Variant report

Variant	esv3438726
Chromosome Location	chr11:66042776-66047874
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:66047671-66047721	HepG2	liver:	n/a	n/a
2	BCL3	chr11:66045256-66045588	GM12878	blood:	n/a	n/a
3	BCL3	chr11:66045213-66045834	GM12878	blood:	n/a	n/a
4	BCLAF1	chr11:66045262-66045585	GM12878	blood:	n/a	n/a
5	CCNT2	chr11:66045191-66045975	K562	blood:	n/a	chr11:66045546-66045555
6	CEBPD	chr11:66045265-66045671	HepG2	liver:	n/a	n/a
7	CHD2	chr11:66046174-66046240	K562	blood:	n/a	n/a
8	CHD2	chr11:66045380-66045544	GM12878	blood:	n/a	n/a
9	CHD2	chr11:66046519-66046529	K562	blood:	n/a	n/a
10	CHD2	chr11:66045263-66045311	HepG2	liver:	n/a	n/a
11	CTCF	chr11:66045234-66045281	GM12892	blood:	n/a	n/a
12	E2F6	chr11:66045567-66045746	K562	blood:	n/a	n/a
13	E2F6	chr11:66045264-66045818	K562	blood:	n/a	n/a
14	E2F6	chr11:66045556-66045728	K562	blood:	n/a	n/a
15	EBF1	chr11:66044306-66044534	GM12878	blood:	n/a	n/a
16	EBF1	chr11:66045118-66045326	GM12878	blood:	n/a	n/a
17	EGR1	chr11:66045515-66045700	K562	blood:	n/a	chr11:66045628-66045642
18	EGR1	chr11:66046057-66046331	K562	blood:	n/a	chr11:66046198-66046207 chr11:66046197-66046210 chr11:66046198-66046209 chr11:66046197-66046207 chr11:66046192-66046214 chr11:66046197-66046210 chr11:66046194-66046208 chr11:66046197-66046210
19	EGR1	chr11:66046112-66046268	GM12878	blood:	n/a	chr11:66046198-66046207 chr11:66046197-66046210 chr11:66046198-66046209 chr11:66046197-66046207 chr11:66046192-66046214 chr11:66046197-66046210 chr11:66046194-66046208 chr11:66046197-66046210
20	EGR1	chr11:66046065-66046272	GM12878	blood:	n/a	chr11:66046198-66046207 chr11:66046197-66046210 chr11:66046198-66046209 chr11:66046197-66046207 chr11:66046192-66046214 chr11:66046197-66046210 chr11:66046194-66046208 chr11:66046197-66046210
21	EGR1	chr11:66045536-66045721	GM12878	blood:	n/a	chr11:66045628-66045642
22	EGR1	chr11:66046034-66046345	K562	blood:	n/a	chr11:66046198-66046207 chr11:66046326-66046336 chr11:66046197-66046210 chr11:66046327-66046337 chr11:66046198-66046209 chr11:66046197-66046207 chr11:66046192-66046214 chr11:66046197-66046210 chr11:66046194-66046208 chr11:66046197-66046210
23	ELF1	chr11:66044883-66045707	GM12878	blood:	n/a	chr11:66045562-66045574
24	ELF1	chr11:66045033-66045842	GM12878	blood:	n/a	chr11:66045562-66045574
25	FOSL2	chr11:66047833-66048218	HepG2	liver:	n/a	chr11:66048077-66048089 chr11:66048025-66048033 chr11:66048078-66048088
26	FOXA2	chr11:66046341-66046534	HepG2	liver:	n/a	n/a
27	HDAC2	chr11:66046285-66046594	HepG2	liver:	n/a	n/a
28	HDAC2	chr11:66045301-66045698	HepG2	liver:	n/a	n/a
29	HMGN3	chr11:66045081-66045977	K562	blood:	n/a	n/a
30	HNF4A	chr11:66045282-66045582	HepG2	liver:	n/a	chr11:66045413-66045427
31	HNF4G	chr11:66045302-66045575	HepG2	liver:	n/a	chr11:66045413-66045427
32	HNF4G	chr11:66046365-66046603	HepG2	liver:	n/a	chr11:66046472-66046487
33	IRF1	chr11:66045513-66045707	K562	blood:	n/a	n/a
34	JUND	chr11:66045545-66045759	H1-hESC	embryonic stem cell:	n/a	n/a
35	JUND	chr11:66045411-66046052	A549	lung:	n/a	n/a
36	MAFK	chr11:66047748-66048174	HepG2	liver:	n/a	chr11:66048077-66048087 chr11:66048076-66048090 chr11:66048080-66048089
37	MAFK	chr11:66047775-66048213	HepG2	liver:	n/a	chr11:66048077-66048087 chr11:66048076-66048090 chr11:66048080-66048089
38	MAX	chr11:66045154-66045458	GM12878	blood:	n/a	n/a
39	MAX	chr11:66045522-66045810	K562	blood:	n/a	n/a
40	MAX	chr11:66045189-66045761	ECC-1	luminal epithelium:	n/a	n/a
41	MAX	chr11:66045550-66045709	K562	blood:	n/a	n/a
42	MAX	chr11:66045399-66045563	HepG2	liver:	n/a	n/a
43	MAX	chr11:66045034-66045869	HepG2	liver:	n/a	n/a
44	MAX	chr11:66044977-66045565	NB4	blood:	n/a	n/a
45	MAX	chr11:66046302-66046612	H1-hESC	embryonic stem cell:	n/a	chr11:66046391-66046401 chr11:66046437-66046446 chr11:66046441-66046450 chr11:66046508-66046518
46	MAZ	chr11:66046310-66046543	K562	blood:	n/a	chr11:66046391-66046401 chr11:66046437-66046446 chr11:66046441-66046450 chr11:66046508-66046518
47	MAZ	chr11:66046455-66046566	HepG2	liver:	n/a	chr11:66046508-66046518
48	MAZ	chr11:66045290-66045779	K562	blood:	n/a	n/a
