Variant report

Variant	esv2763685
Chromosome Location	chr21:15904945-15933282
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:743)
CpG islands
(count:61)
Chromatin interactive
region (count:46)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:15922657-15922941	K562	blood:	n/a	n/a
2	ARID3A	chr21:15920229-15920429	K562	blood:	n/a	n/a
3	ARID3A	chr21:15922300-15922396	K562	blood:	n/a	n/a
4	ARID3A	chr21:15907258-15907450	K562	blood:	n/a	n/a
5	ARID3A	chr21:15905866-15906701	K562	blood:	n/a	n/a
6	ARID3A	chr21:15916297-15916537	K562	blood:	n/a	n/a
7	ARID3A	chr21:15915542-15916058	K562	blood:	n/a	n/a
8	ARID3A	chr21:15913953-15914685	K562	blood:	n/a	n/a
9	ARID3A	chr21:15917206-15917215	K562	blood:	n/a	n/a
10	ARID3A	chr21:15921104-15921404	K562	blood:	n/a	n/a
11	ARID3A	chr21:15918034-15918949	K562	blood:	n/a	n/a
12	ATF1	chr21:15918475-15918878	K562	blood:	n/a	n/a
13	ATF1	chr21:15906176-15906571	K562	blood:	n/a	n/a
14	ATF2	chr21:15920092-15920756	GM12878	blood:	n/a	n/a
15	ATF2	chr21:15906051-15906824	GM12878	blood:	n/a	n/a
16	ATF2	chr21:15920084-15920815	GM12878	blood:	n/a	n/a
17	ATF2	chr21:15906055-15906924	GM12878	blood:	n/a	n/a
18	ATF2	chr21:15918292-15918991	GM12878	blood:	n/a	n/a
19	ATF3	chr21:15918358-15918889	K562	blood:	n/a	n/a
20	ATF3	chr21:15906194-15906673	K562	blood:	n/a	n/a
21	BACH1	chr21:15921741-15921941	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr21:15908205-15908296	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr21:15916463-15916519	K562	blood:	n/a	n/a
24	BACH1	chr21:15908754-15908810	K562	blood:	n/a	n/a
25	BACH1	chr21:15909350-15909434	K562	blood:	n/a	n/a
26	BACH1	chr21:15921610-15921978	K562	blood:	n/a	n/a
27	BATF	chr21:15920482-15920817	GM12878	blood:	n/a	chr21:15920670-15920678
28	BATF	chr21:15906254-15906836	GM12878	blood:	n/a	n/a
29	BATF	chr21:15931495-15931922	GM12878	blood:	n/a	n/a
30	BATF	chr21:15931607-15931920	GM12878	blood:	n/a	n/a
31	BATF	chr21:15918515-15918811	GM12878	blood:	n/a	n/a
32	BATF	chr21:15920187-15920455	GM12878	blood:	n/a	n/a
33	BATF	chr21:15905982-15906869	GM12878	blood:	n/a	n/a
34	BATF	chr21:15918456-15918832	GM12878	blood:	n/a	n/a
35	BCL11A	chr21:15906198-15906816	GM12878	blood:	n/a	n/a
36	BCL11A	chr21:15918476-15918780	GM12878	blood:	n/a	n/a
37	BCL11A	chr21:15918539-15918739	GM12878	blood:	n/a	n/a
38	BCL3	chr21:15910886-15911188	GM12878	blood:	n/a	n/a
39	BCL3	chr21:15920227-15920814	GM12878	blood:	n/a	n/a
40	BCL3	chr21:15906024-15906788	GM12878	blood:	n/a	n/a
41	BCLAF1	chr21:15918290-15918909	GM12878	blood:	n/a	n/a
42	BCLAF1	chr21:15918276-15918932	K562	blood:	n/a	n/a
43	BCLAF1	chr21:15918409-15918766	K562	blood:	n/a	n/a
44	BCLAF1	chr21:15914278-15914649	GM12878	blood:	n/a	n/a
45	BCLAF1	chr21:15906048-15906879	GM12878	blood:	n/a	n/a
46	BHLHE40	chr21:15919813-15920020	GM12878	blood:	n/a	n/a
47	BHLHE40	chr21:15916335-15916682	K562	blood:	n/a	n/a
48	BHLHE40	chr21:15918481-15918856	K562	blood:	n/a	n/a
49	BHLHE40	chr21:15906189-15907287	GM12878	blood:	n/a	n/a
50	BHLHE40	chr21:15931353-15931891	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:15914403-15914453	GM19239	blood:	n/a
2	chr21:15914403-15914453	H1-hESC	embryonic stem cell:	embryo
3	chr21:15914403-15914453	MCF10A-Er-Src	breast:	n/a
4	chr21:15914403-15914453	AG10803	skin:	n/a
5	chr21:15914403-15914453	ovcar-3	ovarian:	n/a
6	chr21:15914403-15914453	ECC-1	luminal epithelium:	n/a
7	chr21:15914403-15914453	NHBE	bronchial:	n/a
8	chr21:15914403-15914453	AG09319	gingival:	n/a
9	chr21:15914403-15914453	A549	lung:	n/a
10	chr21:15914403-15914453	HPAEpiC	pulmonary alveolar:	n/a
11	chr21:15914403-15914453	PFSK-1	brain:	n/a
12	chr21:15914403-15914453	HCPEpiC	choroid plexus:	n/a
13	chr21:15914403-15914453	SAEC	small airway:	n/a
14	chr21:15914403-15914453	RPTEC	kidney:	n/a
15	chr21:15914403-15914453	MCF-7	breast:	n/a
16	chr21:15914403-15914453	PrEC	prostate:	n/a
17	chr21:15914403-15914453	U87	brain:	n/a
18	chr21:15914403-15914453	Hela-S3	cervix:	n/a
19	chr21:15914403-15914453	AG04449	skin:	fetal
20	chr21:15914403-15914453	AG04450	lung:	fetal
21	chr21:15914403-15914453	NT2-D1	testis:	n/a
22	chr21:15914403-15914453	HCM	heart:	n/a
23	chr21:15914403-15914453	T-47D	breast:	n/a
24	chr21:15914403-15914453	K562	blood:	n/a
25	chr21:15914403-15914453	BJ	skin:	n/a
26	chr21:15914403-15914453	CMK	blood:	n/a
27	chr21:15914403-15914453	HL-60	blood:	n/a
