Variant report

Variant	rs6955367
Chromosome Location	chr7:99961194-99961195
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	chr7:99960991-99961403	K562	blood:	n/a	n/a
2	POLR2A	chr7:99961110-99961451	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr7:99960930-99961556	K562	blood:	n/a	n/a
4	PML	chr7:99960386-99961549	K562	blood:	n/a	n/a
5	POLR2A	chr7:99961083-99967399	PFSK-1	brain:	n/a	n/a
6	POLR2A	chr7:99959279-99970406	K562	blood:	n/a	n/a
7	POLR2A	chr7:99961127-99961793	HepG2	liver:	n/a	n/a
8	POLR2A	chr7:99961138-99961452	A549	lung:	n/a	n/a
9	POLR2A	chr7:99961163-99961202	K562	blood:	n/a	n/a
10	POLR2A	chr7:99960959-99961376	HepG2	liver:	n/a	n/a
11	POLR2A	chr7:99961021-99967328	PANC-1	pancreas:	n/a	n/a
12	POLR2A	chr7:99960978-99961574	GM12892	blood:	n/a	n/a
13	POLR2A	chr7:99961086-99961419	GM12891	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:99961125..99963572-chr7:99991510..99993149,2	K562	blood:

Variant related genes	Relation type
PILRA	TF binding region

Extended variants
information (count: 97 )
Associated
traits (count: 68 )

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs1000215	0.86[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.94[MKK][hapmap];1.00[YRI][hapmap];0.84[ASN][1000 genomes]
rs10085549	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10241492	0.85[CEU][hapmap];1.00[JPT][hapmap]
rs1059129	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1063945	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1073	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11559117	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[MKK][hapmap]
rs11760536	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11761253	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11761306	1.00[ASN][1000 genomes]
rs11761426	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11761725	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11761784	0.86[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.81[LWK][hapmap];0.94[MKK][hapmap];1.00[YRI][hapmap]
rs11763414	0.85[CEU][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11763511	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11765869	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11766752	0.85[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];0.96[MKK][hapmap];0.96[YRI][hapmap]
rs11766917	0.83[ASN][1000 genomes]
rs11768933	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11768967	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11769057	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11769700	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11769886	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11771241	0.85[CEU][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11771419	0.84[CEU][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11771799	1.00[ASN][1000 genomes]
rs11771936	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11773661	0.85[CEU][hapmap]
rs1636980	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1962269	0.91[CEU][hapmap]
rs1964242	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2003507	0.84[ASN][1000 genomes]
rs2108269	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2406253	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.93[MKK][hapmap]
rs2406255	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs28401739	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28490152	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]
rs28495773	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28578163	0.93[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap]
rs28660238	0.84[ASN][1000 genomes]
rs28680963	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3087502	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34989573	1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap]
rs35111986	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs35986051	1.00[ASN][1000 genomes]
rs3900792	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs3991498	0.84[EUR][1000 genomes]
rs3991564	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4074838	0.83[CHD][hapmap];1.00[GIH][hapmap]
rs41280971	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4472444	0.93[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];0.96[MKK][hapmap];0.96[YRI][hapmap]
rs61735533	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66632384	0.84[ASN][1000 genomes]
rs67163493	0.84[ASN][1000 genomes]
rs67315960	0.84[ASN][1000 genomes]
rs67471932	0.84[ASN][1000 genomes]
rs68116612	0.84[ASN][1000 genomes]
rs6945952	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6946768	1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6948685	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6953749	0.84[ASN][1000 genomes]
rs6955362	0.85[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap]
rs6957928	0.84[ASN][1000 genomes]
rs6965207	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6965458	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6970806	0.84[ASN][1000 genomes]
rs6975514	0.85[CEU][hapmap]
rs6975563	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6975660	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6975729	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs6979910	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs705866	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73161745	0.85[ASN][1000 genomes]
rs73161759	0.84[ASN][1000 genomes]
rs73161762	0.84[ASN][1000 genomes]
rs73401443	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73401450	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73401451	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7341507	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7783159	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7783550	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7786844	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7787620	0.92[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.80[MKK][hapmap]
rs7792525	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7792959	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7794485	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs7795656	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7795805	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799894	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799901	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7799932	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7803454	0.84[ASN][1000 genomes]
rs7809801	0.85[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[LWK][hapmap];0.96[MKK][hapmap];0.96[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 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	nsv888775	chr7:99940307-99961194	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:68)

