Variant report

Variant	nsv946004
Chromosome Location	chr1:78152199-78160377
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:190)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:190 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD1	chr1:78153440-78153579	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr1:78153424-78153470	HepG2	liver:	n/a	n/a
3	CHD2	chr1:78153277-78153581	H1-hESC	embryonic stem cell:	n/a	chr1:78153407-78153417
4	CTCF	chr1:78153400-78153550	HMEC	breast:	n/a	n/a
5	CTCF	chr1:78153360-78153510	GM06990	blood:	n/a	n/a
6	CTCF	chr1:78153440-78153590	GM12872	blood:	n/a	n/a
7	CTCF	chr1:78153340-78153490	GM12878	blood:	n/a	n/a
8	CTCF	chr1:78153300-78153450	SAEC	small airway:	n/a	n/a
9	CTCF	chr1:78153340-78153490	NHEK	skin:	n/a	n/a
10	CTCF	chr1:78153040-78153190	GM12866	blood:	n/a	n/a
11	CTCF	chr1:78153320-78153470	GM12874	blood:	n/a	n/a
12	CTCF	chr1:78153320-78153470	AG09319	gingival:	n/a	n/a
13	CTCF	chr1:78153360-78153510	AG10803	skin:	n/a	n/a
14	CTCF	chr1:78153380-78153530	GM12874	blood:	n/a	n/a
15	CTCF	chr1:78153418-78153556	GM10248	blood:	n/a	n/a
16	CTCF	chr1:78153300-78153450	HRE	kidney:	n/a	n/a
17	CTCF	chr1:78153340-78153490	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr1:78153320-78153470	GM12864	blood:	n/a	n/a
19	CTCF	chr1:78153340-78153490	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr1:78153375-78153554	GM13976	blood:	n/a	n/a
21	CTCF	chr1:78153300-78153450	HFF	foreskin:	n/a	n/a
22	CTCF	chr1:78153360-78153510	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr1:78153367-78153558	GM12892	blood:	n/a	n/a
24	CTCF	chr1:78153300-78153450	HCT-116	colon:	n/a	n/a
25	CTCF	chr1:78153194-78153640	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr1:78153300-78153450	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr1:78153400-78153550	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr1:78153445-78153461	GM12878	blood:	n/a	n/a
29	CTCF	chr1:78153258-78153601	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:78153360-78153510	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr1:78153340-78153490	GM12865	blood:	n/a	n/a
32	CTCF	chr1:78153400-78153550	GM12872	blood:	n/a	n/a
33	CTCF	chr1:78153360-78153510	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr1:78153340-78153490	AG10803	skin:	n/a	n/a
35	CTCF	chr1:78153580-78153730	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr1:78153340-78153490	GM12869	blood:	n/a	n/a
37	CTCF	chr1:78153340-78153490	A549	lung:	n/a	n/a
38	CTCF	chr1:78153420-78153570	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr1:78153374-78153519	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr1:78153420-78153570	GM12864	blood:	n/a	n/a
41	CTCF	chr1:78153360-78153510	HepG2	liver:	n/a	n/a
42	CTCF	chr1:78153371-78153566	GM19240	blood:	n/a	n/a
43	CTCF	chr1:78153400-78153550	HPF	lung:	n/a	n/a
44	CTCF	chr1:78153412-78153586	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr1:78153280-78153430	HCT-116	colon:	n/a	n/a
46	CTCF	chr1:78153437-78153528	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr1:78153360-78153510	AG04449	skin:	n/a	n/a
48	CTCF	chr1:78153420-78153570	HPF	lung:	n/a	n/a
49	CTCF	chr1:78153360-78153510	Caco-2	colon:	n/a	n/a
50	CTCF	chr1:78153300-78153450	HA-sp	spinal cord:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:78153303-78153353	BE2_C	brain:	n/a
2	chr1:78153303-78153353	GM12891	blood:	n/a
3	chr1:78153303-78153353	AoSMC	blood vessel:	n/a
4	chr1:78153303-78153353	AG09309	skin:	n/a
5	chr1:78153303-78153353	Hela-S3	cervix:	n/a
6	chr1:78153303-78153353	ProgFib	skin:	n/a
7	chr1:78153303-78153353	NHDF-neo	bronchial:	n/a
8	chr1:78153303-78153353	T-47D	breast:	n/a
9	chr1:78153303-78153353	HNPCEpiC	eye:	n/a
10	chr1:78153303-78153353	HCPEpiC	choroid plexus:	n/a
11	chr1:78153303-78153353	NH-A	brain:	n/a
12	chr1:78153303-78153353	HEEpiC	esophagus:	n/a
13	chr1:78153303-78153353	PFSK-1	brain:	n/a
14	chr1:78153303-78153353	GM12878	blood:	n/a
15	chr1:78153303-78153353	HL-60	blood:	n/a
16	chr1:78153303-78153353	K562	blood:	n/a
17	chr1:78153303-78153353	HRE	kidney:	n/a
18	chr1:78153303-78153353	HCT-116	colon:	n/a
19	chr1:78153303-78153353	NHBE	bronchial:	n/a
20	chr1:78153303-78153353	ovcar-3	ovarian:	n/a
21	chr1:78153303-78153353	SKMC	muscle:	n/a
22	chr1:78153303-78153353	Jurkat	blood:	n/a
23	chr1:78153303-78153353	IMR90	lung:	fetal
24	chr1:78153303-78153353	MCF10A-Er-Src	breast:	n/a
25	chr1:78153303-78153353	ECC-1	luminal epithelium:	n/a
26	chr1:78153303-78153353	HepG2	liver:	n/a
27	chr1:78153303-78153353	HIPEpiC	eye:	n/a
28	chr1:78153303-78153353	SK-N-SH	brain:	n/a
29	chr1:78153303-78153353	HCF	heart:	n/a
30	chr1:78153303-78153353	HRPEpiC	eye:	n/a
31	chr1:78153303-78153353	CMK	blood:	n/a
32	chr1:78153303-78153353	NT2-D1	testis:	n/a
33	chr1:78153303-78153353	PANC-1	pancreas:	n/a
34	chr1:78153303-78153353	HUVEC	blood vessel:	n/a
35	chr1:78153303-78153353	SK-N-SH_RA	brain:	n/a
36	chr1:78153303-78153353	GM12892	blood:	n/a
