Variant report

Variant	nsv544377
Chromosome Location	chr21:15896056-15948474
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1031)
CpG islands
(count:61)
Chromatin interactive
region (count:72)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1031 , 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	chr21:15941879-15942072	K562	blood:	n/a	n/a
2	ARID3A	chr21:15917206-15917215	K562	blood:	n/a	n/a
3	ARID3A	chr21:15918034-15918949	K562	blood:	n/a	n/a
4	ARID3A	chr21:15913953-15914685	K562	blood:	n/a	n/a
5	ARID3A	chr21:15948341-15948537	K562	blood:	n/a	n/a
6	ARID3A	chr21:15898648-15900165	K562	blood:	n/a	n/a
7	ARID3A	chr21:15915542-15916058	K562	blood:	n/a	n/a
8	ARID3A	chr21:15921104-15921404	K562	blood:	n/a	n/a
9	ARID3A	chr21:15916297-15916537	K562	blood:	n/a	n/a
10	ARID3A	chr21:15945870-15945930	K562	blood:	n/a	n/a
11	ARID3A	chr21:15922300-15922396	K562	blood:	n/a	n/a
12	ARID3A	chr21:15920229-15920429	K562	blood:	n/a	n/a
13	ARID3A	chr21:15922657-15922941	K562	blood:	n/a	n/a
14	ARID3A	chr21:15907258-15907450	K562	blood:	n/a	n/a
15	ARID3A	chr21:15905866-15906701	K562	blood:	n/a	n/a
16	ARID3A	chr21:15900823-15901417	K562	blood:	n/a	n/a
17	ATF1	chr21:15918475-15918878	K562	blood:	n/a	n/a
18	ATF1	chr21:15906176-15906571	K562	blood:	n/a	n/a
19	ATF1	chr21:15937557-15937915	K562	blood:	n/a	n/a
20	ATF2	chr21:15918292-15918991	GM12878	blood:	n/a	n/a
21	ATF2	chr21:15906051-15906824	GM12878	blood:	n/a	n/a
22	ATF2	chr21:15920092-15920756	GM12878	blood:	n/a	n/a
23	ATF2	chr21:15920084-15920815	GM12878	blood:	n/a	n/a
24	ATF2	chr21:15906055-15906924	GM12878	blood:	n/a	n/a
25	ATF3	chr21:15918358-15918889	K562	blood:	n/a	n/a
26	ATF3	chr21:15899447-15899839	GM12878	blood:	n/a	n/a
27	ATF3	chr21:15937541-15937885	K562	blood:	n/a	n/a
28	ATF3	chr21:15906194-15906673	K562	blood:	n/a	n/a
29	BACH1	chr21:15921741-15921941	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr21:15921610-15921978	K562	blood:	n/a	n/a
31	BACH1	chr21:15908205-15908296	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr21:15908754-15908810	K562	blood:	n/a	n/a
33	BACH1	chr21:15916463-15916519	K562	blood:	n/a	n/a
34	BACH1	chr21:15898648-15899278	K562	blood:	n/a	n/a
35	BACH1	chr21:15909350-15909434	K562	blood:	n/a	n/a
36	BATF	chr21:15904091-15904445	GM12878	blood:	n/a	chr21:15904245-15904256
37	BATF	chr21:15918515-15918811	GM12878	blood:	n/a	n/a
38	BATF	chr21:15920482-15920817	GM12878	blood:	n/a	chr21:15920670-15920678
39	BATF	chr21:15918456-15918832	GM12878	blood:	n/a	n/a
40	BATF	chr21:15920187-15920455	GM12878	blood:	n/a	n/a
41	BATF	chr21:15931495-15931922	GM12878	blood:	n/a	n/a
42	BATF	chr21:15931607-15931920	GM12878	blood:	n/a	n/a
43	BATF	chr21:15944563-15944867	GM12878	blood:	n/a	chr21:15944717-15944728
44	BATF	chr21:15905982-15906869	GM12878	blood:	n/a	n/a
45	BATF	chr21:15944575-15944886	GM12878	blood:	n/a	chr21:15944717-15944728
46	BATF	chr21:15906254-15906836	GM12878	blood:	n/a	n/a
47	BCL11A	chr21:15906198-15906816	GM12878	blood:	n/a	n/a
48	BCL11A	chr21:15918476-15918780	GM12878	blood:	n/a	n/a
49	BCL11A	chr21:15944519-15944866	GM12878	blood:	n/a	n/a
50	BCL11A	chr21:15918539-15918739	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	AG04449	skin:	fetal
2	chr21:15914403-15914453	AG09319	gingival:	n/a
3	chr21:15914403-15914453	AG09309	skin:	n/a
4	chr21:15914403-15914453	RPTEC	kidney:	n/a
5	chr21:15914403-15914453	GM12892	blood:	n/a
6	chr21:15914403-15914453	ovcar-3	ovarian:	n/a
7	chr21:15914403-15914453	NB4	blood:	n/a
8	chr21:15914403-15914453	U87	brain:	n/a
9	chr21:15914403-15914453	IMR90	lung:	fetal
10	chr21:15914403-15914453	HCM	heart:	n/a
11	chr21:15914403-15914453	MCF-7	breast:	n/a
12	chr21:15914403-15914453	SAEC	small airway:	n/a
13	chr21:15914403-15914453	GM12891	blood:	n/a
14	chr21:15914403-15914453	LNCaP	prostate:	n/a
15	chr21:15914403-15914453	HRCEpiC	kidney:	n/a
16	chr21:15914403-15914453	CMK	blood:	n/a
17	chr21:15914403-15914453	BE2_C	brain:	n/a
18	chr21:15914403-15914453	Jurkat	blood:	n/a
19	chr21:15914403-15914453	NH-A	brain:	n/a
20	chr21:15914403-15914453	SK-N-SH_RA	brain:	n/a
21	chr21:15914403-15914453	Caco-2	colon:	n/a
22	chr21:15914403-15914453	HL-60	blood:	n/a
23	chr21:15914403-15914453	HRE	kidney:	n/a
24	chr21:15914403-15914453	HCPEpiC	choroid plexus:	n/a
25	chr21:15914403-15914453	Hepatocyte	liver:	n/a
26	chr21:15914403-15914453	GM19239	blood:	n/a
27	chr21:15914403-15914453	NT2-D1	testis:	n/a
