Variant report

Variant	nsv3755
Chromosome Location	chr1:179998860-180043554
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:195)
CpG islands
(count:61)
Chromatin interactive
region (count:57)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:195 , 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	chr1:180026837-180027685	K562	blood:	n/a	n/a
2	ARID3A	chr1:180022917-180023445	K562	blood:	n/a	n/a
3	ARID3A	chr1:180027943-180027952	K562	blood:	n/a	n/a
4	ARID3A	chr1:180023732-180023861	K562	blood:	n/a	n/a
5	ATF1	chr1:180022859-180023490	K562	blood:	n/a	n/a
6	ATF3	chr1:180023152-180023468	K562	blood:	n/a	n/a
7	BACH1	chr1:180026917-180027441	K562	blood:	n/a	n/a
8	BACH1	chr1:180027050-180027297	H1-hESC	embryonic stem cell:	n/a	n/a
9	CCNT2	chr1:180039551-180039603	K562	blood:	n/a	n/a
10	CCNT2	chr1:180023071-180023396	K562	blood:	n/a	n/a
11	CEBPB	chr1:180023140-180023488	Hela-S3	cervix:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
12	CEBPB	chr1:180023156-180023475	A549	lung:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
13	CEBPB	chr1:180028937-180029135	K562	blood:	n/a	chr1:180029030-180029041
14	CEBPB	chr1:180023128-180023461	HepG2	liver:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
15	CEBPB	chr1:180023126-180023490	K562	blood:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
16	CEBPB	chr1:180027022-180027346	K562	blood:	n/a	n/a
17	CEBPB	chr1:180025022-180025218	K562	blood:	n/a	n/a
18	CEBPB	chr1:180023121-180023491	IMR90	lung:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
19	CEBPB	chr1:180028940-180029169	A549	lung:	n/a	chr1:180029030-180029041
20	CEBPB	chr1:180012982-180013252	K562	blood:	n/a	n/a
21	CEBPB	chr1:180023086-180023473	K562	blood:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
22	CEBPB	chr1:180023114-180023449	K562	blood:	n/a	chr1:180023303-180023316 chr1:180023303-180023316 chr1:180023304-180023315
23	CEBPB	chr1:180012065-180012825	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:180028988-180029094	HepG2	liver:	n/a	chr1:180029030-180029041
25	CTCF	chr1:180034244-180034310	GM20000	blood:	n/a	n/a
26	CTCF	chr1:180012100-180012250	BJ	skin:	n/a	n/a
27	CTCF	chr1:180040498-180040526	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr1:180012180-180012330	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr1:180021878-180021958	Lung_OC	lung:	n/a	n/a
30	CTCF	chr1:180024717-180024789	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr1:180001231-180001311	GM20000	blood:	n/a	n/a
32	CTCF	chr1:180000000-180000150	GM06990	blood:	n/a	n/a
33	CTCF	chr1:180018100-180018250	HRPEpiC	eye:	n/a	n/a
34	CUX1	chr1:180022371-180022382	K562	blood:	n/a	n/a
35	CUX1	chr1:180027777-180027935	K562	blood:	n/a	n/a
36	CUX1	chr1:180030128-180030479	K562	blood:	n/a	n/a
37	CUX1	chr1:180023009-180023416	K562	blood:	n/a	n/a
38	E2F4	chr1:180020331-180020476	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr1:180010342-180010537	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr1:180009233-180009578	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr1:180012304-180012729	MCF10A-Er-Src	breast:	n/a	n/a
42	EBF1	chr1:180026801-180027132	GM12878	blood:	n/a	chr1:180026944-180026955
43	ELF1	chr1:180026938-180027323	K562	blood:	n/a	n/a
44	ELK1	chr1:180027046-180027370	K562	blood:	n/a	n/a
45	EP300	chr1:180002044-180002057	K562	blood:	n/a	n/a
46	EP300	chr1:180026915-180027657	K562	blood:	n/a	n/a
47	EP300	chr1:180022902-180023533	K562	blood:	n/a	chr1:180023301-180023315
48	ESR1	chr1:180009268-180009568	ECC-1	luminal epithelium:	n/a	chr1:180009433-180009450 chr1:180009434-180009451 chr1:180009434-180009449
49	ESR1	chr1:180009282-180009523	ECC-1	luminal epithelium:	n/a	chr1:180009433-180009450 chr1:180009434-180009451 chr1:180009434-180009449
50	ESRRA	chr1:180031105-180032118	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:180012272-180012322	AG09309	skin:	n/a
2	chr1:180012272-180012322	HCPEpiC	choroid plexus:	n/a
3	chr1:180012272-180012322	PrEC	prostate:	n/a
4	chr1:180012272-180012322	K562	blood:	n/a
5	chr1:180012272-180012322	AG09319	gingival:	n/a
6	chr1:180012272-180012322	Hepatocyte	liver:	n/a
7	chr1:180012272-180012322	HNPCEpiC	eye:	n/a
8	chr1:180012272-180012322	NHDF-neo	bronchial:	n/a
9	chr1:180012272-180012322	HepG2	liver:	n/a
10	chr1:180012272-180012322	NH-A	brain:	n/a
11	chr1:180012272-180012322	SAEC	small airway:	n/a
12	chr1:180012272-180012322	SK-N-SH	brain:	n/a
13	chr1:180012272-180012322	RPTEC	kidney:	n/a
14	chr1:180012272-180012322	GM12878	blood:	n/a
15	chr1:180012272-180012322	HL-60	blood:	n/a
16	chr1:180012272-180012322	HCF	heart:	n/a
17	chr1:180012272-180012322	HRE	kidney:	n/a
18	chr1:180012272-180012322	AG04450	lung:	fetal
