Variant report

Variant	rs2428815
Chromosome Location	chr11:67764663-67764664
allele	C/G
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	MAX	chr11:67763874-67765190	H1-hESC	embryonic stem cell:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
2	POLR2A	chr11:67764275-67764709	K562	blood:	n/a	n/a
3	POLR2A	chr11:67764012-67767934	HL-60	blood:	n/a	n/a
4	SP4	chr11:67764142-67764744	H1-hESC	embryonic stem cell:	n/a	chr11:67764437-67764448
5	MAX	chr11:67763921-67765083	A549	lung:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
6	POLR2A	chr11:67764236-67764793	GM18951	blood:	n/a	n/a
7	MAZ	chr11:67764188-67764788	Hela-S3	cervix:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
8	POLR2A	chr11:67764170-67764925	HCT-116	colon:	n/a	n/a
9	HMGN3	chr11:67764102-67764789	K562	blood:	n/a	n/a
10	MAX	chr11:67763973-67764907	H1-hESC	embryonic stem cell:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
11	MAX	chr11:67763889-67765138	H1-hESC	embryonic stem cell:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
12	MAX	chr11:67764156-67764831	Hela-S3	cervix:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
13	BCL3	chr11:67764009-67764693	A549	lung:	n/a	n/a
14	CBX3	chr11:67763950-67764711	K562	blood:	n/a	n/a
15	POLR2A	chr11:67764176-67764718	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr11:67764221-67765106	A549	lung:	n/a	n/a
17	POLR2A	chr11:67764073-67765010	A549	lung:	n/a	n/a
18	SMARCB1	chr11:67764061-67765314	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr11:67764284-67765003	GM12892	blood:	n/a	n/a
20	POLR2A	chr11:67764332-67764910	GM12892	blood:	n/a	n/a
21	E2F6	chr11:67763799-67764724	H1-hESC	embryonic stem cell:	n/a	chr11:67764364-67764373
22	POLR2A	chr11:67764094-67764824	A549	lung:	n/a	n/a
23	USF1	chr11:67763922-67764737	HCT-116	colon:	n/a	n/a
24	MXI1	chr11:67764204-67764815	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr11:67764169-67765246	GM12892	blood:	n/a	n/a
26	SP4	chr11:67764076-67764780	H1-hESC	embryonic stem cell:	n/a	chr11:67764437-67764448
27	ZMIZ1	chr11:67764288-67764716	K562	blood:	n/a	n/a
28	POLR2A	chr11:67764031-67765087	GM12892	blood:	n/a	n/a
29	POLR2A	chr11:67764085-67765115	GM12878	blood:	n/a	n/a
30	POLR2A	chr11:67764098-67764904	HCT-116	colon:	n/a	n/a
31	IRF1	chr11:67764067-67764838	K562	blood:	n/a	chr11:67764360-67764374 chr11:67764602-67764616 chr11:67764313-67764327 chr11:67764435-67764449 chr11:67764380-67764394 chr11:67764760-67764774 chr11:67764621-67764635
32	E2F6	chr11:67764015-67764686	K562	blood:	n/a	chr11:67764364-67764373
33	SMC3	chr11:67764135-67764885	Hela-S3	cervix:	n/a	n/a
34	MAZ	chr11:67764137-67764818	K562	blood:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
35	POLR2A	chr11:67763985-67764978	GM12878	blood:	n/a	n/a
36	TBP	chr11:67764102-67764670	K562	blood:	n/a	n/a
37	SP1	chr11:67764090-67764839	A549	lung:	n/a	chr11:67764437-67764449 chr11:67764822-67764835 chr11:67764363-67764377 chr11:67764363-67764372 chr11:67764625-67764634 chr11:67764383-67764392 chr11:67764315-67764327 chr11:67764383-67764392 chr11:67764383-67764393 chr11:67764364-67764373 chr11:67764624-67764633 chr11:67764437-67764448 chr11:67764362-67764374 chr11:67764382-67764394 chr11:67764624-67764633 chr11:67764438-67764447 chr11:67764383-67764393 chr11:67764316-67764325 chr11:67764815-67764829 chr11:67764438-67764452 chr11:67764382-67764394 chr11:67764362-67764374 chr11:67764384-67764393 chr11:67764623-67764635 chr11:67764315-67764327 chr11:67764605-67764619 chr11:67764437-67764449
38	MAFK	chr11:67764462-67764862	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr11:67763969-67765124	K562	blood:	n/a	n/a
40	BHLHE40	chr11:67763941-67764724	K562	blood:	n/a	n/a
41	POLR2A	chr11:67764558-67764721	A549	lung:	n/a	n/a
42	POLR2A	chr11:67764163-67764815	Hela-S3	cervix:	n/a	n/a
43	MAX	chr11:67763971-67764766	K562	blood:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343
44	USF2	chr11:67764144-67764792	Hela-S3	cervix:	n/a	chr11:67764333-67764344
45	POLR2A	chr11:67763869-67766216	HL-60	blood:	n/a	n/a
46	CCNT2	chr11:67764125-67764664	K562	blood:	n/a	chr11:67764625-67764634 chr11:67764384-67764393
47	POLR2A	chr11:67764197-67764929	GM19193	blood:	n/a	n/a
48	POLR2A	chr11:67764227-67765010	Hela-S3	cervix:	n/a	n/a
49	SP1	chr11:67764054-67764819	H1-hESC	embryonic stem cell:	n/a	chr11:67764437-67764449 chr11:67764363-67764377 chr11:67764363-67764372 chr11:67764625-67764634 chr11:67764383-67764392 chr11:67764315-67764327 chr11:67764383-67764392 chr11:67764383-67764393 chr11:67764364-67764373 chr11:67764624-67764633 chr11:67764437-67764448 chr11:67764362-67764374 chr11:67764382-67764394 chr11:67764624-67764633 chr11:67764438-67764447 chr11:67764383-67764393 chr11:67764316-67764325 chr11:67764438-67764452 chr11:67764382-67764394 chr11:67764362-67764374 chr11:67764384-67764393 chr11:67764623-67764635 chr11:67764315-67764327 chr11:67764605-67764619 chr11:67764437-67764449
50	MAX	chr11:67764025-67764699	ECC-1	luminal epithelium:	n/a	chr11:67764334-67764344 chr11:67764335-67764342 chr11:67764334-67764344 chr11:67764334-67764344 chr11:67764334-67764343 chr11:67764334-67764343