28	chr21:15914403-15914453	HIPEpiC	eye:	n/a
29	chr21:15914403-15914453	SK-N-SH	brain:	n/a
30	chr21:15914403-15914453	HMEC	breast:	n/a
31	chr21:15914403-15914453	HUVEC	blood vessel:	n/a
32	chr21:15914403-15914453	AoSMC	blood vessel:	n/a
33	chr21:15914403-15914453	HEEpiC	esophagus:	n/a
34	chr21:15914403-15914453	BJ	skin:	n/a
35	chr21:15914403-15914453	PFSK-1	brain:	n/a
36	chr21:15914403-15914453	HRPEpiC	eye:	n/a
37	chr21:15914403-15914453	GM06990	blood:	n/a
38	chr21:15914403-15914453	GM12878	blood:	n/a
39	chr21:15914403-15914453	PrEC	prostate:	n/a
40	chr21:15914403-15914453	SK-N-MC	brain:	n/a
41	chr21:15914403-15914453	SKMC	muscle:	n/a
42	chr21:15914403-15914453	Hela-S3	cervix:	n/a
43	chr21:15914403-15914453	AG10803	skin:	n/a
44	chr21:15914403-15914453	K562	blood:	n/a
45	chr21:15914403-15914453	MCF10A-Er-Src	breast:	n/a
46	chr21:15914403-15914453	HCT-116	colon:	n/a
47	chr21:15914403-15914453	H1-hESC	embryonic stem cell:	embryo
48	chr21:15914403-15914453	T-47D	breast:	n/a
49	chr21:15914403-15914453	A549	lung:	n/a
50	chr21:15914403-15914453	ProgFib	skin:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:15919906..15922793-chr21:15932302..15934213,2	K562	blood:
2	chr21:15915395..15917614-chr21:16129062..16131798,2	K562	blood:
3	chr21:15915915..15920125-chr21:15922754..15925442,5	K562	blood:
4	chr21:15915303..15917955-chr21:15967480..15970218,2	K562	blood:
5	chr21:15915978..15918625-chr21:15919465..15922478,3	K562	blood:
6	chr21:15922292..15924126-chr21:15926793..15928319,2	K562	blood:
7	chr21:15940693..15943113-chr21:15945415..15947276,2	K562	blood:
8	chr21:15938738..15940240-chr21:15946079..15949018,2	K562	blood:
9	chr21:15927550..15930394-chr21:15933499..15936075,3	K562	blood:
10	chr21:15904288..15906853-chr21:15912996..15915455,2	K562	blood:
11	chr21:15942072..15943675-chr21:15953537..15956336,2	K562	blood:
12	chr21:15916155..15921451-chr21:15952417..15958327,11	K562	blood:
13	chr21:15905941..15908063-chr21:15951429..15954293,3	K562	blood:
14	chr21:15904847..15907317-chr21:16028940..16030930,2	K562	blood:
15	chr21:15913818..15915789-chr21:15955801..15958160,2	K562	blood:
16	chr21:15942194..15946580-chr21:15946989..15950349,5	K562	blood:
17	chr21:15919672..15922192-chr21:15926866..15928968,2	K562	blood:
18	chr21:15934844..15936651-chr21:15965366..15968076,2	K562	blood:
19	chr21:15916330..15918586-chr21:16097161..16099794,2	K562	blood:
20	chr21:15923906..15926017-chr21:15954257..15957177,2	K562	blood:
21	chr21:15919672..15922192-chr21:15926866..15928968,2	K562	blood:
22	chr21:15916866..15918516-chr21:16085549..16087908,2	K562	blood:
23	chr21:15919365..15921468-chr21:16048127..16050377,2	K562	blood:
24	chr21:15937940..15940141-chr21:15954473..15956452,2	K562	blood:
25	chr21:15927550..15930394-chr21:15933499..15936075,3	K562	blood:
26	chr21:15922292..15924126-chr21:15926793..15928319,2	K562	blood:
27	chr21:15914500..15916247-chr21:15937941..15940190,2	K562	blood:
28	chr21:15919906..15922793-chr21:15932302..15934213,2	K562	blood:
29	chr21:15914500..15916247-chr21:15937941..15940190,2	K562	blood:
30	chr21:15870384..15873192-chr21:15902797..15905377,2	K562	blood:
31	chr21:15910273..15912719-chr21:15913712..15915287,2	K562	blood:
32	chr21:15920671..15923360-chr21:15929340..15932218,2	K562	blood:
33	chr21:15945593..15948533-chr21:15955041..15959412,3	K562	blood:
34	chr21:15920671..15923360-chr21:15929340..15932218,2	K562	blood:
35	chr20:57606873..57607444-chr21:15903062..15903984,2	MCF-7	breast:
36	chr21:15903442..15906073-chr21:15908786..15911014,2	K562	blood:
37	chr21:15904288..15906853-chr21:15912996..15915455,2	K562	blood:
38	chr21:15932451..15935066-chr21:15942952..15944927,2	K562	blood:
39	chr21:15898174..15900938-chr21:15917034..15919951,2	K562	blood:
40	chr21:15870384..15874520-chr21:15900850..15905377,4	K562	blood:
41	chr21:15903442..15906073-chr21:15908786..15911014,2	K562	blood:
42	chr21:15915915..15918568-chr21:15923468..15925442,2	K562	blood:
43	chr21:15912730..15916019-chr21:15916425..15919963,12	K562	blood:
44	chr21:15901318..15902999-chr21:16086127..16088877,2	K562	blood:
45	chr21:15900972..15903079-chr21:15904912..15907876,2	K562	blood:
46	chr21:15919781..15923280-chr21:15954504..15956620,3	K562	blood:
47	chr21:15920124..15923209-chr21:15941679..15944846,3	K562	blood:
48	chr21:15940693..15943113-chr21:15945415..15947276,2	K562	blood:
49	chr21:15916876..15918776-chr21:16125268..16127207,2	K562	blood:
