Variant report

Variant	nsv611832
Chromosome Location	chr8:104400808-104481735
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1347)
CpG islands
(count:1222)
Chromatin interactive
region (count:148)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1347 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:104426866-104427755	HepG2	liver:	n/a	chr8:104427715-104427723
2	ARID3A	chr8:104427398-104427812	K562	blood:	n/a	chr8:104427715-104427723
3	ATF1	chr8:104427062-104427857	K562	blood:	n/a	n/a
4	ATF2	chr8:104426743-104427918	GM12878	blood:	n/a	n/a
5	ATF2	chr8:104426511-104427936	GM12878	blood:	n/a	n/a
6	ATF2	chr8:104426801-104427906	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr8:104426836-104427820	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr8:104427296-104427820	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr8:104427393-104427641	GM12878	blood:	n/a	n/a
10	ATF3	chr8:104427029-104428095	A549	lung:	n/a	n/a
11	ATF3	chr8:104427327-104427741	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr8:104427374-104427690	K562	blood:	n/a	n/a
13	ATF3	chr8:104447915-104448340	HCT-116	colon:	n/a	n/a
14	ATF3	chr8:104427386-104427790	GM12878	blood:	n/a	n/a
15	BACH1	chr8:104426923-104428365	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:104421816-104422006	K562	blood:	n/a	n/a
17	BACH1	chr8:104427238-104427351	K562	blood:	n/a	n/a
18	BACH1	chr8:104457733-104458081	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr8:104416106-104416340	GM12878	blood:	n/a	chr8:104416195-104416206 chr8:104416196-104416206
20	BATF	chr8:104473815-104474033	GM12878	blood:	n/a	n/a
21	BATF	chr8:104416061-104416334	GM12878	blood:	n/a	chr8:104416195-104416206 chr8:104416196-104416206
22	BCL3	chr8:104426840-104427915	A549	lung:	n/a	chr8:104427200-104427209
23	BCL3	chr8:104426809-104427776	GM12878	blood:	n/a	chr8:104427200-104427209
24	BCL3	chr8:104427180-104427880	A549	lung:	n/a	chr8:104427200-104427209
25	BCLAF1	chr8:104426670-104428084	GM12878	blood:	n/a	chr8:104427200-104427209
26	BCLAF1	chr8:104418571-104419110	GM12878	blood:	n/a	chr8:104418644-104418653
27	BCLAF1	chr8:104426457-104427852	GM12878	blood:	n/a	chr8:104427200-104427209
28	BHLHE40	chr8:104457940-104457945	GM12878	blood:	n/a	n/a
29	BHLHE40	chr8:104427297-104427771	A549	lung:	n/a	n/a
30	BHLHE40	chr8:104428488-104428971	GM12878	blood:	n/a	n/a
31	BHLHE40	chr8:104426534-104428035	HepG2	liver:	n/a	n/a
32	BHLHE40	chr8:104426390-104427883	K562	blood:	n/a	n/a
33	BHLHE40	chr8:104426472-104427923	GM12878	blood:	n/a	n/a
34	BHLHE40	chr8:104418496-104418938	GM12878	blood:	n/a	n/a
35	BHLHE40	chr8:104404519-104404555	K562	blood:	n/a	n/a
36	BRCA1	chr8:104427121-104428026	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr8:104427055-104427718	GM12878	blood:	n/a	n/a
38	BRCA1	chr8:104427162-104427797	HepG2	liver:	n/a	n/a
39	BRCA1	chr8:104427314-104427842	H1-hESC	embryonic stem cell:	n/a	n/a
40	CBX3	chr8:104427328-104427694	K562	blood:	n/a	n/a
41	CBX3	chr8:104427009-104427895	K562	blood:	n/a	n/a
42	CCNT2	chr8:104426877-104427870	K562	blood:	n/a	n/a
43	CEBPB	chr8:104477467-104477811	A549	lung:	n/a	n/a
44	CEBPB	chr8:104475142-104475282	H1-hESC	embryonic stem cell:	n/a	chr8:104475189-104475200
45	CEBPB	chr8:104463429-104463646	K562	blood:	n/a	chr8:104463503-104463514
46	CEBPB	chr8:104447962-104448344	ECC-1	luminal epithelium:	n/a	chr8:104448098-104448109
47	CEBPB	chr8:104475065-104475316	K562	blood:	n/a	chr8:104475189-104475200
48	CEBPB	chr8:104447939-104448240	HepG2	liver:	n/a	chr8:104448098-104448109
49	CEBPB	chr8:104426325-104427837	Hela-S3	cervix:	n/a	chr8:104426351-104426363
50	CEBPB	chr8:104429735-104429917	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:104427719-104427769	HCT-116	colon:	n/a
2	chr8:104427260-104427310	U87	brain:	n/a
3	chr8:104427719-104427769	HCT-116	colon:	n/a
4	chr8:104427260-104427310	U87	brain:	n/a
5	chr8:104405508-104405558	SK-N-SH	brain:	n/a
6	chr8:104427069-104427119	HCM	heart:	n/a
7	chr8:104427260-104427310	HAEpiC	amniotic membrane:	n/a
8	chr8:104426828-104426878	GM12878	blood:	n/a
