Variant report

Variant	nsv872208
Chromosome Location	chr1:144560355-144875799
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2553)
CpG islands
(count:1465)
Chromatin interactive
region (count:38)
LncRNA
region (count:155)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2553 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:144853386-144853575	HepG2	liver:	n/a	n/a
2	BATF	chr1:144690283-144690581	GM12878	blood:	n/a	chr1:144690289-144690297 chr1:144690402-144690411
3	BATF	chr1:144583250-144583514	GM12878	blood:	n/a	n/a
4	BATF	chr1:144567866-144568091	GM12878	blood:	n/a	n/a
5	BATF	chr1:144583193-144583534	GM12878	blood:	n/a	n/a
6	BATF	chr1:144822461-144822911	GM12878	blood:	n/a	n/a
7	BATF	chr1:144828408-144829114	GM12878	blood:	n/a	n/a
8	BATF	chr1:144816815-144817082	GM12878	blood:	n/a	n/a
9	BATF	chr1:144618840-144619109	GM12878	blood:	n/a	n/a
10	BATF	chr1:144811689-144812035	GM12878	blood:	n/a	n/a
11	BATF	chr1:144615131-144615468	GM12878	blood:	n/a	n/a
12	BATF	chr1:144829689-144829978	GM12878	blood:	n/a	n/a
13	BATF	chr1:144594992-144595236	GM12878	blood:	n/a	n/a
14	BATF	chr1:144604582-144604786	GM12878	blood:	n/a	n/a
15	BATF	chr1:144572712-144572908	GM12878	blood:	n/a	n/a
16	BATF	chr1:144828481-144829126	GM12878	blood:	n/a	n/a
17	BATF	chr1:144618285-144618435	GM12878	blood:	n/a	n/a
18	BATF	chr1:144617485-144617685	GM12878	blood:	n/a	n/a
19	BATF	chr1:144570308-144570462	GM12878	blood:	n/a	n/a
20	BATF	chr1:144614551-144615001	GM12878	blood:	n/a	n/a
21	BATF	chr1:144822457-144822900	GM12878	blood:	n/a	n/a
22	BATF	chr1:144567749-144568256	GM12878	blood:	n/a	n/a
23	BATF	chr1:144679564-144679880	GM12878	blood:	n/a	n/a
24	BATF	chr1:144614537-144614797	GM12878	blood:	n/a	n/a
25	BATF	chr1:144829153-144829560	GM12878	blood:	n/a	n/a
26	BATF	chr1:144593349-144593687	GM12878	blood:	n/a	n/a
27	BATF	chr1:144839402-144839606	GM12878	blood:	n/a	n/a
28	BATF	chr1:144811804-144812040	GM12878	blood:	n/a	n/a
29	BATF	chr1:144594146-144594619	GM12878	blood:	n/a	n/a
30	BATF	chr1:144816769-144817077	GM12878	blood:	n/a	n/a
31	BATF	chr1:144679543-144679819	GM12878	blood:	n/a	n/a
32	BATF	chr1:144690796-144691031	GM12878	blood:	n/a	n/a
33	BATF	chr1:144615010-144615375	GM12878	blood:	n/a	n/a
34	BATF	chr1:144621396-144621792	GM12878	blood:	n/a	n/a
35	BATF	chr1:144672666-144672904	GM12878	blood:	n/a	n/a
36	BATF	chr1:144618572-144618830	GM12878	blood:	n/a	n/a
37	BATF	chr1:144829180-144829396	GM12878	blood:	n/a	n/a
38	BATF	chr1:144840227-144840482	GM12878	blood:	n/a	n/a
39	BCL11A	chr1:144594234-144594691	GM12878	blood:	n/a	n/a
40	BCL11A	chr1:144690673-144690958	GM12878	blood:	n/a	n/a
41	BCL11A	chr1:144621190-144621435	GM12878	blood:	n/a	n/a
42	BCL11A	chr1:144588906-144589083	GM12878	blood:	n/a	n/a
43	BCL11A	chr1:144840106-144840287	GM12878	blood:	n/a	n/a
44	BCL11A	chr1:144572660-144573001	GM12878	blood:	n/a	chr1:144572970-144572979
45	BCL11A	chr1:144829792-144829953	GM12878	blood:	n/a	n/a
46	BCL11A	chr1:144593207-144593737	GM12878	blood:	n/a	n/a
47	BCL11A	chr1:144614565-144614849	GM12878	blood:	n/a	n/a
48	BCL11A	chr1:144572200-144572437	GM12878	blood:	n/a	n/a
49	BCL11A	chr1:144583227-144583476	GM12878	blood:	n/a	n/a
50	BCL11A	chr1:144828446-144828898	GM12878	blood:	n/a	n/a

