Variant report

Variant	rs371817301
Chromosome Location	chr11:67770792-67770793
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	SIN3AK20	chr11:67770429-67770837	A549	lung:	n/a	n/a
2	CTCF	chr11:67770720-67770870	GM12864	blood:	n/a	n/a
3	MAZ	chr11:67770456-67772155	IMR90	lung:	n/a	n/a
4	CTCF	chr11:67770720-67770870	GM12873	blood:	n/a	n/a
5	RUNX3	chr11:67769945-67771299	GM12878	blood:	n/a	n/a
6	CTCF	chr11:67770720-67770870	AG04449	skin:	n/a	n/a
7	ZEB1	chr11:67770136-67771417	GM12878	blood:	n/a	chr11:67770498-67770510 chr11:67771060-67771068
8	POLR2A	chr11:67770400-67771328	GM12878	blood:	n/a	n/a
9	MAX	chr11:67769976-67772199	MCF-7	breast:	n/a	chr11:67770222-67770231 chr11:67770217-67770236
10	POLR2A	chr11:67770073-67771737	GM19099	blood:	n/a	n/a
11	MXI1	chr11:67770479-67770802	H1-hESC	embryonic stem cell:	n/a	n/a
12	MAX	chr11:67769956-67772210	A549	lung:	n/a	chr11:67770222-67770231 chr11:67770217-67770236
13	SMARCB1	chr11:67770454-67772177	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr11:67770730-67770822	GM12878	blood:	n/a	n/a
15	MTA3	chr11:67769790-67770826	GM12878	blood:	n/a	n/a
16	SPI1	chr11:67770774-67771236	HL-60	blood:	n/a	chr11:67771022-67771035 chr11:67771028-67771037
17	TCF12	chr11:67770494-67771324	ECC-1	luminal epithelium:	n/a	n/a
18	CTCF	chr11:67770660-67770810	WERI-Rb-1	eye:	n/a	n/a
19	ELF1	chr11:67769927-67771310	GM12878	blood:	n/a	chr11:67770351-67770362 chr11:67770352-67770361
20	MXI1	chr11:67770443-67772278	SK-N-SH	brain:	n/a	chr11:67772185-67772194
21	POLR2A	chr11:67770711-67770979	A549	lung:	n/a	n/a
22	POLR2A	chr11:67769911-67771840	GM12892	blood:	n/a	n/a
23	CTCF	chr11:67770700-67770850	GM12868	blood:	n/a	n/a
24	CTCF	chr11:67770553-67770853	GM12891	blood:	n/a	n/a
25	CTCF	chr11:67770660-67770810	GM12878	blood:	n/a	n/a
26	MAX	chr11:67770326-67771324	H1-hESC	embryonic stem cell:	n/a	n/a
27	USF2	chr11:67770698-67770804	GM12878	blood:	n/a	n/a
28	MAX	chr11:67770173-67771206	NB4	blood:	n/a	chr11:67770222-67770231 chr11:67770217-67770236
29	CTCF	chr11:67770712-67770828	MCF-7	breast:	n/a	n/a
30	POLR2A	chr11:67770043-67771729	GM19193	blood:	n/a	n/a
31	CTCF	chr11:67770740-67770890	GM12871	blood:	n/a	n/a
32	CTCF	chr11:67770680-67770830	BJ	skin:	n/a	n/a
33	POLR2A	chr11:67769917-67771750	GM12878	blood:	n/a	n/a
34	CTCF	chr11:67770694-67770817	GM19240	blood:	n/a	n/a
35	SIN3A	chr11:67770465-67771219	H1-hESC	embryonic stem cell:	n/a	chr11:67770755-67770768
36	JUND	chr11:67770393-67770913	A549	lung:	n/a	n/a
37	POLR2A	chr11:67770058-67771749	GM12892	blood:	n/a	n/a
38	POLR2A	chr11:67769905-67772098	HL-60	blood:	n/a	n/a
39	POLR2A	chr11:67770415-67771699	GM10847	blood:	n/a	n/a
40	CTCF	chr11:67770722-67770809	MCF-7	breast:	n/a	n/a
41	POLR2A	chr11:67770041-67771769	GM15510	blood:	n/a	n/a
42	TCF3	chr11:67770696-67771241	GM12878	blood:	n/a	n/a
43	SPI1	chr11:67770387-67771308	GM12878	blood:	n/a	chr11:67771022-67771035 chr11:67771028-67771037
44	MAZ	chr11:67770664-67771879	GM12878	blood:	n/a	n/a
45	ZBTB7A	chr11:67770677-67771722	K562	blood:	n/a	n/a
46	POLR2A	chr11:67770078-67771823	Raji	blood:	n/a	n/a
47	CTCF	chr11:67770653-67770855	GM12892	blood:	n/a	n/a
48	MXI1	chr11:67769684-67771885	GM12878	blood:	n/a	n/a
49	POLR2A	chr11:67770137-67771788	GM18505	blood:	n/a	n/a
50	POLR2A	chr11:67770064-67771768	GM18526	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:67763621..67766711-chr11:67769461..67772575,7	MCF-7	breast:
2	chr11:67770133..67772267-chr11:67796388..67798189,2	K562	blood:
3	chr11:67770218..67773172-chr11:67805064..67808057,3	K562	blood:
4	chr11:67770112..67773137-chr11:67777240..67779852,3	K562	blood:
5	chr11:67762605..67767485-chr11:67767779..67773135,10	K562	blood:
6	chr11:67770129..67772999-chr11:67979313..67982279,4	K562	blood:
7	chr11:67770463..67774040-chr11:67774088..67778740,6	K562	blood:
8	chr11:67770338..67773597-chr11:67780108..67784129,5	K562	blood:
9	chr11:67769721..67772110-chr11:67979489..67981755,3	MCF-7	breast:

Variant related genes	Relation type
UNC93B1	TF binding region
ENSG00000110057	Chromatin interaction
