Variant report

Variant	rs1551889
Chromosome Location	chr11:67273835-67273836
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	POLR2A	chr11:67272463-67273930	Hela-S3	cervix:	n/a	n/a
2	RAD21	chr11:67273267-67274153	SK-N-SH	brain:	n/a	chr11:67273757-67273771 chr11:67273755-67273767 chr11:67273756-67273769 chr11:67273757-67273767 chr11:67273753-67273772
3	FOSL2	chr11:67273412-67273913	A549	lung:	n/a	n/a
4	CTCF	chr11:67273700-67273850	Caco-2	colon:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67273756-67273772 chr11:67273755-67273773
5	MAX	chr11:67273187-67273971	ECC-1	luminal epithelium:	n/a	n/a
6	JUN	chr11:67273633-67273886	H1-hESC	embryonic stem cell:	n/a	n/a
7	TBP	chr11:67273619-67273856	H1-hESC	embryonic stem cell:	n/a	n/a
8	TCF12	chr11:67273565-67273868	GM12878	blood:	n/a	n/a
9	RUNX3	chr11:67272408-67273960	GM12878	blood:	n/a	n/a
10	ARID3A	chr11:67273668-67273868	HepG2	liver:	n/a	n/a
11	HDAC2	chr11:67273269-67274022	MCF-7	breast:	n/a	n/a
12	YY1	chr11:67273631-67273885	K562	blood:	n/a	n/a
13	RELA	chr11:67273519-67273910	GM19099	blood:	n/a	n/a
14	RCOR1	chr11:67273129-67274355	IMR90	lung:	n/a	n/a
15	RAD21	chr11:67273480-67273987	ECC-1	luminal epithelium:	n/a	chr11:67273757-67273771 chr11:67273755-67273767 chr11:67273756-67273769 chr11:67273757-67273767 chr11:67273753-67273772
16	ELF1	chr11:67273193-67273910	K562	blood:	n/a	n/a
17	CTCF	chr11:67273700-67273850	MCF-7	breast:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67273756-67273772 chr11:67273755-67273773
18	CTCF	chr11:67273593-67273919	MCF-7	breast:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67273756-67273772 chr11:67273755-67273773
19	HDAC2	chr11:67273279-67273865	HepG2	liver:	n/a	n/a
20	ZKSCAN1	chr11:67273287-67273890	Hela-S3	cervix:	n/a	chr11:67273330-67273343
21	POLR2A	chr11:67273217-67273934	HCT-116	colon:	n/a	n/a
22	ELF1	chr11:67273648-67273868	HepG2	liver:	n/a	n/a
23	MYC	chr11:67273192-67273940	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr11:67273211-67274402	HCT-116	colon:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67273211-67273224 chr11:67273756-67273772 chr11:67273755-67273773
25	IRF4	chr11:67273499-67273934	GM12878	blood:	n/a	n/a
26	POLR2A	chr11:67272553-67273846	PANC-1	pancreas:	n/a	n/a
27	RCOR1	chr11:67273568-67273905	HepG2	liver:	n/a	n/a
28	POLR2A	chr11:67273620-67274010	K562	blood:	n/a	n/a
29	CTCF	chr11:67273614-67273928	Pancreas_OC	pancreas:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67273756-67273772 chr11:67273755-67273773
30	ZMIZ1	chr11:67273577-67273869	K562	blood:	n/a	n/a
31	CTCF	chr11:67273700-67273850	HPF	lung:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67273756-67273772 chr11:67273755-67273773
32	ATF2	chr11:67273356-67273944	GM12878	blood:	n/a	n/a
33	MXI1	chr11:67272907-67273909	GM12878	blood:	n/a	n/a
34	BATF	chr11:67273570-67273878	GM12878	blood:	n/a	n/a
35	CTCF	chr11:67273700-67273850	A549	lung:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67273756-67273772 chr11:67273755-67273773
36	EP300	chr11:67272715-67274037	ECC-1	luminal epithelium:	n/a	chr11:67272902-67272918
37	CTCF	chr11:67273700-67273850	AG10803	skin:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67273756-67273772 chr11:67273755-67273773
38	EP300	chr11:67273322-67273843	GM12878	blood:	n/a	n/a
39	MYC	chr11:67273246-67273844	MCF10A-Er-Src	breast:	n/a	n/a
40	RAD21	chr11:67273540-67273932	K562	blood:	n/a	chr11:67273757-67273771 chr11:67273755-67273767 chr11:67273756-67273769 chr11:67273757-67273767 chr11:67273753-67273772
41	CTCF	chr11:67273720-67273870	GM12865	blood:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67273756-67273772 chr11:67273755-67273773
42	ZNF143	chr11:67273292-67273937	Hela-S3	cervix:	n/a	chr11:67273699-67273717
43	CTCF	chr11:67273601-67273893	A549	lung:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67273756-67273772 chr11:67273755-67273773
44	CTCF	chr11:67273700-67273850	GM12874	blood:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67273756-67273772 chr11:67273755-67273773
45	CHD2	chr11:67273495-67273927	GM12878	blood:	n/a	n/a
46	ZBTB7A	chr11:67271800-67273994	ECC-1	luminal epithelium:	n/a	chr11:67272728-67272737 chr11:67272109-67272116 chr11:67271941-67271949
47	WRNIP1	chr11:67273489-67273895	GM12878	blood:	n/a	n/a
48	NR2F2	chr11:67272795-67274035	MCF-7	breast:	n/a	n/a
49	TCF12	chr11:67273106-67273929	ECC-1	luminal epithelium:	n/a	n/a
50	CTCF	chr11:67273700-67273850	GM12869	blood:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67273756-67273772 chr11:67273755-67273773

No.	Distal block	Cell Line	Cell type
1	chr11:67118066..67122624-chr11:67272137..67276691,11	MCF-7	breast:
2	chr11:67272970..67273969-chr19:2475840..2476412,2	Hela-S3	cervix:
3	chr11:67247191..67252288-chr11:67270350..67277699,12	MCF-7	breast:
4	chr11:67207904..67210724-chr11:67272140..67274356,2	MCF-7	breast:
5	chr11:67168723..67169834-chr11:67273315..67274170,3	MCF-7	breast:
6	chr11:67234460..67237754-chr11:67271882..67275850,7	MCF-7	breast:
7	chr11:67206947..67211030-chr11:67273670..67277577,4	MCF-7	breast:
8	chr11:67272929..67273871-chr17:46125581..46126100,2	Hela-S3	cervix:
9	chr11:67157498..67160851-chr11:67271704..67276538,6	K562	blood:
10	chr11:67230107..67238941-chr11:67268499..67277838,23	MCF-7	breast:
11	chr11:67168546..67169541-chr11:67273014..67274216,5	K562	blood:
12	chr11:67157917..67161280-chr11:67271512..67274163,3	MCF-7	breast:
13	chr11:67236456..67237113-chr11:67273312..67274146,3	MCF-7	breast:
14	chr11:67164456..67171429-chr11:67268926..67279263,19	K562	blood:
15	chr11:67172030..67174041-chr11:67273255..67275268,2	MCF-7	breast:
16	chr11:67269985..67274388-chr11:67349964..67354078,4	K562	blood:
17	chr11:67232230..67234303-chr11:67273494..67275304,2	K562	blood:
18	chr11:67052872..67055062-chr11:67273802..67275420,2	K562	blood:
19	chr11:67186666..67191064-chr11:67273296..67275634,4	K562	blood:
20	chr11:67182567..67190511-chr11:67270739..67276166,13	MCF-7	breast:
21	chr11:67139414..67143301-chr11:67273275..67276817,6	MCF-7	breast:
22	chr11:67140485..67142430-chr11:67273527..67275502,2	K562	blood:
23	chr11:67273134..67273943-chr9:111775445..111776120,2	Hela-S3	cervix:
24	chr11:67272696..67275492-chr11:67373280..67375901,2	MCF-7	breast:
25	chr11:67272308..67273879-chr17:62223283..62223939,4	Hela-S3	cervix:
26	chr11:67124312..67125028-chr11:67273279..67274094,2	MCF-7	breast:
27	chr11:67166559..67171272-chr11:67271633..67274655,6	MCF-7	breast:
28	chr11:67124281..67124913-chr11:67273353..67273960,2	K562	blood:
29	chr11:67249454..67253550-chr11:67271231..67274487,6	MCF-7	breast:
30	chr11:67124361..67124883-chr11:67273301..67274134,2	MCF-7	breast:
31	chr11:67140165..67142541-chr11:67273740..67276217,2	MCF-7	breast:
32	chr11:67256017..67258793-chr11:67272672..67274747,2	MCF-7	breast:
33	chr11:67271788..67274805-chr11:67372108..67375948,3	K562	blood:
34	chr11:67194364..67200337-chr11:67272800..67277654,9	MCF-7	breast:
35	chr11:67174684..67176198-chr11:67271900..67273931,2	K562	blood:
36	chr11:67201204..67205243-chr11:67272634..67278205,5	MCF-7	breast:
37	chr11:67159421..67161559-chr11:67272153..67274079,2	K562	blood:
38	chr11:67272994..67275730-chr6:26029475..26032362,2	K562	blood:
39	chr11:67164491..67170697-chr11:67268115..67277759,17	MCF-7	breast:
40	chr11:67232230..67238185-chr11:67272105..67277120,9	K562	blood:
41	chr11:67156232..67161608-chr11:67271298..67276147,11	MCF-7	breast:
42	chr11:67201617..67208575-chr11:67270788..67277143,13	K562	blood:
43	chr11:67186666..67189529-chr11:67272076..67275550,4	K562	blood:

Variant related genes	Relation type
PITPNM1	TF binding region
ENSG00000172663	Chromatin interaction
ENSG00000172508	Chromatin interaction
ENSG00000256514	Chromatin interaction
ENSG00000110711	Chromatin interaction
ENSG00000175482	Chromatin interaction
ENSG00000175634	Chromatin interaction
ENSG00000255119	Chromatin interaction
ENSG00000184224	Chromatin interaction
ENSG00000172531	Chromatin interaction
ENSG00000213402	Chromatin interaction
ENSG00000082641	Chromatin interaction
ENSG00000199753	Chromatin interaction
ENSG00000255949	Chromatin interaction
ENSG00000172613	Chromatin interaction
ENSG00000175463	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000167792	Chromatin interaction
ENSG00000084207	Chromatin interaction
ENSG00000266402	Chromatin interaction
ENSG00000172725	Chromatin interaction
ENSG00000119326	Chromatin interaction
ENSG00000175505	Chromatin interaction
ENSG00000099860	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1272686	0.89[CHB][hapmap]
rs57178591	1.00[EUR][1000 genomes]
rs627068	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs627956	0.89[CHB][hapmap]
rs672432	0.88[CHB][hapmap]
rs687058	1.00[ASW][hapmap]
rs687376	0.89[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers 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	271 gene(s)	inside rSNPs	diseases
2	nsv897797	chr11:67023040-67293234	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
3	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
4	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
5	esv1818769	chr11:67138811-67300457	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
6	nsv897805	chr11:67155210-67283891	ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
7	nsv897806	chr11:67155210-67294308	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
8	nsv897807	chr11:67155210-67414492	Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
9	nsv897808	chr11:67155210-67419855	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
