Variant report

Variant	nsv462587
Chromosome Location	chr5:180176005-180226673
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:180212570-180213141	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:180212679-180213244	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr5:180198844-180199194	K562	blood:	n/a	n/a
4	CBX3	chr5:180215613-180215981	K562	blood:	n/a	n/a
5	CBX3	chr5:180208965-180209392	K562	blood:	n/a	n/a
6	CBX3	chr5:180198766-180199290	K562	blood:	n/a	n/a
7	CBX3	chr5:180208858-180209504	K562	blood:	n/a	n/a
8	CEBPB	chr5:180208882-180209430	K562	blood:	n/a	n/a
9	CEBPB	chr5:180209005-180209250	K562	blood:	n/a	n/a
10	CEBPD	chr5:180208780-180209396	K562	blood:	n/a	n/a
11	CEBPD	chr5:180208777-180209303	K562	blood:	n/a	n/a
12	CTCF	chr5:180214240-180214390	K562	blood:	n/a	chr5:180214351-180214360
13	CTCF	chr5:180211553-180211828	MCF-7	breast:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
14	CTCF	chr5:180217019-180217325	MCF-7	breast:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217245-180217258 chr5:180217159-180217172 chr5:180217242-180217260 chr5:180217157-180217173
15	CTCF	chr5:180217040-180217190	AG09319	gingival:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217159-180217172 chr5:180217157-180217173
16	CTCF	chr5:180226300-180226450	HRE	kidney:	n/a	n/a
17	CTCF	chr5:180211620-180211770	SAEC	small airway:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
18	CTCF	chr5:180226280-180226430	RPTEC	kidney:	n/a	n/a
19	CTCF	chr5:180211620-180211770	AoAF	blood vessel:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
20	CTCF	chr5:180217034-180217213	GM10248	blood:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217159-180217172 chr5:180217157-180217173
21	CTCF	chr5:180211600-180211750	HCM	heart:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
22	CTCF	chr5:180226260-180226410	GM12864	blood:	n/a	n/a
23	CTCF	chr5:180226300-180226450	GM12867	blood:	n/a	n/a
24	CTCF	chr5:180211555-180211820	GM13977	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
25	CTCF	chr5:180211600-180211750	GM12868	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
26	CTCF	chr5:180214160-180214310	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr5:180211580-180211730	GM12872	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
28	CTCF	chr5:180226320-180226470	AG10803	skin:	n/a	n/a
29	CTCF	chr5:180226320-180226470	GM12865	blood:	n/a	n/a
30	CTCF	chr5:180211600-180211750	GM12875	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
31	CTCF	chr5:180226247-180226490	GM12891	blood:	n/a	n/a
32	CTCF	chr5:180211640-180211790	BJ	skin:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
33	CTCF	chr5:180214860-180215010	AG04449	skin:	n/a	n/a
34	CTCF	chr5:180217020-180217170	GM12873	blood:	n/a	n/a
35	CTCF	chr5:180226292-180226475	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr5:180217100-180217250	HCM	heart:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217159-180217172 chr5:180217157-180217173
37	CTCF	chr5:180211640-180211790	GM12867	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
38	CTCF	chr5:180217085-180217299	Fibrobl	skin:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217245-180217258 chr5:180217159-180217172 chr5:180217242-180217260 chr5:180217157-180217173
39	CTCF	chr5:180217040-180217190	GM12872	blood:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217159-180217172 chr5:180217157-180217173
40	CTCF	chr5:180217032-180217276	Medullo	brain:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217245-180217258 chr5:180217159-180217172 chr5:180217242-180217260 chr5:180217157-180217173
41	CTCF	chr5:180211555-180211834	HUVEC	blood vessel:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
42	CTCF	chr5:180226324-180226425	GM13977	blood:	n/a	n/a
43	CTCF	chr5:180226320-180226470	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr5:180211620-180211770	GM12871	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
45	CTCF	chr5:180217120-180217270	K562	blood:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217245-180217258 chr5:180217159-180217172 chr5:180217242-180217260 chr5:180217157-180217173
46	CTCF	chr5:180211620-180211770	GM06990	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
47	CTCF	chr5:180211600-180211750	NHLF	lung:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
48	CTCF	chr5:180211547-180211829	Spleen_OC	spleen:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
49	CTCF	chr5:180216160-180216310	NHDF-neo	bronchial:	n/a	chr5:180216211-180216232 chr5:180216214-180216235 chr5:180216219-180216237
50	CTCF	chr5:180226240-180226390	HCM	heart:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180219707-180219757	HAEpiC	amniotic membrane:	n/a
