Variant report

Variant	esv1825207
Chromosome Location	chr7:99552275-99625510
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2596)
CpG islands
(count:2320)
Chromatin interactive
region (count:145)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2596 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99578392-99578401	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:99588561-99588855	K562	blood:	n/a	n/a
3	ARID3A	chr7:99588540-99588839	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:99591808-99592148	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:99573511-99574236	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:99591850-99592144	K562	blood:	n/a	n/a
7	ARID3A	chr7:99612999-99613317	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:99613002-99613272	K562	blood:	n/a	n/a
9	ARID3A	chr7:99553594-99553700	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:99621722-99621985	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:99614020-99614567	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:99595227-99595537	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:99610285-99610671	HepG2	liver:	n/a	n/a
14	ARID3A	chr7:99601325-99601936	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:99577288-99577300	K562	blood:	n/a	n/a
16	ATF1	chr7:99613008-99613355	K562	blood:	n/a	n/a
17	ATF1	chr7:99556328-99556705	K562	blood:	n/a	n/a
18	ATF2	chr7:99588383-99588853	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr7:99612925-99613402	GM12878	blood:	n/a	n/a
20	ATF2	chr7:99595114-99595627	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr7:99595132-99595501	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr7:99623674-99624169	GM12878	blood:	n/a	n/a
23	ATF2	chr7:99612922-99613352	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr7:99588414-99588699	GM12878	blood:	n/a	n/a
25	ATF3	chr7:99612906-99613380	A549	lung:	n/a	n/a
26	ATF3	chr7:99588519-99588908	A549	lung:	n/a	n/a
27	ATF3	chr7:99612938-99613479	K562	blood:	n/a	n/a
28	BACH1	chr7:99612991-99613276	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr7:99588600-99588743	K562	blood:	n/a	n/a
30	BATF	chr7:99623746-99624108	GM12878	blood:	n/a	chr7:99623935-99623946
31	BATF	chr7:99552903-99553159	GM12878	blood:	n/a	chr7:99553049-99553060 chr7:99553050-99553060
32	BATF	chr7:99623677-99624143	GM12878	blood:	n/a	chr7:99623935-99623946
33	BATF	chr7:99612974-99613349	GM12878	blood:	n/a	n/a
34	BCL3	chr7:99612971-99613328	GM12878	blood:	n/a	chr7:99613205-99613214
35	BCL3	chr7:99612943-99613384	A549	lung:	n/a	chr7:99613205-99613214
36	BCLAF1	chr7:99612943-99613345	GM12878	blood:	n/a	chr7:99613205-99613214
37	BCLAF1	chr7:99595032-99595589	GM12878	blood:	n/a	chr7:99595317-99595326
38	BCLAF1	chr7:99623673-99624175	GM12878	blood:	n/a	n/a
39	BCLAF1	chr7:99612895-99613380	GM12878	blood:	n/a	chr7:99613205-99613214
40	BHLHE40	chr7:99595201-99595644	HepG2	liver:	n/a	n/a
41	BHLHE40	chr7:99588564-99588813	K562	blood:	n/a	n/a
42	BHLHE40	chr7:99601366-99601918	HepG2	liver:	n/a	n/a
43	BHLHE40	chr7:99577510-99577734	K562	blood:	n/a	n/a
44	BHLHE40	chr7:99621688-99622047	HepG2	liver:	n/a	n/a
45	BHLHE40	chr7:99576876-99576892	K562	blood:	n/a	n/a
46	BHLHE40	chr7:99577501-99577734	GM12878	blood:	n/a	n/a
47	BHLHE40	chr7:99591934-99592020	K562	blood:	n/a	n/a
48	BHLHE40	chr7:99612987-99613358	K562	blood:	n/a	n/a
49	BHLHE40	chr7:99623878-99624027	GM12878	blood:	n/a	n/a
50	BHLHE40	chr7:99573751-99574031	HepG2	liver:	n/a	n/a

(count:2320 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99613105-99613155	NT2-D1	testis:	n/a
2	chr7:99588561-99588611	HAEpiC	amniotic membrane:	n/a
3	chr7:99613105-99613155	NT2-D1	testis:	n/a
4	chr7:99588561-99588611	HAEpiC	amniotic membrane:	n/a
5	chr7:99616820-99616870	Hela-S3	cervix:	n/a
6	chr7:99574383-99574433	H1-hESC	embryonic stem cell:	embryo
7	chr7:99595276-99595326	A549	lung:	n/a
8	chr7:99613147-99613197	AG04449	skin:	fetal
9	chr7:99588273-99588323	K562	blood:	n/a
10	chr7:99613185-99613235	U87	brain:	n/a
11	chr7:99588561-99588611	GM06990	blood:	n/a
12	chr7:99613147-99613197	SK-N-SH	brain:	n/a
13	chr7:99614209-99614259	HIPEpiC	eye:	n/a
14	chr7:99609831-99609881	H1-hESC	embryonic stem cell:	embryo
15	chr7:99612634-99612684	GM12892	blood:	n/a
16	chr7:99595658-99595708	SKMC	muscle:	n/a
17	chr7:99574420-99574470	NHDF-neo	bronchial:	n/a
18	chr7:99598775-99598825	HAEpiC	amniotic membrane:	n/a
19	chr7:99612634-99612684	NT2-D1	testis:	n/a
20	chr7:99614209-99614259	BJ	skin:	n/a
21	chr7:99574466-99574516	HCPEpiC	choroid plexus:	n/a
22	chr7:99595437-99595487	NHBE	bronchial:	n/a
23	chr7:99612773-99612823	HCPEpiC	choroid plexus:	n/a
