Variant report

Variant	esv2753066
Chromosome Location	chr8:11859740-12443162
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4406)
CpG islands
(count:4949)
Chromatin interactive
region (count:3)
LncRNA
region (count:92)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4406 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:12433133-12433253	K562	blood:	n/a	n/a
2	ARID3A	chr8:11872669-11872691	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:12051904-12051921	HepG2	liver:	n/a	n/a
4	ATF1	chr8:12435183-12435242	K562	blood:	n/a	n/a
5	ATF1	chr8:12051725-12051925	K562	blood:	n/a	n/a
6	ATF1	chr8:12400593-12400794	K562	blood:	n/a	n/a
7	ATF1	chr8:12417563-12417956	K562	blood:	n/a	n/a
8	ATF1	chr8:12307263-12307299	K562	blood:	n/a	n/a
9	ATF1	chr8:12420358-12420412	K562	blood:	n/a	n/a
10	ATF2	chr8:12400579-12400848	GM12878	blood:	n/a	n/a
11	ATF2	chr8:12400598-12400937	GM12878	blood:	n/a	n/a
12	BACH1	chr8:12415419-12415446	K562	blood:	n/a	n/a
13	BATF	chr8:12216425-12216654	GM12878	blood:	n/a	chr8:12216571-12216582
14	BATF	chr8:12037596-12037795	GM12878	blood:	n/a	n/a
15	BATF	chr8:12051326-12051536	GM12878	blood:	n/a	n/a
16	BATF	chr8:12167856-12168080	GM12878	blood:	n/a	n/a
17	BATF	chr8:12046059-12046358	GM12878	blood:	n/a	n/a
18	BATF	chr8:12219374-12219663	GM12878	blood:	n/a	n/a
19	BATF	chr8:11965355-11965780	GM12878	blood:	n/a	n/a
20	BATF	chr8:12282435-12282799	GM12878	blood:	n/a	n/a
21	BATF	chr8:12380131-12380636	GM12878	blood:	n/a	n/a
22	BATF	chr8:12081387-12081678	GM12878	blood:	n/a	n/a
23	BATF	chr8:12052217-12052442	GM12878	blood:	n/a	n/a
24	BATF	chr8:12216425-12216722	GM12878	blood:	n/a	chr8:12216571-12216582
25	BATF	chr8:12142536-12142891	GM12878	blood:	n/a	n/a
26	BATF	chr8:12432790-12433098	GM12878	blood:	n/a	n/a
27	BATF	chr8:11921281-11921530	GM12878	blood:	n/a	n/a
28	BATF	chr8:12355078-12355365	GM12878	blood:	n/a	n/a
29	BATF	chr8:12037531-12037813	GM12878	blood:	n/a	n/a
30	BATF	chr8:12374697-12374930	GM12878	blood:	n/a	n/a
31	BATF	chr8:12294490-12294715	GM12878	blood:	n/a	n/a
32	BATF	chr8:12277703-12278063	GM12878	blood:	n/a	n/a
33	BATF	chr8:11970251-11970426	GM12878	blood:	n/a	chr8:11970334-11970345
34	BATF	chr8:12350272-12350570	GM12878	blood:	n/a	chr8:12350419-12350430
35	BATF	chr8:12400443-12400987	GM12878	blood:	n/a	chr8:12400955-12400964
36	BATF	chr8:12379472-12380084	GM12878	blood:	n/a	n/a
37	BATF	chr8:12437849-12438015	GM12878	blood:	n/a	n/a
38	BATF	chr8:12372870-12373261	GM12878	blood:	n/a	chr8:12372948-12372956
39	BATF	chr8:12211595-12212020	GM12878	blood:	n/a	n/a
40	BATF	chr8:12278913-12279099	GM12878	blood:	n/a	n/a
41	BATF	chr8:12379045-12379257	GM12878	blood:	n/a	n/a
42	BATF	chr8:12409298-12409599	GM12878	blood:	n/a	n/a
43	BATF	chr8:12282063-12282262	GM12878	blood:	n/a	n/a
44	BATF	chr8:12292671-12292987	GM12878	blood:	n/a	n/a
45	BATF	chr8:12355171-12355376	GM12878	blood:	n/a	n/a
46	BATF	chr8:12040152-12040516	GM12878	blood:	n/a	n/a
47	BATF	chr8:12380639-12380871	GM12878	blood:	n/a	n/a
48	BATF	chr8:12375857-12376804	GM12878	blood:	n/a	n/a
49	BATF	chr8:12385574-12385905	GM12878	blood:	n/a	n/a
50	BATF	chr8:12081356-12081721	GM12878	blood:	n/a	n/a

