Variant report

Variant	nsv1010762
Chromosome Location	chr3:101584836-101803821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2318)
CpG islands
(count:428)
Chromatin interactive
region (count:83)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2318 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:101661292-101661422	K562	blood:	n/a	n/a
2	ARID3A	chr3:101587269-101587594	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:101657287-101657657	K562	blood:	n/a	n/a
4	ATF1	chr3:101587567-101587936	K562	blood:	n/a	n/a
5	ATF1	chr3:101620923-101621281	K562	blood:	n/a	n/a
6	ATF1	chr3:101655562-101655712	K562	blood:	n/a	n/a
7	ATF1	chr3:101657342-101657597	K562	blood:	n/a	n/a
8	ATF1	chr3:101659462-101659881	K562	blood:	n/a	n/a
9	ATF2	chr3:101755205-101755759	GM12878	blood:	n/a	n/a
10	ATF2	chr3:101757128-101757841	GM12878	blood:	n/a	n/a
11	ATF2	chr3:101661104-101661715	GM12878	blood:	n/a	n/a
12	ATF2	chr3:101779676-101779966	GM12878	blood:	n/a	n/a
13	ATF2	chr3:101695286-101695807	GM12878	blood:	n/a	n/a
14	ATF2	chr3:101609562-101610011	GM12878	blood:	n/a	n/a
15	ATF2	chr3:101617392-101618142	GM12878	blood:	n/a	n/a
16	ATF2	chr3:101706497-101707277	GM12878	blood:	n/a	n/a
17	ATF2	chr3:101778267-101778830	GM12878	blood:	n/a	n/a
18	ATF2	chr3:101664686-101665244	GM12878	blood:	n/a	n/a
19	ATF2	chr3:101655397-101656094	GM12878	blood:	n/a	n/a
20	ATF2	chr3:101620851-101621349	GM12878	blood:	n/a	n/a
21	ATF2	chr3:101669300-101669842	GM12878	blood:	n/a	n/a
22	ATF2	chr3:101778271-101778853	GM12878	blood:	n/a	n/a
23	ATF2	chr3:101620827-101621352	GM12878	blood:	n/a	n/a
24	ATF2	chr3:101661769-101662193	GM12878	blood:	n/a	n/a
25	ATF2	chr3:101706621-101707731	GM12878	blood:	n/a	n/a
26	ATF2	chr3:101757130-101757887	GM12878	blood:	n/a	n/a
27	ATF2	chr3:101707290-101708048	GM12878	blood:	n/a	n/a
28	ATF2	chr3:101695290-101695865	GM12878	blood:	n/a	n/a
29	ATF2	chr3:101753401-101754014	GM12878	blood:	n/a	n/a
30	ATF2	chr3:101655416-101656196	GM12878	blood:	n/a	n/a
31	ATF2	chr3:101661119-101661721	GM12878	blood:	n/a	n/a
32	ATF2	chr3:101715583-101716171	GM12878	blood:	n/a	n/a
33	ATF2	chr3:101657157-101657821	GM12878	blood:	n/a	n/a
34	ATF2	chr3:101659991-101660694	GM12878	blood:	n/a	n/a
35	ATF2	chr3:101753448-101753954	GM12878	blood:	n/a	n/a
36	ATF2	chr3:101669139-101669996	GM12878	blood:	n/a	n/a
37	ATF2	chr3:101657197-101657791	GM12878	blood:	n/a	n/a
38	ATF2	chr3:101776526-101777328	GM12878	blood:	n/a	n/a
39	ATF2	chr3:101664723-101665293	GM12878	blood:	n/a	n/a
40	ATF2	chr3:101755259-101755652	GM12878	blood:	n/a	n/a
41	ATF2	chr3:101609462-101610018	GM12878	blood:	n/a	n/a
42	ATF2	chr3:101617318-101618220	GM12878	blood:	n/a	n/a
43	ATF3	chr3:101620867-101621416	HCT-116	colon:	n/a	n/a
44	BACH1	chr3:101658528-101658566	K562	blood:	n/a	n/a
45	BATF	chr3:101779682-101779987	GM12878	blood:	n/a	chr3:101779854-101779864
46	BATF	chr3:101594962-101595264	GM12878	blood:	n/a	n/a
47	BATF	chr3:101617545-101618036	GM12878	blood:	n/a	n/a
48	BATF	chr3:101776621-101776939	GM12878	blood:	n/a	n/a
49	BATF	chr3:101778441-101778743	GM12878	blood:	n/a	n/a
50	BATF	chr3:101661219-101661563	GM12878	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:101712884-101712934	HNPCEpiC	eye:	n/a
2	chr3:101712884-101712934	HNPCEpiC	eye:	n/a
3	chr3:101712884-101712934	HCPEpiC	choroid plexus:	n/a
4	chr3:101659687-101659737	T-47D	breast:	n/a
5	chr3:101712884-101712934	U87	brain:	n/a
6	chr3:101659687-101659737	SKMC	muscle:	n/a
7	chr3:101658926-101658976	MCF-7	breast:	n/a
8	chr3:101658926-101658976	HMEC	breast:	n/a
9	chr3:101798142-101798192	CMK	blood:	n/a
10	chr3:101660066-101660116	BJ	skin:	n/a
11	chr3:101798142-101798192	SK-N-SH_RA	brain:	n/a
12	chr3:101798142-101798192	GM19239	blood:	n/a
13	chr3:101712884-101712934	SK-N-MC	brain:	n/a
