Variant report

Variant	esv1825988
Chromosome Location	chr3:19976375-20102773
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3011)
CpG islands
(count:2015)
Chromatin interactive
region (count:152)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:13)

(count:3011 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:19987115-19987639	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:19989243-19989553	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:20008657-20009619	K562	blood:	n/a	n/a
4	ARID3A	chr3:20079145-20079315	K562	blood:	n/a	n/a
5	ARID3A	chr3:20043611-20043819	K562	blood:	n/a	n/a
6	ARID3A	chr3:20002338-20002581	K562	blood:	n/a	n/a
7	ARID3A	chr3:19988883-19988922	K562	blood:	n/a	n/a
8	ARID3A	chr3:20056175-20056432	K562	blood:	n/a	n/a
9	ARID3A	chr3:20082402-20082577	K562	blood:	n/a	n/a
10	ARID3A	chr3:20080060-20080685	K562	blood:	n/a	n/a
11	ARID3A	chr3:19999876-19999936	K562	blood:	n/a	n/a
12	ARID3A	chr3:20081499-20081651	K562	blood:	n/a	n/a
13	ARID3A	chr3:20065245-20065546	K562	blood:	n/a	n/a
14	ARID3A	chr3:19978769-19979488	K562	blood:	n/a	n/a
15	ARID3A	chr3:20063992-20065045	K562	blood:	n/a	n/a
16	ARID3A	chr3:20083156-20083470	K562	blood:	n/a	n/a
17	ARID3A	chr3:19979685-19979859	HepG2	liver:	n/a	n/a
18	ARID3A	chr3:20102456-20102678	HepG2	liver:	n/a	n/a
19	ARID3A	chr3:19988281-19988728	HepG2	liver:	n/a	n/a
20	ARID3A	chr3:19986723-19988668	K562	blood:	n/a	n/a
21	ARID3A	chr3:20096000-20096345	HepG2	liver:	n/a	n/a
22	ARID3A	chr3:20057080-20057584	K562	blood:	n/a	n/a
23	ARID3A	chr3:19999473-19999541	K562	blood:	n/a	n/a
24	ATF1	chr3:20092738-20093002	K562	blood:	n/a	n/a
25	ATF1	chr3:20057033-20057364	K562	blood:	n/a	n/a
26	ATF1	chr3:19987645-19988784	K562	blood:	n/a	n/a
27	ATF1	chr3:20064360-20065076	K562	blood:	n/a	n/a
28	ATF1	chr3:19978931-19979563	K562	blood:	n/a	n/a
29	ATF2	chr3:19988400-19988707	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr3:20081302-20081776	GM12878	blood:	n/a	n/a
31	ATF2	chr3:19987979-19988412	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr3:19987825-19988939	GM12878	blood:	n/a	n/a
33	ATF2	chr3:20082866-20083368	GM12878	blood:	n/a	n/a
34	ATF3	chr3:20052769-20053055	K562	blood:	n/a	n/a
35	ATF3	chr3:20096028-20096490	A549	lung:	n/a	n/a
36	ATF3	chr3:20008679-20009000	K562	blood:	n/a	n/a
37	ATF3	chr3:20064284-20064746	K562	blood:	n/a	n/a
38	ATF3	chr3:19988385-19988823	A549	lung:	n/a	n/a
39	ATF3	chr3:19988926-19989373	K562	blood:	n/a	chr3:19989161-19989169
40	ATF3	chr3:19988976-19989324	K562	blood:	n/a	chr3:19989161-19989169
41	ATF3	chr3:20092643-20092877	K562	blood:	n/a	chr3:20092813-20092828
42	ATF3	chr3:20095973-20096523	HCT-116	colon:	n/a	n/a
43	ATF3	chr3:19988213-19988679	GM12878	blood:	n/a	n/a
44	ATF3	chr3:20095922-20096535	A549	lung:	n/a	n/a
45	ATF3	chr3:19988110-19988819	A549	lung:	n/a	n/a
46	ATF3	chr3:19988313-19988710	K562	blood:	n/a	n/a
47	BACH1	chr3:19988463-19988728	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr3:20035994-20036063	K562	blood:	n/a	n/a
49	BATF	chr3:20090142-20090441	GM12878	blood:	n/a	n/a
50	BATF	chr3:20098660-20098987	GM12878	blood:	n/a	chr3:20098865-20098876

