Variant report

Variant	nsv889488
Chromosome Location	chr7:150926775-150955765
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	chr7:150929395-150929595	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:150929347-150929672	K562	blood:	n/a	n/a
3	ARID3A	chr7:150941405-150941866	K562	blood:	n/a	n/a
4	ATF2	chr7:150929355-150929798	GM12878	blood:	n/a	n/a
5	ATF3	chr7:150944971-150945186	K562	blood:	n/a	n/a
6	BACH1	chr7:150930203-150930526	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:150942108-150942642	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:150930270-150930470	K562	blood:	n/a	n/a
9	BACH1	chr7:150929146-150929630	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:150942909-150943045	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:150946355-150946673	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:150938085-150938459	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:150948637-150948819	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr7:150938082-150938419	K562	blood:	n/a	n/a
15	BATF	chr7:150930204-150930488	GM12878	blood:	n/a	chr7:150930368-150930379 chr7:150930369-150930379
16	BCL11A	chr7:150940448-150940720	GM12878	blood:	n/a	n/a
17	BCL3	chr7:150929081-150929786	A549	lung:	n/a	chr7:150929612-150929621 chr7:150929436-150929449 chr7:150929712-150929721 chr7:150929599-150929612
18	BCLAF1	chr7:150929262-150929769	GM12878	blood:	n/a	chr7:150929612-150929621 chr7:150929436-150929449 chr7:150929712-150929721 chr7:150929599-150929612
19	BHLHE40	chr7:150945774-150945927	K562	blood:	n/a	n/a
20	BHLHE40	chr7:150941284-150941708	K562	blood:	n/a	n/a
21	BHLHE40	chr7:150929885-150930783	K562	blood:	n/a	n/a
22	BHLHE40	chr7:150929277-150929692	GM12878	blood:	n/a	chr7:150929599-150929615
23	BHLHE40	chr7:150929279-150929646	K562	blood:	n/a	chr7:150929599-150929615
24	BHLHE40	chr7:150929228-150929314	HepG2	liver:	n/a	n/a
25	BRCA1	chr7:150929016-150929670	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr7:150930632-150930767	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr7:150929991-150930978	K562	blood:	n/a	n/a
28	CBX3	chr7:150929083-150929751	K562	blood:	n/a	n/a
29	CBX3	chr7:150941299-150941783	K562	blood:	n/a	n/a
30	CCNT2	chr7:150948652-150949244	K562	blood:	n/a	n/a
31	CCNT2	chr7:150930389-150930725	K562	blood:	n/a	n/a
32	CCNT2	chr7:150929265-150930051	K562	blood:	n/a	chr7:150929718-150929727
33	CCNT2	chr7:150934732-150935173	K562	blood:	n/a	n/a
34	CCNT2	chr7:150945698-150946465	K562	blood:	n/a	n/a
35	CCNT2	chr7:150936182-150936226	K562	blood:	n/a	n/a
36	CCNT2	chr7:150942480-150942949	K562	blood:	n/a	chr7:150942843-150942852
37	CCNT2	chr7:150935462-150935643	K562	blood:	n/a	n/a
38	CEBPB	chr7:150939828-150940232	A549	lung:	n/a	chr7:150939998-150940007 chr7:150939997-150940008 chr7:150939996-150940007 chr7:150939996-150940009 chr7:150939996-150940009
39	CEBPB	chr7:150939807-150940211	K562	blood:	n/a	chr7:150939998-150940007 chr7:150939997-150940008 chr7:150939996-150940007 chr7:150939996-150940009 chr7:150939996-150940009
40	CEBPB	chr7:150939812-150940238	HepG2	liver:	n/a	chr7:150939998-150940007 chr7:150939997-150940008 chr7:150939996-150940007 chr7:150939996-150940009 chr7:150939996-150940009
41	CEBPB	chr7:150939817-150940216	HepG2	liver:	n/a	chr7:150939998-150940007 chr7:150939997-150940008 chr7:150939996-150940007 chr7:150939996-150940009 chr7:150939996-150940009
42	CEBPB	chr7:150939889-150940111	K562	blood:	n/a	chr7:150939998-150940007 chr7:150939997-150940008 chr7:150939996-150940007 chr7:150939996-150940009 chr7:150939996-150940009
43	CEBPB	chr7:150939890-150940168	HepG2	liver:	n/a	chr7:150939998-150940007 chr7:150939997-150940008 chr7:150939996-150940007 chr7:150939996-150940009 chr7:150939996-150940009
44	CEBPB	chr7:150939814-150940334	Hela-S3	cervix:	n/a	chr7:150939998-150940007 chr7:150939997-150940008 chr7:150939996-150940007 chr7:150939996-150940009 chr7:150939996-150940009
45	CEBPB	chr7:150939718-150940297	A549	lung:	n/a	chr7:150939998-150940007 chr7:150939997-150940008 chr7:150939996-150940007 chr7:150939996-150940009 chr7:150939996-150940009
46	CEBPB	chr7:150948762-150948990	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr7:150939820-150940292	IMR90	lung:	n/a	chr7:150939998-150940007 chr7:150939997-150940008 chr7:150939996-150940007 chr7:150939996-150940009 chr7:150939996-150940009