(count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144594107-144594157	GM06990	blood:	n/a
2	chr1:144594107-144594157	GM06990	blood:	n/a
3	chr1:144594085-144594135	GM19239	blood:	n/a
4	chr1:144612646-144612696	MCF10A-Er-Src	breast:	n/a
5	chr1:144620428-144620478	LNCaP	prostate:	n/a
6	chr1:144612358-144612408	HCF	heart:	n/a
7	chr1:144619354-144619404	HCM	heart:	n/a
8	chr1:144594107-144594157	LNCaP	prostate:	n/a
9	chr1:144592392-144592442	NB4	blood:	n/a
10	chr1:144620428-144620478	GM12878	blood:	n/a
11	chr1:144594085-144594135	HRE	kidney:	n/a
12	chr1:144815302-144815352	AG04450	lung:	fetal
13	chr1:144596061-144596111	BE2_C	brain:	n/a
14	chr1:144619354-144619404	NB4	blood:	n/a
15	chr1:144594259-144594309	HepG2	liver:	n/a
16	chr1:144592392-144592442	A549	lung:	n/a
17	chr1:144811373-144811423	HAEpiC	amniotic membrane:	n/a
18	chr1:144612646-144612696	SK-N-MC	brain:	n/a
19	chr1:144596061-144596111	CMK	blood:	n/a
20	chr1:144852047-144852097	NT2-D1	testis:	n/a
21	chr1:144612646-144612696	HAEpiC	amniotic membrane:	n/a
22	chr1:144612358-144612408	AG09309	skin:	n/a
23	chr1:144612358-144612408	GM12891	blood:	n/a
24	chr1:144594006-144594056	BE2_C	brain:	n/a
25	chr1:144620428-144620478	HRCEpiC	kidney:	n/a
26	chr1:144615272-144615322	AG04449	skin:	fetal
27	chr1:144592392-144592442	Caco-2	colon:	n/a
28	chr1:144815302-144815352	Jurkat	blood:	n/a
29	chr1:144593341-144593391	SAEC	small airway:	n/a
30	chr1:144592392-144592442	HMEC	breast:	n/a
31	chr1:144594006-144594056	AG04449	skin:	fetal
32	chr1:144612646-144612696	BJ	skin:	n/a
33	chr1:144612646-144612696	GM19239	blood:	n/a
34	chr1:144594259-144594309	H1-hESC	embryonic stem cell:	embryo
35	chr1:144593903-144593953	SK-N-SH	brain:	n/a
36	chr1:144593341-144593391	A549	lung:	n/a
37	chr1:144814628-144814678	T-47D	breast:	n/a
38	chr1:144593903-144593953	HRE	kidney:	n/a
39	chr1:144595718-144595768	AG09319	gingival:	n/a
40	chr1:144593341-144593391	GM12891	blood:	n/a
41	chr1:144567670-144567720	AG04450	lung:	fetal
42	chr1:144593903-144593953	H1-hESC	embryonic stem cell:	embryo
43	chr1:144811373-144811423	HEEpiC	esophagus:	n/a
44	chr1:144593341-144593391	HCF	heart:	n/a
45	chr1:144620428-144620478	A549	lung:	n/a
46	chr1:144594085-144594135	NT2-D1	testis:	n/a
47	chr1:144615272-144615322	SK-N-MC	brain:	n/a
48	chr1:144567670-144567720	RPTEC	kidney:	n/a
49	chr1:144852047-144852097	HCPEpiC	choroid plexus:	n/a
50	chr1:144612646-144612696	SK-N-SH_RA	brain:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:144594105..144596972-chr1:148555192..148558576,3	MCF-7	breast:
2	chr1:144861786..144864624-chr1:144881141..144883484,2	MCF-7	breast:
3	chr1:144866768..144869173-chr1:144870721..144874864,3	K562	blood:
4	chr1:144709036..144711011-chr1:144986149..144988620,2	K562	blood:
5	chr1:144858012..144861709-chr1:144865100..144867014,3	K562	blood:
6	chr1:144589128..144591973-chr1:144594157..144597024,2	MCF-7	breast:
7	chr1:144873625..144876777-chr1:144880154..144883711,4	MCF-7	breast:
8	chr1:144532845..144535745-chr1:144588641..144591361,2	K562	blood:
9	chr1:144590335..144591846-chr1:148550727..148552604,2	MCF-7	breast:
10	chr1:144594107..144594639-chr1:148556298..148556816,2	Hela-S3	cervix:
11	chr1:144566036..144568858-chr1:149222714..149224750,2	MCF-7	breast:
12	chr1:144853163..144855008-chr1:144856698..144858225,2	K562	blood:
13	chr1:144593716..144594289-chr1:148555892..148556883,2	MCF-7	breast:
14	chr1:144861814..144863936-chr1:144885385..144887357,2	MCF-7	breast:
15	chr1:144858012..144861709-chr1:144865100..144867014,3	K562	blood:
16	chr1:144590246..144591117-chr1:148550866..148551429,2	MCF-7	breast:
17	chr1:144708092..144711018-chr1:144989311..144991763,2	K562	blood:
18	chr1:144593856..144595655-chr1:148555098..148556798,2	MCF-7	breast:
19	chr1:144870344..144874042-chr1:144875186..144878291,5	MCF-7	breast:
20	chr1:144870185..144872708-chr1:149042100..149043905,2	MCF-7	breast:
21	chr1:144867331..144870453-chr1:144870555..144873293,3	MCF-7	breast:
22	chr1:144532776..144534883-chr1:144569176..144572167,2	K562	blood:
23	chr1:144858037..144860054-chr1:144867098..144869572,2	K562	blood:
24	chr1:144869766..144871814-chr1:144872899..144874781,2	MCF-7	breast:
25	chr1:144856713..144858353-chr1:144872499..144875477,2	K562	blood:
26	chr1:144696978..144697597-chr1:144972550..144973477,2	MCF-7	breast:
27	chr1:144589128..144591973-chr1:144594157..144597024,2	MCF-7	breast:
28	chr1:144863488..144865055-chr1:144865799..144868536,2	K562	blood:
29	chr1:144569499..144571015-chr1:149221821..149223590,2	MCF-7	breast:
30	chr1:144858037..144860054-chr1:144867098..144869572,2	K562	blood:
31	chr1:144853163..144855008-chr1:144856698..144858225,2	K562	blood:
32	chr1:144866177..144868496-chr1:144870721..144873668,3	K562	blood:
33	chr1:144593744..144594609-chr1:148555862..148556622,3	HCT-116	colon:
34	chr1:144869766..144871814-chr1:144872899..144874781,2	MCF-7	breast:
35	chr1:144856713..144858353-chr1:144872499..144875477,2	K562	blood:
36	chr1:144687969..144690729-chr1:144930762..144933228,2	MCF-7	breast:
37	chr1:144535050..144535880-chr1:144697650..144698167,2	MCF-7	breast:
38	chr1:144859042..144861669-chr1:144863845..144865437,2	MCF-7	breast:

(count:155 , 50 per page) page: 1 2 3 4

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL592284.1-1	chr1:144617150-144617252	ENSG00000225241
2	lnc-AL592284.1-1	chr1:144826933-144827105	NR_102404
3	lnc-AL592284.1-1	chr1:144598512-144598780	ENSG00000225241
4	lnc-PDE4DIP-3	chr1:144833913-144834808	NONHSAT005843
5	lnc-AL592284.1-1	chr1:144617150-144617252	ENSG00000225241
6	lnc-AL592284.1-1	chr1:144814560-144814894	NONHSAT005837
7	lnc-PDE4DIP-1	chr1:144833047-144833912	NONHSAT005841
8	lnc-AL592284.1-1	chr1:144827820-144827928	NR_102404
9	lnc-NBPF9-1	chr1:144858174-144858522	ENSG00000255148.1
10	lnc-PDE4DIP-2	chr1:144837859-144837884	NONHSAT005849
11	lnc-NBPF9-1	chr1:144858639-144858781	ENSG00000255148.1
12	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
13	lnc-AL592284.1-1	chr1:144612349-144612562	NONHSAT005822
14	lnc-AL592284.1-1	chr1:144615096-144615303	ENSG00000225241
15	lnc-AL592284.1-1	chr1:144823128-144823179	NR_102405
16	lnc-AL592284.1-1	chr1:144606369-144606510	ENSG00000225241
17	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
18	lnc-PDE4DIP-2	chr1:144837129-144837429	NONHSAT005846
19	lnc-AL592284.1-1	chr1:144824705-144824756	NR_102405
20	lnc-AL592284.1-1	chr1:144815936-144816008	NR_102404
21	lnc-AL592284.1-1	chr1:144815936-144816008	NONHSAT005838
22	lnc-AL592284.1-1	chr1:144598655-144598780	ENSG00000225241
23	lnc-AL592284.1-1	chr1:144619883-144620094	NR_102404
24	lnc-PDE4DIP-2	chr1:144836655-144836804	NONHSAT005846
25	lnc-AL592284.1-1	chr1:144815936-144816008	NR_102405
26	lnc-AL592284.1-1	chr1:144598651-144598780	ENSG00000225241
27	lnc-AL592284.1-1	chr1:144617150-144617252	ENSG00000225241
28	lnc-AL592284.1-1	chr1:144614840-144614993	ENSG00000225241
29	lnc-AL592284.1-1	chr1:144617150-144617252	ENSG00000225241
30	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
31	lnc-AL592284.1-1	chr1:144826235-144826286	NR_102405
32	lnc-AL592284.1-1	chr1:144604478-144604508	ENSG00000225241
33	lnc-AL592284.1-1	chr1:144614840-144614993	ENSG00000225241
34	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
35	lnc-AL592284.1-1	chr1:144615096-144615303	ENSG00000225241
36	lnc-AL592284.1-1	chr1:144826235-144826286	NR_102404
37	lnc-AL592284.1-1	chr1:144814683-144814894	NONHSAT005838
38	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
39	lnc-AL592284.1-1	chr1:144614388-144614998	ENSG00000225241
40	lnc-AL592284.1-1	chr1:144614532-144614993	ENSG00000225241
41	lnc-AL592284.1-1	chr1:144823813-144823985	NR_102404
42	lnc-AL592284.1-1	chr1:144615096-144615303	ENSG00000225241
43	lnc-AL592284.1-1	chr1:144814680-144814894	NR_102404
44	lnc-PPIAL4B-8	chr1:144847426-144847494	NONHSAT005850
45	lnc-PPIAL4B-8	chr1:144869790-144869871	NONHSAT005850
46	lnc-AL592284.1-1	chr1:144596451-144596473	NONHSAT005825
47	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
48	lnc-AL592284.1-1	chr1:144816316-144816795	NONHSAT005838
49	lnc-AL592284.1-1	chr1:144604410-144604508	ENSG00000225241
50	lnc-PDE4DIP-2	chr1:144837129-144837423	NONHSAT005844

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PDE4DIP	hsa-let-7a-5p	chr1:144851770-144851794

Variant related genes	Relation type
PFN1P2	TF binding region
PDE4DIP	TF binding region
ENSG00000266739	TF binding region
NBPF9	TF binding region
ENSG00000225241	TF binding region
ENSG00000255148	TF binding region
ENSG00000254913	TF binding region
ENSG00000215861	TF binding region
ENSG00000254539	TF binding region
PFN1P2	CpG island
PDE4DIP	CpG island
ENSG00000266739	CpG island
NBPF9	CpG island
ENSG00000225241	CpG island
ENSG00000255148	CpG island
ENSG00000254913	CpG island
ENSG00000215861	CpG island
ENSG00000254539	CpG island
ENSG00000243452	chromatin interactions
ENSG00000266739	chromatin interactions
ENSG00000254913	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000255148	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000201699	chromatin interactions

Extended variants
information (count: 7304 )
Associated
traits (count: 170 )

Variant overlapped rSNPs/rCNVs (count:7304 , 50 per page) page: 1 2 3 4 5 6 7 ... 147

