Variant report

Variant	rs28490152
Chromosome Location	chr7:100020982-100020983
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	MXI1	chr7:100020711-100021311	GM12878	blood:	n/a	n/a
2	RUNX3	chr7:100020932-100021254	GM12878	blood:	n/a	n/a
3	SPI1	chr7:100020915-100021319	GM12891	blood:	n/a	chr7:100021007-100021020
4	RUNX3	chr7:100020896-100021285	GM12878	blood:	n/a	n/a
5	NFE2	chr7:100020966-100021063	GM12878	blood:	n/a	n/a
6	SPI1	chr7:100020844-100021321	GM12878	blood:	n/a	chr7:100021007-100021020
7	SPI1	chr7:100020909-100021328	GM12891	blood:	n/a	chr7:100021007-100021020

No.	Distal block	Cell Line	Cell type
1	chr7:100018468..100021635-chr7:100028917..100032766,4	K562	blood:
2	chr7:100019883..100022700-chr7:100024204..100025806,2	MCF-7	breast:
3	chr7:100020674..100022332-chr7:100031493..100033981,2	MCF-7	breast:
4	chr7:99990597..99992604-chr7:100020661..100023007,2	MCF-7	breast:

Variant related genes	Relation type
ZCWPW1	TF binding region
ENSG00000160813	Chromatin interaction
ENSG00000240211	Chromatin interaction
ENSG00000241357	Chromatin interaction

Extended variants
information (count: 107 )
Associated
traits (count: 56 )

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs1000215	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10085549	0.86[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.96[MKK][hapmap];1.00[YRI][hapmap];0.84[ASN][1000 genomes]
rs10241492	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs1063945	0.84[ASN][1000 genomes]
rs1073	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11559117	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.95[TSI][hapmap]
rs11760536	1.00[CEU][hapmap];1.00[CHD][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap]
rs11761253	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11761306	0.84[ASN][1000 genomes]
rs11761426	0.85[CEU][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11761725	1.00[CEU][hapmap];1.00[CHD][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11761784	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11763414	1.00[CEU][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11763511	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs11764818	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11765869	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11766752	1.00[CEU][hapmap];1.00[CHD][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.95[TSI][hapmap];0.96[YRI][hapmap];0.81[EUR][1000 genomes]
rs11768933	0.84[ASN][1000 genomes]
rs11768967	0.84[ASN][1000 genomes]
rs11769057	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11769700	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs11769886	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11771241	1.00[CEU][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11771419	1.00[CEU][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11771799	0.84[ASN][1000 genomes]
rs11771936	0.84[ASN][1000 genomes]
rs11773661	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs1636980	0.84[ASN][1000 genomes]
rs1962269	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs1964242	0.84[ASN][1000 genomes]
rs2003507	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2108269	0.84[ASN][1000 genomes]
rs2406253	1.00[CEU][hapmap];1.00[CHD][hapmap];0.80[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.95[TSI][hapmap]
rs2406255	1.00[CEU][hapmap];1.00[CHD][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28495773	0.84[ASN][1000 genomes]
rs28578163	0.80[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28629346	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs28660238	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28680963	0.84[ASN][1000 genomes]
rs3087502	0.84[ASN][1000 genomes]
rs34989573	0.93[CEU][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap]
rs35111986	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35986051	0.84[ASN][1000 genomes]
rs3900792	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4074838	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41280971	0.84[ASN][1000 genomes]
rs4472444	1.00[CEU][hapmap];1.00[CHD][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.81[EUR][1000 genomes]
rs4989959	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60257855	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61735533	0.84[ASN][1000 genomes]
rs66632384	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66958101	0.81[EUR][1000 genomes]
rs67163493	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67196635	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67239991	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs67315960	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67471932	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67483801	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs68116612	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6945952	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs6946768	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs6948685	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs6953749	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6955362	1.00[CEU][hapmap];0.83[CHD][hapmap];1.00[TSI][hapmap];0.82[EUR][1000 genomes]
rs6955367	0.86[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];0.94[MKK][hapmap];1.00[YRI][hapmap];0.84[ASN][1000 genomes]
rs6957928	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6962151	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6965207	0.84[ASN][1000 genomes]
rs6965458	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs6970806	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6970828	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6975514	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs6975563	0.84[ASN][1000 genomes]
rs6975660	0.84[ASN][1000 genomes]
rs6975729	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6979910	0.85[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[ASN][1000 genomes]
rs705866	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs73161759	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73161762	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73401443	0.84[ASN][1000 genomes]
rs73401450	0.84[ASN][1000 genomes]
rs73401451	0.84[ASN][1000 genomes]
rs73403312	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7341507	0.85[CEU][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7783159	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7783550	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7786844	0.84[ASN][1000 genomes]
rs7787620	0.92[CEU][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap]
rs7792525	0.85[CEU][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7792959	0.85[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7794485	1.00[CEU][hapmap];1.00[CHD][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes]
rs7795656	0.84[ASN][1000 genomes]
rs7795805	0.84[ASN][1000 genomes]
rs7799894	0.84[ASN][1000 genomes]
rs7799932	0.84[ASN][1000 genomes]
rs7800667	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7803454	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7809801	1.00[CEU][hapmap];1.00[CHD][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.81[EUR][1000 genomes]
rs7811142	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350965	chr7:99747460-100146105	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
2	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
3	nsv831071	chr7:99918025-100113413	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers 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	287 gene(s)	inside rSNPs	diseases
4	nsv527107	chr7:100014711-100064719	Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	269 gene(s)	inside rSNPs	diseases
5	nsv888776	chr7:100014711-100198386	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	297 gene(s)	inside rSNPs	diseases
6	nsv888777	chr7:100014711-100221867	Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
7	nsv888778	chr7:100014711-100236593	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	310 gene(s)	inside rSNPs	diseases
8	nsv888779	chr7:100014711-100313420	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	321 gene(s)	inside rSNPs	diseases

