Variant report

Variant	esv3420380
Chromosome Location	chr13:30168177-30170725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:30170053-30170123	HepG2	liver:	n/a	n/a
2	ATF2	chr13:30168897-30169456	GM12878	blood:	n/a	n/a
3	ATF2	chr13:30168499-30169250	GM12878	blood:	n/a	n/a
4	ATF3	chr13:30168972-30169405	K562	blood:	n/a	chr13:30169089-30169098 chr13:30169217-30169226
5	BACH1	chr13:30169186-30170316	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr13:30168512-30168904	GM12878	blood:	n/a	n/a
7	BATF	chr13:30168926-30169445	GM12878	blood:	n/a	n/a
8	BCL3	chr13:30168831-30169399	GM12878	blood:	n/a	chr13:30169031-30169044 chr13:30169138-30169151 chr13:30169176-30169189 chr13:30169172-30169185 chr13:30169134-30169147
9	BCLAF1	chr13:30168706-30169467	GM12878	blood:	n/a	chr13:30169031-30169044 chr13:30169138-30169151 chr13:30169176-30169189 chr13:30169172-30169185 chr13:30169134-30169147
10	BCLAF1	chr13:30169824-30170286	GM12878	blood:	n/a	chr13:30169938-30169951 chr13:30170162-30170170 chr13:30169927-30169940 chr13:30169934-30169943 chr13:30169932-30169945 chr13:30169960-30169973 chr13:30169937-30169946
11	BHLHE40	chr13:30169596-30169809	GM12878	blood:	n/a	chr13:30169712-30169728
12	BHLHE40	chr13:30169164-30169386	K562	blood:	n/a	n/a
13	BHLHE40	chr13:30169634-30169789	K562	blood:	n/a	chr13:30169712-30169728
14	BHLHE40	chr13:30168371-30169369	GM12878	blood:	n/a	chr13:30169002-30169018
15	BHLHE40	chr13:30168414-30168770	HepG2	liver:	n/a	n/a
16	BHLHE40	chr13:30170060-30170172	K562	blood:	n/a	n/a
17	BRCA1	chr13:30168238-30168664	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr13:30169993-30170255	Hela-S3	cervix:	n/a	n/a
19	CCNT2	chr13:30168898-30170255	K562	blood:	n/a	n/a
20	CEBPB	chr13:30169042-30169478	HepG2	liver:	n/a	chr13:30169284-30169295
21	CEBPB	chr13:30169099-30169456	H1-hESC	embryonic stem cell:	n/a	chr13:30169284-30169295
22	CEBPB	chr13:30168343-30168621	K562	blood:	n/a	chr13:30168508-30168521
23	CEBPB	chr13:30168347-30168785	MCF-7	breast:	n/a	chr13:30168508-30168521
24	CEBPB	chr13:30168325-30168684	K562	blood:	n/a	chr13:30168508-30168521
25	CEBPB	chr13:30169078-30169587	A549	lung:	n/a	chr13:30169284-30169295
26	CEBPB	chr13:30168334-30168752	A549	lung:	n/a	chr13:30168508-30168521
27	CEBPB	chr13:30169114-30169481	A549	lung:	n/a	chr13:30169284-30169295
28	CEBPB	chr13:30168935-30169486	IMR90	lung:	n/a	chr13:30169284-30169295
29	CEBPB	chr13:30169023-30169548	MCF-7	breast:	n/a	chr13:30169284-30169295
30	CEBPB	chr13:30169072-30169453	K562	blood:	n/a	chr13:30169284-30169295
31	CEBPB	chr13:30168221-30168843	A549	lung:	n/a	chr13:30168508-30168521
32	CEBPB	chr13:30169208-30169401	ECC-1	luminal epithelium:	n/a	chr13:30169284-30169295
33	CEBPB	chr13:30169173-30169413	HepG2	liver:	n/a	chr13:30169284-30169295
34	CEBPB	chr13:30169043-30169492	MCF-7	breast:	n/a	chr13:30169284-30169295
35	CEBPB	chr13:30169755-30169796	HepG2	liver:	n/a	n/a
36	CEBPB	chr13:30169121-30169433	K562	blood:	n/a	chr13:30169284-30169295
37	CEBPB	chr13:30168973-30169493	K562	blood:	n/a	chr13:30169284-30169295
38	CEBPB	chr13:30168313-30170146	Hela-S3	cervix:	n/a	chr13:30168508-30168521 chr13:30169284-30169295
39	CEBPB	chr13:30168325-30168754	HepG2	liver:	n/a	chr13:30168508-30168521
40	CEBPB	chr13:30168320-30168725	IMR90	lung:	n/a	chr13:30168508-30168521
41	CEBPB	chr13:30169019-30169486	HepG2	liver:	n/a	chr13:30169284-30169295
42	CEBPB	chr13:30169002-30169477	ECC-1	luminal epithelium:	n/a	chr13:30169284-30169295
43	CEBPB	chr13:30168369-30168725	A549	lung:	n/a	chr13:30168508-30168521
44	CEBPB	chr13:30170234-30170238	A549	lung:	n/a	n/a
45	CEBPD	chr13:30169143-30169344	HepG2	liver:	n/a	n/a
46	CHD1	chr13:30168201-30168983	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr13:30168359-30169492	GM12878	blood:	n/a	chr13:30169129-30169139 chr13:30169090-30169100
48	CHD1	chr13:30169253-30169448	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr13:30167920-30170849	IMR90	lung:	n/a	chr13:30169129-30169139 chr13:30169090-30169100
50	CHD2	chr13:30168925-30169251	H1-hESC	embryonic stem cell:	n/a	chr13:30169129-30169139 chr13:30169090-30169100

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:30169727-30169777	GM19239	blood:	n/a
