Variant report

Variant	esv3417343
Chromosome Location	chr7:105027966-105030814
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:576)
CpG islands
(count:611)
Chromatin interactive
region (count:21)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:105028117-105028318	K562	blood:	n/a	n/a
2	ARID3A	chr7:105029792-105030248	HepG2	liver:	n/a	n/a
3	BACH1	chr7:105027844-105028042	K562	blood:	n/a	n/a
4	BACH1	chr7:105029014-105029308	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:105028171-105028753	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:105029716-105030051	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr7:105029124-105029187	K562	blood:	n/a	n/a
8	BHLHE40	chr7:105029678-105029984	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:105028285-105028701	K562	blood:	n/a	chr7:105028425-105028441
10	BHLHE40	chr7:105029661-105030115	K562	blood:	n/a	chr7:105029666-105029682
11	BHLHE40	chr7:105028352-105028581	GM12878	blood:	n/a	chr7:105028425-105028441
12	BRCA1	chr7:105029780-105029800	GM12878	blood:	n/a	n/a
13	BRCA1	chr7:105029695-105029834	HepG2	liver:	n/a	n/a
14	CCNT2	chr7:105028142-105029984	K562	blood:	n/a	chr7:105028594-105028603 chr7:105029564-105029573
15	CEBPB	chr7:105030782-105031053	K562	blood:	n/a	n/a
16	CHD1	chr7:105029068-105029333	GM12878	blood:	n/a	n/a
17	CHD2	chr7:105029562-105029963	K562	blood:	n/a	n/a
18	CHD2	chr7:105028470-105029337	K562	blood:	n/a	chr7:105028809-105028816
19	CHD2	chr7:105028537-105029884	Hela-S3	cervix:	n/a	chr7:105028809-105028816
20	CHD2	chr7:105029672-105030039	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr7:105028349-105028549	HepG2	liver:	n/a	n/a
22	CHD2	chr7:105028747-105029206	GM12878	blood:	n/a	chr7:105028809-105028816
23	CHD2	chr7:105029054-105029301	HepG2	liver:	n/a	n/a
24	CHD2	chr7:105028531-105028711	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr7:105028300-105028500	GM12878	blood:	n/a	n/a
26	CHD2	chr7:105029588-105030003	HepG2	liver:	n/a	n/a
27	CHD2	chr7:105029647-105029883	GM12878	blood:	n/a	n/a
28	CREB1	chr7:105029014-105029418	A549	lung:	n/a	n/a
29	CREB1	chr7:105028127-105028892	HepG2	liver:	n/a	n/a
30	CTCF	chr7:105029740-105029890	AG10803	skin:	n/a	n/a
31	CTCF	chr7:105028180-105028330	AG04450	lung:	n/a	n/a
32	CTCF	chr7:105029700-105029850	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr7:105029760-105029910	AG09319	gingival:	n/a	n/a
34	CTCF	chr7:105029660-105029810	A549	lung:	n/a	n/a
35	CTCF	chr7:105028126-105028398	IMR90	lung:	n/a	n/a
36	CTCF	chr7:105028248-105028307	GM19238	blood:	n/a	n/a
37	CTCF	chr7:105029080-105029230	AG04449	skin:	n/a	n/a
38	CTCF	chr7:105029860-105030010	HAc	cerebellar:	n/a	n/a
39	CTCF	chr7:105029840-105029990	HMEC	breast:	n/a	n/a
40	CTCF	chr7:105028020-105028170	AG04450	lung:	n/a	n/a
41	CTCF	chr7:105028106-105028405	K562	blood:	n/a	n/a
42	CTCF	chr7:105028180-105028330	RPTEC	kidney:	n/a	n/a
43	CTCF	chr7:105028180-105028330	AG09319	gingival:	n/a	n/a
44	CTCF	chr7:105029780-105029930	AG10803	skin:	n/a	n/a
45	CTCF	chr7:105028260-105028410	GM12867	blood:	n/a	n/a
46	CTCF	chr7:105029800-105029950	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr7:105028340-105028490	GM12866	blood:	n/a	n/a
48	CTCF	chr7:105028191-105028365	A549	lung:	n/a	n/a
49	CTCF	chr7:105028180-105028330	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr7:105029760-105029910	HPAF	blood vessel:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105029385-105029435	AG09309	skin:	n/a
2	chr7:105029385-105029435	AG09309	skin:	n/a
3	chr7:105029499-105029549	HCM	heart:	n/a
4	chr7:105029492-105029542	A549	lung:	n/a
5	chr7:105030168-105030218	Hela-S3	cervix:	n/a
6	chr7:105029499-105029549	HRPEpiC	eye:	n/a
7	chr7:105029485-105029535	IMR90	lung:	fetal
8	chr7:105029125-105029175	RPTEC	kidney:	n/a