19	chr1:180012272-180012322	HCT-116	colon:	n/a
20	chr1:180012272-180012322	HEEpiC	esophagus:	n/a
21	chr1:180012272-180012322	ECC-1	luminal epithelium:	n/a
22	chr1:180012272-180012322	MCF-7	breast:	n/a
23	chr1:180012272-180012322	HRCEpiC	kidney:	n/a
24	chr1:180012272-180012322	CMK	blood:	n/a
25	chr1:180012272-180012322	SK-N-SH_RA	brain:	n/a
26	chr1:180012272-180012322	HMEC	breast:	n/a
27	chr1:180012272-180012322	HEK293	kidney:	embryo
28	chr1:180012272-180012322	HCM	heart:	n/a
29	chr1:180012272-180012322	SKMC	muscle:	n/a
30	chr1:180012272-180012322	NT2-D1	testis:	n/a
31	chr1:180012272-180012322	U87	brain:	n/a
32	chr1:180012272-180012322	NB4	blood:	n/a
33	chr1:180012272-180012322	HRPEpiC	eye:	n/a
34	chr1:180012272-180012322	ProgFib	skin:	n/a
35	chr1:180012272-180012322	BE2_C	brain:	n/a
36	chr1:180012272-180012322	H1-hESC	embryonic stem cell:	embryo
37	chr1:180012272-180012322	IMR90	lung:	fetal
38	chr1:180012272-180012322	ovcar-3	ovarian:	n/a
39	chr1:180012272-180012322	HIPEpiC	eye:	n/a
40	chr1:180012272-180012322	BJ	skin:	n/a
41	chr1:180012272-180012322	MCF10A-Er-Src	breast:	n/a
42	chr1:180012272-180012322	SK-N-MC	brain:	n/a
43	chr1:180012272-180012322	HPAEpiC	pulmonary alveolar:	n/a
44	chr1:180012272-180012322	NHBE	bronchial:	n/a
45	chr1:180012272-180012322	Jurkat	blood:	n/a
46	chr1:180012272-180012322	A549	lung:	n/a
47	chr1:180012272-180012322	GM06990	blood:	n/a
48	chr1:180012272-180012322	HAEpiC	amniotic membrane:	n/a
49	chr1:180012272-180012322	Caco-2	colon:	n/a
50	chr1:180012272-180012322	AoSMC	blood vessel:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:180039217..180042128-chr1:180125172..180126963,2	K562	blood:
2	chr1:179851411..179853011-chr1:180019045..180021728,2	MCF-7	breast:
3	chr1:179921867..179924634-chr1:180042656..180044466,2	MCF-7	breast:
4	chr1:180029884..180031484-chr1:180035395..180037562,2	MCF-7	breast:
5	chr1:179980682..179985119-chr1:179997024..179999746,4	MCF-7	breast:
6	chr1:179998094..180000667-chr1:180001189..180004534,3	MCF-7	breast:
7	chr1:180023147..180025587-chr1:180027128..180029217,2	K562	blood:
8	chr1:180012692..180014319-chr1:180015730..180017884,2	MCF-7	breast:
9	chr1:180009796..180012302-chr1:180015081..180016602,2	MCF-7	breast:
10	chr1:179992324..179995143-chr1:180001757..180004164,2	K562	blood:
11	chr1:180002453..180005081-chr1:180006068..180008636,2	K562	blood:
12	chr1:179998094..180000667-chr1:180001189..180004534,3	MCF-7	breast:
13	chr1:180010589..180013566-chr1:180015108..180016921,2	K562	blood:
14	chr1:180010544..180012138-chr1:180019393..180021137,2	K562	blood:
15	chr1:179994934..179997849-chr1:180033158..180035390,2	MCF-7	breast:
16	chr1:180006459..180008150-chr1:180010486..180012796,2	K562	blood:
17	chr1:180012630..180014181-chr1:180020336..180022043,2	K562	blood:
18	chr1:180011191..180012914-chr1:180032634..180034568,2	K562	blood:
19	chr1:179850167..179851805-chr1:180029319..180031564,2	MCF-7	breast:
20	chr1:180007479..180009332-chr1:180027865..180030769,2	K562	blood:
21	chr1:179988661..179990796-chr1:179997546..179999054,2	K562	blood:
22	chr1:179922873..179925365-chr1:180021771..180024501,3	K562	blood:
23	chr1:179980840..179982638-chr1:180011899..180013783,2	K562	blood:
24	chr1:180004347..180006390-chr1:180011468..180013460,2	K562	blood:
25	chr1:180003860..180005800-chr1:180007847..180009537,2	MCF-7	breast:
26	chr1:180004656..180007316-chr1:180009330..180011103,2	MCF-7	breast:
27	chr1:179850606..179853026-chr1:180024273..180027735,3	K562	blood:
28	chr1:179998356..180000949-chr1:180019994..180021642,2	K562	blood:
29	chr1:179849600..179851970-chr1:180040830..180043217,3	K562	blood:
30	chr1:180002453..180005081-chr1:180006068..180008636,2	K562	blood:
31	chr1:179998356..180000949-chr1:180019994..180021642,2	K562	blood:
32	chr1:179849763..179851404-chr1:180027993..180029985,2	K562	blood:
33	chr1:180006151..180007933-chr1:180048877..180051826,2	K562	blood:
34	chr1:180009163..180012089-chr1:180014307..180016921,2	K562	blood:
35	chr1:179845496..179847681-chr1:180038078..180039850,2	MCF-7	breast:
36	chr1:179999019..180000801-chr1:180002803..180004316,2	K562	blood:
37	chr1:180029884..180031484-chr1:180035395..180037562,2	MCF-7	breast:
38	chr1:179850260..179852147-chr1:180011341..180013974,3	MCF-7	breast:
39	chr1:180037925..180040895-chr1:180041327..180043186,2	K562	blood:
40	chr1:180012692..180014319-chr1:180015730..180017884,2	MCF-7	breast:
41	chr1:179850786..179852448-chr1:180017093..180019020,2	MCF-7	breast:
42	chr1:180023147..180025587-chr1:180027128..180029217,2	K562	blood:
43	chr1:180004347..180006390-chr1:180011468..180013460,2	K562	blood:
44	chr1:180009514..180012969-chr1:180025548..180028168,4	MCF-7	breast:
45	chr1:180039738..180042199-chr1:180043828..180046612,2	K562	blood:
46	chr1:179997127..180001716-chr1:180009044..180014069,5	MCF-7	breast:
47	chr1:179833882..179836832-chr1:180042170..180044941,2	K562	blood:
48	chr1:180032822..180035460-chr1:180037133..180039107,2	K562	blood:
49	chr1:179999019..180000801-chr1:180002803..180004316,2	K562	blood:
50	chr1:179850172..179852530-chr1:180041069..180043217,2	K562	blood:

No data

Variant related genes	Relation type
CEP350	TF binding region
CEP350	CpG island
ENSG00000135837	chromatin interactions
ENSG00000258664	chromatin interactions
ENSG00000260360	chromatin interactions
ENSG00000143337	chromatin interactions
ENSG00000169905	chromatin interactions
ENSG00000272906	chromatin interactions

Extended variants
information (count: 1552 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1552 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559555792	chr1:179998865-179998866	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs58590137	chr1:179998899-179998900	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190266604	chr1:179998940-179998941	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548367681	chr1:179998966-179998967	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs567688541	chr1:179998995-179998996	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567815379	chr1:179998999-179999000	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs143795875	chr1:179999078-179999079	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs181764876	chr1:179999150-179999151	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs550958391	chr1:179999162-179999163	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs570654852	chr1:179999166-179999167	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547703386	chr1:179999173-179999174	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs7538086	chr1:179999203-179999204	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs546792894	chr1:179999279-179999280	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs147246679	chr1:179999340-179999341	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs66494388	chr1:179999349-179999350	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs35905506	chr1:179999350-179999351	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs112078652	chr1:179999355-179999356	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs535659880	chr1:179999364-179999365	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs530408951	chr1:179999365-179999366	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs555127285	chr1:179999376-179999377	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs201156984	chr1:179999415-179999416	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs575298801	chr1:179999444-179999445	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537438650	chr1:179999445-179999446	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs371007302	chr1:179999452-179999453	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201470072	chr1:179999454-179999455	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557774318	chr1:179999459-179999460	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577105199	chr1:179999461-179999462	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs199992801	chr1:179999464-179999465	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs12123402	chr1:179999470-179999471	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs546116835	chr1:179999475-179999476	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200903915	chr1:179999478-179999479	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553274314	chr1:179999490-179999491	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs4651054	chr1:179999512-179999513	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs542420769	chr1:179999525-179999526	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs35042506	chr1:179999574-179999575	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs186343605	chr1:179999618-179999619	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs531082941	chr1:179999632-179999633	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs34466397	chr1:179999645-179999646	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs544273462	chr1:179999759-179999760	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs368089860	chr1:179999765-179999766	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs570255357	chr1:179999828-179999829	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs12124265	chr1:179999848-179999849	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs200640950	chr1:179999867-179999868	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs77876859	chr1:179999909-179999910	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs529031518	chr1:179999940-179999941	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs16855144	chr1:179999978-179999979	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs561460159	chr1:180000044-180000045	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs568849317	chr1:180000048-180000049	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs79593922	chr1:180000071-180000072	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs557447679	chr1:180000096-180000097	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	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
