Variant report

Variant	nsv833681
Chromosome Location	chr2:32652330-32815108
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1018)
CpG islands
(count:244)
Chromatin interactive
region (count:100)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1018 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:32704957-32705557	K562	blood:	n/a	n/a
2	ARID3A	chr2:32667025-32667589	HepG2	liver:	n/a	chr2:32667295-32667311
3	ARID3A	chr2:32678784-32679113	HepG2	liver:	n/a	n/a
4	ATF1	chr2:32661286-32661606	K562	blood:	n/a	n/a
5	ATF1	chr2:32710011-32710380	K562	blood:	n/a	n/a
6	ATF1	chr2:32783652-32783878	K562	blood:	n/a	n/a
7	ATF3	chr2:32709931-32710256	K562	blood:	n/a	n/a
8	BHLHE40	chr2:32705137-32705435	K562	blood:	n/a	n/a
9	BHLHE40	chr2:32653232-32653458	K562	blood:	n/a	n/a
10	CBX3	chr2:32671924-32672171	K562	blood:	n/a	n/a
11	CBX3	chr2:32790916-32791319	K562	blood:	n/a	n/a
12	CCNT2	chr2:32705210-32705391	K562	blood:	n/a	n/a
13	CCNT2	chr2:32660641-32660742	K562	blood:	n/a	n/a
14	CEBPB	chr2:32741798-32741990	K562	blood:	n/a	n/a
15	CEBPB	chr2:32721692-32721985	K562	blood:	n/a	chr2:32721819-32721830
16	CEBPB	chr2:32709920-32710369	A549	lung:	n/a	n/a
17	CEBPB	chr2:32678741-32679160	HepG2	liver:	n/a	chr2:32679093-32679104 chr2:32679001-32679012
18	CEBPB	chr2:32709947-32710739	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:32742536-32742884	HepG2	liver:	n/a	chr2:32742697-32742708
20	CEBPB	chr2:32709980-32710446	HCT-116	colon:	n/a	n/a
21	CEBPB	chr2:32798388-32798611	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:32784249-32784487	K562	blood:	n/a	chr2:32784424-32784435 chr2:32784424-32784437
23	CEBPB	chr2:32778960-32779154	H1-hESC	embryonic stem cell:	n/a	chr2:32779139-32779151
24	CEBPB	chr2:32709884-32710595	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:32722410-32722548	A549	lung:	n/a	n/a
26	CEBPB	chr2:32784260-32784619	HepG2	liver:	n/a	chr2:32784424-32784435 chr2:32784424-32784437
27	CEBPB	chr2:32798415-32798615	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr2:32710090-32710290	K562	blood:	n/a	n/a
29	CEBPB	chr2:32721671-32721990	A549	lung:	n/a	chr2:32721819-32721830
30	CEBPB	chr2:32778859-32779458	A549	lung:	n/a	chr2:32779139-32779151
31	CEBPB	chr2:32806836-32806926	K562	blood:	n/a	n/a
32	CEBPB	chr2:32709838-32710480	A549	lung:	n/a	n/a
33	CEBPB	chr2:32671440-32671756	H1-hESC	embryonic stem cell:	n/a	chr2:32671441-32671452 chr2:32671441-32671454
34	CEBPB	chr2:32785744-32786046	HepG2	liver:	n/a	chr2:32785942-32785955
35	CEBPB	chr2:32785714-32786083	A549	lung:	n/a	chr2:32785942-32785955
36	CEBPB	chr2:32784264-32784570	IMR90	lung:	n/a	chr2:32784424-32784435 chr2:32784424-32784437
37	CEBPB	chr2:32671329-32671776	HepG2	liver:	n/a	chr2:32671441-32671452 chr2:32671441-32671454
38	CEBPB	chr2:32777613-32777857	K562	blood:	n/a	chr2:32777763-32777772 chr2:32777763-32777772 chr2:32777763-32777772 chr2:32777761-32777774
39	CEBPB	chr2:32777580-32777953	Hela-S3	cervix:	n/a	chr2:32777763-32777772 chr2:32777763-32777772 chr2:32777763-32777772 chr2:32777761-32777774
40	CEBPB	chr2:32785720-32786052	IMR90	lung:	n/a	chr2:32785942-32785955
41	CEBPB	chr2:32783668-32783828	K562	blood:	n/a	chr2:32783724-32783737
42	CEBPB	chr2:32745747-32745930	A549	lung:	n/a	chr2:32745834-32745845
43	CEBPB	chr2:32684932-32685189	HepG2	liver:	n/a	chr2:32685049-32685060
44	CEBPB	chr2:32704831-32705344	K562	blood:	n/a	chr2:32704906-32704917
45	CEBPB	chr2:32777580-32777948	A549	lung:	n/a	chr2:32777763-32777772 chr2:32777763-32777772 chr2:32777763-32777772 chr2:32777761-32777774
46	CEBPB	chr2:32784235-32784575	K562	blood:	n/a	chr2:32784424-32784435 chr2:32784424-32784437
47	CEBPB	chr2:32684929-32685182	IMR90	lung:	n/a	chr2:32685049-32685060
48	CEBPB	chr2:32709857-32710476	HCT-116	colon:	n/a	n/a
49	CEBPB	chr2:32784311-32784575	H1-hESC	embryonic stem cell:	n/a	chr2:32784424-32784435 chr2:32784424-32784437
50	CEBPB	chr2:32684883-32685163	K562	blood:	n/a	chr2:32685049-32685060

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:32673206-32673256	HEEpiC	esophagus:	n/a
2	chr2:32673206-32673256	GM12878	blood:	n/a
3	chr2:32678846-32678896	H1-hESC	embryonic stem cell:	embryo
4	chr2:32757069-32757119	BJ	skin:	n/a
5	chr2:32757069-32757119	NHBE	bronchial:	n/a
6	chr2:32757307-32757357	NHBE	bronchial:	n/a
7	chr2:32673206-32673256	AG04449	skin:	fetal
8	chr2:32757307-32757357	ProgFib	skin:	n/a
9	chr2:32757069-32757119	Hepatocyte	liver:	n/a
10	chr2:32757307-32757357	HEK293	kidney:	embryo
11	chr2:32678846-32678896	Caco-2	colon:	n/a
12	chr2:32757307-32757357	Hepatocyte	liver:	n/a
13	chr2:32757307-32757357	MCF-7	breast:	n/a