mRNA abundance (count:56)

SNP	Gene	Cis/trans	Tissue	Source
rs28490152	PILRA	cis	Esophagus Mucosa	GTEx
rs28490152	PILRA	cis	Nerve Tibial	GTEx
rs28490152	STAG3L5P	cis	lung	GTEx
rs28490152	ZCWPW1	cis	cerebellum	SCAN
rs28490152	PVRIG2P	cis	Nerve Tibial	GTEx
rs28490152	GNB2	cis	parietal	SCAN
rs28490152	STAG3L5P	cis	Artery Aorta	GTEx
rs28490152	PILRB	cis	lung	GTEx
rs28490152	PILRA	cis	Thyroid	GTEx
rs28490152	PILRB	cis	Adipose Subcutaneous	GTEx
rs28490152	PILRB	cis	lymphoblastoid	seeQTL
rs28490152	PVRIG2P	cis	Thyroid	GTEx
rs28490152	STAG3L5P	cis	Nerve Tibial	GTEx
rs28490152	STAG3L5P	cis	Esophagus Mucosa	GTEx
rs28490152	PILRA	cis	Esophagus Muscularis	GTEx
rs28490152	PILRA	cis	Artery Tibial	GTEx
rs28490152	PILRB	cis	Artery Aorta	GTEx
rs28490152	MEPCE	cis	lymphoblastoid	seeQTL
rs28490152	PILRB	cis	Skin Sun Exposed Lower leg	GTEx
rs28490152	ZCWPW1	cis	Nerve Tibial	GTEx
rs28490152	STAG3L5P	cis	Skin Sun Exposed Lower leg	GTEx
rs28490152	PILRA	cis	Muscle Skeletal	GTEx
rs28490152	CNPY4	cis	cerebellum	SCAN
rs28490152	STAG3L5P	cis	Muscle Skeletal	GTEx
rs28490152	STAG3L5P	cis	Esophagus Muscularis	GTEx
rs28490152	GATS	cis	parietal	SCAN
rs28490152	PVRIG2P	cis	Artery Tibial	GTEx
rs28490152	ZCWPW1	cis	parietal	SCAN
rs28490152	STAG3L5P	cis	Heart Left Ventricle	GTEx
rs28490152	PVRIG2P	cis	lung	GTEx
rs28490152	PILRB	cis	Whole Blood	GTEx
rs28490152	STAG3L5P	cis	Adipose Subcutaneous	GTEx
rs28490152	PILRA	cis	Artery Aorta	GTEx
rs28490152	STAG3L5P	cis	Artery Tibial	GTEx
rs28490152	PILRA	cis	Skin Sun Exposed Lower leg	GTEx
rs28490152	PVRIG2P	cis	Esophagus Mucosa	GTEx
rs28490152	PILRA	cis	Heart Left Ventricle	GTEx
rs28490152	PILRB	cis	Esophagus Mucosa	GTEx
rs28490152	PILRB	cis	Esophagus Muscularis	GTEx
rs28490152	PILRB	cis	Artery Tibial	GTEx
rs28490152	PILRB	cis	Nerve Tibial	GTEx
rs28490152	PILRB	Cis_1M	lymphoblastoid	RTeQTL
rs28490152	STAG3L5P	cis	Thyroid	GTEx
rs28490152	PILRB	cis	Heart Left Ventricle	GTEx
rs28490152	PILRA	cis	parietal	SCAN
rs28490152	PILRB	cis	Muscle Skeletal	GTEx
rs28490152	PVRIG2P	cis	Adipose Subcutaneous	GTEx
rs28490152	STAG3	Cis_1M	lymphoblastoid	RTeQTL
rs28490152	PVRIG	Cis_1M	lymphoblastoid	RTeQTL
rs28490152	PILRB	cis	cerebellum	SCAN
rs28490152	PILRA	cis	Adipose Subcutaneous	GTEx
rs28490152	PVRIG	cis	cerebellum	SCAN
rs28490152	PILRB	cis	parietal	SCAN
rs28490152	PILRB	cis	multi-tissue	Pritchard
rs28490152	PILRA	cis	cerebellum	SCAN
rs28490152	PILRB	cis	Thyroid	GTEx

