Variant report

Variant	rs7536078
Chromosome Location	chr1:45196754-45196755
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:123)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:123 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:45196086..45196947-chr14:35590878..35591536,2	Hela-S3	cervix:
2	chr1:11967939..11971240-chr1:45194928..45197844,3	K562	blood:
3	chr1:45194515..45198714-chr1:45239955..45244261,13	MCF-7	breast:
4	chr1:45196336..45197048-chr5:176873576..176874340,2	HCT-116	colon:
5	chr1:45190324..45200952-chr1:45272085..45288310,59	MCF-7	breast:
6	chr1:45196394..45197121-chr4:109541480..109542286,2	HCT-116	colon:
7	chr1:45195497..45197976-chr1:46711781..46715025,4	K562	blood:
8	chr1:45196394..45197102-chr4:75023670..75024212,2	Hela-S3	cervix:
9	chr1:45196245..45197123-chr14:54955160..54955765,2	Hela-S3	cervix:
10	chr1:45195509..45198075-chr1:45804039..45807111,4	K562	blood:
11	chr1:45096334..45100885-chr1:45195106..45197628,6	K562	blood:
12	chr1:45187216..45187887-chr1:45195575..45196869,4	MCF-7	breast:
13	chr1:45194189..45198394-chr1:45270401..45277394,13	MCF-7	breast:
14	chr1:45196234..45197183-chr22:24951059..24951922,2	Hela-S3	cervix:
15	chr1:45193444..45198675-chr1:45475617..45480324,16	K562	blood:
16	chr1:45196265..45197015-chr12:72233488..72234280,2	Hela-S3	cervix:
17	chr1:45196249..45197212-chr13:111365516..111366107,2	Hela-S3	cervix:
18	chr1:26559951..26560700-chr1:45196570..45197191,2	Hela-S3	cervix:
19	chr1:45196704..45197222-chr6:31587778..31588630,2	Hela-S3	cervix:
20	chr1:45196303..45197166-chr1:59249336..59250143,2	Hela-S3	cervix:
21	chr1:28974970..28975684-chr1:45196463..45197173,2	HCT-116	colon:
22	chr1:45194988..45198272-chr1:45451491..45453905,3	K562	blood:
23	chr1:45196566..45197074-chr20:33464347..33464934,2	Hela-S3	cervix:
24	chr1:45194867..45196903-chr17:61522851..61524901,2	MCF-7	breast:
25	chr1:45195378..45196913-chr9:74979048..74981622,2	MCF-7	breast:
26	chr1:45196597..45197146-chr2:114513869..114514378,2	HCT-116	colon:
27	chr1:45194156..45199355-chr1:45264282..45268731,9	MCF-7	breast:
28	chr1:45196376..45197118-chrX:48815283..48816112,2	Hela-S3	cervix:
29	chr1:45196596..45197248-chrX:41193334..41193911,2	Hela-S3	cervix:
30	chr1:45196227..45197100-chr6:27860619..27861139,2	Hela-S3	cervix:
31	chr1:45195514..45197967-chr1:78468300..78470449,2	K562	blood:
32	chr1:45196191..45197074-chr17:62503488..62504453,2	Hela-S3	cervix:
33	chr1:45196384..45196925-chr9:136214388..136215199,2	Hela-S3	cervix:
34	chr1:935135..936219-chr1:45196260..45197083,3	Hela-S3	cervix:
35	chr1:45138378..45140523-chr1:45195153..45198091,3	MCF-7	breast:
36	chr1:45194369..45197773-chr1:46046767..46051199,5	K562	blood:
37	chr1:45196548..45197139-chr8:101162507..101163204,2	HCT-116	colon:
38	chr1:45193443..45200768-chr1:45280884..45289784,25	MCF-7	breast:
39	chr1:45195832..45196931-chr1:45805652..45806681,3	Hela-S3	cervix:
40	chr1:45195127..45198642-chr1:45986086..45989017,4	K562	blood:
41	chr1:45196398..45197093-chr10:70847289..70848231,2	NB4	blood:
42	chr1:45194597..45197062-chr16:30076613..30078245,2	K562	blood:
43	chr1:45193557..45198509-chr1:45202622..45207012,16	MCF-7	breast:
44	chr1:45194277..45197109-chr1:45476180..45479040,2	MCF-7	breast:
45	chr1:45196376..45197160-chr9:131418990..131419490,2	Hela-S3	cervix:
46	chr1:45196372..45196898-chr4:75230821..75231749,2	HCT-116	colon:
47	chr1:45196201..45196883-chr10:75173083..75173956,2	Hela-S3	cervix:
48	chr1:45196596..45197171-chr19:5622259..5623063,2	NB4	blood:
49	chr1:45196210..45197177-chr10:121410367..121411032,2	HCT-116	colon:
50	chr1:45195989..45196763-chr6:71276185..71277126,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
ENSG00000126107	Chromatin interaction
ENSG00000264294	Chromatin interaction
ENSG00000134717	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000205913	Chromatin interaction
ENSG00000202031	Chromatin interaction
ENSG00000156508	Chromatin interaction
ENSG00000198668	Chromatin interaction
ENSG00000128917	Chromatin interaction
ENSG00000173451	Chromatin interaction
ENSG00000199568	Chromatin interaction
ENSG00000109475	Chromatin interaction
ENSG00000167186	Chromatin interaction
ENSG00000269559	Chromatin interaction
ENSG00000131188	Chromatin interaction
ENSG00000168209	Chromatin interaction
ENSG00000117425	Chromatin interaction
ENSG00000138867	Chromatin interaction
ENSG00000117862	Chromatin interaction
ENSG00000147669	Chromatin interaction
ENSG00000162298	Chromatin interaction
ENSG00000130695	Chromatin interaction
ENSG00000086300	Chromatin interaction
ENSG00000117448	Chromatin interaction
ENSG00000181924	Chromatin interaction
ENSG00000126088	Chromatin interaction
ENSG00000202444	Chromatin interaction
ENSG00000108654	Chromatin interaction
ENSG00000199347	Chromatin interaction
ENSG00000132780	Chromatin interaction
ENSG00000198520	Chromatin interaction
ENSG00000222009	Chromatin interaction
ENSG00000162415	Chromatin interaction
ENSG00000120159	Chromatin interaction
ENSG00000100028	Chromatin interaction
ENSG00000122862	Chromatin interaction
ENSG00000154079	Chromatin interaction
ENSG00000130254	Chromatin interaction
ENSG00000257718	Chromatin interaction
ENSG00000121274	Chromatin interaction
ENSG00000188290	Chromatin interaction
ENSG00000261821	Chromatin interaction
ENSG00000134905	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000160633	Chromatin interaction
ENSG00000132128	Chromatin interaction
ENSG00000126106	Chromatin interaction
ENSG00000120656	Chromatin interaction
ENSG00000197045	Chromatin interaction
