Variant report

Variant	rs2302055
Chromosome Location	chr19:18684563-18684564
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:18683323-18684665	GM12892	blood:	n/a	n/a
2	POLR2A	chr19:18681493-18689919	HepG2	liver:	n/a	n/a
3	POLR2A	chr19:18681679-18684916	K562	blood:	n/a	n/a
4	POLR2A	chr19:18683961-18684731	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr19:18684544-18684676	HUVEC	blood vessel:	n/a	n/a
6	CTCF	chr19:18684314-18684593	T-47D	breast:	n/a	n/a
7	POLR2A	chr19:18684558-18684563	MCF-7	breast:	n/a	n/a
8	POLR2A	chr19:18681665-18684916	PFSK-1	brain:	n/a	n/a
9	POLR2A	chr19:18682044-18684587	H1-hESC	embryonic stem cell:	n/a	n/a
10	POLR2A	chr19:18682123-18684768	GM12878	blood:	n/a	n/a
11	POLR2A	chr19:18682114-18684802	K562	blood:	n/a	n/a
12	POLR2A	chr19:18683406-18684688	HL-60	blood:	n/a	n/a
13	GATA3	chr19:18684395-18684582	T-47D	breast:	n/a	n/a
14	POLR2A	chr19:18681589-18684803	SK-N-MC	brain:	n/a	n/a
15	POLR2A	chr19:18684394-18684566	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr19:18684236-18684711	K562	blood:	n/a	n/a
17	POLR2A	chr19:18682004-18684809	GM12892	blood:	n/a	n/a
18	POLR2A	chr19:18682063-18684808	GM12878	blood:	n/a	n/a
19	EP300	chr19:18683914-18684650	T-47D	breast:	n/a	n/a
20	POLR2A	chr19:18684369-18684583	H1-hESC	embryonic stem cell:	n/a	n/a
21	SP1	chr19:18683922-18684600	H1-hESC	embryonic stem cell:	n/a	chr19:18684457-18684471

