Variant report

Variant	nsv1031666
Chromosome Location	chr5:177988601-178236068
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3149)
CpG islands
(count:5314)
Chromatin interactive
region (count:174)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3149 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178057206-178058255	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178205915-178206235	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:178214229-178214360	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:178051872-178052821	K562	blood:	n/a	n/a
5	ARID3A	chr5:178157786-178157877	K562	blood:	n/a	n/a
6	ARID3A	chr5:178051788-178051920	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:178110831-178111247	K562	blood:	n/a	n/a
8	ARID3A	chr5:178064518-178064626	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:178053514-178054047	K562	blood:	n/a	n/a
10	ARID3A	chr5:178157633-178157957	HepG2	liver:	n/a	n/a
11	ARID3A	chr5:178052503-178054060	HepG2	liver:	n/a	n/a
12	ATF1	chr5:178110850-178111124	K562	blood:	n/a	n/a
13	ATF1	chr5:178053891-178054277	K562	blood:	n/a	n/a
14	ATF1	chr5:178144690-178144749	K562	blood:	n/a	n/a
15	ATF1	chr5:178157668-178158241	K562	blood:	n/a	n/a
16	ATF1	chr5:177993173-177993348	K562	blood:	n/a	n/a
17	ATF2	chr5:178053813-178054238	H1-hESC	embryonic stem cell:	n/a	chr5:178054159-178054170
18	ATF2	chr5:178157616-178158016	GM12878	blood:	n/a	n/a
19	ATF3	chr5:178053850-178054207	K562	blood:	n/a	chr5:178054159-178054170 chr5:178054159-178054170 chr5:178054158-178054168 chr5:178054160-178054168
20	ATF3	chr5:178157635-178157861	GM12878	blood:	n/a	n/a
21	ATF3	chr5:178054011-178054203	H1-hESC	embryonic stem cell:	n/a	chr5:178054159-178054170 chr5:178054159-178054170 chr5:178054158-178054168 chr5:178054160-178054168
22	ATF3	chr5:178157554-178157898	HepG2	liver:	n/a	n/a
23	ATF3	chr5:178157537-178157936	K562	blood:	n/a	n/a
24	ATF3	chr5:178157671-178158035	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr5:178003565-178003761	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr5:178016327-178016499	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr5:178053118-178053503	K562	blood:	n/a	n/a
28	BACH1	chr5:178157309-178157437	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr5:178053382-178054434	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr5:178214042-178214427	K562	blood:	n/a	n/a
31	BACH1	chr5:178016908-178018114	H1-hESC	embryonic stem cell:	n/a	n/a
32	BATF	chr5:178053782-178054154	GM12878	blood:	n/a	n/a
33	BATF	chr5:178157607-178157972	GM12878	blood:	n/a	n/a
34	BCL11A	chr5:178012458-178012770	GM12878	blood:	n/a	n/a
35	BCL3	chr5:178220955-178221285	GM12878	blood:	n/a	n/a
36	BCL3	chr5:178053449-178054163	A549	lung:	n/a	n/a
37	BCLAF1	chr5:178053422-178054189	GM12878	blood:	n/a	n/a
38	BCLAF1	chr5:178157395-178157998	GM12878	blood:	n/a	chr5:178157397-178157410 chr5:178157688-178157701 chr5:178157489-178157502 chr5:178157396-178157409 chr5:178157641-178157650 chr5:178157728-178157741
39	BCLAF1	chr5:178157439-178158032	GM12878	blood:	n/a	chr5:178157688-178157701 chr5:178157489-178157502 chr5:178157641-178157650 chr5:178157728-178157741
40	BCLAF1	chr5:178053342-178054187	GM12878	blood:	n/a	n/a
41	BHLHE40	chr5:178051853-178052207	K562	blood:	n/a	n/a
42	BHLHE40	chr5:178205860-178206179	HepG2	liver:	n/a	n/a
43	BHLHE40	chr5:178053464-178054266	HepG2	liver:	n/a	chr5:178053688-178053704
44	BHLHE40	chr5:178057474-178058024	HepG2	liver:	n/a	n/a
45	BHLHE40	chr5:178057599-178057607	K562	blood:	n/a	n/a
46	BHLHE40	chr5:178157553-178158038	K562	blood:	n/a	chr5:178157714-178157730
47	BHLHE40	chr5:178017213-178017413	K562	blood:	n/a	n/a
48	BHLHE40	chr5:178223850-178223909	K562	blood:	n/a	chr5:178223892-178223901 chr5:178223891-178223900 chr5:178223893-178223902 chr5:178223892-178223901
49	BHLHE40	chr5:178094647-178094915	K562	blood:	n/a	chr5:178094752-178094761 chr5:178094752-178094761
50	BHLHE40	chr5:178214114-178214477	HepG2	liver:	n/a	n/a

(count:5314 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178054469-178054519	HRCEpiC	kidney:	n/a
