Variant report

Variant	esv3422481
Chromosome Location	chr7:140623508-140626056
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	chr7:140623843-140624299	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:140624812-140624997	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:140624802-140625293	K562	blood:	n/a	n/a
4	ARID3A	chr7:140623879-140624227	K562	blood:	n/a	n/a
5	ATF1	chr7:140623918-140624307	K562	blood:	n/a	n/a
6	ATF1	chr7:140624621-140625482	K562	blood:	n/a	chr7:140624837-140624851
7	ATF2	chr7:140624582-140625195	GM12878	blood:	n/a	chr7:140624837-140624851 chr7:140624821-140624832
8	ATF2	chr7:140623698-140624350	GM12878	blood:	n/a	n/a
9	ATF2	chr7:140624649-140625145	GM12878	blood:	n/a	chr7:140624837-140624851 chr7:140624821-140624832
10	ATF2	chr7:140623893-140624356	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:140624683-140625079	H1-hESC	embryonic stem cell:	n/a	chr7:140624837-140624851 chr7:140624821-140624832
12	ATF2	chr7:140624665-140625114	H1-hESC	embryonic stem cell:	n/a	chr7:140624837-140624851 chr7:140624821-140624832
13	ATF3	chr7:140624737-140625175	K562	blood:	n/a	chr7:140624820-140624833 chr7:140624821-140624834 chr7:140624839-140624850 chr7:140624822-140624830 chr7:140624839-140624850 chr7:140624823-140624834 chr7:140624820-140624833 chr7:140624821-140624832 chr7:140624797-140624811 chr7:140624811-140624831 chr7:140624840-140624848 chr7:140624822-140624842 chr7:140624819-140624834 chr7:140624823-140624830 chr7:140624819-140624832 chr7:140624823-140624831 chr7:140624798-140624809 chr7:140624821-140624832 chr7:140624822-140624833
14	ATF3	chr7:140624658-140625009	K562	blood:	n/a	chr7:140624820-140624833 chr7:140624821-140624834 chr7:140624839-140624850 chr7:140624822-140624830 chr7:140624839-140624850 chr7:140624823-140624834 chr7:140624820-140624833 chr7:140624821-140624832 chr7:140624797-140624811 chr7:140624811-140624831 chr7:140624840-140624848 chr7:140624822-140624842 chr7:140624819-140624834 chr7:140624823-140624830 chr7:140624819-140624832 chr7:140624823-140624831 chr7:140624798-140624809 chr7:140624821-140624832 chr7:140624822-140624833
15	BACH1	chr7:140623360-140623817	K562	blood:	n/a	n/a
16	BACH1	chr7:140624828-140625131	K562	blood:	n/a	n/a
17	BACH1	chr7:140623915-140624103	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr7:140624721-140624951	GM12878	blood:	n/a	chr7:140624820-140624833
19	BCLAF1	chr7:140623561-140624316	GM12878	blood:	n/a	chr7:140624153-140624162 chr7:140624009-140624018 chr7:140624004-140624017 chr7:140624006-140624015
20	BCLAF1	chr7:140624642-140625063	GM12878	blood:	n/a	chr7:140624922-140624931 chr7:140624738-140624751 chr7:140624748-140624761 chr7:140624787-140624800
21	BHLHE40	chr7:140623720-140625154	GM12878	blood:	n/a	n/a
22	BHLHE40	chr7:140623880-140625144	K562	blood:	n/a	n/a
23	BRCA1	chr7:140624150-140624295	HepG2	liver:	n/a	n/a
24	BRCA1	chr7:140624674-140624965	HepG2	liver:	n/a	n/a
25	BRCA1	chr7:140624672-140625005	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr7:140624744-140625017	GM12878	blood:	n/a	n/a
27	BRCA1	chr7:140623590-140623604	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr7:140623386-140624254	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr7:140623964-140624301	GM12878	blood:	n/a	n/a
30	BRCA1	chr7:140624663-140625314	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr7:140624624-140625356	K562	blood:	n/a	n/a
32	CBX3	chr7:140623753-140624315	K562	blood:	n/a	chr7:140624302-140624313
33	CCNT2	chr7:140623430-140625079	K562	blood:	n/a	chr7:140624139-140624148 chr7:140624016-140624025
34	CEBPB	chr7:140624745-140625226	A549	lung:	n/a	n/a
35	CEBPB	chr7:140624018-140624170	K562	blood:	n/a	chr7:140624050-140624058
36	CEBPB	chr7:140624722-140624997	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr7:140624761-140624980	K562	blood:	n/a	n/a
38	CEBPB	chr7:140624687-140625176	A549	lung:	n/a	n/a
39	CEBPB	chr7:140624672-140625128	K562	blood:	n/a	n/a
40	CEBPB	chr7:140624635-140625224	K562	blood:	n/a	n/a
41	CEBPB	chr7:140624662-140625032	IMR90	lung:	n/a	n/a
42	CEBPB	chr7:140623969-140624164	H1-hESC	embryonic stem cell:	n/a	chr7:140624050-140624058