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18684528-18684578	RPTEC	kidney:	n/a
2	chr19:18684528-18684578	HEK293	kidney:	embryo
3	chr19:18684528-18684578	HL-60	blood:	n/a
4	chr19:18684528-18684578	U87	brain:	n/a
5	chr19:18684528-18684578	HIPEpiC	eye:	n/a
6	chr19:18684528-18684578	AG10803	skin:	n/a
7	chr19:18684528-18684578	GM12891	blood:	n/a
8	chr19:18684528-18684578	PFSK-1	brain:	n/a
9	chr19:18684528-18684578	HCPEpiC	choroid plexus:	n/a
10	chr19:18684528-18684578	SKMC	muscle:	n/a
11	chr19:18684528-18684578	GM12892	blood:	n/a
12	chr19:18684528-18684578	Hepatocyte	liver:	n/a
13	chr19:18684528-18684578	GM19239	blood:	n/a
14	chr19:18684528-18684578	HRPEpiC	eye:	n/a
15	chr19:18684528-18684578	AG09309	skin:	n/a
16	chr19:18684528-18684578	NHBE	bronchial:	n/a
17	chr19:18684528-18684578	IMR90	lung:	fetal
18	chr19:18684528-18684578	HEEpiC	esophagus:	n/a
19	chr19:18684528-18684578	GM06990	blood:	n/a
20	chr19:18684528-18684578	SK-N-SH_RA	brain:	n/a
21	chr19:18684528-18684578	HCM	heart:	n/a
22	chr19:18684528-18684578	AG04450	lung:	fetal
23	chr19:18684528-18684578	NB4	blood:	n/a
24	chr19:18684528-18684578	HCF	heart:	n/a
25	chr19:18684528-18684578	AoSMC	blood vessel:	n/a
26	chr19:18684528-18684578	HRE	kidney:	n/a
27	chr19:18684528-18684578	BJ	skin:	n/a
28	chr19:18684528-18684578	A549	lung:	n/a
29	chr19:18684528-18684578	NHDF-neo	bronchial:	n/a
30	chr19:18684528-18684578	HRCEpiC	kidney:	n/a
31	chr19:18684528-18684578	ECC-1	luminal epithelium:	n/a
32	chr19:18684528-18684578	NT2-D1	testis:	n/a
33	chr19:18684528-18684578	T-47D	breast:	n/a
34	chr19:18684528-18684578	LNCaP	prostate:	n/a
35	chr19:18684528-18684578	Hela-S3	cervix:	n/a
36	chr19:18684528-18684578	Jurkat	blood:	n/a
37	chr19:18684528-18684578	ProgFib	skin:	n/a
38	chr19:18684528-18684578	SK-N-SH	brain:	n/a
39	chr19:18684528-18684578	Caco-2	colon:	n/a
40	chr19:18684528-18684578	SK-N-MC	brain:	n/a
41	chr19:18684528-18684578	HPAEpiC	pulmonary alveolar:	n/a
42	chr19:18684528-18684578	MCF10A-Er-Src	breast:	n/a
43	chr19:18684528-18684578	GM12878	blood:	n/a
44	chr19:18684528-18684578	HUVEC	blood vessel:	n/a
45	chr19:18684528-18684578	SAEC	small airway:	n/a
46	chr19:18684528-18684578	PANC-1	pancreas:	n/a
47	chr19:18684528-18684578	PrEC	prostate:	n/a
48	chr19:18684528-18684578	H1-hESC	embryonic stem cell:	embryo
49	chr19:18684528-18684578	MCF-7	breast:	n/a
50	chr19:18684528-18684578	HMEC	breast:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18629832..18635572-chr19:18680910..18686315,11	K562	blood:
2	chr19:18682401..18684687-chr19:18702171..18705609,4	MCF-7	breast:
3	chr19:18666965..18674770-chr19:18676405..18685095,25	K562	blood:
4	chr19:18528984..18533499-chr19:18684426..18687340,4	MCF-7	breast:
5	chr19:18678376..18688390-chr19:18697032..18707656,34	K562	blood:
6	chr19:18585110..18587475-chr19:18684025..18685972,2	MCF-7	breast:
7	chr19:18629832..18634516-chr19:18680910..18685097,11	K562	blood:
8	chr19:18681312..18685117-chr19:18698049..18701447,5	MCF-7	breast:
9	chr19:18651038..18656783-chr19:18680897..18685521,14	K562	blood:

No data

Variant related genes	Relation type
ENSG00000268983	TF binding region
ENSG00000268983	CpG island
ENSG00000130511	Chromatin interaction
ENSG00000105656	Chromatin interaction
ENSG00000105701	Chromatin interaction
ENSG00000268030	Chromatin interaction
ENSG00000105700	Chromatin interaction
ENSG00000006015	Chromatin interaction
ENSG00000006016	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10402321	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10409392	0.86[CHB][hapmap];0.81[CHD][hapmap];0.82[GIH][hapmap];0.82[EUR][1000 genomes]
rs10414427	0.84[EUR][1000 genomes]
rs10425018	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1043192	0.81[JPT][hapmap]
rs11086114	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11086116	0.81[ASN][1000 genomes]
rs11667551	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11672297	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12150991	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12608925	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12609505	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.98[TSI][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1468475	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.98[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1862645	0.81[JPT][hapmap]
rs2057649	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.98[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2058077	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2079015	0.92[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];0.93[GIH][hapmap];0.90[JPT][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2079016	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2238650	0.81[JPT][hapmap]
rs2283616	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2314664	1.00[CHB][hapmap];0.89[CHD][hapmap];0.93[GIH][hapmap];0.90[JPT][hapmap];0.84[TSI][hapmap];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2314665	0.92[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.93[GIH][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2314666	1.00[CHB][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];0.84[JPT][hapmap];0.84[TSI][hapmap];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2314667	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28451415	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28711754	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3170474	0.85[JPT][hapmap]
rs35867875	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35875334	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs36050418	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3761032	0.81[JPT][hapmap]
rs3761034	0.96[CEU][hapmap];0.95[CHB][hapmap];0.94[CHD][hapmap];0.98[GIH][hapmap];0.89[JPT][hapmap];0.91[MEX][hapmap];0.98[TSI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3761036	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3803917	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4629093	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4808137	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4808821	0.91[ASN][1000 genomes]
rs4808839	0.81[JPT][hapmap]
rs55724121	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55888366	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58782998	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59798925	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62137086	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6554	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs709679	0.81[JPT][hapmap]
rs7247557	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7250192	0.81[JPT][hapmap]
rs7250623	0.90[JPT][hapmap]
rs7253088	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7254004	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7256319	0.85[JPT][hapmap]
rs7258480	0.87[ASN][1000 genomes]
rs7648	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8109364	0.82[CEU][hapmap];0.95[CHB][hapmap];0.94[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap]
rs916791	0.81[JPT][hapmap]