28	chr21:15914403-15914453	BE2_C	brain:	n/a
29	chr21:15914403-15914453	HRE	kidney:	n/a
30	chr21:15914403-15914453	ProgFib	skin:	n/a
31	chr21:15914403-15914453	HCF	heart:	n/a
32	chr21:15914403-15914453	HepG2	liver:	n/a
33	chr21:15914403-15914453	HNPCEpiC	eye:	n/a
34	chr21:15914403-15914453	SK-N-MC	brain:	n/a
35	chr21:15914403-15914453	Caco-2	colon:	n/a
36	chr21:15914403-15914453	HAEpiC	amniotic membrane:	n/a
37	chr21:15914403-15914453	HEK293	kidney:	embryo
38	chr21:15914403-15914453	IMR90	lung:	fetal
39	chr21:15914403-15914453	GM12892	blood:	n/a
40	chr21:15914403-15914453	LNCaP	prostate:	n/a
41	chr21:15914403-15914453	AG09309	skin:	n/a
42	chr21:15914403-15914453	HEEpiC	esophagus:	n/a
43	chr21:15914403-15914453	AoSMC	blood vessel:	n/a
44	chr21:15914403-15914453	GM06990	blood:	n/a
45	chr21:15914403-15914453	HUVEC	blood vessel:	n/a
46	chr21:15914403-15914453	NH-A	brain:	n/a
47	chr21:15914403-15914453	HRPEpiC	eye:	n/a
48	chr21:15914403-15914453	HCT-116	colon:	n/a
49	chr21:15914403-15914453	Hepatocyte	liver:	n/a
50	chr21:15914403-15914453	Jurkat	blood:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:15910273..15912719-chr21:15913712..15915287,2	K562	blood:
2	chr21:15919365..15921468-chr21:16048127..16050377,2	K562	blood:
3	chr21:15912730..15916019-chr21:15916425..15919963,12	K562	blood:
4	chr21:15915978..15918625-chr21:15919465..15922478,3	K562	blood:
5	chr21:15915915..15920125-chr21:15922754..15925442,5	K562	blood:
6	chr21:15922292..15924126-chr21:15926793..15928319,2	K562	blood:
7	chr21:15904847..15907317-chr21:16028940..16030930,2	K562	blood:
8	chr21:15920671..15923360-chr21:15929340..15932218,2	K562	blood:
9	chr21:15930237..15934475-chr21:15937814..15942130,5	K562	blood:
10	chr21:15870384..15874520-chr21:15900850..15905377,4	K562	blood:
11	chr21:15900972..15903079-chr21:15904912..15907876,2	K562	blood:
12	chr21:15923906..15926017-chr21:15954257..15957177,2	K562	blood:
13	chr21:15927550..15930394-chr21:15933499..15936075,3	K562	blood:
14	chr21:15913818..15915789-chr21:15955801..15958160,2	K562	blood:
15	chr21:15916384..15919028-chr21:15926638..15928461,2	K562	blood:
16	chr21:15916155..15921451-chr21:15952417..15958327,11	K562	blood:
17	chr21:15919672..15922192-chr21:15926866..15928968,2	K562	blood:
18	chr21:15918667..15923010-chr21:15942455..15946099,5	K562	blood:
19	chr21:15916866..15918516-chr21:16085549..16087908,2	K562	blood:
20	chr21:15916304..15917888-chr21:16008677..16010503,2	K562	blood:
21	chr21:15919672..15922192-chr21:15926866..15928968,2	K562	blood:
22	chr21:15910273..15912719-chr21:15913712..15915287,2	K562	blood:
23	chr21:15915915..15918568-chr21:15923468..15925442,2	K562	blood:
24	chr21:15916876..15918776-chr21:16125268..16127207,2	K562	blood:
25	chr21:15904288..15906853-chr21:15912996..15915455,2	K562	blood:
26	chr21:15903442..15906073-chr21:15908786..15911014,2	K562	blood:
27	chr21:15916860..15919721-chr21:16123639..16127207,4	K562	blood:
28	chr21:15904966..15908708-chr21:15954963..15957807,4	K562	blood:
29	chr21:15919781..15923280-chr21:15954504..15956620,3	K562	blood:
30	chr21:15904847..15906603-chr21:16029430..16031380,2	K562	blood:
31	chr21:15916330..15918586-chr21:16097161..16099794,2	K562	blood:
32	chr21:15922292..15924126-chr21:15926793..15928319,2	K562	blood:
33	chr21:15915395..15917614-chr21:16129062..16131798,2	K562	blood:
34	chr21:15915303..15917955-chr21:15967480..15970218,2	K562	blood:
35	chr21:15905941..15908063-chr21:15951429..15954293,3	K562	blood:
36	chr21:15870384..15873192-chr21:15902797..15905377,2	K562	blood:
37	chr21:15914500..15916247-chr21:15937941..15940190,2	K562	blood:
38	chr21:15920671..15923360-chr21:15929340..15932218,2	K562	blood:
39	chr21:15932451..15935066-chr21:15942952..15944927,2	K562	blood:
40	chr21:15915978..15918625-chr21:15919465..15922478,3	K562	blood:
41	chr21:15903442..15906073-chr21:15908786..15911014,2	K562	blood:
42	chr21:15919906..15922793-chr21:15932302..15934213,2	K562	blood:
43	chr21:15919906..15922793-chr21:15932302..15934213,2	K562	blood:
44	chr21:15915915..15918568-chr21:15923468..15925442,2	K562	blood:
45	chr21:15904288..15906853-chr21:15912996..15915455,2	K562	blood:
46	chr21:15920124..15923209-chr21:15941679..15944846,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AF165138.7.1-5	chr21:15921236-15921459	l_2170_chr21:15869459-15921459_brain
2	lnc-AF165138.7.1-4	chr21:15918526-15918634	NONHSAT081164

