Variant report

Variant	esv1842645
Chromosome Location	chr5:94955602-94962981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:420)
CpG islands
(count:732)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:94956255-94956410	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr5:94956033-94956548	GM12878	blood:	n/a	n/a
3	BCLAF1	chr5:94956738-94957191	GM12878	blood:	n/a	n/a
4	BCLAF1	chr5:94955556-94956455	GM12878	blood:	n/a	chr5:94955667-94955680 chr5:94955902-94955915
5	BHLHE40	chr5:94956200-94956812	HepG2	liver:	n/a	n/a
6	BHLHE40	chr5:94955751-94956678	GM12878	blood:	n/a	n/a
7	CEBPB	chr5:94962592-94962892	HepG2	liver:	n/a	chr5:94962769-94962780 chr5:94962769-94962782 chr5:94962735-94962746
8	CEBPB	chr5:94962672-94962869	A549	lung:	n/a	chr5:94962769-94962780 chr5:94962769-94962782 chr5:94962735-94962746
9	CHD1	chr5:94956205-94956437	GM12878	blood:	n/a	n/a
10	CHD2	chr5:94956081-94956324	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr5:94955610-94956605	GM12878	blood:	n/a	chr5:94955898-94955908
12	CHD2	chr5:94956838-94957147	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr5:94956847-94957456	GM12878	blood:	n/a	n/a
14	CREB1	chr5:94956131-94957568	GM12878	blood:	n/a	n/a
15	CREB1	chr5:94956237-94956602	A549	lung:	n/a	n/a
16	CTBP2	chr5:94955549-94957276	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr5:94957320-94957470	GM12872	blood:	n/a	n/a
18	CTCF	chr5:94956880-94957030	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr5:94956880-94957030	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr5:94955940-94956090	GM12866	blood:	n/a	n/a
21	CTCF	chr5:94956140-94956290	GM06990	blood:	n/a	n/a
22	CTCF	chr5:94957333-94957376	GM12891	blood:	n/a	n/a
23	CTCF	chr5:94956980-94957130	GM12868	blood:	n/a	n/a
24	CTCF	chr5:94956940-94957090	SAEC	small airway:	n/a	n/a
25	CTCF	chr5:94956280-94956430	SAEC	small airway:	n/a	n/a
26	CTCF	chr5:94956280-94956430	GM12871	blood:	n/a	n/a
27	CTCF	chr5:94956982-94957095	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr5:94956320-94956470	AG04449	skin:	n/a	n/a
29	CTCF	chr5:94956840-94956990	AG04449	skin:	n/a	n/a
30	CTCF	chr5:94956080-94956230	GM12873	blood:	n/a	n/a
31	CTCF	chr5:94956220-94956370	GM12866	blood:	n/a	n/a
32	CTCF	chr5:94956071-94956201	GM12891	blood:	n/a	n/a
33	CTCF	chr5:94956960-94957110	GM12864	blood:	n/a	n/a
34	CTCF	chr5:94956140-94956290	WI-38	lung:	n/a	n/a
35	CTCF	chr5:94956243-94956514	GM12891	blood:	n/a	n/a
36	CTCF	chr5:94956301-94956352	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr5:94957000-94957150	SAEC	small airway:	n/a	n/a
38	CTCF	chr5:94956160-94956310	BJ	skin:	n/a	n/a
39	CTCF	chr5:94956260-94956410	AG09319	gingival:	n/a	n/a
40	CTCF	chr5:94956320-94956470	GM12869	blood:	n/a	n/a
41	CTCF	chr5:94956260-94956410	GM12875	blood:	n/a	n/a
42	CTCF	chr5:94956095-94956204	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:94956300-94956450	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr5:94956004-94957185	GM12878	blood:	n/a	n/a
