Variant report

Variant	esv2761235
Chromosome Location	chr8:102613079-102646059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:668)
CpG islands
(count:61)
Chromatin interactive
region (count:93)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:102619918-102620510	HepG2	liver:	n/a	n/a
2	ATF3	chr8:102620079-102620601	A549	lung:	n/a	n/a
3	ATF3	chr8:102619754-102620604	A549	lung:	n/a	n/a
4	BCL3	chr8:102619265-102620729	A549	lung:	n/a	chr8:102620177-102620186
5	BCL3	chr8:102619891-102620734	A549	lung:	n/a	chr8:102620177-102620186
6	BHLHE40	chr8:102644773-102645032	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:102615523-102616317	MCF-7	breast:	n/a	n/a
8	CEBPB	chr8:102616564-102616747	A549	lung:	n/a	n/a
9	CEBPB	chr8:102619509-102620862	MCF-7	breast:	n/a	chr8:102620365-102620376
10	CEBPB	chr8:102616447-102616733	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr8:102644642-102645260	MCF-7	breast:	n/a	n/a
12	CEBPB	chr8:102620184-102620532	HepG2	liver:	n/a	chr8:102620365-102620376
13	CEBPB	chr8:102644779-102645176	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr8:102644779-102645149	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:102644744-102645484	K562	blood:	n/a	n/a
16	CEBPB	chr8:102644772-102645151	A549	lung:	n/a	n/a
17	CEBPB	chr8:102644778-102645105	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:102619871-102620847	HCT-116	colon:	n/a	chr8:102620365-102620376
19	CEBPB	chr8:102644739-102645189	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr8:102644728-102645205	A549	lung:	n/a	n/a
21	CEBPB	chr8:102620185-102620496	IMR90	lung:	n/a	chr8:102620365-102620376
22	CEBPB	chr8:102644511-102645295	HCT-116	colon:	n/a	n/a
23	CEBPB	chr8:102619387-102620819	MCF-7	breast:	n/a	chr8:102620365-102620376
24	CEBPB	chr8:102619737-102620895	A549	lung:	n/a	chr8:102620365-102620376
25	CEBPB	chr8:102619866-102620654	A549	lung:	n/a	chr8:102620365-102620376
26	CEBPB	chr8:102644814-102645095	K562	blood:	n/a	n/a
27	CEBPB	chr8:102644778-102645130	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr8:102644649-102645342	MCF-7	breast:	n/a	n/a
29	CEBPB	chr8:102620106-102620590	ECC-1	luminal epithelium:	n/a	chr8:102620365-102620376
30	CEBPB	chr8:102615742-102616278	MCF-7	breast:	n/a	n/a
31	CEBPB	chr8:102620125-102620511	ECC-1	luminal epithelium:	n/a	chr8:102620365-102620376
32	CEBPB	chr8:102644742-102645161	K562	blood:	n/a	n/a
33	CEBPB	chr8:102644621-102645229	HCT-116	colon:	n/a	n/a
34	CEBPB	chr8:102644658-102645311	A549	lung:	n/a	n/a
35	CEBPB	chr8:102620103-102620599	Hela-S3	cervix:	n/a	chr8:102620365-102620376
36	CEBPB	chr8:102644774-102645157	IMR90	lung:	n/a	n/a
37	CEBPB	chr8:102619848-102620564	A549	lung:	n/a	chr8:102620365-102620376
38	CEBPB	chr8:102644774-102645158	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr8:102644840-102644990	GM12878	blood:	n/a	chr8:102644914-102644935 chr8:102644920-102644936 chr8:102644919-102644937
40	CTCF	chr8:102635868-102635884	GM10248	blood:	n/a	n/a
41	CTCF	chr8:102644815-102645056	LNCaP	prostate:	n/a	chr8:102644914-102644935 chr8:102644920-102644936 chr8:102644919-102644937
42	CTCF	chr8:102644800-102645086	Pancreas_OC	pancreas:	n/a	chr8:102644914-102644935 chr8:102644920-102644936 chr8:102644919-102644937
43	CTCF	chr8:102644845-102645048	LNCaP	prostate:	n/a	chr8:102644914-102644935 chr8:102644920-102644936 chr8:102644919-102644937
44	CTCF	chr8:102644654-102645149	HepG2	liver:	n/a	chr8:102644914-102644935 chr8:102644920-102644936 chr8:102644919-102644937
45	CTCF	chr8:102644860-102645010	HEEpiC	esophagus:	n/a	chr8:102644914-102644935 chr8:102644920-102644936 chr8:102644919-102644937
46	CTCF	chr8:102644769-102645073	HepG2	liver:	n/a	chr8:102644914-102644935 chr8:102644920-102644936 chr8:102644919-102644937
47	CTCF	chr8:102644919-102644927	GM19238	blood:	n/a	n/a
48	CTCF	chr8:102644820-102644970	HCT-116	colon:	n/a	chr8:102644914-102644935 chr8:102644920-102644936 chr8:102644919-102644937
49	CTCF	chr8:102644800-102645062	GM10266	blood:	n/a	chr8:102644914-102644935 chr8:102644920-102644936 chr8:102644919-102644937
50	CTCF	chr8:102644759-102645129	A549	lung:	n/a	chr8:102644914-102644935 chr8:102644920-102644936 chr8:102644919-102644937

