Variant report

Variant	nsv832691
Chromosome Location	chr13:96478098-96659823
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1099)
CpG islands
(count:489)
Chromatin interactive
region (count:40)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:96548454-96548878	K562	blood:	n/a	n/a
2	ARID3A	chr13:96517464-96517648	K562	blood:	n/a	n/a
3	ARID3A	chr13:96632838-96633002	K562	blood:	n/a	n/a
4	ARID3A	chr13:96624887-96625205	HepG2	liver:	n/a	n/a
5	ATF1	chr13:96608880-96609099	K562	blood:	n/a	n/a
6	ATF3	chr13:96608777-96609107	K562	blood:	n/a	n/a
7	BACH1	chr13:96602381-96602390	K562	blood:	n/a	n/a
8	BCL11A	chr13:96606653-96606944	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr13:96632919-96632932	K562	blood:	n/a	n/a
10	BHLHE40	chr13:96486435-96486799	GM12878	blood:	n/a	n/a
11	BRCA1	chr13:96516087-96516280	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr13:96486494-96486815	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr13:96608842-96609006	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr13:96612468-96612822	K562	blood:	n/a	n/a
15	CBX3	chr13:96502134-96502436	K562	blood:	n/a	n/a
16	CCNT2	chr13:96525602-96525816	K562	blood:	n/a	n/a
17	CCNT2	chr13:96608827-96609027	K562	blood:	n/a	n/a
18	CCNT2	chr13:96589983-96590394	K562	blood:	n/a	n/a
19	CEBPB	chr13:96510929-96511193	HepG2	liver:	n/a	n/a
20	CEBPB	chr13:96611144-96611383	K562	blood:	n/a	chr13:96611218-96611229
21	CEBPB	chr13:96534371-96534687	HepG2	liver:	n/a	chr13:96534508-96534519 chr13:96534510-96534519 chr13:96534490-96534501 chr13:96534491-96534502 chr13:96534508-96534521 chr13:96534509-96534520
22	CEBPB	chr13:96510866-96511223	IMR90	lung:	n/a	n/a
23	CEBPB	chr13:96611078-96611376	Hela-S3	cervix:	n/a	chr13:96611218-96611229
24	CEBPB	chr13:96486491-96486798	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr13:96506930-96507159	IMR90	lung:	n/a	n/a
26	CEBPB	chr13:96590049-96590235	K562	blood:	n/a	n/a
27	CEBPB	chr13:96626133-96626333	HepG2	liver:	n/a	chr13:96626229-96626240
28	CEBPB	chr13:96598328-96598528	HepG2	liver:	n/a	chr13:96598419-96598428 chr13:96598418-96598429 chr13:96598419-96598428
29	CEBPB	chr13:96485176-96485688	Hela-S3	cervix:	n/a	chr13:96485484-96485497
30	CEBPB	chr13:96611108-96611320	A549	lung:	n/a	chr13:96611218-96611229
31	CEBPB	chr13:96608843-96609152	K562	blood:	n/a	n/a
32	CEBPB	chr13:96576845-96577189	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr13:96514815-96515026	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr13:96518101-96518321	K562	blood:	n/a	n/a
35	CEBPB	chr13:96608817-96609167	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr13:96608866-96609174	K562	blood:	n/a	n/a
37	CEBPB	chr13:96534415-96534695	ECC-1	luminal epithelium:	n/a	chr13:96534508-96534519 chr13:96534510-96534519 chr13:96534490-96534501 chr13:96534491-96534502 chr13:96534508-96534521 chr13:96534509-96534520
38	CEBPB	chr13:96506900-96507179	HepG2	liver:	n/a	n/a
39	CEBPB	chr13:96611042-96611399	HepG2	liver:	n/a	chr13:96611218-96611229
40	CEBPB	chr13:96510910-96511114	A549	lung:	n/a	n/a
41	CEBPB	chr13:96534378-96534690	A549	lung:	n/a	chr13:96534508-96534519 chr13:96534510-96534519 chr13:96534490-96534501 chr13:96534491-96534502 chr13:96534508-96534521 chr13:96534509-96534520
42	CEBPB	chr13:96548136-96548357	K562	blood:	n/a	n/a
43	CEBPB	chr13:96506907-96507136	A549	lung:	n/a	n/a
44	CEBPB	chr13:96611029-96611416	MCF-7	breast:	n/a	chr13:96611218-96611229
45	CEBPB	chr13:96534445-96534665	K562	blood:	n/a	chr13:96534508-96534519 chr13:96534510-96534519 chr13:96534490-96534501 chr13:96534491-96534502 chr13:96534508-96534521 chr13:96534509-96534520
46	CEBPB	chr13:96534347-96534610	Hela-S3	cervix:	n/a	chr13:96534508-96534519 chr13:96534510-96534519 chr13:96534490-96534501 chr13:96534491-96534502 chr13:96534508-96534521 chr13:96534509-96534520
47	CEBPB	chr13:96576859-96577151	A549	lung:	n/a	n/a
48	CEBPB	chr13:96576845-96577168	HepG2	liver:	n/a	n/a
49	CEBPB	chr13:96632825-96633023	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr13:96611067-96611397	IMR90	lung:	n/a	chr13:96611218-96611229

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96651633-96651683	Hela-S3	cervix:	n/a
2	chr13:96651633-96651683	Hela-S3	cervix:	n/a
3	chr13:96651633-96651683	GM06990	blood:	n/a
4	chr13:96654416-96654466	GM19239	blood:	n/a
5	chr13:96651633-96651683	AG10803	skin:	n/a
6	chr13:96581176-96581226	H1-hESC	embryonic stem cell:	embryo
7	chr13:96583970-96584020	NH-A	brain:	n/a