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374660596	chr1:144563753-144563754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs369167839	chr1:144563802-144563803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs61802528	chr1:144563898-144563899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs587694628	chr1:144564017-144564018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199824773	chr1:144564020-144564021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113717481	chr1:144564050-144564051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201401627	chr1:144564068-144564069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200309587	chr1:144564133-144564134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs587672973	chr1:144564219-144564220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587719371	chr1:144564222-144564223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143240534	chr1:144564235-144564236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587654571	chr1:144564283-144564284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372791831	chr1:144564332-144564333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377149013	chr1:144564404-144564405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148642580	chr1:144564487-144564488	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
16	rs61802529	chr1:144564502-144564503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs587768538	chr1:144564538-144564539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587639025	chr1:144564564-144564565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs587726566	chr1:144564570-144564571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537917	chr1:144564589-144564590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374137503	chr1:144564590-144564591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191358258	chr1:144564596-144564597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141803820	chr1:144564677-144564678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371130923	chr1:144564708-144564709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374470842	chr1:144564734-144564735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587706110	chr1:144564740-144564741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201253994	chr1:144564813-144564814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139988686	chr1:144564856-144564857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201828093	chr1:144564869-144564870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs587606907	chr1:144564872-144564873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs587666901	chr1:144564889-144564890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs61802532	chr1:144564893-144564894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs6661398	chr1:144565022-144565023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs199825284	chr1:144565026-144565027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs200650091	chr1:144565033-144565034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs61802533	chr1:144565040-144565041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs61802534	chr1:144565059-144565060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs587740432	chr1:144565172-144565173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs587619914	chr1:144565178-144565179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs140270413	chr1:144565182-144565183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs587752380	chr1:144565198-144565199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376535471	chr1:144565217-144565218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191615076	chr1:144565220-144565221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs3009721	chr1:144565224-144565225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184807408	chr1:144565228-144565229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587751301	chr1:144565248-144565249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374270867	chr1:144565252-144565253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587620657	chr1:144565253-144565254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587682234	chr1:144565255-144565256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200966136	chr1:144565285-144565286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:170)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	20531469	CNVD

Chromatin state (count:2842 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144563600-144563800	Enhancers	HSMM	muscle
2	chr1:144563800-144567600	Weak transcription	HSMM	muscle
3	chr1:144564600-144565400	Enhancers	HSMMtube	muscle
4	chr1:144565000-144567600	Weak transcription	Pancreas	Pancrea
5	chr1:144565200-144565400	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr1:144565200-144565400	Enhancers	Primary B cells from peripheral blood	blood
7	chr1:144565600-144567400	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr1:144567200-144567400	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr1:144567200-144567400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr1:144567200-144567400	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr1:144567400-144567600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
12	chr1:144567400-144567600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr1:144567400-144567600	Enhancers	Primary T cells fromperipheralblood	blood
14	chr1:144567400-144567600	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr1:144567400-144567600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr1:144567400-144567600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr1:144567400-144567600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:144567400-144567600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:144567400-144567600	Active TSS	Brain Cingulate Gyrus	brain
20	chr1:144567400-144567600	Active TSS	Brain Hippocampus Middle	brain
21	chr1:144567400-144567600	Enhancers	Fetal Lung	lung
22	chr1:144567400-144567600	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr1:144567400-144567600	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr1:144567400-144567600	Enhancers	Osteobl	bone
25	chr1:144567400-144567800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
26	chr1:144567400-144567800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
27	chr1:144567400-144567800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:144567400-144567800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:144567400-144567800	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr1:144567400-144567800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr1:144567400-144567800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
32	chr1:144567400-144567800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr1:144567400-144567800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
34	chr1:144567400-144567800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr1:144567400-144567800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
36	chr1:144567400-144567800	Enhancers	Muscle Satellite Cultured Cells	--
37	chr1:144567400-144567800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr1:144567400-144567800	Enhancers	Fetal Brain Male	brain
39	chr1:144567400-144567800	Enhancers	Fetal Intestine Large	intestine
40	chr1:144567400-144567800	Flanking Active TSS	Fetal Intestine Small	intestine
41	chr1:144567400-144567800	Enhancers	Placenta	Placenta
42	chr1:144567400-144567800	Bivalent Enhancer	Fetal Thymus	thymus
43	chr1:144567400-144567800	Enhancers	Rectal Smooth Muscle	rectum
44	chr1:144567400-144567800	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr1:144567400-144567800	Enhancers	NH-A	brain
46	chr1:144567400-144567800	Enhancers	NHEK	skin
47	chr1:144567400-144568000	Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr1:144567400-144568000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr1:144567400-144568000	Active TSS	H9 Cell Line	embryonic stem cell
50	chr1:144567400-144568000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell

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