37	chr1:78153303-78153353	LNCaP	prostate:	n/a
38	chr1:78153303-78153353	Hepatocyte	liver:	n/a
39	chr1:78153303-78153353	HCM	heart:	n/a
40	chr1:78153303-78153353	AG04449	skin:	fetal
41	chr1:78153303-78153353	HRCEpiC	kidney:	n/a
42	chr1:78153303-78153353	HEK293	kidney:	embryo
43	chr1:78153303-78153353	H1-hESC	embryonic stem cell:	embryo
44	chr1:78153303-78153353	RPTEC	kidney:	n/a
45	chr1:78153303-78153353	BJ	skin:	n/a
46	chr1:78153303-78153353	SAEC	small airway:	n/a
47	chr1:78153303-78153353	AG04450	lung:	fetal
48	chr1:78153303-78153353	PrEC	prostate:	n/a
49	chr1:78153303-78153353	GM19239	blood:	n/a
50	chr1:78153303-78153353	Caco-2	colon:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:78160363..78163155-chr1:78169082..78170861,2	K562	blood:
2	chr1:78155245..78156889-chr1:78160678..78162771,2	K562	blood:
3	chr1:78147657..78150570-chr1:78157305..78159209,2	K562	blood:
4	chr1:78153612..78156248-chr1:78205840..78207802,2	K562	blood:
5	chr1:78147916..78149547-chr1:78151862..78154484,2	MCF-7	breast:
6	chr1:78147132..78149887-chr1:78150193..78152348,2	MCF-7	breast:
7	chr1:78147362..78150738-chr1:78154118..78156119,3	K562	blood:
8	chr1:78150914..78152698-chr1:78165205..78167103,2	K562	blood:
9	chr1:78153418..78155756-chr1:78236442..78239366,2	K562	blood:
10	chr1:78150914..78153442-chr1:78165603..78168568,2	K562	blood:
11	chr1:78148636..78150222-chr1:78153007..78155635,3	MCF-7	breast:

No data

Variant related genes	Relation type
ZZZ3	TF binding region
ZZZ3	CpG island
ENSG00000077254	chromatin interactions
ENSG00000036549	chromatin interactions

Extended variants
information (count: 259 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117397437	chr1:78152249-78152250	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs538869095	chr1:78152265-78152266	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs558783613	chr1:78152393-78152394	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs141835782	chr1:78152395-78152396	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs553420685	chr1:78152451-78152452	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs578104449	chr1:78152455-78152456	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs370341419	chr1:78152463-78152464	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs545278461	chr1:78152470-78152471	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs563347119	chr1:78152509-78152510	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs530616440	chr1:78152577-78152578	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs372116486	chr1:78152641-78152642	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs369449950	chr1:78152646-78152647	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs542783928	chr1:78152657-78152658	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs36021969	chr1:78152661-78152662	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs572226752	chr1:78152665-78152666	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs278844	chr1:78152668-78152669	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs528120112	chr1:78152717-78152718	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs546888838	chr1:78152727-78152728	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs571466695	chr1:78152732-78152733	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs193217805	chr1:78152776-78152777	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs12741347	chr1:78152792-78152793	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs370476510	chr1:78152795-78152796	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs278845	chr1:78152805-78152806	Active TSS Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs554157118	chr1:78152844-78152845	Active TSS Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs112896470	chr1:78152952-78152953	Active TSS Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs537140986	chr1:78152954-78152955	Active TSS Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs543435881	chr1:78152966-78152967	Active TSS Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs555477416	chr1:78153013-78153014	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs567302152	chr1:78153027-78153028	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs534721624	chr1:78153052-78153053	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs369798	chr1:78153082-78153083	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs115363594	chr1:78153097-78153098	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs114306389	chr1:78153175-78153176	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs545728558	chr1:78153186-78153187	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs143085465	chr1:78153250-78153251	Active TSS Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs111661359	chr1:78153273-78153274	Active TSS Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs185574293	chr1:78153341-78153342	Active TSS Strong