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:19987528-19987578	HCF	heart:	n/a
2	chr3:20081367-20081417	GM12878	blood:	n/a
3	chr3:19987528-19987578	HCF	heart:	n/a
4	chr3:20081367-20081417	GM12878	blood:	n/a
5	chr3:20081585-20081635	HL-60	blood:	n/a
6	chr3:20049601-20049651	BJ	skin:	n/a
7	chr3:19990693-19990743	PANC-1	pancreas:	n/a
8	chr3:20049638-20049688	K562	blood:	n/a
9	chr3:19987815-19987865	BJ	skin:	n/a
10	chr3:20081518-20081568	ProgFib	skin:	n/a
11	chr3:19988340-19988390	GM19239	blood:	n/a
12	chr3:20082916-20082966	PrEC	prostate:	n/a
13	chr3:20049601-20049651	GM12878	blood:	n/a
14	chr3:20078165-20078215	PrEC	prostate:	n/a
15	chr3:20053940-20053990	HRCEpiC	kidney:	n/a
16	chr3:19988404-19988454	SK-N-SH_RA	brain:	n/a
17	chr3:19990693-19990743	T-47D	breast:	n/a
18	chr3:20026603-20026653	AG04450	lung:	fetal
19	chr3:19988680-19988730	GM12878	blood:	n/a
20	chr3:19989128-19989178	NH-A	brain:	n/a
21	chr3:20026603-20026653	HRCEpiC	kidney:	n/a
22	chr3:19985031-19985081	HMEC	breast:	n/a
23	chr3:20081367-20081417	GM19239	blood:	n/a
24	chr3:19990693-19990743	PFSK-1	brain:	n/a
25	chr3:19992400-19992450	RPTEC	kidney:	n/a
26	chr3:19988243-19988293	ECC-1	luminal epithelium:	n/a
27	chr3:19990693-19990743	HRPEpiC	eye:	n/a
28	chr3:20082916-20082966	H1-hESC	embryonic stem cell:	embryo
29	chr3:20081585-20081635	HNPCEpiC	eye:	n/a
30	chr3:20081516-20081566	H1-hESC	embryonic stem cell:	embryo
31	chr3:20085136-20085186	SAEC	small airway:	n/a
32	chr3:19987665-19987715	HL-60	blood:	n/a
33	chr3:20081367-20081417	Hela-S3	cervix:	n/a
34	chr3:19988340-19988390	GM12878	blood:	n/a
35	chr3:19988460-19988510	A549	lung:	n/a
36	chr3:20081516-20081566	BE2_C	brain:	n/a
37	chr3:19987528-19987578	PANC-1	pancreas:	n/a
38	chr3:20081516-20081566	GM12878	blood:	n/a
39	chr3:19990693-19990743	ProgFib	skin:	n/a
40	chr3:20085136-20085186	HIPEpiC	eye:	n/a
41	chr3:20081516-20081566	AG09309	skin:	n/a
42	chr3:20026603-20026653	ovcar-3	ovarian:	n/a
43	chr3:19985031-19985081	CMK	blood:	n/a
44	chr3:20082916-20082966	HAEpiC	amniotic membrane:	n/a
45	chr3:20049638-20049688	CMK	blood:	n/a
46	chr3:20026603-20026653	AG09309	skin:	n/a
47	chr3:20049601-20049651	PFSK-1	brain:	n/a
48	chr3:20082285-20082335	Hela-S3	cervix:	n/a
49	chr3:19988340-19988390	AoSMC	blood vessel:	n/a
50	chr3:20026603-20026653	CMK	blood:	n/a

