Variant report

Variant	nsv946484
Chromosome Location	chr1:166458528-166461650
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:177)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:177 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:166458534-166459352	K562	blood:	n/a	n/a
2	ATF1	chr1:166458847-166459789	K562	blood:	n/a	n/a
3	ATF2	chr1:166458800-166459196	GM12878	blood:	n/a	n/a
4	ATF2	chr1:166458732-166459233	GM12878	blood:	n/a	n/a
5	BACH1	chr1:166460805-166460825	K562	blood:	n/a	n/a
6	BACH1	chr1:166458451-166458546	K562	blood:	n/a	n/a
7	BATF	chr1:166459471-166459833	GM12878	blood:	n/a	chr1:166459628-166459639
8	BATF	chr1:166459347-166459847	GM12878	blood:	n/a	chr1:166459628-166459639
9	BCL11A	chr1:166459530-166459768	GM12878	blood:	n/a	chr1:166459647-166459656 chr1:166459628-166459637
10	BCL11A	chr1:166459390-166459731	GM12878	blood:	n/a	chr1:166459647-166459656 chr1:166459628-166459637
11	BHLHE40	chr1:166458772-166460221	K562	blood:	n/a	n/a
12	CBX3	chr1:166458685-166460518	K562	blood:	n/a	n/a
13	CEBPB	chr1:166458565-166459344	K562	blood:	n/a	n/a
14	CHD2	chr1:166458986-166459606	K562	blood:	n/a	n/a
15	CTCF	chr1:166459040-166459190	GM12871	blood:	n/a	n/a
16	CTCF	chr1:166459120-166459270	GM12872	blood:	n/a	n/a
17	CTCF	chr1:166458906-166459488	K562	blood:	n/a	n/a
18	CTCF	chr1:166461380-166461425	K562	blood:	n/a	n/a
19	CTCF	chr1:166459020-166459170	GM12873	blood:	n/a	n/a
20	CUX1	chr1:166458488-166459778	K562	blood:	n/a	n/a
21	CUX1	chr1:166460994-166460998	K562	blood:	n/a	n/a
22	E2F4	chr1:166459632-166459703	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F6	chr1:166458848-166459796	K562	blood:	n/a	chr1:166459592-166459601
24	EBF1	chr1:166459474-166459801	GM12878	blood:	n/a	n/a
25	EGR1	chr1:166458887-166459451	K562	blood:	n/a	n/a
26	ELF1	chr1:166459535-166459861	K562	blood:	n/a	chr1:166459675-166459688
27	ELF1	chr1:166458873-166459389	K562	blood:	n/a	n/a
28	ELK1	chr1:166459775-166459838	GM12878	blood:	n/a	n/a
29	EP300	chr1:166459018-166459507	K562	blood:	n/a	n/a
30	EP300	chr1:166458885-166459308	GM12878	blood:	n/a	n/a
31	EP300	chr1:166458788-166460264	K562	blood:	n/a	chr1:166459628-166459637
32	FOS	chr1:166458891-166459091	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr1:166458881-166459080	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:166459497-166459793	MCF10A-Er-Src	breast:	n/a	chr1:166459627-166459636
35	FOS	chr1:166459473-166459795	MCF10A-Er-Src	breast:	n/a	chr1:166459627-166459636
36	FOS	chr1:166459473-166459794	MCF10A-Er-Src	breast:	n/a	chr1:166459627-166459636
37	FOS	chr1:166459481-166459791	MCF10A-Er-Src	breast:	n/a	chr1:166459627-166459636
38	FOS	chr1:166458988-166459133	MCF10A-Er-Src	breast:	n/a	n/a
39	FOSL1	chr1:166458950-166459892	K562	blood:	n/a	chr1:166459627-166459636
40	FOSL2	chr1:166459341-166459889	HepG2	liver:	n/a	chr1:166459627-166459636 chr1:166459627-166459638
41	FOSL2	chr1:166459390-166459838	HepG2	liver:	n/a	chr1:166459627-166459636 chr1:166459627-166459638
42	GATA1	chr1:166458786-166459572	PBDE	blood:	n/a	n/a
43	GTF2F1	chr1:166458798-166459563	K562	blood:	n/a	n/a
44	HCFC1	chr1:166458798-166460046	K562	blood:	n/a	n/a
45	HDAC2	chr1:166458912-166459487	K562	blood:	n/a	n/a
46	HEY1	chr1:166458744-166459768	K562	blood:	n/a	n/a
47	HEY1	chr1:166458958-166459599	K562	blood:	n/a	n/a
48	IRF1	chr1:166459021-166459615	K562	blood:	n/a	chr1:166459377-166459398 chr1:166459544-166459553 chr1:166459592-166459601
49	IRF1	chr1:166458396-166460911	K562	blood:	n/a	chr1:166459377-166459398 chr1:166459544-166459553 chr1:166459592-166459601
50	IRF1	chr1:166458910-166459862	K562	blood:	n/a	chr1:166459377-166459398 chr1:166459544-166459553 chr1:166459592-166459601

