Variant report

Variant	nsv1024855
Chromosome Location	chr5:180120653-180216254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:727)
CpG islands
(count:427)
Chromatin interactive
region (count:42)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:727 , 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	ATF2	chr5:180212679-180213244	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:180212570-180213141	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:180144959-180145359	GM12878	blood:	n/a	n/a
4	BATF	chr5:180145061-180145379	GM12878	blood:	n/a	chr5:180145207-180145218
5	BATF	chr5:180145040-180145312	GM12878	blood:	n/a	chr5:180145207-180145218
6	BATF	chr5:180169789-180169977	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:180145100-180145299	GM12878	blood:	n/a	chr5:180145235-180145244
8	BCL11A	chr5:180145000-180145348	GM12878	blood:	n/a	chr5:180145235-180145244
9	CBX3	chr5:180127492-180127736	K562	blood:	n/a	n/a
10	CBX3	chr5:180208965-180209392	K562	blood:	n/a	n/a
11	CBX3	chr5:180215613-180215981	K562	blood:	n/a	n/a
12	CBX3	chr5:180198844-180199194	K562	blood:	n/a	n/a
13	CBX3	chr5:180208858-180209504	K562	blood:	n/a	n/a
14	CBX3	chr5:180198766-180199290	K562	blood:	n/a	n/a
15	CEBPB	chr5:180131341-180131657	K562	blood:	n/a	n/a
16	CEBPB	chr5:180209005-180209250	K562	blood:	n/a	n/a
17	CEBPB	chr5:180208882-180209430	K562	blood:	n/a	n/a
18	CEBPD	chr5:180208780-180209396	K562	blood:	n/a	n/a
19	CEBPD	chr5:180131384-180131803	K562	blood:	n/a	n/a
20	CEBPD	chr5:180208777-180209303	K562	blood:	n/a	n/a
21	CREB1	chr5:180144917-180145413	GM12878	blood:	n/a	n/a
22	CREB1	chr5:180144836-180145451	GM12878	blood:	n/a	n/a
23	CTCF	chr5:180211580-180211730	GM12801	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
24	CTCF	chr5:180145820-180145970	GM12871	blood:	n/a	n/a
25	CTCF	chr5:180211600-180211750	Caco-2	colon:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
26	CTCF	chr5:180214294-180214436	K562	blood:	n/a	chr5:180214351-180214360
27	CTCF	chr5:180145920-180146070	A549	lung:	n/a	n/a
28	CTCF	chr5:180145840-180145990	K562	blood:	n/a	n/a
29	CTCF	chr5:180145860-180146010	HMEC	breast:	n/a	n/a
30	CTCF	chr5:180146300-180146450	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr5:180211600-180211750	GM12869	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
32	CTCF	chr5:180211620-180211770	GM12873	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
33	CTCF	chr5:180211563-180211840	Medullo	brain:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
34	CTCF	chr5:180211574-180211799	Fibrobl	skin:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
35	CTCF	chr5:180145840-180145990	HCFaa	heart:	n/a	n/a
36	CTCF	chr5:180145740-180145890	RPTEC	kidney:	n/a	n/a
37	CTCF	chr5:180214280-180214430	BE2_C	brain:	n/a	chr5:180214351-180214360
38	CTCF	chr5:180211473-180211856	H1-hESC	embryonic stem cell:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
39	CTCF	chr5:180146238-180146280	GM12892	blood:	n/a	n/a
40	CTCF	chr5:180211555-180211820	GM13977	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
41	CTCF	chr5:180146220-180146370	GM12865	blood:	n/a	n/a
42	CTCF	chr5:180214240-180214390	K562	blood:	n/a	chr5:180214351-180214360
43	CTCF	chr5:180211600-180211750	A549	lung:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
44	CTCF	chr5:180211620-180211770	GM06990	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
45	CTCF	chr5:180145360-180145510	GM12874	blood:	n/a	n/a
46	CTCF	chr5:180211544-180211827	LNCaP	prostate:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
47	CTCF	chr5:180146100-180146250	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr5:180211552-180211830	GM19238	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
49	CTCF	chr5:180145625-180146627	A549	lung:	n/a	n/a
50	CTCF	chr5:180145820-180145970	GM12874	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180167132-180167182	SKMC	muscle:	n/a
2	chr5:180167132-180167182	GM12892	blood:	n/a
3	chr5:180166492-180166542	PrEC	prostate:	n/a
4	chr5:180167132-180167182	AG09309	skin:	n/a
5	chr5:180213189-180213239	U87	brain:	n/a
6	chr5:180166492-180166542	SK-N-MC	brain:	n/a
7	chr5:180167566-180167616	GM12892	blood:	n/a
8	chr5:180167132-180167182	NT2-D1	testis:	n/a
9	chr5:180166492-180166542	ProgFib	skin:	n/a
10	chr5:180167965-180168015	AG09309	skin:	n/a
11	chr5:180167724-180167774	PFSK-1	brain:	n/a
12	chr5:180166694-180166744	SK-N-SH_RA	brain:	n/a
13	chr5:180167724-180167774	HCM	heart:	n/a
14	chr5:180166492-180166542	NH-A	brain:	n/a
15	chr5:180167566-180167616	BJ	skin:	n/a
