Variant report

Variant	rs308334
Chromosome Location	chr11:67776852-67776853
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	CTCF	chr11:67776841-67779086	A549	lung:	n/a	n/a
2	CTCF	chr11:67776840-67776990	HMF	breast:	n/a	n/a
3	STAT5A	chr11:67776826-67777370	K562	blood:	n/a	n/a
4	GATA1	chr11:67776599-67777966	PBDE	blood:	n/a	n/a
5	EP300	chr11:67776703-67779274	A549	lung:	n/a	n/a
6	KAP1	chr11:67776722-67777238	HEK293	kidney:	n/a	n/a
7	SPI1	chr11:67776439-67776876	HL-60	blood:	n/a	chr11:67776655-67776668 chr11:67776631-67776644
8	NR3C1	chr11:67776798-67777309	A549	lung:	n/a	n/a
9	SP1	chr11:67776718-67782739	A549	lung:	n/a	chr11:67782714-67782728 chr11:67782346-67782355 chr11:67782347-67782356 chr11:67782346-67782360
10	POLR2A	chr11:67775677-67777044	HL-60	blood:	n/a	n/a
11	SPI1	chr11:67776174-67777004	HL-60	blood:	n/a	chr11:67776655-67776668 chr11:67776631-67776644
12	CTCF	chr11:67776760-67776910	HMEC	breast:	n/a	n/a
13	TEAD4	chr11:67776846-67777360	K562	blood:	n/a	n/a
14	SIX5	chr11:67776699-67783266	A549	lung:	n/a	n/a
15	TAL1	chr11:67776795-67777713	K562	blood:	n/a	n/a
16	USF1	chr11:67776789-67777242	K562	blood:	n/a	n/a
17	NR2F2	chr11:67776640-67777894	K562	blood:	n/a	n/a
18	TEAD4	chr11:67776583-67777869	K562	blood:	n/a	n/a
19	MAX	chr11:67775696-67776963	A549	lung:	n/a	chr11:67776499-67776510 chr11:67776500-67776509 chr11:67776025-67776036 chr11:67776182-67776192 chr11:67776026-67776035 chr11:67776026-67776035
20	MAZ	chr11:67776692-67778793	IMR90	lung:	n/a	n/a
21	TRIM28	chr11:67776700-67777405	K562	blood:	n/a	n/a
22	MAX	chr11:67775570-67783343	A549	lung:	n/a	chr11:67776499-67776510 chr11:67776500-67776509 chr11:67776025-67776036 chr11:67779790-67779800 chr11:67776182-67776192 chr11:67776026-67776035 chr11:67776026-67776035
23	BHLHE40	chr11:67776577-67778070	K562	blood:	n/a	n/a
24	FOSL2	chr11:67776553-67778957	A549	lung:	n/a	n/a
25	POLR2A	chr11:67775714-67776984	HL-60	blood:	n/a	n/a
26	POLR2A	chr11:67775887-67778680	PBDE	blood:	n/a	n/a
27	TCF12	chr11:67775698-67783378	A549	lung:	n/a	chr11:67782099-67782109 chr11:67782990-67783000 chr11:67782981-67782991 chr11:67782696-67782706 chr11:67776259-67776269
28	ELF1	chr11:67776489-67776881	K562	blood:	n/a	chr11:67776656-67776667 chr11:67776654-67776667
29	MYC	chr11:67776345-67778567	A549	lung:	n/a	chr11:67776499-67776510 chr11:67776500-67776509
30	RCOR1	chr11:67776824-67777896	K562	blood:	n/a	n/a
31	BCL3	chr11:67776809-67783348	A549	lung:	n/a	chr11:67782268-67782277
32	CBX3	chr11:67776487-67777967	K562	blood:	n/a	n/a
33	NR2F2	chr11:67776764-67777323	K562	blood:	n/a	n/a
34	EP300	chr11:67776757-67778737	A549	lung:	n/a	n/a
35	GATA3	chr11:67776826-67782913	A549	lung:	n/a	n/a
36	CTCF	chr11:67776800-67776950	HL-60	blood:	n/a	n/a
37	ZNF384	chr11:67776846-67777724	K562	blood:	n/a	n/a
38	TBL1XR1	chr11:67776791-67776970	K562	blood:	n/a	n/a
39	NR3C1	chr11:67776793-67777234	A549	lung:	n/a	n/a
40	MAX	chr11:67776784-67777413	K562	blood:	n/a	n/a
41	ATF3	chr11:67776792-67777250	K562	blood:	n/a	n/a
42	SP1	chr11:67776743-67779088	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67776209..67777895-chr11:67887404..67889163,2	K562	blood:
2	chr11:65270883..65271821-chr11:67776699..67777645,2	Hela-S3	cervix:
3	chr11:67776633..67779501-chr11:67798153..67800329,2	K562	blood:
4	chr11:67762444..67764941-chr11:67774417..67777074,2	K562	blood:
5	chr11:67776362..67777982-chr11:67979637..67981259,2	K562	blood:
6	chr11:67776804..67777352-chr11:67788052..67788668,2	MCF-7	breast:
7	chr11:67770463..67774040-chr11:67774088..67778740,6	K562	blood:
8	chr11:67770966..67773282-chr11:67774269..67777181,2	K562	blood:
9	chr11:67776791..67777547-chr11:67788251..67788807,2	MCF-7	breast:

Variant related genes	Relation type
ALDH3B1	TF binding region
UNC93B1	TF binding region
ENSG00000110057	Chromatin interaction
ENSG00000110717	Chromatin interaction
ENSG00000110721	Chromatin interaction
ENSG00000110066	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1636214	1.00[EUR][1000 genomes]
rs1703435	1.00[EUR][1000 genomes]
rs2286171	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs308293	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs308297	1.00[EUR][1000 genomes]
rs308298	1.00[EUR][1000 genomes]
rs308330	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs308333	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs308335	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs308336	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs308337	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs308347	1.00[EUR][1000 genomes]
rs308348	1.00[EUR][1000 genomes]
rs308357	1.00[EUR][1000 genomes]
rs503039	1.00[EUR][1000 genomes]
rs557098	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59143115	1.00[EUR][1000 genomes]
rs6591325	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6591327	1.00[EUR][1000 genomes]
rs7117605	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7118342	1.00[EUR][1000 genomes]
rs7125916	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:36 , 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	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
20	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
21	nsv897839	chr11:67765056-67793014	Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
22	nsv468613	chr11:67765056-67794643	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
23	nsv555277	chr11:67765056-67794643	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
24	nsv468614	chr11:67765056-67799926	ZNF genes & repeats Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
25	nsv897840	chr11:67765056-67804605	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
26	nsv468615	chr11:67765056-67816936	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
27	nsv555278	chr11:67765056-67816936	Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
28	nsv897841	chr11:67765056-67816936	Bivalent Enhancer Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
29	nsv469964	chr11:67765056-67821036	Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
30	nsv897842	chr11:67765056-67821036	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
31	nsv897843	chr11:67765056-67833543	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
32	nsv1046054	chr11:67768796-67819790	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	60 gene(s)	inside rSNPs	diseases
33	nsv897844	chr11:67772729-67793014	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
34	nsv897845	chr11:67774231-67821036	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
35	nsv897846	chr11:67776465-67794643	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
36	nsv897847	chr11:67776465-67804605	Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67771600-67777200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr11:67771600-67797600	Weak transcription	Small Intestine	intestine
3	chr11:67772000-67777000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:67772000-67777200	Weak transcription	Rectal Smooth Muscle	rectum
5	chr11:67772200-67777000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr11:67772200-67777000	Weak transcription	HUVEC	blood vessel
7	chr11:67772200-67777200	Weak transcription	Brain Cingulate Gyrus	brain
8	chr11:67772200-67777200	Weak transcription	Left Ventricle	heart
9	chr11:67772200-67777400	Weak transcription	NHLF	lung
10	chr11:67772200-67777800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr11:67772200-67779200	Enhancers	Primary B cells from peripheral blood	blood
12	chr11:67772400-67777400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr11:67772600-67777400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:67772600-67792400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr11:67772800-67777200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr11:67772800-67777200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr11:67772800-67777200	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr11:67772800-67777800	Weak transcription	Lung	lung
19	chr11:67773600-67777800	Enhancers	Stomach Mucosa	stomach
20	chr11:67775000-67777600	Enhancers	Fetal Muscle Leg	muscle
21	chr11:67775000-67782400	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr11:67775200-67777200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr11:67775200-67777400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr11:67775200-67777400	Enhancers	Placenta	Placenta
25	chr11:67775200-67777600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr11:67775200-67777800	Enhancers	Pancreas	Pancrea
27	chr11:67775400-67777000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:67775400-67777400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr11:67775400-67777400	Enhancers	Fetal Intestine Large	intestine
30	chr11:67775400-67777400	Enhancers	Fetal Intestine Small	intestine
31	chr11:67775400-67777600	Enhancers	Adipose Nuclei	Adipose
32	chr11:67775400-67778200	Enhancers	Primary hematopoietic stem cells	blood
33	chr11:67775400-67778200	Enhancers	Spleen	Spleen
34	chr11:67775600-67777400	Flanking Active TSS	Hela-S3	cervix
35	chr11:67775600-67777600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr11:67775600-67779400	Enhancers	Fetal Heart	heart
37	chr11:67775800-67777400	Flanking Active TSS	HepG2	liver
38	chr11:67775800-67777400	Enhancers	HMEC	breast
39	chr11:67775800-67777400	Enhancers	HSMMtube	muscle
40	chr11:67775800-67777600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr11:67775800-67777600	Enhancers	Brain Anterior Caudate	brain
42	chr11:67775800-67777600	Enhancers	Brain Hippocampus Middle	brain
43	chr11:67775800-67777600	Enhancers	Brain Substantia Nigra	brain
44	chr11:67775800-67777600	Enhancers	Esophagus	oesophagus
45	chr11:67775800-67777800	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr11:67775800-67777800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr11:67775800-67777800	Enhancers	Liver	Liver
48	chr11:67775800-67777800	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr11:67775800-67777800	Enhancers	Thymus	Thymus
50	chr11:67776000-67777000	Flanking Active TSS	Duodenum Mucosa	Duodenum

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