24	chr7:99595276-99595326	HMEC	breast:	n/a
25	chr7:99612634-99612684	HepG2	liver:	n/a
26	chr7:99576539-99576589	PFSK-1	brain:	n/a
27	chr7:99564474-99564524	H1-hESC	embryonic stem cell:	embryo
28	chr7:99613796-99613846	HCM	heart:	n/a
29	chr7:99613796-99613846	Hela-S3	cervix:	n/a
30	chr7:99598775-99598825	ProgFib	skin:	n/a
31	chr7:99576539-99576589	AoSMC	blood vessel:	n/a
32	chr7:99573278-99573328	HCM	heart:	n/a
33	chr7:99574466-99574516	HL-60	blood:	n/a
34	chr7:99613796-99613846	GM06990	blood:	n/a
35	chr7:99559579-99559629	PrEC	prostate:	n/a
36	chr7:99588335-99588385	AG04450	lung:	fetal
37	chr7:99574383-99574433	ProgFib	skin:	n/a
38	chr7:99616820-99616870	NHDF-neo	bronchial:	n/a
39	chr7:99588273-99588323	AoSMC	blood vessel:	n/a
40	chr7:99612715-99612765	RPTEC	kidney:	n/a
41	chr7:99559579-99559629	HRE	kidney:	n/a
42	chr7:99576539-99576589	HIPEpiC	eye:	n/a
43	chr7:99612773-99612823	AG09319	gingival:	n/a
44	chr7:99595458-99595508	CMK	blood:	n/a
45	chr7:99613205-99613255	NT2-D1	testis:	n/a
46	chr7:99613147-99613197	HAEpiC	amniotic membrane:	n/a
47	chr7:99591962-99592012	BJ	skin:	n/a
48	chr7:99595276-99595326	BE2_C	brain:	n/a
49	chr7:99598775-99598825	LNCaP	prostate:	n/a
50	chr7:99613147-99613197	RPTEC	kidney:	n/a

(count:145 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:99624486..99627047-chr7:99678745..99680467,2	K562	blood:
2	chr7:99609246..99610753-chr7:99613622..99615389,2	MCF-7	breast:
3	chr7:99618852..99620390-chr7:99647489..99649484,2	MCF-7	breast:
4	chr7:99552657..99555253-chr7:99568391..99571946,4	MCF-7	breast:
5	chr7:99580447..99583544-chr7:99586500..99589317,4	K562	blood:
6	chr7:99591521..99592480-chr7:99641969..99642586,3	MCF-7	breast:
7	chr7:99516441..99518017-chr7:99556643..99558220,2	MCF-7	breast:
8	chr16:3072904..3075257-chr7:99551706..99553216,2	MCF-7	breast:
9	chr7:99516941..99519594-chr7:99565743..99568567,2	MCF-7	breast:
10	chr7:99600014..99604498-chr7:99605032..99608017,4	MCF-7	breast:
11	chr7:99613224..99616757-chr7:99646903..99650456,6	K562	blood:
12	chr7:99228995..99229922-chr7:99588200..99589102,3	K562	blood:
13	chr7:99599411..99601548-chr7:99605711..99608652,3	MCF-7	breast:
14	chr7:99615508..99617156-chr7:99618905..99620431,2	MCF-7	breast:
15	chr7:99546378..99548989-chr7:99551538..99554041,2	MCF-7	breast:
16	chr7:99607653..99611387-chr7:99613037..99615775,4	K562	blood:
17	chr7:99618314..99620224-chr7:99678750..99680788,2	MCF-7	breast:
18	chr7:99590918..99594546-chr7:99596737..99599787,3	K562	blood:
19	chr7:99552086..99554197-chr7:99560760..99564029,3	MCF-7	breast:
20	chr7:99525542..99528041-chr7:99585746..99587767,2	MCF-7	breast:
21	chr7:99599411..99601548-chr7:99605711..99608652,3	MCF-7	breast:
22	chr7:99564809..99567213-chr7:99568029..99570135,2	K562	blood:
23	chr7:99588733..99590753-chr7:99595568..99598472,2	K562	blood:
24	chr7:99620109..99621730-chr7:99637270..99638942,2	MCF-7	breast:
25	chr7:99515843..99517674-chr7:99586833..99588501,2	MCF-7	breast:
26	chr7:99601553..99605102-chr7:99669434..99672992,3	K562	blood:
27	chr7:99515474..99518311-chr7:99585562..99587097,2	K562	blood:
28	chr7:99561135..99564106-chr7:99572617..99575074,2	K562	blood:
29	chr7:99552086..99554197-chr7:99560760..99564029,3	MCF-7	breast:
30	chr7:99552193..99555165-chr7:99565614..99568546,3	K562	blood:
31	chr7:99591473..99592533-chr7:99642040..99642986,5	MCF-7	breast:
32	chr7:99550695..99553534-chr7:99558845..99560540,2	MCF-7	breast:
33	chr7:99594172..99596915-chr7:99619216..99620782,2	K562	blood:
34	chr7:99612390..99616211-chr7:99697108..99699457,4	K562	blood:
35	chr7:99617125..99619542-chr7:99633323..99635330,2	K562	blood:
36	chr16:56966049..56966601-chr7:99612783..99613720,2	NB4	blood:
37	chr7:99601499..99602018-chr7:99663035..99663790,2	MCF-7	breast:
38	chr7:99587259..99592938-chr7:99645564..99652306,10	MCF-7	breast:
39	chr7:99591475..99592458-chr7:99650846..99651525,3	MCF-7	breast:
40	chr7:99619042..99622957-chr7:99630011..99632854,4	MCF-7	breast:
41	chr7:99609554..99611376-chr7:99679608..99681237,2	K562	blood:
42	chr1:45196470..45197118-chr7:99613158..99613683,2	Hela-S3	cervix:
43	chr7:99601762..99603433-chr7:99603449..99606278,2	K562	blood:
44	chr7:99577524..99578039-chr7:99588237..99589217,3	K562	blood:
45	chr7:99516045..99517602-chr7:99587182..99589911,2	K562	blood:
46	chr7:99584391..99586095-chr7:99609489..99611371,2	K562	blood:
47	chr6:27857861..27860281-chr7:99604688..99606426,2	K562	blood:
48	chr7:99591418..99594065-chr7:99611454..99615168,4	MCF-7	breast:
49	chr7:99510363..99510979-chr7:99592459..99593410,2	K562	blood:
50	chr7:99604525..99607316-chr7:99612606..99614648,4	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