16	chr5:180166694-180166744	HCPEpiC	choroid plexus:	n/a
17	chr5:180167132-180167182	LNCaP	prostate:	n/a
18	chr5:180213189-180213239	HUVEC	blood vessel:	n/a
19	chr5:180166492-180166542	HRE	kidney:	n/a
20	chr5:180166694-180166744	T-47D	breast:	n/a
21	chr5:180167724-180167774	HRCEpiC	kidney:	n/a
22	chr5:180166694-180166744	HCF	heart:	n/a
23	chr5:180167965-180168015	NHDF-neo	bronchial:	n/a
24	chr5:180167724-180167774	NH-A	brain:	n/a
25	chr5:180167132-180167182	HMEC	breast:	n/a
26	chr5:180213189-180213239	NHDF-neo	bronchial:	n/a
27	chr5:180167566-180167616	T-47D	breast:	n/a
28	chr5:180213189-180213239	GM06990	blood:	n/a
29	chr5:180166694-180166744	NB4	blood:	n/a
30	chr5:180213189-180213239	AoSMC	blood vessel:	n/a
31	chr5:180167566-180167616	NHBE	bronchial:	n/a
32	chr5:180167724-180167774	IMR90	lung:	fetal
33	chr5:180213189-180213239	GM19239	blood:	n/a
34	chr5:180167724-180167774	RPTEC	kidney:	n/a
35	chr5:180167965-180168015	HEEpiC	esophagus:	n/a
36	chr5:180166492-180166542	Caco-2	colon:	n/a
37	chr5:180167132-180167182	HCT-116	colon:	n/a
38	chr5:180166694-180166744	SKMC	muscle:	n/a
39	chr5:180166492-180166542	HCPEpiC	choroid plexus:	n/a
40	chr5:180213189-180213239	LNCaP	prostate:	n/a
41	chr5:180166694-180166744	GM12878	blood:	n/a
42	chr5:180213189-180213239	RPTEC	kidney:	n/a
43	chr5:180167566-180167616	PANC-1	pancreas:	n/a
44	chr5:180166694-180166744	HAEpiC	amniotic membrane:	n/a
45	chr5:180167965-180168015	GM06990	blood:	n/a
46	chr5:180213189-180213239	HCM	heart:	n/a
47	chr5:180166492-180166542	HAEpiC	amniotic membrane:	n/a
48	chr5:180167566-180167616	HUVEC	blood vessel:	n/a
49	chr5:180166694-180166744	HCM	heart:	n/a
50	chr5:180167566-180167616	HRPEpiC	eye:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
2	chr5:180212092..180214294-chr5:180453988..180456472,2	K562	blood:
3	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
4	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
5	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
6	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
7	chr5:180211185..180212156-chr5:180225940..180226892,9	MCF-7	breast:
8	chr5:180037911..180038640-chr5:180145288..180145999,2	MCF-7	breast:
9	chr5:179919075..179921338-chr5:180210769..180213087,2	MCF-7	breast:
10	chr5:180154735..180156600-chr5:180159240..180161653,2	MCF-7	breast:
11	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
12	chr5:180209019..180210957-chr5:180453882..180456380,2	K562	blood:
13	chr5:180143140..180144948-chr5:180229622..180231793,2	K562	blood:
14	chr5:180208714..180211260-chr5:180212096..180214924,3	K562	blood:
15	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
16	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
17	chr5:180097643..180098351-chr5:180145367..180146387,3	MCF-7	breast:
18	chr5:180210073..180212750-chr5:180649135..180651698,2	MCF-7	breast:
19	chr5:180147687..180149481-chr5:180151717..180153867,2	K562	blood:
20	chr5:180207548..180210211-chr5:180589188..180591545,3	K562	blood:
21	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
22	chr5:180153993..180156519-chr5:180159947..180161759,2	K562	blood:
23	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
24	chr5:180130605..180132994-chr5:180134010..180136773,2	MCF-7	breast:
25	chr5:180202321..180205166-chr5:180643152..180645917,2	K562	blood:
26	chr5:180207628..180210924-chr5:180228309..180230947,5	MCF-7	breast:
27	chr5:180211375..180212214-chr5:180226180..180226854,2	MCF-7	breast:
28	chr5:180146148..180147851-chr5:180235768..180238086,2	K562	blood:
29	chr5:180210430..180214631-chr5:180286463..180290673,6	MCF-7	breast:
30	chr5:180153993..180156519-chr5:180159947..180161759,2	K562	blood:
31	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
32	chr5:180208930..180211085-chr5:180226767..180229407,2	K562	blood:
33	chr5:180130605..180132994-chr5:180134010..180136773,2	MCF-7	breast:
34	chr5:180136617..180138276-chr5:180153652..180155749,2	K562	blood:
35	chr5:180211281..180211887-chr5:180586366..180586939,2	MCF-7	breast:
36	chr5:180172009..180174376-chr5:180240608..180243076,2	MCF-7	breast:
37	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
38	chr5:180211640..180213961-chr5:180214094..180219248,5	K562	blood:
39	chr5:180147687..180149481-chr5:180151717..180153867,2	K562	blood:
40	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
41	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
42	chr5:180136617..180138276-chr5:180153652..180155749,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR2Y1-2	chr5:180189565-180191201	ucscGeneNc_uc003mmj_1
