Variant report

Variant	esv1845068
Chromosome Location	chr8:39120649-39452805
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1245)
CpG islands
(count:1345)
Chromatin interactive
region (count:30)
LncRNA
region (count:306)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1245 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:39393079-39393534	K562	blood:	n/a	n/a
2	ARID3A	chr8:39424300-39424895	HepG2	liver:	n/a	chr8:39424646-39424662
3	ARID3A	chr8:39184983-39185219	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:39268778-39268961	K562	blood:	n/a	n/a
5	ARID3A	chr8:39391480-39391748	K562	blood:	n/a	n/a
6	ATF1	chr8:39184952-39185134	K562	blood:	n/a	n/a
7	ATF1	chr8:39204094-39204343	K562	blood:	n/a	n/a
8	ATF1	chr8:39187249-39187365	K562	blood:	n/a	n/a
9	ATF1	chr8:39393057-39393338	K562	blood:	n/a	n/a
10	ATF1	chr8:39169144-39169211	K562	blood:	n/a	n/a
11	ATF3	chr8:39390540-39390824	K562	blood:	n/a	n/a
12	BACH1	chr8:39338192-39338414	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:39180150-39180194	K562	blood:	n/a	n/a
14	BCL11A	chr8:39215071-39215373	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:39338201-39338396	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:39215146-39215389	GM12878	blood:	n/a	n/a
17	BCLAF1	chr8:39338104-39338425	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:39135297-39135321	K562	blood:	n/a	n/a
19	BHLHE40	chr8:39338212-39338395	GM12878	blood:	n/a	n/a
20	BHLHE40	chr8:39368980-39370112	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:39439456-39439600	K562	blood:	n/a	n/a
22	BHLHE40	chr8:39393076-39393265	K562	blood:	n/a	n/a
23	BHLHE40	chr8:39379884-39380110	K562	blood:	n/a	n/a
24	CBX3	chr8:39273037-39273388	K562	blood:	n/a	n/a
25	CBX3	chr8:39392968-39393340	K562	blood:	n/a	n/a
26	CBX3	chr8:39403680-39403937	K562	blood:	n/a	n/a
27	CBX3	chr8:39436347-39436562	K562	blood:	n/a	n/a
28	CBX3	chr8:39184878-39185271	HCT-116	colon:	n/a	n/a
29	CBX3	chr8:39268680-39269063	K562	blood:	n/a	n/a
30	CBX3	chr8:39241402-39241706	K562	blood:	n/a	n/a
31	CCNT2	chr8:39379762-39380551	K562	blood:	n/a	n/a
32	CCNT2	chr8:39390615-39390831	K562	blood:	n/a	n/a
33	CEBPB	chr8:39272750-39273063	K562	blood:	n/a	n/a
34	CEBPB	chr8:39393043-39393343	K562	blood:	n/a	n/a
35	CEBPB	chr8:39373801-39373927	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr8:39392971-39393463	K562	blood:	n/a	n/a
37	CEBPB	chr8:39425240-39425556	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr8:39377869-39377951	K562	blood:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
39	CEBPB	chr8:39444323-39444503	A549	lung:	n/a	chr8:39444383-39444394 chr8:39444381-39444394
40	CEBPB	chr8:39172365-39172592	A549	lung:	n/a	chr8:39172538-39172549
41	CEBPB	chr8:39377774-39377967	H1-hESC	embryonic stem cell:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
42	CEBPB	chr8:39340885-39341025	K562	blood:	n/a	n/a
43	CEBPB	chr8:39444289-39444489	IMR90	lung:	n/a	chr8:39444383-39444394 chr8:39444381-39444394
44	CEBPB	chr8:39272719-39273086	K562	blood:	n/a	n/a
45	CEBPB	chr8:39391427-39391768	K562	blood:	n/a	chr8:39391593-39391604
46	CEBPB	chr8:39301112-39301366	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr8:39255330-39255613	K562	blood:	n/a	chr8:39255462-39255475 chr8:39255464-39255475 chr8:39255464-39255473
48	CEBPB	chr8:39169394-39169417	A549	lung:	n/a	n/a
49	CEBPB	chr8:39373729-39373930	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr8:39391451-39391754	IMR90	lung:	n/a	chr8:39391593-39391604

