Variant report

Variant	nsv889139
Chromosome Location	chr7:124600505-124767295
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:934)
CpG islands
(count:305)
Chromatin interactive
region (count:49)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:934 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:124702214-124702414	K562	blood:	n/a	n/a
2	ARID3A	chr7:124700002-124700270	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:124656923-124656953	K562	blood:	n/a	n/a
4	ARID3A	chr7:124699875-124700188	K562	blood:	n/a	n/a
5	ARID3A	chr7:124632397-124633404	K562	blood:	n/a	n/a
6	ARID3A	chr7:124637007-124637167	K562	blood:	n/a	n/a
7	ATF1	chr7:124632844-124633185	K562	blood:	n/a	n/a
8	ATF2	chr7:124738399-124738950	GM12878	blood:	n/a	n/a
9	ATF3	chr7:124702093-124702392	K562	blood:	n/a	n/a
10	ATF3	chr7:124632775-124633232	K562	blood:	n/a	n/a
11	BACH1	chr7:124702235-124702311	K562	blood:	n/a	n/a
12	BACH1	chr7:124632210-124632237	K562	blood:	n/a	n/a
13	BACH1	chr7:124632839-124633414	K562	blood:	n/a	n/a
14	BATF	chr7:124738517-124738718	GM12878	blood:	n/a	chr7:124738608-124738619 chr7:124738609-124738619
15	BATF	chr7:124702173-124702423	GM12878	blood:	n/a	chr7:124702272-124702283
16	BATF	chr7:124702194-124702398	GM12878	blood:	n/a	chr7:124702272-124702283
17	BATF	chr7:124738440-124738777	GM12878	blood:	n/a	chr7:124738608-124738619 chr7:124738609-124738619
18	BCL3	chr7:124702193-124702389	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:124702123-124702446	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:124702000-124702384	K562	blood:	n/a	n/a
21	BHLHE40	chr7:124724253-124724254	GM12878	blood:	n/a	n/a
22	BHLHE40	chr7:124632911-124633233	K562	blood:	n/a	n/a
23	BHLHE40	chr7:124738474-124738831	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:124644549-124644599	K562	blood:	n/a	n/a
25	BHLHE40	chr7:124698048-124698259	K562	blood:	n/a	n/a
26	BHLHE40	chr7:124759668-124759931	GM12878	blood:	n/a	n/a
27	BRCA1	chr7:124700024-124700193	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr7:124702033-124702410	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr7:124632774-124633230	K562	blood:	n/a	n/a
30	CCNT2	chr7:124702118-124702419	K562	blood:	n/a	n/a
31	CCNT2	chr7:124632875-124633179	K562	blood:	n/a	n/a
32	CCNT2	chr7:124745648-124745845	K562	blood:	n/a	n/a
33	CEBPB	chr7:124752861-124753197	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:124705644-124705956	IMR90	lung:	n/a	chr7:124705807-124705818
35	CEBPB	chr7:124705636-124705969	HepG2	liver:	n/a	chr7:124705807-124705818
36	CEBPB	chr7:124705649-124705960	A549	lung:	n/a	chr7:124705807-124705818
37	CEBPB	chr7:124641115-124641235	K562	blood:	n/a	n/a
38	CEBPB	chr7:124632786-124633289	K562	blood:	n/a	n/a
39	CEBPB	chr7:124722882-124722994	A549	lung:	n/a	chr7:124722952-124722961
40	CEBPB	chr7:124663957-124664143	K562	blood:	n/a	n/a
41	CEBPB	chr7:124632938-124633193	K562	blood:	n/a	n/a
42	CEBPB	chr7:124752875-124753279	HCT-116	colon:	n/a	n/a
43	CEBPB	chr7:124632819-124633342	MCF-7	breast:	n/a	n/a
44	CEBPB	chr7:124632741-124633509	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr7:124606210-124606293	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:124632893-124633288	K562	blood:	n/a	n/a
47	CEBPB	chr7:124665488-124665855	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:124752836-124753259	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr7:124760863-124761132	IMR90	lung:	n/a	chr7:124760971-124760984 chr7:124760971-124760984 chr7:124760973-124760984
50	CEBPB	chr7:124632731-124633255	MCF-7	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:124633001-124633051	HUVEC	blood vessel:	n/a
2	chr7:124633001-124633051	HEK293	kidney:	embryo
3	chr7:124765425-124765475	PrEC	prostate:	n/a
4	chr7:124625362-124625412	HRE	kidney:	n/a
5	chr7:124633001-124633051	AG09319	gingival:	n/a
6	chr7:124765450-124765500	PFSK-1	brain:	n/a
7	chr7:124765425-124765475	HL-60	blood:	n/a
8	chr7:124765450-124765500	MCF10A-Er-Src	breast:	n/a
9	chr7:124765450-124765500	RPTEC	kidney:	n/a
10	chr7:124765471-124765521	IMR90	lung:	fetal