ENSG00000188396	Chromatin interaction
ENSG00000136826	Chromatin interaction
ENSG00000143183	Chromatin interaction
ENSG00000270103	Chromatin interaction
ENSG00000201801	Chromatin interaction
ENSG00000151929	Chromatin interaction
ENSG00000173846	Chromatin interaction
ENSG00000177606	Chromatin interaction
ENSG00000159596	Chromatin interaction
ENSG00000159592	Chromatin interaction
ENSG00000124882	Chromatin interaction
ENSG00000138279	Chromatin interaction
ENSG00000085999	Chromatin interaction
ENSG00000115084	Chromatin interaction
ENSG00000107372	Chromatin interaction
ENSG00000132781	Chromatin interaction
ENSG00000117411	Chromatin interaction
ENSG00000132002	Chromatin interaction
ENSG00000112343	Chromatin interaction
ENSG00000186594	Chromatin interaction
ENSG00000273338	Chromatin interaction
ENSG00000225721	Chromatin interaction
ENSG00000008283	Chromatin interaction
ENSG00000173660	Chromatin interaction
ENSG00000215301	Chromatin interaction
ENSG00000143179	Chromatin interaction
ENSG00000100227	Chromatin interaction
ENSG00000149925	Chromatin interaction
ENSG00000164237	Chromatin interaction
ENSG00000153487	Chromatin interaction
ENSG00000229815	Chromatin interaction
ENSG00000133858	Chromatin interaction
ENSG00000068308	Chromatin interaction
ENSG00000211575	Chromatin interaction
ENSG00000065000	Chromatin interaction
ENSG00000261465	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000175575	Chromatin interaction
ENSG00000119333	Chromatin interaction
ENSG00000092020	Chromatin interaction
ENSG00000088888	Chromatin interaction
ENSG00000140459	Chromatin interaction
ENSG00000131069	Chromatin interaction
ENSG00000140943	Chromatin interaction
ENSG00000139117	Chromatin interaction
ENSG00000270022	Chromatin interaction
ENSG00000181904	Chromatin interaction
ENSG00000148297	Chromatin interaction
ENSG00000163738	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000117450	Chromatin interaction
ENSG00000070785	Chromatin interaction
ENSG00000142937	Chromatin interaction
ENSG00000106261	Chromatin interaction
ENSG00000229388	Chromatin interaction
ENSG00000121578	Chromatin interaction
ENSG00000207501	Chromatin interaction
ENSG00000072310	Chromatin interaction
ENSG00000167978	Chromatin interaction
ENSG00000100890	Chromatin interaction
ENSG00000166441	Chromatin interaction
ENSG00000142945	Chromatin interaction
ENSG00000132773	Chromatin interaction
ENSG00000121749	Chromatin interaction
ENSG00000187147	Chromatin interaction
ENSG00000104885	Chromatin interaction
ENSG00000148303	Chromatin interaction
ENSG00000197429	Chromatin interaction
ENSG00000229117	Chromatin interaction
ENSG00000234492	Chromatin interaction
ENSG00000200913	Chromatin interaction
ENSG00000207421	Chromatin interaction
ENSG00000170421	Chromatin interaction
ENSG00000135480	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs11211025	0.84[EUR][1000 genomes]
rs11211026	0.84[EUR][1000 genomes]
rs11211036	0.95[CHB][hapmap];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11211038	0.94[CHB][hapmap];0.81[EUR][1000 genomes]
rs11211040	0.94[CHB][hapmap]
rs11211053	0.84[CHB][hapmap]
rs1140279	0.94[CHB][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11573562	0.90[CHB][hapmap]
rs11578233	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11580010	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11580159	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11582718	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11584440	0.94[CHB][hapmap];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11800505	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11801990	1.00[CHB][hapmap];0.85[JPT][hapmap];0.98[ASN][1000 genomes]
rs11803622	1.00[CHB][hapmap];0.89[JPT][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11806832	0.80[ASN][1000 genomes]
rs11809931	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12139143	0.89[CHB][hapmap]
rs12566610	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12732939	1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12733586	0.95[CHB][hapmap]
rs12733796	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12735728	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12741443	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12746270	1.00[CHB][hapmap];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12746898	0.82[EUR][1000 genomes]
rs16832227	1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16832263	0.90[CHB][hapmap]
rs17881698	0.94[CHB][hapmap];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17883049	0.94[CHB][hapmap];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17886118	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2295997	0.94[CHB][hapmap]
rs34541568	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34639510	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35343809	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35932693	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3795713	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3795714	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3795719	0.95[CHB][hapmap]
rs3820586	1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4342887	1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57995027	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59366549	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59788723	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6429550	0.95[CHB][hapmap]
rs6670449	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6676749	0.94[CHB][hapmap];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6689911	1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6692487	0.94[CHB][hapmap]