8	chr13:96583970-96584020	AG04449	skin:	fetal
9	chr13:96640017-96640067	Hela-S3	cervix:	n/a
10	chr13:96640017-96640067	NHDF-neo	bronchial:	n/a
11	chr13:96583885-96583935	Hepatocyte	liver:	n/a
12	chr13:96624108-96624158	Hepatocyte	liver:	n/a
13	chr13:96583970-96584020	GM12878	blood:	n/a
14	chr13:96583970-96584020	HPAEpiC	pulmonary alveolar:	n/a
15	chr13:96651633-96651683	HMEC	breast:	n/a
16	chr13:96624108-96624158	HIPEpiC	eye:	n/a
17	chr13:96583885-96583935	H1-hESC	embryonic stem cell:	embryo
18	chr13:96583751-96583801	GM19239	blood:	n/a
19	chr13:96624108-96624158	AG04449	skin:	fetal
20	chr13:96640017-96640067	HRE	kidney:	n/a
21	chr13:96640017-96640067	NH-A	brain:	n/a
22	chr13:96651633-96651683	HEEpiC	esophagus:	n/a
23	chr13:96651633-96651683	HCF	heart:	n/a
24	chr13:96651633-96651683	SK-N-SH_RA	brain:	n/a
25	chr13:96583970-96584020	GM19239	blood:	n/a
26	chr13:96583885-96583935	SK-N-SH_RA	brain:	n/a
27	chr13:96583885-96583935	HIPEpiC	eye:	n/a
28	chr13:96640017-96640067	HCT-116	colon:	n/a
29	chr13:96581176-96581226	AG09319	gingival:	n/a
30	chr13:96581176-96581226	AG04450	lung:	fetal
31	chr13:96651633-96651683	ProgFib	skin:	n/a
32	chr13:96654416-96654466	GM06990	blood:	n/a
33	chr13:96583970-96584020	Jurkat	blood:	n/a
34	chr13:96654416-96654466	SK-N-SH_RA	brain:	n/a
35	chr13:96583751-96583801	SKMC	muscle:	n/a
36	chr13:96581176-96581226	GM12892	blood:	n/a
37	chr13:96651633-96651683	HCM	heart:	n/a
38	chr13:96583885-96583935	NB4	blood:	n/a
39	chr13:96581176-96581226	SK-N-SH	brain:	n/a
40	chr13:96654416-96654466	MCF-7	breast:	n/a
41	chr13:96583970-96584020	PANC-1	pancreas:	n/a
42	chr13:96624108-96624158	BJ	skin:	n/a
43	chr13:96651633-96651683	HUVEC	blood vessel:	n/a
44	chr13:96640017-96640067	AG10803	skin:	n/a
45	chr13:96583751-96583801	NH-A	brain:	n/a
46	chr13:96581176-96581226	GM12878	blood:	n/a
47	chr13:96583751-96583801	Hela-S3	cervix:	n/a
48	chr13:96583885-96583935	NT2-D1	testis:	n/a
49	chr13:96624108-96624158	HMEC	breast:	n/a
50	chr13:96654416-96654466	HL-60	blood:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:96520254..96522290-chr13:96547977..96549685,2	MCF-7	breast:
2	chr13:96275906..96276854-chr13:96486114..96486980,5	K562	blood:
3	chr13:96520254..96522290-chr13:96547977..96549685,2	MCF-7	breast:
4	chr13:96548750..96552218-chr13:96554707..96557243,3	K562	blood:
5	chr13:96638885..96641405-chr13:96646337..96648047,2	K562	blood:
6	chr13:96646657..96649376-chr13:96653623..96656450,2	K562	blood:
7	chr13:96506532..96508738-chr13:96509011..96511057,2	K562	blood:
8	chr13:96488916..96491538-chr13:96492775..96495359,2	K562	blood:
9	chr13:96484418..96486030-chr13:96489191..96491096,2	MCF-7	breast:
10	chr13:96646657..96649376-chr13:96653623..96656450,2	K562	blood:
11	chr13:96548750..96552218-chr13:96554707..96557243,3	K562	blood:
12	chr13:96275890..96276432-chr13:96486160..96486773,2	MCF-7	breast:
13	chr13:96632367..96634292-chr13:96635472..96638810,3	K562	blood:
14	chr13:96623472..96625702-chr13:96633366..96635270,2	K562	blood:
15	chr13:96575800..96578505-chr13:96580994..96583120,2	MCF-7	breast:
16	chr13:96275895..96276755-chr13:96486107..96487061,4	MCF-7	breast:
17	chr13:96548785..96550762-chr13:96554235..96556207,2	K562	blood:
18	chr13:96645821..96648157-chr13:96652865..96656450,3	K562	blood:
19	chr13:96645463..96647410-chr13:96650803..96652749,2	K562	blood:
20	chr13:96623472..96625702-chr13:96633366..96635270,2	K562	blood:
21	chr13:96632367..96634450-chr13:96637310..96639783,2	K562	blood:
22	chr13:96642387..96644158-chr13:96654027..96655529,2	K562	blood:
23	chr13:96642387..96644158-chr13:96654027..96655529,2	K562	blood:
24	chr13:96566533..96568077-chr9:100747317..100749032,2	MCF-7	breast:
25	chr13:96654618..96657100-chr13:96704216..96707114,2	MCF-7	breast:
26	chr13:96512925..96513630-chr7:95036382..95037036,2	MCF-7	breast:
27	chr13:96586030..96588095-chr13:96594403..96597240,2	MCF-7	breast:
28	chr13:96548785..96550762-chr13:96554235..96556207,2	K562	blood:
29	chr13:96484418..96486030-chr13:96489191..96491096,2	MCF-7	breast:
30	chr13:96534402..96537608-chr13:96544660..96547266,3	K562	blood:
31	chr13:96506532..96508738-chr13:96509011..96511057,2	K562	blood:
32	chr13:96632367..96634292-chr13:96635472..96638810,3	K562	blood:
33	chr13:96586030..96588095-chr13:96594403..96597240,2	MCF-7	breast:
34	chr13:96632367..96634450-chr13:96637310..96639783,2	K562	blood:
35	chr13:96575800..96578505-chr13:96580994..96583120,2	MCF-7	breast:
36	chr13:96488916..96491538-chr13:96492775..96495359,2	K562	blood:
37	chr13:96645821..96648157-chr13:96652865..96656450,3	K562	blood:
38	chr13:96534402..96536224-chr13:96544660..96547266,2	K562	blood:
39	chr13:96638885..96641405-chr13:96646337..96648047,2	K562	blood:
40	chr13:96471414..96473149-chr13:96476270..96478786,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DZIP1-9	chr13:96622724-96623119	NONHSAT034781
2	lnc-DZIP1-9	chr13:96629582-96629877	NONHSAT034781
3	lnc-DZIP1-3	chr13:96568212-96568330	ENSG00000237822.1
4	lnc-DZIP1-3	chr13:96567601-96567944	ENSG00000237822.1

No data

Variant related genes	Relation type
UGGT2	TF binding region
UGGT2	CpG island
ENSG00000102595	chromatin interactions

Extended variants
information (count: 6692 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:6692 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372924625	chr13:96478161-96478162	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs577019584	chr13:96478189-96478190	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs545864704	chr13:96478190-96478191	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs3101570	chr13:96478219-96478220	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs34679502	chr13:96478238-96478239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531296059	chr13:96478246-96478247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548149915	chr13:96478279-96478280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561882462	chr13:96478280-96478281	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185859587	chr13:96478308-96478309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189052519	chr13:96478310-96478311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370997467	chr13:96478354-96478355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570265712	chr13:96478422-96478423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532492262	chr13:96478506-96478507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140995685	chr13:96478517-96478518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539255248	chr13:96478518-96478519	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142367751	chr13:96478527-96478528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568996268	chr13:96478592-96478593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs151268481	chr13:96478617-96478618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554944073	chr13:96478620-96478621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181142938	chr13:96478697-96478698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374013832	chr13:96478713-96478714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549608253	chr13:96478742-96478743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534465357	chr13:96478756-96478757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140483700	chr13:96478830-96478831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7994753	chr13:96478871-96478872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113985869	chr13:96478873-96478874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375247442	chr13:96478894-96478895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs80355424	chr13:96478902-96478903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138255564	chr13:96478924-96478925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76025114	chr13:96478940-96478941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142642430	chr13:96478962-96478963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374952069	chr13:96479059-96479060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116139135	chr13:96479060-96479061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4147075	chr13:96479064-96479065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541291152	chr13:96479090-96479091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186406944	chr13:96479147-96479148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532995808	chr13:96479162-96479163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555349783	chr13:96479200-96479201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549544604	chr13:96479250-96479251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572027726	chr13:96479253-96479254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190931751	chr13:96479263-96479264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541248966	