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	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
2	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats 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	92 gene(s)	inside rSNPs	diseases
3	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
4	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
5	nsv911281	chr19:18613917-18758255	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
6	nsv911282	chr19:18624964-18928480	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
7	nsv911283	chr19:18626732-18689830	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	nsv833776	chr19:18638028-18782264	Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
9	nsv911286	chr19:18652844-18811112	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription 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 miRNA target site	50 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2302055	UBA52	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18682600-18684600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
2	chr19:18683000-18684600	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
3	chr19:18683600-18684600	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr19:18683600-18684600	Transcr. at gene 5' and 3'	HUES48 Cell Line	embryonic stem cell
5	chr19:18683600-18684600	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
6	chr19:18683600-18684600	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:18683600-18684600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr19:18683600-18684600	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
9	chr19:18683600-18684600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr19:18683600-18684600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr19:18683600-18684600	Enhancers	Right Atrium	heart
12	chr19:18683600-18684600	Transcr. at gene 5' and 3'	A549	lung
13	chr19:18683600-18684600	Transcr. at gene 5' and 3'	Dnd41	blood
14	chr19:18683600-18684600	Transcr. at gene 5' and 3'	HSMM	muscle
15	chr19:18683600-18684600	Transcr. at gene 5' and 3'	K562	blood
16	chr19:18683600-18684600	Transcr. at gene 5' and 3'	NHEK	skin
17	chr19:18683600-18684600	Transcr. at gene 5' and 3'	NHLF	lung
18	chr19:18683600-18684800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr19:18683800-18684600	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr19:18683800-18684600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr19:18683800-18684600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr19:18683800-18684600	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
23	chr19:18683800-18684600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr19:18683800-18684600	Genic enhancers	Placenta	Placenta
25	chr19:18683800-18684600	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
26	chr19:18683800-18684600	Transcr. at gene 5' and 3'	HSMMtube	muscle
27	chr19:18683800-18684600	Transcr. at gene 5' and 3'	Osteobl	bone
28	chr19:18683800-18684800	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
29	chr19:18683800-18684800	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
30	chr19:18683800-18684800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr19:18683800-18687800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr19:18684000-18684600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr19:18684000-18684600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr19:18684000-18684600	Genic enhancers	Primary B cells from peripheral blood	blood
35	chr19:18684000-18684600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
36	chr19:18684000-18684600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr19:18684000-18684600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr19:18684000-18684600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr19:18684000-18684600	Genic enhancers	Brain Cingulate Gyrus	brain
40	chr19:18684000-18684600	Genic enhancers	Fetal Muscle Leg	muscle
41	chr19:18684000-18684600	Genic enhancers	Pancreas	Pancrea
42	chr19:18684000-18684600	Genic enhancers	Placenta Amnion	Placenta Amnion
43	chr19:18684000-18684600	Genic enhancers	Right Ventricle	heart
44	chr19:18684000-18684600	Genic enhancers	Sigmoid Colon	Sigmoid Colon
45	chr19:18684000-18684600	Genic enhancers	Spleen	Spleen
46	chr19:18684000-18684800	Genic enhancers	Primary T cells fromperipheralblood	blood
47	chr19:18684000-18684800	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr19:18684200-18684600	Genic enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr19:18684200-18684600	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr19:18684200-18684600	Genic enhancers	Primary B cells from cord blood	blood

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