Variant report

Variant	nsv831406
Chromosome Location	chr8:99290745-99482076
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2802)
CpG islands
(count:2014)
Chromatin interactive
region (count:262)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2802 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:99318447-99318946	K562	blood:	n/a	n/a
2	ARID3A	chr8:99296511-99296921	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:99309919-99310400	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:99304085-99304477	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:99305347-99305832	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:99345262-99345528	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:99317168-99317874	K562	blood:	n/a	n/a
8	ARID3A	chr8:99466364-99466850	K562	blood:	n/a	n/a
9	ATF1	chr8:99375083-99375259	K562	blood:	n/a	n/a
10	ATF1	chr8:99318425-99318905	K562	blood:	n/a	n/a
11	ATF1	chr8:99317209-99317499	K562	blood:	n/a	n/a
12	ATF1	chr8:99466349-99466891	K562	blood:	n/a	n/a
13	ATF2	chr8:99376914-99377730	GM12878	blood:	n/a	n/a
14	ATF2	chr8:99316992-99317543	GM12878	blood:	n/a	n/a
15	ATF2	chr8:99377855-99378410	GM12878	blood:	n/a	n/a
16	ATF2	chr8:99376915-99377605	GM12878	blood:	n/a	n/a
17	ATF2	chr8:99377908-99378435	GM12878	blood:	n/a	n/a
18	ATF3	chr8:99357521-99357923	K562	blood:	n/a	n/a
19	BACH1	chr8:99305713-99305714	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr8:99439984-99440418	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr8:99397084-99397324	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr8:99439051-99439621	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr8:99334068-99334382	GM12878	blood:	n/a	n/a
24	BATF	chr8:99305384-99305611	GM12878	blood:	n/a	n/a
25	BATF	chr8:99377975-99378323	GM12878	blood:	n/a	chr8:99378143-99378154
26	BATF	chr8:99376997-99377586	GM12878	blood:	n/a	n/a
27	BATF	chr8:99316993-99317510	GM12878	blood:	n/a	n/a
28	BATF	chr8:99334028-99334316	GM12878	blood:	n/a	n/a
29	BATF	chr8:99317010-99317392	GM12878	blood:	n/a	n/a
30	BATF	chr8:99378004-99378312	GM12878	blood:	n/a	chr8:99378143-99378154
31	BATF	chr8:99376867-99377630	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:99334017-99334332	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:99377025-99377493	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:99377968-99378392	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:99479549-99479778	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:99376932-99377581	GM12878	blood:	n/a	n/a
37	BCL3	chr8:99376993-99377707	GM12878	blood:	n/a	n/a
38	BCL3	chr8:99377033-99377508	GM12878	blood:	n/a	n/a
39	BCLAF1	chr8:99376828-99377573	GM12878	blood:	n/a	n/a
40	BHLHE40	chr8:99439044-99439255	K562	blood:	n/a	chr8:99439120-99439136 chr8:99439119-99439135
41	BHLHE40	chr8:99370333-99370664	K562	blood:	n/a	n/a
42	BHLHE40	chr8:99317001-99317352	GM12878	blood:	n/a	n/a
43	BHLHE40	chr8:99317077-99317487	K562	blood:	n/a	n/a
44	BHLHE40	chr8:99396006-99396013	K562	blood:	n/a	n/a
45	BHLHE40	chr8:99439105-99439256	GM12878	blood:	n/a	chr8:99439120-99439136 chr8:99439119-99439135
46	BHLHE40	chr8:99466456-99466833	K562	blood:	n/a	n/a
47	BHLHE40	chr8:99318090-99319115	K562	blood:	n/a	n/a
48	BHLHE40	chr8:99376849-99377602	GM12878	blood:	n/a	n/a
49	BHLHE40	chr8:99394844-99395637	K562	blood:	n/a	chr8:99395138-99395154
50	BHLHE40	chr8:99318751-99319048	HepG2	liver:	n/a	n/a

