Variant report

Variant	esv3422795
Chromosome Location	chr10:21821971-21825319
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:929)
CpG islands
(count:976)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:929 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:21823618-21823737	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:21821834-21823211	HepG2	liver:	n/a	chr10:21821959-21821975
3	ARID3A	chr10:21821685-21822801	K562	blood:	n/a	chr10:21821959-21821975
4	ATF2	chr10:21822598-21823160	GM12878	blood:	n/a	n/a
5	ATF2	chr10:21822338-21823018	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr10:21823643-21824014	K562	blood:	n/a	chr10:21823866-21823875 chr10:21823920-21823929
7	ATF3	chr10:21822317-21822869	A549	lung:	n/a	n/a
8	BACH1	chr10:21823285-21823320	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:21824165-21824172	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:21823919-21823933	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr10:21822460-21822960	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr10:21822173-21822984	A549	lung:	n/a	n/a
13	BCL3	chr10:21822075-21823068	A549	lung:	n/a	n/a
14	BCLAF1	chr10:21822164-21823223	GM12878	blood:	n/a	n/a
15	BCLAF1	chr10:21822313-21823196	GM12878	blood:	n/a	n/a
16	BCLAF1	chr10:21822322-21823212	K562	blood:	n/a	n/a
17	BHLHE40	chr10:21822177-21823358	GM12878	blood:	n/a	n/a
18	BHLHE40	chr10:21822425-21823863	HepG2	liver:	n/a	n/a
19	BHLHE40	chr10:21823643-21824421	K562	blood:	n/a	chr10:21823858-21823874 chr10:21824151-21824167 chr10:21824309-21824325 chr10:21823957-21823973 chr10:21823850-21823866
20	BHLHE40	chr10:21823559-21824392	GM12878	blood:	n/a	chr10:21823858-21823874 chr10:21824151-21824167 chr10:21824309-21824325 chr10:21823957-21823973 chr10:21823850-21823866
21	BHLHE40	chr10:21822528-21823312	K562	blood:	n/a	n/a
22	CBX3	chr10:21822250-21823097	K562	blood:	n/a	n/a
23	CCNT2	chr10:21823570-21824512	K562	blood:	n/a	chr10:21823975-21823984
24	CCNT2	chr10:21822533-21823281	K562	blood:	n/a	chr10:21823239-21823248
25	CEBPB	chr10:21823561-21823733	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:21823558-21823775	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr10:21822782-21823146	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr10:21822351-21823273	HepG2	liver:	n/a	n/a
29	CEBPD	chr10:21822367-21823535	HepG2	liver:	n/a	n/a
30	CEBPD	chr10:21822271-21823359	K562	blood:	n/a	n/a
31	CEBPD	chr10:21822647-21823349	HepG2	liver:	n/a	n/a
32	CHD1	chr10:21824282-21824308	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr10:21823531-21823884	GM12878	blood:	n/a	n/a
34	CHD1	chr10:21822472-21823084	GM12878	blood:	n/a	chr10:21822855-21822865 chr10:21822999-21823009
35	CHD1	chr10:21822113-21822668	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr10:21822289-21823336	HepG2	liver:	n/a	chr10:21822855-21822865 chr10:21823239-21823249 chr10:21822999-21823009
37	CHD2	chr10:21823535-21824613	GM12878	blood:	n/a	n/a
38	CHD2	chr10:21822183-21823199	K562	blood:	n/a	chr10:21822855-21822865 chr10:21822999-21823009
39	CHD2	chr10:21822053-21823287	GM12878	blood:	n/a	chr10:21822855-21822865 chr10:21823239-21823249 chr10:21822999-21823009
40	CHD2	chr10:21823659-21823758	K562	blood:	n/a	n/a
41	CHD2	chr10:21822394-21823869	Hela-S3	cervix:	n/a	chr10:21822855-21822865 chr10:21823239-21823249 chr10:21822999-21823009
42	CHD2	chr10:21822516-21823348	H1-hESC	embryonic stem cell:	n/a	chr10:21822855-21822865 chr10:21823239-21823249 chr10:21822999-21823009
43	CREB1	chr10:21822387-21823467	A549	lung:	n/a	n/a
44	CREB1	chr10:21822623-21823352	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr10:21822445-21823413	GM12878	blood:	n/a	n/a
46	CREB1	chr10:21823544-21824002	K562	blood:	n/a	n/a
47	CREB1	chr10:21822147-21823500	HepG2	liver:	n/a	n/a
48	CREB1	chr10:21822395-21823396	K562	blood:	n/a	n/a
49	CREB1	chr10:21824222-21824493	A549	lung:	n/a	n/a
50	CTCF	chr10:21822340-21822490	GM12865	blood:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:21824447-21824497	RPTEC	kidney:	n/a
2	chr10:21822403-21822453	HRCEpiC	kidney:	n/a
3	chr10:21823297-21823347	AoSMC	blood vessel:	n/a
