr22:30234090-30234547	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr22:30279422-30279568	Hela-S3	cervix:	n/a	n/a

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30279922-30279972	SKMC	muscle:	n/a
2	chr22:30279318-30279368	HRPEpiC	eye:	n/a
3	chr22:30278992-30279042	NB4	blood:	n/a
4	chr22:30279922-30279972	SKMC	muscle:	n/a
5	chr22:30279318-30279368	HRPEpiC	eye:	n/a
6	chr22:30278992-30279042	NB4	blood:	n/a
7	chr22:30283578-30283628	NHDF-neo	bronchial:	n/a
8	chr22:30234293-30234343	K562	blood:	n/a
9	chr22:30230951-30231001	HCF	heart:	n/a
10	chr22:30234222-30234272	GM12892	blood:	n/a
11	chr22:30275995-30276045	NH-A	brain:	n/a
12	chr22:30278992-30279042	Hela-S3	cervix:	n/a
13	chr22:30234304-30234354	U87	brain:	n/a
14	chr22:30275995-30276045	HCT-116	colon:	n/a
15	chr22:30277391-30277441	HRPEpiC	eye:	n/a
16	chr22:30233924-30233974	HRPEpiC	eye:	n/a
17	chr22:30234213-30234263	NT2-D1	testis:	n/a
18	chr22:30234304-30234354	MCF10A-Er-Src	breast:	n/a
19	chr22:30233924-30233974	HRCEpiC	kidney:	n/a
20	chr22:30275995-30276045	A549	lung:	n/a
21	chr22:30234222-30234272	BE2_C	brain:	n/a
22	chr22:30195299-30195349	SK-N-SH	brain:	n/a
23	chr22:30278992-30279042	SK-N-SH	brain:	n/a
24	chr22:30234456-30234506	PFSK-1	brain:	n/a
25	chr22:30275268-30275318	HIPEpiC	eye:	n/a
26	chr22:30275995-30276045	AG09319	gingival:	n/a
27	chr22:30234222-30234272	H1-hESC	embryonic stem cell:	embryo
28	chr22:30234775-30234825	HRPEpiC	eye:	n/a
29	chr22:30230951-30231001	HEEpiC	esophagus:	n/a
30	chr22:30279318-30279368	AG04449	skin:	fetal
31	chr22:30234293-30234343	ovcar-3	ovarian:	n/a
32	chr22:30278876-30278926	NB4	blood:	n/a
33	chr22:30277968-30278018	PFSK-1	brain:	n/a
34	chr22:30275268-30275318	HEEpiC	esophagus:	n/a
35	chr22:30279241-30279291	HNPCEpiC	eye:	n/a
36	chr22:30283578-30283628	RPTEC	kidney:	n/a
37	chr22:30279922-30279972	H1-hESC	embryonic stem cell:	embryo
38	chr22:30234213-30234263	Caco-2	colon:	n/a
39	chr22:30234304-30234354	H1-hESC	embryonic stem cell:	embryo
40	chr22:30279857-30279907	NB4	blood:	n/a
41	chr22:30277968-30278018	MCF-7	breast:	n/a
42	chr22:30234222-30234272	GM12878	blood:	n/a
43	chr22:30237309-30237359	HL-60	blood:	n/a
44	chr22:30234213-30234263	AG04450	lung:	fetal
45	chr22:30278994-30279044	Hela-S3	cervix:	n/a
46	chr22:30234304-30234354	SAEC	small airway:	n/a
47	chr22:30279857-30279907	BJ	skin:	n/a
48	chr22:30277968-30278018	HCT-116	colon:	n/a
49	chr22:30233609-30233659	GM12878	blood:	n/a
50	chr22:30234304-30234354	T-47D	breast:	n/a

