Variant report

Variant	nsv914991
Chromosome Location	chr22:34106384-34293516
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1317)
CpG islands
(count:61)
Chromatin interactive
region (count:51)
LncRNA
region (count:88)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1317 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:34219541-34219836	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:34260707-34261720	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:34263027-34263505	HepG2	liver:	n/a	n/a
4	ATF2	chr22:34267833-34268333	GM12878	blood:	n/a	n/a
5	ATF2	chr22:34291937-34293362	GM12878	blood:	n/a	n/a
6	ATF2	chr22:34292032-34292987	GM12878	blood:	n/a	n/a
7	ATF2	chr22:34292873-34293362	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr22:34267904-34268303	GM12878	blood:	n/a	n/a
9	ATF2	chr22:34185755-34186363	GM12878	blood:	n/a	n/a
10	ATF2	chr22:34183459-34184387	GM12878	blood:	n/a	n/a
11	ATF2	chr22:34183601-34184137	GM12878	blood:	n/a	n/a
12	ATF2	chr22:34237716-34238353	GM12878	blood:	n/a	n/a
13	ATF2	chr22:34185841-34186312	GM12878	blood:	n/a	n/a
14	ATF2	chr22:34181226-34181686	GM12878	blood:	n/a	n/a
15	ATF2	chr22:34237683-34238915	GM12878	blood:	n/a	n/a
16	BACH1	chr22:34244328-34244642	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr22:34221773-34221807	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr22:34225564-34225840	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr22:34267545-34267589	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr22:34135101-34135251	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr22:34279533-34279901	GM12878	blood:	n/a	chr22:34279726-34279737
22	BATF	chr22:34287968-34288282	GM12878	blood:	n/a	n/a
23	BATF	chr22:34183589-34183875	GM12878	blood:	n/a	n/a
24	BATF	chr22:34244253-34244653	GM12878	blood:	n/a	chr22:34244450-34244461
25	BATF	chr22:34185838-34186311	GM12878	blood:	n/a	n/a
26	BATF	chr22:34287933-34288315	GM12878	blood:	n/a	n/a
27	BATF	chr22:34154766-34154993	GM12878	blood:	n/a	n/a
28	BATF	chr22:34237726-34237991	GM12878	blood:	n/a	n/a
29	BATF	chr22:34291932-34292403	GM12878	blood:	n/a	chr22:34292191-34292202
30	BATF	chr22:34279594-34279893	GM12878	blood:	n/a	chr22:34279726-34279737
31	BATF	chr22:34184057-34184349	GM12878	blood:	n/a	n/a
32	BATF	chr22:34292525-34293380	GM12878	blood:	n/a	chr22:34292610-34292623
33	BATF	chr22:34293029-34293343	GM12878	blood:	n/a	n/a
34	BATF	chr22:34185847-34186124	GM12878	blood:	n/a	n/a
35	BCL11A	chr22:34287951-34288299	GM12878	blood:	n/a	n/a
36	BCL11A	chr22:34279521-34279833	GM12878	blood:	n/a	n/a
37	BCL11A	chr22:34279585-34279869	GM12878	blood:	n/a	n/a
38	BCL11A	chr22:34183569-34183918	GM12878	blood:	n/a	n/a
39	BCL3	chr22:34185878-34186387	GM12878	blood:	n/a	n/a
40	BCL3	chr22:34139772-34140140	GM12878	blood:	n/a	n/a
41	BCL3	chr22:34153825-34154068	GM12878	blood:	n/a	n/a
42	BCL3	chr22:34287946-34288297	GM12878	blood:	n/a	n/a
43	BCL3	chr22:34279570-34279880	GM12878	blood:	n/a	n/a
44	BCLAF1	chr22:34291980-34293379	GM12878	blood:	n/a	chr22:34293008-34293017
45	BCLAF1	chr22:34238364-34238878	GM12878	blood:	n/a	n/a
46	BCLAF1	chr22:34237755-34238277	GM12878	blood:	n/a	n/a
47	BCLAF1	chr22:34285684-34286171	GM12878	blood:	n/a	n/a
48	BCLAF1	chr22:34183601-34183918	GM12878	blood:	n/a	n/a
49	BCLAF1	chr22:34292647-34293357	GM12878	blood:	n/a	chr22:34293008-34293017
50	BCLAF1	chr22:34185839-34186424	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:34192387-34192437	HCF	heart:	n/a
2	chr22:34192387-34192437	AG10803	skin:	n/a
3	chr22:34192387-34192437	ovcar-3	ovarian:	n/a
4	chr22:34192387-34192437	HRPEpiC	eye:	n/a
5	chr22:34192387-34192437	HRCEpiC	kidney:	n/a
6	chr22:34192387-34192437	AG09319	gingival:	n/a
7	chr22:34192387-34192437	HL-60	blood:	n/a
8	chr22:34192387-34192437	AG04450	lung:	fetal
9	chr22:34192387-34192437	H1-hESC	embryonic stem cell:	embryo
10	chr22:34192387-34192437	RPTEC	kidney:	n/a
11	chr22:34192387-34192437	SK-N-SH	brain:	n/a
12	chr22:34192387-34192437	PrEC	prostate:	n/a
13	chr22:34192387-34192437	GM12891	blood:	n/a
14	chr22:34192387-34192437	HNPCEpiC	eye:	n/a
15	chr22:34192387-34192437	SAEC	small airway:	n/a
16	chr22:34192387-34192437	HepG2	liver:	n/a
17	chr22:34192387-34192437	BJ	skin:	n/a