9	chr8:104430401-104430451	NT2-D1	testis:	n/a
10	chr8:104427069-104427119	NB4	blood:	n/a
11	chr8:104428676-104428726	GM12891	blood:	n/a
12	chr8:104427370-104427420	Caco-2	colon:	n/a
13	chr8:104430401-104430451	SAEC	small airway:	n/a
14	chr8:104427719-104427769	AoSMC	blood vessel:	n/a
15	chr8:104426895-104426945	AG09309	skin:	n/a
16	chr8:104427696-104427746	T-47D	breast:	n/a
17	chr8:104426895-104426945	NB4	blood:	n/a
18	chr8:104411856-104411906	RPTEC	kidney:	n/a
19	chr8:104427370-104427420	PFSK-1	brain:	n/a
20	chr8:104427320-104427370	GM12891	blood:	n/a
21	chr8:104427320-104427370	U87	brain:	n/a
22	chr8:104426919-104426969	SKMC	muscle:	n/a
23	chr8:104426639-104426689	BJ	skin:	n/a
24	chr8:104427717-104427767	CMK	blood:	n/a
25	chr8:104427069-104427119	HRCEpiC	kidney:	n/a
26	chr8:104427696-104427746	NHBE	bronchial:	n/a
27	chr8:104411856-104411906	Caco-2	colon:	n/a
28	chr8:104427896-104427946	GM12891	blood:	n/a
29	chr8:104405508-104405558	BJ	skin:	n/a
30	chr8:104427655-104427705	PFSK-1	brain:	n/a
31	chr8:104427069-104427119	K562	blood:	n/a
32	chr8:104426895-104426945	HL-60	blood:	n/a
33	chr8:104411856-104411906	AG04450	lung:	fetal
34	chr8:104426828-104426878	K562	blood:	n/a
35	chr8:104426639-104426689	ovcar-3	ovarian:	n/a
36	chr8:104427655-104427705	HEEpiC	esophagus:	n/a
37	chr8:104427717-104427767	HCT-116	colon:	n/a
38	chr8:104426688-104426738	IMR90	lung:	fetal
39	chr8:104426688-104426738	NH-A	brain:	n/a
40	chr8:104427717-104427767	BJ	skin:	n/a
41	chr8:104427717-104427767	SK-N-MC	brain:	n/a
42	chr8:104426919-104426969	U87	brain:	n/a
43	chr8:104427370-104427420	GM12891	blood:	n/a
44	chr8:104427719-104427769	GM06990	blood:	n/a
45	chr8:104426895-104426945	MCF10A-Er-Src	breast:	n/a
46	chr8:104426688-104426738	GM12878	blood:	n/a
47	chr8:104427069-104427119	U87	brain:	n/a
48	chr8:104411856-104411906	HepG2	liver:	n/a
49	chr8:104426895-104426945	NH-A	brain:	n/a
50	chr8:104426639-104426689	HMEC	breast:	n/a

(count:148 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:104462356..104464774-chr8:104466545..104468143,2	K562	blood:
2	chr8:104408959..104409520-chr8:104426871..104427515,2	MCF-7	breast:
3	chr8:104445161..104447747-chr8:104451502..104455112,3	MCF-7	breast:
4	chr8:104437829..104439620-chr8:104450440..104452046,2	MCF-7	breast:
5	chr8:104453549..104455380-chr8:104457133..104459742,2	K562	blood:
6	chr8:104404764..104407750-chr8:104413143..104414836,2	MCF-7	breast:
7	chr6:27777422..27778274-chr8:104426874..104427783,2	Hela-S3	cervix:
8	chr8:104426371..104428380-chr8:104460079..104462602,2	MCF-7	breast:
9	chr8:104446427..104448471-chr8:104458737..104460308,2	MCF-7	breast:
10	chr8:104423857..104432331-chr8:104433396..104440310,16	K562	blood:
11	chr8:104426110..104429898-chr8:104452371..104457146,5	MCF-7	breast:
12	chr8:104425841..104427415-chr8:104438782..104440325,3	K562	blood:
13	chr8:104405652..104407349-chr8:104409170..104411312,2	MCF-7	breast:
14	chr8:104382426..104384366-chr8:104426073..104428422,3	MCF-7	breast:
15	chr8:104427653..104431566-chr8:104442876..104445476,3	K562	blood:
16	chr8:104453143..104455442-chr8:104521985..104524421,2	MCF-7	breast:
17	chr8:104384922..104387635-chr8:104403443..104406734,3	MCF-7	breast:
18	chr8:104409502..104412263-chr8:104415584..104417349,2	K562	blood:
19	chr8:104445161..104447747-chr8:104451502..104455112,3	MCF-7	breast:
20	chr8:104460049..104462766-chr8:104465079..104467156,2	MCF-7	breast:
21	chr8:104426715..104429412-chr8:104458698..104463744,5	MCF-7	breast:
22	chr8:104445021..104448087-chr8:104451150..104453607,3	K562	blood:
23	chr8:104433388..104438523-chr8:104444336..104447964,5	MCF-7	breast:
24	chr4:181363103..181363673-chr8:104455793..104456790,2	MCF-7	breast:
25	chr8:104460049..104462766-chr8:104465079..104467156,2	MCF-7	breast:
26	chr8:104432172..104434830-chr8:104439481..104441243,2	MCF-7	breast:
27	chr8:104409502..104412263-chr8:104415584..104417349,2	K562	blood:
28	chr8:104448646..104450563-chr8:104458852..104463066,3	MCF-7	breast:
29	chr8:104419066..104422515-chr8:104439961..104443732,3	K562	blood:
30	chr8:104414588..104416158-chr8:104422288..104424802,2	MCF-7	breast:
31	chr8:104426168..104429025-chr8:104429349..104431028,2	K562	blood:
32	chr8:104292150..104293871-chr8:104425235..104426887,2	MCF-7	breast:
33	chr8:104427774..104429306-chr8:104457033..104459237,2	MCF-7	breast:
34	chr8:104310642..104313127-chr8:104458418..104460483,2	MCF-7	breast:
35	chr8:104401208..104405161-chr8:104423386..104426686,3	K562	blood:
36	chr6:26156220..26156991-chr8:104426774..104427361,2	Hela-S3	cervix:
37	chr8:104465031..104467717-chr8:104472331..104474521,2	MCF-7	breast:
38	chr8:104309775..104311946-chr8:104402240..104405037,2	MCF-7	breast:
39	chr8:104401208..104405161-chr8:104423386..104426686,3	K562	blood:
40	chr8:104426997..104428750-chr8:104445549..104448139,2	MCF-7	breast:
41	chr8:104403139..104408438-chr8:104419869..104423025,6	K562	blood:
42	chr8:103875054..103878103-chr8:104425943..104429059,5	K562	blood:
43	chr8:104439009..104441617-chr8:104452174..104454970,2	MCF-7	breast:
44	chr8:104412488..104416313-chr8:104425793..104429036,7	MCF-7	breast:
45	chr8:104432523..104434511-chr8:104444027..104445603,2	MCF-7	breast:
46	chr8:104432843..104435364-chr8:104436898..104438979,2	K562	blood:
47	chr8:104410815..104412876-chr8:104413002..104415731,2	MCF-7	breast:
48	chr8:104425937..104427490-chr8:104445696..104447560,2	MCF-7	breast:
49	chr8:104433388..104438523-chr8:104444336..104447964,5	MCF-7	breast:
50	chr8:104384672..104387548-chr8:104409163..104411650,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCAF13-1	chr8:104476617-104481213	ENSG00000261670.1
2	lnc-SLC25A32-2	chr8:104456732-104457496	XLOC_007176
3	lnc-SLC25A32-2	chr8:104456929-104457456	XLOC_007176
4	lnc-SLC25A32-2	chr8:104457713-104457927	XLOC_007176
5	lnc-SLC25A32-3	chr8:104459868-104460278	NONHSAT128187
6	lnc-SLC25A32-2	chr8:104457713-104457916	XLOC_007176

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SLC25A32	hsa-miR-98-5p	chr8:104412434-104412456
2	SLC25A32	hsa-miR-32-5p	chr8:104412255-104412276
3	SLC25A32	hsa-miR-32-5p	chr8:104412261-104412254
4	SLC25A32	hsa-let-7b-5p	chr8:104412434-104412456

Variant related genes	Relation type
ENSG00000266289	TF binding region
ENSG00000261670	TF binding region
SLC25A32	TF binding region
DCAF13	TF binding region
ENSG00000266289	CpG island
ENSG00000261670	CpG island
SLC25A32	CpG island
DCAF13	CpG island
ENSG00000141569	chromatin interactions
ENSG00000207501	chromatin interactions
ENSG00000253320	chromatin interactions
ENSG00000128923	chromatin interactions
ENSG00000164934	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000164930	chromatin interactions
ENSG00000271830	chromatin interactions
ENSG00000104517	chromatin interactions
ENSG00000132305	chromatin interactions
ENSG00000155096	chromatin interactions
ENSG00000253477	chromatin interactions
ENSG00000245975	chromatin interactions
ENSG00000254236	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000129521	chromatin interactions
ENSG00000198355	chromatin interactions
ENSG00000153048	chromatin interactions
ENSG00000168101	chromatin interactions
ENSG00000155097	chromatin interactions
ENSG00000114956	chromatin interactions
ENSG00000273080	chromatin interactions
ENSG00000067334	chromatin interactions
ENSG00000261670	chromatin interactions
ENSG00000164932	chromatin interactions
ENSG00000247081	chromatin interactions
ENSG00000164933	chromatin interactions
ENSG00000176406	chromatin interactions

Extended variants
information (count: 3105 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:3105 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3133803	chr8:104400808-104400809	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573989631	chr8:104400817-104400818	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs369404549	chr8:104400830-104400831	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs116902446	chr8:104400858-104400859	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs372185839	chr8:104400880-104400881	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs71520809	chr8:104400908-104400909	