Variant report

Variant	nsv435860
Chromosome Location	chr7:150923672-150930735
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1202)
CpG islands
(count:1648)
Chromatin interactive
region (count:28)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:150924259-150924615	K562	blood:	n/a	n/a
2	ARID3A	chr7:150924252-150924739	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:150929395-150929595	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:150929347-150929672	K562	blood:	n/a	n/a
5	ATF1	chr7:150924104-150924929	K562	blood:	n/a	n/a
6	ATF2	chr7:150929355-150929798	GM12878	blood:	n/a	n/a
7	ATF3	chr7:150924061-150924797	K562	blood:	n/a	chr7:150924452-150924463 chr7:150924442-150924462 chr7:150924453-150924473
8	ATF3	chr7:150924238-150924662	K562	blood:	n/a	chr7:150924452-150924463 chr7:150924442-150924462 chr7:150924453-150924473
9	ATF3	chr7:150924251-150924588	H1-hESC	embryonic stem cell:	n/a	chr7:150924452-150924463 chr7:150924442-150924462 chr7:150924453-150924473
10	ATF3	chr7:150924103-150924761	HepG2	liver:	n/a	chr7:150924452-150924463 chr7:150924442-150924462 chr7:150924453-150924473
11	ATF3	chr7:150924209-150924601	HepG2	liver:	n/a	chr7:150924452-150924463 chr7:150924442-150924462 chr7:150924453-150924473
12	ATF3	chr7:150924128-150924714	GM12878	blood:	n/a	chr7:150924452-150924463 chr7:150924442-150924462 chr7:150924453-150924473
13	ATF3	chr7:150924318-150924532	GM12878	blood:	n/a	chr7:150924452-150924463 chr7:150924442-150924462 chr7:150924453-150924473
14	ATF3	chr7:150924164-150924730	H1-hESC	embryonic stem cell:	n/a	chr7:150924452-150924463 chr7:150924442-150924462 chr7:150924453-150924473
15	BACH1	chr7:150929146-150929630	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr7:150925383-150925916	K562	blood:	n/a	n/a
17	BACH1	chr7:150924263-150924766	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:150924417-150924447	K562	blood:	n/a	n/a
19	BACH1	chr7:150930270-150930470	K562	blood:	n/a	n/a
20	BACH1	chr7:150930203-150930526	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr7:150930204-150930488	GM12878	blood:	n/a	chr7:150930368-150930379 chr7:150930369-150930379
22	BCL3	chr7:150929081-150929786	A549	lung:	n/a	chr7:150929612-150929621 chr7:150929436-150929449 chr7:150929712-150929721 chr7:150929599-150929612
23	BCLAF1	chr7:150924076-150924626	GM12878	blood:	n/a	chr7:150924225-150924233
24	BCLAF1	chr7:150929262-150929769	GM12878	blood:	n/a	chr7:150929612-150929621 chr7:150929436-150929449 chr7:150929712-150929721 chr7:150929599-150929612
25	BHLHE40	chr7:150929277-150929692	GM12878	blood:	n/a	chr7:150929599-150929615
26	BHLHE40	chr7:150929228-150929314	HepG2	liver:	n/a	n/a
27	BHLHE40	chr7:150924089-150924817	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:150925332-150925701	K562	blood:	n/a	n/a
29	BHLHE40	chr7:150929885-150930783	K562	blood:	n/a	n/a
30	BHLHE40	chr7:150923982-150924591	HepG2	liver:	n/a	n/a
31	BHLHE40	chr7:150929279-150929646	K562	blood:	n/a	chr7:150929599-150929615
32	BHLHE40	chr7:150923970-150924800	K562	blood:	n/a	n/a
33	BRCA1	chr7:150929016-150929670	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr7:150924213-150924631	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr7:150924271-150924630	GM12878	blood:	n/a	n/a
36	BRCA1	chr7:150924179-150924733	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr7:150930632-150930767	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr7:150924242-150924838	HepG2	liver:	n/a	n/a
39	BRCA1	chr7:150923888-150923907	HepG2	liver:	n/a	n/a
40	CBX3	chr7:150929991-150930978	K562	blood:	n/a	n/a
41	CBX3	chr7:150923793-150924954	K562	blood:	n/a	n/a
42	CBX3	chr7:150925259-150925946	K562	blood:	n/a	n/a
43	CBX3	chr7:150929083-150929751	K562	blood:	n/a	n/a
44	CCNT2	chr7:150924216-150924754	K562	blood:	n/a	n/a
45	CCNT2	chr7:150929265-150930051	K562	blood:	n/a	chr7:150929718-150929727
46	CCNT2	chr7:150930389-150930725	K562	blood:	n/a	n/a
47	CEBPB	chr7:150923896-150924719	H1-hESC	embryonic stem cell:	n/a	chr7:150924320-150924328
48	CEBPB	chr7:150924036-150924671	ECC-1	luminal epithelium:	n/a	chr7:150924320-150924328
49	CEBPB	chr7:150923806-150924712	IMR90	lung:	n/a	chr7:150924320-150924328
50	CEBPB	chr7:150924172-150924549	GM12878	blood:	n/a	chr7:150924320-150924328

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150929492-150929542	GM06990	blood:	n/a
2	chr7:150929492-150929542	GM06990	blood:	n/a
3	chr7:150924354-150924404	NT2-D1	testis:	n/a
4	chr7:150927849-150927899	ECC-1	luminal epithelium:	n/a
5	chr7:150925067-150925117	NHBE	bronchial:	n/a
6	chr7:150930536-150930586	ECC-1	luminal epithelium:	n/a
