Variant report

Variant	nsv1053366
Chromosome Location	chr11:48189421-48355981
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	ARID3A	chr11:48194471-48194702	HepG2	liver:	n/a	n/a
2	ATF1	chr11:48292484-48292679	K562	blood:	n/a	n/a
3	ATF3	chr11:48194480-48194676	K562	blood:	n/a	n/a
4	ATF3	chr11:48194364-48194613	K562	blood:	n/a	n/a
5	BHLHE40	chr11:48194470-48194703	GM12878	blood:	n/a	n/a
6	BRCA1	chr11:48194532-48194633	GM12878	blood:	n/a	n/a
7	BRCA1	chr11:48235490-48235559	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr11:48329323-48329679	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr11:48194475-48194742	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr11:48329320-48329744	HCT-116	colon:	n/a	n/a
11	CEBPB	chr11:48232351-48232666	K562	blood:	n/a	chr11:48232504-48232515
12	CEBPB	chr11:48232372-48232647	Hela-S3	cervix:	n/a	chr11:48232504-48232515
13	CEBPB	chr11:48340990-48341301	A549	lung:	n/a	n/a
14	CEBPB	chr11:48232368-48232629	A549	lung:	n/a	chr11:48232504-48232515
15	CEBPB	chr11:48332469-48332671	HepG2	liver:	n/a	chr11:48332598-48332609
16	CEBPB	chr11:48232346-48232660	IMR90	lung:	n/a	chr11:48232504-48232515
17	CEBPB	chr11:48194408-48194759	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:48232376-48232660	HepG2	liver:	n/a	chr11:48232504-48232515
19	CHD1	chr11:48194544-48194553	GM12878	blood:	n/a	n/a
20	CHD2	chr11:48344566-48344658	K562	blood:	n/a	n/a
21	CHD2	chr11:48212930-48213130	K562	blood:	n/a	n/a
22	CHD2	chr11:48199898-48199928	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr11:48194572-48194700	HepG2	liver:	n/a	n/a
24	CREB1	chr11:48194478-48194746	A549	lung:	n/a	n/a
25	CTCF	chr11:48231720-48231870	HEK293	kidney:	n/a	n/a
26	CTCF	chr11:48206128-48206251	Gliobla	brain:	n/a	chr11:48206171-48206192
27	CTCF	chr11:48231688-48231910	MCF-7	breast:	n/a	n/a
28	CTCF	chr11:48194500-48194650	GM12864	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
29	CTCF	chr11:48194520-48194670	HMEC	breast:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
30	CTCF	chr11:48329440-48329590	HRPEpiC	eye:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
31	CTCF	chr11:48329406-48329641	GM20000	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
32	CTCF	chr11:48194520-48194670	SAEC	small airway:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
33	CTCF	chr11:48194520-48194670	Caco-2	colon:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
34	CTCF	chr11:48347233-48347255	Fibrobl	skin:	n/a	n/a
35	CTCF	chr11:48329375-48329656	HepG2	liver:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
36	CTCF	chr11:48194480-48194630	GM12801	blood:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
37	CTCF	chr11:48329440-48329590	WERI-Rb-1	eye:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
38	CTCF	chr11:48231760-48231910	BJ	skin:	n/a	n/a
39	CTCF	chr11:48329400-48329550	GM12866	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
40	CTCF	chr11:48329460-48329610	GM12873	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
41	CTCF	chr11:48194500-48194650	HRE	kidney:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
42	CTCF	chr11:48329460-48329610	GM12872	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
43	CTCF	chr11:48329440-48329590	BJ	skin:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
44	CTCF	chr11:48206240-48206241	K562	blood:	n/a	n/a
45	CTCF	chr11:48194540-48194690	WI-38	lung:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
46	CTCF	chr11:48329420-48329570	GM12869	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