(count:2014 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:99306718-99306768	HepG2	liver:	n/a
2	chr8:99306718-99306768	HepG2	liver:	n/a
3	chr8:99441950-99442000	HCPEpiC	choroid plexus:	n/a
4	chr8:99435204-99435254	T-47D	breast:	n/a
5	chr8:99441950-99442000	CMK	blood:	n/a
6	chr8:99380162-99380212	BE2_C	brain:	n/a
7	chr8:99442883-99442933	HAEpiC	amniotic membrane:	n/a
8	chr8:99305661-99305711	HL-60	blood:	n/a
9	chr8:99306725-99306775	LNCaP	prostate:	n/a
10	chr8:99440522-99440572	AoSMC	blood vessel:	n/a
11	chr8:99306718-99306768	NH-A	brain:	n/a
12	chr8:99306718-99306768	AoSMC	blood vessel:	n/a
13	chr8:99441950-99442000	HNPCEpiC	eye:	n/a
14	chr8:99440331-99440381	GM19239	blood:	n/a
15	chr8:99439441-99439491	IMR90	lung:	fetal
16	chr8:99310335-99310385	HRPEpiC	eye:	n/a
17	chr8:99438624-99438674	BE2_C	brain:	n/a
18	chr8:99442883-99442933	GM12891	blood:	n/a
19	chr8:99338761-99338811	HEK293	kidney:	embryo
20	chr8:99438942-99438992	GM06990	blood:	n/a
21	chr8:99440522-99440572	NHDF-neo	bronchial:	n/a
22	chr8:99435204-99435254	CMK	blood:	n/a
23	chr8:99439441-99439491	AG09309	skin:	n/a
24	chr8:99376661-99376711	HNPCEpiC	eye:	n/a
25	chr8:99380162-99380212	BJ	skin:	n/a
26	chr8:99306870-99306920	NHDF-neo	bronchial:	n/a
27	chr8:99338761-99338811	HCPEpiC	choroid plexus:	n/a
28	chr8:99439685-99439735	Jurkat	blood:	n/a
29	chr8:99422528-99422578	AG10803	skin:	n/a
30	chr8:99439685-99439735	ProgFib	skin:	n/a
31	chr8:99440279-99440329	PFSK-1	brain:	n/a
32	chr8:99440279-99440329	HMEC	breast:	n/a
33	chr8:99440522-99440572	HEEpiC	esophagus:	n/a
34	chr8:99439948-99439998	HCPEpiC	choroid plexus:	n/a
35	chr8:99306725-99306775	AG04450	lung:	fetal
36	chr8:99310335-99310385	SK-N-MC	brain:	n/a
37	chr8:99310335-99310385	NHBE	bronchial:	n/a
38	chr8:99479374-99479424	NHDF-neo	bronchial:	n/a
39	chr8:99438968-99439018	HAEpiC	amniotic membrane:	n/a
40	chr8:99377018-99377068	Hepatocyte	liver:	n/a
41	chr8:99306718-99306768	NB4	blood:	n/a
42	chr8:99440522-99440572	HMEC	breast:	n/a
43	chr8:99440522-99440572	MCF-7	breast:	n/a
44	chr8:99439861-99439911	NHDF-neo	bronchial:	n/a
45	chr8:99303033-99303083	GM06990	blood:	n/a
46	chr8:99338761-99338811	HCF	heart:	n/a
47	chr8:99306718-99306768	SK-N-MC	brain:	n/a
48	chr8:99306748-99306798	HepG2	liver:	n/a
49	chr8:99438942-99438992	AG10803	skin:	n/a
50	chr8:99440522-99440572	HAEpiC	amniotic membrane:	n/a