7	chr7:150924053-150924103	SKMC	muscle:	n/a
8	chr7:150927849-150927899	MCF10A-Er-Src	breast:	n/a
9	chr7:150927849-150927899	LNCaP	prostate:	n/a
10	chr7:150929492-150929542	HIPEpiC	eye:	n/a
11	chr7:150924351-150924401	ProgFib	skin:	n/a
12	chr7:150924409-150924459	AG09309	skin:	n/a
13	chr7:150929295-150929345	HIPEpiC	eye:	n/a
14	chr7:150929509-150929559	LNCaP	prostate:	n/a
15	chr7:150927849-150927899	SK-N-MC	brain:	n/a
16	chr7:150929509-150929559	HIPEpiC	eye:	n/a
17	chr7:150928707-150928757	NHBE	bronchial:	n/a
18	chr7:150929216-150929266	HRPEpiC	eye:	n/a
19	chr7:150928707-150928757	SKMC	muscle:	n/a
20	chr7:150924450-150924500	NHBE	bronchial:	n/a
21	chr7:150924273-150924323	HNPCEpiC	eye:	n/a
22	chr7:150925493-150925543	AG04450	lung:	fetal
23	chr7:150929492-150929542	HCM	heart:	n/a
24	chr7:150929216-150929266	BJ	skin:	n/a
25	chr7:150924356-150924406	BJ	skin:	n/a
26	chr7:150924409-150924459	GM12891	blood:	n/a
27	chr7:150924273-150924323	HMEC	breast:	n/a
28	chr7:150930150-150930200	NHBE	bronchial:	n/a
29	chr7:150924520-150924570	GM12891	blood:	n/a
30	chr7:150924351-150924401	HRPEpiC	eye:	n/a
31	chr7:150924442-150924492	NHBE	bronchial:	n/a
32	chr7:150924409-150924459	LNCaP	prostate:	n/a
33	chr7:150924354-150924404	SK-N-SH	brain:	n/a
34	chr7:150924392-150924442	GM12878	blood:	n/a
35	chr7:150929492-150929542	MCF10A-Er-Src	breast:	n/a
36	chr7:150929492-150929542	HCT-116	colon:	n/a
37	chr7:150929295-150929345	GM12891	blood:	n/a
38	chr7:150924444-150924494	GM12878	blood:	n/a
39	chr7:150924442-150924492	HEK293	kidney:	embryo
40	chr7:150924409-150924459	AoSMC	blood vessel:	n/a
41	chr7:150929216-150929266	HIPEpiC	eye:	n/a
42	chr7:150924392-150924442	ovcar-3	ovarian:	n/a
43	chr7:150924273-150924323	HUVEC	blood vessel:	n/a
44	chr7:150930150-150930200	K562	blood:	n/a
45	chr7:150924356-150924406	LNCaP	prostate:	n/a
46	chr7:150924444-150924494	Jurkat	blood:	n/a
47	chr7:150924450-150924500	LNCaP	prostate:	n/a
48	chr7:150924520-150924570	BJ	skin:	n/a
49	chr7:150924356-150924406	NH-A	brain:	n/a
50	chr7:150927849-150927899	ovcar-3	ovarian:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150929663..150931271-chr7:151251757..151253948,2	MCF-7	breast:
2	chr7:150891570..150894014-chr7:150923322..150926505,4	K562	blood:
3	chr7:150755190..150756692-chr7:150922882..150924419,2	K562	blood:
4	chr17:62502100..62502693-chr7:150924274..150925173,2	HCT-116	colon:
5	chr7:150928143..150930111-chr7:150944656..150946614,2	MCF-7	breast:
6	chr7:150100452..150102413-chr7:150924282..150926650,2	K562	blood:
7	chr7:150755192..150758087-chr7:150922401..150925767,3	K562	blood:
8	chr7:150891632..150894421-chr7:150925445..150927077,2	MCF-7	breast:
9	chr7:150930547..150933438-chr7:151037429..151040414,2	MCF-7	breast:
10	chr7:150776319..150779502-chr7:150929825..150933736,3	K562	blood:
11	chr7:150929647..150931224-chr7:151029766..151031795,2	MCF-7	breast:
12	chr7:150926542..150929326-chr7:151037923..151042316,3	K562	blood:
13	chr7:150923836..150926071-chr7:150936441..150939158,3	MCF-7	breast:
14	chr7:150690495..150692157-chr7:150930437..150932550,2	K562	blood:
15	chr7:150904819..150907851-chr7:150927889..150929495,3	MCF-7	breast:
16	chr7:150725439..150727092-chr7:150922758..150925738,2	K562	blood:
17	chr15:72524051..72524823-chr7:150929953..150930522,2	Hela-S3	cervix:
18	chr7:150925910..150927856-chr7:150934351..150936072,2	MCF-7	breast:
19	chr17:44269917..44270899-chr7:150928967..150929692,2	NB4	blood:
20	chr7:150809563..150811680-chr7:150929692..150931212,2	MCF-7	breast:
21	chr7:150707202..150709348-chr7:150929668..150931245,2	MCF-7	breast:
22	chr7:150922541..150925891-chr7:150969834..150974111,4	K562	blood:
23	chr7:150905206..150906764-chr7:150930054..150932100,2	MCF-7	breast:
24	chr7:150928662..150932139-chr7:150946772..150952684,6	MCF-7	breast:
25	chr7:150923495..150927436-chr7:150940006..150942925,4	MCF-7	breast:
26	chr7:150923377..150925570-chr7:151215684..151217252,2	K562	blood:
27	chr7:150811889..150814867-chr7:150929281..150931083,2	MCF-7	breast:
28	chr7:150862132..150865299-chr7:150928833..150931121,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMARCD3-1	chr7:150923824-150924044	NONHSAT124200
2	lnc-ABCF2-2	chr7:150928545-150930322	NONHSAT124201

No data

Variant related genes	Relation type
ABCF2	TF binding region
MIR671	TF binding region
CHPF2	TF binding region
ABCF2	CpG island
MIR671	CpG island
CHPF2	CpG island
ENSG00000164896	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000120071	chromatin interactions
ENSG00000197150	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000243018	chromatin interactions