45	CTCF	chr5:94956200-94956350	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr5:94956248-94956532	GM19240	blood:	n/a	n/a
47	CTCF	chr5:94956220-94956370	GM12874	blood:	n/a	n/a
48	CTCF	chr5:94956240-94956390	GM12867	blood:	n/a	n/a
49	CTCF	chr5:94956880-94957030	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr5:94956140-94956290	HUVEC	blood vessel:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:94956017-94956067	MCF10A-Er-Src	breast:	n/a
2	chr5:94955816-94955866	GM12891	blood:	n/a
3	chr5:94956175-94956225	HEK293	kidney:	embryo
4	chr5:94955880-94955930	H1-hESC	embryonic stem cell:	embryo
5	chr5:94957269-94957319	LNCaP	prostate:	n/a
6	chr5:94956175-94956225	HMEC	breast:	n/a
7	chr5:94955789-94955839	GM06990	blood:	n/a
8	chr5:94956175-94956225	GM06990	blood:	n/a
9	chr5:94955789-94955839	HIPEpiC	eye:	n/a
10	chr5:94960110-94960160	Jurkat	blood:	n/a
11	chr5:94955816-94955866	U87	brain:	n/a
12	chr5:94955575-94955625	SK-N-MC	brain:	n/a
13	chr5:94960110-94960160	AoSMC	blood vessel:	n/a
14	chr5:94956175-94956225	MCF10A-Er-Src	breast:	n/a
15	chr5:94956175-94956225	SK-N-MC	brain:	n/a
16	chr5:94957269-94957319	RPTEC	kidney:	n/a
17	chr5:94956900-94956950	HRCEpiC	kidney:	n/a
18	chr5:94960110-94960160	ovcar-3	ovarian:	n/a
19	chr5:94955880-94955930	Jurkat	blood:	n/a
20	chr5:94955575-94955625	NT2-D1	testis:	n/a
21	chr5:94955893-94955943	PFSK-1	brain:	n/a
22	chr5:94955789-94955839	GM12878	blood:	n/a
23	chr5:94955756-94955806	NT2-D1	testis:	n/a
24	chr5:94957269-94957319	HCF	heart:	n/a
25	chr5:94957269-94957319	GM19239	blood:	n/a
26	chr5:94957269-94957319	HepG2	liver:	n/a
27	chr5:94955789-94955839	NHBE	bronchial:	n/a
28	chr5:94957269-94957319	AG04449	skin:	fetal
29	chr5:94955816-94955866	T-47D	breast:	n/a
30	chr5:94955816-94955866	HEEpiC	esophagus:	n/a
31	chr5:94955816-94955866	NT2-D1	testis:	n/a
32	chr5:94955880-94955930	HCF	heart:	n/a
33	chr5:94955575-94955625	MCF-7	breast:	n/a
34	chr5:94957269-94957319	Hela-S3	cervix:	n/a
35	chr5:94957269-94957319	HEEpiC	esophagus:	n/a
36	chr5:94957243-94957293	NHBE	bronchial:	n/a
37	chr5:94960110-94960160	NHBE	bronchial:	n/a
38	chr5:94956017-94956067	HUVEC	blood vessel:	n/a
39	chr5:94956017-94956067	GM06990	blood:	n/a
40	chr5:94960110-94960160	GM19239	blood:	n/a
41	chr5:94955893-94955943	Hela-S3	cervix:	n/a
42	chr5:94955816-94955866	ProgFib	skin:	n/a
43	chr5:94956175-94956225	RPTEC	kidney:	n/a
44	chr5:94960110-94960160	HCT-116	colon:	n/a
45	chr5:94955575-94955625	H1-hESC	embryonic stem cell:	embryo
46	chr5:94955756-94955806	Hela-S3	cervix:	n/a
47	chr5:94955816-94955866	AG04450	lung:	fetal
48	chr5:94955756-94955806	NHBE	bronchial:	n/a
49	chr5:94957269-94957319	A549	lung:	n/a
50	chr5:94955880-94955930	SKMC	muscle:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:94959437..94960992-chr5:94968032..94970873,2	K562	blood:
2	chr5:94953878..94956024-chr5:94981084..94983825,2	K562	blood:
3	chr5:94951476..94954294-chr5:94957994..94960881,2	MCF-7	breast:
4	chr5:94889800..94892273-chr5:94955578..94957837,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPATA9-2	chr5:94946081-94955781	NONHSAT102852