ZKSCAN1	TF binding region
ENSG00000235713	TF binding region
AZGP1	TF binding region
AZGP1P1	TF binding region
ZKSCAN1	CpG island
ENSG00000235713	CpG island
AZGP1	CpG island
AZGP1P1	CpG island
ENSG00000237640	chromatin interactions
ENSG00000214252	chromatin interactions
ENSG00000197037	chromatin interactions
ENSG00000166997	chromatin interactions
ENSG00000146833	chromatin interactions
ENSG00000242798	chromatin interactions
ENSG00000235077	chromatin interactions
ENSG00000272373	chromatin interactions
ENSG00000160862	chromatin interactions
ENSG00000106261	chromatin interactions
ENSG00000272888	chromatin interactions
ENSG00000137154	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000106290	chromatin interactions
ENSG00000166526	chromatin interactions
ENSG00000051108	chromatin interactions
ENSG00000221838	chromatin interactions
ENSG00000214309	chromatin interactions
ENSG00000166529	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000176402	chromatin interactions
ENSG00000131652	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000235713	chromatin interactions
ENSG00000103145	chromatin interactions
ENSG00000168090	chromatin interactions
ENSG00000146826	chromatin interactions
ENSG00000197153	chromatin interactions
C11orf82	miRNA target sites
TMEM45A	miRNA target sites
ARSJ	miRNA target sites
NUP153	miRNA target sites
ASCC2	miRNA target sites
KCTD15	miRNA target sites
BRD1	miRNA target sites

Extended variants
information (count: 2980 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2980 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553693074	chr7:99552294-99552295	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs575258030	chr7:99552319-99552320	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs375150299	chr7:99552406-99552407	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs72089988	chr7:99552440-99552441	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs542540610	chr7:99552447-99552448	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs562924501	chr7:99552485-99552486	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs181777360	chr7:99552510-99552511	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs563657628	chr7:99552534-99552535	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs111350538	chr7:99552589-99552590	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs147029363	chr7:99552617-99552618	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs530824205	chr7:99552634-99552635	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs546252849	chr7:99552734-99552735	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs186507523	chr7:99552747-99552748	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs532162598	chr7:99552754-99552755	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs138229375	chr7:99552789-99552790	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs565635130	chr7:99552797-99552798	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs189717344	chr7:99552802-99552803	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs35656988	chr7:99552805-99552806	Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs117296927	chr7:99552806-99552807	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs149585226	chr7:99552837-99552838	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs558602867	chr7:99552871-99552872	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs570494083	chr7:99552874-99552875	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs535227340	chr7:99552886-99552887	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs13223723	chr7:99552892-99552893	Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs182418519	chr7:99552903-99552904	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs116877216	chr7:99552907-99552908	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs188176107	chr7:99552908-99552909	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs374074925	chr7:99552951-99552952	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs575575095	chr7:99552952-99552953	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs545913257	chr7:99553005-99553006	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs117268080	chr7:99553066-99553067	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs528612114	chr7:99553087-99553088	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs79335386	chr7:99553092-99553093	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs114313339	chr7:99553147-99553148	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs115292693	chr7:99553163-99553164	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs2525548	