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39171620-39171670	HCF	heart:	n/a
2	chr8:39196907-39196957	GM12878	blood:	n/a
3	chr8:39328433-39328483	HMEC	breast:	n/a
4	chr8:39171620-39171670	HCF	heart:	n/a
5	chr8:39196907-39196957	GM12878	blood:	n/a
6	chr8:39328433-39328483	HMEC	breast:	n/a
7	chr8:39442347-39442397	H1-hESC	embryonic stem cell:	embryo
8	chr8:39172022-39172072	HCF	heart:	n/a
9	chr8:39172099-39172149	AG04450	lung:	fetal
10	chr8:39223182-39223232	SKMC	muscle:	n/a
11	chr8:39441473-39441523	HepG2	liver:	n/a
12	chr8:39380341-39380391	ECC-1	luminal epithelium:	n/a
13	chr8:39172097-39172147	HUVEC	blood vessel:	n/a
14	chr8:39172022-39172072	ovcar-3	ovarian:	n/a
15	chr8:39171866-39171916	CMK	blood:	n/a
16	chr8:39171866-39171916	HNPCEpiC	eye:	n/a
17	chr8:39172020-39172070	NHBE	bronchial:	n/a
18	chr8:39380592-39380642	HRE	kidney:	n/a
19	chr8:39172022-39172072	AG10803	skin:	n/a
20	chr8:39442347-39442397	PrEC	prostate:	n/a
21	chr8:39441473-39441523	BJ	skin:	n/a
22	chr8:39172120-39172170	NHBE	bronchial:	n/a
23	chr8:39442078-39442128	GM19239	blood:	n/a
24	chr8:39223182-39223232	RPTEC	kidney:	n/a
25	chr8:39171620-39171670	AG09319	gingival:	n/a
26	chr8:39223182-39223232	HMEC	breast:	n/a
27	chr8:39172099-39172149	GM06990	blood:	n/a
28	chr8:39171648-39171698	GM12892	blood:	n/a
29	chr8:39441975-39442025	HIPEpiC	eye:	n/a
30	chr8:39442347-39442397	Hepatocyte	liver:	n/a
31	chr8:39441975-39442025	K562	blood:	n/a
32	chr8:39171648-39171698	NH-A	brain:	n/a
33	chr8:39171866-39171916	HAEpiC	amniotic membrane:	n/a
34	chr8:39380435-39380485	ProgFib	skin:	n/a
35	chr8:39442347-39442397	HAEpiC	amniotic membrane:	n/a
36	chr8:39172097-39172147	Hepatocyte	liver:	n/a
37	chr8:39442347-39442397	AG09319	gingival:	n/a
38	chr8:39172111-39172161	HPAEpiC	pulmonary alveolar:	n/a
39	chr8:39171866-39171916	AG09309	skin:	n/a
40	chr8:39172097-39172147	NHBE	bronchial:	n/a
41	chr8:39172120-39172170	HepG2	liver:	n/a
42	chr8:39172020-39172070	HepG2	liver:	n/a
43	chr8:39171620-39171670	HCPEpiC	choroid plexus:	n/a
44	chr8:39196907-39196957	HEK293	kidney:	embryo
45	chr8:39196907-39196957	HepG2	liver:	n/a
46	chr8:39441968-39442018	AoSMC	blood vessel:	n/a
47	chr8:39172020-39172070	HAEpiC	amniotic membrane:	n/a
48	chr8:39441975-39442025	HAEpiC	amniotic membrane:	n/a
49	chr8:39171620-39171670	AG04450	lung:	fetal
50	chr8:39172120-39172170	AG09309	skin:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39170463..39172530-chr8:39174983..39176968,2	MCF-7	breast:
2	chr8:39204717..39207276-chr8:39207847..39209394,2	K562	blood:
3	chr15:50661566..50662138-chr8:39161334..39161854,2	MCF-7	breast:
4	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
5	chr8:39146560..39148999-chr8:39159680..39162554,2	MCF-7	breast:
6	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
7	chr8:39436752..39438273-chr8:39442880..39445329,2	MCF-7	breast:
8	chr8:38964712..38965432-chr8:39130166..39131088,2	MCF-7	breast:
9	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
10	chr8:39130457..39132494-chr8:39133684..39136395,2	K562	blood:
11	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
12	chr8:38824064..38824622-chr8:39184733..39185545,2	K562	blood:
13	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
14	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
15	chr8:39272566..39275131-chr8:39275897..39277770,2	K562	blood:
16	chr8:39410685..39412216-chr8:39708899..39710030,6	MCF-7	breast:
17	chr8:39410966..39411938-chr8:39709121..39709647,2	MCF-7	breast:
18	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
19	chr8:39436752..39438273-chr8:39442880..39445329,2	MCF-7	breast:
20	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
21	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
22	chr8:39146560..39148999-chr8:39159680..39162554,2	MCF-7	breast:
23	chr6:156717380..156718086-chr8:39158912..39159795,2	MCF-7	breast:
24	chr8:39027799..39028359-chr8:39306044..39306636,2	MCF-7	breast:
25	chr8:39179668..39181798-chr8:39380661..39383115,2	K562	blood:
26	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
27	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
28	chr8:39130457..39132494-chr8:39133684..39136395,2	K562	blood:
29	chr8:39204717..39207276-chr8:39207847..39209394,2	K562	blood:
30	chr8:38964583..38965453-chr8:39130431..39131111,2	MCF-7	breast:

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126163
2	lnc-ADAM2-4	chr8:39274731-39274897	XLOC_007062
3	lnc-ADAM32-1	chr8:39274733-39274897	NONHSAT126150
4	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126165
5	lnc-TM2D2-6	chr8:39167428-39167962	NONHSAT126147
6	lnc-ADAM18-1	chr8:39435933-39435990	ENSG00000254082
7	lnc-ADAM18-1	chr8:39437484-39437653	NONHSAT126175
8	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT126151
9	lnc-ADAM32-1	chr8:39172182-39172236	NONHSAT126154
10	lnc-ADAM2-6	chr8:39380272-39380508	NONHSAT126165
11	lnc-ADAM2-6	chr8:39371620-39371674	NONHSAT126169
12	lnc-ADAM2-6	chr8:39331452-39331539	NONHSAT126167
13	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126155
14	lnc-ADAM2-6	chr8:39312858-39313023	NONHSAT126163
15	lnc-ADAM18-1	chr8:39437484-39437653	ENSG00000254082
16	lnc-ADAM9-1	chr8:39128394-39128433	NONHSAT126144
17	lnc-ADAM32-1	chr8:39239023-39239254	NONHSAT126150
18	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126168
19	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126169
20	lnc-ADAM18-1	chr8:39433100-39433157	NONHSAT126174
21	lnc-ADAM9-1	chr8:39133347-39133385	NONHSAT126144
22	lnc-ADAM2-6	chr8:39362860-39363037	NONHSAT126163
23	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126166
24	lnc-ADAM32-1	chr8:39172151-39172236	NONHSAT126150
25	lnc-ADAM32-1	chr8:39176971-39177024	NONHSAT126153
26	lnc-ADAM2-6	chr8:39325142-39325219	NONHSAT126165
27	lnc-ADAM9-1	chr8:39141105-39141143	NONHSAT126143
28	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126166
29	lnc-ADAM32-1	chr8:39274733-39274745	NONHSAT126155
30	lnc-ADAM32-1	chr8:39238308-39238398	NONHSAT126153
31	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126164
32	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126168
33	lnc-ADAM2-4	chr8:39274730-39274897	NONHSAT126161
34	lnc-ADAM18-1	chr8:39430763-39430927	NONHSAT126174
35	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126165
36	lnc-ADAM2-6	chr8:39362860-39363037	NONHSAT126166
37	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126152
38	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126171
39	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126148
40	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT126152
41	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126153
42	lnc-ADAM2-6	chr8:39335215-39335616	NONHSAT126167
43	lnc-ADAM32-1	chr8:39238308-39238398	NONHSAT147628
44	lnc-ADAM32-1	chr8:39274733-39274897	NONHSAT126148
45	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT126148
46	lnc-ADAM18-1	chr8:39435933-39435990	NONHSAT126175
47	lnc-ADAM18-1	chr8:39424224-39424336	ENSG00000254082
48	lnc-ADAM2-6	chr8:39361493-39361558	NONHSAT126166
49	lnc-ADAM32-1	chr8:39260325-39260375	NONHSAT126148
50	lnc-ADAM2-6	chr8:39308564-39308680	NONHSAT126164

No data

Variant related genes	Relation type
ADAM32	TF binding region
ENSG00000253160	TF binding region
ENSG00000252176	TF binding region
ADAM18	TF binding region
ADAM5	TF binding region
ENSG00000254067	TF binding region
ENSG00000254082	TF binding region
ADAM3A	TF binding region
ADAM32	CpG island
ENSG00000253160	CpG island
ENSG00000252176	CpG island
ADAM18	CpG island
ADAM5	CpG island
ENSG00000254067	CpG island
ENSG00000254082	CpG island
ADAM3A	CpG island
ENSG00000197140	chromatin interactions
ENSG00000196115	chromatin interactions

