Variant report

Variant	rs4072037
Chromosome Location	chr1:155162067-155162068
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:155161721-155162735	H1-neurons	neurons:	n/a	n/a
2	POLR2A	chr1:155161817-155168780	MCF10A-Er-Src	breast:	n/a	n/a
3	POLR2A	chr1:155161754-155168618	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:155096309..155104200-chr1:155157595..155166389,23	MCF-7	breast:
2	chr1:155161998..155167332-chr1:155208163..155212538,6	K562	blood:
3	chr1:155160177..155166575-chr1:155191666..155199927,14	MCF-7	breast:
4	chr1:155092552..155095095-chr1:155160179..155163739,4	MCF-7	breast:
5	chr1:155161998..155164147-chr1:155209813..155212664,2	K562	blood:
6	chr1:154944711..154947532-chr1:155161851..155164798,3	MCF-7	breast:
7	chr1:155106609..155109409-chr1:155161242..155164268,3	MCF-7	breast:
8	chr1:154943189..154945318-chr1:155161226..155163403,2	K562	blood:
9	chr1:154974390..154976020-chr1:155161759..155163515,2	MCF-7	breast:
10	chr1:155161598..155164529-chr1:155278690..155280381,2	MCF-7	breast:
11	chr1:155161236..155164985-chr1:155290580..155295192,7	K562	blood:
12	chr1:155105295..155110704-chr1:155161873..155165835,7	K562	blood:
13	chr1:155160293..155162117-chr1:155291803..155294447,2	K562	blood:
14	chr1:155160377..155162781-chr1:155242739..155244795,2	MCF-7	breast:
15	chr1:155098824..155101489-chr1:155162030..155163615,2	K562	blood:
16	chr1:155160390..155165295-chr1:155194589..155199400,14	K562	blood:
17	chr1:155106165..155110704-chr1:155161873..155165835,8	K562	blood:
18	chr1:155161177..155163523-chr1:155219674..155222613,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KRTCAP2-2	chr1:155161654-155162101	NONHSAT006696