14	chr2:32673206-32673256	HRPEpiC	eye:	n/a
15	chr2:32757069-32757119	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:32678846-32678896	GM19239	blood:	n/a
17	chr2:32678846-32678896	MCF-7	breast:	n/a
18	chr2:32673206-32673256	HRE	kidney:	n/a
19	chr2:32757307-32757357	SK-N-SH_RA	brain:	n/a
20	chr2:32757069-32757119	IMR90	lung:	fetal
21	chr2:32678846-32678896	SK-N-SH_RA	brain:	n/a
22	chr2:32757307-32757357	NH-A	brain:	n/a
23	chr2:32757307-32757357	PrEC	prostate:	n/a
24	chr2:32673206-32673256	LNCaP	prostate:	n/a
25	chr2:32678846-32678896	AG04449	skin:	fetal
26	chr2:32678846-32678896	BE2_C	brain:	n/a
27	chr2:32757069-32757119	LNCaP	prostate:	n/a
28	chr2:32757307-32757357	BJ	skin:	n/a
29	chr2:32678846-32678896	HIPEpiC	eye:	n/a
30	chr2:32757307-32757357	LNCaP	prostate:	n/a
31	chr2:32673206-32673256	HEK293	kidney:	embryo
32	chr2:32757307-32757357	K562	blood:	n/a
33	chr2:32757069-32757119	HRCEpiC	kidney:	n/a
34	chr2:32757307-32757357	HUVEC	blood vessel:	n/a
35	chr2:32757307-32757357	SKMC	muscle:	n/a
36	chr2:32678846-32678896	AG09309	skin:	n/a
37	chr2:32678846-32678896	HMEC	breast:	n/a
38	chr2:32757307-32757357	HCM	heart:	n/a
39	chr2:32678846-32678896	PrEC	prostate:	n/a
40	chr2:32757069-32757119	AG04450	lung:	fetal
41	chr2:32757069-32757119	ECC-1	luminal epithelium:	n/a
42	chr2:32673206-32673256	HRCEpiC	kidney:	n/a
43	chr2:32757307-32757357	AG10803	skin:	n/a
44	chr2:32678846-32678896	HRCEpiC	kidney:	n/a
45	chr2:32673206-32673256	NHDF-neo	bronchial:	n/a
46	chr2:32757069-32757119	Hela-S3	cervix:	n/a
47	chr2:32673206-32673256	SK-N-SH_RA	brain:	n/a
48	chr2:32757069-32757119	HRE	kidney:	n/a
49	chr2:32757307-32757357	HMEC	breast:	n/a
50	chr2:32757307-32757357	AG04450	lung:	fetal

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:32690803..32693344-chr2:32695188..32697337,2	K562	blood:
2	chr2:32651894..32653691-chr2:32654473..32656959,2	K562	blood:
3	chr2:32690803..32693344-chr2:32695188..32697337,2	K562	blood:
4	chr2:32651894..32653691-chr2:32654473..32656959,2	K562	blood:
5	chr2:32778978..32780786-chr2:32851895..32854475,2	K562	blood:
6	chr2:32785634..32788035-chr2:32791375..32793905,2	K562	blood:
7	chr2:32728272..32730412-chr2:32730528..32733099,2	MCF-7	breast:
8	chr2:32638863..32640718-chr2:32652115..32654346,2	MCF-7	breast:
9	chr2:32728272..32730412-chr2:32730528..32733099,2	MCF-7	breast:
10	chr2:32726916..32730767-chr2:32738166..32740838,4	K562	blood:
11	chr2:32705619..32707758-chr2:32716833..32718434,2	K562	blood:
12	chr2:32769209..32771746-chr2:32772996..32775659,2	K562	blood:
13	chr2:32814146..32816317-chr2:32853032..32854719,2	K562	blood:
14	chr2:32650702..32653420-chr2:32683411..32685638,2	MCF-7	breast:
15	chr2:32801178..32803170-chr2:32805443..32807726,2	K562	blood:
16	chr2:32582006..32583703-chr2:32658464..32660440,2	K562	blood:
17	chr2:32795969..32798734-chr2:32800957..32802571,2	MCF-7	breast:
18	chr2:32766200..32768668-chr2:32771192..32774567,4	K562	blood:
19	chr2:32705619..32707758-chr2:32716833..32718434,2	K562	blood:
20	chr2:32655375..32657837-chr2:32663152..32664844,2	K562	blood:
21	chr2:32785634..32788035-chr2:32791375..32793905,2	K562	blood:
22	chr2:32773195..32775185-chr2:33170524..33173451,2	K562	blood:
23	chr2:32772967..32775818-chr2:32777845..32779821,2	K562	blood:
24	chr2:32779834..32781544-chr2:32785286..32788159,2	K562	blood:
25	chr2:32809505..32811336-chr2:32812287..32814125,2	K562	blood:
26	chr2:32692267..32694137-chr2:32700993..32702587,2	MCF-7	breast:
27	chr2:32809505..32811336-chr2:32812287..32814125,2	K562	blood:
28	chr2:32692267..32694137-chr2:32700993..32702587,2	MCF-7	breast:
29	chr2:32655316..32658127-chr2:32662690..32665444,3	K562	blood:
30	chr2:32742615..32744223-chr2:32774053..32776106,2	K562	blood:
31	chr2:32736775..32738278-chr2:32740099..32741901,2	K562	blood:
32	chr2:32648680..32650262-chr2:32651820..32653321,2	MCF-7	breast:
33	chr2:32666229..32669442-chr2:32676026..32679242,3	K562	blood:
34	chr2:32733215..32738320-chr2:32742218..32745168,5	K562	blood:
35	chr2:32713396..32715355-chr2:32717113..32719991,2	K562	blood:
36	chr2:32762219..32764200-chr2:32765014..32767388,2	MCF-7	breast:
37	chr2:32675460..32677596-chr2:32681562..32684315,2	MCF-7	breast:
38	chr2:32653224..32654777-chr2:32659583..32661293,2	MCF-7	breast:
39	chr2:32775412..32777093-chr2:32778223..32780162,2	MCF-7	breast:
40	chr2:32754921..32756453-chr2:32757614..32759528,2	K562	blood:
41	chr2:32628910..32631702-chr2:32651764..32653919,2	MCF-7	breast:
42	chr2:32769209..32771746-chr2:32772996..32775659,2	K562	blood:
43	chr2:32779834..32781544-chr2:32785286..32788159,2	K562	blood:
44	chr2:32754921..32756453-chr2:32757614..32759528,2	K562	blood:
45	chr2:32753629..32756308-chr2:32762346..32764743,2	MCF-7	breast:
46	chr2:32770330..32771989-chr2:32772579..32774228,2	MCF-7	breast:
47	chr2:32663362..32665357-chr2:32667579..32669468,2	K562	blood:
48	chr2:32655530..32658471-chr2:32661173..32663842,2	MCF-7	breast:
49	chr2:32675460..32677596-chr2:32681562..32684315,2	MCF-7	breast:
50	chr2:32742615..32744223-chr2:32774053..32776106,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-558	chr2:32757280-32757298	MIMAT0003222

No data

Variant related genes	Relation type
MIR558	TF binding region
BIRC6	TF binding region
MIR558	CpG island
BIRC6	CpG island
ENSG00000049323	chromatin interactions
ENSG00000018699	chromatin interactions
ENSG00000115760	chromatin interactions
ENSG00000185608	chromatin interactions

Extended variants
information (count: 6573 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6573 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141725724	chr2:32652332-32652333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs376329450	chr2:32652358-32652359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs55982624	chr2:32652362-32652363	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs549464487	chr2:32652363-32652364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77854496	chr2:32652367-32652368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560580576	chr2:32652371-32652372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189370390	chr2:32652381-32652382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146277018	chr2:32652415-32652416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572696531	chr2:32652443-32652444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182080705	chr2:32652481-32652482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537981324	chr2:32652505-32652506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551438529	chr2:32652511-32652512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138099452	chr2:32652569-32652570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533893703	chr2:32652573-32652574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543284156	chr2:32652577-32652578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141957598	chr2:32652596-32652597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535732943	chr2:32652613-32652614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4569523	chr2:32652627-32652628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575490272	chr2:32652641-32652642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561429681	chr2:32652653-32652654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544343793	chr2:32652659-32652660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs72798788	chr2:32652665-32652666	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs550670676	chr2:32652789-32652790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577719979	chr2:32652791-32652792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs367894620	chr2:32652807-32652808	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs372393510	chr2:32652808-32652809	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539794513	chr2:32652816-32652817	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115666450	chr2:32652849-32652850	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529600249	chr2:32652913-32652914	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543289429	chr2:32652925-32652926	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11686349	chr2:32652926-32652927	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs375563551	chr2:32652937-32652938	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34315035	chr2:32652984-32652985	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531756397	chr2:32652992-32652993	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183746173	chr2:32653064-32653065	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115213463	chr2:32653137-32653138	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148508028	chr2:32653190-32653191	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547517562	chr2:32653240-32653241	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs188123108	chr2:32653247-32653248	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs534049668	chr2:32653286-32653287	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs78713323	chr2:32653382-32653383	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs555673807	chr2:32653389-32653390	