Variant report

Variant	nsv831151
Chromosome Location	chr7:137711447-137865471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1862)
CpG islands
(count:917)
Chromatin interactive
region (count:51)
LncRNA
region (count:3)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1862 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:137771010-137771910	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:137805182-137805415	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:137843324-137844196	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:137748104-137748763	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:137836674-137837544	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:137822296-137822442	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:137750508-137751465	HepG2	liver:	n/a	chr7:137750854-137750870
8	ARID3A	chr7:137714786-137714985	K562	blood:	n/a	n/a
9	ARID3A	chr7:137801681-137801977	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:137777428-137777492	K562	blood:	n/a	n/a
11	ARID3A	chr7:137733989-137735077	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:137749521-137750060	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:137774018-137774708	HepG2	liver:	n/a	n/a
14	ARID3A	chr7:137774401-137774720	K562	blood:	n/a	n/a
15	ARID3A	chr7:137729730-137729868	HepG2	liver:	n/a	n/a
16	ARID3A	chr7:137751675-137753045	HepG2	liver:	n/a	n/a
17	ARID3A	chr7:137832489-137832563	K562	blood:	n/a	n/a
18	ARID3A	chr7:137782093-137782734	HepG2	liver:	n/a	n/a
19	ARID3A	chr7:137810323-137810515	K562	blood:	n/a	n/a
20	ARID3A	chr7:137846294-137846901	HepG2	liver:	n/a	n/a
21	ARID3A	chr7:137715442-137715584	K562	blood:	n/a	n/a
22	ARID3A	chr7:137828569-137829154	HepG2	liver:	n/a	n/a
23	ARID3A	chr7:137781060-137781211	HepG2	liver:	n/a	n/a
24	ATF1	chr7:137849683-137849800	K562	blood:	n/a	n/a
25	ATF1	chr7:137729694-137730047	K562	blood:	n/a	n/a
26	ATF1	chr7:137777073-137777147	K562	blood:	n/a	n/a
27	ATF1	chr7:137810396-137810695	K562	blood:	n/a	n/a
28	ATF1	chr7:137793583-137793622	K562	blood:	n/a	n/a
29	ATF1	chr7:137730387-137730470	K562	blood:	n/a	n/a
30	ATF1	chr7:137800983-137801203	K562	blood:	n/a	n/a
31	ATF1	chr7:137778567-137778679	K562	blood:	n/a	n/a
32	ATF1	chr7:137832201-137832540	K562	blood:	n/a	n/a
33	ATF2	chr7:137854994-137855477	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF2	chr7:137852470-137852943	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr7:137853725-137854739	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr7:137853816-137854566	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr7:137854928-137855569	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF2	chr7:137810335-137810890	GM12878	blood:	n/a	n/a
39	ATF2	chr7:137852557-137853424	H1-hESC	embryonic stem cell:	n/a	n/a
40	ATF3	chr7:137846218-137846596	K562	blood:	n/a	n/a
41	BATF	chr7:137846324-137846588	GM12878	blood:	n/a	n/a
42	BATF	chr7:137822566-137822769	GM12878	blood:	n/a	n/a
43	BCL11A	chr7:137854172-137854421	H1-hESC	embryonic stem cell:	n/a	n/a
44	BCL11A	chr7:137855039-137855245	H1-hESC	embryonic stem cell:	n/a	n/a
45	BCL11A	chr7:137855068-137855336	H1-hESC	embryonic stem cell:	n/a	n/a
46	BCL11A	chr7:137810391-137810691	GM12878	blood:	n/a	n/a
47	BHLHE40	chr7:137849728-137849775	K562	blood:	n/a	n/a
48	BHLHE40	chr7:137806536-137806568	K562	blood:	n/a	n/a
49	BHLHE40	chr7:137846298-137846597	GM12878	blood:	n/a	n/a
50	BHLHE40	chr7:137822602-137822802	GM12878	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:137801780-137801830	HL-60	blood:	n/a
2	chr7:137854552-137854602	AG04449	skin:	fetal
3	chr7:137801780-137801830	HL-60	blood:	n/a
4	chr7:137854552-137854602	AG04449	skin:	fetal
5	chr7:137757578-137757628	A549	lung:	n/a
6	chr7:137775882-137775932	T-47D	breast:	n/a
7	chr7:137807365-137807415	NB4	blood:	n/a
8	chr7:137807164-137807214	HNPCEpiC	eye:	n/a
9	chr7:137760128-137760178	GM06990	blood:	n/a
10	chr7:137757578-137757628	SK-N-MC	brain:	n/a
11	chr7:137757578-137757628	GM12878	blood:	n/a
12	chr7:137775104-137775154	HNPCEpiC	eye:	n/a
13	chr7:137761047-137761097	HCPEpiC	choroid plexus:	n/a
14	chr7:137760128-137760178	PFSK-1	brain:	n/a
15	chr7:137760331-137760381	HL-60	blood:	n/a
16	chr7:137801780-137801830	HCF	heart:	n/a
17	chr7:137775104-137775154	HCF	heart:	n/a
18	chr7:137775882-137775932	GM06990	blood:	n/a
19	chr7:137807365-137807415	BE2_C	brain:	n/a
20	chr7:137761289-137761339	RPTEC	kidney:	n/a
21	chr7:137757578-137757628	SK-N-SH	brain:	n/a
22	chr7:137807421-137807471	ovcar-3	ovarian:	n/a
23	chr7:137801780-137801830	ProgFib	skin:	n/a
24	chr7:137807365-137807415	AG04449	skin:	fetal
25	chr7:137760331-137760381	HIPEpiC	eye:	n/a
26	chr7:137830988-137831038	NB4	blood:	n/a
27	chr7:137830988-137831038	GM06990	blood:	n/a
28	chr7:137761289-137761339	PrEC	prostate:	n/a
29	chr7:137854552-137854602	H1-hESC	embryonic stem cell:	embryo