50	chr21:15893314..15896057-chr21:15897268..15899492,2	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
ENSG00000228600	chromatin interactions
ENSG00000155307	chromatin interactions
ENSG00000232884	chromatin interactions
ENSG00000124172	chromatin interactions
ENSG00000243440	chromatin interactions
ENSG00000223662	chromatin interactions

Extended variants
information (count: 2310 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2310 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567191589	chr21:15896079-15896080	Enhancers Flanking Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs190996336	chr21:15896081-15896082	Enhancers Flanking Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs377541995	chr21:15896092-15896093	Enhancers Flanking Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575605578	chr21:15896104-15896105	Enhancers Flanking Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537893974	chr21:15896127-15896128	Enhancers Flanking Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558280730	chr21:15896157-15896158	Enhancers Flanking Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370746324	chr21:15896189-15896190	Enhancers Flanking Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182509755	chr21:15896211-15896212	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540795714	chr21:15896223-15896224	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554428215	chr21:15896236-15896237	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138173069	chr21:15896239-15896240	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2822726	chr21:15896281-15896282	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs149088147	chr21:15896309-15896310	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531332511	chr21:15896313-15896314	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574205503	chr21:15896344-15896345	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368394993	chr21:15896376-15896377	Enhancers Weak transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544704801	chr21:15896401-15896402	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2822727	chr21:15896422-15896423	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs574542382	chr21:15896464-15896465	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs143106718	chr21:15896507-15896508	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2822728	chr21:15896516-15896517	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs567128840	chr21:15896518-15896519	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188022070	chr21:15896528-15896529	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148336473	chr21:15896547-15896548	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560162564	chr21:15896552-15896553	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192691747	chr21:15896564-15896565	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546065438	chr21:15896585-15896586	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141462054	chr21:15896586-15896587	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76961776	chr21:15896595-15896596	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371887797	chr21:15896633-15896634	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184685535	chr21:15896639-15896640	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35969431	chr21:15896696-15896697	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs66748730	chr21:15896697-15896698	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534289900	chr21:15896698-15896699	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554365043	chr21:15896699-15896700	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574165862	chr21:15896700-15896701	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542896312	chr21:15896701-15896702	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187197152	chr21:15896710-15896711	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs74608483	chr21:15896711-15896712	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544573677	chr21:15896712-15896713	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548405569	chr21:15896754-15896755	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564563529	chr21:15896760-15896761	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs116072670	chr21:15896784-15896785	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146312107	