Variant report

Variant	nsv1041918
Chromosome Location	chr12:124115035-124184855
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1293)
CpG islands
(count:1834)
Chromatin interactive
region (count:101)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:124118134-124118531	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:124118202-124118430	K562	blood:	n/a	n/a
3	ATF1	chr12:124118054-124118572	K562	blood:	n/a	n/a
4	ATF2	chr12:124118133-124118718	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr12:124118041-124118671	GM12878	blood:	n/a	n/a
6	ATF2	chr12:124172381-124172960	GM12878	blood:	n/a	n/a
7	ATF2	chr12:124144752-124145277	GM12878	blood:	n/a	n/a
8	ATF2	chr12:124172426-124172866	GM12878	blood:	n/a	n/a
9	ATF2	chr12:124117993-124118726	GM12878	blood:	n/a	n/a
10	ATF2	chr12:124165973-124166596	GM12878	blood:	n/a	n/a
11	ATF2	chr12:124165813-124166609	GM12878	blood:	n/a	n/a
12	ATF2	chr12:124118102-124118636	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr12:124118019-124118526	HepG2	liver:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
14	ATF3	chr12:124118016-124118688	GM12878	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
15	ATF3	chr12:124118086-124118563	K562	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
16	ATF3	chr12:124118039-124118550	H1-hESC	embryonic stem cell:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
17	ATF3	chr12:124117982-124118633	HepG2	liver:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
18	ATF3	chr12:124118019-124118591	H1-hESC	embryonic stem cell:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
19	ATF3	chr12:124117986-124118648	A549	lung:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
20	ATF3	chr12:124118087-124118409	GM12878	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
21	ATF3	chr12:124118056-124118549	K562	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
22	ATF3	chr12:124118070-124118525	K562	blood:	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	chr12:124166177-124166501	GM12878	blood:	n/a	n/a
27	BATF	chr12:124144875-124145201	GM12878	blood:	n/a	chr12:124145072-124145083
28	BATF	chr12:124144904-124145195	GM12878	blood:	n/a	chr12:124145072-124145083
29	BATF	chr12:124118055-124118499	GM12878	blood:	n/a	n/a
30	BATF	chr12:124172432-124172890	GM12878	blood:	n/a	n/a
31	BATF	chr12:124166147-124166490	GM12878	blood:	n/a	n/a
32	BCL11A	chr12:124172504-124172853	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:124172540-124172846	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:124166091-124166461	GM12878	blood:	n/a	n/a
35	BCL3	chr12:124117820-124118863	A549	lung:	n/a	n/a
36	BCL3	chr12:124117744-124118749	A549	lung:	n/a	n/a
37	BCL3	chr12:124117997-124118571	GM12878	blood:	n/a	n/a
38	BCLAF1	chr12:124139925-124140367	GM12878	blood:	n/a	n/a
39	BCLAF1	chr12:124117968-124118680	GM12878	blood:	n/a	n/a
40	BCLAF1	chr12:124117938-124119147	K562	blood:	n/a	chr12:124119093-124119101
41	BCLAF1	chr12:124172411-124172914	GM12878	blood:	n/a	n/a
42	BCLAF1	chr12:124117899-124118589	GM12878	blood:	n/a	n/a
43	BCLAF1	chr12:124166045-124166526	GM12878	blood:	n/a	n/a
44	BHLHE40	chr12:124118125-124118468	A549	lung:	n/a	n/a
45	BHLHE40	chr12:124139600-124140393	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:124146182-124146377	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:124117548-124118596	K562	blood:	n/a	n/a
48	BHLHE40	chr12:124166226-124166361	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:124118012-124118609	GM12878	blood:	n/a	n/a
50	BHLHE40	chr12:124172483-124172783	GM12878	blood:	n/a	n/a

(count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124155594-124155644	PFSK-1	brain:	n/a
2	chr12:124155594-124155644	NT2-D1	testis:	n/a
3	chr12:124156170-124156220	RPTEC	kidney:	n/a
4	chr12:124119250-124119300	GM19239	blood:	n/a
5	chr12:124155594-124155644	PFSK-1	brain:	n/a
6	chr12:124155594-124155644	NT2-D1	testis:	n/a
7	chr12:124156170-124156220	RPTEC	kidney:	n/a
8	chr12:124119250-124119300	GM19239	blood:	n/a
9	chr12:124118360-124118410	SAEC	small airway:	n/a
10	chr12:124155579-124155629	CMK	blood:	n/a
11	chr12:124118178-124118228	BJ	skin:	n/a
12	chr12:124115280-124115330	PANC-1	pancreas:	n/a
13	chr12:124118336-124118386	RPTEC	kidney:	n/a
14	chr12:124158499-124158549	AG09319	gingival:	n/a
15	chr12:124144432-124144482	BJ	skin:	n/a
16	chr12:124155880-124155930	T-47D	breast:	n/a
17	chr12:124156170-124156220	MCF10A-Er-Src	breast:	n/a
18	chr12:124118178-124118228	SK-N-SH_RA	brain:	n/a
19	chr12:124118329-124118379	GM06990	blood:	n/a
20	chr12:124156159-124156209	HNPCEpiC	eye:	n/a
21	chr12:124145110-124145160	IMR90	lung:	fetal
