Variant report

Variant	nsv608003
Chromosome Location	chr7:102105566-102110938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102107670-102107707	HepG2	liver:	n/a	n/a
2	ATF2	chr7:102105214-102105642	GM12878	blood:	n/a	n/a
3	ATF3	chr7:102105079-102105666	K562	blood:	n/a	chr7:102105134-102105143
4	BACH1	chr7:102105152-102105627	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:102105195-102105583	K562	blood:	n/a	n/a
6	BATF	chr7:102106969-102107235	GM12878	blood:	n/a	chr7:102107141-102107152
7	BCL3	chr7:102105600-102105954	A549	lung:	n/a	n/a
8	BCLAF1	chr7:102105109-102105696	K562	blood:	n/a	n/a
9	BCLAF1	chr7:102105007-102105737	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:102105028-102105670	K562	blood:	n/a	chr7:102105343-102105359 chr7:102105409-102105425
11	BRCA1	chr7:102107666-102107866	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr7:102105131-102105589	HepG2	liver:	n/a	n/a
13	BRCA1	chr7:102107676-102107680	HepG2	liver:	n/a	n/a
14	CBX3	chr7:102104440-102105788	K562	blood:	n/a	n/a
15	CCNT2	chr7:102105109-102105718	K562	blood:	n/a	n/a
16	CCNT2	chr7:102109140-102109266	K562	blood:	n/a	n/a
17	CEBPB	chr7:102105268-102105644	Hela-S3	cervix:	n/a	n/a
18	CEBPD	chr7:102105226-102105633	HepG2	liver:	n/a	n/a
19	CHD1	chr7:102105332-102105854	GM12878	blood:	n/a	n/a
20	CHD1	chr7:102105968-102105976	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr7:102104946-102105631	HepG2	liver:	n/a	n/a
22	CHD2	chr7:102105044-102105606	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr7:102105035-102105755	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr7:102104973-102105628	GM12878	blood:	n/a	n/a
25	CHD2	chr7:102107547-102107747	GM12878	blood:	n/a	n/a
26	CREB1	chr7:102105108-102105614	A549	lung:	n/a	n/a
27	CREB1	chr7:102105174-102105661	ECC-1	luminal epithelium:	n/a	n/a
28	CREB1	chr7:102104730-102105812	HepG2	liver:	n/a	n/a
29	CTCF	chr7:102105420-102105570	GM12873	blood:	n/a	n/a
30	CTCF	chr7:102105440-102105590	SAEC	small airway:	n/a	n/a
31	CTCF	chr7:102107640-102107790	NHDF-neo	bronchial:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
32	CTCF	chr7:102107660-102107810	WI-38	lung:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
33	CTCF	chr7:102107660-102107810	HFF-Myc	foreskin:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
34	CTCF	chr7:102107620-102107770	HepG2	liver:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
35	CTCF	chr7:102107600-102107750	HRPEpiC	eye:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
36	CTCF	chr7:102107580-102107730	GM12869	blood:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
37	CTCF	chr7:102107680-102107830	HMF	breast:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
38	CTCF	chr7:102107540-102107544	ProgFib	skin:	n/a	n/a
39	CTCF	chr7:102105460-102105610	GM12874	blood:	n/a	n/a
40	CTCF	chr7:102105740-102105890	GM12875	blood:	n/a	n/a
41	CTCF	chr7:102107559-102107801	MCF-7	breast:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
42	CTCF	chr7:102107660-102107810	Hela-S3	cervix:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
43	CTCF	chr7:102107625-102107775	HepG2	liver:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
44	CTCF	chr7:102107360-102107510	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr7:102107640-102107790	MCF-7	breast:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
46	CTCF	chr7:102107380-102107530	GM12873	blood:	n/a	n/a
47	CTCF	chr7:102107640-102107790	WI-38	lung:	n/a	chr7:102107690-102107711 chr7:102107688-102107706 chr7:102107691-102107704 chr7:102107689-102107705 chr7:102107691-102107699
48	CTCF	chr7:102105720-102105870	BJ	skin:	n/a	n/a
49	CTCF	chr7:102105440-102105590	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr7:102107340-102107490	WI-38	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102107737-102107787	NHDF-neo	bronchial:	n/a
2	chr7:102107737-102107787	NHDF-neo	bronchial:	n/a
3	chr7:102109446-102109496	HCT-116	colon:	n/a
4	chr7:102105781-102105831	HCF	heart:	n/a
5	chr7:102109247-102109297	HRCEpiC	kidney:	n/a
6	chr7:102107737-102107787	HMEC	breast:	n/a
7	chr7:102109247-102109297	HL-60	blood:	n/a
8	chr7:102105781-102105831	LNCaP	prostate:	n/a
9	chr7:102109446-102109496	HAEpiC	amniotic membrane:	n/a
10	chr7:102107737-102107787	Caco-2	colon:	n/a
11	chr7:102105641-102105691	HMEC	breast:	n/a
12	chr7:102109446-102109496	HCM	heart:	n/a
13	chr7:102105753-102105803	HNPCEpiC	eye:	n/a
14	chr7:102105641-102105691	Hepatocyte	liver:	n/a
15	chr7:102105781-102105831	NT2-D1	testis:	n/a
16	chr7:102109247-102109297	PFSK-1	brain:	n/a
17	chr7:102105781-102105831	Jurkat	blood:	n/a
18	chr7:102105753-102105803	K562	blood:	n/a
19	chr7:102105781-102105831	AG09309	skin:	n/a
20	chr7:102109446-102109496	MCF10A-Er-Src	breast:	n/a
21	chr7:102109095-102109145	PFSK-1	brain:	n/a
22	chr7:102109446-102109496	GM12892	blood:	n/a
23	chr7:102105781-102105831	AG09319	gingival:	n/a
24	chr7:102109247-102109297	BE2_C	brain:	n/a
25	chr7:102109247-102109297	SK-N-MC	brain:	n/a
26	chr7:102109247-102109297	HCT-116	colon:	n/a
27	chr7:102105781-102105831	A549	lung:	n/a
28	chr7:102109446-102109496	SK-N-SH	brain:	n/a
29	chr7:102105781-102105831	HEK293	kidney:	embryo
30	chr7:102109446-102109496	HL-60	blood:	n/a
31	chr7:102105641-102105691	LNCaP	prostate:	n/a