30	chr7:137807421-137807471	HCPEpiC	choroid plexus:	n/a
31	chr7:137807164-137807214	PANC-1	pancreas:	n/a
32	chr7:137760128-137760178	HEEpiC	esophagus:	n/a
33	chr7:137854552-137854602	AG09319	gingival:	n/a
34	chr7:137854552-137854602	GM19239	blood:	n/a
35	chr7:137807164-137807214	HEEpiC	esophagus:	n/a
36	chr7:137766315-137766365	HUVEC	blood vessel:	n/a
37	chr7:137807164-137807214	NB4	blood:	n/a
38	chr7:137807365-137807415	SK-N-SH_RA	brain:	n/a
39	chr7:137760331-137760381	HepG2	liver:	n/a
40	chr7:137760331-137760381	H1-hESC	embryonic stem cell:	embryo
41	chr7:137757578-137757628	HAEpiC	amniotic membrane:	n/a
42	chr7:137760222-137760272	GM12892	blood:	n/a
43	chr7:137775104-137775154	Hepatocyte	liver:	n/a
44	chr7:137775882-137775932	A549	lung:	n/a
45	chr7:137761289-137761339	T-47D	breast:	n/a
46	chr7:137807421-137807471	NH-A	brain:	n/a
47	chr7:137761289-137761339	BE2_C	brain:	n/a
48	chr7:137807421-137807471	HAEpiC	amniotic membrane:	n/a
49	chr7:137757578-137757628	T-47D	breast:	n/a
50	chr7:137775882-137775932	ECC-1	luminal epithelium:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:137795035..137796778-chr7:137799284..137801134,2	MCF-7	breast:
2	chr7:137745328..137748047-chr7:137765457..137767555,2	K562	blood:
3	chr7:137747667..137753748-chr7:137756655..137760355,9	MCF-7	breast:
4	chr7:137758486..137761270-chr7:137763871..137767061,3	K562	blood:
5	chr7:137795035..137796778-chr7:137799284..137801134,2	MCF-7	breast:
6	chr7:137761079..137762998-chr7:137763211..137766028,2	MCF-7	breast:
7	chr7:137785512..137789009-chr7:137789748..137791579,3	K562	blood:
8	chr7:137782212..137782802-chr7:138410795..138411700,2	MCF-7	breast:
9	chr7:137776778..137778514-chr7:137780065..137781935,2	K562	blood:
10	chr7:137801785..137804367-chr7:137806016..137808191,2	K562	blood:
11	chr7:137846378..137846934-chr7:138144707..138145358,2	MCF-7	breast:
12	chr7:137816714..137818662-chr7:137822102..137823677,2	K562	blood:
13	chr7:137588092..137589015-chr7:137746698..137747545,2	K562	blood:
14	chr7:137852078..137854915-chr7:138143824..138145867,3	MCF-7	breast:
15	chr7:137782066..137784344-chr7:137794480..137797336,2	MCF-7	breast:
16	chr7:137776778..137778514-chr7:137780065..137781935,2	K562	blood:
17	chr7:137641166..137642974-chr7:137749095..137751251,2	MCF-7	breast:
18	chr7:137746837..137750836-chr7:137772601..137775949,4	MCF-7	breast:
19	chr7:137845964..137846544-chr7:138410692..138411250,3	K562	blood:
20	chr7:137845735..137846635-chr7:138201766..138202517,3	MCF-7	breast:
21	chr7:137745328..137748047-chr7:137765457..137767555,2	K562	blood:
22	chr7:137759066..137761270-chr7:137763871..137766101,2	K562	blood:
23	chr7:137710320..137713234-chr7:137749902..137751982,2	K562	blood:
24	chr7:137769402..137771015-chr7:137771922..137774982,3	MCF-7	breast:
25	chr7:137709286..137711862-chr7:137713310..137716482,3	MCF-7	breast:
26	chr7:137588115..137589032-chr7:137782020..137782614,2	K562	blood:
27	chr7:137774765..137777637-chr7:138144590..138146200,2	MCF-7	breast:
28	chr7:137686258..137688306-chr7:137772925..137775024,2	MCF-7	breast:
29	chr7:137782171..137782778-chr7:138423201..138423786,2	K562	blood:
30	chr7:137692957..137695430-chr7:137713449..137716116,2	K562	blood:
31	chr7:137782066..137784344-chr7:137794480..137797336,2	MCF-7	breast:
32	chr7:137816714..137818662-chr7:137822102..137823677,2	K562	blood:
33	chr7:137709286..137711862-chr7:137713310..137716482,3	MCF-7	breast:
34	chr7:137808206..137811036-chr7:137813988..137816221,2	K562	blood:
35	chr7:137801995..137804884-chr7:137807459..137809542,2	MCF-7	breast:
36	chr7:137854218..137856013-chr7:137925326..137928137,2	MCF-7	breast:
37	chr7:137843474..137846683-chr7:138143795..138145728,3	K562	blood:
38	chr7:137845962..137846888-chr7:138422836..138424129,6	K562	blood:
39	chr7:137769402..137771015-chr7:137771922..137774982,3	MCF-7	breast:
40	chr7:137705059..137708002-chr7:137713112..137715556,2	MCF-7	breast:
41	chr7:137746837..137750836-chr7:137772601..137775949,4	MCF-7	breast:
42	chr7:137742841..137745511-chr7:137746371..137748103,2	K562	blood:
43	chr7:137774458..137776682-chr7:137779682..137782164,2	K562	blood:
44	chr7:137750905..137753391-chr7:137753701..137756369,2	MCF-7	breast:
45	chr7:137785512..137787638-chr7:137789748..137791579,2	K562	blood:
46	chr20:52194951..52195553-chr7:137774107..137774609,2	MCF-7	breast:
47	chr7:137791459..137793672-chr7:138145071..138146706,2	MCF-7	breast:
48	chr7:137710320..137713234-chr7:137749902..137751982,2	K562	blood:
49	chr7:137588282..137589029-chr7:137845978..137846860,2	K562	blood:
50	chr7:137785512..137787638-chr7:137789748..137791579,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM24-5	chr7:137732000-137732643	NONHSAT123592
2	lnc-TRIM24-4	chr7:137744802-137745039	NONHSAT123593
3	lnc-TRIM24-5	chr7:137731400-137731454	NONHSAT123592