(count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr8:99411379..99414219-chr8:99414803..99416412,2	K562	blood:
2	chr5:31736992..31739495-chr8:99347589..99350230,2	MCF-7	breast:
3	chr8:99344297..99345235-chr8:99357703..99358227,2	MCF-7	breast:
4	chr8:99389616..99393006-chr8:99411002..99413447,3	MCF-7	breast:
5	chr8:99181890..99183854-chr8:99347309..99350010,2	MCF-7	breast:
6	chr8:99305095..99308077-chr8:99325429..99329049,3	MCF-7	breast:
7	chr8:99344297..99345235-chr8:99357703..99358227,2	MCF-7	breast:
8	chr8:99294576..99297304-chr8:99298018..99299770,2	MCF-7	breast:
9	chr8:99356606..99360601-chr8:99368413..99371833,4	MCF-7	breast:
10	chr8:99351707..99353474-chr8:99355817..99358709,2	MCF-7	breast:
11	chr8:99304071..99306084-chr8:99410525..99412832,2	MCF-7	breast:
12	chr8:99271786..99273294-chr8:99302806..99304675,2	MCF-7	breast:
13	chr8:99304623..99310031-chr8:99366806..99371417,6	MCF-7	breast:
14	chr8:99339898..99346485-chr8:99480859..99484990,7	MCF-7	breast:
15	chr8:99410786..99412684-chr8:99420186..99422700,2	MCF-7	breast:
16	chr8:99373069..99375307-chr8:99379575..99381805,2	K562	blood:
17	chr12:27340912..27341732-chr8:99449571..99450562,2	MCF-7	breast:
18	chr8:99476761..99480533-chr8:99480952..99484066,4	MCF-7	breast:
19	chr8:99418180..99421038-chr8:99421150..99423251,2	K562	blood:
20	chr8:99304071..99306084-chr8:99410525..99412832,2	MCF-7	breast:
21	chr8:99371126..99375307-chr8:99376656..99381075,4	K562	blood:
22	chr8:99177794..99180485-chr8:99476278..99478549,2	MCF-7	breast:
23	chr8:99176613..99177756-chr8:99370117..99370793,5	MCF-7	breast:
24	chr8:99481593..99484303-chr8:99484870..99487403,2	K562	blood:
25	chr6:26204334..26206803-chr8:99304596..99307549,2	MCF-7	breast:
26	chr8:99389611..99391541-chr8:99393502..99396031,2	K562	blood:
27	chr8:99375676..99377993-chr8:99381556..99384314,2	MCF-7	breast:
28	chr8:99306604..99309572-chr8:99429728..99432541,2	MCF-7	breast:
29	chr8:99317402..99318955-chr8:99321562..99323926,2	K562	blood:
30	chr8:99343429..99346182-chr8:99476403..99480248,3	MCF-7	breast:
31	chr8:99399092..99403051-chr8:99412315..99417483,4	K562	blood:
32	chr8:99305275..99307120-chr8:99422089..99423858,2	MCF-7	breast:
33	chr8:99373585..99375762-chr8:99389237..99391103,2	K562	blood:
34	chr8:99348334..99350137-chr8:99356726..99359108,2	MCF-7	breast:
35	chr1:234745047..234747067-chr8:99344812..99347699,2	MCF-7	breast:
36	chr8:99318271..99319945-chr8:99351260..99353325,2	MCF-7	breast:
37	chr8:99457417..99459146-chr8:99461965..99464100,2	K562	blood:
38	chr8:99405535..99409022-chr8:99413535..99417090,3	MCF-7	breast:
39	chr8:99373069..99375307-chr8:99379575..99381805,2	K562	blood:
40	chr8:99328599..99331093-chr8:99335692..99337383,2	MCF-7	breast:
41	chr8:99321286..99323579-chr8:99343349..99347132,3	MCF-7	breast:
42	chr8:99270989..99273601-chr8:99316752..99319337,2	MCF-7	breast:
43	chr8:99347365..99349416-chr8:99356232..99359153,2	K562	blood:
44	chr8:99400709..99403673-chr8:99405478..99407358,2	MCF-7	breast:
45	chr8:99397844..99400010-chr8:99411059..99412585,2	MCF-7	breast:
46	chr8:99423861..99425965-chr8:99426065..99427627,2	MCF-7	breast:
47	chr8:99181135..99183759-chr8:99296172..99297898,2	MCF-7	breast:
48	chr8:99420942..99422686-chr8:99431232..99433617,2	K562	blood:
49	chr8:99363750..99366423-chr8:99367673..99369509,2	MCF-7	breast:
50	chr8:99396216..99398380-chr8:99401301..99403521,3	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NIPAL2-2	chr8:99425532-99426012	NONHSAT127924
2	lnc-STK3-1	chr8:99401092-99401181	XLOC_007169
3	lnc-STK3-1	chr8:99400420-99400475	ENSG00000254267
4	lnc-STK3-1	chr8:99383583-99383906	ENSG00000254267
5	lnc-NIPAL2-2	chr8:99425110-99425215	NONHSAT127924
6	lnc-STK3-1	chr8:99391381-99391435	ENSG00000254267
7	lnc-STK3-1	chr8:99391381-99391435	XLOC_007169
8	lnc-STK3-1	chr8:99374348-99374358	XLOC_007169
9	lnc-NIPAL2-1	chr8:99327931-99328120	XLOC_007168
10	lnc-STK3-1	chr8:99400420-99400475	XLOC_007169
11	lnc-KCNS2-2	chr8:99448897-99451518	ENSG00000272321.1
12	lnc-NIPAL2-1	chr8:99333181-99333207	XLOC_007168

No data

Variant related genes	Relation type
ENSG00000254267	TF binding region
ENSG00000253468	TF binding region
RNU6-748P	TF binding region
KCNS2	TF binding region
NIPAL2	TF binding region
ENSG00000272321	TF binding region
ENSG00000254267	CpG island
ENSG00000253468	CpG island
RNU6-748P	CpG island
KCNS2	CpG island
NIPAL2	CpG island
ENSG00000272321	CpG island
ENSG00000207378	chromatin interactions
ENSG00000254024	chromatin interactions
ENSG00000156486	chromatin interactions
ENSG00000104361	chromatin interactions
ENSG00000261437	chromatin interactions
ENSG00000249114	chromatin interactions
ENSG00000112308	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000272321	chromatin interactions
ENSG00000156482	chromatin interactions
ENSG00000132305	chromatin interactions
ENSG00000198518	chromatin interactions
ENSG00000168264	chromatin interactions
ENSG00000160191	chromatin interactions
ENSG00000254267	chromatin interactions
ENSG00000273080	chromatin interactions
ENSG00000253468	chromatin interactions

