Variant report

Variant	nsv831297
Chromosome Location	chr8:39301121-39434693
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:482)
CpG islands
(count:244)
Chromatin interactive
region (count:13)
LncRNA
region (count:149)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:39391480-39391748	K562	blood:	n/a	n/a
2	ARID3A	chr8:39424300-39424895	HepG2	liver:	n/a	chr8:39424646-39424662
3	ARID3A	chr8:39393079-39393534	K562	blood:	n/a	n/a
4	ATF1	chr8:39393057-39393338	K562	blood:	n/a	n/a
5	ATF3	chr8:39390540-39390824	K562	blood:	n/a	n/a
6	BACH1	chr8:39338192-39338414	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr8:39338201-39338396	GM12878	blood:	n/a	n/a
8	BCLAF1	chr8:39338104-39338425	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:39338212-39338395	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:39368980-39370112	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:39379884-39380110	K562	blood:	n/a	n/a
12	BHLHE40	chr8:39393076-39393265	K562	blood:	n/a	n/a
13	CBX3	chr8:39403680-39403937	K562	blood:	n/a	n/a
14	CBX3	chr8:39392968-39393340	K562	blood:	n/a	n/a
15	CCNT2	chr8:39379762-39380551	K562	blood:	n/a	n/a
16	CCNT2	chr8:39390615-39390831	K562	blood:	n/a	n/a
17	CEBPB	chr8:39391429-39391709	HepG2	liver:	n/a	chr8:39391593-39391604
18	CEBPB	chr8:39301088-39301411	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:39390555-39390826	K562	blood:	n/a	n/a
20	CEBPB	chr8:39391451-39391754	IMR90	lung:	n/a	chr8:39391593-39391604
21	CEBPB	chr8:39417758-39418058	IMR90	lung:	n/a	chr8:39417873-39417884 chr8:39417830-39417841
22	CEBPB	chr8:39417741-39418065	HepG2	liver:	n/a	chr8:39417873-39417884 chr8:39417830-39417841
23	CEBPB	chr8:39393010-39393254	K562	blood:	n/a	n/a
24	CEBPB	chr8:39373801-39373927	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:39377869-39377951	K562	blood:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
26	CEBPB	chr8:39377774-39377967	H1-hESC	embryonic stem cell:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
27	CEBPB	chr8:39391427-39391768	K562	blood:	n/a	chr8:39391593-39391604
28	CEBPB	chr8:39373655-39374022	IMR90	lung:	n/a	n/a
29	CEBPB	chr8:39373790-39373924	K562	blood:	n/a	n/a
30	CEBPB	chr8:39340885-39341025	K562	blood:	n/a	n/a
31	CEBPB	chr8:39392971-39393463	K562	blood:	n/a	n/a
32	CEBPB	chr8:39425240-39425556	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr8:39417791-39417944	K562	blood:	n/a	chr8:39417873-39417884 chr8:39417830-39417841
34	CEBPB	chr8:39393043-39393343	K562	blood:	n/a	n/a
35	CEBPB	chr8:39301112-39301366	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr8:39390600-39390943	K562	blood:	n/a	n/a
37	CEBPB	chr8:39373729-39373930	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr8:39377723-39378059	IMR90	lung:	n/a	chr8:39377888-39377905 chr8:39377891-39377900 chr8:39377889-39377900 chr8:39377889-39377902
39	CEBPD	chr8:39392925-39393295	K562	blood:	n/a	n/a
40	CEBPD	chr8:39392946-39393345	K562	blood:	n/a	n/a
41	CEBPD	chr8:39390559-39390864	K562	blood:	n/a	n/a
42	CEBPD	chr8:39390527-39390847	K562	blood:	n/a	n/a
43	CHD1	chr8:39338195-39338500	GM12878	blood:	n/a	n/a
44	CHD2	chr8:39338173-39338614	GM12878	blood:	n/a	n/a
45	CHD2	chr8:39328713-39329005	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr8:39411046-39411240	Hela-S3	cervix:	n/a	chr8:39411141-39411149 chr8:39411138-39411156 chr8:39411141-39411154 chr8:39411141-39411154
47	CTCF	chr8:39411040-39411190	MCF-7	breast:	n/a	chr8:39411141-39411149 chr8:39411138-39411156 chr8:39411141-39411154 chr8:39411141-39411154
48	CTCF	chr8:39411080-39411230	MCF-7	breast:	n/a	chr8:39411141-39411149 chr8:39411138-39411156 chr8:39411141-39411154 chr8:39411141-39411154
49	CTCF	chr8:39304020-39304170	NHLF	lung:	n/a	n/a
50	CTCF	chr8:39411048-39411252	MCF-7	breast:	n/a	chr8:39411141-39411149 chr8:39411138-39411156 chr8:39411141-39411154 chr8:39411141-39411154