chr21:15896877-15896878	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530206145	chr21:15896880-15896881	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550344226	chr21:15896893-15896894	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs192005975	chr21:15896947-15896948	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529897584	chr21:15896966-15896967	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138192902	chr21:15896997-15896998	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569917784	chr21:15897026-15897027	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:834 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15853400-15905400	Weak transcription	HUVEC	blood vessel
2	chr21:15883200-15898600	Weak transcription	Spleen	Spleen
3	chr21:15893000-15896200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr21:15893000-15899400	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr21:15893200-15898600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr21:15893400-15896200	Enhancers	Primary B cells from peripheral blood	blood
7	chr21:15894000-15897800	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr21:15894200-15899200	Weak transcription	Thymus	Thymus
9	chr21:15894800-15896200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr21:15895000-15896200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr21:15895000-15896200	Enhancers	Fetal Thymus	thymus
12	chr21:15895200-15896200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr21:15895200-15896200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr21:15895200-15896200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr21:15895200-15896200	Enhancers	Duodenum Mucosa	Duodenum
16	chr21:15895200-15896200	Flanking Active TSS	Dnd41	blood
17	chr21:15895200-15896600	Flanking Active TSS	GM12878-XiMat	blood
18	chr21:15895200-15897400	Genic enhancers	K562	blood
19	chr21:15895400-15896200	Enhancers	Primary T cells from cord blood	blood
20	chr21:15895400-15896200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
21	chr21:15895600-15896200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr21:15895600-15896200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
23	chr21:15895800-15896200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr21:15895800-15896400	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr21:15895800-15898600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr21:15896000-15896200	Genic enhancers	Primary T cells fromperipheralblood	blood
27	chr21:15896000-15896200	Enhancers	Primary hematopoietic stem cells	blood
28	chr21:15896000-15896200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
29	chr21:15896000-15896400	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr21:15896000-15896800	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr21:15896000-15897800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr21:15896000-15898400	Weak transcription	Primary B cells from cord blood	blood
33	chr21:15896200-15897000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr21:15896200-15897000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr21:15896200-15897400	Weak transcription	Primary T cells from cord blood	blood
36	chr21:15896200-15897400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr21:15896200-15897400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr21:15896200-15897600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr21:15896200-15898200	Weak transcription	Primary B cells from peripheral blood	blood
40	chr21:15896200-15898200	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr21:15896200-15898200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr21:15896200-15898600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr21:15896200-15898800	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr21:15896200-15899000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr21:15896200-15899000	Weak transcription	Duodenum Mucosa	Duodenum
46	chr21:15896200-15899200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr21:15896200-15899200	Enhancers	Dnd41	blood
48	chr21:15896200-15899600	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr21:15896200-15904200	Weak transcription	Primary hematopoietic stem cells	blood
50	chr21:15896200-15906200	Weak transcription	Fetal Thymus	thymus

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