32	chr7:102109446-102109496	HRCEpiC	kidney:	n/a
33	chr7:102109247-102109297	RPTEC	kidney:	n/a
34	chr7:102109247-102109297	Hepatocyte	liver:	n/a
35	chr7:102109446-102109496	Caco-2	colon:	n/a
36	chr7:102105641-102105691	GM12891	blood:	n/a
37	chr7:102105781-102105831	HMEC	breast:	n/a
38	chr7:102105641-102105691	HCT-116	colon:	n/a
39	chr7:102107737-102107787	PANC-1	pancreas:	n/a
40	chr7:102105641-102105691	HCPEpiC	choroid plexus:	n/a
41	chr7:102107737-102107787	ProgFib	skin:	n/a
42	chr7:102109247-102109297	IMR90	lung:	fetal
43	chr7:102109446-102109496	AG10803	skin:	n/a
44	chr7:102109446-102109496	Hela-S3	cervix:	n/a
45	chr7:102105781-102105831	T-47D	breast:	n/a
46	chr7:102107737-102107787	AG04449	skin:	fetal
47	chr7:102107737-102107787	RPTEC	kidney:	n/a
48	chr7:102109095-102109145	T-47D	breast:	n/a
49	chr7:102109446-102109496	HepG2	liver:	n/a
50	chr7:102107737-102107787	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:101929851..101931493-chr7:102106221..102107741,2	MCF-7	breast:
2	chr7:101935058..101937626-chr7:102103527..102105838,2	MCF-7	breast:
3	chr7:102073875..102075484-chr7:102103725..102106348,2	MCF-7	breast:
4	chr7:102035604..102038403-chr7:102105375..102107150,2	K562	blood:
5	chr7:102074336..102076927-chr7:102105688..102108273,2	K562	blood:
6	chr6:82462024..82463020-chr7:102105257..102105953,2	NB4	blood:
7	chr16:90039038..90039558-chr7:102105289..102105810,2	Hela-S3	cervix:
8	chr7:102110628..102112535-chr8:144951000..144953117,2	MCF-7	breast:
9	chr7:102085730..102086410-chr7:102110585..102111557,2	K562	blood:
10	chr7:102110592..102113197-chr7:102117853..102119354,2	MCF-7	breast:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5090	chr7:102106199-102106221	MIMAT0021082

Variant related genes	Relation type
MIR5090	TF binding region
MIR4467	TF binding region
LRWD1	TF binding region
ALKBH4	TF binding region
MIR5090	CpG island
MIR4467	CpG island
LRWD1	CpG island
ALKBH4	CpG island
ENSG00000112773	chromatin interactions
ENSG00000005075	chromatin interactions
ENSG00000223959	chromatin interactions
ENSG00000227184	chromatin interactions
ENSG00000264675	chromatin interactions
ENSG00000128563	chromatin interactions
ENSG00000239480	chromatin interactions
ENSG00000160991	chromatin interactions

Extended variants
information (count: 341 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79978502	chr7:102105566-102105567	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs553520557	chr7:102105593-102105594	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs571987032	chr7:102105617-102105618	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs113009525	chr7:102105620-102105621	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs542580225	chr7:102105671-102105672	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs142288913	chr7:102105682-102105683	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs576315564	chr7:102105704-102105705	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs543596956	chr7:102105713-102105714	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs565070541	chr7:102105714-102105715	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs375932908	chr7:102105782-102105783	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs533306289	chr7:102105789-102105790	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs118047026	chr7:102105828-102105829	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	mRNA abundance
13	rs10953367	chr7:102105916-102105917	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs576550297	chr7:102105936-102105937	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs10953368	chr7:102105984-102105985	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs542769824	chr7:102106013-102106014	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs73712497	chr7:102106050-102106051	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs560838083	chr7:102106055-102106056	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs183948178	chr7:102106057-102106058	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs146877659	chr7:102106092-102106093	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs549999146	chr7:102106113-102106114	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs567975415	chr7:102106158-102106159	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs538380556	chr7:102106167-102106168	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs3823658	chr7:102106201-102106202	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region miRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs532015107	chr7:102106217-102106218	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region miRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs111295263	chr7:102106224-102106225	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs187641533	chr7:102106234-102106235	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs368120898	chr7:102106238-102106239	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs370869046	chr7:102106239-102106240	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs147183285	chr7:102106265-102106266	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs200711890	chr7:102106277-102106278	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs11538919	