Variant report

Variant	rs11577338
Chromosome Location	chr1:155240077-155240078
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:155238212..155240823-chr1:155276858..155278738,2	K562	blood:
2	chr1:155167345..155170267-chr1:155238790..155240384,2	MCF-7	breast:
3	chr1:155236269..155241954-chr1:155291931..155295779,5	K562	blood:
4	chr1:155239466..155241223-chr1:155241628..155244752,3	MCF-7	breast:
5	chr1:155237070..155244636-chr1:155291827..155295779,11	K562	blood:
6	chr1:155239314..155245036-chr1:155288379..155297041,21	MCF-7	breast:

Variant related genes	Relation type
ENSG00000231064	Chromatin interaction
ENSG00000176444	Chromatin interaction
ENSG00000225855	Chromatin interaction
ENSG00000160752	Chromatin interaction
ENSG00000160753	Chromatin interaction
ENSG00000169231	Chromatin interaction

Extended variants
information (count: 108 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10128085	0.82[ASN][1000 genomes]
rs1045253	0.85[ASN][1000 genomes]
rs1046188	0.97[ASN][1000 genomes]
rs1052176	0.95[ASN][1000 genomes]
rs1052177	0.95[ASN][1000 genomes]
rs1076556	0.98[ASN][1000 genomes]
rs1078699	0.97[ASN][1000 genomes]
rs10796940	0.85[ASN][1000 genomes]
rs10908459	0.87[ASN][1000 genomes]
rs11264343	0.85[ASN][1000 genomes]
rs11264345	0.86[ASN][1000 genomes]
rs11264346	0.96[ASN][1000 genomes]
rs11264348	0.97[ASN][1000 genomes]
rs11264349	0.97[ASN][1000 genomes]
rs11264351	0.90[ASN][1000 genomes]
rs11264352	0.97[ASN][1000 genomes]
rs11264353	0.97[ASN][1000 genomes]
rs11264354	0.90[ASN][1000 genomes]
rs11264355	0.88[ASN][1000 genomes]
rs1142287	0.97[ASN][1000 genomes]
rs12034326	0.86[ASN][1000 genomes]
rs12042020	0.94[ASN][1000 genomes]
rs12044063	0.95[ASN][1000 genomes]
rs12049375	0.98[ASN][1000 genomes]
rs12067675	0.90[ASN][1000 genomes]
rs12407919	0.85[ASN][1000 genomes]
rs12563994	0.99[ASN][1000 genomes]
rs12723761	0.84[ASN][1000 genomes]
rs12724449	0.97[ASN][1000 genomes]
rs12732972	0.85[ASN][1000 genomes]
rs12748155	0.88[ASN][1000 genomes]
rs12749306	0.99[ASN][1000 genomes]
rs1546818	0.92[ASN][1000 genomes]
rs1800438	0.86[ASN][1000 genomes]
rs1800442	0.82[ASN][1000 genomes]
rs1807042	0.87[ASN][1000 genomes]
rs2009578	0.86[ASN][1000 genomes]
rs2071053	0.95[ASN][1000 genomes]
rs2072647	0.90[ASN][1000 genomes]
rs2075566	0.95[ASN][1000 genomes]
rs2075569	0.86[ASN][1000 genomes]
rs2236863	0.99[ASN][1000 genomes]
rs2236864	0.80[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2242576	0.96[ASN][1000 genomes]
rs2242577	0.95[ASN][1000 genomes]
rs2361536	0.90[ASN][1000 genomes]
rs2361543	0.98[ASN][1000 genomes]
rs28373017	0.80[ASN][1000 genomes]
rs3020781	0.85[ASN][1000 genomes]
rs34906309	0.91[ASN][1000 genomes]
rs3754485	0.86[ASN][1000 genomes]
rs3762272	0.88[ASN][1000 genomes]
rs3768566	0.85[ASN][1000 genomes]
rs3814318	0.94[ASN][1000 genomes]
rs3814319	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4043	0.85[ASN][1000 genomes]
rs4620533	0.95[ASN][1000 genomes]
rs4971072	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs56310840	0.85[ASN][1000 genomes]
rs59062514	0.87[ASN][1000 genomes]
rs59352002	0.82[ASN][1000 genomes]
rs734073	0.92[ASN][1000 genomes]
rs734074	0.90[ASN][1000 genomes]
rs741756	0.88[ASN][1000 genomes]
rs7520184	0.98[ASN][1000 genomes]
rs7543234	0.90[ASN][1000 genomes]
rs7549276	0.99[ASN][1000 genomes]
rs7554780	0.99[ASN][1000 genomes]
rs762488	0.86[ASN][1000 genomes]
rs8177968	0.93[ASN][1000 genomes]
rs8847	0.95[ASN][1000 genomes]
rs932972	0.95[ASN][1000 genomes]
rs9628662	0.86[ASN][1000 genomes]
rs9729564	0.95[ASN][1000 genomes]