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:102613838-102613888	NHBE	bronchial:	n/a
2	chr8:102613838-102613888	GM06990	blood:	n/a
3	chr8:102613838-102613888	HCT-116	colon:	n/a
4	chr8:102613838-102613888	Hela-S3	cervix:	n/a
5	chr8:102613838-102613888	PANC-1	pancreas:	n/a
6	chr8:102613838-102613888	AG10803	skin:	n/a
7	chr8:102613838-102613888	MCF-7	breast:	n/a
8	chr8:102613838-102613888	BJ	skin:	n/a
9	chr8:102613838-102613888	Hepatocyte	liver:	n/a
10	chr8:102613838-102613888	Caco-2	colon:	n/a
11	chr8:102613838-102613888	SAEC	small airway:	n/a
12	chr8:102613838-102613888	HIPEpiC	eye:	n/a
13	chr8:102613838-102613888	HAEpiC	amniotic membrane:	n/a
14	chr8:102613838-102613888	HUVEC	blood vessel:	n/a
15	chr8:102613838-102613888	CMK	blood:	n/a
16	chr8:102613838-102613888	GM19239	blood:	n/a
17	chr8:102613838-102613888	HNPCEpiC	eye:	n/a
18	chr8:102613838-102613888	ovcar-3	ovarian:	n/a
19	chr8:102613838-102613888	A549	lung:	n/a
20	chr8:102613838-102613888	AG09319	gingival:	n/a
21	chr8:102613838-102613888	K562	blood:	n/a
22	chr8:102613838-102613888	NT2-D1	testis:	n/a
23	chr8:102613838-102613888	HepG2	liver:	n/a
24	chr8:102613838-102613888	AG09309	skin:	n/a
25	chr8:102613838-102613888	IMR90	lung:	fetal
26	chr8:102613838-102613888	HEK293	kidney:	embryo
27	chr8:102613838-102613888	ProgFib	skin:	n/a
28	chr8:102613838-102613888	HRPEpiC	eye:	n/a
29	chr8:102613838-102613888	GM12892	blood:	n/a
30	chr8:102613838-102613888	HL-60	blood:	n/a
31	chr8:102613838-102613888	BE2_C	brain:	n/a
32	chr8:102613838-102613888	HCPEpiC	choroid plexus:	n/a
33	chr8:102613838-102613888	RPTEC	kidney:	n/a
34	chr8:102613838-102613888	AG04449	skin:	fetal
35	chr8:102613838-102613888	SK-N-MC	brain:	n/a
36	chr8:102613838-102613888	SKMC	muscle:	n/a
37	chr8:102613838-102613888	AG04450	lung:	fetal
38	chr8:102613838-102613888	HRE	kidney:	n/a
39	chr8:102613838-102613888	HCF	heart:	n/a
40	chr8:102613838-102613888	HEEpiC	esophagus:	n/a
41	chr8:102613838-102613888	HPAEpiC	pulmonary alveolar:	n/a
42	chr8:102613838-102613888	LNCaP	prostate:	n/a
43	chr8:102613838-102613888	U87	brain:	n/a
44	chr8:102613838-102613888	Jurkat	blood:	n/a
45	chr8:102613838-102613888	PFSK-1	brain:	n/a
46	chr8:102613838-102613888	SK-N-SH	brain:	n/a
47	chr8:102613838-102613888	NB4	blood:	n/a
48	chr8:102613838-102613888	HRCEpiC	kidney:	n/a
49	chr8:102613838-102613888	NHDF-neo	bronchial:	n/a
50	chr8:102613838-102613888	SK-N-SH_RA	brain:	n/a