chr7:102106306-102106307	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs550399566	chr7:102106309-102106310	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs200209552	chr7:102106310-102106311	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs370174818	chr7:102106319-102106320	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs117376828	chr7:102106362-102106363	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs151171497	chr7:102106369-102106370	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs371342787	chr7:102106371-102106372	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs11538921	chr7:102106375-102106376	Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs139115115	chr7:102106412-102106413	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs571827042	chr7:102106426-102106427	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs572352133	chr7:102106433-102106434	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs201713941	chr7:102106434-102106435	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs143977682	chr7:102106444-102106445	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs560935249	chr7:102106453-102106454	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs146433593	chr7:102106459-102106460	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs140741148	chr7:102106462-102106463	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs138888097	chr7:102106483-102106484	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs373947079	chr7:102106559-102106560	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs118132583	chr7:102106567-102106568	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:630 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102104000-102106200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:102104000-102106400	Flanking Active TSS	Primary hematopoietic stem cells	blood
3	chr7:102104200-102105800	Active TSS	Muscle Satellite Cultured Cells	--
4	chr7:102104200-102106000	Active TSS	Fetal Kidney	kidney
5	chr7:102104200-102106200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr7:102104200-102106200	Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr7:102104200-102106400	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr7:102104200-102106400	Active TSS	H9 Cell Line	embryonic stem cell
9	chr7:102104200-102106400	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr7:102104200-102106600	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr7:102104400-102106200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
12	chr7:102104400-102106200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:102104400-102106200	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr7:102104400-102106400	Active TSS	NHDF-Ad	bronchial
15	chr7:102104400-102106600	Active TSS	H1 Cell Line	embryonic stem cell
16	chr7:102104400-102106800	Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr7:102104600-102105800	Active TSS	HMEC	breast
18	chr7:102104600-102106000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:102104600-102106000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:102104600-102106000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:102104600-102106000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:102104600-102106000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:102104600-102106000	Active TSS	Aorta	Aorta
24	chr7:102104600-102106000	Active TSS	Brain Hippocampus Middle	brain
25	chr7:102104600-102106000	Active TSS	Sigmoid Colon	Sigmoid Colon
26	chr7:102104600-102106000	Bivalent/Poised TSS	HepG2	liver
27	chr7:102104600-102106000	Active TSS	HUVEC	blood vessel
28	chr7:102104600-102106000	Active TSS	K562	blood
29	chr7:102104600-102106000	Active TSS	Osteobl	bone
30	chr7:102104600-102106200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr7:102104600-102106200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr7:102104600-102106200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr7:102104600-102106200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:102104600-102106200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr7:102104600-102106200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr7:102104600-102106200	Active TSS	Fetal Intestine Large	intestine
37	chr7:102104600-102106200	Active TSS	Gastric	stomach
38	chr7:102104600-102106200	Active TSS	Lung	lung
39	chr7:102104600-102106200	Active TSS	Stomach Mucosa	stomach
40	chr7:102104600-102106200	Active TSS	A549	lung
41	chr7:102104600-102106200	Active TSS	GM12878-XiMat	blood
42	chr7:102104600-102106200	Active TSS	HSMM	muscle
43	chr7:102104600-102106200	Active TSS	HSMMtube	muscle
44	chr7:102104600-102106200	Active TSS	NHLF	lung
45	chr7:102104600-102106400	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr7:102104600-102106800	Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr7:102104800-102105600	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr7:102104800-102105800	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
49	chr7:102104800-102105800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr7:102104800-102105800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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