Variant report

Variant	esv2754685
Chromosome Location	chr12:835074-936468
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2960)
CpG islands
(count:916)
Chromatin interactive
region (count:119)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2960 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:860968-861705	HepG2	liver:	n/a	chr12:861103-861119
2	ARID3A	chr12:904508-904691	K562	blood:	n/a	n/a
3	ARID3A	chr12:860435-860729	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:864137-864680	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:859850-860665	K562	blood:	n/a	n/a
6	ARID3A	chr12:835577-835922	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:899446-899520	K562	blood:	n/a	n/a
8	ARID3A	chr12:888927-889307	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:861036-861605	K562	blood:	n/a	chr12:861103-861119
10	ARID3A	chr12:899820-900011	K562	blood:	n/a	n/a
11	ARID3A	chr12:886012-886221	HepG2	liver:	n/a	n/a
12	ARID3A	chr12:925667-926004	K562	blood:	n/a	n/a
13	ARID3A	chr12:914118-914158	HepG2	liver:	n/a	n/a
14	ARID3A	chr12:863980-864603	K562	blood:	n/a	n/a
15	ARID3A	chr12:925672-925952	HepG2	liver:	n/a	n/a
16	ARID3A	chr12:923375-923763	HepG2	liver:	n/a	n/a
17	ARID3A	chr12:923400-923725	K562	blood:	n/a	n/a
18	ATF1	chr12:864177-864588	K562	blood:	n/a	n/a
19	ATF1	chr12:861326-861689	K562	blood:	n/a	n/a
20	ATF2	chr12:916459-916858	GM12878	blood:	n/a	n/a
21	ATF2	chr12:919620-920364	GM12878	blood:	n/a	n/a
22	ATF2	chr12:861296-861837	GM12878	blood:	n/a	n/a
23	ATF2	chr12:916414-916900	GM12878	blood:	n/a	n/a
24	ATF2	chr12:919616-920278	GM12878	blood:	n/a	n/a
25	ATF2	chr12:860111-860867	GM12878	blood:	n/a	n/a
26	ATF2	chr12:852485-853543	GM12878	blood:	n/a	n/a
27	ATF2	chr12:860317-860903	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr12:932098-932901	GM12878	blood:	n/a	n/a
29	ATF2	chr12:860099-860870	GM12878	blood:	n/a	n/a
30	ATF2	chr12:932136-932907	GM12878	blood:	n/a	n/a
31	ATF2	chr12:860283-860868	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr12:852433-853559	GM12878	blood:	n/a	n/a
33	ATF3	chr12:860217-860784	A549	lung:	n/a	n/a
34	ATF3	chr12:860183-860817	A549	lung:	n/a	n/a
35	ATF3	chr12:861305-861867	A549	lung:	n/a	n/a
36	ATF3	chr12:861345-861689	GM12878	blood:	n/a	n/a
37	ATF3	chr12:861395-861668	K562	blood:	n/a	n/a
38	ATF3	chr12:861424-861712	HepG2	liver:	n/a	n/a
39	BACH1	chr12:922636-922643	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr12:927295-927341	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr12:864141-864402	K562	blood:	n/a	n/a
42	BACH1	chr12:860059-860703	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr12:839594-839599	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr12:927893-928274	H1-hESC	embryonic stem cell:	n/a	n/a
45	BATF	chr12:860308-860675	GM12878	blood:	n/a	n/a
46	BATF	chr12:919759-920261	GM12878	blood:	n/a	n/a
47	BATF	chr12:852571-853389	GM12878	blood:	n/a	n/a
48	BATF	chr12:898909-899396	GM12878	blood:	n/a	chr12:899377-899386
49	BATF	chr12:901667-901904	GM12878	blood:	n/a	chr12:901756-901767
50	BATF	chr12:919770-920232	GM12878	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:861469-861519	GM06990	blood:	n/a
2	chr12:861469-861519	GM06990	blood:	n/a
3	chr12:862975-863025	NH-A	brain:	n/a
4	chr12:863472-863522	HUVEC	blood vessel:	n/a
5	chr12:861715-861765	ECC-1	luminal epithelium:	n/a
6	chr12:863605-863655	GM12891	blood:	n/a
7	chr12:862793-862843	GM12892	blood:	n/a
8	chr12:862975-863025	CMK	blood:	n/a
9	chr12:860787-860837	Hela-S3	cervix:	n/a
10	chr12:861469-861519	MCF10A-Er-Src	breast:	n/a
11	chr12:862663-862713	HRE	kidney:	n/a
12	chr12:886615-886665	SK-N-SH	brain:	n/a
13	chr12:858759-858809	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:860520-860570	MCF10A-Er-Src	breast:	n/a
15	chr12:863605-863655	ProgFib	skin:	n/a
16	chr12:861787-861837	T-47D	breast:	n/a
17	chr12:861469-861519	Caco-2	colon:	n/a
18	chr12:860520-860570	RPTEC	kidney:	n/a
19	chr12:860480-860530	ovcar-3	ovarian:	n/a
20	chr12:861715-861765	HAEpiC	amniotic membrane:	n/a
21	chr12:860480-860530	GM19239	blood:	n/a
22	chr12:863605-863655	AG09319	gingival:	n/a
23	chr12:858759-858809	HNPCEpiC	eye:	n/a
24	chr12:858759-858809	GM12891	blood:	n/a
25	chr12:863605-863655	HRCEpiC	kidney:	n/a
26	chr12:861715-861765	Caco-2	colon:	n/a
27	chr12:861715-861765	SAEC	small airway:	n/a