ENSG00000110717	Chromatin interaction
ENSG00000110719	Chromatin interaction
ENSG00000110066	Chromatin interaction
ENSG00000255306	Chromatin interaction
ENSG00000006534	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:34 , 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	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	esv3372157	chr11:67769401-67772749	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67765000-67770800	Weak transcription	K562	blood
2	chr11:67766200-67771400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr11:67766400-67770800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr11:67766400-67770800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr11:67767800-67771200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:67769000-67770800	Weak transcription	Osteobl	bone
7	chr11:67769200-67771000	Flanking Active TSS	Primary B cells from cord blood	blood
8	chr11:67769800-67770800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr11:67770000-67770800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:67770000-67770800	Flanking Active TSS	Adipose Nuclei	Adipose
11	chr11:67770000-67770800	Enhancers	Colon Smooth Muscle	Colon
12	chr11:67770000-67770800	Flanking Active TSS	Duodenum Mucosa	Duodenum
13	chr11:67770000-67770800	Flanking Active TSS	Fetal Lung	lung
14	chr11:67770000-67771000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr11:67770000-67771000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr11:67770000-67771000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr11:67770000-67771000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr11:67770000-67771800	Active TSS	Rectal Smooth Muscle	rectum
19	chr11:67770000-67772400	Enhancers	Stomach Mucosa	stomach
20	chr11:67770200-67770800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr11:67770200-67770800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
22	chr11:67770200-67771000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr11:67770200-67771800	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr11:67770200-67771800	Active TSS	Brain Anterior Caudate	brain
25	chr11:67770200-67772200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
26	chr11:67770400-67770800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
27	chr11:67770400-67770800	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr11:67770400-67770800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:67770400-67770800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr11:67770400-67770800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr11:67770400-67770800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
32	chr11:67770400-67770800	Active TSS	Fetal Kidney	kidney
33	chr11:67770400-67770800	Flanking Active TSS	Gastric	stomach
34	chr11:67770400-67770800	Active TSS	Left Ventricle	heart
35	chr11:67770400-67770800	Flanking Active TSS	Pancreas	Pancrea
36	chr11:67770400-67771000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
37	chr11:67770400-67771000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
38	chr11:67770400-67771000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr11:67770400-67771000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr11:67770400-67771000	Flanking Active TSS	Colonic Mucosa	Colon
41	chr11:67770400-67771000	Flanking Active TSS	Placenta	Placenta
42	chr11:67770400-67771200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr11:67770400-67771400	Weak transcription	Fetal Heart	heart
44	chr11:67770400-67771400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
45	chr11:67770400-67771600	Active TSS	Liver	Liver
46	chr11:67770400-67771600	Active TSS	Brain Cingulate Gyrus	brain
47	chr11:67770400-67771600	Active TSS	Brain Hippocampus Middle	brain
48	chr11:67770400-67771800	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr11:67770400-67771800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
50	chr11:67770400-67771800	Active TSS	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links