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:102612038..102613685-chr8:102646133..102647980,2	MCF-7	breast:
2	chr8:102579608..102581495-chr8:102645973..102648635,2	MCF-7	breast:
3	chr8:102584389..102586925-chr8:102611656..102613755,2	MCF-7	breast:
4	chr8:102619068..102621889-chr8:103209199..103211504,2	MCF-7	breast:
5	chr8:102577206..102577740-chr8:102644735..102645456,2	MCF-7	breast:
6	chr8:102614548..102616839-chr8:102636990..102639158,2	K562	blood:
7	chr8:102619314..102627249-chr8:102640943..102646440,7	MCF-7	breast:
8	chr8:102478978..102481456-chr8:102614668..102616210,2	MCF-7	breast:
9	chr8:102503909..102508497-chr8:102637267..102642010,6	MCF-7	breast:
10	chr8:102576342..102577944-chr8:102615348..102618284,2	MCF-7	breast:
11	chr8:102577611..102578416-chr8:102644647..102645261,2	MCF-7	breast:
12	chr8:102557068..102559432-chr8:102644756..102646494,2	MCF-7	breast:
13	chr8:102619702..102621730-chr8:103818248..103820356,2	MCF-7	breast:
14	chr8:102553740..102555578-chr8:102612921..102614753,2	MCF-7	breast:
15	chr8:102447454..102450323-chr8:102645181..102647136,2	MCF-7	breast:
16	chr8:102446688..102449567-chr8:102612575..102615399,2	MCF-7	breast:
17	chr8:102338951..102340127-chr8:102644504..102645388,3	K562	blood:
18	chr8:102344261..102346988-chr8:102617766..102619760,2	MCF-7	breast:
19	chr8:102618432..102620239-chr8:103613397..103615204,2	MCF-7	breast:
20	chr8:102517484..102520449-chr8:102641469..102644392,2	MCF-7	breast:
21	chr8:102481107..102483505-chr8:102620149..102622971,2	MCF-7	breast:
22	chr8:102591202..102591897-chr8:102618452..102619177,2	MCF-7	breast:
23	chr8:102617550..102620194-chr8:102645723..102647723,2	MCF-7	breast:
24	chr8:102599624..102601949-chr8:102615535..102617652,3	MCF-7	breast:
25	chr8:102611534..102613191-chr8:102616243..102617957,2	K562	blood:
26	chr8:102371583..102375357-chr8:102617580..102619595,4	MCF-7	breast:
27	chr8:102539558..102541965-chr8:102618200..102620922,2	MCF-7	breast:
28	chr8:102624784..102626996-chr8:102628052..102630610,2	MCF-7	breast:
29	chr8:102448412..102450698-chr8:102617075..102619900,3	MCF-7	breast:
30	chr8:102618309..102622005-chr8:102635683..102639742,4	MCF-7	breast:
31	chr8:102570444..102572768-chr8:102615878..102617763,2	MCF-7	breast:
32	chr8:102503148..102509288-chr8:102639386..102649682,19	MCF-7	breast:
33	chr8:102618200..102620350-chr8:102623909..102626355,2	K562	blood:
34	chr8:102590604..102593500-chr8:102619061..102620861,2	MCF-7	breast:
35	chr8:102611534..102613191-chr8:102616243..102617957,2	K562	blood:
36	chr8:102613840..102615756-chr8:102643274..102644834,2	MCF-7	breast:
37	chr8:102503101..102510814-chr8:102611042..102623761,44	MCF-7	breast:
38	chr8:102607733..102610045-chr8:102616611..102619932,3	MCF-7	breast:
39	chr8:102504779..102507162-chr8:102627473..102630274,3	MCF-7	breast:
40	chr8:102617550..102620194-chr8:102645723..102647723,2	MCF-7	breast:
41	chr8:102503334..102507333-chr8:102630459..102637316,8	MCF-7	breast:
42	chr8:102588119..102597900-chr8:102614552..102624670,18	MCF-7	breast:
43	chr8:102525449..102527790-chr8:102621194..102623795,2	MCF-7	breast:
44	chr8:102618937..102621907-chr8:102637698..102639886,2	MCF-7	breast:
45	chr8:102626664..102629265-chr8:102631491..102634297,2	MCF-7	breast:
46	chr8:102630738..102634360-chr8:102636671..102639236,3	MCF-7	breast:
47	chr8:102631475..102633589-chr8:102642485..102645272,3	MCF-7	breast:
48	chr8:102618200..102620350-chr8:102623909..102626355,2	K562	blood:
49	chr8:102624784..102626996-chr8:102628052..102630610,2	MCF-7	breast:
50	chr8:102594059..102599317-chr8:102614223..102621570,11	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KB-1980E6.3.1-9	chr8:102633033-102633418	NONHSAT128066

No data

Variant related genes	Relation type
GRHL2	TF binding region
GRHL2	CpG island
ENSG00000228224	chromatin interactions
ENSG00000253320	chromatin interactions
ENSG00000253669	chromatin interactions
ENSG00000155096	chromatin interactions
ENSG00000254957	chromatin interactions
ENSG00000258701	chromatin interactions
ENSG00000253991	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000155090	chromatin interactions
ENSG00000120963	chromatin interactions
ENSG00000254024	chromatin interactions