28	chr12:861787-861837	PFSK-1	brain:	n/a
29	chr12:863472-863522	LNCaP	prostate:	n/a
30	chr12:862975-863025	U87	brain:	n/a
31	chr12:863472-863522	SK-N-SH	brain:	n/a
32	chr12:862793-862843	SKMC	muscle:	n/a
33	chr12:862663-862713	MCF10A-Er-Src	breast:	n/a
34	chr12:860787-860837	AoSMC	blood vessel:	n/a
35	chr12:863472-863522	GM12878	blood:	n/a
36	chr12:862975-863025	H1-hESC	embryonic stem cell:	embryo
37	chr12:860520-860570	NB4	blood:	n/a
38	chr12:861715-861765	Jurkat	blood:	n/a
39	chr12:862793-862843	HCF	heart:	n/a
40	chr12:862793-862843	PFSK-1	brain:	n/a
41	chr12:861752-861802	SK-N-SH_RA	brain:	n/a
42	chr12:861787-861837	PANC-1	pancreas:	n/a
43	chr12:858759-858809	PFSK-1	brain:	n/a
44	chr12:862793-862843	HNPCEpiC	eye:	n/a
45	chr12:886615-886665	BJ	skin:	n/a
46	chr12:858759-858809	HAEpiC	amniotic membrane:	n/a
47	chr12:862663-862713	HIPEpiC	eye:	n/a
48	chr12:866289-866339	Caco-2	colon:	n/a
49	chr12:860787-860837	RPTEC	kidney:	n/a
50	chr12:860787-860837	GM19239	blood:	n/a

(count:119 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:845151..847111-chr12:848367..852019,3	MCF-7	breast:
2	chr12:864121..866273-chr12:867871..870258,2	K562	blood:
3	chr12:849337..852194-chr12:853558..856397,3	K562	blood:
4	chr12:860874..861474-chr8:121823843..121824589,2	HCT-116	colon:
5	chr12:751792..752466-chr12:860118..860688,2	Hela-S3	cervix:
6	chr12:857339..858842-chr12:859156..860743,2	MCF-7	breast:
7	chr12:851480..853426-chr12:857104..859711,2	K562	blood:
8	chr12:867638..869974-chr12:870964..872822,2	K562	blood:
9	chr12:861880..864242-chr12:927799..930624,2	K562	blood:
10	chr12:919540..922758-chr12:931539..933937,3	K562	blood:
11	chr12:751484..754177-chr12:833162..836032,2	MCF-7	breast:
12	chr12:881327..884915-chr12:893641..898608,4	K562	blood:
13	chr12:678017..679838-chr12:873854..876600,2	K562	blood:
14	chr12:824399..827215-chr12:865443..868265,2	K562	blood:
15	chr10:31607443..31608369-chr12:861345..862098,2	Hela-S3	cervix:
16	chr12:684050..686927-chr12:859603..861672,3	K562	blood:
17	chr12:825603..828799-chr12:857363..861650,3	K562	blood:
18	chr12:739334..741511-chr12:860709..863370,3	MCF-7	breast:
19	chr12:723353..724122-chr12:860374..861153,4	MCF-7	breast:
20	chr12:864121..866273-chr12:867871..870258,2	K562	blood:
21	chr12:749128..755954-chr12:858463..864495,7	MCF-7	breast:
22	chr12:749727..757562-chr12:858273..868886,17	MCF-7	breast:
23	chr12:860587..863557-chr12:905754..908662,2	MCF-7	breast:
24	chr12:862748..867412-chr12:867871..873426,6	K562	blood:
25	chr12:851908..854303-chr12:860165..862567,2	MCF-7	breast:
26	chr12:860210..861203-chr12:922611..923577,2	Hela-S3	cervix:
27	chr12:876367..879119-chr12:880594..883556,3	K562	blood:
28	chr12:861431..862176-chr14:103800047..103800564,2	MCF-7	breast:
29	chr12:751010..752994-chr12:848617..851185,2	MCF-7	breast:
30	chr12:925748..927383-chr12:929410..931068,2	K562	blood:
31	chr12:684961..685544-chr12:860128..860643,2	K562	blood:
32	chr12:902748..905210-chr12:909004..911043,2	K562	blood:
33	chr12:689801..692487-chr12:897629..900163,2	K562	blood:
34	chr12:860770..863546-chr12:920587..924774,4	MCF-7	breast:
35	chr12:846994..850450-chr12:851888..854645,3	K562	blood:
36	chr12:862748..867412-chr12:867871..873426,6	K562	blood:
37	chr12:838287..839811-chr12:861670..863793,2	MCF-7	breast:
38	chr12:860489..863381-chr12:877011..880566,3	MCF-7	breast:
39	chr12:851480..853426-chr12:857104..859711,2	K562	blood:
40	chr12:860140..862854-chr12:919115..921823,2	K562	blood:
41	chr12:831910..837502-chr12:858732..864374,10	MCF-7	breast:
42	chr12:860770..861524-chr9:131102541..131103389,2	Hela-S3	cervix:
43	chr12:855985..857857-chr12:859146..862006,3	K562	blood:
44	chr12:852835..854793-chr12:856754..858401,2	K562	blood:
45	chr12:860213..861917-chr12:1056995..1059720,2	MCF-7	breast:
46	chr12:685032..685901-chr12:859937..861024,3	MCF-7	breast:
47	chr12:869508..871876-chr12:1056862..1059672,2	MCF-7	breast:
48	chr12:925748..927383-chr12:929410..931068,2	K562	blood:
49	chr12:678986..679579-chr12:860176..860988,2	MCF-7	breast:
50	chr12:678673..679595-chr12:860437..861048,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WNK1-1	chr12:837176-837499	XLOC_009614
2	lnc-NINJ2-3	chr12:890139-890879	predAs_chen_BU787457_1

No data

Variant related genes	Relation type
WNK1	TF binding region
RNU4ATAC16P	TF binding region
WNK1	CpG island