No data

Variant related genes	Relation type
SAMSN1	TF binding region
SAMSN1	CpG island
ENSG00000155307	chromatin interactions
ENSG00000232884	chromatin interactions
ENSG00000223662	chromatin interactions
ENSG00000243440	chromatin interactions
ENSG00000228600	chromatin interactions

Extended variants
information (count: 1215 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1215 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369702350	chr21:15905065-15905066	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs555418944	chr21:15905070-15905071	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs574488857	chr21:15905113-15905114	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs543440276	chr21:15905137-15905138	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs573549455	chr21:15905158-15905159	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs541901931	chr21:15905193-15905194	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs191289730	chr21:15905209-15905210	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs535104918	chr21:15905222-15905223	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs368558941	chr21:15905223-15905224	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs116813389	chr21:15905242-15905243	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs546033424	chr21:15905257-15905258	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs183826209	chr21:15905294-15905295	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs559906056	chr21:15905325-15905326	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs369558229	chr21:15905375-15905376	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs186370433	chr21:15905406-15905407	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs528719056	chr21:15905504-15905505	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs145629962	chr21:15905515-15905516	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs79468283	chr21:15905553-15905554	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs4817236	chr21:15905580-15905581	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs550609103	chr21:15905605-15905606	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs35009227	chr21:15905610-15905611	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs539524714	chr21:15905632-15905633	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs369101838	chr21:15905633-15905634	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs566653743	chr21:15905673-15905674	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs535337639	chr21:15905730-15905731	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs139662538	chr21:15905752-15905753	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs555613987	chr21:15905868-15905869	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs372538673	chr21:15905936-15905937	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs537014137	chr21:15905949-15905950	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs189637128	chr21:15905970-15905971	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs200089751	chr21:15905971-15905972	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs576884258	chr21:15906018-15906019	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs146482609	chr21:15906020-15906021	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs377081907	chr21:15906084-15906085	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs543388460	chr21:15906127-15906128	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs553238179	chr21:15906168-15906169	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs114837297	chr21:15906208-15906209	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs141312790	chr21:15906229-15906230	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs181670496	chr21:15906237-15906238	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs531251957	chr21:15906241-15906242	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs544182383	chr21:15906248-15906249	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs564082660	chr21:15906250-15906251	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs111407996	chr21:15906280-15906281	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs151265550	chr21:15906336-15906337	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs566473647	chr21:15906368-15906369	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs529070019	chr21:15906382-15906383	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs186871872	chr21:15906474-15906475	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs190586210	chr21:15906492-15906493	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs537757347	chr21:15906503-15906504	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs544617563	chr21:15906514-15906515	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell lymphomas	19863542	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
