Variant report

Variant	esv1826763
Chromosome Location	chr7:99583219-99626295
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2102)
CpG islands
(count:1709)
Chromatin interactive
region (count:125)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2102 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99595227-99595537	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:99613002-99613272	K562	blood:	n/a	n/a
3	ARID3A	chr7:99612999-99613317	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:99614020-99614567	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:99601325-99601936	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:99621722-99621985	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:99588540-99588839	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:99591850-99592144	K562	blood:	n/a	n/a
9	ARID3A	chr7:99610285-99610671	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:99591808-99592148	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:99588561-99588855	K562	blood:	n/a	n/a
12	ATF1	chr7:99613008-99613355	K562	blood:	n/a	n/a
13	ATF2	chr7:99588383-99588853	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr7:99588414-99588699	GM12878	blood:	n/a	n/a
15	ATF2	chr7:99612925-99613402	GM12878	blood:	n/a	n/a
16	ATF2	chr7:99595132-99595501	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr7:99595114-99595627	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr7:99612922-99613352	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr7:99623674-99624169	GM12878	blood:	n/a	n/a
20	ATF3	chr7:99612938-99613479	K562	blood:	n/a	n/a
21	ATF3	chr7:99612906-99613380	A549	lung:	n/a	n/a
22	ATF3	chr7:99588519-99588908	A549	lung:	n/a	n/a
23	BACH1	chr7:99588600-99588743	K562	blood:	n/a	n/a
24	BACH1	chr7:99612991-99613276	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr7:99623746-99624108	GM12878	blood:	n/a	chr7:99623935-99623946
26	BATF	chr7:99623677-99624143	GM12878	blood:	n/a	chr7:99623935-99623946
27	BATF	chr7:99612974-99613349	GM12878	blood:	n/a	n/a
28	BCL3	chr7:99612943-99613384	A549	lung:	n/a	chr7:99613205-99613214
29	BCL3	chr7:99612971-99613328	GM12878	blood:	n/a	chr7:99613205-99613214
30	BCLAF1	chr7:99612943-99613345	GM12878	blood:	n/a	chr7:99613205-99613214
31	BCLAF1	chr7:99595032-99595589	GM12878	blood:	n/a	chr7:99595317-99595326
32	BCLAF1	chr7:99623673-99624175	GM12878	blood:	n/a	n/a
33	BCLAF1	chr7:99612895-99613380	GM12878	blood:	n/a	chr7:99613205-99613214
34	BHLHE40	chr7:99588564-99588813	K562	blood:	n/a	n/a
35	BHLHE40	chr7:99623878-99624027	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:99591934-99592020	K562	blood:	n/a	n/a
37	BHLHE40	chr7:99595199-99595648	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:99612987-99613358	K562	blood:	n/a	n/a
39	BHLHE40	chr7:99595201-99595644	HepG2	liver:	n/a	n/a
40	BHLHE40	chr7:99621688-99622047	HepG2	liver:	n/a	n/a
41	BHLHE40	chr7:99601366-99601918	HepG2	liver:	n/a	n/a
42	BRCA1	chr7:99612967-99613336	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr7:99601493-99601826	HepG2	liver:	n/a	n/a
44	BRCA1	chr7:99591862-99592076	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr7:99588462-99588995	K562	blood:	n/a	n/a
46	CBX3	chr7:99612836-99613459	K562	blood:	n/a	n/a
47	CBX3	chr7:99588497-99588920	K562	blood:	n/a	n/a
48	CBX3	chr7:99612953-99613313	K562	blood:	n/a	n/a
49	CCNT2	chr7:99613083-99613301	K562	blood:	n/a	n/a
50	CCNT2	chr7:99588638-99588787	K562	blood:	n/a	n/a

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99616820-99616870	AG09309	skin:	n/a
2	chr7:99616820-99616870	AG09309	skin:	n/a
3	chr7:99591962-99592012	HMEC	breast:	n/a
4	chr7:99612634-99612684	ovcar-3	ovarian:	n/a
5	chr7:99588273-99588323	HEEpiC	esophagus:	n/a
6	chr7:99598775-99598825	K562	blood:	n/a
7	chr7:99588335-99588385	A549	lung:	n/a
8	chr7:99595276-99595326	HRPEpiC	eye:	n/a