48	CEBPB	chr7:150939820-150940359	MCF-7	breast:	n/a	chr7:150939998-150940007 chr7:150939997-150940008 chr7:150939996-150940007 chr7:150939996-150940009 chr7:150939996-150940009
49	CEBPB	chr7:150941520-150941753	A549	lung:	n/a	n/a
50	CEBPB	chr7:150939848-150940230	H1-hESC	embryonic stem cell:	n/a	chr7:150939998-150940007 chr7:150939997-150940008 chr7:150939996-150940007 chr7:150939996-150940009 chr7:150939996-150940009

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150934650-150934700	HL-60	blood:	n/a
2	chr7:150949204-150949254	MCF10A-Er-Src	breast:	n/a
3	chr7:150936167-150936217	AG09309	skin:	n/a
4	chr7:150942958-150943008	HCF	heart:	n/a
5	chr7:150937303-150937353	Hepatocyte	liver:	n/a
6	chr7:150945607-150945657	ovcar-3	ovarian:	n/a
7	chr7:150942352-150942402	GM06990	blood:	n/a
8	chr7:150934650-150934700	HL-60	blood:	n/a
9	chr7:150949204-150949254	MCF10A-Er-Src	breast:	n/a
10	chr7:150936167-150936217	AG09309	skin:	n/a
11	chr7:150942958-150943008	HCF	heart:	n/a
12	chr7:150937303-150937353	Hepatocyte	liver:	n/a
13	chr7:150945607-150945657	ovcar-3	ovarian:	n/a
14	chr7:150942352-150942402	GM06990	blood:	n/a
15	chr7:150930536-150930586	SAEC	small airway:	n/a
16	chr7:150945869-150945919	LNCaP	prostate:	n/a
17	chr7:150942958-150943008	NHBE	bronchial:	n/a
18	chr7:150930150-150930200	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:150941389-150941439	H1-hESC	embryonic stem cell:	embryo
20	chr7:150933506-150933556	SK-N-SH_RA	brain:	n/a
21	chr7:150945937-150945987	HRE	kidney:	n/a
22	chr7:150937303-150937353	HUVEC	blood vessel:	n/a
23	chr7:150929295-150929345	HRPEpiC	eye:	n/a
24	chr7:150951482-150951532	Hepatocyte	liver:	n/a
25	chr7:150929389-150929439	SAEC	small airway:	n/a
26	chr7:150936167-150936217	HCPEpiC	choroid plexus:	n/a
27	chr7:150929389-150929439	SK-N-SH_RA	brain:	n/a
28	chr7:150945937-150945987	AG04450	lung:	fetal
29	chr7:150929295-150929345	PANC-1	pancreas:	n/a
30	chr7:150948324-150948374	PrEC	prostate:	n/a
31	chr7:150935770-150935820	NT2-D1	testis:	n/a
32	chr7:150949204-150949254	BE2_C	brain:	n/a
33	chr7:150943825-150943875	AG04449	skin:	fetal
34	chr7:150945607-150945657	HL-60	blood:	n/a
35	chr7:150932495-150932545	SK-N-MC	brain:	n/a
36	chr7:150929389-150929439	HIPEpiC	eye:	n/a
37	chr7:150945869-150945919	NB4	blood:	n/a
38	chr7:150928707-150928757	SK-N-SH_RA	brain:	n/a
39	chr7:150946199-150946249	NHDF-neo	bronchial:	n/a
40	chr7:150946114-150946164	H1-hESC	embryonic stem cell:	embryo
41	chr7:150929216-150929266	AG09309	skin:	n/a
42	chr7:150945607-150945657	A549	lung:	n/a
43	chr7:150945607-150945657	HUVEC	blood vessel:	n/a
44	chr7:150935476-150935526	NH-A	brain:	n/a
45	chr7:150942732-150942782	NB4	blood:	n/a
46	chr7:150937303-150937353	HL-60	blood:	n/a
47	chr7:150927849-150927899	NT2-D1	testis:	n/a
48	chr7:150939592-150939642	SKMC	muscle:	n/a
49	chr7:150936167-150936217	PFSK-1	brain:	n/a
50	chr7:150942352-150942402	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:150948703..150950863-chr7:150952432..150955323,2	K562	blood:
2	chr7:150775206..150778180-chr7:150932374..150934759,2	MCF-7	breast:
3	chr7:150923495..150927436-chr7:150940006..150942925,4	MCF-7	breast:
4	chr7:150869379..150870234-chr7:150941055..150942048,8	MCF-7	breast:
5	chr7:150901645..150902197-chr7:150940945..150941682,2	K562	blood:
6	chr7:150929663..150931271-chr7:151251757..151253948,2	MCF-7	breast:
7	chr7:150949363..150951350-chr7:150953823..150956264,2	K562	blood:
8	chr7:150820602..150821298-chr7:150941184..150941993,2	MCF-7	breast:
9	chr7:150865018..150866330-chr7:150941109..150942155,6	K562	blood:
10	chr7:150938571..150942838-chr7:150950941..150954111,4	MCF-7	breast:
11	chr7:150928662..150932139-chr7:150946772..150952684,6	MCF-7	breast:
12	chr7:150941406..150944514-chr7:150945051..150947075,3	MCF-7	breast:
13	chr7:150931216..150932896-chr7:150955646..150957462,2	K562	blood:
14	chr7:150869400..150870347-chr7:150941097..150942121,7	K562	blood:
15	chr7:150932407..150934552-chr7:151037359..151040324,2	K562	blood:
16	chr7:150888388..150889316-chr7:150941010..150942053,3	K562	blood:
17	chr7:150891632..150894421-chr7:150925445..150927077,2	MCF-7	breast:
18	chr7:150941689..150943266-chr7:150971664..150974365,2	K562	blood:
19	chr7:150929647..150931224-chr7:151029766..151031795,2	MCF-7	breast:
20	chr15:72524051..72524823-chr7:150929953..150930522,2	Hela-S3	cervix:
21	chr7:150707202..150709348-chr7:150929668..150931245,2	MCF-7	breast:
22	chr7:150910425..150912295-chr7:150932793..150934367,2	MCF-7	breast:
23	chr7:150952243..150954405-chr7:150956858..150959573,2	K562	blood:
24	chr7:150928662..150932139-chr7:150946772..150952684,6	MCF-7	breast:
25	chr7:150953242..150955142-chr7:150956991..150958505,2	K562	blood:
26	chr7:150811889..150814867-chr7:150929281..150931083,2	MCF-7	breast:
27	chr7:150954107..150956387-chr7:150957972..150959934,2	MCF-7	breast:
28	chr7:150942010..150944289-chr7:150955333..150957192,2	K562	blood:
29	chr7:150948703..150950863-chr7:150952432..150955323,2	K562	blood:
30	chr7:150705057..150707030-chr7:150948019..150950739,2	K562	blood:
31	chr7:150926542..150929326-chr7:151037923..151042316,3	K562	blood:
32	chr7:150820748..150821377-chr7:150941500..150942022,2	MCF-7	breast:
33	chr7:150819780..150822617-chr7:150940406..150943194,3	MCF-7	breast:
34	chr7:150809563..150811680-chr7:150929692..150931212,2	MCF-7	breast:
35	chr7:150933071..150935607-chr7:151215540..151217863,2	K562	blood:
36	chr7:150928143..150930111-chr7:150944656..150946614,2	MCF-7	breast:
37	chr7:150820799..150821593-chr7:150941510..150942032,2	K562	blood:
38	chr7:150776319..150779502-chr7:150929825..150933736,3	K562	blood:
39	chr7:150928143..150930111-chr7:150944656..150946614,2	MCF-7	breast:
40	chr17:44269917..44270899-chr7:150928967..150929692,2	NB4	blood:
41	chr7:150949363..150951350-chr7:150953823..150956264,2	K562	blood:
42	chr7:150925910..150927856-chr7:150934351..150936072,2	MCF-7	breast:
43	chr7:150955167..150957625-chr7:150960069..150962944,2	K562	blood:
44	chr7:150949835..150952279-chr7:150953865..150957966,4	MCF-7	breast:
45	chr7:150944159..150946342-chr7:150972887..150975150,2	MCF-7	breast:
46	chr7:150862132..150865299-chr7:150928833..150931121,3	MCF-7	breast:
47	chr7:150863343..150865061-chr7:150947610..150949922,2	MCF-7	breast:
48	chr7:150923495..150927436-chr7:150940006..150942925,4	MCF-7	breast:
49	chr7:150930547..150933438-chr7:151037429..151040414,2	MCF-7	breast:
50	chr7:150954098..150959160-chr7:150959832..150962944,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHPF2-1	chr7:150946411-150946548	ENSG00000243018.1
2	lnc-ABCF2-2	chr7:150928545-150930322	NONHSAT124201
3	lnc-CHPF2-1	chr7:150951399-150951476	ENSG00000243018.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-671-5p	chr7:150935535-150935557	MIMAT0003880
hsa-miR-671-3p	chr7:150935574-150935594	MIMAT0004819

Variant related genes	Relation type
ENSG00000243018	TF binding region
ABCF2	TF binding region
MIR671	TF binding region
SMARCD3	TF binding region
ENSG00000272661	TF binding region
CHPF2	TF binding region
ENSG00000243018	CpG island
ABCF2	CpG island
MIR671	CpG island
SMARCD3	CpG island
ENSG00000272661	CpG island
CHPF2	CpG island
ENSG00000164867	chromatin interactions
ENSG00000120071	chromatin interactions
ENSG00000183016	chromatin interactions
ENSG00000164900	chromatin interactions
ENSG00000133612	chromatin interactions
ENSG00000211517	chromatin interactions
ENSG00000033050	chromatin interactions
ENSG00000033100	chromatin interactions
ENSG00000243018	chromatin interactions
ENSG00000164896	chromatin interactions
ENSG00000082014	chromatin interactions
ENSG00000106615	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000013374	chromatin interactions
KIFAP3	Mature miRNA region
CDC123	Mature miRNA region
HIST2H2AA4	Mature miRNA region
XRCC6	Mature miRNA region
ERGIC2	Mature miRNA region
GPI	Mature miRNA region
NACA	Mature miRNA region
DIS3L	Mature miRNA region
LCT	Mature miRNA region
CAPN15	Mature miRNA region
TXNRD2	Mature miRNA region
PRR14L	Mature miRNA region
BAZ2A	Mature miRNA region
ATP2A2	Mature miRNA region
METTL23	Mature miRNA region
INPPL1	Mature miRNA region
LGALS3BP	Mature miRNA region
C17orf58	Mature miRNA region
UBE2C	Mature miRNA region
OGT	Mature miRNA region
HDAC1	Mature miRNA region
SLC7A5	Mature miRNA region
COA4	Mature miRNA region
LRRN2	Mature miRNA region
RREB1	Mature miRNA region
U2AF2	Mature miRNA region
HJURP	Mature miRNA region
HMGA1	Mature miRNA region
CEP85	Mature miRNA region
OXA1L	Mature miRNA region
UBFD1	Mature miRNA region
FBRS	Mature miRNA region
HNRNPUL1	Mature miRNA region
CRLF3	Mature miRNA region
MEPCE	Mature miRNA region
TMEM223	Mature miRNA region
RPL23A	Mature miRNA region
SSPO	Mature miRNA region
SLC7A1	Mature miRNA region