(count:4949 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:12033377-12033427	HCPEpiC	choroid plexus:	n/a
2	chr8:11973495-11973545	CMK	blood:	n/a
3	chr8:12027122-12027172	PFSK-1	brain:	n/a
4	chr8:11947722-11947772	NB4	blood:	n/a
5	chr8:11872882-11872932	Jurkat	blood:	n/a
6	chr8:12294380-12294430	SK-N-SH_RA	brain:	n/a
7	chr8:12236258-12236308	ECC-1	luminal epithelium:	n/a
8	chr8:12040795-12040845	AG09319	gingival:	n/a
9	chr8:12033377-12033427	HCPEpiC	choroid plexus:	n/a
10	chr8:11973495-11973545	CMK	blood:	n/a
11	chr8:12027122-12027172	PFSK-1	brain:	n/a
12	chr8:11947722-11947772	NB4	blood:	n/a
13	chr8:11872882-11872932	Jurkat	blood:	n/a
14	chr8:12294380-12294430	SK-N-SH_RA	brain:	n/a
15	chr8:12236258-12236308	ECC-1	luminal epithelium:	n/a
16	chr8:12040795-12040845	AG09319	gingival:	n/a
17	chr8:12052924-12052974	HEEpiC	esophagus:	n/a
18	chr8:12048124-12048174	H1-hESC	embryonic stem cell:	embryo
19	chr8:11977206-11977256	ECC-1	luminal epithelium:	n/a
20	chr8:12052102-12052152	HRPEpiC	eye:	n/a
21	chr8:12272982-12273032	SK-N-MC	brain:	n/a
22	chr8:11986501-11986551	RPTEC	kidney:	n/a
23	chr8:12296542-12296592	HEK293	kidney:	embryo
24	chr8:12426340-12426390	SK-N-SH_RA	brain:	n/a
25	chr8:11870338-11870388	HCM	heart:	n/a
26	chr8:12293513-12293563	ProgFib	skin:	n/a
27	chr8:11946498-11946548	AG04450	lung:	fetal
28	chr8:11947722-11947772	CMK	blood:	n/a
29	chr8:12033377-12033427	HAEpiC	amniotic membrane:	n/a
30	chr8:12237900-12237950	RPTEC	kidney:	n/a
31	chr8:12052164-12052214	AG09319	gingival:	n/a
32	chr8:12435562-12435612	SKMC	muscle:	n/a
33	chr8:12435562-12435612	HepG2	liver:	n/a
34	chr8:12033377-12033427	T-47D	breast:	n/a
35	chr8:12236258-12236308	GM12878	blood:	n/a
36	chr8:11973029-11973079	BJ	skin:	n/a
37	chr8:12244544-12244594	SK-N-MC	brain:	n/a
38	chr8:12429581-12429631	HCT-116	colon:	n/a
39	chr8:11872659-11872709	H1-hESC	embryonic stem cell:	embryo
40	chr8:11970655-11970705	PANC-1	pancreas:	n/a
41	chr8:11876646-11876696	AG04450	lung:	fetal
42	chr8:11991521-11991571	T-47D	breast:	n/a
43	chr8:12237780-12237830	K562	blood:	n/a
44	chr8:11996327-11996377	HRCEpiC	kidney:	n/a
45	chr8:12237626-12237676	GM12892	blood:	n/a
46	chr8:11973029-11973079	SKMC	muscle:	n/a
47	chr8:11907551-11907601	HNPCEpiC	eye:	n/a
48	chr8:12256259-12256309	HCF	heart:	n/a
49	chr8:11870063-11870113	AG04450	lung:	fetal
50	chr8:11972998-11973048	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr11:64863606..64864139-chr8:11882400..11882963,2	Hela-S3	cervix:
2	chr10:101006536..101007134-chr8:11906757..11907257,2	MCF-7	breast:
3	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:

(count:92 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC130352.1-5	chr8:12263898-12264442	ucscGeneNc_uc010lsi_1
2	lnc-ZNF705D-2	chr8:12298509-12298570	NONHSAT125147
3	lnc-USP17L2-1	chr8:11985367-11986806	NONHSAT125118
4	lnc-ZNF705D-2	chr8:12423395-12424354	NONHSAT125127
5	lnc-ZNF705D-3	chr8:12295784-12296020	XLOC_006721
6	lnc-ZNF705D-2	chr8:12059991-12060129	NONHSAT125127
7	lnc-AC130352.1-5	chr8:12270119-12270182	ucscGeneNc_uc010lsi_1
8	lnc-ZNF705D-2	chr8:12245250-12245374	ENSG00000227888.3
9	lnc-AC130352.1-5	chr8:12290147-12290214	ucscGeneNc_uc010lsi_1
10	lnc-ZNF705D-2	chr8:12426979-12428991	NONHSAT125162
11	lnc-AC130352.1-4	chr8:12270336-12271882	ENSG00000270074.1
12	lnc-AC130352.1-5	chr8:12312845-12312881	ucscGeneNc_uc010lsi_1
13	lnc-AC130352.1-5	chr8:12289838-12289899	ucscGeneNc_uc010lsi_1
14	lnc-ZNF705D-2	chr8:12294522-12295219	NONHSAT125148
15	lnc-ZNF705D-2	chr8:12053400-12053457	XLOC_006719
16	lnc-ZNF705D-2	chr8:12423395-12424354	NONHSAT125147
17	lnc-ZNF705D-2	chr8:12298478-12298570	NONHSAT125148
18	lnc-ZNF705D-2	chr8:12056213-12056305	XLOC_006719
19	lnc-AC130352.1-3	chr8:12435815-12438798	NONHSAT125164
20	lnc-ZNF705D-2	chr8:11998190-11998224	NONHSAT125119
21	lnc-ZNF705D-3	chr8:12298509-12298570	XLOC_006721
22	lnc-ZNF705D-2	chr8:12245250-12245374	NONHSAT125138
23	lnc-ZNF705D-2	chr8:12428214-12428329	NONHSAT125158
24	lnc-ZNF705D-3	chr8:12299097-12299198	XLOC_006721
25	lnc-ZNF705D-3	chr8:12295801-12296020	XLOC_006721
26	lnc-ZNF705D-2	chr8:12002932-12003176	NONHSAT125119
27	lnc-ZNF705D-2	chr8:12388452-12388540	NONHSAT125147
28	lnc-ZNF705D-2	chr8:12355092-12355358	NONHSAT125148
29	lnc-ZNF705D-2	chr8:12245467-12245528	NONHSAT125138
30	lnc-ZNF705D-2	chr8:12295673-12296020	NONHSAT125148
31	lnc-ZNF705D-2	chr8:12423395-12423557	NONHSAT125158
32	lnc-ZNF705D-2	chr8:12053400-12053747	XLOC_006719
33	lnc-ZNF705D-3	chr8:12295920-12296020	XLOC_006721
34	lnc-ZNF705D-2	chr8:12388452-12388540	NONHSAT125148
35	lnc-ZNF705D-2	chr8:12276651-12276793	NONHSAT125139
36	lnc-ZNF705D-2	chr8:12225748-12225811	ENSG00000227888.3
37	lnc-ZNF705D-3	chr8:12295112-12295219	XLOC_006721
38	lnc-ZNF705D-2	chr8:12277210-12279968	NONHSAT125139
39	lnc-ZNF705D-2	chr8:12388452-12388540	NONHSAT125127
40	lnc-ZNF705D-3	chr8:12298509-12298570	XLOC_006721
41	lnc-ZNF705D-2	chr8:12219891-12220071	ENSG00000227888.3
42	lnc-AC130352.1-2	chr8:12306848-12307964	ENSG00000215248
43	lnc-ZNF705D-2	chr8:12228304-12228337	NONHSAT125138
44	lnc-ZNF705D-3	chr8:12295112-12295219	XLOC_006721
45	lnc-ZNF705D-2	chr8:12245760-12245843	NONHSAT125138
46	lnc-ZNF705D-2	chr8:12034891-12035004	NONHSAT125117
47	lnc-ZNF705D-2	chr8:12355092-12355358	NONHSAT125127
48	lnc-ZNF705D-3	chr8:12302265-12302380	XLOC_006721
49	lnc-ZNF705D-3	chr8:12298478-12298570	XLOC_006721
50	lnc-ZNF705D-2	chr8:12408261-12408540	NONHSAT125158