14	chr3:101683592-101683642	IMR90	lung:	fetal
15	chr3:101659687-101659737	HRCEpiC	kidney:	n/a
16	chr3:101658926-101658976	AG10803	skin:	n/a
17	chr3:101659630-101659680	CMK	blood:	n/a
18	chr3:101658926-101658976	NB4	blood:	n/a
19	chr3:101659630-101659680	Caco-2	colon:	n/a
20	chr3:101659687-101659737	NHDF-neo	bronchial:	n/a
21	chr3:101658926-101658976	Jurkat	blood:	n/a
22	chr3:101660066-101660116	HL-60	blood:	n/a
23	chr3:101660066-101660116	HRCEpiC	kidney:	n/a
24	chr3:101659630-101659680	GM12878	blood:	n/a
25	chr3:101712884-101712934	AG10803	skin:	n/a
26	chr3:101683592-101683642	NB4	blood:	n/a
27	chr3:101683592-101683642	AG04450	lung:	fetal
28	chr3:101659630-101659680	HUVEC	blood vessel:	n/a
29	chr3:101798142-101798192	HCPEpiC	choroid plexus:	n/a
30	chr3:101683592-101683642	HRCEpiC	kidney:	n/a
31	chr3:101659687-101659737	SK-N-SH	brain:	n/a
32	chr3:101658926-101658976	SK-N-MC	brain:	n/a
33	chr3:101659687-101659737	SAEC	small airway:	n/a
34	chr3:101659630-101659680	A549	lung:	n/a
35	chr3:101658926-101658976	PANC-1	pancreas:	n/a
36	chr3:101798142-101798192	NT2-D1	testis:	n/a
37	chr3:101798142-101798192	GM12891	blood:	n/a
38	chr3:101659630-101659680	BJ	skin:	n/a
39	chr3:101659687-101659737	SK-N-MC	brain:	n/a
40	chr3:101712884-101712934	GM12891	blood:	n/a
41	chr3:101660066-101660116	SK-N-SH	brain:	n/a
42	chr3:101658926-101658976	PFSK-1	brain:	n/a
43	chr3:101683592-101683642	MCF10A-Er-Src	breast:	n/a
44	chr3:101660066-101660116	ProgFib	skin:	n/a
45	chr3:101659630-101659680	PANC-1	pancreas:	n/a
46	chr3:101712884-101712934	GM19239	blood:	n/a
47	chr3:101659687-101659737	A549	lung:	n/a
48	chr3:101712884-101712934	HCF	heart:	n/a
49	chr3:101660066-101660116	SKMC	muscle:	n/a
50	chr3:101659687-101659737	SK-N-SH_RA	brain:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:101664188..101666694-chr3:101667013..101668837,2	MCF-7	breast:
2	chr3:101738065..101740879-chr3:101940382..101942538,2	MCF-7	breast:
3	chr3:101664188..101666694-chr3:101667013..101668837,2	MCF-7	breast:
4	chr3:101604292..101607119-chr3:101609303..101612287,2	MCF-7	breast:
5	chr3:101661155..101664150-chr3:101664624..101666610,2	K562	blood:
6	chr3:101609413..101611144-chr3:101614360..101616706,2	MCF-7	breast:
7	chr3:101583187..101585591-chr3:101588676..101591535,3	MCF-7	breast:
8	chr3:101611977..101614577-chr3:101618423..101621104,2	K562	blood:
9	chr3:101566961..101569726-chr3:101642997..101646954,3	MCF-7	breast:
10	chr3:101587884..101589425-chr3:101596987..101599237,2	K562	blood:
11	chr3:101567616..101569184-chr3:101621763..101623602,2	K562	blood:
12	chr3:101567124..101569055-chr3:101716434..101718714,2	MCF-7	breast:
13	chr3:101568338..101570388-chr3:101616291..101618191,2	K562	blood:
14	chr3:101716217..101718460-chr3:101885237..101888035,2	MCF-7	breast:
15	chr3:101678379..101679165-chr6:48381606..48382388,2	MCF-7	breast:
16	chr3:101655492..101658302-chr3:101660937..101663877,2	MCF-7	breast:
17	chr3:101661155..101664150-chr3:101664624..101666610,2	K562	blood:
18	chr3:101568745..101570435-chr3:101718037..101719941,2	K562	blood:
19	chr3:101611977..101614577-chr3:101618423..101621104,2	K562	blood:
20	chr3:101583187..101585591-chr3:101588676..101591535,3	MCF-7	breast:
21	chr3:101587093..101588701-chr3:101591968..101594547,2	MCF-7	breast:
22	chr3:101567492..101571608-chr3:101590460..101594047,4	K562	blood:
23	chr3:101571126..101574195-chr3:101601068..101603657,3	K562	blood:
24	chr3:101681933..101682716-chr3:122473612..122474290,2	MCF-7	breast:
25	chr3:101589284..101592114-chr3:101593162..101595895,2	MCF-7	breast:
26	chr3:101711972..101714062-chr3:101716715..101719526,2	MCF-7	breast:
27	chr3:101642851..101646450-chr3:101646744..101649155,3	MCF-7	breast:
28	chr3:101567314..101569899-chr3:101785470..101789586,5	MCF-7	breast:
29	chr3:101567750..101569822-chr3:101667491..101670371,3	K562	blood:
30	chr3:101612357..101614518-chr3:101615231..101617299,2	K562	blood:
31	chr3:101586222..101589351-chr3:101592520..101595732,3	K562	blood:
32	chr3:101654323..101656814-chr3:101941741..101943329,2	MCF-7	breast:
33	chr3:101587093..101588701-chr3:101591968..101594547,2	MCF-7	breast:
34	chr3:101569504..101571608-chr3:101590460..101592111,2	K562	blood:
35	chr3:101568351..101575418-chr3:101783867..101789752,8	MCF-7	breast:
36	chr3:101566748..101570087-chr3:101596631..101600244,5	MCF-7	breast:
37	chr3:101587884..101589425-chr3:101596987..101599237,2	K562	blood:
38	chr3:101571381..101573933-chr3:101586598..101588197,2	K562	blood:
39	chr3:101567204..101569919-chr3:101592318..101595246,2	MCF-7	breast:
40	chr3:101704688..101706460-chr3:101721589..101723644,2	MCF-7	breast:
41	chr3:101601882..101603837-chr3:101610958..101613952,2	MCF-7	breast:
42	chr3:101683624..101685727-chr3:101697646..101699483,2	MCF-7	breast:
43	chr3:101586222..101589351-chr3:101592319..101595732,4	K562	blood:
44	chr3:101589284..101592114-chr3:101593162..101595895,2	MCF-7	breast:
45	chr3:101609413..101611144-chr3:101614360..101616706,2	MCF-7	breast:
46	chr3:101570052..101571665-chr3:101611707..101614656,2	MCF-7	breast:
47	chr3:101586222..101589351-chr3:101592319..101595732,4	K562	blood:
48	chr3:101567030..101569894-chr3:101796236..101798456,2	MCF-7	breast:
49	chr3:101658485..101660497-chr3:101661357..101663143,2	MCF-7	breast:
50	chr3:101618062..101619983-chr3:101666275..101668883,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NFKBIZ-1	chr3:101659703-101659869	XLOC_002741
2	lnc-NFKBIZ-1	chr3:101713405-101713741	XLOC_002741
3	lnc-NFKBIZ-1	chr3:101713658-101713741	XLOC_002741
4	lnc-NFKBIZ-4	chr3:101652775-101653063	NONHSAT090918
5	lnc-NFKBIZ-1	chr3:101679206-101679306	XLOC_002741
6	lnc-NFKBIZ-1	chr3:101713405-101713741	XLOC_002741
7	lnc-NFKBIZ-1	chr3:101679230-101679575	XLOC_002741
8	lnc-ZPLD1-3	chr3:101782506-101782794	NONHSAT090924
9	lnc-NFKBIZ-1	chr3:101679202-101679306	XLOC_002741
10	lnc-NFKBIZ-1	chr3:101715325-101716770	XLOC_002741
11	lnc-NFKBIZ-1	chr3:101715325-101715376	XLOC_002741
12	lnc-NFKBIZ-1	chr3:101715325-101715502	XLOC_002741
13	lnc-ZPLD1-3	chr3:101771495-101771570	NONHSAT090924
14	lnc-NFKBIZ-1	chr3:101678830-101680760	NONHSAT090921
15	lnc-NFKBIZ-1	chr3:101715325-101716770	XLOC_002741
16	lnc-NFKBIZ-1	chr3:101678176-101678586	NONHSAT090921
17	lnc-NFKBIZ-1	chr3:101713405-101713512	XLOC_002741
18	lnc-NFKBIZ-4	chr3:101645751-101646147	NONHSAT090918

No data

Variant related genes	Relation type
ENSG00000241280	TF binding region
ENSG00000214407	TF binding region
ENSG00000202177	TF binding region
ENSG00000241280	CpG island
ENSG00000214407	CpG island
ENSG00000202177	CpG island
ENSG00000214407	chromatin interactions
ENSG00000144802	chromatin interactions
ENSG00000114391	chromatin interactions
NXN	miRNA target sites
CAPRIN2	miRNA target sites
ANKS1B	miRNA target sites

Extended variants
information (count: 8145 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:8145 , 50 per page) page: 1 2 3 4 5 6 7 ... 163

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs681573	chr3:101584861-101584862	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567749784	chr3:101584870-101584871	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs372205323	chr3:101584876-101584877	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs150846638	chr3:101584884-101584885	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs592779	chr3:101584944-101584945	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs533672482	chr3:101584960-101584961	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139327368	chr3:101584968-101584969	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs9844218	