2	chr5:178054017-178054067	CMK	blood:	n/a
3	chr5:178017300-178017350	GM19239	blood:	n/a
4	chr5:178017853-178017903	K562	blood:	n/a
5	chr5:178195589-178195639	ovcar-3	ovarian:	n/a
6	chr5:178017853-178017903	SK-N-MC	brain:	n/a
7	chr5:178157550-178157600	MCF-7	breast:	n/a
8	chr5:178054469-178054519	HRCEpiC	kidney:	n/a
9	chr5:178054017-178054067	CMK	blood:	n/a
10	chr5:178017300-178017350	GM19239	blood:	n/a
11	chr5:178017853-178017903	K562	blood:	n/a
12	chr5:178195589-178195639	ovcar-3	ovarian:	n/a
13	chr5:178017853-178017903	SK-N-MC	brain:	n/a
14	chr5:178157550-178157600	MCF-7	breast:	n/a
15	chr5:178053231-178053281	BJ	skin:	n/a
16	chr5:178052578-178052628	AG09319	gingival:	n/a
17	chr5:178199408-178199458	HCF	heart:	n/a
18	chr5:178199408-178199458	HUVEC	blood vessel:	n/a
19	chr5:178213543-178213593	LNCaP	prostate:	n/a
20	chr5:178157956-178158006	AG09309	skin:	n/a
21	chr5:178017879-178017929	Jurkat	blood:	n/a
22	chr5:178157801-178157851	HAEpiC	amniotic membrane:	n/a
23	chr5:178057845-178057895	AG10803	skin:	n/a
24	chr5:178054172-178054222	SK-N-SH	brain:	n/a
25	chr5:178157792-178157842	AG09309	skin:	n/a
26	chr5:178157825-178157875	HCF	heart:	n/a
27	chr5:178018968-178019018	HRCEpiC	kidney:	n/a
28	chr5:178017879-178017929	HRPEpiC	eye:	n/a
29	chr5:178204766-178204816	LNCaP	prostate:	n/a
30	chr5:178160252-178160302	Jurkat	blood:	n/a
31	chr5:178054298-178054348	HCT-116	colon:	n/a
32	chr5:178213543-178213593	HCT-116	colon:	n/a
33	chr5:178053533-178053583	HepG2	liver:	n/a
34	chr5:178018186-178018236	HCPEpiC	choroid plexus:	n/a
35	chr5:178157792-178157842	BJ	skin:	n/a
36	chr5:178012716-178012766	SK-N-MC	brain:	n/a
37	chr5:178004091-178004141	Hepatocyte	liver:	n/a
38	chr5:178157518-178157568	HRCEpiC	kidney:	n/a
39	chr5:178043484-178043534	MCF10A-Er-Src	breast:	n/a
40	chr5:178199408-178199458	CMK	blood:	n/a
41	chr5:178153430-178153480	AoSMC	blood vessel:	n/a
42	chr5:178049773-178049823	NHDF-neo	bronchial:	n/a
43	chr5:178054017-178054067	K562	blood:	n/a
44	chr5:178017827-178017877	HL-60	blood:	n/a
45	chr5:178017667-178017717	HL-60	blood:	n/a
46	chr5:178204763-178204813	Hepatocyte	liver:	n/a
47	chr5:178157809-178157859	HCT-116	colon:	n/a
48	chr5:178018186-178018236	AG09319	gingival:	n/a
49	chr5:178043484-178043534	ProgFib	skin:	n/a
50	chr5:178017879-178017929	MCF-7	breast:	n/a

(count:174 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr5:178053391..178055177-chr5:178285758..178288394,2	MCF-7	breast:
2	chr5:178082180..178084775-chr5:178097053..178099400,3	MCF-7	breast:
3	chr5:178119500..178121494-chr5:178122164..178124985,2	MCF-7	breast:
4	chr5:178063122..178065248-chr5:178068092..178070072,3	K562	blood:
5	chr5:178135141..178137270-chr5:178138560..178140664,2	K562	blood:
6	chr5:178032038..178034320-chr5:178042432..178044449,2	K562	blood:
7	chr5:178051814..178054054-chr5:178071532..178073696,2	MCF-7	breast:
8	chr5:178056292..178058896-chr5:178156268..178158313,2	MCF-7	breast:
9	chr5:178157437..178158143-chr5:178214195..178215016,4	MCF-7	breast:
10	chr5:178060070..178062652-chr5:178068693..178071518,2	MCF-7	breast:
11	chr5:178035433..178037862-chr5:178050507..178052447,2	K562	blood:
12	chr5:178052435..178056379-chr5:178060810..178069102,10	MCF-7	breast:
13	chr5:178067993..178069564-chr5:178084194..178086392,2	K562	blood:
14	chr5:170259431..170263893-chr5:178180791..178183224,3	MCF-7	breast:
15	chr5:178058360..178060808-chr5:178094532..178097215,2	K562	blood:
16	chr5:178135141..178137270-chr5:178138560..178140664,2	K562	blood:
17	chr5:178039292..178042196-chr5:178044380..178046432,3	K562	blood:
18	chr5:178052822..178055819-chr5:178156143..178158096,2	MCF-7	breast:
19	chr5:178219922..178220838-chr5:178920668..178921270,2	MCF-7	breast:
20	chr5:177630932..177632998-chr5:178042770..178045637,2	K562	blood:
21	chr5:178030104..178033077-chr5:178039867..178042129,2	K562	blood:
22	chr5:178042026..178043855-chr5:178045474..178048004,2	K562	blood:
23	chr5:178054153..178056905-chr5:178057584..178060537,3	K562	blood:
24	chr5:177650184..177652351-chr5:178050731..178052958,2	K562	blood:
25	chr5:178051446..178054153-chr5:178157357..178158910,2	MCF-7	breast:
26	chr1:149207614..149210594-chr5:178225995..178227496,2	MCF-7	breast:
27	chr5:177629964..177631778-chr5:178045699..178047442,2	K562	blood:
28	chr5:178219841..178220793-chr5:178920740..178921735,2	MCF-7	breast:
29	chr5:178053433..178053933-chrX:41193160..41193798,2	Hela-S3	cervix:
30	chr5:178001407..178003756-chr5:178005377..178007780,2	K562	blood:
31	chr5:178119500..178121494-chr5:178122164..178124985,2	MCF-7	breast:
32	chr5:177997965..178000895-chr5:178002250..178003802,2	MCF-7	breast:
33	chr5:178029668..178031491-chr5:178050533..178053383,2	K562	blood:
34	chr5:178001407..178003756-chr5:178005377..178007780,2	K562	blood:
35	chr5:177775560..177777498-chr5:178072805..178075321,2	MCF-7	breast:
36	chr5:178067993..178069564-chr5:178084194..178086392,2	K562	blood:
37	chr5:178006099..178008478-chr5:178010854..178012707,2	MCF-7	breast:
38	chr5:178022246..178024591-chr5:178025333..178028233,2	MCF-7	breast:
39	chr5:178006099..178008478-chr5:178010854..178012707,2	MCF-7	breast:
40	chr5:178145453..178147162-chr5:178151776..178154712,2	MCF-7	breast:
41	chr5:178223973..178226497-chr5:178266303..178268866,2	MCF-7	breast:
42	chr5:178026410..178028805-chr5:178033864..178036012,2	K562	blood:
43	chr5:177995855..177997941-chr5:178001993..178004774,2	K562	blood:
44	chr5:178157230..178157844-chr5:178286636..178287441,3	MCF-7	breast:
45	chr5:178024210..178026391-chr5:178026680..178028373,2	K562	blood:
46	chr5:178072351..178074150-chr5:178081295..178082959,2	MCF-7	breast:
47	chr5:178085944..178088842-chr5:178089934..178092038,2	K562	blood:
48	chr5:178054847..178056678-chr5:178067285..178069085,2	K562	blood:
49	chr5:178028596..178031589-chr5:178051913..178055707,3	MCF-7	breast:
50	chr5:178219910..178220433-chr5:178257274..178257901,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLK4-2	chr5:177989599-177989727	NONHSAT105537
2	lnc-COL23A1-2	chr5:178046729-178046999	NONHSAT105542
3	lnc-ZNF354A-2	chr5:178178077-178178301	NONHSAT105546
4	lnc-ZNF354A-2	chr5:178176203-178176293	NONHSAT105546
5	lnc-ZNF354A-3	chr5:178181044-178181218	NONHSAT105547
6	lnc-ZNF354A-1	chr5:178122288-178122599	XLOC_005102
7	lnc-ZNF354A-1	chr5:178121721-178121948	XLOC_005102
8	lnc-ZNF354A-1	chr5:178133940-178134039	XLOC_005102
9	lnc-CLK4-2	chr5:177988845-177989007	NONHSAT105537
10	lnc-ZNF354A-1	chr5:178123098-178123182	XLOC_005102
11	lnc-ZNF354A-1	chr5:178124587-178124696	XLOC_005102
12	lnc-ZNF354A-3	chr5:178178352-178178894	NONHSAT105547

No data

Variant related genes	Relation type
RN7SKP70	TF binding region
ZNF354A	TF binding region
COL23A1	TF binding region
AACSP1	TF binding region
CLK4	TF binding region
RN7SKP70	CpG island
ZNF354A	CpG island
COL23A1	CpG island
AACSP1	CpG island
CLK4	CpG island
ENSG00000178338	chromatin interactions
ENSG00000252464	chromatin interactions
ENSG00000215301	chromatin interactions
ENSG00000214046	chromatin interactions
ENSG00000268790	chromatin interactions
ENSG00000250420	chromatin interactions
ENSG00000113240	chromatin interactions
ENSG00000169131	chromatin interactions
ENSG00000101193	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000253725	chromatin interactions
ENSG00000101191	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000050767	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000175309	chromatin interactions
ENSG00000113262	chromatin interactions

Extended variants
information (count: 10998 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:10998 , 50 per page) page: 1 2 3 4 5 6 7 ... 220

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114404905	chr5:177988656-177988657	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs573841564	chr5:177988682-177988683	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs555598795	chr5:177988703-177988704	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs540874438	chr5:177988795-177988796	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs78055108	chr5:177988816-177988817	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs559473603	chr5:177988821-177988822	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs10903227	chr5:177988888-177988889	Enhancers Weak transcription Bivalent Enhancer	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs546345662	chr5:177988974-177988975	Enhancers Weak transcription Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