rs6695350	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6697153	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6702415	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6703452	0.89[CHB][hapmap]
rs6704436	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67742332	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7517439	0.94[CHB][hapmap]
rs7517639	0.94[CHB][hapmap]
rs7534487	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7539538	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7546285	0.93[CHB][hapmap];0.85[JPT][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533037	chr1:44361728-45333408	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
2	nsv1004861	chr1:44843654-45210176	Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	346 gene(s)	inside rSNPs	diseases
3	nsv534940	chr1:44843654-45210176	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	346 gene(s)	inside rSNPs	diseases
4	nsv998476	chr1:45001278-45311757	Flanking Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases
5	nsv534941	chr1:45001278-45311757	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases
6	nsv1014894	chr1:45139123-45397943	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	414 gene(s)	inside rSNPs	diseases
7	nsv529677	chr1:45179509-45748571	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS 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 lncRNA miRNA target site	424 gene(s)	inside rSNPs	diseases
8	nsv1002026	chr1:45187594-45758048	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	386 gene(s)	inside rSNPs	diseases
9	nsv998871	chr1:45196587-45251179	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	171 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs7536078	UROD	cis	Artery Tibial	GTEx
rs7536078	UROD	cis	lung	GTEx
rs7536078	UROD	cis	Thyroid	GTEx

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45189800-45205000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:45192800-45196800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr1:45192800-45197200	Weak transcription	HSMM	muscle
4	chr1:45192800-45197600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:45192800-45198200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:45192800-45198800	Weak transcription	HMEC	breast
7	chr1:45193200-45197600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr1:45193400-45196800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:45193400-45200400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr1:45194800-45196800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr1:45194800-45197600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr1:45195000-45196800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr1:45195000-45196800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr1:45195200-45196800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:45195800-45196800	Active TSS	Hela-S3	cervix
16	chr1:45195800-45197000	Enhancers	H1 Cell Line	embryonic stem cell
17	chr1:45195800-45197200	Enhancers	Placenta	Placenta
18	chr1:45196000-45196800	Enhancers	HepG2	liver
19	chr1:45196000-45197000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
20	chr1:45196000-45197000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr1:45196000-45197200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
22	chr1:45196000-45197200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
23	chr1:45196000-45197200	Weak transcription	NHEK	skin
24	chr1:45196000-45197600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
25	chr1:45196200-45196800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr1:45196200-45196800	Flanking Active TSS	Brain Anterior Caudate	brain
27	chr1:45196200-45197000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr1:45196200-45197000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:45196200-45197000	Flanking Active TSS	Primary T cells from cord blood	blood
30	chr1:45196200-45197000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr1:45196200-45197000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
32	chr1:45196200-45197000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:45196200-45197000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:45196200-45197000	Active TSS	Brain Angular Gyrus	brain
35	chr1:45196200-45197000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
36	chr1:45196200-45197000	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr1:45196200-45197000	Flanking Active TSS	Fetal Thymus	thymus
38	chr1:45196200-45197000	Active TSS	Placenta Amnion	Placenta Amnion
39	chr1:45196200-45197000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
40	chr1:45196200-45197200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:45196200-45197200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
42	chr1:45196200-45197200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
43	chr1:45196200-45197200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:45196200-45197200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr1:45196200-45197200	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr1:45196200-45197200	Active TSS	Fetal Kidney	kidney
47	chr1:45196200-45197200	Enhancers	NHLF	lung
48	chr1:45196200-45197800	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr1:45196200-45199800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:45196400-45196800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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