chr7:99553167-99553168	Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs532103703	chr7:99553234-99553235	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs550424782	chr7:99553239-99553240	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs563139684	chr7:99553335-99553336	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs530516873	chr7:99553336-99553337	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs143365014	chr7:99553360-99553361	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs191365439	chr7:99553361-99553362	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs570465003	chr7:99553434-99553435	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs35180763	chr7:99553437-99553438	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs562661782	chr7:99553507-99553508	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs183619425	chr7:99553528-99553529	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs553116272	chr7:99553529-99553530	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs199796601	chr7:99553541-99553542	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs564339619	chr7:99553595-99553596	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs148347774	chr7:99553616-99553617	Enhancers	Chromatin interactive region	3 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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:2159 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99546400-99552800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:99550400-99553800	Enhancers	Liver	Liver
3	chr7:99550800-99553200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr7:99551400-99552800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:99551400-99552800	Weak transcription	HepG2	liver
6	chr7:99551800-99552400	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr7:99552200-99553000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr7:99552800-99553000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:99552800-99553800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:99552800-99553800	Enhancers	GM12878-XiMat	blood
11	chr7:99552800-99554000	Enhancers	HepG2	liver
12	chr7:99553000-99553800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr7:99553800-99563200	Weak transcription	Liver	Liver
14	chr7:99554000-99565000	Weak transcription	HepG2	liver
15	chr7:99556400-99556600	Bivalent/Poised TSS	K562	blood
16	chr7:99560400-99560600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
17	chr7:99561600-99564000	Weak transcription	Pancreas	Pancrea
18	chr7:99562600-99573000	Weak transcription	Left Ventricle	heart
19	chr7:99563200-99567000	Strong transcription	Liver	Liver
20	chr7:99563400-99572800	Weak transcription	Brain Substantia Nigra	brain
21	chr7:99563400-99573000	Weak transcription	Gastric	stomach
22	chr7:99564000-99565600	Strong transcription	Pancreas	Pancrea
23	chr7:99564600-99564800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr7:99564800-99567600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:99565000-99565800	Strong transcription	HepG2	liver
26	chr7:99565400-99571600	Weak transcription	Adipose Nuclei	Adipose
27	chr7:99565600-99567600	Weak transcription	Pancreas	Pancrea
28	chr7:99565800-99568200	Weak transcription	HepG2	liver
29	chr7:99566000-99572400	Weak transcription	Right Ventricle	heart
30	chr7:99566800-99567000	Enhancers	Lung	lung
31	chr7:99567000-99569000	Weak transcription	Lung	lung
32	chr7:99567000-99570600	Genic enhancers	Liver	Liver
33	chr7:99567600-99567800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr7:99567600-99567800	Enhancers	Pancreas	Pancrea
35	chr7:99567800-99568200	Weak transcription	Pancreas	Pancrea
36	chr7:99567800-99578000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:99568200-99569600	Strong transcription	HepG2	liver
38	chr7:99568200-99570000	Genic enhancers	Pancreas	Pancrea
39	chr7:99568400-99568800	Weak transcription	Brain Anterior Caudate	brain
40	chr7:99569000-99569600	Enhancers	Lung	lung
41	chr7:99569600-99571600	Weak transcription	HepG2	liver
42	chr7:99570000-99570400	Enhancers	Pancreas	Pancrea
43	chr7:99570400-99572600	Weak transcription	Pancreas	Pancrea
44	chr7:99570600-99570800	Enhancers	Liver	Liver
45	chr7:99570800-99571400	Flanking Active TSS	Liver	Liver
46	chr7:99571400-99573800	Active TSS	Liver	Liver
47	chr7:99571600-99571800	Enhancers	Adipose Nuclei	Adipose
48	chr7:99571600-99572400	Enhancers	HepG2	liver
49	chr7:99571800-99572400	Weak transcription	Adipose Nuclei	Adipose
50	chr7:99572400-99572600	Flanking Active TSS	Adipose Nuclei	Adipose

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