NDUFA3	Mature miRNA region
USP21	Mature miRNA region
CRTC3	Mature miRNA region
POR	Mature miRNA region
NRSN2	Mature miRNA region
R3HDM2	Mature miRNA region
RPL3	Mature miRNA region
HDGF	Mature miRNA region
GJC1	Mature miRNA region
CHPF2	Mature miRNA region
MOSPD3	Mature miRNA region
ZFP36L2	Mature miRNA region
AGO2	Mature miRNA region

Extended variants
information (count: 1255 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1255 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6464134	chr7:150926775-150926776	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs2446064	chr7:150926776-150926777	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs552318750	chr7:150926780-150926781	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs377308352	chr7:150926794-150926795	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs76707991	chr7:150926817-150926818	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs538101405	chr7:150926902-150926903	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs554850448	chr7:150926908-150926909	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs181565227	chr7:150926946-150926947	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs376661745	chr7:150926973-150926974	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs201332990	chr7:150926978-150926979	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs35194500	chr7:150926979-150926980	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs397734104	chr7:150926989-150926990	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs150659858	chr7:150926999-150927000	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs553950247	chr7:150927019-150927020	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs577299140	chr7:150927024-150927025	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs185357832	chr7:150927025-150927026	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs562646901	chr7:150927060-150927061	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs33997833	chr7:150927078-150927079	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs576309381	chr7:150927122-150927123	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs189414571	chr7:150927143-150927144	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs542107440	chr7:150927205-150927206	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs71533524	chr7:150927231-150927232	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs56776814	chr7:150927285-150927286	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs536832938	chr7:150927290-150927291	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs547398001	chr7:150927310-150927311	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs564011357	chr7:150927345-150927346	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs532836302	chr7:150927347-150927348	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs182015910	chr7:150927378-150927379	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs569067584	chr7:150927425-150927426	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs117460099	chr7:150927466-150927467	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs548595761	chr7:150927519-150927520	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs568760921	chr7:150927553-150927554	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs570525197	chr7:150927592-150927593	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs372641173	chr7:150927692-150927693	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs111407002	chr7:150927698-150927699	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs574673358	chr7:150927731-150927732	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs2792432	chr7:150927763-150927764	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs577192437	chr7:150927784-150927785	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs77488196	chr7:150927850-150927851	Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs552942840	chr7:150928030-150928031	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs556705828	chr7:150928032-150928033	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs576296855	chr7:150928048-150928049	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs542093345	chr7:150928066-150928067	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs141026348	chr7:150928107-150928108	