chr3:101584983-101584984	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs143989212	chr3:101584988-101584989	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs147299848	chr3:101585019-101585020	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs592332	chr3:101585035-101585036	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs370162392	chr3:101585064-101585065	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs545439859	chr3:101585074-101585075	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560499901	chr3:101585075-101585076	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs527670519	chr3:101585129-101585130	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs9840222	chr3:101585135-101585136	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs561432468	chr3:101585147-101585148	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs529083516	chr3:101585170-101585171	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs550712717	chr3:101585175-101585176	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562658474	chr3:101585176-101585177	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs533032674	chr3:101585217-101585218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs62703860	chr3:101585292-101585293	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs35391641	chr3:101585303-101585304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563896224	chr3:101585311-101585312	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs73145713	chr3:101585340-101585341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs182960236	chr3:101585342-101585343	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs9821333	chr3:101585442-101585443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs188106222	chr3:101585443-101585444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs564529086	chr3:101585448-101585449	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs688058	chr3:101585467-101585468	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs192716108	chr3:101585499-101585500	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543360914	chr3:101585517-101585518	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556696996	chr3:101585555-101585556	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs578197500	chr3:101585566-101585567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs536922856	chr3:101585570-101585571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs144938604	chr3:101585575-101585576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs74439930	chr3:101585719-101585720	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs144877219	chr3:101585735-101585736	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs546991687	chr3:101585738-101585739	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs148605549	chr3:101585841-101585842	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561263631	chr3:101585861-101585862	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs182711491	chr3:101585892-101585893	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544101606	chr3:101585934-101585935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562722718	chr3:101585938-101585939	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs577032758	chr3:101586045-101586046	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs369090486	chr3:101586064-101586065	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532925249	chr3:101586067-101586068	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs665374	chr3:101586143-101586144	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs186860907	chr3:101586144-101586145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs527329758	chr3:101586162-101586163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1818 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:101570400-101598400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:101576400-101586400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:101576400-101586800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:101576600-101586200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr3:101577200-101586200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:101579200-101586400	Weak transcription	Fetal Kidney	kidney