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99987800-100025400	Weak transcription	Right Ventricle	heart
2	chr7:99995000-100025400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr7:99995000-100026000	Weak transcription	Primary T cells from cord blood	blood
4	chr7:99996200-100025400	Weak transcription	Brain Substantia Nigra	brain
5	chr7:99997400-100025600	Weak transcription	Aorta	Aorta
6	chr7:99998800-100025400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr7:99999000-100025400	Weak transcription	Left Ventricle	heart
8	chr7:99999400-100025400	Weak transcription	Psoas Muscle	Psoas
9	chr7:100000200-100025400	Weak transcription	Liver	Liver
10	chr7:100002800-100025400	Weak transcription	Brain Anterior Caudate	brain
11	chr7:100005400-100024800	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr7:100011000-100021200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr7:100011600-100026000	Weak transcription	Primary hematopoietic stem cells	blood
14	chr7:100011800-100025400	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr7:100011800-100025400	Weak transcription	Primary B cells from cord blood	blood
16	chr7:100011800-100025400	Weak transcription	Primary B cells from peripheral blood	blood
17	chr7:100011800-100025400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:100013000-100022000	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr7:100015000-100025400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr7:100015000-100025400	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr7:100017000-100025400	Weak transcription	Brain Angular Gyrus	brain
22	chr7:100017400-100025400	Weak transcription	Brain Hippocampus Middle	brain
23	chr7:100017600-100025600	Weak transcription	Duodenum Mucosa	Duodenum
24	chr7:100017800-100025200	Weak transcription	Osteobl	bone
25	chr7:100017800-100025400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr7:100017800-100025400	Weak transcription	Adipose Nuclei	Adipose
27	chr7:100017800-100025600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr7:100018000-100025400	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr7:100018200-100025400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:100019000-100025400	Weak transcription	Fetal Brain Male	brain
31	chr7:100019200-100025400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:100019600-100025400	Weak transcription	HSMMtube	muscle
33	chr7:100019800-100021000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:100019800-100021400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr7:100020400-100025600	Weak transcription	Fetal Lung	lung
36	chr7:100020600-100021200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr7:100020600-100022000	Strong transcription	Duodenum Smooth Muscle	Duodenum
38	chr7:100020600-100025400	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr7:100020600-100025400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr7:100020800-100021200	Flanking Active TSS	GM12878-XiMat	blood

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