Variant report

Variant	nsv2610
Chromosome Location	chr1:120451060-120471049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:80)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:12)

(count:80 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:120462961-120463475	K562	blood:	n/a	n/a
2	BHLHE40	chr1:120462981-120463318	K562	blood:	n/a	n/a
3	CEBPB	chr1:120458293-120458452	HepG2	liver:	n/a	chr1:120458392-120458403
4	CEBPD	chr1:120462831-120463263	K562	blood:	n/a	n/a
5	CEBPD	chr1:120462907-120463321	K562	blood:	n/a	n/a
6	CHD1	chr1:120470129-120470186	GM12878	blood:	n/a	n/a
7	CTCF	chr1:120452940-120453090	HCPEpiC	choroid plexus:	n/a	n/a
8	CTCF	chr1:120464900-120465050	AG09309	skin:	n/a	n/a
9	CUX1	chr1:120452254-120452257	K562	blood:	n/a	n/a
10	ELK1	chr1:120452165-120452224	GM12878	blood:	n/a	n/a
11	EP300	chr1:120455642-120455979	SK-N-SH_RA	brain:	n/a	n/a
12	EP300	chr1:120462930-120463377	K562	blood:	n/a	n/a
13	EP300	chr1:120455624-120456004	SK-N-SH_RA	brain:	n/a	n/a
14	GATA2	chr1:120462849-120463192	K562	blood:	n/a	chr1:120463106-120463116 chr1:120463107-120463116
15	GATA2	chr1:120462868-120463277	K562	blood:	n/a	chr1:120463106-120463116 chr1:120463107-120463116
16	GTF2F1	chr1:120460979-120460991	K562	blood:	n/a	n/a
17	JUND	chr1:120462980-120463251	K562	blood:	n/a	n/a
18	MAFF	chr1:120454422-120454780	K562	blood:	n/a	chr1:120454594-120454612
19	MAFF	chr1:120454413-120454787	HepG2	liver:	n/a	chr1:120454594-120454612
20	MAFF	chr1:120463811-120463814	K562	blood:	n/a	n/a
21	MAFF	chr1:120463251-120463565	HepG2	liver:	n/a	chr1:120463389-120463403 chr1:120463383-120463401
22	MAFF	chr1:120463213-120463572	K562	blood:	n/a	chr1:120463389-120463403 chr1:120463383-120463401
23	MAFK	chr1:120454419-120454782	IMR90	lung:	n/a	chr1:120454595-120454610
24	MAFK	chr1:120454403-120454777	H1-hESC	embryonic stem cell:	n/a	chr1:120454595-120454610
25	MAFK	chr1:120463219-120463552	HepG2	liver:	n/a	chr1:120463389-120463403 chr1:120463355-120463372 chr1:120463385-120463400
26	MAFK	chr1:120463231-120463581	HepG2	liver:	n/a	chr1:120463389-120463403 chr1:120463355-120463372 chr1:120463385-120463400
27	MAFK	chr1:120463250-120463547	K562	blood:	n/a	chr1:120463389-120463403 chr1:120463355-120463372 chr1:120463385-120463400
28	MAFK	chr1:120454413-120454783	HepG2	liver:	n/a	chr1:120454595-120454610
29	MAFK	chr1:120457675-120457903	HepG2	liver:	n/a	n/a
30	MAFK	chr1:120463226-120463523	IMR90	lung:	n/a	chr1:120463389-120463403 chr1:120463355-120463372 chr1:120463385-120463400
31	MAFK	chr1:120454390-120454806	Hela-S3	cervix:	n/a	chr1:120454595-120454610
32	MAFK	chr1:120454420-120454775	K562	blood:	n/a	chr1:120454595-120454610
33	MAFK	chr1:120454422-120454787	HepG2	liver:	n/a	chr1:120454595-120454610
34	MAFK	chr1:120463295-120463542	Hela-S3	cervix:	n/a	chr1:120463389-120463403 chr1:120463355-120463372 chr1:120463385-120463400
35	MAX	chr1:120453004-120453824	NB4	blood:	n/a	n/a
36	MXI1	chr1:120454839-120454843	GM12878	blood:	n/a	n/a
37	MXI1	chr1:120458041-120458200	Hela-S3	cervix:	n/a	n/a
38	MXI1	chr1:120459534-120459553	GM12878	blood:	n/a	n/a
39	MXI1	chr1:120459862-120459877	GM12878	blood:	n/a	n/a
40	MYC	chr1:120452931-120453779	NB4	blood:	n/a	n/a
41	MYC	chr1:120465025-120465194	MCF10A-Er-Src	breast:	n/a	n/a
42	MYC	chr1:120466724-120466867	MCF10A-Er-Src	breast:	n/a	n/a
43	MYC	chr1:120458587-120458719	H1-hESC	embryonic stem cell:	n/a	n/a
44	NR2F2	chr1:120462887-120463214	K562	blood:	n/a	n/a
45	NRF1	chr1:120470473-120470673	H1-hESC	embryonic stem cell:	n/a	n/a
46	NRF1	chr1:120452153-120452315	GM12878	blood:	n/a	n/a
47	POLR2A	chr1:120455634-120455751	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr1:120452489-120453728	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr1:120452843-120452869	ProgFib	skin:	n/a	n/a