9	chr7:99601692-99601742	Hepatocyte	liver:	n/a
10	chr7:99616820-99616870	HL-60	blood:	n/a
11	chr7:99613796-99613846	SK-N-MC	brain:	n/a
12	chr7:99601692-99601742	LNCaP	prostate:	n/a
13	chr7:99613517-99613567	HCM	heart:	n/a
14	chr7:99613185-99613235	HCPEpiC	choroid plexus:	n/a
15	chr7:99613192-99613242	HRCEpiC	kidney:	n/a
16	chr7:99595348-99595398	HRCEpiC	kidney:	n/a
17	chr7:99613244-99613294	RPTEC	kidney:	n/a
18	chr7:99595348-99595398	IMR90	lung:	fetal
19	chr7:99598775-99598825	GM12892	blood:	n/a
20	chr7:99595095-99595145	AG10803	skin:	n/a
21	chr7:99598775-99598825	A549	lung:	n/a
22	chr7:99613244-99613294	HRCEpiC	kidney:	n/a
23	chr7:99613244-99613294	GM12878	blood:	n/a
24	chr7:99588273-99588323	HAEpiC	amniotic membrane:	n/a
25	chr7:99591962-99592012	IMR90	lung:	fetal
26	chr7:99614209-99614259	PrEC	prostate:	n/a
27	chr7:99609831-99609881	Jurkat	blood:	n/a
28	chr7:99601692-99601742	NHBE	bronchial:	n/a
29	chr7:99613517-99613567	NT2-D1	testis:	n/a
30	chr7:99609831-99609881	Hela-S3	cervix:	n/a
31	chr7:99587136-99587186	PFSK-1	brain:	n/a
32	chr7:99595458-99595508	PrEC	prostate:	n/a
33	chr7:99613517-99613567	U87	brain:	n/a
34	chr7:99613105-99613155	HL-60	blood:	n/a
35	chr7:99598775-99598825	HEEpiC	esophagus:	n/a
36	chr7:99588273-99588323	AoSMC	blood vessel:	n/a
37	chr7:99613796-99613846	CMK	blood:	n/a
38	chr7:99614209-99614259	GM12878	blood:	n/a
39	chr7:99612715-99612765	HEEpiC	esophagus:	n/a
40	chr7:99595437-99595487	PFSK-1	brain:	n/a
41	chr7:99612773-99612823	ProgFib	skin:	n/a
42	chr7:99588273-99588323	SAEC	small airway:	n/a
43	chr7:99614209-99614259	SK-N-SH	brain:	n/a
44	chr7:99609831-99609881	PrEC	prostate:	n/a
45	chr7:99595658-99595708	NH-A	brain:	n/a
46	chr7:99616820-99616870	Caco-2	colon:	n/a
47	chr7:99591962-99592012	Hela-S3	cervix:	n/a
48	chr7:99588657-99588707	BJ	skin:	n/a
49	chr7:99588657-99588707	Hela-S3	cervix:	n/a
50	chr7:99613796-99613846	NHBE	bronchial:	n/a

(count:125 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:99592003..99594227-chr7:99676787..99679509,2	K562	blood:
2	chr7:99600927..99603522-chr7:99678013..99680469,2	MCF-7	breast:
3	chr7:99618852..99620390-chr7:99647489..99649484,2	MCF-7	breast:
4	chr7:99603071..99604678-chr7:99629876..99631429,2	MCF-7	breast:
5	chr7:99588733..99590753-chr7:99595568..99598472,2	K562	blood:
6	chr7:99591418..99594065-chr7:99611454..99615168,4	MCF-7	breast:
7	chr7:99613052..99614661-chr7:99625234..99626812,2	MCF-7	breast:
8	chr7:99592424..99598434-chr7:99598646..99605571,11	MCF-7	breast:
9	chr7:99616524..99619632-chr7:99677690..99679745,3	K562	blood:
10	chr7:99591473..99592533-chr7:99642040..99642986,5	MCF-7	breast:
11	chr7:99591491..99592473-chr7:99650892..99651464,2	K562	blood:
12	chr7:99586340..99588249-chr7:99590043..99591844,2	K562	blood:
13	chr7:99588806..99591548-chr7:99620634..99622161,2	MCF-7	breast:
14	chr7:99598705..99603395-chr7:99611992..99615824,4	MCF-7	breast:
15	chr7:99528952..99531320-chr7:99615014..99616984,2	K562	blood:
16	chr7:99580447..99583544-chr7:99586500..99589317,4	K562	blood:
17	chr7:99617125..99619542-chr7:99633323..99635330,2	K562	blood:
18	chr7:99587817..99590250-chr7:99755042..99756960,2	K562	blood:
19	chr7:99591119..99593503-chr7:99676787..99678586,2	K562	blood:
20	chr7:99599411..99601548-chr7:99605711..99608652,3	MCF-7	breast:
21	chr7:99590547..99592612-chr7:99626360..99629032,2	K562	blood:
22	chr7:99607653..99611387-chr7:99613037..99615775,4	K562	blood:
23	chr7:99613224..99616757-chr7:99646903..99650456,6	K562	blood:
24	chr7:99591947..99592458-chr7:99728297..99729231,2	K562	blood:
25	chr7:99626268..99629732-chr7:99646321..99649999,3	MCF-7	breast:
26	chr7:99586340..99588249-chr7:99590043..99591844,2	K562	blood:
27	chr7:99588477..99590075-chr7:99697467..99699544,2	K562	blood:
28	chr7:99590918..99594546-chr7:99596737..99599787,3	K562	blood:
29	chr7:99601356..99603407-chr7:99644840..99648336,3	MCF-7	breast:
30	chr7:99577524..99578039-chr7:99588237..99589217,3	K562	blood:
31	chr7:99618848..99621935-chr7:99625446..99628535,4	MCF-7	breast:
32	chr6:27857861..27860281-chr7:99604688..99606426,2	K562	blood:
33	chr7:99592424..99598434-chr7:99598646..99605571,11	MCF-7	breast:
34	chr7:99590918..99594546-chr7:99596737..99599787,3	K562	blood:
35	chr7:99524861..99526650-chr7:99605841..99607428,2	MCF-7	breast:
36	chr10:43133589..43134241-chr7:99612910..99613726,2	NB4	blood:
37	chr7:99589288..99591810-chr7:99612834..99614804,4	MCF-7	breast:
38	chr16:56966049..56966601-chr7:99612783..99613720,2	NB4	blood:
39	chr7:99580447..99585207-chr7:99587129..99590928,6	K562	blood:
40	chr7:99601965..99606251-chr7:99612417..99615707,8	K562	blood:
41	chr7:99590363..99592421-chr7:99597136..99600060,2	MCF-7	breast:
42	chr7:99612131..99615242-chr7:99723277..99726662,3	K562	blood:
43	chr7:99596904..99604482-chr7:99611016..99614805,10	MCF-7	breast:
44	chr7:99514062..99516474-chr7:99604675..99606310,2	MCF-7	breast:
45	chr7:99626167..99629081-chr7:99640250..99642340,2	K562	blood:
46	chr7:99608355..99609979-chr7:99641023..99642646,2	MCF-7	breast:
47	chr1:45196470..45197118-chr7:99613158..99613683,2	Hela-S3	cervix:
48	chr7:99595238..99600680-chr7:99611222..99614830,6	K562	blood:
49	chr15:93425219..93426130-chr7:99613026..99613921,3	Hela-S3	cervix:
50	chr7:99600014..99604498-chr7:99605032..99608017,4	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZKSCAN1-1	chr7:99597123-99597186	XLOC_006188
2	lnc-ZKSCAN1-1	chr7:99597006-99597115	XLOC_006188
3	lnc-ZKSCAN1-1	chr7:99608999-99609247	XLOC_006188
4	lnc-ZKSCAN1-1	chr7:99608999-99609239	XLOC_006188
5	lnc-ZKSCAN1-1	chr7:99606205-99606730	XLOC_006188
6	lnc-ZKSCAN1-2	chr7:99587971-99588326	expReg_chr7_6373_+
7	lnc-ZKSCAN1-1	chr7:99608999-99609249	XLOC_006188
8	lnc-ZKSCAN1-1	chr7:99594667-99594733	XLOC_006188
9	lnc-ZKSCAN1-1	chr7:99605744-99605862	XLOC_006188
10	lnc-ZKSCAN1-1	chr7:99608999-99609247	XLOC_006188
11	lnc-ZKSCAN1-1	chr7:99597002-99597115	XLOC_006188
12	lnc-ZKSCAN1-1	chr7:99605669-99605945	XLOC_006188
13	lnc-ZKSCAN1-1	chr7:99605931-99605945	XLOC_006188
14	lnc-ZKSCAN1-1	chr7:99595355-99595546	XLOC_006188

No data

Variant related genes	Relation type
ZKSCAN1	TF binding region
ENSG00000235713	TF binding region
ZKSCAN1	CpG island
ENSG00000235713	CpG island
ENSG00000237640	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000166529	chromatin interactions
ENSG00000214309	chromatin interactions
ENSG00000242798	chromatin interactions
ENSG00000106290	chromatin interactions
ENSG00000197037	chromatin interactions
ENSG00000272373	chromatin interactions
ENSG00000235077	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000146826	chromatin interactions
ENSG00000166526	chromatin interactions
ENSG00000106261	chromatin interactions
ENSG00000051108	chromatin interactions
ENSG00000235713	chromatin interactions
ENSG00000137154	chromatin interactions
ENSG00000272888	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000176402	chromatin interactions
ENSG00000168090	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000221838	chromatin interactions
ENSG00000166997	chromatin interactions
ENSG00000146833	chromatin interactions
C11orf82	miRNA target sites
NUP153	miRNA target sites
ASCC2	miRNA target sites
TMEM45A	miRNA target sites
BRD1	miRNA target sites
KCTD15	miRNA target sites
ARSJ	miRNA target sites

Extended variants