2	chr5:180220005-180220055	RPTEC	kidney:	n/a
3	chr5:180219707-180219757	HAEpiC	amniotic membrane:	n/a
4	chr5:180220005-180220055	RPTEC	kidney:	n/a
5	chr5:180213189-180213239	NHBE	bronchial:	n/a
6	chr5:180218509-180218559	A549	lung:	n/a
7	chr5:180219008-180219058	NB4	blood:	n/a
8	chr5:180218509-180218559	HEEpiC	esophagus:	n/a
9	chr5:180220005-180220055	NH-A	brain:	n/a
10	chr5:180213189-180213239	HPAEpiC	pulmonary alveolar:	n/a
11	chr5:180217700-180217750	BE2_C	brain:	n/a
12	chr5:180216985-180217035	PFSK-1	brain:	n/a
13	chr5:180219412-180219462	Hela-S3	cervix:	n/a
14	chr5:180219008-180219058	LNCaP	prostate:	n/a
15	chr5:180219707-180219757	MCF10A-Er-Src	breast:	n/a
16	chr5:180219008-180219058	AG10803	skin:	n/a
17	chr5:180219008-180219058	RPTEC	kidney:	n/a
18	chr5:180219412-180219462	AoSMC	blood vessel:	n/a
19	chr5:180219882-180219932	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:180218509-180218559	PrEC	prostate:	n/a
21	chr5:180217700-180217750	NB4	blood:	n/a
22	chr5:180219008-180219058	AG09309	skin:	n/a
23	chr5:180219412-180219462	GM12878	blood:	n/a
24	chr5:180219707-180219757	K562	blood:	n/a
25	chr5:180217700-180217750	HNPCEpiC	eye:	n/a
26	chr5:180220005-180220055	AG04449	skin:	fetal
27	chr5:180213189-180213239	HIPEpiC	eye:	n/a
28	chr5:180219412-180219462	ProgFib	skin:	n/a
29	chr5:180219882-180219932	H1-hESC	embryonic stem cell:	embryo
30	chr5:180218509-180218559	HRE	kidney:	n/a
31	chr5:180219707-180219757	SAEC	small airway:	n/a
32	chr5:180213189-180213239	H1-hESC	embryonic stem cell:	embryo
33	chr5:180218509-180218559	HIPEpiC	eye:	n/a
34	chr5:180216985-180217035	HRCEpiC	kidney:	n/a
35	chr5:180216985-180217035	HL-60	blood:	n/a
36	chr5:180219707-180219757	AG04449	skin:	fetal
37	chr5:180220005-180220055	BE2_C	brain:	n/a
38	chr5:180220005-180220055	ProgFib	skin:	n/a
39	chr5:180217700-180217750	HCPEpiC	choroid plexus:	n/a
40	chr5:180219412-180219462	NT2-D1	testis:	n/a
41	chr5:180219707-180219757	U87	brain:	n/a
42	chr5:180219882-180219932	HRPEpiC	eye:	n/a
43	chr5:180213189-180213239	SAEC	small airway:	n/a
44	chr5:180219008-180219058	AG04450	lung:	fetal
45	chr5:180220005-180220055	AG04450	lung:	fetal
46	chr5:180219412-180219462	AG04449	skin:	fetal
47	chr5:180219008-180219058	SK-N-MC	brain:	n/a
48	chr5:180216985-180217035	ECC-1	luminal epithelium:	n/a
49	chr5:180218509-180218559	SKMC	muscle:	n/a
50	chr5:180220005-180220055	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
2	chr5:180208930..180211085-chr5:180226767..180229407,2	K562	blood:
3	chr5:180216578..180217657-chr5:180225674..180226614,3	MCF-7	breast:
4	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
5	chr5:180207628..180210924-chr5:180228309..180230947,5	MCF-7	breast:
6	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
7	chr5:180211185..180212156-chr5:180225940..180226892,9	MCF-7	breast:
8	chr5:180211375..180212214-chr5:180226180..180226854,2	MCF-7	breast:
9	chr5:180211375..180212214-chr5:180226180..180226854,2	MCF-7	breast:
10	chr5:180225360..180227126-chr5:180650048..180652695,2	MCF-7	breast:
11	chr5:180202321..180205166-chr5:180643152..180645917,2	K562	blood:
12	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
13	chr5:180211281..180211887-chr5:180586366..180586939,2	MCF-7	breast:
14	chr5:180210430..180214631-chr5:180286463..180290673,6	MCF-7	breast:
15	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
16	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
17	chr5:180217957..180220948-chr5:180429295..180431970,2	K562	blood:
18	chr5:180210073..180212750-chr5:180649135..180651698,2	MCF-7	breast:
19	chr5:180217067..180219759-chr5:180269419..180271439,2	K562	blood:
20	chr5:179919075..179921338-chr5:180210769..180213087,2	MCF-7	breast:
21	chr5:180217057..180217623-chr5:180228458..180229188,2	MCF-7	breast:
22	chr5:180216578..180217657-chr5:180225674..180226614,3	MCF-7	breast:
23	chr5:180224924..180227171-chr5:180287379..180289877,3	MCF-7	breast:
24	chr5:180208714..180211260-chr5:180212096..180214924,3	K562	blood:
25	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
26	chr5:180219008..180221127-chr5:180221660..180224233,2	MCF-7	breast:
27	chr5:180226030..180229620-chr5:180255411..180258955,4	K562	blood:
28	chr5:180207548..180210211-chr5:180589188..180591545,3	K562	blood:
29	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
30	chr5:180209019..180210957-chr5:180453882..180456380,2	K562	blood:
31	chr5:180211185..180212156-chr5:180225940..180226892,9	MCF-7	breast:
32	chr5:180219008..180221127-chr5:180221660..180224233,2	MCF-7	breast:
33	chr5:180223525..180226490-chr5:180609242..180611026,2	K562	blood:
34	chr5:180212092..180214294-chr5:180453988..180456472,2	K562	blood:
35	chr5:180211640..180213961-chr5:180214094..180219248,5	K562	blood:
36	chr5:180221672..180224385-chr5:180256701..180259508,2	K562	blood:
37	chr5:180222666..180225025-chr5:180609526..180611478,2	K562	blood:
38	chr5:180216327..180219256-chr5:180485099..180486798,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP62-3	chr5:180222430-180222875	NONHSAT105810
2	lnc-OR2Y1-2	chr5:180189565-180191201	ucscGeneNc_uc003mmj_1
3	lnc-BTNL8-8	chr5:180190563-180190835	ucscGeneNc_uc003mmk_2
4	lnc-BTNL8-8	chr5:180192279-180192466	ucscGeneNc_uc003mmk_2
5	lnc-ZFP62-3	chr5:180222406-180222875	NONHSAT105809
6	lnc-BTNL8-8	chr5:180193918-180195284	ucscGeneNc_uc003mmk_2

Variant related genes	Relation type
ENSG00000260841	TF binding region
ENSG00000260841	CpG island
ENSG00000146063	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000196670	chromatin interactions
ENSG00000245060	chromatin interactions
ENSG00000260841	chromatin interactions
ENSG00000264732	chromatin interactions

Extended variants
information (count: 1270 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1270 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs607108	chr5:180189572-180189573	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566217626	chr5:180189587-180189588	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs192641317	chr5:180189595-180189596	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs183350647	chr5:180189621-180189622	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs187606446	chr5:180189627-180189628	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs115343003	chr5:180189628-180189629	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs75383691	chr5:180189657-180189658	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs571953138	chr5:180189658-180189659	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs145385268	chr5:180189664-180189665	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs537472225	chr5:180189680-180189681	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs541740008	chr5:180189741-180189742	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs673132	chr5:180189792-180189793	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs555357053	chr5:180189811-180189812	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs565640444	chr5:180189857-180189858	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs534712702	chr5:180189889-180189890	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs192103202	chr5:180189909-180189910	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs577951216	chr5:180189918-180189919	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs605721	chr5:180189920-180189921	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs375207775	chr5:180189929-180189930	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs557002616	chr5:180189947-180189948	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs185154676	chr5:180189961-180189962	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs573897605	chr5:180190025-180190026	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs188077762	chr5:180190039-180190040	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs559704323	chr5:180190050-180190051	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs140749864	chr5:180190057-180190058	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs545140317	chr5:180190058-180190059	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs548722773	chr5:180190071-180190072	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs200372660	chr5:180190262-180190263	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs531039566	chr5:180190327-180190328	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs10066216	chr5:180190328-180190329	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs376204644	chr5:180190340-180190341	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs192826838	chr5:180190383-180190384	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs200985018	chr5:180190396-180190397	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs184386892	chr5:180190427-180190428	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs112872153	chr5:180190462-180190463	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs546931153	chr5:180190481-180190482	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs565728835	chr5:180190504-180190505	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs150085921	chr5:180190523-180190524	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs659703	chr5:180190532-180190533	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs571342100	chr5:180190553-180190554	