47	CTCF	chr11:48329365-48329661	GM13977	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
48	CTCF	chr11:48234402-48234440	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr11:48194520-48194670	AG09319	gingival:	n/a	chr11:48194577-48194585 chr11:48194574-48194595 chr11:48194572-48194590 chr11:48194575-48194588 chr11:48194573-48194589
50	CTCF	chr11:48329460-48329610	HCM	heart:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48237353-48237403	SK-N-SH_RA	brain:	n/a
2	chr11:48237353-48237403	SK-N-SH_RA	brain:	n/a
3	chr11:48345815-48345865	HCT-116	colon:	n/a
4	chr11:48345361-48345411	AG10803	skin:	n/a
5	chr11:48285200-48285250	ovcar-3	ovarian:	n/a
6	chr11:48346680-48346730	AoSMC	blood vessel:	n/a
7	chr11:48284249-48284299	ProgFib	skin:	n/a
8	chr11:48328132-48328182	PANC-1	pancreas:	n/a
9	chr11:48285821-48285871	NHDF-neo	bronchial:	n/a
10	chr11:48285821-48285871	HRE	kidney:	n/a
11	chr11:48191068-48191118	Caco-2	colon:	n/a
12	chr11:48284249-48284299	RPTEC	kidney:	n/a
13	chr11:48266856-48266906	HRE	kidney:	n/a
14	chr11:48238296-48238346	SK-N-SH	brain:	n/a
15	chr11:48346680-48346730	U87	brain:	n/a
16	chr11:48284249-48284299	PFSK-1	brain:	n/a
17	chr11:48285821-48285871	AG10803	skin:	n/a
18	chr11:48238724-48238774	AG09309	skin:	n/a
19	chr11:48345361-48345411	SAEC	small airway:	n/a
20	chr11:48326388-48326438	Hepatocyte	liver:	n/a
21	chr11:48326388-48326438	HEEpiC	esophagus:	n/a
22	chr11:48345361-48345411	NHDF-neo	bronchial:	n/a
23	chr11:48238724-48238774	HIPEpiC	eye:	n/a
24	chr11:48285821-48285871	AoSMC	blood vessel:	n/a
25	chr11:48346680-48346730	PFSK-1	brain:	n/a
26	chr11:48238296-48238346	NT2-D1	testis:	n/a
27	chr11:48238724-48238774	HCF	heart:	n/a
28	chr11:48284249-48284299	AG09319	gingival:	n/a
29	chr11:48326388-48326438	MCF-7	breast:	n/a
30	chr11:48346680-48346730	MCF10A-Er-Src	breast:	n/a
31	chr11:48238724-48238774	HEEpiC	esophagus:	n/a
32	chr11:48237353-48237403	SK-N-MC	brain:	n/a
33	chr11:48327164-48327214	SAEC	small airway:	n/a
34	chr11:48284249-48284299	SK-N-SH_RA	brain:	n/a
35	chr11:48345361-48345411	AG04449	skin:	fetal
36	chr11:48191068-48191118	A549	lung:	n/a
37	chr11:48327164-48327214	HAEpiC	amniotic membrane:	n/a
38	chr11:48237358-48237408	ProgFib	skin:	n/a
39	chr11:48266856-48266906	HNPCEpiC	eye:	n/a
40	chr11:48327164-48327214	A549	lung:	n/a
41	chr11:48237353-48237403	HPAEpiC	pulmonary alveolar:	n/a
42	chr11:48238296-48238346	NHDF-neo	bronchial:	n/a
43	chr11:48266856-48266906	HRPEpiC	eye:	n/a
44	chr11:48285200-48285250	AG09319	gingival:	n/a
45	chr11:48285821-48285871	H1-hESC	embryonic stem cell:	embryo
46	chr11:48266856-48266906	BE2_C	brain:	n/a
47	chr11:48327164-48327214	IMR90	lung:	fetal
48	chr11:48266856-48266906	K562	blood:	n/a
49	chr11:48284249-48284299	HUVEC	blood vessel:	n/a
50	chr11:48327164-48327214	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
2	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
3	chr11:48194206..48195039-chr11:49190936..49191807,2	MCF-7	breast:
4	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
5	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
6	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
7	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
8	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
9	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
10	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
11	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
12	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
13	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:

No.	miRNA target gene	miRNA name	Chromosome Location
1	PTPRJ	hsa-miR-328-3p	chr11:48191725-48191748
2	PTPRJ	hsa-miR-16-5p	chr11:48190236-48190242
3	PTPRJ	hsa-miR-155-5p	chr11:48190367-48190373
4	PTPRJ	hsa-miR-124-3p	chr11:48189431-48189437
5	PTPRJ	hsa-miR-124-3p	chr11:48189418-48189438
6	PTPRJ	hsa-miR-155-5p	chr11:48190351-48190373
7	PTPRJ	hsa-miR-26b-5p	chr11:48190233-48190256
8	PTPRJ	hsa-miR-16-5p	chr11:48190225-48190243

Variant related genes	Relation type
OR4X2	TF binding region
OR4B2P	TF binding region
OR4X1	TF binding region
OR4C3	TF binding region
OR4S1	TF binding region
OR4B1	TF binding region
OR4X2	CpG island
OR4B2P	CpG island
OR4X1	CpG island
OR4C3	CpG island
OR4S1	CpG island
OR4B1	CpG island

Extended variants
information (count: 3022 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3022 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373842274	chr11:48189449-48189450	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs546441888	chr11:48189474-48189475	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562936929	chr11:48189487-48189488	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528488829	chr11:48189497-48189498	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186948486	chr11:48189513-48189514	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1058417	chr11:48189604-48189605	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7951730	chr11:48189606-48189607	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs1058416	chr11:48189627-48189628	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561979015	chr11:48189686-48189687	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs117902837	chr11:48189911-48189912	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544055903	chr11:48189951-48189952	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs3071027	chr11:48190083-48190084	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573714428	chr11:48190085-48190086	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10607467	chr11:48190086-48190087	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs71045551	chr11:48190129-48190130	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7131268	chr11:48190133-48190134	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs1983072	chr11:48190134-48190135	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs115355320	chr11:48190138-48190139	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560036006	chr11:48190154-48190155	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184241728	chr11:48190209-48190210	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188676138	chr11:48190230-48190231	Weak transcription Strong transcription Enhancers Genic enhancers	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
22	rs200439577	chr11:48190266-48190267	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs59306113	chr11:48190275-48190276	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565393556	chr11:48190289-48190290	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551984371	chr11:48190316-48190317	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7115597	chr11:48190383-48190384	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs531355208	chr11:48190390-48190391	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs193023074	chr11:48190448-48190449	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530997480	chr11:48190496-48190497	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2174127	chr11:48190527-48190528	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs372474850	chr11:48190551-48190552	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569847416	chr11:48190566-48190567	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141898589	chr11:48190612-48190613	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554479344	chr11:48190649-48190650	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571176510	chr11:48190650-48190651	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35318681	chr11:48190681-48190682	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185657283	chr11:48190689-48190690	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556842628	chr11:48190713-48190714	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576472694	chr11:48190717-48190718	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535786244	chr11:48190718-48190719	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146272819	chr11:48190725-48190726	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139364012	chr11:48190731-48190732	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs74823631	chr11:48190737-48190738	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541427691	chr11:48190766-48190767	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12798703	chr11:48190777-48190778	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs532303587	chr11:48190782-48190783	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570608413	chr11:48190862-48190863	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs75367689	chr11:48190899-48190900	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs190583556	chr11:48190903-48190904	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs531543941	chr11:48190953-48190954	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:519 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48131600-48191600	Weak transcription	Small Intestine	intestine
2	chr11:48138200-48192600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr11:48149800-48190600	Weak transcription	Right Ventricle	heart
4	chr11:48151400-48191600	Weak transcription	Stomach Mucosa	stomach
5	chr11:48156400-48191400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr11:48163400-48192400	Weak transcription	Colon Smooth Muscle	Colon
7	chr11:48174000-48190800	Strong transcription	Liver	Liver
8	chr11:48175200-48191200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr11:48175400-48192400	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr11:48175600-48191000	Strong transcription	Primary T cells fromperipheralblood	blood
11	chr11:48175800-48190800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr11:48175800-48190800	Weak transcription	HSMMtube	muscle
13	chr11:48175800-48191600	Weak transcription	Rectal Smooth Muscle	rectum
14	chr11:48176000-48190800	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr11:48176000-48194600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr11:48176200-48191000	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr11:48176200-48191200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr11:48176200-48192000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr11:48176600-48190600	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr11:48176600-48191800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr11:48177000-48190400	Weak transcription	Fetal Muscle Trunk	muscle
22	chr11:48177600-48191000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:48177600-48191000	Weak transcription	Fetal Kidney	kidney
24	chr11:48177600-48191200	Strong transcription	Primary B cells from peripheral blood	blood
25	chr11:48177600-48191400	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr11:48178000-48191200	Strong transcription	Primary B cells from cord blood	blood
27	chr11:48178200-48190800	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr11:48179200-48190800	Weak transcription	Left Ventricle	heart
29	chr11:48179200-48193200	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr11:48179400-48191000	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr11:48179400-48192200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr11:48183400-48191000	Strong transcription	Primary T helper cells PMA-I stimulated	--
33	chr11:48184000-48189800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr11:48184000-48190000	Strong transcription	Sigmoid Colon	Sigmoid Colon
35	chr11:48184000-48191600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr11:48184200-48190800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr11:48184200-48191000	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr11:48184400-48190600	Weak transcription	NHLF	lung
39	chr11:48184400-48191200	Weak transcription	Ovary	ovary
40	chr11:48184400-48191200	Weak transcription	HUVEC	blood vessel
41	chr11:48184600-48190600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr11:48184800-48191000	Strong transcription	Placenta	Placenta
43	chr11:48185000-48192000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr11:48185600-48192600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr11:48185800-48192400	Weak transcription	Fetal Brain Female	brain
46	chr11:48186000-48190400	Weak transcription	Colonic Mucosa	Colon
47	chr11:48186000-48190600	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr11:48186000-48191000	Weak transcription	Brain Cingulate Gyrus	brain
49	chr11:48186000-48191000	Weak transcription	Fetal Lung	lung
50	chr11:48186000-48191000	Weak transcription	HSMM	muscle

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