4	chr10:21823297-21823347	HAEpiC	amniotic membrane:	n/a
5	chr10:21823423-21823473	GM06990	blood:	n/a
6	chr10:21823475-21823525	MCF-7	breast:	n/a
7	chr10:21822977-21823027	IMR90	lung:	fetal
8	chr10:21823447-21823497	PANC-1	pancreas:	n/a
9	chr10:21823437-21823487	T-47D	breast:	n/a
10	chr10:21823423-21823473	Caco-2	colon:	n/a
11	chr10:21823475-21823525	IMR90	lung:	fetal
12	chr10:21823455-21823505	ECC-1	luminal epithelium:	n/a
13	chr10:21823447-21823497	CMK	blood:	n/a
14	chr10:21824407-21824457	NHDF-neo	bronchial:	n/a
15	chr10:21823423-21823473	HRE	kidney:	n/a
16	chr10:21824407-21824457	HEK293	kidney:	embryo
17	chr10:21822303-21822353	HNPCEpiC	eye:	n/a
18	chr10:21824447-21824497	H1-hESC	embryonic stem cell:	embryo
19	chr10:21822303-21822353	HRCEpiC	kidney:	n/a
20	chr10:21822787-21822837	AG04449	skin:	fetal
21	chr10:21822272-21822322	NHBE	bronchial:	n/a
22	chr10:21823423-21823473	BJ	skin:	n/a
23	chr10:21822968-21823018	PANC-1	pancreas:	n/a
24	chr10:21822403-21822453	GM19239	blood:	n/a
25	chr10:21823423-21823473	HMEC	breast:	n/a
26	chr10:21822977-21823027	HCF	heart:	n/a
27	chr10:21822272-21822322	AG09309	skin:	n/a
28	chr10:21824158-21824208	NT2-D1	testis:	n/a
29	chr10:21823437-21823487	Caco-2	colon:	n/a
30	chr10:21822787-21822837	HCT-116	colon:	n/a
31	chr10:21823447-21823497	SK-N-MC	brain:	n/a
32	chr10:21823423-21823473	AG04450	lung:	fetal
33	chr10:21822977-21823027	AG09319	gingival:	n/a
34	chr10:21822787-21822837	BJ	skin:	n/a
35	chr10:21822968-21823018	ovcar-3	ovarian:	n/a
36	chr10:21824158-21824208	SAEC	small airway:	n/a
37	chr10:21823447-21823497	AG04449	skin:	fetal
38	chr10:21822303-21822353	BJ	skin:	n/a
39	chr10:21823437-21823487	H1-hESC	embryonic stem cell:	embryo
40	chr10:21823475-21823525	HIPEpiC	eye:	n/a
41	chr10:21824158-21824208	GM19239	blood:	n/a
42	chr10:21823437-21823487	PrEC	prostate:	n/a
43	chr10:21824158-21824208	PFSK-1	brain:	n/a
44	chr10:21822977-21823027	NHBE	bronchial:	n/a
45	chr10:21824407-21824457	LNCaP	prostate:	n/a
46	chr10:21824158-21824208	SK-N-SH	brain:	n/a
47	chr10:21824158-21824208	CMK	blood:	n/a
48	chr10:21822272-21822322	PFSK-1	brain:	n/a
49	chr10:21823437-21823487	AG04450	lung:	fetal
50	chr10:21823475-21823525	MCF10A-Er-Src	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:6844565..6845211-chr10:21822402..21823399,2	NB4	blood:
2	chr10:21824097..21826874-chr10:22615041..22617499,2	K562	blood:
3	chr10:21824380..21826372-chr10:21842074..21844777,3	K562	blood:
4	chr10:21784774..21789957-chr10:21820858..21826220,9	MCF-7	breast:
5	chr10:21784105..21788419-chr10:21820020..21825934,15	K562	blood:
6	chr10:21823004..21824663-chr10:22608853..22611559,3	K562	blood:
7	chr10:21822045..21822922-chr14:50065370..50066027,2	Hela-S3	cervix:
8	chr10:21784405..21786921-chr10:21820578..21824484,6	MCF-7	breast:
9	chr10:21462486..21464752-chr10:21822711..21824780,2	MCF-7	breast:
10	chr10:21763967..21765915-chr10:21820410..21823036,2	MCF-7	breast:
11	chr10:21822674..21823308-chr16:68271100..68271892,2	Hela-S3	cervix:
12	chr10:21821191..21822728-chr10:22232911..22234926,2	MCF-7	breast:
13	chr10:21822396..21823232-chr20:50727562..50728298,2	MCF-7	breast:
14	chr10:21819973..21822184-chr10:22292181..22294416,2	K562	blood:
15	chr10:21821950..21822940-chr11:65728654..65729654,2	HCT-116	colon:
16	chr10:21814321..21814920-chr10:21822442..21823074,2	Hela-S3	cervix:
17	chr10:21779286..21780842-chr10:21820192..21822090,2	K562	blood:
18	chr10:21822623..21823131-chr19:49999677..50000261,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
MLLT10	TF binding region
MLLT10	CpG island
ENSG00000180592	chromatin interactions
ENSG00000233347	chromatin interactions
ENSG00000261469	chromatin interactions
ENSG00000165501	chromatin interactions
ENSG00000213741	chromatin interactions
ENSG00000204682	chromatin interactions
ENSG00000136770	chromatin interactions
ENSG00000231920	chromatin interactions
ENSG00000168283	chromatin interactions
ENSG00000175467	chromatin interactions
ENSG00000142534	chromatin interactions
ENSG00000237436	chromatin interactions
ENSG00000078114	chromatin interactions
ENSG00000222071	chromatin interactions
