Variant report

Variant	nsv1051986
Chromosome Location	chr12:33962656-34457196
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3420)
CpG islands
(count:4519)
Chromatin interactive
region (count:75)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3420 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:34372445-34372838	K562	blood:	n/a	n/a
2	ARID3A	chr12:34417095-34417295	K562	blood:	n/a	n/a
3	ARID3A	chr12:34186859-34187191	K562	blood:	n/a	chr12:34187070-34187086 chr12:34187069-34187085
4	ARID3A	chr12:34174917-34175527	HepG2	liver:	n/a	chr12:34175026-34175042 chr12:34175027-34175043
5	ARID3A	chr12:34276092-34276305	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:34098056-34098330	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:34186930-34187207	HepG2	liver:	n/a	chr12:34187070-34187086 chr12:34187069-34187085
8	ARID3A	chr12:34174965-34175535	K562	blood:	n/a	chr12:34175026-34175042 chr12:34175027-34175043
9	ARID3A	chr12:34367118-34367148	K562	blood:	n/a	n/a
10	ARID3A	chr12:34276078-34276334	K562	blood:	n/a	n/a
11	ATF1	chr12:34280414-34280639	K562	blood:	n/a	n/a
12	ATF1	chr12:34276078-34276281	K562	blood:	n/a	n/a
13	ATF1	chr12:34407159-34407233	K562	blood:	n/a	n/a
14	ATF1	chr12:34372443-34372838	K562	blood:	n/a	n/a
15	ATF1	chr12:34250260-34250470	K562	blood:	n/a	n/a
16	ATF1	chr12:34175112-34175525	K562	blood:	n/a	n/a
17	ATF1	chr12:34430831-34430993	K562	blood:	n/a	n/a
18	ATF1	chr12:34340026-34340130	K562	blood:	n/a	n/a
19	ATF2	chr12:34175128-34175510	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr12:34175036-34175597	GM12878	blood:	n/a	n/a
21	ATF2	chr12:34174909-34175573	GM12878	blood:	n/a	n/a
22	ATF2	chr12:34175155-34175514	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr12:34175027-34175625	A549	lung:	n/a	n/a
24	ATF3	chr12:34372398-34372788	A549	lung:	n/a	n/a
25	ATF3	chr12:34280320-34280675	K562	blood:	n/a	n/a
26	ATF3	chr12:34275984-34276254	GM12878	blood:	n/a	n/a
27	ATF3	chr12:34372504-34372902	A549	lung:	n/a	n/a
28	ATF3	chr12:34175051-34175608	A549	lung:	n/a	n/a
29	BACH1	chr12:34186566-34186928	K562	blood:	n/a	chr12:34186742-34186756
30	BACH1	chr12:34428886-34428914	K562	blood:	n/a	n/a
31	BACH1	chr12:34369832-34370042	K562	blood:	n/a	n/a
32	BACH1	chr12:34417965-34418172	K562	blood:	n/a	n/a
33	BACH1	chr12:34186563-34186928	H1-hESC	embryonic stem cell:	n/a	chr12:34186742-34186756
34	BACH1	chr12:34417075-34417361	K562	blood:	n/a	n/a
35	BACH1	chr12:34429537-34429559	K562	blood:	n/a	n/a
36	BACH1	chr12:34429857-34430227	K562	blood:	n/a	n/a
37	BATF	chr12:34372475-34372720	GM12878	blood:	n/a	n/a
38	BATF	chr12:34374801-34375081	GM12878	blood:	n/a	n/a
39	BATF	chr12:34207885-34208102	GM12878	blood:	n/a	n/a
40	BATF	chr12:34175171-34175544	GM12878	blood:	n/a	n/a
41	BATF	chr12:34387277-34387522	GM12878	blood:	n/a	n/a
42	BATF	chr12:34207658-34207839	GM12878	blood:	n/a	n/a
43	BATF	chr12:34279173-34279432	GM12878	blood:	n/a	n/a
44	BCL11A	chr12:34175171-34175530	GM12878	blood:	n/a	n/a
45	BCL11A	chr12:34367954-34368142	GM12878	blood:	n/a	n/a
46	BCL3	chr12:34174944-34175580	A549	lung:	n/a	n/a
47	BCL3	chr12:34372532-34372732	GM12878	blood:	n/a	n/a
48	BCL3	chr12:34175028-34175635	A549	lung:	n/a	n/a
49	BCL3	chr12:34372500-34372832	A549	lung:	n/a	n/a
50	BCLAF1	chr12:34275971-34276281	GM12878	blood:	n/a	n/a

(count:4519 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:34456631-34456681	RPTEC	kidney:	n/a
2	chr12:34175262-34175312	MCF10A-Er-Src	breast:	n/a
3	chr12:34362315-34362365	HMEC	breast:	n/a
4	chr12:34175454-34175504	PANC-1	pancreas:	n/a
5	chr12:34363872-34363922	Caco-2	colon:	n/a
6	chr12:34456631-34456681	RPTEC	kidney:	n/a
7	chr12:34175262-34175312	MCF10A-Er-Src	breast:	n/a
8	chr12:34362315-34362365	HMEC	breast:	n/a
9	chr12:34175454-34175504	PANC-1	pancreas:	n/a
10	chr12:34363872-34363922	Caco-2	colon:	n/a