11	chr7:124765425-124765475	HUVEC	blood vessel:	n/a
12	chr7:124765425-124765475	CMK	blood:	n/a
13	chr7:124633001-124633051	HL-60	blood:	n/a
14	chr7:124765471-124765521	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:124765450-124765500	ovcar-3	ovarian:	n/a
16	chr7:124765425-124765475	HepG2	liver:	n/a
17	chr7:124765471-124765521	HCM	heart:	n/a
18	chr7:124765450-124765500	PANC-1	pancreas:	n/a
19	chr7:124765471-124765521	Jurkat	blood:	n/a
20	chr7:124625362-124625412	A549	lung:	n/a
21	chr7:124765425-124765475	HCPEpiC	choroid plexus:	n/a
22	chr7:124625362-124625412	SK-N-SH	brain:	n/a
23	chr7:124765471-124765521	RPTEC	kidney:	n/a
24	chr7:124625362-124625412	Caco-2	colon:	n/a
25	chr7:124765471-124765521	PANC-1	pancreas:	n/a
26	chr7:124765450-124765500	AG04450	lung:	fetal
27	chr7:124765471-124765521	HRCEpiC	kidney:	n/a
28	chr7:124765471-124765521	AG10803	skin:	n/a
29	chr7:124625362-124625412	SK-N-MC	brain:	n/a
30	chr7:124625362-124625412	LNCaP	prostate:	n/a
31	chr7:124625362-124625412	NHBE	bronchial:	n/a
32	chr7:124765425-124765475	AoSMC	blood vessel:	n/a
33	chr7:124625362-124625412	U87	brain:	n/a
34	chr7:124765425-124765475	AG09319	gingival:	n/a
35	chr7:124765450-124765500	NH-A	brain:	n/a
36	chr7:124633001-124633051	HepG2	liver:	n/a
37	chr7:124633001-124633051	NB4	blood:	n/a
38	chr7:124765471-124765521	BE2_C	brain:	n/a
39	chr7:124765471-124765521	SK-N-SH	brain:	n/a
40	chr7:124625362-124625412	AG04449	skin:	fetal
41	chr7:124633001-124633051	AoSMC	blood vessel:	n/a
42	chr7:124633001-124633051	NT2-D1	testis:	n/a
43	chr7:124765471-124765521	GM06990	blood:	n/a
44	chr7:124765471-124765521	HCPEpiC	choroid plexus:	n/a
45	chr7:124633001-124633051	ECC-1	luminal epithelium:	n/a
46	chr7:124765425-124765475	K562	blood:	n/a
47	chr7:124633001-124633051	SK-N-SH_RA	brain:	n/a
48	chr7:124625362-124625412	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:124633001-124633051	SAEC	small airway:	n/a
50	chr7:124765425-124765475	H1-hESC	embryonic stem cell:	embryo

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:124699717..124700520-chr7:124956250..124957181,4	MCF-7	breast:
2	chr7:124666403..124669373-chr7:124671418..124674369,2	MCF-7	breast:
3	chr7:124652094..124654102-chr7:124655952..124659375,3	K562	blood:
4	chr7:124651129..124654102-chr7:124654805..124659375,5	K562	blood:
5	chr7:124610367..124612617-chr7:124646921..124649703,2	K562	blood:
6	chr7:124715890..124718550-chr7:124819406..124822329,2	MCF-7	breast:
7	chr7:124699688..124701477-chr7:124956011..124957871,2	MCF-7	breast:
8	chr7:124738749..124741628-chr7:124743456..124745788,2	K562	blood:
9	chr7:124611698..124614462-chr7:124706318..124708451,2	K562	blood:
10	chr7:124641428..124646399-chr7:124650390..124654210,4	K562	blood:
11	chr7:124701246..124703610-chr7:124820642..124822320,2	MCF-7	breast:
12	chr7:124704352..124706297-chr7:124709672..124711396,2	K562	blood:
13	chr7:124495485..124496005-chr7:124636684..124637532,2	MCF-7	breast:
14	chr7:124568419..124570704-chr7:124629136..124631296,2	MCF-7	breast:
15	chr7:124720373..124721901-chr7:124740400..124743244,2	K562	blood:
16	chr7:124641428..124646399-chr7:124650390..124654210,4	K562	blood:
17	chr7:124699671..124700472-chr7:125310284..125311293,4	MCF-7	breast:
18	chr7:124610367..124612617-chr7:124646921..124649703,2	K562	blood:
19	chr7:124738749..124741628-chr7:124743456..124745788,2	K562	blood:
20	chr7:124682680..124683208-chr7:124956334..124957073,2	MCF-7	breast:
21	chr7:124674442..124676696-chr7:124676789..124679518,2	MCF-7	breast:
22	chr7:124570010..124572071-chr7:124632097..124634842,3	MCF-7	breast:
23	chr7:124559307..124561381-chr7:124633111..124635066,2	MCF-7	breast:
24	chr7:124611698..124614462-chr7:124706318..124708451,2	K562	blood:
25	chr7:124652094..124654102-chr7:124655952..124659375,3	K562	blood:
26	chr7:124704797..124707787-chr7:124709672..124712293,2	K562	blood:
27	chr7:124656588..124658906-chr7:124962987..124965229,2	K562	blood:
28	chr7:124709051..124711137-chr7:124712296..124713913,2	K562	blood:
29	chr7:124625632..124627676-chr7:124628734..124631039,2	MCF-7	breast:
30	chr7:124651129..124654102-chr7:124654805..124659375,5	K562	blood:
31	chr7:124606875..124608614-chr7:124609059..124611420,2	MCF-7	breast:
32	chr7:124697959..124699891-chr7:124704188..124706087,2	K562	blood:
33	chr7:124709051..124711137-chr7:124712296..124713913,2	K562	blood:
34	chr7:124728103..124730281-chr7:124737035..124739420,2	K562	blood:
35	chr7:124699558..124701618-chr7:125055753..125057701,2	K562	blood:
36	chr7:124674442..124676696-chr7:124676789..124679518,2	MCF-7	breast:
37	chr7:124701709..124702473-chr7:124956278..124956931,2	MCF-7	breast:
38	chr7:124735275..124737095-chr7:124743479..124745063,2	K562	blood:
39	chr7:124720373..124721901-chr7:124740400..124743244,2	K562	blood:
40	chr7:124735275..124737095-chr7:124743479..124745063,2	K562	blood:
41	chr7:124699605..124700536-chr7:124955869..124957164,4	MCF-7	breast:
42	chr7:124697959..124699891-chr7:124704188..124706087,2	K562	blood:
43	chr7:124728103..124730281-chr7:124737035..124739420,2	K562	blood:
44	chr7:124708792..124711418-chr7:124715743..124718371,2	K562	blood:
45	chr7:124625632..124627676-chr7:124628734..124631039,2	MCF-7	breast:
46	chr7:124704352..124706297-chr7:124709672..124711396,2	K562	blood:
47	chr7:124708792..124711418-chr7:124715743..124718371,2	K562	blood:
48	chr7:124704797..124707787-chr7:124709672..124712293,2	K562	blood:
49	chr7:124606875..124608614-chr7:124609059..124611420,2	MCF-7	breast:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-4	chr7:124633062-124633253	ENSG00000224897
2	lnc-SPAM1-4	chr7:124765879-124766031	ENSG00000224897
3	lnc-SPAM1-4	chr7:124763035-124763129	ENSG00000224897
4	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
5	lnc-SPAM1-4	chr7:124756928-124757082	ENSG00000224897
6	lnc-SPAM1-4	chr7:124720766-124720867	ENSG00000224897
7	lnc-SPAM1-4	chr7:124640736-124641124	XLOC_006231
8	lnc-SPAM1-4	chr7:124660387-124660535	NONHSAT123092
9	lnc-SPAM1-4	chr7:124756928-124757082	ENSG00000224897
10	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
11	lnc-SPAM1-4	chr7:124758683-124758776	ENSG00000224897
12	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
13	lnc-SPAM1-7	chr7:124627790-124627842	NONHSAT123095
14	lnc-POT1-3	chr7:124673634-124673820	ucscGeneNc_uc010lky_1
15	lnc-SPAM1-4	chr7:124756928-124757082	NONHSAT123098
16	lnc-POT1-3	chr7:124656869-124658131	ucscGeneNc_uc010lky_1
17	lnc-SPAM1-4	chr7:124729744-124729830	ENSG00000224897
18	lnc-SPAM1-4	chr7:124742014-124742104	ENSG00000224897
19	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
20	lnc-SPAM1-4	chr7:124729744-124729830	ENSG00000224897
21	lnc-SPAM1-4	chr7:124761696-124761897	ENSG00000224897
22	lnc-POT1-3	chr7:124675591-124675731	ucscGeneNc_uc010lky_1
23	lnc-SPAM1-4	chr7:124739458-124739567	ENSG00000224897
24	lnc-SPAM1-4	chr7:124765879-124766031	NONHSAT123098
25	lnc-SPAM1-4	chr7:124660387-124660467	ENSG00000224897
26	lnc-SPAM1-7	chr7:124631917-124632152	NONHSAT123095
27	lnc-SPAM1-4	chr7:124739410-124739567	NONHSAT123098
28	lnc-SPAM1-4	chr7:124765879-124766031	ENSG00000224897
29	lnc-SPAM1-4	chr7:124720766-124720867	ENSG00000224897
30	lnc-SPAM1-4	chr7:124765879-124765961	ENSG00000224897
31	lnc-SPAM1-4	chr7:124638324-124638458	XLOC_006231
32	lnc-POT1-3	chr7:124691333-124691581	ucscGeneNc_uc010lky_1
33	lnc-POT1-3	chr7:124677270-124677347	ucscGeneNc_uc010lky_1
34	lnc-SPAM1-4	chr7:124640736-124641066	ENSG00000224897

No data

Variant related genes	Relation type
POT1-AS1	TF binding region
EEF1GP1	TF binding region
POT1-AS1	CpG island
EEF1GP1	CpG island
ENSG00000128513	chromatin interactions
ENSG00000186676	chromatin interactions
ENSG00000224897	chromatin interactions
YIPF5	miRNA target sites
CKAP5	miRNA target sites
SACM1L	miRNA target sites
ENC1	miRNA target sites
ARHGAP19	miRNA target sites
ING3	miRNA target sites
NUDT15	miRNA target sites
FGL2	miRNA target sites
CREBZF	miRNA target sites
ZNF238	miRNA target sites
MYO5C	miRNA target sites
IMPA1	miRNA target sites
RRBP1	miRNA target sites
MCL1	miRNA target sites
XYLT2	miRNA target sites
SPRY2	miRNA target sites
PITX1	miRNA target sites