Glioblastoma multiforme	21080181	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
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
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	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
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1373 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179941400-180031800	Weak transcription	Spleen	Spleen
2	chr1:179964000-180014200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:179965800-180013200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr1:179970800-180076800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr1:179973000-180010800	Weak transcription	Psoas Muscle	Psoas
6	chr1:179976200-180063600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr1:179979400-179999600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:179979600-180002000	Strong transcription	Fetal Intestine Large	intestine
9	chr1:179979800-179999000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr1:179979800-179999400	Strong transcription	Fetal Thymus	thymus
11	chr1:179979800-180008400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr1:179980200-180007800	Strong transcription	Primary B cells from cord blood	blood
13	chr1:179980400-180027400	Strong transcription	Dnd41	blood
14	chr1:179980600-179999000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:179980600-179999200	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr1:179980600-179999800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr1:179980600-180008000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:179981000-180027200	Strong transcription	Primary B cells from peripheral blood	blood
19	chr1:179981000-180059000	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr1:179981600-180012000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr1:179982400-179999000	Strong transcription	Skeletal Muscle Female	skeletal muscle
22	chr1:179983000-179999000	Strong transcription	Primary T cells from cord blood	blood
23	chr1:179983600-180083400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr1:179985600-180024800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr1:179989000-180000000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr1:179989000-180008800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
27	chr1:179989200-179999800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr1:179989800-180034200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr1:179990000-180010200	Weak transcription	NHEK	skin
30	chr1:179990000-180012000	Weak transcription	Gastric	stomach
31	chr1:179990000-180012200	Weak transcription	Stomach Mucosa	stomach
32	chr1:179990000-180025600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr1:179990200-180025400	Weak transcription	Pancreas	Pancrea
34	chr1:179990600-180002600	Weak transcription	A549	lung
35	chr1:179990800-180003600	Weak transcription	Small Intestine	intestine
36	chr1:179992400-180001000	Weak transcription	Left Ventricle	heart
37	chr1:179992400-180009200	Weak transcription	Brain Cingulate Gyrus	brain
38	chr1:179992400-180009200	Weak transcription	HMEC	breast
39	chr1:179992400-180012000	Weak transcription	Right Ventricle	heart
40	chr1:179992400-180031400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:179992400-180032200	Weak transcription	Esophagus	oesophagus
42	chr1:179992600-180000800	Weak transcription	HepG2	liver
43	chr1:179992600-180010800	Weak transcription	Colonic Mucosa	Colon
44	chr1:179993000-180010000	Weak transcription	Fetal Brain Male	brain
45	chr1:179993200-180002800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr1:179993800-180000800	Weak transcription	Fetal Kidney	kidney
47	chr1:179993800-180005000	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr1:179993800-180010800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr1:179994000-180005400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr1:179995000-180000600	Weak transcription	Placenta Amnion	Placenta Amnion

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