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67764654-67764704	PANC-1	pancreas:	n/a
2	chr11:67764654-67764704	HCPEpiC	choroid plexus:	n/a
3	chr11:67764654-67764704	ProgFib	skin:	n/a
4	chr11:67764654-67764704	SK-N-MC	brain:	n/a
5	chr11:67764654-67764704	AG04449	skin:	fetal
6	chr11:67764654-67764704	U87	brain:	n/a
7	chr11:67764654-67764704	RPTEC	kidney:	n/a
8	chr11:67764654-67764704	AG09319	gingival:	n/a
9	chr11:67764654-67764704	NHDF-neo	bronchial:	n/a
10	chr11:67764654-67764704	AG04450	lung:	fetal
11	chr11:67764654-67764704	HMEC	breast:	n/a
12	chr11:67764654-67764704	GM12892	blood:	n/a
13	chr11:67764654-67764704	SK-N-SH	brain:	n/a
14	chr11:67764654-67764704	T-47D	breast:	n/a
15	chr11:67764654-67764704	PFSK-1	brain:	n/a
16	chr11:67764654-67764704	SKMC	muscle:	n/a
17	chr11:67764654-67764704	HEEpiC	esophagus:	n/a
18	chr11:67764654-67764704	H1-hESC	embryonic stem cell:	embryo
19	chr11:67764654-67764704	AoSMC	blood vessel:	n/a
20	chr11:67764654-67764704	MCF-7	breast:	n/a
21	chr11:67764654-67764704	GM19239	blood:	n/a
22	chr11:67764654-67764704	Hepatocyte	liver:	n/a
23	chr11:67764654-67764704	NB4	blood:	n/a
24	chr11:67764654-67764704	AG09309	skin:	n/a
25	chr11:67764654-67764704	SAEC	small airway:	n/a
26	chr11:67764654-67764704	GM12878	blood:	n/a
27	chr11:67764654-67764704	Jurkat	blood:	n/a
28	chr11:67764654-67764704	HAEpiC	amniotic membrane:	n/a
29	chr11:67764654-67764704	HNPCEpiC	eye:	n/a
30	chr11:67764654-67764704	HCT-116	colon:	n/a
31	chr11:67764654-67764704	K562	blood:	n/a
32	chr11:67764654-67764704	HRCEpiC	kidney:	n/a
33	chr11:67764654-67764704	PrEC	prostate:	n/a
34	chr11:67764654-67764704	Hela-S3	cervix:	n/a
35	chr11:67764654-67764704	HPAEpiC	pulmonary alveolar:	n/a
36	chr11:67764654-67764704	BJ	skin:	n/a
37	chr11:67764654-67764704	BE2_C	brain:	n/a
38	chr11:67764654-67764704	HL-60	blood:	n/a
39	chr11:67764654-67764704	GM12891	blood:	n/a
40	chr11:67764654-67764704	HIPEpiC	eye:	n/a
41	chr11:67764654-67764704	IMR90	lung:	fetal
42	chr11:67764654-67764704	HRPEpiC	eye:	n/a
43	chr11:67764654-67764704	SK-N-SH_RA	brain:	n/a
44	chr11:67764654-67764704	HCF	heart:	n/a
45	chr11:67764654-67764704	HEK293	kidney:	embryo
46	chr11:67764654-67764704	CMK	blood:	n/a
47	chr11:67764654-67764704	ovcar-3	ovarian:	n/a
48	chr11:67764654-67764704	ECC-1	luminal epithelium:	n/a
49	chr11:67764654-67764704	AG10803	skin:	n/a
50	chr11:67764654-67764704	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67764595..67767102-chr11:67888272..67890683,2	K562	blood:
2	chr11:67763621..67766711-chr11:67769461..67772575,7	MCF-7	breast:
3	chr11:67763215..67765770-chr11:68037604..68039605,2	K562	blood:
4	chr11:67762605..67767485-chr11:67767779..67773135,10	K562	blood:
5	chr11:67762444..67764941-chr11:67774417..67777074,2	K562	blood:

Variant related genes	Relation type
UNC93B1	TF binding region
UNC93B1	CpG island
ENSG00000110057	Chromatin interaction
ENSG00000006534	Chromatin interaction
ENSG00000171067	Chromatin interaction
ENSG00000110721	Chromatin interaction
ENSG00000255236	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs308292	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs308295	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs308296	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs308326	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs308327	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs308328	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs524442	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs589391	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1036101	chr11:67346813-67828351	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
2	nsv541079	chr11:67346813-67828351	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
3	nsv468606	chr11:67352689-67816936	Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
4	nsv555269	chr11:67352689-67816936	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
5	nsv427892	chr11:67451649-67926562	Bivalent Enhancer Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
6	esv2757450	chr11:67472905-67891289	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
7	esv2759835	chr11:67472905-67891289	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
8	nsv428260	chr11:67524937-67797669	Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	80 gene(s)	inside rSNPs	diseases
9	esv2758275	chr11:67524937-67859490	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	87 gene(s)	inside rSNPs	diseases
10	nsv469856	chr11:67639037-67859490	Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
11	nsv482760	chr11:67639037-67859490	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
12	nsv1038960	chr11:67727827-67785555	Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
13	nsv1047567	chr11:67747160-67819790	Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	62 gene(s)	inside rSNPs	diseases
14	nsv8836	chr11:67752879-67819799	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
15	nsv983037	chr11:67756642-67778389	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
16	nsv897836	chr11:67757350-67816936	Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
17	nsv897837	chr11:67757350-67821036	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
18	nsv897838	chr11:67757350-67833543	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
19	nsv482160	chr11:67758575-67771593	Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
20	nsv825963	chr11:67763676-68197054	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
21	nsv1050471	chr11:67764068-67821610	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
22	esv3348305	chr11:67764314-67764715	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2428815	UNC93B1	cis	Nerve Tibial	GTEx

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67759000-67766000	Weak transcription	Liver	Liver
2	chr11:67759200-67770400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr11:67759200-67770400	Weak transcription	Right Atrium	heart
4	chr11:67760200-67767600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr11:67761400-67769800	Genic enhancers	Primary B cells from peripheral blood	blood
6	chr11:67761600-67765600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr11:67761800-67764800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr11:67761800-67765200	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr11:67761800-67765200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr11:67761800-67765400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr11:67761800-67765600	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr11:67761800-67765600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr11:67762000-67770400	Weak transcription	NHLF	lung
14	chr11:67762200-67764800	Weak transcription	Primary hematopoietic stem cells	blood
15	chr11:67762400-67764800	Weak transcription	Fetal Thymus	thymus
16	chr11:67762400-67765200	Weak transcription	Thymus	Thymus
17	chr11:67762400-67765600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr11:67762600-67765400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr11:67762800-67767000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr11:67762800-67767200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr11:67763400-67765200	Enhancers	Fetal Intestine Large	intestine
22	chr11:67763400-67767000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:67763600-67766000	Genic enhancers	A549	lung
24	chr11:67763600-67766200	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr11:67763600-67769800	Genic enhancers	Primary monocytes fromperipheralblood	blood
26	chr11:67763800-67766200	Genic enhancers	Primary B cells from cord blood	blood
27	chr11:67763800-67770400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr11:67764000-67764800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
29	chr11:67764000-67764800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr11:67764000-67764800	Active TSS	H9 Cell Line	embryonic stem cell
31	chr11:67764000-67764800	Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr11:67764000-67764800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr11:67764000-67764800	Flanking Active TSS	K562	blood
34	chr11:67764000-67765000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr11:67764000-67765000	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr11:67764000-67765000	Enhancers	Stomach Mucosa	stomach
37	chr11:67764000-67765400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr11:67764000-67765600	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr11:67764000-67767400	Enhancers	Primary T cells fromperipheralblood	blood
40	chr11:67764000-67768400	Genic enhancers	GM12878-XiMat	blood
41	chr11:67764200-67764800	Active TSS	iPS-15b Cell Line	embryonic stem cell
42	chr11:67764200-67764800	Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr11:67764200-67764800	Genic enhancers	Esophagus	oesophagus
44	chr11:67764200-67765000	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr11:67764200-67765000	Active TSS	HUES48 Cell Line	embryonic stem cell
46	chr11:67764200-67765000	Flanking Active TSS	Hela-S3	cervix
47	chr11:67764200-67765000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr11:67764200-67765200	Enhancers	Lung	lung
49	chr11:67764200-67765200	Enhancers	Pancreas	Pancrea
50	chr11:67764200-67765400	Enhancers	Colonic Mucosa	Colon

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