11	chr12:34361006-34361056	LNCaP	prostate:	n/a
12	chr12:34320121-34320171	AG10803	skin:	n/a
13	chr12:34443659-34443709	GM12891	blood:	n/a
14	chr12:34261436-34261486	AG09309	skin:	n/a
15	chr12:34175262-34175312	NHBE	bronchial:	n/a
16	chr12:34453757-34453807	HRE	kidney:	n/a
17	chr12:34448038-34448088	PFSK-1	brain:	n/a
18	chr12:34317983-34318033	H1-hESC	embryonic stem cell:	embryo
19	chr12:34362315-34362365	CMK	blood:	n/a
20	chr12:34318527-34318577	HNPCEpiC	eye:	n/a
21	chr12:34175445-34175495	SAEC	small airway:	n/a
22	chr12:34318527-34318577	ovcar-3	ovarian:	n/a
23	chr12:34259098-34259148	BE2_C	brain:	n/a
24	chr12:34457023-34457073	CMK	blood:	n/a
25	chr12:34448038-34448088	Caco-2	colon:	n/a
26	chr12:34457072-34457122	GM19239	blood:	n/a
27	chr12:34175443-34175493	SKMC	muscle:	n/a
28	chr12:34457023-34457073	NHBE	bronchial:	n/a
29	chr12:34371529-34371579	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:34317983-34318033	PFSK-1	brain:	n/a
31	chr12:34261436-34261486	SK-N-MC	brain:	n/a
32	chr12:34318704-34318754	PrEC	prostate:	n/a
33	chr12:34371529-34371579	GM12878	blood:	n/a
34	chr12:34453300-34453350	HAEpiC	amniotic membrane:	n/a
35	chr12:34362315-34362365	BJ	skin:	n/a
36	chr12:34457023-34457073	RPTEC	kidney:	n/a
37	chr12:34367440-34367490	AG10803	skin:	n/a
38	chr12:34453300-34453350	SK-N-SH_RA	brain:	n/a
39	chr12:34361006-34361056	SAEC	small airway:	n/a
40	chr12:34455326-34455376	HRCEpiC	kidney:	n/a
41	chr12:34441774-34441824	BJ	skin:	n/a
42	chr12:34362315-34362365	ovcar-3	ovarian:	n/a
43	chr12:34001319-34001369	HCM	heart:	n/a
44	chr12:34317983-34318033	PANC-1	pancreas:	n/a
45	chr12:34261006-34261056	GM12892	blood:	n/a
46	chr12:34367670-34367720	HRE	kidney:	n/a
47	chr12:34448038-34448088	AoSMC	blood vessel:	n/a
48	chr12:34320121-34320171	GM19239	blood:	n/a
49	chr12:34441774-34441824	HCPEpiC	choroid plexus:	n/a
50	chr12:34323943-34323993	NHBE	bronchial:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:34098748..34102292-chr12:49653830..49659564,5	MCF-7	breast:
2	chr12:33975803..33979098-chr12:33979674..33983619,4	MCF-7	breast:
3	chr1:227730297..227731134-chr12:34260025..34260625,2	MCF-7	breast:
4	chr12:33984638..33987420-chr12:33995374..33998517,3	MCF-7	breast:
5	chr12:34191233..34191868-chr12:34777963..34778741,2	MCF-7	breast:
6	chr12:34053367..34054987-chr12:34055066..34057564,2	MCF-7	breast:
7	chr12:34372126..34372636-chr12:127650618..127651388,2	MCF-7	breast:
8	chr1:91852282..91853087-chr12:34372625..34373157,6	MCF-7	breast:
9	chr12:34367163..34367683-chr14:88237196..88237802,3	MCF-7	breast:
10	chr12:34371140..34372648-chr12:127650511..127652141,3	MCF-7	breast:
11	chr12:34275679..34276702-chr12:34339057..34340086,5	MCF-7	breast:
12	chr12:34095993..34098950-chr12:34112537..34115292,2	MCF-7	breast:
13	chr12:34275776..34276287-chr12:34445928..34446780,2	MCF-7	breast:
14	chr1:91852330..91853034-chr12:34372628..34373167,11	MCF-7	breast:
15	chr12:32908405..32909605-chr12:34174701..34175708,3	MCF-7	breast:
16	chr1:91852355..91852916-chr12:34372634..34373168,4	MCF-7	breast:
17	chr12:34275751..34276656-chr12:34370666..34371823,3	MCF-7	breast:
18	chr12:34372145..34372649-chr9:79186173..79186679,2	MCF-7	breast:
19	chr12:34275679..34276702-chr12:34339057..34340086,5	MCF-7	breast:
20	chr12:34416748..34417268-chr2:133025884..133026405,2	MCF-7	breast:
21	chr12:34372661..34373161-chrX:108297704..108298236,2	HCT-116	colon:
22	chr12:34008981..34009786-chr2:33211553..33212456,2	MCF-7	breast:
23	chr12:33990071..33993034-chr8:42750325..42752539,2	MCF-7	breast:
24	chr12:33977547..33980480-chr12:33992605..33994282,2	K562	blood:
25	chr12:33590585..33592422-chr12:34176176..34177683,2	MCF-7	breast:
26	chr12:34277684..34281105-chr12:34367413..34370316,3	K562	blood:
27	chr12:34097991..34100054-chr12:60091596..60093323,2	MCF-7	breast:
28	chr12:34275135..34276661-chr12:34371105..34372093,8	K562	blood:
29	chr12:34372136..34372665-chr12:127650606..127651138,2	MCF-7	breast:
30	chr12:34095993..34098950-chr12:34112537..34115292,2	MCF-7	breast:
31	chr1:91851344..91853074-chr12:34372634..34374167,5	MCF-7	breast:
32	chr12:34009182..34012663-chr12:34013902..34015537,3	MCF-7	breast:
33	chr12:34275660..34276572-chr12:34778082..34778680,2	MCF-7	breast:
34	chr12:34247375..34249864-chr12:34256794..34259523,2	MCF-7	breast:
35	chr12:34275803..34276751-chr12:34446099..34446740,3	K562	blood:
36	chr12:34145843..34147953-chr17:56709056..56711203,2	MCF-7	breast:
37	chr12:32905758..32908162-chr12:34183695..34185541,2	K562	blood:
38	chr1:91852303..91852973-chr12:34372638..34373146,2	HCT-116	colon:
39	chr12:34277684..34280343-chr12:34367543..34370316,2	K562	blood:
40	chr12:34279057..34280887-chr12:34440053..34441876,2	K562	blood:
41	chr12:34275785..34276629-chr12:34339119..34339912,4	MCF-7	breast:
42	chr12:34275803..34276751-chr12:34446099..34446740,3	K562	blood:
43	chr12:34276079..34276686-chr12:34371078..34371813,4	MCF-7	breast:
44	chr12:34241238..34243550-chr12:38853316..38855678,2	MCF-7	breast:
45	chr12:34053367..34054987-chr12:34055066..34057564,2	MCF-7	breast:
46	chr12:34372131..34372654-chr9:79186162..79186868,3	MCF-7	breast:
47	chr12:34275776..34276287-chr12:34445928..34446780,2	MCF-7	breast:
48	chr12:34277684..34280343-chr12:34367543..34370316,2	K562	blood:
49	chr12:33977547..33980480-chr12:33992605..33994282,2	K562	blood:
50	chr12:32907346..32909769-chr12:34153874..34155673,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-1	chr12:34208992-34209394	XLOC_009707
2	lnc-ALG10-1	chr12:34190373-34190583	ENSG00000256538
3	lnc-ALG10-1	chr12:34209496-34209675	ENSG00000256538
4	lnc-ALG10-1	chr12:34208992-34209394	ENSG00000256538
5	lnc-ALG10-1	chr12:34209496-34209704	XLOC_009707
6	lnc-ALG10-1	chr12:34190307-34190583	XLOC_009707
7	lnc-ALG10-5	chr12:34421984-34422141	NONHSAT027661
8	lnc-ALG10-3	chr12:34315397-34315903	NONHSAT027653
9	lnc-ALG10-2	chr12:34315112-34315173	ENSG00000255628
10	lnc-ALG10-5	chr12:34430929-34431017	NONHSAT027661
11	lnc-ALG10-2	chr12:34309116-34309255	ENSG00000255628
12	lnc-ALG10-4	chr12:34402416-34402893	NONHSAT140067
13	lnc-ALG10-2	chr12:34302774-34303105	ENSG00000255628

No data

Variant related genes	Relation type
ENSG00000201624	TF binding region
ENSG00000264446	TF binding region
ENSG00000245482	TF binding region
ENSG00000256986	TF binding region
ENSG00000272435	TF binding region
ENSG00000258794	TF binding region
TUBB8P4	TF binding region
ENSG00000255628	TF binding region
RNU6-472P	TF binding region
ENSG00000255652	TF binding region
ENSG00000256614	TF binding region
ENSG00000256538	TF binding region
ALG10	TF binding region
ENSG00000201624	CpG island
ENSG00000264446	CpG island
ENSG00000245482	CpG island
ENSG00000256986	CpG island
ENSG00000272435	CpG island
ENSG00000258794	CpG island
TUBB8P4	CpG island
ENSG00000255628	CpG island
RNU6-472P	CpG island
ENSG00000255652	CpG island
ENSG00000256614	CpG island
ENSG00000256538	CpG island
ALG10	CpG island
ENSG00000175548	chromatin interactions
ENSG00000168172	chromatin interactions
ENSG00000239776	chromatin interactions
ENSG00000226958	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000120925	chromatin interactions
ENSG00000266044	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000139133	chromatin interactions
ENSG00000139131	chromatin interactions
ENSG00000255652	chromatin interactions
ENSG00000241781	chromatin interactions
ENSG00000258101	chromatin interactions
PPARGC1A	miRNA target sites

Extended variants
information (count: 10438 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:10438 , 50 per page) page: 1 2 3 4 5 6 7 ... 209