2	lnc-OR2Y1-1	chr5:180155280-180155484	expReg_chr5_11028_-
3	lnc-BTNL8-8	chr5:180192279-180192466	ucscGeneNc_uc003mmk_2
4	lnc-BTNL8-8	chr5:180193918-180195284	ucscGeneNc_uc003mmk_2
5	lnc-BTNL8-8	chr5:180190563-180190835	ucscGeneNc_uc003mmk_2

No data

Variant related genes	Relation type
RNU1-17P	TF binding region
ENSG00000260841	TF binding region
OR2Y1	TF binding region
OR2AI1P	TF binding region
RNU1-17P	CpG island
ENSG00000260841	CpG island
OR2Y1	CpG island
OR2AI1P	CpG island
ENSG00000196670	chromatin interactions
ENSG00000260841	chromatin interactions
ENSG00000264732	chromatin interactions
ENSG00000146063	chromatin interactions
ENSG00000199892	chromatin interactions
ENSG00000131446	chromatin interactions

Extended variants
information (count: 2261 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:2261 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543241792	chr5:180120662-180120663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs559671015	chr5:180120699-180120700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528841171	chr5:180120723-180120724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10073529	chr5:180120738-180120739	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs570475017	chr5:180120795-180120796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181525395	chr5:180120822-180120823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532912158	chr5:180120824-180120825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568116401	chr5:180120871-180120872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549925121	chr5:180120894-180120895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533970602	chr5:180120981-180120982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs72824470	chr5:180121017-180121018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376164125	chr5:180121023-180121024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546465988	chr5:180121127-180121128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565725008	chr5:180121148-180121149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528432820	chr5:180121300-180121301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534613077	chr5:180121301-180121302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10073887	chr5:180121337-180121338	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs142841309	chr5:180121401-180121402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536690713	chr5:180121421-180121422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147399866	chr5:180121428-180121429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543376854	chr5:180121455-180121456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557063564	chr5:180121461-180121462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77534160	chr5:180121512-180121513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559939170	chr5:180121614-180121615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184292146	chr5:180121665-180121666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545721675	chr5:180121717-180121718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372585007	chr5:180121754-180121755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189903325	chr5:180121781-180121782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181178039	chr5:180121802-180121803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549775042	chr5:180121826-180121827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140018616	chr5:180121847-180121848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529022034	chr5:180121904-180121905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186122792	chr5:180121990-180121991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7443346	chr5:180121991-180121992	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs372738992	chr5:180122048-180122049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374271353	chr5:180122049-180122050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs60419380	chr5:180122068-180122069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190747574	chr5:180122073-180122074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75820289	chr5:180122142-180122143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142881278	chr5:180122370-180122371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs151049883	chr5:180122381-180122382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3912996	chr5:180122392-180122393	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs375469942	