2	chr13:30169825-30169875	NH-A	brain:	n/a
3	chr13:30169727-30169777	T-47D	breast:	n/a
4	chr13:30169727-30169777	GM19239	blood:	n/a
5	chr13:30169825-30169875	NH-A	brain:	n/a
6	chr13:30169727-30169777	T-47D	breast:	n/a
7	chr13:30170122-30170172	SAEC	small airway:	n/a
8	chr13:30169825-30169875	U87	brain:	n/a
9	chr13:30170094-30170144	T-47D	breast:	n/a
10	chr13:30169482-30169532	AG04449	skin:	fetal
11	chr13:30169727-30169777	AG04449	skin:	fetal
12	chr13:30169825-30169875	IMR90	lung:	fetal
13	chr13:30169727-30169777	HEK293	kidney:	embryo
14	chr13:30169249-30169299	AG10803	skin:	n/a
15	chr13:30170129-30170179	HRPEpiC	eye:	n/a
16	chr13:30170094-30170144	HCT-116	colon:	n/a
17	chr13:30169825-30169875	BE2_C	brain:	n/a
18	chr13:30169249-30169299	IMR90	lung:	fetal
19	chr13:30169482-30169532	ECC-1	luminal epithelium:	n/a
20	chr13:30170122-30170172	PANC-1	pancreas:	n/a
21	chr13:30169727-30169777	HEEpiC	esophagus:	n/a
22	chr13:30169825-30169875	GM12891	blood:	n/a
23	chr13:30169727-30169777	GM12892	blood:	n/a
24	chr13:30169482-30169532	SKMC	muscle:	n/a
25	chr13:30169825-30169875	K562	blood:	n/a
26	chr13:30170094-30170144	HIPEpiC	eye:	n/a
27	chr13:30169825-30169875	GM12878	blood:	n/a
28	chr13:30170129-30170179	GM12878	blood:	n/a
29	chr13:30169249-30169299	HRCEpiC	kidney:	n/a
30	chr13:30169727-30169777	K562	blood:	n/a
31	chr13:30170129-30170179	HL-60	blood:	n/a
32	chr13:30170129-30170179	Hela-S3	cervix:	n/a
33	chr13:30169727-30169777	PrEC	prostate:	n/a
34	chr13:30170122-30170172	NB4	blood:	n/a
35	chr13:30170094-30170144	HepG2	liver:	n/a
36	chr13:30169727-30169777	HRE	kidney:	n/a
37	chr13:30170122-30170172	HNPCEpiC	eye:	n/a
38	chr13:30170129-30170179	HNPCEpiC	eye:	n/a
39	chr13:30169249-30169299	AG04449	skin:	fetal
40	chr13:30169825-30169875	AoSMC	blood vessel:	n/a
41	chr13:30170129-30170179	GM12891	blood:	n/a
42	chr13:30170129-30170179	AG09319	gingival:	n/a
43	chr13:30170094-30170144	HCM	heart:	n/a
44	chr13:30169249-30169299	CMK	blood:	n/a
45	chr13:30169249-30169299	AoSMC	blood vessel:	n/a
46	chr13:30170129-30170179	PrEC	prostate:	n/a
47	chr13:30169727-30169777	MCF-7	breast:	n/a
48	chr13:30170129-30170179	NB4	blood:	n/a
49	chr13:30169249-30169299	K562	blood:	n/a
50	chr13:30169482-30169532	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:30168293..30169921-chr13:31039031..31041940,2	K562	blood:
2	chr13:30169260..30170181-chr14:23398301..23399025,2	HCT-116	colon:
3	chr13:30168290..30169281-chr3:119814085..119814597,2	Hela-S3	cervix:
4	chr13:30169255..30170193-chr3:73159968..73160573,2	Hela-S3	cervix:
5	chr13:30170246..30170891-chr4:53525300..53526271,2	MCF-7	breast:
6	chr12:49525036..49525582-chr13:30168706..30169410,2	Hela-S3	cervix:
7	chr13:30093611..30096522-chr13:30167989..30170777,2	MCF-7	breast:
8	chr13:30086955..30089041-chr13:30166781..30169428,2	MCF-7	breast:
9	chr13:30091097..30092804-chr13:30167943..30169459,2	K562	blood:
10	chr13:30168902..30170623-chr13:47369921..47372567,2	MCF-7	breast:
11	chr13:30069723..30071518-chr13:30169502..30172461,2	MCF-7	breast:
12	chr13:30168942..30169620-chr2:220094024..220094805,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTUS2-2	chr13:30170020-30170280	XLOC_010330

Variant related genes	Relation type
SLC7A1	TF binding region
SLC7A1	CpG island
ENSG00000223247	chromatin interactions
ENSG00000163516	chromatin interactions
ENSG00000242622	chromatin interactions
ENSG00000109189	chromatin interactions
ENSG00000139684	chromatin interactions
ENSG00000189403	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000198925	chromatin interactions
ENSG00000139514	chromatin interactions
ENSG00000132938	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000100462	chromatin interactions
ENSG00000248866	chromatin interactions
ENSG00000257285	chromatin interactions

Extended variants