(count:153 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr22:30197601..30198103-chr22:30207199..30208176,2	MCF-7	breast:
2	chr22:30211412..30212970-chr22:30236507..30238739,2	K562	blood:
3	chr22:30228546..30230856-chr22:30232707..30235317,4	MCF-7	breast:
4	chr22:30194639..30195376-chr22:30212522..30213417,5	MCF-7	breast:
5	chr22:30205102..30207625-chr22:30210050..30212988,2	MCF-7	breast:
6	chr22:30218166..30221158-chr22:30224343..30226322,2	K562	blood:
7	chr22:30194639..30195376-chr22:30212522..30213417,5	MCF-7	breast:
8	chr22:30192738..30197507-chr22:30207918..30212414,7	MCF-7	breast:
9	chr22:30224439..30228420-chr22:30233600..30235751,3	K562	blood:
10	chr22:30161269..30163676-chr22:30230353..30231980,2	MCF-7	breast:
11	chr22:30194688..30196951-chr22:30207949..30209520,2	K562	blood:
12	chr22:30294545..30297116-chr22:30298361..30301240,2	K562	blood:
13	chr22:30226492..30228224-chr22:30228706..30231451,2	K562	blood:
14	chr22:30288615..30290652-chr22:30302494..30304851,2	MCF-7	breast:
15	chr22:30182549..30186689-chr22:30188373..30192437,4	K562	blood:
16	chr22:30224439..30228420-chr22:30233600..30235751,3	K562	blood:
17	chr22:30182549..30185414-chr22:30188242..30189873,2	K562	blood:
18	chr22:30174951..30177454-chr22:30180789..30183545,2	MCF-7	breast:
19	chr22:30196978..30199682-chr22:30207664..30209469,2	K562	blood:
20	chr22:30207717..30211289-chr22:30214169..30217331,4	K562	blood:
21	chr22:30200496..30202537-chr22:30212324..30214845,2	MCF-7	breast:
22	chr22:30210116..30212715-chr22:30390306..30391990,2	MCF-7	breast:
23	chr22:30301235..30303561-chr22:30313115..30315333,2	MCF-7	breast:
24	chr22:30163203..30165019-chr22:30216595..30218999,2	MCF-7	breast:
25	chr22:30280125..30281940-chr22:30289079..30291294,2	MCF-7	breast:
26	chr22:30183374..30186087-chr22:30189628..30192258,4	MCF-7	breast:
27	chr22:30190305..30192087-chr22:30205014..30207322,2	MCF-7	breast:
28	chr22:30185624..30189974-chr22:30192313..30194980,5	MCF-7	breast:
29	chr16:46723531..46724116-chr22:30233901..30234633,2	Hela-S3	cervix:
30	chr22:30303958..30305806-chr22:30307869..30310153,2	K562	blood:
31	chr22:30238896..30240450-chr22:30246132..30247997,2	K562	blood:
32	chr22:30277721..30280339-chr22:30399364..30402748,3	K562	blood:
33	chr22:30238285..30239003-chr9:140485780..140486690,2	MCF-7	breast:
34	chr22:30191639..30194644-chr22:30194985..30199113,4	K562	blood:
35	chr22:30174951..30177454-chr22:30180789..30183545,2	MCF-7	breast:
36	chr22:30191459..30193505-chr22:30210545..30213247,2	MCF-7	breast:
37	chr22:30233635..30235405-chr22:30235774..30238672,2	MCF-7	breast:
38	chr22:30203646..30205505-chr22:30211553..30214467,2	K562	blood:
39	chr22:30201897..30203976-chr22:30208446..30210144,3	MCF-7	breast:
40	chr22:30232954..30235817-chr22:30277750..30279574,2	MCF-7	breast:
41	chr22:30182549..30185414-chr22:30188242..30189873,2	K562	blood:
42	chr22:30161121..30163790-chr22:30207742..30209725,2	MCF-7	breast:
43	chr22:30211621..30214094-chr22:30399623..30401520,2	K562	blood:
44	chr22:30203989..30206698-chr22:30207811..30209768,4	MCF-7	breast:
45	chr22:30266018..30267537-chr22:30271072..30273991,2	K562	blood:
46	chr22:30265481..30267590-chr22:30272869..30274738,2	MCF-7	breast:
47	chr22:30298737..30301803-chr22:30302494..30306350,3	K562	blood:
48	chr22:30185624..30189974-chr22:30192313..30194980,5	MCF-7	breast:
49	chr22:30206160..30207800-chr22:30209309..30211288,2	K562	blood:
50	chr22:30229506..30231085-chr22:30279535..30281040,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HORMAD2-6	chr22:30279168-30279348	NONHSAT084740

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ASCC2	hsa-miR-124-3p	chr22:30184806-30184825
2	ASCC2	hsa-miR-320a	chr22:30184879-30184902
3	ASCC2	hsa-miR-124-3p	chr22:30184812-30184805

Variant related genes	Relation type
MTMR3	TF binding region
ASCC2	TF binding region
RNU6-331P	TF binding region
MTMR3	CpG island
ASCC2	CpG island
RNU6-331P	CpG island
ENSG00000207455	chromatin interactions
ENSG00000200976	chromatin interactions
ENSG00000184076	chromatin interactions
ENSG00000091651	chromatin interactions
ENSG00000100319	chromatin interactions
ENSG00000100325	chromatin interactions
ENSG00000100330	chromatin interactions

