Variant report

Variant	esv1803951
Chromosome Location	chr8:99922754-100191783
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3814)
CpG islands
(count:5010)
Chromatin interactive
region (count:259)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3814 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:100038356-100038875	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:100046312-100046577	K562	blood:	n/a	n/a
3	ARID3A	chr8:100025752-100025948	K562	blood:	n/a	n/a
4	ARID3A	chr8:100124728-100124858	K562	blood:	n/a	n/a
5	ARID3A	chr8:100149959-100150472	K562	blood:	n/a	n/a
6	ARID3A	chr8:100025256-100025507	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:100103092-100103687	K562	blood:	n/a	n/a
8	ARID3A	chr8:100023747-100023947	K562	blood:	n/a	n/a
9	ARID3A	chr8:100046132-100046815	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:100058615-100058867	K562	blood:	n/a	n/a
11	ARID3A	chr8:100010143-100010485	K562	blood:	n/a	n/a
12	ARID3A	chr8:99953361-99953710	HepG2	liver:	n/a	n/a
13	ARID3A	chr8:100025358-100025487	K562	blood:	n/a	n/a
14	ARID3A	chr8:99979696-99979755	HepG2	liver:	n/a	n/a
15	ATF1	chr8:100135547-100135703	K562	blood:	n/a	n/a
16	ATF1	chr8:100103355-100103611	K562	blood:	n/a	n/a
17	ATF1	chr8:99989189-99989309	K562	blood:	n/a	n/a
18	ATF1	chr8:99943657-99943981	K562	blood:	n/a	n/a
19	ATF1	chr8:99922773-99923250	K562	blood:	n/a	n/a
20	ATF1	chr8:100150113-100150549	K562	blood:	n/a	n/a
21	ATF1	chr8:99939428-99939464	K562	blood:	n/a	n/a
22	ATF1	chr8:100058613-100058861	K562	blood:	n/a	n/a
23	ATF1	chr8:100177666-100177787	K562	blood:	n/a	n/a
24	ATF2	chr8:99986670-99987066	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr8:100093166-100093626	GM12878	blood:	n/a	n/a
26	ATF2	chr8:100024655-100026274	GM12878	blood:	n/a	n/a
27	ATF2	chr8:100025069-100025608	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr8:99956232-99956831	GM12878	blood:	n/a	n/a
29	ATF2	chr8:100025121-100025659	GM12878	blood:	n/a	n/a
30	ATF2	chr8:100092901-100093701	GM12878	blood:	n/a	n/a
31	ATF3	chr8:100025143-100025741	A549	lung:	n/a	n/a
32	ATF3	chr8:100024993-100025682	A549	lung:	n/a	n/a
33	ATF3	chr8:100150017-100150481	K562	blood:	n/a	n/a
34	ATF3	chr8:99953212-99953610	A549	lung:	n/a	n/a
35	ATF3	chr8:100103253-100103550	K562	blood:	n/a	n/a
36	BACH1	chr8:99956255-99957045	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr8:100150185-100150441	K562	blood:	n/a	n/a
38	BACH1	chr8:100182411-100182437	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr8:99957290-99957855	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr8:100025132-100025563	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr8:99960886-99961005	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr8:99960325-99960638	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr8:99950930-99950997	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr8:99986624-99986995	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr8:99952263-99955172	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr8:99924713-99925020	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr8:99951944-99951982	H1-hESC	embryonic stem cell:	n/a	n/a
48	BATF	chr8:99956234-99956577	GM12878	blood:	n/a	chr8:99956446-99956456
49	BATF	chr8:100093290-100093609	GM12878	blood:	n/a	n/a
50	BATF	chr8:99934137-99934602	GM12878	blood:	n/a	chr8:99934227-99934236

(count:5010 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:99962118-99962168	HRPEpiC	eye:	n/a
2	chr8:100025000-100025050	HepG2	liver:	n/a
3	chr8:99960580-99960630	HMEC	breast:	n/a
4	chr8:99959723-99959773	NH-A	brain:	n/a
5	chr8:100025604-100025654	SK-N-SH_RA	brain:	n/a
6	chr8:100025487-100025537	U87	brain:	n/a
7	chr8:99961874-99961924	HNPCEpiC	eye:	n/a
8	chr8:99957225-99957275	NT2-D1	testis:	n/a
9	chr8:99962118-99962168	HRPEpiC	eye:	n/a
10	chr8:100025000-100025050	HepG2	liver:	n/a
11	chr8:99960580-99960630	HMEC	breast:	n/a
12	chr8:99959723-99959773	NH-A	brain:	n/a
13	chr8:100025604-100025654	SK-N-SH_RA	brain:	n/a
14	chr8:100025487-100025537	U87	brain:	n/a