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:166459325-166459375	NHDF-neo	bronchial:	n/a
2	chr1:166459325-166459375	GM12892	blood:	n/a
3	chr1:166459325-166459375	Jurkat	blood:	n/a
4	chr1:166459325-166459375	HRPEpiC	eye:	n/a
5	chr1:166459325-166459375	AG09309	skin:	n/a
6	chr1:166459325-166459375	HEK293	kidney:	embryo
7	chr1:166459325-166459375	AoSMC	blood vessel:	n/a
8	chr1:166459325-166459375	Hela-S3	cervix:	n/a
9	chr1:166459325-166459375	Caco-2	colon:	n/a
10	chr1:166459325-166459375	HCPEpiC	choroid plexus:	n/a
11	chr1:166459325-166459375	AG09319	gingival:	n/a
12	chr1:166459325-166459375	HCF	heart:	n/a
13	chr1:166459325-166459375	NH-A	brain:	n/a
14	chr1:166459325-166459375	AG04450	lung:	fetal
15	chr1:166459325-166459375	A549	lung:	n/a
16	chr1:166459325-166459375	T-47D	breast:	n/a
17	chr1:166459325-166459375	PrEC	prostate:	n/a
18	chr1:166459325-166459375	NHBE	bronchial:	n/a
19	chr1:166459325-166459375	IMR90	lung:	fetal
20	chr1:166459325-166459375	GM12878	blood:	n/a
21	chr1:166459325-166459375	HCM	heart:	n/a
22	chr1:166459325-166459375	RPTEC	kidney:	n/a
23	chr1:166459325-166459375	PFSK-1	brain:	n/a
24	chr1:166459325-166459375	SK-N-SH_RA	brain:	n/a
25	chr1:166459325-166459375	NB4	blood:	n/a
26	chr1:166459325-166459375	GM12891	blood:	n/a
27	chr1:166459325-166459375	HNPCEpiC	eye:	n/a
28	chr1:166459325-166459375	HepG2	liver:	n/a
29	chr1:166459325-166459375	H1-hESC	embryonic stem cell:	embryo
30	chr1:166459325-166459375	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:166459325-166459375	K562	blood:	n/a
32	chr1:166459325-166459375	HMEC	breast:	n/a
33	chr1:166459325-166459375	HAEpiC	amniotic membrane:	n/a
34	chr1:166459325-166459375	SKMC	muscle:	n/a
35	chr1:166459325-166459375	BE2_C	brain:	n/a
36	chr1:166459325-166459375	AG10803	skin:	n/a
37	chr1:166459325-166459375	HIPEpiC	eye:	n/a
38	chr1:166459325-166459375	SAEC	small airway:	n/a
39	chr1:166459325-166459375	HCT-116	colon:	n/a
40	chr1:166459325-166459375	MCF-7	breast:	n/a
41	chr1:166459325-166459375	Hepatocyte	liver:	n/a
42	chr1:166459325-166459375	MCF10A-Er-Src	breast:	n/a
43	chr1:166459325-166459375	HEEpiC	esophagus:	n/a
44	chr1:166459325-166459375	SK-N-MC	brain:	n/a
45	chr1:166459325-166459375	ProgFib	skin:	n/a
46	chr1:166459325-166459375	NT2-D1	testis:	n/a
47	chr1:166459325-166459375	ovcar-3	ovarian:	n/a
48	chr1:166459325-166459375	BJ	skin:	n/a
49	chr1:166459325-166459375	HRE	kidney:	n/a
50	chr1:166459325-166459375	GM06990	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:166455370..166456980-chr1:166459569..166461512,2	K562	blood:
2	chr1:166457611..166459186-chr1:166459770..166461312,2	K562	blood:
3	chr1:166458815..166461765-chr1:166845065..166847210,2	MCF-7	breast:
4	chr1:166447978..166448509-chr1:166458216..166458981,2	K562	blood:
5	chr1:166449687..166451198-chr1:166457189..166459099,2	K562	blood:
6	chr1:166457611..166459186-chr1:166459770..166461312,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM78B-2	chr1:166459098-166459276	ENSG00000234142

No data

Variant related genes	Relation type
ENSG00000234142	TF binding region
ENSG00000234142	CpG island
ENSG00000152382	chromatin interactions