information (count: 1615 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1615 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6960542	chr7:99583219-99583220	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536508760	chr7:99583262-99583263	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs563017863	chr7:99583271-99583272	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs533456257	chr7:99583273-99583274	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs4729561	chr7:99583286-99583287	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs191514201	chr7:99583311-99583312	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs572502986	chr7:99583338-99583339	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs528393193	chr7:99583357-99583358	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs546834351	chr7:99583403-99583404	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs567967646	chr7:99583434-99583435	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs182980007	chr7:99583513-99583514	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373966136	chr7:99583540-99583541	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs150377473	chr7:99583565-99583566	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs558604834	chr7:99583581-99583582	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs368172723	chr7:99583590-99583591	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs4729562	chr7:99583650-99583651	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs35766848	chr7:99583662-99583663	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs557954019	chr7:99583666-99583667	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs562834274	chr7:99583682-99583683	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs567017494	chr7:99583707-99583708	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs534231795	chr7:99583719-99583720	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs532464507	chr7:99583773-99583774	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs544310514	chr7:99583782-99583783	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs555976675	chr7:99583959-99583960	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs187737684	chr7:99583976-99583977	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562502837	chr7:99584082-99584083	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs544657122	chr7:99584126-99584127	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs192653077	chr7:99584159-99584160	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs578162606	chr7:99584196-99584197	Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs147630872	chr7:99584208-99584209	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs374968752	chr7:99584209-99584210	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs368439248	chr7:99584210-99584211	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs372813432	chr7:99584215-99584216	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs542142094	chr7:99584224-99584225	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs35065773	chr7:99584253-99584254	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs78375248	chr7:99584266-99584267	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs80211368	chr7:99584267-99584268	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs142350506	chr7:99584318-99584319	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs562056478	chr7:99584336-99584337	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs183269260	chr7:99584350-99584351	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs118126374	chr7:99584410-99584411	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs550997668	chr7:99584434-99584435	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs568487755	chr7:99584465-99584466	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs544879376	chr7:99584501-99584502	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs146318201	chr7:99584548-99584549	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs571634350	chr7:99584588-99584589	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs376964710	chr7:99584698-99584699	Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567540117	chr7:99584760-99584761	Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534448403	chr7:99584792-99584793	Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532468585	chr7:99584807-99584808	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2038 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99581400-99584200	Genic enhancers	Liver	Liver
