Variant report

Variant	rs7107191
Chromosome Location	chr11:66140397-66140398
allele	A/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	chr11:66138316-66140447	MCF-7	breast:	n/a	chr11:66138849-66138859 chr11:66139400-66139410 chr11:66138998-66139008
2	TBP	chr11:66139704-66140502	Hela-S3	cervix:	n/a	n/a
3	EGR1	chr11:66138427-66140449	HCT-116	colon:	n/a	chr11:66139411-66139424 chr11:66138920-66138944 chr11:66139414-66139424 chr11:66138835-66138846 chr11:66139411-66139424 chr11:66139149-66139162 chr11:66139414-66139423 chr11:66139450-66139464 chr11:66139411-66139424 chr11:66138835-66138845 chr11:66138831-66138845 chr11:66139412-66139426 chr11:66139411-66139425 chr11:66139435-66139449 chr11:66139411-66139424 chr11:66139413-66139423
4	ATF1	chr11:66139805-66140467	K562	blood:	n/a	n/a
5	PRDM1	chr11:66140253-66140638	Hela-S3	cervix:	n/a	n/a
6	NR2F2	chr11:66138215-66140563	K562	blood:	n/a	n/a
7	EGR1	chr11:66138427-66140569	HCT-116	colon:	n/a	chr11:66139411-66139424 chr11:66138920-66138944 chr11:66139414-66139424 chr11:66138835-66138846 chr11:66139411-66139424 chr11:66139149-66139162 chr11:66139414-66139423 chr11:66139450-66139464 chr11:66139411-66139424 chr11:66138835-66138845 chr11:66138831-66138845 chr11:66139412-66139426 chr11:66139411-66139425 chr11:66139435-66139449 chr11:66139411-66139424 chr11:66139413-66139423
8	RCOR1	chr11:66140150-66140463	K562	blood:	n/a	n/a
9	GTF3C2	chr11:66139352-66140543	K562	blood:	n/a	n/a
10	MAX	chr11:66138354-66140435	NB4	blood:	n/a	chr11:66138849-66138859 chr11:66139400-66139410 chr11:66138998-66139008
11	SETDB1	chr11:66140062-66140433	U2OS	brain:	n/a	n/a
12	GTF2F1	chr11:66139727-66140465	Hela-S3	cervix:	n/a	n/a
13	RCOR1	chr11:66138574-66140453	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr11:66138310-66140426	K562	blood:	n/a	n/a
15	ZNF384	chr11:66140375-66140419	K562	blood:	n/a	n/a
16	CBX3	chr11:66138988-66140559	K562	blood:	n/a	n/a
17	RPC155	chr11:66140093-66140400	Hela-S3	cervix:	n/a	n/a
18	ELK1	chr11:66139841-66140474	GM12878	blood:	n/a	n/a
19	POLR2A	chr11:66140328-66142568	K562	blood:	n/a	n/a
20	BRCA1	chr11:66140033-66140447	Hela-S3	cervix:	n/a	n/a
21	GTF3C2	chr11:66139660-66140484	Hela-S3	cervix:	n/a	n/a
22	KAP1	chr11:66139482-66140495	U2OS	brain:	n/a	n/a
23	EP300	chr11:66140365-66140454	K562	blood:	n/a	n/a
24	NR2F2	chr11:66138336-66140433	MCF-7	breast:	n/a	n/a
25	CEBPB	chr11:66139840-66140414	Hela-S3	cervix:	n/a	n/a
26	TEAD4	chr11:66138969-66140503	K562	blood:	n/a	n/a
27	ZC3H11A	chr11:66140105-66140475	K562	blood:	n/a	n/a
28	IRF1	chr11:66138385-66140710	K562	blood:	n/a	chr11:66139335-66139349 chr11:66139153-66139167 chr11:66139415-66139429
29	MAZ	chr11:66138410-66140408	K562	blood:	n/a	chr11:66138849-66138859 chr11:66139400-66139410 chr11:66138998-66139008
30	CTCF	chr11:66140256-66140463	K562	blood:	n/a	n/a
31	RCOR1	chr11:66138576-66140528	K562	blood:	n/a	n/a
32	TBP	chr11:66138433-66140445	K562	blood:	n/a	n/a
33	POLR2A	chr11:66138475-66140398	HCT-116	colon:	n/a	n/a
34	MYC	chr11:66138322-66140399	K562	blood:	n/a	chr11:66138849-66138859 chr11:66139400-66139410 chr11:66138998-66139008
35	IRF1	chr11:66138760-66140567	K562	blood:	n/a	chr11:66139335-66139349 chr11:66139153-66139167 chr11:66139415-66139429
36	MAX	chr11:66138254-66140472	HCT-116	colon:	n/a	chr11:66138849-66138859 chr11:66139400-66139410 chr11:66138998-66139008
37	CUX1	chr11:66140358-66140494	K562	blood:	n/a	n/a
38	RFX5	chr11:66140235-66140407	Hela-S3	cervix:	n/a	n/a
39	EP300	chr11:66138756-66140585	K562	blood:	n/a	chr11:66139256-66139272 chr11:66138971-66138987 chr11:66139122-66139138
40	RFX5	chr11:66140291-66140501	K562	blood:	n/a	n/a
41	MXI1	chr11:66139999-66140471	Hela-S3	cervix:	n/a	n/a
42	KAP1	chr11:66140294-66140588	K562	blood:	n/a	n/a
43	JUND	chr11:66138485-66140442	K562	blood:	n/a	chr11:66139370-66139379 chr11:66138852-66138861 chr11:66139153-66139162 chr11:66138703-66138714
44	BHLHE40	chr11:66138538-66140425	K562	blood:	n/a	chr11:66139619-66139635
45	MTA3	chr11:66139706-66140491	GM12878	blood:	n/a	n/a
46	HCFC1	chr11:66137127-66141321	Hela-S3	cervix:	n/a	n/a
47	ZNF274	chr11:66140265-66140822	K562	blood:	n/a	n/a
48	CEBPB	chr11:66139983-66140556	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:66138830..66140876-chr11:66445335..66446976,2	K562	blood:
2	chr11:66078412..66081908-chr11:66138198..66140974,6	K562	blood:
3	chr11:66102581..66106910-chr11:66137391..66141246,5	MCF-7	breast:
4	chr11:66137724..66140546-chr11:66233440..66235364,2	MCF-7	breast:
5	chr11:66024034..66026694-chr11:66139002..66141879,3	K562	blood:
6	chr11:66138351..66141046-chr11:66154511..66157251,2	K562	blood:
7	chr11:66108426..66118730-chr11:66133678..66141000,25	MCF-7	breast:
8	chr11:66102037..66105089-chr11:66137738..66140850,8	MCF-7	breast:
9	chr11:66137544..66141665-chr11:66155643..66157959,3	MCF-7	breast:
10	chr11:66049515..66053153-chr11:66136549..66141980,4	K562	blood:
11	chr11:66139563..66141244-chr11:66219589..66221744,2	MCF-7	breast:
12	chr11:66054859..66059696-chr11:66135983..66141726,7	K562	blood:
13	chr11:66138363..66140696-chr11:66204293..66206330,3	MCF-7	breast:
14	chr11:66138177..66141064-chr11:66382767..66386168,3	MCF-7	breast:
15	chr11:66139196..66140787-chr11:66233339..66235193,2	MCF-7	breast:
16	chr11:66052361..66057023-chr11:66137906..66140994,4	MCF-7	breast:
17	chr11:66139168..66140849-chr11:66177644..66179339,2	K562	blood:
18	chr11:66103854..66118324-chr11:66119048..66141728,55	K562	blood:

Variant related genes	Relation type
SLC29A2	TF binding region
ENSG00000174684	Chromatin interaction
ENSG00000174791	Chromatin interaction
ENSG00000179292	Chromatin interaction
ENSG00000254510	Chromatin interaction
ENSG00000174996	Chromatin interaction
ENSG00000174547	Chromatin interaction
ENSG00000174516	Chromatin interaction
ENSG00000254736	Chromatin interaction
ENSG00000173914	Chromatin interaction
ENSG00000174871	Chromatin interaction
ENSG00000174744	Chromatin interaction
ENSG00000239306	Chromatin interaction
ENSG00000255468	Chromatin interaction
ENSG00000248643	Chromatin interaction
ENSG00000254458	Chromatin interaction
ENSG00000254596	Chromatin interaction
ENSG00000174851	Chromatin interaction

Extended variants
information (count: 74 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs1039594	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1047029	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10750784	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10791869	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10791872	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10791874	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10791876	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10896111	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10896112	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10896115	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10896116	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11227465	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11601396	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11823140	0.85[EUR][1000 genomes]
rs12416747	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12576293	0.80[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs12576299	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12577196	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12785321	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12785651	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12786563	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12794121	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1546358	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1784029	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs1785633	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1785639	0.87[EUR][1000 genomes]
rs1892940	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2236679	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2279861	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2279862	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2282530	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2282531	0.86[EUR][1000 genomes]
rs3016767	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3177514	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34043951	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4244813	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4930177	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4930178	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4930179	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4930181	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4930360	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4930362	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4930363	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4930366	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4930368	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55998145	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56123976	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56321771	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61891449	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6591213	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6591215	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6591217	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs66810040	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs67780191	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7104253	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7104570	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7105015	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7105401	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7110944	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7117630	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7126018	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73489638	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7938676	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7939111	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7940980	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs905770	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs947978	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3335923	chr11:65741698-66175759	Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