15	chr8:99961874-99961924	HNPCEpiC	eye:	n/a
16	chr8:99957225-99957275	NT2-D1	testis:	n/a
17	chr8:99952217-99952267	PFSK-1	brain:	n/a
18	chr8:99961768-99961818	HCF	heart:	n/a
19	chr8:99953809-99953859	GM12878	blood:	n/a
20	chr8:100028166-100028216	SAEC	small airway:	n/a
21	chr8:100025487-100025537	Caco-2	colon:	n/a
22	chr8:99952031-99952081	RPTEC	kidney:	n/a
23	chr8:99957472-99957522	AG04449	skin:	fetal
24	chr8:99949391-99949441	SK-N-SH_RA	brain:	n/a
25	chr8:99982385-99982435	SKMC	muscle:	n/a
26	chr8:99983622-99983672	HEEpiC	esophagus:	n/a
27	chr8:99954432-99954482	Hela-S3	cervix:	n/a
28	chr8:100028166-100028216	NH-A	brain:	n/a
29	chr8:99952217-99952267	HMEC	breast:	n/a
30	chr8:100023123-100023173	T-47D	breast:	n/a
31	chr8:99956751-99956801	PrEC	prostate:	n/a
32	chr8:99953809-99953859	SK-N-SH_RA	brain:	n/a
33	chr8:99986964-99987014	BJ	skin:	n/a
34	chr8:99986344-99986394	SK-N-MC	brain:	n/a
35	chr8:99952047-99952097	GM12878	blood:	n/a
36	chr8:99956055-99956105	MCF10A-Er-Src	breast:	n/a
37	chr8:100023123-100023173	PFSK-1	brain:	n/a
38	chr8:99957472-99957522	HepG2	liver:	n/a
39	chr8:99956467-99956517	AG04450	lung:	fetal
40	chr8:100026087-100026137	AoSMC	blood vessel:	n/a
41	chr8:99952591-99952641	BJ	skin:	n/a
42	chr8:99953809-99953859	GM19239	blood:	n/a
43	chr8:99962118-99962168	HEEpiC	esophagus:	n/a
44	chr8:100104103-100104153	MCF10A-Er-Src	breast:	n/a
45	chr8:99957607-99957657	AG09309	skin:	n/a
46	chr8:99943905-99943955	AG09319	gingival:	n/a
47	chr8:99959602-99959652	T-47D	breast:	n/a
48	chr8:99951420-99951470	HNPCEpiC	eye:	n/a
49	chr8:99961376-99961426	H1-hESC	embryonic stem cell:	embryo
50	chr8:99955610-99955660	AG10803	skin:	n/a

(count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr8:99986955..99988754-chr8:99989038..99991100,2	K562	blood:
2	chr8:100024345..100027040-chr8:100106649..100108605,2	MCF-7	breast:
3	chr8:99713408..99715331-chr8:99956897..99958843,2	MCF-7	breast:
4	chr8:99956762..99958304-chr8:100013613..100016438,2	K562	blood:
5	chr8:99962872..99965221-chr8:99992608..99995397,2	MCF-7	breast:
6	chr8:99983465..99985131-chr8:99988953..99990808,2	K562	blood:
7	chr8:100048867..100050500-chr8:100268956..100271777,2	MCF-7	breast:
8	chr8:99952762..99963438-chr8:100019139..100031293,37	MCF-7	breast:
9	chr8:99981927..99983914-chr8:100024309..100025891,2	MCF-7	breast:
10	chr1:153584358..153587308-chr8:99979640..99981391,2	MCF-7	breast:
11	chr8:99994497..99999202-chr8:100022431..100027300,8	MCF-7	breast:
12	chr8:99835847..99838422-chr8:99986795..99989582,2	K562	blood:
13	chr8:100025833..100028756-chr8:100100624..100103335,2	MCF-7	breast:
14	chr8:100023165..100025763-chr8:100036969..100038746,2	K562	blood:
15	chr8:99962836..99965114-chr8:99973570..99976399,2	K562	blood:
16	chr8:99942235..99943803-chr8:99945712..99947725,2	K562	blood:
17	chr8:99945155..99947475-chr8:100009371..100011688,2	MCF-7	breast:
18	chr8:99931677..99933733-chr8:99937087..99939527,3	MCF-7	breast:
19	chr8:100025901..100029663-chr8:100033487..100035486,3	K562	blood:
20	chr8:99955273..99957309-chr8:100023910..100025896,2	K562	blood:
21	chr8:100179836..100180811-chr8:101138118..101138640,2	MCF-7	breast:
22	chr8:100180149..100180921-chr8:100370671..100371459,2	MCF-7	breast:
23	chr8:99677331..99680175-chr8:100027131..100030033,2	K562	blood:
24	chr8:99901798..99904036-chr8:99961157..99963131,2	K562	blood:
25	chr8:100024436..100026482-chr8:100177416..100178944,2	MCF-7	breast:
26	chr8:100162823..100164704-chr8:100167097..100169098,2	K562	blood:
27	chr8:99717164..99718794-chr8:100022848..100024966,2	K562	blood:
28	chr8:99852770..99853592-chr8:100009889..100010836,2	MCF-7	breast:
29	chr8:99661906..99664329-chr8:99956094..99958895,2	MCF-7	breast:
30	chr14:24316655..24319371-chr8:99990741..99993144,2	MCF-7	breast:
31	chr8:99949821..99952393-chr8:99958605..99960379,2	K562	blood:
32	chr8:100067262..100071049-chr8:100071737..100074698,3	MCF-7	breast:
33	chr8:99952913..99953621-chr8:100370794..100371379,2	MCF-7	breast:
34	chr8:100038785..100041042-chr8:100044049..100045799,2	K562	blood:
35	chr8:99965681..99968140-chr8:100024075..100026959,2	MCF-7	breast:
36	chr8:99956069..99958668-chr8:99982298..99983994,2	K562	blood:
37	chr8:99951388..99953620-chr8:100021426..100022985,2	K562	blood:
38	chr8:99942235..99943803-chr8:99945712..99947725,2	K562	blood:
39	chr8:100000931..100003067-chr8:100022088..100023611,2	K562	blood:
40	chr8:100144557..100146496-chr8:100147591..100149372,3	MCF-7	breast:
41	chr8:100043126..100045218-chr8:100045409..100048093,2	K562	blood:
42	chr8:100024340..100026866-chr8:100052293..100056237,3	MCF-7	breast:
43	chr8:100115261..100117016-chr8:100117428..100119133,2	K562	blood:
44	chr8:99922248..99926179-chr8:99930900..99934447,3	MCF-7	breast:
45	chr8:100011207..100013044-chr8:100013955..100016177,3	K562	blood:
46	chr8:100181985..100183886-chr8:100189568..100191594,2	MCF-7	breast:
47	chr8:99967373..99970274-chr8:99997572..100000017,2	K562	blood:
48	chr8:99942466..99945481-chr8:99954331..99957519,4	K562	blood:
49	chr8:100144557..100146496-chr8:100147591..100149372,3	MCF-7	breast:
50	chr8:99967373..99970274-chr8:99997572..100000017,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OSR2-1	chr8:99980150-99980512	ENSG00000229625
2	lnc-OSR2-2	chr8:100131580-100131696	ENSG00000253532.1
3	lnc-STK3-2	chr8:100008991-100009194	ENSG00000253948.1
4	lnc-OSR2-1	chr8:99977692-99977735	ENSG00000229625
5	lnc-STK3-2	chr8:100025097-100025462	NONHSAT127943
6	lnc-STK3-3	chr8:100106157-100106288	ENSG00000253562.1
7	lnc-OSR2-1	chr8:99973656-99973712	ENSG00000229625
8	lnc-OSR2-3	chr8:99958259-99958530	NONHSAT127938
9	lnc-OSR2-4	chr8:99955823-99956326	ENSG00000271930.1
10	lnc-STK3-2	chr8:100008558-100009194	NONHSAT127943
11	lnc-OSR2-3	chr8:99956631-99957051	NONHSAT127938
12	lnc-VPS13B-1	chr8:100014060-100015451	NONHSAT127942
13	lnc-STK3-5	chr8:100018891-100019738	l_3657_chr8:100017408-100021457_testes
14	lnc-VPS13B-1	chr8:100008217-100013862	NONHSAT127942
15	lnc-NIPAL2-7	chr8:99933461-99933778	NONHSAT127937
16	lnc-OSR2-2	chr8:100132332-100132809	ENSG00000253532.1
17	lnc-STK3-5	chr8:100020741-100021457	l_3657_chr8:100017408-100021457_testes
18	lnc-STK3-5	chr8:100017409-100018868	l_3657_chr8:100017408-100021457_testes
19	lnc-NIPAL2-5	chr8:99954606-99954873	NONHSAT127935
20	lnc-STK3-2	chr8:100025097-100025272	ENSG00000253948.1
21	lnc-STK3-3	chr8:100103966-100104326	ENSG00000253562.1

No data

Variant related genes	Relation type
ENSG00000263842	TF binding region
STK3	TF binding region
VPS13B	TF binding region
ENSG00000229625	TF binding region
ENSG00000253948	TF binding region
ENSG00000253562	TF binding region
MRP63P7	TF binding region
ENSG00000253180	TF binding region
RN7SKP85	TF binding region
ENSG00000253532	TF binding region
OSR2	TF binding region
ENSG00000253415	TF binding region
ENSG00000271930	TF binding region
ENSG00000263842	CpG island
STK3	CpG island
VPS13B	CpG island
ENSG00000229625	CpG island
ENSG00000253948	CpG island
ENSG00000253562	CpG island
MRP63P7	CpG island
ENSG00000253180	CpG island
RN7SKP85	CpG island
ENSG00000253532	CpG island
OSR2	CpG island
ENSG00000253415	CpG island
ENSG00000271930	CpG island
ENSG00000188643	chromatin interactions
ENSG00000253180	chromatin interactions
ENSG00000089157	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000271930	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000253532	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000140157	chromatin interactions
ENSG00000254312	chromatin interactions
ENSG00000263842	chromatin interactions
ENSG00000001167	chromatin interactions
ENSG00000104361	chromatin interactions
ENSG00000164924	chromatin interactions
ENSG00000203865	chromatin interactions
ENSG00000229625	chromatin interactions
ENSG00000253415	chromatin interactions
ENSG00000124596	chromatin interactions
ENSG00000223281	chromatin interactions
ENSG00000104375	chromatin interactions
ENSG00000103769	chromatin interactions
ENSG00000164919	chromatin interactions

Extended variants
information (count: 8953 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:8953 , 50 per page) page: 1 2 3 4 5 6 7 ... 180