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183539012	chr8:104400921-104400922	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs13278537	chr8:104400991-104400992	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs533290508	chr8:104400998-104400999	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs185924031	chr8:104401023-104401024	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532483240	chr8:104401028-104401029	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200108516	chr8:104401208-104401209	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs35542814	chr8:104401211-104401212	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs386413541	chr8:104401215-104401216	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201352260	chr8:104401218-104401219	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs56873685	chr8:104401221-104401222	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs3098250	chr8:104401239-104401240	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs142346878	chr8:104401271-104401272	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs116916779	chr8:104401307-104401308	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs150975967	chr8:104401367-104401368	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs35392014	chr8:104401398-104401399	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs191861234	chr8:104401411-104401412	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs565850429	chr8:104401441-104401442	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539175533	chr8:104401476-104401477	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557792816	chr8:104401478-104401479	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs569552631	chr8:104401577-104401578	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs371819060	chr8:104401607-104401608	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs140519481	chr8:104401610-104401611	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs574026379	chr8:104401628-104401629	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144497991	chr8:104401644-104401645	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs553170157	chr8:104401682-104401683	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs578095025	chr8:104401706-104401707	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs545178076	chr8:104401740-104401741	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs563853410	chr8:104401790-104401791	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs530901079	chr8:104401804-104401805	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112960301	chr8:104401827-104401828	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs561246397	chr8:104401912-104401913	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs78872158	chr8:104401916-104401917	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs182847952	chr8:104401982-104401983	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs559291646	chr8:104401983-104401984	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs533101401	chr8:104402031-104402032	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs551282105	chr8:104402136-104402137	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs79994759	chr8:104402142-104402143	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs534729996	chr8:104402225-104402226	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs569771742	chr8:104402236-104402237	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554807565	chr8:104402298-104402299	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs560644429	chr8:104402323-104402324	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs536731718	chr8:104402371-104402372	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs117288711	chr8:104402372-104402373	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs147857700	chr8:104402373-104402374	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:123)

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
