Variant report

Variant	nsv878624
Chromosome Location	chr4:8656976-9371116
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4567)
CpG islands
(count:1343)
Chromatin interactive
region (count:116)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4567 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9154835-9154872	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:9155684-9155703	HepG2	liver:	n/a	n/a
3	ATF1	chr4:9154438-9155046	K562	blood:	n/a	n/a
4	ATF3	chr4:8854977-8855363	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr4:9154337-9154466	K562	blood:	n/a	n/a
6	ATF3	chr4:8854995-8855309	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr4:8855081-8855244	K562	blood:	n/a	n/a
8	BACH1	chr4:8894725-8895016	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:8862268-8862627	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:8689946-8690325	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:8857031-8857091	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:8893693-8893726	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:8857632-8857756	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:8874989-8875170	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr4:8861399-8861529	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:8862941-8863709	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr4:8859610-8859971	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr4:8858777-8858889	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr4:8869917-8869990	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr4:8875855-8875971	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr4:8686570-8686574	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr4:8873787-8873987	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr4:9019180-9019377	GM12878	blood:	n/a	n/a
24	BATF	chr4:9155849-9156145	GM12878	blood:	n/a	n/a
25	BATF	chr4:9069049-9069339	GM12878	blood:	n/a	n/a
26	BATF	chr4:9075036-9075407	GM12878	blood:	n/a	n/a
27	BATF	chr4:9016052-9016284	GM12878	blood:	n/a	chr4:9016178-9016189
28	BATF	chr4:9167731-9168069	GM12878	blood:	n/a	n/a
29	BATF	chr4:9125270-9125602	GM12878	blood:	n/a	n/a
30	BATF	chr4:8947322-8947571	GM12878	blood:	n/a	chr4:8947446-8947457
31	BATF	chr4:9172276-9172654	GM12878	blood:	n/a	n/a
32	BATF	chr4:9167836-9168045	GM12878	blood:	n/a	n/a
33	BATF	chr4:9078511-9078942	GM12878	blood:	n/a	n/a
34	BATF	chr4:8962972-8963416	GM12878	blood:	n/a	n/a
35	BATF	chr4:9050779-9051110	GM12878	blood:	n/a	n/a
36	BATF	chr4:9027943-9028103	GM12878	blood:	n/a	n/a
37	BATF	chr4:8877064-8877233	GM12878	blood:	n/a	chr4:8877125-8877134
38	BATF	chr4:9027580-9027939	GM12878	blood:	n/a	n/a
39	BATF	chr4:9074518-9074764	GM12878	blood:	n/a	n/a
40	BATF	chr4:9075010-9075406	GM12878	blood:	n/a	n/a
41	BATF	chr4:8977979-8978183	GM12878	blood:	n/a	n/a
42	BATF	chr4:9170428-9170639	GM12878	blood:	n/a	n/a
43	BATF	chr4:8947373-8947544	GM12878	blood:	n/a	chr4:8947446-8947457
44	BATF	chr4:9078532-9078952	GM12878	blood:	n/a	n/a
45	BATF	chr4:9059496-9059973	GM12878	blood:	n/a	n/a
46	BATF	chr4:9155872-9156200	GM12878	blood:	n/a	n/a
47	BATF	chr4:9160170-9160447	GM12878	blood:	n/a	n/a
48	BATF	chr4:9050852-9051138	GM12878	blood:	n/a	n/a
49	BATF	chr4:9172306-9172654	GM12878	blood:	n/a	n/a
50	BATF	chr4:8911262-8911579	GM12878	blood:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8689975-8690025	GM12892	blood:	n/a
2	chr4:8689975-8690025	GM12892	blood:	n/a
3	chr4:8687955-8688005	PFSK-1	brain:	n/a
4	chr4:8702535-8702585	NB4	blood:	n/a
5	chr4:8690489-8690539	SK-N-SH	brain:	n/a
6	chr4:8687039-8687089	T-47D	breast:	n/a
7	chr4:8702397-8702447	HCPEpiC	choroid plexus:	n/a
8	chr4:8689852-8689902	AoSMC	blood vessel:	n/a
9	chr4:9355351-9355401	HEEpiC	esophagus:	n/a
10	chr4:8689975-8690025	CMK	blood:	n/a
11	chr4:8689975-8690025	AG09309	skin:	n/a
12	chr4:8687039-8687089	RPTEC	kidney:	n/a
13	chr4:8690035-8690085	SKMC	muscle:	n/a
14	chr4:9355351-9355401	Caco-2	colon:	n/a
15	chr4:8666871-8666921	Hela-S3	cervix:	n/a
16	chr4:9352827-9352877	AoSMC	blood vessel:	n/a
17	chr4:8687039-8687089	LNCaP	prostate:	n/a