18	chr22:34192387-34192437	HEK293	kidney:	embryo
19	chr22:34192387-34192437	BE2_C	brain:	n/a
20	chr22:34192387-34192437	AG09309	skin:	n/a
21	chr22:34192387-34192437	HEEpiC	esophagus:	n/a
22	chr22:34192387-34192437	HPAEpiC	pulmonary alveolar:	n/a
23	chr22:34192387-34192437	HAEpiC	amniotic membrane:	n/a
24	chr22:34192387-34192437	ECC-1	luminal epithelium:	n/a
25	chr22:34192387-34192437	HUVEC	blood vessel:	n/a
26	chr22:34192387-34192437	AG04449	skin:	fetal
27	chr22:34192387-34192437	A549	lung:	n/a
28	chr22:34192387-34192437	MCF-7	breast:	n/a
29	chr22:34192387-34192437	Hela-S3	cervix:	n/a
30	chr22:34192387-34192437	MCF10A-Er-Src	breast:	n/a
31	chr22:34192387-34192437	NH-A	brain:	n/a
32	chr22:34192387-34192437	Jurkat	blood:	n/a
33	chr22:34192387-34192437	GM12892	blood:	n/a
34	chr22:34192387-34192437	HIPEpiC	eye:	n/a
35	chr22:34192387-34192437	NHBE	bronchial:	n/a
36	chr22:34192387-34192437	T-47D	breast:	n/a
37	chr22:34192387-34192437	K562	blood:	n/a
38	chr22:34192387-34192437	NT2-D1	testis:	n/a
39	chr22:34192387-34192437	PFSK-1	brain:	n/a
40	chr22:34192387-34192437	HCM	heart:	n/a
41	chr22:34192387-34192437	NB4	blood:	n/a
42	chr22:34192387-34192437	CMK	blood:	n/a
43	chr22:34192387-34192437	GM12878	blood:	n/a
44	chr22:34192387-34192437	GM06990	blood:	n/a
45	chr22:34192387-34192437	U87	brain:	n/a
46	chr22:34192387-34192437	LNCaP	prostate:	n/a
47	chr22:34192387-34192437	ProgFib	skin:	n/a
48	chr22:34192387-34192437	AoSMC	blood vessel:	n/a
49	chr22:34192387-34192437	SKMC	muscle:	n/a
50	chr22:34192387-34192437	SK-N-SH_RA	brain:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr22:34269817..34272444-chr22:34314882..34316654,2	MCF-7	breast:
2	chr22:34265653..34267240-chr22:34270322..34272194,2	MCF-7	breast:
3	chr22:34210266..34212147-chr22:34215786..34217625,2	MCF-7	breast:
4	chr22:34248231..34249994-chr22:34261049..34263874,2	MCF-7	breast:
5	chr22:34277917..34281628-chr22:34285820..34288664,3	MCF-7	breast:
6	chr22:34153944..34154522-chr22:34255921..34256610,2	MCF-7	breast:
7	chr22:34153944..34154522-chr22:34255921..34256610,2	MCF-7	breast:
8	chr22:34243203..34243910-chr9:5087187..5087998,2	MCF-7	breast:
9	chr22:34260736..34263686-chr22:34313890..34318281,7	MCF-7	breast:
10	chr22:34226044..34229431-chr22:34231299..34234951,3	MCF-7	breast:
11	chr22:34246562..34250566-chr22:34253925..34258689,11	MCF-7	breast:
12	chr22:34276961..34279522-chr22:34313897..34317110,3	MCF-7	breast:
13	chr22:34188517..34191299-chr22:34192329..34196152,3	MCF-7	breast:
14	chr22:34261283..34264105-chr22:34285527..34288136,2	MCF-7	breast:
15	chr22:34277917..34281628-chr22:34285820..34288664,3	MCF-7	breast:
16	chr22:34262180..34264985-chr22:34291444..34294296,2	MCF-7	breast:
17	chr22:34210266..34212147-chr22:34215786..34217625,2	MCF-7	breast:
18	chr22:34188517..34191299-chr22:34192329..34196152,3	MCF-7	breast:
19	chr22:34265653..34267240-chr22:34270322..34272194,2	MCF-7	breast:
20	chr22:34259639..34261419-chr22:34267116..34269181,2	MCF-7	breast:
21	chr22:34255181..34259842-chr22:34260995..34265736,9	MCF-7	breast:
22	chr22:34287867..34289464-chr22:34291655..34293352,2	MCF-7	breast:
23	chr22:34167046..34169223-chr22:34170241..34173338,3	MCF-7	breast:
24	chr22:34247616..34248584-chr22:34315645..34316533,2	MCF-7	breast:
25	chr22:34255630..34257426-chr22:34307549..34309607,2	MCF-7	breast:
26	chr22:34245347..34248923-chr22:34315491..34319689,7	MCF-7	breast:
27	chr22:34264153..34267717-chr22:34273021..34274940,3	MCF-7	breast:
28	chr22:34248240..34252170-chr22:34315347..34319641,4	MCF-7	breast:
29	chr22:34283903..34286858-chr22:34289207..34290909,2	MCF-7	breast:
30	chr22:34248614..34251924-chr22:34259957..34262591,3	MCF-7	breast:
31	chr22:34172664..34173221-chr22:34313368..34314036,2	MCF-7	breast:
32	chr22:34261283..34264105-chr22:34285527..34288136,2	MCF-7	breast:
33	chr22:34270457..34273179-chr22:34316799..34318425,2	MCF-7	breast:
34	chr22:34259639..34261419-chr22:34267116..34269181,2	MCF-7	breast:
35	chr22:34255666..34258346-chr22:34316396..34318049,2	MCF-7	breast:
36	chr22:34167046..34169223-chr22:34170241..34173338,3	MCF-7	breast:
37	chr22:34248231..34249994-chr22:34261049..34263874,2	MCF-7	breast:
38	chr22:34264153..34267717-chr22:34273021..34274940,3	MCF-7	breast:
39	chr22:34279207..34280839-chr22:34295025..34297477,2	MCF-7	breast:
40	chr22:34270428..34272649-chr22:34273804..34275941,2	MCF-7	breast:
41	chr22:34247996..34248570-chr22:34261032..34261815,2	MCF-7	breast:
42	chr22:34262180..34264985-chr22:34291444..34294296,2	MCF-7	breast:
43	chr22:34247996..34248570-chr22:34261032..34261815,2	MCF-7	breast:
44	chr22:34226044..34229431-chr22:34231299..34234951,3	MCF-7	breast:
45	chr22:34143232..34145432-chr22:34315745..34318657,2	MCF-7	breast:
46	chr22:34248614..34251924-chr22:34259957..34262591,3	MCF-7	breast:
47	chr22:34287867..34289464-chr22:34291655..34293352,2	MCF-7	breast:
48	chr22:34270428..34272649-chr22:34273804..34275941,2	MCF-7	breast:
49	chr22:34181411..34183196-chr22:34314966..34317332,2	MCF-7	breast:
50	chr22:34283913..34285789-chr22:34315526..34317915,2	MCF-7	breast:

(count:88 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TIMP3-6	chr22:34146591-34146729	ENSG00000224973.1
2	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085012
3	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085015
4	lnc-TIMP3-6	chr22:34143657-34143811	NONHSAT085018
5	lnc-TIMP3-6	chr22:34139122-34139185	ENSG00000224973.1
6	lnc-TIMP3-6	chr22:34128242-34129671	ENSG00000224973.1
7	lnc-SYN3-4	chr22:34119818-34120265	ENSG00000232081.1
8	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085015
9	lnc-TIMP3-6	chr22:34120972-34121087	NONHSAT085012
10	lnc-TIMP3-6	chr22:34146591-34146803	NONHSAT085011
11	lnc-TIMP3-6	chr22:34133550-34133761	ENSG00000224973.1
12	lnc-TIMP3-6	chr22:34146591-34146644	ENSG00000224973.1
13	lnc-TIMP3-6	chr22:34122102-34122183	ENSG00000224973.1
14	lnc-TIMP3-6	chr22:34121013-34121087	ENSG00000224973.1
15	lnc-TIMP3-6	chr22:34146591-34146670	ENSG00000224973.1
16	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085012
17	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085014
18	lnc-TIMP3-6	chr22:34139996-34140315	ENSG00000224973.1
19	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085015
20	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085011
21	lnc-TIMP3-6	chr22:34140116-34140315	ENSG00000224973.1
22	lnc-TIMP3-6	chr22:34121055-34121087	ENSG00000224973.1
23	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085013
24	lnc-TIMP3-6	chr22:34142402-34142444	ENSG00000224973.1
25	lnc-TIMP3-6	chr22:34140116-34140315	ENSG00000224973.1
26	lnc-TIMP3-6	chr22:34128242-34129671	NONHSAT085013
27	lnc-SYN3-4	chr22:34120789-34120898	ENSG00000232081.1
28	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085011
29	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085011
30	lnc-TIMP3-6	chr22:34122102-34122183	ENSG00000224973.1
31	lnc-TIMP3-6	chr22:34121003-34121087	NONHSAT085015
32	lnc-TIMP3-6	chr22:34121058-34121087	ENSG00000224973.1
33	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085015
34	lnc-TIMP3-6	chr22:34142402-34142444	ENSG00000224973.1
35	lnc-TIMP3-6	chr22:34122102-34122183	NONHSAT085011
36	lnc-TIMP3-6	chr22:34121000-34121087	ENSG00000224973.1
37	lnc-TIMP3-6	chr22:34121598-34121742	ENSG00000224973.1
38	lnc-TIMP3-6	chr22:34121003-34121087	NONHSAT085014
39	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085015
40	lnc-TIMP3-6	chr22:34123477-34123574	ENSG00000224973.1
41	lnc-TIMP3-6	chr22:34128242-34128488	ENSG00000224973.1
42	lnc-TIMP3-6	chr22:34121598-34121742	ENSG00000224973.1
43	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
44	lnc-TIMP3-6	chr22:34143657-34143811	ENSG00000224973.1
45	lnc-TIMP3-6	chr22:34146591-34146803	NONHSAT085012
46	lnc-TIMP3-6	chr22:34128242-34129671	NONHSAT085011
47	lnc-TIMP3-6	chr22:34122102-34122183	NONHSAT085015
48	lnc-TIMP3-6	chr22:34133550-34133769	ENSG00000224973.1
49	lnc-TIMP3-6	chr22:34121598-34121742	ENSG00000224973.1
50	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1

No data

Variant related genes	Relation type
LARGE-AS1	TF binding region
LARGE	TF binding region
LARGE-IT1	TF binding region
LARGE-AS1	CpG island
LARGE	CpG island
LARGE-IT1	CpG island
ENSG00000133424	chromatin interactions
ENSG00000273082	chromatin interactions

Extended variants