50	POLR2A	chr1:120458054-120458059	ProgFib	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120457856-120457906	MCF-7	breast:	n/a
2	chr1:120457856-120457906	AG09319	gingival:	n/a
3	chr1:120457856-120457906	HAEpiC	amniotic membrane:	n/a
4	chr1:120457856-120457906	Caco-2	colon:	n/a
5	chr1:120457856-120457906	HNPCEpiC	eye:	n/a
6	chr1:120457856-120457906	HCPEpiC	choroid plexus:	n/a
7	chr1:120457856-120457906	CMK	blood:	n/a
8	chr1:120457856-120457906	HIPEpiC	eye:	n/a
9	chr1:120457856-120457906	HMEC	breast:	n/a
10	chr1:120457856-120457906	HL-60	blood:	n/a
11	chr1:120457856-120457906	MCF10A-Er-Src	breast:	n/a
12	chr1:120457856-120457906	A549	lung:	n/a
13	chr1:120457856-120457906	NT2-D1	testis:	n/a
14	chr1:120457856-120457906	SK-N-SH	brain:	n/a
15	chr1:120457856-120457906	U87	brain:	n/a
16	chr1:120457856-120457906	T-47D	breast:	n/a
17	chr1:120457856-120457906	HRPEpiC	eye:	n/a
18	chr1:120457856-120457906	IMR90	lung:	fetal
19	chr1:120457856-120457906	HRE	kidney:	n/a
20	chr1:120457856-120457906	GM12892	blood:	n/a
21	chr1:120457856-120457906	AG04450	lung:	fetal
22	chr1:120457856-120457906	HEEpiC	esophagus:	n/a
23	chr1:120457856-120457906	Hepatocyte	liver:	n/a
24	chr1:120457856-120457906	NH-A	brain:	n/a
25	chr1:120457856-120457906	AoSMC	blood vessel:	n/a
26	chr1:120457856-120457906	Jurkat	blood:	n/a
27	chr1:120457856-120457906	LNCaP	prostate:	n/a
28	chr1:120457856-120457906	AG10803	skin:	n/a
29	chr1:120457856-120457906	GM12891	blood:	n/a
30	chr1:120457856-120457906	HCM	heart:	n/a
31	chr1:120457856-120457906	SK-N-SH_RA	brain:	n/a
32	chr1:120457856-120457906	NB4	blood:	n/a
33	chr1:120457856-120457906	HCT-116	colon:	n/a
34	chr1:120457856-120457906	ProgFib	skin:	n/a
35	chr1:120457856-120457906	GM19239	blood:	n/a
36	chr1:120457856-120457906	HRCEpiC	kidney:	n/a
37	chr1:120457856-120457906	K562	blood:	n/a
38	chr1:120457856-120457906	AG04449	skin:	fetal
39	chr1:120457856-120457906	ECC-1	luminal epithelium:	n/a
40	chr1:120457856-120457906	GM06990	blood:	n/a
41	chr1:120457856-120457906	PFSK-1	brain:	n/a
42	chr1:120457856-120457906	NHDF-neo	bronchial:	n/a
43	chr1:120457856-120457906	GM12878	blood:	n/a
44	chr1:120457856-120457906	ovcar-3	ovarian:	n/a
45	chr1:120457856-120457906	BE2_C	brain:	n/a
46	chr1:120457856-120457906	Hela-S3	cervix:	n/a
47	chr1:120457856-120457906	HepG2	liver:	n/a
48	chr1:120457856-120457906	PANC-1	pancreas:	n/a
49	chr1:120457856-120457906	HUVEC	blood vessel:	n/a
50	chr1:120457856-120457906	HCF	heart:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:120461841..120464545-chr1:120468138..120469880,2	MCF-7	breast:
2	chr1:120445705..120448547-chr1:120448757..120452152,3	MCF-7	breast:
3	chr1:120444002..120446345-chr1:120453344..120455730,3	MCF-7	breast:
4	chr1:120456262..120460550-chr1:120460767..120463877,3	K562	blood:
5	chr1:120436002..120438494-chr1:120462381..120464792,2	MCF-7	breast:
6	chr1:120449760..120452245-chrX:18130620..18132924,2	MCF-7	breast:
7	chr1:120461834..120464698-chr1:120475865..120478415,2	MCF-7	breast:
8	chr1:120466619..120469104-chr1:120488906..120491795,2	K562	blood:
9	chr1:120450368..120452473-chr1:120481049..120483944,2	K562	blood:
10	chr1:120461841..120464545-chr1:120468138..120469880,2	MCF-7	breast:
11	chr1:120449201..120451980-chr1:120452971..120455460,2	MCF-7	breast:
12	chr1:120452541..120455108-chr1:120461853..120464281,3	K562	blood:
13	chr1:120467969..120469676-chr1:120469960..120472021,2	MCF-7	breast:
14	chr1:120455729..120458677-chr1:120465147..120468544,4	MCF-7	breast:
15	chr1:120454474..120456790-chr1:120460931..120463931,3	MCF-7	breast:
16	chr1:120454474..120456790-chr1:120460931..120463931,3	MCF-7	breast:
17	chr1:120456262..120460550-chr1:120460767..120463877,3	K562	blood:
18	chr1:120467969..120469676-chr1:120469960..120472021,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOTCH2-1	chr1:120451878-120453236	ENSG00000261662.1