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs574257931	chr7:150928119-150928120	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs73727124	chr7:150928177-150928178	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs572339005	chr7:150928180-150928181	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs540989047	chr7:150928188-150928189	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs564063048	chr7:150928202-150928203	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs115128218	chr7:150928233-150928234	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2826 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150924800-150928800	Weak transcription	Spleen	Spleen
2	chr7:150925000-150929200	Weak transcription	Gastric	stomach
3	chr7:150925200-150928600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr7:150925200-150928800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr7:150925200-150928800	Weak transcription	Esophagus	oesophagus
6	chr7:150925200-150929000	Weak transcription	Right Atrium	heart
7	chr7:150925400-150927800	Weak transcription	NH-A	brain
8	chr7:150925400-150928400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr7:150925400-150928600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr7:150925400-150928600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr7:150925400-150928600	Weak transcription	Primary B cells from peripheral blood	blood
12	chr7:150925400-150928600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr7:150925400-150928600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr7:150925400-150928600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr7:150925400-150928600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:150925400-150928600	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr7:150925400-150928600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr7:150925400-150928600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:150925400-150928600	Weak transcription	Brain Germinal Matrix	brain
20	chr7:150925400-150928600	Weak transcription	Brain Substantia Nigra	brain
21	chr7:150925400-150928600	Weak transcription	Fetal Brain Female	brain
22	chr7:150925400-150928600	Weak transcription	Left Ventricle	heart
23	chr7:150925400-150928600	Weak transcription	Right Ventricle	heart
24	chr7:150925400-150928600	Weak transcription	GM12878-XiMat	blood
25	chr7:150925400-150928800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr7:150925400-150928800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr7:150925400-150928800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:150925400-150928800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr7:150925400-150928800	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr7:150925400-150928800	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr7:150925400-150928800	Weak transcription	Primary T cells from cord blood	blood
32	chr7:150925400-150928800	Weak transcription	Primary hematopoietic stem cells	blood
33	chr7:150925400-150928800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr7:150925400-150928800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr7:150925400-150928800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:150925400-150928800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr7:150925400-150928800	Weak transcription	Brain Hippocampus Middle	brain
38	chr7:150925400-150928800	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr7:150925400-150928800	Weak transcription	Fetal Brain Male	brain
40	chr7:150925400-150928800	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr7:150925400-150928800	Weak transcription	Lung	lung
42	chr7:150925400-150928800	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr7:150925400-150928800	Weak transcription	Small Intestine	intestine
44	chr7:150925400-150929000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:150925400-150929000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr7:150925400-150929000	Weak transcription	Fetal Muscle Trunk	muscle
47	chr7:150925400-150929000	Weak transcription	Fetal Muscle Leg	muscle
48	chr7:150925400-150929000	Weak transcription	Pancreas	Pancrea
49	chr7:150925400-150929000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr7:150925400-150929000	Weak transcription	Psoas Muscle	Psoas

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