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39328433-39328483	PrEC	prostate:	n/a
2	chr8:39380341-39380391	HRPEpiC	eye:	n/a
3	chr8:39380435-39380485	GM12891	blood:	n/a
4	chr8:39380435-39380485	GM06990	blood:	n/a
5	chr8:39328433-39328483	HMEC	breast:	n/a
6	chr8:39380592-39380642	MCF-7	breast:	n/a
7	chr8:39380592-39380642	SKMC	muscle:	n/a
8	chr8:39380435-39380485	HRE	kidney:	n/a
9	chr8:39328433-39328483	AoSMC	blood vessel:	n/a
10	chr8:39380435-39380485	CMK	blood:	n/a
11	chr8:39380435-39380485	AG09319	gingival:	n/a
12	chr8:39328433-39328483	HNPCEpiC	eye:	n/a
13	chr8:39380341-39380391	CMK	blood:	n/a
14	chr8:39380341-39380391	GM06990	blood:	n/a
15	chr8:39380435-39380485	NHBE	bronchial:	n/a
16	chr8:39328433-39328483	NH-A	brain:	n/a
17	chr8:39380341-39380391	K562	blood:	n/a
18	chr8:39380592-39380642	MCF10A-Er-Src	breast:	n/a
19	chr8:39380592-39380642	HepG2	liver:	n/a
20	chr8:39380341-39380391	HCM	heart:	n/a
21	chr8:39380341-39380391	HMEC	breast:	n/a
22	chr8:39380592-39380642	NH-A	brain:	n/a
23	chr8:39328433-39328483	SK-N-SH_RA	brain:	n/a
24	chr8:39380592-39380642	GM12892	blood:	n/a
25	chr8:39380435-39380485	Hela-S3	cervix:	n/a
26	chr8:39380435-39380485	HEEpiC	esophagus:	n/a
27	chr8:39380592-39380642	NHBE	bronchial:	n/a
28	chr8:39380592-39380642	HCF	heart:	n/a
29	chr8:39380592-39380642	IMR90	lung:	fetal
30	chr8:39380592-39380642	ovcar-3	ovarian:	n/a
31	chr8:39380592-39380642	LNCaP	prostate:	n/a
32	chr8:39328433-39328483	AG04449	skin:	fetal
33	chr8:39380435-39380485	AG04450	lung:	fetal
34	chr8:39328433-39328483	CMK	blood:	n/a
35	chr8:39328433-39328483	GM12878	blood:	n/a
36	chr8:39380435-39380485	A549	lung:	n/a
37	chr8:39328433-39328483	BJ	skin:	n/a
38	chr8:39328433-39328483	Jurkat	blood:	n/a
39	chr8:39380435-39380485	HAEpiC	amniotic membrane:	n/a
40	chr8:39380435-39380485	GM12892	blood:	n/a
41	chr8:39380341-39380391	Hela-S3	cervix:	n/a
42	chr8:39328433-39328483	NHDF-neo	bronchial:	n/a
43	chr8:39380435-39380485	HIPEpiC	eye:	n/a
44	chr8:39380341-39380391	NHBE	bronchial:	n/a
45	chr8:39380341-39380391	NHDF-neo	bronchial:	n/a
46	chr8:39380435-39380485	HRPEpiC	eye:	n/a
47	chr8:39380592-39380642	GM06990	blood:	n/a
48	chr8:39328433-39328483	GM12891	blood:	n/a
49	chr8:39328433-39328483	AG09319	gingival:	n/a
50	chr8:39328433-39328483	HEK293	kidney:	embryo

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
2	chr8:39027799..39028359-chr8:39306044..39306636,2	MCF-7	breast:
3	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
4	chr8:39410685..39412216-chr8:39708899..39710030,6	MCF-7	breast:
5	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
6	chr8:39330052..39332420-chr8:39336777..39338505,2	K562	blood:
7	chr8:39410966..39411938-chr8:39709121..39709647,2	MCF-7	breast:
8	chr8:39381512..39383756-chr8:39389034..39392927,3	K562	blood:
9	chr8:39382256..39384894-chr8:39388828..39390534,2	K562	blood:
10	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
11	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
12	chr8:39383877..39386094-chr8:39398092..39400099,2	K562	blood:
13	chr8:39179668..39181798-chr8:39380661..39383115,2	K562	blood:

(count:149 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126165
2	lnc-ADAM2-6	chr8:39331001-39331181	NONHSAT126168
3	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126169
4	lnc-ADAM18-1	chr8:39430763-39430927	ENSG00000254082
5	lnc-ADAM2-6	chr8:39358434-39358505	NONHSAT126164
6	lnc-ADAM2-6	chr8:39380272-39380390	NONHSAT126171
7	lnc-ADAM2-6	chr8:39380272-39380508	NONHSAT126165
8	lnc-ADAM2-6	chr8:39331452-39331539	NONHSAT126166
9	lnc-ADAM2-6	chr8:39362860-39363037	NONHSAT126168
10	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126163
11	lnc-ADAM18-2	chr8:39415511-39415698	NONHSAT126172
12	lnc-ADAM2-6	chr8:39312858-39313023	NONHSAT126164
13	lnc-ADAM2-6	chr8:39371620-39371674	NONHSAT126169
14	lnc-ADAM2-6	chr8:39380272-39380508	NONHSAT126166
15	lnc-ADAM2-6	chr8:39332029-39332224	NONHSAT126167
16	lnc-ADAM2-6	chr8:39358434-39358505	NONHSAT126166
17	lnc-ADAM2-6	chr8:39380272-39380344	NONHSAT126168
18	lnc-ADAM18-1	chr8:39433100-39433157	NONHSAT126174
19	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126166
20	lnc-ADAM2-6	chr8:39371620-39371674	NONHSAT126164
21	lnc-ADAM2-6	chr8:39361493-39361558	NONHSAT126168
22	lnc-ADAM2-6	chr8:39380272-39380508	NONHSAT126164
23	lnc-ADAM2-6	chr8:39332029-39332224	NONHSAT126164
24	lnc-ADAM2-6	chr8:39311569-39311619	NONHSAT126168
25	lnc-ADAM2-6	chr8:39323364-39323478	NONHSAT126166
26	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126165
27	lnc-ADAM2-6	chr8:39331001-39331181	NONHSAT126164
28	lnc-ADAM2-6	chr8:39363315-39363391	NONHSAT126165
29	lnc-ADAM2-6	chr8:39356853-39356934	NONHSAT126165
30	lnc-ADAM18-1	chr8:39433100-39433157	ENSG00000254082
31	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126164
32	lnc-ADAM2-6	chr8:39349344-39349527	NONHSAT126166
33	lnc-ADAM2-6	chr8:39308567-39308680	NONHSAT126168
34	lnc-ADAM2-6	chr8:39371620-39371674	NONHSAT126171
35	lnc-ADAM2-6	chr8:39370097-39370175	NONHSAT126171
36	lnc-ADAM2-6	chr8:39325142-39325219	NONHSAT126168
37	lnc-ADAM2-6	chr8:39361493-39361558	NONHSAT126165
38	lnc-ADAM2-6	chr8:39358434-39358505	NONHSAT126165
39	lnc-ADAM2-6	chr8:39380272-39380508	NONHSAT126163
40	lnc-ADAM2-6	chr8:39332942-39333040	NONHSAT126169
41	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126166
42	lnc-ADAM2-6	chr8:39371620-39371674	NONHSAT126163
43	lnc-ADAM2-6	chr8:39350630-39350766	NONHSAT126164
44	lnc-ADAM2-6	chr8:39347782-39347876	NONHSAT126165
45	lnc-ADAM2-6	chr8:39380272-39380371	NONHSAT126169
46	lnc-ADAM18-1	chr8:39424224-39424336	ENSG00000254082
47	lnc-ADAM2-6	chr8:39308564-39308680	NONHSAT126166
48	lnc-ADAM2-6	chr8:39361493-39361558	NONHSAT126163
49	lnc-ADAM2-6	chr8:39332029-39332224	NONHSAT126166
50	lnc-ADAM2-6	chr8:39358011-39358177	NONHSAT126169

No data

Variant related genes	Relation type
ENSG00000254067	TF binding region
ENSG00000254082	TF binding region
ADAM3A	TF binding region
ENSG00000252176	TF binding region
ENSG00000254067	CpG island
ENSG00000254082	CpG island
ADAM3A	CpG island
ENSG00000252176	CpG island
ENSG00000196115	chromatin interactions