No data

(count:12 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NOTCH2	hsa-miR-34a-5p	chr1:120455462-120455456
2	NOTCH2	hsa-miR-181a-5p	chr1:120454955-120454976
3	NOTCH2	hsa-miR-181c-5p	chr1:120454955-120454976
4	NOTCH2	hsa-miR-107	chr1:120457885-120457879
5	NOTCH2	hsa-miR-1	chr1:120454297-120454318
6	NOTCH2	hsa-miR-181a-5p	chr1:120454961-120454954
7	NOTCH2	hsa-miR-107	chr1:120457879-120457900
8	NOTCH2	hsa-miR-181c-5p	chr1:120454961-120454954
9	NOTCH2	hsa-miR-16-5p	chr1:120457884-120457878
10	NOTCH2	hsa-miR-34a-5p	chr1:120455456-120455477
11	NOTCH2	hsa-miR-326	chr1:120454916-120454935
12	NOTCH2	hsa-miR-16-5p	chr1:120457878-120457901

Variant related genes	Relation type
NOTCH2	TF binding region
ENSG00000261662	TF binding region
NOTCH2	CpG island
ENSG00000261662	CpG island
ENSG00000261662	chromatin interactions
ENSG00000134250	chromatin interactions

Extended variants
information (count: 719 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112186790	chr1:120451075-120451076	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs148993563	chr1:120451107-120451108	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143753206	chr1:120451132-120451133	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs3897478	chr1:120451190-120451191	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	disease
5	rs74115392	chr1:120451209-120451210	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs587769125	chr1:120451216-120451217	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs587644942	chr1:120451226-120451227	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs587726442	chr1:120451239-120451240	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs587604279	chr1:120451240-120451241	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs587651471	chr1:120451295-120451296	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs587714932	chr1:120451348-120451349	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs947273	chr1:120451352-120451353	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs386635147	chr1:120451389-120451390	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs74115395	chr1:120451390-120451391	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs587625297	chr1:120451428-120451429	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs587627650	chr1:120451475-120451476	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs587682675	chr1:120451484-120451485	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs368257099	chr1:120451501-120451502	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs182749558	chr1:120451532-120451533	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs587617961	chr1:120451577-120451578	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372826222	chr1:120451711-120451712	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs587693313	chr1:120451815-120451816	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs587733159	chr1:120451827-120451828	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs587632430	chr1:120451869-120451870	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs55787603	chr1:120451917-120451918	Weak transcription Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs113221155	chr1:120451985-120451986	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs115019697	chr1:120452036-120452037	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs181244488	chr1:120452060-120452061	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs587645029	chr1:120452095-120452096	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs141212912	chr1:120452180-120452181	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs587754754	chr1:120452188-120452189	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs587636113	chr1:120452193-120452194	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs145320878	chr1:120452227-120452228	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs587594437	chr1:120452236-120452237	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs587670743	chr1:120452243-120452244	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs587727676	chr1:120452293-120452294	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs587625414	chr1:120452335-120452336	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs117109211	chr1:120452338-120452339	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs587755289	chr1:120452366-120452367	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs2793828	chr1:120452415-120452416	