SNP	Gene	Cis/trans	Tissue	Source
rs6955367	PILRB	cis	lung	GTEx
rs6955367	PVRIG2P	cis	lung	GTEx
rs6955367	PILRA	cis	Heart Left Ventricle	GTEx
rs6955367	PILRB	cis	brain	seeQTL
rs6955367	PVRIG2P	cis	Artery Tibial	GTEx
rs6955367	STAG3	cis	lymphoblastoid	seeQTL
rs6955367	PILRA	cis	Nerve Tibial	GTEx
rs6955367	PILRB	cis	Thyroid	GTEx
rs6955367	PMS2	trans	multi-tissue	Pritchard
rs6955367	STAG3L5P	cis	Artery Aorta	GTEx
rs6955367	STAG3L5P	cis	Nerve Tibial	GTEx
rs6955367	ZCWPW1	cis	cerebellum	SCAN
rs6955367	STAG3L5P	cis	Esophagus Mucosa	GTEx
rs6955367	PILRB	cis	Esophagus Mucosa	GTEx
rs6955367	PILRA	cis	Thyroid	GTEx
rs6955367	PVRIG2P	cis	Nerve Tibial	GTEx
rs6955367	PILRB	cis	parietal	SCAN
rs6955367	STAG3L5P	cis	Adipose Subcutaneous	GTEx
rs6955367	PILRA	cis	Skin Sun Exposed Lower leg	GTEx
rs6955367	PILRB	cis	cerebellum	SCAN
rs6955367	GATS	cis	multi-tissue	Pritchard
rs6955367	PILRA	cis	Muscle Skeletal	GTEx
rs6955367	GNB2	cis	parietal	SCAN
rs6955367	PILRA	cis	Stomach	GTEx
rs6955367	PVRIG	cis	multi-tissue	Pritchard
rs6955367	PILRB	cis	Artery Aorta	GTEx
rs6955367	PVRIG2P	cis	Esophagus Mucosa	GTEx
rs6955367	STAG3L5P	cis	Artery Tibial	GTEx
rs6955367	PVRIG	cis	cerebellum	SCAN
rs6955367	PILRA	cis	cerebellum	SCAN
rs6955367	PILRB	cis	Nerve Tibial	GTEx
rs6955367	PVRIG	Cis_1M	lymphoblastoid	RTeQTL
rs6955367	MEPCE	trans	brain	seeQTL
rs6955367	ORAI2	cis	cerebellum	SCAN
rs6955367	STAG3L5P	cis	Stomach	GTEx
rs6955367	PILRB	Cis_1M	lymphoblastoid	RTeQTL
rs6955367	STAG3L5P	cis	lung	GTEx
rs6955367	PILRA	cis	Adipose Subcutaneous	GTEx
rs6955367	CNPY4	cis	cerebellum	SCAN
rs6955367	PVRIG2P	cis	Adipose Subcutaneous	GTEx
rs6955367	PILRB	cis	Artery Tibial	GTEx
rs6955367	PILRB	cis	Muscle Skeletal	GTEx
rs6955367	STAG3L5P	cis	Thyroid	GTEx
rs6955367	PILRB	cis	lymphoblastoid	seeQTL
rs6955367	PVRIG2P	cis	Heart Left Ventricle	GTEx
rs6955367	PILRB	cis	Skin Sun Exposed Lower leg	GTEx
rs6955367	PILRA	cis	multi-tissue	Pritchard
rs6955367	STAG3L5P	cis	Skin Sun Exposed Lower leg	GTEx
rs6955367	ZCWPW1	cis	parietal	SCAN
rs6955367	PILRB	cis	Esophagus Muscularis	GTEx
rs6955367	STAG3L5P	cis	Esophagus Muscularis	GTEx
rs6955367	STAG3L5P	cis	Heart Left Ventricle	GTEx
rs6955367	GATS	cis	parietal	SCAN
rs6955367	PVRIG2P	cis	Thyroid	GTEx
rs6955367	STAG3L5P	cis	Muscle Skeletal	GTEx
rs6955367	MEPCE	cis	brain	seeQTL
rs6955367	PILRB	cis	multi-tissue	Pritchard
rs6955367	PILRB	trans	brain	seeQTL
rs6955367	PILRA	cis	Esophagus Mucosa	GTEx
rs6955367	PILRB	cis	Adipose Subcutaneous	GTEx
rs6955367	PILRA	cis	Artery Tibial	GTEx
rs6955367	TRIM4	cis	multi-tissue	Pritchard
rs6955367	PILRA	cis	parietal	SCAN
rs6955367	PILRB	cis	Heart Left Ventricle	GTEx
rs6955367	PILRA	cis	Esophagus Muscularis	GTEx
rs6955367	PILRB	cis	Whole Blood	GTEx
rs6955367	PILRA	cis	Artery Aorta	GTEx
rs6955367	PVRIG	cis	lymphoblastoid	seeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99934000-99977600	Weak transcription	Fetal Brain Male	brain
2	chr7:99934400-99963400	Weak transcription	Psoas Muscle	Psoas
3	chr7:99934800-99963800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:99935400-99962200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:99935400-99962400	Strong transcription	HUES48 Cell Line	embryonic stem cell
6	chr7:99937600-99967800	Strong transcription	Fetal Stomach	stomach