18	chr4:8687039-8687089	CMK	blood:	n/a
19	chr4:8693400-8693450	CMK	blood:	n/a
20	chr4:9352827-9352877	AG09309	skin:	n/a
21	chr4:8687955-8688005	HEK293	kidney:	embryo
22	chr4:8689975-8690025	BJ	skin:	n/a
23	chr4:8687039-8687089	AG09309	skin:	n/a
24	chr4:8689852-8689902	T-47D	breast:	n/a
25	chr4:9355372-9355422	HCF	heart:	n/a
26	chr4:9355351-9355401	GM06990	blood:	n/a
27	chr4:8702475-8702525	RPTEC	kidney:	n/a
28	chr4:8702475-8702525	U87	brain:	n/a
29	chr4:8696173-8696223	Hepatocyte	liver:	n/a
30	chr4:8702279-8702329	Hepatocyte	liver:	n/a
31	chr4:8692854-8692904	BE2_C	brain:	n/a
32	chr4:8702279-8702329	NHBE	bronchial:	n/a
33	chr4:8666871-8666921	NHBE	bronchial:	n/a
34	chr4:8696173-8696223	HRCEpiC	kidney:	n/a
35	chr4:8687039-8687089	NT2-D1	testis:	n/a
36	chr4:8692935-8692985	HRPEpiC	eye:	n/a
37	chr4:8693400-8693450	AG04449	skin:	fetal
38	chr4:8693400-8693450	Jurkat	blood:	n/a
39	chr4:8696173-8696223	GM12892	blood:	n/a
40	chr4:8666871-8666921	NHDF-neo	bronchial:	n/a
41	chr4:8692854-8692904	GM19239	blood:	n/a
42	chr4:8702279-8702329	SK-N-SH	brain:	n/a
43	chr4:8702535-8702585	HCT-116	colon:	n/a
44	chr4:8696173-8696223	K562	blood:	n/a
45	chr4:9352827-9352877	GM19239	blood:	n/a
46	chr4:8692854-8692904	SK-N-SH_RA	brain:	n/a
47	chr4:8666871-8666921	HEEpiC	esophagus:	n/a
48	chr4:8727474-8727524	AG09309	skin:	n/a
49	chr4:8702397-8702447	CMK	blood:	n/a
50	chr4:8692935-8692985	SAEC	small airway:	n/a

(count:116 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:8667609..8668516-chr4:8887656..8888210,2	MCF-7	breast:
2	chr4:8689272..8690551-chr4:8887541..8888216,4	MCF-7	breast:
3	chr4:8854005..8855600-chr4:8858236..8860977,2	MCF-7	breast:
4	chr4:8841775..8843355-chr4:8852105..8854658,2	MCF-7	breast:
5	chr4:8781022..8782784-chr4:8786066..8789038,2	K562	blood:
6	chr4:8887461..8890172-chr4:8891389..8893910,2	MCF-7	breast:
7	chr4:8689272..8690551-chr4:8887541..8888216,4	MCF-7	breast:
8	chr4:8720313..8722738-chr4:8763583..8766332,2	MCF-7	breast:
9	chr4:8709792..8713378-chr4:8726638..8730577,3	K562	blood:
10	chr4:8847923..8849486-chr4:8849539..8851969,2	K562	blood:
11	chr4:8871272..8873108-chr4:8879640..8882009,2	MCF-7	breast:
12	chr4:8778847..8780683-chr4:8898052..8900103,2	MCF-7	breast:
13	chr4:8690025..8690993-chr4:8919534..8920174,2	MCF-7	breast:
14	chr4:8723681..8726595-chr4:8727045..8729022,2	MCF-7	breast:
15	chr4:8690025..8690993-chr4:8919534..8920174,2	MCF-7	breast:
16	chr4:8727792..8729635-chr4:8777761..8780174,2	MCF-7	breast:
17	chr4:8743350..8745103-chr4:8747922..8749875,2	MCF-7	breast:
18	chr4:8887461..8890172-chr4:8891389..8893910,2	MCF-7	breast:
19	chr4:8785973..8787809-chr4:8789851..8791798,2	MCF-7	breast:
20	chr4:8987440..8989215-chr4:9123032..9125625,2	MCF-7	breast:
21	chr4:8781022..8782784-chr4:8786066..8789038,2	K562	blood:
22	chr4:9155081..9155863-chr4:79696788..79697581,2	HCT-116	colon:
23	chr4:8707817..8709520-chr4:8713049..8714741,2	MCF-7	breast:
24	chr4:8917493..8920418-chr4:8922098..8924605,3	K562	blood:
25	chr4:8778847..8780683-chr4:8898052..8900103,2	MCF-7	breast:
26	chr4:8654425..8657330-chr7:61967859..61969474,2	MCF-7	breast:
27	chr4:8722609..8725304-chr4:8746886..8749545,2	MCF-7	breast:
28	chr4:8689949..8690495-chr4:8884145..8884993,2	MCF-7	breast:
29	chr4:8709795..8712592-chr4:8714328..8716618,2	MCF-7	breast:
30	chr4:8738768..8740939-chr4:8744102..8745703,2	MCF-7	breast:
31	chr4:8667609..8668516-chr4:8887656..8888210,2	MCF-7	breast:
32	chr4:8827560..8829523-chr4:8830683..8833064,2	K562	blood:
33	chr4:8732091..8733640-chr4:8882099..8884528,2	MCF-7	breast:
34	chr4:8875731..8878681-chr4:8880679..8882236,2	K562	blood:
35	chr4:8728690..8730772-chr4:10106539..10108201,2	K562	blood:
36	chr4:8483492..8484345-chr4:8919742..8920371,2	MCF-7	breast:
37	chr4:8707817..8709520-chr4:8713049..8714741,2	MCF-7	breast:
38	chr4:8889120..8890631-chr4:8897595..8899572,2	MCF-7	breast:
39	chr4:8677416..8680217-chr4:8770931..8773550,2	K562	blood:
40	chr4:8442251..8443878-chr4:8907020..8909362,2	MCF-7	breast:
41	chr4:8836102..8838665-chr4:8853304..8855667,2	MCF-7	breast:
42	chr4:8836102..8838665-chr4:8853304..8855667,2	MCF-7	breast:
43	chr4:8847923..8849486-chr4:8849539..8851969,2	K562	blood:
44	chr4:8732091..8733640-chr4:8882099..8884528,2	MCF-7	breast:
45	chr4:8850333..8852547-chr4:8858670..8860391,2	MCF-7	breast:
46	chr4:8916094..8919081-chr4:8922098..8925711,3	K562	blood:
47	chr4:8852857..8854871-chr4:8860134..8862966,2	K562	blood:
48	chr4:8874973..8877231-chr4:8879936..8882236,2	K562	blood:
49	chr4:8709792..8713378-chr4:8726638..8730577,3	K562	blood:
50	chr4:8649831..8652641-chr4:8656604..8658458,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMX1-4	chr4:9036310-9037271	NONHSAT095124
2	lnc-HMX1-4	chr4:9065968-9066056	NONHSAT095123
3	lnc-ACOX3-3	chr4:8860441-8860823	ENSG00000258507.1
4	lnc-HMX1-1	chr4:8749072-8749394	NONHSAT095114
5	lnc-HMX1-4	chr4:9036251-9037271	NONHSAT095123
6	lnc-HMX1-4	chr4:9083355-9083373	NONHSAT095123
7	lnc-RP11-1286E23.8.1-1	chr4:9173538-9173895	XLOC_003448
8	lnc-HMX1-1	chr4:8747672-8747863	NONHSAT095113
9	lnc-HMX1-1	chr4:8747165-8747482	NONHSAT095114
10	lnc-HMX1-1	chr4:8747123-8747482	ENSG00000250915
11	lnc-HMX1-4	chr4:9036251-9037271	NONHSAT095122
12	lnc-RP11-1286E23.8.1-1	chr4:9174843-9174908	XLOC_003448
13	lnc-ACOX3-3	chr4:8862375-8862553	ENSG00000258507.1
14	lnc-HMX1-1	chr4:8749072-8749394	NONHSAT095113
15	lnc-HMX1-4	chr4:9065968-9066056	NONHSAT095124
16	lnc-HMX1-3	chr4:9053568-9053777	NONHSAT095125
17	lnc-HMX1-4	chr4:9065968-9066056	NONHSAT095122
18	lnc-HMX1-2	chr4:9022583-9022887	NONHSAT095120
19	lnc-HMX1-4	chr4:9072963-9073140	NONHSAT095124
20	lnc-HMX1-4	chr4:9074628-9074691	NONHSAT095122
21	lnc-HMX1-1	chr4:8747165-8747482	NONHSAT095113
22	lnc-HMX1-1	chr4:8747656-8747863	NONHSAT095114
23	lnc-HMX1-1	chr4:8747656-8747759	ENSG00000250915

No data

Variant related genes	Relation type
USP17L11	TF binding region
USP17L22	TF binding region
ENSG00000264372	TF binding region
ENSG00000250804	TF binding region
ENSG00000197468	TF binding region
USP17L19	TF binding region
USP17L9P	TF binding region
USP17L5	TF binding region
ALG1L14P	TF binding region
USP17L10	TF binding region
FAM90A26	TF binding region
USP17L17	TF binding region
USP17L15	TF binding region
USP17L26	TF binding region
USP17L23	TF binding region
USP17L25	TF binding region
USP17L6P	TF binding region
USP17L27	TF binding region
USP17L20	TF binding region
FAM86KP	TF binding region
ENSG00000258507	TF binding region
USP17L18	TF binding region
ENSG00000250342	TF binding region
ENSG00000271057	TF binding region
ENSG00000251313	TF binding region
USP17L24	TF binding region
USP17L29	TF binding region
USP17L13	TF binding region
HMX1	TF binding region
USP17L14P	TF binding region
USP17L12	TF binding region
ENSG00000238726	TF binding region
UNC93B8	TF binding region
USP17L30	TF binding region
ENSG00000250915	TF binding region
USP17L16P	TF binding region
ENPP7P10	TF binding region
USP17L21	TF binding region
ENSG00000249347	TF binding region
USP17L28	TF binding region
USP17L11	CpG island
USP17L22	CpG island
ENSG00000264372	CpG island
ENSG00000250804	CpG island
ENSG00000197468	CpG island
USP17L19	CpG island
USP17L9P	CpG island
USP17L5	CpG island
ALG1L14P	CpG island
USP17L10	CpG island
FAM90A26	CpG island
USP17L17	CpG island
USP17L15	CpG island
USP17L26	CpG island
USP17L23	CpG island
USP17L25	CpG island
USP17L6P	CpG island
USP17L27	CpG island
USP17L20	CpG island
FAM86KP	CpG island
ENSG00000258507	CpG island
USP17L18	CpG island
ENSG00000250342	CpG island
ENSG00000271057	CpG island
ENSG00000251313	CpG island
USP17L24	CpG island
USP17L29	CpG island
USP17L13	CpG island
HMX1	CpG island
USP17L14P	CpG island
USP17L12	CpG island
ENSG00000238726	CpG island
UNC93B8	CpG island
USP17L30	CpG island
ENSG00000250915	CpG island
USP17L16P	CpG island
ENPP7P10	CpG island
USP17L21	CpG island
ENSG00000249347	CpG island
USP17L28	CpG island
ENSG00000071127	chromatin interactions
ENSG00000205959	chromatin interactions
ENSG00000260278	chromatin interactions
ENSG00000087008	chromatin interactions
ENSG00000155275	chromatin interactions
ENSG00000170142	chromatin interactions