22	chr12:124119657-124119707	HIPEpiC	eye:	n/a
23	chr12:124119250-124119300	GM06990	blood:	n/a
24	chr12:124118386-124118436	HAEpiC	amniotic membrane:	n/a
25	chr12:124155594-124155644	ECC-1	luminal epithelium:	n/a
26	chr12:124118052-124118102	GM06990	blood:	n/a
27	chr12:124155880-124155930	HRCEpiC	kidney:	n/a
28	chr12:124155594-124155644	HRCEpiC	kidney:	n/a
29	chr12:124155594-124155644	NB4	blood:	n/a
30	chr12:124155451-124155501	ProgFib	skin:	n/a
31	chr12:124116920-124116970	PrEC	prostate:	n/a
32	chr12:124144432-124144482	MCF10A-Er-Src	breast:	n/a
33	chr12:124118346-124118396	NHDF-neo	bronchial:	n/a
34	chr12:124118346-124118396	HNPCEpiC	eye:	n/a
35	chr12:124118326-124118376	Jurkat	blood:	n/a
36	chr12:124155579-124155629	SK-N-SH	brain:	n/a
37	chr12:124118336-124118386	HCF	heart:	n/a
38	chr12:124145110-124145160	HCM	heart:	n/a
39	chr12:124145110-124145160	HNPCEpiC	eye:	n/a
40	chr12:124121050-124121100	BJ	skin:	n/a
41	chr12:124144432-124144482	HRPEpiC	eye:	n/a
42	chr12:124118052-124118102	HPAEpiC	pulmonary alveolar:	n/a
43	chr12:124118329-124118379	AG10803	skin:	n/a
44	chr12:124118360-124118410	RPTEC	kidney:	n/a
45	chr12:124118360-124118410	MCF-7	breast:	n/a
46	chr12:124118173-124118223	K562	blood:	n/a
47	chr12:124155620-124155670	BE2_C	brain:	n/a
48	chr12:124158499-124158549	MCF10A-Er-Src	breast:	n/a
49	chr12:124118184-124118234	GM12891	blood:	n/a
50	chr12:124118360-124118410	HRE	kidney:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:124117612..124120056-chr12:124127858..124130457,4	K562	blood:
2	chr12:124130507..124132191-chr12:124132895..124134450,2	MCF-7	breast:
3	chr12:124084509..124086598-chr12:124112180..124115159,2	K562	blood:
4	chr12:124157626..124159857-chr12:124196461..124198464,2	MCF-7	breast:
5	chr12:124084988..124092992-chr12:124114351..124121638,14	K562	blood:
6	chr12:124143980..124146532-chr12:124155769..124157495,2	MCF-7	breast:
7	chr12:123866683..123868660-chr12:124118535..124120956,2	K562	blood:
8	chr12:124117920..124120001-chr12:124129132..124130798,2	MCF-7	breast:
9	chr12:124119450..124122240-chr12:124131405..124134508,3	MCF-7	breast:
10	chr12:124127308..124129753-chr12:124158031..124160799,2	K562	blood:
11	chr12:124105722..124107597-chr12:124119086..124122015,4	K562	blood:
12	chr12:124085496..124088026-chr12:124116630..124119648,4	MCF-7	breast:
13	chr12:124105043..124107387-chr12:124113363..124115205,2	K562	blood:
14	chr12:124123949..124126710-chr12:124128875..124131426,2	K562	blood:
15	chr12:124120301..124122353-chr12:124128299..124130201,3	K562	blood:
16	chr12:124128608..124131370-chr12:124135245..124137740,4	K562	blood:
17	chr12:124085449..124088387-chr12:124115552..124120028,6	MCF-7	breast:
18	chr12:124112176..124115481-chr12:124118258..124122183,5	K562	blood:
19	chr12:124157962..124160129-chr12:124161284..124163771,2	MCF-7	breast:
20	chr12:124095180..124096998-chr12:124140972..124143607,2	MCF-7	breast:
21	chr12:124141910..124144216-chr12:124195360..124197441,2	MCF-7	breast:
22	chr12:124084914..124087862-chr12:124122413..124125179,2	K562	blood:
23	chr12:124117633..124120865-chr12:124133499..124139438,5	K562	blood:
24	chr12:124118155..124119851-chr12:124120256..124121890,2	MCF-7	breast:
25	chr12:123716817..123718990-chr12:124117809..124119418,3	K562	blood:
26	chr12:124116659..124120709-chr12:124455290..124460616,5	K562	blood:
27	chr12:124143980..124146532-chr12:124155769..124157495,2	MCF-7	breast:
28	chr12:124112554..124115997-chr12:124116047..124118023,3	MCF-7	breast:
29	chr12:123847301..123849584-chr12:124117443..124120110,3	K562	blood:
30	chr12:124120951..124123869-chr12:124130412..124132116,2	K562	blood:
31	chr12:124117633..124119272-chr12:124133499..124136176,2	K562	blood:
32	chr12:124130618..124132144-chr12:124154341..124156246,2	MCF-7	breast:
33	chr12:124155436..124158746-chr12:124195101..124198299,4	MCF-7	breast:
34	chr12:124117107..124120837-chr12:124123304..124127842,5	MCF-7	breast:
35	chr12:124155686..124156232-chr17:56084289..56085093,2	HCT-116	colon:
36	chr12:124126711..124128243-chr12:124132496..124134774,2	MCF-7	breast:
37	chr12:124181824..124184450-chr12:124186002..124188364,2	K562	blood:
38	chr12:124105734..124108451-chr12:124133249..124135719,2	K562	blood:
39	chr12:123753793..123756876-chr12:124117523..124121813,4	K562	blood:
40	chr12:124127308..124129753-chr12:124158031..124160799,2	K562	blood:
41	chr12:124117495..124119400-chr12:124126684..124128895,2	MCF-7	breast:
42	chr12:124067567..124070616-chr12:124116717..124118360,3	K562	blood:
43	chr12:124171218..124172882-chr12:124173161..124174693,2	K562	blood:
44	chr12:124157620..124159905-chr12:124196914..124199226,2	K562	blood:
45	chr12:124134030..124137334-chr12:124197093..124199913,4	MCF-7	breast:
46	chr12:124086664..124088557-chr12:124117448..124120033,4	K562	blood:
47	chr12:124157024..124160371-chr12:124188986..124191737,3	MCF-7	breast:
48	chr12:124171218..124172882-chr12:124173161..124174693,2	K562	blood:
49	chr12:124128608..124131370-chr12:124135245..124137740,4	K562	blood:
50	chr12:124137852..124140530-chr12:124458317..124460698,2	K562	blood:

No data

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

Extended variants
information (count: 2789 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2789 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202096209	chr12:124115084-124115085	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs200972398	chr12:124115098-124115099	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs189474095	chr12:124115108-124115109	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs191202290	chr12:124115119-124115120	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs376839100	chr12:124115130-124115131	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs141755541	chr12:124115136-124115137	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs551605617	chr12:124115146-124115147	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs569727268	chr12:124115181-124115182	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs3748270	chr12:124115200-124115201	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs555489008	chr12:124115202-124115203	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs370486321	chr12:124115247-124115248	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs139642766	chr12:124115271-124115272	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs534649769	chr12:124115280-124115281	Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs183748807	chr12:124115281-124115282	Strong transcription Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs577936933	chr12:124115284-124115285	Strong transcription Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs371234055	chr12:124115326-124115327	Strong transcription Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs545148674	chr12:124115397-124115398	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs562862101	chr12:124115469-124115470	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs114155449	chr12:124115491-124115492	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs542751186	chr12:124115492-124115493	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs149750508	chr12:124115501-124115502	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs561460731	chr12:124115613-124115614	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs528459320	chr12:124115675-124115676	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs73416222	chr12:124115695-124115696	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs559641830	chr12:124115700-124115701	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs533276758	chr12:124115708-124115709	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs146291673	chr12:124115722-124115723	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs569747619	chr12:124115734-124115735	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs139525041	chr12:124115737-124115738	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs144292556	chr12:124115741-124115742	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs11057310	chr12:124115811-124115812	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs1004583	chr12:124115838-124115839	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs571566039	chr12:124115862-124115863	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs546709485	chr12:124115895-124115896	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs538933952	chr12:124115921-124115922	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs557277339	chr12:124115941-124115942	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs189530512	chr12:124115969-124115970	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs566617100	chr12:124115988-124115989	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs371048480	chr12:124115990-124115991	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs112174307	chr12:124115995-124115996	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs367620678	chr12:124116008-124116009	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs61611881	chr12:124116034-124116035	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs57890199	chr12:124116037-124116038	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs138412125	chr12:124116064-124116065	