9	rs564566183	chr5:177988975-177988976	Enhancers Weak transcription Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
10	rs531778662	chr5:177989028-177989029	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs11249552	chr5:177989103-177989104	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs76592681	chr5:177989153-177989154	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs114582223	chr5:177989174-177989175	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs186306484	chr5:177989178-177989179	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs566297768	chr5:177989209-177989210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369573389	chr5:177989239-177989240	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs191317835	chr5:177989250-177989251	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs190327651	chr5:177989278-177989279	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs569403329	chr5:177989285-177989286	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs6859361	chr5:177989335-177989336	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs78719159	chr5:177989337-177989338	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs112398897	chr5:177989371-177989372	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs6898605	chr5:177989373-177989374	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs529461691	chr5:177989411-177989412	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs182970224	chr5:177989412-177989413	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs549199785	chr5:177989415-177989416	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs552968226	chr5:177989428-177989429	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs577812322	chr5:177989437-177989438	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs559669383	chr5:177989487-177989488	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs564578536	chr5:177989496-177989497	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs531791055	chr5:177989512-177989513	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs6880593	chr5:177989516-177989517	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs4452575	chr5:177989534-177989535	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs566788938	chr5:177989538-177989539	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs377385199	chr5:177989565-177989566	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs6880618	chr5:177989573-177989574	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs76569222	chr5:177989579-177989580	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs566240718	chr5:177989592-177989593	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs533390013	chr5:177989613-177989614	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs192975195	chr5:177989641-177989642	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs174438	chr5:177989644-177989645	Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs372804960	chr5:177989662-177989663	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs140583377	chr5:177989667-177989668	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs554962643	chr5:177989680-177989681	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs539395139	chr5:177989681-177989682	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs262038	chr5:177989689-177989690	Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs534317325	chr5:177989697-177989698	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs553281982	chr5:177989707-177989708	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs370458159	chr5:177989717-177989718	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs115953131	chr5:177989721-177989722	Weak transcription	TF binding region lncRNA	1 gene(s)	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