information (count: 8196 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:8196 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12158758	chr22:34106384-34106385	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533400263	chr22:34106443-34106444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540830922	chr22:34106474-34106475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560433963	chr22:34106491-34106492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529409157	chr22:34106500-34106501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12159427	chr22:34106504-34106505	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs141839258	chr22:34106513-34106514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540684959	chr22:34106523-34106524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2267267	chr22:34106551-34106552	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs368792470	chr22:34106556-34106557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550508056	chr22:34106588-34106589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570407340	chr22:34106714-34106715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs6518838	chr22:34106745-34106746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553137195	chr22:34106749-34106750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566170817	chr22:34106750-34106751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73170537	chr22:34106751-34106752	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs558008331	chr22:34106755-34106756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183615252	chr22:34106756-34106757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368807001	chr22:34106767-34106768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575355209	chr22:34106782-34106783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150651793	chr22:34106793-34106794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs5999067	chr22:34106827-34106828	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs2267268	chr22:34106853-34106854	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs139761195	chr22:34106867-34106868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188706328	chr22:34106869-34106870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs116235265	chr22:34106872-34106873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542741766	chr22:34106954-34106955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562639642	chr22:34106970-34106971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531638589	chr22:34107014-34107015	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551373134	chr22:34107015-34107016	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192813843	chr22:34107038-34107039	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184072459	chr22:34107059-34107060	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557334961	chr22:34107063-34107064	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567567952	chr22:34107095-34107096	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9609858	chr22:34107137-34107138	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573554101	chr22:34107152-34107153	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs62225398	chr22:34107220-34107221	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs240091	chr22:34107247-34107248	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs376703463	chr22:34107250-34107251	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535639754	chr22:34107252-34107253	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539169125	chr22:34107253-34107254	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111287093	chr22:34107277-34107278	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537892535	chr22:34107314-34107315	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566366133	chr22:34107363-34107364	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528205066	chr22:34107364-34107365	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535459900	chr22:34107365-34107366	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs117760161	chr22:34107392-34107393	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577529787	chr22:34107404-34107405	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs371738020	chr22:34107413-34107414	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534544729	chr22:34107462-34107463	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