transcription Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs563845199	chr1:78153355-78153356	Active TSS Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs189304054	chr1:78153381-78153382	Active TSS Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs542721034	chr1:78153456-78153457	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs146834067	chr1:78153468-78153469	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs278846	chr1:78153501-78153502	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs539850890	chr1:78153524-78153525	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs369150440	chr1:78153550-78153551	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs114922089	chr1:78153552-78153553	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs532294935	chr1:78153566-78153567	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs180833793	chr1:78153572-78153573	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs34933676	chr1:78153684-78153685	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs550897401	chr1:78153790-78153791	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs278847	chr1:78153821-78153822	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	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
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
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:78149600-78175000	Weak transcription	Gastric	stomach
2	chr1:78149600-78177800	Weak transcription	Spleen	Spleen
3	chr1:78149800-78152600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:78149800-78152600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:78149800-78152600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:78149800-78153000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:78149800-78153000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr1:78149800-78153000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr1:78149800-78153200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr1:78149800-78153200	Weak transcription	Placenta	Placenta
11	chr1:78149800-78153200	Weak transcription	Right Atrium	heart
12	chr1:78149800-78153400	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr1:78149800-78157400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:78149800-78157600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr1:78149800-78158800	Weak transcription	Left Ventricle	heart
16	chr1:78149800-78159800	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr1:78149800-78165600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr1:78149800-78165600	Weak transcription	Esophagus	oesophagus
19	chr1:78149800-78165600	Weak transcription	Lung	lung
20	chr1:78149800-78171800	Weak transcription	Fetal Brain Male	brain
21	chr1:78149800-78173000	Weak transcription	Colonic Mucosa	Colon
22	chr1:78149800-78173800	Weak transcription	Aorta	Aorta
23	chr1:78149800-78178000	Weak transcription	Small Intestine	intestine
24	chr1:78150000-78152600	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr1:78150000-78153400	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr1:78150000-78153400	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr1:78150000-78153400	Weak transcription	Fetal Kidney	kidney
28	chr1:78150000-78153400	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr1:78150000-78158600	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr1:78150000-78158800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr1:78150000-78158800	Weak transcription	Fetal Brain Female	brain
32	chr1:78150000-78160800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr1:78150000-78160800	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr1:78150000-78161600	Weak transcription	Brain Cingulate Gyrus	brain
35	chr1:78150000-78162000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr1:78150000-78163000	Weak transcription	Stomach Smooth Muscle	stomach
37	chr1:78150000-78165200	Weak transcription	Brain Angular Gyrus	brain
38	chr1:78150000-78166000	Weak transcription	HSMMtube	muscle
39	chr1:78150000-78172800	Weak transcription	Colon Smooth Muscle	Colon
40	chr1:78150000-78173000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr1:78150000-78173000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr1:78150000-78173600	Weak transcription	Psoas Muscle	Psoas
43	chr1:78150000-78174000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr1:78150000-78175600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr1:78150200-78152200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr1:78150200-78152200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr1:78150200-78152200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr1:78150200-78152200	Enhancers	Fetal Heart	heart
49	chr1:78150200-78152400	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr1:78150200-78152400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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