ENSG00000243433	chromatin interactions
ENSG00000164885	chromatin interactions
ENSG00000183016	chromatin interactions
ENSG00000211517	chromatin interactions
ENSG00000013374	chromatin interactions
ENSG00000196456	chromatin interactions
ENSG00000082014	chromatin interactions
ENSG00000164900	chromatin interactions
ENSG00000106615	chromatin interactions
ENSG00000272661	chromatin interactions
ENSG00000133612	chromatin interactions
ENSG00000164889	chromatin interactions
ENSG00000164867	chromatin interactions

Extended variants
information (count: 284 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:284 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542198184	chr7:150923683-150923684	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs534864854	chr7:150923705-150923706	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs552897819	chr7:150923751-150923752	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs575735077	chr7:150923815-150923816	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs572771512	chr7:150923876-150923877	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
6	rs543070741	chr7:150923891-150923892	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
7	rs545040391	chr7:150923905-150923906	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
8	rs11973593	chr7:150923942-150923943	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185458201	chr7:150923946-150923947	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
10	rs544058646	chr7:150924019-150924020	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
11	rs3823589	chr7:150924030-150924031	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs141589811	chr7:150924069-150924070	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
13	rs576400179	chr7:150924087-150924088	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
14	rs35887483	chr7:150924092-150924093	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
15	rs540900733	chr7:150924097-150924098	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
16	rs150743106	chr7:150924134-150924135	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
17	rs549721707	chr7:150924142-150924143	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
18	rs566019563	chr7:150924159-150924160	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
19	rs541387125	chr7:150924162-150924163	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
20	rs528489721	chr7:150924201-150924202	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs377348400	chr7:150924215-150924216	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs112829219	chr7:150924219-150924220	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs551846280	chr7:150924240-150924241	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs571694762	chr7:150924265-150924266	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs536825952	chr7:150924279-150924280	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs550392993	chr7:150924283-150924284	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
27	rs567138711	chr7:150924284-150924285	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
28	rs536112137	chr7:150924288-150924289	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
29	rs552994867	chr7:150924293-150924294	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
30	rs62489654	chr7:150924302-150924303	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs373516672	chr7:150924329-150924330	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs572757718	chr7:150924342-150924343	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs78862637	chr7:150924350-150924351	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs66696522	chr7:150924351-150924352	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs10689344	chr7:150924356-150924357	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs111419502	chr7:150924358-150924359	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs149304903	chr7:150924367-150924368	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs111694512	chr7:150924394-150924395	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs558598726	chr7:150924396-150924397	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs546666206	chr7:150924407-150924408	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs115866277	chr7:150924453-150924454	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs143600315	chr7:150924470-150924471	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs182833558	chr7:150924494-150924495	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs371471426	chr7:150924502-150924503	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs574289054	chr7:150924521-150924522	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs374973911	chr7:150924528-150924529	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs542406530	chr7:150924545-150924546	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs148070685	chr7:150924555-150924556	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs144409624	chr7:150924634-150924635	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
