Variant report

Variant	nsv1040356
Chromosome Location	chr12:124094758-124172731
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1874)
CpG islands
(count:1953)
Chromatin interactive
region (count:128)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1874 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:124118202-124118430	K562	blood:	n/a	n/a
2	ARID3A	chr12:124118134-124118531	HepG2	liver:	n/a	n/a
3	ATF1	chr12:124118054-124118572	K562	blood:	n/a	n/a
4	ATF2	chr12:124118041-124118671	GM12878	blood:	n/a	n/a
5	ATF2	chr12:124165973-124166596	GM12878	blood:	n/a	n/a
6	ATF2	chr12:124118133-124118718	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr12:124165813-124166609	GM12878	blood:	n/a	n/a
8	ATF2	chr12:124172381-124172960	GM12878	blood:	n/a	n/a
9	ATF2	chr12:124172426-124172866	GM12878	blood:	n/a	n/a
10	ATF2	chr12:124117993-124118726	GM12878	blood:	n/a	n/a
11	ATF2	chr12:124118102-124118636	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr12:124144752-124145277	GM12878	blood:	n/a	n/a
13	ATF3	chr12:124118056-124118549	K562	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
14	ATF3	chr12:124118070-124118525	K562	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
15	ATF3	chr12:124117986-124118648	A549	lung:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
16	ATF3	chr12:124118016-124118688	GM12878	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
17	ATF3	chr12:124118019-124118591	H1-hESC	embryonic stem cell:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
18	ATF3	chr12:124118087-124118409	GM12878	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
19	ATF3	chr12:124118039-124118550	H1-hESC	embryonic stem cell:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
20	ATF3	chr12:124118086-124118563	K562	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
21	ATF3	chr12:124118019-124118526	HepG2	liver:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
22	ATF3	chr12:124117982-124118633	HepG2	liver:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
23	ATF3	chr12:124117981-124118734	A549	lung:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
24	BACH1	chr12:124118432-124118786	K562	blood:	n/a	n/a
25	BATF	chr12:124172484-124172812	GM12878	blood:	n/a	n/a
26	BATF	chr12:124166147-124166490	GM12878	blood:	n/a	n/a
27	BATF	chr12:124118055-124118499	GM12878	blood:	n/a	n/a
28	BATF	chr12:124166177-124166501	GM12878	blood:	n/a	n/a
29	BATF	chr12:124144904-124145195	GM12878	blood:	n/a	chr12:124145072-124145083
30	BATF	chr12:124144875-124145201	GM12878	blood:	n/a	chr12:124145072-124145083
31	BATF	chr12:124172432-124172890	GM12878	blood:	n/a	n/a
32	BCL11A	chr12:124172540-124172846	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:124172504-124172853	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:124166091-124166461	GM12878	blood:	n/a	n/a
35	BCL3	chr12:124117744-124118749	A549	lung:	n/a	n/a
36	BCL3	chr12:124117820-124118863	A549	lung:	n/a	n/a
37	BCL3	chr12:124106088-124107034	A549	lung:	n/a	n/a
38	BCL3	chr12:124117997-124118571	GM12878	blood:	n/a	n/a
39	BCLAF1	chr12:124117899-124118589	GM12878	blood:	n/a	n/a
40	BCLAF1	chr12:124117968-124118680	GM12878	blood:	n/a	n/a
41	BCLAF1	chr12:124166045-124166526	GM12878	blood:	n/a	n/a
42	BCLAF1	chr12:124139925-124140367	GM12878	blood:	n/a	n/a
43	BCLAF1	chr12:124117938-124119147	K562	blood:	n/a	chr12:124119093-124119101
44	BCLAF1	chr12:124172411-124172914	GM12878	blood:	n/a	n/a
45	BHLHE40	chr12:124103165-124103399	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:124139600-124140393	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:124146182-124146377	GM12878	blood:	n/a	n/a
48	BHLHE40	chr12:124172483-124172783	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:124103108-124103341	HepG2	liver:	n/a	n/a
50	BHLHE40	chr12:124117548-124118596	K562	blood:	n/a	n/a

(count:1953 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124118326-124118376	HepG2	liver:	n/a
2	chr12:124118326-124118376	HepG2	liver:	n/a
3	chr12:124118326-124118376	HUVEC	blood vessel:	n/a
4	chr12:124155458-124155508	AoSMC	blood vessel:	n/a
5	chr12:124118386-124118436	MCF-7	breast:	n/a
6	chr12:124118346-124118396	IMR90	lung:	fetal
7	chr12:124118052-124118102	H1-hESC	embryonic stem cell:	embryo
8	chr12:124155620-124155670	U87	brain:	n/a
9	chr12:124155451-124155501	LNCaP	prostate:	n/a
10	chr12:124118336-124118386	PFSK-1	brain:	n/a
11	chr12:124118184-124118234	GM19239	blood:	n/a
12	chr12:124118346-124118396	HRPEpiC	eye:	n/a
13	chr12:124154378-124154428	IMR90	lung:	fetal
14	chr12:124118173-124118223	AG10803	skin:	n/a
15	chr12:124155451-124155501	RPTEC	kidney:	n/a
16	chr12:124118184-124118234	AoSMC	blood vessel:	n/a
17	chr12:124105880-124105930	SK-N-MC	brain:	n/a
18	chr12:124119053-124119103	HRE	kidney:	n/a
19	chr12:124118264-124118314	HCPEpiC	choroid plexus:	n/a
20	chr12:124118173-124118223	Jurkat	blood:	n/a
21	chr12:124158499-124158549	A549	lung:	n/a
22	chr12:124156159-124156209	HCF	heart:	n/a