49	MAZ	chr11:66045376-66045676	HepG2	liver:	n/a	n/a
50	MAZ	chr11:66045248-66045709	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:66045500-66045550	A549	lung:	n/a
2	chr11:66045500-66045550	A549	lung:	n/a
3	chr11:66046770-66046820	HAEpiC	amniotic membrane:	n/a
4	chr11:66045494-66045544	A549	lung:	n/a
5	chr11:66045512-66045562	HRPEpiC	eye:	n/a
6	chr11:66046083-66046133	K562	blood:	n/a
7	chr11:66045718-66045768	AG04450	lung:	fetal
8	chr11:66046770-66046820	ovcar-3	ovarian:	n/a
9	chr11:66046083-66046133	HPAEpiC	pulmonary alveolar:	n/a
10	chr11:66045351-66045401	HIPEpiC	eye:	n/a
11	chr11:66045564-66045614	Jurkat	blood:	n/a
12	chr11:66045718-66045768	HNPCEpiC	eye:	n/a
13	chr11:66046083-66046133	GM12878	blood:	n/a
14	chr11:66045351-66045401	Caco-2	colon:	n/a
15	chr11:66045564-66045614	AG09309	skin:	n/a
16	chr11:66044596-66044646	HRE	kidney:	n/a
17	chr11:66045560-66045610	Hepatocyte	liver:	n/a
18	chr11:66044596-66044646	ovcar-3	ovarian:	n/a
19	chr11:66045506-66045556	NB4	blood:	n/a
20	chr11:66045486-66045536	ProgFib	skin:	n/a
21	chr11:66045486-66045536	HCT-116	colon:	n/a
22	chr11:66045500-66045550	PrEC	prostate:	n/a
23	chr11:66045564-66045614	HCM	heart:	n/a
24	chr11:66045500-66045550	BE2_C	brain:	n/a
25	chr11:66045494-66045544	T-47D	breast:	n/a
26	chr11:66045351-66045401	A549	lung:	n/a
27	chr11:66045506-66045556	HEK293	kidney:	embryo
28	chr11:66045486-66045536	Hela-S3	cervix:	n/a
29	chr11:66046770-66046820	HRE	kidney:	n/a
30	chr11:66045486-66045536	HRCEpiC	kidney:	n/a
31	chr11:66044596-66044646	HL-60	blood:	n/a
32	chr11:66045560-66045610	RPTEC	kidney:	n/a
33	chr11:66045506-66045556	HUVEC	blood vessel:	n/a
34	chr11:66045564-66045614	HEEpiC	esophagus:	n/a
35	chr11:66045506-66045556	HepG2	liver:	n/a
36	chr11:66045932-66045982	HMEC	breast:	n/a
37	chr11:66045494-66045544	HUVEC	blood vessel:	n/a
38	chr11:66045718-66045768	HIPEpiC	eye:	n/a
39	chr11:66046770-66046820	NHDF-neo	bronchial:	n/a
40	chr11:66045560-66045610	HCM	heart:	n/a
41	chr11:66044596-66044646	Hepatocyte	liver:	n/a
42	chr11:66046770-66046820	PFSK-1	brain:	n/a
43	chr11:66045512-66045562	NT2-D1	testis:	n/a
44	chr11:66045486-66045536	GM12878	blood:	n/a
45	chr11:66044596-66044646	NH-A	brain:	n/a
46	chr11:66045932-66045982	HL-60	blood:	n/a
47	chr11:66045718-66045768	AoSMC	blood vessel:	n/a
48	chr11:66045494-66045544	GM12878	blood:	n/a
49	chr11:66046838-66046888	SK-N-SH	brain:	n/a
50	chr11:66044326-66044376	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65818576..65820605-chr11:66044652..66046444,2	MCF-7	breast:
2	chr11:66043530..66045792-chr11:66110035..66112602,2	MCF-7	breast:
3	chr11:65999678..66002038-chr11:66045531..66047368,2	K562	blood:
4	chr11:66045260..66048745-chr11:66100560..66104011,3	K562	blood:
5	chr11:66041439..66043181-chr11:66053492..66056458,2	MCF-7	breast:
6	chr1:227578119..227581046-chr11:66042464..66044320,2	MCF-7	breast:
7	chr11:66047213..66049788-chr11:66097470..66100241,3	K562	blood:
8	chr11:66023062..66027568-chr11:66043406..66047432,6	MCF-7	breast:
9	chr11:66047571..66049763-chr11:66079162..66081273,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-YIF1A-1	chr11:66044250-66044514	ENSG00000254452.1
2	lnc-YIF1A-1	chr11:66044640-66044963	ENSG00000254452.1
3	lnc-YIF1A-1	chr11:66044340-66044495	ENSG00000254452.1
4	lnc-YIF1A-1	chr11:66044771-66044958	ENSG00000254452.1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RAB1B	hsa-miR-103a-3p	chr11:66044024-66044045
2	RAB1B	hsa-miR-103a-3p	chr11:66044038-66044045
3	RAB1B	hsa-miR-107	chr11:66044024-66044045
4	RAB1B	hsa-miR-107	chr11:66044038-66044045
5	RAB1B	hsa-miR-185-5p	chr11:66044039-66044059

Variant related genes	Relation type
ENSG00000254452	TF binding region
ENSG00000245156	TF binding region
CNIH2	TF binding region
ENSG00000254452	CpG island
ENSG00000245156	CpG island
CNIH2	CpG island
ENSG00000254756	chromatin interactions
ENSG00000175115	chromatin interactions
ENSG00000174744	chromatin interactions
ENSG00000174791	chromatin interactions
ENSG00000087365	chromatin interactions
ENSG00000174996	chromatin interactions
ENSG00000254458	chromatin interactions

Extended variants