(count:152 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:20063707..20066137-chr3:20066791..20068854,2	K562	blood:
2	chr3:20061429..20065762-chr3:20080168..20083220,6	K562	blood:
3	chr3:20087468..20090751-chr3:20095333..20097422,3	MCF-7	breast:
4	chr3:20046912..20049769-chr3:20052524..20055370,2	K562	blood:
5	chr3:20036427..20038510-chr3:20080865..20083451,2	K562	blood:
6	chr3:19967166..19969606-chr3:20013917..20016357,2	MCF-7	breast:
7	chr14:24899081..24899637-chr3:19988552..19989514,2	Hela-S3	cervix:
8	chr3:20002226..20004591-chr3:20006312..20009350,3	MCF-7	breast:
9	chr3:19998852..20001425-chr3:20020103..20022422,2	MCF-7	breast:
10	chr3:20066355..20070620-chr3:20073671..20078413,5	K562	blood:
11	chr3:20069120..20070627-chr3:20076892..20079468,2	K562	blood:
12	chr3:20092001..20094712-chr3:20096791..20098373,2	K562	blood:
13	chr3:19987059..19990115-chr3:20012573..20015556,4	MCF-7	breast:
14	chr3:20022682..20025378-chr3:20026127..20028940,2	MCF-7	breast:
15	chr3:19975611..19979082-chr3:19987774..19990681,3	MCF-7	breast:
16	chr14:23770618..23772878-chr3:20077291..20079103,2	MCF-7	breast:
17	chr3:20050259..20051981-chr3:20063056..20065911,2	K562	blood:
18	chr3:20089290..20092094-chr3:20224764..20226931,2	K562	blood:
19	chr3:19188168..19190474-chr3:19988134..19989911,2	MCF-7	breast:
20	chr3:19999385..20001229-chr3:20001451..20003044,2	K562	blood:
21	chr3:20064379..20066103-chr3:20069480..20072008,2	MCF-7	breast:
22	chr3:20010598..20012211-chr3:20015468..20017013,2	K562	blood:
23	chr3:19998852..20001425-chr3:20020103..20022422,2	MCF-7	breast:
24	chr3:20058205..20061001-chr3:20066769..20068692,2	K562	blood:
25	chr3:19986647..19989004-chr3:20010739..20012359,2	K562	blood:
26	chr3:20002287..20004974-chr3:20006037..20009711,3	K562	blood:
27	chr3:20079279..20082964-chr3:20226299..20229620,6	K562	blood:
28	chr3:19999505..20001254-chr3:20002139..20004557,2	MCF-7	breast:
29	chr3:20067539..20069733-chr3:20073671..20076293,2	K562	blood:
30	chr3:19987782..19990680-chr3:20013275..20017779,4	K562	blood:
31	chr3:19988069..19990118-chr3:20020900..20023827,2	MCF-7	breast:
32	chr3:20079527..20082964-chr3:20226742..20229620,4	K562	blood:
33	chr17:8076548..8077059-chr3:19987723..19988396,2	Hela-S3	cervix:
34	chr3:20029851..20032501-chr3:20180308..20182516,2	K562	blood:
35	chr3:20007536..20010825-chr3:20014102..20016831,3	K562	blood:
36	chr3:20005781..20007385-chr3:20012300..20014395,2	K562	blood:
37	chr3:19991110..19993492-chr3:20053410..20056377,2	K562	blood:
38	chr3:20094893..20096727-chr3:20227964..20230863,2	MCF-7	breast:
39	chr3:20027470..20029591-chr3:20033923..20036338,3	K562	blood:
40	chr3:19979250..19980946-chr3:19981520..19983771,2	K562	blood:
41	chr3:20071377..20073447-chr3:20074855..20077238,2	K562	blood:
42	chr3:20071336..20075491-chr3:20077751..20082913,7	K562	blood:
43	chr3:19996748..19999658-chr3:20007262..20009565,3	K562	blood:
44	chr3:20035142..20037256-chr3:20064733..20066737,2	K562	blood:
45	chr3:20082249..20087148-chr3:20090873..20095169,4	K562	blood:
46	chr3:20050259..20051981-chr3:20063056..20065911,2	K562	blood:
47	chr3:20002287..20004974-chr3:20006037..20009711,3	K562	blood:
48	chr3:20096569..20098445-chr3:20104189..20106827,2	MCF-7	breast:
49	chr3:19985145..19990136-chr3:20225418..20228312,6	K562	blood:
50	chr3:20007751..20010574-chr3:20010896..20013275,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EFHB-4	chr3:20042522-20043588	NR_027694
2	lnc-EFHB-4	chr3:20053542-20053765	NR_027694
3	lnc-EFHB-2	chr3:19987406-19987746	NONHSAT088605
4	lnc-EFHB-2	chr3:19988411-19988517	NONHSAT088605
5	lnc-EFHB-4	chr3:20025686-20025788	NR_027694
6	lnc-EFHB-3	chr3:20049344-20049739	NONHSAT088609
7	lnc-EFHB-4	chr3:20053542-20053749	NONHSAT088608
8	lnc-EFHB-4	chr3:20042467-20043588	NONHSAT088608
9	lnc-EFHB-4	chr3:20021453-20021666	NR_027694