No data

Variant related genes	Relation type
MIR92B	TF binding region
ENSG00000231064	TF binding region
ENSG00000273088	TF binding region
MUC1	TF binding region
ENSG00000173207	Chromatin interaction
ENSG00000225855	Chromatin interaction
ENSG00000160767	Chromatin interaction
ENSG00000169242	Chromatin interaction
ENSG00000176444	Chromatin interaction
ENSG00000160685	Chromatin interaction
ENSG00000160752	Chromatin interaction
ENSG00000160753	Chromatin interaction
ENSG00000202027	Chromatin interaction
ENSG00000160766	Chromatin interaction
ENSG00000160691	Chromatin interaction
ENSG00000169241	Chromatin interaction
ENSG00000177628	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 21 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10157801	0.92[CHB][hapmap];0.96[CHD][hapmap]
rs10908458	0.92[CHB][hapmap]
rs11264337	0.84[ASW][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.91[JPT][hapmap];0.83[YRI][hapmap]
rs11264338	0.84[ASW][hapmap];0.92[CHB][hapmap];0.96[CHD][hapmap];0.91[JPT][hapmap];0.83[YRI][hapmap]
rs11264339	0.84[ASW][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs12025371	0.92[CHB][hapmap]
rs12028043	0.92[CHB][hapmap];1.00[CHD][hapmap]
rs12411216	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12904	0.92[CHB][hapmap];0.96[CHD][hapmap]
rs2049805	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2066981	0.92[ASW][hapmap];0.92[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.90[JPT][hapmap];0.87[LWK][hapmap];0.95[MEX][hapmap];0.98[MKK][hapmap];0.98[TSI][hapmap];0.85[YRI][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2075570	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2075571	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs28445596	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2974929	0.83[EUR][1000 genomes]
rs2974930	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2974931	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2974935	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2974937	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2990220	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2990245	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs370545	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3814316	0.82[CHD][hapmap];0.91[JPT][hapmap]
rs4246529	0.92[CHB][hapmap];0.96[CHD][hapmap]
rs4276913	0.92[CHB][hapmap];0.93[CHD][hapmap]
rs4421576	0.84[ASW][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs4460629	0.92[ASW][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap]
rs4745	0.92[CHB][hapmap];0.96[CHD][hapmap]
rs4971052	0.81[CHB][hapmap]
rs4971059	0.84[CHD][hapmap];0.91[JPT][hapmap]
rs4971066	0.81[CHD][hapmap]
rs4971073	0.87[CHD][hapmap]
rs4971076	0.85[CHB][hapmap]
rs4971079	0.84[ASW][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.80[YRI][hapmap]
rs4971085	0.92[CHB][hapmap];0.91[JPT][hapmap];0.83[YRI][hapmap]
rs4971088	0.92[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs4971100	0.86[CHB][hapmap];0.82[CHD][hapmap];0.91[JPT][hapmap]
rs497829	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7364524	0.85[CHB][hapmap]
rs7556304	0.84[ASW][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.91[JPT][hapmap];0.83[YRI][hapmap]
rs760077	0.86[ASN][1000 genomes]
rs914615	0.92[ASW][hapmap];0.96[CEU][hapmap];0.92[CHB][hapmap];0.82[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];0.95[MEX][hapmap];0.96[MKK][hapmap];0.98[TSI][hapmap];0.93[YRI][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9297	0.92[CHB][hapmap];0.96[CHD][hapmap]
rs9426886	0.86[CHB][hapmap];0.90[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:24 , 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	esv1823746	chr1:154965207-155231904	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS 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	469 gene(s)	inside rSNPs	diseases
3	nsv464084	chr1:155082298-155194980	Weak transcription Bivalent Enhancer Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	366 gene(s)	inside rSNPs	diseases
4	nsv547961	chr1:155082298-155194980	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	366 gene(s)	inside rSNPs	diseases
5	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
6	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
7	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
8	nsv470741	chr1:155115260-155230131	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	381 gene(s)	inside rSNPs	diseases
9	nsv1010146	chr1:155119096-155201064	ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers 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 miRNA target site	368 gene(s)	inside rSNPs	diseases
10	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
11	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
12	nsv872458	chr1:155146102-155180466	Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	316 gene(s)	inside rSNPs	diseases
13	nsv872459	chr1:155149718-155169633	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	308 gene(s)	inside rSNPs	diseases
14	nsv527682	chr1:155149718-155197462	Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	361 gene(s)	inside rSNPs	diseases
15	nsv872460	chr1:155151493-155163181	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
16	nsv872461	chr1:155151493-155169633	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	308 gene(s)	inside rSNPs	diseases
17	nsv872462	chr1:155151493-155172177	Strong transcription Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	308 gene(s)	inside rSNPs	diseases
18	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
19	nsv872463	chr1:155155731-155169633	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	308 gene(s)	inside rSNPs	diseases
20	nsv872464	chr1:155157853-155163181	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
21	nsv872465	chr1:155157853-155169633	Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	308 gene(s)	inside rSNPs	diseases
22	esv3338339	chr1:155159128-155163626	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	63 gene(s)	inside rSNPs	diseases
23	esv3381155	chr1:155160128-155162626	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
24	esv3331596	chr1:155160553-155162301	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

Variant related diseases (count:2)

Disease	PMID	Source
Esophageal cancer and gastric cancer	20729852	GWAS catalog
Magnesium levels	20700443	GWAS catalog

mRNA abundance (count:19)