No data

Variant related genes	Relation type
FAM86B2	TF binding region
DEFB109P3	TF binding region
ENSG00000238460	TF binding region
DEFB108P3	TF binding region
FAM66A	TF binding region
ENPP7P6	TF binding region
RNA5SP253	TF binding region
USP17L7	TF binding region
ENSG00000255016	TF binding region
LINC00965	TF binding region
ENSG00000270154	TF binding region
ALG1L11P	TF binding region
USP17L2	TF binding region
FAM90A2P	TF binding region
DEFB109P1	TF binding region
FAM66D	TF binding region
ENSG00000221714	TF binding region
ENSG00000255122	TF binding region
DEFB108P4	TF binding region
ZNF705D	TF binding region
ENSG00000254923	TF binding region
FAM85A	TF binding region
ENSG00000265826	TF binding region
ENPP7P12	TF binding region
RPS3AP34	TF binding region
ENSG00000254507	TF binding region
ENSG00000233050	TF binding region
ALG1L12P	TF binding region
FAM86B1	TF binding region
ENSG00000255098	TF binding region
RNA5SP254	TF binding region
ENSG00000255556	TF binding region
ZNF705C	TF binding region
DEFB130	TF binding region
OR7E160P	TF binding region
ENSG00000237215	TF binding region
ENSG00000254423	TF binding region
FAM90A25P	TF binding region
ENSG00000254700	TF binding region
ENSG00000266637	TF binding region
FAM86B2	CpG island
DEFB109P3	CpG island
ENSG00000238460	CpG island
DEFB108P3	CpG island
FAM66A	CpG island
ENPP7P6	CpG island
RNA5SP253	CpG island
USP17L7	CpG island
ENSG00000255016	CpG island
LINC00965	CpG island
ENSG00000270154	CpG island
ALG1L11P	CpG island
USP17L2	CpG island
FAM90A2P	CpG island
DEFB109P1	CpG island
FAM66D	CpG island
ENSG00000221714	CpG island
ENSG00000255122	CpG island
DEFB108P4	CpG island
ZNF705D	CpG island
ENSG00000254923	CpG island
FAM85A	CpG island
ENSG00000265826	CpG island
ENPP7P12	CpG island
RPS3AP34	CpG island
ENSG00000254507	CpG island
ENSG00000233050	CpG island
ALG1L12P	CpG island
FAM86B1	CpG island
ENSG00000255098	CpG island
RNA5SP254	CpG island
ENSG00000255556	CpG island
ZNF705C	CpG island
DEFB130	CpG island
OR7E160P	CpG island
ENSG00000237215	CpG island
ENSG00000254423	CpG island
FAM90A25P	CpG island
ENSG00000254700	CpG island
ENSG00000266637	CpG island
ENSG00000149823	chromatin interactions
ZNF597	miRNA target sites
C9orf150	miRNA target sites
TMEM30B	miRNA target sites

Extended variants
information (count: 11139 )
Associated
traits (count: 151 )

Variant overlapped rSNPs/rCNVs (count:11139 , 50 per page) page: 1 2 3 4 5 6 7 ... 223