Extended variants
information (count: 140 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:140 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144237403	chr1:166458538-166458539	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs371973271	chr1:166458566-166458567	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs10918487	chr1:166458590-166458591	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs547013808	chr1:166458597-166458598	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs78975883	chr1:166458627-166458628	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs538574232	chr1:166458647-166458648	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs11584555	chr1:166458651-166458652	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs558417033	chr1:166458676-166458677	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs191926505	chr1:166458680-166458681	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs34858711	chr1:166458686-166458687	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs553150771	chr1:166458705-166458706	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs11583236	chr1:166458826-166458827	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
13	rs183883377	chr1:166458836-166458837	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574514280	chr1:166458863-166458864	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs376245540	chr1:166458864-166458865	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs553755878	chr1:166458881-166458882	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs146548122	chr1:166458911-166458912	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538869882	chr1:166458927-166458928	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545731992	chr1:166459006-166459007	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs368628772	chr1:166459008-166459009	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs57391743	chr1:166459009-166459010	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545078563	chr1:166459010-166459011	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149691865	chr1:166459014-166459015	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs145463227	chr1:166459019-166459020	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs202204061	chr1:166459025-166459026	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs200304228	chr1:166459026-166459027	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs186189002	chr1:166459032-166459033	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs531129397	chr1:166459094-166459095	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs190511673	chr1:166459117-166459118	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs561316099	chr1:166459119-166459120	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs530261623	chr1:166459131-166459132	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs546757146	chr1:166459210-166459211	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs141279806	chr1:166459223-166459224	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs532341156	chr1:166459249-166459250	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs182805243	chr1:166459251-166459252	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs12732576	chr1:166459262-166459263	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs72689841	chr1:166459285-166459286	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs528328318	chr1:166459289-166459290	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs372850385	chr1:166459290-166459291	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs543749958	chr1:166459295-166459296	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs12731435	chr1:166459298-166459299	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs12731436	chr1:166459300-166459301	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs557084147	chr1:166459344-166459345	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs568137865	chr1:166459375-166459376	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs10918488	chr1:166459430-166459431	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs553549501	chr1:166459439-166459440	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs576934984	chr1:166459525-166459526	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs150224957	chr1:166459547-166459548	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs200299967	chr1:166459552-166459553	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs187089388	chr1:166459553-166459554	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166455200-166458800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:166456400-166458600	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr1:166457000-166458800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr1:166457000-166458800	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr1:166457000-166458800	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr1:166457200-166458600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
7	chr1:166457400-166458600	Enhancers	Primary hematopoietic stem cells	blood
8	chr1:166457400-166458600	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr1:166457600-166458600	Enhancers	Primary B cells from peripheral blood	blood
10	chr1:166457600-166458600	Enhancers	Primary T cells fromperipheralblood	blood
11	chr1:166457600-166458600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr1:166457600-166458800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr1:166457800-166458600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr1:166458000-166458600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr1:166458000-166458800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr1:166458000-166458800	Weak transcription	Liver	Liver
17	chr1:166458000-166459200	Flanking Active TSS	K562	blood
18	chr1:166458000-166460000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:166458000-166460000	Flanking Active TSS	Dnd41	blood
20	chr1:166458000-166460000	Active TSS	GM12878-XiMat	blood
21	chr1:166458200-166458600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr1:166458200-166458600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:166458400-166458600	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr1:166458400-166458800	Enhancers	Primary T cells from cord blood	blood
25	chr1:166458400-166458800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr1:166458400-166458800	Enhancers	Adipose Nuclei	Adipose
27	chr1:166458400-166459000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr1:166458600-166458800	Enhancers	Primary B cells from cord blood	blood
29	chr1:166458600-166458800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
30	chr1:166458600-166458800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr1:166458600-166458800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
32	chr1:166458600-166458800	Active TSS	Duodenum Mucosa	Duodenum
33	chr1:166458600-166459000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
34	chr1:166458600-166459000	Flanking Active TSS	Primary hematopoietic stem cells	blood
35	chr1:166458600-166459000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
36	chr1:166458600-166459000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
37	chr1:166458600-166459200	Flanking Active TSS	Primary B cells from peripheral blood	blood
38	chr1:166458600-166459200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
39	chr1:166458600-166459200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr1:166458600-166459200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
41	chr1:166458600-166459800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr1:166458800-166459000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:166458800-166459000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
44	chr1:166458800-166459000	Flanking Active TSS	Primary T cells from cord blood	blood
45	chr1:166458800-166459000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
46	chr1:166458800-166459000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
47	chr1:166458800-166459000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr1:166458800-166459000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
49	chr1:166458800-166459000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
50	chr1:166458800-166459000	Enhancers	Pancreas	Pancrea

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