43	CEBPB	chr7:140624611-140625112	MCF-7	breast:	n/a	n/a
44	CEBPB	chr7:140624674-140625043	HepG2	liver:	n/a	n/a
45	CEBPB	chr7:140623851-140624274	Hela-S3	cervix:	n/a	chr7:140624050-140624058
46	CEBPB	chr7:140624654-140625142	Hela-S3	cervix:	n/a	n/a
47	CEBPD	chr7:140623978-140624271	HepG2	liver:	n/a	n/a
48	CEBPD	chr7:140624283-140624880	HepG2	liver:	n/a	n/a
49	CEBPD	chr7:140623770-140625203	K562	blood:	n/a	n/a
50	CEBPD	chr7:140624282-140625185	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:140625651-140625701	HIPEpiC	eye:	n/a
2	chr7:140625651-140625701	HIPEpiC	eye:	n/a
3	chr7:140624194-140624244	PFSK-1	brain:	n/a
4	chr7:140625651-140625701	SK-N-SH_RA	brain:	n/a
5	chr7:140624194-140624244	HMEC	breast:	n/a
6	chr7:140624470-140624520	HRPEpiC	eye:	n/a
7	chr7:140626003-140626053	PFSK-1	brain:	n/a
8	chr7:140625247-140625297	U87	brain:	n/a
9	chr7:140625365-140625415	SK-N-SH	brain:	n/a
10	chr7:140624462-140624512	T-47D	breast:	n/a
11	chr7:140624462-140624512	AG04449	skin:	fetal
12	chr7:140625106-140625156	GM06990	blood:	n/a
13	chr7:140625651-140625701	ECC-1	luminal epithelium:	n/a
14	chr7:140625247-140625297	AG04449	skin:	fetal
15	chr7:140624470-140624520	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:140624470-140624520	AoSMC	blood vessel:	n/a
17	chr7:140624976-140625026	HEK293	kidney:	embryo
18	chr7:140624462-140624512	HEK293	kidney:	embryo
19	chr7:140624470-140624520	HAEpiC	amniotic membrane:	n/a
20	chr7:140623924-140623974	RPTEC	kidney:	n/a
21	chr7:140625106-140625156	PANC-1	pancreas:	n/a
22	chr7:140625510-140625560	LNCaP	prostate:	n/a
23	chr7:140623924-140623974	GM12878	blood:	n/a
24	chr7:140624462-140624512	ovcar-3	ovarian:	n/a
25	chr7:140625365-140625415	Caco-2	colon:	n/a
26	chr7:140626003-140626053	ECC-1	luminal epithelium:	n/a
27	chr7:140625365-140625415	BJ	skin:	n/a
28	chr7:140624468-140624518	SAEC	small airway:	n/a
29	chr7:140623924-140623974	HCM	heart:	n/a
30	chr7:140626003-140626053	HMEC	breast:	n/a
31	chr7:140624468-140624518	RPTEC	kidney:	n/a
32	chr7:140624468-140624518	SKMC	muscle:	n/a
33	chr7:140624194-140624244	SK-N-MC	brain:	n/a
34	chr7:140625510-140625560	HRPEpiC	eye:	n/a
35	chr7:140624057-140624107	GM12892	blood:	n/a
36	chr7:140624462-140624512	GM12892	blood:	n/a
37	chr7:140624905-140624955	Hepatocyte	liver:	n/a
38	chr7:140625247-140625297	ProgFib	skin:	n/a
39	chr7:140625365-140625415	SAEC	small airway:	n/a
40	chr7:140625783-140625833	GM12892	blood:	n/a
41	chr7:140625510-140625560	GM12878	blood:	n/a
42	chr7:140624976-140625026	HRPEpiC	eye:	n/a
43	chr7:140625365-140625415	LNCaP	prostate:	n/a
44	chr7:140624057-140624107	HCM	heart:	n/a
45	chr7:140624468-140624518	NHDF-neo	bronchial:	n/a
46	chr7:140624468-140624518	BJ	skin:	n/a
47	chr7:140624470-140624520	NT2-D1	testis:	n/a
48	chr7:140624470-140624520	NHDF-neo	bronchial:	n/a
49	chr7:140623924-140623974	GM19239	blood:	n/a
50	chr7:140625510-140625560	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:140625504..140628313-chr7:140642636..140644756,2	K562	blood:
2	chr7:140532465..140534919-chr7:140622566..140624357,2	K562	blood:
3	chr7:140621424..140625828-chr7:140713150..140716057,6	K562	blood:
4	chr7:140395805..140398704-chr7:140623265..140626329,4	K562	blood:
5	chr11:62608794..62609409-chr7:140624415..140625261,2	NB4	blood:
6	chr7:140621971..140623569-chr7:140707032..140709391,2	MCF-7	breast:
7	chr7:140554945..140557362-chr7:140625940..140628286,2	K562	blood:
8	chr7:140624883..140626746-chr7:140635141..140637023,2	K562	blood:
9	chr7:77325504..77326093-chr7:140624035..140624792,2	NB4	blood:
10	chr7:140621424..140625988-chr7:140712136..140716057,7	K562	blood:
11	chr7:140395267..140398426-chr7:140622802..140626309,6	K562	blood:
12	chr7:140621726..140624133-chr7:141216889..141219173,2	K562	blood:
13	chr7:140572911..140575551-chr7:140622620..140624458,2	MCF-7	breast:
14	chr7:140624233..140624974-chr9:33510596..33511369,2	NB4	blood:
15	chr7:140625343..140628260-chr7:140713839..140715821,2	MCF-7	breast:

Variant related genes	Relation type
BRAF	TF binding region
BRAF	CpG island
ENSG00000240889	chromatin interactions
ENSG00000226823	chromatin interactions
ENSG00000187257	chromatin interactions
ENSG00000090266	chromatin interactions