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
Oral squamous cell carcinoma	21853135	CNVD
Developmental delay	21147756	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Prostate cancer	22341455	CNVD
Autism	20531469	CNVD
Congenital heart defect	22969434	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:2440 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104384400-104412200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr8:104384600-104409400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:104384600-104418600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:104385000-104408800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr8:104385000-104415600	Weak transcription	Placenta	Placenta
6	chr8:104385600-104405400	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr8:104385600-104408400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr8:104385600-104423600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr8:104385600-104424600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr8:104385800-104409000	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr8:104385800-104409000	Weak transcription	Stomach Smooth Muscle	stomach
12	chr8:104386000-104409800	Weak transcription	NHLF	lung
13	chr8:104386000-104418600	Weak transcription	Aorta	Aorta
14	chr8:104386000-104425600	Weak transcription	HSMMtube	muscle
15	chr8:104386200-104405600	Weak transcription	HUVEC	blood vessel
16	chr8:104388200-104412200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:104393200-104423600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr8:104393600-104409800	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr8:104394800-104421800	Weak transcription	Small Intestine	intestine
20	chr8:104397400-104412400	Weak transcription	Brain Hippocampus Middle	brain
21	chr8:104398200-104409200	Weak transcription	Thymus	Thymus
22	chr8:104398600-104413000	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr8:104399000-104401000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr8:104399200-104401200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr8:104399200-104403000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr8:104399400-104412200	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr8:104399600-104401200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:104399800-104401000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
29	chr8:104399800-104401000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr8:104399800-104401000	ZNF genes & repeats	Primary T cells from cord blood	blood
31	chr8:104399800-104401000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr8:104399800-104401000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr8:104399800-104401000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr8:104399800-104401200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr8:104399800-104401200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:104399800-104401600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr8:104399800-104401800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr8:104399800-104402600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr8:104400000-104401000	Weak transcription	Brain Angular Gyrus	brain
40	chr8:104400000-104408600	Weak transcription	Fetal Stomach	stomach
41	chr8:104400000-104426000	Weak transcription	Stomach Mucosa	stomach
42	chr8:104400200-104401000	ZNF genes & repeats	GM12878-XiMat	blood
43	chr8:104400200-104401000	Strong transcription	HSMM	muscle
44	chr8:104400200-104401200	ZNF genes & repeats	Dnd41	blood
45	chr8:104400200-104401400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:104400200-104401400	Strong transcription	Fetal Thymus	thymus
47	chr8:104400200-104425600	Weak transcription	Colonic Mucosa	Colon
48	chr8:104400400-104401000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr8:104400400-104401200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
50	chr8:104400400-104401200	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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