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
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	20729466	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	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Deafness	17160897	CNVD
Bipolar disorder	19114987	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Prostate cancer	22341455	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:3845 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34076200-34106400	Weak transcription	Psoas Muscle	Psoas
2	chr22:34087000-34109400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr22:34091600-34115800	Weak transcription	Pancreas	Pancrea
4	chr22:34092400-34109200	Weak transcription	Fetal Intestine Large	intestine
5	chr22:34097000-34110000	Weak transcription	Ovary	ovary
6	chr22:34097200-34108000	Weak transcription	Fetal Intestine Small	intestine
7	chr22:34097200-34109200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr22:34097200-34109200	Weak transcription	Fetal Brain Female	brain
9	chr22:34097200-34109400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr22:34097400-34107400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr22:34097600-34110200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr22:34097600-34114600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr22:34098200-34110600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr22:34100400-34109000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr22:34100600-34108200	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr22:34100800-34110000	Weak transcription	Primary B cells from peripheral blood	blood
17	chr22:34101200-34108800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr22:34101200-34109600	Weak transcription	Fetal Stomach	stomach
19	chr22:34101200-34110000	Weak transcription	Aorta	Aorta
20	chr22:34102400-34106400	Weak transcription	Brain Angular Gyrus	brain
21	chr22:34103200-34106400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr22:34103200-34110600	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr22:34104000-34106400	Weak transcription	Brain Anterior Caudate	brain
24	chr22:34104000-34107400	Weak transcription	Stomach Mucosa	stomach
25	chr22:34104000-34110000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr22:34104200-34118800	Weak transcription	Right Ventricle	heart
27	chr22:34104600-34109400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr22:34105000-34106400	Weak transcription	Left Ventricle	heart
29	chr22:34105000-34109800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr22:34105200-34106600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr22:34105200-34109800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr22:34105600-34133400	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr22:34105800-34107400	Enhancers	HSMMtube	muscle
34	chr22:34106000-34106600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr22:34106000-34106600	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr22:34106000-34106600	Enhancers	Brain Cingulate Gyrus	brain
37	chr22:34106000-34107200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr22:34106000-34107200	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr22:34106000-34107200	Enhancers	HSMM	muscle
40	chr22:34106200-34106600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr22:34106200-34106600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr22:34106200-34106600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr22:34106200-34106600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr22:34106200-34106600	Enhancers	Brain Hippocampus Middle	brain
45	chr22:34106200-34106600	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr22:34106200-34107200	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr22:34106200-34107400	Weak transcription	Fetal Heart	heart
48	chr22:34106400-34106600	Enhancers	Left Ventricle	heart
49	chr22:34106400-34106800	Enhancers	Brain Anterior Caudate	brain
50	chr22:34106400-34107200	Enhancers	H1 Cell Line	embryonic stem cell

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