RNU4ATAC16P	CpG island
ENSG00000272502	chromatin interactions
ENSG00000079999	chromatin interactions
ENSG00000256672	chromatin interactions
ENSG00000100664	chromatin interactions
ENSG00000237036	chromatin interactions
ENSG00000136897	chromatin interactions
ENSG00000177406	chromatin interactions
ENSG00000120647	chromatin interactions
ENSG00000135185	chromatin interactions
ENSG00000079805	chromatin interactions
ENSG00000171840	chromatin interactions
ENSG00000172164	chromatin interactions
ENSG00000073614	chromatin interactions
ENSG00000002016	chromatin interactions
ENSG00000060237	chromatin interactions
ENSG00000136870	chromatin interactions
ENSG00000255825	chromatin interactions
ENSG00000148516	chromatin interactions
ENSG00000207972	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000167114	chromatin interactions

Extended variants
information (count: 3693 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3693 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7315904	chr12:835074-835075	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs549279757	chr12:835092-835093	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs146411724	chr12:835170-835171	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs114863404	chr12:835173-835174	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs117799794	chr12:835256-835257	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs577605906	chr12:835278-835279	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs10849542	chr12:835317-835318	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs74471551	chr12:835318-835319	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs55688852	chr12:835328-835329	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs117578776	chr12:835354-835355	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs576253663	chr12:835359-835360	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs78965713	chr12:835360-835361	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs554420761	chr12:835381-835382	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs576232612	chr12:835382-835383	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs148289951	chr12:835387-835388	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs543536284	chr12:835417-835418	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs532122416	chr12:835444-835445	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs185484930	chr12:835466-835467	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs141357090	chr12:835493-835494	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs116411183	chr12:835505-835506	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs548272851	chr12:835570-835571	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs567757321	chr12:835586-835587	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs150785260	chr12:835589-835590	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs115852225	chr12:835661-835662	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs138058009	chr12:835662-835663	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs189913090	chr12:835691-835692	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs553716569	chr12:835729-835730	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs114204379	chr12:835836-835837	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs370015899	chr12:835896-835897	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs111490997	chr12:835909-835910	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs79229101	chr12:835968-835969	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs11064470	chr12:835987-835988	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs543668216	chr12:836186-836187	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs558806095	chr12:836222-836223	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs558782985	chr12:836226-836227	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs377475656	chr12:836242-836243	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs577171932	chr12:836244-836245	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs375426283	chr12:836289-836290	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs142548221	chr12:836302-836303	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs35781306	chr12:836326-836327	