chr13:96479264-96479265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs75803386	chr13:96479282-96479283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146903560	chr13:96479293-96479294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139286647	chr13:96479298-96479299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149400364	chr13:96479312-96479313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182599401	chr13:96479331-96479332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556023121	chr13:96479344-96479345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116651537	chr13:96479383-96479384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187225579	chr13:96479483-96479484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2406 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96444400-96485600	Weak transcription	NHDF-Ad	bronchial
2	chr13:96445800-96490000	Weak transcription	HepG2	liver
3	chr13:96452000-96490600	Weak transcription	Fetal Kidney	kidney
4	chr13:96462600-96485600	Weak transcription	Hela-S3	cervix
5	chr13:96465600-96481200	Weak transcription	Psoas Muscle	Psoas
6	chr13:96466200-96480800	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr13:96466200-96481400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr13:96466400-96485400	Weak transcription	NHEK	skin
9	chr13:96466400-96486000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr13:96466600-96485800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr13:96466800-96485800	Weak transcription	Brain Anterior Caudate	brain
12	chr13:96467000-96485200	Weak transcription	HUVEC	blood vessel
13	chr13:96467400-96490800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr13:96468200-96489800	Weak transcription	GM12878-XiMat	blood
15	chr13:96468800-96486000	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr13:96475400-96481200	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr13:96475800-96485600	Weak transcription	HMEC	breast
18	chr13:96476000-96478600	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr13:96476000-96502600	Weak transcription	Fetal Heart	heart
20	chr13:96476400-96489800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr13:96476600-96478200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr13:96476600-96478200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr13:96476800-96480000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr13:96477000-96481200	Weak transcription	Brain Substantia Nigra	brain
25	chr13:96477200-96478200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr13:96477200-96478200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr13:96477200-96478200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr13:96477200-96478200	Strong transcription	Brain Germinal Matrix	brain
29	chr13:96477200-96478200	Strong transcription	Brain Hippocampus Middle	brain
30	chr13:96477200-96478200	Strong transcription	Fetal Lung	lung
31	chr13:96477200-96478200	Strong transcription	Fetal Muscle Trunk	muscle
32	chr13:96477200-96478600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr13:96477200-96479600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr13:96477200-96479800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr13:96477400-96478200	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr13:96477400-96478200	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
37	chr13:96477400-96478200	Strong transcription	Muscle Satellite Cultured Cells	--
38	chr13:96477400-96478200	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr13:96477400-96478200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr13:96477400-96478200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr13:96477400-96478200	Strong transcription	Liver	Liver
42	chr13:96477400-96478200	Strong transcription	Brain Inferior Temporal Lobe	brain
43	chr13:96477400-96478200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr13:96477400-96478200	Strong transcription	Fetal Intestine Large	intestine
45	chr13:96477400-96478200	Strong transcription	Fetal Muscle Leg	muscle
46	chr13:96477400-96478200	Strong transcription	Fetal Stomach	stomach
47	chr13:96477400-96478200	Strong transcription	Gastric	stomach
48	chr13:96477400-96478200	Strong transcription	Ovary	ovary
49	chr13:96477400-96478200	Strong transcription	Pancreas	Pancrea
50	chr13:96477400-96478200	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links