ENSG00000253459	chromatin interactions

Extended variants
information (count: 117 )
Associated
traits (count: 37 )

Variant overlapped rSNPs/rCNVs (count:117 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528756821	chr10:21821984-21821985	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs114796320	chr10:21821994-21821995	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs183398564	chr10:21822061-21822062	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs150228461	chr10:21822071-21822072	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs548892644	chr10:21822091-21822092	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs188329666	chr10:21822097-21822098	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs546906530	chr10:21822107-21822108	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs139119665	chr10:21822178-21822179	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs531247376	chr10:21822203-21822204	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs536226286	chr10:21822227-21822228	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs552806729	chr10:21822264-21822265	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs572865591	chr10:21822391-21822392	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs550822792	chr10:21822409-21822410	Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs368864434	chr10:21822475-21822476	Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs558289253	chr10:21822518-21822519	Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs575085486	chr10:21822528-21822529	Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs544129394	chr10:21822536-21822537	Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs560845613	chr10:21822540-21822541	Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs528413865	chr10:21822599-21822600	Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs190673849	chr10:21822613-21822614	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs28364865	chr10:21822698-21822699	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs118163926	chr10:21822711-21822712	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs532608687	chr10:21822788-21822789	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs552817746	chr10:21822806-21822807	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs563107180	chr10:21822818-21822819	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs10828247	chr10:21822856-21822857	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs548943688	chr10:21822872-21822873	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
28	rs568699912	chr10:21822877-21822878	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
29	rs535875852	chr10:21822900-21822901	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
30	rs578119507	chr10:21822938-21822939	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs546549200	chr10:21822974-21822975	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs566462203	chr10:21822976-21822977	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs182925975	chr10:21823000-21823001	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs187623788	chr10:21823200-21823201	Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs558209609	chr10:21823240-21823241	Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs575143252	chr10:21823241-21823242	Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs200909217	chr10:21823243-21823244	Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs537640120	chr10:21823249-21823250	Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs554451902	chr10:21823292-21823293	Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs113634034	chr10:21823312-21823313	Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs574628420	chr10:21823326-21823327	Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs540288638	chr10:21823327-21823328	Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs527697532	chr10:21823339-21823340	Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs554100603	chr10:21823348-21823349	Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs577151744	