information (count: 80 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:80 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538710320	chr13:30168217-30168218	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs577545479	chr13:30168228-30168229	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs540365373	chr13:30168273-30168274	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs545330348	chr13:30168311-30168312	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs528949426	chr13:30168319-30168320	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs548809312	chr13:30168325-30168326	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs76949676	chr13:30168326-30168327	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs539658565	chr13:30168378-30168379	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs678844	chr13:30168388-30168389	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs368451566	chr13:30168392-30168393	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs570788660	chr13:30168446-30168447	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs9579415	chr13:30168482-30168483	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs148177866	chr13:30168494-30168495	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs533844552	chr13:30168589-30168590	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs555206329	chr13:30168676-30168677	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs9508501	chr13:30168693-30168694	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs534335929	chr13:30168702-30168703	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs548790084	chr13:30168742-30168743	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs144079641	chr13:30168766-30168767	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs191355500	chr13:30168787-30168788	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs367940523	chr13:30168803-30168804	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs566630600	chr13:30168804-30168805	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs535518698	chr13:30168854-30168855	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs183811304	chr13:30168859-30168860	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs555290359	chr13:30168902-30168903	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs145014058	chr13:30168926-30168927	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs537779666	chr13:30168987-30168988	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs558018500	chr13:30169036-30169037	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs369331946	chr13:30169050-30169051	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs4769763	chr13:30169098-30169099	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs111324208	chr13:30169140-30169141	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs140166390	chr13:30169174-30169175	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs114917727	chr13:30169192-30169193	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs368867170	chr13:30169232-30169233	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs573796049	chr13:30169250-30169251	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs12872613	chr13:30169307-30169308	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs555731742	chr13:30169314-30169315	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs35499262	chr13:30169459-30169460	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs542678731	chr13:30169467-30169468	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs372160330	chr13:30169498-30169499	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs77871962	chr13:30169521-30169522	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs544617158	chr13:30169533-30169534	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs73454246	chr13:30169550-30169551	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs533397262	chr13:30169634-30169635	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs546601066	chr13:30169638-30169639	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs140060217	chr13:30169644-30169645	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs555770903	chr13:30169662-30169663	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs76676938	chr13:30169666-30169667	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs566497537	chr13:30169799-30169800	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs61947180	chr13:30169861-30169862	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	18698080	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Squamous cell cancer	20885788	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Malignant glioma	17146433	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Retinoblastoma	22278416	CNVD