23	chr12:124119250-124119300	SAEC	small airway:	n/a
24	chr12:124154378-124154428	HL-60	blood:	n/a
25	chr12:124144432-124144482	GM19239	blood:	n/a
26	chr12:124145110-124145160	K562	blood:	n/a
27	chr12:124155880-124155930	AG04450	lung:	fetal
28	chr12:124118052-124118102	NT2-D1	testis:	n/a
29	chr12:124155451-124155501	HPAEpiC	pulmonary alveolar:	n/a
30	chr12:124118346-124118396	HRE	kidney:	n/a
31	chr12:124118346-124118396	PrEC	prostate:	n/a
32	chr12:124155458-124155508	HNPCEpiC	eye:	n/a
33	chr12:124118360-124118410	HL-60	blood:	n/a
34	chr12:124158499-124158549	SK-N-SH	brain:	n/a
35	chr12:124119250-124119300	HepG2	liver:	n/a
36	chr12:124119250-124119300	BE2_C	brain:	n/a
37	chr12:124118052-124118102	AG10803	skin:	n/a
38	chr12:124118346-124118396	HepG2	liver:	n/a
39	chr12:124118178-124118228	NHBE	bronchial:	n/a
40	chr12:124115280-124115330	Caco-2	colon:	n/a
41	chr12:124118052-124118102	HRPEpiC	eye:	n/a
42	chr12:124118184-124118234	AG09319	gingival:	n/a
43	chr12:124105880-124105930	T-47D	breast:	n/a
44	chr12:124118052-124118102	PrEC	prostate:	n/a
45	chr12:124119250-124119300	IMR90	lung:	fetal
46	chr12:124154378-124154428	HUVEC	blood vessel:	n/a
47	chr12:124118184-124118234	PrEC	prostate:	n/a
48	chr12:124105880-124105930	Hela-S3	cervix:	n/a
49	chr12:124156159-124156209	HRE	kidney:	n/a
50	chr12:124158499-124158549	H1-hESC	embryonic stem cell:	embryo

(count:128 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:124116825..124119400-chr12:124154444..124157055,3	MCF-7	breast:
2	chr12:124105043..124107387-chr12:124113363..124115205,2	K562	blood:
3	chr12:124098297..124101264-chr12:124101448..124103367,2	MCF-7	breast:
4	chr12:124128608..124131370-chr12:124135245..124137740,4	K562	blood:
5	chr12:124155020..124157089-chr12:124215035..124217819,2	MCF-7	breast:
6	chr12:124085496..124088026-chr12:124116630..124119648,4	MCF-7	breast:
7	chr12:124068831..124072178-chr12:124116882..124120107,5	K562	blood:
8	chr12:124103214..124105859-chr12:124106055..124109639,4	MCF-7	breast:
9	chr12:124117557..124118523-chr17:78120518..78121066,2	Hela-S3	cervix:
10	chr12:124128608..124131370-chr12:124135245..124137740,4	K562	blood:
11	chr12:124115420..124119615-chr12:124195159..124199573,8	MCF-7	breast:
12	chr12:124141910..124144216-chr12:124195360..124197441,2	MCF-7	breast:
13	chr12:124117774..124119426-chr12:124160532..124162075,2	K562	blood:
14	chr12:124086555..124088221-chr12:124100026..124101762,2	K562	blood:
15	chr12:124119450..124122240-chr12:124131405..124134508,3	MCF-7	breast:
16	chr12:124119318..124121767-chr12:124194183..124197056,2	MCF-7	breast:
17	chr12:124154247..124158137-chr12:124158575..124163340,6	K562	blood:
18	chr12:123847883..123849879-chr12:124118467..124120545,3	K562	blood:
19	chr12:124123949..124126710-chr12:124128875..124131426,2	K562	blood:
20	chr12:124090198..124092919-chr12:124093242..124095991,2	MCF-7	breast:
21	chr12:124143980..124146532-chr12:124155769..124157495,2	MCF-7	breast:
22	chr12:124090616..124092389-chr12:124114546..124116542,2	MCF-7	breast:
23	chr12:124116659..124120709-chr12:124455290..124460616,5	K562	blood:
24	chr12:124120301..124122353-chr12:124128299..124130201,3	K562	blood:
25	chr12:124091509..124094120-chr12:124098771..124100606,2	MCF-7	breast:
26	chr12:124117920..124120001-chr12:124129132..124130798,2	MCF-7	breast:
27	chr12:123753772..123755288-chr12:124118042..124119686,2	MCF-7	breast:
28	chr12:123752175..123754799-chr12:124094511..124096299,2	K562	blood:
29	chr12:124123949..124126710-chr12:124128875..124131426,2	K562	blood:
30	chr12:124068850..124070943-chr12:124092800..124095066,2	MCF-7	breast:
31	chr12:124157962..124160129-chr12:124161284..124163771,2	MCF-7	breast:
32	chr12:124127308..124129753-chr12:124158031..124160799,2	K562	blood:
33	chr12:124150313..124152080-chr12:124154611..124157419,2	MCF-7	breast:
34	chr12:124131124..124134135-chr12:124154416..124157411,3	K562	blood:
35	chr12:124138422..124140008-chr12:124142075..124144430,2	MCF-7	breast:
36	chr12:124157620..124159905-chr12:124196914..124199226,2	K562	blood:
37	chr12:124118193..124121025-chr12:124132767..124136539,4	MCF-7	breast:
38	chr12:124095180..124096998-chr12:124140972..124143607,2	MCF-7	breast:
39	chr12:124109158..124110697-chr12:124113991..124116759,2	K562	blood:
40	chr12:124118155..124119851-chr12:124120256..124121890,2	MCF-7	breast:
41	chr12:124127308..124129753-chr12:124158031..124160799,2	K562	blood:
42	chr12:124107998..124110847-chr12:124196796..124199749,2	MCF-7	breast:
43	chr12:124107277..124111165-chr12:124113286..124117641,5	MCF-7	breast:
44	chr12:124102971..124106526-chr12:124116602..124119947,4	MCF-7	breast:
45	chr12:124137919..124140915-chr12:124140949..124142983,2	MCF-7	breast:
46	chr12:124117633..124120865-chr12:124133499..124139438,5	K562	blood:
47	chr12:124125615..124128872-chr12:124133075..124135751,3	MCF-7	breast:
48	chr12:123875063..123876805-chr12:124118427..124120711,2	K562	blood:
49	chr12:124084509..124086598-chr12:124112180..124115159,2	K562	blood:
50	chr12:123755830..123757417-chr12:124116609..124118455,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	EIF2B1	hsa-miR-26b-5p	chr12:124105615-124105637
2	EIF2B1	hsa-miR-30b-5p	chr12:124105656-124105681
3	EIF2B1	hsa-miR-30a-5p	chr12:124105656-124105677

Variant related genes	Relation type
ENSG00000206897	TF binding region
EIF2B1	TF binding region
GTF2H3	TF binding region
DDX55	TF binding region
TCTN2	TF binding region
ENSG00000206897	CpG island
EIF2B1	CpG island
GTF2H3	CpG island
DDX55	CpG island
TCTN2	CpG island
ENSG00000247373	chromatin interactions
ENSG00000139697	chromatin interactions
ENSG00000111361	chromatin interactions
ENSG00000188026	chromatin interactions
ENSG00000111328	chromatin interactions
ENSG00000179195	chromatin interactions
ENSG00000168778	chromatin interactions
ENSG00000184575	chromatin interactions
ENSG00000111358	chromatin interactions
ENSG00000141543	chromatin interactions
ENSG00000119242	chromatin interactions
ENSG00000111364	chromatin interactions
ENSG00000256092	chromatin interactions
ENSG00000136450	chromatin interactions
ENSG00000206897	chromatin interactions
ENSG00000178882	chromatin interactions
ENSG00000270095	chromatin interactions
ENSG00000130921	chromatin interactions
ENSG00000183955	chromatin interactions
ENSG00000051825	chromatin interactions
ENSG00000086598	chromatin interactions
ENSG00000185344	chromatin interactions

Extended variants
information (count: 3198 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3198 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554303975	chr12:124094802-124094803	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs11610332	chr12:124094881-124094882	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs7977314	chr12:124094896-124094897	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs111846418	chr12:124094973-124094974	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs114623334	chr12:124094991-124094992	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs533867480	chr12:124095035-124095036	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs73414268	chr12:124095037-124095038	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs566346327	chr12:124095071-124095072	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs192983556	chr12:124095098-124095099	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs36098639	chr12:124095101-124095102	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs540152374	chr12:124095107-124095108	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs558343348	chr12:124095108-124095109	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs376723067	chr12:124095113-124095114	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs370156052	chr12:124095152-124095153	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs183069326	chr12:124095185-124095186	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs537696500	chr12:124095222-124095223	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs555570519	chr12:124095230-124095231	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs574113037	chr12:124095276-124095277	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs541006083	chr12:124095308-124095309	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs552972055	chr12:124095309-124095310	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs571977897	chr12:124095316-124095317	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs545703052	chr12:124095319-124095320	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs564262941	chr12:124095384-124095385	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs576157003	chr12:124095385-124095386	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs543634344	chr12:124095386-124095387	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs561604447	chr12:124095388-124095389	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs188552916	chr12:124095402-124095403	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs11057304	chr12:124095426-124095427	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs559399218	chr12:124095427-124095428	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs533620296	chr12:124095432-124095433	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs552099315	chr12:124095433-124095434	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs150494192	chr12:124095443-124095444	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs570368924	chr12:124095444-124095445	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs11057305	chr12:124095447-124095448	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs376659381	chr12:124095455-124095456	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs567627814	chr12:124095456-124095457	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs192105904	chr12:124095514-124095515	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs576160358	chr12:124095517-124095518	