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17373806	chr8:99922754-99922755	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573853509	chr8:99922773-99922774	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs147890969	chr8:99922804-99922805	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs377551679	chr8:99922808-99922809	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs535084161	chr8:99922825-99922826	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs370226172	chr8:99922839-99922840	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs141553791	chr8:99922883-99922884	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs145385757	chr8:99922944-99922945	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs147662133	chr8:99922975-99922976	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs141116620	chr8:99922982-99922983	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs373400634	chr8:99923069-99923070	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs577095188	chr8:99923171-99923172	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs150262271	chr8:99923209-99923210	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs180900149	chr8:99923219-99923220	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs73279717	chr8:99923229-99923230	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs572514950	chr8:99923409-99923410	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs542972308	chr8:99923411-99923412	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs561840775	chr8:99923466-99923467	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs184703863	chr8:99923485-99923486	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs542969595	chr8:99923487-99923488	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs544027314	chr8:99923541-99923542	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs562787434	chr8:99923597-99923598	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs563826141	chr8:99923607-99923608	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs10715541	chr8:99923612-99923613	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs138390674	chr8:99923616-99923617	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs201242993	chr8:99923637-99923638	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs532899275	chr8:99923648-99923649	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs552915903	chr8:99923671-99923672	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs567898575	chr8:99923712-99923713	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs566035998	chr8:99923743-99923744	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs188871401	chr8:99923744-99923745	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs548359395	chr8:99923752-99923753	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs138903934	chr8:99923763-99923764	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs568576410	chr8:99923770-99923771	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs536822283	chr8:99923811-99923812	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs111956755	chr8:99923825-99923826	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs181580097	chr8:99923841-99923842	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs570402904	chr8:99923853-99923854	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs112816314	chr8:99923856-99923857	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs186229438	chr8:99923873-99923874	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs190950234	chr8:99923874-99923875	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs181836578	chr8:99923904-99923905	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs572474859	chr8:99923954-99923955	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs187236966	chr8:99923979-99923980	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs551294431	chr8:99924025-99924026	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs113410166	chr8:99924026-99924027	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs555152002	