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4468	chr7:137808549-137808566	MIMAT0018995

No data

Variant related genes	Relation type
ENSG00000225559	TF binding region
ENSG00000239145	TF binding region
ENSG00000252820	TF binding region
ENSG00000231931	TF binding region
ENSG00000231923	TF binding region
RN7SKP223	TF binding region
RCC2P3	TF binding region
MIR4468	TF binding region
ENSG00000221558	TF binding region
ENSG00000238984	TF binding region
AKR1D1	TF binding region
ENSG00000225559	CpG island
ENSG00000239145	CpG island
ENSG00000252820	CpG island
ENSG00000231931	CpG island
ENSG00000231923	CpG island
RN7SKP223	CpG island
RCC2P3	CpG island
MIR4468	CpG island
ENSG00000221558	CpG island
ENSG00000238984	CpG island
AKR1D1	CpG island
ENSG00000233951	chromatin interactions
ENSG00000222514	chromatin interactions
ENSG00000234639	chromatin interactions
ENSG00000221558	chromatin interactions
ENSG00000266193	chromatin interactions
ENSG00000122787	chromatin interactions
ENSG00000231931	chromatin interactions
ENSG00000182158	chromatin interactions
ENSG00000122779	chromatin interactions

Extended variants
information (count: 5364 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:5364 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373184571	chr7:137711450-137711451	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs149891131	chr7:137711462-137711463	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs565532718	chr7:137711540-137711541	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs376382362	chr7:137711557-137711558	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs547783617	chr7:137711599-137711600	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs567699828	chr7:137711612-137711613	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs17169503	chr7:137711614-137711615	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs144882451	chr7:137711619-137711620	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs570166255	chr7:137711635-137711636	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs149016489	chr7:137711640-137711641	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs4732282	chr7:137711644-137711645	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs572279393	chr7:137711665-137711666	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs534642196	chr7:137711712-137711713	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs562025993	chr7:137711733-137711734	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs554126629	chr7:137711769-137711770	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs10259708	chr7:137711814-137711815	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs370284079	chr7:137711829-137711830	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs35661518	chr7:137711872-137711873	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs6955277	chr7:137711893-137711894	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs562996925	chr7:137711908-137711909	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs115103624	chr7:137711951-137711952	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs545548508	chr7:137712014-137712015	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs565359453	chr7:137712015-137712016	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs527972257	chr7:137712039-137712040	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs6948821	chr7:137712058-137712059	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs561264768	chr7:137712102-137712103	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs530070376	chr7:137712118-137712119	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs145905048	chr7:137712119-137712120	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs570103722	chr7:137712127-137712128	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs532522688	chr7:137712150-137712151	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs552329940	chr7:137712163-137712164	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs191894221	chr7:137712211-137712212	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs534593865	chr7:137712221-137712222	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs554486640	chr7:137712227-137712228	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs183913166	chr7:137712285-137712286	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs536608487	chr7:137712292-137712293	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs146628553	chr7:137712296-137712297	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs141350285	chr7:137712311-137712312	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs187540961	chr7:137712339-137712340	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs559098416	chr7:137712365-137712366	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs572599771	chr7:137712400-137712401	