ISM2	miRNA target sites
CA2	miRNA target sites
GTF2A2	miRNA target sites

Extended variants
information (count: 2870 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2870 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12538587	chr7:124600505-124600506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs540696083	chr7:124600526-124600527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10954056	chr7:124600534-124600535	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs188689666	chr7:124600582-124600583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149818168	chr7:124600608-124600609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs377664206	chr7:124600611-124600612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145822151	chr7:124600612-124600613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199587619	chr7:124600615-124600616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12536146	chr7:124600631-124600632	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs12538641	chr7:124600671-124600672	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs371255573	chr7:124600704-124600705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77589873	chr7:124600710-124600711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369412552	chr7:124600711-124600712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200256820	chr7:124600714-124600715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113608728	chr7:124600715-124600716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527500637	chr7:124600716-124600717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs193228185	chr7:124600735-124600736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536734705	chr7:124600786-124600787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183346587	chr7:124600797-124600798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74379695	chr7:124600809-124600810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539059638	chr7:124600839-124600840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556165085	chr7:124600854-124600855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569427726	chr7:124600861-124600862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs13307657	chr7:124600864-124600865	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs187242003	chr7:124600869-124600870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376338005	chr7:124600914-124600915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575044595	chr7:124600921-124600922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540830663	chr7:124600927-124600928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73617415	chr7:124600944-124600945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554301795	chr7:124600951-124600952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542066417	chr7:124600985-124600986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78967966	chr7:124601052-124601053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs80088023	chr7:124601059-124601060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs74787645	chr7:124601066-124601067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577305415	chr7:124601074-124601075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545859710	chr7:124601087-124601088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs200490531	chr7:124601094-124601095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534925841	chr7:124601135-124601136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376578133	chr7:124601146-124601147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562932265	chr7:124601260-124601261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs3955485	chr7:124601266-124601267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192098801	chr7:124601272-124601273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370727477	chr7:124601287-124601288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531632289	chr7:124601293-124601294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541689446	chr7:124601298-124601299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557731821	chr7:124601319-124601320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183973733	chr7:124601347-124601348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577787538	chr7:124601348-124601349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561659806	chr7:124601355-124601356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527439648	chr7:124601378-124601379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Autism	20858243	CNVD