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs373918960	chr2:32653444-32653445	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142887317	chr2:32653450-32653451	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs150637551	chr2:32653487-32653488	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs557887592	chr2:32653493-32653494	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs577857554	chr2:32653511-32653512	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567604654	chr2:32653563-32653564	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs74574368	chr2:32653636-32653637	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs573557790	chr2:32653644-32653645	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Neurocytoma	17123091	CNVD
Breast cancer	22522925	CNVD
Autism	22549408	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4537 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:32583600-32653200	Weak transcription	Gastric	stomach
2	chr2:32602000-32653000	Weak transcription	Stomach Mucosa	stomach
3	chr2:32605400-32652800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr2:32621000-32669800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr2:32621200-32664600	Weak transcription	Fetal Brain Male	brain
6	chr2:32621600-32693400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr2:32630000-32653000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:32640800-32656000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:32640800-32663200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr2:32641000-32653000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr2:32641200-32656600	Weak transcription	Fetal Brain Female	brain
12	chr2:32641200-32664000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr2:32641200-32664000	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr2:32641400-32653200	Weak transcription	Brain Germinal Matrix	brain
15	chr2:32641400-32660600	Weak transcription	Colonic Mucosa	Colon
16	chr2:32641400-32664200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr2:32641600-32655800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr2:32642800-32656000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr2:32642800-32656000	Weak transcription	Fetal Kidney	kidney
20	chr2:32643000-32653200	Weak transcription	Primary B cells from cord blood	blood
21	chr2:32643000-32655800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr2:32643000-32656000	Weak transcription	Primary T cells from cord blood	blood
23	chr2:32643000-32660000	Weak transcription	Stomach Smooth Muscle	stomach
24	chr2:32643200-32656000	Weak transcription	Fetal Lung	lung
25	chr2:32643200-32656600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr2:32643400-32654200	Weak transcription	Primary hematopoietic stem cells	blood
27	chr2:32643400-32655800	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr2:32643400-32656000	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr2:32643600-32652800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:32643600-32656600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr2:32643800-32655400	Weak transcription	Primary B cells from peripheral blood	blood
32	chr2:32644000-32653000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr2:32644000-32656000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr2:32644000-32656000	Weak transcription	Fetal Stomach	stomach
35	chr2:32644200-32655800	Weak transcription	Fetal Thymus	thymus
36	chr2:32644800-32655200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr2:32645200-32653200	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr2:32645400-32654600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:32645400-32656000	Weak transcription	Fetal Intestine Large	intestine
40	chr2:32646600-32656000	Weak transcription	Fetal Intestine Small	intestine
41	chr2:32647400-32652800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr2:32647400-32654600	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr2:32647400-32655600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr2:32647400-32656000	Weak transcription	NHEK	skin
45	chr2:32647800-32652800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr2:32647800-32656000	Weak transcription	Hela-S3	cervix
47	chr2:32649000-32653200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:32649000-32653200	Weak transcription	K562	blood
49	chr2:32649000-32654400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr2:32650000-32652800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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