50	rs528480621	chr7:150924636-150924637	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:964 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150922600-150924000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
2	chr7:150922800-150923800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:150922800-150923800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr7:150922800-150923800	Flanking Active TSS	Fetal Brain Female	brain
5	chr7:150922800-150923800	Flanking Active TSS	Psoas Muscle	Psoas
6	chr7:150922800-150923800	Flanking Active TSS	Stomach Smooth Muscle	stomach
7	chr7:150922800-150924000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:150923000-150923800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
9	chr7:150923000-150923800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
10	chr7:150923000-150923800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
11	chr7:150923000-150923800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
12	chr7:150923000-150923800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:150923000-150923800	Flanking Active TSS	Brain Angular Gyrus	brain
14	chr7:150923000-150923800	Flanking Active TSS	Brain Anterior Caudate	brain
15	chr7:150923000-150923800	Flanking Active TSS	Brain Germinal Matrix	brain
16	chr7:150923000-150923800	Flanking Active TSS	Colon Smooth Muscle	Colon
17	chr7:150923000-150923800	Flanking Active TSS	Duodenum Mucosa	Duodenum
18	chr7:150923000-150923800	Flanking Active TSS	Fetal Lung	lung
19	chr7:150923000-150923800	Flanking Active TSS	Rectal Smooth Muscle	rectum
20	chr7:150923000-150923800	Flanking Active TSS	HUVEC	blood vessel
21	chr7:150923000-150923800	Flanking Active TSS	NH-A	brain
22	chr7:150923000-150923800	Flanking Active TSS	Osteobl	bone
23	chr7:150923000-150924000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
24	chr7:150923000-150924000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
25	chr7:150923000-150924000	Flanking Active TSS	Adipose Nuclei	Adipose
26	chr7:150923000-150924000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
27	chr7:150923000-150924200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:150923000-150924200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:150923000-150924200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr7:150923000-150925200	Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr7:150923200-150923800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr7:150923200-150923800	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
33	chr7:150923200-150923800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
34	chr7:150923200-150923800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr7:150923200-150923800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
36	chr7:150923200-150923800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr7:150923200-150923800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:150923200-150923800	Flanking Active TSS	Brain Hippocampus Middle	brain
39	chr7:150923200-150923800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
40	chr7:150923200-150923800	Flanking Active TSS	Brain Substantia Nigra	brain
41	chr7:150923200-150923800	Flanking Active TSS	Colonic Mucosa	Colon
42	chr7:150923200-150923800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
43	chr7:150923200-150923800	Flanking Active TSS	Fetal Heart	heart
44	chr7:150923200-150923800	Flanking Active TSS	Fetal Intestine Large	intestine
45	chr7:150923200-150923800	Flanking Active TSS	Fetal Intestine Small	intestine
46	chr7:150923200-150923800	Flanking Active TSS	Fetal Muscle Trunk	muscle
47	chr7:150923200-150923800	Flanking Active TSS	Fetal Muscle Leg	muscle
48	chr7:150923200-150923800	Flanking Active TSS	Fetal Thymus	thymus
49	chr7:150923200-150924000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr7:150923200-150924000	Flanking Active TSS	Primary T cells from cord blood	blood

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