7	chr7:99938600-99967400	Strong transcription	Fetal Brain Female	brain
8	chr7:99938800-99962400	Strong transcription	Dnd41	blood
9	chr7:99940800-100014600	Weak transcription	Right Atrium	heart
10	chr7:99942800-99963600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr7:99942800-99966400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:99942800-99966400	Strong transcription	A549	lung
13	chr7:99942800-99967000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:99942800-99967400	Strong transcription	Fetal Intestine Small	intestine
15	chr7:99943200-99962000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
16	chr7:99943200-99962600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr7:99943200-99965400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:99943400-99961400	Strong transcription	Liver	Liver
19	chr7:99943400-99961600	Strong transcription	HepG2	liver
20	chr7:99943400-99962400	Strong transcription	H1 Cell Line	embryonic stem cell
21	chr7:99943400-99963200	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr7:99943400-99963200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr7:99943400-99966800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:99943400-99967200	Strong transcription	Fetal Intestine Large	intestine
25	chr7:99943600-99962200	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr7:99943600-99962400	Strong transcription	Brain Hippocampus Middle	brain
27	chr7:99943600-99962400	Strong transcription	Duodenum Mucosa	Duodenum
28	chr7:99943600-99962400	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr7:99943800-99962400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr7:99943800-99962600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr7:99943800-99963200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr7:99943800-99963800	Strong transcription	Placenta	Placenta
33	chr7:99944000-99961400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr7:99944000-99961600	Strong transcription	Stomach Smooth Muscle	stomach
35	chr7:99944000-99962400	Strong transcription	Placenta Amnion	Placenta Amnion
36	chr7:99944000-99967000	Strong transcription	Brain Anterior Caudate	brain
37	chr7:99944200-99961400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:99944200-99961600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr7:99944200-99967400	Strong transcription	Brain Germinal Matrix	brain
40	chr7:99945400-99961400	Strong transcription	Skeletal Muscle Female	skeletal muscle
41	chr7:99945400-99969400	Weak transcription	Fetal Heart	heart
42	chr7:99945600-99966000	Strong transcription	Fetal Muscle Leg	muscle
43	chr7:99946000-99961400	Strong transcription	Skeletal Muscle Male	skeletal muscle
44	chr7:99946000-99966800	Strong transcription	Fetal Muscle Trunk	muscle
45	chr7:99946400-99967400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr7:99949400-99961200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr7:99950000-99961200	Strong transcription	NHEK	skin
48	chr7:99950400-99962400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr7:99950400-99962600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:99950800-99961400	Strong transcription	Brain Substantia Nigra	brain

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