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541327214	chr8:11860938-11860939	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs560039460	chr8:11860959-11860960	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs374497879	chr8:11860981-11860982	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs542245247	chr8:11860995-11860996	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs563611238	chr8:11860998-11860999	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs144043529	chr8:11861000-11861001	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs549969660	chr8:11861018-11861019	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs571477340	chr8:11861077-11861078	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs532401686	chr8:11861083-11861084	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs377757882	chr8:11861101-11861102	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs556603951	chr8:11861129-11861130	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs565998902	chr8:11861135-11861136	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs535850142	chr8:11861137-11861138	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs554570757	chr8:11861151-11861152	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs569615489	chr8:11861211-11861212	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs556670318	chr8:11861220-11861221	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs536757396	chr8:11861263-11861264	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs10107274	chr8:11861280-11861281	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs577017104	chr8:11861285-11861286	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs538997230	chr8:11861332-11861333	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs374225174	chr8:11861341-11861342	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs553377744	chr8:11861365-11861366	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs575107858	chr8:11861403-11861404	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs552688298	chr8:11861497-11861498	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs10107517	chr8:11861501-11861502	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs530987261	chr8:11861526-11861527	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs184899634	chr8:11861527-11861528	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs564618108	chr8:11861565-11861566	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs188515107	chr8:11861578-11861579	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs576957217	chr8:11861583-11861584	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs111897736	chr8:11863174-11863175	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs550262306	chr8:11863192-11863193	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs72496203	chr8:11863206-11863207	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs200015107	chr8:11863253-11863254	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs544375523	chr8:11864032-11864033	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs530469382	chr8:11866812-11866813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552241891	chr8:11866860-11866861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570490098	chr8:11866861-11866862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7823991	chr8:11866862-11866863	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs546902491	chr8:11866863-11866864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568736359	chr8:11866879-11866880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536166169	chr8:11866893-11866894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557347068	chr8:11866897-11866898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs386722355	chr8:11866906-11866907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138780537	chr8:11866907-11866908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558208851	chr8:11866908-11866909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573278035	chr8:11866912-11866913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566399012	chr8:11866915-11866916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541186520	chr8:11866920-11866921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368822152	chr8:11866934-11866935	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:151)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Osteosarcoma	21215367	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20688739	CNVD
Pancreatic cancer	17952125	CNVD
Intracranial tumor	22048656	CNVD
Ollier disease	21235737	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1552 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11866800-11867200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:11867000-11867200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:11867000-11867400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:11867000-11869800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr8:11867200-11868000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:11868000-11869800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:11869000-11869200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr8:11869800-11870200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:11869800-11870400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr8:11870200-11871000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:11870400-11872800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr8:11870800-11871200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:11871000-11871200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr8:11871200-11872800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr8:11871400-11871600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr8:11871400-11871800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:11871400-11872600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
18	chr8:11871600-11871800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:11871600-11871800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr8:11871600-11871800	Enhancers	Stomach Smooth Muscle	stomach
21	chr8:11871600-11872000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
22	chr8:11871600-11872000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr8:11871600-11872000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:11871600-11872000	Bivalent Enhancer	Fetal Stomach	stomach
25	chr8:11871600-11872000	Enhancers	HMEC	breast
26	chr8:11871800-11872000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr8:11871800-11872200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
28	chr8:11871800-11872200	Enhancers	Colon Smooth Muscle	Colon
29	chr8:11871800-11872400	Enhancers	Primary B cells from cord blood	blood
30	chr8:11871800-11872400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr8:11871800-11872400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr8:11871800-11872600	Active TSS	H9 Cell Line	embryonic stem cell
33	chr8:11871800-11872600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
34	chr8:11871800-11872600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr8:11871800-11872600	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr8:11871800-11872600	Active TSS	Brain Anterior Caudate	brain
37	chr8:11871800-11872600	Active TSS	Stomach Smooth Muscle	stomach
38	chr8:11871800-11872800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
39	chr8:11871800-11873000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr8:11872000-11872200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:11872000-11872200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:11872000-11872200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr8:11872000-11872200	Enhancers	Primary hematopoietic stem cells	blood
44	chr8:11872000-11872200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr8:11872000-11872200	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr8:11872000-11872200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr8:11872000-11872200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr8:11872000-11872200	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr8:11872000-11872200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr8:11872000-11872200	Enhancers	Fetal Brain Male	brain

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