No data

(count:13 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RAB5A	hsa-miR-130a-3p	chr3:20026128-20026150
2	RAB5A	hsa-miR-33a-5p	chr3:20026130-20026148
3	RAB5A	hsa-miR-101-3p	chr3:20026185-20026206
4	RAB5A	hsa-miR-130b-3p	chr3:20026477-20026484
5	RAB5A	hsa-miR-101-3p	chr3:20026199-20026206
6	RAB5A	hsa-miR-33a-5p	chr3:20026571-20026591
7	RAB5A	hsa-miR-130b-3p	chr3:20026461-20026484
8	RAB5A	hsa-miR-101-3p	chr3:20025772-20025793
9	RAB5A	hsa-miR-130b-3p	chr3:20026129-20026150
10	RAB5A	hsa-miR-130a-3p	chr3:20026477-20026484
11	RAB5A	hsa-miR-18a-5p	chr3:20025965-20025987
12	RAB5A	hsa-miR-101-3p	chr3:20026272-20026293
13	RAB5A	hsa-miR-130a-3p	chr3:20026463-20026484

Variant related genes	Relation type
KAT2B	TF binding region
ENSG00000229468	TF binding region
RNU4-85P	TF binding region
EFHB	TF binding region
ENSG00000230697	TF binding region
HSPA8P18	TF binding region
RAB5A	TF binding region
PP2D1	TF binding region
KAT2B	CpG island
ENSG00000229468	CpG island
RNU4-85P	CpG island
EFHB	CpG island
ENSG00000230697	CpG island
HSPA8P18	CpG island
RAB5A	CpG island
PP2D1	CpG island
ENSG00000230697	chromatin interactions
ENSG00000144566	chromatin interactions
ENSG00000100441	chromatin interactions
ENSG00000267321	chromatin interactions
ENSG00000163576	chromatin interactions
ENSG00000183977	chromatin interactions
ENSG00000114166	chromatin interactions
ENSG00000235194	chromatin interactions
ENSG00000169241	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000229468	chromatin interactions
ENSG00000183960	chromatin interactions
ENSG00000201545	chromatin interactions
ENSG00000129810	chromatin interactions