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566192638	chr12:33962661-33962662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375204455	chr12:33962669-33962670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181857229	chr12:33962676-33962677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186363315	chr12:33962693-33962694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191208297	chr12:33962724-33962725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537124822	chr12:33962761-33962762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557066603	chr12:33962763-33962764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576939914	chr12:33962771-33962772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs149200828	chr12:33962847-33962848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs116108537	chr12:33962868-33962869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572242224	chr12:33962878-33962879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182252573	chr12:33962888-33962889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554451005	chr12:33962898-33962899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1852226	chr12:33962940-33962941	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs185339666	chr12:33962957-33962958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7304339	chr12:33962959-33962960	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs10844713	chr12:33962970-33962971	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs191005370	chr12:33962975-33962976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1852225	chr12:33963004-33963005	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs183368009	chr12:33963005-33963006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528776036	chr12:33963028-33963029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs80303888	chr12:33963030-33963031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1852224	chr12:33963080-33963081	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs188247176	chr12:33963099-33963100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550783774	chr12:33963110-33963111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565243128	chr12:33963111-33963112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs193081769	chr12:33963132-33963133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1352205	chr12:33963179-33963180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539962639	chr12:33963303-33963304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201654511	chr12:33963316-33963317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536187776	chr12:33963318-33963319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs5797551	chr12:33963319-33963320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs397783630	chr12:33963330-33963331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375143227	chr12:33963355-33963356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573219572	chr12:33963400-33963401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148343854	chr12:33963407-33963408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141585000	chr12:33963441-33963442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533103746	chr12:33963443-33963444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199755022	chr12:33963455-33963456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574810088	chr12:33963458-33963459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147104110	chr12:33963497-33963498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182986820	chr12:33963508-33963509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551159869	chr12:33963533-33963534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75646612	chr12:33963551-33963552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs201876855	chr12:33963564-33963565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545928654	