Enhancers Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs587598048	chr1:120452516-120452517	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs587675933	chr1:120452588-120452589	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs116365973	chr1:120452589-120452590	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs587634407	chr1:120452595-120452596	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs60648337	chr1:120452643-120452644	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs17024486	chr1:120452676-120452677	Enhancers Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs587624416	chr1:120452706-120452707	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs587674721	chr1:120452728-120452729	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs587761260	chr1:120452763-120452764	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs587609919	chr1:120452787-120452788	Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120444600-120453000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:120446400-120452000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:120446400-120454400	Weak transcription	NH-A	brain
4	chr1:120446600-120453400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:120448200-120452600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr1:120448200-120471000	Weak transcription	Right Atrium	heart
7	chr1:120448400-120453200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:120448400-120457400	Weak transcription	Fetal Brain Female	brain
9	chr1:120448800-120454800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:120448800-120455800	Weak transcription	NHLF	lung
11	chr1:120448800-120456000	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr1:120449000-120456600	Weak transcription	Aorta	Aorta
13	chr1:120449200-120452800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:120449200-120457200	Weak transcription	Gastric	stomach
15	chr1:120449400-120453000	Weak transcription	Esophagus	oesophagus
16	chr1:120449400-120453400	Weak transcription	Fetal Muscle Leg	muscle
17	chr1:120449600-120456200	Weak transcription	Fetal Muscle Trunk	muscle
18	chr1:120449600-120457800	Weak transcription	Fetal Intestine Small	intestine
19	chr1:120449800-120453400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr1:120450000-120453400	Weak transcription	Osteobl	bone
21	chr1:120450000-120473000	Strong transcription	HSMM	muscle
22	chr1:120450200-120452600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:120450200-120453000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr1:120450200-120456200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr1:120450200-120457800	Weak transcription	Colonic Mucosa	Colon
26	chr1:120450200-120458600	Weak transcription	HepG2	liver
27	chr1:120450400-120453000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:120450400-120455200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:120450400-120455600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr1:120450400-120456800	Weak transcription	Fetal Intestine Large	intestine
31	chr1:120450400-120456800	Weak transcription	Pancreas	Pancrea
32	chr1:120450600-120453000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr1:120450600-120453000	Weak transcription	Fetal Stomach	stomach
34	chr1:120450600-120454400	Weak transcription	NHDF-Ad	bronchial
35	chr1:120450600-120455800	Weak transcription	Liver	Liver
36	chr1:120450800-120453400	Weak transcription	HSMMtube	muscle
37	chr1:120450800-120454400	Weak transcription	Primary B cells from cord blood	blood
38	chr1:120450800-120456600	Weak transcription	Thymus	Thymus
39	chr1:120451000-120452600	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr1:120451000-120454800	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr1:120451000-120455200	Weak transcription	Placenta	Placenta
42	chr1:120451000-120456600	Weak transcription	Spleen	Spleen
43	chr1:120451000-120458400	Weak transcription	Small Intestine	intestine
44	chr1:120451000-120466800	Weak transcription	Fetal Brain Male	brain
45	chr1:120451400-120451600	Enhancers	Psoas Muscle	Psoas
46	chr1:120451400-120453000	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr1:120451400-120456600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr1:120451400-120457200	Weak transcription	Hela-S3	cervix
49	chr1:120451600-120455600	Weak transcription	Fetal Lung	lung
50	chr1:120451600-120480000	Weak transcription	Psoas Muscle	Psoas

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