Extended variants
information (count: 5092 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5092 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535594448	chr22:30171786-30171787	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs372989950	chr22:30171827-30171828	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs372649878	chr22:30171895-30171896	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs112481907	chr22:30172061-30172062	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs568846883	chr22:30172076-30172077	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs545299885	chr22:30172085-30172086	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs182739504	chr22:30172149-30172150	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs559221672	chr22:30172162-30172163	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs577142946	chr22:30172172-30172173	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs143487156	chr22:30172173-30172174	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs553188768	chr22:30172194-30172195	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs551254458	chr22:30172200-30172201	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs737721	chr22:30172254-30172255	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs189055611	chr22:30172282-30172283	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs548359345	chr22:30172315-30172316	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs372626887	chr22:30172326-30172327	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs530949989	chr22:30172376-30172377	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs545906833	chr22:30172390-30172391	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs16987142	chr22:30172404-30172405	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528438605	chr22:30172466-30172467	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs147146125	chr22:30172505-30172506	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs370569094	chr22:30172506-30172507	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs113405529	chr22:30172530-30172531	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs550123655	chr22:30172565-30172566	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs9614051	chr22:30172568-30172569	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs2018808	chr22:30172589-30172590	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs5763487	chr22:30172648-30172649	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs5763488	chr22:30172666-30172667	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs737728	chr22:30172693-30172694	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs568733865	chr22:30172720-30172721	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs192533309	chr22:30172772-30172773	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs572665401	chr22:30172783-30172784	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs527879182	chr22:30172829-30172830	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs370048408	chr22:30172835-30172836	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs142477147	chr22:30172848-30172849	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs570799111	chr22:30172906-30172907	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs535186051	chr22:30173022-30173023	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs75992869	chr22:30173033-30173034	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs5763489	chr22:30173079-30173080	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs184385720	chr22:30173106-30173107	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs140143	chr22:30173109-30173110	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs558492093	chr22:30173122-30173123	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs187555861	chr22:30173130-30173131	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs575684283	chr22:30173157-30173158	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs5997520	chr22:30173177-30173178	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs367581858	chr22:30173217-30173218	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs373184171	chr22:30173335-30173336	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs375080957	chr22:30173388-30173389	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs371121817	chr22:30173389-30173390	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs543065813	chr22:30173390-30173391	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
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
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
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
Melanoma	17363583	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4306 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30164600-30183800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr22:30164600-30185000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr22:30164600-30188600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr22:30165000-30172400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr22:30165400-30176800	Weak transcription	Fetal Brain Male	brain
6	chr22:30166000-30176800	Weak transcription	Fetal Kidney	kidney
7	chr22:30166400-30176800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr22:30166600-30176800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr22:30166600-30177000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr22:30166600-30183800	Weak transcription	Aorta	Aorta
11	chr22:30166800-30172600	Weak transcription	K562	blood
12	chr22:30166800-30174200	Weak transcription	Pancreas	Pancrea
13	chr22:30166800-30176400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr22:30166800-30176400	Weak transcription	Colon Smooth Muscle	Colon
15	chr22:30166800-30176400	Weak transcription	Small Intestine	intestine
16	chr22:30166800-30176800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr22:30166800-30176800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr22:30166800-30182800	Weak transcription	Primary T cells from cord blood	blood
19	chr22:30166800-30183000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr22:30166800-30183400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr22:30166800-30183800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr22:30166800-30184200	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr22:30166800-30194400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr22:30167000-30174800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr22:30167000-30175000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr22:30167000-30176400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr22:30167000-30176400	Weak transcription	Brain Angular Gyrus	brain
28	chr22:30167000-30176400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr22:30167000-30176600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr22:30167000-30176800	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr22:30167000-30176800	Weak transcription	Brain Germinal Matrix	brain
32	chr22:30167000-30180400	Weak transcription	Fetal Brain Female	brain
33	chr22:30167000-30183400	Weak transcription	Primary B cells from cord blood	blood
34	chr22:30167000-30183600	Weak transcription	Dnd41	blood
35	chr22:30167200-30173800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr22:30167200-30174200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr22:30167200-30174800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr22:30167200-30175000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr22:30167200-30175000	Weak transcription	Spleen	Spleen
40	chr22:30167200-30176600	Weak transcription	Brain Hippocampus Middle	brain
41	chr22:30167200-30176600	Weak transcription	Brain Substantia Nigra	brain
42	chr22:30167200-30176600	Weak transcription	Ovary	ovary
43	chr22:30167200-30176800	Weak transcription	Rectal Smooth Muscle	rectum
44	chr22:30167200-30177200	Weak transcription	Lung	lung
45	chr22:30167200-30183000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr22:30167200-30183200	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr22:30167200-30183200	Weak transcription	GM12878-XiMat	blood
48	chr22:30167200-30184000	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr22:30167200-30184000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr22:30167200-30187800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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