ENSG00000090263	chromatin interactions
ENSG00000214293	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 109 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:109 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143786335	chr7:140623527-140623528	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs377019772	chr7:140623531-140623532	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs6968623	chr7:140623555-140623556	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs71645940	chr7:140623630-140623631	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs566088303	chr7:140623703-140623704	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs71645939	chr7:140623712-140623713	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs145862578	chr7:140623784-140623785	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs533642336	chr7:140623843-140623844	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs182862184	chr7:140623874-140623875	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs187538177	chr7:140623879-140623880	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs568887381	chr7:140623882-140623883	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs529722201	chr7:140623898-140623899	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs548175241	chr7:140623930-140623931	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs566795675	chr7:140624046-140624047	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs534059228	chr7:140624076-140624077	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs371851738	chr7:140624079-140624080	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs558822460	chr7:140624095-140624096	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs192417684	chr7:140624106-140624107	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs538385194	chr7:140624118-140624119	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs556387066	chr7:140624128-140624129	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs71645938	chr7:140624140-140624141	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs541840926	chr7:140624149-140624150	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs549752436	chr7:140624201-140624202	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs550987073	chr7:140624204-140624205	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs71645937	chr7:140624205-140624206	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs553726719	chr7:140624245-140624246	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs572436924	chr7:140624262-140624263	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs546076145	chr7:140624286-140624287	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs571199067	chr7:140624300-140624301	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs548737688	chr7:140624311-140624312	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs373133922	chr7:140624314-140624315	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs397515331	chr7:140624403-140624404	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs397507459	chr7:140624404-140624405	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs397516906	chr7:140624412-140624413	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs371877084	chr7:140624426-140624427	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs397507457	chr7:140624428-140624429	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs543953468	chr7:140624438-140624439	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs397507456	chr7:140624440-140624441	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs397507455	chr7:140624463-140624464	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs397507454	chr7:140624468-140624469	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs562457397	chr7:140624502-140624503	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs71645936	chr7:140624508-140624509	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs397507453	chr7:140624521-140624522	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs71645935	chr7:140624522-140624523	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs560175142	chr7:140624621-140624622	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs527625447	chr7:140624627-140624628	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs71645934	chr7:140624676-140624677	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs570681770	chr7:140624696-140624697	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs71645933	chr7:140624738-140624739	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs71645932	chr7:140624765-140624766	Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	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