Extended variants
information (count: 4310 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:4310 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6986118	chr8:39120664-39120665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551477111	chr8:39120688-39120689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535777841	chr8:39120705-39120706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555398511	chr8:39120738-39120739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181861247	chr8:39120748-39120749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537863352	chr8:39120809-39120810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558188171	chr8:39120812-39120813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577759937	chr8:39120857-39120858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185695157	chr8:39120859-39120860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553978000	chr8:39120917-39120918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573971496	chr8:39120951-39120952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117760900	chr8:39120983-39120984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534324227	chr8:39120997-39120998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563054405	chr8:39121006-39121007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530485133	chr8:39121070-39121071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543868379	chr8:39121077-39121078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189413136	chr8:39121079-39121080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181054486	chr8:39121086-39121087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546794814	chr8:39121087-39121088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570403344	chr8:39121097-39121098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149287106	chr8:39121103-39121104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577190456	chr8:39121230-39121231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368144357	chr8:39121256-39121257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371337025	chr8:39121263-39121264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529115338	chr8:39121270-39121271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549217226	chr8:39121309-39121310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76575227	chr8:39121343-39121344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538231372	chr8:39121371-39121372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557909273	chr8:39121407-39121408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556196898	chr8:39121493-39121494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186307079	chr8:39121509-39121510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534058577	chr8:39121511-39121512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76679777	chr8:39121512-39121513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78711566	chr8:39121566-39121567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111916981	chr8:39121663-39121664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541756775	chr8:39121704-39121705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190140632	chr8:39121753-39121754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556770624	chr8:39121765-39121766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368701949	chr8:39121767-39121768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559941543	chr8:39121798-39121799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571892289	chr8:39121811-39121812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144625619	chr8:39121813-39121814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13260825	chr8:39121817-39121818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148474736	chr8:39121818-39121819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181406971	chr8:39121822-39121823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13260826	chr8:39121824-39121825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185941360	chr8:39121829-39121830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554933045	chr8:39121831-39121832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545506737	chr8:39121836-39121837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74339891	chr8:39121841-39121842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	21979893	CNVD
Prostate cancer	16573809	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
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	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
Colorectal cancer	16272173	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
Melanoma	18172304	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
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Breast cancer	16620391	CNVD
Adrenocortical carcinoma	18281524	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Lung cancer	21569311	CNVD
Prader-willi syndrome	20588305	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Chordoma	21215367	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Medulloblastoma	21163964	CNVD
Cancer	21249187	CNVD
Autism	19287141	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Rett syndrome	21593744	CNVD
Recurrent pregnancy loss	19789632	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39099800-39124600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:39122000-39123000	Enhancers	Hela-S3	cervix
3	chr8:39122200-39122800	Enhancers	NHEK	skin
4	chr8:39124400-39124800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr8:39124600-39125600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:39125200-39125800	Enhancers	HepG2	liver
7	chr8:39125600-39129200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:39129200-39131200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr8:39129400-39130000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr8:39129400-39130600	Enhancers	HMEC	breast
11	chr8:39129600-39130600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:39129800-39130600	Enhancers	NHEK	skin
13	chr8:39135000-39135200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:39135000-39135200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr8:39135200-39135400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:39135600-39135800	Enhancers	HepG2	liver
17	chr8:39137200-39137600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr8:39137400-39137800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:39140600-39141000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr8:39146000-39146400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr8:39163200-39163600	Enhancers	Gastric	stomach
22	chr8:39163200-39163800	Enhancers	Fetal Intestine Small	intestine
23	chr8:39171400-39171600	Bivalent Enhancer	Fetal Lung	lung
24	chr8:39171600-39171800	Enhancers	Fetal Brain Female	brain
25	chr8:39171600-39172000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
26	chr8:39171600-39172000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
27	chr8:39171600-39172400	Bivalent/Poised TSS	Fetal Lung	lung
28	chr8:39171800-39172000	Bivalent/Poised TSS	NH-A	brain
29	chr8:39171800-39172200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr8:39171800-39172200	Active TSS	Brain Anterior Caudate	brain
31	chr8:39171800-39172400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr8:39171800-39172400	Active TSS	Brain Angular Gyrus	brain
33	chr8:39171800-39172400	Active TSS	Brain Germinal Matrix	brain
34	chr8:39171800-39172400	Bivalent/Poised TSS	Fetal Brain Male	brain
35	chr8:39171800-39172400	Active TSS	Fetal Brain Female	brain
36	chr8:39172000-39172200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
37	chr8:39172000-39172200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr8:39172000-39172200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
39	chr8:39172000-39172200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr8:39172000-39172200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr8:39172000-39172200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr8:39172000-39172200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr8:39172000-39172200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
44	chr8:39172000-39172200	Enhancers	Fetal Heart	heart
45	chr8:39172000-39172200	Bivalent Enhancer	Psoas Muscle	Psoas
46	chr8:39172000-39172200	Active TSS	Rectal Smooth Muscle	rectum
47	chr8:39172000-39172200	Bivalent Enhancer	NHDF-Ad	bronchial
48	chr8:39172000-39172400	ZNF genes & repeats	Aorta	Aorta
49	chr8:39172000-39172400	Enhancers	Placenta	Placenta
50	chr8:39172000-39172600	Active TSS	Stomach Smooth Muscle	stomach

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