7	chr3:101579200-101586400	Weak transcription	K562	blood
8	chr3:101579400-101586200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:101579400-101586400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr3:101579400-101586400	Weak transcription	Small Intestine	intestine
11	chr3:101579400-101586600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr3:101579400-101587200	Weak transcription	NHEK	skin
13	chr3:101579400-101587400	Weak transcription	Fetal Muscle Leg	muscle
14	chr3:101579400-101587600	Weak transcription	Aorta	Aorta
15	chr3:101579400-101587600	Weak transcription	Gastric	stomach
16	chr3:101579400-101587600	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr3:101579400-101587800	Weak transcription	Brain Hippocampus Middle	brain
18	chr3:101579400-101588600	Weak transcription	Esophagus	oesophagus
19	chr3:101580000-101587400	Weak transcription	Fetal Lung	lung
20	chr3:101580400-101587600	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr3:101580600-101586000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:101580800-101587400	Weak transcription	HMEC	breast
23	chr3:101580800-101587600	Weak transcription	Placenta	Placenta
24	chr3:101580800-101588600	Weak transcription	NHDF-Ad	bronchial
25	chr3:101581000-101586200	Weak transcription	Rectal Smooth Muscle	rectum
26	chr3:101581000-101586400	Weak transcription	Colon Smooth Muscle	Colon
27	chr3:101581200-101586400	Weak transcription	Pancreas	Pancrea
28	chr3:101581200-101587400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr3:101581200-101587400	Weak transcription	Primary B cells from cord blood	blood
30	chr3:101581200-101587600	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr3:101581400-101586400	Weak transcription	Duodenum Mucosa	Duodenum
32	chr3:101581400-101586400	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr3:101581400-101586400	Weak transcription	Stomach Smooth Muscle	stomach
34	chr3:101581400-101586600	Weak transcription	Primary B cells from peripheral blood	blood
35	chr3:101581400-101587200	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr3:101581400-101587400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr3:101581400-101587600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr3:101581600-101586200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr3:101581600-101587200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr3:101581600-101587400	Weak transcription	Adipose Nuclei	Adipose
41	chr3:101581600-101587600	Weak transcription	GM12878-XiMat	blood
42	chr3:101581800-101587000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr3:101581800-101587200	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr3:101582000-101585000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr3:101582000-101585600	Weak transcription	HSMM	muscle
46	chr3:101582000-101586000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr3:101582000-101586600	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr3:101582000-101587000	Weak transcription	Left Ventricle	heart
49	chr3:101582000-101587200	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr3:101582000-101587600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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