chr12:33963571-33963572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559062515	chr12:33963592-33963593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528121545	chr12:33963620-33963621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187750368	chr12:33963635-33963636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs562016465	chr12:33963645-33963646	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chordoma	18071362	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:1265 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33962200-33964600	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr12:33972400-33972800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:33977800-33979000	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr12:33978000-33979200	Enhancers	HMEC	breast
5	chr12:33978000-33979400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr12:33978400-33978800	Enhancers	HSMM	muscle
7	chr12:33979000-33979800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr12:33979000-33980800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr12:33979200-33983000	Weak transcription	HMEC	breast
10	chr12:33980800-33981000	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr12:33983000-33983400	Enhancers	HMEC	breast
12	chr12:33983400-33986600	Weak transcription	HMEC	breast
13	chr12:33986600-33987200	Enhancers	HMEC	breast
14	chr12:33987200-33988000	Weak transcription	HMEC	breast
15	chr12:33988000-33988200	Enhancers	HMEC	breast
16	chr12:33999800-34000400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr12:34060400-34063400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr12:34061200-34062800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr12:34061200-34062800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:34061400-34062800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr12:34061400-34062800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr12:34061400-34063400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr12:34061600-34062600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr12:34061800-34062000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr12:34061800-34062800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr12:34062000-34062400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr12:34062000-34062800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr12:34062400-34062600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr12:34062800-34067600	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr12:34067600-34068000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr12:34067600-34068000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr12:34090000-34090400	Enhancers	Liver	Liver
33	chr12:34090400-34090800	Weak transcription	Liver	Liver
34	chr12:34090800-34092000	Enhancers	Liver	Liver
35	chr12:34092000-34096800	Weak transcription	Liver	Liver
36	chr12:34093800-34130400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr12:34096800-34098000	Enhancers	HMEC	breast
38	chr12:34096800-34098200	Enhancers	Liver	Liver
39	chr12:34097800-34098200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr12:34097800-34098400	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr12:34098200-34098600	Flanking Active TSS	Liver	Liver
42	chr12:34098600-34098800	Enhancers	Liver	Liver
43	chr12:34099800-34100000	ZNF genes & repeats	Psoas Muscle	Psoas
44	chr12:34120200-34120800	Enhancers	HMEC	breast
45	chr12:34120400-34120800	Enhancers	NHEK	skin
46	chr12:34127800-34128000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:34130400-34130800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr12:34130800-34141200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:34131200-34131800	Enhancers	Liver	Liver
50	chr12:34140600-34142000	Enhancers	HMEC	breast

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