Chromatin state (count:225 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124599400-124601000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:124600000-124600600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr7:124600000-124600600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr7:124600400-124602400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:124601000-124601200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:124602400-124602600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:124604800-124605400	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr7:124612400-124612800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr7:124629600-124632600	Weak transcription	Stomach Mucosa	stomach
10	chr7:124629800-124630400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:124630000-124630400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:124630200-124630400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr7:124630200-124630400	Enhancers	Hela-S3	cervix
14	chr7:124630200-124630600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:124630200-124630600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr7:124630200-124630600	Enhancers	NH-A	brain
17	chr7:124630400-124632800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:124630400-124633200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:124630600-124631000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr7:124630600-124631800	Weak transcription	Hela-S3	cervix
21	chr7:124630600-124632200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr7:124630600-124632400	Weak transcription	NH-A	brain
23	chr7:124631000-124631200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:124631000-124631200	Enhancers	Aorta	Aorta
25	chr7:124631200-124632800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr7:124631800-124632800	Enhancers	Hela-S3	cervix
27	chr7:124632200-124633200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:124632400-124632800	Enhancers	NH-A	brain
29	chr7:124632600-124633600	Enhancers	Stomach Mucosa	stomach
30	chr7:124632800-124633000	Flanking Active TSS	Hela-S3	cervix
31	chr7:124632800-124633000	Flanking Active TSS	K562	blood
32	chr7:124632800-124633000	Flanking Active TSS	NH-A	brain
33	chr7:124632800-124633200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr7:124632800-124633200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:124632800-124633200	Enhancers	Osteobl	bone
36	chr7:124632800-124633600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr7:124632800-124633800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:124632800-124633800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr7:124632800-124633800	Enhancers	HUVEC	blood vessel
40	chr7:124633000-124633200	Active TSS	K562	blood
41	chr7:124633000-124633400	Active TSS	Hela-S3	cervix
42	chr7:124633000-124633400	Active TSS	NH-A	brain
43	chr7:124633200-124633600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr7:124633200-124633600	Weak transcription	Aorta	Aorta
45	chr7:124633200-124633600	Flanking Active TSS	K562	blood
46	chr7:124633200-124633600	Active TSS	Osteobl	bone
47	chr7:124633200-124633800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:124633200-124633800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr7:124633200-124634000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:124633200-124634200	Enhancers	Placenta Amnion	Placenta Amnion

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