information (count: 219 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:219 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562693223	chr11:66042878-66042879	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs546008953	chr11:66042886-66042887	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs551029387	chr11:66042894-66042895	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs562997258	chr11:66042897-66042898	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs192871206	chr11:66042931-66042932	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs115491790	chr11:66042933-66042934	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs576399012	chr11:66042935-66042936	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs541832559	chr11:66042946-66042947	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs184964093	chr11:66042960-66042961	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs2298468	chr11:66042962-66042963	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs189422661	chr11:66042979-66042980	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs549854717	chr11:66042987-66042988	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs180722413	chr11:66042990-66042991	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs185096268	chr11:66043002-66043003	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs527604938	chr11:66043029-66043030	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs547257228	chr11:66043082-66043083	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs534268759	chr11:66043090-66043091	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs554063090	chr11:66043110-66043111	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs574180074	chr11:66043154-66043155	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs542726381	chr11:66043158-66043159	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs148716081	chr11:66043187-66043188	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs372955261	chr11:66043235-66043236	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs55931871	chr11:66043253-66043254	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs368722305	chr11:66043259-66043260	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs373293659	chr11:66043268-66043269	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs149085050	chr11:66043283-66043284	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs143206894	chr11:66043318-66043319	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs372476957	chr11:66043334-66043335	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs371245994	chr11:66043339-66043340	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs199961685	chr11:66043364-66043365	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs61734075	chr11:66043388-66043389	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs376818036	chr11:66043416-66043417	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs374208171	chr11:66043429-66043430	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs201011194	chr11:66043430-66043431	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs560874766	chr11:66043433-66043434	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs571905895	chr11:66043437-66043438	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs529924364	chr11:66043440-66043441	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs549578116	chr11:66043456-66043457	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs569398947	chr11:66043462-66043463	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs538375727	chr11:66043465-66043466	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs549647643	chr11:66043466-66043467	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs368074010	chr11:66043480-66043481	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs551753819	chr11:66043502-66043503	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs148276108	chr11:66043527-66043528	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs61730423	chr11:66043553-66043554	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs375241856	