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs536719490	chr5:180190575-180190576	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs188120103	chr5:180190578-180190579	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs573711821	chr5:180190616-180190617	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs536548911	chr5:180190630-180190631	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs138359704	chr5:180190654-180190655	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs370108538	chr5:180190670-180190671	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs572938523	chr5:180190675-180190676	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs373186851	chr5:180190677-180190678	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs377409479	chr5:180190713-180190714	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs564908771	chr5:180190718-180190719	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
early-passage human iPS cells	21368824	CNVD
Cancer	17440070	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1087 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180196600-180197200	Enhancers	HepG2	liver
2	chr5:180202000-180202800	Enhancers	K562	blood
3	chr5:180202800-180203000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:180202800-180206000	Weak transcription	K562	blood
5	chr5:180203000-180212400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:180204400-180215400	Weak transcription	Primary B cells from cord blood	blood
7	chr5:180205200-180209800	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr5:180205600-180211800	Weak transcription	Liver	Liver
9	chr5:180205800-180212400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr5:180206000-180208400	Enhancers	K562	blood
11	chr5:180206000-180212200	Weak transcription	Lung	lung
12	chr5:180206200-180209800	Weak transcription	Primary T cells from cord blood	blood
13	chr5:180206600-180212400	Weak transcription	Aorta	Aorta
14	chr5:180206800-180210800	Weak transcription	Esophagus	oesophagus
15	chr5:180207000-180207200	Enhancers	Right Atrium	heart
16	chr5:180207000-180214600	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr5:180207200-180212200	Weak transcription	Right Atrium	heart
18	chr5:180207200-180212400	Weak transcription	Fetal Intestine Large	intestine
19	chr5:180207800-180210800	Weak transcription	Placenta	Placenta
20	chr5:180208000-180212000	Weak transcription	Stomach Smooth Muscle	stomach
21	chr5:180208000-180212400	Weak transcription	Psoas Muscle	Psoas
22	chr5:180208400-180208600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:180208400-180210000	Flanking Active TSS	K562	blood
24	chr5:180209200-180214000	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr5:180209200-180214800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr5:180209400-180209800	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr5:180209400-180209800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr5:180209400-180210200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr5:180209600-180210000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr5:180209600-180210000	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr5:180209600-180210200	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr5:180209600-180210400	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr5:180209800-180210400	Enhancers	Primary T cells from cord blood	blood
34	chr5:180209800-180211000	Enhancers	Primary T cells fromperipheralblood	blood
35	chr5:180209800-180212200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr5:180209800-180213200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr5:180210000-180210200	Enhancers	Colon Smooth Muscle	Colon
38	chr5:180210000-180210400	Enhancers	Thymus	Thymus
39	chr5:180210000-180211200	Enhancers	K562	blood
40	chr5:180210000-180214000	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr5:180210000-180217800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr5:180210200-180210400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr5:180210200-180210600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr5:180210200-180211200	Enhancers	Fetal Thymus	thymus
45	chr5:180210200-180212400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr5:180210200-180212400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr5:180210200-180217400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr5:180210400-180210600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr5:180210400-180210800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr5:180210400-180211000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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