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140620200-140625400	Active TSS	GM12878-XiMat	blood
2	chr7:140620800-140625200	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr7:140622000-140623600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:140622000-140625400	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr7:140622200-140623800	Flanking Active TSS	Dnd41	blood
6	chr7:140622200-140625600	Active TSS	Breast Myoepithelial Primary Cells	Breast
7	chr7:140622400-140623800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:140622400-140624000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:140622600-140623800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:140622600-140624000	Flanking Active TSS	Primary B cells from cord blood	blood
11	chr7:140622600-140624000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
12	chr7:140622600-140624000	Active TSS	Right Atrium	heart
13	chr7:140622600-140625200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:140622600-140625200	Active TSS	Fetal Intestine Large	intestine
15	chr7:140622600-140625400	Active TSS	Aorta	Aorta
16	chr7:140622600-140625400	Active TSS	Colonic Mucosa	Colon
17	chr7:140622600-140625400	Active TSS	Fetal Brain Female	brain
18	chr7:140622600-140625600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr7:140622800-140623600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr7:140622800-140624800	Active TSS	HMEC	breast
21	chr7:140622800-140625200	Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr7:140622800-140625400	Active TSS	NHLF	lung
23	chr7:140622800-140625600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr7:140622800-140625600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr7:140622800-140625600	Active TSS	K562	blood
26	chr7:140623000-140623600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr7:140623000-140623600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
28	chr7:140623000-140623600	Active TSS	Brain Germinal Matrix	brain
29	chr7:140623000-140623600	Flanking Active TSS	Duodenum Mucosa	Duodenum
30	chr7:140623000-140623600	Flanking Active TSS	Fetal Kidney	kidney
31	chr7:140623000-140623600	Flanking Active TSS	NHEK	skin
32	chr7:140623000-140623800	Flanking Active TSS	HUVEC	blood vessel
33	chr7:140623000-140625000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:140623000-140625200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:140623000-140625200	Active TSS	A549	lung
36	chr7:140623000-140625200	Active TSS	Hela-S3	cervix
37	chr7:140623000-140625400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr7:140623000-140625600	Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr7:140623000-140625600	Active TSS	Brain Anterior Caudate	brain
40	chr7:140623000-140625600	Active TSS	Duodenum Smooth Muscle	Duodenum
41	chr7:140623200-140623600	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:140623200-140623600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr7:140623200-140623600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr7:140623200-140623600	Flanking Active TSS	Adipose Nuclei	Adipose
45	chr7:140623200-140623600	Flanking Active TSS	Brain Cingulate Gyrus	brain
46	chr7:140623200-140623600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
47	chr7:140623200-140623600	Flanking Active TSS	Fetal Muscle Leg	muscle
48	chr7:140623200-140623600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr7:140623200-140623600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
50	chr7:140623200-140623600	Flanking Active TSS	HSMM	muscle

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