ENSG00000258507	chromatin interactions
ENSG00000250915	chromatin interactions
ENSG00000138756	chromatin interactions

Extended variants
information (count: 19275 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:19275 , 50 per page) page: 1 2 3 4 5 6 7 ... 386

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12511120	chr4:8656976-8656977	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557534904	chr4:8656994-8656995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575809405	chr4:8657030-8657031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs75216143	chr4:8657054-8657055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs59229016	chr4:8657056-8657057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182202149	chr4:8657073-8657074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112623262	chr4:8657104-8657105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559205643	chr4:8657120-8657121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375963938	chr4:8657156-8657157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529683442	chr4:8657176-8657177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547780431	chr4:8657188-8657189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370859454	chr4:8657216-8657217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112530068	chr4:8657233-8657234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373081375	chr4:8657265-8657266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552217446	chr4:8657292-8657293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs80052843	chr4:8657294-8657295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139118698	chr4:8657320-8657321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547353975	chr4:8657325-8657326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186762078	chr4:8657328-8657329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs71635970	chr4:8657343-8657344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12511251	chr4:8657344-8657345	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs575556875	chr4:8657357-8657358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114324119	chr4:8657396-8657397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558210504	chr4:8657407-8657408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576997460	chr4:8657412-8657413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540816026	chr4:8657413-8657414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559269770	chr4:8657419-8657420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190842028	chr4:8657420-8657421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567892071	chr4:8657447-8657448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183348675	chr4:8657475-8657476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188179339	chr4:8657482-8657483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531858343	chr4:8657501-8657502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550078177	chr4:8657555-8657556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143969936	chr4:8657558-8657559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73800340	chr4:8657600-8657601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528724904	chr4:8657671-8657672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547216285	chr4:8657693-8657694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6817709	chr4:8657711-8657712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529627348	chr4:8657720-8657721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551267255	chr4:8657737-8657738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs193162159	chr4:8657768-8657769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185311698	chr4:8657782-8657783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs151012689	chr4:8657803-8657804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558009096	chr4:8657809-8657810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370629120	chr4:8657812-8657813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566954754	chr4:8657814-8657815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533984775	chr4:8657815-8657816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139597730	chr4:8657834-8657835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574259187	chr4:8657855-8657856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541746660	chr4:8657856-8657857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Autism	21865298	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	21858162	CNVD