chr5:180122394-180122395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182033950	chr5:180122408-180122409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573942519	chr5:180122440-180122441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536762224	chr5:180122465-180122466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186175415	chr5:180122491-180122492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190640519	chr5:180122529-180122530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572482368	chr5:180122567-180122568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575356785	chr5:180122569-180122570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	17440070	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:561 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180116600-180130800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:180117000-180120800	Enhancers	Fetal Thymus	thymus
3	chr5:180117200-180121400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr5:180125800-180126400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr5:180126200-180127000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr5:180126200-180127200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr5:180127200-180134800	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr5:180130800-180131600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:180131000-180131600	Enhancers	K562	blood
10	chr5:180131200-180131400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:180131200-180131600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr5:180131200-180131600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr5:180131400-180131800	Enhancers	A549	lung
14	chr5:180131600-180134800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr5:180131600-180134800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:180131600-180135000	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr5:180134800-180135200	Enhancers	H1 Cell Line	embryonic stem cell
18	chr5:180134800-180135200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:180134800-180137200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr5:180134800-180138000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr5:180135000-180135200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr5:180135200-180135600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr5:180135200-180137200	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr5:180135200-180137200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr5:180135200-180137400	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr5:180135600-180137400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr5:180136000-180136200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr5:180136200-180138200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr5:180136400-180137400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr5:180137200-180137400	Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr5:180137200-180138000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr5:180137200-180138600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:180137400-180137600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr5:180137400-180137600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr5:180137400-180137800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr5:180137400-180138000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr5:180137400-180138000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr5:180137600-180139600	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr5:180137800-180138400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr5:180138000-180140000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr5:180144600-180145400	Bivalent Enhancer	Primary T cells from cord blood	blood
42	chr5:180144600-180146600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr5:180144800-180146200	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr5:180144800-180146200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr5:180144800-180146400	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr5:180144800-180146400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr5:180144800-180146400	Enhancers	Fetal Thymus	thymus
48	chr5:180144800-180146400	Enhancers	Dnd41	blood
49	chr5:180144800-180146800	Enhancers	GM12878-XiMat	blood
50	chr5:180145000-180146200	Enhancers	Primary T killer memory cells from peripheral blood	blood

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