Extended variants
information (count: 5262 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:5262 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115005690	chr3:19976384-19976385	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs543249911	chr3:19976403-19976404	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs147749359	chr3:19976407-19976408	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs79072115	chr3:19976418-19976419	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs200587668	chr3:19976421-19976422	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs550401461	chr3:19976434-19976435	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs145771569	chr3:19976454-19976455	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs9818022	chr3:19976468-19976469	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs566050648	chr3:19976479-19976480	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs530132575	chr3:19976492-19976493	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548636096	chr3:19976505-19976506	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs570277073	chr3:19976515-19976516	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs113600966	chr3:19976551-19976552	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs139910418	chr3:19976552-19976553	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs570758065	chr3:19976623-19976624	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs12638170	chr3:19976648-19976649	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs376974358	chr3:19976649-19976650	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs538329475	chr3:19976657-19976658	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs111423853	chr3:19976676-19976677	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs149402861	chr3:19976678-19976679	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs193001111	chr3:19976697-19976698	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs535823557	chr3:19976713-19976714	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs556866315	chr3:19976732-19976733	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs576248460	chr3:19976763-19976764	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs546797716	chr3:19976770-19976771	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576699795	chr3:19976811-19976812	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs146344721	chr3:19976814-19976815	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs139627480	chr3:19976878-19976879	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs566626709	chr3:19976889-19976890	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs576989895	chr3:19976914-19976915	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs184184956	chr3:19976970-19976971	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs9878068	chr3:19977011-19977012	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs370863839	chr3:19977029-19977030	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs535964461	chr3:19977059-19977060	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs548597385	chr3:19977063-19977064	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs563738955	chr3:19977076-19977077	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs9822900	chr3:19977120-19977121	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs552859341	chr3:19977129-19977130	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs116328675	chr3:19977132-19977133	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs534875926	chr3:19977164-19977165	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs117433726	chr3:19977165-19977166	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs545409636	chr3:19977214-19977215	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs188982896	chr3:19977225-19977226	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs9878676	chr3:19977226-19977227	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs554104437	chr3:19977230-19977231	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs9878688	chr3:19977254-19977255	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs536918652	chr3:19977262-19977263	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs558828071	chr3:19977275-19977276	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs577096433	chr3:19977299-19977300	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs541204744	chr3:19977300-19977301	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	19363497	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:3721 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:19973600-19979200	Weak transcription	HMEC	breast
2	chr3:19973600-19987200	Weak transcription	Primary B cells from peripheral blood	blood
3	chr3:19973800-19978400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr3:19973800-19979000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr3:19974200-19979200	Weak transcription	Hela-S3	cervix
6	chr3:19975000-19976400	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr3:19975200-19976400	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr3:19975200-19976400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
9	chr3:19975600-19987400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr3:19976000-19976800	Enhancers	K562	blood
11	chr3:19976000-19979000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr3:19976000-19979200	Weak transcription	HepG2	liver
13	chr3:19976000-19987400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:19976200-19979000	Weak transcription	A549	lung
15	chr3:19976400-19976800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr3:19976800-19977600	Weak transcription	K562	blood
17	chr3:19977600-19978800	Enhancers	K562	blood
18	chr3:19978400-19979800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr3:19978600-19979800	Enhancers	NH-A	brain
20	chr3:19978800-19979600	Enhancers	Stomach Mucosa	stomach
21	chr3:19978800-19979600	Flanking Active TSS	K562	blood
22	chr3:19978800-19979800	Enhancers	Osteobl	bone
23	chr3:19979000-19979400	Enhancers	A549	lung
24	chr3:19979000-19979600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr3:19979000-19979600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr3:19979000-19979600	Enhancers	Placenta Amnion	Placenta Amnion
27	chr3:19979200-19979400	Enhancers	HMEC	breast
28	chr3:19979200-19979600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr3:19979200-19979800	Enhancers	Hela-S3	cervix
30	chr3:19979200-19980000	Enhancers	HepG2	liver
31	chr3:19979400-19979800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr3:19979600-19980000	Enhancers	K562	blood
33	chr3:19979600-19987600	Weak transcription	Fetal Muscle Trunk	muscle
34	chr3:19979600-19987800	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr3:19980000-19986600	Weak transcription	K562	blood
36	chr3:19982200-19987200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr3:19983200-19987400	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr3:19983800-19987600	Weak transcription	Aorta	Aorta
39	chr3:19984200-19984800	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr3:19984400-19984600	ZNF genes & repeats	Brain Germinal Matrix	brain
41	chr3:19984600-19987400	Weak transcription	Brain Germinal Matrix	brain
42	chr3:19984800-19987200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr3:19984800-19987200	Weak transcription	Adipose Nuclei	Adipose
44	chr3:19984800-19987600	Weak transcription	Esophagus	oesophagus
45	chr3:19985000-19987000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr3:19985000-19987400	Weak transcription	HSMM	muscle
47	chr3:19985600-19987600	Weak transcription	Fetal Lung	lung
48	chr3:19985800-19987400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr3:19985800-19987400	Weak transcription	NH-A	brain
50	chr3:19986200-19986400	Enhancers	Muscle Satellite Cultured Cells	--

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