SNP	Gene	Cis/trans	Tissue	Source
rs4072037	GBAP1	cis	Artery Aorta	GTEx
rs4072037	GBA	cis	Esophagus Mucosa	GTEx
rs4072037	GBAP1	cis	Artery Tibial	GTEx
rs4072037	IVL	cis	parietal	SCAN
rs4072037	GNAI2	trans	lymphoblastoid	RTeQTL
rs4072037	THBS3	cis	Whole Blood	GTEx
rs4072037	RP11-263K19.4	cis	Whole Blood	GTEx
rs4072037	GBAP1	cis	Adipose Subcutaneous	GTEx
rs4072037	GBAP1	cis	Esophagus Muscularis	GTEx
rs4072037	LASS2	cis	parietal	SCAN
rs4072037	YY1AP1	cis	cerebellum	SCAN
rs4072037	SPRR4	cis	parietal	SCAN
rs4072037	GBA///GBAP	Cis_1M	lymphoblastoid	RTeQTL
rs4072037	GBAP1	cis	lung	GTEx
rs4072037	THEM5	cis	parietal	SCAN
rs4072037	GBAP1	cis	parietal	SCAN
rs4072037	GBAP1	cis	Esophagus Mucosa	GTEx
rs4072037	GBAP1	cis	Heart Left Ventricle	GTEx
rs4072037	GBAP1	cis	Thyroid	GTEx

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155146600-155163000	Weak transcription	Aorta	Aorta
2	chr1:155149600-155162600	Weak transcription	Small Intestine	intestine
3	chr1:155149600-155162800	Weak transcription	NHDF-Ad	bronchial
4	chr1:155149800-155162200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr1:155150000-155163000	Weak transcription	Fetal Brain Male	brain
6	chr1:155150200-155162400	Weak transcription	Dnd41	blood
7	chr1:155152200-155162800	Weak transcription	Osteobl	bone
8	chr1:155152400-155163000	Weak transcription	HUVEC	blood vessel
9	chr1:155152600-155162200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr1:155152600-155162400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:155152600-155162800	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr1:155152600-155163000	Weak transcription	Brain Substantia Nigra	brain
13	chr1:155152800-155162200	Weak transcription	Fetal Thymus	thymus
14	chr1:155152800-155162400	Weak transcription	Brain Anterior Caudate	brain
15	chr1:155152800-155163000	Weak transcription	NH-A	brain
16	chr1:155153000-155162400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr1:155154800-155162200	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr1:155155000-155162200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:155155000-155162200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:155155000-155162800	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr1:155155400-155162200	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr1:155155400-155162400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr1:155156600-155162800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:155156600-155163000	Weak transcription	Brain Cingulate Gyrus	brain
25	chr1:155156800-155163000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr1:155157000-155163000	Weak transcription	Brain Angular Gyrus	brain
27	chr1:155157600-155162200	Weak transcription	Primary T cells from cord blood	blood
28	chr1:155157800-155162200	Weak transcription	Fetal Brain Female	brain
29	chr1:155157800-155162400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr1:155157800-155163000	Weak transcription	Brain Hippocampus Middle	brain
31	chr1:155158000-155162400	Weak transcription	Right Atrium	heart
32	chr1:155158200-155162200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr1:155158200-155162400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr1:155158200-155162800	Weak transcription	HSMM	muscle
35	chr1:155158400-155162400	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr1:155158400-155162400	Weak transcription	HSMMtube	muscle
37	chr1:155158400-155162800	Weak transcription	Brain Germinal Matrix	brain
38	chr1:155158400-155162800	Weak transcription	Left Ventricle	heart
39	chr1:155158400-155162800	Weak transcription	Psoas Muscle	Psoas
40	chr1:155158600-155162200	Weak transcription	Primary B cells from cord blood	blood
41	chr1:155158800-155162200	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr1:155158800-155162200	Weak transcription	Right Ventricle	heart
43	chr1:155158800-155162200	Weak transcription	Spleen	Spleen
44	chr1:155158800-155162200	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr1:155158800-155162400	Weak transcription	GM12878-XiMat	blood
46	chr1:155158800-155162800	Weak transcription	Fetal Heart	heart
47	chr1:155159000-155162400	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr1:155159000-155162800	Weak transcription	HMEC	breast
49	chr1:155159200-155162200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr1:155159200-155162400	Weak transcription	Primary B cells from peripheral blood	blood

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