chr11:66043574-66043575	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs140356034	chr11:66043578-66043579	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs367843963	chr11:66043586-66043587	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs375965398	chr11:66043643-66043644	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs371996451	chr11:66043646-66043647	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66037400-66044600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr11:66037400-66044800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:66037600-66043600	Strong transcription	Osteobl	bone
4	chr11:66037600-66044600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr11:66037600-66045000	Genic enhancers	Fetal Thymus	thymus
6	chr11:66037800-66044000	Strong transcription	NHEK	skin
7	chr11:66037800-66044200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr11:66037800-66044600	Strong transcription	Fetal Intestine Small	intestine
9	chr11:66037800-66044800	Strong transcription	Fetal Stomach	stomach
10	chr11:66038000-66042800	Strong transcription	K562	blood
11	chr11:66038000-66043000	Genic enhancers	Primary T cells fromperipheralblood	blood
12	chr11:66038000-66043200	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr11:66038000-66043600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr11:66038000-66044200	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr11:66038000-66044200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr11:66038000-66044200	Strong transcription	Brain Cingulate Gyrus	brain
17	chr11:66038000-66044200	Strong transcription	Fetal Intestine Large	intestine
18	chr11:66038000-66044200	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr11:66038000-66044200	Strong transcription	NHLF	lung
20	chr11:66038000-66044600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr11:66038000-66044600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:66038000-66044800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr11:66038200-66042800	Strong transcription	Fetal Lung	lung
24	chr11:66038200-66043600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr11:66038200-66043800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr11:66038200-66044200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr11:66038200-66044200	Strong transcription	Primary B cells from peripheral blood	blood
28	chr11:66038200-66044200	Strong transcription	Colonic Mucosa	Colon
29	chr11:66038200-66044200	Strong transcription	Lung	lung
30	chr11:66038200-66044200	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr11:66038200-66044600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr11:66038200-66045000	Weak transcription	Right Atrium	heart
33	chr11:66038400-66044000	Strong transcription	Brain Anterior Caudate	brain
34	chr11:66038400-66044400	Strong transcription	Muscle Satellite Cultured Cells	--
35	chr11:66038400-66044800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:66038400-66045000	Weak transcription	Fetal Heart	heart
37	chr11:66038400-66045000	Strong transcription	Gastric	stomach
38	chr11:66038400-66045200	Weak transcription	Psoas Muscle	Psoas
39	chr11:66038600-66044000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr11:66038600-66044000	Strong transcription	Duodenum Mucosa	Duodenum
41	chr11:66038600-66044000	Strong transcription	Placenta	Placenta
42	chr11:66038600-66044000	Strong transcription	Dnd41	blood
43	chr11:66038600-66044400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr11:66038800-66044200	Strong transcription	Primary neutrophils fromperipheralblood	blood
45	chr11:66038800-66044200	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr11:66039000-66042800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr11:66039000-66043600	Strong transcription	HepG2	liver
48	chr11:66039000-66043800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr11:66039000-66044000	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr11:66039000-66044000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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