10	nsv897809	chr11:67156875-67276235	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
11	nsv555254	chr11:67164495-67288594	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
12	nsv534229	chr11:67164667-67411909	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
13	nsv897813	chr11:67175692-67283891	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
14	nsv521723	chr11:67175692-67311258	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
15	nsv468604	chr11:67186000-67283891	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
16	nsv555256	chr11:67186000-67283891	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
17	nsv527056	chr11:67207426-67294308	Genic enhancers Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	115 gene(s)	inside rSNPs	diseases
18	esv2422195	chr11:67234322-67626901	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
19	nsv1052919	chr11:67252337-67306030	Active TSS Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS 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	70 gene(s)	inside rSNPs	diseases
20	nsv541078	chr11:67252337-67306030	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67270600-67276600	Enhancers	Fetal Heart	heart
2	chr11:67271000-67276800	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr11:67271200-67275400	Flanking Active TSS	Pancreas	Pancrea
4	chr11:67271200-67275600	Flanking Active TSS	Colonic Mucosa	Colon
5	chr11:67272200-67274000	Active TSS	Right Ventricle	heart
6	chr11:67272600-67274800	Weak transcription	Fetal Kidney	kidney
7	chr11:67272600-67276400	Enhancers	Fetal Brain Male	brain
8	chr11:67272800-67274000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr11:67272800-67274000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
10	chr11:67272800-67274000	Flanking Active TSS	Brain Cingulate Gyrus	brain
11	chr11:67272800-67274000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
12	chr11:67272800-67274200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
13	chr11:67272800-67274200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
14	chr11:67272800-67274400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr11:67272800-67274800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr11:67272800-67274800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr11:67272800-67274800	Enhancers	Spleen	Spleen
18	chr11:67272800-67275000	Weak transcription	Small Intestine	intestine
19	chr11:67272800-67275200	Weak transcription	Ovary	ovary
20	chr11:67273000-67274000	Flanking Active TSS	Primary T cells from cord blood	blood
21	chr11:67273000-67274000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
22	chr11:67273000-67274000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr11:67273000-67274000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr11:67273000-67274000	Flanking Active TSS	Brain Angular Gyrus	brain
25	chr11:67273000-67274000	Flanking Active TSS	Brain Anterior Caudate	brain
26	chr11:67273000-67274000	Flanking Active TSS	Brain Hippocampus Middle	brain
27	chr11:67273000-67274000	Flanking Active TSS	Duodenum Mucosa	Duodenum
28	chr11:67273000-67274000	Flanking Active TSS	Thymus	Thymus
29	chr11:67273000-67274000	Flanking Active TSS	HSMMtube	muscle
30	chr11:67273000-67274000	Flanking Active TSS	NHEK	skin
31	chr11:67273000-67274200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr11:67273000-67274200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr11:67273000-67274200	Flanking Active TSS	Fetal Intestine Large	intestine
34	chr11:67273000-67274200	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr11:67273000-67274600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr11:67273000-67274800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr11:67273000-67274800	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr11:67273000-67275000	Flanking Active TSS	GM12878-XiMat	blood
39	chr11:67273000-67275000	Flanking Active TSS	HepG2	liver
40	chr11:67273000-67275400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
41	chr11:67273000-67275400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
42	chr11:67273200-67274000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:67273200-67274000	Flanking Active TSS	Rectal Smooth Muscle	rectum
44	chr11:67273200-67274600	Weak transcription	Fetal Brain Female	brain
45	chr11:67273200-67274800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr11:67273200-67275000	Enhancers	Primary hematopoietic stem cells	blood
47	chr11:67273200-67275000	Enhancers	Fetal Muscle Trunk	muscle
48	chr11:67273400-67274000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr11:67273400-67274000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr11:67273400-67274000	Weak transcription	Gastric	stomach

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