Chromatin state (count:2197 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8655600-8665800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:8659600-8660200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:8662400-8662800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr4:8662800-8666000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:8665800-8666400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr4:8665800-8666600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:8665800-8667000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr4:8665800-8667200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:8666000-8666600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr4:8666000-8666600	Enhancers	H9 Cell Line	embryonic stem cell
11	chr4:8666000-8666600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:8666000-8666600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
13	chr4:8666000-8666800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr4:8666000-8666800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:8666000-8667800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr4:8666200-8666600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
17	chr4:8666600-8666800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
18	chr4:8666600-8667200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:8666800-8667000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
20	chr4:8667000-8667200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
21	chr4:8667200-8667400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:8667200-8667600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:8674400-8674600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:8676200-8676600	Enhancers	Brain Anterior Caudate	brain
25	chr4:8676600-8676800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr4:8676800-8677600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:8677000-8677600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr4:8677000-8677600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
29	chr4:8677000-8677600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr4:8681600-8682200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:8683200-8685200	Enhancers	Left Ventricle	heart
32	chr4:8684400-8684600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:8684400-8684600	Bivalent Enhancer	Adipose Nuclei	Adipose
34	chr4:8684400-8685000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr4:8684800-8685000	Bivalent Enhancer	Fetal Muscle Leg	muscle
36	chr4:8686600-8694200	Weak transcription	Right Atrium	heart
37	chr4:8687800-8689000	Bivalent Enhancer	Right Ventricle	heart
38	chr4:8688200-8688400	Weak transcription	Gastric	stomach
39	chr4:8688400-8688600	Enhancers	Gastric	stomach
40	chr4:8688400-8688800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:8688400-8689000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:8688600-8688800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:8688600-8689000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr4:8688600-8689000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr4:8688600-8689000	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
46	chr4:8688600-8689000	Bivalent/Poised TSS	Fetal Kidney	kidney
47	chr4:8688600-8689000	Flanking Active TSS	Gastric	stomach
48	chr4:8688600-8689000	Enhancers	K562	blood
49	chr4:8688600-8689200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:8688800-8689000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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