chr8:99924046-99924047	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs575345673	chr8:99924063-99924064	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs386728138	chr8:99924072-99924073	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs200634455	chr8:99924075-99924076	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Prostate cancer	22341455	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cohen syndrome	20461111	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:5698 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99914400-99923000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:99914400-99924600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr8:99918800-99923000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:99918800-99924400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:99918800-99926400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:99922600-99923400	Enhancers	Dnd41	blood
7	chr8:99922600-99923400	Enhancers	NHEK	skin
8	chr8:99922800-99923200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr8:99922800-99923200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:99922800-99923200	Enhancers	GM12878-XiMat	blood
11	chr8:99922800-99923400	Enhancers	HMEC	breast
12	chr8:99922800-99923400	Enhancers	K562	blood
13	chr8:99922800-99925400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:99923000-99923200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr8:99923000-99923400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:99923000-99923400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr8:99923000-99923400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr8:99923000-99923600	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr8:99923200-99923400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr8:99923200-99924600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:99923200-99924800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:99923400-99924400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr8:99923400-99924400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:99923400-99924600	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr8:99923400-99924600	Weak transcription	HMEC	breast
26	chr8:99923400-99924600	Weak transcription	NHEK	skin
27	chr8:99923400-99925000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:99923600-99924200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr8:99923600-99924600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr8:99924200-99924600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr8:99924200-99924800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr8:99924200-99925000	Enhancers	H1 Cell Line	embryonic stem cell
33	chr8:99924400-99924600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr8:99924400-99925000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:99924400-99925000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr8:99924400-99927200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr8:99924600-99924800	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr8:99924600-99924800	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr8:99924600-99924800	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr8:99924600-99925000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr8:99924600-99925000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr8:99924600-99925000	Enhancers	NHEK	skin
43	chr8:99924600-99925200	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr8:99924600-99925400	Enhancers	HMEC	breast
45	chr8:99924600-99925800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr8:99924600-99925800	Enhancers	A549	lung
47	chr8:99924800-99925000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr8:99924800-99925000	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr8:99924800-99925200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr8:99924800-99925400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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