9	chr7:105030168-105030218	A549	lung:	n/a
10	chr7:105029385-105029435	SK-N-SH	brain:	n/a
11	chr7:105029499-105029549	ECC-1	luminal epithelium:	n/a
12	chr7:105028539-105028589	ECC-1	luminal epithelium:	n/a
13	chr7:105029125-105029175	SK-N-SH	brain:	n/a
14	chr7:105029385-105029435	U87	brain:	n/a
15	chr7:105029385-105029435	PANC-1	pancreas:	n/a
16	chr7:105029497-105029547	H1-hESC	embryonic stem cell:	embryo
17	chr7:105029492-105029542	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:105028539-105028589	HRPEpiC	eye:	n/a
19	chr7:105030168-105030218	AG04449	skin:	fetal
20	chr7:105029125-105029175	AG09319	gingival:	n/a
21	chr7:105029125-105029175	SK-N-MC	brain:	n/a
22	chr7:105028539-105028589	GM12891	blood:	n/a
23	chr7:105029499-105029549	NHBE	bronchial:	n/a
24	chr7:105029499-105029549	PANC-1	pancreas:	n/a
25	chr7:105029895-105029945	GM06990	blood:	n/a
26	chr7:105028539-105028589	HCF	heart:	n/a
27	chr7:105029499-105029549	GM12892	blood:	n/a
28	chr7:105029499-105029549	HUVEC	blood vessel:	n/a
29	chr7:105030168-105030218	HAEpiC	amniotic membrane:	n/a
30	chr7:105029492-105029542	BJ	skin:	n/a
31	chr7:105030752-105030802	SK-N-SH	brain:	n/a
32	chr7:105028539-105028589	U87	brain:	n/a
33	chr7:105029385-105029435	GM19239	blood:	n/a
34	chr7:105029492-105029542	GM06990	blood:	n/a
35	chr7:105029492-105029542	NT2-D1	testis:	n/a
36	chr7:105029125-105029175	Hepatocyte	liver:	n/a
37	chr7:105029385-105029435	GM12891	blood:	n/a
38	chr7:105029497-105029547	ECC-1	luminal epithelium:	n/a
39	chr7:105029497-105029547	GM19239	blood:	n/a
40	chr7:105028539-105028589	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:105030752-105030802	HRPEpiC	eye:	n/a
42	chr7:105029492-105029542	HEK293	kidney:	embryo
43	chr7:105029492-105029542	HL-60	blood:	n/a
44	chr7:105030752-105030802	AG04450	lung:	fetal
45	chr7:105030752-105030802	HNPCEpiC	eye:	n/a
46	chr7:105030752-105030802	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:105030752-105030802	HEK293	kidney:	embryo
48	chr7:105029497-105029547	MCF-7	breast:	n/a
49	chr7:105029492-105029542	NB4	blood:	n/a
50	chr7:105029385-105029435	SK-N-MC	brain:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:104971088..104973665-chr7:105027778..105030280,2	K562	blood:
2	chr5:144628686..144629379-chr7:105027367..105028166,2	MCF-7	breast:
3	chr7:104757007..104759673-chr7:105027481..105029991,2	MCF-7	breast:
4	chr7:105030763..105032789-chr7:105035167..105036681,2	K562	blood:
5	chr7:105026529..105029377-chr7:105162488..105165118,2	MCF-7	breast:
6	chr7:105027932..105031943-chr7:105036648..105042469,7	K562	blood:
7	chr7:105028215..105030486-chr7:105171271..105172847,2	K562	blood:
8	chr7:104650837..104656019-chr7:105026206..105030997,7	K562	blood:
9	chr7:105027206..105036314-chr7:105036751..105044757,13	K562	blood:
10	chr7:104652744..104654842-chr7:105028526..105031470,2	MCF-7	breast:
11	chr7:104652893..104655901-chr7:105027705..105031319,8	MCF-7	breast:
12	chr7:104649601..104653676-chr7:105029497..105032094,4	K562	blood:
13	chr7:104653211..104654776-chr7:105027099..105029228,2	K562	blood:
14	chr7:104715799..104718256-chr7:105026783..105029016,2	K562	blood:
15	chr7:105027174..105029032-chr7:105171146..105173908,2	K562	blood:
16	chr7:105019571..105021474-chr7:105027326..105029018,2	MCF-7	breast:
17	chr7:105029252..105029910-chr9:3525726..3526715,2	NB4	blood:
18	chr7:105027746..105030082-chr7:105160759..105163665,5	MCF-7	breast:
19	chr7:105029590..105031238-chr7:105038445..105041248,2	MCF-7	breast:
20	chr7:104937663..104939344-chr7:105026759..105029557,2	MCF-7	breast:
21	chr7:105007315..105010553-chr7:105026431..105029268,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRPK2-5	chr7:105029095-105029149	NONHSAT122614
2	lnc-SRPK2-5	chr7:105029691-105029837	NONHSAT122614