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs541646832	chr7:137712419-137712420	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561525944	chr7:137712420-137712421	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145085539	chr7:137712443-137712444	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563715982	chr7:137712449-137712450	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563562100	chr7:137712456-137712457	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529130850	chr7:137712463-137712464	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532914011	chr7:137712561-137712562	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148334978	chr7:137712577-137712578	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532738723	chr7:137712603-137712604	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	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
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Bladder cancer	21909424	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute promyelocytic leukemia	20824076	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:650 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137708200-137715000	Enhancers	Primary B cells from cord blood	blood
2	chr7:137708400-137714000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:137708800-137712800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
4	chr7:137709800-137712000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:137710000-137712400	Flanking Active TSS	GM12878-XiMat	blood
6	chr7:137710200-137711600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
7	chr7:137711000-137715200	Enhancers	Primary B cells from peripheral blood	blood
8	chr7:137711200-137711800	Enhancers	H9 Cell Line	embryonic stem cell
9	chr7:137711200-137712600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr7:137711200-137712800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr7:137711200-137712800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:137711400-137712200	Enhancers	H1 Cell Line	embryonic stem cell
13	chr7:137711400-137712800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr7:137711600-137711800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:137711600-137712800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr7:137711600-137714000	Enhancers	Primary hematopoietic stem cells	blood
17	chr7:137711600-137714200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr7:137711800-137713800	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr7:137711800-137714000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:137711800-137714000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr7:137712000-137712200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr7:137712000-137714000	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr7:137712200-137713800	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr7:137712200-137714200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:137712400-137713000	Enhancers	GM12878-XiMat	blood
26	chr7:137712600-137713400	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr7:137712600-137714200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr7:137712800-137713800	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr7:137712800-137713800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr7:137712800-137714800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr7:137712800-137717600	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr7:137713000-137713400	Flanking Active TSS	GM12878-XiMat	blood
33	chr7:137713400-137713800	Enhancers	GM12878-XiMat	blood
34	chr7:137713800-137714000	Flanking Active TSS	GM12878-XiMat	blood
35	chr7:137713800-137714400	Enhancers	H9 Cell Line	embryonic stem cell
36	chr7:137713800-137714400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:137713800-137714400	Enhancers	K562	blood
38	chr7:137713800-137715000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr7:137714000-137714200	Enhancers	GM12878-XiMat	blood
40	chr7:137714000-137714800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:137714000-137715000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:137714000-137715800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr7:137714000-137716600	Enhancers	Hela-S3	cervix
44	chr7:137714000-137716800	Enhancers	Fetal Intestine Large	intestine
45	chr7:137714000-137718200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr7:137714200-137714400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:137714200-137714400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr7:137714200-137714400	Flanking Active TSS	GM12878-XiMat	blood
49	chr7:137714200-137715200	Enhancers	H1 Cell Line	embryonic stem cell
50	chr7:137714200-137716400	Enhancers	Placenta	Placenta

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