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs373500985	chr12:124116077-124116078	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs540593052	chr12:124116078-124116079	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs181187403	chr12:124116083-124116084	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs142418988	chr12:124116093-124116094	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs545304522	chr12:124116098-124116099	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs563637016	chr12:124116124-124116125	Weak transcription Strong transcription	Chromatin interactive region	2 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:2901 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124088200-124116000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr12:124088200-124117000	Strong transcription	Fetal Stomach	stomach
3	chr12:124088400-124116000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:124088400-124116000	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr12:124088400-124116000	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr12:124088400-124116000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr12:124088400-124116000	Strong transcription	Sigmoid Colon	Sigmoid Colon
8	chr12:124088400-124116200	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr12:124088400-124116800	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr12:124088400-124117000	Strong transcription	Fetal Intestine Small	intestine
11	chr12:124088600-124116000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr12:124088600-124116000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
13	chr12:124088600-124116000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr12:124088600-124116000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:124088600-124116000	Strong transcription	Duodenum Smooth Muscle	Duodenum
16	chr12:124088600-124116000	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr12:124088600-124116200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr12:124088600-124116200	Strong transcription	Fetal Thymus	thymus
19	chr12:124088600-124116800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:124088600-124116800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr12:124088600-124116800	Strong transcription	Fetal Muscle Trunk	muscle
22	chr12:124088600-124117000	Strong transcription	Primary B cells from peripheral blood	blood
23	chr12:124088800-124116000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr12:124088800-124116000	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr12:124088800-124116000	Strong transcription	Fetal Intestine Large	intestine
26	chr12:124089000-124116000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr12:124089000-124116200	Strong transcription	Brain Germinal Matrix	brain
28	chr12:124089200-124115400	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr12:124089200-124116000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr12:124089200-124116000	Strong transcription	Primary T helper cells PMA-I stimulated	--
31	chr12:124089200-124116000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:124089200-124116200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr12:124089200-124116400	Strong transcription	Liver	Liver
34	chr12:124089200-124116600	Strong transcription	Stomach Smooth Muscle	stomach
35	chr12:124089600-124116000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr12:124089600-124116000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr12:124089600-124116000	Strong transcription	Duodenum Mucosa	Duodenum
38	chr12:124089800-124116200	Strong transcription	Thymus	Thymus
39	chr12:124089800-124117000	Strong transcription	Placenta	Placenta
40	chr12:124090000-124115600	Strong transcription	GM12878-XiMat	blood
41	chr12:124090000-124116000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr12:124090000-124116000	Strong transcription	Primary B cells from cord blood	blood
43	chr12:124090000-124116000	Strong transcription	Primary T cells from cord blood	blood
44	chr12:124090200-124116000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr12:124090200-124116000	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr12:124090200-124116000	Strong transcription	Rectal Smooth Muscle	rectum
47	chr12:124090200-124116200	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr12:124090200-124116200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr12:124090200-124116200	Strong transcription	Brain Anterior Caudate	brain
50	chr12:124090200-124116800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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