No data

Variant related genes	Relation type
GPR150	TF binding region
GPR150	CpG island
ENSG00000198677	chromatin interactions
ENSG00000164291	chromatin interactions
ENSG00000175449	chromatin interactions

Extended variants
information (count: 247 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:247 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2194051	chr5:94955602-94955603	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73147988	chr5:94955626-94955627	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs539470296	chr5:94955649-94955650	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs76724318	chr5:94955670-94955671	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs541303981	chr5:94955736-94955737	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs191179596	chr5:94955757-94955758	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs10038242	chr5:94955783-94955784	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs555171670	chr5:94955789-94955790	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs574979809	chr5:94955828-94955829	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs543870263	chr5:94955853-94955854	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs557453667	chr5:94955878-94955879	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs182664853	chr5:94955891-94955892	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs369430862	chr5:94955894-94955895	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs539859258	chr5:94955941-94955942	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs199778484	chr5:94955944-94955945	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs141886145	chr5:94956002-94956003	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs528827248	chr5:94956016-94956017	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs542417744	chr5:94956025-94956026	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs577545347	chr5:94956031-94956032	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs562300310	chr5:94956060-94956061	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs531142520	chr5:94956107-94956108	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551064639	chr5:94956145-94956146	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs370724717	chr5:94956167-94956168	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs202159323	chr5:94956181-94956182	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs377374612	chr5:94956203-94956204	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs533317407	chr5:94956204-94956205	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs546718334	chr5:94956261-94956262	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs112840250	chr5:94956313-94956314	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs566737769	chr5:94956329-94956330	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs7733295	chr5:94956345-94956346	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs13169194	chr5:94956396-94956397	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs548880276	chr5:94956427-94956428	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs568682063	chr5:94956468-94956469	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs537651968	chr5:94956496-94956497	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs557387695	chr5:94956550-94956551	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs564827254	chr5:94956555-94956556	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs113272282	chr5:94956619-94956620	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs201254414	chr5:94956634-94956635	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs376668578	chr5:94956727-94956728	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs369838352	chr5:94956781-94956782	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs573469225	chr5:94956782-94956783	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs116554559	chr5:94956783-94956784	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs562391621	chr5:94956857-94956858	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs575862620	chr5:94956921-94956922	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs201990735	chr5:94956923-94956924	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs544830129	chr5:94956941-94956942	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs367933080	chr5:94956983-94956984	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs564595317	chr5:94956991-94956992	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs151062094	chr5:94956993-94956994	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs546956925	chr5:94957041-94957042	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Breast cancer	21858162	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
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Williams Syndrome	20824207	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94953800-94955800	Weak transcription	HMEC	breast
2	chr5:94954600-94955800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
3	chr5:94954800-94955800	Enhancers	Dnd41	blood
4	chr5:94954800-94958600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr5:94955000-94956000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
6	chr5:94955000-94956400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
7	chr5:94955000-94957600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr5:94955000-94957600	Active TSS	Brain Inferior Temporal Lobe	brain
9	chr5:94955200-94955800	Flanking Active TSS	Primary T cells from cord blood	blood
10	chr5:94955200-94955800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
11	chr5:94955200-94955800	Flanking Active TSS	Brain Hippocampus Middle	brain
12	chr5:94955200-94955800	Flanking Active TSS	NHDF-Ad	bronchial
13	chr5:94955200-94956000	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
14	chr5:94955200-94956200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr5:94955200-94956200	Flanking Active TSS	Osteobl	bone
16	chr5:94955200-94956400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
17	chr5:94955200-94957000	Flanking Active TSS	HUVEC	blood vessel
18	chr5:94955200-94957200	Active TSS	Rectal Mucosa Donor 29	rectum
19	chr5:94955200-94957200	Flanking Active TSS	NH-A	brain
20	chr5:94955200-94957400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
21	chr5:94955200-94957600	Flanking Active TSS	Primary B cells from cord blood	blood
22	chr5:94955200-94957600	Flanking Active TSS	Primary hematopoietic stem cells	blood
23	chr5:94955200-94957800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
24	chr5:94955400-94955800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
25	chr5:94955400-94955800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:94955400-94955800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
27	chr5:94955400-94955800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr5:94955400-94955800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
29	chr5:94955400-94955800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
30	chr5:94955400-94955800	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
31	chr5:94955400-94955800	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
32	chr5:94955400-94955800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
33	chr5:94955400-94955800	Bivalent Enhancer	Stomach Mucosa	stomach
34	chr5:94955400-94955800	Flanking Active TSS	NHLF	lung
35	chr5:94955400-94956000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
36	chr5:94955400-94956000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:94955400-94956000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr5:94955400-94956000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
39	chr5:94955400-94956000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr5:94955400-94956000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
41	chr5:94955400-94956000	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
42	chr5:94955400-94956000	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
43	chr5:94955400-94956000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
44	chr5:94955400-94956000	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
45	chr5:94955400-94956000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
46	chr5:94955400-94956000	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
47	chr5:94955400-94956200	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
48	chr5:94955400-94956200	Flanking Active TSS	Primary B cells from peripheral blood	blood
49	chr5:94955400-94956200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
50	chr5:94955400-94956200	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood

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