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs184551548	chr12:124095529-124095530	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs371650397	chr12:124095569-124095570	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs577620264	chr12:124095572-124095573	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs189478097	chr12:124095663-124095664	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs139817539	chr12:124095705-124095706	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs576310579	chr12:124095721-124095722	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs143220715	chr12:124095760-124095761	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs561933322	chr12:124095791-124095792	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs374333673	chr12:124095821-124095822	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs118104666	chr12:124095829-124095830	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs567288173	chr12:124095892-124095893	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs370794084	chr12:124095893-124095894	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2970 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124087800-124102000	Weak transcription	Stomach Mucosa	stomach
2	chr12:124087800-124109600	Weak transcription	Right Atrium	heart
3	chr12:124088000-124099200	Weak transcription	Fetal Heart	heart
4	chr12:124088000-124107200	Strong transcription	K562	blood
5	chr12:124088200-124098800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr12:124088200-124116000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr12:124088200-124117000	Strong transcription	Fetal Stomach	stomach
8	chr12:124088400-124096800	Strong transcription	Ovary	ovary
9	chr12:124088400-124097400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr12:124088400-124102400	Strong transcription	HUVEC	blood vessel
11	chr12:124088400-124103000	Strong transcription	Left Ventricle	heart
12	chr12:124088400-124105800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr12:124088400-124108000	Strong transcription	H1 Cell Line	embryonic stem cell
14	chr12:124088400-124116000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:124088400-124116000	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr12:124088400-124116000	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr12:124088400-124116000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr12:124088400-124116000	Strong transcription	Sigmoid Colon	Sigmoid Colon
19	chr12:124088400-124116200	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr12:124088400-124116800	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr12:124088400-124117000	Strong transcription	Fetal Intestine Small	intestine
22	chr12:124088600-124096800	Strong transcription	Spleen	Spleen
23	chr12:124088600-124099200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr12:124088600-124103000	Strong transcription	Lung	lung
25	chr12:124088600-124104800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr12:124088600-124107400	Strong transcription	H9 Cell Line	embryonic stem cell
27	chr12:124088600-124116000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr12:124088600-124116000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
29	chr12:124088600-124116000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr12:124088600-124116000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:124088600-124116000	Strong transcription	Duodenum Smooth Muscle	Duodenum
32	chr12:124088600-124116000	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr12:124088600-124116200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr12:124088600-124116200	Strong transcription	Fetal Thymus	thymus
35	chr12:124088600-124116800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr12:124088600-124116800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr12:124088600-124116800	Strong transcription	Fetal Muscle Trunk	muscle
38	chr12:124088600-124117000	Strong transcription	Primary B cells from peripheral blood	blood
39	chr12:124088800-124098000	Strong transcription	A549	lung
40	chr12:124088800-124102800	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr12:124088800-124107600	Strong transcription	NH-A	brain
42	chr12:124088800-124116000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr12:124088800-124116000	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr12:124088800-124116000	Strong transcription	Fetal Intestine Large	intestine
45	chr12:124089000-124105800	Strong transcription	Fetal Muscle Leg	muscle
46	chr12:124089000-124107400	Strong transcription	Fetal Lung	lung
47	chr12:124089000-124116000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr12:124089000-124116200	Strong transcription	Brain Germinal Matrix	brain
49	chr12:124089200-124098000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr12:124089200-124098200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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