Extended variants
information (count: 6691 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:6691 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534156367	chr8:99290766-99290767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561134887	chr8:99290769-99290770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112445179	chr8:99290857-99290858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149795652	chr8:99290880-99290881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13264971	chr8:99290881-99290882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs187734750	chr8:99290895-99290896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35688636	chr8:99290978-99290979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564040754	chr8:99290995-99290996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532681182	chr8:99291065-99291066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552846395	chr8:99291069-99291070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566272554	chr8:99291079-99291080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192240910	chr8:99291094-99291095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528196913	chr8:99291157-99291158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548264078	chr8:99291185-99291186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184678177	chr8:99291290-99291291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs55958946	chr8:99291448-99291449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11782558	chr8:99291450-99291451	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs113176365	chr8:99291469-99291470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373640917	chr8:99291498-99291499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531126975	chr8:99291563-99291564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs62524195	chr8:99291589-99291590	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs556661449	chr8:99291590-99291591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545378207	chr8:99291612-99291613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570757635	chr8:99291668-99291669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71514985	chr8:99291723-99291724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141648521	chr8:99291796-99291797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79542204	chr8:99291806-99291807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532163776	chr8:99291808-99291809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs541142917	chr8:99291845-99291846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs78564181	chr8:99291929-99291930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574819095	chr8:99291970-99291971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551838326	chr8:99291978-99291979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73698771	chr8:99292094-99292095	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs532905442	chr8:99292111-99292112	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546470523	chr8:99292140-99292141	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559995757	chr8:99292173-99292174	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528658763	chr8:99292179-99292180	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548000249	chr8:99292189-99292190	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568175602	chr8:99292231-99292232	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs115371107	chr8:99292256-99292257	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147025588	chr8:99292305-99292306	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570349370	chr8:99292335-99292336	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528173975	chr8:99292336-99292337	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528414866	chr8:99292355-99292356	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548461123	chr8:99292357-99292358	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567941758	chr8:99292366-99292367	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs112864857	chr8:99292402-99292403	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs138308692	chr8:99292445-99292446	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs189544465	chr8:99292479-99292480	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs142607855	chr8:99292498-99292499	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
head and neck squamous cell carcinoma	19451471	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
Breast cancer	21611746	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Prostate cancer	22341455	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	21215367	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2674 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99240600-99294200	Weak transcription	Ovary	ovary
2	chr8:99260400-99304400	Weak transcription	Duodenum Mucosa	Duodenum
3	chr8:99265400-99298400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr8:99265400-99304200	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr8:99284600-99304600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr8:99284800-99304600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr8:99287600-99305000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr8:99287800-99303600	Weak transcription	Fetal Stomach	stomach
9	chr8:99289000-99292000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr8:99289000-99297800	Weak transcription	Primary B cells from peripheral blood	blood
11	chr8:99289000-99303400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr8:99290800-99305400	Weak transcription	Aorta	Aorta
13	chr8:99291000-99297800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:99291200-99295800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr8:99291400-99305400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:99291600-99291800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr8:99291800-99292000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr8:99291800-99292200	Enhancers	NHDF-Ad	bronchial
19	chr8:99291800-99298400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr8:99291800-99304000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:99292000-99292600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:99292000-99297000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:99292200-99292400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
24	chr8:99292400-99292600	Enhancers	Esophagus	oesophagus
25	chr8:99292400-99292600	Active TSS	Spleen	Spleen
26	chr8:99292400-99293400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr8:99292600-99294400	Weak transcription	Esophagus	oesophagus
28	chr8:99292600-99295800	Weak transcription	Pancreas	Pancrea
29	chr8:99292600-99296000	Weak transcription	Spleen	Spleen
30	chr8:99292600-99298200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:99292800-99296200	Weak transcription	Gastric	stomach
32	chr8:99293200-99293400	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr8:99293400-99293600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr8:99293400-99293600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr8:99293400-99293600	Enhancers	Lung	lung
36	chr8:99293400-99304600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr8:99293600-99295800	Weak transcription	Lung	lung
38	chr8:99293600-99303800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr8:99293600-99304000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr8:99293800-99294800	Enhancers	Fetal Intestine Large	intestine
41	chr8:99294000-99295000	Enhancers	Fetal Intestine Small	intestine
42	chr8:99294200-99294600	Genic enhancers	Ovary	ovary
43	chr8:99294200-99294600	Enhancers	HepG2	liver
44	chr8:99294400-99294600	Enhancers	Right Ventricle	heart
45	chr8:99294400-99294800	Enhancers	Esophagus	oesophagus
46	chr8:99294400-99294800	Enhancers	Right Atrium	heart
47	chr8:99294400-99295200	Enhancers	Left Ventricle	heart
48	chr8:99294400-99296600	Enhancers	Fetal Heart	heart
49	chr8:99294600-99295400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:99294600-99295800	Weak transcription	Ovary	ovary

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