2	esv3407551	chr11:65794503-66158322	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
3	esv3392427	chr11:65981489-66273695	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
4	nsv897771	chr11:66011280-66362997	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	124 gene(s)	inside rSNPs	diseases
5	nsv897772	chr11:66018155-66254085	Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
6	nsv897780	chr11:66083129-66362997	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
7	nsv832193	chr11:66120339-66278805	Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7107191	RIN1	cis	Whole Blood	GTEx

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66137600-66140400	Active TSS	H9 Cell Line	embryonic stem cell
2	chr11:66137600-66140400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:66137800-66140400	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr11:66137800-66140400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr11:66137800-66140400	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr11:66137800-66140400	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr11:66137800-66140400	Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr11:66137800-66140400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr11:66138000-66140400	Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr11:66138000-66140400	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr11:66138400-66140400	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr11:66138400-66140400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
13	chr11:66138600-66140400	Active TSS	Brain Angular Gyrus	brain
14	chr11:66138600-66140600	Flanking Active TSS	Dnd41	blood
15	chr11:66139400-66140400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chr11:66139600-66140400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr11:66139600-66140400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr11:66139800-66140400	Flanking Active TSS	Primary B cells from peripheral blood	blood
19	chr11:66139800-66140400	Flanking Active TSS	Primary T cells from cord blood	blood
20	chr11:66139800-66140400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
21	chr11:66139800-66140400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr11:66139800-66140400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
23	chr11:66139800-66140400	Flanking Active TSS	Duodenum Mucosa	Duodenum
24	chr11:66139800-66140400	Flanking Active TSS	Fetal Thymus	thymus
25	chr11:66139800-66140400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
26	chr11:66139800-66140600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:66139800-66140600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
28	chr11:66139800-66141000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr11:66140000-66140400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
30	chr11:66140000-66140400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
31	chr11:66140000-66140400	Flanking Active TSS	Primary hematopoietic stem cells	blood
32	chr11:66140000-66140400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
33	chr11:66140000-66140400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
34	chr11:66140000-66140400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr11:66140000-66140400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
36	chr11:66140000-66140400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr11:66140000-66140400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr11:66140000-66140400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
39	chr11:66140000-66140400	Bivalent Enhancer	Fetal Brain Male	brain
40	chr11:66140000-66140400	Flanking Active TSS	Left Ventricle	heart
41	chr11:66140000-66140400	Flanking Active TSS	Pancreas	Pancrea
42	chr11:66140000-66140400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
43	chr11:66140000-66140400	Flanking Active TSS	Thymus	Thymus
44	chr11:66140000-66140400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
45	chr11:66140000-66140600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:66140000-66140600	Bivalent Enhancer	NH-A	brain
47	chr11:66140000-66141000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr11:66140000-66141000	Enhancers	Esophagus	oesophagus
49	chr11:66140200-66140400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
50	chr11:66140200-66140400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links