Extended variants
information (count: 1298 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1298 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs118182005	chr8:102613096-102613097	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs567328481	chr8:102613110-102613111	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs2470625	chr8:102613145-102613146	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs7816116	chr8:102613152-102613153	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs531988044	chr8:102613255-102613256	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs550613593	chr8:102613262-102613263	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs544727048	chr8:102613306-102613307	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs569159888	chr8:102613323-102613324	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs149513784	chr8:102613388-102613389	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs34987085	chr8:102613389-102613390	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs201631357	chr8:102613404-102613405	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs374021936	chr8:102613416-102613417	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs57471873	chr8:102613417-102613418	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs200432210	chr8:102613418-102613419	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs140404462	chr8:102613437-102613438	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs199927254	chr8:102613440-102613441	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs5010126	chr8:102613443-102613444	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs372708190	chr8:102613446-102613447	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs559180488	chr8:102613475-102613476	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs558753744	chr8:102613476-102613477	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs149472075	chr8:102613504-102613505	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs540995508	chr8:102613508-102613509	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs375896472	chr8:102613510-102613511	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs187127011	chr8:102613519-102613520	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs35257717	chr8:102613550-102613551	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs35890104	chr8:102613554-102613555	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs9649995	chr8:102613555-102613556	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs35001063	chr8:102613590-102613591	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs374221991	chr8:102613624-102613625	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs535784902	chr8:102613689-102613690	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs568230595	chr8:102613733-102613734	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs4734544	chr8:102613747-102613748	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs572503230	chr8:102613817-102613818	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs4734545	chr8:102613928-102613929	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs564797073	chr8:102614029-102614030	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs576908600	chr8:102614046-102614047	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs188259334	chr8:102614100-102614101	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs114422462	chr8:102614176-102614177	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs531518672	chr8:102614214-102614215	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs376264197	chr8:102614235-102614236	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs145870078	chr8:102614243-102614244	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs138767136	chr8:102614282-102614283	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs143194228	chr8:102614355-102614356	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs527459279	chr8:102614402-102614403	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs180925098	chr8:102614404-102614405	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs370960059	chr8:102614421-102614422	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs7821380	chr8:102614434-102614435	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs147518461	chr8:102614490-102614491	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs4734546	chr8:102614570-102614571	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs148579263	chr8:102614598-102614599	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Oral squamous cell carcinoma	21853135	CNVD

Chromatin state (count:580 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:102552200-102620600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:102590600-102631600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr8:102590600-102635200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:102596000-102615000	Weak transcription	Stomach Mucosa	stomach
5	chr8:102597400-102616000	Weak transcription	Gastric	stomach
6	chr8:102597400-102620600	Weak transcription	Colonic Mucosa	Colon
7	chr8:102600600-102619200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr8:102601600-102616200	Weak transcription	Fetal Kidney	kidney
9	chr8:102604000-102614600	Weak transcription	Fetal Lung	lung
10	chr8:102607000-102616600	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr8:102607800-102617000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr8:102609200-102616000	Weak transcription	Rectal Smooth Muscle	rectum
13	chr8:102609800-102614400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr8:102611000-102613800	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr8:102611200-102613400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr8:102611400-102613200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:102611400-102613400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:102611400-102613600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:102611400-102613800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr8:102611600-102613200	Strong transcription	Fetal Intestine Small	intestine
21	chr8:102611600-102617200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr8:102612200-102613200	Strong transcription	Fetal Stomach	stomach
23	chr8:102612200-102613400	Enhancers	Placenta	Placenta
24	chr8:102612200-102613600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr8:102612400-102613200	Enhancers	Osteobl	bone
26	chr8:102612400-102613800	Enhancers	NHDF-Ad	bronchial
27	chr8:102612400-102614400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:102612600-102613200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr8:102612600-102613200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr8:102612600-102613200	Genic enhancers	Esophagus	oesophagus
31	chr8:102612600-102613400	Enhancers	Adipose Nuclei	Adipose
32	chr8:102612600-102613800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr8:102612600-102615000	Weak transcription	Fetal Brain Male	brain
34	chr8:102612800-102613200	Enhancers	Lung	lung
35	chr8:102612800-102614600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr8:102612800-102614600	Weak transcription	NHEK	skin
37	chr8:102612800-102615000	Weak transcription	Right Atrium	heart
38	chr8:102612800-102615800	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr8:102612800-102616600	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr8:102612800-102617000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:102612800-102617600	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr8:102612800-102623000	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr8:102613000-102614000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:102613000-102615000	Weak transcription	HMEC	breast
45	chr8:102613000-102615800	Weak transcription	Duodenum Mucosa	Duodenum
46	chr8:102613000-102615800	Weak transcription	Fetal Intestine Large	intestine
47	chr8:102613000-102616000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr8:102613000-102617000	Enhancers	Placenta Amnion	Placenta Amnion
49	chr8:102613000-102618800	Weak transcription	Pancreas	Pancrea
50	chr8:102613200-102614800	Weak transcription	Esophagus	oesophagus

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