chr10:21823376-21823377	Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs546345707	chr10:21823395-21823396	Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs7477898	chr10:21823432-21823433	Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs562965377	chr10:21823440-21823441	Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs531954553	chr10:21823464-21823465	Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs542397508	chr10:21823494-21823495	Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:37)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21816600-21822400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:21816600-21822400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:21817000-21822200	Weak transcription	Placenta	Placenta
4	chr10:21818000-21822000	Weak transcription	Osteobl	bone
5	chr10:21818000-21822200	Weak transcription	Small Intestine	intestine
6	chr10:21818200-21822000	Weak transcription	Fetal Muscle Leg	muscle
7	chr10:21818200-21822200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr10:21821000-21822000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr10:21821000-21822000	Enhancers	HSMM	muscle
10	chr10:21821200-21822000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr10:21821200-21822000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr10:21821200-21822000	Enhancers	Primary T cells from cord blood	blood
13	chr10:21821200-21822000	Enhancers	Fetal Heart	heart
14	chr10:21821200-21822000	Enhancers	Fetal Intestine Large	intestine
15	chr10:21821200-21822000	Enhancers	Fetal Kidney	kidney
16	chr10:21821200-21822200	Enhancers	H9 Cell Line	embryonic stem cell
17	chr10:21821200-21822200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:21821200-21822200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr10:21821200-21822600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr10:21821200-21822800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr10:21821200-21824600	Active TSS	Psoas Muscle	Psoas
22	chr10:21821400-21824400	Active TSS	A549	lung
23	chr10:21821600-21822000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr10:21821600-21822000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr10:21821600-21822000	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr10:21821600-21822000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr10:21821600-21822000	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr10:21821600-21822000	Enhancers	HMEC	breast
29	chr10:21821600-21822200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr10:21821600-21822200	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr10:21821600-21822200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr10:21821600-21822200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr10:21821600-21822200	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr10:21821600-21822200	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr10:21821600-21822200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr10:21821600-21822400	Flanking Active TSS	Liver	Liver
37	chr10:21821600-21822600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr10:21821600-21822600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr10:21821600-21822600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr10:21821600-21822600	Flanking Active TSS	NHEK	skin
41	chr10:21821600-21822800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr10:21821600-21822800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
43	chr10:21821600-21824400	Active TSS	Stomach Smooth Muscle	stomach
44	chr10:21821600-21824400	Active TSS	K562	blood
45	chr10:21821800-21822000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:21821800-21822000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
47	chr10:21821800-21822000	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr10:21821800-21822000	Enhancers	Primary B cells from cord blood	blood
49	chr10:21821800-21822000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr10:21821800-21822000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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