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	nsv532579	chr1:154548165-155262692	Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	575 gene(s)	inside rSNPs	diseases
2	nsv831614	chr1:155094978-155275031	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	434 gene(s)	inside rSNPs	diseases
3	esv2757756	chr1:155094978-155314807	Bivalent Enhancer Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	452 gene(s)	inside rSNPs	diseases
4	esv2758971	chr1:155094978-155314807	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	452 gene(s)	inside rSNPs	diseases
5	nsv872457	chr1:155135335-155310443	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	407 gene(s)	inside rSNPs	diseases
6	nsv831625	chr1:155145634-155313409	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer 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 miRNA target site	407 gene(s)	inside rSNPs	diseases
7	nsv529709	chr1:155154933-155757219	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	450 gene(s)	inside rSNPs	diseases
8	esv1832331	chr1:155213136-155271366	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
9	esv1826485	chr1:155214478-155264270	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
10	esv1824971	chr1:155215985-155260869	Genic enhancers Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
11	nsv831636	chr1:155219223-155444864	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer 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	67 gene(s)	inside rSNPs	diseases
12	esv33869	chr1:155223283-155917961	Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers 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 miRNA target site	187 gene(s)	inside rSNPs	diseases
13	esv1832799	chr1:155226846-155261543	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
14	esv17013	chr1:155227059-155262674	Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
15	esv1797617	chr1:155228592-155264270	Genic enhancers Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
16	esv1829849	chr1:155228592-155264270	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
17	esv1832093	chr1:155230444-155253599	Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	29 gene(s)	inside rSNPs	diseases
18	esv1826500	chr1:155230444-155261567	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
19	esv1831471	chr1:155230444-155261567	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
20	esv1826924	chr1:155230444-155271566	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription 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	31 gene(s)	inside rSNPs	diseases
21	esv1830821	chr1:155230610-155265661	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
22	esv1831955	chr1:155230610-155265661	Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
23	esv1826761	chr1:155230622-155262613	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
24	esv1826280	chr1:155230622-155262851	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
25	esv1832100	chr1:155230622-155269896	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
26	esv1830793	chr1:155230644-155261367	Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
27	esv1827811	chr1:155230644-155271366	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
28	esv1827924	chr1:155230644-155271366	Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
29	esv1826306	chr1:155232074-155261777	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
30	esv1832706	chr1:155232647-155261567	Active TSS Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
31	esv1831149	chr1:155233501-155252122	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	27 gene(s)	inside rSNPs	diseases
32	esv1829673	chr1:155235493-155261280	Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
33	esv1831963	chr1:155239116-155267459	Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
34	esv1830532	chr1:155239128-155267471	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs11577338	THBS3	cis	Whole Blood	GTEx
rs11577338	GBA	cis	Esophagus Mucosa	GTEx
rs11577338	FDPS	Cis_1M	lymphoblastoid	RTeQTL
rs11577338	GBAP1	cis	Artery Tibial	GTEx
rs11577338	RIT1	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155232000-155242400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:155232200-155242200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:155232400-155241000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:155232400-155241600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:155232600-155240600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:155232600-155240600	Strong transcription	Primary T killer memory cells from peripheral blood	blood
7	chr1:155232600-155240800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:155232600-155240800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr1:155232600-155240800	Strong transcription	Gastric	stomach
10	chr1:155232600-155241000	Strong transcription	HMEC	breast
11	chr1:155232600-155241200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:155232600-155241400	Strong transcription	H1 Cell Line	embryonic stem cell
13	chr1:155232600-155241400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:155232600-155241400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr1:155232600-155241600	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr1:155232600-155241600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr1:155232600-155241600	Strong transcription	Fetal Thymus	thymus
18	chr1:155232600-155241600	Strong transcription	Osteobl	bone
19	chr1:155232600-155241800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
20	chr1:155232600-155241800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr1:155232600-155241800	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr1:155232600-155241800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:155232600-155241800	Strong transcription	Fetal Muscle Trunk	muscle
24	chr1:155232600-155242000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:155232600-155242000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr1:155232600-155242200	Weak transcription	Right Atrium	heart
27	chr1:155232800-155240400	Strong transcription	GM12878-XiMat	blood
28	chr1:155232800-155240600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:155232800-155240600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr1:155232800-155240600	Strong transcription	Primary T helper cells fromperipheralblood	blood
31	chr1:155232800-155240600	Strong transcription	Brain Germinal Matrix	brain
32	chr1:155232800-155240800	Strong transcription	Primary T helper cells PMA-I stimulated	--
33	chr1:155232800-155240800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:155232800-155240800	Strong transcription	Fetal Intestine Large	intestine
35	chr1:155232800-155240800	Strong transcription	Thymus	Thymus
36	chr1:155232800-155240800	Strong transcription	HepG2	liver
37	chr1:155232800-155241000	Strong transcription	Primary neutrophils fromperipheralblood	blood
38	chr1:155232800-155241000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:155232800-155241000	Strong transcription	Adipose Nuclei	Adipose
40	chr1:155232800-155241000	Strong transcription	Liver	Liver
41	chr1:155232800-155241000	Strong transcription	Fetal Brain Female	brain
42	chr1:155232800-155241000	Strong transcription	Fetal Intestine Small	intestine
43	chr1:155232800-155241000	Strong transcription	Placenta Amnion	Placenta Amnion
44	chr1:155232800-155241000	Strong transcription	NH-A	brain
45	chr1:155232800-155241200	Strong transcription	Fetal Muscle Leg	muscle
46	chr1:155232800-155241200	Strong transcription	NHLF	lung
47	chr1:155232800-155241400	Strong transcription	HUES64 Cell Line	embryonic stem cell
48	chr1:155232800-155241400	Strong transcription	Primary B cells from peripheral blood	blood
49	chr1:155232800-155241400	Strong transcription	Muscle Satellite Cultured Cells	--
50	chr1:155232800-155241400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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