No data

Variant related genes	Relation type
SRPK2	TF binding region
SRPK2	CpG island
ENSG00000239569	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000201179	chromatin interactions
ENSG00000080298	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000135250	chromatin interactions

Extended variants
information (count: 113 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:113 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs398067142	chr7:105027972-105027973	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs572516409	chr7:105028028-105028029	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs374909203	chr7:105028042-105028043	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs4727620	chr7:105028132-105028133	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs566000919	chr7:105028135-105028136	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs368758746	chr7:105028139-105028140	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs528387742	chr7:105028160-105028161	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs181506703	chr7:105028164-105028165	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs568118569	chr7:105028167-105028168	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs537008509	chr7:105028189-105028190	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs185698630	chr7:105028196-105028197	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs62484715	chr7:105028219-105028220	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs367732914	chr7:105028233-105028234	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs3087867	chr7:105028238-105028239	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs370225352	chr7:105028248-105028249	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs540057917	chr7:105028278-105028279	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs376208093	chr7:105028293-105028294	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs553305828	chr7:105028336-105028337	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs573446286	chr7:105028362-105028363	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs4727621	chr7:105028370-105028371	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs113706131	chr7:105028380-105028381	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs556053144	chr7:105028425-105028426	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs574523916	chr7:105028492-105028493	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs543436767	chr7:105028500-105028501	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs563427165	chr7:105028540-105028541	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs556502970	chr7:105028581-105028582	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs374082321	chr7:105028628-105028629	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs576850566	chr7:105028645-105028646	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs545851430	chr7:105028659-105028660	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs559308820	chr7:105028660-105028661	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs377154706	chr7:105028707-105028708	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs548089219	chr7:105028763-105028764	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs561640123	chr7:105028818-105028819	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs530861424	chr7:105028829-105028830	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs1917046	chr7:105028838-105028839	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs550683536	chr7:105028850-105028851	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs6978496	chr7:105028852-105028853	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs539571030	chr7:105028936-105028937	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs560402880	chr7:105028953-105028954	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs372623675	chr7:105029032-105029033	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs567077075	chr7:105029076-105029077	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs201468375	chr7:105029079-105029080	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs146307731	chr7:105029121-105029122	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
44	rs368165566	chr7:105029134-105029135	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
45	rs139958323	chr7:105029137-105029138	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
46	rs202092463	chr7:105029163-105029164	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs373130871	chr7:105029166-105029167	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs369530914	chr7:105029176-105029177	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs372921365	chr7:105029190-105029191	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs201149905	chr7:105029199-105029200	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
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
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16573809	CNVD
Myxofibrosarcoma	20639860	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104995200-105028200	Weak transcription	Esophagus	oesophagus
2	chr7:104995400-105028000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:105000000-105028200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:105008200-105028200	Weak transcription	Pancreas	Pancrea
5	chr7:105009200-105028000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr7:105009200-105028000	Weak transcription	Psoas Muscle	Psoas
7	chr7:105018000-105028000	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr7:105018200-105028000	Weak transcription	Left Ventricle	heart
9	chr7:105018600-105028000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr7:105020800-105028000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr7:105025800-105028000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:105026200-105028200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr7:105026400-105028200	Weak transcription	Gastric	stomach
14	chr7:105026400-105028200	Weak transcription	Spleen	Spleen
15	chr7:105027200-105028000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:105027200-105028000	Enhancers	Primary B cells from peripheral blood	blood
17	chr7:105027200-105028000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr7:105027200-105028000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr7:105027200-105028000	Enhancers	Fetal Heart	heart
20	chr7:105027200-105028200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
21	chr7:105027200-105028200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
22	chr7:105027200-105028200	Flanking Active TSS	Dnd41	blood
23	chr7:105027200-105028600	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr7:105027200-105030000	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr7:105027400-105028000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:105027400-105028000	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr7:105027400-105028000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:105027400-105028000	Enhancers	Brain Angular Gyrus	brain
29	chr7:105027400-105028000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr7:105027400-105028000	Enhancers	Fetal Brain Male	brain
31	chr7:105027400-105028000	Active TSS	Rectal Mucosa Donor 29	rectum
32	chr7:105027400-105028000	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr7:105027400-105028200	Flanking Active TSS	Primary T cells from cord blood	blood
34	chr7:105027400-105028200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr7:105027400-105028200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:105027400-105028200	Flanking Active TSS	Osteobl	bone
37	chr7:105027400-105028400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:105027600-105028000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
39	chr7:105027600-105028000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr7:105027600-105028000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr7:105027600-105028000	Weak transcription	Brain Germinal Matrix	brain
42	chr7:105027600-105028000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr7:105027600-105028000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr7:105027600-105028000	Enhancers	Rectal Smooth Muscle	rectum
45	chr7:105027600-105028200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
46	chr7:105027600-105028200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr7:105027600-105028200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
48	chr7:105027600-105028200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
49	chr7:105027600-105028200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr7:105027600-105028200	Flanking Active TSS	A549	lung

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