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs145979205	chr12:836332-836333	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs115780805	chr12:836392-836393	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs541552773	chr12:836440-836441	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs139852955	chr12:836450-836451	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs531768384	chr12:836464-836465	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs116247728	chr12:836488-836489	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs542378142	chr12:836491-836492	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs571524177	chr12:836531-836532	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs532619846	chr12:836584-836585	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs76544554	chr12:836601-836602	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22844521	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3870 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:822000-835600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr12:828600-835200	Weak transcription	Spleen	Spleen
3	chr12:828600-838400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr12:828800-835200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr12:828800-835400	Weak transcription	Brain Angular Gyrus	brain
6	chr12:828800-835400	Weak transcription	Colon Smooth Muscle	Colon
7	chr12:828800-835600	Weak transcription	Brain Hippocampus Middle	brain
8	chr12:831400-840600	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr12:831600-838000	Enhancers	Primary T cells from cord blood	blood
10	chr12:832000-835200	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr12:832000-835400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr12:832000-835400	Weak transcription	Brain Cingulate Gyrus	brain
13	chr12:832000-835600	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr12:832600-837800	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr12:832600-839200	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr12:832600-840400	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr12:832800-836000	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr12:832800-836000	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr12:832800-840000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr12:832800-840200	Enhancers	Fetal Thymus	thymus
21	chr12:833000-840000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr12:833000-841200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr12:833200-837600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:833400-836800	Enhancers	Fetal Heart	heart
25	chr12:833400-836800	Enhancers	Fetal Muscle Leg	muscle
26	chr12:833400-837000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr12:833400-837000	Enhancers	NHEK	skin
28	chr12:833400-838600	Enhancers	HSMM	muscle
29	chr12:833400-839000	Enhancers	Primary hematopoietic stem cells	blood
30	chr12:833800-835200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:834000-835200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr12:834000-835400	Weak transcription	HMEC	breast
33	chr12:834000-835600	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr12:834000-836000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr12:834000-836600	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr12:834000-836800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr12:834000-837400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr12:834200-836200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr12:834600-835600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr12:834600-835600	Weak transcription	Left Ventricle	heart
41	chr12:834600-836600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr12:834600-838000	Weak transcription	GM12878-XiMat	blood
43	chr12:834800-837600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr12:834800-840400	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr12:835000-835800	Enhancers	Right Atrium	heart
46	chr12:835000-836000	Enhancers	Thymus	Thymus
47	chr12:835000-836200	Enhancers	Muscle Satellite Cultured Cells	--
48	chr12:835000-836400	Enhancers	Brain Substantia Nigra	brain
49	chr12:835000-836800	Enhancers	A549	lung
50	chr12:835000-838200	Enhancers	HSMMtube	muscle

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