Peters Plus syndrome	16909395	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Ovarian cancer	19047089	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30128800-30168200	Weak transcription	Primary T cells from cord blood	blood
2	chr13:30152600-30168200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:30156400-30168400	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr13:30156800-30168200	Weak transcription	Fetal Brain Female	brain
5	chr13:30156800-30168400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr13:30157200-30168400	Weak transcription	Brain Germinal Matrix	brain
7	chr13:30157600-30168200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr13:30157600-30168200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr13:30157800-30168200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr13:30157800-30168400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr13:30157800-30168400	Weak transcription	Small Intestine	intestine
12	chr13:30157800-30168600	Weak transcription	Ovary	ovary
13	chr13:30158000-30168600	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr13:30158200-30168400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr13:30159400-30168200	Weak transcription	Brain Angular Gyrus	brain
16	chr13:30160000-30168400	Weak transcription	Psoas Muscle	Psoas
17	chr13:30162000-30168400	Weak transcription	Aorta	Aorta
18	chr13:30162200-30168400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr13:30162600-30168200	Weak transcription	Primary B cells from cord blood	blood
20	chr13:30162600-30168200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr13:30164000-30168400	Weak transcription	Fetal Stomach	stomach
22	chr13:30164000-30168600	Weak transcription	Right Atrium	heart
23	chr13:30164000-30168600	Weak transcription	Thymus	Thymus
24	chr13:30164400-30168200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr13:30164400-30168200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr13:30164400-30168400	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr13:30164400-30168400	Weak transcription	Brain Hippocampus Middle	brain
28	chr13:30164400-30168400	Weak transcription	Fetal Muscle Trunk	muscle
29	chr13:30164400-30168600	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr13:30164600-30168200	Weak transcription	Colon Smooth Muscle	Colon
31	chr13:30164800-30168200	Weak transcription	Fetal Intestine Small	intestine
32	chr13:30164800-30168200	Weak transcription	Rectal Smooth Muscle	rectum
33	chr13:30164800-30168400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr13:30164800-30168400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr13:30164800-30168400	Weak transcription	Brain Cingulate Gyrus	brain
36	chr13:30164800-30168400	Weak transcription	Fetal Muscle Leg	muscle
37	chr13:30164800-30168400	Weak transcription	Gastric	stomach
38	chr13:30165000-30168200	Weak transcription	Stomach Smooth Muscle	stomach
39	chr13:30165400-30168600	Transcr. at gene 5' and 3'	NHEK	skin
40	chr13:30166400-30168200	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr13:30166600-30168200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr13:30166800-30168400	Weak transcription	NHLF	lung
43	chr13:30166800-30169000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr13:30167000-30168200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr13:30167000-30168200	Weak transcription	Right Ventricle	heart
46	chr13:30167000-30168400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr13:30167000-30168400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr13:30167200-30168400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr13:30167200-30168400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr13:30167200-30168400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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