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	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
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
small cell lung cancer	20016488	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
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:3683 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177982200-177990200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:177983200-177991000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:177987200-177989000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr5:177987200-177989200	Enhancers	H1 Cell Line	embryonic stem cell
5	chr5:177987200-177989200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr5:177987200-177989200	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr5:177987400-177988800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr5:177987400-177989000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr5:177987400-177989200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr5:177987400-177989200	Enhancers	Fetal Thymus	thymus
11	chr5:177987600-177989200	Enhancers	Fetal Stomach	stomach
12	chr5:177987600-177989200	Enhancers	Dnd41	blood
13	chr5:177987800-177989000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr5:177987800-177989000	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr5:177987800-177989000	Enhancers	Fetal Lung	lung
16	chr5:177988000-177989200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr5:177988200-177989200	Enhancers	Fetal Muscle Leg	muscle
18	chr5:177988400-177989200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
19	chr5:177988600-177989200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:177988600-177989200	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr5:177988600-177989200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr5:177988600-177989200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr5:177988600-177990000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr5:177988600-177990200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr5:177988600-177990200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:177988600-177990200	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr5:177988800-177989000	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr5:177988800-177989000	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr5:177988800-177989200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
30	chr5:177988800-177989200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
31	chr5:177988800-177991000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr5:177989000-177990800	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr5:177989000-177990800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr5:177989000-177990800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr5:177989000-177990800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr5:177989200-177990000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr5:177989200-177990200	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr5:177989200-177990400	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr5:177989200-177990800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr5:177989200-177991600	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr5:177989200-177992000	Weak transcription	Fetal Muscle Leg	muscle
42	chr5:177990000-177990400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr5:177990000-177990600	Bivalent Enhancer	Fetal Stomach	stomach
44	chr5:177990000-177992600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:177990200-177990400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr5:177990200-177990400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr5:177990200-177990400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr5:177990200-177990400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:177990200-177991600	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr5:177990400-177990600	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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