XY gonadal dysgenesis	20685758	CNVD

Chromatin state (count:580 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15853400-15905400	Weak transcription	HUVEC	blood vessel
2	chr21:15896200-15906200	Weak transcription	Fetal Thymus	thymus
3	chr21:15899800-15906000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr21:15900000-15905200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr21:15900000-15906000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr21:15900000-15906000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr21:15901000-15906000	Weak transcription	Primary T cells from cord blood	blood
8	chr21:15901200-15905800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr21:15901200-15905800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr21:15902600-15906600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr21:15902800-15905800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr21:15903800-15906600	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr21:15904000-15905800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr21:15904000-15906600	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr21:15904200-15905800	Enhancers	GM12878-XiMat	blood
16	chr21:15904200-15906000	Enhancers	Primary T cells fromperipheralblood	blood
17	chr21:15904200-15906000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr21:15904200-15908000	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr21:15904200-15908400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr21:15904400-15905000	Transcr. at gene 5' and 3'	K562	blood
21	chr21:15904400-15906600	Enhancers	Primary B cells from peripheral blood	blood
22	chr21:15904600-15905200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr21:15904600-15907400	Enhancers	Dnd41	blood
24	chr21:15904600-15907400	Enhancers	Hela-S3	cervix
25	chr21:15904600-15913600	Weak transcription	Primary hematopoietic stem cells	blood
26	chr21:15904800-15905400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr21:15904800-15905400	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr21:15904800-15905800	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr21:15904800-15905800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr21:15904800-15905800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr21:15904800-15906000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr21:15904800-15906200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr21:15904800-15906600	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr21:15905000-15905800	Weak transcription	K562	blood
35	chr21:15905200-15906600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr21:15905200-15907200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr21:15905400-15905800	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr21:15905400-15905800	Enhancers	NHEK	skin
39	chr21:15905400-15906400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
40	chr21:15905400-15907400	Enhancers	HUVEC	blood vessel
41	chr21:15905800-15906000	Genic enhancers	K562	blood
42	chr21:15905800-15906200	Flanking Active TSS	NHEK	skin
43	chr21:15905800-15906400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr21:15905800-15906400	Flanking Active TSS	GM12878-XiMat	blood
45	chr21:15905800-15906400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr21:15905800-15906800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr21:15905800-15906800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr21:15905800-15906800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr21:15905800-15906800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
50	chr21:15905800-15906800	Enhancers	Muscle Satellite Cultured Cells	--

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