2	chr7:99582800-99588400	Weak transcription	Right Atrium	heart
3	chr7:99584200-99585400	Strong transcription	Liver	Liver
4	chr7:99584600-99584800	Enhancers	Fetal Brain Female	brain
5	chr7:99584800-99587200	Weak transcription	Fetal Brain Female	brain
6	chr7:99585400-99586000	Genic enhancers	Liver	Liver
7	chr7:99585600-99585800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr7:99585800-99588000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:99586000-99587000	Weak transcription	Liver	Liver
10	chr7:99586400-99587200	Enhancers	HepG2	liver
11	chr7:99587000-99587200	Enhancers	Liver	Liver
12	chr7:99587200-99587600	Weak transcription	Liver	Liver
13	chr7:99587200-99588000	Weak transcription	HepG2	liver
14	chr7:99587200-99588800	Active TSS	Fetal Brain Female	brain
15	chr7:99587600-99588400	Enhancers	Liver	Liver
16	chr7:99587800-99588000	Enhancers	Brain Anterior Caudate	brain
17	chr7:99587800-99588000	Enhancers	Brain Hippocampus Middle	brain
18	chr7:99587800-99588000	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr7:99587800-99588000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr7:99587800-99588000	Enhancers	Brain Substantia Nigra	brain
21	chr7:99587800-99588200	Flanking Active TSS	Fetal Brain Male	brain
22	chr7:99587800-99588800	Active TSS	Brain Germinal Matrix	brain
23	chr7:99588000-99588200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr7:99588000-99588200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:99588000-99588200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
26	chr7:99588000-99588200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
27	chr7:99588000-99588200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
28	chr7:99588000-99588200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr7:99588000-99588200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:99588000-99588200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:99588000-99588200	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr7:99588000-99588200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
33	chr7:99588000-99588200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr7:99588000-99588200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
35	chr7:99588000-99588200	Enhancers	Stomach Smooth Muscle	stomach
36	chr7:99588000-99588200	Bivalent Enhancer	NHEK	skin
37	chr7:99588000-99588400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
38	chr7:99588000-99588400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr7:99588000-99588400	Flanking Active TSS	Brain Anterior Caudate	brain
40	chr7:99588000-99588400	Flanking Active TSS	Brain Hippocampus Middle	brain
41	chr7:99588000-99588400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr7:99588000-99588400	Flanking Active TSS	Brain Substantia Nigra	brain
43	chr7:99588000-99588400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr7:99588000-99588600	Active TSS	H9 Cell Line	embryonic stem cell
45	chr7:99588000-99588600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:99588000-99588600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
47	chr7:99588000-99588600	Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr7:99588000-99588600	Active TSS	Brain Cingulate Gyrus	brain
49	chr7:99588000-99588600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
50	chr7:99588000-99588600	Active TSS	Pancreatic Islets	Pancreatic Islet

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