Extended variants
information (count: 2380 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:2380 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573124399	chr8:39301138-39301139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561360158	chr8:39301146-39301147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530415439	chr8:39301174-39301175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182007184	chr8:39301235-39301236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563646358	chr8:39301251-39301252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372001265	chr8:39301287-39301288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201184477	chr8:39301306-39301307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531171922	chr8:39301310-39301311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550983987	chr8:39301323-39301324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77558119	chr8:39301347-39301348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79529013	chr8:39301352-39301353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373130747	chr8:39301398-39301399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561212226	chr8:39301442-39301443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185060072	chr8:39301496-39301497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190798928	chr8:39301586-39301587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183111956	chr8:39301593-39301594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546675583	chr8:39301660-39301661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569990582	chr8:39301681-39301682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372404484	chr8:39301704-39301705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539015112	chr8:39301740-39301741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375665838	chr8:39301784-39301785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559030319	chr8:39301802-39301803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572558655	chr8:39301825-39301826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541210468	chr8:39301851-39301852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555047235	chr8:39301967-39301968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565224337	chr8:39301980-39301981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188043255	chr8:39301984-39301985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12541734	chr8:39301999-39302000	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs550364272	chr8:39302010-39302011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568682400	chr8:39302019-39302020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369724805	chr8:39302067-39302068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112259909	chr8:39302086-39302087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs6998557	chr8:39302187-39302188	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs532694073	chr8:39302189-39302190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544588212	chr8:39302196-39302197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs377528270	chr8:39302226-39302227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191722363	chr8:39302260-39302261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558361116	chr8:39302272-39302273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527285788	chr8:39302317-39302318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557873288	chr8:39302357-39302358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs12677366	chr8:39305423-39305424	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs569571090	chr8:39305424-39305425	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs142173014	chr8:39305461-39305462	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs146359214	chr8:39305467-39305468	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs544188906	chr8:39305474-39305475	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs139782221	chr8:39305522-39305523	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs533172881	chr8:39305523-39305524	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs201592227	chr8:39305533-39305534	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs573291223	chr8:39305571-39305572	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs186207767	chr8:39305609-39305610	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Prader-willi syndrome	20588305	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Cancer	20164919	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
Non-syndromic sensorineural hearing loss	21293372	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:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39301000-39301200	Enhancers	Fetal Lung	lung
2	chr8:39301200-39302200	Weak transcription	Fetal Lung	lung
3	chr8:39302000-39302400	Enhancers	Spleen	Spleen
4	chr8:39302200-39302400	Enhancers	Fetal Lung	lung
5	chr8:39305400-39306400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:39317600-39318000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr8:39328200-39328600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:39328400-39328800	Enhancers	H1 Cell Line	embryonic stem cell
9	chr8:39328400-39329200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:39328400-39329400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
11	chr8:39328600-39329000	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr8:39328600-39329000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr8:39328600-39329200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:39328600-39329400	Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr8:39328600-39334800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:39328800-39329200	Active TSS	H1 Cell Line	embryonic stem cell
17	chr8:39328800-39329200	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr8:39329200-39329400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr8:39329200-39329400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:39334800-39335000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr8:39335000-39335800	Enhancers	Fetal Lung	lung
22	chr8:39335000-39340400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr8:39335400-39336400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr8:39335600-39337200	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr8:39335800-39336400	Flanking Active TSS	Fetal Lung	lung
26	chr8:39336000-39337200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:39336200-39336800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr8:39336200-39337200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr8:39336200-39337200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr8:39336400-39337000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr8:39336400-39337000	Active TSS	Fetal Lung	lung
32	chr8:39336800-39337200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr8:39338000-39338400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:39340400-39341000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:39343000-39345400	Enhancers	Fetal Lung	lung
36	chr8:39363600-39364000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr8:39368800-39369600	Enhancers	GM12878-XiMat	blood
38	chr8:39369200-39369600	Enhancers	Fetal Intestine Large	intestine
39	chr8:39374400-39375200	Enhancers	Spleen	Spleen
40	chr8:39378200-39378600	Enhancers	Fetal Lung	lung
41	chr8:39379600-39381800	Active TSS	K562	blood
42	chr8:39380200-39380600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr8:39381800-39392400	Weak transcription	K562	blood
44	chr8:39390200-39390400	Enhancers	Fetal Intestine Large	intestine
45	chr8:39390200-39390600	Enhancers	Fetal Intestine Small	intestine
46	chr8:39390400-39390600	Enhancers	Fetal Heart	heart
47	chr8:39390400-39391600	Weak transcription	Fetal Intestine Large	intestine
48	chr8:39391400-39391600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr8:39391400-39392400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:39391600-39394000	Enhancers	Fetal Intestine Large	intestine

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